Title of Invention

PERFUME CONTAINING SURFACTANT COMPOSITIONS HAVING PERFUME BURST WHEN DILUTED AND PROCESS THEROF

Abstract Compositions yielding a maximum fragrance burst of one or more of the fragrance components of at least 20%, relative to an undiluted product, wherein said composition is defined by perfume burst index PBI: 4>-1.4/CMC PBI = K wherein . <|> = oil/water partition coefficient of a selected perfume or perfume components in a mixture; CMC=critical micellization concentration (wt./wt.) of selected surfactant system or mixture of surfactant system in diluent or continuous phase; K=volatility constant of selected perfume from said continuous phase or diluent (atmospheres); wherein said perfume or at least one component of said perfume mixture and wherein said surfactant system or said mixture of surfactant systems are selected such that variables are calculated to provide a PBI that is greater than about 3; wherein by maximum fragrance burst of at least 20% is meant that the perfume concentration in the headspace above said fragrance or fragrance components increases at least 20% relative to the perfume concentration in the headspace of an undiluted product comprising the same fragrance or fragrance components measured as the composition comprising said fragrance or fragrance components is diluted below the critical micelle concentration (CMC) of the fragrance, surfactant and water system.
Full Text FORM -2
THE PATENTS ACT, 1970 (39 of 1970)
COMPLETE SPECIFICATION
(See Section 10)
PERFUME CONTAINING SURFACTANT COMPOSITIONS
HAVING PERFUME BURST WHEN DILUTED AND
PROCESS THEREOF
HINDUSTAN LEVER LIMITED, a company incorporated under , * the Indian Companies Act, 1913 and having its registered office at Hindustan Lever House, 165/166, Backbay Reclamation, Mumbai -400 020, Maharashtra, India
The following specification particularly describes the nature of the invention and the manner in which it is to be performed.

ORIGINAL
450/MUMNP/2004
16/8/04

GRANTED
16-10-2006


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PERFUME CONTAINING SURFACTANT COMPOSITIONS HAVING PERFUME BURST WHEN DILUTED AND PROCESS THEREOF
The invention relates to compositions, e.g., personal wash
5 perfume-containing compositions, which are able to deliver
perfume benefits (i.e., "urst" or increase in perfume
headspace relative to undiluted composition) upon dilution
in water. The invention further relates to process for
i : preparing such compositions. Further the invention relates
10 to enhanced deposition of one or more fragrance components
on surfaces with which the compositions come into contact.
More specifically, by; being aware of which properties of the perfume and of the surfactant systems in which they are
15 found are responsible:for perfume release on dilution, the applicants have been able to provide both specific compositions and processes for selecting perfumes and/or surfactant systems in said compositions which meet defined criteria (as defined, for example, in perfume burst index),
20 and thereby provide aroma burst of at least defined levels upon dilution. The invention further may relate to methods of changing fragrance note and/or introducing smell after dilution.
25 Perfume is a key component for a favorable consumer
experience with home and personal care products. It is also often the most costly component of the formulation. Typically most of the fragrance is quickly lost as the product is used, because most of the perfume is trapped in
30 the surfactant system. There has been a long-standing need to improve the utilization of perfumes, and to design

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compositions that provide maximum and prolonged impact in use. It is one objective of this invention to develop a means by which products can be developed to provide greater fragrance impact and novel fragrance characteristics in use. 5
To this end, the applicant has found that perfume activity (e.g., the aroma of the perfume) both in a product (e.g., surfactant containing product) and upon use (e.g., dilution of product in shower) can be correlated to the thermodynamic 10 characteristics of (1) the perfume itself and (2) the formulation in which the perfume is found.
For example, the degree to which a perfume will partition into oil or water (measured by a so-called "artition
15 coefficient", and a reflection of the hydrophobicity of the perfume) and the degree to which the perfume evaporates (measured by "volatility constant" and a reflection of the volatility of the perfume) are two significant characteristics of the perfume which strongly affect the
20 potential perfume "burst" when said product is diluted. By burst is meant an increase in the concentration of perfume in the vapor phase above the solution (i.e., this is also known as perfume headspace) with respect to the undiluted product and composition. The vapor phase can of course vary
25 depending on product, for example, from a small area above a bottle of perfume to an area in a shower stall.
As noted, the perfume burst is affected not only by the perfume properties, but also by properties of the 30 formulation in which the perfume is found. Thus, the number and type of surfactant micelles found in a surfactant

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solution also has an effect. For example, in a surfactant with high critical micellization concentration (CMC) (in compositions of high CMC, micelles do not form as readily) perfume "burst" would occur more readily and less dilution 5 is required. The critical micellization concentration is defined as the surfactant concentration at which micelles begin to form from unassociated surfactant monomers (M.J. Rosen, Surfactants and Interfacial Phenomena, 2nd Ed., 1989).
*
Conversely, in a surfactant with low critical micelle 10 concentration (e.g., one where micelles do form easily or, stated differently, don't break apart as readily once formed), a perfume, being generally more hydrophobic, tends to stay in the surfactant more readily. As a result, the perfume will tend not to "burst" (increase perfume 15 headspace) as readily and to achieve more headspace, more dilution may be required.
Other important formulation factors which may affect the "burst" of the perfume may include, but are not limited to 20 perfume content in solution, and the surfactant to water ratio.
Still another factor which can affect perfume "burst" is the environment in which it is found, for example such 25 environmental factors as (1) overall sample amount; (2) vapor volume and (3) temperature.
According to the subject invention, the applicants have succeeded in putting together a thermodynamic model which 30 can be used to select the types of perfume and formulations which should be used in order to maximize this perfume burst

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or actual headspace (actual concentration of perfume in vapor phase) when a formulation (e.g., personal wash or shampoo formulation) is diluted in use. Also, the applicants have found, since perfume burst correlates with 5 perfume deposition, the model can be used to select perfumes in surfactant systems with enhanced disposition.
More specifically, the applicants have defined a perfume burst index which defines compositions which can deliver a
10 perfume burst upon dilution of at least a certain amount relative to undiluted composition; and further allows the applicants to define a process for obtaining such compositions and methods for enhancing deposition, as well as a method of changing"fragrance note and/or introducing
15 smell after dilution.
In general, burst is achieved by diluting a surfactant system (e.g., an aqueous surfactant system) whereupon the burst begins upon dilution, and maximum burst is obtained
20 upon reaching CMC, therefore, releasing all of the perfume from the surfactant system. Thus, a composition yielding a maximum fragrance burst of 20% means the perfume concentration in the headspace increases by about 20% relative to the undiluted product when the solution is
25 diluted through the CMC. The CMC is the point where the perfume-surfactant-water system changes to a perfume-water system (i.e., the system is too dilute for micelles to form).
30 A surfactant system is defined as a surfactant and/or
surfactant mixtures which may include ingredients selected

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to manipulate the CMC in a continuous phase. These selected ingredients can include urea; glycerine; C1-C12 straight-chained or branched alcohols or diols; water soluble polymers such as polyvinylpyrolidone, polyvinylalcohol, 5 polyethyleneglycol, polypropyleneglycol; multivalent
electrolytes such as magnesium, calcium and aluminum salts; and sugars such as dextrose, glucose, maltose, galactose, sucrose. The continuous phase is typically water, but may
also include C1-C8 straight-chained or branched alcohols or 10 dipls, glycerine, C1-C8 esters and combinations thereof.
Generally, surfactants which may be used include anionic, nonionic, amphoteric/zwitterionic and cationic surfactants as discussed in more detail below.
15
In one embodiment, the invention relates to a composition having a fragrance burst, as measured by a "perfume burst index", of about 20% relative to a composition containing surfactant systems;and perfume/fragrance prior to dilution
20 of said product. The invention also relates to processes to prepare such composition. The process is also to prepare or select a composition having enhanced deposition of one or more fragrance components on surface (e.g., skin) with which the composition comes into contact.
25
More specifically, the invention relates to specific compositions (and processes to obtain the composition) obtained by selecting perfume and/or perfumes and surfactant systems and/or mixtures of surfactant systems and

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calculating therefrom a perfume burst index (PBI) according to the following formula:

PBI =

p - 1.4/CMC
K

wherein p = oil/water partition coefficient of
selected perfumes or perfume components
10 in a mixture;
CMC = critical micellization concentration of surfactant systems or mixture of surfactant systems (wt./wt.); and K=' volatility constant of perfume or
15 perfume components in a mixture from the
continuous phase (atmospheres).
The perfumes and surfactant systems are specifically selected to ensure that the PBI calculated is greater than 20 about 3.
It should be understood that the PBI defines the maximum potential fragrance burst which is achieved at the CMC for the surfactant or surfactant mixture. For example, a
25 relatively low PBI (e.g., about 3) will obtain a "burst" of at least 20% as noted. However, if the PBI is higher, much higher fragrance burst can be expected. Thus, for example, a burst of 20% may be achieved upon immediate dilution (assuming high enough PBI), and may continue up to 700% or
30 800% or more at CMC (which as noted is point of maximum potential burst).

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As far as the applicants are aware, there is no art which specifically discloses that such burst can be obtained with such compositions or processes, or which discloses a way of predicting when and under what circumstances such fragrance 5 "burst" will occur based on the dilution behavior of a perfume-surfactant-water system. Further no art of which the applicants are aware discloses how such compositions are in turn related, for.example, to properties of the perfume (e.g., partition coefficient, volatility) as well as to 10 properties of the formulation (e.g., surfactant concentration and surfactant CMC).
The invention relates; to surfactant compositions, preferably aqueous surfactant compositions (e.g., bars, personal wash
15 liquids, shampoos) in- which perfume and surfactant are
selected as to provide a fragrance burst, when diluted, of at least about 20% relative to undiluted product. Compositions must have a perfume burst index, as defined, of about 3.0 or greater, preferably 4.0 or greater.
20
The invention further relates to a process for selecting such compositions by selecting perfumes and choosing surfactant system or manipulating CMC of surfactant system to ensure the PBI is at least about 3.0.
25
The invention is based on the applicants' observation that variations in perfume impact ("burst") on dilution are essentially caused by the competition between a decrease in overall fragrance concentration upon dilution;"and an
30 increase in fragrance concentration in the continuous phase as the fragrance is released during disassociation of

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surfactant micelles which occurs during dilution. More specifically, and without wishing to be bound by theory, applicants have observed and shown that only perfumes with relatively large oil/water partition coefficient (very
5 hydrophobic) possess the potential to produce a fragrance burst upon dilution. Other parameters which are important to minimum burst include (1) volatility constant of perfume; (2) surfactant concentration; (3) type of surfactant system; (e.g., CMC) etc.
0
Specifically, the applicants have developed a theoretical mathematical equation based on the various variables noted above. More specifically, they have developed a perfume burst index which both defines compositions having a maximum
5 burst of at least 20% and further provides a process for selecting such compositions based on properties of perfume and surfactant system.
The relationships are defined in more detail below. 20 The invention will now be described by way of example only with reference to the accompanying drawings, in which:
- Figure 1 is a chart showing various product
25 parameters that influence perfume performance in diluted products (e.g., diluted personal wash products);
- Figure 2 shows theoretical calculation of fragrance
burst for 3 types of perfume (as per Table 1) -with-.dilution;

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--
- Figure 3 shows fragrance burst profiles of different perfumes in surfactant solution;
- Figure 4 discloses an example of 2-component
5 fragrances which would change note upon dilution as one
component increases in concentration and another decreases;
- Figure 5 shows theoretical models of fragrance burst
with changes in surfa'ctant concentration;
10
- Figure 6 shows experimental results of fragrance
burst with changes in surfactant concentration;
- Figure 7 shows theoretical model of fragrance burst
15 with change in surfact CMC;
- Figure 8 shows experimental results of fragrance
burst with change in surfactant CMC;
20 - Figure 9 shows normalized dilution curve for component in a perfume mixture;
- Figure 10 shows the result of sensory scores averaged
overall panellists in a panel study of single perfume;
25
- Figure 11 shows the results of sensory scores
averaged over all panellists panel study of multi-component
perfume;
30 - Figure 12 shows how deposition of perfume varies with CMC of surfactant; and

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- Figure 13 shows deposition results for a multi component perfume from surfactant systems having different CMC. 5
According to the subject invention, the applicants have identified surfactant compositions in which the perfume and/or perfumes and the surfactant system and/or surfactant systems are selected 'to provide a fragrance burst when
10 diluted. The invention also provides a process for preparing or selecting such composition with defined fragrance burst by selecting perfume and/or perfumes and surfactant system and/or systems to provide such a burst when diluted. The burst is at least 20% at dilution,
15 although it can be much higher and reaches maximum strength at CMC. The applicants have further developed a process for, determining (using defined perfume burst index) how to identify these compositions.
20 That is, when a perfume is in a perfume-surfactant-water system (where some portion of perfume will be associated with surfactant micelles and some portion will be in water) and the formulation is diluted, a fragrance "burst" is produced when parameters are properly chosen. The intensity
25 of the burst will depend, for example, on how much of the
perfume is released from micelles as dilution occurs; and on the volatility of the perfume.
More specifically, some factors which affect perfume
30 headspace concentration, upon dilution, are "(a) -various
perfume properties (e.g., oil/water partition coefficient;

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p, which is a measurement of the partitioning of the perfume or of the perfume components in a mixture between the oil and water phases, thereby reflecting the hydrophobicity of perfume; and volatility constant, K, which is a measure of
5 the partial pressure of the perfume or of the perfume components in a mixture in the vapor phase above the continuous phase of the composition, thereby reflecting the volatility of the perfume); (b) surfactant concentration in the formulation (e.g. lower surfactant concentration tends
0 to result in higher perfume headspace over initial
formulation and more intense "burst" around CMC with fewer required dilutions); and (c) CMC of surfactant system (e.g., higher surfactant system CMC tends to provide more intense fragrance "burst" around CMC with fewer required dilutions).
15
As noted earlier, in general, for a fragrance "burst" or increase in perfume headspace concentration to occur during product use, the amount of fragrance released from micelles as they dissociate must compensate for overall decrease in
20 perfume concentration upon dilution. Compositions having a Perfume Burst Index (PBI) greater than about 3 clearly meet the necessary criteria.
Typically, a cleansing composition (e.g., a personal wash 25 cleansing composition) containing perfume can be thought of
as a perfume-oil-water system with the oil phase comprising
surfactant micelles and water forming the continuous phase.
Any perfume will distribute between the surfactant micelles
and water phase as governed by the perfume's 30 surfactant/water partition coefficient. In-addition, the
equilibrium perfume headspace concentration is proportional

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to the perfume concentration in the aqueous phase as governed by the volatility constant, K. The presence of a surfactant micelle phase impacts perfume headspace concentration by solubilizing the perfume, and thereby 5 affecting perfume concentration in the aqueous phase (e.g., more is in the micelles, less is in the water).
Use of, for example, a personal wash cleansing product in bath or shower causes dilution. This dilution leads to a 10 decrease in micelle concentration forcing the perfume into the aqueous phase and, accordingly, affecting the headspace concentration or perfume "burst".
However, dilution causes the quantity of surfactant micelles 15 in a surfactant composition to decrease until gradually
reaching critical micellization concentration (CMC). Below CMC, surfactant is present only as monomers or other small aggregates not large enough to form micelles. At this point, all perfume which was previously present in micelles 20 is totally released.
More specifically, it should be understood, CMC is the point of maximum potential burst (e.g., where release of perfume is complete because there are no more micelles). The 25 release of perfume, however, begins as soon as dilution occurs, and the burst gradually increases from first dilution up until CMC.
In measuring perfume headspace (using, for example, gas 30 chromatography headspace measurement), the applicants
observed that dilution of certain compositions containing

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perfume or perfume components in a perfume mixture led to an increase in perfume headspace and that, upon reaching the CMC, maximum perfume headspace was achieved. It is precisely this "burst" or increase in headspace (e.g., from 5 start of dilution up until CMC) and methods for determining in what compositions it will occur that is the basis of the subject invention.
The different parameters that affect perfume concentration 10 in the vapor phase can be controlled by manipulating the
formulation, the perfume itself or the environment in which
the product dilution is occurring as shown in Figure 1.
Understanding how each variable affects the overall
fragrance performance in a personal product composition in 15 use is critical to designing optimum systems for enhanced
perfume benefits (e.g. fragrance burst, enhanced perfume
deposition).
More specifically, applicants have found compositions which 20 yield a maximum fragrance burst of at least about 20%, relative to undiluted product. These compositions are defined by establishing a perfume burst index (PBI) which is defined below:
25 p - 1.4/CMC
PBI = =—
K
wherein

30 perfume or perfume components in a mixture;
CMC = critical micellization concentration (wt./wt.) of surfactant systems;

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K = volatility constant of perfume or perfume components in a mixture from the continuous phase (atmospheres); 5
wherein variables are selected such that PBI is greater than
about 3.
As noted, perfume headspace behavior of a perfume-10 surfactant-water system is governed by different
thermodynamic principles above or below CMC upon dilution. The perfume headspace behavior upon dilution is closely related to the oil/wafer partition coefficent (o) and the volatility constant (K) of perfume, which reflect the 15 hydrophobicity and volatility of the perfume respectively.
In Table 1 below, perfumes are classified into four categories according to their oil/water partition coefficients (o) and their volatility constants (K) . Since 20 two of the three factors contributing to the PBI value for fragrance molecules, are the partition coefficient and volatility constant, one can predict the extent of " perfume burst" these different types of perfume should exhibit in the proper surfactant system.



Table 1: Classification of Perfume Molecules
00

Examples of partition Coefficient

Volatility
Constant
k * Volatility Initial headspace Burst
upon
dilution
For
Perfume
Type 1 50 (1.7) Low 50 High Very high No
For Perfume Type 2 1000 (3) High 1 Low Very low High
For
Perfume
Type 3 1000 (3) High 250 High High Medium
For Perfume Type 4 50 (1.7) Low 1 Low Low No

* K is generally measured in units of atmosphere.
OS

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Fragrance molecules that fall into the Type 1 category are
actually very rare, but due to their low partition
coefficient (0) and their high volatility constant, one
would predict no fragrance burst upon dilution. The low
5 solubility in the surfactant phase would result in very
small release of fragrance upon dilution, so a typical
dilution profile (e.g., where perfume headspace decreases
continuously with dilution) would be expected. That is,
t . such molecules would normally tend to be found in the water
10 phase anyway. So any action (dilution) causing release of
perfume from surfactant micelles would be largely
irrelevant.
In general, type 1 perfumes have oil/water partition 15 coefficient [o) of 1 to about 200, preferably 2 to 100; and volatility constant (K) of 2 to 1000, preferably 50 to 1000 -atmospheres.
Type 2 perfumes would be anticipated to produce the most 20 intense "perfume burst" upon dilution. These molecules are typically fragrance base notes and are very hydrophobic although their overall volatility is low resulting in low fragrance impact in a typical full formulation, i.e., before dilution. Therefore upon dilution, these molecules are 25 released from the surfactant micelles, and the noted
increase in fragrance intensity is quite large. That is, because of their hydrophobicity, the perfume molecules tend to stay in micelles until release upon dilution, and ...this release combined with the low volatility of the perfume in 30 the initial formulation causes a high burst. In general, Type 2 perfumes have oil/water partition coefficients

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greater than 500, preferably greater than 700 and volatility constant less than about 20, preferably less than about 15.
Specific examples of Type 2 perfume molecules include allyl 5 cyclohexane propionate, ambrettolide, Ambrox DL
(dodecahydro-3a, 6,6,9a-tetramethyl-naphtho[2,1-b]furan), amyl benzoate, amyl cinnamate, amyl cinnamic aldehyde, amyl salicylate, anethol, aurantiol, benzophenone, benzyl butyrate, benzyl iso-valerate, benzyl salicylate, cadinene,
10 campylcyclohexal, cedrol, cedryl acetate, cinnamyl
cinnamate, citronellyl acetate, citronellyl isobutyrate, citronellyl propionate, cuminic aldehyde,
cyclohexylsalicylate, cyclamen aldehyde, cyclomyral, dihydro isojasmonate, diphenyl"methane, diphenyl oxide, dodecanal,
15 dodecalactone, ethylen® brassylate, ethylmethyl phenylglycidate, ethyl undecylenate, exaltolide,
Galoxilide™ {1,3,4,6,7, 8-hexhydro, 4, 6, 6, 7, 8, 8-hexamethyl-
cyclopenta-y-2-benzopyran), geranyl acetate, geranyl isobutyrate, hexadecanolide, hexenyl salicylate, hexyl 20 cinnamic aldehyde, hexyl salicylate, a-ionone, p-ionone, y-ionone, a-irone, isobutyl benzoate, isobutyl quinoline, Iso
E Super™ (7-acettl,1,2,3,4,5, 6,7,8-octahydro,1,1,6,7-
tetramethyl napthalene), cis-jasmone, lilial, linalyl benzoate, 20 methoxy naphthaline, methyl cinnamate, methyl 25 eugenol, y-methylionone, methyl linolate, methyl linolenate, musk indanone, musk ketone, musk tibetine, myristicin, neryl acetate, 5-nonalactone, y-nonalactone, patchouli alcohol, phantolide, phenylethyl benzoate, phenylethylphenylacetate, phenyl heptanol, phenyl hexanol, a-santalol, thibetolide,

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tonalid, 8-undecalactone, y-undecalactone, vertenex, vetiveryl acetate, yara-yara and ylangene.
Hydrophobic, volatile fragrances fall into the Type 3 5 perfume category. Since these molecules have high oil/water partition coefficients, they will be solubilized by the surfactant system and then be released upon dilution providing a "perfume burst". The actual extent of this burst will not be. as large as that for Type 2 perfumes
10 because the fragrances are so volatile in the first place, hence the PBI values will be lower, but great enough to provide a perceivable burst. In general, they will have an oil/water partition coefficient of greater than about 500, preferably greater than 700; and a volatility constant of
15 about 20 to 1000.
Type 3 fragrance molecules fall into the top and middle note categories and include allo-ocimene, allyl caproate, allyl heptoate, anisole, camphene, carvacrol, carvone, citral,
20 citronellal, citronellol, citronellyl nitrile, coumarin,
cyclohexyl ethylacetate, p-cymene, decanal, dihydromyrcenol, dihydromyrcenyl acetate, dimethyl octanol, ethyllinalool, ethylhexyl ketone, eucalyptol, fenchyl acetate, geraniol, gernyl formate, hexenyl isobutyrate, hexyl acetate, hexyl
25 neopentanoate, heptanal, isobornyl acetate, isoeugenol,
isomenthone, isononyl acetate, isononyl alcohol, isomenthol, isopulegol, limonene, linalool, linalyl acetate, menthyl acetate, methyl chavicol, methyl octyl acetaldehyde, myrcene, napthalene, nerol, neral, nonanal, 2-nonanone,
30 nonyl acetate, octanol, octanal, a-pinene, p-pinene, rose oxide, a-terpinene, y-terpinene, a-terpinenol, terpinolene,

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terpinyl acetate, tetrahydrolinalool, tetrahydromyrcenol, undecenal, veratrol, and verdox.
Finally, Type A perfume components which again are 5 classified as top and middle notes, have very low- oil/water partition coefficients and therefore like Type 1 components would not be expected to release significantly upon dilution to provide a perfume burst". While these molecules will
t
not add to the intensity of the fragrance burst in a fully 10 formulated perfume, they are still very important fragrance components. By combining perfume molecules that decrease in intensity upon dilution with those that "burst" upon dilution, the overall, fragrance note during use will change. Fragrance note is defined as the type of odor a perfume or

15 mixture of perfume components produces.
For example, phenethylalcohol provides a floral rose note, methylionone produces a woody note, and bergomot and limonene produces citrusy, fruity notes. The fragrance
20 could smell different' in-use to that of the original
product. Typically these perfumes will have an oil/water partition coefficient of about 1 to about 200, preferably 2 to 100 and a volatility constant of less than about 20, preferably less than about 15.
25
Fragrance Type 4 molecules include acetanisol; amyl acetate; anisic aldehyde; anisylalcohol; benzaldehyde; benzyl acetate; benzyl acetone; benzyl alcohol; benzyl formate; hexenol; Iaevo-carveol; d-carvone; cinnamaldehyde; cinnamic
30 alcohol; cinnamyl acetate; cinnamyl formate; cis-3-hexenyl acetate; Cyclal C (2,4-dimethyl-3-cyclohexen-l-

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carbaldehyde) ; dihydroxyindole; dimethyl benzyl carbinol; ethyl acetate; ethyl acetoacetate; ethyl butanoate; ethyl butyrate; ethyl vanillin; tricyclo decenyl propionate; furfural; hexanal; hexenol; hydratropic alcohol; 5 hydroxycitronellal; indole; isoamyl alcohol; isopulegyl acetate; isoquinoline; ligustral; linalool oxide; methyl acetophenone; methyl amyl ketone; methyl anthranilate; methyl benzoate; methyl benzyl acetate; methyl heptenone;
t
methyl heptyl ketone; methyl phenyl carbinyl acetate; methyl
10 salicylate; octalactone; para-cresol; para-methoxy
acetophenone; para-methyl acetophenone; phenethylalcohol; phenoxy ethanol; phenyl acetaldehyde; phenyl ethyl acetate; phenyl ethyl alcohol; prenyl acetate; propyl butyrate; safrole; vanillin and viridine.
15
In general, as noted above, it can be seen that molecules with higher oil/water partition coefficient (e.g., Type 2 and 3) will have a greater burst. This may be, without wishing to be bound by theory, because the perfume is highly
20 soluble in the surfact ant micelles and upon dilution, which triggers the dissociation of these micelles, a large amount of perfume is released thereby compensating for the decrease in overall perfume concentration in the diluted system. As noted from perfume Type 3 versus 2, this is balanced to some
25 extent by volatility (volatility constant) of the perfume since, for two perfumes otherwise having same partition coefficient, the one which is less volatile (Type 2) will be expected to have larger burst.
30 The CMC of the surfactant system also affects "perfume burst". Thus, for example, a surfactant system of

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-
relatively low CMC (e.g., sodium lauryl ether sulfate, also known as SLES) lowers the PBI and can greatly reduce the expected "perfume burst" on dilution. By contrast, surfactant systems of relatively higher CMC (e.g., sodium 5 laurate compared to SLES) would raise PBI, and can thus increase '"perfume burst" on dilution. Examples of CMC for various individual surfactants are set forth in Table 2 below.


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Table 2: The Critical Micellization Concentration (CMC) of Surfactants

Surfactant CMC (wt./wt.)
C8H17S03~Na+ 0.0346*
C10H2lS03~Na+ 0.0105*
Cl2H25S03~Na+
t 0.0034*
C8H17S04~Na+ 0.0325*
C10H21SO4 Na 0.00858*
C11H23S04~Na 0.00438*
C10H2lOC2S03~Na 0.00452*
C6H13OOCCH2S03~Na+ 0.0412*
C8H1700CCH2S03"Na+ 0.0181*
C8H1700C(CH2)2S03~Na+ 0.0132*
C12H2500C(CH2)2S03~Na+ (SCI) 0.00076* (30 °C)
C4H9OOCCH2CH(S03~Na+)COO C4H9 0.0664*
C5H11OOCH2(S03"Na+.)COO C5H11 0.0178*
C6H1300CH2CH(S03~Na+)COO C6H13 0.0053*
n-C6H13(OC2H4)60H 0.0271*
(C2H5)2CHCH2(OC2H4)6OH 0.0366*
(C3H7)2CHCH2(OC2H4)60H 0.0091*
C6H13[OCH2CH(CH3)]2(OC2H4)9.90H 0.0307*
n-octyl-B-D-glucoside 0.0111*
Pluronic E037P058E037 0.0065**
5 (continued ...)

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- ?3 -

Sodium laureth sulfonate (2EO) (50°C) 0.0.011***
Sodium laureth sulfonate (3EO) (50°C) 0.00084***
Linear alkylbenzene sulfonate 0.00171***
Sodium oleate 0.0008***
Potassium laurate 0.00607***
Sodium laurate
* 0.0052***
Caprylamidopropyl betaine 0.00032
Reference:
* M. J. Rosen, Surfactants and Interfacial Phenomena, 2nd 5 ed., 1989
** P. Alexandridis, L. Yang, Macromolecules, 2000, 33,
5574-5587. *** P. Mukerjee, K. J Mysels, Critical Micelle
Concentrations of Aqueous Surfactant Systems, 1971 10
The CMC of the surfactant or surfactant system mixture can itself be manipulated (e.g., to help control "perfume burst") by using various components which can be added to 15 affect the CMC.
Non-limiting examples of such component include urea; glycerine; C1-C12 straight-chained or branched alcohols or diols, water soluble polymers such as polyvinylpyrolidone 20 polyvinylalcohol polyethylene glycol, or
polypropyleneglycol, multivalent electrolytes (e.g., magnesium, calcium and aluminum salts); and sugars such as dextrose, glucose, maltose, galactose and sucrose.

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In general, the surfactant system or surfactant system mixture are selected to have a CMC greater than about 0.0001 (wt./wt.).
5 In general, however, there is no limitation to the
surfactant or surfactant system which can be used. That is, the surfactant system of the invention may comprise anionic, nonionic, amphoteric/zwitterionic and/or cationic surfactant and/or mixtures of any of these. That is, the invention is 10 not dependent on type of surfactant system, but only on CMC of surfactant or surfactant systems.
Among anionic surfactants which may be used are included aliphatic surfactants (e.g., non-limiting examples include
15 C8 to C22 alkane sulfonate or disulfonate, alkene sulfonate,
hydroxy alkane sulfonate, alkyl glyceryl ether sulfonate); and aromatic sulfonate (e.g., alkyl benzene sulfonate).
Also included are alkyl sulfates (e.g., C12-C18 20 alkylsulfate); alkyl ether sulfates; alkyl sulfosuccinates; alkyl and acyl taurates; alkyl and acyl sarcosinates; sulfoacetates; alkyl phosphates; phosphate esters; acyl
lactates; C8to C22 monoalkyl succinates and maleates; sulfoacetates; and acyl isethionates. Also included are 25 carboxylates. Salts of anionic surfactants (which can include fatty acid soaps) may also be included.
Zwitterionic surfactants can be broadly described as derivatives of aliphatic quaternary ammonium, phosphonium 30 and sulfonium compounds in which aliphatic radicals can be

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straight or branched chain and wherein at least one aliphatic substituent contains about 8 to about 18 carbons and at least one contains an anionic group, e.g., carboxy, sulfonate, sulfate, phosphate or phosphonate. 5
Amphoteric surfactants include at least one acid group (e.g., carboxylic or sulfonic). They include quaternary nitrogen and may include quaternary amido acids as acid group. They also generally include alkyl or alkeny group of 10 7 to 18 carbons. Examples include simple betaines, amido betaines and sulfobetaines.
Nonionic surfactants which may be used include reaction product of compounds having a hydrophobic group and a 15 reactive hydrogen (for example, aliphatic alcohols, acids, amides or alkyl phenols) with alkylene oxide, especially ethylene oxide either alone or with propylene oxide. Examples include alkylphenols-ethylene oxide condensates and
condensation products of aliphatic (C8-C18) primary or
20 secondary linear or branched alcohols with ethylene oxide. They may also be sugar amides and alkylpolyglycosides.
Cationic surfactants include quaternary ammonium compounds such as, for example, alkyldimethyl ammonium halogenides.
25
Some examples of surfactants which may be used in surfactant systems of the invention include sodium lauryl ether sulfate, sodium laurate, potassium lauride, sodium oleate, potassium oleate, triethanolamine laurate,
30 alkylpolyglucosides, sodium lauryl sulfate,
caprylamidopropyl betaine and sodium cocoylisethionate. As

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noted, however, there is theoretically no limit as to which surfactant or surfactant systems may be used.
The compositions of the invention also have enhanced 5 deposition of perfume or perfume components onto the surfaces with which the compositions come into contact.
Generally, for compositions with higher PBI, perfume headspace increases with dilution due to higher perfume
10 concentration in the continuous phase. The higher
concentration in the continuous phase also favors greater surface contact, and hence greater perfume deposition. Thus, perfume deposition is correlated to perfume burst. In this way, it can be seen that PBI can be used to predict
15 fragrance delivery or deposition. Those surfactant systems which facilitate perfume burst will, in other words, have enhanced deposition relative to surfactant systems which do not favor burst as much.
20 In another embodiment, the invention relates to a
composition wherein the fragrance note can be changed subsequent to dilution by (1) selecting a fragrance with a mixture of perfume components wherein some have PBI greater than 3.0 and some have PBI less than 3.0; and (2) assuring
25 selection of fragrance components such that the components desired in the new fragrance (i.e., notes with desired fragrance after dilution) have a PBI greater than about 3.
In yet another embodiment, the invention relates to a 30 composition wherein a desired fragrance note can be subsequent to dilution by ensuring that fragrance or

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fragrance components having the desired aroma and which are selected for the composition have a PBI greater than about 3 so that, upon dilution, the perfume headspace concentration exceeds the odor threshold. Odor threshold is the minimum 5 concentration of fragrance in the vapor phase required for human detection.
Except in the operating and comparative examples, or where
otherwise explicitly indicated, all numbers in this
20 description indicating amounts or ratios of materials or
conditions or reaction, physical properties of materials
and/or use are to be understood as modified by the word
" about" . ;
25 Where used in the specification, the term " comprising" is intended to include the presence of stated features, integers, steps, components, but not to preclude the presence or addition of one or more features, integers, steps, components or groups thereof.
The following examples are intended to further illustrate the invention and are not intended to limit the invention in any way.
25 Unless indicated otherwise, all percentages are intended to be percentages by weight.

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EXAMPLES
Example 1
5 Fragrance molecules vary quite a bit in their physical
properties, and can therefore provide a variety of different effects depending on properties such as hydrophobicity, water solubility, volatility, molecular weight, etc. As shown in Example 1, some perfume components with specific
10 physical parameters will provide a fragrance burst" upon dilution of surfactant containing products such as shampoos, shower gels, soap bars, etc. A "perfume burst index" has been developed to determine which fragrance molecules will provide a burst or an' increase in perfume in the air upon
15 dilution of the product (which typically happens during
standard use of shampoos, shower gels, soap bars, light duty liquids, etc.).
This "perfume burst index" (PBI) is a function of several 20 physical properties of- the perfume and of the surfactant system. Depending on the amount of fragrance burst one desires, certain PBI is required.
pBI = O-1.4/CMC K
25 perfume or perfume components of a mixture; CMC = critical micellization concentration (wt/wt) of surfactant system; and

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K = volatility constant of perfume or perfume components of the mixture from the continuous phase.
5 To achieve a small, but potentially noticeable maximum
fragrance burst of 20% from a product containing surfactant,
the PBI of the perfume should be greater than about 3.0. To
produce a 50% enhancement of the fragrance, the PBI needs to
be greater than about 11 and to double the amount of
10 fragrance upon use, the PBI should be greater than about 27.
A perfume burst index" can be calculated for any desired
perfume molecule in a surfactant system. Table 3 contains a
list of fragrance molecules and their PBI's in a product
with CMC of 0.005 wt/wt (i.e. sodium laurate).

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Table 3: PBI Values for Various Perfumes

Perfume Molecule PBI "20% Burst"?
Acetanisol -31,000 No
p-Cresol -27,778 No
Indole -5,209 No
Benzyl Acetate -819 No
2-Phenoxyethanol -156 No
2-heptanone -153 No
Acetaldehyde -130 No
Cinnamyl Acetate;. -122 No
Hexanal -109 No
Methyl Benzoate -13 No
Anisole -5 No
Limonene 12 Yes
p-Cymene 12.2 Yes
a-pinene 20 Yes
Isoeugenol 58 Yes
Menthone 61 Yes
Napthalene 107 Yes
2-Nonanone 180 Yes
Tetrahydrolinolool 202 Yes
Linalool 240 Yes
Dihydromyrcenol 307 Yes
Nonanal 502 Yes
Ethyl Undecylenate 624 Yes
Decanal 942 Yes
a-ionone 1,692 Yes
y-methyl ionone 1,677 Yes
1-nonanol 24,164 Yes
Methyl Linolenate 771,304 Yes
Methyl Linolate 61149428 Yes
5 Example 2
As noted in Table 1, perfume may have various properties depending on hydrophobicity oil/water (oil/water-partition coefficient), volatility (volatility constant), etc.

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Figures 2(a) - 2(c) show calculated fragrance concentration profile in the headspace for three different types of perfume in a 5% surfactant product containing surfactant system with a CMC of 0.5% (i.e., sodium laurate). Hence, 5 maximum fragrance burst is obtained with 10 dilutions (around CMC). Figure 2(a) is "type 2" perfume (high hydrophobicity, low volatility), where one would expect high burst at CMC; Figure,2(b) is "type 3" perfume (high hydrophobicity, high'volatility), where burst at dilution is 10 less than for Type 2; and Figure 2(c) is "type 4" perfume
(low hydrophobicity, low volatility) , where no "burst" would be expected.
In general, fragrances "with high "perfume burst index" (PBI) 15 will produce much larger burst upon dilution than those with medium PBI. Perfume molecules with PBI less than about 3 will essentially produce no perceivable enhancement in smell on dilution, and simply show a standard dilution curve with decreasing perfume concentration in the headspace (see 20 Figure 2(c) ) .
In general, it may be noted that one key to "burst" is that the perfume must have high hydrophobicity.
.25 Example 3
Several different fragrance molecules were tested experimentally to validate the theoretical predictions. Limonene, p-cymene, a-pinene, tetrahydrolinolool, a-ionone, 30 Y-methyl ionone, benzyl acetate and 2-phenoxylethanol -were tested in a 5% sodium laurate shower product and diluted a

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number of times through the CMC (Figure 3). The PBI of limonene is 12, p-cymene is 12.2, cc-pinene is 20, tetrahydrolinolool is 202, a-ionone is 1692, y-methyl ionone is 1677, benzyl acetate is -819 and 2-phenoxylethanol is -5 156. As predicted, limonene, p-cymene and cc-pinene with a moderate positive PBI show moderate fragrance bursts of ~95%, 120% and 50% respectively. Tetrahydrolinolool, a-ionone and y_methyl ionone with large PBI values give quite large fragrance bursts of 320%, 430% and 460%, while benzyl 10 acetate and 2-phenoxylethanol with low, negative PBI values show no fragrance burst at all.
Example 4
15 Besides simply obtaining a "fragrance burst" upon dilution of these surfactant-containing products, one can also produce a change in fragrance note. Many perfumes are a combination of many different fragrance molecules. Depending on the combination of molecules and the amount of
20 each fragrance component in the mixture, one can obtain both a "fragrance burst"', i.e. an overall increase in fragrance concentration in the air around the product, and/or a change in fragrance note, i.e. a change from a "floral/green" note to a citrus note. The reason this change in fragrance note
25 can be obtained is because upon product dilution, those
molecules with a PBI greater than 3 will actually increase in concentration, while those compounds with a PBI less than 3 will simply dilute and decrease in concentration.
30 Therefore the concentration of the different--fragrance
components smelled with product use will change from that

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smelled over the fully formulated "original" product, and hence the overall character or "note" of the fragrance will be modified.
5 A few examples of fragrance mixtures that would be predicted to change note upon product dilution or use are shown in Tables 4-5. Figure 4 shows examples of two 2-component fragrances which would definitely change note upon dilution as one component increases in concentration and the other 10 decreases.
Table 4: Perfume that Could Change "Note" on Dilution in Surfactant Containing Product

Fragrance Component • PBI Dilution Behavior
Benzyl Acetate -881 Decrease headspace (HS)
Cinnamyl Acetate -43.3 Decrease HS
Limonene 12 Increase HS (50%)
Dihydromycenol 86 Increase HS (>3 times)
a-ionone 366 Increase HS (>3 times)
15
Table 5; Perfume that Could Change "Note" on Dilution in Surfactant Containing Product
20
Fragrance Component PBI Dilution Behavior
2-heptanone -153 Decrease HS
Menthone -71.4 Decrease HS
Isoeugenol 58 Increase HS (>3 times)
Tetrahydrolinalool 202 Increase HS (>3 times)
Linalool 240 Increase HS (>3 times)

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- Example 5 ,
It is also possible to take advantage of the technology of the invention to provide the introduction of a smell during 5 dilution of the surfactant-containing product. This can be achieved by formulating a fragrance ingredient into the product at a concentration just below the odor threshold. Therefore this component will not be perceived by the consumer in the original product, but as dilution occurs, if 10 the PBI is large enough to supply a concentration of that
component into the headspace above the product to exceed the
odor threshold, the fragrance molecule will now be perceived
upon use.
15 This concept can be used to provide a product that is
essentially " fragrance-free", but produces a light fragrance, with product dilution. This concept can also be utilized to , change fragrance note, but providing a new smell upon product dilution to combine with the other perfume molecules
20 to produce a new overall perfume mixture with use.
Example 6
As suggested by the theoretical predictions, formulation 25 factors also play a role in controlling the fragrance burst from the surfactant containing product in use. Two very important factors are the surfactant concentration in the original product, and the CMC of the surfactant mixture used in the formulation. 30

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The effect of surfactant concentration can be predicted from the theoretical predictions in Example 1. The charts in Figure 5 show the result of two different perfumes with PBI of ~700 and ~12 with varying surfactant concentration 5 (surfactant CMC = 0.005 wt/wt). As the graphs indicate, with a lower surfactant concentration in the original formulation, the initial fragrance concentration above the product will be higher (e.g., because fewer fragrance molecules are in surfactant micelles), and maximum fragrance
10 burst can be reached with fewer dilutions. This is
especially important, because the actual amount of dilution that typically occurs during product use is variable, depending on the type'of product and the consumer's habits. If the fragrance burst occurs with minimal dilution, the
15 effect is more likely to be noticed by the product user.
The other distinct advantage of products with low surfactant levels is that the absolute amount of fragrance available during the fragrance burst is greater, therefore the 20 consumer will experience more fragrance during product use.
Example 7
Experiments performed on actual perfumes in products with 25 different surfactant concentrations are shown in Figure 6. Limonene (PBI=12.2) was tested in shower liquids containing sodium laurate at 5, 10, 15 and 20 wt.%; gamma-methyl ionone and menthone were tested in sodium laurate at 5, 10 and 15 wt.% (Figure 6) . As noted in the theoretical.calculation 30 in Example 6, the maximum fragrance burst is reached with fewer dilutions in the 5% soap product, and the overall

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amount of fragrance available during the burst is also greater for the 5% product.
Thus, as seen, lower surfactant concentration is highly 5 beneficial.
Example 8
t
As noted in Examples 2. and 6, another variable that affects 10 the fragrance burst properties of a formulation is the
critical micellization concentration (CMC) of the surfactant system. The CMC is actually used to calculate the PBI for various fragrance molecules. As the CMC of the surfactant system is decreased,the PBI values for different fragrance 15 molecules also decreases as shown in Table 6. Therefore in products with surfactant systems with low CMC values, the expected extent of the fragrance burst for different fragrances will be less.

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Table 6: Fragrance Burst Potential in Surfactants with Different CMC's

5


Fragrance PBI CMC=0.005 Burst PBI CMC=0.0025 Burst PBI CMC=0.001 Burst
Benzyl Acetate -819 No -1694 No -4319 No
Hexanal -109 No -268 No -599 No
Methyl Benzoate -13
i No -32 No -89 No
2-Octanone -5 No -178 No -697 No
Isoeugenol 58 Yes 21 Yes -90 No
Hexyl Acetate 86 Yes -119 No -188 No
Napthalene 107 Yes 78 Yes -10 No
2-Nonanone 194 Yes -94 No -190 No
Linanool 24,0' Yes 147 Yes -133 No
Limonene 1.2 Yes 9 Yes 1 No
a-Ionone 1692; Yes 1261 Yes -30 No
a-Pinene 20 Yes 19 Yes 16 Yes
Tetrahydrolinolool 202 Yes 183 Yes 127 Yes
Dihydromyrcenol 307 Yes 267 Yes 145 Yes
Ethyl Undecylenate 624' Yes 557 Yes 357 Yes
Decanal 942 Yes 916 Yes 847 Yes
Methyl linolenate 771304 Yes 771283 Yes 771222 Yes

As expected, the lower the CMC of the surfactant systems, the lower the fragrance burst potential. Also, since the 10 CMC is lower and the maximum burst is found around the CMC, as one moves to products with lower CMC's, the consumer will have to dilute the product more to actually experience higher fragrance concentrations.

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Example 9 .
Limonene and gamma-Methyl Ionone were tested in two different shower liquid samples. One product was formulated 5 with 5% sodium laurate (CMC = 0.005 wt/wt) and the second with 5% sodium laureth sulfate (CMC = 0.0011 wt/wt) (Figure 8). These results validate the theoretical results in Figure 7. The product with the lower CMC gives a lower overall fragrance burst, and more dilutions are required to 10 reach the maximum burst potential.
Example 10
A typical fully formulated perfume used in a commercial 15 product, e.g., personalm wash formulation, usually is a
multi-component composition in which the properties of each perfume component can vary dramatically. A typical perfume mixture in a 5 wt.% sodium laurate formulation was tested for its "perfume burst" behaviour upon dilution. The PBI 20 values of the componerits in this perfume mixture vary from a large negative number (e.g., benzyl acetate, PBI = -819; PEA, PBI = -200 in sodium laurate solution) to a large positive number (e.g., gamma-methyl-ionone, PBI = 1,677 in sodium laurate solution). The dilution behaviour of each 25 component in this perfume mixture is shown in Figure 9 (the graph represents a normalized GC measurement so the amount of burst of each molecule is clearly indicated).
In this perfume mixture of twelve components, the dilution 30 behaviour of each component is different. Each component has a unique dilution curve (GC headspace vs. dilution

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factor) governed by the factors (hydrophobicity, volatility, etc) discussed previously. For instance, for those perfumes with a negative PBI (e.g., benzyl acetate), the perfume headspaces decrease upon dilution. For those perfumes with 5 a moderate positive PBI (e.g., limonene, PBI = 12; p-cymene = 12.2 in sodium laurate solution), the perfume headspaces increases 1-2 times upon dilution. For those fragrance components with a very large positive PBI (e.g., gamma-methyl-ionone), the "perfume burst" can be as high as seven 10 times. The results shown in Figure 9 indicated that in a fully formulated perfume, in terms of dilution behaviour, the performance of each component is mostly determined by its own individual physical properties.
15 Example 11
Trained sensory panel analyses were carried out to validate the "perfume burst" phenomena. A group of 20 to 30 expert sensory panellists were asked to rate the intensity of the
20 fragrance over formulations and anchor their scores to a perfume standard supplied for each test. Formulations containing a single perfume (gamma-methyl-ionone) and multi-component perfume were studied in two separate panels. The multi-component perfume contains four perfumes of equal
25 weight percentage, menthone, tetra-hydro-linalool, a-ionone, y-methyl-ionone, that will all "burst" in a sodium laurate product, but will not "burst" (e.g., menthone, a-ionone) or will give a moderate "burst" (e.g., tetra-hydro-linaiooi, y-methyl-ionone) in an SLES product with dilution.
30

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Each sample was tested in duplicate and the sample information and the panel study results are shown in Tables 7 and 8, and Figures 10 and 11. As shown in Tables 7 and 8, perfumes at two different initial concentrations were tested 5 in the sodium laurate solution. The scores shown in Figures 10 and 11 are the panel averages for each sample.
The results of the panel analyses indicate that as expected, both the single perfume and the perfume mixture (Figure 10
10 and 11) in a sodium laurate product (a surfactant of high CMC, CMC = 0.5 wt.%), have higher sensory scores for the 10 times diluted solution compared to the original undiluted formulations. In the :SLES formulations (a surfactant of relatively low CMC, CMC = 0.1 wt.%), both single perfume and
15 perfume mixture (Figure'10 and 11) have lower sensory scores for the 10 times diluted solution compared to the original undiluted product. These results are consistent with the discussion and data presented in Example 8, which indicate that a surfactant of low CMC lowers the PBI of the perfume
20 and can greatly reduce the expected "perfume burst" upon dilution.
The panel studies indicate that this "perfume burst" upon dilution can be perceived quite easily by the human nose if 25 the formulation is designed according to the rules listed in this specification.

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Table 7: Sample Information of the Single Perfume (y-methyl-ionone) System for Panel Study

Sample Name Information
1 0.0649 wt.% y-methyl-ionone in 4.5 wt.% sodium laurate
2 10 times dilution of 0.064 9 wt.% y-methyl-ionone in 4.5 wt.% sodium laurate
3 0.2193 wt.%. y-methyl-ionone in 4.5 wt.% sodium laurate
4 10 times dilution of 0.2193 wt.% y-methyl-ionone in 4.5 wt.% sodium laurate
5 0.2200 wt.% y-methyl-ionone in 4.5 wt.% SLES
6 10 times dilution of 0.2200 wt.% y-methyl-ionone in 4.5 wt.% SLES
Table 8: Sample Information of the Multi-Component Perfume (menthone, tetra-hydro-linalool, a-ionone, y-methyl-ionone) System for Panel Study
10

Sample Name Information
7 0.2404 wt.% perfume mixture in 5 wt.% sodium laurate
8 10 times dilution of 0.2404 wt.% perfume mixture in 5 wt.% sodium laurate
9 0.6022 wt.% perfume mixture in 5 wt.% sodium laurate
10 10 times dilution of 0.6022 wt.% perfume mixture in 5 wt.% sodium laurate
11 0.2433 wt.% perfume mixture in 5 wt.% SLES
12 10 times dilution of 0.2433 wt.% perfume mixture in 5 wt.% SLES
Example 12
15 There are any number of surfactant containing formulations that should provide a "perfume burst" in use. These include

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personal wash products (i.e. shower gels, soap bars), shampoos, household cleaners, light duty detergents, fabric washing products, etc. All of these products undergo some dilution with use which could potentially cause release of 5 fragrance molecules from the surfactant micelles and provide a *burst" of fragrance intensity. As explained in the previous examples, the CMC of the surfactant mixture, the amount of surfactant in the product and the perfume ingredients used in the fragrance formulation all contribute 10 to the type and intensity of the "perfume burst" during product use.
The following formulations are just a few examples of products that would be, expected to provide a "fragrance 15 burst" or change in fragrance note, assuming the perfume was properly designed (i.e. a fragrance containing a fraction of components with high PBI values).

Table 9


Formulation Ingredients (%) Form. #1 Form. #2 Form. #3 Form. #4 Form. #5 Form. #6 Form. #7 Form. #8
Sodium Laurate 10 5 8 4 4 5
TEA Laurate 5 5
Sodium Laureth Sulfonate 2 4 8
Sodium Lauryl Sulfate 8
Alkylpoly Glucoside 7
Nonionic Polymeric Surfactant Containing Mixture of Alkylene Oxides 2 5
Caprylamido Propylbetaine 1 1 2 1
Sodium Cocoylisethionate 10
Laurie Acid 3 2 2 3
Amine Oxide 1
Xanthan Gum 1 0.8
Jaguar S13 (Cationic Polymer) 0.4
Polyacrylates (e.g., Structuring Agent) 0.6 0.6
Polymer JR (Cationic Polymer) 0.3
Triclosan 0.5
Trichlorocarbanilide 0.5
Propylene Glycol 10
Glycerine: 30
Vitamin E 0.05
Perfume 1 1 1.3. 1 1 1.2 0.8 1
Water To 100 To 100 To 100 To 100 To 100 To 100 To 100 To 100






O H
o


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As noted, these are examples of the many formulations in which the perfume burst concept can be used.
Example 13 5
The deposition of the fragrance components onto a surface (e.g., skin) upon dilution of a surfactant containing product is also closely related to the thermodynamic characteristics of theperfume (e.g.,- oil/water partition coefficient, O, and
10 volatility constant, K) and the formulation (e.g., the
surfactant CMC). For a perfume-containing composition that has a high PBI, the perfume headspace will increase upon dilution due to the increase of the perfume concentration in the continuous phase caused by surfactant demicellization.
15
This increase in perfume concentration in the continuous phase will also favor the deposition of the perfume onto the surface that the product comes into contact with due to the enhanced chemical potential of the perfume in the continuous phase
20 which is in direct 'contact with the surface. Since perfume deposition is directly correlated with perfume burst, the PBI can also be used to predict fragrance delivery to a substrate during product use. Therefore, for a certain perfume, the surfactant systems which facilitate perfume burst upon
25 dilution can also enhance the deposition of perfume onto the surface in contact, compared to the surfactant systems which less favor the burst.
The deposition of a Type 2 perfume which-typically have high 30 PBI values was tested in two surfactant systems with
different CMCs (sodium laurate, CMC=0.5 wt. %, and SLES,

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CMC=0.1 wt. %) on a synthetic skin substrate (e.g., Vitro-Skin®) . The recovery of the perfume, which is the ratio of
the amount of perfume extracted after deposition to that originally dosed onto the surface, is used to reflect the 5 deposition efficiency of the perfume. The results of the recovery of y-methyl-ionone are plotted vs. the dilution factor for both sodium laurate and SLES surfactant systems (Figure 12).
10 The recovery of y-methyl-ionone from the skin washed with the undiluted sodium laurate and SLES surfactant systems (the surfactant concentration in both systems is 5%) is not significantly different. Upon dilution, the recovery of the perfume is enhancedin both surfactant systems, however, the
15 sodium laurate surfactant system, which has a higher PBI due
to the higher CMC of the surfactant, provides a much higher
deposition efficiency upon dilution than the SLES surfactant
system. These results correlate as expected with the perfume
burst results.
20
Example 14
The deposition of a multi-component "burst" perfume composed of perfumes with relatively high PBI's (i.e. high oil/water
25 partition coefficient (O) and low volatility constant (K) ) was tested on vitro-skin from sodium laurate surfactant system (high CMC) and SLES surfactant system (low CMC). The results were plotted in Figure 13. It was found that the recoveries of the perfumes from this mixture after
30 deposition from the undiluted sodium laurate and SLES
surfactant systems (the surfactant concentration in both

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systems is 5%) are very similar. An enhanced recovery of the perfume in both diluted surfactant systems (sodium laurate and SLES) is observed compared with that of the perfume in the undiluted surfactant systems. However, after 5 10 times dilution, the perfume recoveries were higher in sodium laurate surfactant system than that in SLES. These results again correlate with the perfume burst measurements, indicating that the BBI can be a useful tool for predicting fragrance deposition from surfactant containing products.

WE CLAIM
1. Compositions yielding a maximum fragrance burst of one or more of the fragrance components of at least 20%, relative to an undiluted product, wherein said composition is defined by perfume burst index PBI:
4>-1.4/CMC
PBI =
K
wherein . = oil/water partition coefficient of a selected perfume or perfume components in a mixture; CMC=critical micellization concentration (wt./wt.) of selected surfactant system or mixture of surfactant system in diluent or continuous phase; K=volatility constant of selected perfume from said continuous phase or diluent (atmospheres);
wherein said perfume or at least one component of said perfume mixture and wherein said surfactant system or said mixture of surfactant systems are selected such that variables are calculated to provide a PBI that is greater than about 3; wherein by maximum fragrance burst of at least 20% is meant that the perfume concentration in the headspace above said fragrance or fragrance components increases at least 20% relative to the perfume concentration in the headspace of an undiluted product comprising the same fragrance or fragrance components measured as the composition comprising said fragrance or fragrance components is diluted below the critical micelle concentration (CMC) of the fragrance, surfactant and water system.
2. A composition according to claim 1, wherein said perfume is a type 2 perfume selected to have an oil/water partition coefficient greater than about 500 and volatility constant of less than about 20.


A composition according to claim 2, wherein said perfume is selected from the group consisting of allyl cyclohexane propionate, ambrettolide, Ambrox DL (dodecahydro-3a,6,6,9a-tetramethyl-naphtho[2,l-b]furan), amyl benzoate, amyl cinnamate, amyl cinnamic aldehyde, amyl salicylate, anethol, aurantiol, benzophenone, benzyl butyrate, benzyl iso-valerate, benzyl salicylate, cadinene, campylcyclohexal, cedrol, cedryl acetate, cinnamyl cinnamate, citronellyl acetate, citronellyl isobutyrate, citronellyl propionate, cuminic aldehyde, cyclohexylsalicylate, cyclamen aldehyde, cyclomyral, dihydro isojamonate, diphenyl methane, diphenyl oxide, dodecanal, dodecalactone, ethylene brassylate, ethylmethyl phenylglycidate, ethyl undecylenate, exaltolide, Galoxilide.™-(l,3,4,6,7,8-hexhydro,4,6,6,7,8,8-hexamethyl-cyclopenta-.gamma.-2-benzopyr an), geranyl acetate, geranyl isobutyrate, hexadecanolide, hexenyl salicylate, hexyl cinnamic aldehyde, hexyl salicylate, a.-ionone, P-ionone, y-ionone, a.-irone, isobutyl benzoate, isobutyl quinoline, Iso E Super.™. (7-acettl,l,2,3,4,5,6,7,8-octahydro,l,l,6,7-tetramethyl napthalene), cis-jasmine, lilial, linalyl benzoate, 20 methoxy naphthaline, methyl cinnamate, methyl eugenol, .gamma.-methylionone, methyl linolate, methyl linolenate, musk indanone, musk ketone, musk tibetine, myristicin, neryl acetate, .8-nonalactone, .gamma.-nonalactone, patchouli alcohol, phantolide, phenylethyl benzoate, phenylethylphenylacetate, phenyl heptanol, phenyl hexanol, a-santalol, thibetolide, tonalid, . 8 -undecalactone, y-undecalactone, vertenex, vetiveryl acetate, yara-yara, ylangene, and mixtures thereof.
A composition according to claim 1, wherein said perfume is a type 3 perfume selected to have a partition coefficient of greater than about 500 and volatility constant of about 20 to about 1000.
A composition according to claim 4, wherein said perfume is selected from the group consisting of allo-ocimene, allyl caproate, allyl heptoate, anisole, camphene, carvacrol, carvone, citral, citronellal, citronellol, citronellyl nitrile, coumarin, cyclohexyl ethylacetate, p-cymene, decanal, dihydromyrcenol,

dihydromyrcenyl acetate, dimethyl octanol, ethyllinalool, ethylhexyl ketone, eucalyptol, fenchyl acetate, geraniol, gernyl formate, hexenyl isobutyrate, hexyl acetate, hexyl neopentanoate, heptanal, isobornyl acetate, isoeugenol, isomenthone, isononyl acetate, isononyl alcohol, isomenthol, isopulegol, limonene, linalool, linalyl acetate, menthyl acetate, methyl chavicol, methyl octyl acetaldehyde, myrcene, napthalene, nerol, neral, nonanal, 2-nonanone, nonyl acetate, octanol, octanal, . a-pinene, p-pinene, rose oxide, a-terpinene, y-terpinene, a-terpinenol, terpinolene, terpinyl acetate, tetrahydrolinalool, tetrahydromyrcenol, undecenal, veratrol, verdox, and mixtures thereof.
6. A composition according to claim 1 yielding maximum fragrance burst of at least 25%.
7. A composition according to claim 1, wherein said surfactant or mixture of surfactant system has CMC greater than about 0.0001 wt. to wt.,.
8. A composition according to claim 1, wherein surfactant systems contain surfactants selected from the group consisting of sodium lauryl ether sulfate, sodium laurate, potassium laurate, sodium oleate, potassium oleate, triethanolamine laurate, alkylpolyglucosides, sodium lauryl sulfate, caprylamidopropyl betaine, sodiumcocoylisethionate and mixtures thereof.
9. A composition according to claim 8, wherein the diluent or continuous phase in which said surfactant systems or surfactant system mixtures is found additionally comprises CMC modifying ingredients selected from the group consisting of urea; glycerine; C1-C12 straight-chained or branched alcohols or diols; water soluble polymers selected from polyvinylpyrolidone, polyvinylalcohol, polyethyleneglycol, polypropyleneglycol; multivalent electrolytes selected from magnesium, calcium and aluminum salts; sugars selected from dextrose, glucose, maltose, galactose, sucrose and mixtures thereof.

A process for selecting a composition yielding a maximum fragrance burst of one or more of the fragrance components of at least 20%, when it is diluted, wherein said composition is defined by perfume burst index PBI:
0-1.4/CMC
PBI =
K
wherein (j)=oil/water partition coefficient of a selected perfume or perfume components in a mixture; CMC=critical micellization concentration (wt./wt.) of selected surfactant systems or mixture of surfactant systems in diluent or continuous phase; K=volatility constant of selected perfume from said continuous phase or diluent (atmospheres);
wherein said process comprises selecting a first perfume or at least one component of a first perfume mixture and selecting a first surfactant system or mixture of surfactant systems such that the above-noted variables are calculated to provide a PBI that is greater than about 3; wherein by maximum fragrance burst of at least 20% is meant that the perfume concentration in the headspace above said fragrance or fragrance components increases at least 20%, when it is diluted, relative to the perfume concentration in the headspace of a second composition, differing in perfume properties, surfactant concentration and/or CMC of a surfactant system with a PBI less than that of the first composition, both compositions measured as the compositions comprising said fragrance or fragrance components are diluted below the critical micelle concentration (CMC) of the fragrance, surfactant and water system.
A method for changing fragrance note in a composition subsequent to dilution by (1) selection a fragrance with mixture perfume components wherein one or more of the perfume components have a PBI of greater than 3 and one or more components have a PBI of less than 3; and (2) assuring the selection of fragrance

components such that the components desired in a new fragrance have a PBI greater than 3.
12. A method for introducing a fragrance to a composition subsequent to dilution by ensuring desired fragrance or fragrance components have a PBI of greater than about 3 so that, upon dilution, the concentration of desired fragrance components in a vapour phase exceeds an odour threshold of the desired components.
13. A process according to claim 10 for providing enhanced deposition of one or more fragrance components on to surfaces on which the composition comes into contact.

Dated this 16th day of August 2004.


Abhishek Sen
OfS.Majumdar&Co.
Applicant's Agent



Documents:

00450-mumnp-2004 claim (granted) - (16-10-2006).doc

00450-mumnp-2004 form 2(granted) - (16-10-2006).doc

00450-mumnp-2004-cancelled page(16-10-2006).pdf

00450-mumnp-2004-claim(granted)-(16-10-2006).pdf

00450-mumnp-2004-correspondence 1(12-10-2004).pdf

00450-mumnp-2004-correspondence 2(05-02-2007).pdf

00450-mumnp-2004-correspondence(ipo)-(03-01-2007).pdf

00450-mumnp-2004-drawing(16-08-2004).pdf

00450-mumnp-2004-form 19(12-10-2004).pdf

00450-mumnp-2004-form 1a(16-08-2004).pdf

00450-mumnp-2004-form 2(granted)-(16-10-2006).pdf

00450-mumnp-2004-form 3(16-08-2004).pdf

00450-mumnp-2004-form 5(16-08-2004).pdf

00450-mumnp-2004-form-pct-ipea-409 (16-08-2004).pdf

00450-mumnp-2004-form-pct-isa-210 (16-08-2004).pdf

00450-mumnp-2004-power of attorney (13-03-2006).pdf

450-MUMNP-2004-CORRESPONDENCE(8-2-2012).pdf

abstract1.jpg


Patent Number 206544
Indian Patent Application Number 450/MUMNP/2004
PG Journal Number 43/2008
Publication Date 24-Oct-2008
Grant Date 30-Apr-2007
Date of Filing 16-Aug-2004
Name of Patentee HINDUSTAN UNILEVER LIMITED
Applicant Address 165-166 BACKBAY RECLAMATION, MUMBAI - 400 020,
Inventors:
# Inventor's Name Inventor's Address
1 YANG, LIN (CHINESE) UNILEVER R & D EDGEWATER, 45 RIVER ROAD, EDGEWATER, NEW JERSEY 07020,
2 KERSCHNER, JUDITH LYNNE 22 RAVINE DRIVE W., HAWTHORNE, NEW JERSEY 07506,
PCT International Classification Number A61K 7/46
PCT International Application Number PCT/EP03/01692
PCT International Filing date 2003-02-19
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 10 / 085736 2002-02-28 U.S.A.