EP2793837A2 - Agents de mise en forme de fibres kératiniques conférant un bon maintien et un aspect naturel - Google Patents

Agents de mise en forme de fibres kératiniques conférant un bon maintien et un aspect naturel

Info

Publication number
EP2793837A2
EP2793837A2 EP12781358.2A EP12781358A EP2793837A2 EP 2793837 A2 EP2793837 A2 EP 2793837A2 EP 12781358 A EP12781358 A EP 12781358A EP 2793837 A2 EP2793837 A2 EP 2793837A2
Authority
EP
European Patent Office
Prior art keywords
formula
structural unit
group
hydrogen atom
agent
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
EP12781358.2A
Other languages
German (de)
English (en)
Inventor
Burkhard Müller
Susanne Schmarje
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 EP2793837A2 publication Critical patent/EP2793837A2/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)
    • 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
    • A61K2800/74—Biological properties of particular ingredients

Definitions

  • Forming agent for keratin fibers provides strong hold and natural appearance
  • the invention relates to the technical field of temporary transformation keratin inconveniencer fibers, especially human hair. It relates in particular to hair treatment compositions containing a special polymer combination, the use of these agents for the temporary shaping and / or care of keratin-containing fibers and aerosol sprays or aerosol foams based on these agents.
  • styling agent The first most important property of a composition for the temporary deformation of keratinic fibers, also referred to below as styling agent, is to give the treated fibers in the produced form the strongest possible 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 tackiness and a balanced conditioning effect.
  • 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 on a small amount when applied to 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 hair coated with a firming polymer often feels harsh.
  • 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 mica particles.
  • Glossy particles have the disadvantage that they detach with time from the hair and after some time, for example, on the clothing or facial skin again. 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.
  • the object of the present invention was therefore to provide a means for the temporary deformation of keratin-containing fibers, which is characterized by a high degree of hold, does not matt the keratin-containing fibers and effects good sensor technology of the keratin-containing fibers (in particular a soft hair feel).
  • 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
  • R is a hydrogen atom or a methyl group
  • R 2 represents a hydrogen atom or a methyl group
  • R 3 is a branched (C 1 to C 2 o) -alkyl group, a branched (C 2 to C 6 ) -
  • R 4 and R 5 are each a hydrogen atom or one of the two radicals
  • a chemical bond marked with the symbol * stands for a "free valence" of the corresponding structural fragment, to which "free valence” bind further structural fragments in the corresponding copolymer.
  • 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. As a test method for the firming effect of a polymer, the so-called curl retention test is often used.
  • 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.
  • 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.
  • 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 takes place through a bridging polysiloxane molecule fragment.
  • the cross-linking polysiloxane molecule fragment binds to the polymer chains bridged by the molecule fragment, each by means of covalent chemical bonding.
  • an anionic polymer is understood as meaning a polymer which, in standard conditions, contains structural units with anionic groups which have to be compensated by counterions while maintaining the electroneutrality in a protic solvent and has no structural units with permanently cationic or cationizable groups.
  • Anionic groups include carboxyl and sulfonic acid groups.
  • the reinforcing anionic copolymer comprises 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)
  • the radical R is a hydrogen atom, therefore, styrene is a preferred monomer in the copolymers used according to the invention.
  • Preferred agents according to the invention contain, as structural unit (II), esters of acrylic acid or methacrylic acid with branched alcohols, the acrylic esters being preferred, so that in preferred agents R 2 is a hydrogen atom.
  • the setting anionic copolymers have not only one structural unit of the formula (II) in which acrylic acid or methacrylic acid are esterified with branched alcohols, but additionally one Have structural unit in which acrylic acid or methacrylic acid are esterified with unbranched alcohols.
  • the reinforcing anionic copolymer comprises at least one structural unit of the formula (I) and at least one structural unit of the formula (IIa) and at least one structural unit of the formula (IIb) and at least one structural unit of the formula (III)
  • R is a hydrogen atom
  • R 2 is a hydrogen atom
  • R 3 is an ethylhexyl group
  • R 2 is a hydrogen atom
  • R 3 is a butyl group
  • R 4 and R 5 stand for a hydrogen atom or one of the two radicals for a hydrogen atom and the other for a methyl group.
  • compositions of the invention As a third mandatory structural unit used in the compositions of the invention
  • Very particularly preferred agents according to the invention contain as strengthening (s) anionic (s)
  • Copolymers of styrene with isopropyl acrylate and n-butyl acrylate and methacrylic acid Copolymers of styrene with sec-butyl acrylate and n-butyl acrylate and methacrylic acid Copolymers of styrene with tert-butyl acrylate and n-butyl acrylate and methacrylic acid
  • the composition according to the invention preferably contains the first reinforcing anionic copolymer in an amount of from 0.01 to 29.99% by weight, particularly preferably from 0.1 to 14.9% by weight, very particularly preferably from 0.1 to 9.5% by weight. -%, and most preferably from 0.2 to 7.0 wt .-%, each based on the total weight of the composition according to the invention.
  • the agent according to the invention necessarily contains as component (b) a polymer having at least one caprolactam structural unit of the above formula (M1).
  • the polymers of component (b) are preferably present in the composition according to the invention in an amount of 0.05 to 15.0% by weight, particularly preferably 0.1 to 7.0% by weight, in each case based on the total weight of the composition , contain.
  • the polymers according to the invention of component (b) of the agent according to the invention are preferably nonionic or cationic.
  • Cationic polymers are to be understood as meaning polymers which have a group in the main and / or side chain which may be “temporary” or “permanent” cationic.
  • "permanently cationic” refers to those polymers which have a cationic group, irrespective of the pH of the agent. These are usually polymers containing a quaternary nitrogen atom, for example in the form of an ammonium group.
  • Preferred cationic groups are quaternary ammonium groups.
  • those polymers in which the quaternary ammonium group is bonded via a C 1-4 hydrocarbon group to a polymer main chain constructed from acrylic acid, methacrylic acid or derivatives thereof have proven to be suitable.
  • cationic, fixing polymers preferably used in the compositions according to the invention are the so-called "temporary cationic" polymers. These polymers are preferred cationic polymers. They usually contain an amino group which is present in protic solvents as a protonated ammonium group and thus cationic. The degree of cationization depends on the pH.
  • the polymers according to the invention of component (b) of the agent according to the invention are particularly preferably nonionic or temporarily cationic.
  • a homopolymer of N-vinylcaprolactam is suitable.
  • Such polymers are nonionic and are marketed, for example, by BASF SE under the trade name Luviskol Plus (INCI name: polyvinylcaprolactam, 50% by weight of active substance in ethanol).
  • Luviskol Plus INCI name: polyvinylcaprolactam, 50% by weight of active substance in ethanol.
  • Particularly preferred agents are characterized in that the polymer of component (b) comprises at least one structural unit of the formula (M1) and at least one structural unit of the formula (M2) and at least one structural unit of the formula (M3),
  • R is a hydrogen atom or a methyl group
  • X 1 represents an oxygen atom or a group NH
  • A is a group of ethane-1, 2-diyl, propane-1, 3-diyl or butane-1, 4-diyl,
  • R 2 and R 3 independently of one another represent a (C 1 -C 4 ) -alkyl group.
  • R in formula (M3) is preferably a methyl group.
  • Examples of (C 1 to C 4 ) -alkyl groups according to formula (M3) are methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, isobutyl and tert-butyl.
  • R 2 and R 3 in formula (M3) are preferably a methyl group.
  • Especially suitable polymers of this embodiment have at least one structural unit of the formula (M3) in which A is an ethane-1,2-diyl group and X 1 is an oxygen atom.
  • such a polymer preferably comprises at least one structural unit of the formula (M1) and at least one structural unit of the formula (M2) and at least one structural unit of the formula (M3-1)
  • R 2 and R 3 independently of one another are a (C 1 -C 4 ) -alkyl group, in particular methyl.
  • Examples of (C 1 to C 4 ) -alkyl groups according to formula (M3-1) are methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, isobutyl and tert-butyl.
  • the agent according to the invention contains as component (b) of the agent according to the invention a terpolymer of N-vinylcaprolactam, N-vinylpyrrolidone and N, N-dimethylaminoethyl methacrylate.
  • Such copolymers may, for example, under the trade name Advantage LC-E (INCI name:
  • the agents according to the invention contain as component (b) at least one polymer comprising at least one structural unit of the formula (M2) and at least one structural unit of the formula (M3)
  • R is a hydrogen atom or a methyl group
  • X 1 stands for a group NH
  • A is a propane-1, 3-diyl group
  • R 2 and R 3 independently of one another are a (C 1 to C 4 ) -alkyl group, in particular methyl.
  • the composition according to the invention of this embodiment contains as polymer of component (b) of the composition according to the invention a terpolymer of N-vinylpyrrolidone, N-vinylcaprolactam and N, N-dimethylaminopropylmethacrylamide.
  • a terpolymer of N-vinylpyrrolidone, N-vinylcaprolactam and N, N-dimethylaminopropylmethacrylamide 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.
  • the agent according to the invention contains as polymer of component (b) a cationic polymer comprising at least one structural unit of formula (M1) and at least one structural unit of formula (M2) and at least one structural unit of formula (M3) and at least one Structural unit of the formula (M4),
  • R and R 4 independently of one another represent a hydrogen atom or a methyl group
  • X 1 and X 2 independently of one another represent an oxygen atom or a group NH
  • a and A 2 independently of one another represent a group 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 represent a (C 1 to C 4 ) -alkyl group
  • R 7 is a (C 8 to C 30 ) alkyl group
  • a cationic polymer preferably present as component (b) in the context of this embodiment comprises at least one structural unit of the formula (M1), at least one structural unit of the formula (M2), at least one structural unit of the formula (M3-2) and at least one Structural unit of the formula (M4-1),
  • R 7 is octyl (capryl), decyl (caprinyl), dodecyl (lauryl), tetradecyl (myristyl), hexadecyl (cetyl), octadecyl (stearyl), eicosyl (arachyl) or docosyl (behenyl).
  • Another preferred cationic polymer according to the invention is the copolymer of N-vinylpyrrolidone, N-vinylcaprolactam, N- (3-dimethylaminopropyl) methacrylamide and 3- (methacryloylamino) propyl-lauryl-dimethylammonium chloride (INCI name: Polyquaternium-69), which is described, for example, in US Pat the trade name Aqua style ® 300 marketed (28-32 wt .-% of active substance in ethanol-water mixture, molecular weight 350,000) by the company ISP.
  • copolymers of the component (c) contained in the agent of the invention in this embodiment of the invention are preferably in an amount of 0.1 to 10.0% by weight, more preferably 0.3 to 8.0% by weight, respectively based on the total weight of the agent
  • the agent according to the invention additionally contains at least one copolymer as component (c) which contains at least one structural unit of the formula (M5), at least one structural unit of the formula (M6) and at least one structural unit of the formula (M7),
  • R 3 represents a hydrogen atom or a methyl group
  • R 4 is an alkyl group having 4 carbon atoms (especially n-butyl, sec-butyl, iso-butyl or tert-butyl).
  • the copolymer of component (c) additionally contains at least one structural unit of the formula (M8) in addition to the above structural units of the formulas (M5), (M6) and (M7)
  • R 5 represents a hydrogen atom or a methyl group
  • R 6 is a (C 1 -C 4 ) -alkyl group (in particular a methyl group or an ethyl group).
  • Preferred copolymers of component (c) of this type are selected from the group consisting of:
  • the copolymer of the component (c) is that available under the trade name Amphomer ® 28-4910 from Akzo Nobel powdered polymer having the INCI name
  • Agents preferred according to the invention are characterized in that, based in each case on the weight of the total ready-to-use agent, they contain 0.05 to 5% by weight, preferably 0, 1 to 2.5% by weight and in particular 0, 15 to 0, Contain 5 wt .-% of at least one alkyl ester of a hydroxy acid.
  • At least one compound of the formula E) is the (C 2 to C 6 ) trialkyl citrates. Therefore, it is preferred according to the invention if the agents additionally contain at least one compound of the formula E),
  • R, 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-
  • 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.
  • Particularly preferred agents according to the invention are characterized in that they are based on the weight of the entire ready-to-use
  • 0.05 to 5 wt.% Preferably 0, 1 to 2.5 wt.% And in particular 0, 15 to 0.5 wt.
  • 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, 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.
  • Very particularly preferred agents according to the invention are characterized in that, based in each case on the weight of the entire ready-to-use agent, they are from 10 to 70% by weight, preferably from 20 to 65% by weight, more preferably from 30 to 60% by weight and in particular 35 to 50 wt .-% ethanol and / or isopropanol.
  • 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 of 40 wt .-% to 50 wt .-%, each based on the weight of the cosmetic composition containing.
  • organic solvents or a mixture of solvents having a boiling point below 400 ° C in an amount of 0, 1 to 15 weight percent, preferably from 1 to 10 weight percent based on the total agent may be included.
  • 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 agent according to the invention formed polymer film.
  • 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 1 1.
  • 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.
  • the agents according to the invention preferably additionally comprise at least one surfactant, nonionic, anionic, cationic and ampholytic surfactants in particular being suitable.
  • 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
  • Polyol fatty acid esters such as the commercial product Hydagen ® HSP (Cognis) or
  • R is 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 alkyl radicals having 1 to 4 carbon atoms and w is from 1 to 20,
  • Hydroxy mixed ethers as described, for example, in DE-OS 19738866, sorbitan fatty acid esters and addition products of ethylene oxide onto sorbitan fatty acid esters, for example the polysorbates,
  • 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 preferred alkyl and / or alkenyl oligoglycosides are 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.
  • 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 can be 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. Examples of suitable 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,
  • 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 R-O (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,
  • R 2 is hydrogen, a radical (CH 2 CH 2 0) nR or X, n is from 1 to 10 and X is hydrogen, an alkali 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,
  • R 7 CO- for a linear or branched, aliphatic, saturated and / or unsaturated acyl radical having 6 to 22 carbon atoms, Alk for CH 2 CH 2 , CHCH 3 CH 2 and / or CH 2 CHCH 3 , n for numbers from 0.5 to 5 and M is a cation,
  • Condensation products of C 8 - C 30 - fat 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.
  • 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.
  • cetyl trimethyl ammonium chloride stearyl trimethyl ammonium chloride, distearyl dimethyl ammonium chloride, lauryl dimethyl ammonium chloride, lauryl dimethyl benzyl ammonium chloride and tricetylmethyl ammonium chloride.
  • Further preferred cationic surfactants are the imidazolium compounds known under the INCI names Quaternium-27 and Quaternium-83.
  • Zwitterionic surfactants are surface-active compounds which contain at least one quaternary ammonium group and at least one -COO ⁇ _) in the molecule - Wear group - or -S0 3 ⁇ _).
  • Particularly suitable zwitterionic surfactants are the so-called betaines such as N-alkyl-N, N-dimethylammonium glycinates, for example cocoalkyl dimethylammonium glycinate, N-acylaminopropyl N, N-dimethylammonium glycinates, for example cocoacylaminopropyldimethylammonium glycinate, and 2-alkyl-3-carboxymethyl-3-hydroxyethyl-imidazolines having 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, have at least one free amino group and at least one Contain -COOH- or -S0 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 the d 2 -C 8 -acylsarcosine.
  • compositions of the invention may further contain the auxiliaries and additives which are usually added to conventional styling agents.
  • 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.
  • ⁇ -amino acids and their derivatives 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.
  • amino acid mixtures otherwise obtained may be used in their place, if appropriate.
  • 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.
  • 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 nicotinamide 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.
  • the compositions according to the invention may further contain at least one plant extract.
  • these 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.
  • 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. Furthermore, it may be preferred to use in the compositions according to the invention mixtures of several, especially two, different plant extracts.
  • the 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.
  • 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. According to preferred means according to the invention, in each case based on the weight of the entire ready-to-use agent, 0.05 to 5 wt .-%, preferably 0, 1 to 2.5 wt .-% and in particular 0, 15 to 0.5 wt .-% UV filter substances.
  • 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, cinnamates and o-aminobenzoic acid esters. Preference is given to those UV filters whose molar extinction coefficient at the absorption maximum is above 15,000, in particular above 20,000.
  • compositions according to the invention contain, based in each case on the weight of the total ready-to-use agent, from 0.05 to 5% by weight, preferably from 0.1 to 2.5% by weight and in particular from 0.15 to 0.5% by weight.
  • % Benzophenone-4 and / or isoamyl-p-methoxycinnamate 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. For example, methylcellulose, hydroxyalkylcellulose and carboxymethylcellulose, starch fractions and derivatives such as amylose, amylopectin and dextrins, clays such. 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 a compressed gas container ("aerosol container”) additionally filled with a propellant or a non-aerosol container Valve is distributed, is called by definition as "aerosol container”.
  • a container under normal pressure is defined as a "non-aerosol container” with the aid of which a product is distributed by means of a mechanical action by means of a pumping or squeezing system.
  • 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.
  • the desired amount of blowing agent is introduced.
  • a second subject of the present invention is therefore a kit-of-parts comprising an aerosol delivery device, in particular an aerosol spray device, and a composition based on their weight
  • suitable blowing agents are for example selected from N 2 0, dimethyl ether, C0 2 , air, alkanes having 3 to 5 carbon atoms, such as propane, n-butane, iso-butane, 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.
  • dimethyl ether or 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.
  • the mixtures are again preferably used in the compositions according to the invention in an amount of from 30 to 55% by weight. based on 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.
  • dimethyl ether will be used as the sole blowing agent
  • 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 star 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.
  • suitable propellants are for example selected from N 2 0, dimethyl ether, C0 2 , air, alkanes having 3 to 5 carbon atoms, such as propane, n-butane, isobutane, n-pentane and iso-pentane, and their mixtures.
  • the invention expressly also includes the concomitant use of propellants of the type of chlorofluorocarbons, but in particular of fluorocarbons.
  • the alkanes mentioned, mixtures of said alkanes or mixtures of said alkanes with dimethyl ether are preferably used as the sole blowing agent.
  • Particularly preferred blowing agents are dimethyl ether, propane, n-butane, isobutane and mixtures thereof.
  • the sizes of the foam bubbles and the respective size distribution can be set for a given spraying device.
  • aerosol foam products When conventional aerosol containers are used, aerosol foam products preferably contain the propellant in amounts of from 1 to 35% by weight, 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.
  • at least one further propellant other than isopentane is made up, 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, C0 2 , air, alkanes having 3 or 4 carbon atoms (such as propane, n-butane, iso-butane) and mixtures thereof.
  • compositions according to the invention and products which contain the agents according to the invention, in particular aerosol hair sprays and aerosol hair foams, are distinguished, in particular, by giving treated hair a very natural gloss and strong hold.
  • a second subject of the invention is the use of a composition of the first invention agent for the production of gloss on keratin fibers, in particular human hair.
  • the products according to the invention which contain these agents, in particular aerosol hair sprays, are distinguished in particular by the fact that they give treated hair a very strong, lasting hairstyle hold, although the hair remains flexible.
  • the invention therefore relates to the use of a composition of the first subject of the invention for the temporary deformation of keratin-containing fibers, in particular human hair.
  • Another object of the invention is a method for treating keratin fibers, in particular human hair, wherein a means according to the first subject of the invention is applied as a spray on the keratin-containing fibers using a dispenser.
  • 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.
  • inventively preferred apply the aforementioned dispensing devices or
  • Another object 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 into a foam using a dispenser and the resulting foam is applied to the keratin 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, ie, it is not rinsed out again.
  • inventively preferred are the aforementioned dispensing devices.
  • compositions of the invention After application of funds E1 to E3 on each strand of hair caused these compositions of the invention excellent hairstyle hold. The hair received a pronounced shine and felt supple.

Landscapes

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

Abstract

L'invention concerne des agents pour le traitement de fibres kératiniques, notamment de cheveux humains, contenant dans un véhicule cosmétiquement acceptable : (a) au moins un copolymère anionique fixant, 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), formules dans lesquelles R1 représente un atome d'hydrogène ou un groupe méthyle, R2 représente un atome d'hydrogène ou un groupe méthyle, R3 représente un groupe alkyle (C1 à C20) ramifié, un groupe hydroxyalkyle (C2 à C6) ramifié ou un groupe *-(CH2CH2O)n-R6, R6 représentant un groupe alkyle (C1 à C20) ramifié et n étant compris entre 1 et 30, R4 et R5 représentent un atome d'hydrogène ou un des deux radicaux représente un atome d'hydrogène et l'autre un groupe méthyle, et (b) au moins un polymère comprenant au moins un motif structural de formule (M1). Ces agents confèrent un excellent maintien à une forme appliquée à la fibre, par exemple une coiffure. Ils donnent aux fibres kératiniques un brillant prononcé et un toucher souple.
EP12781358.2A 2011-12-22 2012-11-09 Agents de mise en forme de fibres kératiniques conférant un bon maintien et un aspect naturel Ceased EP2793837A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102011089578A DE102011089578A1 (de) 2011-12-22 2011-12-22 Umformungsmittel für keratinhaltige Fasern vermittelt starken Halt und natürliche Erscheinung
PCT/EP2012/072246 WO2013091993A2 (fr) 2011-12-22 2012-11-09 Agents de mise en forme de fibres kératiniques conférant un bon maintien et un aspect naturel

Publications (1)

Publication Number Publication Date
EP2793837A2 true EP2793837A2 (fr) 2014-10-29

Family

ID=47143140

Family Applications (1)

Application Number Title Priority Date Filing Date
EP12781358.2A Ceased EP2793837A2 (fr) 2011-12-22 2012-11-09 Agents de mise en forme de fibres kératiniques conférant un bon maintien et un aspect naturel

Country Status (4)

Country Link
US (1) US20140348770A1 (fr)
EP (1) EP2793837A2 (fr)
DE (1) DE102011089578A1 (fr)
WO (1) WO2013091993A2 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018073066A1 (fr) * 2016-10-19 2018-04-26 Unilever Plc Spray capillaire comprimé
JP2019532732A (ja) * 2016-10-19 2019-11-14 ユニリーバー・ナームローゼ・ベンノートシヤープ 圧縮ヘアスプレー
DE102017217455A1 (de) * 2017-09-29 2019-04-04 Henkel Ag & Co. Kgaa Mittel und Verfahren zur temporären Verformung keratinhaltiger Fasern
DE102018222047A1 (de) 2018-12-18 2020-06-18 Henkel Ag & Co. Kgaa Zusammensetzung und Verfahren zur temporären Verformung keratinhaltiger Fasern

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7029661B1 (en) * 1995-08-11 2006-04-18 L'oreal Cosmetic composition with a fixing and/or conditioning polymer containing a specific acrylic copolymer
DE19738866A1 (de) 1997-09-05 1999-03-11 Henkel Kgaa Schaumarme Tensidmischungen mit Hydroxymischethern
FR2840208B1 (fr) * 2002-05-31 2005-08-05 Oreal Compositions capillaires contenant au moins un copolymere diblocs amphiphile non-epaississant et au moins un polymere filmogene benefique pour les cheveux
FR2848430B1 (fr) * 2002-12-13 2006-06-23 Composition capillaire comprenant un copolymere filmogene a gradient, composition aerosol la comprenant et procedes de traitement
FR2858979B1 (fr) * 2003-08-22 2005-11-11 Oreal Utilisation d'un copolymere a gradient de composition dans un dispositif aerosol a deux compartiments et dispositif aerosol le comprenant associe a un gaz
DE10357532A1 (de) * 2003-12-08 2005-07-07 Basf Ag Verwendung von Polymerisaten auf Basis von N-Vinylcaprolactam für die Haarkosmetik
US8241616B2 (en) * 2008-04-03 2012-08-14 Rohm And Haas Company Hair styling composition
DE102009020553A1 (de) * 2009-05-08 2010-11-11 Henkel Ag & Co. Kgaa Polymerkombination aus mindestens zwei verschiedenen N-Vinylpyrrolidon/N-Vinylcaprolactam-Copolymeren für glanzgebende kosmetische Haarbehandlungsmittel
DE102009054516A1 (de) * 2009-12-10 2011-06-16 Henkel Ag & Co. Kgaa Polymerkombination für glanzgebende kosmetische Haarbehandlungsmittel mit starkem Halt und gutem Haargefühl

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
None *
See also references of WO2013091993A2 *

Also Published As

Publication number Publication date
WO2013091993A3 (fr) 2014-05-15
WO2013091993A2 (fr) 2013-06-27
DE102011089578A1 (de) 2013-06-27
US20140348770A1 (en) 2014-11-27

Similar Documents

Publication Publication Date Title
EP2509574B1 (fr) Combinaison de polymères pour des agents cosmétiques de traitement capillaire donnant de la brillance, permettant d'obtenir un maintien ferme et un bon toucher des cheveux
EP2717846A1 (fr) Agents de mise en forme des cheveux donnant du brillant, permettant d'obtenir une tenue ferme et un bon toucher des cheveux
EP2717845A1 (fr) Agent de mise en forme à tenue maximale
EP2793837A2 (fr) Agents de mise en forme de fibres kératiniques conférant un bon maintien et un aspect naturel
EP2272499B1 (fr) Produits de coiffage apportant une tenue forte en atmosphère humide
EP2934675A2 (fr) Utilisation d'un agent pour fibres kératiniques, contenant au moins une association de polymeres speciale pour améliorer la tenue de colorations oxydatives de cheveux
WO2011009815A2 (fr) Agents pour fibres kératiniques, contenant au moins un copolymère acrylate/glycérylacrylate, au moins un polymère filmogène et/ou renforçateur et au moins une huile-ester
EP2427171A2 (fr) 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
WO2014095163A2 (fr) Mousse aerosol pour augmenter le volume des cheveux
EP2313078B1 (fr) Préparation pour fibres kératiniques, contenant au moins un polymère cationique amphiphile spécial et au moins un polymère non ionique additionnel spécial filmogène et/ou fixant
WO2010000607A2 (fr) Agent pour fibres kératiniques, comprenant au moins une cellulose spéciale et au moins un polymère supplémentaire filmogène et/ou fixateur
EP2785418B1 (fr) Produits de traitement pour donner du brillant aux cheveux
DE102009045841A1 (de) Kosmetisches Mittel zur Reduktion von überkraustem, störrischem Haar
EP2489345B1 (fr) Produits de coiffage apportant une tenue forte en atmosphère humide III
EP1900772B1 (fr) Fixation de forme de matériaux contenant des fibres à l'aide de polymères
WO2010000608A1 (fr) Agent pour fibres kératiniques, contenant au moins un composé spécial de bétaïne et au moins un polymère filmogène et/ou renforçateur
EP2214624B1 (fr) Produit de coiffage
EP3082745B1 (fr) Produit cosmétique de soin capillaire contenant un agent propulseur
WO2014095162A2 (fr) Mousse aerosol pour augmenter le volume des cheveux
WO2011047943A2 (fr) Polyamides de dimères d'acides gras et de diamines en association avec des copolymères d'acrylamide spéciaux pour la fixation d'une coiffure
WO2009027238A1 (fr) Procédé de mise en forme

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20140226

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

RIN1 Information on inventor provided before grant (corrected)

Inventor name: MUELLER, BURKHARD

Inventor name: SCHMARJE, SUSANNE

DAX Request for extension of the european patent (deleted)
17Q First examination report despatched

Effective date: 20161018

REG Reference to a national code

Ref country code: DE

Ref legal event code: R003

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 20170403