WO1996003967A1 - Hair cosmetic compositions - Google Patents

Hair cosmetic compositions Download PDF

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Publication number
WO1996003967A1
WO1996003967A1 PCT/US1995/008336 US9508336W WO9603967A1 WO 1996003967 A1 WO1996003967 A1 WO 1996003967A1 US 9508336 W US9508336 W US 9508336W WO 9603967 A1 WO9603967 A1 WO 9603967A1
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WO
WIPO (PCT)
Prior art keywords
hair
hair cosmetic
cosmetic composition
composition according
gelling agent
Prior art date
Application number
PCT/US1995/008336
Other languages
French (fr)
Inventor
Stevan David Jones
Philip John Marchant
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 MX9700667A priority Critical patent/MX9700667A/en
Priority to CA002192799A priority patent/CA2192799A1/en
Priority to US08/776,453 priority patent/US5922312A/en
Priority to EP95925443A priority patent/EP0768864A4/en
Priority to JP8506495A priority patent/JPH10503514A/en
Publication of WO1996003967A1 publication Critical patent/WO1996003967A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/042Gels
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8164Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical, and containing at least one other carboxyl radical in the molecule, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers, e.g. poly (methyl vinyl ether-co-maleic anhydride)
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8194Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/06Preparations for styling the hair, e.g. by temporary shaping or colouring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5424Polymers characterized by specific structures/properties characterized by the charge anionic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5426Polymers characterized by specific structures/properties characterized by the charge cationic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/594Mixtures of polymers

Abstract

A hair cosmetic composition comprising: (a) from about 0.01 % to about 3 % by weight of gelling agent comprising a copolymer of methyl vinyl ether/maleic anhydride, cross-linked with C4-C16 alkadiene or hydrolysis products thereof; (b) from about 0.1 % to about 10 % by weight of hair fixative polymer comprising a cationic copolymer of nonionic cellulose and diallyl dimethyl ammonium chloride; and (c) the balance comprising a carrier suitable for application to hair. The liquid hair cosmetic products have an improved non-tacky on-hair and on-hand feel, demonstrate excellent hair styling benefits in addition to ease of brush-out.

Description

HATR COSMETTC CO POSTTIOIVS
Technical Field
The present invention relates to hair cosmetic compositions. More particularly, this invention relates to hair cosmetic compositions containing a gelling agent and a hair fixative/conditioning polymer and having improved "in-use" and "on-hair" feel properties in addition to manageability and style retention benefits.
Background Of The Invention
The desire to have the hair retain a particular shape is widely held. A common methodology for accomplishing this is applying hair styling, or "setting" compositions to the hair, typically to damp or dry hair. These compositions provide temporary setting benefits, and should be removable by water and/or by shampooing. The materials used in the compositions to provide the setting benefits are generally applied in the form of mousses, gels, lotions or sprays.
High levels of style retention, or hold, are typically expected from hair compositions whether applied as a gel or a spray. Style retention in gel products is typically achieved by use of one or more hair fixative polymers, such as polyvinylpyrollidone (PVP) and the copolymer of PVP with vinyl acetate (PVP/VA) in combination with a gelling agent. A commonly used gelling agent is crosslinked polyacrylic acid, known by the CTFA name of Carbomer. When such polymers are incorporated into hair fixative compositions containing conventional gelling agents they can provide suitable style retention attributes. However, such compositions can give a sticky feel on the hair and hands during and after application as well as leaving the hair feeling stiff and unnatural.
It has now been found that certain combinations of gelling agents and hair fixative polymers can deliver excellent styling benefits without the sticky and stiff feel usually associated with conventional styling gels.
Thus a need exists for hair styling compositions which deliver effective style retention, impart a hair conditioning effect, have a non-sticky hair and on-hand feel, are easily brushed out, are resistant to flakiness and at the same time have stable product and viscosity characteristics and remain fully stable under long term and stressed temperature storage.
Summary of the Invention
According to one aspect of the invention, there is provided a hair cosmetic composition comprising:-
(a) from about 0.01% to about 3% by weight of gelling agent comprising a copolymer of methyl vinyl ether/maleic anhydride, crosslinked with C4-C 16 alkadiene or hydrolysis products thereof;
(b) from about 0.1% to about 10% by weight of hair fixative polymer comprising a cationic copolymer of nonionic cellulose and diallyl dimethyl ammonium chloride; and
(c) the balance comprising a carrier suitable for application to hair. The essential, as well as the optional, components of the present invention are described below. All levels and ratios are on a weight basis unless otherwise specified.
Gelling Agent
The compositions of the present invention contain from about 0.01% to about 3% preferably from about 0.05% to about 2%, more preferably from about 0.5% to about 1.5%, most preferably from about 0.6% to about 1% by weight of gelling agent. It is this gelling agent which in combination with a cationic hair fixative polymer imparts hair setting and conditioning benefits without the tacky dry-hair feel and on-hand stickiness normally associated with hair styling cosmetics. The gelling agents suitable for use in the present invention comprise a copolymer of methyl vinyl ether/maleic anhydride, and hydrolysis products thereof, crosslinked with C4-C16, preferably C6-C12, more preferably Cg-Cjo alkadiene. The gelling agents typically have a viscosity in the region of from about 50,000 cps to about 150,000 cps, preferably from about 70,000 cps to about 100,000 cps (measured as 0.5% gelling agent in non-alcoholic solution at pH7; Brookfield RVT, Spindle TE, 10 φm).
In its broadest aspect, the copolymer utilised in the present application comprise a copolymer of methyl vinyl ether/maleic anhydride (hereafter identified as A) crosslinked with C4-C16, preferably C6-C12, more preferably Cg-Cio alkadiene (hereafter identified as B). Examples of suitable polymers and their preparations are described in detail in "Polymers and Thickeners" Vol. 108, May 1993, p61-67, S.L. Kopolow, Y.T. Kwak and M.Helioff. These polymers comprise part A and B as defined above. In preferred embodiments, B comprises C6-C14 alkadiene, more preferably a C -C\2 alkadiene, most preferably a Cg-C^o alkadiene.
The preferred gelling agent for use herein is methyl vinyl ether/maleic anhydride, crosslinked with 1 ,9-decadiene (PVM/MA decadiene crosspolymer), available from ISP as Stabileze 06 (RTM). The hair gelling agents, herein are preferably utilised in at least partially neutralised form in order to obtain the required gel structure and overall pH of the hair cosmetic compositions.
The gelling agent can be neutralised to a level of from about 30% to about 100%, preferably from about 40% to about 98%, more preferably from about 50% to about 95% with base. Any conventionally used base, organic or inorganic, may be used for neutralisation of the acidic gelling agents. Hydroxides of alkali and alkaline earth metals and amino alcohols are suitable neutralisers for use in the present hair cosmetic compositions.
Examples of suitable organic neutralising agents which may be included in the hair cosmetic compositions of the present invention include amines, especially amino alcohols such as 2-amino-2-methyl- 1 ,3-propanediol (AMPD), 2-amine-2-ethyl-l,3-propanediol (AEPD), 2-amino-2-methyl-l- propanol (AMP), 2-amino-l-butanol (AB), monethanolamine (ME A), diethanolamine (DEA), triethanolamine (TEA), monoisopropanolamine (MIPA), diisopropanolamine (DIPA), triisopropanolamine (TIPA), dimethyl steramine (DMS) and amino methyl propanol (AMP) and mixtures thereof.
Preferred neutralising agents for use in compositions of the present invention are potassium and sodium hydroxides, aminomethyl propanol (AMP) and triethanolamine (TEA) and mixtures thereof.
In addition to the specific gelling agents as detailed supra such compositions may optionally include an auxiliary gelling agent at from about 0.01% to about 1%, preferqably from about 0.1% to about 0.5% by weight. Suitable auxiliary gelling agents can be selected from any conventional gelling agent such as a crosslinked polyacrylic acid copolymer, ethylene maleic anhydride copolymers or hydroxyethylcellulose and its derivatives. The preferred auxiliary gelling for use herein is hydroxyethylcellulose. Carrier The hair cosmetic compositions of the present invention also include a carrier which can be aqueouse or non-aqueous and mixtures thereof. This can comprise any of those conventionally used in polymer containing hair cosmetic formulations. The carrier is generally present in the hair cosmetic compositions at from about 70% to about 99.89%, preferably from about 78% to about 99.5% by weight. More preferably, the carrier is present at from about 80% to about 99% by weight of the total composition.
Organic solvents suitable for use in the carrier in compositions according to the present invention include C\~Cβ alkanols, carbitol, acetone and mixtures thereof. C\-C alkanols preferred for use in the present compositions are C2-C4 monohydric alcohols such as ethanol, isopropanol and mixtures thereof.
The preferred hair compositions according to the present invention contain from 70% to about 99.89% by weight of water, preferably from 78% to about 99.5%, more preferably from about 80% to about 99% by weight of water as the carrier.
Cationic Hair Fixative Polymer
In addition to the gelling agent the compositions according to the present invention comprise, as a second essential component, a hair fixative polymer. This hair fixative polymer is preferably solubilized or colloidally dispersed in the hair cosmetic carrier along with the gelling agent copolymer.
The preferred hair fixative polymer component of the hair cosmetic compositions of the present invention comprises a cationic copolymer of hydroxyethyl cellulose and diallyl dimethyl ammonium chloride which is known by the CTFA name Polyquaternium 4 and marketed under the trade names Celquat L200 (RTM) and Celquat HI 00 (RTM) by National Starch and Chemical Ltd. The hair fixative polymer is present in an amount of from about 0.1% to about 10%, preferably from about 0.3% to about 8%, more preferably from about 0.5% to about 6%, most preferably from about 0.8% to about 3% by weight of composition. In compositions according to the present invention the weight ratio of gelling agent:hair fixative polymer is in the range of from about 10: 1 to about 1 : 10.
Other hair fixative polymers suitable for use herein in conjunction with the above material include any polymer which is soluble or colloidally dispersible in the hair cosmetic carrier. Solubility and dispersibility are determined at ambient conditions of temperature and pressure (25°C and at 101.3 kPa (1 Atm)). Such copolymers may be cationic or nonionic in character. Copolymers suitable for use herein have a molecular weight in the range of from about 1,000 to about 5,000,000, preferably from about 50,000 to about 4,000,000, more preferably from about 100,000 to about 3,000,000, most preferably from about 500,000 to about 2,000,000.
In addition cationic and nonionic resins may be utilised as detailed below. Polycationic hair conditioning polymer resins suitable for use herein are described below. For convenience in describing the polymers hereof, monomeric units present in the polymers may be referred to as the monomers from which they can be derived. The cationic monomers can be derived from polymerizable cationic starting monomers, or from polymerizable nonionic monomers which are modified subsequent to polymerization to be of cationic character.
These 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 quaternizing agent (eg. ethyl monochloroacetate, diemethyl sulfate, etc.). Preferred cationic monomers include dimethylaminoethyl methacrylate, quaternized dimethylaminoethyl methacrylate, diallyldimethyl ammonium chloride, vinylimidazolium quaternary ammonium monomers and mixtures thereof.
Respresentative examples of nonionic monomers are acrylic or methacrylic acid esters of C 1-C24 alcohols, such as methanol, ethanol, 1- propanol, 2-proρanol, 1-butanol, 2-methyl-l -propanol, 1-pentanol, 2- pentanol, 3-pentanol, 2-methyl- l-butanol, 1 -methyl- 1-butanol, 3-methyl-l- butanol, 1 -methyl- 1 -pentanol, 2-methyl-l -pentanol, 3-methyl-l -pentanol, t-butaonl, cyclohexanol, 2-ethyl-l -butanol, 3-heptanol, benzyl alcohol, 2- octanol, 6-methyl-l-heptanol, 2-ethyl-l -hexanol, 3,5-dimethyl-l-hexanol, 3,5,5-trimethyl-l-hexanol, 1-decanol, 1-dodecanol, 1-hexadecanol, 1- octadecanol, and the like, the alcohols having from about 1-24 preferably from about 4-18, more preferably from about 4-12 carbon atoms; styrene; chlorostyrene; vinyl estes such as vinyl acetate; vinyl chloride; vinylidene chloride; acrylonitrile; alpha-methylstyrene; t-butylstyrene; butadiene; cyclohexadiene; ethylene; propylene; vinyl toluene; alkoxyalkyl (meth)acrylate, such as methoxy ethyl (meth)acrylate and butoxytheyl (meth)acrylate; and mixtures thereof. Other nonionic monomers include acrylate and methacrylate derivatives such as allyl acrylate and methacrylate, cyclohexyl acrylate and methacrylate, oleyl acrylate and methacrylate, benzyl acrylate and methacylate, tetrahydrofurfuryl acrylate and methacrylate, ethylene glycol di-acrylate and -methacrylate, 1,3- butyleneglycol di-acrylate and -methacrylate, diacetonacylamide, isobornyl (meth)acrylate, and the like.
Preferred nonionic monomers include n-butyl methacrylate, isobutyl methacrylate, 2-ethylhexyl methacrylate, methyl methacrylate, t- butylacrylate, t-butylmethacrylate, and mixtures thereof.
Representative polar nonionic monomers include acrylamide, N,N- dimethylacrylamide, methacrylamide, N-t-butyl acylamide, methacrylonitrile, acrylamide, acrylate alcohols (eg. C2-C6 acrylate alcohols such as hydroxyethyl acrylate, hydroxyproxyl acrylate), hydroxyethyl methacrylate, hydroxpropyl methacrylate, vinyl pyrrolidone, vinyl ethers, such as methyl vinyl ether, acyl lactones and vinyl pyridine, allyl alcohols, vinyl alcohols and vinyl caprolactam.
Preferred polycationic polymer resins for use herein include cationic guar gum, cationic polysaccharides, homopolymers of dimethyldiallyl ammonium chloride, copolymers of dimethyldiallyl ammonium chloride and acrylamide, cationic amino-functional homopolymers and copolymers derived from acrylic acid and/or methacrylic acid, especially from alkylaminoalkyl acrylate and methacrylate monomers such as dimethylacmonoethyl acrylate and methacrylate, polyalkylene imines and ethoxy polyalkylene imines, vinylimidazolium vinylpyrrolidone quaternary ammonium copolymers, and mixtures thereof.
The auxilliary hair fixative polymer is incorporated with the Polyquaternium 4 at levels of from about 0.01% to about 10%, preferably from about 0.15 to about 5% by weight. The combination of Polyquat 4 and auxilliary hair fixative polymer is valuable for providing overall hair feel benefits, particularity with respect to flakiness.
The present compositions can be formulated as leave-in hair cosmetic compositions such as gels or creams. Methods of making the hair cosmetic compositions of the present invention are described more specifically in the examples.
The hair cosmetic compositions of the present invention may contain a chelating agent at a level of from about 0.01% to about 5%, preferably from about 0.5% to about 3%, more preferably from about 0.08% to about 1% by weight. Chelating agents suitable for the compositions according to the present invention include salts of ethylenediamine tetraacetic acid including ethylenediamine tetraacetic acid, disodium ethylenediamine tetraacetic acid and pentasodium pentatate. The preferred chelating agent for use in compositions according to the present invention is tetrasodium ethylenediamine tetraacetic acid.
The hair cosmetic compositions of the present invention can also contain a variety of non-essential, optional components such as preservatives, surfactants, block polymers, thickeners and viscosity modifiers, electrolytes, fatty alcohols, pH adjusting agents, perfume oils; UV screening agents; hair conditioning agents, Pearlescants, emollients; lubricants and penetrants such as various lanolin components; protein hydrolysates and other protein derivatives; ethylene adducts and polv oxyethylene cholesterol; volatile and non-volatile silicone fluids. Such conventional optional ingredients are well known to a person skilled in the art, e.g. surfactants used as perfume solubilizing agents such as anionics (e.g., sodium alkyl sulphates, nonionics (a ine oxides); amphoterics (aliphatic secondary or tertiary amine derivatives) zwitterionics (aliphatic quaternary ammonium; phosphonium or sulphonium derivatives) and fluorinated surfactants (e.g. Zonyl FSK) (RTM), preferred surfactants for use herein being nonionics such as polyethylene glycol fatty acid esters, isosteareth-20, polysorbate-20, PPG- 12-PEG-65 lanolin oil, PEG-40 hydrogenated caster oil, polysorbate 80, Oleth-20 and Nonoxynol- 10, thickeners and viscosity modifiers such as diethanolamides of long chain fatty acids, sodium chloride, sodium sulphate, and ethyl alcohol; block polymers of ethylene oxide and propylene oxide such as Pluronic (RTM) F88 offered by BASF Wyandotte; preservatives such as DMDM hydantoin, methyl paraben, propyl paraben and diaxolidinyl urea; fatty alcohols such as cetearyl alcohol; electrolyte such as earth and alkaline-earth metal salts; quaternary ammonium ions and cationic amines and halogen ions; pH adjusting agents such as citric acid, succinic acid, sodium hydroxide and triethanolamine; perfume oils such as Florasynth (RTM) perfumes ; hair conditioning agents such as panthenol/pantyl B and pearlescing agents such as ethylene glycol distearate and mica and UV screening agents such as benzophenone-4 and benzophenone-10. Each of these optional materials can be present at a level of from about 0.01% to about 5%, preferably from about 0.05% to about 3%, most preferably from about 0.08% to about 1%, by weight of composition.
The hair cosmetic compositions of the present invention are used in conventional ways to provide the hair styling/holding benefits of the present invention in combination with reduced on-hair and on-hand tack. Such methods can involve applying an effective amount of the product to dry or damp hair before or after the hair is styled, or both. By "effective amount" is meant an amount sufficient to provide the hair volume and style benefits desired considering the length and texture of the hair. The hair cosmetic compositions according to the present invention may be effectively applied to the hair using the hands, using a comb or brush or by applying with a sponge or 'wipe'. The invention is illustrated by the following non-limiting examples.
Gelling agent Stablileze 06 (RTM) Neutralising agent Triethanolamine (TEA) Hair fixative polymer A - Polyquaternium 4 (RTM) Hair fixative polymer B - PVP VA Chelating agent tetra sodium ethylenediamine tetracetic acid
EDTA (Na)4
Examples I II ill
Stabileze 06 0.6 0.4 0.3
Carbomer 980/201 - 0.2
TEA 0.6 0.6 0.3
Polyquat 4 1.0 0.5 1.0
PVP/VA - 0.5 0.5
EDTA (Na)4 0.1 0.1 0.1
Ethanol - - 10.0
Water To balance To balance To balai
The hair cosmetic formulations are prepared by (a) dispersing the gelling agent(s) into water, allowing sufficient time for hydration of the gelling agent (30 minutes to 1 hour), then partially neutralising the gelling agent with a suitable base and (b) in a separate step, solubilising the fixative polymer(s) in water along with any non-essential optional ingredients and the chelating agent. The premixes (a) and (b) are combined and the resulting mixture is modified to the desired viscosity and pH characteristics using the remainder of the neutralising base.
The above compositions provide effective style retention, deliver a hair conditioning effect with low on-hand and on-hair tack.

Claims

1. A hair cosmetic composition comprising:-
(a) from about 0.01% to about 3% by weight of gelling agent comprising a copolymer of methyl vinyl ether/maleic anhydride, crosslinked with C4-C16 alkadiene or hydrolysis products thereof:
(b) from about 0.1% to about 10% by weight of hair fixative polymer comprising a cationic copolymer of nonionic cellulose and diallyl dimethyl ammonium chloride; and
(c) the balance comprising a carrier suitable for application to hair.
2. A hair cosmetic composition according to Claim 1 wherein the viscosity of the gelling agent at 25°C is in the region of from about 70,000 cps to about 100,000 cps (measured as 0.5% gelling agent in non-alcholic solution at pH7; Brookfield RVT, Spindle TE, lOrpm).
3. A hair cosmetic composition according to Claims 1 or 2 wherein the level of gelling agent is from 0.05% to about 2%, preferably from about 0.5% to about 1.5%, more preferably from about 0.6% to about 1.0% by weight.
4. A hair cosmetic composition according to any of Claims 1 to 3 wherein the gelling agent is neutralized to a level of from about 30% to about 95%, preferably from about 40% to about 80%, more preferably from about 50% to about 60% with base.
5. A hair cosmetic composition according to Claim 4 wherein the base is selected from alkali metal, alkaline earth metal and ammonium hydroxides, amines and amino alcohols and mixtures thereof and in particular is selected from triethanolamine, sodium hydroxide and mixtures thereof.
6. A hair cosmetic composition according to any of Claims 1 to 5 wherein the weight average molecular weight of the cationic copolymer is in the range of from about 1,000 to about 5,000,000.
7. A hair cosmetic composition according to any of Claims 1 to 6 wherein the cationic copolymer comprises a copolymer of hydroxy ethyl cellulose and diallyldimethyl ammonium chloride.
8. A hair cosmetic composition according to any of Claims 1 to 7 wherein the hair fixative polymer is present at a level of from about 0.5% to about 8%, preferably from about 0.8% to about 6%, more preferably from about 1% to about 3% by weight.
9. A hair cosmetic composition according to any of Claims 1 to 8 wherein the weight ratio of gelling agent: hair fixative polymer(s) is in the range of from about 10:1 to about 1 :10.
10. A hair cosmetic composition according to any of Claims 1 to 9 wherein the carrier system comprises water and optionally organic solvent selected from C i-C^ alkanols, diols, polyols, carbitols, acetone and mixtures thereof.
1 1. A hair cosmetic composition according to any of Claims 1 to 10 wherein the gelling agent copolymer crosslinking agent is an alkadiene selected from C4-C16 alkadienes, preferably C6-C14 alkadienes, more preferably C6-C12 alkadienes, most preferably a Cg-Cio alkadiene such as 1 ,9-decadiene.
12. A hair cosmetic composition according to any of Claims 1 to 11 wherein the gelling agent is a copolymer of methyl vinyl ether/maleic anhydride crosslinked with 1,9-decadiene.
PCT/US1995/008336 1994-07-29 1995-06-30 Hair cosmetic compositions WO1996003967A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
MX9700667A MX9700667A (en) 1994-07-29 1995-06-30 Hair cosmetic compositions.
CA002192799A CA2192799A1 (en) 1994-07-29 1995-06-30 Hair cosmetic compositions
US08/776,453 US5922312A (en) 1994-07-29 1995-06-30 Hair cosmetic compositions
EP95925443A EP0768864A4 (en) 1994-07-29 1995-06-30 Hair cosmetic compositions
JP8506495A JPH10503514A (en) 1994-07-29 1995-06-30 Hair cosmetic composition

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB9415324.4 1994-07-29
GB9415324A GB9415324D0 (en) 1994-07-29 1994-07-29 Hair cosmetic compositions

Publications (1)

Publication Number Publication Date
WO1996003967A1 true WO1996003967A1 (en) 1996-02-15

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EP (1) EP0768864A4 (en)
JP (1) JPH10503514A (en)
CN (1) CN1086936C (en)
CA (1) CA2192799A1 (en)
GB (1) GB9415324D0 (en)
MX (1) MX9700667A (en)
WO (1) WO1996003967A1 (en)

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5714135A (en) * 1996-03-18 1998-02-03 Chesebrough-Pond' S Usa Co., Division Of Conopco, Inc. Hair treatment compostion
FR2755607A1 (en) * 1996-11-08 1998-05-15 Oreal COSMETIC COMPOSITION BASED ON FIXING POLYMER AND GELIFYING AGENT, METHOD AND USE
WO1999053890A1 (en) * 1998-04-22 1999-10-28 Amway Corporation Conditioning shampoo
WO2000048555A2 (en) * 1999-02-19 2000-08-24 The Procter & Gamble Company Leave-on cosmetic compositions containing a cationic polymer
FR2833487A1 (en) * 2001-12-18 2003-06-20 Oreal Cosmetic composition for treating keratinic materials comprises two polymers that have complementary non-photoactivatable functional groups
WO2003053379A1 (en) * 2001-12-18 2003-07-03 L'oreal Cosmetic composition forming an adhesive film comprising a polymer with silicone-free skeleton including reactive functions
EP2319491A1 (en) * 2009-06-29 2011-05-11 L'oreal S.A. Refreshing cream foundation in gel form
EP2319487A1 (en) * 2009-06-29 2011-05-11 L'oreal S.A. Refreshing cream foundation in gel form
US8475816B2 (en) 2008-12-16 2013-07-02 L'oreal S.A. Emulsion lipstick composition
US8551461B2 (en) 2008-12-09 2013-10-08 L'oreal Moisturizing and shine-imparting emulsion lip compositions
US8597626B2 (en) 2009-06-29 2013-12-03 L'oreal Long wear, waterproof mascara composition with water washability
US8597621B2 (en) 2008-12-16 2013-12-03 L'oreal Shine-imparting hydrating and moisturizing emulsion lipstick composition
US8647611B2 (en) 2009-06-29 2014-02-11 L'oréal Composition containing a polyol and a reaction product
US8652451B2 (en) 2009-06-29 2014-02-18 L'oreal Composition comprising a sugar silicone surfactant and a oil-soluble polar modified polymer
US8663609B2 (en) 2009-06-29 2014-03-04 L'oreal Composition comprising a polyol, a sugar silicone surfactant and a oil-soluble polar modified polymer
US8663667B2 (en) 2009-06-29 2014-03-04 L'oreal Refreshing cream foundation in gel form
US8747868B2 (en) 2010-12-30 2014-06-10 L'oreal Reaction product of a polar modified polymer and an alkoxysilane and a composition containing the reaction product
US8778316B2 (en) 2008-12-11 2014-07-15 L'oreal Non-sticky, hydrating and moisturizing aqueous lip gloss composition
US8828366B2 (en) 2009-06-29 2014-09-09 L'oreal Hydrating cream foundation in emulsion form
US8932566B2 (en) 2009-06-29 2015-01-13 L'oreal Composition comprising a polyol and a oil-soluble polar modified polymer
US9023387B2 (en) 2008-12-09 2015-05-05 L'oreal Transfer-resistant emulsion containing a surfactant
US9040593B2 (en) 2008-12-16 2015-05-26 L'oreal Water-insoluble reaction product of a polyamine and an oil-soluble high carbon polar modified polymer
US9308396B2 (en) 2008-12-16 2016-04-12 L'oreal Transfer-resistant and long wear foundation in emulsion form containing oil absorbing powders

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011008532A2 (en) * 2009-06-29 2011-01-20 L'oreal S.A. Composition comprising a polar modified polymer
JP6879904B2 (en) * 2014-09-03 2021-06-02 ユニリーバー・ナームローゼ・ベンノートシヤープ Transparent, cosmetic and personal care compositions

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5066481A (en) * 1990-11-05 1991-11-19 Isp Investments Inc. Mousse hair composition
US5118498A (en) * 1990-11-19 1992-06-02 Isp Investments Inc. Hair setting shampoo composition
US5194260A (en) * 1990-08-23 1993-03-16 L'oreal Cosmetic composition for the hair contains a film forming polymer and a silicone incorporated in a wax microdispersion and a cosmetic treatment using the same

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LU83349A1 (en) * 1981-05-08 1983-03-24 Oreal AEROSOL FOAM COMPOSITION BASED ON CATIONIC POLYMER AND ANIONIC POLYMER
US5085856A (en) * 1990-07-25 1992-02-04 Elizabeth Arden Co., Division Of Conopco, Inc. Cosmetic water-in-oil emulsion lipstick comprising a phospholipid and glycerol fatty acid esters emulsifying system
US5254636A (en) * 1992-05-28 1993-10-19 Isp Investments Inc. Rapid hydrolysis of crosslinked maleic anhydride/lower alkyl vinyl ether copolymers
DE4232944A1 (en) * 1992-10-01 1994-04-07 Wella Ag Hair treatment products and methods for use
FR2702958B1 (en) * 1993-03-24 1995-05-24 Oreal Cosmetic composition containing at least one nonionic surfactant of the alkylpolyglycoside and / or polyglycerolated type and at least one crosslinked copolymer of maleic anhydride / alkyl (C1-C5) vinyl ether.

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5194260A (en) * 1990-08-23 1993-03-16 L'oreal Cosmetic composition for the hair contains a film forming polymer and a silicone incorporated in a wax microdispersion and a cosmetic treatment using the same
US5066481A (en) * 1990-11-05 1991-11-19 Isp Investments Inc. Mousse hair composition
US5118498A (en) * 1990-11-19 1992-06-02 Isp Investments Inc. Hair setting shampoo composition

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP0768864A4 *

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5714135A (en) * 1996-03-18 1998-02-03 Chesebrough-Pond' S Usa Co., Division Of Conopco, Inc. Hair treatment compostion
FR2755607A1 (en) * 1996-11-08 1998-05-15 Oreal COSMETIC COMPOSITION BASED ON FIXING POLYMER AND GELIFYING AGENT, METHOD AND USE
WO1998020846A1 (en) * 1996-11-08 1998-05-22 L'oreal Cosmetic composition with fixing polymer and gelling agent base, method and use
WO1999053890A1 (en) * 1998-04-22 1999-10-28 Amway Corporation Conditioning shampoo
WO2000048555A2 (en) * 1999-02-19 2000-08-24 The Procter & Gamble Company Leave-on cosmetic compositions containing a cationic polymer
WO2000048555A3 (en) * 1999-02-19 2001-01-11 Procter & Gamble Leave-on cosmetic compositions containing a cationic polymer
AU771906B2 (en) * 1999-02-19 2004-04-08 Procter & Gamble Company, The Cosmetic compositions
FR2833487A1 (en) * 2001-12-18 2003-06-20 Oreal Cosmetic composition for treating keratinic materials comprises two polymers that have complementary non-photoactivatable functional groups
EP1321126A1 (en) * 2001-12-18 2003-06-25 L'Oreal Cosmetic compositions comprising polymers having complementary chemical functions
WO2003053379A1 (en) * 2001-12-18 2003-07-03 L'oreal Cosmetic composition forming an adhesive film comprising a polymer with silicone-free skeleton including reactive functions
US8551461B2 (en) 2008-12-09 2013-10-08 L'oreal Moisturizing and shine-imparting emulsion lip compositions
US9023387B2 (en) 2008-12-09 2015-05-05 L'oreal Transfer-resistant emulsion containing a surfactant
US8778316B2 (en) 2008-12-11 2014-07-15 L'oreal Non-sticky, hydrating and moisturizing aqueous lip gloss composition
US8597621B2 (en) 2008-12-16 2013-12-03 L'oreal Shine-imparting hydrating and moisturizing emulsion lipstick composition
US8475816B2 (en) 2008-12-16 2013-07-02 L'oreal S.A. Emulsion lipstick composition
US9308396B2 (en) 2008-12-16 2016-04-12 L'oreal Transfer-resistant and long wear foundation in emulsion form containing oil absorbing powders
US9040593B2 (en) 2008-12-16 2015-05-26 L'oreal Water-insoluble reaction product of a polyamine and an oil-soluble high carbon polar modified polymer
US8562961B2 (en) 2009-06-29 2013-10-22 L'oreal Refreshing cream foundation in gel form
US8647611B2 (en) 2009-06-29 2014-02-11 L'oréal Composition containing a polyol and a reaction product
US8652451B2 (en) 2009-06-29 2014-02-18 L'oreal Composition comprising a sugar silicone surfactant and a oil-soluble polar modified polymer
US8663609B2 (en) 2009-06-29 2014-03-04 L'oreal Composition comprising a polyol, a sugar silicone surfactant and a oil-soluble polar modified polymer
US8663667B2 (en) 2009-06-29 2014-03-04 L'oreal Refreshing cream foundation in gel form
US8597626B2 (en) 2009-06-29 2013-12-03 L'oreal Long wear, waterproof mascara composition with water washability
US8828366B2 (en) 2009-06-29 2014-09-09 L'oreal Hydrating cream foundation in emulsion form
US8932566B2 (en) 2009-06-29 2015-01-13 L'oreal Composition comprising a polyol and a oil-soluble polar modified polymer
EP2319487A1 (en) * 2009-06-29 2011-05-11 L'oreal S.A. Refreshing cream foundation in gel form
EP2319491A1 (en) * 2009-06-29 2011-05-11 L'oreal S.A. Refreshing cream foundation in gel form
US8540973B2 (en) 2009-06-29 2013-09-24 L'oréal Refreshing cream foundation in gel form
US8747868B2 (en) 2010-12-30 2014-06-10 L'oreal Reaction product of a polar modified polymer and an alkoxysilane and a composition containing the reaction product
US8846062B2 (en) 2010-12-30 2014-09-30 L'oreal Reaction product of a polar modified polymer and an alkoxysilane and a composition containing the reaction product

Also Published As

Publication number Publication date
CA2192799A1 (en) 1996-02-15
CN1086936C (en) 2002-07-03
MX9700667A (en) 1997-04-30
EP0768864A1 (en) 1997-04-23
EP0768864A4 (en) 1997-08-20
JPH10503514A (en) 1998-03-31
CN1154651A (en) 1997-07-16
GB9415324D0 (en) 1994-09-21

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