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WO1996019188A1 - Agent moussant pour compositions cosmetiques moussantes - Google Patents

Agent moussant pour compositions cosmetiques moussantes Download PDF

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Publication number
WO1996019188A1
WO1996019188A1 PCT/US1995/016050 US9516050W WO9619188A1 WO 1996019188 A1 WO1996019188 A1 WO 1996019188A1 US 9516050 W US9516050 W US 9516050W WO 9619188 A1 WO9619188 A1 WO 9619188A1
Authority
WO
WIPO (PCT)
Prior art keywords
foaming
alkyl
foaming agent
hair mousse
composition according
Prior art date
Application number
PCT/US1995/016050
Other languages
English (en)
Inventor
Takanori Nambu
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to AU45139/96A priority Critical patent/AU4513996A/en
Publication of WO1996019188A1 publication Critical patent/WO1996019188A1/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/046—Aerosols; Foams
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/442—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
    • C09K23/017—Mixtures of compounds
    • C09K23/018—Mixtures of two or more different organic oxygen-containing compounds

Definitions

  • the present invention relates to a foaming agent comprising an amphoteric surfactant and an N-acylamino acid surfactant which provides voluminous and stable foaming, and smooth and mild touch to foaming cosmetic compositions.
  • the present invention relates to leave-on hair mousse products comprising this foaming agent.
  • Cosmetic compositions such as shaving creams, hair mousses, spray foams, foaming lotions and foaming creams are aimed to be dispensed or sprayed as foams and applied on the human skin or hair. These products are described in the present invention as "leave-on foaming cosmetic products”.
  • One common characteristic desired for these leave-on foaming cosmetic products is a foam having favorable characteristics to the consumer such as voluminous and stable foaming, with smooth and mild touch to the skin and hair.
  • Hair mousses Leave-on foaming cosmetic compositions for hair are usually referred to as "mousses", which term will be used in the present invention. Hair mousses were bom in Europe in the early 1980s. Hair mousses are fundamentally an aerosol foam, however, non-aerosol foams are also known. The general appeal of hair mousses can be largely attributed to the ease of application and controlled amount of product which are possible from mousse formulations. Hair mousse compositions are generally dispensed by a compressible dispenser or a valve and applied to the user's hand or a specifically designed comb and spread through the hair. Alternatively, hair mousse compositions can be directly applied to the hair by dispensing through nozzles. Hair mousses are formulated for the pu ⁇ ose of styling, setting, and arranging, or for other purposes such as shampooing, conditioning, treating, dyeing, and combinations thereof.
  • alcohol refers to volatile primary alcohols having about 1 to 6 carbons, particularly ethanol. Alcohol is used in mousses for a number of reasons. First, the presence of volatile alcohol can aid styling by decreasing drying time. However, it is assumed that this drying has raised the concerns of some consumers that alcohol is also drying hair. Second, alcohol aids foam breakage as the mousse is spread throughout the hair. It is known that foam breakage is a result of the ability of alcohol to act as a defoaming agent. Third, alcohol itself improves product ability of alcohol to act as a defoaming agent.
  • alcohol itself improves product preservation.
  • alcohol enhances the compatibility of the concentrate with the propellant, and acts as a solubility bridge between the resin and the water base.
  • alcohol is a good solvent for dissolving oil base ingredients such as conditioning fatty s alcohols. Consequently, elimination of alcohol from the formulation may affect product performance.
  • a foaming agent which can be used in hair mousse compositions with or without alcohol.
  • Preservatives such as DMDM Hydantoin (dimethylol dimethyl hydantoin) 0 and Kathon CG (mixture of methylchloro-isothiazolinone and methyl isothiazolinone) are known as effective preservatives at low levels, however, are not approved for use in leave- on cosmetic products in a number of countries. Phenoxyethanol and EDTA are widely accepted for use, however, are not satisfactorily effective at low levels.
  • Parabens such as methyl paraben, propyl paraben, butyl paraben, and LiquaPar oil (mixture of isobutyl s paraben, isopropyl paraben, and butyl paraben) are also widely accepted for use.
  • parabens are lipophilic, they cannot dissolve in water, and thus have some formulation constraints.
  • Methyl paraben and propyl paraben are difficult to formulate at high levels, for they are solid at room temperature.
  • the type of propellents are also known to affect product performance. It is known that fluorohydrocarbons such as difluoroethane 152a (supplied by DuPont) can be used for a wide range of formulations. Propane and dimethyl ether can also be used for a wide range of formulations. However, propane is relatively combustible. Dimethyl ether when 5 used at high levels can be corrosive. LPG (liquefied petroleum gas) is a mixture of mainly isc-butane, n-butane, and propane, and is available in different pressure grades. LPG is a relatively safe propellant, however, have some formulation constraints.
  • foaming agent which foams by being dispensed or sprayed, and provides voluminous and stable foaming, smooth and mild touch, and styling/conditioning effect to foaming cosmetic compositions.
  • foaming cosmetic composition such as a hair mousse composition
  • said foaming agent which provides a foam having appropriate foam breakdown (foam breakability) under shear and is easy to spread on hair, has a smooth, soft and creamy texture, and has a mild touch.
  • foaming cosmetic 0 composition such as a hair mousse composition
  • a foaming cosmetic 0 composition such as a hair mousse composition
  • said foaming agent which can be formulated in combination with a wide range of solvents, preservatives, and propellants.
  • foaming cosmetic composition such as a hair mousse composition
  • a hair mousse composition comprising said foaming agent which provides quick, voluminous foam expansion and reduced pooling upon dispensing.
  • a hair mousse composition comprising said foaming agent which provides good style control, conditioning effect, and good feel to the hair.
  • the present invention relates to a foaming agent comprising an amphoteric 5 surfactant and an N-acylamino acid surfactant which foams by being dispensed or sprayed, and provides improved foaming characteristics to foaming cosmetic compositions.
  • the present invention also relates to a foaming cosmetic composition such as a hair mousse composition comprising the foaming agent and further comprising a solvent and a propellant.
  • the hair mousse composition comprises the foaming agent which comprises amphoteric surfactant and an N-acylamino acid surfactant at a weight ratio of 15:85 to 99:1 and further comprises a polymer, a solvent, a preservative, and a propellant.
  • the present invention relates to a foaming agent for use in a foaming cosmetic composition which foams by being dispensed or sprayed, comprising an amphoteric surfactant and an N-acylamino acid anionic surfactant and salts thereof.
  • the present invention also relates to a foaming composition such as a hair mousse composition comprising the foaming agent and further comprising a solvent and a propellant. All percentages and ratios are based on weight unless otherwise specified.
  • the total of components except for propellant is defined as a concentrate. For non-aerosol products containing no propellant, the concentrate is equal to the entire composition.
  • the foaming agent of the present invention comprises an amphoteric surfactant and an N-acylamino acid surfactant and salts thereof.
  • the foaming agent of the present invention preferably comprises the amphoteric surfactant and the N-acylamino acid surfactant at a ratio of 15:85 to 99:1 , more preferably 25:75 to 99:1 , and typically comprising 50%- 100% by weight of the combination of the amphoteric surfactant and the N-acylamino acid surfactant.
  • Other components of a foaming agent include solvents such as water, lower alcohol, polyhydric alcohols, and mixture thereof.
  • Amphoteric surfactants useful in the present invention are those having the following general formulae (I) (II), (III) and (IV) and mixtures thereof:
  • R 1 is an alkyl, alkenyl, aryl, or hydroxyalkyi radical of from about 8 to about 22 carbon atoms, optionally interrupted with up to about 10 ethylene oxide moieties and/or 1 glyceryl moiety
  • R 2 and R 3 are individually selected from alkyl and monohydroxyalkyl groups containing from about 1 to about 3 carbon atoms
  • R 4 is alkylene, or hydroxyalkylene of from about 1 to about 4 carbon atoms
  • Z is a radical selected from carboxylate, sulfonate, sulfate, phosphate, or phosphonate
  • x is 0 or 1
  • n is from about 1 to about 6
  • m is 0 or 1.
  • R 1 is an alkyl, alkenyl, or hydroxyalkyi radical of from 11 to 17 carbon atoms
  • R 2 and R 3 are individually selected from alkyl groups containing of from 1 to 3 carbon atoms
  • R 4 is alkylene or hydroxyalkylene of from 1 to 2 carbon atoms
  • Z 1 is a radical selected from carboxylate, sulfonate
  • x is 0 or 1
  • n is 1 to 3
  • m is 0 or 1.
  • R 8 R 6 wherein R ⁇ is C8-C22 alkyl, alkenyl, aryl, or hydroxyalkyi, preferably C8-C22.
  • R 6 is hydrogen or CH2CO2M 1
  • R 7 is CH2CH2OH or CH2CH2OCH2CH2COOM 1
  • R 8 is hydrogen, CH2CH2OH, or CH2CH2OCH2CH2COOM 1
  • Z 2 is CO2M 1 or CH2CO2M 1
  • y is 2 or 3, preferably 2
  • M 1 is hydrogen or a cation, such as alkali metal, alkaline earth metal, ammonium, alkanol ammonium, sulfate, sulfonate, phosphate, or phosphonate.
  • amphoteric surfactants useful for hair mousse compositions having general formula (I) are amide betaines, amide sulfo betaines, alkyl betaines, alkenyl betaines, sultaines (sulfo betaines), and imidazolinium betaines.
  • amphoteric surfactants particulariy useful for hair mousse compositions are high alkyl betaines, such as coco dimethyl carboxy methyl betaine, cocamidopropyl betaine under the trade name of TEGO BETAINE, coco betaine, lauryl betaine under the trade name REWOTERIC AM DML-35, lauryl amidopropyl betaine, oleyl betaine, lauryl dimethyl carboxy methyl betaine, lauryl dimethyl alpha-carboxyethyl betaine, cetyl dimethyl carboxymethyl betaine, lauryl bis-(2-hydroxyethyl) carboxymethyl betaine, stearyl bis-(2-hydroxypropyl) carboxymethyl betaine, oleyl dimethyl gamma-carboxypropyl betaine, lauryl bis-(2-hydroxypropyl) alpha- carboxyethyl betaine, cocamidopropyl hydroxy sultaine (sulfobetaine), lauryl sultaine (lau
  • amphoteric surfactants useful for hair mousse compositions having general formula (II) are marketed under the trade name MIRANOL and are understood to comprise a complex mixture of species, and can exist in protonated and non-protonated species depending upon pH with respect to species that can have a hydrogen at R 6 .
  • the imidazolinium amphoteric surfactant hereof can be derived via an imidazolinium intermediate.
  • Preferred amphoteric surfactants of formula (II) are monocarboxylates and dicarboxylates. Examples of these materials include cocoamphocarboxypropionate, cocoamphocarboxypropionic acid, cocoamphocarboxyglycinate (alternately referred to as cocoamphodiacetate), and cocoamphoacetate.
  • Specific commercial products providing the imidazolinium derivative component of the present compositions include those sold under the trade names MIRANOL C2M CONC. N.P., MIRANOL C2M CONC. O.P., MIRANOL C2M SF, MIRANOL CM SPECIAL (Miranol, Inc.); ALKATERIC 2CIP (Alkaril Chemicals); cocoamphocarboxy propionate under the trade name NIKKOL AM-101 , AMPHOTERGE W-2 (Lonza, Inc.); MONATERIC CDX-38, MONATERIC CSH-32 (Mona Industries); REWOTERIC AM-2C (Rewo Chemical Group); and SCHEROTERIC MS-2 (Scher Chemicals).
  • MIRANOL C2M CONC. N.P. MIRANOL C2M CONC. O.P.
  • MIRANOL C2M SF MIRANOL CM SPECIAL
  • ALKATERIC 2CIP Alkaril Chemicals
  • cocoamphocarboxy propionate under the
  • amphoteric surfactants useful for hair mousse compositions having general formulae (III) and (IV) include n-alkylaminopropionates and n- alkyliminodipropionates. Such materials are sold under the trade name DERIPHAT by Henkel and MIRATAINE by Miranol, Inc. Specific examples include N-lauryl-beta-amino propionic acid or salts thereof, and N-lauryl-beta-imino-dipropionic acid or salts thereof. N-Acylamino Acid Surfactant
  • N-acyl amino acid surfactants for purposes hereof, include N-acyl hydrocarbyl acids and salts thereof, such as those represented by Formula (V), as follows:
  • R 10 is a C8-C24 alkyl or alkenyl radical, preferably C ⁇ rj-C-*8 alkyl-
  • R1 1 is " ⁇ "• ⁇ c 1" C4 alkyl, phenyl, or -C ⁇ COOM, preferably C1-C4 alkyl, more preferably C1-C2 alkyl
  • R 12 is -CR 13 2- or C-J-C2 alkoxy, wherein each R 13 independently is -H or C ⁇ -Cg alkyl or alkylester, and n is from 1 to 4, preferably 1 or 2
  • M is -H or a soluble salt-forming cation such as ammonium, alkanolamine, such triethanolamine, monovalent metals, such as sodium and potassium, and polyvalent metal cations, such as magnesium and calcium, preferably an alkali metal such as sodium or potassium.
  • N-acyl acid surfactants A wide variety of N-acyl acid surfactants and their synthesis are described in Anionic Surfactants, Part II, Surfactant Science Series, Vol. VII, edited by Warner M. Linfield, Marcel Dekker, Inc. (New York and Basel), 1976; pp 581-617.
  • R 1 1 is methyl and R 12 is -CH2-, and n is 1 or 2, which are known as the N-acyl sarcosinates, propionates and acids thereof.
  • Specific examples include lauroyl sarcosinate, myristoyl sarcosinate, cocoyi sarcosinate, oleoyl sarcosinate, lauroyl methyl aminopropionate, and cocoyi methyl aminopropionate preferably in their sodium and potassium salt forms.
  • alkyl or “alkenyl” include mixtures of radicals which may contain one or more intermediate linkages such as ether or polyether linkages or non-functional substituents such as hydroxyl or halogen radicals wherein the radical remains of hydrophobic character.
  • a foaming cosmetic conposition of the present invention comprises a concentrate which is a foamable liquid which produces a foam when mixed an external source of air or gas, and is dispensed as a foam.
  • a concentrate (by weight) of the foaming cosmetic composition of the present invention comprises 0.01-20%, more preferably 0.01-10%, most preferably 0.01-6%, of the foaming agent.
  • the concentrate (by weight) of the foaming cosmetic composition of the present invention comprises from about 0.005% to 5%, preferably from about 0.01% to about 3%, of amphoteric surfactant, and comprise from about 0.005% to about 5%, preferably from about 0.01% to about 3% of N-acyl amino acid surfactant as the foaming agent of the present invention .
  • the foaming cosmetic compositions further preferably comprises a solvent for the foaming agent.
  • Solvents used in a foaming cosmetic composition of the present invention are selected depending on variables such as the remainder components, viscosity, and desired foaming characteristic of the composition.
  • the solvent is preferably comprised at a level of
  • Non-limiting examples of solvents useful in the present invention are: water, lower alcohols having 1 to 6 carbons such as ethanol and isopropanol, and polyhydric alcohols such as propylene glycol, hexylene glycol, glycerin, and propane diol, and mixtures thereof.
  • solvents useful in the present invention are: water, lower alcohols having 1 to 6 carbons such as ethanol and isopropanol, and polyhydric alcohols such as propylene glycol, hexylene glycol, glycerin, and propane diol, and mixtures thereof.
  • the foaming cosmeitc compositions further preferably comprises a propellant so mixing with the concentrate to foam the foam.
  • Propellents when used in a foaming cosmetic composition in the present invention are selected depending on variables such as the remainder components, the package, and how the product is designed to be used (standing or invert).
  • the propellant is preferably comprised at a level of 0-60%, more preferably 0-30% of the entire composition.
  • the hair mousse composition is usually provided in a package equipped with an air or gas mixing device.
  • Non-limiting examples of propellents useful in the present invention are: fluorohydrocarbons such as difluoroethane 152a (supplied by DuPont), dimethyl ether, carbon dioxide, nitrogen, and hydrocarbons such as propane, iso-butane, n-butane, and mixtures of hydrocarbons such as LPG (liquefied petroleum gas).
  • fluorohydrocarbons such as difluoroethane 152a (supplied by DuPont), dimethyl ether, carbon dioxide, nitrogen, and hydrocarbons such as propane, iso-butane, n-butane, and mixtures of hydrocarbons such as LPG (liquefied petroleum gas).
  • a suitable vessel such as a pressed dispensing package which is well known in the art(for example, a package for Vidal Sassoon Styling Mousse Extra Body/ The Procter & Gample Company).
  • a suitable vessel such as a pressed dispensing package which is well known in the art(for example, a package for Vidal Sassoon Styling Mousse Extra Body/ The Procter & Gample Company).
  • Optional components can be included in the foaming cosmetic compositions of the present invention, depending on the needs of the product.
  • optional components include additional surfactants, ultraviolet and infrared screening and absorbing agents, hair conditioning agents, skin conditioning agents, perfume, color, pH adjusters, polymers, dyes, vitamins, proteins, plant extracts, and nutrients.
  • a foaming cosmetic composition such as a hair mousse compositions can comprise a polymer for hair styling and conditioning, and a preservative, and can further comprise other optional components.
  • a foaming cosmetic composition such as a hair mousse compositions may further comprise a polymer.
  • Such polymer comprise cationic, nonionic, anionic, and amphoteric polymers.
  • Polymer is typically included by weight at a level of 0-15%, preferably 0-10% of the concentrate.
  • Polymers suitable for use herein include any polymers soluble or colloidaliy dispersible in the aqueous phase (if water is the only solvent in the aqueous phase, the polymer should be soluble or dispersible in water; if an optional cosolvent such as ethanol is present the polymer should be soluble or dispersible in the combined solvent system). Solubility/dispersibility is determined at ambient conditions of temperature and pressure (25°C at 1At).
  • Polymers for use in the compositions of the present invention include cationic, anionic, nonionic, and amphoteric resins.
  • Non-limiting examples of cationic polymers useful in the present invention include quatemized cellulose ethers such as Polyquatemium 10 (hydroxyethylcellulose hydroxypropyl trimethylammonium chloride ether) under the trade name Ucare Polymer LR and Polyquatemium 4 (hydroxyethylcellulose dimethyldiallyl ammonium chloride copolymer) under the trade name Celquat, quatemized vinyl pyrrolidone/alkylaminoacrylate or methacrylate copoiymers such as Polyquatemium 11 (polyvinylpyrrolidone N.N'-dimethylaminoethylmethacrylic acid copolymer diethyl sulfate salt) under the trade name Gafquat, methylvinylimidazolium vinylpyrrolidone quaternary ammonium copoiymers commercial
  • cationic polymers are cationic guar gums, for example, hydroxypropyltrimethylammonium guar gum, quatemized cellulose ethers such as copoiymers of hydroxyethylcellulose with diallyldimethyl ammonium chloride or with trimethyl ammonium substituted epoxides, homopolymers of lower alkylamino alkyl acrylate or methacrylate monomers (e.g.
  • dimethyl aminoethylmethacrylate and copoiymers thereof with compatible monomers such as N-vinylpyrrolidone or with methacrylate derivatives such as methyl, ethyl, abietyl and oleyl methacrylates and mixtures thereof and/or with alkyl acrylates such as methyl and butyl acrylates and mixtures thereof, copoiymers of dimethyldiallyl ammonium chloride and acrylamide, homopolymers of dimethyldiallyl ammonium chloride, vinylimidazolium/vinyl pyrrolidone copoiymers, and mixtures thereof.
  • compatible monomers such as N-vinylpyrrolidone or with methacrylate derivatives such as methyl, ethyl, abietyl and oleyl methacrylates and mixtures thereof and/or with alkyl acrylates such as methyl and butyl acrylates and mixtures thereof
  • Polycationic hair conditioning polymers can be derived from polymerizable cationic starting monomers, or from polymerizable nonionic monomers which are modified subsequent to polymerization to be of cationic character.
  • Examples of the cationic monomers include:
  • amine derivatives of (meth)acrylic acid or amine derivatives of (meth)acrylamide derived from (meth)acrylic acid or (meth)acrylamide and a dialkylalkanolamine have C1-C4 alkyl groups such as dimethylaminoethyl (meth)acrylate, diethylaminoethyl (meth)acrylate, dimethylaminopropyl (meth)acrylate, or dimethylaminopropyl (meth)acrylamide; and (iii) derivatives of the products of the group (ii) above by (1) neutralization with an inorganic or organic acid, such as hydrochloric acid, or lactic acid, (2) modification with a halogenated alkyl, such as methyl chloride, ethyl chloride, methyl bromide, or ethyl iodide, (3) modification with a halogenated fatty acid ester such as ethyl monochloroacetate, or methyl mono
  • cationic unsaturated monomers can be polymerized in cationic form, or as an alternative they can be polymerized in the form of their precursors, which are then modified to be cationic, for example, by a quatemizing agent (eg. ethyl monochloroacetate, dimethyl sulfate, etc.)
  • a quatemizing agent eg. ethyl monochloroacetate, dimethyl sulfate, etc.
  • Non-limiting examples of nonionic monomers are acrylic or methacrylic acid esters of C1-C24 alcohols, such as methanol, ethanol, 1-propanol, 2-propanol, 1 -butanol, 2- methyl-1-propanol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1 -butanol, 1-methyM- butanol, 3-methyl-1 -butanol, 1-methyl-1-pentanol, 2-methyl-1-pentanol, 3-methyl-1- pentanol, t-butanol, cyclohexanol, 2-ethyl-1 -butanol, 3-heptanol, benzyl alcohol, 2-octanol, 6-methyl-1-heptanol, 2-ethyl-1-hexanol, 3,5-dimethyl-1-hexanol, 3,5,5-trimethyl-1-hexanol, 1-decan
  • nonionic monomers include acrylate and methacrylate derivatives such as allyl acrylate and methacrylate, cyclohexyl acrylate and methacrylate, oleyl acrylate and methacrylate, benzyl acrylate and methacrylate, tetrahydrofurfuryl acrylate and methacrylate, ethylene glycol di-acrylate and -methacrylate, 1 ,3-butyleneglycol d-acrylate and -methacrylate, diacetonacrylamide, isobornyl (meth)acrylate, and the like.
  • acrylate and methacrylate derivatives such as allyl acrylate and methacrylate, cyclohexyl acrylate and methacrylate, oleyl acrylate and methacrylate, benzyl acrylate and methacrylate, tetrahydrofurfuryl acrylate and methacrylate, ethylene glycol di-acrylate and -meth
  • Non-limiting examples of polar nonionic monomers include acrylamide, N,N- dimethylacrylamide, methacrylamide, N-t-butyl acrylamide, methacryionitrile, acrylamide, acrylate alcohols (eg.C2-C ⁇ acrylate alcohols such as hydroxyethyl acrylate, hydroxy proxy I acrylate), hydroxyethyl methacrylate, hydroxypropyl methacrylate, vinyl pyrrolidone, vinyl ethers, such as methyl vinyl ether, acyl lactones and vinyl pyridine, allyl alcohols, vinyl alcohols and vinyl caprolactam.
  • acrylate alcohols eg.C2-C ⁇ acrylate alcohols such as hydroxyethyl acrylate, hydroxy proxy I acrylate
  • vinyl pyrrolidone vinyl ethers, such as methyl vinyl ether, acyl lactones and vinyl pyridine, allyl alcohols, vinyl alcohols and vinyl caprolactam.
  • Non-limiting examples of polycationic polymers include cationic polysaccharides, homopolymers of dimethyldiallyl ammonium chloride, copoiymers of dimethyldiallyl ammonium chloride and acrylamide, cationic amino-functional homopolymers and copoiymers derived from acrylic acid and/or methacrylic acid, especially from alkylaminoalkyl acrylate and methacrylate monomers such as dimethylaminoethyl acrylate and methacrylate, polyalkylene imines and ethoxy polyaikylene imines, vinylimidazolium/vinylpyrrolidone quaternary ammonium copoiymers, and mixtures thereof.
  • Non-limiting examples of amphoteric polymers include N-methacrylol ethyl-N,N'- dimethyl ammonium gamma-N-methyl carboxy betaine butyl methacrylate copolymer which is sold under the trade name Yukaformer AM-75; Octylacrylamide/Acrylates/Butylaminoethyl Methacrylate Copolymer which is sold under the trade name Amphomer 4910; and Octylacrylamide/Hydroxypropyl Acrylates/Butylaminoethyl Methacrylate Copolymer which is sold under the trade name Amphomer LV-71.
  • anionic polymers include the anionic, i.e. salt-neutralized forms of the following: VA Crotonates/Vinyl Neodecanoate Copolymer which is sold under the trade name Resyn 28-2930; VA/Crotonates Copolymer which is sold under the trade name Resyn 28-1310; Terpolymer of t-butylacrylate, ethylacrylate and methacrylic acid which is sold under the trade name Luvimer 100P; Acrylates/Octylacrylamide Copolymer which is sold under the trade name Dermacryl 79.
  • VA Crotonates/Vinyl Neodecanoate Copolymer which is sold under the trade name Resyn 28-2930
  • VA/Crotonates Copolymer which is sold under the trade name Resyn 28-1310
  • Terpolymer of t-butylacrylate, ethylacrylate and methacrylic acid which is sold under the trade name Luvimer 100P
  • Non-limiting examples of bases suitable for forming the salt-neutralized forms of these copoiymers include sodium hydroxide, potassium hydroxide, ammonium hydroxide, triethanolamine, trimethylamine, and 2- amino-2-methyl-1-propanol. Preservative
  • Hair mousse compositions can further comprise a preservative.
  • a preservative is preferably included at a level of 0-5%, more preferably 0-3% of the concentrate.
  • preservatives useful in the present invention are DMDM
  • Hydantoin (dimethylol dimethyl hydantoin) Kathon CG, (mixture of methylchloro- isothiazolinone and methyl isothiazolinone), imidazolidinyl urea, phenoxyethanol, EDTA and its salts, benzyl alcohol, and parabens such as methyl paraben, propyl paraben, butyl paraben, and LiquaPar oil (mixture of isobutyl paraben, isopropyl paraben, and butyl paraben).
  • Hair mousse compositions can further comprise additional surfactants.
  • additional surfactants comprise nonionic, cationic, anionic, and other amphoteric surfactants which do not affect the foaming agent of the present invention.
  • additional surfactants include sodium cocoyi isethionate (sodium cocoyi ethyl ester sulfonate), isosteareth 10, polyoxyethylene alkyl ether, and Geropon TC-42 (Na- N-cocoyl N-methyl taurate), lauric acid dimethanolamide.
  • Additional surfactant is typically included at a level of less than 50%, preferably less than 33% of the foaming agent.
  • Hair mousse compositions may further comprise a variety of optional components.
  • optional components include; thickeners and viscosity modifiers such as diethanolamides of long chain fatty acids, sodium chloride, and sodium sulfate, hair conditioning agents such as cetyl alcohol, stearyl alcohol, oleyl alcohol, and panthenol, ultraviolet absorbing agents such as octyl salicylate, pH adjusting agents such as citric acid, succinic acid, sodium hydroxide and triethanolamine, coloring agents, hair oxidizing agents such as hydrogen peroxide, perborate salts and persulfate salts, hair reducing agents such as thioglycolates, perfumes, perfume solubilizing agents such as polyethylene glycol fatty acid esters, sequestering agents, polymer plasticizing agents such as glycerin and propylene glycol, and volatile and non-volatile silicone fluids.
  • Such optional ingredients are typically included at a level of 0.01-20%, preferably from 0.01-10% of the concentrate.
  • Disodium Cocoamphodipropionate *4 0.05 Sodium Cocoyi Sarcosinate *5 0.05 0.30 Sodium N-cocoyl N-methyl ⁇ Aminopropionate *6 0.02 0.05 Sodium N-lauroyl N-methylaminopropionate *8 0.45 0.05 Isosteareth 10 *10 0.02 Lauramide DEA *11 Polyquatemium 4 1.00 2.00 Polyquatemium 7 1.20 Polyquatemium 11 0.30 Ethyl ether of PVM/MA copolymer - - 0.80 - Ethanol - 0.30 5.00 5.00
  • composition 8 The foaming rheology of a foaming composition of the present invention (composition 8) against compositions A (as being example of the composition of co-pending U.S. application serial No. 08/154231),B (0.6% by weight of Cocamidopropyl Betaine) and C (0.05% by weight of Sodium Cocoyi Sarcosinate), measured by using the Carri-Med CSL 100 Controlled stress rheometer (Carri-Med Ltd., England), under the following conditions.
  • the gap between two plates is 1mm.
  • the time between foam dispensing and commencement of measurement is no more than 10 seconds
  • Polyquatemium 4 1.00 1.00 1.00 1.00 Methyl Paraben 0.15 0.15 0.15 0.15 Phenoxyethanol 0.25 0.25 0.25 0.25 Disodium EDTA 0.10 0.10 0.10 Dimethicone Copolyol 0.17 0.17 0.17 Dimethicone 0.83 0.83 0.83 0.83 0.83 0.83 0.83 0.83 Perfume 0.05 0.05 0.05 0.05 Propylene Glycol 0.10 0.10 0.10 0.10 Dl Water q.s. q.s. q.s. q.S.
  • the Fig.1 shows the result of the comparison of the foaming rtieology of the composition 8 of the present invention and comparative examples A, B and C.
  • the vertical axis shows shear stress (Pa of Nm" 2 ) and represents foam stiffness
  • the horizontal axis shows shear rate (1/S) and represents foam breakability.
  • composition 8 in Fig.1 shows similar rtieology to conparatife example A, and better foam rheology compared to comparative examples B and C.
  • the compositions shown in Tables 1 , 2 and 3 can be prepared by any conventional method well known in the art. A suitable method is as follows:
  • Polymers and preservatives are added into distilled water under agitation at room temperature.
  • the obtained mixture is heated up to 70-75°C until homogenized.
  • Other optional components are added to the heated mixture, and agitated until homogenized.
  • the obtained mixture is allowed to cool to 30-40°C, and amphoteric surfactant, N-acyl acid surfactant, perfume and other heat sensitive components are added.
  • the obtained concentrate is packed into cans with propellant.

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Abstract

Agent moussant comprenant un tensioactif amphotère et un tensioactif d'acide N-acylaminé, et moussant lorsqu'il est dispersé ou pulvérisé et permettant d'améliorer les caractéristiques de moussage de compositions cosmétiques moussantes. Dans un mode de réalisation préféré, l'agent moussant fait partie d'une composition cosmétique moussante, telle qu'une mousse coiffante incorporant un solvant et des compositions optiques, telles qu'un polymère, un conservateur et un propulseur. Comme l'illustre la figure 1, cette composition moussante (8) contenant de la bétaïne de cocamidopropyle et du sarcosinate de sodium laurylé présente une rhéologie similaire à celle de l'exemple comparatif (A) et une rhéologie de moussage supérieure à celle des exemples comparatifs (B) et (C).
PCT/US1995/016050 1994-12-20 1995-12-12 Agent moussant pour compositions cosmetiques moussantes WO1996019188A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU45139/96A AU4513996A (en) 1994-12-20 1995-12-12 Foaming agent for foaming cosmetic compositions

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AUPN0153 1994-12-20
AUPN0153A AUPN015394A0 (en) 1994-12-20 1994-12-20 Foaming agent for foaming cosmetic compositions

Publications (1)

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WO1996019188A1 true WO1996019188A1 (fr) 1996-06-27

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AU (1) AUPN015394A0 (fr)
TR (1) TR199501602A2 (fr)
WO (1) WO1996019188A1 (fr)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1000606A3 (fr) * 1998-11-13 2000-08-02 Shiseido Company Limited Produit de nettoyage à faible acidité comprenant un sel alkalin d'un amino-acide N-acylé
US6551970B2 (en) 1996-05-06 2003-04-22 L'oréal Detergent cosmetic compositions for hair-care application and use thereof
WO2003097005A1 (fr) * 2002-05-16 2003-11-27 Beiersdorf Ag Gel nettoyant a fort pouvoir moussant, contenant des tensioactifs d'acide acylamine
DE10236063A1 (de) * 2002-08-07 2004-02-19 Beiersdorf Ag Milde Reinigungszubereitung
WO2009024362A1 (fr) * 2007-08-20 2009-02-26 Henkel Ag & Co. Kgaa Agents de traitement capillaires contenant un dérivé d'acide acylaminé, une hydroxyalkylamine et une 2-(2-hydroxyéthyle)-p-phénylènediamine
US9993419B2 (en) 2014-06-16 2018-06-12 The Procter & Gamble Company Method of treating hair with a concentrated conditioner
US9993420B2 (en) 2014-06-16 2018-06-12 The Procter & Gamble Company Method of treating hair with a concentrated conditioner
US10124951B2 (en) 2015-12-15 2018-11-13 The Procter And Gamble Company Method of treating hair
US10123963B2 (en) 2014-06-16 2018-11-13 The Procter And Gamble Company Method of treating hair with a concentrated conditioner
US10258548B2 (en) 2015-04-23 2019-04-16 The Procter And Gamble Company Hair care conditioning composition
US10265255B2 (en) 2015-12-15 2019-04-23 The Procter And Gamble Company Method of treating hair
US10265256B2 (en) 2015-12-15 2019-04-23 The Procter And Gamble Company Method of treating hair
US10265251B2 (en) 2015-12-15 2019-04-23 The Procter And Gamble Company Method of treating hair
US10285925B2 (en) 2015-12-15 2019-05-14 The Procter & Gamble Company Method of treating hair
US10294013B2 (en) 2015-12-21 2019-05-21 The Procter And Gamble Plaza Package to dispense a foaming composition
US10322072B2 (en) 2015-12-15 2019-06-18 The Procter And Gamble Company Method of treating hair
CN110270270A (zh) * 2019-07-02 2019-09-24 宜兴市中大凯水处理有限公司 一种新型mto水洗塔用分散剂及其制备方法
US10828248B2 (en) 2016-04-22 2020-11-10 The Procter And Gamble Company Method of forming a silicone layer
US10835480B2 (en) 2016-04-22 2020-11-17 The Procter And Gamble Company Method of forming a silicone layer
US11464724B2 (en) 2018-11-08 2022-10-11 The Procter & Gamble Company Low shear stress conditioner composition with spherical gel network vesicles

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4526781A (en) * 1984-04-25 1985-07-02 Revlon, Inc. Hair care compositions
US4713182A (en) * 1986-11-06 1987-12-15 Mine Safety Appliances Company Fire-fighting foam
US5217652A (en) * 1991-10-04 1993-06-08 The Gillette Company Conditioning shampoo

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4526781A (en) * 1984-04-25 1985-07-02 Revlon, Inc. Hair care compositions
US4713182A (en) * 1986-11-06 1987-12-15 Mine Safety Appliances Company Fire-fighting foam
US5217652A (en) * 1991-10-04 1993-06-08 The Gillette Company Conditioning shampoo

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6551970B2 (en) 1996-05-06 2003-04-22 L'oréal Detergent cosmetic compositions for hair-care application and use thereof
EP1000606A3 (fr) * 1998-11-13 2000-08-02 Shiseido Company Limited Produit de nettoyage à faible acidité comprenant un sel alkalin d'un amino-acide N-acylé
WO2003097005A1 (fr) * 2002-05-16 2003-11-27 Beiersdorf Ag Gel nettoyant a fort pouvoir moussant, contenant des tensioactifs d'acide acylamine
DE10236063A1 (de) * 2002-08-07 2004-02-19 Beiersdorf Ag Milde Reinigungszubereitung
WO2009024362A1 (fr) * 2007-08-20 2009-02-26 Henkel Ag & Co. Kgaa Agents de traitement capillaires contenant un dérivé d'acide acylaminé, une hydroxyalkylamine et une 2-(2-hydroxyéthyle)-p-phénylènediamine
US9993419B2 (en) 2014-06-16 2018-06-12 The Procter & Gamble Company Method of treating hair with a concentrated conditioner
US9993420B2 (en) 2014-06-16 2018-06-12 The Procter & Gamble Company Method of treating hair with a concentrated conditioner
US10123963B2 (en) 2014-06-16 2018-11-13 The Procter And Gamble Company Method of treating hair with a concentrated conditioner
US10258548B2 (en) 2015-04-23 2019-04-16 The Procter And Gamble Company Hair care conditioning composition
US10265255B2 (en) 2015-12-15 2019-04-23 The Procter And Gamble Company Method of treating hair
US10124951B2 (en) 2015-12-15 2018-11-13 The Procter And Gamble Company Method of treating hair
US10265256B2 (en) 2015-12-15 2019-04-23 The Procter And Gamble Company Method of treating hair
US10265251B2 (en) 2015-12-15 2019-04-23 The Procter And Gamble Company Method of treating hair
US10285925B2 (en) 2015-12-15 2019-05-14 The Procter & Gamble Company Method of treating hair
US10322072B2 (en) 2015-12-15 2019-06-18 The Procter And Gamble Company Method of treating hair
US10294013B2 (en) 2015-12-21 2019-05-21 The Procter And Gamble Plaza Package to dispense a foaming composition
US10828248B2 (en) 2016-04-22 2020-11-10 The Procter And Gamble Company Method of forming a silicone layer
US10835480B2 (en) 2016-04-22 2020-11-17 The Procter And Gamble Company Method of forming a silicone layer
US11464724B2 (en) 2018-11-08 2022-10-11 The Procter & Gamble Company Low shear stress conditioner composition with spherical gel network vesicles
CN110270270A (zh) * 2019-07-02 2019-09-24 宜兴市中大凯水处理有限公司 一种新型mto水洗塔用分散剂及其制备方法

Also Published As

Publication number Publication date
TR199501602A2 (tr) 1996-07-21
AUPN015394A0 (en) 1995-01-19

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