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WO2010000361A2 - Produit de fixation et de coiffage volumisant - Google Patents

Produit de fixation et de coiffage volumisant Download PDF

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Publication number
WO2010000361A2
WO2010000361A2 PCT/EP2009/003957 EP2009003957W WO2010000361A2 WO 2010000361 A2 WO2010000361 A2 WO 2010000361A2 EP 2009003957 W EP2009003957 W EP 2009003957W WO 2010000361 A2 WO2010000361 A2 WO 2010000361A2
Authority
WO
WIPO (PCT)
Prior art keywords
preparation
preparation according
polymer
total weight
cationic
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/EP2009/003957
Other languages
German (de)
English (en)
Other versions
WO2010000361A3 (fr
WO2010000361A9 (fr
Inventor
Wiebke Krieger
Viola Sass
Björn HEUER
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.)
Beiersdorf AG
Original Assignee
Beiersdorf AG
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 Beiersdorf AG filed Critical Beiersdorf AG
Priority to EP09772061A priority Critical patent/EP2310096A2/fr
Publication of WO2010000361A2 publication Critical patent/WO2010000361A2/fr
Publication of WO2010000361A3 publication Critical patent/WO2010000361A3/fr
Anticipated expiration legal-status Critical
Publication of WO2010000361A9 publication Critical patent/WO2010000361A9/fr
Ceased legal-status Critical Current

Links

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
    • A61K8/81—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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • A61K8/585—Organosilicon compounds
    • 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
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5422—Polymers characterized by specific structures/properties characterized by the charge nonionic
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54—Polymers characterized by specific structures/properties
    • A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5428—Polymers characterized by specific structures/properties characterized by the charge amphoteric or zwitterionic

Definitions

  • styling agents For temporary shaping and stabilization of the hairstyle, products are used which are known as styling agents. These include hair sprays, mousses, liquid fixatives, gels, waxes and more.
  • the formulations are diverse, the ingredients must be compatible in ethanolic, aqueous-ethanolic or aqueous medium.
  • these hair strengthening agents consist of solutions of film-forming natural or synthetic polymers or polymer combinations. These are nonionic, anionic, cationic or amphoteric polymers. These leave a transparent colorless film on the hair after application. There are a number of requirements placed on these films: they should be clear, glossy, insensitive to moisture, firming, long-lasting, flexible, non-sticky, do not affect the natural feel of the hair and can also easily be washed out with commercially available shampoos. Hairstyles have a special position in the group of styling products. Not only the film properties (hold, flexibility) are in the foreground, but also the care performance on the hair (combability, well-kept grip).
  • a major disadvantage of the holding polymers in hair fixatives are the insufficient care properties: the hair can be combed bad and feels dull, rough and poorly maintained. After drying, the films are then relatively hard, brittle and inflexible.
  • a disadvantage for the consumer are the tactile properties of the film and the formation of residues during combing (film splicing). These trickle on shoulders or clothes and make the user look neglected.
  • BESTATIGUNGSKOPIE ren cationic surfactants or silicones (for example, cyclic polydimethylsiloxanes (cycromethicone), silicone surfactants (polyether-modified siloxanes) of the dimethicone type).
  • silicones for example, cyclic polydimethylsiloxanes (cycromethicone), silicone surfactants (polyether-modified siloxanes) of the dimethicone type).
  • foam stabilizing additives e.g. nonionic surfactants.
  • At least one cationic amphoteric polymer composed of the monomers vinylpyrrolidone, te / t-butyl acrylate, methacrylic acid, dimethylaminopropylmethacrylamide and methacryloylethyldimethylethyl ammonium ethylsulfate, the proportion of methacrylic acid being less than the proportion of dimethylaminopropylmethacrylamide and the polymer having a suitable one Acid is neutralized,
  • the cationic or the amphoteric polymers has an active content of 0.01 to 10 wt .-%, preferably 0.05 to 5 wt .-% based on the total weight of the preparation. It is furthermore advantageous if the cationically amphoteric polymer is a random, linear copolymer of vinylpyrrolidone, tert-butyl acrylate, methacrylic acid, dimethylaminopropylmethacrylamide and methacryloylethyldimethylethylammonium ethyl sulfate neutralized with phosphoric acid to pH 6.0.
  • the one or more nonionic polymers have an active content of 0.01 to 10 wt .-%, preferably 0.1 to 5 wt .-% based on the total weight of the preparation. Further, it is advantageous if the nonionic polymer is a copolymer of vinylpyrrolidone and vinyl acetate. It is furthermore advantageous if the silicone oil (s) has an active content of 0.01 to 5% by weight, preferably 0.05 to 2.5% by weight, based on the total weight of the preparation. It is also advantageous if the silicone oil or oils are selected from linear or cyclic silicones, PEG- and / or PPG-modified silicones.
  • the preparation contains 0 to 95% by weight, preferably 5 to 60% by weight, of ethanol, based on the total weight of the preparation. Further, it is advantageous if the preparation contains 0 to 25 wt .-%, preferably 1 to 15 wt .-% propellant based on the total weight of the preparation. It is also advantageous if the preparation is present as blowing agent-containing mousse, pump foam stabilizer or pump spray for use in the hair. Furthermore, it is advantageous if additionally at least one further anionic, cationic, nonionic or amphoteric film-forming polymer is present in a concentration of 0 to 10% by weight, preferably 1 to 5% by weight, based on the total weight of the preparation.
  • UV filter antioxidants, oils, extracts, proteins and / or protein hydrolysates, pigments and / or perfume is included.
  • the invention also encompasses the use of one of the preparations described for shaping the hairstyle of the human and / or the animal.
  • Inventive styling agents may contain other cosmetic adjuncts having different functions, e.g. Conditioners, preservatives, bactericides, perfumes, emulsifiers, propellants, softening, moisturizing and / or moisturizing substances, fats, oils, waxes, fatty alcohols, fatty acid esters or other usual constituents of a cosmetic or dermatological formulation such as alcohols, polyols, polymers, electrolytes, organic solvents or silicone derivatives.
  • Conditioners preservatives, bactericides, perfumes, emulsifiers, propellants, softening, moisturizing and / or moisturizing substances, fats, oils, waxes, fatty alcohols, fatty acid esters or other usual constituents of a cosmetic or dermatological formulation such as alcohols, polyols, polymers, electrolytes, organic solvents or silicone derivatives.
  • a silicone oil and / or a silicone gum can additionally be used.
  • the agents contain at least one silicone oil and / or a silicone gum.
  • Silicone oils or silicone gums which are suitable according to the invention are, in particular, dialkyl and alkylaryl siloxanes, for example dimethylpolysiloxane and methylphenylpolysiloxane, and also their alkoxylated, quaternized or else anionic derivatives. Preference is given to cyclic and linear polydialkylsiloxanes, their alkoxylated and / or aminated derivatives, dihydroxypolydimethylsiloxanes and polyphenylalkylsiloxanes. Silicone oils cause a wide variety of effects. For example, at the same time they influence the dry and wet combability, the grip of dry and wet hair and the shine.
  • the term "silicone oils" is understood by the person skilled in the art as meaning several structures of silicon-organic compounds.
  • Examples of such products include the following commercial products: Botanisil NU-150M (Botanigenics), Dow Coming 1-1254 Fluid, Dow Corning 2-9023 Fluid, Dow Corning 2-9026 Fluid, Ultrapure Dimethiconol (Ultra Chemical), Unisil SF- R (Universal Preserve), X-21-5,619 (Shin-Etsu Chemical Co.), Abil OSW 5 (Degussa Care Specialties), ACC DL-9430 Emulsion (Taylor Chemical Company, AEC Dimethiconol & Sodium Dodecylbenzenesulfonate (A & E Connock (A) Perfumery & Cosmetics) Ltd.), BC Dimethiconol Emulsion 95 (Basildon Chemical Company, Ltd.), Cosmetic Fluid 1401, Cosmetic Fluid 1403, Cosmetic Fluid 1501, Cosmetic Fluid 1401DC (all aforementioned Chemsil Silicones, Inc.), Dow Corning 1401 Dow Coming 1403 Fluid, Dow Coming 1501 Fluid, Dow Coming 1784 HVF Emul
  • Suitable silicones are, for example, oligomeric polydimethylcyclosiloxanes (INCI name: cyclomethicone), in particular the tetrameric and the pentameric compound, which are available as commercial products DC 245 fluid, DC
  • Hexamethyl disiloxane (INCI name: Hexamethyldisiloxane), z. B. the product sold under the name Abil K 520,
  • Polyphenylmethylsiloxanes (INCI name: phenyl trimethicone), z.
  • anionic silicone oils such as the Dow Corning 1784 product
  • the agent may contain a protein hydrolyzate and / or one of its derivatives.
  • Protein hydrolysates are product mixtures obtained by acid, alkaline or enzymatically catalyzed degradation of proteins (proteins).
  • the term protein hydrolyzates also means total hydrolyzates as well as individual amino acids and their derivatives as well as mixtures of different amino acids.
  • polymers made up of amino acids and amino acid derivatives are understood by the term protein hydrolyzates. The latter include, for example, polyalanine, polyasparagine, polyserine, etc.
  • Further examples of compounds which can be used according to the invention are L-alanyl-L-proline, polyglycine, glycyl-L-glutamine or D / L-methionine-S-methylsulfonium chloride.
  • [beta] -amino acids and their derivatives such as [beta] -alanine, anthranilic acid or hippuric acid can also be used according to the invention.
  • the molecular weight of the protein hydrolysates which can be used according to the invention is between 75, the molecular weight for glycine, and 200,000, preferably the molecular weight is 75 to 50,000 and very particularly preferably 75 to 20,000 daltons.
  • protein hydrolysates of both plant and animal or marine or synthetic origin can be used.
  • Animal protein hydrolysates are, for example, elastin, collagen, keratin, silk and milk protein protein hydrolysates, which may also be present in the form of salts.
  • Such products are sold, for example, under the trade names Dehylan (Cognis), Promois (Interorgana), Collapuron (Cognis), Nutrilan (Cognis), Gelita-Sol (German Gelatine Factories Stoess & Co), Lexein (Inolex), Sericin (Pentapharm) and Kerasol (Croda).
  • vinyl lactams (vinyl pyrrolidone, vinyl caprolactam), vinyl acetate, alkyl (meth) acrylates (methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n-butyl (meth) acrylate, tert-butyl (meth ) acrylate, cyclohexyl (meth) acrylate, etc.), styrene, (meth) acrylamide, alkyl (meth) acrylamides, functionalized alkyl (meth) acrylates (eg hydroxyethyl (meth) acrylate, dimethylaminoethyl (meth) acrylate) , Dimethylaminopropyl (meth) acrylate), functionalized alkyl (meth) acrylamides (dimethylaminopropyl (meth) acrylamide), (meth) acrylic acid, maleic acid,
  • polymers of this type used in hair setting agents are, for example, polymers with INCI Acrylates Copolymer (Luvimer®, Luviflex® Soft from BASF, Balance CR®, Balance 0/55® from National Starch, Avila AC® from Lubrizol), acrylates / Hydroxyesters Acrylates Copolymer (Acudyne® from Rohm & Haas), Acrylates / Octylacrylamide Copolymer (Amphomer® or Resyn XP from National Starch), AMP Acrylates / Allyl Methacrylate Copolymer (Fixate® from Lubrizol), Butyl Ester of PVM / MA Copolymer (Gantrez ® from ISP), ethyl esters of PVM / MA Copoylmer (Gantrez®, Omnrez® or Advantage® from ISP), acrylamides / sodium acryloyldimethyltaurate / acrylic acid polymer (Acudyne SCP
  • Polyurethanes e.g. Polyurethane-1 (Luviset PUR® from BASF), Polyurethane-2 (Avalure UR® from Lubrizol), Polyurethane-6 (Luviset Sl PUR® from BASF), polyesters, e.g. Polyester-5 (Eastman AQ polymers), polyimides, e.g. Polyimide-1 (Aquaflex XL-30® from ISP), and many more.
  • Suitable cationic surfactants are selected from the group of the quaternary ammonium compounds, in particular benzyltrialkylammonium salts or alkyltrimethylammonium salts, for example cetyltrimethylammonium chloride or bromide, alkyldimethylhydroxyethylammonium chlorides or bromides, dialkyldimethylammonium chlorides or bromides, alkylaminoethyltrimethylammonium ether sulfates, hydroxyethyl cetyldimonium phosphates, alkylpyridinium salts, for example Lauryl or cetylpyrimidinium chloride, imidazoline derivatives and compounds having a cationic character, such as amine oxides, for example alkyldimethylamine oxides or alkylaminoethyldimethylamine oxides.
  • benzyltrialkylammonium salts or alkyltrimethylammonium salts for example cetyltrimethyl
  • Suitable cationic polymers are polymers described under the name Polyquaternium, such as quaternized copolymers of vinylimidazole, vinylpyrrolidone and / or vinylcaprolactam (Polyquaternium-16, -44 or -46), quaternized vinylpyrrolidone /
  • Dimethylaminoethyl methacrylate copolymer (Polyquaternium-11), homopolymers and copolymers of dimethyldiallylammonium chloride (Polyquaternium-6, -7 or -22), quaternized cellulose polymers (Polyquaternium-4, -10), copolymers of cationic cellulose and starch (polyquaternium) 4 / hydroxypropyl starch copolymer), quaternized vinylpyrrolidone / dimethylaminopropyl methacrylate / lauryl dimethylaminopropyl methacrylate copolymer (Polyquaternium-55), vinylpyrrolidone / vinylimidazole / methacrylamide / quaternized vinylimidazole (Polyquatemium-68), quaternized vinylcaprolactam / vinylpyrrolidone / dimethylaminopropylmethacrylamide / Methacryloylaminopropyllauryldi
  • Nonionic polymers suitable according to the invention are e.g. Homopolymers of vinylpyrrolidone, e.g. Luviskol K from BASF or homopolymers of N-vinylformamide e.g. PVF from National Starch.
  • polymers are copolymers of vinylpyrrolidone and vinyl acetate, e.g. Luviskol VA types from BASF, terpolymers from vinylpyrrolidone, vinyl acetate and propionate such as e.g. Luviskol VAP from BASF, polyvinylcaprolactam, polyvinylamides and their salts, as well as copolymers of vinylpyrrolidone and dimethylaminoethyl methacrylate, terpolymers of vinylcaprolactam, vinylpyrrolidone and dimethylaminomethacrylate; Polysiloxanes and the like.
  • Suitable nonionic surfactants according to the invention are alcohols, alkanolamides, such as cocamide MEA / DEA / MIPA, amine oxides, such as cocoamidopropylamine oxide, esters which are formed by esterification of carboxylic acids with ethylene oxide, glycerol, sorbitan or other alcohols, ethers, for example ethoxylated / propoxylated alcohols, ethoxylated / propoxylated esters, ethoxylated / propoxylated glycerol esters, ethoxylated / propoxylated cholesterols, ethoxylated / propoxylated triglyceride esters, ethoxylated propoxylated lanolin, ethoxylated / propoxylated polysiloxanes, propoxylated POE ethers and alkyl polyglycosides such as lauryl glucoside, decyl glycoside and cocogly
  • Suitable propellants according to the invention are hydrocarbons such as butane, isobutane and propane, dimethyl ether or fluorohydrocarbons such.
  • Other blowing agents are nitrogen, carbon dioxide, nitrous oxide or compressed air.
  • Polymer 1 random, linear copolymer of vinylpyrrolidone, terf-butyl acrylate, methacrylic acid, dimethylaminopropylmethacrylamide and methacryloylethyldimethylethyl ammonium ethyl sulfate, neutralized with phosphoric acid to pH 6.0.
  • Polymer 1 random, linear copolymer of vinylpyrrolidone, tert-butyl acrylate, methacrylic acid, dimethylaminopropylmethacrylamide and methacryloylethyldimethylethyl ammonium ethyl sulfate, neutralized with phosphoric acid to pH 6.0.
  • Polymer 1 random, linear copolymer of vinylpyrrolidone, terf-butyl acrylate, methacrylic acid, dimethylaminopropylmethacrylamide and methacryloylethyldimethylethyl ammonium ethyl sulfate, neutralized with phosphoric acid to pH 6.0.

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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)
  • Cosmetics (AREA)

Abstract

L'invention concerne une préparation pour le traitement de fibres kératiniques, en particulier un produit de fixation et de coiffage cosmétique, qui contient a) au moins un polymère amphotère cationique constitué des monomères vinylpyrrolidone, tert-butylacrylate, acide méthacrylique, diméthylaminopropylméthacrylamide et méthacryloyléthyldiméthyléthyl ammonium éthylsulfate, la teneur en acide méthacrylique étant inférieure à la teneur en diméthylaminopropylméthacrylamide et le polymère étant neutralisé à l'aide d'un acide approprié, b) au moins un polymère non ionique et c) au moins une huile de silicone.
PCT/EP2009/003957 2008-07-03 2009-06-03 Produit de fixation et de coiffage volumisant Ceased WO2010000361A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP09772061A EP2310096A2 (fr) 2008-07-03 2009-06-03 Produit de fixation et de coiffage volumisant

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102008040102.1 2008-07-03
DE200810040102 DE102008040102A1 (de) 2008-07-03 2008-07-03 Volumengebender Haarfestiger

Publications (3)

Publication Number Publication Date
WO2010000361A2 true WO2010000361A2 (fr) 2010-01-07
WO2010000361A3 WO2010000361A3 (fr) 2010-03-11
WO2010000361A9 WO2010000361A9 (fr) 2011-04-28

Family

ID=41130333

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2009/003957 Ceased WO2010000361A2 (fr) 2008-07-03 2009-06-03 Produit de fixation et de coiffage volumisant

Country Status (4)

Country Link
EP (1) EP2310096A2 (fr)
CN (1) CN101617997A (fr)
DE (1) DE102008040102A1 (fr)
WO (1) WO2010000361A2 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020064252A1 (fr) 2018-09-27 2020-04-02 Beiersdorf Ag Préparation pompable pour la mise en forme des cheveux

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102488629B (zh) * 2011-12-21 2012-11-14 广州好迪集团有限公司 一种发用定型剂及发用定型品
CN106176288A (zh) * 2015-05-27 2016-12-07 株式会社爱茉莉太平洋 增强毛发的蓬松感的毛发或头皮用组合物
EP3275422B1 (fr) 2016-07-26 2019-11-20 Kao Germany GmbH Composition de coiffure aqueuse contenant de grandes quantités de cires et composés graisseux
CN106420402A (zh) * 2016-11-15 2017-02-22 九江天赐高新材料有限公司 一种头发造型组合物
CN107157807A (zh) * 2017-06-08 2017-09-15 广州天赐高新材料股份有限公司 一种毛发定型组合物及其制备方法
DE102018216625A1 (de) * 2018-09-27 2020-04-02 Beiersdorf Ag Kosmetische Zubereitung für die Haare freigesetzt in Aerosolform

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2441029C2 (ru) * 2006-09-15 2012-01-27 Басф Се Амфолитный сополимер на основе кватернизованных азотсодержащих мономеров
DE102008006227A1 (de) * 2008-01-25 2009-07-30 Beiersdorf Ag Haarspray mit besonders hohem Langzeithalt
DE102008012959A1 (de) * 2008-03-06 2009-09-10 Beiersdorf Ag Haarspray mit besonders hohem Langzeithalt
DE202008004924U1 (de) * 2008-03-06 2008-06-26 Beiersdorf Ag Haarspray mit besonders hohem Langzeithalt
DE102008013171A1 (de) * 2008-03-07 2009-09-10 Beiersdorf Ag Volumengebender Haarfestiger mit ampholytischem Copolymer
DE102008001661A1 (de) * 2008-05-08 2009-11-12 Beiersdorf Ag Haarpflegeformulierungen mit kationisch amphoteren Polymeren
EP2116225A1 (fr) * 2008-10-16 2009-11-11 Beiersdorf AG Produit de soin capillaire à rinçage pour l'augmentation du volume de la coiffure

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020064252A1 (fr) 2018-09-27 2020-04-02 Beiersdorf Ag Préparation pompable pour la mise en forme des cheveux

Also Published As

Publication number Publication date
DE102008040102A1 (de) 2010-01-07
WO2010000361A3 (fr) 2010-03-11
WO2010000361A9 (fr) 2011-04-28
EP2310096A2 (fr) 2011-04-20
CN101617997A (zh) 2010-01-06

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