EP2427171A2 - Association de polymères comprenant au moins deux copolymères n-vinylpyrrolidone/n-vinylcaprolactame différents pour produits cosmétiques de traitement capillaire destinés à donner de la brillance - Google Patents

Association de polymères comprenant au moins deux copolymères n-vinylpyrrolidone/n-vinylcaprolactame différents pour produits cosmétiques de traitement capillaire destinés à donner de la brillance

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Publication number
EP2427171A2
EP2427171A2 EP10713333A EP10713333A EP2427171A2 EP 2427171 A2 EP2427171 A2 EP 2427171A2 EP 10713333 A EP10713333 A EP 10713333A EP 10713333 A EP10713333 A EP 10713333A EP 2427171 A2 EP2427171 A2 EP 2427171A2
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EP
European Patent Office
Prior art keywords
formula
weight
structural unit
copolymer
group
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
EP10713333A
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German (de)
English (en)
Inventor
Susanne Schmarje
Uwe Bergemann
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Henkel AG and Co KGaA
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Henkel AG and Co KGaA
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Publication of EP2427171A2 publication Critical patent/EP2427171A2/fr
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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—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
    • A61K8/02—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
    • 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
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/12—Preparations containing hair conditioners
    • 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 hair treatment compositions containing a specific amount of a polymer combination of at least two different N-vinylpyrrolidone / N-vinylcaprolactam copolymers, the use of these agents for temporary deformation and / or care keratin inconveniencer fibers and aerosol sprays or aerosol foams based on this Medium.
  • all animal hair e.g. Wool, horsehair, angora hair, furs, feathers and products or textiles made from them.
  • the keratinic fibers are human hairs.
  • Corresponding temporary shaping agents usually contain synthetic polymers as the shaping component.
  • Preparations containing a dissolved or dispersed polymer can be applied to the hair by means of propellant gases or by a pumping mechanism.
  • hair gels and hair waxes are generally not applied directly to the hair, but distributed by means of a comb or hands in the hair.
  • the first most important property of a composition for the temporary deformation of keratinic fibers is to give the treated fibers in the produced form the strongest possible hold. If the keratin fibers are human hair, it is also referred to as a strong hairstyle or the high degree of retention of the styling agent.
  • the hairstyle hold is essentially determined by the type and amount of the synthetic polymer used, but also an influence of the other constituents of the styling agent may be given. In addition to a high degree of hold, styling agents must meet a whole range of other requirements.
  • properties on the hair may be broadly subdivided into properties on the hair, properties of the particular formulation, eg properties of the foam, of the gel or of the sprayed aerosol, and of properties which affect the handling of the styling agent, whereby the properties on the hair are of particular importance. Particularly noteworthy are moisture resistance, low tackiness and a balanced conditioning effect. Furthermore, a styling agent should be universally applicable as possible for all hair types.
  • the polymers can be subdivided into cationic, anionic, nonionic and amphoteric film-forming and / or setting polymers.
  • the polymers yield a polymer film even when used on a small amount on the hair, which on the one hand gives the hairstyle a strong hold, but on the other hand is sufficiently flexible so as not to break under stress. If the polymer film is too brittle, it results in the formation of so-called Filmpiaken, that is residues that detach during the movement of the hair and give the impression that the user of the corresponding styling agent would dandruff.
  • the temporarily styled hair should look healthy and natural next to the strong hairstyle.
  • the hair shine plays an outstanding role.
  • the hair styling agents so-called brighteners are added in sufficient quantity.
  • These brighteners are, for example, oils or gloss pigments such as e.g. Mica particles.
  • Glossy particles have the disadvantage of detaching themselves from the hair over time and, after some time, e.g. find again on clothes or facial skin. Oils complain the hair and sometimes lead to a deteriorated adhesion of the film-forming or firming polymers on the hair. This possibly leads to the disadvantage that the imprinted hairstyle can not be fixed by the film-forming or setting polymers over a sufficient duration. The hairstyle hangs faster.
  • Object of the present invention was therefore to provide a means for temporary deformation and / or care keratinic fibers available, which is characterized by a high degree of retention and cause excellent gloss on the keratin fibers.
  • a first subject of the present invention is therefore an agent for treating keratin-containing fibers, especially human hair, contained in a cosmetically acceptable carrier (i) 1, 0 wt .-% to 2.8 wt .-%, particularly preferably from 1, 5 wt .-% to 2.8 wt .-%, each based on the weight of the cosmetic composition, at least one copolymer (a) comprising at least one structural unit of the formula (I) and at least one structural unit of the formula (II) and at least one structural unit of the formula (III)
  • R 1 represents a hydrogen atom or a methyl group
  • X 1 represents an oxygen atom or a group NH
  • R 2 and R 3 are independently (C 1 to C 4 ) alkyl
  • R represents a hydrogen atom or a methyl group
  • X 2 represents an oxygen atom or a group NH
  • R 5 and R 6 independently represent a (C 1 to C 4 ) alkyl group.
  • Examples of (C 1 to C 4 ) -alkyl groups according to formula (III) and (IV) are methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, isobutyl and tert-butyl.
  • Agents preferred according to the invention comprise at least one such copolymer (a) which according to formula (III) fulfills at least one of the following parameters (particularly preferably all three together):
  • R 1 is a methyl group
  • X 1 is an oxygen atom
  • R 2 and R 3 are a methyl group.
  • composition according to the invention contains as copolymer (a) a terpolymer of N-vinylpyrrolidone, N-vinylcaprolactam and N, N-dimethylaminoethyl methacrylate.
  • Such copolymers can be synthesized, for example, under the trade name Advantage LC-E (INCI name: vinylcaprolactam / VP / dimethylaminoethyl methacrylate copolymer, laurylpyrrolidone, 37% by weight of active substance in ethanol with the addition of N-laurylpyrrolidone) or Advantage LC-A (INCI name: Vinylcaprolactam / VP / dimethylaminoethyl methacrylate copolymer, 37% by weight of active substance in ethanol) from ISP.
  • Advantage LC-E ICI name: vinylcaprolactam / VP / dimethylaminoethyl methacrylate copolymer, laurylpyrrolidone, 37% by weight of active substance in ethanol with the addition of N-laurylpyrrolidone
  • Advantage LC-A INCI name: Vinylcaprolactam / VP / dimethylaminoethyl methacrylate
  • Agents preferred according to the invention comprise at least one copolymer (b) which according to formula (IV) fulfills at least one of the following parameters (particularly preferably all three together):
  • R 4 is a methyl group
  • X 2 is a group NH
  • R 5 and R 6 are a methyl group.
  • composition according to the invention contains as copolymer (b) a terpolymer of N-vinylpyrrolidone, N-vinylcaprolactam and N, N-dimethylaminopropylmethacrylamide.
  • copolymers are available, for example, under the trade name Aquaflex SF 40 (INCI name: VP / Vinyl Caprolactam / DMAPA Acrylates Copolymer, Alcohol Denat, 38-42% by weight of active substance in ethanol) from ISP.
  • This mixing ratio is of course preferred for all embodiments of the copolymers (a) and (b). This applies and also with the addition of at least one of the following preferred additional ingredients.
  • a particularly preferred means of treating keratinous fibers, especially human hair, is in a cosmetically acceptable carrier
  • R and R independently of one another represent a (C 1 to C 4 ) -alkyl group, and (ii) from 0.4% by weight to 1.4% by weight, in particular from 0.6% by weight to 1, 3% by weight, in each case based on the weight of the cosmetic agent, of at least one copolymer (b) comprising at least one structural unit of the formula (I) and at least one structural unit of the formula
  • R 5 and R 6 independently of one another are a (C 1 to C 4 ) -alkyl group.
  • Examples of (C 1 to C 4 ) -alkyl groups according to formula (III-1) and (IV-1) are methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, isobutyl and tert-butyl.
  • Very particularly preferred according to the invention means for the treatment of keratin fibers, in particular human hair, containing in a cosmetically acceptable carrier (i) 1, 0 wt .-% to 2.8 wt .-%, particularly preferably from 1, 5 wt .-% to 2.8 wt .-%, each based on the weight of the cosmetic composition, as a copolymer ( a) at least one terpolymer of N-vinylpyrrolidone, N-vinylcaprolactam and N, N-
  • a particularly preferred means of treating keratinous fibers, especially human hair, is in a cosmetically acceptable carrier
  • R 2 and R 3 independently of one another are a (C 1 to C 4 ) -alkyl group, and (ii) from 0.4% by weight to 1.4% by weight, in particular from 0.6% by weight to 1 , 3 wt .-%, each based on the weight of the cosmetic composition, of at least one copolymer (b) comprising at least one structural unit of the formula (I) and at least one structural unit of the formula
  • R 5 and R 6 independently represent a (C 1 to C 4 ) alkyl group, wherein copolymer (a) and copolymer (b) in a weight ratio range (i) to (ii) of 1 to 1 to 1 to 5, in particular from 1 to 1.5 to 1 to 2.5 are included.
  • Examples of (C 1 to C 4 ) -alkyl groups according to formula (III-1) and (IV-1) are methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, isobutyl and tert-butyl.
  • Very particularly preferred according to the invention means for the treatment of keratin fibers, in particular human hair, containing in a cosmetically acceptable carrier
  • copolymer (b ) at least one terpolymer of N-vinylpyrrolidone, N-vinylcaprolactam and N, N-dimethylaminopropylmethacrylamide, wherein copolymer (a) and copolymer (b) in a weight ratio range (i) to (ii) from 1 to 1 to 1 to 5, in particular of 1 to 1.5 to 1 to 2.5 are included.
  • compositions according to the invention contain the ingredients or active substances 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, based on the total agent.
  • 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.
  • the agent therefore additionally contains at least one alcohol which has 2 to 6 carbon atoms and 1 to 3 hydroxyl groups.
  • This additional alcohol is again preferably selected from at least one compound of the group formed from ethanol, ethylene glycol, isopropanol, 1,2-propylene glycol, 1,3-propylene glycol, glycerol, n-butanol, 1,3-butylene glycol.
  • a most preferred alcohol is ethanol.
  • the additional alcohol having 2 to 6 carbon atoms and 1 to 3 hydroxyl groups is preferably in the agent according to the invention (in particular in the presence of at least one propellant) in an amount of 40 wt .-% to 65 wt .-%, in particular from 40 wt .-% to 50 wt .-%, each based on the weight of the cosmetic composition containing.
  • Particularly suitable as additional co-solvents are unbranched or branched hydrocarbons such as pentane, hexane, isopentane and cyclic hydrocarbons such as cyclopentane and cyclohexane.
  • particularly preferred water-soluble solvents are polyethylene glycol and propylene glycol in an amount of up to 30 wt .-% based on the total agent.
  • the addition of propylene glycol and / or polyethylene glycol and / or polypropylene glycol increases the flexibility of the polymer film formed when the agent according to the invention is used. If, therefore, a flexible hold is desired, the agents according to the invention preferably contain from 0.01 to 30% by weight of polyethylene glycol and / or polypropylene glycol, based on the total agent.
  • the agents preferably have a pH of 2 to 11.
  • the pH range between 2 and 8 is particularly preferred.
  • the pH value in the context of this document refers to the pH at 25 ° C., unless stated otherwise.
  • composition of the invention optionally additionally contains at least one N- (C 6 to C 2 o) -Alkylpyrrolidon.
  • N-Laurylpyrrolidone is an inventively preferred N- (C 6 to C 2 o) alkylpyrrolidone.
  • the effects according to the invention can be increased by adding at least one (C 2 to C 6 ) trialkyl citrate to the composition according to the invention. It is therefore preferred according to the invention if the agents additionally contain at least one compound of the formula (E)
  • R 1 , R 2 and R 3 independently represent a (C 2 to C 6 ) alkyl group.
  • Examples of a (C 2 to C 6 ) -alkyl group according to formula (E) are methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, neopentyl, isopentyl, n hexyl.
  • the agent according to the invention preferably contains the compounds of the formula (E) in an amount of from 0.01 to 1% by weight, in particular from 0.05 to 0.3% by weight, based in each case on the weight of the entire composition.
  • isopropyl myristate is added to the inventive compositions preferably in an amount of 0.01 to 1 wt .-%, in particular from 0.05 to 0.3 wt .-%, each based on the weight of the total composition - included.
  • the agents according to the invention preferably additionally contain at least one surfactant, nonionic, anionic, cationic, ampholytic surfactants being suitable in principle.
  • the group of ampholytic or amphoteric surfactants includes zwitterionic surfactants and ampholytes.
  • the surfactants according to the invention may already have emulsifying activity.
  • the use of at least one nonionic surfactant and / or at least one cationic surfactant is preferred in this embodiment of the invention.
  • the additional surfactants are in the inventive composition preferably in an amount of 0.01 wt .-% to 5 wt .-%, particularly preferably from 0.05 wt .-% to 0.5 wt .-%, each based on the Weight of the agent, included.
  • agents according to the invention additionally comprise at least one nonionic surfactant.
  • Nonionic surfactants contain as hydrophilic group e.g. a polyol group, a polyalkylene glycol ether group, or a combination of polyol and polyglycol ether groups.
  • hydrophilic group e.g. a polyol group, a polyalkylene glycol ether group, or a combination of polyol and polyglycol ether groups.
  • Such compounds are, for example
  • R 1 CO for a linear or branched, saturated and / or unsaturated acyl radical having 6 to 22 carbon atoms
  • R 2 is hydrogen or methyl
  • R 3 is linear or branched
  • R 4 is an alkyl or alkenyl radical having 4 to 22 carbon atoms
  • G is a sugar radical having 5 or 6 carbon atoms
  • p is a number from 1 to 10. They can be obtained by the relevant methods of preparative organic chemistry.
  • the alkyl and alkenyl oligoglycosides can be derived from aldoses or ketoses with 5 or 6 carbon atoms, preferably glucose.
  • the preferred alkyl and / or alkenyl oligoglycosides are thus alkyl and / or alkenyl oligoglucosides.
  • the index number p in the general formula (T-II) indicates the degree of oligomerization (DP), ie the distribution of mono- and oligoglycosides and stands for a number between 1 and 10.
  • the value p for a given alkyloligoglycoside is an analytically determined arithmetic quantity, which usually represents a fractional number. Preference is given to using alkyl and / or alkenyl oligoglycosides having an average degree of oligomerization p of from 1.1 to 3.0. From an application point of view, those alkyl and / or alkenyl oligoglycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.4 are preferred.
  • the alkyl or alkenyl radical R 4 can be derived from primary alcohols having 4 to 11, preferably 8 to 10 carbon atoms. Typical examples are butanol, caproic alcohol, capryl alcohol, capric alcohol and undecyl alcohol and their technical mixtures, as they are For example, be obtained in the hydrogenation of technical fatty acid methyl esters or in the course of the hydrogenation of aldehydes from the Roelen oxo synthesis.
  • the alkyl or alkenyl radical R 15 can also be derived from primary alcohols having 12 to 22, preferably 12 to 14 carbon atoms.
  • Typical examples are lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol, brassidyl alcohol, and technical mixtures thereof which can be obtained as described above.
  • Alkyl oligoglucosides based on hydrogenated C12 / -i 4 coconut alcohol with a DP of 1 to 3
  • R 5 is CO for an aliphatic acyl radical having 6 to 22 carbon atoms
  • R 6 is hydrogen, an alkyl or hydroxyalkyl radical having 1 to 4 carbon atoms
  • [Z] is a linear or branched polyhydroxyalkyl radical having 3 to 12 carbon atoms and 3 to 10 hydroxyl groups stands.
  • the fatty acid N-alkyl polyhydroxyalkylamides are known substances which can usually be obtained by reductive amination of a reducing sugar with ammonia, an alkylamine or an alkanolamine and subsequent acylation with a fatty acid, a fatty acid alkyl ester or a fatty acid chloride.
  • the fatty acid N-alkylpolyhydroxyalkylamides are derived from reducing sugars having 5 or 6 carbon atoms, especially glucose.
  • the preferred fatty acid N-alkylpolyhydroxyalkylamides are therefore fatty acid N-alkylglucamides as represented by the formula (T-IV):
  • the fatty acid N-alkylpolyhydroxyalkylamides used are preferably glucamides of the formula (IV) in which R 8 is hydrogen or an alkyl group and R 7 is CO for the acyl radical of caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, palmitic acid, Stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, arachidic acid, gadoleic acid, behenic acid or erucic acid or technical mixtures of these acids.
  • R 8 is hydrogen or an alkyl group and R 7 is CO for the acyl radical of caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, palmitic acid, Stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid
  • fatty acid N- Alkylglucamide of formula (T-IV) which are obtained by reductive amination of glucose with methylamine and subsequent acylation with lauric acid or C12 / 14 coconut fatty acid or a corresponding derivative.
  • the polyhydroxyalkylamides can also be derived from maltose and palatinose.
  • alkylene oxide addition products of saturated linear fatty alcohols and fatty acids with in each case 2 to 100 mol of ethylene oxide per mole of fatty alcohol or fatty acid have proven to be very particularly preferred nonionic surfactants. Preparations with excellent properties are also obtained when they contain as nonionic surfactants C 2 -C 30 fatty acid mono- and diesters of addition products of 1 to 30 moles of ethylene oxide with glycerol and / or addition products of 5 to 60 moles of ethylene oxide with castor oil and hydrogenated castor oil ,
  • both products with a "normal” homolog distribution and those with a narrow homolog distribution can be used.
  • "normal” homolog distribution are meant mixtures of homologs obtained in the reaction of fatty alcohol and alkylene oxide using alkali metals, alkali metal hydroxides or alkali metal alcoholates as catalysts. Narrowed homolog distributions are obtained when, for example, hydrotalcites, alkaline earth metal salts of ether carboxylic acids, alkaline earth metal oxides, hydroxides or alkoxides are used as catalysts. The use of products with narrow homolog distribution may be preferred.
  • the agents according to the invention as surfactant very particularly preferably contain at least one addition product of from 15 to 100 mol of ethylene oxide, in particular from 15 to 50 mol of ethylene oxide, to a linear or branched (in particular linear) fatty alcohol having from 8 to 22 carbon atoms.
  • ethylene oxide in particular from 15 to 50 mol of ethylene oxide
  • linear or branched (in particular linear) fatty alcohol having from 8 to 22 carbon atoms.
  • These are very particularly preferably Ceteareth-15, Ceteareth-25 or Ceteareth- 50, which are marketed as Eumulgin ® CS 15 (Cognis), Cremophor A25 (BASF SE) or Eumulgin ® CS 50 (Cognis).
  • Suitable anionic surfactants are in principle all anionic surfactants suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as. As a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group having about 8 to 30 carbon atoms. In addition, glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups may be present in the molecule.
  • anionic surfactants are, in each case in the form of the sodium, potassium and ammonium as well as the mono-, di- and trialkanolammonium salts having 2 to 4 C atoms in the alkanol group, linear and branched fatty acids with 8 to 30 carbon atoms (soaps),
  • Ethercarbon Acid the formula R-O- (CH2-CH2O) x-CH2-COOH, in which R is a linear
  • Alkyl group having 8 to 30 C atoms and x 0 or 1 to 16,
  • Alpha-sulfofatty acid methyl esters of fatty acids having 8 to 30 carbon atoms are alpha-sulfofatty acids having 8 to 30 carbon atoms.
  • Alkyl sulfates and alkyl polyglycol ether sulfates of the formula RO (CH 2 -CH 2 O) x -OSO 3 H, in which R is a preferably linear alkyl group having 8 to 30 C atoms and x 0 or 1 to 12,
  • esters of tartaric acid and citric acid with alcohols the addition products of about 2-15
  • R 1 is preferably an aliphatic hydrocarbon radical having 8 to 30 carbon atoms
  • R 2 is hydrogen, a radical (CH 2 CH 2 O) n R 1 or X, n is from 1 to 10 and X is hydrogen, an alkali metal radical or alkaline earth metal or NR 3 R 4 R 5 R 6 , where R 3 to R 6 independently of one another represent hydrogen or a C 1 to C 4 hydrocarbon radical, is a sulfated fatty acid alkylene glycol ester of the formula (T-VI)
  • R 8 CO is a linear or branched acyl radical having 6 to 22 carbon atoms
  • x, y and z are in total O or numbers from 1 to 30, preferably 2 to 10
  • X is an alkali or alkaline earth metal.
  • monoglyceride (ether) sulfates suitable for the purposes of the invention are the reaction products of lauric acid monoglyceride, coconut fatty acid monoglyceride, palmitic acid monoglyceride, stearic acid monoglyceride, oleic acid monoglyceride and tallow fatty acid monoglyceride and their ethylene oxide adducts with sulfur trioxide or chlorosulfonic acid in the form of their sodium salts. It is preferred to use monoglyceride sulfates of the formula (T-VII) in which R 8 CO is a linear acyl radical having 8 to 18 carbon atoms, amide-ether carboxylic acids,
  • Condensation products of C 8 - C 30 - fatty alcohols with protein hydrolysates and / or amino acids and their derivatives which are known to the skilled person as protein fatty acid condensates, such as Lamepon ® - types Gluadin ® - types Hostapon ® KCG or Amisoft ® - types.
  • Preferred anionic surfactants are alkyl sulfates, alkyl polyglycol ether sulfates and ether carboxylic acids having 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in the molecule, sulfosuccinic acid mono- and dialkyl esters having 8 to 18 carbon atoms in the alkyl group and sulfosuccinic monoalkylpolyoxyethylester with 8 to 18 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups, Monoglycerdisulfate, alkyl and Alkenyletherphosphate and Eiweissfettkladensate.
  • cationic surfactants of the quaternary ammonium compound type are ammonium halides, in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides.
  • the long alkyl chains of these surfactants preferably have 10 to 18 carbon atoms, such as.
  • cetyltrimethylammonium chloride stearyltrimethylammonium chloride, distearyldimethyl ammonium chloride, lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetylmethylammonium chloride.
  • Further preferred cationic surfactants are the imidazolium compounds known under the INCI names Quaternium-27 and Quaternium-83.
  • Zwitterionic surfactants are those surface-active compounds which carry at least one quaternary ammonium group and at least one -COO () or -SO 3 ' " ' group in the molecule
  • Particularly suitable zwitterionic surfactants are the so-called betaines such as N-alkyl-N , N-dimethylammonium glycinates, for example, the cocoalkyl dimethylammonium glycinate, N-acyl-aminopropyl-N, N-dimethylammoniumglycinate, for example, the Kokosacyl- aminopropyl-dimethylammoniumglycinat, and 2-alkyl-3-carboxymethyl-3-hydroxyethyl-imidazoline with in each case 8 to 18 C atoms in the alkyl or acyl group and the cocoacylaminoethylhydroxyethylcarboxymethylglycinate
  • a preferred zwitterionic surfactant is the fatty acid
  • Ampholytes are understood as meaning those surface-active compounds which, apart from a C 8 -C 24 -alkyl or -acyl group in the molecule, contain at least one free amino group and at least one -COOH or -SO 3 H group and are capable of forming internal salts.
  • ampholytes are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids each having about 8 to 24 C atoms in the alkyl group.
  • Particularly preferred ampholytes are N-cocoalkylaminopropionate, cocoacylaminoethylaminopropionate and C 12 -C 18 acylsarcosine.
  • the agents according to the invention may optionally additionally contain at least one film-forming polymer and / or setting polymer. These additional polymers are different from copolymer (a) and copolymer (b).
  • the optionally added film-forming and / or setting polymers are preferably cationic and / or nonionic.
  • Film-forming polymers are polymers which leave a continuous film on the skin, the hair or the nails when drying.
  • Such film formers can be used in a wide variety of cosmetic products, such as for example face masks, make-up, hair fixatives, hair sprays, hair gels, hair waxes, hair treatments, shampoos or nail varnishes.
  • Particular preference is given to polymers which have a sufficient solubility in water or water / alcohol mixtures in order to be present in completely completely dissolved form in the agent according to the invention.
  • the film-forming polymers may be of synthetic or natural origin. According to the invention, film-forming polymers are understood as meaning polymers which, when used in 0.01 to 20% strength by weight aqueous, alcoholic or aqueous-alcoholic solution, are capable of depositing a transparent polymer film on the hair.
  • Firming polymers contribute to the maintenance and / or build-up of the hair volume and hair fullness of the overall hairstyle. These polymers are at the same time also film-forming polymers and therefore generally typical substances for shaping hair treatment agents such as hair fixatives, hair foams, hair waxes, hair sprays.
  • the film formation can be quite selective and connect only a few fibers.
  • composition according to the invention may contain at least one film-forming cationic and / or setting cationic polymer.
  • the additional film-forming cationic and / or setting cationic polymers have at least one structural unit containing at least one permanently cationized nitrogen atom.
  • Permanently cationized nitrogen atoms are to be understood as meaning those nitrogen atoms which carry a positive charge and thereby form a quaternary ammonium compound.
  • Quaternary ammonium compounds are most commonly prepared by reacting tertiary amines with alkylating agents, e.g. Methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also produced ethylene oxide.
  • alkylating agents e.g. Methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also produced ethylene oxide.
  • alkylating agents e.g. Methyl chloride, benzyl chloride, dimethyl sulfate, dodecyl bromide, but also produced
  • Preferred agents in the context of this embodiment comprise the film-forming cationic and / or setting cationic polymers in an amount of from 0.1% by weight to 20.0% by weight, particularly preferably from 0.2% by weight to 10.0 Wt .-%, most preferably from 0.5 wt .-% to 5.0 wt .-%, each based on the weight of the composition.
  • the cationic film-forming and / or cationic fixing polymers can be selected according to the invention from cationic, quaternized cellulose derivatives.
  • such cationic, quaternized celluloses prove to be advantageous in the sense of the embodiment which carries more than one permanent cationic charge in a side chain.
  • the cationic cellulose derivatives are those which are prepared from the reaction of hydroxyethylcellulose with a dimethyldiallylammonium reactant (in particular dimethyldiallylammonium chloride), if appropriate in the presence of further reactants.
  • a dimethyldiallylammonium reactant in particular dimethyldiallylammonium chloride
  • these cationic celluloses such cationic celluloses with the INCI name Polyquaternium-4 in turn, are particularly suitable, which are sold for example under the names of Celquat ® H 100, Celquat L 200 ® by the company National Starch.
  • cationic film-forming and / or cationic fixing polymers which comprise at least one structural unit of the formula (I) and at least one structural unit of the formula (VI) and optionally at least one structural unit of the formula (V)
  • R 1 and R 4 independently of one another represent a hydrogen atom or a methyl group
  • a 1 and A 2 independently of one another represent a group of ethane-1,2-diyl, propane-1,3-diyl or butane-1,4-diyl,
  • R 2 , R 3 , R 5 and R 6 independently of one another are a (C 1 to C 4 ) -alkyl group, R 7 is a (C 8 to C 30 ) -alkyl group.
  • ком ⁇ онент (VI) To compensate for the positive charge of the monomer (VI) are all possible physiologically acceptable anions, such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • Suitable compounds are, for example, as
  • R is a (C 1 to C 4 ) -alkyl group, in particular a methyl group, and additionally has at least one further cationic and / or nonionic structural element.
  • At least one copolymer (c1) is present in the inventive cationic film-forming and / or cationic setting polymer which, in addition to at least one structural element of the formula (M1), additionally contains a structural element of the formula (I) includes
  • R is a (C 1 to C 4 ) -alkyl group, in particular a methyl group.
  • the copolymers (c1) are all possible physiologically acceptable anions, such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • Very particularly preferred cationic film-forming and / or cationic fixing polymers as copolymers (c1) contain 10 to 30 mol%, preferably 15 to 25 mol% and in particular 20 mol% of structural units of the formula (M1) and 70 to 90 mol .-%, preferably 75 to 85 MoI.-% and in particular 80 mol .-% of structural units according to formula (I). It is particularly preferred if the copolymers (c1) in addition to polymer units resulting from the incorporation of said structural units of the formula (M1) and (I) in the copolymer, a maximum of 5 wt .-%, preferably at most 1 wt .-%, Contain polymer units, which are due to the incorporation of other monomers.
  • these N-Methylvinylimidazol ⁇ are / inylpyrrolidon copolymers are referred to as Polyquaternium-16, according to INCI Nomenclature and are, for example, from BASF under the trade names Luviquat ® Style , Luviquat.RTM ® FC 370, Luviquat.RTM ® FC 550, FC 905 and Luviquat.RTM ® Luviquat.RTM ® HM 552
  • agents according to the invention of this embodiment contain a copolymer (c1), in particular of the formula (poly), which has molar masses within a certain range.
  • agents according to the invention are preferred in which the copolymer (c1) has a molecular weight of 50 to 400 kDa, preferably 100 to 300 kDa, more preferably 150 to 250 kDa and in particular 190 to 210 kDa.
  • the agents according to the invention may also contain copolymers (c2) which, starting from the copolymer (d), have structural units of the formula (II) as additional structural units
  • compositions according to this embodiment are thus characterized in that they contain as cationic film-forming and / or cationic setting polymer at least one copolymer (c2) which has at least one structural unit of the formula (M1-a) and at least one structural unit of the formula (I) and at least structural unit according to formula (II)
  • the copolymers (c2) in addition to polymer units resulting from the incorporation of said structural units of the formula (M1-a), (I) and (II) in the copolymer, a maximum of 5 wt .-%, preferably at most 1 wt .-%, contain polymer units, which go back to the incorporation of other monomers.
  • the copolymers (c2) are composed exclusively of structural units of the formulas (M1-a), (I) and (II) and can be represented by the general formula (Poly 2)
  • indices m, n and p vary depending on the molecular weight of the polymer and should not mean that they are block copolymers. Rather, structural units of said formulas can be present in the molecule in a statistically distributed manner.
  • component (c2) To compensate for the positive polymer charge of component (c2) are all possible physiologically acceptable anions, such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • a methosulfate be used refer to those N-methylvinylimidazole / vinylpyrrolidone / vinylcaprolactam copolymers, according to INCI nomenclature as Polyquaternium-46 and are for example available under the trade names Luviquat ® Hold by BASF ,
  • Very particularly preferred copolymers (c2) contain 1 to 20 mol%, preferably 5 to 15 mol% and in particular 10 mol% of structural units of the formula (M1-a) and 30 to 50 mol%, preferably 35 to 45 mol .-% and in particular 40 mol .-% of structural units of the formula (I) and 40 to 60 mol .-%, preferably 45 to 55 mol .-% and in particular 60 mol .-% of structural units of the formula (II).
  • agents of this embodiment contain a copolymer (c2) having molecular weights within a certain range.
  • agents according to the invention are preferred in which the copolymer (c2) has a molecular weight of 100 to 1000 kDa, preferably from 250 to 900 kDa, more preferably from 500 to 850 kDa and in particular from 650 to 710 kDa.
  • the agents according to the invention may also contain copolymers (c3) as structural units forming cationic and / or setting cationic polymers which contain structural units as structural units of the formulas (M1-a) and (I), as well as further structural units from the group of the vinylimidazole units and further structural units from the group of the acrylamide and / or methacrylamide units.
  • Further particularly preferred agents according to this embodiment are characterized in that they contain as additional cationic film-forming and / or cationic setting polymer at least one copolymer (c3) which contains at least one structural unit of formula (M1-a) and at least one further structural unit of formula (I ) and at least one further structural unit according to formula (VII) and at least one further structural unit according to formula (VIII)
  • the copolymers (c3) in addition to polymer units resulting from the incorporation of said structural units of the formula (M1-a), (I), (VII) and (VIII) in the copolymer , maximum 5% by weight, preferably at most 1 wt .-%, polymer units, which go back to the incorporation of other monomers.
  • the copolymers (c3) are composed exclusively of structural units of the formula (M1-a), (I), (VII) and (VIII) and can be represented by the general formula (Poly 3)
  • component (c2) To compensate for the positive polymer charge of component (c2) are all possible physiologically acceptable anions, such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • a methosulfate be used refer to those N-Methylvinylimidazol ⁇ / inylpyrrolidon ⁇ / inylimidazol / methacrylamide copolymers, according to INCI nomenclature as Polyquaternium-68 and are, for example, from BASF under the tradename Luviquat ® Supreme available.
  • Very particularly preferred copolymers (c3) contain 1 to 12 mol%, preferably 3 to 9 mol% and in particular 6 mol% of structural units of the formula (M1-a) and 45 to 65 mol%, preferably 50 to 60 mol .-% and in particular 55 mol .-% of structural units of the formula (I) and 1 to 20 mol .-%, preferably 5 to 15 mol .-% and in particular 10 mol .-% of structural units of the formula (VII) and 20 to 40 mol .-%, preferably 25 to 35 mol .-% and in particular 29 mol .-% of structural units of the formula (VIII).
  • agents of this embodiment contain a copolymer (c3) having molecular weights within a certain range.
  • agents according to the invention are preferred in which the copolymer (c3) has a molecular weight of 100 to 500 kDa, preferably from 150 to 400 kDa, more preferably from 250 to 350 kDa and in particular from 290 to 310 kDa.
  • the additional film-forming cationic and / or setting polymers selected from the cationic polymers having at least one structural element of the above formula (M 1) the following are preferred:
  • Vinylpyrrolidone / i-vinyl-S-methyl-I H-imidazolium chloride copolymers (such as for example that with the INCI name Polyquaternium-16 under the trade names Luviquat ® Style, Luviquat ® FC 370, Luviquat ® FC 550, Luviquat ® FC 905 and Luviquat ® HM 552 (BASF SE)),
  • Vinylpyrrolidone / i-vinyl-S-methyl-I H-imidazolium copolymers (such as for example that with the INCI name Polyquaternium-44 under the trade names Luviquat Care ® (BASF SE)),
  • Vinylpyrrolidone / vinyl caprolactam / i-vinyl-S-methyl-I H-imidazolium terpolymer (such as for example that with the INCI name Polyquaternium-46 under the trade names Luviquat ® Care or Luviquat Hold ® (BASF SE)),
  • Vinylpyrrolidone / methacrylamide / vinylimidazole / i-vinyl-S-methyl-I H-imidazoliummethylsulfat- copolymer (such as (with the INCI name Polyquaternium-68 under the trade name Luviquat ® Supreme BASF SE)), as well as mixtures of these polymers.
  • composition according to the invention may comprise as additional film-forming and / or setting polymer at least one film-forming nonionic and / or setting nonionic polymer.
  • a nonionic polymer is understood as meaning a polymer which carries in a protic solvent under standard conditions substantially no structural units with permanently cationic or anionic groups which have to be compensated by counterions while maintaining the electroneutrality. Quaternized ammonium groups, however, do not include protonated amines under cationic groups. Examples of anionic groups include carboxyl and sulfonic acid groups.
  • the film-forming nonionic and / or setting nonionic polymers are preferably present in the composition according to the invention of this embodiment in an amount of from 0.1% by weight to 20.0% by weight, particularly preferably from 0.2% by weight to 15. 0 wt .-%, most preferably from 0.5 wt .-% to 10.0 wt .-%, each based on the weight of the composition according to the invention.
  • such film-forming nonionic and / or strengthening nonionic polymers having at least one structural element of the formula (M2)
  • R '(M2) preferably suitable which according to formula (M2) as R 'is a hydrogen atom, an acetyl group or a propanoyl group, in particular an acetyl group bear.
  • the film-forming nonionic and / or setting nonionic polymers are preferably selected from at least one polymer of the group that is formed
  • Suitable polyvinylpyrrolidones are, for example, commercial products such as Luviskol ® K 90 or Luviskol ® K 85 from BASF SE.
  • Suitable polyvinyl alcohols are marketed under the trade names Elvanol.RTM ® from DuPont or Vinol ® 523/540 by Air Products.
  • Suitable polyvinyl acetate is marketed under the trade name Vinac ® as an emulsion from Air Products.
  • Means comprising as film-forming nonionic and / or setting nonionic polymer at least one polymer selected from the group formed from
  • Copolymers of N-vinylpyrrolidone with N 1 N-di (C 1 to C 4) alkylamino (C 2 to C 4) -alkylacrylamid, copolymers of N-vinylpyrrolidone with N 1 N-di (C 1 to C 4) - Alkylamino (C 2 to C 4 ) alkylacrylamide are very particularly preferred according to the invention.
  • compositions according to the invention of this embodiment are characterized in that they contain at least one copolymer (c4) as nonionic film-forming and / or nonionic fixing polymer, the at least one further structural unit of formula (I) and at least one structural unit of formula (VII) and at least one Structural unit according to formula (VIII) contains
  • copolymers (c4) are preferably composed exclusively of structural units of the formulas (M1-a), (I), (VII) and (VIII) and can be distinguished by the general formula (poly4)
  • a particularly preferred polymer is selected from the polymers of the INCI name VP / methacrylamide / vinyl imidazole copolymer, which are obtainable, for example, under the trade name Luviset Clear from BASF SE.
  • additional co-solvents can agents of the invention organic solvent or a mixture of solvents with a boiling point below 400 0 C in an amount of 0.1 to 15 weight percent, preferably from 1 to 10 weight percent be present on the total composition.
  • Particularly suitable as additional co-solvents are unbranched or branched hydrocarbons such as pentane, hexane, isopentane and cyclic hydrocarbons such as cyclopentane and cyclohexane.
  • particularly preferred water-soluble solvents are glycerol, ethylene glycol and propylene glycol in an amount of up to 30% by weight, based on the total agent.
  • the addition of glycerol and / or propylene glycol and / or polyethylene glycol and / or polypropylene glycol increases the flexibility of the polymer film formed when the agent according to the invention is used.
  • the compositions according to the invention preferably contain from 0.01 to 30% by weight of glycerol and / or propylene glycol and / or polyethylene glycol and / or polypropylene glycol, based on the total agent.
  • the agents preferably have a pH of 2 to 11.
  • the pH range between 2 and 8 is particularly preferred.
  • the pH value in the context of this document refers to the pH at 25 ° C., unless stated otherwise.
  • compositions of the invention may further contain the auxiliaries and additives which are usually added to conventional styling.
  • auxiliaries and additives in particular additional care substances are mentioned.
  • 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 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.
  • ⁇ -amino acids and their derivatives such as ⁇ -alanine, anthranilic acid or hippuric acid can also be used.
  • 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 vegetable and animal or marine or synthetic origin can be used.
  • Animal protein hydrolysates are, for example, elastin, collagen, keratin, silk and milk protein hydrolysates, which may also be present in the form of salts.
  • Such products are, for example, under the trademarks Dehylan ® (Cognis), Promois® ® (Interorgana) Collapuron ® (Cognis), Nutrilan® ® (Cognis), Gelita-Sol ® (German Gelatinefabriken Stoess and Co), Lexein ® (Inolex) sericin (Pentapharm) and kerasol tm ® (Croda) sold.
  • silk protein hydrolysates By silk one understands the fibers of the cocoon of the mulberry silkworm (Bombyx mori L.).
  • the raw silk fiber consists of a double thread fibroin.
  • sericin keeps this double thread together.
  • Silk consists of 70-80% by weight of fibroin, 19-28% by weight of sericin, 0.5-1% by weight of fat and 0.5-1% by weight of dyes and mineral constituents.
  • the essential components of sericin are with about 46 wt.% Hydroxyamino acids.
  • the sericin consists of a group of 5 to 6 proteins.
  • the essential amino acids of the sericin are serine (Ser, 37% by weight), aspartate (Asp, 26% by weight), glycine (Gly, 17% by weight), alanine (Ala), leucine (Leu) and tyrosine (Tyr) ,
  • the water-insoluble fibroin belongs to the skieroproteins with a long-chain molecular structure.
  • the main components of the fibroin are glycine (44% by weight), alanine (26% by weight), and tyrosine (13% by weight).
  • Another essential structural feature of the fibroin is the hexapeptide sequence SerGIy-AIa-GIy-AIa-Gly.
  • an active ingredient complex consisting of the active ingredient (A1) selected from sericin, sericin hydrolysates and / or derivatives thereof, and mixtures thereof, and an active ingredient (A2) selected from fibroin, and / or fibroin hydrolysates and / or derivatives thereof and / or mixtures thereof.
  • the active ingredient complex (A) significantly synergistically improves the above-described essential internal and external structural features and the strength and elasticity of human hair.
  • Particularly good nourishing properties can be achieved if one of the two active ingredient components of the active ingredient complex (A) is used in the native or at most solubilized form. It is also possible to use a mixture of several active substances (A1) and / or (A2).
  • the two active compounds (A1) and (A2) in the ratio of 10:90 to 70:30, in particular 15:85 to 50:50 and very particularly 20:80 to 40:60, based on their respective Contents of active substance can be used in the inventive compositions.
  • Protein hydrolysates of vegetable origin eg. As soybean, almond, pea, potato and wheat protein hydrolysates are, for example, under the trademarks Gluadin ® (Cognis), DiaMin ® (Diamalt), Lexein ® (Inolex), Hydrosoy ® (Croda), Hydrolupin ® (Croda) , hydro Sesame ® (Croda), Hydro tritium ® (Croda) and Crotein ® (Croda) available.
  • protein hydrolysates Although the use of the protein hydrolysates is preferred as such, amino acid mixtures otherwise obtained may be used in their place, if appropriate. Also possible is the use of derivatives of protein hydrolysates, for example in the form of their fatty acid condensation products. Such products are marketed for example under the names Lamepon ® (Cognis), Lexein ® (Inolex), Crolastin ® (Croda), Crosilk ® (Croda) or Crotein ® (Croda).
  • the protein hydrolysates may be present in the agents according to the invention, for example in concentrations of from 0.01% by weight to 20% by weight, preferably from 0.05% by weight up to 15% by weight and most preferably in amounts of from 0 , 05 wt .-% up to 5 wt .-%, in each case based on the total application preparation.
  • the agent according to the invention may further comprise at least one vitamin, a provitamin, a vitamin precursor and / or one of their derivatives.
  • vitamins, provitamins and vitamin precursors are preferred, which are usually assigned to groups A, B, C, E, F and H.
  • vitamin A includes retinol (vitamin A 1 ) and 3,4-didehydroretinol (vitamin A 2 ).
  • the ß-carotene is the provitamin of retinol.
  • vitamin A component for example, vitamin A acid and its esters, vitamin A aldehyde and vitamin A alcohol and its esters such as the palmitate and the acetate into consideration.
  • the agents preferably contain the vitamin A component in amounts of 0.05-1% by weight, based on the total application preparation.
  • the vitamin B group or the vitamin B complex include vitamin B 1 (thiamine) vitamin B 2 (riboflavin)
  • Vitamin B 3 the compounds nicotinic acid and nicotinamide (niacinamide) are often performed.
  • Preferred according to the invention is the nicotinic acid amide, which is preferably contained in the agents according to the invention in amounts of from 0.05 to 1% by weight, based on the total application preparation.
  • Vitamin B 5 pantothenic acid, panthenol and pantolactone. Panthenol and / or pantolactone are preferably used in the context of this group.
  • Derivatives of panthenol which can be used according to the invention are, in particular, the esters and ethers of panthenol and also cationically derivatized panthenols. Individual representatives are, for example, panthenol triacetate, panthenol monoethyl ether and its monoacetate, as well as cationic panthenol derivatives.
  • the said compounds of the vitamin B 5 type are preferably present in the agents according to the invention in amounts of 0.05-10% by weight, based on the total application preparation. Amounts of 0.1-5 wt .-% are particularly preferred.
  • Vitamin B 6 (pyridoxine and pyridoxamine and pyridoxal).
  • the compounds of the vitamin B 6 type mentioned are preferably contained in the agents according to the invention in amounts of 0.01-5% by weight, based on the total application preparation. Levels of 0.05-1 wt% are particularly preferred.
  • Vitamin C (ascorbic acid). Vitamin C is used in the inventive compositions preferably in amounts of 0.1 to 3 wt .-%, based on the total application preparation. Use in the form of palmitic acid ester, glucosides or phosphates may be preferred. The use in combination with tocopherols may also be preferred.
  • Vitamin E tocopherols, especially ⁇ -tocopherol.
  • Tocopherol and its derivatives which include in particular the esters such as acetate, nicotinate, phosphate and succinate, are in the inventive compositions preferably in amounts of 0.05-1 wt .-%, based on the total application preparation included.
  • Vitamin F is usually understood as meaning essential fatty acids, in particular linoleic acid, linolenic acid and arachidonic acid.
  • Vitamin H is the compound (3aS, 4S, 6aR) -2-oxohexahydrothienol [3,4-c /] -imidazole-4-valeric acid, for which, however, the trivial name biotin has meanwhile prevailed.
  • Biotin is contained in the agents according to the invention preferably in amounts of 0.0001 to 1, 0 wt .-%, in particular in amounts of 0.001 to 0.01 wt .-%, each based on the total application preparation.
  • the agents according to the invention preferably contain vitamins, provitamins and vitamin precursors from groups A, B, C, E and H.
  • Panthenol, pantolactone, pyridoxine and its derivatives as well as nicotinic acid amide and biotin are particularly preferred.
  • the addition of panthenol increases the flexibility of the polymer film formed using the composition of the present invention.
  • the compositions according to the invention may contain panthenol instead of or in addition to glycerol and / or propylene glycol.
  • the agents according to the invention contain panthenol, preferably in an amount of 0.05 to 10% by weight, particularly preferably 0.1 to 5% by weight, in each case based on the total agent.
  • compositions according to the invention may further contain at least one plant extract.
  • extracts are produced by extraction of the whole plant. However, in individual cases it may also be preferred to prepare the extracts exclusively from flowers and / or leaves of the plant.
  • extracts of green tea, almond, aloe vera, coconut, mango, apricot, lime, wheat, kiwi and melon are especially suitable.
  • alcohols and mixtures thereof can be used as extraction agent for the preparation of said plant extracts water.
  • the alcohols are lower alcohols such as ethanol and isopropanol, but especially polyhydric alcohols such as ethylene glycol and propylene glycol, both as sole extractant and in admixture with water, are preferred.
  • Plant extracts based on water / propylene glycol in a ratio of 1:10 to 10: 1 have proven to be particularly suitable. It is possible according to the invention to use water-containing plant extracts within the given amount of water. However, this is not preferred according to the invention.
  • the plant extracts can be used according to the invention both in pure and in diluted form. If they are used in diluted form, they usually contain about 2 to 80 wt .-% of active substance and as a solvent used in their extraction agent or extractant mixture.
  • compositions according to the invention mixtures of several, especially two, different plant extracts.
  • compositions of the invention contain these care substances preferably in amounts of 0.001 to 2, in particular from 0.01 to 0.5 wt .-%, each based on the total application preparation.
  • Mono- or oligosaccharides can also be used as a care substance in the compositions according to the invention. Both monosaccharides and oligosaccharides, such as cane sugar, lactose and raffinose, can be used. The use of monosaccharides is preferred according to the invention. Among the monosaccharides, in turn, those compounds which contain 5 or 6 carbon atoms are preferred.
  • Suitable pentoses and hexoses are, for example, ribose, arabinose, xylose, lyxose, allose, altrose, glucose, mannose, gulose, idose, galactose, talose, fucose and fructose.
  • Arabinose, glucose, galactose and fructose are preferably used carbohydrates; Very particular preference is given to using glucose which is suitable both in the D - (+) or L - (-) configuration or as a racemate.
  • derivatives of these pentoses and hexoses can also be used according to the invention.
  • Preferred sugars are gluconic acid, glucuronic acid, sugar acid, mannose acid and mucic acid.
  • Preferred sugar alcohols are sorbitol, mannitol and dulcitol.
  • Preferred glycosides are the methylglucosides.
  • the monosaccharides or oligosaccharides used are usually obtained from natural raw materials such as starch, they usually have the configurations corresponding to these raw materials (for example D-glucose, D-fructose and D-galactose).
  • the mono- or oligosaccharides are preferably present in the compositions according to the invention in an amount of from 0.1 to 8% by weight, particularly preferably from 1 to 5% by weight, based on the total application preparation.
  • UV filters are not subject to any general restrictions with regard to their structure and their physical properties. On the contrary, all UV filters which can be used in the cosmetics sector and whose absorption maximum lies in the UVA (315-400 nm), in the UVB (280-315 nm) or in the UVC ( ⁇ 280 nm) range are suitable. UV filters with an absorption maximum in the UVB range, in particular in the range from about 280 to about 300 nm, are particularly preferred.
  • the UV filters preferred according to the invention can be selected, for example, from substituted benzophenones, p-aminobenzoic acid esters, diphenylacrylic acid esters, cinnamic acid esters, salicylic acid esters, benzimidazoles and o-aminobenzoic acid esters.
  • UV filters which can be used according to the invention are 4-aminobenzoic acid, N, N, N-trimethyl-4- (2-oxoborn-3-ylidenemethyl) aniline-methyl sulfate, S.S.S-trinnethylcyclohexylsalicylate
  • water-insoluble UV filters are to be understood which at 20 ° C. do not amount to more than 1% by weight, in particular to not more than 0.1% by weight, dissolve in water.
  • these compounds should be soluble in common cosmetic oil components at room temperature to at least 0.1, in particular at least 1 wt .-%. The use of water-insoluble UV filters may therefore be preferred according to the invention.
  • the UV filters are usually contained in amounts of 0.01-5 wt .-%, based on the total application preparation. Amounts of 0.1-2.5 wt .-% are preferred.
  • the composition according to the invention also contains one or more substantive dyes. This allows the treated keratin fiber not only to be temporarily patterned when the agent is applied, but also dyed at the same time. This may be particularly desirable if only a temporary dyeing is desired, for example, with eye-catching fashion colors, which can be removed again by simple washing from the keratinic fiber.
  • Direct dyes are usually nitrophenylenediamines, nitroaminophenols, azo dyes, anthraquinones or indophenols.
  • Preferred substantive dyes are those having the international designations or trade names HC Yellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, HC Yellow 12, Acid Yellow 1, Acid Yellow 10, Acid Yellow 23, Acid Yellow 36, HC Orange Disperse Orange 3, Acid Orange 7, HC Red 1, HC Red 3, HC Red 10, HC Red 11, HC Red 13, Acid Red 33, Acid Red 52, HC Red BN, Pigment Red 57: 1, HC Blue 2, HC Blue 11, HC Blue 12, Disperse Blue 3, Acid Blue 7, Acid Green 50, HC Violet 1, Disperse Violet 1, Disperse Violet 4, Acid Violet 43, Disperse Black 9, Acid Black 1, and Acid Black 52 known compounds as well as 1,4-diamino-2-nitrobenzene, 2-amino-4-nitrophenol, 1,4-bis- ( ⁇ -hydroxyethyl) -amino-2-nitrobenzene, 3-nitro
  • aromatic systems substituted with a quaternary nitrogen group such as Basic Yellow 57, Basic Red 76, Basic Blue 99, Basic Brown 16 and Basic Brown 17, as well as (C) substantive dyes containing a heterocycle having at least one quaternary nitrogen atom, as mentioned for example in EP-A2-998 908, to which reference is explicitly made at this point in claims 6 to 11 are called.
  • Very particularly preferred cationic substantive dyes of group (c) are the dyes known under the names Basic Yellow 87, Basic Orange 31 and Basic Red 51.
  • the cationic direct dyes which are sold under the trademark Arianor ®, according to the invention are also very particularly preferred cationic direct dyes.
  • the agents according to the invention according to this embodiment preferably contain the substantive dyes in an amount of 0.001 to 20 wt .-%, based on the total agent.
  • the agents of the invention may also contain naturally occurring dyes, such as those in henna red, henna neutral, henna black, chamomile flower, sandalwood, black tea, buckthorn bark, sage, bluewood, madder root, Catechu, Sedre and alkano root are included.
  • naturally occurring dyes such as those in henna red, henna neutral, henna black, chamomile flower, sandalwood, black tea, buckthorn bark, sage, bluewood, madder root, Catechu, Sedre and alkano root are included.
  • the substantive dyes each represent uniform compounds. Rather, in the inventive compositions, due to the production process for the individual dyes, in minor amounts, other components may be included, as far as they do not adversely affect the styling result or for other reasons, e.g. toxicological, must be excluded.
  • the agents according to the invention are free of oxidation dye precursors.
  • Oxidation dye precursors are classified into so-called developer components and coupler components.
  • the developer components form the actual dyes under the influence of oxidizing agents or of atmospheric oxygen with one another or with coupling with one or more coupler components.
  • the agents may furthermore contain all active ingredients, additives and auxiliaries known for such preparations.
  • Thickeners such as agar-agar, guar gum, alginates, xanthan gum, gum arabic, karaya gum, locust bean gum, linseed gums, dextrans, cellulose derivatives, e.g. Methylcellulose, hydroxyalkylcellulose and carboxymethylcellulose, starch fractions and Derivatives such as amylose, amylopectin and dextrins, clays such.
  • B. bentonite fully synthetic
  • Hydrocolloids such as e.g. Polyvinyl alcohol, and optionally crosslinked polyacrylates,
  • Structurants such as maleic acid and lactic acid
  • Anti-dandruff agents such as Piroctone Olamine, Zinc Omadine and Climbazole,
  • Bodying agents such as sugar esters, polyol esters or polyol alkyl ethers,
  • Swelling and penetration substances such as glycerol, propylene glycol monoethyl ether, carbonates,
  • Opacifiers such as latex, styrene / PVP and styrene / acrylamide copolymers
  • Pearlescing agents such as ethylene glycol mono- and distearate and PEG-3-distearate,
  • compositions according to the invention can be carried out in all forms customary for styling agents, for example in the form of solutions which can be applied to the hair as a lotion or pump or aerosol spray, or other preparations which are suitable for use on the hair.
  • the agents according to the invention are preferably designed as pump spray, aerosol spray, pump foam or aerosol foam.
  • the agents according to the invention are packaged in a dispensing device, which is either an additionally filled with a propellant compressed gas container ("aerosol container”) or a non-aerosol container.
  • a dispensing device which is either an additionally filled with a propellant compressed gas container ("aerosol container”) or a non-aerosol container.
  • the pressurized gas containers are defined as “aerosol containers”.
  • aerosol container a container under normal pressure is defined in reverse to the aerosol definition, with the aid of which a product is distributed by means of mechanical action by a pumping system.
  • the agents according to the invention are present as aerosol hair foam or aerosol hair spray.
  • the agent according to the invention therefore preferably additionally contains at least one propellant.
  • compositions according to the invention which are in the form of an aerosol product, can be prepared in a customary manner.
  • all constituents of the composition according to the invention with the exception of the blowing agent, are introduced into a suitable pressure-resistant container. This is then closed with a valve. By conventional techniques, finally, the desired amount of blowing agent is introduced.
  • suitable blowing agents are, for example, selected from N 2 O, dimethyl ether, CO 2 , air, alkanes having 3 to 5 carbon atoms, such as propane, n-butane, isobutane, n-pentane and iso-pentane, and their mixtures. Preference is given to dimethyl ether, propane, n-butane, isobutane and mixtures thereof. According to a preferred embodiment, said alkanes, mixtures of said alkanes or mixtures of said alkanes with dimethyl ether are used as sole blowing agent. However, the invention expressly also includes the concomitant use of propellants of the type of chlorofluorocarbons, but in particular of fluorocarbons.
  • the propellant is in the inventive compositions of the embodiment as aerosol spray preferably in an amount of 30 to 60 wt .-% - based on the weight of the total composition - included.
  • mixtures of propane and butane as the sole blowing agent in a weight ratio of propane to butane of from 20:80 to 15:85. These mixtures are again preferably present in the compositions according to the invention in an amount of from 30 to 55% by weight the weight of the entire agent - used.
  • Butane according to the invention is understood to mean n-butane, isobutane and mixtures of n-butane and isobutane.
  • a particularly preferred aerosol spray of this invention is an agent packaged in an aerosol container contained in a cosmetically acceptable carrier
  • R 2 and R 3 are independently (C 1 to C 4 ) alkyl
  • R 5 and R 6 independently of one another are a (C 1 to C 4 ) -alkyl group, and (iii) at least one blowing agent, (in particular as the sole blowing agent 30 to 55% by weight of a
  • Examples of (C 1 to C 4 ) -alkyl groups according to formula (III-1) and (IV-1) are methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, isobutyl and tert-butyl.
  • a most preferred aerosol spray of this invention is an agent packaged in an aerosol container containing in a cosmetically acceptable carrier (i) 1, 0 wt .-% to 2.8 wt .-%, particularly preferably from 1, 5 wt .-% to 2.8 wt .-%, each based on the weight of the cosmetic composition, as a copolymer ( a) at least one terpolymer of N-vinylpyrrolidone, N-vinylcaprolactam and N, N-
  • copolymer (a) and copolymer (b) are in a weight ratio range (i) to (ii) of 1 to 1 to 1 to 5, in particular from 1 to 1.5 to 1 to 2.5 are included.
  • the sizes of the aerosol droplets and the respective size distribution can be set for a given spraying device.
  • the spray rate of the sprays according to the invention is preferably 6.5 to 10.0 g / 10 s.
  • agents according to the invention are packaged in an aerosol container with a stem valve with a bore of 0.27 to 0.35 mm diameter.
  • Such valves are sold, for example, as valves of the type KE or KEN from the company. Coster.
  • Vortex nozzles in the embodiment of the so-called vortex nozzle are particularly well suited for the embodiment according to the invention as an aerosol spray.
  • Vortex nozzles have a channel guide known to those skilled in the art to the center of the center within the nozzle.
  • Vortex nozzles of this type are sold, for example, under the name "standard micromist insert" by the company. Coster.
  • a particularly preferred aerosol spray of this invention is an agent packaged in an aerosol container contained in a cosmetically acceptable carrier
  • R and R independently of one another represent a (C 1 to C 4 ) -alkyl group, and (ii) from 0.4% by weight to 1.4% by weight, in particular from 0.6% by weight to 1, 3% by weight, in each case based on the weight of the cosmetic agent, of at least one copolymer (b) comprising at least one structural unit of the formula (I) and at least one structural unit of the formula
  • R 5 and R 6 independently of one another are a (C 1 to C 4 ) -alkyl group and (iii) at least one blowing agent, (in particular as the sole blowing agent 30 to 55% by weight of a
  • the aerosol container has a stem valve with a Stembohrung 0.27 to 0.35 mm in diameter and preferably additionally carries a vortex nozzle.
  • a most preferred aerosol spray of this invention is therefore an agent packaged in an aerosol container containing in a cosmetically acceptable carrier
  • the aerosol canister has a star valve with a Stubenbohrung 0.27 to 0.35 mm in diameter and preferably additionally carries a vortex nozzle.
  • a particularly preferred aerosol spray of this invention is an agent packaged in an aerosol container contained in a cosmetically acceptable carrier
  • R 2 and R 3 independently of one another are a (C 1 to C 4 ) -alkyl group, and (ii) from 0.4% by weight to 1.4% by weight, in particular from 0.6% by weight to 1 , 3 wt .-%, each based on the weight of the cosmetic composition, of at least one copolymer (b) comprising at least one structural unit of the formula (I) and at least one structural unit of the formula
  • R 5 and R 6 independently of one another are a (C 1 to C 4 ) -alkyl group, and (iii) at least one blowing agent, (in particular as the sole blowing agent 30 to 55 wt .-% of a
  • the aerosol container having a Stem valve with a Stembohrung 0.27 to 0.35 mm in diameter and preferably additionally carries a vortex nozzle and
  • Copolymer (a) and copolymer (b) in a weight ratio range (i) to (ii) from 1 to 1 to 1 to 5, in particular from 1 to 1.5 to 1 to 2.5 are included.
  • Examples of (C 1 to C 4 ) -alkyl groups according to formula (III-1) and (IV-1) are methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, isobutyl and tert-butyl.
  • a most preferred aerosol spray of this invention is an agent packaged in an aerosol container containing in a cosmetically acceptable carrier
  • the aerosol container has a stem valve with a bore of 0.27 to 0.35 mm in diameter and preferably additionally carries a vortex nozzle and wherein copolymer (a) and copolymer (b) in a weight ratio range (i) to (ii) of 1 to
  • 1 to 1 to 5 in particular from 1 to 1.5 to 1 to 2.5 are included.
  • the aerosol sprays of all embodiments according to the invention preferably have a spray rate of 6.5 to 10.0 g / 10 s.
  • Propellants suitable for producing an aerosol foam according to the invention are selected, for example, from N 2 O, dimethyl ether, CO 2 , air, alkanes having from 3 to 5 carbon atoms, such as propane, n-butane, isobutane, n-pentane and isopentane, and their mixtures. Preference is given to dimethyl ether, propane, n-butane, isobutane and mixtures thereof.
  • suitable blowing agents are for example selected from N 2 O, dimethyl ether, CO 2 , air, alkanes having 3 to 5 carbon atoms, such as propane, n-butane, iso-butane, n-pentane and iso-pentane, and their mixtures.
  • alkanes, mixtures of said alkanes or mixtures of said alkanes with dimethyl ether are used as sole blowing agent.
  • the invention expressly also includes the concomitant use of propellants of the type of chlorofluorocarbons, but in particular of fluorocarbons.
  • the sizes of the foam bubbles and the respective size distribution can be set for a given spraying device.
  • Aerosolschau m When using conventional aerosol container Aerosolschau m. contain the propellant preferably in amounts of 1 to 35 wt .-%, based on the total product. Amounts of 2 to 30 wt .-%, in particular from 3 to 15 wt .-% are particularly preferred.
  • isopentane is preferably suitable as a propellant, which is incorporated into the compositions according to the invention and is packaged in the first chamber of the two-chamber aerosol container.
  • the second Chamber of the two-chamber aerosol container is made up of at least one other, different from isopentane blowing agent, which builds up a higher pressure in the two-chamber aerosol container than the isopentane.
  • the blowing agents of the second chamber are preferably selected from N 2 O, dimethyl ether, CO 2 , air, alkanes having 3 or 4 carbon atoms (such as propane, n-butane, isobutane) and mixtures thereof.
  • compositions according to the invention and products which contain these agents are distinguished, in particular, by giving treated hair a very natural gloss and strong hold.
  • a second object of the invention is the use of a composition of the first subject of the invention for producing gloss on keratin-containing fibers, in particular human hair.
  • the products according to the invention containing these agents are characterized in particular by the fact that they give treated hair a very strong, permanent hairstyle hold, although the hair remains flexible.
  • a third aspect of the invention is therefore the use of a composition of the first subject of the invention for the temporary deformation of keratin-containing fibers, in particular human hair.
  • a fourth subject of the invention is a method for treating keratin-containing fibers, in particular human hair, wherein an agent according to the first subject of the invention is applied as a spray to the keratin-containing fibers using a dispensing device. It is inventively preferred that the keratin-containing fibers are brought into shape and this form is fixed by the means of the first subject of the invention.
  • the agent according to the invention remains from the keratin-containing fibers, i. is not rinsed out again.
  • a fifth subject of the invention is a method for treating keratin-containing fibers, in particular human hair, wherein a means according to the first subject of the invention is foamed to a foam using a dispenser and the resulting foam is applied to the keratin-containing fibers.
  • the keratin-containing fibers are brought into shape and this form is fixed by the means of the first subject of the invention.
  • the agent according to the invention remains from the keratin-containing fibers, i. is not rinsed out again.
  • Preferred according to the invention are the abovementioned dispensers (vide supra).

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  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Cosmetics (AREA)

Abstract

L'invention concerne des produits pour le traitement de fibres kératiniques, en particulier des cheveux humains, contenant dans un support cosmétiquement acceptable : (i) entre 1,0 et 2,8 % en poids, idéalement entre 1,5 et 2,8 % en poids, d'au moins un copolymère (a) comprenant au moins un motif structural de formule (I), au moins un motif structural de formule (II) et au moins un motif structural de formule (III), dans laquelle R1 représente un atome d'hydrogène ou un groupe méthyle, X1 désigne un atome d'oxygène ou un groupe NH, R2 et R3 représentent indépendamment l'un de l'autre un groupe alkyle en C1-C4, et (ii) entre 0,4 et 1,4 % en poids, en particulier entre 0,6 et 1,3 % en poids, d'au moins un copolymère (b) comprenant au moins un motif structural de formule (I), au moins un motif structural de formule (II) et au moins un motif structural de formule (IV) dans laquelle R4 représente un atome d'hydrogène ou un groupe méthyle, X2 désigne un atome d'oxygène ou un groupe NH, R5 et R6 représentent indépendamment l'un de l'autre un groupe alkyle en C1-C4. Ces produits servent à réaliser une déformation temporaire des cheveux et à leur donner de la brillance, et se présentent en particulier sous forme de spray aérosol ou de mousse aérosol.
EP10713333A 2009-05-08 2010-04-09 Association de polymères comprenant au moins deux copolymères n-vinylpyrrolidone/n-vinylcaprolactame différents pour produits cosmétiques de traitement capillaire destinés à donner de la brillance Ceased EP2427171A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102009020552A DE102009020552A1 (de) 2009-05-08 2009-05-08 Polymerkombination aus mindestens zwei verschiedenen N-Vinylpyrrolidon/N-Vinylcaprolactam-Copolymeren für glanzgebende kosmetische Haarbehandlungsmittel
PCT/EP2010/054679 WO2010127921A2 (fr) 2009-05-08 2010-04-09 Association de polymères comprenant au moins deux copolymères n-vinylpyrrolidone/n-vinylcaprolactame différents pour produits cosmétiques de traitement capillaire destinés à donner de la brillance

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EP2427171A2 true EP2427171A2 (fr) 2012-03-14

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US (1) US20120052020A1 (fr)
EP (1) EP2427171A2 (fr)
DE (1) DE102009020552A1 (fr)
WO (1) WO2010127921A2 (fr)

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DE102010055842A1 (de) * 2010-12-23 2012-06-28 Henkel Ag & Co. Kgaa Treibmittelhaltige Haarstylingzusammensetzungen
DE102011077373A1 (de) * 2011-06-10 2012-12-13 Henkel Ag & Co. Kgaa Glanzgebende Haarumformungsmittel mit starkem Halt und gutem Haargefühl
DE102012222769A1 (de) * 2012-12-11 2014-06-12 Henkel Ag & Co. Kgaa Haarpflegemittel mit Silikonen enthaltend Zuckerstrukturen und ausgewählte weitere Silikone
DE102012222773A1 (de) * 2012-12-11 2014-06-12 Henkel Ag & Co. Kgaa Haarpflegemittel mit ausgewählten quarternären Ammoniumverbindungen und Silikonen enthaltend Zuckerstrukturen
DE102012222768A1 (de) * 2012-12-11 2014-06-12 Henkel Ag & Co. Kgaa Haarpflegemittel mit ausgewählten und/oder ausgewählten Oligopeptiden und/oder ausgewählten kationischen Proteinhydrolysaten und Silikonen enthaltend Zuckerstrukturen

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DE3139438A1 (de) 1981-10-03 1983-04-21 Henkel KGaA, 4000 Düsseldorf Verwendung kolloidaler loesungen von seidenfibroin in haarkosmetischen mitteln und haarshampoo
US5658558A (en) * 1994-10-03 1997-08-19 Rohm And Haas Company Hair styling compositions and method of enhancing the performance of hair fixative resins
US5626836A (en) * 1994-12-28 1997-05-06 Isp Investments Inc. Low VOC hair spray compositions containing terpolymers of vinyl pyrrolidone, vinyl caprolactam and 3-(N-dimethylaminopropyl) methacrylamide
DE19738866A1 (de) 1997-09-05 1999-03-11 Henkel Kgaa Schaumarme Tensidmischungen mit Hydroxymischethern
FR2785183B1 (fr) 1998-11-04 2002-04-05 Oreal COMPOSITION TINCTORIALE CONTENANT UN COLORANT DIRECT CATIONIQUE ET UNE PYRAZOLO-[1,5-a]- PYRIMIDINE A TITRE DE BASE D'OXYDATION, ET PROCEDES DE TEINTURE
DE19937386A1 (de) * 1999-08-07 2001-02-15 Wella Ag Volumengebendes Haarbehandlungsmittel
DE19937434C2 (de) * 1999-08-07 2002-02-21 Wella Ag Haarbehandlungsmittel mit langanhaltendem Volumeneffekt
DE19957947C1 (de) * 1999-12-02 2001-08-09 Wella Ag Polymerkombination für Haarbehandlungsmittel
DE10240757A1 (de) 2002-08-30 2003-07-24 Henkel Kgaa Synergistische Kombination von Seidenproteinen
DE10358587A1 (de) * 2003-12-12 2005-07-07 Hans Schwarzkopf & Henkel Gmbh & Co. Kg Volumengebendes kosmetisches Mittel

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US20120052020A1 (en) 2012-03-01
DE102009020552A1 (de) 2010-11-18
WO2010127921A3 (fr) 2012-01-26
WO2010127921A2 (fr) 2010-11-11

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