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EP3267972A1 - Produit et procédé de mise en en forme temporaire de fibres kératiniques - Google Patents

Produit et procédé de mise en en forme temporaire de fibres kératiniques

Info

Publication number
EP3267972A1
EP3267972A1 EP15797040.1A EP15797040A EP3267972A1 EP 3267972 A1 EP3267972 A1 EP 3267972A1 EP 15797040 A EP15797040 A EP 15797040A EP 3267972 A1 EP3267972 A1 EP 3267972A1
Authority
EP
European Patent Office
Prior art keywords
copolymer
cosmetic composition
composition according
hair
meth
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
EP15797040.1A
Other languages
German (de)
English (en)
Inventor
Julia Bibiane Lange
Anna PULS
Cyrielle Martinez
Bernd Richters
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.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP3267972A1 publication Critical patent/EP3267972A1/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
    • A61K8/8141—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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; 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
    • A61K8/72—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
    • 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
    • A61K2800/59—Mixtures
    • A61K2800/594—Mixtures of polymers

Definitions

  • the present invention relates to a cosmetic composition for the hair setting or for the temporary reshaping of keratinic fibers, in particular human hair, wherein the composition contains a combination of two anionic acrylate polymers.
  • Hair treatment products which serve a temporary shaping of the hair, an important role.
  • Corresponding temporary deformation agents usually contain synthetic polymers and / or waxes as the setting agent.
  • Means for supporting the temporary shaping keratin braver fibers can be formulated for example as a hair spray, hair wax, hair gel, hair foam.
  • a hair temporary deformation agent hereafter called a styling agent
  • a styling agent The most important property of a hair temporary deformation agent, hereafter called a styling agent, is to treat the treated fibers in the newly modeled form - i. a form imprinted on the hair - to give as strong a hold as possible.
  • the hairstyle hold is essentially determined by the type and amount of setting agents used, but also an influence of the other ingredients of the styling agent may be given.
  • styling agents In addition to a high degree of hold, styling agents must meet a whole range of other requirements. These may be broad in properties on the hair, properties of the particular formulation, e.g. Properties of the foam, the gel or the sprayed aerosol, and properties that affect the handling of the styling agent, are subdivided, with the properties of the hair is of particular importance. Particularly noteworthy are moisture resistance, low tack and a balanced conditioning effect. Furthermore, a styling agent should be universally applicable for all hair types and mild to hair and skin.
  • the polymers In order to meet the different requirements, a variety of synthetic polymers have been developed as setting agents, which are used in styling agents.
  • the polymers can be subdivided into cationic, anionic, nonionic and amphoteric setting polymers.
  • the polymers when applied to hair, the polymers give a polymer film which, on the one hand, gives the hairstyle strong hold but, on the other hand, is sufficiently flexible not to break under stress. If the polymer film is too brittle, it leads to the formation of so-called film plaques, that is, residues that detach during the movement of the hair and give the impression that the user of the corresponding styling agent would have dandruff. Similar problems arise when waxes as a firming agent in the Styling agent find use. If the styling agent is a gel or a paste, the polymers should also have thickening properties.
  • anionic polymers which find use in hair fixation products are crosslinked anionic amphiphilic polymers which contain a (meth) acrylic acid unit and a
  • BALANCE® RTF (INCI: Acrylates / Ceteareth-20 Methacrylate Crosspolymer), the function of which is described in U.S. Pat
  • hydrophobically modified acrylate copolymers (INCI: Acrylates Copolymer (and) Water) are commercially available, which act essentially as a thickening agent.
  • the data sheet Aquastyle ® SH-100 polymer (Ashland Inc.) describes such an acrylate copolymer and its use in combination with carbomers. It describes suitability for crystal clear hair gels, good initial stiffness, moisture resistance and long-term performance.
  • An object of the present invention was to provide further suitable polymer combinations which are distinguished by good film-forming and / or setting properties, have a very high degree of retention, without sacrificing flexibility and good moisture resistance, in particular perspiration and water resistance would and should also be suitable for the production of stable viscous and stable transparent cosmetic compositions.
  • currently available styling agents can be improved to the extent that a good combination of stiffness (Stiffness) and long-term (High Humidity Curl Retention) is not always sufficiently guaranteed. It is therefore an object of the present invention to provide such styling agents, which in addition to the above-mentioned properties, in particular both a good stiffness and a good
  • a cosmetic composition for the temporary transformation of keratinous fibers which contains:
  • Structural units (a1) and (a2) is constructed:
  • R 1 represents a hydrogen atom or a methyl group
  • R 3 is a (C 8 -C 30) -alkyl group
  • M + represents a physiologically compatible cation
  • x is an integer from 5 to 35
  • (B) at least one anionic acrylate copolymer (b), which at least from the following
  • Monomer units is constructed:
  • composition according to one of the preceding points, wherein the anionic acrylate copolymer (b) comprises methacrylic acid as monomer unit (b1) and ethyl acrylate as monomer unit (b2).
  • composition according to one of the preceding points, wherein the anionic acrylate copolymer (a) is one with the INCI name Acrylates / Ceteareth-20 Methacrylate Crosspolymer, in particular BALANCE® RCF (AkzoNobel).
  • composition according to one of the preceding points, wherein the anionic acrylate copolymer (b) is one having the INCI name Acrylates Copolyme (and) Water, in particular AquaStyle SH-100 (Ashland Inc.).
  • composition according to one of the preceding points, wherein the anionic acrylate copolymer (a) is one with the INCI name Acrylates / Ceteareth-Methacrylate Crosspolymer and the anionic acrylate copolymer (b) one with the INCI name Acrylates Copolymer (and) Water. 12. The cosmetic composition of any preceding points, wherein the anionic acrylate copolymer (a) BALANCE ® RCF (AkzoNobel) and the anionic acrylate copolymer (b) Aquastyle ® SH-100 (Ashland Inc.) is.
  • Cosmetic composition according to one of the preceding points which, based on the total weight of the cosmetic composition, contains:
  • Cosmetic composition according to one of the preceding points containing, based on the total weight of the cosmetic composition:
  • Composition further at least one of the acrylate copolymers (a) and (b)
  • Cosmetic composition according to one of the preceding points characterized in that it continues to be based on its total weight
  • Cosmetic composition according to item 16 characterized in that the
  • Composition water in a proportion of 50 and 95 wt .-%, preferably between 60 and 90 wt .-% and in particular between 65 and 85 wt .-%, based on the
  • Composition as a hair gel, hair spray, hair foam or hair wax, in particular as a hair gel is present. 20. Use of a cosmetic composition according to any one of items 1 to 19 for the temporary transformation of keratinous fibers.
  • keratinic fibers according to the invention comprises furs, wool and feathers, but in particular human hair.
  • the essential constituents of the cosmetic composition according to the invention are the crosslinked acrylate copolymer (a) and the anionic acrylate copolymer (b) other than the acrylate copolymer (a).
  • the crosslinked anionic acrylate copolymer (a) is composed at least of the following structural units (a1) and (a2):
  • R 1 represents a hydrogen atom or a methyl group
  • R 3 is a (C 8 -C 30) -alkyl group
  • M + represents a physiologically compatible cation
  • x is an integer from 5 to 35.
  • the crosslinked acrylate copolymer (a) is amphiphilic due to the structural units it contains.
  • amphiphilic the skilled person generally understands the fact that the same molecule hydrophilic structural elements (for example, those of the formula (a1)) and lipophilic
  • Structural elements for example those of the formula (a2)
  • physiologically compatible cations M + for compensating the negative charge of the amphiphilic, anionic polymers are metal cations of the physiologically acceptable metals from groups Ia, Ib, IIa, IIb, IIIb, Via or VIII of the Periodic Table of the Elements, ammonium ions and cationic organic compounds suitable with quaternized nitrogen atom.
  • the latter are formed, for example, by protonation of primary, secondary or tertiary organic amines with an acid, or by permanent quaternization of said organic amines.
  • these cationic organic ammonium compounds are 2-ammonioethanol and 2-trimethylammonioethanol.
  • crosslinked is the linking of polymer chains to one another by covalent chemical bonding to form a network.
  • This covalent linkage of the polymer chains may be effected by means of direct covalent bonding or mediated by a molecular fragment bridging the polymer chains.
  • the Molecule fragment binds to the polymer chains bridged by the molecule fragment, each by means of covalent chemical bonding.
  • the crosslinking of the crosslinked amphiphilic anionic polymers (a) may preferably be accomplished by using at least one crosslinking monomer.
  • the crosslinking monomers from at least one compound of the group formed from polyunsaturated aromatic monomers (such as divinylbenzene, divinylnaphthalene, trivinylbenzene), polyunsaturated alicyclic monomers (such as 1,2,4-trivinylcyclohexane), di-functional esters of phthalic acid (such as diallyl phthalate), polyunsaturated aliphatic monomers (such as dienes, trienes, tetraenes such as isoprene, 1,3-butadiene, 1,5-hexadiene, 1, 5,9-decatriene, 1, 9- Decadiene, 1,5-heptadiene), polyalkenyl ethers (such as triallyl pentaerythritol, diallyl pentaerythrito
  • Polyethylene glycol di (meth) acrylates such as ethylene glycol di (meth) acrylate,
  • the copolymer (a) can be constructed according to the invention from further structural units. In a preferred embodiment, the copolymer (a) is at least 30% by weight,
  • the copolymer (a) is composed only of units (a1), and (a2) and crosslinking units, i. H. it consists of these structural units.
  • the at least one unit (a1) is a (meth) acrylic acid unit and can be a methacrylic acid and / or acrylic acid unit according to the invention.
  • x in the unit (a2) of the crosslinked acrylate copolymer (a) is an integer from 10 to 24, more preferably from 16 to 22, most preferably 20.
  • R 3 in the unit (a2) of the crosslinked acrylate copolymer (a) is a (C 12 -C 20) -alkyl group, more preferably (C 4 -C 20) -alkyl group, likewise preferably (C 1 -C 8 -alkyl).
  • the alkyl group is preferably linear but may also be branched.
  • R 3 is more preferably a combination of linear C 16 and C 18 -alkyl groups, ie stearyl and cetyl groups (INCI:
  • the crosslinked acrylate copolymer (a) is one containing the INCI name Acrylates / Ceteareth-20 Methacrylate Crosspolymer.
  • the crosslinked acrylate copolymer (a) is one available under the trade name BALANCE® RCF (AkzoNobel). The latter is an about 30% by weight dispersion in water.
  • crosslinked acrylate copolymers (a) bear the INCI name Acrylates / Steareth-20 Methacrylate Crosspolymer.
  • the at least one unit (a1) is a (meth) acrylic acid unit and can according to the invention a methacrylic acid and / or
  • Be acrylic acid unit They have 20 units of ethylene oxide and are etherified with stearyl alcohol.
  • Such a polymer is erannetlich example, under the trade name Aculyn ® 88 (Rohm & Haas). This has in the commercially available form a solids content of about 28 to 33 wt .-% and a pH of 3.3 to 4.3.
  • compositions according to the invention contain as the second essential constituent an anionic acrylate copolymer (b).
  • the anionic acrylate copolymer (b) is composed of at least the following monomer units: at least one (meth) acrylic acid unit (b1), at least one (meth) acrylic acid ethyl ester unit (b2) and at least one (meth) acrylic ester unit (b3) derived from the
  • the copolymer (b) can be constructed according to the invention from further monomer units.
  • the copolymer (b) is composed only of the units (b1), (b2) and (b3), i. H. it consists of units derived from these monomer units.
  • the at least one (meth) acrylic acid unit (b1) may be a methacrylic acid or
  • Acrylic acid unit with a methacrylic acid unit is preferred.
  • the at least one (meth) acrylic acid ethyl ester unit (b2) can be a
  • Ethyl acrylate is preferred.
  • the at least one (meth) acrylic ester unit (b3) can according to the invention a
  • the alkyl group of the (meth) acrylic acid alkyl ester unit serves to control the hydrophobicity of the copolymer.
  • the alkyl group is preferably a linear or branched alkyl group having 2 to 30 carbon atoms, more preferably 3 to 12
  • the hydrophobic group according to the invention may also be a hydrophobic other than an alkyl group, for.
  • Acrylate copolymer (b) at a solids content of 2% by weight and neutralized solution at 25 ° C. is preferably at most 60,000 to 120,000 cps.
  • Suitable anionic acrylate copolymers (b) are commercially available under the INCI name Acrylates Copolymer (and) Water. On Rushzugtesten the anionic acrylate copolymer (b) is Aquastyle ® SH-100 polymer from Ashland, Inc. This has in the commercially available form of a solids content of about 28 to 32 wt .-% and a pH of 2.1 to 4 , 0th
  • the cosmetic composition of the present invention contains the acrylate copolymer (a) and acrylate copolymer (b) in suitable and appropriate amounts for styling agents, which can be adapted for specific application and packaging.
  • composition according to the invention may comprise the crosslinked acrylate copolymer (a), for example, in an amount of from 0.1 to 5.0% by weight, based on the total weight of the novel compounds Composition, included. More preferred are proportions of the copolymer (a) from 1, 0 to 4.0 wt .-% and in particular from 1, 5 to 3.0 wt .-%, each expressed as the solids content of active substance in the cosmetic composition.
  • the cosmetic composition of the invention contains the acrylate copolymer (b), based on the total weight of the cosmetic composition, for. B. in an amount of 0.1 to 5.0 wt .-%, preferably 1, 0 to 4.0 wt .-%, further preferably 1, 5 to 3.0 wt .-%, each stated as the solids content active Substance in the cosmetic composition.
  • the cosmetic compositions according to the invention are distinguished, in particular, by improved long-term preservation in comparison to alternative cosmetic agents.
  • a weight ratio of the polymers a) and b) in the cosmetic has proved to be 5: 1 to 1: 5, preferably 3: 1 to 1: 3 and in particular 2: 1 to 1: 2 ,
  • the cosmetic composition contains as the crosslinked anionic acrylate copolymer (a) the copolymer commercially available under the name BALANCE® RCF and as the anionic one
  • Acrylate copolymer (b) the commercially available under the name AquaStyle ® SH-100 copolymer. In this combination were particularly good results in terms of a
  • the acrylate copolymers (a) and (b) are preferably used in the cosmetic composition in partially neutralized or neutralized form.
  • at least one alkanolamine is preferably used.
  • Alkanolamines are preferably selected from primary amines having a C2-C6-Alkylgrund Sciences carrying at least one hydroxyl group. Particularly preferred alkanolamines are selected from the group formed from 2-aminoethane-1-ol (monoethanolamine), tris (2-hydroxyethyl) amine (triethanolamine), 3-aminopropan-1-ol, 4-aminobutane-1 -ol, 5-aminopentan-1-ol, 1-aminopropan-2-ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1-aminopentan-3-ol, 1-aminopentan-4-ol , 3-Amino-2-methylpropan-1-ol, 1-amino-2-methylpropan-2-ol, 3-aminopropane-1, 2-diol, 2-amino-2-methylpropane-1,3-diol.
  • Very particularly preferred alkanolamines according to the invention are selected from the group consisting of 2-aminoethane-1-ol, 2-amino-2-methylpropan-1-ol and 2-amino-2-methyl-propane-1,3-diol.
  • 2-aminoethane-1-ol 2-amino-2-methylpropan-1-ol
  • 2-amino-2-methyl-propane-1,3-diol are selected from the group consisting of 2-aminoethane-1-ol, 2-amino-2-methylpropan-1-ol and 2-amino-2-methyl-propane-1,3-diol.
  • Neutralizing agent has proven to be 2-amino-2-methylpropanol. According to the invention therefore, preferred cosmetic agents contain 2-amino-2-methylpropanol.
  • the 2-amino-2-methylpropanol is preferably used in the compositions according to the invention in an amount which does not exceed the amount needed to neutralize the acrylate copolymers (a) and (b).
  • the amounts of 2-amino-2-methylpropanol used in the compositions according to the invention are preferably from 80 to 100%, particularly preferably from 90 to 100% and in particular from 95 to 100% of the amount required for complete neutralization of the acrylate copolymers (a) and (b).
  • the proportion by weight of 2-amino-2-methylpropanol in the total weight of the cosmetic agent is from 0.05 to 7.0% by weight, preferably from 0.1 to 5.0% by weight and in particular from 0.1 to 3 , 0% by weight.
  • a preferred cosmetic composition for the temporary transformation of keratinic fibers based on their total weight comprises:
  • R 1 represents a hydrogen atom or a methyl group
  • R 3 is a (C 8 -C 30) -alkyl group
  • M + represents a physiologically compatible cation
  • x is an integer from 5 to 35
  • Acrylic ethyl ester unit (b2) is different and has a hydrophobic group as an ester group.
  • the cosmetic composition of the present invention contains one or more further thickening or gelling component (s) other than the acrylate copolymer (a) and (b) and also promoting film formation.
  • s further thickening or gelling component
  • Examples are cationic, anionic, nonionic or amphoteric polymers.
  • the proportion by weight of this further component in the total weight of the cosmetic composition can be comparatively low owing to the presence of components (a) and (b) and amounts, for example, to 0.02 to 3% by weight, preferably 0.05 to 1.5% by weight. %, and more preferably 0.2 to 0.8% by weight.
  • Examples are acrylamide / ammonium acrylate copolymer, acrylamide / DMAPA
  • Methacrylates / Glycol Dimethacrylate Crosspolymer MEA Sulfites, Methacrylic Acid / Sodium
  • Dimethicone / Acrylates Copolymer PEG-8 / SMDI Copolymer, Polyacrylamides, Polyacrylates-6, Polybeta-Alanine / Glutaric Acid Crosspolymer, Polybutylene Terephthalate, Polyester-1,
  • Polyethylacrylate polyethylene terephthalate, polymethacryloyl ethyl betaine, polypentaerythrityl terephthalate, polyperfluoroperhydrophenanthrenes, polyquaternium-1, polyquaternium-2, polyquaternium-4, polyquaternium-5, polyquaternium-6, polyquaternium-7, polyquaternium-8, polyquaternium-9, polyquaternium-10, Polyquaternium-1 1, Polyquaternium-12, Polyquaternium-13, Polyquaternium-14, Polyquaternium-15, Polyquaternium-16, Polyquaternium-17, Polyquaternium-18, Polyquaternium-19, Polyquaternium-20, Polyquaternium-22, Polyquaternium-24,
  • Polyurethane-10 Polyvinyl Acetate, Polyvinyl Butyral, Polyvinyl Caprolactam, Polyvinylformamide, Polyvinyl Imidazolinium Acetate, Polyvinyl Methyl Ether, Potassium Butyl Ester of PVM / MA Copolymer, Potassium Ethyl Ester of PVM / MA Copolymer, PPG-70 Polyglyceryl-10 Ether, PPG 12 / SMDI copolymer, PPG-51 / SMDI copolymer, PPG-10 sorbitol, PVM / MA copolymer, PVP, PVP / VA / itaconic acid copolymer, PVP / VA / vinyl propionate copolymer, Rhizobian gum, Rosin acrylate, Shellac, sodium butyl Ester of PVM / MA Copolymer, Sodium Ethyl Ester of PVM / MA Copolymer, Sodium Polyacrylate, Sterculi
  • nonionic polymers examples are:
  • Cellulose ethers such as hydroxypropylcellulose, hydroxyethylcellulose and Methylhydroxypropylcellulose, as for example sold under the trademarks Culminal and Benecel (AQUALON).
  • siloxanes can be both water-soluble and water-insoluble. Both volatile and nonvolatile siloxanes are suitable, nonvolatile siloxanes being understood as meaning those compounds whose boiling point is above 200 ° C. under normal pressure.
  • Preferred siloxanes are polydialkylsiloxanes, such as, for example, polydimethylsiloxane,
  • Polyalkylarylsiloxane such as polyphenylmethylsiloxane, ethoxylated polydialkylsiloxanes and polydialkylsiloxanes containing amine and / or hydroxyl groups.
  • Carbopol ® which is available in different versions commercially available under the name Carbopol ®: the other acting as a gelling agent component is a homopolyacrylic (Carbomer INCI) is preferred.
  • the carbomer is preferably in an amount of 0.02 to 3% by weight, preferably 0.05 to 1.5% by weight, and more preferably 0.2 to 0.8% by weight, based on the total weight of the cosmetic composition.
  • the film-forming polymers preferably used according to the invention are in particular the
  • Polyvinylpyrrolidone (INCI name: PVP) and the vinylpyrrolidone / vinyl acetate copolymers (INCI name VP / VA copolymer), wherein the weight fraction of these polymers is preferably limited to amounts between 1, 0 and 10 wt .-%.
  • PVP Polyvinylpyrrolidone
  • VP / VA copolymer vinyl acetate copolymers
  • the weight fraction of these polymers is preferably limited to amounts between 1, 0 and 10 wt .-%.
  • Cosmetic compositions according to the invention are therefore characterized in that, based on their total weight, they furthermore contain 1.0 to 10% by weight of polyvinylpyrrolidone and / or vinylpyrrolidone / vinyl acetate copolymer, preferably polyvinylpyrrolidone.
  • Particularly preferred cosmetic compositions have a weight fraction of the polyvinylpyrrolidone and / or vinylpyrrolidone / vinyl acetate copolymer c) in the total weight of the cosmetic composition of from 2.0 to 8.5% by weight, preferably from 3.0 to 7.0% by weight. on.
  • the cosmetic composition according to the invention may contain other conventional substances
  • Styling products included.
  • Other suitable auxiliaries and additives are in particular additional care substances.
  • the agent may contain, for example, at least one 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 hydrolysates also includes total hydrolysates and individual amino acids and their derivatives as well as mixtures of different amino acids understood.
  • 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.
  • the agent according to the invention may further comprise at least one vitamin
  • Provitamin a vitamin precursor and / or derivatives thereof.
  • vitamins, provitamins and vitamin precursors are preferred, which are usually assigned to the groups A, B, C, E, F and H.
  • panthenol increases the flexibility of the polymer film formed using the composition of the present invention.
  • compositions according to the invention may further contain at least one plant extract, but also mono- or oligosaccharides and / or lipids.
  • oil bodies are suitable as a care substance.
  • the natural and synthetic cosmetic oil bodies include, for example, vegetable oils, liquid paraffin oils, isoparaffin oils and synthetic hydrocarbons and di-n-alkyl ethers having a total of between 12 and 36 carbon atoms, in particular 12 to 24 carbon atoms.
  • Preferred cosmetic agents according to the invention contain at least one oil body, preferably at least one oil body from the group of silicone oils.
  • the group of silicone oils includes in particular the dimethicones, to which the cyclomethicones are also to be expected, the amino-functional silicones and the dimethiconols.
  • the dimethicones may be both linear and branched as well as cyclic or cyclic and branched.
  • Suitable silicone oils or silicone gums 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,
  • Ester oils that is esters of 6-C30 fatty acids with C2-C30 fatty alcohols, preferably
  • Isopropyl myristate (IPM Rilanit ®), isononanoic acid C16-18 alkyl ester (Cetiol ® SN), 2-ethylhexyl palmitate (Cegesoft ® 24), stearic acid-2-ethylhexyl ester (Cetiol ® 868), cetyl oleate, glycerol tricaprylate, cocofatty alcohol caprate / caprylate (Cetiol ® LC), n-butyl stearate, oleyl erucate (Cetiol ® J 600), isopropyl palmitate (Rilanit ® IPP), oleyl Oleate (Cetiol ®), hexyl laurate (Cetiol ® A), di-n-butyl adipate (Cetiol ® B), myristyl myristate (Cet
  • dicarboxylic acid esters symmetrical, unsymmetrical or cyclic esters of carbonic acid with fatty alcohols
  • Fatty acid partial glycerides which are understood to mean monoglycerides, diglycerides and their technical mixtures.
  • composition according to the invention emulsifiers or
  • PEG derivatives of hydrogenated castor oil the z. B are available under the name PEG Hydrogenated Castor Oil, e.g. PEG-30 Hydrogenated Castor Oil, PEG-33 Hydrogenated Castor Oil, PEG-35 Hydrogenated Castor Oil, PEG-36
  • PEG-40 Hydrogenated Castor Oil Hydrogenated Castor Oil or PEG-40 Hydrogenated Castor Oil.
  • PEG-40 hydrogenated castor oil are preferably contained in an amount of 0.05 to 1.5% by weight, more preferably 0.1 to 1.0% by weight, and also preferably 0.2 to 0.8% by weight or 0.3 to 0.6% by weight.
  • compositions of the invention contain the ingredients or active ingredients in a cosmetically acceptable carrier.
  • Preferred cosmetically acceptable carriers are aqueous, alcoholic or aqueous-alcoholic media with preferably at least 10% by weight of water, calculated on the total weight of the agent.
  • the cosmetic carrier according to the invention particularly preferably comprises water, in particular in the amount, that the cosmetic agent, calculated on the total weight of the composition, is at least 10% by weight, in particular at least 20.0% by weight, most preferably at least 40% by weight. Contains% water. Very particularly preferred cosmetic agents have a water content of between 50 and 95% by weight, preferably between 60 and 90% by weight and in particular between 65 and 85% by weight, based on their total weight.
  • alcohols it is possible in particular to include the lower alcohols having 1 to 4 carbon atoms usually used for cosmetic purposes, such as, for example, ethanol and isopropanol.
  • water-soluble solvents as cosolvent are glycerol and / or ethylene glycol and / or 1, 2-propylene glycol in an amount of 0 to 30 wt .-% based on the total agent.
  • composition of some preferred cosmetic agents can be found in the following tables (data in% by weight based on the total weight of the cosmetic agent, unless stated otherwise).
  • Formula 6a Formula 7a Formula 8a Formula 9a Formula 10a Copolymer a): 0.1 to 5.0 1.0 to 4.0 1.0 to 4.0 1.5 to 3.0 1.5 to 3.0 acrylates / ceteareth-20
  • Carbomer 0.02 to 3.0 0.05 to 2.0 0.05 to 1.5 0.2 to 1.0 0.4 to 0.8
  • Carbomer 0.02 to 3.0 0.05 to 2.0 0.05 to 1.5, 0.2 to 1.0, 0.4 to 0.8 Water 50 to 95 50 to 95 60 to 90 60 to 90 65 to 85
  • Mise add 100 add 100 add 100 add 100 add 100 add 100 According to the invention, "Mise” is to be understood as a cosmetic carrier, in particular (if not stated separately) water and optionally further customary constituents of styling products.
  • the cosmetic composition of the present invention may be formulated in the forms customary for the temporary shaping of hair, e.g. B. as a hair gel, hair spray hair foam or hair wax. Preference is given to the preparation as a hair gel.
  • Hydrocarbons are used. Propane, propane / butane mixtures and dimethyl ether are particularly suitable blowing agents according to the invention.
  • the present invention also relates to the use of cosmetic compositions according to the invention for the temporary transformation of keratinic fibers, in particular of human hair, as well as a method for the temporary deformation of keratinic fibers, in particular human hair, in which the inventive cosmetic
  • Composition is applied to keratinic fibers.
  • a further subject of this patent application is the use of a cosmetic composition according to the invention for improving the moisture resistance of temporarily deformed keratinic fibers.
  • the moisture resistance was determined by means of an HHCR test (High Humidity Curl Retention Test: 6 h) on cleaned Kerling hair strands (mean value determined on 5 hair strands each):
  • the polymer combination E1 according to the invention therefore showed a clearly superadditive, synergistic effect in terms of moisture resistance.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Abstract

La présente invention concerne une composition cosmétique pour la mise en forme temporaire de cheveux, ladite composition contenant une association de deux copolymères d'acrylate anioniques spécifiques. Ladite composition cosmétique confère une excellente résistance à l'humidité.
EP15797040.1A 2015-03-09 2015-11-11 Produit et procédé de mise en en forme temporaire de fibres kératiniques Ceased EP3267972A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102015204148.4A DE102015204148A1 (de) 2015-03-09 2015-03-09 "Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern"
PCT/EP2015/076330 WO2016142013A1 (fr) 2015-03-09 2015-11-11 Produit et procédé de mise en en forme temporaire de fibres kératiniques

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EP3267972A1 true EP3267972A1 (fr) 2018-01-17

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US (1) US10668003B2 (fr)
EP (1) EP3267972A1 (fr)
DE (1) DE102015204148A1 (fr)
WO (1) WO2016142013A1 (fr)

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GB2568792A (en) * 2017-09-29 2019-05-29 Henkel Ag & Co Kgaa Agent and method for the temporary deformation of keratin-containing fibers

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102015204149A1 (de) * 2015-03-09 2016-09-15 Henkel Ag & Co. Kgaa "Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern"
DE102015204150A1 (de) * 2015-03-09 2016-09-15 Henkel Ag & Co. Kgaa "Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern"
DE102015204146A1 (de) * 2015-03-09 2016-09-15 Henkel Ag & Co. Kgaa "Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern"
DE102016225467A1 (de) * 2016-12-19 2018-06-21 Henkel Ag & Co. Kgaa Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern
DE102016225465A1 (de) * 2016-12-19 2018-06-21 Henkel Ag & Co. Kgaa Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern
DE102016225472A1 (de) * 2016-12-19 2018-06-21 Henkel Ag & Co. Kgaa Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern

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EP0897711B1 (fr) 1997-07-31 2000-10-25 Wella Aktiengesellschaft Produit pour augmenter la façonnage et le brillant des cheveux
DE10109820A1 (de) * 2001-03-01 2002-09-12 Goldwell Gmbh Haarbehandlungsmittel
DE102007008089A1 (de) * 2007-02-13 2008-08-14 Beiersdorf Ag Haarstylinggel mit hohem Langzeithalt
DE102009001978A1 (de) 2009-03-30 2010-10-07 Henkel Ag & Co. Kgaa Mittel für keratinhaltige Fasern, enthaltend mindestens ein spezielles vernetztes amphiphiles, anionisches Polymer und mindestens ein weiteres spezielles unvernetztes amphiphiles, anionisches Polymer
DE102011077364A1 (de) * 2011-06-10 2012-12-13 Henkel Ag & Co. Kgaa Stylingmittel mit höchstem Halt
DE102013225753A1 (de) * 2013-12-12 2014-05-08 Henkel Ag & Co. Kgaa Kosmetisches Mittel
DE102015204150A1 (de) * 2015-03-09 2016-09-15 Henkel Ag & Co. Kgaa "Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern"
DE102016225465A1 (de) * 2016-12-19 2018-06-21 Henkel Ag & Co. Kgaa Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2568792A (en) * 2017-09-29 2019-05-29 Henkel Ag & Co Kgaa Agent and method for the temporary deformation of keratin-containing fibers
US10736834B2 (en) 2017-09-29 2020-08-11 Henkel Ag & Co. Kgaa Agent and method for the temporary deformation of keratin-containing fibers
GB2568792B (en) * 2017-09-29 2021-07-28 Henkel Ag & Co Kgaa Agent and method for the temporary deformation of keratin-containing fibers

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Publication number Publication date
US20180049967A1 (en) 2018-02-22
WO2016142013A1 (fr) 2016-09-15
DE102015204148A1 (de) 2016-09-15
US10668003B2 (en) 2020-06-02

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