EP2405974A2 - Produit de traitement capillaire contenant de la gelée royale - Google Patents

Produit de traitement capillaire contenant de la gelée royale

Info

Publication number
EP2405974A2
EP2405974A2 EP10707886A EP10707886A EP2405974A2 EP 2405974 A2 EP2405974 A2 EP 2405974A2 EP 10707886 A EP10707886 A EP 10707886A EP 10707886 A EP10707886 A EP 10707886A EP 2405974 A2 EP2405974 A2 EP 2405974A2
Authority
EP
European Patent Office
Prior art keywords
agent
amino
color
hair
composition according
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.)
Withdrawn
Application number
EP10707886A
Other languages
German (de)
English (en)
Inventor
Astrid Kleen
Anja Reichert
Christa Hartwich
Stephan Schwartz
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 EP2405974A2 publication Critical patent/EP2405974A2/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • A61Q5/10—Preparations for permanently dyeing the hair
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/86—Polyethers
    • 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
    • A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
    • A61K8/98—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution of animal origin
    • A61K8/987—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution of animal origin of species other than mammals or birds
    • A61K8/988—Honey; Royal jelly, Propolis
    • 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
    • A61Q5/04—Preparations for permanent waving or straightening the hair
    • 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
    • A61K2800/42—Colour properties
    • A61K2800/43—Pigments; Dyes
    • A61K2800/432—Direct dyes
    • A61K2800/4324—Direct dyes in preparations for permanently dyeing the hair

Definitions

  • the invention relates to an agent for the color and / or permanent change in shape of keratinic fibers, characterized in that it contains in a cosmetic carrier at least one color and / or shape-changing component and an animal care product, in particular royal jelly, in combination with a polyalkoxylated Contains fat body.
  • the compositions according to the invention are particularly suitable for the reduction of hair damage which occurs in connection with the oxidative hair treatment, such as oxidative hair coloring, hair lightening and perming treatment. Therefore, the invention relates to a method of such agents on keratin-containing fibers.
  • the invention relates to the use of the dyeing agent and / or permanent change in shape to reduce hair damage.
  • oxidation colorants For permanent, intensive colorations with corresponding fastness properties, so-called oxidation colorants are used. Such colorants usually contain oxidation dye precursors, so-called developer components and coupler components which form the actual dyes with one another under the influence of oxidizing agents or of atmospheric oxygen.
  • the oxidation dyes are characterized by excellent, long-lasting dyeing results.
  • dyeing or tinting agents For temporary dyeings usually dyeing or tinting agents are used which contain so-called direct drawers as a coloring component. These are dye molecules that attach directly to the substrate and do not require an oxidative process to form the paint.
  • Another dyeing process has received great attention, in the precursors of the natural hair dye melanin on the substrate, eg. As hair, are applied, these then form in the context of oxidative processes in the hair natural analog dyes.
  • the dyes coloring the substrate are usually decolorized oxidatively using appropriate oxidizing agents, such as hydrogen peroxide.
  • oxidizing agents such as hydrogen peroxide.
  • the permanent deformation of keratin fibers is usually carried out by mechanically deforming the fiber and defining the deformation by suitable means.
  • the fiber Before and / or after this deformation, the fiber is treated with the aqueous preparation of a keratin-reducing substance, which part of the disulfide bonds of the keratin to thiol groups, so that it splits to a loosening of the peptide cross-linking and it due to the stress the fiber undergoes a reorientation of the keratinous structure due to the mechanical deformation and rinses after exposure to water or an aqueous solution.
  • the fiber is then treated with the aqueous preparation of an oxidizing agent, under the influence of which disulfide bonds are again knotted, and the keratin structure is then refixed in the predetermined deformation.
  • the fiber of the mechanical deformation aids (winder, Papilloten) freed.
  • One such such method is the permanent wave treatment of human hair. This can be used both to create curls and waves in straight hair and to smooth ruffled hair.
  • the fibers In order to improve the care condition of the fibers, it has long been customary to subject the fibers to a special aftertreatment following the dyeing or shape-changing treatment.
  • the hair is treated with special active ingredients, for example quaternary ammonium salts or special polymers, usually in the form of a rinse.
  • this treatment improves combability, hold and fullness of the hair and reduces the splitting rate.
  • oxidative hair treatment agents are disadvantageous to the user despite their advantageous dyeing, whitening and / or shape-changing properties.
  • the use of oxidants leads to damage in the hair structure and on the hair surface. The hair becomes brittle, its elasticity decreases and the combability decreases. This damage increases with the duration of use.
  • oxidative colorants usually require a basic pH for coloration, in particular between pH 9.0 and pH 10.5.
  • the spread of the outer cuticle layer of the hair associated with the basic pH leads to an unpleasant surface sensation of the hair and thus to a deteriorated combability in the wet and dry state.
  • additional aftertreatment agents such as conditioning agents.
  • the hair structure is also affected by external environmental influences. These include mechanical and thermal effects, such as combing and blow-drying. Likewise, weather influences, such as wind, rain and UV radiation in sunlight, and additional external stresses, such as chlorinated swimming pool water or sweat, contribute to damage to the hair structure and the hair surface.
  • Object of the present invention is therefore to provide a color and / or shape-changing agent, by which the above Disadvantages of conventional color and / or shape-changing agents are lowered.
  • color and / or shape-changing agents hair which has just been attacked and has been damaged by external influences should experience as little additional damage as possible due to changes in color and / or shape.
  • protection against oxidative damage to the hair structure and the hair surface should be achieved by the color and / or shape-changing agents.
  • Nursing properties of the compositions are particularly desirable, so that the user can do without the use of additional conditioning and aftertreatment agents.
  • color and / or shape-changing agents which contain, in addition to a color and / or shape-changing component, at least one polyalkoxylated fatty body and at least one animal care component avoid the abovementioned disadvantages. Due to the protective effect when using the composition according to the invention, the hair damage can be minimized or even a hair care can be achieved.
  • a first subject of the invention is therefore an agent for the color and / or shape change of keratinic fibers, in particular human hair, containing in a cosmetic carrier at least one color and / or shape-changing component, characterized in that the agent additionally at least one polyalkoxylated fatty body and at least one animal care component contains.
  • compositions according to the invention are primarily suitable for dyeing keratin fibers, in principle there is nothing to prevent their use in other fields as well.
  • the agents according to the invention contain the active ingredients in a cosmetic carrier.
  • this cosmetic carrier is aqueous, alcoholic or aqueous-alcoholic.
  • hair coloring such carriers are, for example, creams, emulsions, gels or surfactant-containing foaming solutions, such as shampoos, foam aerosols or other preparations which are suitable for use on the hair.
  • aqueous-alcoholic carriers are water-containing compositions containing 3 to 70% by weight of a C 1 -C 4 -alcohol, based on the total weight of the application mixture, in particular ethanol or isopropanol.
  • an aqueous carrier contains at least 30% by weight, in particular at least 50% by weight, of water, based on the total weight of the application mixture.
  • the agent according to the invention contains an animal care component.
  • animal care component are preferably care substances which are insecticidal products to let win.
  • silk proteins and bee products such as honey, beeswax and royal jelly.
  • Preferred agents according to the invention are characterized in that they contain royal jelly as the animal care component.
  • Royal Jelly is a product of the honey bee and is used as a special feed to raise the queens of the bee colonies. It contains in addition to water about 4 to 5 wt .-% lipids, about 14-16 wt .-% sugar, especially glucose, fructose and sucrose, about 13-14 wt .-% proteins and amino acids and lower levels of vitamins, provitamins and trace elements.
  • This combination of ingredients means that royal jelly develops its care effect even in small amounts on the hair treatment agent.
  • Preferred agents are therefore characterized in that royal jelly is present in an amount of from 0.00001 to 5%, in particular from 0.0001 to 1%, very particularly preferably from 0.01 to 0.5%, in each case based on the total weight of the ready-to-use agent , is included.
  • the agent according to the invention contains at least one polyalkoxylated fatty body.
  • this is understood as meaning a fatty body which has been etherified or esterified at least via one hydroxyl and / or carboxy group with one or more units of ethylene oxide, propylene oxide and or glycerol.
  • polyalkoxylated fatty substances are a) addition products of 4 to 30 moles of ethylene oxide and / or 0 to 5 moles of propylene oxide with linear or branched, saturated or unsaturated fatty alcohols having 8 to 22 carbon atoms, with linear or branched, saturated or unsaturated fatty acids with 12 to 22 C atoms and to alkylphenols having 8 to 15 C atoms in the alkyl group; b) mono- or polyglycerylated linear or branched, saturated or unsaturated fatty alcohols having 8 to 22 C atoms; c) Polyethoxylated fatty acid alkyl esters of the formula RCOO- (C 2 H 4 O) n -R ', where R is a linear or branched, saturated or unsaturated alkyl radical having 7 to 21 C atoms, n is an integer between 1 and 50 and R 'is alkyl of 1 to 30 carbon atoms, preferably 1 to 4 carbon atoms; d
  • Preferred saturated and unsaturated fatty alcohols are capryl alcohol, 2-ethylhexyl alcohol, capric alcohol, lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, linolyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachyl alcohol , Gadoleyl alcohol, behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures.
  • Preferred fatty acids are lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, elaeostearic acid, arachidic acid, gadoleic acid, behenic acid and erucic acid and their natural and / or technical mixtures.
  • Preferred agents are characterized in that the polyalkoxylated fatty body is selected from the group consisting of addition products of polyethylene oxide with fatty alcohols and / or hydroxyl-containing fatty acid triglycerides and with mono- or polyglycerylated fatty alcohols.
  • Examples of mono- or polyglycerylated fatty alcohols are the compounds listed under the INCI names polyglyceryl-4 lauryl ether or polyglyceryl-2 oleyl ether.
  • Particularly preferred agents contain as polyalkoxylated fatty body a polyalkoxylated, hydroxyl-containing fatty acid triglyceride, in particular a polyethylene oxide adduct of hydrogenated and / or hydrogenated castor oil.
  • An addition product of polyethylene oxide onto hydrogenated castor oil has proven to be particularly advantageous, the average degree of ethoxylation being between 1 and 100, preferably between 10 and 75 and in particular between 20 and 60.
  • Preferred examples of such compounds are those under the INCI name PEG-5 hydrogenated Castor OiI, PEG-7 hydrogenated Castor OiI, PEG-10 hydrogenated Castor OiI, PEG-20 hydrogenated Castor OiI, PEG-25 hydrogenated Castor OiI, PEG-40 hydrogenated Castor OiI, PEG-45 hydrogenated Castor OiI, PEG-54 hydrogenated Castor OiI and PEG-60 hydrogenated Castor OiI known compounds, with PEG-40 hydrogenated Castor OiI is particularly preferred.
  • Agents preferred according to the invention comprise the polyalkoxylated fatty body in an amount of from 0.001 to 20% by weight, in particular from 0.01 to 15% by weight, in each case based on the total weight of the ready-to-use agent. It has been found that by the addition of a water-soluble, organic solvent in the composition according to the invention the hair damage can be further reduced and the care performance can be improved.
  • the agent further contains at least one water-soluble, organic solvent.
  • the organic solvents are liquid at room temperature under normal pressure.
  • Preferred organic solvents are d-C ⁇ -alcohols which optionally carry further functional groups for improving the water solubility, such as, for example, 4-methoxybutanol, ethyldiglycol, 1,2-propylene glycol, n-propanol, n-butanol, n-butylene glycol, glycerol, Diethylene glycol monoethyl ether, and diethylene glycol mono-n-butyl ether.
  • Preferred water-soluble organic solvents contain at least two hydroxyl groups.
  • 1,2-ethanediol 1,2-propanediol (1,2-propylene glycol), 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1 , 4-butanediol, 2,3-butanediol, 1, 6-hexanediol, 2- (2-hydroxyethoxy) ethanol and glycerol.
  • 1, 2-propanediol and glycerol Particular preference is given to 1, 2-propanediol and glycerol.
  • agents according to the invention are used particularly advantageously for the color change of keratinic fibers.
  • Agents which are preferred according to the invention are therefore characterized in that the agent contains at least one oxidation dye precursor and / or at least one substantive dye and / or at least one precursor of naturally-analogous dyes and / or at least one brightening agent as a color-changing component.
  • the color-changing components are selected from oxidation dye precursors.
  • the oxidation dye precursors are preferably used in an amount of 0.005 to 20 wt .-%, preferably from 0.05 to 5 wt .-% and particularly preferably from 0.1 to 5 wt .-%, each based on the ready-to-use oxidation colorant.
  • compositions according to the invention contain at least one oxidation dye precursor of the developer type and / or coupler type.
  • the colorants of the present invention contain at least one developer type oxidation dye precursor and at least one coupler type oxidation dye precursor.
  • the developer and coupler components are usually used in free form. In the case of substances having amino groups, however, it may be preferable to use them in salt form, in particular in the form of the hydrochlorides and hydrobromides or the sulfates.
  • Inventive developer components are selected from p-phenylenediamine, binuclear developer components, p-aminophenol, o-aminophenol, heterocyclic developer components and / or the derivatives of the above classes of substances.
  • the developer Components are preferably used in an amount of 0.005 to 20 wt .-%, preferably 0.1 to 5 wt .-%, each based on the ready-to-use oxidation colorant.
  • Preferred p-phenylenediamines are selected from one or more compounds of the group formed from p-phenylenediamine, p-toluenediamine, 2-chloro-p-phenylenediamine, 2,3-dimethyl-p-phenylenediamine, 2,6-dimethyl -p-phenylenediamine, 2,6-diethyl-p-phenylenediamine, 2,5-dimethyl-p-phenylenediamine, N, N-dimethyl-p-phenylenediamine, N, N-diethyl-p-phenylenediamine, N, N-dipropyl -p-phenylenediamine, 4-amino-3-methyl- (N, N-diethyl) aniline, N, N-bis- (2-hydroxyethyl) -p-phenylenediamine, 4-N, N-bis (2-hydroxyethyl ) amino-2-methylaniline, 4-N, N-bis (2
  • Particularly preferred p-phenylenediamine derivatives according to the invention are selected from at least one compound of the group p-phenylenediamine, p-toluenediamine, 2- (2-hydroxyethyl) -p-phenylenediamine, 2- (1, 2-dihydroxyethyl) -p-phenylenediamine, N, N-bis (2-hydroxyethyl) -p-phenylenediamine, N- (4-amino-3-methylphenyl) -N- [3- (1 H -imidazol-1-yl) propyl] amine, 2-methoxymethyl -p-phenylenediamine and the physiologically acceptable salts of these compounds.
  • developer component compounds which contain at least two aromatic nuclei which are substituted by amino and / or hydroxyl groups.
  • preferred binuclear developer components are selected from at least one of the following compounds: N, N'-bis (2-hydroxyethyl) -N, N'-bis (4'-aminophenyl) -1, 3-diamino-propane-2 ol, N, N'-bis (2-hydroxyethyl) -N, N'-bis (4'-aminophenyl) ethylenediamine, N, N'-bis (4'-aminophenyl) tetramethylenediamine, N, N ' Bis (2-hydroxyethyl) -N, N'-bis (4'-aminophenyl) tetramethylenediamine, N, N'-bis [4- (methylamino) phenyl] tetramethylenediamine, N, N'-diethyl-N
  • binuclear developer components are selected from N, N'-bis (2-hydroxyethyl) -N, N'-bis (4-aminophenyl) -1,3-diamino-propan-2-ol, bis ( 2-hydroxy-5-aminophenyl) methane, 1, 3-bis (2,5-diaminophenoxy) propan-2-ol, N, N'-bis (4-aminophenyl) -1, 4-diazacycloheptane, 1, 10-bis (2,5-diaminophenyl) -1, 4,7,10-tetraoxadecane or one of the physiologically acceptable salts of these compounds.
  • p-amino phenol derivative or one of its physiologically tolerable salts.
  • Particularly preferred p-aminophenols are p-aminophenol, N-methyl-p-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 2-hydroxymethylamino-4-aminophenol, 4-amino-3-ol hydroxymethylphenol, 4-amino-2- (2-hydroxyethoxy) phenol, 4-amino-2-methylphenol, 4-amino-2-hydroxy-methylphenol, 4-amino-2-methoxymethyl-phenol, 4-amino-2 -aminomethylphenol, 4-amino-2 - [(2-hydroxyethyl) aminomethyl] phenol, 4-amino-2- (1, 2-dihydroxyethyl) phenol, 4-amino-2-fluorophenol, 4-amino-2-chlorophenol, 4-amino-2,6-dichlorophenol
  • Particularly preferred compounds of the formula (E3) are p-aminophenol, 4-amino-3-methylphenol, 4-amino-2-aminomethylphenol, 4-amino-2- (1, 2-dihydroxyethyl) phenol and 4-amino-2-ol (diethylaminomethyl) phenol.
  • the developer component may be selected from o-aminophenol and its derivatives such as 2-amino-4-methylphenol, 2-amino-5-methylphenol or 2-amino-4-chlorophenol.
  • the developer component may be selected from heterocyclic developer components, such as pyrimidine derivatives, pyrazole derivatives, pyrazolopyrimidine derivatives or their physiologically acceptable salts.
  • Preferred pyrimidine derivatives are the compounds 2,4,5,6-tetraaminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 2-dimethylamino-4,5,6-triaminopyrimidine , 2,4-dihydroxy-5,6-diaminopyrimidine and 2,5,6-triaminopyrimidine.
  • Preferred pyrazole derivatives are the compounds selected from 4,5-diamino-1-methylpyrazole, 4,5-diamino-1- (2-hydroxyethyl) pyrazole, 3,4-diamino-pyrazole, 4,5-diamino-1 - (4'-chlorobenzyl) pyrazole, 4,5-diamino-1,3-dimethylpyrazole, 4,5-diamino-3-methyl-1-phenylpyrazole, 4,5-diamino-1-methyl-3-phenylpyrazole, 4 -Amino-1,3-dimethyl-5-hydrazino-pyrazole, 1-benzyl-4,5-diamino-3-methylpyrazole, 4,5-diamino-3-t-butyl-1-methylpyrazole, 4,5-diamino 1-t-butyl-3-methylpyrazole, 4,5-diamino-1- (2-hydroxyethyl)
  • Preferred pyrazolopyrimidine derivatives are in particular the derivatives of pyrazolo [1, 5-a] pyrimidine and its tautomeric forms, provided that a tautomeric equilibrium exists.
  • the pyrazolo [1,5-a] pyrimidines are in particular selected from pyrazolo [1,5-a] pyrimidine-3,7-diamine, 2,5-dimethylpyrazolo [1,5-a] pyrimidin-3, 7-diamine, pyrazolo [1,5-a] pyrimidine-3,5-diamine, 2,7-dimethylpyrazolo [1,5-a] pyrimidine-3,5-diamine, 3-aminopyrazolo [1, 5 a] pyrimidin-7-ol, 3-amino-pyrazolo [1,5-a] pyrimidin-5-ol, 2- (3-aminopyrazolo [1,5-a] pyrimidin-7-ylamino) ethanol,
  • Very particularly preferred developer components are selected from at least one compound from the group formed from p-phenylenediamine, p-toluenediamine, 2- (2-hydroxyethyl) -p-phenylenediamine, 2- (1, 2-dihydroxyethyl) -p phenylenediamine, N, N-bis- (2-hydroxy-ethyl) -p-phenylenediamine, 2-methoxymethyl-p-phenylenediamine, N- (4-amino-3-methylphenyl) -N- [3- (1H- imidazol-1-yl) propyl] amine, N, N'-bis (2-hydroxyethyl) -N, N'-bis (4-aminophenyl) -1, 3-diamino-propan-2-ol, bis- (2-hydroxy-5-aminophenyl) methane, 1, 3-bis (2,5-diaminophenoxy) -propan-2-ol, N, N
  • Coupler components do not form a significant color within the framework of the oxidative dyeing alone, but always require the presence of developer components. Therefore, it is preferred according to the invention that at least one developer component is additionally used when using at least one coupler component.
  • Coupler components according to the invention are preferably selected from m-aminophenol, m-diaminobenzene, o-diaminobenzene, o-aminophenol, naphthalene derivatives having at least one hydroxyl group, di- or trihydroxybenzene, pyridine, pyrimidine, monohydroxy- or monoaminoindole, monohydroxy- or monoaminoindoline, pyrazolone , Benzomorpholine, quinoxaline and / or the derivatives of the preceding classes of substances.
  • the coupler components are preferably used in an amount of 0.005 to 20 wt .-%, preferably 0.1 to 5 wt .-%, each based on the ready-to-use oxidation colorant.
  • the inventively preferred m-aminophenols or derivatives thereof are selected from at least one compound from the group formed from m-aminophenol, 5-amino-2-methylphenol, N-cyclopentyl-3-aminophenol, 3-amino-2 chloro-6-methylphenol, 2-hydroxy-4-aminophenoxyethanol, 2,6-dimethyl-3-aminophenol, 3-trifluoroacetylamino-2-chloro-6-methylphenol, 5-amino-4-chloro-2-methylphenol, 5-amino-4-methoxy-2-methylphenol, 5- (2'-hydroxyethyl) amino-2-methylphenol, 3-diethylaminophenol, N-cyclopentyl-3-aminophenol, 1, 3-dihydroxy-5-methylaminobenzene, 3-ethylamino-4-methylphenol, 2,4-dichloro-3-aminophenol and the physiologically acceptable salts of all the compounds mentioned above.
  • the inventively preferred m-diaminobenzenes or derivatives thereof are selected from at least one compound from the group formed from m-phenylenediamine, 2- (2,4-diaminophenoxy) ethanol, 1, 3-bis (2,4-diaminophenoxy ) propane, 1-methoxy-2-amino-4- (2'- hydroxyethylamino) benzene, 1, 3-bis (2,4-diaminophenyl) propane, 2,6-bis (2'-hydroxyethylamino) -1-methylbenzene, 2 - ( ⁇ 3 - [(2-hydroxyethyl) amino] -4 -methoxy-5-methylphenyl ⁇ amino) ethanol, 2 - ( ⁇ 3 - [(2-hydroxyethyl) amino] -2-methoxy-5-methylphenyl ⁇ amino) ethanol, 2 - ( ⁇ 3 - [(2-hydroxyethyl) amino] -2-methoxy-5-methylphenyl ⁇ amino)
  • inventively preferred o-diaminobenzenes or derivatives thereof are selected from at least one compound from the group which is formed from 3,4-diaminobenzoic acid and 2,3-diamino-1-methylbenzene and the physiologically acceptable salts of said compounds.
  • Preferred di- or trihydroxybenzenes and their derivatives are selected from at least one compound of the group formed from resorcinol, resorcinol monomethyl ether, 2-methylresorcinol, 5-methylresorcinol, 2,5-dimethylresorcinol, 2-chlororesorcinol, 4-chlororesorcinol, pyrogallol and 1, 2,4-trihydroxybenzene.
  • the preferred pyridine derivatives according to the invention are selected from at least one compound of the group formed from 2,6-dihydroxypyridine, 2-amino-3-hydroxypyridine, 2-amino-5-chloro-3-hydroxypyridine, 3-amino-2-methylamino 6-methoxypyridine, 2,6-dihydroxy-3,4-dimethylpyridine, 2,6-dihydroxy-4-methylpyridine, 2,6-diaminopyridine, 2,3-diamino-6-methoxypyridine, 3,5-diamino 2,6-dimethoxypyridine, 3,4-diaminopyridine, 2- (2-methoxyethyl) amino-3-amino-6-methoxypyridine, 2- (4'-methoxyphenyl) amino-3-aminopyridine, and the physiologically acceptable salts of aforementioned compounds.
  • Preferred naphthalene derivatives having at least one hydroxy group are selected from at least one compound of the group formed from 1-naphthol, 2-methyl-1-naphthol, 2-hydroxymethyl-1-naphthol, 2-hydroxyethyl-1-naphthol, 1, 3 Dihydroxynaphthalene, 1, 5-dihydroxynaphthalene, 1, 6-dihydroxynaphthalene, 1, 7-dihydroxynaphthalene, 1, 8-dihydroxynaphthalene, 2,7-dihydroxynaphthalene and 2,3-dihydroxynaphthalene.
  • inventively preferred indole derivatives are selected from at least one compound of the group which is formed from 4-hydroxyindole, 6-hydroxyindole and 7-hydroxyindole and the physiologically acceptable salts of the aforementioned compounds.
  • inventively preferred indoline derivatives are selected from at least one compound of the group which is formed from 4-hydroxyindoline, 6-hydroxyindoline and 7-hydroxyindoline and the physiologically acceptable salts of the aforementioned compounds.
  • Preferred pyrimidine derivatives are selected from at least one compound of the group formed from 4,6-diaminopyrimidine, 4-amino-2,6-dihydroxypyrimidine, 2,4-diamino-6- hydroxypyrimidine, 2,4,6-trihydroxypyrimidine, 2-amino-4-methylpyrimidine, 2-amino-4-hydroxy-6-methylpyrimidine and 4,6-dihydroxy-2-methylpyrimidine and the physiologically acceptable salts of the abovementioned compounds.
  • coupler components according to the invention are selected from 3-aminophenol, 5-amino-2-methylphenol, 3-amino-2-chloro-6-methylphenol, 2-hydroxy-4-aminophenoxyethanol, 5-amino-4-chloro-2 methylphenol, 5- (2-hydroxyethyl) amino-2-methylphenol, 2,4-dichloro-3-aminophenol, 2-aminophenol, 3-phenylenediamine, 2- (2,4-diaminophenoxy) ethanol, 1, 3 Bis (2,4-diaminophenoxy) propane, 1-methoxy-2-amino-4- (2-hydroxyethylamino) benzene, 1, 3-bis (2,4-diaminophenyl) propane, 2,6-bis (2'-bis) hydroxyethylamino) -1-methylbenzene, 2 - ( ⁇ 3 - [(2-hydroxyethyl) amino] -4-methoxy-5-methylphenyl ⁇ amino) ethanol, 2 - ( ⁇ (2-
  • developer components and coupler components are generally used in approximately molar amounts to each other.
  • a certain excess of individual oxidation dye precursors is not disadvantageous, so that developer components and coupler components in a molar ratio of 1: 0.5 to 1: 3, in particular 1: 1 to 1: 2 , can stand.
  • the agents according to the invention may contain as dye-changing component at least one substantive dye.
  • These are dyes that raise directly on the hair and do not require an oxidative process to form the color.
  • Direct dyes are usually nitrophenylenediamines, nitroaminophenols, azo dyes, anthraquinones or indophenols.
  • the substantive dyes are each preferably used in an amount of 0.001 to 20 wt .-%, based on the total application preparation. The total amount of substantive dyes is preferably at most 20% by weight.
  • Direct dyes are known as anionic, cationic and nonionic substantive dyes.
  • Preferred anionic substantive dyes are those under the international designations or trade names Acid Yellow 1, Yellow 10, Acid Yellow 23, Acid Yellow 36, Acid Orange 7, Acid Red 33, Acid Red 52, Pigment Red 57: 1, Acid Blue 7, Acid Green 50, Acid Violet 43, acid black 1, acid black 52, bromophenol blue and tetrabromophenol blue known compounds.
  • Preferred cationic substantive dyes are cationic triphenylmethane dyes such as Basic Blue 7, Basic Blue 26, Basic Violet 2 and Basic Violet 14, 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 direct dyes which contain a heterocycle which has at least one quaternary nitrogen atom, in particular Basic Yellow 87, Basic Orange 31 and Basic Red 51.
  • the cationic direct dyes that sold under the trademark Arianor ® are also very particularly preferred cationic substantive dyes according to the invention.
  • Suitable nonionic substantive dyes are in particular nonionic nitro and quinone dyes and neutral azo dyes.
  • Preferred nonionic substantive dyes are those under the international designations or trade names HC Yellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, HC Yellow 12, HC Orange 1, Disperse Orange 3, HC Red 1, HC Red 3, HC HC Red 11, HC Red 11, HC Red 11, HC Blue 11, HC Blue 2, HC Blue 11, HC Blue 12, Disperse Blue 3, HC Violet 1, Disperse Violet 1, Disperse Violet 4, Disperse Black 9 well-known compounds, as well 1,4-diamino-2-nitrobenzene, 2-amino-4-nitrophenol, 1,4-bis (2-hydroxyethyl) amino-2-nitrobenzene, 3-nitro-4- (2-hydroxyethyl) aminophenol, 2 - (2-hydroxyethyl) amino-4,6-dinitrophenol, 4 - [(2-hydroxyethyl) amino] -3-nitro-1-methylbenzene, 1-a
  • the color-modifying component is selected from dye precursors of naturally-analogous dyes.
  • the dyestuff precursors of naturally-analogous dyes are preferably indoles and indolines which have at least two groups selected from hydroxy and / or amino groups, preferably as a substituent on the six-membered ring. These groups can carry further substituents, eg. In the form of etherification or esterification of the hydroxyl group or alkylation of the amino group.
  • the colorants contain at least one indole and / or indoline derivative.
  • Compositions according to the invention which comprise precursors of naturally-analogous dyes are preferably used as air-oxidative colorants. Consequently, in this embodiment said compositions are not added with an additional oxidizing agent.
  • the dye precursors of naturally-analogous dyes are each preferably in an amount of 0.001 to 5 wt .-%, based on the total Application preparation, used. The total amount of substantive dyes is preferably at most 3% by weight.
  • Preferred derivatives of indoline are 5,6-dihydroxyindoline, N-methyl-5,6-dihydroxyindoline, N-ethyl-5,6-dihydroxyindoline, N-propyl-5,6-dihydroxyindoline, N-butyl-5,6- dihydroxyindoline and 5,6-dihydroxyindoline-2-carboxylic acid, especially N-methyl-5,6-dihydroxyindoline, N-ethyl-5,6-dihydroxyindoline, N-propyl-5,6-dihydroxyindoline, N-butyl-5,6 dihydroxyindoline, and more preferably 5,6-dihydroxyindoline.
  • Preferred derivatives of indole are 5,6-dihydroxyindole, N-methyl-5,6-dihydroxyindole, N-ethyl-5,6-dihydroxyindole, N-propyl-5,6-dihydroxyindole, N-butyl-5,6-dihydroxyindole , 5,6-dihydroxyindole-2-carboxylic acid, preferably N-methyl-5,6-dihydroxyindole, N-ethyl-5,6-dihydroxyindole, N-propyl-5,6-dihydroxyindole, N-butyl-5,6- dihydroxyindole and in particular 5,6-dihydroxyindole.
  • oxidation dye precursors direct dyes or naturally-analogous dyes to be each one of the same compounds. Rather, 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 dyeing or for other reasons, eg. As toxicological, must be excluded.
  • the color changing component is selected from brighteners.
  • lightening agents are usually chemical oxidants which help to break down natural and artificial dyes in the hair and bleach the hair.
  • brighteners therefore, come persulfates, Peroxomonosulfate, chlorites, hypochlorites and in particular hydrogen peroxide or its addition products of urea, melamine and sodium borate in question.
  • compositions according to the invention may also contain blonding and / or bleaching agents and thus be provided as agents which simultaneously have a coloring and lightening effect.
  • agents will hereinafter be referred to as "colorants”, as “whitening colorants” or as “colorants and whiteners”.
  • Hydrogen peroxide is preferably used as oxidizing agent.
  • the amount of hydrogen peroxide in the ready-to-use agent is preferably from 0.5 to 12% by weight, preferably from 0.8 to 6% by weight, in each case based on the ready-to-use agent.
  • Such oxidizer formulations are preferably aqueous, flowable oxidizer formulations.
  • Preferred preparations are characterized in that the flowable oxidizing agent preparation - based on their weight - 40 to 90 wt .-%, preferably 50 to 85 wt .-%, particularly preferably 55 to 80 wt .-%, more preferably 60 to 77, 5 wt .-% and in particular 65 to 75 wt .-% water.
  • the development of the color can in principle be done with atmospheric oxygen.
  • a chemical oxidizing agent is used, especially if, in addition to the coloring, a lightening effect on human hair is desired.
  • the color-changing agent can also be applied to the hair as an oxidation dye together with a catalyst which activates the oxidation of the dye precursors, for example by atmospheric oxygen.
  • a catalyst which activates the oxidation of the dye precursors, for example by atmospheric oxygen.
  • Such catalysts are z.
  • Preferred persulfate salt are ammonium peroxodisulfate, potassium peroxodisulfate and sodium peroxodisulfate.
  • the peroxodisulfate salts may be contained in an amount of from 0.1 to 25% by weight, in particular in an amount of from 0.5 to 15% by weight, based on the total weight of the ready-to-use agent.
  • the use of persulfate salts or peroxodisulfate salts is generally carried out in the form of an optionally dedusted powder or a molding pressed into the mold.
  • the actual coloring and / or brightening agent is expediently prepared immediately before use by mixing a preparation according to the invention comprising at least one oxidation dye precursor in a cosmetic carrier and a preparation containing the additional oxidizing agent, in particular hydrogen peroxide.
  • the agent according to the invention may contain the combination of royal jelly and at least one polyalkoxylated fatty substance in the preparation with oxidation dye precursors and / or in the oxidizing agent preparation.
  • the preparation with oxidation dye precursors preferably contains a combination of royal jelly and at least one polyalkoxylated fatty body.
  • a bleaching preparation containing at least one inorganic compound is admixed with the oxidizing agent preparation before mixing with the dyeing preparation according to the invention.
  • compositions according to the invention are furthermore used particularly advantageously for changing the shape of keratinic fibers.
  • Agents which are preferred according to the invention are therefore characterized in that the agent contains as the shape-modifying component at least one keratin-reducing substance, preferably mercaptans.
  • Means for changing the shape usually consist of two or three preparations, which are successively applied to the fibers. The following terms are used below:
  • the corrugating agents according to the invention necessarily contain at least one keratin-reducing substance as a shape-changing component, preferably mercaptans.
  • a shape-changing component preferably mercaptans.
  • Such compounds are, for example, thioglycolic acid, thiolactic acid, thiomalic acid, mercaptoethanesulfonic acid and its salts and esters, cysteamine, cysteine, Bunte salts and salts of sulfurous acid.
  • suitable as shape-changing components are the alkali metal or ammonium salts of thioglycolic acid and / or thiolactic acid and the free acids.
  • the corrugating agents according to the invention usually contain alkalizing agents such as ammonia, alkali metal and ammonium carbonates and bicarbonates or organic amines such as monoethanolamine.
  • the corrugated lotions according to the invention may contain components which enhance the power, preferably selected from heterocyclic compounds such as imidazole, pyrrolidine, piperidine, dioxolane, dioxane, morpholine, piperazine and derivatives of these compounds, in particular 1-methylimidazole, 2-methylimidazole, 4 (5) -methylimidazole, 1 , 2-dimethylimidazole, 2-ethylimidazole, 2-isopropylimidazole, N-methylpyrrolidone, 1-methylpiperidine, 4-methylpiperidine, 2-ethylpiperidine, 4-methylmorpholine, 4- (2-hydroxyethyl) morpholine, 1-ethylpiperazine, 1- (2-hydroxyethyl) piperazine, 1- (2-aminoethyl) piperazine, biotin, hydantoin and benzimidazole, with imidazole being particularly preferred;
  • heterocyclic compounds such as imidazo
  • Amino acids such as in particular arginine, citrulline, histidine, ornithine, lysine, oligopeptides from an average of 2-3 amino acids, which have a high proportion (> 50%, especially> 70%) of the amino acids mentioned, and their salts, preferably arginine and its salts and arginine-rich oligopeptides;
  • Diols such as 2-ethyl-1, 3-hexanediol, 1, 3-butanediol, 1, 4-butanediol, 1, 2-propanediol, 1, 3-propanediol, neopentyl glycol and ethylene glycol, wherein 1, 3-diols, especially 2 Ethyl-1, 3-hexanediol and 1, 3-butanediol are particularly preferred.
  • the wellenverstärverEntnden compounds may be present in the corrugated lotions according to the invention in amounts of 0.5 to 5 wt .-%, based on the total wave lotion. Amounts of 1 to 4 wt .-%, in the case of the diols of 0.5 to 3 wt .-%, have been found to be sufficient, which is why these amounts are particularly preferred.
  • oxidizing agents for.
  • Aqueous H 2 O 2 preparations which can be used according to the invention contain about 0.5 to 15% by weight, usually about 0.5 to 3% by weight, hydrogen peroxide, ready for use.
  • the pH of such aqueous H 2 O 2 preparations is preferably from 2 to 6, in particular from 2 to 4, and is adjusted by inorganic acids, preferably phosphoric acid.
  • Bromate-based fixatives are usually used in concentrations of from 1 to 10% by weight and the pH of the solutions is adjusted to 4 to 7.
  • enzymatic-based fixatives eg peroxidases
  • corrugating agents or fixing agents according to the invention are usually formulated in a single phase, including by this term are systems which have a continuous phase, such as, for example, pure oil-in-water or water-in-oil emulsions. It has been found that two-phase and multi-phase systems according to the invention are also preferred. These are systems where there are at least two separate, continuous phases.
  • oxidizing agent preparations of oxidation colorants, brightening agents and / or fixing agents of shape-changing agents contain at least one stabilizer or complexing agent.
  • Customary and preferred chelating agents in the context of the present invention are, for example, polycarboxylic acids, nitrogen-containing mono- or polycarboxylic acids, especially ethylenediaminetetraacetic acid (EDTA), ethylenediamine disuccinic acid (EDDS) and nitrilotriacetic acid (NTA), geminal diphosphonic acids, in particular 1-hydroxyethane-1,1-diphosphonic acid (HEDP), aminophosphonic acids, such as ethylenediaminetetra (methylenephosphonic acid) (EDTMP), diethylenetriaminepenta- (methylenephosphonic acid) (DTPMP), phosphonopolycarboxylic acids, such as 2-phosphonobutane-1, 2,4-tricarboxylic acid, and cyclodextrins, alkali
  • compositions of the invention contain other auxiliaries and additives.
  • the ready-to-use agents are flowable preparations.
  • the flowable preparations preferably additionally comprise as surfactant an emulsifier or a surfactant, surface-active substances being referred to as surfactants or as emulsifiers, depending on the field of application, and of anionic, cationic, amphoteric, zwitterionic and nonionic surfactants and emulsifiers are selected. These substances will be described in detail below.
  • Suitable anionic surfactants in preparations according to the invention are all anionic surfactants suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic, saturated or unsaturated alkyl group having about 8 to 30 carbon atoms and 0, 1, 2 or 3 double bonds ,
  • anionic group such as a carboxylate, sulfate, sulfonate or phosphate group
  • a lipophilic, saturated or unsaturated alkyl group having about 8 to 30 carbon atoms and 0, 1, 2 or 3 double bonds
  • glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups may be present in the molecule.
  • Alkyl sulfates and alkyl ether sulfates of the formula RO (CH 2 CH 2 O) x SO 3 H, in which R is a preferably linear alkyl group and x 0 or a number from 1 to 12,
  • Esters of tartaric acid and citric acid with alcohols the addition products of about 2 to 15 molecules of ethylene oxide and / or propylene oxide with fatty alcohols,
  • RO (C 2 H 4 O) ⁇ P-OR 'OH in the R is preferably an aliphatic, optionally unsaturated hydrocarbon radical having 8 to 30 carbon atoms
  • R' is hydrogen
  • a radical (CH 2 CH 2 O) y R and x and y is independently a number from 1 to 10
  • sulfated fatty acid alkylene glycol esters of the formula RC (O) O (alkO) n SO 3 H in which R is a linear alkyl radical, alk is CH 2 CH 2 , CHCH 3 CH 2 and / or CH 2 CHCH 3 and n is a number from 0.5 to 5, monoglyceride sulfates and monoglyceride ether sulfates.
  • Preferred anionic surfactants are alkyl sulfates, alkyl ether sulfates, each having from 10 to 18 carbon atoms in the alkyl group, and polyalkoxylated ether carboxylic acids having from 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in the molecule.
  • Zwitterionic surfactants are surface-active compounds which carry at least one quaternary ammonium group and at least one carboxylate, sulfonate or sulfate group in the molecule.
  • Particularly suitable zwitterionic surfactants are the so-called betaines such as N-alkyl-N, N-dimethylammonium glycinates, for example cocoalkyldimethylammonium glycinate, N-acylaminopropyl N, N-dimethylammonium glycinates, for example cocoacylaminopropyldimethylammonium glycinate, and Alkyl-3-carboxymethyl-3-hydroxyethyl imidazolines having in each case 8 to 18 C atoms in the alkyl or acyl group and the coco acylaminoethylhydroxyethylcarboxymethylglycinate.
  • a preferred zwitterionic surfactant is the fatty acid amide derivative known by the INCI
  • the agent further contains at least one amphoteric surfactant.
  • Amphoteric surfactants are understood to mean 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 which are capable of forming internal salts .
  • suitable amphoteric surfactants 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.
  • amphoteric surfactants are sold under the INCI name Dime cocoamphodipropionate with the trade names Miranol C2M SF conc. (Rhodia), Amphoterge K-2 (Lonza) and Monateric CEM-38 (Unichema) and designation Disodium Cocoamphoacetate with the trade names Dehyton (Cognis), Miranol C2M (Rhodia) and Ampholak XCO 30 (Akzo Nobel).
  • composition according to the invention produces an excellent finish, in particular improved wet combability.
  • the brightening agents according to the invention in addition to the above-described polyalkoxylated fatty bodies contain additional nonionic surfactants.
  • Such compounds are for example C 2 -C 3 o-fatty acid mono- and - diesters of addition products of 1 to 30 mol ethylene oxide onto glycerol; Polyglycerol esters and alkoxylated polyglycerol esters, such as poly (3) glycerol diisostearate (commercial product: Lameform ® TGI (Henkel)) and poly (2) glycerinpolyhydroxy stearate (commercial product: Dehymuls ® PGPH (Henkel)); alkoxylated, preferably propoxylated and in particular ethoxylated, mono-, di- and triglycerides, such as, for example, glycerol monolaurate + 20 EO (mol of ethylene oxide) and glycerol monostearate + 20 EO; Amine oxides
  • Suitable nonionic surfactants are, in particular, C 8 -C 22 -alkyl mono- and -oligoglycosides and their ethoxylated analogs.
  • the nonethoxylated compounds have been found to be particularly suitable.
  • R consists essentially of C 8 and C 14 alkyl groups from C 8 -C 6 alkyl groups, from Ci 2 -Ci 6 alkyl groups or Ci 6 -Ci 8 alkyl groups.
  • sugar building block Z it is possible to use any desired mono- or oligosaccharides.
  • sugars with 5 or 6 carbon atoms and the corresponding oligosaccharides are used.
  • Such sugars are, for example, glucose, fructose, galactose, arabinose, ribose, xylose, lyxose, allose, altrose, mannose, gulose, idose, talose and sucrose.
  • Preferred sugar building blocks are glucose, fructose, galactose, arabinose and sucrose; Glucose is particularly preferred.
  • the alkyl polyglycosides which can be used according to the invention contain on average from 1.1 to 5 sugar units. Alkyl polyglycosides having x values of 1.1 to 2.0 are preferred. Very particular preference is given to alkyl glycosides in which x is 1: 1 to 1, 8.
  • the anionic, additional nonionic, zwitterionic and amphoteric surfactants are in preferably in a total amount of 0.1 to 45 wt.%, Preferably 1 to 30 wt.% And most preferably from 1 to 20 wt.%, Based on the total amount of ready-to-use agent.
  • quaternary ammonium compounds are ammonium halides, in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides, eg.
  • the long alkyl chains of the above-mentioned surfactants preferably have 10 to 18 carbon atoms.
  • Further cationic surfactants which can be used according to the invention are the quaternized protein hydrolysates.
  • esterquats are known substances which contain at least one ester function as well as at least one quaternary ammonium group as a structural element.
  • Preferred ester quats are quaternized ester salts of fatty acids with triethanolamine, quaternized ester salts of fatty acids with diethanolalkylamines and quaternized ester salts of fatty acids with 1,2-dihydroxypropyldialkylamines, such as N, N-bis (2-palmitoyloxyethyl) dimethylammonium chloride.
  • Such products are sold, for example, under the trademarks Stepantex, Dehyquart and Armocare.
  • the cationic surfactants are contained in the compositions according to the invention preferably in amounts of 0.05 to 10 wt .-%, based on the total agent. Levels of 0.1 to 5% by weight are particularly preferred.
  • agents contain at least one thickener.
  • thickeners there are no fundamental restrictions. Both organic and purely inorganic thickening agents can be used.
  • the thickener is an anionic, synthetic polymer.
  • Preferred anionic polymers are acrylic acid and / or methacrylic acid polymers or copolymers which are preferably used in the compositions according to the invention in an amount of from 0.1 to 10% by weight, particularly preferably from 1 to 5% by weight, based in each case on the weight of the agent, are included.
  • the thickener is a cationic synthetic polymer.
  • Preferred cationic groups are quaternary ammonium groups. In particular, such polymers in which the quaternary ammonium group are bonded via a C 1 -C 4 -hydrocarbon group to a polymer main chain composed of acrylic acid, methacrylic acid or derivatives thereof have proven to be particularly suitable.
  • Such polymers can also be used as copolymers with nonionic monomer units, preferably acrylamide, methacrylamide, acrylic acid-C 1 -C 4 -alkyl ester and methacrylic acid-C 1 -C 4 -alkyl ester.
  • nonionic, fully synthetic polymers such as polyvinyl alcohol or polyvinylpyrrolidinone, are also useful as thickeners of the invention. Preference is furthermore given to using naturally occurring, optionally modified thickening agents.
  • guar gums such as gum arabic, ghatti gum, karaya gum, tragacanth gum, carrageenan gum, agar agar, locust bean gum, pectins, alginates, starch, starch fractions and derivatives such as Amylose, amylopectin and dextrins, cellulose derivatives, for example methylcellulose, carboxyalkylcelluloses and hydroxyalkylcelluloses.
  • phyllosilicates polymeric, crystalline sodium disilicates
  • the agents additionally contain at least one further active substance which synergistically improves the care properties of the agents.
  • This active ingredient is preferably selected from the group consisting of amino acids, oligopeptides and protein hydrolysates; Silicone derivatives; Polyphenols and (pseudo) ceramides.
  • the agent according to the invention additionally contains at least one further active ingredient selected from the group consisting of amino acids, oligopeptides and protein hydrolysates.
  • active ingredient refers to amino acids themselves and their oligomers and polymers linked via peptical bonds, in particular oligopeptides and protein hydrolysates.
  • An amino acid in the context of the invention is an organic compound which carries in its structure at least one protonatable amino group and at least one carboxylic acid or sulfonic acid group.
  • Preferred amino acids are aminocarboxylic acids, in particular ⁇ -aminocarboxylic acids and ⁇ -amino-carboxylic acids, ⁇ -aminocarboxylic acids being preferred.
  • the active ingredient of at least one amino acid, an oligopeptide or a protein hydrolyzate is preferably present in the agents according to the invention in amounts of from 0.01 to 10% by weight, in particular from 0.05 to 5% by weight, based on the total weight of the application mixture, contain.
  • Preferred silicone derivatives are functionalized and nonfunctionalized, optionally branched polyalkylsiloxanes, polyarylsiloxanes, polyalkylarylsiloxanes, such as dimethicones, amodimethicones, cyclomethicones and dimethicone copolyols.
  • Preferred agents contain silicone derivatives preferably in amounts of 0.01 to 5 wt .-%, preferably from 0.05 to 2 wt .-%, each based on the ready-to-use agent.
  • Polyphenols are generally compounds which contain more than two phenol (polyol) or phenol ether groups, which belong to different substance classes.
  • the polyphenols are preferably selected from at least one member of the group formed from hydroxy cinnamic acids, 6,7-dihydroxycumarines, hydroxybenzoic acids, catechins, leucoanthocyanidines, anthocyanidines, flavanones, flavones and flavonols.
  • Preferred ceramides are the sphingolipids.
  • Preferred compounds according to the invention are the compounds ceramides I, ceramides II, ceramides 1, ceramides 2, ceramides 3, ceramides 5 and ceramides 6 known under the INCI names as the active ingredient. Particular preference is given to using mixtures of such compounds, which are obtainable, for example, under the trade names SK-Influx and Ceramide III from Degussa Care Specialties, respectively, and the commercial product Ceramide TIC-001, which is marketed by Takasago International Corporation. These compounds are preferably used in an amount of 0.01 to 1.0% by weight, based on the weight of the ready-to-use cosmetic product.
  • the agents according to the invention may contain further active ingredients, auxiliaries and additives, such as nonionic polymers, cationic polymers, zwitterionic and amphoteric polymers, anionic polymers, structurants such as glucose, maleic acid and lactic acid, hair conditioning compounds such as phospholipids, fiber-structure-improving active ingredients, in particular Mono-, di- and oligosaccharides such as glucose, galactose, fructose, fructose and lactose, defoamers such as silicones, preferably dimethicone, dyes for staining the agent, anti-dandruff agents, light stabilizers, drugs such as panthenol, pantothenic acid, pantolactone, allantoin, Pyrrolidinoncarbonklaren and salts thereof and bisabolol, vitamins, provitamins and vitamin precursors, in particular those of the groups A, B 3 , B 5 , B 6 , C, E, F and H, plant extract
  • the ready-to-use agent has a pH between 4.0 and 12.0, preferably between 5.0 and 11, 5, particularly preferably between 6.0 and 11, 0.
  • the pH values for the purposes of the present invention are pH values which were measured at a temperature of 22 ° C.
  • the pH is adjusted with pH adjusters. In order to adjust the pH, those skilled in the art are familiar with common acidifying and alkalizing agents.
  • the alkalizing agents which can be used for adjusting the pH are typically selected from inorganic salts, in particular the alkali metals and alkaline earth metals, organic alkalizing agents, in particular amines, basic amino acids and alkanolamines, and ammonia.
  • Acidifying agents which are preferred according to the invention are pleasure acids, such as, for example, citric acid, acetic acid, malic acid or tartaric acid, and also dilute mineral acids.
  • Alkaliating agents which are preferred according to the invention are selected from the group formed from sodium hydroxide, potassium hydroxide, calcium hydroxide, barium hydroxide, sodium phosphate, potassium phosphate, sodium silicate, potassium silicate, sodium carbonate, potassium carbonate, 2-aminoethane-1.
  • ol monoethanolamine
  • triethanolamine triethanolamine, ammonia, 1-aminopropan-2-ol and 2-amino-2-methyl-propan-1-ol.
  • the formulation of the inventive color and shape-changing agents is subject in principle to no restrictions.
  • the agents according to the invention are formulated as 1-component agents, which are optionally mixed with a second preparation containing, for example, an oxidizing agent immediately before use.
  • a second preparation containing, for example, an oxidizing agent immediately before use.
  • the product is formulated as a 2-component agent.
  • the means according to the invention are therefore made up in such a way that one of the components essential to the invention is packaged separately. According to the invention, it does not initially matter which of the components according to the invention is packaged separately; however, it may be preferable to package the preparation containing the animal care component separately until use.
  • Agents preferred according to the invention are characterized in that the agent is prepared immediately before use by mixing at least two preparations, wherein the at least two preparations are provided in at least two separate prefabricated containers and wherein a container is a colorant, which in a cosmetic carrier at least one oxidation dye precursor and at least one polyalkoxylated fatty body and at least one animal care component, preferably royal jelly, contains and has a pH between 5.0 and 12.0, preferably between 6.0 and 1 1, 0, and another container contains an oxidizing agent containing at least one oxidizing agent.
  • a container is a colorant, which in a cosmetic carrier at least one oxidation dye precursor and at least one polyalkoxylated fatty body and at least one animal care component, preferably royal jelly, contains and has a pH between 5.0 and 12.0, preferably between 6.0 and 1 1, 0, and another container contains an oxidizing agent containing at least one oxidizing agent.
  • Another object of the present invention is a process for the color and / or permanent change in shape keratinic fibers, in which an inventive composition according to the above specifications is applied to the hair, for a contact time of 2 to 45 minutes, preferably from 15 to 30 minutes the hair is left, and then the hair is rinsed out.
  • a preferred embodiment of the process according to the invention for the color change of keratinic fibers is when a composition in a cosmetic carrier containing at least one oxidation dye precursor and at least one polyalkoxylated fatty body and at least one animal care component, preferably royal jelly, with an oxidizing agent preparation containing hydrogen peroxide, to a homogeneous Composition, this is applied to the hair, is left on the hair for a contact time of 2 to 45 minutes, preferably 15 to 30 minutes, and then the hair is rinsed.
  • the application temperatures for the inventive color change of keratinic fibers may be in a range between 15 and 45 0 C.
  • the hair dye is removed by rinsing off the hair to be dyed. removed.
  • the washing with a shampoo can be omitted if a strong surfactant-containing carrier, eg. As a dyeing shampoo was used.
  • a further preferred embodiment of the method according to the invention for permanently modifying keratinous fibers is when a composition in a cosmetic carrier containing at least one keratin-reducing substance and at least one polyalkoxylated fatty body and at least one animal care component, preferably royal jelly, is applied to the hair an exposure time of 2 to 45 minutes, preferably 15 to 30 minutes left on the hair, and then optionally the hair is rinsed out. Subsequently, a fixing agent containing at least one oxidizing agent, preferably hydrogen peroxide, and preferably additionally at least one stabilizer or complexing agent, applied to the hair, for a contact time of 2 to 45 minutes, preferably 15 to 30 minutes left on the hair, and then the Hair is rinsed out.
  • a fixing agent containing at least one oxidizing agent, preferably hydrogen peroxide, and preferably additionally at least one stabilizer or complexing agent, applied to the hair, for a contact time of 2 to 45 minutes, preferably 15 to 30 minutes left on the hair, and then the Hair is rinsed out
  • the application temperatures in the permanent change in shape of keratinic fibers according to the invention can be in a range between 15 and 45 ° C.
  • the fixative is removed by rinsing off the hair.
  • the washing with a shampoo can be omitted if a strong surfactant-containing carrier was used.
  • compositions according to the invention can also be prepared directly before use from two or more separately packaged preparations. This is particularly useful for the separation of incompatible ingredients to avoid premature reaction.
  • the ready-to-use agent in such systems is manufactured by the consumer just prior to application by mixing the components.
  • a further subject of the present invention is therefore a multicomponent packaging unit (kit-of-parts) containing at least two separately assembled containers, wherein a container at least one container a color and / or shape-changing compound and at least one polyalkoxylated fat body and at least one animal care component, preferably royal jelly, contains and a container an Oxidationsstoff- setting, containing at least one chemical oxidizing agent, in particular hydrogen peroxide containing.
  • kit-of-parts containing at least two separately assembled containers, wherein a container at least one container a color and / or shape-changing compound and at least one polyalkoxylated fat body and at least one animal care component, preferably royal jelly, contains and a container an Oxidationsmittel- setting, containing at least one chemical oxidizing agent, in particular hydrogen peroxide containing.
  • a preferred embodiment of this subject matter of the present invention is therefore a multi-component packaging unit (kit-of-parts) comprising at least two separate containers, one container comprising a coloring mixture in a cosmetic carrier containing at least one coloring component, in particular at least one oxidation dye precursor, at least one polyalkoxylated fatty body and at least one animal care component, preferably royal jelly, and a container containing an oxidizing agent composition containing at least one chemical oxidizing agent, in particular hydrogen peroxide.
  • kit-of-parts comprising at least two separate containers, one container comprising a coloring mixture in a cosmetic carrier containing at least one coloring component, in particular at least one oxidation dye precursor, at least one polyalkoxylated fatty body and at least one animal care component, preferably royal jelly, and a container containing an oxidizing agent composition containing at least one chemical oxidizing agent, in particular hydrogen peroxide.
  • the multicomponent packaging unit according to the invention (kit-of-parts) in the form of an optionally dusted powder or a molding pressed in the form of a separately packed, additional component to add.
  • a further preferred embodiment of the subject of the invention is a multi-component packaging unit (kit-of-parts) containing at least two separate prefabricated containers, one container comprising a shape-change mixture in a cosmetic carrier comprising at least one shape-modifying component and at least one polyalkoxylated fatty body and at least one animal Care component, preferably royal jelly, and a container containing an oxidizing agent composition containing at least one chemical oxidizing agent, in particular hydrogen peroxide.
  • kit-of-parts containing at least two separate prefabricated containers, one container comprising a shape-change mixture in a cosmetic carrier comprising at least one shape-modifying component and at least one polyalkoxylated fatty body and at least one animal Care component, preferably royal jelly, and a container containing an oxidizing agent composition containing at least one chemical oxidizing agent, in particular hydrogen peroxide.
  • the damage to hair can be reduced by color and / or shape-changing agents and their care state can be improved if the hair following a color and shape change with an aftertreatment agent containing at least one polyalkoxylated fatty body and at least an animal care component, preferably royal jelly, are treated.
  • an aftertreatment agent containing at least one polyalkoxylated fatty body and at least an animal care component, preferably royal jelly.
  • following here is in particular the period of immediately up to 2 hours, preferably up to 1 hour, after completion of the dyeing and / or shaping change treatment more than 2 hours after changing the color and / or shape of the hair with this aftertreatment agent, the reduction of hair damage and the care performance by the aftertreatment agent significantly less fails or is no longer recognizable.
  • a further subject of the present invention is therefore a multicomponent packaging unit (kit-of-parts) containing at least two separately assembled containers, one container comprising at least one color and / or shape-changing preparation and one container at least one aftertreatment agent containing at least one polyalkoxylated Fat body and at least one animal care component, preferably royal jelly, contains.
  • kit-of-parts containing at least two separately assembled containers, one container comprising at least one color and / or shape-changing preparation and one container at least one aftertreatment agent containing at least one polyalkoxylated Fat body and at least one animal care component, preferably royal jelly, contains.
  • the color and / or shape-changing component for special embodiments of the color and / or shape-changing component, the polyalkoxylierter fat body and the animal care component, and other additives in color and / or shape-changing preparations and in the aftertreatment applies mutatis mutandis said to the means according to the first subject of the invention.
  • the multi-component packaging unit (kit-of-parts) next to a container with at least one color and / or shape-changing preparation and next to a container with at least one post-treatment agent containing at least one polyalkoxylated fatty body and at least one animal care component, preferably royal jelly, additionally comprising a container with an oxidizing agent composition containing at least one chemical oxidizing agent, in particular hydrogen peroxide.
  • the oxidizing agent the previously described preferred embodiments apply mutatis mutandis.
  • the multi-component packaging unit (kit-of-parts) preferably additionally contains an instruction manual which explains the application and, if appropriate, the mixing sequence of the individual preparations.
  • an application aid such as a comb or brush
  • personal protective equipment such as disposable gloves
  • Another object of the invention is the use of a prepared by mixing the components of a multi-component packaging unit means for reducing the damage to hair in the color and / or permanent change in shape of human hair.
  • Another object of the present invention is finally the use of the components of a multi-component packaging unit in a predetermined time sequence to reduce the damage to hair in the color and / or permanent change in shape of human hair.
  • Raw materials used Lanette D Ci 6 -C 8 fatty alcohol (INCI name: Cetearyl alcohol) (Cognis) Lorol tech. C 2 -C 8 fatty alcohol (INCI name: coconut alcohol) (Cognis) eumulgin B 2 C 6 -C 8 fatty alcohol, ethoxylated (20 EO) (INCI name: ceteareth-20) (Cognis)
  • Eumulgin B1 C 6 -C 8 fatty alcohol ethoxylated (12 EO) (INCI name: Ceteareth- 12)
  • Lanette D, Lorol, Eumulgin B2 and Eumulgin B1 and Lamesoft PO 65 were melted together at 80 0C, dispersed with a portion of the amount of water, the remaining ingredients were incorporated, made up with water and the formulation was stirred cold.
  • the ready-to-use colorants are prepared by mixing equal proportions by weight of the respective cream (E1 to E5) with the following developer dispersion:
  • Dye mixture containing 59.1 wt .-% p-toluenediamine sulfate, 6.6 wt .-% of 3-aminophenol, 22.7 wt .-% resorcinol, 0.8 wt .-% 2-amino-4-hydroxyethylaminoanisolsulfat and 10.8 wt .-% silica, pyrogenic, in each case based on the total weight of the dye mixture.
  • Lanette E powder C 16 -C 18 fatty alcohol sulfate, sodium salt (INCI name: Sodium Cetearyl Sulfate) (Cognis)
  • Texapon NSF 27% Ci ⁇ fatty alcohol sulfate, ethoxylated (2 EO) sodium salt (INCI name: Sodium Laureth Sulfate) (Cognis)
  • Phospholipid EFA zwitterionic phospholide (INCI name: Linoleamidopropyl PG-dimonium Chloride phosphate) (Uniqema) Hydrovance Hydroxyethyl urea (about 50%, INCI name: Hydroxyethylura, Aqua) (National Starch)
  • the fat base was melted together at 80 0 C and dispersed with a portion of the amount of water. Subsequently, the remaining recipe ingredients were incorporated with stirring in order. It was then made up to 100% by weight with water and the formulation was stirred cold.
  • the ready-to-use dyeing cream was mixed in a weight ratio of 1: 1 with a developer dispersion composed as follows.
  • Genamin STAC Trimethylstearylammonium chloride (about 80% active ingredient, INCI name: Steartrimonium Chloride) (Clariant)
  • strands of bleached buffalo belly hair of about 0.7 g in weight were applied with 4 times the amount of the finished application mixtures. After the tresses were dyed for 30 min at 32 0 C, they were washed with a commercial shampoo and dried with a hair dryer. The stained strands were characterized by brilliant colors and a pleasant feel.

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

Abstract

L'invention porte sur un produit pour la modification de la couleur et/ou la modification durable de la forme de fibres kératiniques, caractérisé en ce qu'il contient, dans un support cosmétique, au moins un composant modifiant la coloration et/ou la forme, ainsi qu'un produit de soin animal, en particulier la gelée royale, en combinaison avec un corps gras polyalcoxylé. Les produits selon l'invention conviennent en particulier pour la réduction de la détérioration des cheveux, qui apparaît en liaison avec le traitement oxydant des cheveux, tel qu'une coloration oxydante, une décoloration et une permanente.
EP10707886A 2009-03-11 2010-03-03 Produit de traitement capillaire contenant de la gelée royale Withdrawn EP2405974A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102009001484A DE102009001484A1 (de) 2009-03-11 2009-03-11 Haarbehandlungsmittel mit Gelee Royale
PCT/EP2010/052663 WO2010102928A2 (fr) 2009-03-11 2010-03-03 Produit de traitement capillaire contenant de la gelée royale

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EP2405974A2 true EP2405974A2 (fr) 2012-01-18

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US (1) US20110318293A1 (fr)
EP (1) EP2405974A2 (fr)
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WO (1) WO2010102928A2 (fr)

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Publication number Priority date Publication date Assignee Title
DE102009003002A1 (de) * 2009-05-11 2010-11-18 Henkel Ag & Co. Kgaa Färbemittel mit Tensid/Emulgator-Kombination
DE102009026775A1 (de) * 2009-06-05 2010-12-09 Henkel Ag & Co. Kgaa Tensidhaltiges kosmetisches Reinigungsmittel mit Gelee Royale
US10238588B2 (en) 2012-12-20 2019-03-26 Kao Germany Gmbh Aqueous oxidizing composition for hair
US11413231B2 (en) * 2018-04-24 2022-08-16 Revlon Consumer Products Corporation Cosmetic hair dyeing and/or bleaching composition, method, use and kit thereof

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DE4436065A1 (de) 1994-10-10 1996-04-11 Henkel Kgaa Mittel und Verfahren zur dauerhaften Verformung von Keratinfasern
JP2002537307A (ja) * 1999-02-19 2002-11-05 ベー・エル・アー・ハー・エム・エス・ディアグノスティカ・ゲーエムベーハー 甲状腺機能亢進症の治療におけるブロッキング抗ｔｓｈレセプター抗体の使用およびかかる使用のためのモノクローナル抗体
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WO2010102928A3 (fr) 2012-06-21
US20110318293A1 (en) 2011-12-29
DE102009001484A1 (de) 2010-09-16
WO2010102928A2 (fr) 2010-09-16

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