Indian Patents
Title of Invention

METHOD AND DEVICE FOR PROTECTING TOBACCO
Abstract Abstract A method for protecting tobacco trom during, comprises the step or the tobacco with a material preferably a net, which has a protective activity against the harmful organ¬isms.
Full Text AS ORIGINALLY FILED
Method and Device for Protecting Tobacco
The invention relates to a method of protecting tobacco tbacco bales or other tobacco products Iron harmful organisms during harvesting, drying, curing, transport and storage. The invention further relates to a device for carrying out the method.
Tobacco is a valuable cash crop, and is the most widely grown non-food crop in the world.
After harvesting, the tobacco leaves are subjected to the stages of curing, fermenting and aging as part of the process of producing tobaccos suitable for smoking or chewing by hu¬mans. All of these stages require extended storage periods, in the last case up to several years. During these storage periods, the tobacco leaves have to be protected from pests, specifically from insect pests
Nevertheless, contamination of the tobacco with pesticides has to be avoided to create no additional health hazards for the human consumers.
Currently, a common method of pest control in the storage of tobacco is the use of gaseous pesticides, specifically methyl bromide and phosphin (PH3). However, the use of methyl bromide is not desirable from an ecological point of view as this substance is ozone deplet¬ing. Phosphine, on the other hand, is highly toxic and - if not properly handled - is a poten¬tial health hazard for the workers engaged in the production of tobacco.
Accordingly, there is a continuous demand to provide new methods for protecting tobacco leaves from harmful organisms, while avoiding pesticide residues in the tobacco and health
hazards for the workers.
It has now been found that this demand can be met by providing a method for protecting tobacco from harmful organisms during storage comprising the step of covering the to¬bacco with a material which has a protective activity against the harmful organisms.
WO 2005/064072 discloses a composition for the impregnation of fibers, fabrics and net¬tings imparting a protective activity against pests, however, the use of such a composition for protecting tobacco is not contemplated.

According to the invention, tobacco can be protected from harmful organisms in an easy and efficient way without health hazard to workers and without causing residues of pesti¬cides in the tobacco products.
In a further aspect ot ttie invention there is provided the use of a material which has a pro¬tective activity against harmful organisms for protecting tobacco.
In yet a further aspect of the invention there is provided a device for protecting tobacco from harmful organisms comprising a device for storing the tobacco and a material which has a protective activity against harmful organisms, for covering the tobacco.
The term "tobacco" as used herein means tobacco plants or parts thereof in any stage after and during harvesting, specifically in the stages of curing, fermentation and aging.
The terms "protection" or "protecting" as used herein means a controlling or repelling ac¬tion.
The term "harmful organism" as used herein means pests, specifically arthropod pests, including insects and arachnids, and harmful micro-organisms, specifically fungi including spores, microbes and viruses.
The term "covering" as used herein means that the fabric or netting forms a physical barrier between the tobacco to be protected and the harmful organism, but does not imply that the tobacco is in physical contact with the cover materiat.
The material is preferably a non-rigid material. It is preferably a textile material or plastics material selected from the group consisting of yarn, fibers, fabric, knitgoods, nonwovens, netting material, foils, tarpaulins and coatings. The netting material may be prepared by any method known in the art, for example by circular knitting or warp knitting, or by sewing parts of a netting to obtain the desired nettings.
The textile material or plastics material may be made form a variety of natural and synthetic fibers, also as textile blends in woven or non-woven form, as knit goods, yarns or fibers. Natural fibers are for example cotton, wool, silk or bast fibers, like jute, linen, ramie, hemp and kenaf. Synthetic fibers are for example polyamides, polyesters, polyacryl nitriles, Doly-

olefines, for example polypropylene or polyethylene, Teflon, and mixtures of fibers, for ex¬ample mixtures of synthetic and natural fibers. Polyamides, potyolefins and polyesters are preferred. Polyethylene terephthalate is especially preferred.
The term material also includes non-textile substrates such as coatings, leathers, synthetic adaptions of leather, flocked fabrics, sheetings, foils, perforated foils and packaging male-rial.
Further, the term material includes cellulose-containing materials e.g. cotton materials such as garment or cotton nets and also wooden materials such a& bouses, trees, board fences, or sleepers and also paper.
Preferably, the material is a textile material or plastics material, e.g. polypropylene, poly¬ethylene, polyester or polyamide.
Preferably the textile material is a netting.
Suitable mesh sizes are well known to those skilled In the art and may be chosen in view of the size of the prevailing pests. While the mesh size should be small enough to present an obstacle to the pest it is usually preferred to have an exchange of air and humidity.
Suitable mesh sizes are in the range of 5 x 5 mm, preferably 2.5 x 2.5 mm, more preferred 1.5 X 1.5 mm as an upper limit and 0.1 x 0.1 mm, preferably 0.25 x 0.25 mm, more pre¬ferred 0.5 X 0,5 mm, in particular 0.75 x 0.75 mm as a lower limit. In the case of very small pests a wide-meshed woven fabric may be preferred as a textile material.
More preferred are nettings made from polyester, especially polyethylene terephthalate. In a further preferred embodiment the material is a cellulose containing material.
Preferably, the material is treated with a composition comprising a pesticide, however, the invention is not limited to such embodiments. E.g., the pesticide can also be incorporated into a fiber during the production of the fiber.
Such materials show good results in controlling the pests and provide long lasting protec¬tion to the stored tobacco.

In a preferred embodiment, the pesticide is incorporated into the material (e.g. into the plastics matrix) or applied to the surface of the material or both.
In a most preferred embodiment, the material is treated with a composition comprising;
a) at least one pesticide (component A), and
b) at (east one polymeric binder (component B).
The pesticidal composition comprises in general 0.001 to 95 % by weight preferably 0.1 to 45 % by weight, more preferably 0.5 to 30 % by weight, most preferably 0.5 to 25 % by weight, based on the weight of the composition, of at least one pesticide.
The pesticidal composition preferably comprises the following components, based on the solids content of the composition
a) 0.1 to 45 % by weight, preferably 0.5 to 30% by weight, more preferably 1 to 25 % by weight of at least one pesticide (component A), and
b) 55 to 99 % by weight, preferably 70 to 98 % by weight, more preferably 75 to 90 by weight of at least one polymeric binder (component B),
wherein the sum of the components is 100 % by weight of solids content of the insecticide composition.
In a further preferred embodiment the pesticidal composition comprises the following com¬ponents, based on the solids content of the composition,
a) 20 to 70 % by weight, preferably 25 to 65 % by weight, more preferably 30 to 65 % by
weight of at least one pesticide (component A), and
b) 30 to 80 % by weight, preferably 35 to 75 % by weight, more preferably 35 to 70 by
weight of at least one polymeric binder (component B),
wherein the sum of the components is 100 % by weight of solids content of the pesticidal
composition.
The term "pesticide" as used herein comprises insecticides, repellents and fungicides.
The term "insecticides" as used herein comprises agents with arthropodicidal (specifically, insecticidal, acaricidal and miticidal), molluscicidal and rodenticidal activity, if not otherwise stated in the context.

The term 'lungicides" as used herein comprises agents with fungicidal, microbicidal and viricidai activity, if not otherwise stated in the context.
Preferably, the pesticide is an insecticide or repellent.
The pesticidal composition is particularly suitable for application to polyester nettings as used for mosquito nets.
The pesticidal composition of the present invention may be applied to textile materials or plastics material, before their formation into the desired products, i.e. while still a yarn or in sheet torm, or after formation of the desired products.
Pesticide (component A)
Preferably, the pesticide is an insecticide and/or repellent with a fast paralyzing or l Preferred insecticides and/or repellents are mentioned below:
pyrethroid compounds such as
Etofenprox: 2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzyl ether,
Chlorfenapyr: 4-bromo-2-(4-chlorophenyl)-1-ethoxymethy(-5-(trifIuoromethyI)pyrrole-3-
carbonitrile,
Fenvalerate: (RS)-alpha-cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3 methylbutyrate,
Esfenvalerate: (S)-alpha-cyano-3-phenoxybenzyl (S)-2-{4-chlorophenyl)-3-methylbuty-rate,
Fenpropathrin; (RS)-alpha-cyano-3-phenoxybenzyl 2,2,3,3-tetramethylcyclopropane-
carboxylate,
Cypermethrin: (RS)-alpha-cyano-3-phenoxyben2yl (IRS)-cis, trans-3-(2,2-dichlorovinyl)-
2,2-dimethylcyclopropanecarboxylate,
alpha-Cypermethhn: racemate comprising the (S)-a-(1R) and (R)-a-{lS) diastereomers,
Permethrin: 3-phenoxybenzyl (IRS)-cis, trans-3-(2,2-dichlorovinyl)-2,2-
dimethylcyclopropanecarboxylate,

Cyhalothrin: {RS)-alpha-cyano-3-phenoxybenzyl (Z)-{1RS}-cis-3-{2-chloro-3,3,3-
trifluoroprop-1 -eny[)-2,2-dimethylcyclopro panecarboxylate, lambda-cyhalothrin,
Deltamethrin: (S)-alpha-cyano-3-phenoxybenzyl (lR)-cis-3-(2,2-dibromovinyl)-2,2-
dimethylcyclopropanecarboxylate,
Cycloprothrin: (RS}-alpha-cyano-3-phenoxyb6nzyl (RS)-2,2-dichloro-1-(4-
ethoxyphenyl)cyclopropanecarboxylate,
Fluvalinate: alpha-cyano>3-phenoxybenzyl N-(2-chloro-alpha, alpha, alpha, alpha-trifluoro-p-tolyl)-D-valinate,
Bifenthrin: (2-methylblphenyl-3-ylnnethyl)0(Z)-{1RS)-cis-3-(2-chloro-3,3,3-trifluoro-1-
propenyl)-2,2-dimethylcyclopropanecarboxylate,
2-methyl-2-(4-bromodifluoromethoxyphenyl) propyl (3-phenoxybenzyl)ether, Tralomethrin: (S)-alpha-cyano-3-phenoxybenzyl {1 R-cis)3((1 'RS)(1', 2', 2', 2'-tetrabromoethyl))-2,2-dimethylcyclopropanecarboxylate, Silafluofen: 4-ethoxyphenyl(3-{4-fluoro-3-phenoxyphenyl)propyl}dimethylsilanc, D-tenothrin: 3-phenoxybenzyl {1R)-cis, trans)-chrysanthemate,
Cyphenothrin: CRS)-alpha-cyano-3-phenoxyb6nzyl {1 R-cis, trans)-chrysanthemate, D-
resmethrin: 5-benzyl-3-furylmethyl (1 R-cis, trans)-chrysanthemate,
Acrinathrin: {S)-alpha-cyano-3-phenoxybenzyl (1R-cis(Z))-(2,2-dimethyl-3-(oxo-3-
(1,1,1,3,3,3-hexafluoropropyloxy)propenyl{cyclopropanecarboxylate,
Cyfluthrin: (RS)-alpha-cyano-4-(luoro-3-phenoxybenzyl 3-(2,2-dichlorovinyl)-2.2-
dimethylcyclopropanecarboxylate,
Tefluthrin: 2,3,5,6-tetrafluoro-4-methylbenzyl (IRS-cis {Z))-3-(2-chloro-3,3,3-trifluoro-prop-1-enyl)-2,2-dimethylcyclopropanecarboxylate,
Transfluthrin: 2,3,5,6-tetrafluorobenzyl (1R-trans)-3-(2,2-dichlorovinyl)-2,2-dimettiyl-cyclopropanecarboxylate,
Tetramethrin: 3,4,5,6-tetrahydrophthatimidomethyl (IRS)-cis, trans-chrysanthemate, Aljethrin: (RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (IRS)-cis, trans-clirysanthemate, Prailethrin: (S)-2-methyl-4-oxo-3-{2-propynyl)cyclopent-2-enyl (1 R)-cis, trans-chrysanthemate,
Empenthrin: (RS)-1 -ethynyl-2-methy)-2-pentenyI (1 R)-cis,trans-chrysanthemate, Imiprothrin: 2,5-dioxo-3-(prop-2-ynyl)imidazolidin-1-ylmethyl (1R)-cis, trans-2,2-dimethyl-3-(2-methyl-l-prDpenyl)-cyclopropanecarboxylate,
D-flamethrin: 5-(2-propynyl)-furfuryl (1R)-cis, trans-chrysanthemate, and 5-(2-propynyl)furiuryl2,2,3,3-tetramethyicyclopropanecarboxylate; Pyriproxyfen: 4-phenoxyphenyl (RS)-2-(2-pyridyloxy)propyl ether; pyrethrum;

d-d, trans-cyphenothrin: (RS)-a-cyano-3-phenoxybenzyl (1RS,3RS;1RS,?SR)-2,2-dimethyi-
3-(2-methylprop-1-enyl)cyclopropanecarboxyiate;
DDT;.
Carbamate compounds such as
Alanycarb: S-methyl-N[[N-methyl-N-[N-ben2yl-N{2-ethoxy-carbonylethyl)amino-
thio]carbamoyl]thioacetimidate,
Bendiocarb: 2,2-dimethyl-1,3-benzodioxol-4-y!-methylcarbamate),
Carbaryl(1 -naphthyl N-methylcarbamate,
Isoprocarb: 2-(1-methylethyl)phenyl methylcarbamate,
Carbosulfan: 2,3 dihydro-2,2-dimethyl-7-benzofuranyl[(dibutylamino)thio]methyl-carbamate,
Fenoxycarb; Ethyl[2-(4-phenoxyphenoxy)ethyl]carbamate,
Indoxacarb: Methyl-7-chloro-22,3,4',5-tetrahydro-2-[methoxycarbonyl (-4-
trifluoromethoxyphenyl)]
Propoxur: 2-isopropyloxyphenol methylcarbamate,
Pirimicarb: 2-dimethylamino-5,6-dlmethyl-4-pyrimidinyl-dimethylcarbamate,
Thiodiocarb: Dimethyl N,N'(thiobis((mefhy(imino)carbonoyloxy)bisethanimidiothioate).
Methomyl: S-methyl N-((methylcarbamoyl)oxy)thioacetamidate,
Ethiofencarb: 2-((ethyithio)methyl)phenyl methylcarbamate,
Fenothiocarb: S-(4-phenoxybutyl)-N,N-dimethyl thiocarbamate,
Cartap: S,S'-{2-5 d(methy(am(na)trimethylene)bis (thiocarbamate)hydrochlonde,
Fenobucarb: 2-sec-butylphenylmethyl carbamate,
XMC: 3,5-dimethylphenyt-methyl carbamate,
Xylylcarb: 3,4-dlmethy[phenylmethylcarbamate;
organophosphorous compounds such as
Trichlorfon: Phosphoric acid, (2,2,2-trich!oro-1-hydroxyethyl)-, dimethyl ester
Fenitrothion; 0,0-dimethyl 0-(4-nitro-m-tolyl)phosphorothioate,
Diazinon: 0,0-diethyl-0-(2-isopropyl-6-methyl-4-pyrimidinyl)phosphorothioate,
Pyridaphenthion: 0-(1,6-dihydro-6-oxo-1-phenylpyrazidin-3-yi) 0,0-diethyl phosphorothioa-
te,
Pirimiphos-Etyl: 0,O-diethyl 0-(2-(diethylamino)6-methyl-pyrimidinyl)phosphorothioate,
Pirimiphos-Methyl: 0-[2-(diethylamino)-6-melhyl-4 pyrimidinyl] 0,0-dimethyl phosphoro-
thioate,
Etrimphos: 0-6-ethoxy-2-ethyl-pyrimidin-4-yl-0,0-dimethyl-phosphorothioate,

Fenthion: 0,0-dimethyl-0-[-3-methy[-4-(methylthio)pheny( phosphorothioate, Phoxlm: 2-(diethoxyphosphinothoyloxyimino)-2-phenylacetonitrile, Chlorpyrifos: 0,0-diethyi-0-(3,5,6-trichloro-2-pyrinyl)phosphorothioate, Chiorpyriphosmethyl: 0,0-dimethyl 0-(3,5,6-trichloro-2-pyridinyl)phosphorothioate, Cyanophos: 0,0-dimethyl 0-(4 cyanophenyl)phosphDrottiioa1e, Pyradofos: {R,S)[4-ch!orophenyl)-pyrazDl-4-yl]-0-ethyl-S-n-propyl phosphorothioate, Acephate: O, S-dimethyl acetylphosphoroamidothioate,
Azamethiphos: S-(6-chloro-2,3-dihydro-oxo-l,3-oxa2olo[4,5-blpyridine-3-ylmethyl phos¬phorothioate,
Malathion: 0,0-dimethyl phosphorodithloate ester of diethyl mercaptosuccinate, Temephos: (0,0'(thiodi-4-l-phGnylene) 0,0,O,O~tetramethyl phosphorodithloate, Dimethoate: ({0,0-dimethyl S-(n-methylcarbamoylethyl)phosphorodithioate, Formothion: S[2-formylmethylamino]-2-oxoethyl]-0,0-dimethyl phosphorodithioate, Phenthoate: 0,0-dimethyl S-(alpha-ethoxycarbonylbenzal)-phosphorodithioate; lodofenphos: 0-(2,5-dichloro-4-iodophenyl)-0,0-dimethyl-phosphorthioate.
Insecticides with a sterilising effect on adult mosquitoes such as
1-(alfa-(chloro-alpha-cyclopropylben2ylidenamino-oxy)-p-tolyl)-3-{2,6-difluorobenzoyl)urea,
Diflubenzuron: N-(((3,5-dichloro-4-(1,1,2,2-tetra{louroethoxy)phenylamino)carbonyl)2,6 di-
tluoro benzamid,
Triflumuron; 2-Chloro-N-(((4-(trifluoromethoxy)phenyl}-amino-)carbonyl)benzamide, or a
triazin such as N-cyclopropyl-1,3,5-triazine-2,4,6-triamin; and
Lambda-cyhaloth rine:
a^cyano-3-phenoxybenzyl-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropane carboxylate, as a 1:1 mixture of {Z)-{1R,3R), R-esterand (Z)-{1S,3S), S-ester.
The repellent is preferably selected from N,N-Diethyl-meta-toluamide (DEET), N,N-diethylphenylacetamidG (DEPA), 1-(3-cyclohexan-1-yl-carbonyl)-2-methylpip6rine, (2-hydroxymethylcyclohexyl) acetic acid lactone, 2-ethyl-1,3-hexandiol, indalone, Methyl-neodecanamide (MNDA), a pyrethroid not used for insect control such as {(+/-)-3-allyl-2-melhy)-4-oxocyclopent-2-{+)-enyl-(+)-trans-chfysantemate (Esbiothrin), a repellent derived from or identical with plant extracts like limonene, eugenol, (+)-Eucamalol (1), {-)-1-epi-eucamalol or crude plant extracts from plants like Eucalyptus maculata, Vitex rotundifolia, Cymbopogan martinii, Cymbopogan citratus (lemon grass), Cymopogan nartdus (citro-

nella), IR3535 (ethyl butylacetylaminopropionate), icaridin (1-piperidinecarboxylic acid 2-(2-hydroxyethyl)-1-methylpropylester).
A suitable molluscicide is for example niclosamide.
Suitable rodenticides are first generation anticoagulant rodenticides and second generation anticoagulant rodenticides, where second generation rodenticides are preferred. Examples for first generation anticoagulant rodenticides are warfarin, chlorphacinone, coumatetralyt, suitable second generation anticoagulant rodenticides are for example flocoumafen, brodi-facoum, difenacoum, bromadialone, difethialone, and bromethalin.
Suitable fungicides are for example
Azofes sucfi as Bitertanol, Bromoconazole, Cyproconazole, Difenoconazole, Oinitrocona-
zole, Epoxiconazole, Fenbuconazole, Fluquiconazole, Flusilazole, Flutriatol, Hexacona-
zole, Imazalil, Ipconazole, Metconazole, Myclobutanil, Penconazole, Rropiconazole,
Prochloraz, Prothioconazole, Simeconazole, Tebuconazole Tetraconazol, Triadimefon,
Triadimenol, Triflumizol, Triticonazol;
Strofailurines such as Azoxystrobin, Dimoxystrobin, Ruoxastrobin, KresoJtim-methyl. Me-
tominostrobin, Orysastrobin, Picoxystrobin, Pyraclostrobin and Trifloxystrobin;
Acylalanines such as Benalaxyl, Metalaxyl, Mefenoxam, Ofurace, Oxadixyl;
Aminderivatives such as Aldimorph, Dodine, Dodemorph, Fenpropimorph, Fenpropidin,
Guazatine, Iminoctadine, Spiroxamin, Tridemoiph;
Anilinopyrimidines such as Pyrimethanil, Mepanipyrim, Cyprodinil;
Dicarboximide such as Iprodion, Myclozolin, Procymidon, Vinciozolin;
Cinnamic amides and derivatives such as Dimethomorph, Flumetover, Flumorph;
Antibiotics as Cycloheximide, Griseofulvin, Kasugamycin, Natamycin, Polyoxin,
Streptomycine;
Dithiocarbamates such as Ferbam, Nabam, f\flaneb, Mancozeb, Metam, Metiram,
Propineb, Polycarbamat, Thiram, Ziram Zineb;
Heterocyclic compounds such as Aniiazin, Benomyl, Boscalid, Carbendazim, Carboxin,
Oxycarboxin, Cyazofamid, Dazomet, Dithianon, Famoxadon, Fenamidon, Fenarimol,
Fuberidazol, Flutolanil, Furametpyr, Isoprothiolan, f^epronil, Nuarimol, Picobenzamid,
Probenazol, Proquinazid, Pyrifenox, Pyroquilon, Quinoxyfen, Silthioiam, Thiabendazol,
Thifluzamid, Thiophanat-methyl. Tiadinil, Tricyclazol, Triforine M Anorganika;
Nitrophenylderivatives such as Binapacryl, Dinocap, Dinobuton, Nitrophthal-isopropyt;
Phenylpyrroles such as Fenpiclonil, Fludioxonil;

Derivatives of sulfenic acid such as Captafol, Captan, Dichloffuanid, Folpet, Tolyifluanid; Other fungicides such as Acibenzolar-S-methyl, Benthiavalicarb, Carpropamid, Chlorofhalonil, Cyflufenamid, Cymoxanil, Dazomet, Diclomezin, Diclocymet, Diclofluanid, Diethofencarb, Edifenphos, Ethaboxam, Fenhexamid, Fentin-Acetat, Fenoxanil, Ferimzone, Fluazinam, Fosetyl, Fosetyl-Alumintum, Phosphoric Acid, Iprovalicarb, Hexachlorbenzene, Metrafenon, Pencycuron, Propamocarb, Phthaiid, Toloclofos- methyl, Quintozene, Zoxamid.
In a further preferred embodiment, the pesticide is at least one N-aryihydrazine derivative, preferably of formula I,


(I)

wherein
A is C-R^ or N;
B is C-R^ or N;

D is C-R" or N;
with the proviso that at least one of A, B or D must be other than N;
Z is halogen, CN, NOa, C-Ce-alkyl, C-Ce-haloalkyl, Ci-Ce-alkoxy or Ci-Cg-haloalkoxy;
n is an integer of 0, 1 or 2;
Qis
NR^R' X^
R . R
R^
or N^O R
wherein Ris
hydrogen;
C,-Cio-alkyl, optionally substituted with one or more halogens; Cs-Ce-cycloalkyI; C1-C4-alkoxy; CrC4-haloalkoxy; (Ci-C4-alkyl)S0,; {Ci-C4-haloalkyl)SO,; phenyl, optionally substi¬tuted with one to three halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy, C,-C4-haloalkoxy, (Ci-C4-alkyl)S0x, {C,-C4-haloalkyl)SOx, NOg or ON groups; phenoxy, optionally substituted with one to three halogen, C,-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy, 0,-04-haloalkoxy, (Ci-C4-alkyl)S0„ (C,-C4-haloalkyl)SOx, NOj or CN groups;

C3-C,2-cyc(oa(kyl, optionally substituted with one or more halogens, Ci-C6-alkyl, Ci-Cg-
haloalkyi, CrC^-alkoxy. Ci-Ca-haloalkoxy, (CrC4-alkyl)S0„ (CI-C4-haloalkyl)SOx; phenyl,
optionally substituted with one to three halogen, CrC4-alkyl, Ci-C4-haloa!ky(, Ci-Ci-alkoxy,
C,-C4-haloalkoxy, NOj or CN groups; phenoxy, optionally substituted with one to three
halogen, CrC4-alkyl, C-C^-haloalkyl, C,-C4-alkoxy, Ci-C^-haloalkoxy, NOgorCN groups;
or
phenyl, optionally substituted with one or more halogens, d-C^-alkyl, CrC^-haloalkyl, C|-
C4-alkoxy, Ci-C4-haloaikoxy, N02 or CN groups;
or
R" and R'^ are each independently CrCe-alkyl, Ca-Cg-alkenyl, Ca-Cg-alkynyl, or C3-C6-
cycloalkyl which may be substituted with 1 to 3 halogen atoms;
R^^ is hydrogen or Ci-Ce-alkyI;
R^ and R^ are each independently hydrogen or Ci-Ci-alkyI;
R^ and R^ are each independently
hydrogen;
Ci-Cio-alkyl, optionally substituted with one or more halogen, hydroxy, Ci-C4-alkoxy, (C,-
C4-alkyl}S0„ CONR^R^, CO^R'", R", R'^;
C3-Cio-alkenyl, optionally substituted with one or more halogen, hydroxy, Ci-C4-alkoxy, (Ci-
C4-alky()S0„, CONR^R^ COaR'", R", R'^;
Ca-Cio-alkynyl, optionally substituted with one or more halogen, hydroxy, Ci-C4-alkoxy, (C,-
C4-alkyl)S0„ CONR^R^ CO^R'", R^\ R^';
C3-Ci2-cycloalkyl, optionally substituted with one or more halogen, hydroxy, C,'C4-alkoxy,
(CrC,-alkyl)SO„ CONR^R^ CO^R'", R", R^^-
Cs-Ce-cycloalkyI, optionally substituted with one to three halogen, C,-C4-alkyl, C1-C4-
haloalkyl, CrC^-alkoxy, CrC4-haloalkoxy, NO? or CN groups;
phenyl, optionally substituted with one or more halogen, Ci-C4-alkyl, Ci-C4-haioalkyl, C1-C4-
alkoxy, CrCa-haloalkoxy, NO? or CN groups;
pyridyl, optionally substituted with one or more halogen, Ci-C4-alkyl, Ci-Ca-haloalkyI, C1-C4-
alkoxy, CrCa-haloalkoxy, NO2 or CN groups;
R^ and R^ may be taken together to form a ring represented by the structure

R^ R^ and R" are each independently hydrogen, halogen, CN, NOg, (Ci-C4-alkyI)S0x, (C,-C4-haloalkyl)SOx, C,-C6-aikyl, CrCe-haloaikyl, Ci-C6-alkoxy or Ci-Ce-haloalkoxy; R®, R^ aad R'" are each independently hydrogen or Ci-C4-alkyl; R'^sMR'^R'",

\CH,)/\_ \CH,)/-'
N, .X. CH, .X,
or

R'^is
,16
-R'
jry
N
R'^, R'', R'^ and R'^ are each independently hydrogen or Ci-C4-alkyl;
XisO, SorNR^^
X' is chlorine, bromine or fluorine;
r is an integer of 0 or 1;
p and m are each independently an integer of 0, 1, 2 or 3, with the proviso that only one of
p, m or r can be 0 and with the further proviso that the sum of p + m + r must be 4, 5 or 6;
X is an integer of 0, 1 or 2; or
the enantiomers or the salts thereof.
In a preferred embodiment Q in fomiula I is
NR^R^
R More preferably, the least one N-arylhydrazine derivative is a compound of formula la

wherein
R^ is chlorine or thfluoromethyl;
Z^ and Z^ are each independently chlorine or bromine;

R^ is Ci-Cs-alkyI, Ca-Ce-alkenyl, Cg-Ce-alkynyl, or Ca-Ce-cycioalkyl which may be substituted
witti 1 to 3 halogen atoms, or C2-C4-alkyl which is substituted by Ci-C4-alkoxy;
R"' and R^^ are each independently Ci-Ce-alkyl, Ca-Cg-alkenyl, Cg-Ce-alkynyl, or Cj-Ce-
cycloalkyl which may be substituted with 1 to 3 halogen atoms;
R'^ is hydrogen or d-Cs-alkyl;
or enantiomers or salts thereof.
In the definition of formula I and formula la shown above, the substituents have the follow¬ing meanings:
"Halogen" will be taken to mean fluoro, chloro, bromo and iodo.
The term "alkyl" as used herein refers to a branched or unbranched saturated hydrocarbon group having 1 to 4 or 6 carbon atoms, especially Ci-C6-alkyl such as methyl, ethyj, propyl, 1 -methyfethyl, butyl, 1 -methylpropyl, 2-methy(propyl, 1,1 -dimethylethyl, pentyl, 1 -methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyi, 1,2-dimethylpropyl, t-methylpentyl, 2-methy(pentyl, 3-methylpenty(, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethyfbutyl, 1,1,2-trtmethylpropyl, 1,2,2-tri methyl propyl, 1-ethyl-l-methylpropyi and 1-ethyl-2-methylpropyl.
"Alkoxy" refers to a straight-chain or branched alkyl group having 1 to 4 carbon atoms (methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyi, 1,1-dimethylethyl) bonded through an oxygen linkage, at any bond in the alkyl group. Examples include methoxy, ethoxy, propoxy, and isopropoxy.
"Cycloalkyl" refers to a monocyclic 3- to 6-membered saturated carbon atom ring, i.e. cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
With respect to the intended use of the compounds of formula 1, particular preference is given to the following meanings of the substituents, in each case on their own or in combi¬nation:
Preference is given to compounds of formula I wherein R* is trifluoromethyl.
Preference is further given to compounds of formula I wherein Z^ and Z^ are both chlorine.

Moreover, preferred are compounds of formula I wherein R^ is CrCe-alkyI, especially ethyl. Preference is further given to compounds of formula I wherein R^^ and R'* are both methyl.
Moreover, preferred are compounds of formula I wherein R^' and R'^ form a cyclopropyl
ring which is unsubstituted or substituted by 1 to 3 halogen atoms, especially chlorine and bromine.
Moreover, particularly preferred are compounds of formula I wherein R^^ and R^^ form a cyclopropyl ring which is substituted by 2 halogen atoms.
Moreover, particularly preferred are compounds of formula I wherein R^^ and R'^ form a cyclopropyl ring which is substituted by 2 chlorine atoms.
Particularly preferred are compounds of formula I wherein R" and R'^ form a 2,2-dichlorocyclopropyl ring.
Preference is further given to compounds of formula I wherein R'^ is Ci-Ce alkyl, especially methyl.
Particularly preferred are compounds of formula I wherein R^^, R'^ and R'^ are all methyl.
Moreover, particularly preferred are compounds of formula I wherein R'^, R'° and R'^ form a moiety 1-methyl-2,2-dlchlorocyclopropyl.
Preference is further given to compounds of formula I wherein
R"* is trifluoromethyl;
Z' and Z^ are each independently chlorine or bromine;
R^isCrCe-alkyl;
R" and R'^ are CrCe-alkyl or may be taken together to fonn Ca-Ce-cydoalkyl which is
substituted by 1 to 2 halogen atoms;
R^^ is C-Ce-alkyI;
or the enantiomers or salts thereof.

Particular preference is given to N-ethyl-2,2-dimethylproptonamide-2-(2,6-dichloro-a,a,a-trifiuoro-p-tolyl)hydrazone and N-ethyl-2,2-dichIoro-1-methylcyclopropane-carboxamide, 2-{2,6-dichloro-a,a ,a -trif|uoro-p-tolyl)hydrazone.
Furthermore, particular preference with respect to the use in the present invention is given to the compound of formula la-1 (N-ethyl-2,2-dimethylpropionamide-2-{2,6-dichloro-a,a,a -tnftuorQ-p-tolyl)-hydrazone):


•^3^ CH,
(la-l)

Moreover, particular preference with respect to the use in the present invention is given to the compound of formula ia-2 (N-Ethyl-2,2-dichloro-1-methylcyclo-propanecarboxamide-2-
(2,6-dichlorq-a,a,a -tri-fluoro-p-toiyl)hydrazone):


CI CI C!
(la-ll)

With respect to their use, particular preference is given to the compounds la-A compiled in the tables below. Moreover, the groups mentioned for a substituent in the tables are on their own, independently of the combination in which they are mentioned, a particularly pre¬ferred embodiment of the substituent in question.
With respect to their use, particular preference is also given to the hydrochloric acid, maieic acid, dimaleic acid, fumaric acid, difumaric acid, methane sulfenic acid, methane sulfonic acid, and succinic acid adducts of the compounds of the tables below.


(la-A)

Table A
No. R^ R" Rl« R19 Z' z=
A-1 CH3 2,2-dichlorocyclopropvl H CI CI
A-2 CH3 2,2-dibromocvclopro 3Vl H CI CI
A-3 CH3 CH3 CH3 CH3 CI CI
A-4 CH3 Cn2Crl3 CHa CH3 CI CI
A-5 CH3 2,2-dichlorocyclopropvl CHa CI CI
A-6 CH3 2,2-dibromocvclopropvl CH3 CI CI
A-7 CH3 2,2-dichlorocyclopropvl H Br Br
A-8 CH3 2,2-dibromocvclopro pyl H Br Br
A-9 CH3 CH3 CH3 CHa Br Br
A-10 CH3 Cn2Cn3 CH3 CHa Br Br
A-11 CHa 2,2-dichlo rocyclop ropyl CH3 Br Br
A-12 CH3 2,2-dibromocvclopropvl CH3 Br Br
A-13 CH2CH3 2,2-dichlorocyclopropvl H CI CI
A-M Cn2Crl3 2,2-dibromocyclopro pyl H C\ cA-15 CHjCHs CH3 CH3 CHa CI CI
A-16 CH2CH3 CH2CH3 CH3 CH3 CI CI
A-17 CH2CH3 2,2-dichlorocvclop ropyl CH3 CI CI
A-18 CH2CH3 2,2-dib romocyclopropyl CH3 CI CI
A-19 CH2CH3 2,2-dichlorocyclop ropyl H Br Br
A-20 CH2CH3 2,2-dibromocyclop ro pyl H Br Br
A-21 CH£CH3 CH3 CH3 CHa Br Br
A-22 CHgCHs Cn2CH3 CH3 CH3 Br Br
A-23 CHjCHs 2,2-dichlorocvclopropvl CH3 Br Br
A-24 CrljCrlg 2,2-dibromocyclopropvl CH3 Br Br
A-25 CH2CH2CH3 2,2-dichlorocyclopropyl H CI CI
A-26 CH2Cn2CH3 2,2-dibromocycloprc ipyl H CI CI
A-27 CH2CH2CH3 CH3 CH3 CH3 CI CI
A-28 CH2CH2CH3 CH2CH3 CH3 CH3 CI CI

No. R^ R^^ RI8 p19 Z' Z^
A-29 CH2CH5CH3 2,2-dichlorocyclopropvl CHa CI 1 CI
A-30 CHgCHgCHs 2,2-dibromocyclopropyl CH3 CI CI
A-31 OH2Cr1pCH3 2,2-dichlorocyclopropvl H Br Br
A-32 CHgCH^CHs 2,2-dibromocvclopropvl H Br Br
A-33 CH2Cn?Cn3 CH3 CH3 CH3 Br Br
Preferred insecticides and/or repellents of the pesticidal composition of the invention may be either one or a mixture. Preferred mixtures of pesticides are mixtures of insecticides and/or repellents with similar diffusion/migration properties. This group of insecticides and/or repellents may include synthetic pyrethroids such as alphacypermethrin, cyfluthrin, deltamethrin, etofenprox and permethrin, other pyrethroids such as bifenthrine, and non-pyrethroids such as carbosulphane.
The pesticide can also be included in the pesticidal composition as one of a water-based pesticide concentrate or a solvent, preferably an organic solvent, based pesticide concen¬trate or a concentrate based on a mixture of water and a solvent, preferably an organic solvent. Water-based concentrates may be in the form of suspensions or dispersions com¬prising suitable dispersing agents if necessary or in the form of emulsions comprising emulsifiers, solvents and co-solvents if appropriate. Nanoparticular pesticidal formulations may be obtained by dissolving solid solutions of pesticidal in a polar organic solvent, e.g. poly vinyl pyrrolidone (PVP). The concentration of the pesticide in the water based or sol¬vent based concentrates is in general between 0.5 to 60 %, preferably 1 to 40 %, more preferably 3 to 20 %.
The particle size of the pesticide in water-based suspensions or dispersions is in general between 50 nm to 20 fjm, preferably 50 nm to 8 pm, more preferably 50 nm to 4 pm, most preferably 50 nm to 500 nm, or 1 pm to 3 pm.
Polymeric binder (component B)
The polymeric binder (component B) may be any polymeric binder known in the art. Espe¬cially preferred are polymeric binders used in the area of impregnating or coating textile materials or plastics materials.

Preferred binders are for example binders obtainable by polymerization, preferably radical polymerization, of at least one ethylenically unsaturated monomer selected from the group consisting of acrylates, preferably CrCi2-esters of acrylic acid or acrylates having crosslinked ester functionalities, methacrylates, preferably Ci-Ci2-esters of methacrylic acid or methacrylates having crosslinked ester functionalities, acrylic acid, methacrylic acid, acrylonitrile, maleic acid, maleic acid anhydride, mono or diesters of maleic acid, styrene, derivatives of styrene such as methyl styrene, butadiene, vinyl acetate, vinyl alcohol, ethyl¬ene, propylene, allylic alcohol, vinyl pyrrolidone, vinyl chloride and vinyl dichloride.
The polymerization, preferably radical polymerization, may be carried out for example as bulk polymerization, gas phase polymerization, solvent polymerization, emulsion polymeri¬zation or suspension polymerization.
The conditions and further necessary and suitable components for the preparation of suit¬able polymers by polymerization, preferably radical polymerization, of the monomers men¬tioned above are known by a person skilled in the art.
Suitable polymeric binders obtained by polymerization, preferably radical polymerization, of the above-mentioned monomers are homopolymers or copolymers, preferably selected from the group consisting of polyacrylates, poly methacrylates, polyacrylonitrlle, polymaleic acid anhydride, polystyrene, po[y{methyl)styrene, polybutadiene, polyvinylacetate, polyvi-nylalcohol as well as copolymers obtained by polymerization of at least two different ethylenically unsaturated monomers of the group of monomers mentioned above and blends of said homopolymers and/or copolymers, for example poly{styrene-acrylates), poly(styrene-butadiene), ethylene-acrylate-copolymers, ethylene-vinylacetate-copolymers, which may be partially or completely hydrolyzed.
Further suitable polymeric binders are selected from polyurethanes and/or polyiso-
cyanurates, blends comprising polyurethanes and/or polyisocyanu rates, preferable blends
comprising polyurethanes and/or polyisocyan urates and polycarbonates;
mineral waxes, zirconium waxes, silicones, polysiloxanes, fluorinated polyacrylates and
methacrylates, fluorosilicones, and
fluorocarbon resins (as disclosed e.g. in WO 01/37662 and WO 92/16103);
melamine formaldehyde condensation resins, methylol urea derivatives; and
curable polyesters;
or

blends or preparations comprising at least one of said polymeric binders.
The polymeric binders mentioned above are known in the art and are either commercially available or can be prepared by preparation processes known in the art.
Further suitable polymeric binders are polyvinytacetates in a formulation comprising a thickener like carboxymethyl cellulose and optionally a cross linking agent like a melamine resin; curable polyesters; formulations comprising reactive silicones (organic polysilox-anes), polyvinyl alcohol, polyvinyl acetate or an acrylic copolymer.
The crosslinking may be carried out thermally or by UV-light or by the dual cure technique. Optionally, a catalyst or a crosslinking agent may be used together with the polymeric
binder.
Preferred polymeric binders are selected from the group consisting of acrylic binders and polyurethane and/or polyisocyanurate binders.
Most preferred polymeric binders are acrylic binders, which are optionally fluorinated. Es¬pecially preferred acrylic binders are mentioned below (component B1).
Acrylic binders (Component B1)
Most preferred are actylic binders, which may be hompolymers or copolymers, wherein the copolymers are preferred.
The acrylic binders are preferably obtained by radical polymerization, more preferably radi¬cal emulsion polymerization, of at least one monomer of formula II as component Bl A

^ on
H'

wherein
R^°, R^' and R^^ are independently selected from Ci- to Cio-alkyl, which is optionally fluoro substituted and which may be linear or branched, for example methyl, ethyl, n-propyl. i-propyl. n-butyl, i-butyl, sec-butyl, t-butyl, n-pentyl, l-pentyl, sec-pentyl, neo-pentyl, 1,2-

dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, preferably Cr to C4-alkyl, for example methyl, ethyl, n-propyl, i-propyl, ri-butyi, i-butyl, sec-butyl, tert-butyl; substituted or unsubstituted aryl, preferably substituted or un¬substituted Cg- to C,o-aryt, more preferably substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;
R'" and R^' may further be H.
Preferably R^" Is H or methyl. R^' is preferably H; R^^ is preferably methyl, ethyl, n-butyl or 2-ethylhexyl.
More preferably R^°is H or methyl, R^' is H and R^ is methyl, ethyl, n-butyl or 2-ethylhexyl.
Most preferably the monomer of formula II (component BA) is selected from the group con¬sisting of 2-ethylhexylacrylate, n-butylacrylate, methylacrylate, methyl methacrylate and ethylacrylate. Most preferably a copolymer obtainable by polymerization of at least two dif¬ferent acrylic monomers of formula II is employed.
Most preferably an acrylic binder is used as component B obtainable by emulsion polym¬erization of b1 a) at least one monomer of formula II as component B1A

°.
R% VOR^'

\ (II)
wherein
R^", R^' and R^^ are independently selected from Ci- to Cio-alkyl which may be linear OT branched, for example methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, preferably Ci- to Cd-alkyI, for example methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl; substituted or unsubstituted aryl, preferably substituted or unsubstituted Cg-to C,o-aryl, more preferably substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;

R^° and R^' may further be H.
Preferably R^° is H or methyl. R^' is preferably H; R^^ is preferably methyl, ethyl, n-butyl or 2-ethylhexyl.
More preferably R^" is H or methyl, R^' is H and R^^ is methyl, ethyl, n-butyl or 2-ethylhexyl;
b1 b) at least one monomer of formula III as component B1B
(111)
wherein
R^^, R^', R^^and R^ are independently selected from the group consisting of H, Ci¬te Cio-a!kyl which may be linear or branched, for example, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyi and n-decyl; preferably R^^, R^', R^^ and R^ are selected from the group consisting of H, Ci- to C4-alkyl, which may be linear or branched, for example methyl, ethyl, n-propyl, iso-propyl, n-butyl, i-butyl, sec-butyl and tert-butyl; substituted or un-substituted aryl, preferably substituted or unsubstituted Ce- to do-aryl, more prefera¬bly substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;
more preferably R^^ is H or methyl, R^", R^^ and R^ are preferably H;
most preferably R^^ is H or methyl and R^*, R^^ and R^^ are H;
bic) optionally at least one monomer of formula IV as component B1C



(IV)
wherein
R^' and R^^ are independently selected Irom the group consisting of H, C,- to C,o-alkyl which may be linear or branched, for example, methyi, ethyl, n-propyl, i-propyi, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyi, i-amyl, n-hexyl, i-hexyl, sec-hexyi, n-heptyl, n-octyi, 2-ethylhexyl, n-nonyi and n-decyl; preferably R" and R^' are selected from the group consisting of H, C,- to C4-alkyl, which may be linear or branched, for example methyl, ethyl, n-propyl, iso-propyl, n-butyt, i-butyl, sec-butyl and tert-butyl; substituted or unsubstituted aryl, preferably substituted or unsubstituted Cg- to Cio-aryl, more preferably substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;
most preferably R^' and R^^ are H;
X is selected from the group consisting of H, OH, NH2, OR^^OH, glycidyl, hydroxypro-
pyf,
—O
V
■0
V
groups of the fomiula
OR^
-°vA^o
O
wherein
R^ is selected from the group consisting of C,- to Cio-alkyl which may be branched or linear, for example meUiyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyi, n-octyt, 2-ethy(hexyl, n-nonyl, n-decyl; preferably Cr to C4-alkyl, which may be branched or linear, for example methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyt and tert-butyl; substituted or unsubstituted aryl.

preferably substituted or unsubstitutir-' Cg- to Cio-aryl, more preferably substituted or unsubstituted Ce-aryl, for example phenyl or tolyl;
R^^ is selected from the group consisting of Cr to Cio-alkylene, for example methyl¬ene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, non-ylene, decylene; preferably C,- to C4-alkylene, for example methylene, ethylene, pro¬pylene, butylenes; substituted or unsubstituted arylenes, preferably substituted or un¬substituted Cg- to Co-arylene, more preferably substituted or unsubstituted Ce-arylene, for example phenylene; most preferably X ist acetoacetyl;
bid) further monomers which are copolymerizable with the monomers mentioned above
selected from
bidl) polar monomers, preferably (meth)acrylic nitrlle and/or methyl{metti)acrylate as component B1D1; and/or
b1d2) non polar monomers, preferably styrene and/or a-methylstyrene as compo¬nent B1D2.
The acrylic binder is preferably obtainable by emulsion polymerization of
b1 a) 10 to 95 % by weight, preferably 30 to 95 % by weight, more preferably 50 to 90 % by
weight of component 81 A; bib) 1 to 5 % by weight of component BIB; bic) 0 to 5 % by weight, preferably 1 to 4 % by weight, more preferably 0.2 to 3% by
weight of component B1C;
bid) further monomers which are copolymerizable with the monomers mentioned above
selected from
bidl) 0 to 30 % by weight, preferably 0 to 25 % by weight, more preferably 5 to
20 % by weight of component B1D1; and/or
bld2) 0 to 40 % by weight, preferably 0 to 30 % by weight, more preferably 5 to
20 % by weight of component B1D2; wherein the sum of the components B1A, BIB and optionally BIC and BID is 100 % by weight.
In a further preferred embodiment the acrylic binder is obtainable by emulsion polymeriza¬tion of

bla) 10 to 95 % by weight, preferably 30 to 95 % by weight, more preferably 50 to 90 by weight of at least one acrylic binder (component B1 A) as defined above, comprising; bla]) 10 to 90% by weight, preferably 15 to 85% by weight, more preferably 30 to
85% by weight based on the acrylic binder of n-butyl acrylate; b1a2) 10 to 90% by weight, preferably 12 to 85% by weight, more preferably 15 to 65% by weight based on the acrylic binder of at least one monomer of formula II, different from n-butyl acrylate; bib) 1 to 5 % by weight based on the acrylic binder of at least one monomer of formula III
(component BIB); bic) 0 to 5 % by weight, preferably 0.1 to 4 % by weight, more preferably 0.2 to 3% by weight based on the acrylic binder of at least one monomer of formula III (component BIC); bid) further monomers which are copolymerizable with the monomers mentioned (com¬ponent BID) above selected from
b1d1) 0 to 30 % by weight, preferably 0 to 25 % by weight, more preferably 5 to 20 % by weight based on the acrylic binder of at least one polar mono¬mer, preferably (meth)acrylic nitrile and/or methyl(meth)acrylate (compo-r^ent 8101); and/or b1d2) 0 to 40 % by weight, preferably 0 to 30 % by weight, more preferably 5 to 20 % by weight based on the acrylic binder of at least one non polar monomer, preferably styrene and/or a-methylstyrene (component B1D2);
wherein the sum of the components B1A, BIB and optionally BIC and BID is 100 % by weight.
The acrylic binder may comprise further additives as known by a person skilled in the art, for example film forming agents and plasticizers, e.g. adipate, phlhalate, butyl diglycol, mix¬tures of diesters preparable by reaction of dicarboxyiic acids and alcohols which may be linear or branched. Suitable dicarboxyiic acids and alcohols are known by a person skilled in the art.
The insecticide compositions comprising the binder as claimed in the present invention are wash resistant while permitting continuous release of the insecticide at a controlled rate, in order to provide the required bioavailability of the insecticide. It is not necessary to add for example a dispersing agent that, after application of the composition to a fabric and upon wetting of the fabric, reduces the hydrophobicity imparted to the insecticide by the binder to

permit limited insecticide release. Preferably, the insecticide composition of the present invention does therefore not comprise a dispersing agent in addition to the polymeric binder.
Most preferably the acrylic binder is obtainable by emulsion polymerization of the following
components:
bla) 50 to 90 % by weight of at least one monomer of formula II as component B1A
^= wherein
R™ is H or methyl, R^^ is H and R^^ is methyl, ethyl, n-butyl, or 2-ethylhexyl, as com¬ponent B1A, most preferably component B1A is 2-ethylhexylacrylate, n-butylacrylate, methylacrylate, methylmethacrylate or ethylacrylate; bib) 1 to 5% by weight of at least one monomer of formula III
O^ V-OH
\ no
R^^
(III)
wherein R^^ is H or methyl, R^^ R" and R^^ each are H as component BIB;
bic) 1 to 10 % by weight, preferably 1 to 7 % by weight, more preferably 2 to 5 % by
weight of at least one monomer of formula IV
O.

(IV)
wherein R" and R^^ are H and X is H, OH, NHE, OR^^OH, glycldyl or a group of the formula

OR^
—o
o o
wherein
R^ is selected from the group consisting of C,- to Cio-alKyl which may be branched or linear, for example methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyi, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyi, 2-ethylhexyl, n-nonyl, n-decyl; preferably Ci- to C4-alkyl, which may be branched or linear, for example methyl, ethyl, n-propyt, iso-propyl, n-butyl, iso-butyl, sec-butyl and tert-butyl; substituted or unsubstituted aryl, preferably substituted or unsubstituted Ce- to Cjo-aryl, more preferably substituted or unsubstituted Ce-aryl, for example phenyl or tolyl;

R^^ is selected from the group consisting of d- to C,o-afkylene, for example methyl¬ene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, non-y)ene, decylene; preferably C,- to C4-alkyIene, for example methylene, ethylene, pro¬pylene, butylenes; substituted or unsubstituted arylenes, preferably substituted or un¬substituted Ce- to Cio-arylene, more preferably substituted or unsubstituted Gg-arylene, for example phenylene;
as component BIC, most preferably X is acetoacetyl;

bid) further monomers which are copolymerizable with the monomers mentioned above selected from
b1d1) 0 to 30 % by weight, preferably 0 to 25 % by weight, more preferably 5 to 20 % by weight of component B1D1, preferably (meth)acrylic nitrile and/or methyt{meth)acrylate; and/or
bld2) 0 to 40 % by weight, preferably 0 to 30 % by weigtit, more preferably 5 to
20 % by weight of component BD2, preferably styrene and/or a-methylstyrene; wherein the sum of components BA, BB and optionally BC and BD is 100 % by weight.

In a further most preferred embodiment the amount of n-butylacrylate as component BA is from 30 to 90 % by weight, and the other components BIB and optionally a further mono-

mer of formula 11 (component B1A), B1C and BID are chosen as mentioned before, wherein the sum of components BIA, BIB and optionally BIG and BID is 100 % by weight.
The acrylic binder of the present invention is preferably obtainable by emulsion polymeriza¬tion of the monomers mentioned before. Suitable process conditions are known by a per¬son skilled in the art, and are disclosed e.g., in WO-A 2005/064072.
In the acrylic binder according to the invention, it is possible to add in general up to 10 % by weight, preferably 0.05 to 5 % by weight of mono- or di-olefinically unsaturated mono¬mers containing reactive or cross-linking groups. Examples of such monomers are in par¬ticular the amides of a,p-olefinically unsaturated Cg-a-carboxylic acids, particularly acryl amides, methacryl amides and maleic diamides, and their N-methylol derivatives such as N-methylol acrylic amide, N-methylo! methacrylic amide, N-alkoxy methyl amides of a,|3-monoolefinically unsaturated Cs-s-carboxylic acids such as N-methoxy methacrylic amide and N-n-butoxymethylactylic amide, vinyl sulfonic acid, monoesters of acrylic and methacrylic acids with alkanediols such as glycol, butan0diol-1,4, hexane diol-1,6, and 3-chloropropanediol-1,2, and also allyl and methallyl esters of a,p-otefinically unsaturated mono- and di-carboxylic acids such as diallyl maleate, dimethyl allyl fumarate, allyl acrylate and allyl methacrylate, diallyl phthalate, diallyl terephthalate, p-di-vinyl benzene, methyl-ene-bis-acrylamide and ethylene glycol di-allylether.
The molecular weight of the non crosslinked emulsion polymers obtained is in general 40,000 to 250,000 (determined by GPC). The molecular weight is usually controlled by the use of conventional chain stoppers in conventional amounts. Conventional chain stoppers are for example sulfoorganic compounds.
The acrylic binder of the present invention is obtained in form of its aqueous dispersion and is preferably employed in the insecticide compositions ot the present invention in form of the aqueous dispersion.
Polyurethane binders and/or Polyisocyanurate binders (Component B2)
In a further preferred embodiment the polymeric binders are polyurethanes and/or polyiso-cyanurates. Said polyurethanes and/or poiyisocyanu rates may be employed either alone as polymeric binders or in combination with further polymeric binders, especially polymeric

binders mentioned before, for example in combination with the acrylic binders mentioned before.
Suitable polymeric binders are therefore:
at least one polyurethane as component B2, obtainable by reaction of the following compo¬nents:
b2a} at least one diisocyanate or polyisocyanate as component B2A, preferably aliphatic, cycloaliphatic, araliphatic and/or aromatic insocyanates, more preferably diisocy-anates, which are optionally biuretisized and/or isocyanurized, most preferably 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylene cyclohexane (IPDI) and hexame-thylene diisocyanate-1,6 (HMDI); b2b) at least one diol, triol or poiyol as component B2B, preferably aliphatic, cycloaliphatic and/or araliphatic diols having 2 to 14, preferably 4 to 10 carbon atoms, more pref¬erably 1,6-hexanediot or neopentyl glycol; b2c) optionally further components as component B2C, preferably adipic acid or carbonyl diimidazole (GDI); and b2d) optionally further additives as component B2D.
The polyurethane is preferably obtainable by reaction of the following components:
b2a) 55 to 99 % by weight, preferably 70 to 98 % by weight, more preferably 75 to 90 by .weight based on the polyurethane of at least one diisocyanate or polyisocyanate (component B2a), preferably aliphatic, cycloaliphatic, araliphatic and/or aromatic in¬socyanates, more preferably diisocyanates, which are optionally biuretisized and/or isocyanurized, more preferably alkylene diisocyanates having from 4 to 12 carbon at¬oms in the alkylene unit, like 1,12-dodecane diisocyanate, 2-ethyltetramethylene diisocyanate-1,4, 2-methylpentamethy!ene diisocyanate-1,5, tetramethylene diisocy-anate-1,4, lysinester diisocyanate (LDI), hexamethyfene diisocyanate-1,6 (HMDI), cyclohexane-1,3-and/or-1,4-diisocyanate, 2,4-and 2,6-hexahydro-toiuylene diisocy¬anate as well as the corresponding isomeric mixtures 4,4'-2,2'- and 2,4'-dicyclohexylmethane diisocyanate as well as the corresponding mixtures, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl cyclohexane (IPDI), 2,4- and/or 2,6-toluylene diisocyanate, 4,4'-, 2,4' and/or 2,2'-diphenylmethane diisocyanate (mono-meric MDI), polyphenylpolymethylene polyisocyanate (polymeric MDI) and/or mix¬tures comprising at least 2 of the isocyanates mentioned before; further ester-, urea-, allophanate-, carbodiimid-, uretdione- and/or urethane groups comprising di- and/or

polyisocyanates may be used; most preferably 1-(socyanato-3,3,5-trimethyl-5-isocyanatomethyiene cyclohexane (IPDI) and hexamethylene diisocyanate-1,6 (HMDI);
b2b} 10 to 90% by weight, preferably 12 to 85% by weight, more preferably 15 to 65% by weight based on the polyurethane of at least one diol, triol or polyol (component B2B), preferably aliphatic, cycloaliphatic and/or araliphatic diols having 2 to 14, pref¬erably 4 to 10 carbon atoms, more preferably polyols, selected from the group con¬sisting of polyetherols, e.g. polytetrahydrofurane, polyesterols, polythioetherpolyols, hydroxyl group containing polyacetales and hydroxyl group containing aliphatic poly¬carbonates or mixtures of at least 2 o^ the polyols mentioned before. Preferred are polyesterols and/or polyetherols. The hydroxyl number of the polyhydroxy com¬pounds is in general from 20 to 850 mg KOH/g and preferably 25 to 80 mg KOH/g. Further, diols and/or triols having a molecular weight of from in general 60 to b2c} 0 to 10 % by weight, preferably 0.1 to 5 % by weight, more preferably 1 to 5 % by weight based on the polyurethane of further components (component B2C), prefera¬bly adipic acid or carbonyl diimidazole (GDI); and
b2d) 0 to 10 % by weight, preferably 0.1 to 5 % by weight, more preferably 0.5 to 5 % by weight based on the polyurethane of further additives (component B2D);
wherein the sum of the components B2A, B2B, B2C and B2D is 100 % by weight.
The polyurethanes are prepared by methods known in the art. Further, additives as known by a person skilled in the art may be used in the process for preparing the polyurethanes.

Component B may also be a polyisocyanurate or a mixture of a polyisocyanurate and a polyurethane, preferably a polyurethane as mentioned above.
Polyisocyanurates are polymers comprising groups of the following formula:

wherein R' is an alkylene or arylene residue depending on the isocyanate employed in the preparation of the isocyanurate.
Polyisocyanurates are usually prepared by cyclotrimerization of isocyanates. Preferred iso-cyanates are the same isocyanates as mentioned before (component B2A), Preparation processes and conditions for the preparation of polyisocyanu rates are known by a person skilled in the art.
Pesticidal compositions
The pesticidal compositions of the invention may be aqueous compositions or dry composi¬tions, i.e. compositions which do not comprise water.
In a preferred embodiment the pesticidal compositions are aqueous compositions, prefera¬bly comprising 55 to 97 % by weight, more preferably 85 to 95 % by weight of water, and 3 to 45 % by weight, preferably 5 to 15 % by weight of solids, based on the total of the com¬ponents in the insecticide compositions of the present invention, wherein the total is 100 % by weight. The solids are preferably selected from the group consisting of at least one pes¬ticide as component A as defined above, and at least one polymeric binder as component B as defined above, and optionally at least one fixative agent as component C as defined below, and optionally further components depending on the use of the final product as de¬fined above.

The treatment baths from which the pesticidal compositions are applied to the materia! are preferably aqueous formulations comprising 95 to 99.5 % by weight, preferably 95 to 99 % by weight, more preferably 97 to 99 % by weight of water, and 0.5 to 5 % by weight, pref¬erably 1 to 5 % by weight of solids, based on the total of the components in the insecticidal compositions of the present invention. The solids are preferably selected from the group consisting of at least one pesticidal of formula I as component A as defined above, and at least one polymeric binder as component B as defined above, and optionally at least one fixative agent as component C as defined below, and optionally further components de¬pending on the use of the final product as defined above.
The polymeric binder may advantageously be applied with a fixative agent C for improved attachment of the pesticide on the material. The fixative agent may comprise free isocy-anate groups.
Suitable fixable agents are for example isocyanates or isocyanurates comprising free iso-cyanate groups. Preferably the isocyanurates are based on aikylene diisocyanates having from 4 to 12 carbon atoms in the alkylene unit, like 1,12-dodecane diisocyanate, 2-ethyltetramethylene diisocyanate-1,4, 2-methylpentamethylene diisocyanate-1,5, tetrame-thylene diisocyanate-1,4, lysinester diisocyanate (LDI), hexamethylene diisocyanate-1,6 (HMDI), cyclohe)iane-1,3-and/or-1,4-diisocyanate, 2,4-and 2,6-hexahydrotoluytene diisocy¬anate as well as the corresponding isomeric mixtures 4,4'-2,2'- and 2,4'-dicyclohexylmethane diisocycuiate as well as the corresponding mixtures, 1-isocyanato-3,3,5-trimethyl-5-isQcyanatomethyl cydohexane (IPDI), 2,4- and/or 2,6-toluylene diisocy¬anate, 4,4'-, 2,4' and/or 2,2'-diphenylmethane diisocyanate (monomeric MDI), polyphenyl-polymethylene polyisocyanate (polymeric MDI) and/or mixtures comprising at least 2 of the isocyanates mentioned before. More preferably the isocyanurates are based on hexame¬thylene diisocyanate-1,6 (HMDI).
More preferably the isocyanurate is a isocyanurate which is hydrophilized with a polyal-kylene oxide based on ethylene oxide and/or 1,2-propylene oxide, preferably polyethylene oxide.
The isocyanurate used as a fixative agent can be prepared by methods known in the art. Preferably 5 to 25% by weight, more preferably 7 to 20% by weight, most preferably 10 to 15% by weight ot the isocyanate groups based on the amount of isocyanate used as star¬ing material for the preparation of the isocyanurate are free isocyanate groups.

Most preferably the isocyanurate used as a fixative agent is dissolved in a polar aprotic solvent, e.g. THF, DMF or propylene or ethylene carbonate.
The most preferred fixative agent used is an isocyanurate based on HMDI which are hy-drophilized with a polyethylene oxide and which is dissolved in propylene carbonate (70% by weight of HMDI in 30% by weight of propylene carbonate). The amount of free isocy-anate groups is 11 to 12 % by weight, based on the amount of isocyanate used as staring material for the preparation of the isocyanurate.
The pesticidal composition preferably comprises the following components, based on the solids content of the composition, if a fixative agent is used:
a) 20 to 70 % by weight, preferably 25 to 65 % by weight, more preferably 30 to 65 % by weight of at least one pesticide (component A), and
b) 29 to 72 % by weight, preferably 34 to 70 % by weight, more preferably 33 to 66 by weight of at least one polymeric binder (component B) as defined above;
c) 1 to 8 % by weight, preferably 1 to 5% by weight, more preferably 2 to 4 % by weight of at least one fixative agent (component C);
wherein the sum of the components is 100 % by weight of solids content of the pesticide composition.
Depending on the use of the final product the pesticidal composition may further comprise one or- more components selected from water, preservatives, detergents, fillers, impact modifiers, anti-fogging agents, blowing agents, clarifiers, nucleating agents, coupling agents, conductivity-enhancing agents (antistats), stabilizers such as anti-oxidants, carbon and oxygen radical scavengers and peroxide decomposing agents and the like, flame re-tardants, mould release agents, agents having UV protecting properties, optical bright-eners, spreading agents, anti-blocking agents, arrti-migrating agents, foam-forming agents, anti-soiling agents, thicKeners, further biocides, wetting agents, plasticizers and film form¬ing agents, adhesive or anti-adhesive agents, optical brightening (fluorescent whitening} agents, fragrance, pigments and dyestuffs.
Suitable anti-foam agents are for example silicon anti-foam agents. Suitable UV-protecting agents for protecting UV-sensitive insecticides and/or repellents are for example para-aminobenzoic acids (PABA), octylmethoxysinameth, stilbenes, styryl or benzotriazole de¬rivatives, benzoxazol derivatives, hydroxy-substituted benzophenones, salicylates, substi-■ tuted triazines, cinnamic acid derivatives (optionally substituted by 2-cyano groups), pyra-

zoline derivatives, 1,1'-biphenyl-4,4'-bis-2-(methoxyphenyl)-ethenyl or other UV protecting agents. Suitable optical brighteners are dthydroquinolinone derivatives, 1,3-diaryl pyra-zoline derivatives, pyrenes, naphthalic acid imides, 4,4'- diystyryl biphenylene, 4,4'-diamino-2,2'-stilbene disulphonic acids, cumarin derivatives and benzoxazole, benzisoxa-zole or benzimidazole systems which are linked by -CH=CH-bridges or other fluorescent whitening agents.
Typical pigments used in the pestidical compositions of the present invention are pigments which are used in pigment dyeing or printing processes or are applied for the coloration of plastics and are known by a person skilled in the art.
Pigments may be inorganic or organic by their chemical nature. Inorganic pigments are mainly used as white pigments (e.g., titanium dioxide in the form of rutile or anatas, ZnO, chalk) or black pigments (e.g., carbon black). Colored inorganic pigments may be used as well but are not preferred because of potential toxicologic hazards. For imparting color, organic pigments or dyestuffs are preferred. Organic pigments may be mono or disazo, naphthol, benzimidcizolone, (thio) indigoid, dioxazine, quinacridone, phthalocyanine, isoin-dolinone, perylene, perinone, metal complex or diketo pyrrole pyrrole type pigments. Pig¬ments may be used in powder or liquid form (i.e., as a dispersion). Preferred pigments are Pigment Yellow 83, Pigment Yellow 138, Pigment Orange 34, Pigment Red 170, Pigment Red 146, Pigment Violet 19, Pigment Violet 23, Pigment Blue 15/1, Pigment Blue 15/3, Pigment Green 7, Pigment Black 7. Other suitable pigments are known to a person skilled in the art.
Typical dyestuffs which may be used in the present invention are vat dyes, cationic dyes and disperse dyes in powder or liquid form. Vat dyes may be used as pigments or following the vatting (reduction) and oxidation procedure. Using the vat pigment form is preferred. Vat dyes may be of the indanthrone type, e.g. C.l. Vat Blue 4. 6 or 14; or of the flavan-throne type, e.g. C.l. Vat Yellow 1; or of the pyranthrone type, e.g. C.i. Vat Orange 2 and 9; or of the isobenzanthrone (isoviolanthrone) type, e.g. C.l. Vat Violet 1; or of the dibenzan-throne (violanthrone) type, e.g. C.l. Vat Blue 16, 19, 20 and 22, C.l. Vat Green 1, 2 and 9, C.l. Vat Black 9; or of the anthraquinone carbazole type, e.g. CI. Vat Orange 11 and 15, C.l. Vat Brown 1, 3 and 44, C.l. Vat Green 8 and C.l. Vat Black 27; or of the benzanthrone acridone type, e.g. C.l. Vat Green 3 and 13 and C.l. Vat Black 25; or of the anthraquinone oxazole type, e.g. C.l. Vat Red 10; or of the perylene tetra carbonic acid diimide type, e.g. C.l. Vat Red 23 and 32; or imidazole derivatives, e.g. C.l. Vat Yellow 46; or amino triazine

derivatives, e.g. C.I. Vat Blue 66. Other suitable vat dyes are known by a person skilled in the art.
Typical disperse and cationic dyestuffs are known by a person skilled in the art.
If cellulosic substrates are employed as material, said cellulosic substrates are preferably dyed with vat, direct, realative or sulphur dyestuffs.
In a further embodiment the pesticidal compositions of the present invention are pesticidal compositions as mentioned before comprising at least one pigment and/or at least one dyestuff. The pesticidal compositions of the present invention preferably comprise 10 to 300 % by weight, more preferably 20 to 150 % by weight of the pigment and/or dyestuff relating to the total weight of the solids content of the pesticide.
The material, for example textile material or plastics material, may be impregr\ated prior to use if the composition is delivered in the form of a kit.
In a further embodiment, the impregnated material according to the present invention fur¬ther comprises one or more components selected from preservatives, detergents, stabiliz¬ers, agents having UV-protecting properties, optical brighteners, spreading agents, anti-migrating agents, foam-forming agente, wetting agents, anti-soiling agents, thickeners, fur¬ther biocides, plasticizers, adhesive agents, pigments and dyestuffs. Suitable examples of the components mentioned above are known to a person skilled in the art.
In a further embodiment of the present invention the impregnated material comprises be¬sides the at least one pesticide and the at least one polymeric binder as described before at least one pigment and/or at least one dyestuff. The amount of the at least one pigment is in general from 0.05 to 10 % by weight, preferably 0.1 to 5 % by weight, more preferably 0.2 to 3.5 % by weight of the (dry) weight of the non-living material. The amount of the at least one dyestuff is in general from 0.05 to 10 % by weight, preferably 0.1 to 5 % by weight, more preferably 0.2 to 3.5 % by weight of the (dry) weight of the material. The ma¬terial comprises preferably either at least one pigment or at least one dyestuff. Suitable pigments and dyestuffs are mentioned before.
Process for impregnation of a protective material

In a further embodiment, the present invention relates to a process for impregnation of a material, for example a textile material or plastics material, comprising i) forming an aqueous formulation or a melt, wherein an aqueous formulation is pre¬ferred, comprising at least one pesticide and at least one polymeric binder, preferably a polymeric binder as defined above, and optionally further ingredients;
ii) applying the aqueous formulation to the material by
iia) passing the material through the aqueous formulation;
or
iib) bringing the material in contact with a roller that is partly or fully dipped into the
aqueous formulation and drawing the aqueous formulation to the side of the
material in contact with the roller, or
lie) double-side coating of the material or iid) spraying the aqueous formulation onto the material, wherein the spraying is
carried out with any suitable device for spraying by hand or automatically, for
example with an aerosol can or devices usually used in a factory; or
lie) applying the aqueous formulation in fomi of a foam; or
iif) submerging the material into the aqueous formulation; or
iig) brushing the aqueous formulation onto or into the material; or
iih) pouring the aqueous formulation onto the material; or applying the melt by calendaring or with a doctor-blade;
iii) optionally removing surplus aqueous formulation or surplus; and iv) drying and/or curing the material.
In the context of the invention, an aqueous formulation may be a solution, an emulsion or a suspension/dispersion.

The aqueous formulation or the melt preferably comprises the pesticidal composition, which is preferably employed in form of an aqueous formulation.
In the context of the invention "impregnation" is a process for applying the pesticidal com¬position. This process may include a process for curing the applied pestidical composition to achieve a coating onto the material, if desired. An "impregnated material" is a material onto which the pesticidal composition is applied. The "impregnated material" may be coated by curing the applied pesticidal composition, it desired.
The pesticidal composition may also be applied onto the material by transfer printing, Inkjet printing, a screen process, and powder printing.
Details of the application of the pesticidal composition are well known to someone skilled in the art and are disclosed, e.g.. in WO 2005/064072.
The method according to the invention is useful for protecting tobacco, tobacco bales or other tobacco products. It can be used for protecting any kind of tobacco, such as e.g. tobacco produced from Nicotiana rostica and Nicotiana tabacum, specifically dark tobacco, bright tobacco, burley tobacco, shade tobacco and Perique.
The method is useful for protecting, the tobacco from any kind of pests and disease en¬countered in the transport and storage of tobacco, specifically from storage pests, like bugs, beetles and moths, mites, mice and tobacco diseases.
Such pests include:
Cigarette beetle (Lasioderma serricorne), tobacco moth (Ephespha elutella), confused flour beetle (Tribolium confusum), red flour beetle {Tribolium castaneum), saw-toothed grain beetle {Oryzaephilus surinamensis), yellow meal worm (Tenebrio molitor), lesser meal worm (Alphitobius diaperinus), granary weevil (Sitophilus granarius), lesser grain borer (Rhyzopertha dominica), maize weevil (Sitophilus zeamais), rice weevil (Sitophilus oryzae), angoumois grain moth (Sitotroga cerealella), Indian meal moth (Plodia interpunctella), drugstore beetle (Stegobium paniceum), cadelle beetle (Tenebroides mauritanicus), long¬headed flour beetle (Latheticus orizae), dark mealworm (Tenebrio obscurus), denmestid beetles such as: black carpet beetle, larder beetle, wardrobe beetle, odd beetle, hide bee¬tle, warehouse beetle, spider beetles, weevils, especially the bean weevil, grain mite, black

flour beetle, flat grain beetles, fruit flies, vinegar flies, rusty grain beetle, hairy fungus bee¬tle, flat grain beetle, sap beetles, deathwatch beetles, darkling beetles, and fungus beetles.
The method according to the invention is specifically useful for the control of the cigarette beetle (Lasioderma serricorne), and the tobacco moth (Ephespha elutella), the two main pests in tobacco storage.
The methods according to the invention can be applied in all stages and types of tobacco processing, where a storage period is required.
Such processing includes the curing of tobacco after harvesting, specifically the yellowing, leaf drying and stem drying stage.
It includes any type of curing, such as air-curing, sun-curing, fire-curing and, in particular, flue-curing. In the flue-curing, the method can be used in direct-fired systems as indirect fired systems, working, e.g., with heat exchangers.
The method according to the invention is further useful in the fermenting and aging steps of tobacco processing. Depending on the kind and quality of the final tobacco product, these steps range from a couple of days to several years - during which the tobacco has to be protected from pests.
Accordingly, the method according to the invention is useful in the production of any kind of tobacco product for human consumption, such as cigarettes, cigars, pipe tobacco, cigarette tobacco, snuff, chewing tobacco, snuff, gutka and creamy snuff.
The device according to the invention comprises means for spreading out the tobacco leaves, such as a rack or an open framework where sticks of tied leaves or the whole stalk is hung, a material, which has protective activity against harmful organism, and which cov¬ers the tobacco to be protected, and, optionally means for attaching the material to the means for spreading out the tobacco.
The material is preferably a net, because this does not disturb the drying or curing process - which requires an exchange of air, humidity and heat between the tobacco and its envi¬ronment - while it still affords good protection against pests.

Surprisingly, the use of nets leads to a good protection even in the case of fungal diseases.
The invention is further illustrated by the following examples without limiting it thereby.
Examples
1. Binder:
A) Preparation of polymer dispersions
General procedure:
250 g of water and 3 g of a styrene seed (33 % by weight) having a medium particle diame¬ter of 30 nm are heated to 85 "C and 5 % by weight of feed 2 are added. After 10 mIn. addi¬tion of feed 1 comprising the monomers mentioned below and feed 2 is started.
Feed 2 comprises 3.0 g sodiumperoxidsulfate dissolved in 39.9 g of water.
The composition of feed 1 is listed in table 1.
Feed 1 and 2 are added in 3 h, and it was polymerized for further 0.5 h.

Table 1: Composition of feed 1 in % by weight pphm (parts per hundred monomers)

Monomer compositions MMA S AN EHA BA EA HPMA GMA MaMol AMol AM AS FI-1 BMA-Acac
A1 27.0 3.1 65.0 2.0 1.0 1.9
A2 23.9 5.0 5.3 60.0 1.2 0,6 4.0
A3 16.6 30.0 30.0 20.0 3.0 0.4
A4 25.7 5.0 5.3 60.0 3.5 0.5
A5 14.7 11.0 70.0 3.5 0.5 0.3
A6 30.0 13.0 8.0 .45^ 3.0 0.5 0.3
A7 30.0 13.0 8.0 44.5 0.5 0.3 3.7
A8 33.0 60.0 3.9 1.0 0.5 1.6
A9 20.0 20.0 17.0 23.0 15.3 3.5 1.2
A 10 20.0 20.0 17.0 23.0 15.3 0.4 0.3 4.0
All 10.0 10.0 25.5 50.0 2.5 2.0
A 12 10.0 10.0 25.5 47.7 2.5 3.5 0.7 0.1
A 13 10.0 11.0 60.0 ^14.7 4.0 0.2 0.1
A 14 20.0 8.0 55.0 12.5 3.0 1.5
A 15 26.0 13.0 57.0 3.0 1.0
A16 15.0 13.0 68.0 3.0 1.0
A 17 16.0 81.0 2.0 1.0

The amount of initiator sodium peroxidisulfate is 0.3 parts by weight, the emulsifier com¬prises 0,4 parts by weight of Dowfax 2A1 (Dow) und 0.6 parts by weight of Lumiten IRA (BASF AG), relating to 100 parts by weight of the monomer composition of table 1.
Abbreviations:
MMA: methyl methacrylate
S: styrene
AN: acrylic nitril
EA: ethyl acrylate
EHA: 2-ethylhexylacrylate
BA: n-butyl acrylate
Fl: copolymerizable benzophenone having an acrylic group
GMA: glycidy I methacrylate
B^AA-Acac■. bitandiolmonoacvylate acetylacetate
Amol: N-methylol acrylamide
MAMol: N-methylol methacrylamide
HPMA: hydroxypropyl methacrylate
AS: acrylic acid
AM: acrylic amide
Dowfax 2A1:
^25*^12
-SOgNa
Lumiten IRA:
O O

SOgNa
Examples A1 and A8
Aqueous polymer dispersions comprising Fl - 1 polymerizable photo initiator which is later useful as crosslinking agent is a photo initiator of formula

R^

O 0'
o
wherein
R^ IS an organic radical having from 1 to 30 carbon atoms,
R^ is H or a methyl group, and
H^° is a phenyl group which is optionally substituted or a Cr to C4-all I(. Examples of use
a) Preparation of long-lasting insecticidai nets (LLINs)
The insecticidai treatment was performed with aqueous dispersions according to examples A1 - A17 on commercially available white polyester netting material (fiber titer 75 denier, 156 mesh, weight 28-32 g/m^) without prior washing. The aqueous treatment baths were prepared by mixing the aqueous dispersions with commercially available emulsions of in¬secticide and/or repellent, setting pH with buffer solutions and adding a fixative (if needed). The concentrations of the treatment baths were adjusted according to the liquor uptake possible (LU between 60 and 100 %). The treatment baths were applied by using a padder-stenter equipment on a laboratory scale {Mathis AG, Switzerland). The netting material is fully immersed into the treatment bath and excess liquor is removed by passing it through cylinders which move in counter-direction. By choosing a defined distance between these cylinders (and thus a defined pressure) the liquor uptake can be controlled. The liquor up¬take is measured by weighing an impregnated piece of netting and subtracting the weight of the dry, untreated netting and is given as % weight of liquor on weight of netting. The drying/curing step was performed in a laboratory stenter which allows to control the tem¬perature and time of the treatment.
b) Testing Methodologies
Limited Forced Exposure Assay:
Aiphacypermethrin-impregnated long-lasting insecticidai nets (LLINs, 200 mg ai/m^) were cut to fit 150 X 25 mm Petri dishes. LLINs were placed on the bottom of the dishes and 10 adult cigarette beetles, Lasioderma serricome, were introduced into each dish onto the

nets. Beetles were exposed to the nets for 10, 30, or 60 minutes and the nets were then removed. Mortality/knockdown was evaluated at the time of net removal. Ten replicates were performed per treatment.
Behavioral Assay:
Cardboard shipping tubers (457 mm pieces of 76 mm diameter) were covered on one end with aiphacypermethrin-impregnated long-lasting insecticidal net (LLIN, 200 mg ai/m^), which was secured with a rubber band and electrical tape. The end of the tube with the LLIN was attached to a clear plastic cup (76 mm diameter x 89 mm height) with electrical tape filled with 20.0 g of toasted oat cereal to serve as a food source. Ten adutt tobacco moths, Ephestia elutella, (Table 3) or ten adult cigarette beetles, Lasiodeima serricorne, (Table 2) were introduced into the tubes on the opposite end of the LLIN and food source. The opposite (open) end of each tube was then sealed. Location and mortality of the moths/beetles were evaluated at 1 and 2 days (E elutella) or 1 and 4 days (L serricorne) after treatment (DAT). Ten replications were performed per trea^ent with E..elutella and eight replications were performed per treatment with L serricorne-
c) Results
1. Aiphacypermethrin-impregnated long-lasting insecticidal nets (LLlNs) were efficacious against cigarette beetles, resulting in 87% knockdown + mortality after 10 minutes ex¬posure and 100% mortality after 60 minutes exposure in a forced exposure assay (Ta¬ble 1, Figures 1 and 2). Knocked down beetles were un^le to recover:

Table 1 -
Efficacy of alphacypermethrin-impregnated long-iasting insecticidal nets (LLIN) against
cigarette beetles, Lasioderma serricorne. in a limited forced exposure assay



2. LLlNs caused significantly greater mortality ot cigarette beetles (93% at 1 day after treatment (DAT) and 100% at 4 DAT) compared to the untreated net in a behavioral assay where the beetles had to pass through the net to reach a food/light source:
Table 2.
Efficacy of alphacypemiethrin-impregnated long-lasting insecticidal nets (LLIN) against cigarette beetle, Lasioderma semcorne, adults in a behavioral assay



3. LLiNs caused significantly greater mortality of tobacco moths (89 % at 1 DAT and 94 % at 2 DAT) compared to the untreated net in a behavioral assay where the moths had to pass through the net to reach a food/light source. Very few moths able to pass through the untreated net or LLIN, indicating utility of (2 mm x 2 mm) LLINs for use as a physical and chemical barrier for protection of stored tobacco from tobacco moth in¬festations (Table 3, Figure 4):
Table 3.
Efficacy of alphacypermethrin-impregnated long-lasting insecticidal nets (LLIN) against
tobacco moth, Ephestia elutella, adults in a behavioral assay



4. LUNs caused significantly greater mortality of to cigarette beetles compared to the untreated net in a beliavioral assay wfiere the beetles had to pass through the net to reach a food/light source. No beetles were able to pass through the untreated net or LLIN, indicating utility of (1 mm x 1 mm) LLINs at different a.!, levels for use as a physical and chemical barrier for protection of stored tobacco cigarette beetle infesta¬tions (Table 4, Figure 5):






AS ORIGINALLY FILED
Method and Device for Protecting Tobacco
The invention relates to a method of protecting tobacco tbacco bales or other tobacco products Iron harmful organisms during harvesting, drying, curing, transport and storage. The invention further relates to a device for carrying out the method.
Tobacco is a valuable cash crop, and is the most widely grown non-food crop in the world.
After harvesting, the tobacco leaves are subjected to the stages of curing, fermenting and aging as part of the process of producing tobaccos suitable for smoking or chewing by hu¬mans. All of these stages require extended storage periods, in the last case up to several years. During these storage periods, the tobacco leaves have to be protected from pests, specifically from insect pests
Nevertheless, contamination of the tobacco with pesticides has to be avoided to create no additional health hazards for the human consumers.
Currently, a common method of pest control in the storage of tobacco is the use of gaseous pesticides, specifically methyl bromide and phosphin (PH3). However, the use of methyl bromide is not desirable from an ecological point of view as this substance is ozone deplet¬ing. Phosphine, on the other hand, is highly toxic and - if not properly handled - is a poten¬tial health hazard for the workers engaged in the production of tobacco.
Accordingly, there is a continuous demand to provide new methods for protecting tobacco leaves from harmful organisms, while avoiding pesticide residues in the tobacco and health
hazards for the workers.
It has now been found that this demand can be met by providing a method for protecting tobacco from harmful organisms during storage comprising the step of covering the to¬bacco with a material which has a protective activity against the harmful organisms.
WO 2005/064072 discloses a composition for the impregnation of fibers, fabrics and net¬tings imparting a protective activity against pests, however, the use of such a composition for protecting tobacco is not contemplated.

According to the invention, tobacco can be protected from harmful organisms in an easy and efficient way without health hazard to workers and without causing residues of pesti¬cides in the tobacco products.
In a further aspect ot ttie invention there is provided the use of a material which has a pro¬tective activity against harmful organisms for protecting tobacco.
In yet a further aspect of the invention there is provided a device for protecting tobacco from harmful organisms comprising a device for storing the tobacco and a material which has a protective activity against harmful organisms, for covering the tobacco.
The term "tobacco" as used herein means tobacco plants or parts thereof in any stage after and during harvesting, specifically in the stages of curing, fermentation and aging.
The terms "protection" or "protecting" as used herein means a controlling or repelling ac¬tion.
The term "harmful organism" as used herein means pests, specifically arthropod pests, including insects and arachnids, and harmful micro-organisms, specifically fungi including spores, microbes and viruses.
The term "covering" as used herein means that the fabric or netting forms a physical barrier between the tobacco to be protected and the harmful organism, but does not imply that the tobacco is in physical contact with the cover materiat.
The material is preferably a non-rigid material. It is preferably a textile material or plastics material selected from the group consisting of yarn, fibers, fabric, knitgoods, nonwovens, netting material, foils, tarpaulins and coatings. The netting material may be prepared by any method known in the art, for example by circular knitting or warp knitting, or by sewing parts of a netting to obtain the desired nettings.
The textile material or plastics material may be made form a variety of natural and synthetic fibers, also as textile blends in woven or non-woven form, as knit goods, yarns or fibers. Natural fibers are for example cotton, wool, silk or bast fibers, like jute, linen, ramie, hemp and kenaf. Synthetic fibers are for example polyamides, polyesters, polyacryl nitriles, Doly-

olefines, for example polypropylene or polyethylene, Teflon, and mixtures of fibers, for ex¬ample mixtures of synthetic and natural fibers. Polyamides, potyolefins and polyesters are preferred. Polyethylene terephthalate is especially preferred.
The term material also includes non-textile substrates such as coatings, leathers, synthetic adaptions of leather, flocked fabrics, sheetings, foils, perforated foils and packaging male-rial.
Further, the term material includes cellulose-containing materials e.g. cotton materials such as garment or cotton nets and also wooden materials such a& bouses, trees, board fences, or sleepers and also paper.
Preferably, the material is a textile material or plastics material, e.g. polypropylene, poly¬ethylene, polyester or polyamide.
Preferably the textile material is a netting.
Suitable mesh sizes are well known to those skilled In the art and may be chosen in view of the size of the prevailing pests. While the mesh size should be small enough to present an obstacle to the pest it is usually preferred to have an exchange of air and humidity.
Suitable mesh sizes are in the range of 5 x 5 mm, preferably 2.5 x 2.5 mm, more preferred 1.5 X 1.5 mm as an upper limit and 0.1 x 0.1 mm, preferably 0.25 x 0.25 mm, more pre¬ferred 0.5 X 0,5 mm, in particular 0.75 x 0.75 mm as a lower limit. In the case of very small pests a wide-meshed woven fabric may be preferred as a textile material.
More preferred are nettings made from polyester, especially polyethylene terephthalate. In a further preferred embodiment the material is a cellulose containing material.
Preferably, the material is treated with a composition comprising a pesticide, however, the invention is not limited to such embodiments. E.g., the pesticide can also be incorporated into a fiber during the production of the fiber.
Such materials show good results in controlling the pests and provide long lasting protec¬tion to the stored tobacco.

In a preferred embodiment, the pesticide is incorporated into the material (e.g. into the plastics matrix) or applied to the surface of the material or both.
In a most preferred embodiment, the material is treated with a composition comprising;
a) at least one pesticide (component A), and
b) at (east one polymeric binder (component B).
The pesticidal composition comprises in general 0.001 to 95 % by weight preferably 0.1 to 45 % by weight, more preferably 0.5 to 30 % by weight, most preferably 0.5 to 25 % by weight, based on the weight of the composition, of at least one pesticide.
The pesticidal composition preferably comprises the following components, based on the solids content of the composition
a) 0.1 to 45 % by weight, preferably 0.5 to 30% by weight, more preferably 1 to 25 % by weight of at least one pesticide (component A), and
b) 55 to 99 % by weight, preferably 70 to 98 % by weight, more preferably 75 to 90 by weight of at least one polymeric binder (component B),
wherein the sum of the components is 100 % by weight of solids content of the insecticide composition.
In a further preferred embodiment the pesticidal composition comprises the following com¬ponents, based on the solids content of the composition,
a) 20 to 70 % by weight, preferably 25 to 65 % by weight, more preferably 30 to 65 % by
weight of at least one pesticide (component A), and
b) 30 to 80 % by weight, preferably 35 to 75 % by weight, more preferably 35 to 70 by
weight of at least one polymeric binder (component B),
wherein the sum of the components is 100 % by weight of solids content of the pesticidal
composition.
The term "pesticide" as used herein comprises insecticides, repellents and fungicides.
The term "insecticides" as used herein comprises agents with arthropodicidal (specifically, insecticidal, acaricidal and miticidal), molluscicidal and rodenticidal activity, if not otherwise stated in the context.

The term 'lungicides" as used herein comprises agents with fungicidal, microbicidal and viricidai activity, if not otherwise stated in the context.
Preferably, the pesticide is an insecticide or repellent.
The pesticidal composition is particularly suitable for application to polyester nettings as used for mosquito nets.
The pesticidal composition of the present invention may be applied to textile materials or plastics material, before their formation into the desired products, i.e. while still a yarn or in sheet torm, or after formation of the desired products.
Pesticide (component A)
Preferably, the pesticide is an insecticide and/or repellent with a fast paralyzing or l Preferred insecticides and/or repellents are mentioned below:
pyrethroid compounds such as
Etofenprox: 2-(4-ethoxyphenyl)-2-methylpropyl-3-phenoxybenzyl ether,
Chlorfenapyr: 4-bromo-2-(4-chlorophenyl)-1-ethoxymethy(-5-(trifIuoromethyI)pyrrole-3-
carbonitrile,
Fenvalerate: (RS)-alpha-cyano-3-phenoxybenzyl (RS)-2-(4-chlorophenyl)-3 methylbutyrate,
Esfenvalerate: (S)-alpha-cyano-3-phenoxybenzyl (S)-2-{4-chlorophenyl)-3-methylbuty-rate,
Fenpropathrin; (RS)-alpha-cyano-3-phenoxybenzyl 2,2,3,3-tetramethylcyclopropane-
carboxylate,
Cypermethrin: (RS)-alpha-cyano-3-phenoxyben2yl (IRS)-cis, trans-3-(2,2-dichlorovinyl)-
2,2-dimethylcyclopropanecarboxylate,
alpha-Cypermethhn: racemate comprising the (S)-a-(1R) and (R)-a-{lS) diastereomers,
Permethrin: 3-phenoxybenzyl (IRS)-cis, trans-3-(2,2-dichlorovinyl)-2,2-
dimethylcyclopropanecarboxylate,

Cyhalothrin: {RS)-alpha-cyano-3-phenoxybenzyl (Z)-{1RS}-cis-3-{2-chloro-3,3,3-
trifluoroprop-1 -eny[)-2,2-dimethylcyclopro panecarboxylate, lambda-cyhalothrin,
Deltamethrin: (S)-alpha-cyano-3-phenoxybenzyl (lR)-cis-3-(2,2-dibromovinyl)-2,2-
dimethylcyclopropanecarboxylate,
Cycloprothrin: (RS}-alpha-cyano-3-phenoxyb6nzyl (RS)-2,2-dichloro-1-(4-
ethoxyphenyl)cyclopropanecarboxylate,
Fluvalinate: alpha-cyano>3-phenoxybenzyl N-(2-chloro-alpha, alpha, alpha, alpha-trifluoro-p-tolyl)-D-valinate,
Bifenthrin: (2-methylblphenyl-3-ylnnethyl)0(Z)-{1RS)-cis-3-(2-chloro-3,3,3-trifluoro-1-
propenyl)-2,2-dimethylcyclopropanecarboxylate,
2-methyl-2-(4-bromodifluoromethoxyphenyl) propyl (3-phenoxybenzyl)ether, Tralomethrin: (S)-alpha-cyano-3-phenoxybenzyl {1 R-cis)3((1 'RS)(1', 2', 2', 2'-tetrabromoethyl))-2,2-dimethylcyclopropanecarboxylate, Silafluofen: 4-ethoxyphenyl(3-{4-fluoro-3-phenoxyphenyl)propyl}dimethylsilanc, D-tenothrin: 3-phenoxybenzyl {1R)-cis, trans)-chrysanthemate,
Cyphenothrin: CRS)-alpha-cyano-3-phenoxyb6nzyl {1 R-cis, trans)-chrysanthemate, D-
resmethrin: 5-benzyl-3-furylmethyl (1 R-cis, trans)-chrysanthemate,
Acrinathrin: {S)-alpha-cyano-3-phenoxybenzyl (1R-cis(Z))-(2,2-dimethyl-3-(oxo-3-
(1,1,1,3,3,3-hexafluoropropyloxy)propenyl{cyclopropanecarboxylate,
Cyfluthrin: (RS)-alpha-cyano-4-(luoro-3-phenoxybenzyl 3-(2,2-dichlorovinyl)-2.2-
dimethylcyclopropanecarboxylate,
Tefluthrin: 2,3,5,6-tetrafluoro-4-methylbenzyl (IRS-cis {Z))-3-(2-chloro-3,3,3-trifluoro-prop-1-enyl)-2,2-dimethylcyclopropanecarboxylate,
Transfluthrin: 2,3,5,6-tetrafluorobenzyl (1R-trans)-3-(2,2-dichlorovinyl)-2,2-dimettiyl-cyclopropanecarboxylate,
Tetramethrin: 3,4,5,6-tetrahydrophthatimidomethyl (IRS)-cis, trans-chrysanthemate, Aljethrin: (RS)-3-allyl-2-methyl-4-oxocyclopent-2-enyl (IRS)-cis, trans-clirysanthemate, Prailethrin: (S)-2-methyl-4-oxo-3-{2-propynyl)cyclopent-2-enyl (1 R)-cis, trans-chrysanthemate,
Empenthrin: (RS)-1 -ethynyl-2-methy)-2-pentenyI (1 R)-cis,trans-chrysanthemate, Imiprothrin: 2,5-dioxo-3-(prop-2-ynyl)imidazolidin-1-ylmethyl (1R)-cis, trans-2,2-dimethyl-3-(2-methyl-l-prDpenyl)-cyclopropanecarboxylate,
D-flamethrin: 5-(2-propynyl)-furfuryl (1R)-cis, trans-chrysanthemate, and 5-(2-propynyl)furiuryl2,2,3,3-tetramethyicyclopropanecarboxylate; Pyriproxyfen: 4-phenoxyphenyl (RS)-2-(2-pyridyloxy)propyl ether; pyrethrum;

d-d, trans-cyphenothrin: (RS)-a-cyano-3-phenoxybenzyl (1RS,3RS;1RS,?SR)-2,2-dimethyi-
3-(2-methylprop-1-enyl)cyclopropanecarboxyiate;
DDT;.
Carbamate compounds such as
Alanycarb: S-methyl-N[[N-methyl-N-[N-ben2yl-N{2-ethoxy-carbonylethyl)amino-
thio]carbamoyl]thioacetimidate,
Bendiocarb: 2,2-dimethyl-1,3-benzodioxol-4-y!-methylcarbamate),
Carbaryl(1 -naphthyl N-methylcarbamate,
Isoprocarb: 2-(1-methylethyl)phenyl methylcarbamate,
Carbosulfan: 2,3 dihydro-2,2-dimethyl-7-benzofuranyl[(dibutylamino)thio]methyl-carbamate,
Fenoxycarb; Ethyl[2-(4-phenoxyphenoxy)ethyl]carbamate,
Indoxacarb: Methyl-7-chloro-22,3,4',5-tetrahydro-2-[methoxycarbonyl (-4-
trifluoromethoxyphenyl)]
Propoxur: 2-isopropyloxyphenol methylcarbamate,
Pirimicarb: 2-dimethylamino-5,6-dlmethyl-4-pyrimidinyl-dimethylcarbamate,
Thiodiocarb: Dimethyl N,N'(thiobis((mefhy(imino)carbonoyloxy)bisethanimidiothioate).
Methomyl: S-methyl N-((methylcarbamoyl)oxy)thioacetamidate,
Ethiofencarb: 2-((ethyithio)methyl)phenyl methylcarbamate,
Fenothiocarb: S-(4-phenoxybutyl)-N,N-dimethyl thiocarbamate,
Cartap: S,S'-{2-5 d(methy(am(na)trimethylene)bis (thiocarbamate)hydrochlonde,
Fenobucarb: 2-sec-butylphenylmethyl carbamate,
XMC: 3,5-dimethylphenyt-methyl carbamate,
Xylylcarb: 3,4-dlmethy[phenylmethylcarbamate;
organophosphorous compounds such as
Trichlorfon: Phosphoric acid, (2,2,2-trich!oro-1-hydroxyethyl)-, dimethyl ester
Fenitrothion; 0,0-dimethyl 0-(4-nitro-m-tolyl)phosphorothioate,
Diazinon: 0,0-diethyl-0-(2-isopropyl-6-methyl-4-pyrimidinyl)phosphorothioate,
Pyridaphenthion: 0-(1,6-dihydro-6-oxo-1-phenylpyrazidin-3-yi) 0,0-diethyl phosphorothioa-
te,
Pirimiphos-Etyl: 0,O-diethyl 0-(2-(diethylamino)6-methyl-pyrimidinyl)phosphorothioate,
Pirimiphos-Methyl: 0-[2-(diethylamino)-6-melhyl-4 pyrimidinyl] 0,0-dimethyl phosphoro-
thioate,
Etrimphos: 0-6-ethoxy-2-ethyl-pyrimidin-4-yl-0,0-dimethyl-phosphorothioate,

Fenthion: 0,0-dimethyl-0-[-3-methy[-4-(methylthio)pheny( phosphorothioate, Phoxlm: 2-(diethoxyphosphinothoyloxyimino)-2-phenylacetonitrile, Chlorpyrifos: 0,0-diethyi-0-(3,5,6-trichloro-2-pyrinyl)phosphorothioate, Chiorpyriphosmethyl: 0,0-dimethyl 0-(3,5,6-trichloro-2-pyridinyl)phosphorothioate, Cyanophos: 0,0-dimethyl 0-(4 cyanophenyl)phosphDrottiioa1e, Pyradofos: {R,S)[4-ch!orophenyl)-pyrazDl-4-yl]-0-ethyl-S-n-propyl phosphorothioate, Acephate: O, S-dimethyl acetylphosphoroamidothioate,
Azamethiphos: S-(6-chloro-2,3-dihydro-oxo-l,3-oxa2olo[4,5-blpyridine-3-ylmethyl phos¬phorothioate,
Malathion: 0,0-dimethyl phosphorodithloate ester of diethyl mercaptosuccinate, Temephos: (0,0'(thiodi-4-l-phGnylene) 0,0,O,O~tetramethyl phosphorodithloate, Dimethoate: ({0,0-dimethyl S-(n-methylcarbamoylethyl)phosphorodithioate, Formothion: S[2-formylmethylamino]-2-oxoethyl]-0,0-dimethyl phosphorodithioate, Phenthoate: 0,0-dimethyl S-(alpha-ethoxycarbonylbenzal)-phosphorodithioate; lodofenphos: 0-(2,5-dichloro-4-iodophenyl)-0,0-dimethyl-phosphorthioate.
Insecticides with a sterilising effect on adult mosquitoes such as
1-(alfa-(chloro-alpha-cyclopropylben2ylidenamino-oxy)-p-tolyl)-3-{2,6-difluorobenzoyl)urea,
Diflubenzuron: N-(((3,5-dichloro-4-(1,1,2,2-tetra{louroethoxy)phenylamino)carbonyl)2,6 di-
tluoro benzamid,
Triflumuron; 2-Chloro-N-(((4-(trifluoromethoxy)phenyl}-amino-)carbonyl)benzamide, or a
triazin such as N-cyclopropyl-1,3,5-triazine-2,4,6-triamin; and
Lambda-cyhaloth rine:
a^cyano-3-phenoxybenzyl-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropane carboxylate, as a 1:1 mixture of {Z)-{1R,3R), R-esterand (Z)-{1S,3S), S-ester.
The repellent is preferably selected from N,N-Diethyl-meta-toluamide (DEET), N,N-diethylphenylacetamidG (DEPA), 1-(3-cyclohexan-1-yl-carbonyl)-2-methylpip6rine, (2-hydroxymethylcyclohexyl) acetic acid lactone, 2-ethyl-1,3-hexandiol, indalone, Methyl-neodecanamide (MNDA), a pyrethroid not used for insect control such as {(+/-)-3-allyl-2-melhy)-4-oxocyclopent-2-{+)-enyl-(+)-trans-chfysantemate (Esbiothrin), a repellent derived from or identical with plant extracts like limonene, eugenol, (+)-Eucamalol (1), {-)-1-epi-eucamalol or crude plant extracts from plants like Eucalyptus maculata, Vitex rotundifolia, Cymbopogan martinii, Cymbopogan citratus (lemon grass), Cymopogan nartdus (citro-

nella), IR3535 (ethyl butylacetylaminopropionate), icaridin (1-piperidinecarboxylic acid 2-(2-hydroxyethyl)-1-methylpropylester).
A suitable molluscicide is for example niclosamide.
Suitable rodenticides are first generation anticoagulant rodenticides and second generation anticoagulant rodenticides, where second generation rodenticides are preferred. Examples for first generation anticoagulant rodenticides are warfarin, chlorphacinone, coumatetralyt, suitable second generation anticoagulant rodenticides are for example flocoumafen, brodi-facoum, difenacoum, bromadialone, difethialone, and bromethalin.
Suitable fungicides are for example
Azofes sucfi as Bitertanol, Bromoconazole, Cyproconazole, Difenoconazole, Oinitrocona-
zole, Epoxiconazole, Fenbuconazole, Fluquiconazole, Flusilazole, Flutriatol, Hexacona-
zole, Imazalil, Ipconazole, Metconazole, Myclobutanil, Penconazole, Rropiconazole,
Prochloraz, Prothioconazole, Simeconazole, Tebuconazole Tetraconazol, Triadimefon,
Triadimenol, Triflumizol, Triticonazol;
Strofailurines such as Azoxystrobin, Dimoxystrobin, Ruoxastrobin, KresoJtim-methyl. Me-
tominostrobin, Orysastrobin, Picoxystrobin, Pyraclostrobin and Trifloxystrobin;
Acylalanines such as Benalaxyl, Metalaxyl, Mefenoxam, Ofurace, Oxadixyl;
Aminderivatives such as Aldimorph, Dodine, Dodemorph, Fenpropimorph, Fenpropidin,
Guazatine, Iminoctadine, Spiroxamin, Tridemoiph;
Anilinopyrimidines such as Pyrimethanil, Mepanipyrim, Cyprodinil;
Dicarboximide such as Iprodion, Myclozolin, Procymidon, Vinciozolin;
Cinnamic amides and derivatives such as Dimethomorph, Flumetover, Flumorph;
Antibiotics as Cycloheximide, Griseofulvin, Kasugamycin, Natamycin, Polyoxin,
Streptomycine;
Dithiocarbamates such as Ferbam, Nabam, f\flaneb, Mancozeb, Metam, Metiram,
Propineb, Polycarbamat, Thiram, Ziram Zineb;
Heterocyclic compounds such as Aniiazin, Benomyl, Boscalid, Carbendazim, Carboxin,
Oxycarboxin, Cyazofamid, Dazomet, Dithianon, Famoxadon, Fenamidon, Fenarimol,
Fuberidazol, Flutolanil, Furametpyr, Isoprothiolan, f^epronil, Nuarimol, Picobenzamid,
Probenazol, Proquinazid, Pyrifenox, Pyroquilon, Quinoxyfen, Silthioiam, Thiabendazol,
Thifluzamid, Thiophanat-methyl. Tiadinil, Tricyclazol, Triforine M Anorganika;
Nitrophenylderivatives such as Binapacryl, Dinocap, Dinobuton, Nitrophthal-isopropyt;
Phenylpyrroles such as Fenpiclonil, Fludioxonil;

Derivatives of sulfenic acid such as Captafol, Captan, Dichloffuanid, Folpet, Tolyifluanid; Other fungicides such as Acibenzolar-S-methyl, Benthiavalicarb, Carpropamid, Chlorofhalonil, Cyflufenamid, Cymoxanil, Dazomet, Diclomezin, Diclocymet, Diclofluanid, Diethofencarb, Edifenphos, Ethaboxam, Fenhexamid, Fentin-Acetat, Fenoxanil, Ferimzone, Fluazinam, Fosetyl, Fosetyl-Alumintum, Phosphoric Acid, Iprovalicarb, Hexachlorbenzene, Metrafenon, Pencycuron, Propamocarb, Phthaiid, Toloclofos- methyl, Quintozene, Zoxamid.
In a further preferred embodiment, the pesticide is at least one N-aryihydrazine derivative, preferably of formula I,


(I)

wherein
A is C-R^ or N;
B is C-R^ or N;

D is C-R" or N;
with the proviso that at least one of A, B or D must be other than N;
Z is halogen, CN, NOa, C-Ce-alkyl, C-Ce-haloalkyl, Ci-Ce-alkoxy or Ci-Cg-haloalkoxy;
n is an integer of 0, 1 or 2;
Qis
NR^R' X^
R . R
R^
or N^O R
wherein Ris
hydrogen;
C,-Cio-alkyl, optionally substituted with one or more halogens; Cs-Ce-cycloalkyI; C1-C4-alkoxy; CrC4-haloalkoxy; (Ci-C4-alkyl)S0,; {Ci-C4-haloalkyl)SO,; phenyl, optionally substi¬tuted with one to three halogen, Ci-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy, C,-C4-haloalkoxy, (Ci-C4-alkyl)S0x, {C,-C4-haloalkyl)SOx, NOg or ON groups; phenoxy, optionally substituted with one to three halogen, C,-C4-alkyl, Ci-C4-haloalkyl, Ci-C4-alkoxy, 0,-04-haloalkoxy, (Ci-C4-alkyl)S0„ (C,-C4-haloalkyl)SOx, NOj or CN groups;

C3-C,2-cyc(oa(kyl, optionally substituted with one or more halogens, Ci-C6-alkyl, Ci-Cg-
haloalkyi, CrC^-alkoxy. Ci-Ca-haloalkoxy, (CrC4-alkyl)S0„ (CI-C4-haloalkyl)SOx; phenyl,
optionally substituted with one to three halogen, CrC4-alkyl, Ci-C4-haloa!ky(, Ci-Ci-alkoxy,
C,-C4-haloalkoxy, NOj or CN groups; phenoxy, optionally substituted with one to three
halogen, CrC4-alkyl, C-C^-haloalkyl, C,-C4-alkoxy, Ci-C^-haloalkoxy, NOgorCN groups;
or
phenyl, optionally substituted with one or more halogens, d-C^-alkyl, CrC^-haloalkyl, C|-
C4-alkoxy, Ci-C4-haloaikoxy, N02 or CN groups;
or
R" and R'^ are each independently CrCe-alkyl, Ca-Cg-alkenyl, Ca-Cg-alkynyl, or C3-C6-
cycloalkyl which may be substituted with 1 to 3 halogen atoms;
R^^ is hydrogen or Ci-Ce-alkyI;
R^ and R^ are each independently hydrogen or Ci-Ci-alkyI;
R^ and R^ are each independently
hydrogen;
Ci-Cio-alkyl, optionally substituted with one or more halogen, hydroxy, Ci-C4-alkoxy, (C,-
C4-alkyl}S0„ CONR^R^, CO^R'", R", R'^;
C3-Cio-alkenyl, optionally substituted with one or more halogen, hydroxy, Ci-C4-alkoxy, (Ci-
C4-alky()S0„, CONR^R^ COaR'", R", R'^;
Ca-Cio-alkynyl, optionally substituted with one or more halogen, hydroxy, Ci-C4-alkoxy, (C,-
C4-alkyl)S0„ CONR^R^ CO^R'", R^\ R^';
C3-Ci2-cycloalkyl, optionally substituted with one or more halogen, hydroxy, C,'C4-alkoxy,
(CrC,-alkyl)SO„ CONR^R^ CO^R'", R", R^^-
Cs-Ce-cycloalkyI, optionally substituted with one to three halogen, C,-C4-alkyl, C1-C4-
haloalkyl, CrC^-alkoxy, CrC4-haloalkoxy, NO? or CN groups;
phenyl, optionally substituted with one or more halogen, Ci-C4-alkyl, Ci-C4-haioalkyl, C1-C4-
alkoxy, CrCa-haloalkoxy, NO? or CN groups;
pyridyl, optionally substituted with one or more halogen, Ci-C4-alkyl, Ci-Ca-haloalkyI, C1-C4-
alkoxy, CrCa-haloalkoxy, NO2 or CN groups;
R^ and R^ may be taken together to form a ring represented by the structure

R^ R^ and R" are each independently hydrogen, halogen, CN, NOg, (Ci-C4-alkyI)S0x, (C,-C4-haloalkyl)SOx, C,-C6-aikyl, CrCe-haloaikyl, Ci-C6-alkoxy or Ci-Ce-haloalkoxy; R®, R^ aad R'" are each independently hydrogen or Ci-C4-alkyl; R'^sMR'^R'",

\CH,)/\_ \CH,)/-'
N, .X. CH, .X,
or

R'^is
,16
-R'
jry
N
R'^, R'', R'^ and R'^ are each independently hydrogen or Ci-C4-alkyl;
XisO, SorNR^^
X' is chlorine, bromine or fluorine;
r is an integer of 0 or 1;
p and m are each independently an integer of 0, 1, 2 or 3, with the proviso that only one of
p, m or r can be 0 and with the further proviso that the sum of p + m + r must be 4, 5 or 6;
X is an integer of 0, 1 or 2; or
the enantiomers or the salts thereof.
In a preferred embodiment Q in fomiula I is
NR^R^
R More preferably, the least one N-arylhydrazine derivative is a compound of formula la

wherein
R^ is chlorine or thfluoromethyl;
Z^ and Z^ are each independently chlorine or bromine;

R^ is Ci-Cs-alkyI, Ca-Ce-alkenyl, Cg-Ce-alkynyl, or Ca-Ce-cycioalkyl which may be substituted
witti 1 to 3 halogen atoms, or C2-C4-alkyl which is substituted by Ci-C4-alkoxy;
R"' and R^^ are each independently Ci-Ce-alkyl, Ca-Cg-alkenyl, Cg-Ce-alkynyl, or Cj-Ce-
cycloalkyl which may be substituted with 1 to 3 halogen atoms;
R'^ is hydrogen or d-Cs-alkyl;
or enantiomers or salts thereof.
In the definition of formula I and formula la shown above, the substituents have the follow¬ing meanings:
"Halogen" will be taken to mean fluoro, chloro, bromo and iodo.
The term "alkyl" as used herein refers to a branched or unbranched saturated hydrocarbon group having 1 to 4 or 6 carbon atoms, especially Ci-C6-alkyl such as methyl, ethyj, propyl, 1 -methyfethyl, butyl, 1 -methylpropyl, 2-methy(propyl, 1,1 -dimethylethyl, pentyl, 1 -methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, hexyl, 1,1-dimethylpropyi, 1,2-dimethylpropyl, t-methylpentyl, 2-methy(pentyl, 3-methylpenty(, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethyfbutyl, 1,1,2-trtmethylpropyl, 1,2,2-tri methyl propyl, 1-ethyl-l-methylpropyi and 1-ethyl-2-methylpropyl.
"Alkoxy" refers to a straight-chain or branched alkyl group having 1 to 4 carbon atoms (methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyi, 1,1-dimethylethyl) bonded through an oxygen linkage, at any bond in the alkyl group. Examples include methoxy, ethoxy, propoxy, and isopropoxy.
"Cycloalkyl" refers to a monocyclic 3- to 6-membered saturated carbon atom ring, i.e. cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
With respect to the intended use of the compounds of formula 1, particular preference is given to the following meanings of the substituents, in each case on their own or in combi¬nation:
Preference is given to compounds of formula I wherein R* is trifluoromethyl.
Preference is further given to compounds of formula I wherein Z^ and Z^ are both chlorine.

Moreover, preferred are compounds of formula I wherein R^ is CrCe-alkyI, especially ethyl. Preference is further given to compounds of formula I wherein R^^ and R'* are both methyl.
Moreover, preferred are compounds of formula I wherein R^' and R'^ form a cyclopropyl
ring which is unsubstituted or substituted by 1 to 3 halogen atoms, especially chlorine and bromine.
Moreover, particularly preferred are compounds of formula I wherein R^^ and R^^ form a cyclopropyl ring which is substituted by 2 halogen atoms.
Moreover, particularly preferred are compounds of formula I wherein R^^ and R'^ form a cyclopropyl ring which is substituted by 2 chlorine atoms.
Particularly preferred are compounds of formula I wherein R" and R'^ form a 2,2-dichlorocyclopropyl ring.
Preference is further given to compounds of formula I wherein R'^ is Ci-Ce alkyl, especially methyl.
Particularly preferred are compounds of formula I wherein R^^, R'^ and R'^ are all methyl.
Moreover, particularly preferred are compounds of formula I wherein R'^, R'° and R'^ form a moiety 1-methyl-2,2-dlchlorocyclopropyl.
Preference is further given to compounds of formula I wherein
R"* is trifluoromethyl;
Z' and Z^ are each independently chlorine or bromine;
R^isCrCe-alkyl;
R" and R'^ are CrCe-alkyl or may be taken together to fonn Ca-Ce-cydoalkyl which is
substituted by 1 to 2 halogen atoms;
R^^ is C-Ce-alkyI;
or the enantiomers or salts thereof.

Particular preference is given to N-ethyl-2,2-dimethylproptonamide-2-(2,6-dichloro-a,a,a-trifiuoro-p-tolyl)hydrazone and N-ethyl-2,2-dichIoro-1-methylcyclopropane-carboxamide, 2-{2,6-dichloro-a,a ,a -trif|uoro-p-tolyl)hydrazone.
Furthermore, particular preference with respect to the use in the present invention is given to the compound of formula la-1 (N-ethyl-2,2-dimethylpropionamide-2-{2,6-dichloro-a,a,a -tnftuorQ-p-tolyl)-hydrazone):


•^3^ CH,
(la-l)

Moreover, particular preference with respect to the use in the present invention is given to the compound of formula ia-2 (N-Ethyl-2,2-dichloro-1-methylcyclo-propanecarboxamide-2-
(2,6-dichlorq-a,a,a -tri-fluoro-p-toiyl)hydrazone):


CI CI C!
(la-ll)

With respect to their use, particular preference is given to the compounds la-A compiled in the tables below. Moreover, the groups mentioned for a substituent in the tables are on their own, independently of the combination in which they are mentioned, a particularly pre¬ferred embodiment of the substituent in question.
With respect to their use, particular preference is also given to the hydrochloric acid, maieic acid, dimaleic acid, fumaric acid, difumaric acid, methane sulfenic acid, methane sulfonic acid, and succinic acid adducts of the compounds of the tables below.


(la-A)

Table A
No. R^ R" Rl« R19 Z' z=
A-1 CH3 2,2-dichlorocyclopropvl H CI CI
A-2 CH3 2,2-dibromocvclopro 3Vl H CI CI
A-3 CH3 CH3 CH3 CH3 CI CI
A-4 CH3 Cn2Crl3 CHa CH3 CI CI
A-5 CH3 2,2-dichlorocyclopropvl CHa CI CI
A-6 CH3 2,2-dibromocvclopropvl CH3 CI CI
A-7 CH3 2,2-dichlorocyclopropvl H Br Br
A-8 CH3 2,2-dibromocvclopro pyl H Br Br
A-9 CH3 CH3 CH3 CHa Br Br
A-10 CH3 Cn2Cn3 CH3 CHa Br Br
A-11 CHa 2,2-dichlo rocyclop ropyl CH3 Br Br
A-12 CH3 2,2-dibromocvclopropvl CH3 Br Br
A-13 CH2CH3 2,2-dichlorocyclopropvl H CI CI
A-M Cn2Crl3 2,2-dibromocyclopro pyl H C\ cA-15 CHjCHs CH3 CH3 CHa CI CI
A-16 CH2CH3 CH2CH3 CH3 CH3 CI CI
A-17 CH2CH3 2,2-dichlorocvclop ropyl CH3 CI CI
A-18 CH2CH3 2,2-dib romocyclopropyl CH3 CI CI
A-19 CH2CH3 2,2-dichlorocyclop ropyl H Br Br
A-20 CH2CH3 2,2-dibromocyclop ro pyl H Br Br
A-21 CH£CH3 CH3 CH3 CHa Br Br
A-22 CHgCHs Cn2CH3 CH3 CH3 Br Br
A-23 CHjCHs 2,2-dichlorocvclopropvl CH3 Br Br
A-24 CrljCrlg 2,2-dibromocyclopropvl CH3 Br Br
A-25 CH2CH2CH3 2,2-dichlorocyclopropyl H CI CI
A-26 CH2Cn2CH3 2,2-dibromocycloprc ipyl H CI CI
A-27 CH2CH2CH3 CH3 CH3 CH3 CI CI
A-28 CH2CH2CH3 CH2CH3 CH3 CH3 CI CI

No. R^ R^^ RI8 p19 Z' Z^
A-29 CH2CH5CH3 2,2-dichlorocyclopropvl CHa CI 1 CI
A-30 CHgCHgCHs 2,2-dibromocyclopropyl CH3 CI CI
A-31 OH2Cr1pCH3 2,2-dichlorocyclopropvl H Br Br
A-32 CHgCH^CHs 2,2-dibromocvclopropvl H Br Br
A-33 CH2Cn?Cn3 CH3 CH3 CH3 Br Br
Preferred insecticides and/or repellents of the pesticidal composition of the invention may be either one or a mixture. Preferred mixtures of pesticides are mixtures of insecticides and/or repellents with similar diffusion/migration properties. This group of insecticides and/or repellents may include synthetic pyrethroids such as alphacypermethrin, cyfluthrin, deltamethrin, etofenprox and permethrin, other pyrethroids such as bifenthrine, and non-pyrethroids such as carbosulphane.
The pesticide can also be included in the pesticidal composition as one of a water-based pesticide concentrate or a solvent, preferably an organic solvent, based pesticide concen¬trate or a concentrate based on a mixture of water and a solvent, preferably an organic solvent. Water-based concentrates may be in the form of suspensions or dispersions com¬prising suitable dispersing agents if necessary or in the form of emulsions comprising emulsifiers, solvents and co-solvents if appropriate. Nanoparticular pesticidal formulations may be obtained by dissolving solid solutions of pesticidal in a polar organic solvent, e.g. poly vinyl pyrrolidone (PVP). The concentration of the pesticide in the water based or sol¬vent based concentrates is in general between 0.5 to 60 %, preferably 1 to 40 %, more preferably 3 to 20 %.
The particle size of the pesticide in water-based suspensions or dispersions is in general between 50 nm to 20 fjm, preferably 50 nm to 8 pm, more preferably 50 nm to 4 pm, most preferably 50 nm to 500 nm, or 1 pm to 3 pm.
Polymeric binder (component B)
The polymeric binder (component B) may be any polymeric binder known in the art. Espe¬cially preferred are polymeric binders used in the area of impregnating or coating textile materials or plastics materials.

Preferred binders are for example binders obtainable by polymerization, preferably radical polymerization, of at least one ethylenically unsaturated monomer selected from the group consisting of acrylates, preferably CrCi2-esters of acrylic acid or acrylates having crosslinked ester functionalities, methacrylates, preferably Ci-Ci2-esters of methacrylic acid or methacrylates having crosslinked ester functionalities, acrylic acid, methacrylic acid, acrylonitrile, maleic acid, maleic acid anhydride, mono or diesters of maleic acid, styrene, derivatives of styrene such as methyl styrene, butadiene, vinyl acetate, vinyl alcohol, ethyl¬ene, propylene, allylic alcohol, vinyl pyrrolidone, vinyl chloride and vinyl dichloride.
The polymerization, preferably radical polymerization, may be carried out for example as bulk polymerization, gas phase polymerization, solvent polymerization, emulsion polymeri¬zation or suspension polymerization.
The conditions and further necessary and suitable components for the preparation of suit¬able polymers by polymerization, preferably radical polymerization, of the monomers men¬tioned above are known by a person skilled in the art.
Suitable polymeric binders obtained by polymerization, preferably radical polymerization, of the above-mentioned monomers are homopolymers or copolymers, preferably selected from the group consisting of polyacrylates, poly methacrylates, polyacrylonitrlle, polymaleic acid anhydride, polystyrene, po[y{methyl)styrene, polybutadiene, polyvinylacetate, polyvi-nylalcohol as well as copolymers obtained by polymerization of at least two different ethylenically unsaturated monomers of the group of monomers mentioned above and blends of said homopolymers and/or copolymers, for example poly{styrene-acrylates), poly(styrene-butadiene), ethylene-acrylate-copolymers, ethylene-vinylacetate-copolymers, which may be partially or completely hydrolyzed.
Further suitable polymeric binders are selected from polyurethanes and/or polyiso-
cyanurates, blends comprising polyurethanes and/or polyisocyanu rates, preferable blends
comprising polyurethanes and/or polyisocyan urates and polycarbonates;
mineral waxes, zirconium waxes, silicones, polysiloxanes, fluorinated polyacrylates and
methacrylates, fluorosilicones, and
fluorocarbon resins (as disclosed e.g. in WO 01/37662 and WO 92/16103);
melamine formaldehyde condensation resins, methylol urea derivatives; and
curable polyesters;
or

blends or preparations comprising at least one of said polymeric binders.
The polymeric binders mentioned above are known in the art and are either commercially available or can be prepared by preparation processes known in the art.
Further suitable polymeric binders are polyvinytacetates in a formulation comprising a thickener like carboxymethyl cellulose and optionally a cross linking agent like a melamine resin; curable polyesters; formulations comprising reactive silicones (organic polysilox-anes), polyvinyl alcohol, polyvinyl acetate or an acrylic copolymer.
The crosslinking may be carried out thermally or by UV-light or by the dual cure technique. Optionally, a catalyst or a crosslinking agent may be used together with the polymeric
binder.
Preferred polymeric binders are selected from the group consisting of acrylic binders and polyurethane and/or polyisocyanurate binders.
Most preferred polymeric binders are acrylic binders, which are optionally fluorinated. Es¬pecially preferred acrylic binders are mentioned below (component B1).
Acrylic binders (Component B1)
Most preferred are actylic binders, which may be hompolymers or copolymers, wherein the copolymers are preferred.
The acrylic binders are preferably obtained by radical polymerization, more preferably radi¬cal emulsion polymerization, of at least one monomer of formula II as component Bl A

^ on
H'

wherein
R^°, R^' and R^^ are independently selected from Ci- to Cio-alkyl, which is optionally fluoro substituted and which may be linear or branched, for example methyl, ethyl, n-propyl. i-propyl. n-butyl, i-butyl, sec-butyl, t-butyl, n-pentyl, l-pentyl, sec-pentyl, neo-pentyl, 1,2-

dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, preferably Cr to C4-alkyl, for example methyl, ethyl, n-propyl, i-propyl, ri-butyi, i-butyl, sec-butyl, tert-butyl; substituted or unsubstituted aryl, preferably substituted or un¬substituted Cg- to C,o-aryt, more preferably substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;
R'" and R^' may further be H.
Preferably R^" Is H or methyl. R^' is preferably H; R^^ is preferably methyl, ethyl, n-butyl or 2-ethylhexyl.
More preferably R^°is H or methyl, R^' is H and R^ is methyl, ethyl, n-butyl or 2-ethylhexyl.
Most preferably the monomer of formula II (component BA) is selected from the group con¬sisting of 2-ethylhexylacrylate, n-butylacrylate, methylacrylate, methyl methacrylate and ethylacrylate. Most preferably a copolymer obtainable by polymerization of at least two dif¬ferent acrylic monomers of formula II is employed.
Most preferably an acrylic binder is used as component B obtainable by emulsion polym¬erization of b1 a) at least one monomer of formula II as component B1A

°.
R% VOR^'

\ (II)
wherein
R^", R^' and R^^ are independently selected from Ci- to Cio-alkyl which may be linear OT branched, for example methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, preferably Ci- to Cd-alkyI, for example methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl; substituted or unsubstituted aryl, preferably substituted or unsubstituted Cg-to C,o-aryl, more preferably substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;

R^° and R^' may further be H.
Preferably R^° is H or methyl. R^' is preferably H; R^^ is preferably methyl, ethyl, n-butyl or 2-ethylhexyl.
More preferably R^" is H or methyl, R^' is H and R^^ is methyl, ethyl, n-butyl or 2-ethylhexyl;
b1 b) at least one monomer of formula III as component B1B
(111)
wherein
R^^, R^', R^^and R^ are independently selected from the group consisting of H, Ci¬te Cio-a!kyl which may be linear or branched, for example, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyi and n-decyl; preferably R^^, R^', R^^ and R^ are selected from the group consisting of H, Ci- to C4-alkyl, which may be linear or branched, for example methyl, ethyl, n-propyl, iso-propyl, n-butyl, i-butyl, sec-butyl and tert-butyl; substituted or un-substituted aryl, preferably substituted or unsubstituted Ce- to do-aryl, more prefera¬bly substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;
more preferably R^^ is H or methyl, R^", R^^ and R^ are preferably H;
most preferably R^^ is H or methyl and R^*, R^^ and R^^ are H;
bic) optionally at least one monomer of formula IV as component B1C



(IV)
wherein
R^' and R^^ are independently selected Irom the group consisting of H, C,- to C,o-alkyl which may be linear or branched, for example, methyi, ethyl, n-propyl, i-propyi, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyi, i-amyl, n-hexyl, i-hexyl, sec-hexyi, n-heptyl, n-octyi, 2-ethylhexyl, n-nonyi and n-decyl; preferably R" and R^' are selected from the group consisting of H, C,- to C4-alkyl, which may be linear or branched, for example methyl, ethyl, n-propyl, iso-propyl, n-butyt, i-butyl, sec-butyl and tert-butyl; substituted or unsubstituted aryl, preferably substituted or unsubstituted Cg- to Cio-aryl, more preferably substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;
most preferably R^' and R^^ are H;
X is selected from the group consisting of H, OH, NH2, OR^^OH, glycidyl, hydroxypro-
pyf,
—O
V
■0
V
groups of the fomiula
OR^
-°vA^o
O
wherein
R^ is selected from the group consisting of C,- to Cio-alkyl which may be branched or linear, for example meUiyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyi, n-octyt, 2-ethy(hexyl, n-nonyl, n-decyl; preferably Cr to C4-alkyl, which may be branched or linear, for example methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyt and tert-butyl; substituted or unsubstituted aryl.

preferably substituted or unsubstitutir-' Cg- to Cio-aryl, more preferably substituted or unsubstituted Ce-aryl, for example phenyl or tolyl;
R^^ is selected from the group consisting of Cr to Cio-alkylene, for example methyl¬ene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, non-ylene, decylene; preferably C,- to C4-alkylene, for example methylene, ethylene, pro¬pylene, butylenes; substituted or unsubstituted arylenes, preferably substituted or un¬substituted Cg- to Co-arylene, more preferably substituted or unsubstituted Ce-arylene, for example phenylene; most preferably X ist acetoacetyl;
bid) further monomers which are copolymerizable with the monomers mentioned above
selected from
bidl) polar monomers, preferably (meth)acrylic nitrlle and/or methyl{metti)acrylate as component B1D1; and/or
b1d2) non polar monomers, preferably styrene and/or a-methylstyrene as compo¬nent B1D2.
The acrylic binder is preferably obtainable by emulsion polymerization of
b1 a) 10 to 95 % by weight, preferably 30 to 95 % by weight, more preferably 50 to 90 % by
weight of component 81 A; bib) 1 to 5 % by weight of component BIB; bic) 0 to 5 % by weight, preferably 1 to 4 % by weight, more preferably 0.2 to 3% by
weight of component B1C;
bid) further monomers which are copolymerizable with the monomers mentioned above
selected from
bidl) 0 to 30 % by weight, preferably 0 to 25 % by weight, more preferably 5 to
20 % by weight of component B1D1; and/or
bld2) 0 to 40 % by weight, preferably 0 to 30 % by weight, more preferably 5 to
20 % by weight of component B1D2; wherein the sum of the components B1A, BIB and optionally BIC and BID is 100 % by weight.
In a further preferred embodiment the acrylic binder is obtainable by emulsion polymeriza¬tion of

bla) 10 to 95 % by weight, preferably 30 to 95 % by weight, more preferably 50 to 90 by weight of at least one acrylic binder (component B1 A) as defined above, comprising; bla]) 10 to 90% by weight, preferably 15 to 85% by weight, more preferably 30 to
85% by weight based on the acrylic binder of n-butyl acrylate; b1a2) 10 to 90% by weight, preferably 12 to 85% by weight, more preferably 15 to 65% by weight based on the acrylic binder of at least one monomer of formula II, different from n-butyl acrylate; bib) 1 to 5 % by weight based on the acrylic binder of at least one monomer of formula III
(component BIB); bic) 0 to 5 % by weight, preferably 0.1 to 4 % by weight, more preferably 0.2 to 3% by weight based on the acrylic binder of at least one monomer of formula III (component BIC); bid) further monomers which are copolymerizable with the monomers mentioned (com¬ponent BID) above selected from
b1d1) 0 to 30 % by weight, preferably 0 to 25 % by weight, more preferably 5 to 20 % by weight based on the acrylic binder of at least one polar mono¬mer, preferably (meth)acrylic nitrile and/or methyl(meth)acrylate (compo-r^ent 8101); and/or b1d2) 0 to 40 % by weight, preferably 0 to 30 % by weight, more preferably 5 to 20 % by weight based on the acrylic binder of at least one non polar monomer, preferably styrene and/or a-methylstyrene (component B1D2);
wherein the sum of the components B1A, BIB and optionally BIC and BID is 100 % by weight.
The acrylic binder may comprise further additives as known by a person skilled in the art, for example film forming agents and plasticizers, e.g. adipate, phlhalate, butyl diglycol, mix¬tures of diesters preparable by reaction of dicarboxyiic acids and alcohols which may be linear or branched. Suitable dicarboxyiic acids and alcohols are known by a person skilled in the art.
The insecticide compositions comprising the binder as claimed in the present invention are wash resistant while permitting continuous release of the insecticide at a controlled rate, in order to provide the required bioavailability of the insecticide. It is not necessary to add for example a dispersing agent that, after application of the composition to a fabric and upon wetting of the fabric, reduces the hydrophobicity imparted to the insecticide by the binder to

permit limited insecticide release. Preferably, the insecticide composition of the present invention does therefore not comprise a dispersing agent in addition to the polymeric binder.
Most preferably the acrylic binder is obtainable by emulsion polymerization of the following
components:
bla) 50 to 90 % by weight of at least one monomer of formula II as component B1A
^= wherein
R™ is H or methyl, R^^ is H and R^^ is methyl, ethyl, n-butyl, or 2-ethylhexyl, as com¬ponent B1A, most preferably component B1A is 2-ethylhexylacrylate, n-butylacrylate, methylacrylate, methylmethacrylate or ethylacrylate; bib) 1 to 5% by weight of at least one monomer of formula III
O^ V-OH
\ no
R^^
(III)
wherein R^^ is H or methyl, R^^ R" and R^^ each are H as component BIB;
bic) 1 to 10 % by weight, preferably 1 to 7 % by weight, more preferably 2 to 5 % by
weight of at least one monomer of formula IV
O.

(IV)
wherein R" and R^^ are H and X is H, OH, NHE, OR^^OH, glycldyl or a group of the formula

OR^
—o
o o
wherein
R^ is selected from the group consisting of C,- to Cio-alKyl which may be branched or linear, for example methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyi, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyi, 2-ethylhexyl, n-nonyl, n-decyl; preferably Ci- to C4-alkyl, which may be branched or linear, for example methyl, ethyl, n-propyt, iso-propyl, n-butyl, iso-butyl, sec-butyl and tert-butyl; substituted or unsubstituted aryl, preferably substituted or unsubstituted Ce- to Cjo-aryl, more preferably substituted or unsubstituted Ce-aryl, for example phenyl or tolyl;

R^^ is selected from the group consisting of d- to C,o-afkylene, for example methyl¬ene, ethylene, propylene, butylene, pentylene, hexylene, heptylene, octylene, non-y)ene, decylene; preferably C,- to C4-alkyIene, for example methylene, ethylene, pro¬pylene, butylenes; substituted or unsubstituted arylenes, preferably substituted or un¬substituted Ce- to Cio-arylene, more preferably substituted or unsubstituted Gg-arylene, for example phenylene;
as component BIC, most preferably X is acetoacetyl;

bid) further monomers which are copolymerizable with the monomers mentioned above selected from
b1d1) 0 to 30 % by weight, preferably 0 to 25 % by weight, more preferably 5 to 20 % by weight of component B1D1, preferably (meth)acrylic nitrile and/or methyt{meth)acrylate; and/or
bld2) 0 to 40 % by weight, preferably 0 to 30 % by weigtit, more preferably 5 to
20 % by weight of component BD2, preferably styrene and/or a-methylstyrene; wherein the sum of components BA, BB and optionally BC and BD is 100 % by weight.

In a further most preferred embodiment the amount of n-butylacrylate as component BA is from 30 to 90 % by weight, and the other components BIB and optionally a further mono-

mer of formula 11 (component B1A), B1C and BID are chosen as mentioned before, wherein the sum of components BIA, BIB and optionally BIG and BID is 100 % by weight.
The acrylic binder of the present invention is preferably obtainable by emulsion polymeriza¬tion of the monomers mentioned before. Suitable process conditions are known by a per¬son skilled in the art, and are disclosed e.g., in WO-A 2005/064072.
In the acrylic binder according to the invention, it is possible to add in general up to 10 % by weight, preferably 0.05 to 5 % by weight of mono- or di-olefinically unsaturated mono¬mers containing reactive or cross-linking groups. Examples of such monomers are in par¬ticular the amides of a,p-olefinically unsaturated Cg-a-carboxylic acids, particularly acryl amides, methacryl amides and maleic diamides, and their N-methylol derivatives such as N-methylol acrylic amide, N-methylo! methacrylic amide, N-alkoxy methyl amides of a,|3-monoolefinically unsaturated Cs-s-carboxylic acids such as N-methoxy methacrylic amide and N-n-butoxymethylactylic amide, vinyl sulfonic acid, monoesters of acrylic and methacrylic acids with alkanediols such as glycol, butan0diol-1,4, hexane diol-1,6, and 3-chloropropanediol-1,2, and also allyl and methallyl esters of a,p-otefinically unsaturated mono- and di-carboxylic acids such as diallyl maleate, dimethyl allyl fumarate, allyl acrylate and allyl methacrylate, diallyl phthalate, diallyl terephthalate, p-di-vinyl benzene, methyl-ene-bis-acrylamide and ethylene glycol di-allylether.
The molecular weight of the non crosslinked emulsion polymers obtained is in general 40,000 to 250,000 (determined by GPC). The molecular weight is usually controlled by the use of conventional chain stoppers in conventional amounts. Conventional chain stoppers are for example sulfoorganic compounds.
The acrylic binder of the present invention is obtained in form of its aqueous dispersion and is preferably employed in the insecticide compositions ot the present invention in form of the aqueous dispersion.
Polyurethane binders and/or Polyisocyanurate binders (Component B2)
In a further preferred embodiment the polymeric binders are polyurethanes and/or polyiso-cyanurates. Said polyurethanes and/or poiyisocyanu rates may be employed either alone as polymeric binders or in combination with further polymeric binders, especially polymeric

binders mentioned before, for example in combination with the acrylic binders mentioned before.
Suitable polymeric binders are therefore:
at least one polyurethane as component B2, obtainable by reaction of the following compo¬nents:
b2a} at least one diisocyanate or polyisocyanate as component B2A, preferably aliphatic, cycloaliphatic, araliphatic and/or aromatic insocyanates, more preferably diisocy-anates, which are optionally biuretisized and/or isocyanurized, most preferably 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylene cyclohexane (IPDI) and hexame-thylene diisocyanate-1,6 (HMDI); b2b) at least one diol, triol or poiyol as component B2B, preferably aliphatic, cycloaliphatic and/or araliphatic diols having 2 to 14, preferably 4 to 10 carbon atoms, more pref¬erably 1,6-hexanediot or neopentyl glycol; b2c) optionally further components as component B2C, preferably adipic acid or carbonyl diimidazole (GDI); and b2d) optionally further additives as component B2D.
The polyurethane is preferably obtainable by reaction of the following components:
b2a) 55 to 99 % by weight, preferably 70 to 98 % by weight, more preferably 75 to 90 by .weight based on the polyurethane of at least one diisocyanate or polyisocyanate (component B2a), preferably aliphatic, cycloaliphatic, araliphatic and/or aromatic in¬socyanates, more preferably diisocyanates, which are optionally biuretisized and/or isocyanurized, more preferably alkylene diisocyanates having from 4 to 12 carbon at¬oms in the alkylene unit, like 1,12-dodecane diisocyanate, 2-ethyltetramethylene diisocyanate-1,4, 2-methylpentamethy!ene diisocyanate-1,5, tetramethylene diisocy-anate-1,4, lysinester diisocyanate (LDI), hexamethyfene diisocyanate-1,6 (HMDI), cyclohexane-1,3-and/or-1,4-diisocyanate, 2,4-and 2,6-hexahydro-toiuylene diisocy¬anate as well as the corresponding isomeric mixtures 4,4'-2,2'- and 2,4'-dicyclohexylmethane diisocyanate as well as the corresponding mixtures, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethyl cyclohexane (IPDI), 2,4- and/or 2,6-toluylene diisocyanate, 4,4'-, 2,4' and/or 2,2'-diphenylmethane diisocyanate (mono-meric MDI), polyphenylpolymethylene polyisocyanate (polymeric MDI) and/or mix¬tures comprising at least 2 of the isocyanates mentioned before; further ester-, urea-, allophanate-, carbodiimid-, uretdione- and/or urethane groups comprising di- and/or

polyisocyanates may be used; most preferably 1-(socyanato-3,3,5-trimethyl-5-isocyanatomethyiene cyclohexane (IPDI) and hexamethylene diisocyanate-1,6 (HMDI);
b2b} 10 to 90% by weight, preferably 12 to 85% by weight, more preferably 15 to 65% by weight based on the polyurethane of at least one diol, triol or polyol (component B2B), preferably aliphatic, cycloaliphatic and/or araliphatic diols having 2 to 14, pref¬erably 4 to 10 carbon atoms, more preferably polyols, selected from the group con¬sisting of polyetherols, e.g. polytetrahydrofurane, polyesterols, polythioetherpolyols, hydroxyl group containing polyacetales and hydroxyl group containing aliphatic poly¬carbonates or mixtures of at least 2 o^ the polyols mentioned before. Preferred are polyesterols and/or polyetherols. The hydroxyl number of the polyhydroxy com¬pounds is in general from 20 to 850 mg KOH/g and preferably 25 to 80 mg KOH/g. Further, diols and/or triols having a molecular weight of from in general 60 to b2c} 0 to 10 % by weight, preferably 0.1 to 5 % by weight, more preferably 1 to 5 % by weight based on the polyurethane of further components (component B2C), prefera¬bly adipic acid or carbonyl diimidazole (GDI); and
b2d) 0 to 10 % by weight, preferably 0.1 to 5 % by weight, more preferably 0.5 to 5 % by weight based on the polyurethane of further additives (component B2D);
wherein the sum of the components B2A, B2B, B2C and B2D is 100 % by weight.
The polyurethanes are prepared by methods known in the art. Further, additives as known by a person skilled in the art may be used in the process for preparing the polyurethanes.

Component B may also be a polyisocyanurate or a mixture of a polyisocyanurate and a polyurethane, preferably a polyurethane as mentioned above.
Polyisocyanurates are polymers comprising groups of the following formula:

wherein R' is an alkylene or arylene residue depending on the isocyanate employed in the preparation of the isocyanurate.
Polyisocyanurates are usually prepared by cyclotrimerization of isocyanates. Preferred iso-cyanates are the same isocyanates as mentioned before (component B2A), Preparation processes and conditions for the preparation of polyisocyanu rates are known by a person skilled in the art.
Pesticidal compositions
The pesticidal compositions of the invention may be aqueous compositions or dry composi¬tions, i.e. compositions which do not comprise water.
In a preferred embodiment the pesticidal compositions are aqueous compositions, prefera¬bly comprising 55 to 97 % by weight, more preferably 85 to 95 % by weight of water, and 3 to 45 % by weight, preferably 5 to 15 % by weight of solids, based on the total of the com¬ponents in the insecticide compositions of the present invention, wherein the total is 100 % by weight. The solids are preferably selected from the group consisting of at least one pes¬ticide as component A as defined above, and at least one polymeric binder as component B as defined above, and optionally at least one fixative agent as component C as defined below, and optionally further components depending on the use of the final product as de¬fined above.

The treatment baths from which the pesticidal compositions are applied to the materia! are preferably aqueous formulations comprising 95 to 99.5 % by weight, preferably 95 to 99 % by weight, more preferably 97 to 99 % by weight of water, and 0.5 to 5 % by weight, pref¬erably 1 to 5 % by weight of solids, based on the total of the components in the insecticidal compositions of the present invention. The solids are preferably selected from the group consisting of at least one pesticidal of formula I as component A as defined above, and at least one polymeric binder as component B as defined above, and optionally at least one fixative agent as component C as defined below, and optionally further components de¬pending on the use of the final product as defined above.
The polymeric binder may advantageously be applied with a fixative agent C for improved attachment of the pesticide on the material. The fixative agent may comprise free isocy-anate groups.
Suitable fixable agents are for example isocyanates or isocyanurates comprising free iso-cyanate groups. Preferably the isocyanurates are based on aikylene diisocyanates having from 4 to 12 carbon atoms in the alkylene unit, like 1,12-dodecane diisocyanate, 2-ethyltetramethylene diisocyanate-1,4, 2-methylpentamethylene diisocyanate-1,5, tetrame-thylene diisocyanate-1,4, lysinester diisocyanate (LDI), hexamethylene diisocyanate-1,6 (HMDI), cyclohe)iane-1,3-and/or-1,4-diisocyanate, 2,4-and 2,6-hexahydrotoluytene diisocy¬anate as well as the corresponding isomeric mixtures 4,4'-2,2'- and 2,4'-dicyclohexylmethane diisocycuiate as well as the corresponding mixtures, 1-isocyanato-3,3,5-trimethyl-5-isQcyanatomethyl cydohexane (IPDI), 2,4- and/or 2,6-toluylene diisocy¬anate, 4,4'-, 2,4' and/or 2,2'-diphenylmethane diisocyanate (monomeric MDI), polyphenyl-polymethylene polyisocyanate (polymeric MDI) and/or mixtures comprising at least 2 of the isocyanates mentioned before. More preferably the isocyanurates are based on hexame¬thylene diisocyanate-1,6 (HMDI).
More preferably the isocyanurate is a isocyanurate which is hydrophilized with a polyal-kylene oxide based on ethylene oxide and/or 1,2-propylene oxide, preferably polyethylene oxide.
The isocyanurate used as a fixative agent can be prepared by methods known in the art. Preferably 5 to 25% by weight, more preferably 7 to 20% by weight, most preferably 10 to 15% by weight ot the isocyanate groups based on the amount of isocyanate used as star¬ing material for the preparation of the isocyanurate are free isocyanate groups.

Most preferably the isocyanurate used as a fixative agent is dissolved in a polar aprotic solvent, e.g. THF, DMF or propylene or ethylene carbonate.
The most preferred fixative agent used is an isocyanurate based on HMDI which are hy-drophilized with a polyethylene oxide and which is dissolved in propylene carbonate (70% by weight of HMDI in 30% by weight of propylene carbonate). The amount of free isocy-anate groups is 11 to 12 % by weight, based on the amount of isocyanate used as staring material for the preparation of the isocyanurate.
The pesticidal composition preferably comprises the following components, based on the solids content of the composition, if a fixative agent is used:
a) 20 to 70 % by weight, preferably 25 to 65 % by weight, more preferably 30 to 65 % by weight of at least one pesticide (component A), and
b) 29 to 72 % by weight, preferably 34 to 70 % by weight, more preferably 33 to 66 by weight of at least one polymeric binder (component B) as defined above;
c) 1 to 8 % by weight, preferably 1 to 5% by weight, more preferably 2 to 4 % by weight of at least one fixative agent (component C);
wherein the sum of the components is 100 % by weight of solids content of the pesticide composition.
Depending on the use of the final product the pesticidal composition may further comprise one or- more components selected from water, preservatives, detergents, fillers, impact modifiers, anti-fogging agents, blowing agents, clarifiers, nucleating agents, coupling agents, conductivity-enhancing agents (antistats), stabilizers such as anti-oxidants, carbon and oxygen radical scavengers and peroxide decomposing agents and the like, flame re-tardants, mould release agents, agents having UV protecting properties, optical bright-eners, spreading agents, anti-blocking agents, arrti-migrating agents, foam-forming agents, anti-soiling agents, thicKeners, further biocides, wetting agents, plasticizers and film form¬ing agents, adhesive or anti-adhesive agents, optical brightening (fluorescent whitening} agents, fragrance, pigments and dyestuffs.
Suitable anti-foam agents are for example silicon anti-foam agents. Suitable UV-protecting agents for protecting UV-sensitive insecticides and/or repellents are for example para-aminobenzoic acids (PABA), octylmethoxysinameth, stilbenes, styryl or benzotriazole de¬rivatives, benzoxazol derivatives, hydroxy-substituted benzophenones, salicylates, substi-■ tuted triazines, cinnamic acid derivatives (optionally substituted by 2-cyano groups), pyra-

zoline derivatives, 1,1'-biphenyl-4,4'-bis-2-(methoxyphenyl)-ethenyl or other UV protecting agents. Suitable optical brighteners are dthydroquinolinone derivatives, 1,3-diaryl pyra-zoline derivatives, pyrenes, naphthalic acid imides, 4,4'- diystyryl biphenylene, 4,4'-diamino-2,2'-stilbene disulphonic acids, cumarin derivatives and benzoxazole, benzisoxa-zole or benzimidazole systems which are linked by -CH=CH-bridges or other fluorescent whitening agents.
Typical pigments used in the pestidical compositions of the present invention are pigments which are used in pigment dyeing or printing processes or are applied for the coloration of plastics and are known by a person skilled in the art.
Pigments may be inorganic or organic by their chemical nature. Inorganic pigments are mainly used as white pigments (e.g., titanium dioxide in the form of rutile or anatas, ZnO, chalk) or black pigments (e.g., carbon black). Colored inorganic pigments may be used as well but are not preferred because of potential toxicologic hazards. For imparting color, organic pigments or dyestuffs are preferred. Organic pigments may be mono or disazo, naphthol, benzimidcizolone, (thio) indigoid, dioxazine, quinacridone, phthalocyanine, isoin-dolinone, perylene, perinone, metal complex or diketo pyrrole pyrrole type pigments. Pig¬ments may be used in powder or liquid form (i.e., as a dispersion). Preferred pigments are Pigment Yellow 83, Pigment Yellow 138, Pigment Orange 34, Pigment Red 170, Pigment Red 146, Pigment Violet 19, Pigment Violet 23, Pigment Blue 15/1, Pigment Blue 15/3, Pigment Green 7, Pigment Black 7. Other suitable pigments are known to a person skilled in the art.
Typical dyestuffs which may be used in the present invention are vat dyes, cationic dyes and disperse dyes in powder or liquid form. Vat dyes may be used as pigments or following the vatting (reduction) and oxidation procedure. Using the vat pigment form is preferred. Vat dyes may be of the indanthrone type, e.g. C.l. Vat Blue 4. 6 or 14; or of the flavan-throne type, e.g. C.l. Vat Yellow 1; or of the pyranthrone type, e.g. C.i. Vat Orange 2 and 9; or of the isobenzanthrone (isoviolanthrone) type, e.g. C.l. Vat Violet 1; or of the dibenzan-throne (violanthrone) type, e.g. C.l. Vat Blue 16, 19, 20 and 22, C.l. Vat Green 1, 2 and 9, C.l. Vat Black 9; or of the anthraquinone carbazole type, e.g. CI. Vat Orange 11 and 15, C.l. Vat Brown 1, 3 and 44, C.l. Vat Green 8 and C.l. Vat Black 27; or of the benzanthrone acridone type, e.g. C.l. Vat Green 3 and 13 and C.l. Vat Black 25; or of the anthraquinone oxazole type, e.g. C.l. Vat Red 10; or of the perylene tetra carbonic acid diimide type, e.g. C.l. Vat Red 23 and 32; or imidazole derivatives, e.g. C.l. Vat Yellow 46; or amino triazine

derivatives, e.g. C.I. Vat Blue 66. Other suitable vat dyes are known by a person skilled in the art.
Typical disperse and cationic dyestuffs are known by a person skilled in the art.
If cellulosic substrates are employed as material, said cellulosic substrates are preferably dyed with vat, direct, realative or sulphur dyestuffs.
In a further embodiment the pesticidal compositions of the present invention are pesticidal compositions as mentioned before comprising at least one pigment and/or at least one dyestuff. The pesticidal compositions of the present invention preferably comprise 10 to 300 % by weight, more preferably 20 to 150 % by weight of the pigment and/or dyestuff relating to the total weight of the solids content of the pesticide.
The material, for example textile material or plastics material, may be impregr\ated prior to use if the composition is delivered in the form of a kit.
In a further embodiment, the impregnated material according to the present invention fur¬ther comprises one or more components selected from preservatives, detergents, stabiliz¬ers, agents having UV-protecting properties, optical brighteners, spreading agents, anti-migrating agents, foam-forming agente, wetting agents, anti-soiling agents, thickeners, fur¬ther biocides, plasticizers, adhesive agents, pigments and dyestuffs. Suitable examples of the components mentioned above are known to a person skilled in the art.
In a further embodiment of the present invention the impregnated material comprises be¬sides the at least one pesticide and the at least one polymeric binder as described before at least one pigment and/or at least one dyestuff. The amount of the at least one pigment is in general from 0.05 to 10 % by weight, preferably 0.1 to 5 % by weight, more preferably 0.2 to 3.5 % by weight of the (dry) weight of the non-living material. The amount of the at least one dyestuff is in general from 0.05 to 10 % by weight, preferably 0.1 to 5 % by weight, more preferably 0.2 to 3.5 % by weight of the (dry) weight of the material. The ma¬terial comprises preferably either at least one pigment or at least one dyestuff. Suitable pigments and dyestuffs are mentioned before.
Process for impregnation of a protective material

In a further embodiment, the present invention relates to a process for impregnation of a material, for example a textile material or plastics material, comprising i) forming an aqueous formulation or a melt, wherein an aqueous formulation is pre¬ferred, comprising at least one pesticide and at least one polymeric binder, preferably a polymeric binder as defined above, and optionally further ingredients;
ii) applying the aqueous formulation to the material by
iia) passing the material through the aqueous formulation;
or
iib) bringing the material in contact with a roller that is partly or fully dipped into the
aqueous formulation and drawing the aqueous formulation to the side of the
material in contact with the roller, or
lie) double-side coating of the material or iid) spraying the aqueous formulation onto the material, wherein the spraying is
carried out with any suitable device for spraying by hand or automatically, for
example with an aerosol can or devices usually used in a factory; or
lie) applying the aqueous formulation in fomi of a foam; or
iif) submerging the material into the aqueous formulation; or
iig) brushing the aqueous formulation onto or into the material; or
iih) pouring the aqueous formulation onto the material; or applying the melt by calendaring or with a doctor-blade;
iii) optionally removing surplus aqueous formulation or surplus; and iv) drying and/or curing the material.
In the context of the invention, an aqueous formulation may be a solution, an emulsion or a suspension/dispersion.

The aqueous formulation or the melt preferably comprises the pesticidal composition, which is preferably employed in form of an aqueous formulation.
In the context of the invention "impregnation" is a process for applying the pesticidal com¬position. This process may include a process for curing the applied pestidical composition to achieve a coating onto the material, if desired. An "impregnated material" is a material onto which the pesticidal composition is applied. The "impregnated material" may be coated by curing the applied pesticidal composition, it desired.
The pesticidal composition may also be applied onto the material by transfer printing, Inkjet printing, a screen process, and powder printing.
Details of the application of the pesticidal composition are well known to someone skilled in the art and are disclosed, e.g.. in WO 2005/064072.
The method according to the invention is useful for protecting tobacco, tobacco bales or other tobacco products. It can be used for protecting any kind of tobacco, such as e.g. tobacco produced from Nicotiana rostica and Nicotiana tabacum, specifically dark tobacco, bright tobacco, burley tobacco, shade tobacco and Perique.
The method is useful for protecting, the tobacco from any kind of pests and disease en¬countered in the transport and storage of tobacco, specifically from storage pests, like bugs, beetles and moths, mites, mice and tobacco diseases.
Such pests include:
Cigarette beetle (Lasioderma serricorne), tobacco moth (Ephespha elutella), confused flour beetle (Tribolium confusum), red flour beetle {Tribolium castaneum), saw-toothed grain beetle {Oryzaephilus surinamensis), yellow meal worm (Tenebrio molitor), lesser meal worm (Alphitobius diaperinus), granary weevil (Sitophilus granarius), lesser grain borer (Rhyzopertha dominica), maize weevil (Sitophilus zeamais), rice weevil (Sitophilus oryzae), angoumois grain moth (Sitotroga cerealella), Indian meal moth (Plodia interpunctella), drugstore beetle (Stegobium paniceum), cadelle beetle (Tenebroides mauritanicus), long¬headed flour beetle (Latheticus orizae), dark mealworm (Tenebrio obscurus), denmestid beetles such as: black carpet beetle, larder beetle, wardrobe beetle, odd beetle, hide bee¬tle, warehouse beetle, spider beetles, weevils, especially the bean weevil, grain mite, black

flour beetle, flat grain beetles, fruit flies, vinegar flies, rusty grain beetle, hairy fungus bee¬tle, flat grain beetle, sap beetles, deathwatch beetles, darkling beetles, and fungus beetles.
The method according to the invention is specifically useful for the control of the cigarette beetle (Lasioderma serricorne), and the tobacco moth (Ephespha elutella), the two main pests in tobacco storage.
The methods according to the invention can be applied in all stages and types of tobacco processing, where a storage period is required.
Such processing includes the curing of tobacco after harvesting, specifically the yellowing, leaf drying and stem drying stage.
It includes any type of curing, such as air-curing, sun-curing, fire-curing and, in particular, flue-curing. In the flue-curing, the method can be used in direct-fired systems as indirect fired systems, working, e.g., with heat exchangers.
The method according to the invention is further useful in the fermenting and aging steps of tobacco processing. Depending on the kind and quality of the final tobacco product, these steps range from a couple of days to several years - during which the tobacco has to be protected from pests.
Accordingly, the method according to the invention is useful in the production of any kind of tobacco product for human consumption, such as cigarettes, cigars, pipe tobacco, cigarette tobacco, snuff, chewing tobacco, snuff, gutka and creamy snuff.
The device according to the invention comprises means for spreading out the tobacco leaves, such as a rack or an open framework where sticks of tied leaves or the whole stalk is hung, a material, which has protective activity against harmful organism, and which cov¬ers the tobacco to be protected, and, optionally means for attaching the material to the means for spreading out the tobacco.
The material is preferably a net, because this does not disturb the drying or curing process - which requires an exchange of air, humidity and heat between the tobacco and its envi¬ronment - while it still affords good protection against pests.

Surprisingly, the use of nets leads to a good protection even in the case of fungal diseases.
The invention is further illustrated by the following examples without limiting it thereby.
Examples
1. Binder:
A) Preparation of polymer dispersions
General procedure:
250 g of water and 3 g of a styrene seed (33 % by weight) having a medium particle diame¬ter of 30 nm are heated to 85 "C and 5 % by weight of feed 2 are added. After 10 mIn. addi¬tion of feed 1 comprising the monomers mentioned below and feed 2 is started.
Feed 2 comprises 3.0 g sodiumperoxidsulfate dissolved in 39.9 g of water.
The composition of feed 1 is listed in table 1.
Feed 1 and 2 are added in 3 h, and it was polymerized for further 0.5 h.

Table 1: Composition of feed 1 in % by weight pphm (parts per hundred monomers)

Monomer compositions MMA S AN EHA BA EA HPMA GMA MaMol AMol AM AS FI-1 BMA-Acac
A1 27.0 3.1 65.0 2.0 1.0 1.9
A2 23.9 5.0 5.3 60.0 1.2 0,6 4.0
A3 16.6 30.0 30.0 20.0 3.0 0.4
A4 25.7 5.0 5.3 60.0 3.5 0.5
A5 14.7 11.0 70.0 3.5 0.5 0.3
A6 30.0 13.0 8.0 .45^ 3.0 0.5 0.3
A7 30.0 13.0 8.0 44.5 0.5 0.3 3.7
A8 33.0 60.0 3.9 1.0 0.5 1.6
A9 20.0 20.0 17.0 23.0 15.3 3.5 1.2
A 10 20.0 20.0 17.0 23.0 15.3 0.4 0.3 4.0
All 10.0 10.0 25.5 50.0 2.5 2.0
A 12 10.0 10.0 25.5 47.7 2.5 3.5 0.7 0.1
A 13 10.0 11.0 60.0 ^14.7 4.0 0.2 0.1
A 14 20.0 8.0 55.0 12.5 3.0 1.5
A 15 26.0 13.0 57.0 3.0 1.0
A16 15.0 13.0 68.0 3.0 1.0
A 17 16.0 81.0 2.0 1.0

The amount of initiator sodium peroxidisulfate is 0.3 parts by weight, the emulsifier com¬prises 0,4 parts by weight of Dowfax 2A1 (Dow) und 0.6 parts by weight of Lumiten IRA (BASF AG), relating to 100 parts by weight of the monomer composition of table 1.
Abbreviations:
MMA: methyl methacrylate
S: styrene
AN: acrylic nitril
EA: ethyl acrylate
EHA: 2-ethylhexylacrylate
BA: n-butyl acrylate
Fl: copolymerizable benzophenone having an acrylic group
GMA: glycidy I methacrylate
B^AA-Acac■. bitandiolmonoacvylate acetylacetate
Amol: N-methylol acrylamide
MAMol: N-methylol methacrylamide
HPMA: hydroxypropyl methacrylate
AS: acrylic acid
AM: acrylic amide
Dowfax 2A1:
^25*^12
-SOgNa
Lumiten IRA:
O O

SOgNa
Examples A1 and A8
Aqueous polymer dispersions comprising Fl - 1 polymerizable photo initiator which is later useful as crosslinking agent is a photo initiator of formula

R^

O 0'
o
wherein
R^ IS an organic radical having from 1 to 30 carbon atoms,
R^ is H or a methyl group, and
H^° is a phenyl group which is optionally substituted or a Cr to C4-all I(. Examples of use
a) Preparation of long-lasting insecticidai nets (LLINs)
The insecticidai treatment was performed with aqueous dispersions according to examples A1 - A17 on commercially available white polyester netting material (fiber titer 75 denier, 156 mesh, weight 28-32 g/m^) without prior washing. The aqueous treatment baths were prepared by mixing the aqueous dispersions with commercially available emulsions of in¬secticide and/or repellent, setting pH with buffer solutions and adding a fixative (if needed). The concentrations of the treatment baths were adjusted according to the liquor uptake possible (LU between 60 and 100 %). The treatment baths were applied by using a padder-stenter equipment on a laboratory scale {Mathis AG, Switzerland). The netting material is fully immersed into the treatment bath and excess liquor is removed by passing it through cylinders which move in counter-direction. By choosing a defined distance between these cylinders (and thus a defined pressure) the liquor uptake can be controlled. The liquor up¬take is measured by weighing an impregnated piece of netting and subtracting the weight of the dry, untreated netting and is given as % weight of liquor on weight of netting. The drying/curing step was performed in a laboratory stenter which allows to control the tem¬perature and time of the treatment.
b) Testing Methodologies
Limited Forced Exposure Assay:
Aiphacypermethrin-impregnated long-lasting insecticidai nets (LLINs, 200 mg ai/m^) were cut to fit 150 X 25 mm Petri dishes. LLINs were placed on the bottom of the dishes and 10 adult cigarette beetles, Lasioderma serricome, were introduced into each dish onto the

nets. Beetles were exposed to the nets for 10, 30, or 60 minutes and the nets were then removed. Mortality/knockdown was evaluated at the time of net removal. Ten replicates were performed per treatment.
Behavioral Assay:
Cardboard shipping tubers (457 mm pieces of 76 mm diameter) were covered on one end with aiphacypermethrin-impregnated long-lasting insecticidal net (LLIN, 200 mg ai/m^), which was secured with a rubber band and electrical tape. The end of the tube with the LLIN was attached to a clear plastic cup (76 mm diameter x 89 mm height) with electrical tape filled with 20.0 g of toasted oat cereal to serve as a food source. Ten adutt tobacco moths, Ephestia elutella, (Table 3) or ten adult cigarette beetles, Lasiodeima serricorne, (Table 2) were introduced into the tubes on the opposite end of the LLIN and food source. The opposite (open) end of each tube was then sealed. Location and mortality of the moths/beetles were evaluated at 1 and 2 days (E elutella) or 1 and 4 days (L serricorne) after treatment (DAT). Ten replications were performed per trea^ent with E..elutella and eight replications were performed per treatment with L serricorne-
c) Results
1. Aiphacypermethrin-impregnated long-lasting insecticidal nets (LLlNs) were efficacious against cigarette beetles, resulting in 87% knockdown + mortality after 10 minutes ex¬posure and 100% mortality after 60 minutes exposure in a forced exposure assay (Ta¬ble 1, Figures 1 and 2). Knocked down beetles were un^le to recover:

Table 1 -
Efficacy of alphacypermethrin-impregnated long-iasting insecticidal nets (LLIN) against
cigarette beetles, Lasioderma serricorne. in a limited forced exposure assay



2. LLlNs caused significantly greater mortality ot cigarette beetles (93% at 1 day after treatment (DAT) and 100% at 4 DAT) compared to the untreated net in a behavioral assay where the beetles had to pass through the net to reach a food/light source:
Table 2.
Efficacy of alphacypemiethrin-impregnated long-lasting insecticidal nets (LLIN) against cigarette beetle, Lasioderma semcorne, adults in a behavioral assay



3. LLiNs caused significantly greater mortality of tobacco moths (89 % at 1 DAT and 94 % at 2 DAT) compared to the untreated net in a behavioral assay where the moths had to pass through the net to reach a food/light source. Very few moths able to pass through the untreated net or LLIN, indicating utility of (2 mm x 2 mm) LLINs for use as a physical and chemical barrier for protection of stored tobacco from tobacco moth in¬festations (Table 3, Figure 4):
Table 3.
Efficacy of alphacypermethrin-impregnated long-lasting insecticidal nets (LLIN) against
tobacco moth, Ephestia elutella, adults in a behavioral assay



4. LUNs caused significantly greater mortality of to cigarette beetles compared to the untreated net in a beliavioral assay wfiere the beetles had to pass through the net to reach a food/light source. No beetles were able to pass through the untreated net or LLIN, indicating utility of (1 mm x 1 mm) LLINs at different a.!, levels for use as a physical and chemical barrier for protection of stored tobacco cigarette beetle infesta¬tions (Table 4, Figure 5):







Claims for further prosecution in IN
1. A method tor protecting tobacco from harmful organisms during storage omprising the step of covering the tobacco with a matenal which has a protective activity against the harmful organisms, wherein the material is a netting with a mesh size of 1.5 X 1.5 mm as an upper limit.
2. The method as claimed in claim 1, wherein the material is a textile material, plastic material, a leather material, a flocked fabric, a sheeting, foil, a packaging material or a cellulose containing material.
3. The method as claimed in claim 1 or 2, wherein the material is treated with a compo¬sition comprising:
a. at least one pesticide (component A), and
b. at least one polymeric binder {component B).
4. The method as claimed in claim 3, wherein the composition comprises (based on the total content of A and B), 0.001 to 95 wt.-% of at least one pesticide, and 5 to 99.999 wt.-% of at least one polymeric binder.
5. The method as claimed in claim 3 or 4, wherein the pesticide is selected from pyre-throid compounds, carbamate compounds, organophosphorous compounds, N-arythydrazine derivatives, molluscicides, rodenticides, and fungicides.
6. The method as claimed in any of claims 3 to 5, wherein the polymer binder is se¬lected from the group consisting of polyacrylates, potymethacrylates, polyacryloni-trile, polymaleic acid anhydride, polystyrene, poly(methyl)styrene, polybutadiene, polyvinylacetate, polyvinyl alcohol as well as copolymers obtained by polymerization of at least two different ethylenically unsaturated monomers of the group of mono¬mers mentioned above and blends of said homopolymers and/or copolymers, for ex¬ample, poly(styrene-acrylates), poly(styrene-butadiene), ethylene-acrylate-copolymers, ethylene-vinylacetate-copolymers which may be partially or completely hydrolyzed, polyurethanes and/or or polyisocyanurates, blends comprising polyure-thanes and/or polyisocyanurates, preferably blends comprising polyurethanes and/or polyisocyanu rates and polycarbonates; mineral waxes, zirconium waxes, silicones.

polysiloxanes, fluorinated polyacrylates and methacrylates, fluorosilicones, and fluorocarbon resins
melamine formaldehyde condensation resins, methyiol urea derivatives; and curable
polyesters
and
blends or preparations comprising at least one of said polymeric binders.
7. The method as claimed in any of claims 3 to 6, wherein the polymeric binder is an
acrylic binder, obtained by radical polymerization of at least one monomer of formula
II

wherein
R1", R1' and R11 are independently selected from C1 to C10lkyl, which is optionally fluoro substituted and which may be linear or branched, for example methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, t-butyl, n-pentyl, i-pentyl, sec-pentyl, neo-pentyl, 1,2-dimethylpropyl, i-amyl, n-hexyl, i-hexyl, sec-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl, preferably C,- to C4-alkyl, for example methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, sec-butyl, tert-butyl; substituted or unsubstituted aryl, preferably substituted or unsubstituted Cg- to C,o-aryl, more preferably substituted or unsubstituted Cg-aryl, for example phenyl or tolyl;
R1 and R1' may further be H.
8. A method of use for a material according to any of claims 1 to 7 which has a protec¬
tive activity against harmful organisms hich comprises the steps of covering to¬
bacco with the material.

Documents:

6855-CHENP-2008 CORRESPONDENCE OTHERS 13-01-2014.pdf

6855-CHENP-2008 FORM-3 13-01-2014.pdf

6855-CHENP-2008 OTHERS 15-10-2013.pdf

6855-CHENP-2008 AMENDED CLAIMS 03-07-2014.pdf

6855-CHENP-2008 AMENDED PAGES OF SPECIFICATION 03-07-2014.pdf

6855-CHENP-2008 CORRESPONDENCE OTHERS 15-10-2013.pdf

6855-CHENP-2008 FORM-1 03-07-2014.pdf

6855-CHENP-2008 FORM-3 03-07-2014.pdf

6855-chenp-2008 abstract.pdf

6855-chenp-2008 claims.pdf

6855-CHENP-2008 CORRESPONDENCE OTHERS 03-07-2014.pdf

6855-chenp-2008 correspondence others.pdf

6855-chenp-2008 correspondence-others.pdf

6855-chenp-2008 description (complete).pdf

6855-chenp-2008 drawings.pdf

6855-chenp-2008 form-1.pdf

6855-chenp-2008 form-18.pdf

6855-chenp-2008 form-26.pdf

6855-chenp-2008 form-3.pdf

6855-chenp-2008 form-5.pdf

6855-chenp-2008 pct.pdf

Form 13.pdf

Petition for POR.pdf


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Patent Number 263503
Indian Patent Application Number 6855/CHENP/2008
PG Journal Number 44/2014
Publication Date 31-Oct-2014
Grant Date 30-Oct-2014
Date of Filing 12-Dec-2008
Name of Patentee BASF SE
Applicant Address 67056 LUDWIGSHAFEN,
Inventors:
# Inventor's Name Inventor's Address
1 LEININGER, HARTMUT, KAISERSTUHL 10, 67434 NEUSTADT,
2 HUFF, JURGEN, HAGELLOCHSTRASSE 48, 67063 LUDWIGSHAFEN
3 KARL, ULRICH, BORDOLLORING 29, 67269 GRUNSTADT,
4 HARMSEN, SVEN, AHORNWEG 27, 67311 TIEFENTHAL,
5 BREJC, ANDREJ JOHANN GEORGE LEHMANN STR.4, 67273 WEISENHEIM, AM BERG,
PCT International Classification Number A01N25/34
PCT International Application Number PCT/EP07/55891
PCT International Filing date 2007-06-14
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 06115497.7 2006-06-14 EUROPEAN UNION