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WO2006042588A1 - Produit de coiffure moussant ou pulverisable, contenant des esters de silicones polyalcoxyles - Google Patents

Produit de coiffure moussant ou pulverisable, contenant des esters de silicones polyalcoxyles Download PDF

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Publication number
WO2006042588A1
WO2006042588A1 PCT/EP2005/009639 EP2005009639W WO2006042588A1 WO 2006042588 A1 WO2006042588 A1 WO 2006042588A1 EP 2005009639 W EP2005009639 W EP 2005009639W WO 2006042588 A1 WO2006042588 A1 WO 2006042588A1
Authority
WO
WIPO (PCT)
Prior art keywords
copolymers
hair
acid
product according
esters
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/EP2005/009639
Other languages
German (de)
English (en)
Inventor
Monika Mönks
Jan Baumeister
Sarah Maillefer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Procter and Gamble Deutschland GmbH
Procter and Gamble Co
Original Assignee
Wella GmbH
Procter and Gamble Co
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 Wella GmbH, Procter and Gamble Co filed Critical Wella GmbH
Priority to CA002587086A priority Critical patent/CA2587086A1/fr
Priority to JP2007536010A priority patent/JP2008515934A/ja
Priority to BRPI0516599-7A priority patent/BRPI0516599A/pt
Priority to EP05783363A priority patent/EP1799182A1/fr
Priority to MX2007004557A priority patent/MX2007004557A/es
Priority to AU2005297520A priority patent/AU2005297520A1/en
Publication of WO2006042588A1 publication Critical patent/WO2006042588A1/fr
Priority to US11/731,990 priority patent/US20080178899A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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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
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89—Polysiloxanes
    • A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
    • A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/731—Cellulose; Quaternized cellulose derivatives
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73—Polysaccharides
    • A61K8/732—Starch; Amylose; Amylopectin; Derivatives thereof
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8164—Compositions 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)
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions 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 single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • 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
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/817—Compositions 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 single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
    • A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
    • 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
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/927—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of insects, e.g. shellac
    • 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
    • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring

Definitions

  • Hair waxes are known products for hair treatment. They are used in particular to bring short to medium-long hair trend-oriented in shape and give the hairstyle hold, stand and consolidation and shine. Hair growth can also create contours and texture in the hairstyle. The hair retains a characteristic haptic, a typical "wax grip" and, due to the persistence of residual tackiness, a restyle-possibility results as a typical hair waxing property.
  • Conventional hair waxes have a waxy solid consistency and are usually offered in crucibles. The application is based on the following principle of action: The removal of the product mass is done with the fingers. The wax, which is solid at room temperature, is distributed in the palms of the hands and melted or at least strongly softened by hand warming and shearing.
  • the zeit ⁇ Liche course in particular the onset, the strength and the duration of the bonding phase, during which the optimal Stylingmög ⁇ opportunities are given in conventional products such as hair waxes, wax foams, spray waxing or styling foams not completely satisfactory.
  • the task was to develop a product, which on the one hand has typical product performances of a solid hair wax, eg the hairstyle improved hold and stand and gives a typical wax grip and the hair wax specific Restyle-possibility allows as well as gives the hair a natural, semi-gloss and which on the other hand has a good adhesive phase, easily distributed and well incorporated into the hair, ensures a simple and clean handling and an innovative, the user positive associations , has a pleasant feel during incorporation and is easy to wash out.
  • a product which on the one hand has typical product performances of a solid hair wax, eg the hairstyle improved hold and stand and gives a typical wax grip and the hair wax specific Restyle-possibility allows as well as gives the hair a natural, semi-gloss and which on the other hand has a good adhesive phase, easily distributed and well incorporated into the hair, ensures a simple and clean handling and an innovative, the user positive associations , has a pleasant feel during incorporation and is easy to wash out.
  • the invention relates to hairstyling products containing a foamable or sprayable, gelatinous emulsion containing
  • Gel-shaped compositions are usually distinguished from liquids in that they have elastic properties, ie the elastic portion of the storage modulus (elastic modulus) G 'exceeds the value of the loss modulus G 1 '.
  • G ' is greater than G 11 in at least one partial range (eg at 20 Hz), preferably in the entire range of normal measurement frequencies such as 0.01 to 40 Hz, measurable eg with a Bohlin CS System rheometer.
  • Polyalkoxylated polydimethylsiloxanes have one or more terminal or lateral polyalkylene oxide groups, preferably polyethylene oxide (polyethylene glycol) and / or polypropylene oxide (polypropylene glycol).
  • the degree of alkoxylation is preferably 2 to 40, in particular 5 to 30, 7 to 20 or 10 to 15.
  • the polyalkoxylated polydimethylsiloxanes are preferably esterified with organic carboxylic acids, in particular with fatty acids.
  • the fatty acids are preferably monocarboxylic acids, dicarboxylic acids or hydroxycarboxylic acids having at least 8, preferably 10 to 32 C atoms. Particular preference is given to fatty acids from natural waxes, for example fatty acids from beeswax or candelilla wax.
  • PEG-7 undecylenates Particular preference is given to fatty acid esters of bis (polyethylene oxide) polydimethylsiloxanes.
  • Natural-based polymers in particular polysaccharides and their derivatives, e.g. Sclerotium gum, starch,
  • Anionic surfactants may e.g. be selected from alkali metal or alkaline earth metal salts of ClO to C18 alkyl sulfates, the ClO to C18 alkyl sulfonates, the ClO to C18 Alkylbenzolsulfona- te, the ClO to C18 xylene sulfonates and with 1 to 10
  • R i _ ⁇ M (R 2 ) ⁇ -CH 2 -R 3 -Z (“ 'where R 1 is a linear or branched alkyl, alkenyl or hydroxyalkyl group having 8 to 18 C atoms and 0 to 10 Ethylene oxide units and 0 to 1 glycerol unit; Y is an N-, P- or S-containing group; R 2 is an alkyl or monohydroxyalkyl group having 1 to 3 C atoms; x is 1 if Y is an S atom and x is 2 if Y is an N or a P atom; R3 is an alkyl or hydroxyalkyl group having 1 to 4 carbon atoms and Z represents a carboxylate, sulfate, phosphonate or phosphate group.
  • Lauryl bis (2-hydroxyethyl) sulfopropyl betaine the carboxyl derivatives of the imidazole, the C8 to C18 alkyl dimethylammonium acetates, the C8 to C18 alkyl-dimethyldimethylcarbonylmethylammonium salts and also the C8 to C18 fatty acid alkylamido betaines, such as, for example, the coconut fatty acid amidopropyl betaine (INCI name: cocamidopropyl betaine) and the N-coconut fatty acid amidoethyl N- [2- (carboxymethoxy) ethyl] glycerol (INCI name: cocoamphocarboxyglycinate).
  • x is a number from 10 to 1000, preferably from 10 to 500, particularly preferably from 20 to 200 and y is a number from 0 to 100, preferably 1 to 50, with the proviso that the compound is at least one
  • R 2 (OC n H 2n ) ra R 3 where R 2 is a divalent group which binds the oxyalkylene unit to the siloxane chain, preferably C p H 2p where p is 2-8, preferably 2-6, more preferably 3 -6; R 3 is a monofunctional end group for the oxyalkylene unit, for example H, OH, C 1 -C 6 -alkyl, aryl, C 1 -C 6 -alkoxy, C 1 -C 6 -acyloxy, preferably OH; n is a number from 2 to 4, preferably 2 or 3, and m is a number of at least one, wherein the sum of m for all oxyalkylene groups is 2 to 40, preferably 10 to 30.
  • PPG-y dimethicone where y is the degree of propoxylation and e.g. Values from 2 to 30, especially the values
  • Bis-PEG-x Dimethicone where x is the degree of ethoxylation and e.g. Values from 2 to 30, in particular the values 4, 12 and 20 may have;
  • Carbon dioxide is preferably contained in an amount of at least 0.5% by weight, more preferably from 0.5 to 5% by weight or from 1 to 4% by weight, based on the total composition. Carbon dioxide is preferably combined with at least 0.5% by weight, more preferably from 0.5 to 10 or from 1 to 5% by weight of at least one further blowing agent, in particular propane, butane, DME and / or fluorinated hydrocarbons (eg 1 , 1-difluoroethane).
  • propane, butane, DME and / or fluorinated hydrocarbons eg 1 , 1-difluoroethane
  • the agent is foamed immediately before use and incorporated as a foam in the hair and can then be rinsed or left without rinsing in the hair.
  • the hair styling product according to the invention is a pump spray product and has a mechanical pump spray device.
  • the composition according to the invention contains at least one hair-setting and / or at least one hair-care polymer.
  • the hair-setting or hair-care polymers are preferably contained in an amount of 0.01 to 20 wt.% Or from 0.05 to 10 wt.%, Particularly preferably from 0.1 to 5 wt.%. They may be anionic polymers, ie polymers with anionic or anionizable groups, cationic polymers, ie polymers with cationic or cationizable groups, zwitterionic polymers, ie polymers with cationic and anionic groups, amphoteric polymers, ie polyols. mers with acidic and basic groups or nonionic polymers.
  • Acid groups include sulfonic acid, phosphoric acid and carboxylic acid groups, of which the carboxylic acid groups are preferred.
  • Suitable acid group-containing monomers are, for example, acrylic acid, methacrylic acid, crotonic acid, maleic acid or maleic anhydride, maleic acid monoesters, in particular the mono-C 1 -C 7 -alkyl esters of maleic acid and also aldehydocarboxylic acids or ketocarboxylic acids.
  • Suitable polymers having acid groups are in particular non-crosslinked or crosslinked with polyfunctional agents homopolymers of acrylic acid or methacrylic acid, copolymers of acrylic acid or methacrylic acid with monomers selected from acrylic or methacrylic acid esters, acrylamides, methacrylamides and vinylpyrrolidone, homopolymers of crotonic acid and copolymers of crotonic acid with monomers selected from vinyl esters, acrylic or methacrylic esters, acrylamides and methacrylamides.
  • a suitable natural polymer is, for example, shellac.
  • Suitable cationic monomers are unsaturated, radically polymerizable compounds which carry at least one cationic group, in particular ammonium-substituted vinyl monomers, for example trialkylmethacryloxyalkylammonium.
  • the alkyl groups of these monomers are preferably lower alkyl groups, for example C 1 - to C 7 -alkyl groups, more preferably C 1 - to C 3 -alkyl groups.
  • Dimethylaminoethyl methacrylate methosulfate copolymer e.g.
  • Gafquat ® 755 N, Gafquat ® 734 quaternary ammonium polymers of methylvinylimidazolium chloride and vinylpyrrolidone (eg
  • Suitable cationic polymers derived from natural polymers are, in particular, cationic derivatives of polysaccharides, for example cationic derivatives of cellulose, starch or guar. Are suitable also chitosan and chitosan derivatives.
  • Cationic polysaccharides have, for example, the general formula
  • GOBN + R a R b R c X-G is an anhydroglucose residue, for example starch or cellulose anhydroglucose;
  • B is a divalent linking group, for example, alkylene, oxyalkylene, polyoxyalkylene or hydroxyalkylene;
  • R a , R b and R c are independently alkyl, aryl, alkylaryl, arylalkyl, alkoxyalkyl or alkoxyaryl each having up to 18 carbon atoms, wherein the total number of carbon atoms in R a , R b and R c is preferably not more than 20 is;
  • X is a common counter anion, for example a halogen, acetate, phosphate, nitrate or alkyl sulfate, preferably a chloride.
  • Cationic celluloses are, for example, those with the INCI names Polyquaternium-10 or Polyquaternium-24.
  • a suitable cationic guar derivative has, for example, the INCI name Guar Hydroxypropyltrimonium Chloride.
  • Particularly preferred cationic substances are chitosan, chitosan salts and chitosan derivatives.
  • the chitosans to be used according to the invention are completely or partially deacetylated chitins.
  • the molecular weight can be distributed over a broad spectrum, for example from 20,000 to about 5 million g / mol, for example from 30,000 to 70,000 g / mol. Preferably, however, the molecular weight is above 100,000 g / mol, more preferably from 200,000 to 700,000 g / mol.
  • the degree of deacetylation is preferably 10 to 99%, more preferably 60 to 99%.
  • a preferred chitosan salt is Chitosoniumpyrrolidoncarboxylat, eg Kytamer ® PC with a molecular weight of about 200,000 to 300,000 g / mol and deacetylation of 70 to 85%.
  • Chito sanderivate are quaternized, alkylated or hydroxyalkylated derivatives, for example hydroxyethyl, hydroxypropyl or hydroxybutyl chitosan into consideration.
  • the chitosans or chitosan derivatives are preferably in neutralized or partially neutralized form.
  • the degree of neutralization is preferably at least 50%, more preferably between 70 and 100%, based on the number of free base groups.
  • all cosmetically acceptable inorganic or organic acids such as, for example, formic acid, can be used as the neutralizing agent.
  • Natural-based preferred cationic polymers cationic cellulose derivatives of hydroxyethyl cellulose and diallyldimethyl ammonium chloride; cationic cellulose derivatives of hydroxyethyl cellulose and trimethyl ammonium substituted epoxy, chitosan and its salts; Hydroxyalkyl chitosans and their salts; Alkylhydroxyalkylchitosans and their
  • Suitable nonionic polymers are homopolymers or copolymers which are composed of at least one of the following monomers: vinylpyrrolidone, vinylcaprolactam, vinyl esters such as vinyl acetate, vinyl alcohol, acrylamide, methacrylamide, alkyl and dialkylacrylamide, alkyl and dialkylmethacrylamide, alkyl acrylate, alkyl methacrylate, propylene glycol or Ethylene glycol, where the alkyl groups of these monomers are preferably C 1 - to C 7 -alkyl groups, particularly preferably C 1 - to C 3 -alkyl groups. Are alkyl groups.
  • homopolymers of vinylcaprolactam, of vinylpyrrolidone or of N-vinylformamide are suitable.
  • suitable synthetic film-forming, nonionic, hair-fixing polymers are, for example, copolymers of vinylpyrrolidone and vinyl acetate, terpolymers of vinylpyrrolidone, vinyl acetate and vinyl propionate, polyacrylamides; Polyvinyl alcohols and polyethylene glycol / polypropylene glycol copolymers.
  • Suitable natural film-forming polymers are, for example, cellulose derivatives, for example hydroxyalkylcellulose.
  • Preferred nonionic polymers are:
  • Composition in the hydrophobic phase of the emulsion at least one additional hydrophobic fat, wax or oil.
  • the additional hydrophobic substances are preferably contained in an amount of from 0.5 to 20% by weight or from 1 to 10% by weight. Particular preference is given to mineral oils, fatty alcohols and fatty acid triglycerides.
  • Suitable fats and waxes or waxy substances have a solidification or dropping point, which is greater than or equal to 25 ° C, preferably in the range of 30 to 100 0 C, in particular in the range of 40 to 90 0 C.
  • Fats and waxy substances are, for example, animal waxes, vegetable waxes, mineral waxes, synthetic waxes, microcrystalline crystalline waxes, macrocrystalline waxes, paraffin waxes, ozokerite, montan waxes, Fischer-Tropsch waxes, polyolefin waxes (eg polyethylene, polybutene and the like), amide waxes, silicone waxes, beeswax, wool wax (lanolin) and its derivatives such as wool wax alcohols (lanolin alcohols ), Candelilla wax, carnauba wax, Japan wax, fats, Fettkla ⁇ esters, fatty acid glycerides, long-chain carboxylic acids or long-chain (ClO to C22) alcohols, each with melting,
  • the additives can be selected, for example, from plant and herb extracts, protein and silk hydrolysates, light stabilizers, antioxidants, radical scavengers, antidandruff active ingredients, gloss generators, vitamins, panthenol, plasticizers, combability improvers, proteins, bactericides, virucides, antimicrobial, proteolytic or keratolytic effective substances, keratin-reducing Substances, oxidizing agents, direct hair dyes, oxidation dye precursors.
  • the preparation takes place as described above.
  • the emulsions are filled with the blowing agents in pressure-resistant packaging with foam head.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Insects & Arthropods (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Zoology (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)

Abstract

L'invention concerne des produits de coiffure contenant une émulsion sous forme de gel, moussante ou pulvérisable. Elle concerne également un dispositif pour faire mousser ou pulvériser l'émulsion. Cette dernière contient des esters de polydiméthylsiloxanes polyalcoxylés, notamment des esters de polydiméthylsiloxanes polyalcoxylés et des acides gras comportant au moins 8 atomes de carbone; des gélifiants ou des épaississants, de préférence du carraghénane; des émulsifiants, de préférence des tensioactifs de silicone alcoxylés et de l'eau. Dans des modes de réalisation préférés, lesdits produits se présentent sous la forme de mousses en aérosol ou de matières pulvérisables au moyen d'une pompe. Ces produits peuvent être utilisés pour les soins et la coiffure des cheveux humains.
PCT/EP2005/009639 2004-10-15 2005-09-08 Produit de coiffure moussant ou pulverisable, contenant des esters de silicones polyalcoxyles Ceased WO2006042588A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA002587086A CA2587086A1 (fr) 2004-10-15 2005-09-08 Produit de coiffure moussant ou pulverisable, contenant des esters de silicones polyalcoxyles
JP2007536010A JP2008515934A (ja) 2004-10-15 2005-09-08 発泡又はスプレー可能なポリアルコキシル化シリコーンエステルを含有するヘアスタイリング製品
BRPI0516599-7A BRPI0516599A (pt) 2004-10-15 2005-09-08 produto para pentear os cabelos, sob a forma de espuma ou aspersão, contendo éster de silicone polialcoxilado
EP05783363A EP1799182A1 (fr) 2004-10-15 2005-09-08 Produit de coiffure moussant ou pulverisable, contenant des esters de silicones polyalcoxyles
MX2007004557A MX2007004557A (es) 2004-10-15 2005-09-08 Producto para el peinado aplicable como espuma o rocio con esteres de silicona polialcoxilados.
AU2005297520A AU2005297520A1 (en) 2004-10-15 2005-09-08 Foamable or sprayable hair styling product comprising polyalkoxylated silicone esters
US11/731,990 US20080178899A1 (en) 2004-10-15 2007-04-02 Foamable or sprayable hair styling product with polyalkoxylated silicone esters

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102004050211.0 2004-10-15
DE200410050211 DE102004050211A1 (de) 2004-10-15 2004-10-15 Verschäum- oder versprühbares Haarstylingprodukt mit polyalkoxylierten Silikonestern

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/731,990 Continuation US20080178899A1 (en) 2004-10-15 2007-04-02 Foamable or sprayable hair styling product with polyalkoxylated silicone esters

Publications (1)

Publication Number Publication Date
WO2006042588A1 true WO2006042588A1 (fr) 2006-04-27

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Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2005/009639 Ceased WO2006042588A1 (fr) 2004-10-15 2005-09-08 Produit de coiffure moussant ou pulverisable, contenant des esters de silicones polyalcoxyles

Country Status (9)

Country Link
EP (1) EP1799182A1 (fr)
JP (1) JP2008515934A (fr)
CN (1) CN101043917A (fr)
AU (1) AU2005297520A1 (fr)
BR (1) BRPI0516599A (fr)
CA (1) CA2587086A1 (fr)
DE (1) DE102004050211A1 (fr)
MX (1) MX2007004557A (fr)
WO (1) WO2006042588A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7670615B2 (en) 2004-12-21 2010-03-02 Stockhausen Gmbh Alcoholic pump foam
US7683018B2 (en) 2003-09-29 2010-03-23 Deb Worldwide Healthcare Inc. High alcohol content gel-like and foaming compositions comprising an anionic phosphate fluorosurfactant
WO2011032728A1 (fr) 2009-09-21 2011-03-24 Cargill, Incorporated Mélanges de carraghénane utilisés comme ingrédients cosmétiques et gels de coiffage des cheveux comprenant lesdits mélanges
US8263098B2 (en) 2005-03-07 2012-09-11 Deb Worldwide Healthcare Inc. High alcohol content foaming compositions with silicone-based surfactants
WO2017107175A1 (fr) * 2015-12-25 2017-06-29 Henkel (China) Investment Co., Ltd. Composition de gel pulvérisable et utilisation de celle-ci

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080059313A1 (en) * 2006-08-30 2008-03-06 Oblong John E Hair care compositions, methods, and articles of commerce that can increase the appearance of thicker and fuller hair
JP5002433B2 (ja) * 2007-11-27 2012-08-15 花王株式会社 毛髪化粧料
JP5797507B2 (ja) * 2011-09-29 2015-10-21 株式会社マンダム 化粧料用組成物
CN103239366B (zh) * 2013-05-03 2015-07-08 肇庆迪彩日化科技有限公司 一种液体整发剂
JP6284895B2 (ja) * 2015-03-20 2018-02-28 富士フイルム株式会社 エアゾル化粧料
CN106806157A (zh) * 2016-11-01 2017-06-09 田鹏新 一种气雾型摩丝及其制作方法
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CN106806253A (zh) * 2016-11-01 2017-06-09 田鹏新 一种定型发胶及其制作方法
CN106758190A (zh) * 2016-12-28 2017-05-31 湖州品创孵化器有限公司 一种用于羊毛纤维拉伸后的定型剂
CN107822904B (zh) * 2017-11-16 2020-06-05 广州旭妆生物科技有限公司 喷雾乳组合物及其制备方法

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US7683018B2 (en) 2003-09-29 2010-03-23 Deb Worldwide Healthcare Inc. High alcohol content gel-like and foaming compositions comprising an anionic phosphate fluorosurfactant
US8569219B2 (en) 2003-09-29 2013-10-29 Deb Worldwide Healthcare Inc. High alcohol content foaming compositions comprising an anionic phosphate fluorosurfactant
US7670615B2 (en) 2004-12-21 2010-03-02 Stockhausen Gmbh Alcoholic pump foam
US8124115B2 (en) 2004-12-21 2012-02-28 Dep Ip Limited Alcoholic pump foam
US8263098B2 (en) 2005-03-07 2012-09-11 Deb Worldwide Healthcare Inc. High alcohol content foaming compositions with silicone-based surfactants
US8309111B2 (en) 2005-03-07 2012-11-13 Deb Worldwide Healthcare Inc. High alcohol content foaming compositions with silicone-based surfactants
US8313758B2 (en) 2005-03-07 2012-11-20 Deb Worldwide Healthcare Inc. Method of producing high alcohol content foaming compositions with silicone-based surfactants
WO2011032728A1 (fr) 2009-09-21 2011-03-24 Cargill, Incorporated Mélanges de carraghénane utilisés comme ingrédients cosmétiques et gels de coiffage des cheveux comprenant lesdits mélanges
WO2017107175A1 (fr) * 2015-12-25 2017-06-29 Henkel (China) Investment Co., Ltd. Composition de gel pulvérisable et utilisation de celle-ci
US10716746B2 (en) 2015-12-25 2020-07-21 Henkel Ag & Co. Kgaa Sprayable gel composition and use thereof

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EP1799182A1 (fr) 2007-06-27
CA2587086A1 (fr) 2006-04-27
DE102004050211A1 (de) 2006-04-20
CN101043917A (zh) 2007-09-26
AU2005297520A1 (en) 2006-04-27
BRPI0516599A (pt) 2008-09-16
JP2008515934A (ja) 2008-05-15

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