Title of Invention | "A PROCESS FOR MAKING PARTICLES OF AMINE REACTION PRODUCT" |
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Abstract | There is provided a process for producing particles of amine reaction product by means of a carrier having a melting point between 30 °C and 135 °C, optionally followed by a coating step. Processed amine reaction products and finished compositions incorporating such processed product are also herein provided. |
Full Text | There is provided a process for producing particles of amine reaction product by means of a carrier having a melting point between 30°C and 135°C, optionally followed by a coating step, processed amine reaction products and finished compositions incorporating such processed product are also herein provided. WE CLAIM: 1. A process for making particles of amine reaction product of a compound containing a primary and/or secondary amine functional group an active component containing active ketone or aldehyde of the kind hereinbefore described and which comprises the step of: a) providing an amine reaction product comprising from 10% to 90% by weight of said active ketone or aldehyde containing component and having a viscosity greater than lOOOcps. b) mixing therewith, at a temperature just above the carrier melting point, a carrier having a melting point of between 30°C and 135°C in the ratio of 3-95% to produce particles of processed amine reaction product containing from 1% to 75% by weight of said amine reaction product, and c) optionally treating the particle by conventional manner to form a coated particle. 2. A process as claimed in any of the preceding claims, wherein the amine reaction product comprises from 30% to 85% of said active ketone or aldehyde containing component. 3. A process as claimed in any of the preceding claims, wherein the primary and/or secondary amine is selected from aminoaryl derivatives, polymers, amino acids and derivatives thereof, polyaminoacides, cross-linked polyamilaoacides, substituted polyvinylalcohol with a MW ranging from 400-300,00 polyoxyethylene bis[amine]; polyoxyethylene bis [6-aminohexyl]; N,N-bis-(3-aminopropyl)-l,3-propanedlamine linear or branched; l,4-bis-(3-aminopropyl) piperazine, and mixture thereof, preferably selected from ethyl-4 amino benzoate, polyethylenamine polymers; glucamine; the diaminobutane dendrimers, amino substituted polyvinulalcohol with a MW ranging from 400-3—,000; polyoxyethylene bis [amine]; polyoxyethylene bis [6-aminohexyl]; N,N'-bis-(3- aminopropyl),3-propanediemine linear or branched; a,4-biz-(3-aminopropyl)piperazine, and mixture thereof; more preferably selected from ethyl-4-amino benzoate, polyethyleneimine polymers; the diaminobutane dendrimers, N,N'-bis-(3-aminopropyl)-l,3-propanediamine linear to branched; l,4-bis(3-aminopropyl) piperazine, and mixtures thereof, most preferably selected from ethyl-4-amino benzoate, polyethyleneimine polymers; polylysine, cross-linked polylysine, N,N'-bis-(3-aminopropyl)-l,3-propanediamine linear or branched, l,4-bis-(3-aminopropyl) piperazine, and mixtures thereof. 4. A process as claimed in any of the preceding claims, wherein the active component is selected from a flavour ketone or aldehyde ingredient, a pharmaceutical ketone or aldehyde active, a biocontrol ketone or aldehyde agent, a perfume ketone or aldehyde component, a refreshing cooling ketone or aldehyde agent and/or mixtures thereof. 5. A process as claimed in any of the preceding claims, wherein said active component is an insect and/or moth repellant, preferably selected from citronellal, citral, N, N diethyl meta toluamide, Rotundial, 8-acetoxycarvotanacenone, and mixtures thereof. 6. A process as claimed in any of the preceding claims, wherein said active component is an antimicrobial, preferably selected from Glutaraldehyde, Cinnamaldehyde, and mixtures thereof. 7. A process as claimed in any of the preceding claims, wherein the active is a perfume preferably selected from alpha-damascone, delta damascone, Carvone, Gamma-Methyl- lonone; Damascenone, hedione, 2.4-dimethyl-3-cyclohexen-l-carboxaldehydel, Florhydral, Lilial, heliotropine, trans-2-nonenal, citral, and mixtures thereof. 8. A process as claimed in any of the preceding claims, wherein the amount of amine reaction product ranges from 5 to 30%, by weight of the processes amine reaction product. 9. A process as claimed in any of the preceding claims, wherein the carrier has a melting point between 45°C and 85°C. 10. A process as Claimed in any of the preceding claims, wherein said carrier is selected from organic polymeric compounds, waxes, paraffins, oils, glycerides, monoglycerides, diglycerides, triglycerides, anionic surfactants; nonionic surfactants, cationic surfactants, zwitterionic surfactants, and mixtures thereof, preferably selected from organic polymeric compound, nonionic surfactants, and mixtures thereof, more preferably nonionic surfactants selected from nonionic ethoxylated alcohols. 11. A process as claimed in any of the preceding claims, wherein the amount of carrier material range from 15 to 80% and preferably from 25 to 75%, by weight of the produced particles of the processed amine reaction product. 12. A process as claimed in any of the preceding claims, wherein the coating is made of water-soluble agglomerating agent. 13. A process as claimed in any claim 12, wherein the water-soluble agglomerating agent is selected from water soluble organic polymeric compounds, water soluble monomeric polycarboxylates, or their acid forms, home or copolymeric polycarboxylic acids or their salts in which the polycarboxylic acid comprises at least two carboxylic radicals separated from each other by not more that two carbon atoms, carbonates, bicarbonates, borates, phosphates, sulfate salts, inorganic perhydrate salts, silicates, starch, cyclodextrin, and mixtures thereof, preferably selected from starch, carbonate, cyclodextrin, and mixtures thereof. 14. A process as claimed in any of the preceding claims, wherein the amount of amine reaction product ranges from 1 to 75%, preferably 5 to 30% by weight of the coated particle. 15. A processed amine reaction product as obtainable by the process as claimed in claims 1-14. 16. A process for making particles of amine reaction product of a compound, substantially as hereinbefore described with reference to the foregoing examples. |
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in-pct-2000-00335-del-abstract.pdf
in-pct-2000-00335-del-claims.pdf
in-pct-2000-00335-del-correspondence-others.pdf
in-pct-2000-00335-del-correspondence-po.pdf
in-pct-2000-00335-del-description (complete).pdf
in-pct-2000-00335-del-form-1.pdf
in-pct-2000-00335-del-form-19.pdf
in-pct-2000-00335-del-form-2.pdf
in-pct-2000-00335-del-form-26.pdf
in-pct-2000-00335-del-form-3.pdf
in-pct-2000-00335-del-form-5.pdf
in-pct-2000-00335-del-pct-304.pdf
in-pct-2000-00335-del-pct-409.pdf
in-pct-2000-00335-del-pct-416.pdf
in-pct-2000-00335-del-petition-137.pdf
in-pct-2000-00335-del-petition-138.pdf
IN-PCT-2000-335-DEL-Correspondence Others-(21-06-2011).pdf
IN-PCT-2000-335-DEL-Form-27-(21-06-2011).pdf
IN-PCT-2000-335-DEL-Petition-137-(21-06-2011).pdf
Patent Number | 214560 | ||||||||||||||||||||||||
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Indian Patent Application Number | IN/PCT/2000/00335/DEL | ||||||||||||||||||||||||
PG Journal Number | 08/2008 | ||||||||||||||||||||||||
Publication Date | 22-Feb-2008 | ||||||||||||||||||||||||
Grant Date | 12-Feb-2008 | ||||||||||||||||||||||||
Date of Filing | 15-Nov-2000 | ||||||||||||||||||||||||
Name of Patentee | THE PROCTER & GAMBLE COMPANY | ||||||||||||||||||||||||
Applicant Address | ONE PROCTOR & GAMBLE PLAZA, CINCINNATI, STATE OF OHIO, UNITED STATES OF AMERICA | ||||||||||||||||||||||||
Inventors:
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PCT International Classification Number | C11D 3/20 | ||||||||||||||||||||||||
PCT International Application Number | PCT/US99/15679 | ||||||||||||||||||||||||
PCT International Filing date | 1999-07-12 | ||||||||||||||||||||||||
PCT Conventions:
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