Background to the Invention Skin is made up of several layers of cells which coat and protect the keratin and collagen fibrous proteins that form the skeleton of its structure. The outermost of these layers, referred to as the stratum corneum, is known to be composed of 25nm protein bundles surrounded by 8nm thick layers. Anionic surfactants and organic solvents typically penetrate the stratum corneum membrane and, by delipidization (i. e. removal of the lipids from the stratum corneum), destroy its integrity. This destruction of the skin surface topography leads to a rough feel and may eventually permit the surfactant or solvent to interact with the keratin, creating irritation. Many people expose their skin to this type of insult every day.

In addition, the skin can be damaged by other factors such as exposure to cold air or wind, mechanical abrasion, immersion in water etc. Thus, there exists a need for a way of mitigating or ameliorating this damage.

In the past compositions have been formulated that are claimed to assist the stratum corneum in maintaining its barrier and water-retention functions at optimum performance in spite of deleterious interactions which the skin may encounter in washing, work, and recreation. Desirable properties for such compositions are that they have good skin feel, water retention, moisturisation, absorption, and/or rub-in characteristics. Prior art compositions have attempted to deliver these properties by the use of one or more'skin benefit agents'. For example, one way of delivering high moisturisation to the skin is to incorporate polyhydric alcohol-like humectant materials such as glycerine into a composition.

Skin compositions with high levels of polyhydric alcools and therefore high levels of moisturisation, however, are often perceived by the consumer as unpleasant as such compositions can feel sticky when applied to the skin.

Another way of delivering desirable skin benefits to the skin is to incorporate emollient materials such as polyol carboxylic acid esters into skin care compositions. However, such compositions can suffer from undesirable negatives in terms of skin feel (i. e. they often feel very greasy on the skin) as well as having poor rub-in, absorption and residue characteristics.

There appears to be a direct relationship between the amount of the skin benefit agent and the effectiveness of the composition at delivering benefits to the skin.

However, it is also the case that the higher the level of skin benefit agent the higher the risk of the associated negatives. Therefore, to date, it has been necessary to balance the benefits of compositions comprising high levels of the skin benefit agents against the negatives associated with such high levels.

Thus, there remains a need for compositions which contain high levels of skin benefit agents, and therefore provide high levels of the associated benefits such as skin feel, skin softness and skin smoothness, but show low levels of the associated negatives such as greasiness, stickiness or tackiness.

Polyol polyester oils are known for use in cosmetic compositions. See, for example, US-A-6,013,271 which discloses a skin care composition in the form of an oil-in-water emulsion comprising an oil phase which includes liquid polyol carboxylic acid ester, water; and an organic liquid crystal-forming amphiphilic emulsifier material. Also, US-A-5,916,575 which discloses a non-emulsified personal cleansing composition comprising a lathering surfactant, water and an insoluble skin conditioning component which can be a solid polyol carboxylic acid ester and an insoluble skin conditioning oil. Ester derivatives of lanolin are also known for use in cosmetic compositions. See, for example, EP-A-913146 and EP-A-777465.

Quaternary ammonium agents are also known for use in cosmetic compositions.

See, for example, WO-A-99/27904, WO-A-96/32089, and EP-A-789,076. Also, US-A-5,804,205 which discloses skin care compositions which are claimed to provide a high degree of moisturisation without leaving a"tacky"or"sticky" residue. The compositions contain quaternary ammonium compounds having two alkyl groups of 16-22 carbon atoms, humectant and non-irritating hydrophobic micrcspheres having an average particle size of less than 50 um. It is claimed that the hydrophobic polymeric microspheres significantly reduce the "tackiness"associated with high humectant levels. The compositions of US-A- 5,804,205 may also contain low levels of emollients such as petrolatum or mineral oil.

It has now been unexpectedly found that compositions comprising at least one quaternary ammonium agent and an emollient selected from polyol polyester oils and/or ester derivatives of lanolin provide high levels of the associated benefits such as skin feel, skin softness and skin smoothness, but show low levels of the associated negatives such as greasiness, stickiness or tackiness.

While not wishing to be bound by theory, it is believed that the quaternary ammonium agents of the present invention can emulsify the polyol polyester oils and/or ester derivatives of lanolin which ensures that the emollients are more uniformly applied to the skin and the greasiness/tackiness/stickiness is minimised. Also, the quaternary ammonium agents help reduce the loss of the emollients from the skin due to environmental factors such as water or abrasion.

Moreover, it is believed that the quaternary ammonium agents themselves deliver skin care benefits, such as good moisturisation, good skin feel, good skin softness.

Summarv of the Invention According to the present invention there is provided a cosmetic composition comprising: (a) at least one quaternary ammonium agent; and (b) an emollient selected from polyol polyester oils, ester derivatives of lanolin and mixtures thereof.

The compositions of the present invention give good skin care benefits, such as good moisturisation, good hydration, good skin feel, good skin softness and/or good skin smoothness, with low levels of negatives such as greasiness, stickiness or tack.

Detailed Description of the Invention The compositions of the present invention comprise at least one quaternary ammonium agent and an emollient selected from polyol polyester oils and/or cholesterol esters. These elements will be described in more detail below.

The present compositions can be used for any suitable purpose. In particular, the present compositions are suitable for topical application to the skin. In particular, the skin care compositions can be in the form of creams, lotions, gels, and the like. Preferably the cosmetic compositions herein are in the form of an oil-in-water emulsion of one or more oil phases in an aqueous continuous phase, each oil phase comprising a single oily component or a mixture of oily components in miscible or homogeneous form but said different oil phases containing different materials or combinations of materials from each other.

Preferably the compositions of the present invention comprise less than 10%, preferably less than 5%, more preferably less than 3%, even more preferably 0%, by weight, of anionic surfactant.

The compositions of the present invention are preferably formulated so as to have a product viscosity of at least about 1,000 mPa. s and preferably in the range from about 1,000 to about 300,000 mPa. s, more preferably from about 2,500 to about 250,000 mPa. s and especially from about 5,000 to about 200,000 mPa. s (26.8°C, neat, Brookfield DV-I I+ Spindle CP52/CP41).

Quaternary Ammonium Axent The compositions of the present invention must comprise at least one quaternary ammonium agent. Any quaternary ammonium agent suitable for use in cosmetic compositions may be used herein. As used herein the term "quaternary ammonium agent'means a compound or mixture of compounds having a quaternary nitrogen atom substituted with one or more, preferably two, moieties containing six or more carbon atoms. Preferably the quaternary ammonium agents for use herein are selected from those having a quaternary nitrogen substituted with two moieties wherein each moiety comprises ten or more, preferably 12 or more, carbon atoms. Highly preferred quaternary ammonium agents for use herein are selected from those which are able to form vesicles in polar solvents, as detected by microscopic analysis (polarised light microscopy at a magnification of x60 using a Nikon Eclipse E800 microscope).

Preferably, said vesicles comprise quaternary ammonium agent and emollient. As used herein the term"vesicle"means one or more bilayers arranged in a closed, usually spherical geometry, said bilayer comprises quaternary ammonium agent as described hereinbelow.

Preferably the present compositions comprise at least 0.01 %, more preferably at least 0.1%, even more preferably at least 1%, still more preferably at least 3%, by weight, of quaternary ammonium agent.

Preferably the quaternary ammonium agents for use herein are selected from: (a) quaternary ammonium compounds according to general formula (I): wherein, Ri & R2 are each Ci-C4 alkyl or Ci-C4 hydroxyalkyl groups or hydrogen.

R3 & R4 are each alkyl or alkenyl groups having from about 8 to about 22 carbon atoms. X-is a salt forming anion, compatible with quaternary ammonium compounds and other adjunct ingredients.

Preferred quaternary ammonium compounds of this type are quaternised amines having the general formula (I) where Ri & R2 are methyl or hydroxyethyl and R3 & R4 are linear or branched alkyl or alkenyl chains comprising at least 11 atoms, preferably at least 15 carbon atoms.

(b) quaternary ammonium compounds according to general formula (II) or (III): wherein, each R5 unit is independently selected from hydrogen, branched or straight chain Ci-Ce alkyl, branched or straight chain Ci-Ce hydroxyalkyl and mixtures thereof, preferably methyl and hydroxyethyl; each R6 unit is independently linear or branched C11-C22 alkyl, linear or branched C1,-C22 alkenyl, and mixtures thereof; X- is an anion which is compatible with skin care actives and adjunct ingredients; m is from 1 to 4, preferably 2; n is from 1 to 4, preferably 2 and Q is a carbonyl unit selected from: wherein R7 is hydrogen, Ci-C4 alkyl, C1-C4 hydroxyalkyl, and mixtures thereof.

In the above quaternary ammonium compound example, the unit-QR6 contains a fatty acyl unit which is typically derived from a triglyceride source. The triglyceride source is preferably derived from tallow, partially hydrogenated tallow, lard, partially hydrogenated lard, vegetable oils and/or partially hydrogenated vegetable oils, such as, canola oil, safflower oil, peanut oil, rapeseed oil, sunflower oil, corn oil, soybean oil, tall oil, rice bran oil, etc. and mixtures of these oils.

The counterion, X-in the above compounds, can be any compatible anion, preferably the anion of a strong acid, for example, chloride, bromide, methylsulfate, ethylsulfate, sulfate, nitrate and the like, more preferably chloride or methyl sulfate. The anion can also, but less preferably, carry a double charge in which case X-represents half a group.

The preferred quaternary ammonium compounds of the present invention are the diester and/or diamide Quaternary Ammonium (DEQA) compounds, the diesters and diamides having general formula (II), wherein the carbonyl group Q is selected from: Tallow, canola and palm oil are convenient and inexpensive sources of fatty acyl units which are suitable for use in the present invention as R6 units.

The counterion, X-, can be chloride, bromide, methylsulfate, formate, sulfate, nitrate, and mixtures thereof. In fact, the anion, X, is merely present as a counterion of the positively charged quaternary ammonium compounds. The scope of this invention is not considered limited to any particular anion.

As used herein, when the diester is specified, it will include the monoester and triester that are normally present as a result of the manufacture process.

(c) quaternary ammonium compounds according to general formula (IV) or (V): wherein Rg is an acyclic aliphatic ¬15-621 hydrocarbon group and Rr0 is a Ci-Ce alkyl or alkylene group.

These ammonium compounds, having a pKa value of not greater than about 4, are able to generate a cationic charge in situ when dispersed in an aqueous solution, providing that the pH of the final composition is not greater than about 6.

(d) quaternary ammonium compounds according to general formula (VI) or (Vll): wherein Rg & Rio are as specified hereinabove and Rn is selected from Ci-C4 alkyl and hydroxyalkyl groups.

The counterion, X-, can be chloride, bromide, methylsulfate, formate, sulfate, nitrate, and mixtures thereof. In fact, the anion, X, is merely present as a counterion of the positively charged quaternary ammonium compounds. The scope of this invention is not considered limited to any particular anion.

(e) quaternary ammonium compounds according to general formula (VIII) or (IX): wherein, n is from 1 to 6, Rg is selected from acyclic aliphatic Cis-C2i hydrocarbon groups and R12 is selected from Ci-C4 alkyl and hydroxyalkyl groups.

These ammonium compounds (VIII), having a pKa value of not greater than about 4, are able to generate a cationic charge in situ when dispersed in an aqueous solution, providing that the pH of the final composition is not greater than about 6.

The counterion, X- (IX), can be chloride, bromide, methylsulfate, formate, sulfate, nitrate, and mixtures thereof. In fact, the anion, X, is merely present as a counterion of the positively charged quaternary ammonium compounds. The scope of this invention is not considered limited to any particular anion.

(f) diquaternary ammonium compounds according to general formula (X), (XI), (XII) or (XIII): wherein R5, R6, Q, n & X- are as defined hereinabove in relation to general formula (II) and (III), R13 is selected from Ci-Ce alkylene groups, preferably an ethylene group and z is from 0 to 4.

(g) mixtures of the above quaternary ammonium compounds.

The preferred quaternary ammonium agents for use in the present invention are those described in section (b) hereinabove. In particular, diester and/or diamide quaternary ammonium (DEQA) compounds according to general formula (II) hereinabove are preferred. Preferred diesters for use herein are those according to general formula (II) wherein R5, R6, and X-are as defined hereinabove and Q is: Preferred diamides for use herein are those according to general formula (II) wherein R5, R6, and X-are as defined hereinabove and Q is: Preferred examples of quaternary ammonium compounds suitable for use in the compositions of the present invention are N, N-di (canolyl-oxy-ethyl)-N, N-dimethyl ammonium chloride, N, N- di (canolyl-oxy-ethyl)-N-methyl, N- (2-hydroxyethyl) ammonium methyl sulfate, N, N-di (canolyl-oxy-ethyl)-N-methyl, N- (2- hydroxyethyl) ammonium chloride and mixtures thereof. Particularly preferred for use herein is N, N-di (canolyl-oxy-ethyl)-N-methyl, N- (2-hydroxyethyl) ammonium methyl sulfate.

Although quaternary ammonium compounds are derived from"canolyl"fatty acyl groups are preferred, other suitable examples of quaternary ammonium compounds are derived from fatty acyl groups wherein the term"canolyl"in the above examples is replace by the terms"tallowyl, cocoyl, palmyl, lauryl, oleyl, ricinoleyl, stearyl, palmityl"which correspond to the triglyceride source from which the fatty acyl units are derived. These alternative fatty acyl sources can comprise either fully saturated, or preferably at least partly unsaturated chains.

Emollients A second essential element of the compositions of the present invention is that they comprise an emollient selected from polyol polyester oils, ester derivatives of lanolin and mixtures thereof. Preferably the compositions of the present invention comprise an emollient selected from polyol polyester oils. Preferably the compositions of the present invention comprise at least 1 %, more preferably at least 5%, even more preferably at least 10%, more preferably still at least 20%, by weight, of polyol polyester oils, cholesterol esters or mixtures thereof.

Polyol Polyester Oils Any polyol polyester oil suitable for use in cosmetic compositions may be used in the present compositions. Preferably the compositions of the present invention comprise at least 1 %, more preferably at least 5%, even more preferably at least 10%, more preferably still at least 20%, by weight, of polyol polyester oils. These esters are derived from a sugar or polyol moiety and one or more carboxylic acid moieties. Depending on the constituent acid and sugar, these esters can be in either liquid or solid form at room temperature. Examples of liquid esters include: glucose tetraoleate, the glucose tetraesters of soybean oil fatty acids (unsaturated), the mannose tetraesters of mixed soybean oil fatty acids, the galactose tetraesters of oleic acid, the arabinose tetraesters of linoleic acid, xylose tetralinoleate, galactose pentaoleate, sorbitol tetraoleate, the sorbitol hexaesters of unsaturated soybean oil fatty acids, xylitol pentaoleate, sucrose tetraoleate, sucrose pentaoletate, sucrose hexaoleate, sucrose hepatoleate, sucrose octaoleate, and mixtures thereof. Examples of solid esters include: sorbitol hexaester in which the carboxylic acid ester moieties are palmitoleate and arachidate in a 1: 2 molar ratio; the octaester of raffinose in which the carboxylic acid ester moieties are linoleate and behenate in a 1: 3 molar ratio; the heptaester of maltose wherein the esterifying carboxylic acid moieties are sunflower seed oil fatty acids and lignocerate in a 3: 4 molar ratio; the octaester of sucrose wherein the esterifying carboxylic acid moieties are oleate and behenate in a 2: 6 molar ratio; and the octaester of sucrose wherein the esterifying carboxylic acid moieties are laurate, linoleate and behenate in a 1: 3: 4 molar ratio. A preferred solid material is sucrose polyester in which the degree of esterification is 7-8, and in which the fatty acid moieties are C18 mono-and/or di-unsaturated and behenic, in a molar ratio of unsaturates: behenic of 1: 7 to 3: 5. A particularly preferred solid sugar polyester is the octaester of sucrose in which there are about 7 behenic fatty acid moieties and about 1 oleic acid moiety in the molecule. Other materials include cottonseed oil or soybean oil fatty acid esters of sucrose. The ester materials are further described in, U. S. Patent No. 2,831,854, U. S. Patent No. 4,005,196, to Jandacek, issued January 25,1977; U. S. Patent No. 4,005,195, to Jandacek, issued January 25,1977, U. S. Patent No. 5,306,516, to Letton et al., issued April 26,1994; U. S. Patent No. 5,306,515, to Letton et al., issued April 26, 1994; U. S. Patent No. 5,305,514, to Letton et al., issued April 26,1994; U. S. Patent No. 4,797,300, to Jandacek et al., issued January 10,1989; U. S. Patent No. 3,963,699, to Rizzi et al, issued June 15,1976; U. S. Patent No. 4,518,772, to Volpenhein, issued May 21,1985; and U. S. Patent No. 4,517,360, to Volpenhein, issued May 21,1985.

The polyol fatty acid polyesters suitable for use herein can be prepared by a variety of methods well known to those skilled in the art. These methods include: transesterification of the polyol with methyl, ethyl or glycerol fatty acid esters using a variety of catalysts; acylation of the polyol with a fatty acid chloride; acylation of the polyol with a fatty acid anhydride; and acylation of the polyol with a fatty acid, per se. See, for example, U. S. Patent No. 2,831,854; U. S. Patent No. 4,005,196, to Jandacek, issued January 25,1977.

An especially preferred material is known by the INCI name sucrose polycottonseedate.

Ester Derivatives of Lanolin Any ester derivative of lanolin suitable for use in cosmetic compositions may be used in the compositions of the present invention. As used herein the term "ester derivative of lanolin"means any ester or mixture of esters that is derived from reacting C10-C30 acids with lanolin alcohol or with a blend of cholesterol and lanosterol. Preferably the compositions of the present invention comprise at least 0.1%, more preferably at least 0.5%, even more preferably at least 1%, more preferably still at least 5%, by weight, of ester derivatives of lanolin.

Optional Inqredients The compositions herein can contain a variety of optional components suitable for rendering the present compositions more cosmetically or aesthetically acceptable or to provide them with addition usage benefits. Such conventional optional ingredients are well-known to those skilled in the art. These include any cosmetically acceptable ingredients such as those found in the CTFA International Cosmetic Ingredient Dictionary and Handbook, 7th edition, edited by Wenninger and McEwen, (The Cosmetic, Toiletry, and Fragrance Association, Inc., Washington, D. C., 1997). Some non-limiting examples of these optional ingredients are given below.

Humectant A highly preferred optional ingredient for the compositions of the present invention is humectant. As used herein the term"humectant"means a substance which provides the skin with water-retention benefits. Preferably, the compositions of the present invention comprise at least 1%, more preferably at least 5%, even more preferably at least 10%, even more still preferably at least 20%, by weight of humectant.

Any humectant suitable for use in cosmetic compositions may be used herein.

Non-limiting examples of suitable humectants for use in the present invention are described in W098/22085, W098/18444 and W097/01326. Preferably the humectants for use herein are selected from, but not limited to; amino acids and derivatives thereof such as proline and arginine aspartate, 1,3-butylene glycol, propylene glycol and water and codium tomentosum extract, collagen amino acids or peptides, creatinine, diglycerol, biosaccharide gum-1, glucamine salts, glucuronic acid salts, glutamic acid salts, polyethylene glycol ethers of glycerine (e. g. glycereth 20), glycerine, glycerol monopropoxylate, glycogen, hexylene glycol, honey, and extracts or derivatives thereof, hydrogenated starch hydrolysates, hydrolyzed mucopolysaccharides, inositol, keratin amino acids, urea, LAREX A-200 (available from Larex), glycosaminoglycans, methoxy PEG 10, methyl gluceth-10 and-20 (both commercially available from Amerchol located in Edison, NJ), methyl glucose, 3-methyl-1, 3-butanediol, N-acetyl glucosamine salts, polyethylene glycol and derivatives thereof (such as PEG 15 butanediol, PEG 4, PEG 5 pentaerythitol, PEG 6, PEG 8, PEG 9), pentaerythitol, 1,2 pentanediol, PPG-1 glyceryl ether, PPG-9,2-pyrrolidone-5-carboxylic acid and its salts such as glyceryl pca, saccharide isomerate, SEACARE (available from Secma), sericin, silk amino acids, sodium acetylhyaluronate, sodium hyaluronate, sodium poly-aspartate, sodium polyglutamate, sorbeth 20, sorbeth 6, sugar and sugar alcools and derivatives thereof such as glucose, mannose and polyglycerol sorbitol, trehalose, triglycerol, trimethyolpropane, tris (hydroxymethyl) amino methane salts, and yeast extract, and mixtures thereof.

More preferably, the humectants for use herein are selected from glycerine, urea, butylene glycol, polyethylene glycol and derivatives thereof, or mixtures thereof. Even more preferably, the humectants for use herein are selected from glycerine, urea and mixtures thereof, especially glycerine.

Emollients In addition to the emollients discussed hereinabove, the compositions of the present invention can also comprise other emollient materials. Emollients tend to lubricate the skin, increase the smoothness and suppleness of the skin, prevent or relieve dryness of the skin, and/or protect the skin. A wide variety of suitable additional emollients are known and may be used herein. Sagarin, Cosmetics, Science and Technology, 2nd Edition, Vol. 1, pp. 32-43 (1972) contains numerous examples of materials suitable for use as emollients. Preferably, if present, the compositions of the present invention comprise at least 1 %, more preferably at least 5%, by weight, of other emollient material.

Preferably the emollients for use herein are selected from: i) Straight and branched chain hydrocarbons having from about 7 to about 40 carbon atoms, such as dodecane, squalane, petrolatum, cholesterol, hydrogenated polyisobutylene, isohexadecane and the C7-C40 isoparaffins, which are C7-C40 branched hydrocarbons. ii) C1-C30 alcohol esters of Cl-C30 carboxylic acids and of C2-C3o dicarboxylic acids, e. g. isononyl isononanoate, isopropyl myristate, myristyl propionate, isopropyl stearate, behenyl behenate, dioctyl maleate, diisopropyl adipate, and diisopropyl dilinoleate. iii) mono-, di-and tri-glycerides of C1-C30 carboxylic acids and ethoxylated derivatives thereof. Suitable polyethylene glycol derivatives of glycerides include PEG-20 almond glycerides, PEG-60 almond glycerides, PEG-11 avocado glycerides, PEG-6 capric/caprylic glycerides, PEG-8 capric/caprylic glycerides, PEG-20 corn glycerides, PEG-60 corn glycerides, PEG-60 evening primose glycerides, PEG-7 glyceryl cocoate, PEG-30 glyceryl cocoate, PEG-40 glyceryl cocoate, PEG-78 glyceryl cocoate, PEG-80 glyceryl cocoate, PEG-12 glyceryl dioleate, PEG-15 glyceryl isostearate, PEG-20 glyceryl isostearate, PEG-30 glyceryl isostearate, PEG-75 cocoa butter glycerides, PEG-20 hydrogenated palm oil glycerides, PEG-70 mango glycerides, PEG-13 mink glycerides, PEG-75 shorea butter glycerides, PEG- 10 olive glycerides, PEG-12 palm kernal glycerides, PEG-45 palm kernal glycerides, PEG-8 glyceryl laurate and PEG-30 glyceryl laurate. Mixtures of polyethylene glycol derivatives of glycerides can also be used herein. iv) alkylene glycol esters of Cl-C30 carboxylic acids, e. g. ethylene glycol mono- and di-esters, and propylene glycol mono-and di-esters of Cl-C30 carboxylic acids e. g., ethylene glycol distearate. v) Organopolysiloxane oils. The organopolysiloxane oil may be volatile, non- volatile, or a mixture of volatile and non-volatile silicones. The term"non- volatile"as used in this context refers to those silicones that are liquid under ambient conditions and have a flash point (under one atmospheric of pressure) of or greater than about 100°C. The term"volatile"as used in this context refers to all other silicone oils. Suitable organopolysiloxanes can be selected from a wide variety of silicones spanning a broad range of volatilities and viscosities. Non-volatile polysiloxanes are preferred.

Suitable silicones are disclosed in U. S. Patent No. 5,069,897, issued December 3,1991. Preferred for use herein are organopolysiloxanes selected from polyalkylsiloxanes, alkyl substituted dimethicones, dimethiconols, polyalkylaryl siloxanes, and mixtures thereof. More preferred for use herein are polyalkylsiloxanes and cyclomethicones. Preferred among the polyalkylsiloxanes are dimethicones. vi) Vegetable oils and hydrogenated vegetable oils. Examples of vegetable oils and hydrogenated vegetable oils include safflower oil, castor oil, coconut oil, cottonseed oil, menhaden oil, palm kernel oil, palm oil, peanut oil, soybean oil, rapeseed oil, linseed oil, rice bran oil, pine oil, sesame oil, sunflower seed oil, partially and fully hydrogenated oils from the foregoing sources, and mixtures thereof. vii) animal fats and oils, e. g. cod liver oil, lanolin and derivatives thereof such as acetylated lanolin and isopropyl lanolate. Lanolin oil is preferred. viii) Also useful are C4-C20 alkyl ethers of polypropylene glycols, C1-C20 carboxylic acid esters of polypropylene glycols, and di-C8-C30 alkyl ethers, examples of which include PPG-14 butyl ether, PPG-15 stearyl ether, dioctyl ether, dodecyl octyl ether, and mixtures thereof. ix) mixtures of the above.

Preferred other emollients for use in the compositions herein are selected from dodecane, squalane, cholesterol, isohexadecane, isononyl isononanoate, petrolatum, lanolin and derivatives thereof, safflower oil, castor oil, coconut oil, cottonseed oil, palm kernel oil, palm oil, peanut oil, soybean oil and mixtures thereof.

Other Skin Benefit Agents Other skin benefit agents may be useful in the compositions of the present invention. Examples of other skin benefit agents that may be used in the present compositions include: (a) Vitamin Compound The present compositions may comprise vitamin compounds, precursors, and derivatives thereof. These vitamin compounds may be in either natural or synthetic form. Suitable vitamin compounds include, Vitamin A (e. g., beta carotene, retinoic acid, retinol, retinoids, retinyl palmitate, retinyl proprionate, etc.), Vitamin B (e. g., niacin, niacinamide, riboflavin, pantothenic acid, etc.), Vitamin C (e. g., ascorbic acid, etc.), Vitamin D (e. g., ergosterol, ergocalciferol, cholecalciferol, etc.), Vitamin E (e. g., tocopherol acetate, etc.), and Vitamin K (e. g., phytonadione, menadione, phthiocol, etc.) compounds. Preferred vitamin compounds for use in the compositions of the present invention are vitamin B3 compounds. Vitamin B3 compounds are particularly useful for regulating skin condition as described WO-A-97/39733. When present, the compositions of the present invention preferably comprise from about 0.01% to about 50%, more preferably from about 0.1% to about 10%, even more preferably from about 0.5% to about 5%, by weight, of the vitamin B3 compound.

As used herein,"vitamin B3 compound"means a compound having the formula: wherein R is-CONH2 (i. e., niacinamide),-COOH (i. e., nicotinic acid) or-CH20H (i. e., nicotinyl alcohol); derivatives thereof; and salts of any of the foregoing.

Exemplary derivatives of the foregoing vitamin B3 compounds include nicotinic acid esters, including non-vasodilating esters of nicotinic acid, nicotinyl amino acids, nicotinyl alcohol esters of carboxylic acids, nicotinic acid N-oxide and niacinamide N-oxide.

Examples of suitable vitamin B3 compounds are well known in the art and are commercially available from a number of sources, e. g., the Sigma Chemical Company (St. Louis, MO); ICN Biomedicals, Inc. (Irvin, CA) and Aldrich Chemical Company (Milwaukee, WI).

The vitamin compounds may be included as the substantially pure material, or as an extract obtained by suitable physical and/or chemical isolation from natural (e. g., plant) sources.

(b) Anti-Wrinkle and Anti-Skin Atrophy Actives Examples of anti-wrinkle and anti-skin atrophy actives that may be used in the compositions of the present invention include, but are not limited to, lactic acid and derivatives thereof, retinoic acid and its derivatives (e. g., cis and trans); retinol; retinyl esters; niacinamide, salicylic acid and derivatives thereof; sulfur- containing D and L amino acids and their derivatives and salts, particularly the N-acetyl derivatives, a preferred example of which is N-acetyl-L-cysteine; thiols, e. g., ethane thiol; hydroxy acids, phytic acid, lipoic acid; lysophosphatidic acid, and skin peel agents (e. g., phenol and the like).

(c) Antimicrobial and Antifungal Actives Examples of antimicrobial and antifungal actives that may be used in the compositions of the present invention include, but are not limited to, R-lactam drugs, quinolone drugs, ciprofloxacin, norfloxacin, tetracycline, erythromycin, amikacin, 2,4,4'-trichloro-2'-hydroxy diphenyl ether, 3,4,4'-trichlorocarbanilide, phenoxyethanol, phenoxy propanol, phenoxyisopropanol, doxycycline, capreomycin, chlorhexidine, chlortetracycline, oxytetracycline, clindamycin, ethambutol, hexamidine isethionate, metronidazole, pentamidine, gentamicin, kanamycin, lineomycin, methacycline, methenamine, minocycline, neomycin, netilmicin, paromomycin, streptomycin, tobramycin, miconazole, tetracycline hydrochloride, erythromycin, zinc erythromycin, erythromycin estolate, erythromycin stearate, amikacin sulfate, doxycycline hydrochloride, capreomycin sulfate, chlorhexidine gluconate, chlorhexidine hydrochloride, chlortetracycline hydrochloride, oxytetracycline hydrochloride, clindamycin hydrochloride, ethambutol hydrochloride, metronidazole hydrochloride, pentamidine hydrochloride, gentamicin sulfate, kanamycin sulfate, lineomycin hydrochloride, methacycline hydrochloride, methenamine hippurate, methenamine mandelate, minocycline hydrochloride, neomycin sulfate, netilmicin sulfate, paromomycin sulfate, streptomycin sulfate, tobramycin sulfate, miconazole hydrochloride, amanfadine hydrochloride, amanfadine sulfate, octopirox, parachlorometa xylenol, nystatin, tolnaftate, zinc pyrithione and clotrimazole.

(d) Sunscreen Actives The compositions herein may also comprise sunscreening actives. A wide variety of sunscreen agents are useful herein. These sunscreen agents include both organic compounds and their salts as well as inorganic particulate materials. Without being limited by theory, it is believed that sunscreen agents provide protection from ultraviolet radiation by one or more of the following mechanisms including absorption, scattering, and reflection of the ultraviolet radiation. Nonlimiting examples of these sunscreen agents are described in U. S. Patent No. 5,087,445, to Haffey et al., issued February 11,1992; U. S. Patent No. 5,073,372, to Turner et al., issued December 17,1991; U. S. Patent No. 5,073,371, to Turner et al. issued December 17,1991; U. S. Patent No. 5,160,731, to Sabatelli et al., issued November 3,1992; U. S. Patent No. 5,138,089, to Sabatelli, issued August 11,1992; U. S. Patent No. 5,041,282, to Sabatelli, issued August 20,1991; U. S. Patent No. 4,999,186, to Sabatelli et al., issued March 12,1991; U. S. Patent No. 4,937,370, to Sabatelli, issued June 26, 1990; and Segarin, et al., at Chapter VIII, pages 189 et seq., of Cosmetics Science and Technoloqv. Preferred among the sunscreen agents are those selected from the group consisting of 2-ethylhexyl p-methoxycinnamate, octyl salicylate, octocrylene, oxybenzone, 2-ethylhexyl N, N-dimethylaminobenzoate, p-aminobenzoic acid, 2-phenyl-benzimidazole-5-sulfonic acid, homomenthyl salicylate, DEA p-methoxycinnamate, 4,4'methoxy-t-butyidibenzoyl methane, 4- isopropyldibenzoylmethane, 3- (4-methylbenzylidene) camphor, 3-benzylidene camphor, 4-N, N-dimethylaminobenzoic acid ester with 2,4- dihydroxybenzophenone, 4-N, N-dimethylaminobenzoic acid ester with 2- hydroxy-4- (2-hydroxyethoxy) benzophenone, 4-N, N-dimethylaminobenzoic acid ester with 4-hydroxydibenzoyl-methane, 4-N, N-dimethylaminobenzoic acid ester with 4- roxyeth-oxy) d ibenzoyl methane, 4-N, N-di (2-ethylhexyl)- aminobenzoic acid ester with 2,4-dihydroxybenzophenone, 4-N, N-di (2- ethylhexyl) aminobenzoic acid ester with 2-hydroxy-4- (2- hydroxyethoxy) benzophenone, 4-N, N-di (2-ethylhexyl) aminobenzoic acid ester with 4-hy-d roxyd ibenzoyl methane, 4-N, N-di (2-ethylhexyl) aminobenzoic acid ester with 4- (2-hydroxyeth-oxy) dibenzoylmethane, 4-N, N- (2- ethylhexyl) methylaminobenzoic acid ester with 2,4-dihydroxybenzophenone, 4- N, N- (2-ethylhexyl) methylaminobenzoic acid ester with 2-hydroxy-4- (2- hydroxyethoxy) benzophenone, 4-N, N- (2-ethylhexyl) methylaminobenzoic acid ester with 4-hy-droxydibenzoylmethane, 4-N, N- (2- ethylhexyl) methylaminobenzoic acid ester with 4- (2-hydroxyeth- oxy) dibenzoylmethane, titanium dioxide, zinc oxide, iron oxide, and mixtures thereof.

More preferred for use in the compositions described herein are the sunscreen agents selected from the group consisting of 2-ethylhexyl N, N-dimethyl-p- aminobenzoate, 2-ethylhexyl p-methoxycinnamate, octocrylene, octyl salicylate, homomenthyl salicylate, p-aminobenzoic acid, oxybenzone, 2- phenylbenzimidazole-5-sulfonic acid, DEA p-methoxycinnamate, 4,4'-methoxy-t- butyldibenzoylmethane, 4-isopropyl dibenzoylmethane, 3- (4-methylbenzylidene) camphor, 3-benzylidene camphor, 4-N, N-(2-ethylhexyl) methylaminobenzoic acid ester with 4- (2-hydroxyeth-oxy) dibenzoylmethane, titanium dioxide, zinc oxide, iron oxide, and mixtures thereof.

Exact amounts of sunscreens which can be employed will vary depending upon the sunscreen chosen and the desired Sun Protection Factor (SPF) to be achieved. SPF is a commonly used measure of photoprotection of a sunscreen against erythema. See Federal Registe, Vol. 43, No. 166, pp. 38206-38269, August 25,1978.

Polar Solvent The compositions of the present invention may also comprise polar solvent. Any polar solvent suitable for use in cosmetic compositions may be used herein. However, the polar solvent must be sufficiently polar to drive the formation of vesicles in the present invention. Preferably the polar solvent used in the compositions of the present invention is water.

Preferably comprise the present compositions will comprise from 10% to 90%, more preferably from 20% to 80%, even more preferably from 30% to 60%, by weight, of polar solvent.

Thickeners The compositions of the present invention preferably comprise thickeners. Any thickener suitable for use in cosmetic compositions can be used herein.

Preferred thickeners are selected from nonionic water-soluble polymers, fatty alcools and mixtures thereof. Suitable nonionic polymers include such water soluble polymers as cellulose ethers (e. g. hydroxybutyl methyl cellulose, hydroxypropylcellulose, hydroxypropyl methyl cellulose, ethylhydroxy ethyl cellulose, hydrophobically modified hydroxyethyl cellulose and hydroxyethylcellulose), poly (ethylene oxide), polyvinyl alcool, polyvinylpyrrolidone, hydroxypropyl guar gum, amulose, hydroxyethyl amylose, starch, and starch derivatives. Suitable fatty alcools are higher molecular weight, nonvolatile, primary alcools having the general formula RCH20H wherein R is a C8-20 alkyl. They can be produced from natural fats or oils by reduction of the fatty acid COOH-grouping to the hydroxyl function. Alternatively, identical or similarly structured fatty alcools can be produced according to conventional synthetic methods known in the art. Suitable fatty alcohols include, but are not limited to behenylalcohol, Cg-Cn alcohols, C12-C13 alcohols, C12-C15 <BR> <BR> <BR> alcohols, C12-Cr6 alcohols, C14-C15 alcohols, caprylic alcohol, cetearyl alcohol, coconut alcohol, decyl alcohol, isocetyl alcohol, isostearyl alcohol, lauryl alcohol, oleyl alcohol, palm kernel alcohol, stearyl alcohol, cetyl alcohol, tallow alcohol, tridecyl alcohol or myristyl alcool.

Other Optional Ingredients The compositions of the present invention can comprise a wide range of other optional components. These additional components should be pharmaceutically acceptable. Non-limiting examples of functional classes of ingredients suitable for use in the compositions of the present invention include: abrasives, absorbents, anti-acne actives, anticaking agents, anti-dandruff agents, anti- perspirant agents, antioxidants, anti-viral actives, artificial tanning actives and accelerators, biological additives, bleach, bleach activators, brighteners, builders, buffering agents, chelating agents, chemical additives, colorants, cosmetics, cleansers, cosmetic astringents, cosmetic biocides, denaturants, deodorants, desquamation actives, depilatories, drug astringents, dyes, dye transfer agents, enzymes, external analgesics, foam generators, flavours, film formers, fragrance components, insect repellents, mildewcides, non-steroidal anti-inflammatory active, opacifying agents, oxidative dyes, oxidising agents, pest control ingredients, pH adjusters such as citric acid, pH buffers, pharmaceutical actives, plasticizers, preservatives, radical scavengers, skin, hair or nail bleaching agents, skin, hair or nail conditioners, skin, hair or nail penetration enhancers, stabilisers, surfactants, surface conditioners, reducing agents, temperature depressors, viscosity modifiers, and warmth generators such as exothermic zeolites. Also useful herein are aesthetic components such as colourings, essential oils, and skin healing agents. Other optional materials herein include pigments. Pigments suitable for use in the compositions of the present invention can be organic and/or inorganic. Also included within the term pigment are materials having a low colour or lustre such as matte finishing agents, and also light scattering agents. Examples of suitable pigments are iron oxides, acyglutamate iron oxides, titanium dioxide, ultramarine blue, D&C dyes, carmine, and mixtures thereof.

Formulation Process Preferably the compositions of the present invention are preferably prepared in such a way that the quaternary ammonium compound forms vesicles. It is preferred that said vesicles also comprise emollient. Preferably said vesicles also comprise humectant. In order to ensure optimal performance characteristics it is preferred that the compositions of the present invention are prepared as follows: (i) all or part of the quaternary ammonium agent is mixed with humectant, water soluble skin care actives (where included), and, preferably, polar solvent at a temperature which is higher than the melting point of the quaternary ammonium agent; (ii) optionally, the mixture is vigorously agitated; (iii) In a separate vessel the emulsion is prepared as follows; The oil phase containing the emollients, the relevant thickener in case the said thickener is oil soluble, and any remaining quaternary ammonium agent are mixed together at a temperature which is higher than the melting point of the quaternary ammonium compound. The aqueous phase is prepared separately. The water, the relevant thickener in case the said thickener is water soluble, and any remaining water soluble ingredients are heated to the same temperature as the oil phase.

(iv) the temperature of the oil and aqueous phases of the emulsion are then approximately equalised and the aqueous phase is combined with the oil phase with agitation.

(v) On production of the emulsion the mixture formed in step (i) is added to the aforementioned emulsion with agitation.

Method of Use The cosmetic compositions of the present invention may be used in a conventional manner for the treatment of skin. An effective amount of the composition, typically from about 0.1 grams to about 50 grams, preferably from about 1 gram to about 20 grams, is applied to wet or dry, preferably wet, skin.

Application of the composition typically includes working the composition into the skin, generally with the hands and fingers. The composition is then left on the skin or, preferably, the skin is rinsed.

The preferred method of treating the skin, therefore, comprises the steps of: (a) applying an effective amount of the cosmetic composition to the skin, (b) rinsing the skin.

A preferred aspect of the present invention involves the above method with an application of the composition on dry skin before an application on wet skin.

Therefore, a preferred method comprises: (i) applying to dry skin an effective amount of the cosmetic composition; (ii) rinsing the skin under a shower; (iii) further application of said composition; and (iv) further rinsing.

Much of the damage to human skin is caused by repeated exposure to surfactant containing compositions during washing routines. It has been found that this damage can be mitigated using the present compositions. Therefore, another preferred method comprises: (i) washing the skin using a composition comprising surfactants; (ii) rinsing the skin; (iii) applying to the wet skin a composition according to the present invention; (iv) rinsing the skin.

It has also been found that the present compositions are particularly useful when incorporated as part of a regular routine. Therefore, another preferred method comprises: (i) applying to the skin a composition comprising: (a) at least one quaternary ammonium compound; (b) humectant; and (ii) rinsing the skin; (iii) repeating steps (i) and (ii) within 48 hours.

The present compositions can also be useful in mitigating damage caused by exposure of the skin to ultra violet radiation, damage caused by exposure of the skin to water during swimming or similar water based exercise, damage caused by shaving or exfoliation or damage caused by exposure of the skin to water during bathing.

Examples The following examples further illustrate the preferred embodiments within the scope of the present invention. The examples are given solely for the purposes of illustration and are not to be construed as limitations of the present invention as many variations of the invention are possible without departing from its spirit or scope. Unless otherwise indicated, all ingredients are expressed on a weight percentage of the active ingredient. 2345678910111213Example1 Weight % Quat. Amm. Agent 3 3 3 3 3 3 3 3 3 3 3 3 3 A see notes below Glycerine 32 32 32 32 32 32 32------A Urea - - - - - - - 22 22 22 22 22 22 A Petrolatum 10-12----10-12-B Lanolin'7.5 15 15---10 10 15 B 5 CoronetLanolin---5 B Super Sterol Esters---5 B Sefa Cottonate 21 21 12 12---21 21 12 12--B Dimethicone 10Cst-0.0.0.-0.0.0.---0.5 0. B 5555555 Oimethlcone 1000Cst - 1. 1.---1.0 1. B 0000000 Cyclomethicone-2.2.2.-2.2.2.---2.5 2. B 5 5 5 5 5 5 5 Florasun PEG-10 2-2-2-3-1-13--B Methyl Paraben 0.0.5 0.5 0.5 0. A 5 5 5 5 5 5 5 5 5 5 Propyl Paraben 0.0.0.0.0.0.0.0.0.0.5 0.5 0.5 0. B 5555555555 Disodium EDTA 0.0.0.0.0.0.0.0.0.0.1 0.1 0.1 0. A 1 1 1 1 1 1 1 1 1 1 Sodium Benzoate 0.0.0.0.0.0.0.0.0.0. 3 0.3 0.3 0. B 3 3 3 3 3 3 3 3 3 3 53-55535--55ANiacinamide5 Panthenol 3 3 1-3 3 3 1 3--3 3 A Tocopherol Acetate 2 2 0.-2 2 2 0.2--2 2 8 55 Retinol -----0.--0.1---B0. 05 -1-10.-0.-1-1-1BParsol17893 51 -5-52.-0.-5-5-5BParsolMCX3 55 Citric acid 1 0.1 0.0.1 0.1 0.0.7 1 1 1 A 55355 5 Salicylic acid-0. 0. 0.-0.-0.---A 55755 Triethanolamine 0. - - 0. 0. - - - 0. - - 0. 9 0. C 11511 Sodium Hydroxide - - 0. 0.0.--0.-0. 1---C 1 1 1 1 _ --1.--0.-0.---0.BPolyquaternium10 0 5 6 5 Polymer KG 30 4-0.--0.----0. 8---B 77 Fragrance 0.0.5 0.5 0.5 0. E 5 5 5 5 5 5 5 5 5 Cetyl Alcohol 3---2.--2.-2. 2-2. 5-C 6 2 Stearyl Alcohol 2---1.--3.-1. 1-1. 6-C 5 2 --4-0.---3.---3.CCetearylAlcohol 444 2-2----0.-0.7---CBehenylAlcohol 6 Natrosol 330 Plus 1 - - - 0. - - 0. 0. - - 0. 5 0. C 4 7 6 25 Natrosol 250 HHR--1-0.----1. 2--0. C 33 1055-1.--------0.8--DJaguarHP 2 ---1---------DJaguarC14S5 Jaguar C13S 5-----1.------. D 2 Xanthan Gum------2.------D 0 --0.---0.0.-0.3---ASodiumChloride 15 2 qsqsqsqsWaterqs qs qs qs qs qs qs qs qs A Example 14 15 16 17 18 19 20 21 22 23 24 25 26 Weight% Quat. Amm. Agent 8 8 8 8 8 8 8 8 8 8 8 8 8 A see notes below Glycerine 32 32 32 32 32 32 32------A Urea - - - - - - - 22 22 22 22 22 22 A Petrolatum--10-12----10-12-B Lanolin'7.5 15 15---10 10 15 B 5 CoronetLanolin 5--------B Esters1------5------BSuperSterol Sefa Cottonate 21 21 12 12---21 21 12 12--B Dimethicone 10Cst - 0. 0. 0. - 0. 5 0.5 B 55555 Dimethicone 1000Cst - 1. 1. 1. - 1. 0 1. 1. - - - 1. 0 1.0 B 00000 Cyclomethicone - 2. 2.5 B 5 5 5 5 5 FlorasunPEG-10 2-2-2-3-1--3--B Methyl Paraben 0.0.0.0.0.0.5 0.0.0.0.5 0.5 0.5 0.5 A 5 5 5 5 5 5 5 5 Propyl Paraben 0.0.0.0.0.0.5 0.0.0.0.5 0.5 0.5 0.5 B -5 5 5 5 5 5 5 5 Disodium EDTA 0.0.0.0.0.0.1 0.0.0.0.1 0.1 0.1 0.1 A 11111111 Sodium Benzoate 0.0.0.0.0.0.3 0.0.0.0.3 0.3 0.3 0.3 B 33333333 Niacinamide 5 5 3-5 5 5 3 5 - - 5 5 A Panthenol 3 3 1-3 3 3 1 3 - - 3 3 A Tocopherol Acetate 2 2 0.-2 2 2 0.2 2 2 B 55 Retinol Palmitate 0.----0. 05------0.1 B 15 Parsol 1789 3-1-1 0.-0.-1-1-1 B 51 Parsol MCX'-5-5 2.-0.-5-5-5 B 55 Citric acid 1 0.1 0.0.1 0.1 0.0.7 1 1 1 A 55355 Salicylic acid-0.-0. 0.-0.-0.----A 5 5 5 5 7 Triethanolamine 0.--0. 0.---0.--0.9 0.5 C 1111 Sodium Hydroxide--0.0.0.--0.-0. 1---C 1 1 1 Polyquaternium 10---1.--0.-0.---0.5 B 0 5 6 304-0.--0.---0.8---BPolymerKG 77 Fragrance 5 0.5 0.5 0.5 E 55555555 Cetyl Alcohol 3---2.--2.-2. 2-2. 5-C 6 2 Stearyl Alcohol 2---1.--3.-1. 1-1. 6-C 5 2 --4-0.---3.---3.4CCetearylAlcohol 4 4 Behenyl Alcohol 2-2----0.-0. 7---C 6 Natrosol 330 Plus 1 - - - 0. - - 0. 0. - 0. 5 0.2 C 6547 Natrosol 250 HHR - - 1 - 0. - - - - 1.2 - - 0. 3 C 3 1055-1.--------0.8--DJaguarHP 2 ---1---------DJaguarC14S5 -----1.2-------DJaguarC13S5 Xanthan Gum------2.------D 0 Sodium Chloride--0.---0. 0.-0. 3---A 215 Water qs qs qs qs qs qs qs qs qs qs qs qs qs A Example 27 28 29 30 31 32 33 34 35 36 37 38 Weight % Quat. Amm. Agt (see 3 3 3 3 3 3 3 3 3 3 3 3 A notes) Glycerine 15 16 22 9 8 9-32 32 32 32 32 A 116---512-----APropyleneGlycol --88-812-----AButyleneGlycol urea 12 2 9 A -10-12---47.5--BPetrlatum- Lanolin1 - - - 7. 5 7.5 15 15-3. 5-3 12 B Coronet-------7-6.7-B- Super Sterol Esters'--------3. 5-6. 5-B --------5-3BIsohexadecane- ---------3-5BIsononylIsono0nanoate Sefa Cottonate21 211212---13-8--B Sefa Behenate 9 3 B -0.50.0.5-0.50.50.5---0.5BDimethlcone10Cst 5 Dimethlcone 1000Cst - 1.0 1. 1.0 1. 0 - - - 1. 0 B 0 Cyclomethicone-2. 5 2.2.5-2.5 2.5 2. 5 - - - 2. 5 B 5 PorasunPEG-10-2-2-3-1--3-B Methyl Paraben 0.5 5 0.5 0.5 0.5 0.5 0.5 0.5 0. 5 0. 5 A 5 Propyl Paraben 0. 5 0.5 0. 0.5 0.5 0.5 0.5 0.5 0.5 0.5 0. 5 0.5 B 5 0.10.10.0.10.10.10.10.10.10.10.10.1ADisodiumEDTA 1 Sodium Benzoate 0.3 0.3 0. 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0. 3 0. 3 B 3 55--55533-5ANiacinamide3 Panthenol 1 3 3--3 3 3 1 1-3 A 0.522--2220.50.5-2BTocopherlAcetate ---0.1-0.0--0.1---BRetinolPalmitate 5 Parsol1-10.5-1-1-1-B- Parsol5-52.5-5-5-5-B- Citric acid 1 0.5 1 0. 5 1 0. 3 0. 7 1 1 A 5 -0.5-0.50.5-0.5-0.7---ASalicylicacid --0.10.1---0-.1--0.9CTriethanolamine0.1 Sodium Hydroxide - - 0. 0.1 0.1--0. 1-0. 1--C 1 ---1.0--0.5-0.6---BPolyquaternium10 Polymer KG 0.7--0.7---0.8--B- Fragrance 0.5 5 0.5 0.5 0.5 0.5 0.5 E 5 3---2.6--2.2-2.2-2.5CCetylAlcohol 2---1.5--3.2-1.1-1.6CStearylAlcohol Cetearyl Alcohol--4-0. 4---3. 4---C 2-2----0.6-0.7--CSehenylAlcohol Natrosol 330 Plus 1 - - 0.4 - - 0. 7 0. 6 - 0. 5 C Natrosol 250 -1-0.3----1.2--C- Jaguar HP 1.2--------0.8-D- ---1--------DJaguarC14S5 -----1.2------DJaguarC13S6 XanthanGum3. 0-----D Sodium Chloride-0. 0.5 0. 2 - 0.3 - - A 1 Water qs qs qs qs qs qs qs qs qs qs qs qs A Example 39 40 41 42 43 45 46 47 48 49 Weight % Quat. Amm. Agt (see 8 8 8 8 8 8 8 8 8 8 A notes) Glycerine 15 16 22 9 8 9-32 32 32 A -16---512---APropyleneGlycol --88-812---AButyleneGlycol --12-29---AUrea- Petrolatum - - 10 - 12 - - - 4 7.5 B Lanolin1 - - - 7. 5 7.5 15 15 3. 5 B CoronetLanolin'7 B Esters1--------3.5-BSuperSterol Isohexadecane---------5 B ---------3BIsononylIsononanoale Sefa 211212---13-8B21 Sefa Behenate-----9--B Dimethicone 10Cst - 0.5 0. 0.5 0. 5 - - B 5 Dimethicone 1000Cst - 1.0 1. 1.0 1. 0 - - B0 0 Cyclomethicone - 2.5 2. 2.5 2. 5 - - B 5 Florasun PEG-10 -2-2-3-1--B Methyl Paraben 0.5 5 0.5 0.5 0.5 0.5 0.5 0.5 A 5 Propyl Paraben 0.5 5 0.5 0.5 0.5 0.5 0.5 0.5 B 5 Disodium EDTA 0.1 1 0.1 0.1 0.1 0.1 0.1 0.1 A 1 Sodium Benzoate 0.3 3 0.3 0.3 0.3 0.3 0.3 0.3 B 3 55--55533ANiacinamide3 Panthenol 1 3 3 3 3 1 1 A Tocopherol Acetate 0.5 2 2-2 2 2 0.5 0.5 B RetinolPalmitate------0. 0- 5 Parsol1-10.5-1-1-B- Parsol MCX 3-5-5 2. 5 - 5 - 5 - B Citric acid 1 0. 5 1 0. 5 0.5 1 0.5 1 0.3 0.75 A Salicylic acid - 0.5 - 0. 5 0.5-0. 5-0. 7-A Triethanolamine 0. 1--0.1 0. 1 - - - 0.1 - C Sodium Hydroxide - - 0. 0.1 0. 1 - - 0.1 - 0. 1 C 1 ---1.0--0.5-0.6-BPolyquatemium10 Polymer KG 30 4 - 0.7 - - 0.7 - - - 0. 8 B Fragrance 0.5 0. 5 0. 0. 5 0.5 0.5 0.5 0.5 0.5 E 5 3---2.6--2.2-2.2CCetylAlcohol 2---1.5--3.2-1.1CStearylAlcohol --4-0.4---3.4-CCetearylAlcohol 2-2----0.6-0.7CBehenylAlcohol Natrosol 330 Plus 1 - - - 0.4 - - 0. 7 0.6-C Natrosol 250 HHR - - 1 - 0.3 - - - - 1. 2 C Jaguar HP 1.2--------D- ---1------DJaguarC14S5 Jaguar C13S 5--1. 2-D Xanthan-----3.0---D- Sodium Chloride - - 0. - - - 0. 5 A 1 Water qs qs qs qs qs qs qs qs qs qs A Example 50 51 52 53 54 Quat 8 8 8 8 8 A Glycerine 32 32 32 32 32 A -5-6BPetrolatum- Lanolin'3 12---B CoronetLanolin 6. 7--6-B Esters16.5-3SuperSterol 6 3 B 3--3BIsohexadecane- -5---BIsononylIsononanoate Sefa Cottonate - - 8 12 10 B Sefa-5--B3 Dimethicone 10Cst-0. 5 0.--B 5 -1.01.--BDimethicone1000Cst 0 2.52.--BCyclomethicone- 5 3--2.5-BFlorasunPEG-102 Methyl Paraben 0.5 5 0.5 A 5 Propyl Paraben 0.5 5 0.5 B 5 Disodium EDTA 0.1 1 0.1 A 1 Sodium Benzoate 0.3 3 0.3 B 3 5553ANiacinamide- Panthenol 3 3 3 1 A -2220.5BTocopherolAcetate Retinol0.1---B- Parsol 1789 3 1-0. 1-B 1 5-90.5-BParsolMCX3 5 Citric acid 11-A1 ----0.5ASalicylicacid Triethanolamine-0. 9 0.--C 5 Sodium Hydroxide----0. 6 C Polyquaternium 10--0.1. 0 - B 5 Polymer KG ---0.8B- Fragrance 0.5 5 0.5 E 5 -2.5--3.2CCetylAlcohol -1.6--2.6CStearylAlcohol Cetearyl Alcohol--3.--C 4 ----0.2CBehenylAlcohol Natrosol 330 Plus-0. 5 0.-0. 6 C 25 Natrosol 250 HHR 0. C 3 Jaguar HP 105 0. 8 ! | S Jaguar Cl 3S 5 0. 8 D Sodium Chloride--0.2 0.1 A Water qs qs qs qs qs A 1; Available from Croda 2; Available from Floratech, AZ, USA 3: Available from Hoffman La Roche, NJ, USA 4; Available from Amerchol, NJ, USA 5; Available from Rhodia, NJ, USA Notes In examples 1,4,7,9,17,20,22,24,28,36,38,47,49,53, the quaternary ammonium compound used is Distearyl Dimethyl Ammonium Chloride supplied by Goldschmidt, trade name Varisoft TA100.

. In examples 2,3,5,6,8,10,15,16,18,19,21,23,26,27,31,33,34,35,37,41,45,46 ,48,50,51,52,5 4, the quaternary ammonium compounds used is N, N-di (canolyl-oxy-ethyl)-N methyl, N- (2-hydroxyethyl) Ammonium Methyl Sulfate supplied by Goldschmidt, trade name Rewoquat V3620.

. In Example 11 the quaternary ammonium compound used is N, N-di (canolyl- oxy-ethyl)-N methyl, N- (2-hydroxyethyl) Ammonium Methyl Sulfate supplied by Goldschmidt, trade name Rewoquat WE18 . In Example 12 the quaternary ammonium compound used is N, N-di (canolyl- oxy-ethyl)-N methyl, N- (2-hydroxyethyl) Ammonium Chloride supplied by Goldschmidt, developmental material (WE25) In Example13 the quaternary ammonium compound used is Methyl bis (hydrogenated tallowamidoethyl) (2-hydroxyethyl) ammonium methyl sulfate supplied by Goldschmidt, trade name Varisoft 110.

. In Example 14 the quaternary ammonium compound used is Methylbis (tallowamidoethyl) (2-hydroxyethyl) ammonium methyl sulfate supplied by Goldschmidt, trade name Varisoft 222. In Example 25 the quaternary ammonium compound used is Methyl-1- tallowoylethyl-2-tallowimidazoline supplied by Goldschmidt, developmental material In Example 29 the quaternary ammonium compound used is Methyl-1- tallowamidoethyl-2-tallowimidazoline supplied by Goldschmidt, developmental material In Example 30 the quaternary ammonium compound used is Methyl-1- tallowoylethyl-2-tallowimidazolinium methyl sulfate supplied by Goldschmidt, In Example 32 the quaternary ammonium compound used is Methyl-1- tallowamidoethyl-2-tallowimidazolinium methyl sulfate supplied by Goldschmidt, trade name Varisoft 475, Varisoft 445 In Example 39 the quaternary ammonium compound used is N, N-Dimethyl-N- (canolyl-oxy-ethyl)-N- (canolamidoethyl) amine, supplied by Kao.

In Example 40 the quaternary ammonium compound used is N, N-Dimethyl-N- (canolyl-oxy-ethyl)-N-(canolamidoethyl) Ammonium Methyl Sulfate, supplied by Kao In Example 42 the quaternary ammonium compound used is N, N'-Bis (2- talloyloxyethyl)-N, N, N', N'-Tetramethylene Diammonium Dichloride, as disclosed in patents US 4728337, US 4721512, US 4906413 from Ciba-Geigy Corporation In Example 43 the quaternary ammonium compound used is N, N'-Bis (2- canolyloxyethyl)-N, N'-Dimethyl-N, N'- (2-Hydroxyethyl)-1,6-Hexane Diammonium Methyl Sulfate, as disclosed in patents EP 0503155A1 & EP 0803498 from Goldschmidt-Witco.

In Example 44 the quaternary ammonium compound used is the di and oligo ester quats made by the reaction of fatty acid, di functional (or multi functional) acid and triethanolamine followed by quaternisation as disclosed in W098/49132 by Kao and US 5880289 by Henkel.

Process For those examples includinq component C : 1. Premix 1: Combine components of group A together at a temperature greater than the transition temperature of the chosen quaternary ammonium compound, keeping back a predetermined part of the quaternary ammonium compound and water. Vigorously agitate this premix. 2. Premix 2: Combine components of groups B and C with the remaining parts of the quaternary ammonium compounds and water not previously used in premix 1. Heat above the melting point of the quat and the oils.

3. Combine Premix 1 & 2 and allow to cool until 40°C, stir in the perfume.

For those examPies includinq component D : 1. Premix 1: Combine components of group A together at a temperature greater than the transition temperature of the chosen quaternary ammonium compound, keeping back a predetermined part of the water. Vigorously agitate this premix.

2. Premix 2: Combine with agitation the components of group D with the water not previously used in premix 1.

3. Combine Premix 1 & 2 and components of groups B & E. Vigorously agitate.

The compositions of the above examples provide good skin care benefits, such as good moisturisation, good hydration, good skin feel, good skin softness and/or good skin smoothness, with low levels of negatives such as greasiness, stickiness or tack.