DE10057545A1 - Composition for dyeing keratinic fibers, especially for oxidation dyeing of human hair, comprises a phenol-oxidizing enzyme derived from an Acremonium fungus - Google Patents

Abstract

Composition for dyeing keratinic fibers, comprising one or more dye precursors in a cosmetically acceptable vehicle, includes a phenol-oxidizing enzyme derived from an Acremonium fungus.

Description

The present invention relates to agents for dyeing keratinic fibers which are at least a phenol-oxidizing enzyme derived from fungi of the genus Acremonium can be included, appropriate methods for dyeing keratinous fibers as well the use of a phenol oxidizing enzyme derived from fungi of the genus Acremonium can be obtained for oxidative hair coloring.

Human hair is used today in a variety of ways with hair cosmetic preparations treated. These include cleaning the hair with shampoos, taking care and re generation with rinses and cures, as well as the bleaching, dyeing and shaping of the Hair with coloring, tinting, waving and styling preparations. Play it Means for changing or nuancing the color of the hair of the head an outstanding Role.

For temporary dyeings usually dyeing or tinting agents are used, the as a coloring component so-called Direktzieher included. This is Dye molecules that grow directly on the hair and no oxidative process for Need training of the paint. For example, these dyes already belong Henna known from ancient times for coloring body and hair. These dyes are generally much more sensitive to shampooing than oxidative dyeing gene, so that much faster then a much undesirable nuance shift or even a visible "discoloration" occurs.  

For permanent, intense colorations with corresponding fastness properties so-called oxidation colorants used. Such colorants usually contain Oxidation dye precursors, so-called developer components and Kupplerkom components. The developer components form under the influence of oxidants or of atmospheric oxygen with each other or under coupling with one or more Coupler components from the actual dyes. Draw the oxidation colorants characterized by excellent, long lasting staining results. For natural looking Dyeing is usually a mixture of a larger number of oxidation color substance precursors are used; in many cases will continue to be substantive Dyes used for shade.

The oxidative development of the dyeing can in principle be carried out with atmospheric oxygen. Preferably, however, a chemical oxidizing agent is used. As oxidizing agent come persulfates, chlorites and in particular hydrogen peroxide or its plant tion products of urea, melamine and sodium borate in question. Usually will used an approximately 2-9% aqueous hydrogen peroxide solution. Under the influence such high oxidant concentrations, the keratinic fibers, in particular however, if they are already permed or bleached, they are damaged and rare Cases can also cause skin irritation due to these high concentrations.

An essential solution to this problem is the reduction of the Oxi dationsmittelkonzentration. It was therefore in the past on the one hand by color fabric precursors, due to their chemical structure already by lower Amounts of hydrogen peroxide or can be oxidized by atmospheric oxygen. other The use of enzymes as biocatalysts has been proposed desired oxidation process with very little or no hydrogen peroxide only in can catalyze the presence of atmospheric oxygen.

In the German patent application DE-OS 21 55 390 an enzyme-activated, oxida tive hair dyeing method is described, are used in the small amounts of H ₂ O ₂ in combination with a peroxidase. EP-A1-0 310 675 also discloses enzymatic hair treatment compositions containing at least one electron-reducing oxidase which uses oxygen as the acceptor. EP-B 1-0 548 620 describes enzymatic hair dyes in which the oxidation of the dye precursors is catalyzed by using a peroxidase. Finally, EP-A2-0 795 313 describes enzymatic hair dyes which contain an oxygen oxidoreductase / substrate system and a peroxidase and, as coupler components, a m-phenylenediamine derivative. However, all of these colorants can not fully convince regarding the achievable dyeing power (intensity, nuance, gloss, fastness properties).

The technique of easily oxidizable dye precursors as well as the previously be described enzymatic color development the disadvantage that in comparison to the her conventional methods, in particular with regard to the intensity, the gloss and the real properties of the dyeings worse results can be achieved.

The present invention is therefore based on the object of colorants for keratinische To provide fibers that allow a gentle fiber treatment and at the same time guarantee excellent dyeing performance.

A first object of the present invention are therefore agents for dyeing kerati nischer fibers, the at least one Farbstoffvor in a cosmetically acceptable carrier product and at least one phenol oxidizing enzyme selected from fungi of the genus Acremonium can be obtained.

According to the invention, keratinic fibers include furs, wool, feathers and in particular to understand human hair.

Among phenol-oxidizing enzymes derived from fungi of the genus Acremonium According to the invention, besides the naturally produced enzymes, In particular, to understand equivalent enzymes derived from organisms which do not belong to the genus Acremonium. Furthermore, this term should According to the invention also include mutants, variants and derivatives of these enzymes, as they for example, in International Publication WO-A1-00 / 05349 become. In particular to the disclosure of this document for recovery and purification of these enzymes and their extraction also from sources that are not of the genus  Acremonium, is explicitly referred to here. According to the invention For example, purified enzyme preparations are preferred.

Particularly suitable according to the invention is the enzyme which is Acremonium murorum (DSMZ accession number DSM63375) can be obtained. Also suitable is the Enzyme that can be obtained from Acremonium obclavatum. Furthermore, that is also Enzyme derived from Acremonium murorum var. Murorum with the CBS approval number 157.72 can be obtained, according to the invention preferred.

The enzyme can be incorporated into the colorant itself or separated from the Prepared dye precursors and immediately before use the Colorants are added. In a third embodiment, the enzyme may also be in Form of a post-treatment agent separately from dye precursors on the fibers be applied.

The enzyme is preferably used in an amount of 0.001-2% by weight, especially 0.001 -1 wt .-%, based on the protein amount of the enzyme and the entire colorant, used.

With regard to the dye preproducts used in the colorants according to the invention, the present invention is subject to no restrictions. The erfindungsge MAESSEN colorants can be used as dye precursors

• - Developer and / or coupler type oxidation dye precursors, and
• Precursors of nature-analogous dyes, such as indole and indoline derivatives,

and mixtures of representatives of these groups.

As developer components are usually primary aromatic amines with a further, in the para or ortho position, free or substituted hydroxy or amino group, diaminopyridine derivatives, heterocyclic hydrazones, 4-aminopyra zolderivate and 2,4,5,6-tetraaminopyrimidine and its derivatives used.  

It may be preferred according to the invention to use a p-phenylenediamine derivative or one of its physiologically tolerated salts as the developer component. Particular preference is given to p-phenylenediamine derivatives of the formula (I)

in which

• G ¹ represents a hydrogen atom, a C ₁ to C ₄ alkyl radical, a C ₁ to C ₄ monohydroxyalkyl radical, a C ₂ to C ₄ polyhydroxyalkyl radical, a C ₁ to C ₄ alkoxy radical (C ₁ - to C ₄ ) -alkyl radical, a 4'-aminophenyl radical or a C ₁ - to C ₄ -alkyl radical which is substituted by a nitrogen-containing group, a phenyl or a 4'-aminophenyl radical;
• G ² is a hydrogen atom, a C ₁ to C ₄ alkyl radical, a C ₁ to C ₄ monohydroxyalkyl radical, a C ₂ to C ₄ polyhydroxyalkyl radical, a C ₁ to C ₄ alkoxy radical C ₁ - to C ₄ ) -alkyl radical or a C ₁ - to C ₄ -alkyl radical substituted with a nitrogen-containing group;
• G ³ represents a hydrogen atom, a halogen atom such as a chlorine, bromine, iodine or fluorine atom, a C ₁ to C ₄ alkyl radical, a C ₁ to C ₄ monohydroxyalkyl radical, a C ₁ to C ₄ -Hydroxyalkoxyradikal, a C ₁ - to C ₄ -Acetylaminoalkoxyradikal, a C ₁ - to C ₄ - Mesylaminoalkoxyradikal or a C ₁ - to C ₄ -Carbamoylaminoalkoxyradikal;
• - G ⁴ represents a hydrogen atom, a halogen atom or a C ₁ - to C ₄ -alkyl radical

or

• - When G ³ and G ⁴ are ortho to each other, they may together form a bridging α, ω-alkylenedioxy group, such as an ethylenedioxy group.

Examples of the C ₁ -C ₄ -alkyl radicals mentioned as substituents in the compounds according to the invention are the groups methyl, ethyl, propyl, isopropyl and butyl. Ethyl and methyl are preferred alkyl radicals. C ₁ -C ₄ -alkoxy radicals which are preferred according to the invention are, for example, a methoxy or an ethoxy group. Furthermore, as preferred examples of a C ₁ - to C ₄ -hydroxyalkyl group, a hydroxy methyl, a 2-hydroxyethyl, a 3-hydroxypropyl or a 4-hydroxybutyl group may be mentioned. A 2-hydroxyethyl group is particularly preferred. Examples of halo genatome according to the invention F, Cl or Br atoms, Cl atoms are very particularly preferred. The other terms used are derived according to the invention from the definitions given here. Examples of nitrogen-containing groups of the formula (I) are, in particular, the amino groups, C ₁ - to C ₄ -monoalkylamino groups, C ₁ - to C ₄ -dialylamino groups, C ₁ - to C ₄ -trialkylammonium groups, C ₁ - to C ₄ -monohydroxy alkylamino groups, imidazolinium and ammonium.

Particularly preferred p-phenylenediamines of the formula (I) are selected from p-phenylene diamine, 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 (β-Hy droxyethyl) -p-phenylenediamine, 4-N, N-bis (β-hydroxyethyl) amino-2-methylaniline, 4-N, N- bis (β-hydroxyethyl) amino-2-chloroaniline, 2- (β-hydroxyethyl) -p-phenylenediamine, 2-fluoro p-phenylenediamine, 2-isopropyl-p-phenylenediamine, N- (β-hydroxypropyl) -p-phenylene diamine, 2-hydroxymethyl-p-phenylenediamine, N, N-dimethyl-3-methyl-p-phenylenediamine, N, N- (ethyl, -β-hydroxyethyl) -p-phenylenediamine, N- (β, γ-dihydroxypropyl) -p-phenylene diamine, N- (4'-aminophenyl) -p-phenylenediamine, N-phenyl-p-phenylenediamine, 2- (β-Hy droxyethyloxy) -p-phenylenediamine, 2- (β-acetylaminoethyloxy) -p-phenylenediamine, N- (β-) Methoxyethyl) -p-phenylenediamine and 5,8-diaminobenzo-1,4-dioxane and their physio logically compatible salts.

Very particularly preferred p-phenylenediamine derivatives of the formula (I) according to the invention are p-phenylenediamine, p-toluenediamine, 2- (β-hydroxyethyl) -p-phenylenediamine and N, N-bis (β-hydroxyethyl) -p-phenylenediamine.

It may further be preferred according to the invention, as a developer component verbin use at least two aromatic nuclei containing amino acids and / or hydroxyl groups are substituted.  

Among the binuclear developer components which can be used in the dyeing compositions according to the invention, mention may be made, in particular, of the compounds corresponding to the following formula (II) and their physiologically tolerable salts:

in which:

• - Z ¹ and Z ² independently represent a hydroxyl or NH ₂ radical, which is optionally kylradikal by a C ₁ - to C ₄ -alkyl radical, by a C ₁ - to C ₄ -Hydroxyal and / or by a bridge Y. is substituted or are part of a bridging ring system,
• - The bridge Y is an alkylene group having 1 to 14 carbon atoms, such as a linear or branched alkylene chain or an alkylene ring, which interrupted by one or more nitrogen-containing groups and / or one or more heteroatoms such as oxygen, sulfur or nitrogen atoms or may be terminated and may be optionally substituted by one or more hydroxyl or C ₁ to C ₈ alkoxy radicals,
• G ⁵ and G ⁶ independently of one another represent a hydrogen or halogen atom, a C ₁ - to C ₄ -alkyl radical, a C ₁ - to C ₄ -monohydroxyalkyl radical, a C ₂ - to C ₄ -polyhydroxyalkyl radical, a C ₁ - to C ₄ -aminoalkyl radical or a direct compound for bridging Y,
• - G ⁷ , G ⁸ , G ⁹ , G ¹⁰ , G ¹¹ and G ¹² independently represent a hydrogen atom, a direct bond to the bridge Y or a C ₁ - to C ₄ -alkyl radical, with the provisos that
• - The compounds of formula (II) only one bridge Y per molecule included and  
• The compounds of the formula (II) contain at least one amino group which carries at least one hydrogen atom.

The substituents used in formula (II) are analogous to the above according to the invention Executions defined.

Preferred binuclear developer components of the formula (II) are in particular: N, N'- bis- (β-hydroxyethyl) -N, N'-bis (4'-aminophenyl) -1,3-diamino-propan-2-ol, N, N'-bis- (β-) Hydroxyethyl) -N, N'-bis (4'-aminophenyl) ethylenediamine, N, N'-bis (4-aminophenyl) - tetramethylenediamine, N, N'-bis (β-hydroxyethyl) -N, N'-bis (4-aminophenyl) tetram thylenediamine, N, N'-bis (4-methylaminophenyl) tetramethylenediamine, N, N'-bis (ethyl) - N, N'-bis (4'-amino-3'-methylphenyl) ethylenediamine, bis (2-hydroxy-5-aminophenyl) - methane, 1,4-bis (4'-aminophenyl) diaza-cycloheptane and 1,10-bis (2 ', 5'-diaminophenyl) - 1,4,7,10-tetraoxadecane and its physiologically acceptable salts.

Very particularly preferred binuclear developer components of the formula (II) are N, N'-bis- (β-hydroxyethyl) -N, N'-bis (4'-aminophenyl) -1,3-diamino-propan-2-ol, bis (2- hydroxy-5-aminophenyl) methane, N, N'-bis (4'-aminophenyl) -1,4-diazacycloheptane and 1,10-bis- (2 ', 5'-diaminophenyl) -1,4,7,10-tetraoxadecane or one of its physiologically ver suitable salts.

Furthermore, it may be preferred according to the invention to use as the developer component a p-aminophenol derivative or one of its physiologically tolerable salts. Particular preference is given to p-aminophenol derivatives of the formula (III)

in which:

• G ¹³ represents a hydrogen atom, a halogen atom, a C ₁ - to C ₄ -alkyl radical, a C ₁ - to C ₄ -monohydroxyalkyl radical, a (C ₁ - to C ₄ ) -alkoxy- (C ₁ - to C ₄ ) alkyl radical, a C ₁ to C ₄ aminoalkyl radical, a hydroxy (C ₁ to C ₄ ) alkyl amino radical, a C ₁ to C ₄ hydroxyalkoxy radical, a C ₁ to C ₄ hydroxyalkyl (C ₁ -C ₄ ) -aminoalkyl radical or a (di-C ₁ - to C ₄ -alkylamino) - (C ₁ - to C ₄ ) -alkyl radical, and
• G ¹⁴ is a hydrogen or halogen atom, a C ₁ to C ₄ alkyl radical, a C ₁ to C ₄ monohydroxyalkyl radical, a C ₂ to C ₄ polyhydroxyalkyl radical, a C ₁ to C ₄ Alkoxy (C ₁ to C ₄ ) alkyl radical, a C ₁ to C ₄ aminoalkyl radical or a C ₁ to C ₄ cyanoalkyl radical,
• G ¹⁵ is hydrogen, a C ₁ to C ₄ alkyl radical, a C ₁ to C ₄ monohydroxyalkyl radical, a C ₂ to C ₄ polyhydroxyalkyl radical, a phenyl radical or a benzyl radical, and
• - G ¹⁶ is hydrogen or a halogen atom.

The substituents used in formula (III) are according to the invention analogous to the above Executions defined.

Preferred p-aminophenols of the formula (III) are in particular p-aminophenol, N-Me ethyl-p-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 2-hydroxyme thylamino-4-amino-phenol, 4-amino-3-hydroxymethylphenol, 4-amino-2- (2-hydroxy ethoxy) -phenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2- methoxymethyl-phenol, 4-amino-2-aminomethylphenol, 4-amino-2- (β-hydroxyethyl aminomethyl) phenol, 4-amino-2-fluorophenol, 4-amino-2-chlorophenol, 2,6-dichloro-4- aminophenol, 4-amino-2 - ((diethylamino) methyl) phenol and their physiologically compatible salts.

Very particularly preferred compounds of the formula (III) are p-aminophenol, 4-amino 3-methylphenol, 4-amino-2-chlorophenol, 4-amino-2,6-dichlorophenol, 4-amino-2-amino methylphenol and 4-amino-2 - ((diethylamino) methyl) phenol.

Further, the developer component may be selected from o-aminophenol and its Derivatives such as 2-amino-4-methylphenol or 2-amino-4-chlorophenol.  

Furthermore, the developer component may be selected from heterocyclic Ent Winder components, such as the pyridine, pyrimidine, pyrazole, pyrazole Py rimidine derivatives and their physiologically acceptable salts.

Preferred pyridine derivatives are in particular the compounds described in the patents GB 1 026 978 and GB 1 153 196, such as 2,5-diamino-pyridine, 2- (4- Methoxyphenyl) amino-3-amino-pyridine, 2,3-diamino-6-methoxy-pyridine, 2- (β- Methoxyethyl) amino-3-amino-6-methoxy-pyridine and 3,4-diamino-pyridine.

Preferred pyrimidine derivatives are in particular the compounds described in the German Patent DE 23 59 399, Japanese Patent Laid-Open JP-A2-02 / 019576 or in the Offenlegungsschrift WO 96/15765, such as 2,4,5,6-tetraaminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 2-dimethyl amino-4,5,6-triaminopyrimidine, 2,4-dihydroxy-5,6-diaminopyrimidine and 2,5,6-triamino pyrimidine.

Preferred pyrazole derivatives are in particular the compounds described in the patents DE 38 43 892, DE 41 33 957 and Laid-open WO 94/08969, WO 94/08970, EP 0 740 931 and DE 195 43 988, such as 4,5-diamino-1-methylpyrazole, 4,5-diamino-1- (β-hydroxyethyl) pyrazole, 3,4-diaminopyrazole, 4,5-diamino-1- (4'-chloro benzyl) pyrazole, 4,5-diamino-1,3-dimethylpyrazole, 4,5-diamino-3-methyl-1-phenylpyra zol, 4,5-diamino-1-methyl-3-phenylpyrazole, 4-amino-1,3-dimethyl-5-hydrazinopyrazole, 1-Benzyl-4,5-diamino-3-methylpyrazole, 4,5-diamino-3-tert-butyl-1-methylpyrazole, 4,5- Diamino-1-tert-butyl-3-methylpyrazole, 4,5-diamino-1- (β-hydroxyethyl) -3-methylpyrazole, 4,5-diamino-1-ethyl-3-methylpyrazole, 4,5-diamino-1-ethyl-3- (4'-methoxyphenyl) -pyrazole, 4,5-diamino-1-ethyl-3-hydroxymethylpyrazole, 4,5-diamino-3-hydroxymethyl-1 methylpyrazole, 4,5-diamino-3-hydroxymethyl-1-isopropylpyrazole, 4,5-diamino-3-methyl 1-isopropylpyrazole, 4-amino-5- (2'-aminoethyl) amino-1,3-dimethylpyrazole, 3,4,5-tri aminopyrazole, 1-methyl-3,4,5-triaminopyrazole, 3,5-diamino-1-methyl-4-methylaminopy razole and 3,5-diamino-4 (β-hydroxyethyl) amino-1-methylpyrazole.

Preferred pyrazole-pyrimidine derivatives are, in particular, the derivatives of the pyrazolo [1,5-a] pyrimidine of the following formula (IV) and their tautomeric forms, if a tau tomeric equilibrium exists:

in which:

• - G ¹⁷ , G ¹⁸ , G ¹⁹ and G ²⁰ independently represent a hydrogen atom, a
• - C ₁ - to C ₄ -alkyl radical, an aryl radical, a C ₁ - to C ₄ -Hydroxyalkylradikal, a C ₂ - to C ₄ -Polyhydroxyalkylradikal a (C ₁ - to C ₄₎ alkoxy (C ₁ - to C ₄ ) -alkyl radical, a C ₁ - to C ₄ -aminoalkyl radical which may optionally be protected by an acetyl-ureide or sulfonyl radical, a (C ₁ - to C ₄ ) -alkylamino- (C ₁ - to C ₄ ) -alkyl radical, a di - [(C ₁ - to C ₄ ) -alkyl] - (C ₁ - to C ₄ ) -aminoalkyl radical, wherein the dialkyl radicals optionally have a carbon cycle or a heterocycle with 5 or 6 chain members form a C ₁ to C ₄ hydroxyalkyl or a di (C ₁ to C ₄ ) hydroxyalkyl (C ₁ to C ₄ ) aminoalkyl radical;
• the X radicals independently of one another represent a hydrogen atom, a C ₁ to C ₄ alkyl radical, an aryl radical, a C ₁ to C ₄ hydroxyalkyl radical, a C ₂ to C ₄ polyhydroxyalkyl radical, a C ₁ to C ₄ aminoalkyl radical, a (C ₁ to C ₄ ) alkylamino (C ₁ to C ₄ ) alkyl radical, a di - [(C ₁ to C ₄ ) alkyl] - (C ₁ to C ₄ ) -aminoalkyl radical, where the dialkyl radicals optionally form a carbon cycle or a heterocycle having 5 or 6 chain members, a C ₁ - to C ₄ - hydroxyalkyl or a di- (C ₁ - to C ₄ -hydroxyalkyl) - aminoalkyl radical, an amino radical, a C ₁ - to C ₄ -alkyl or di (C ₁ - to C ₄ -hydroxyalkyl) -aminoradi cal, a halogen atom, a carboxylic acid group or a sulfonic acid group,
• - i has the value 0, 1, 2 or 3,
• - p has the value 0 or 1,
• - q has the value 0 or 1 and
• - n has the value 0 or 1,

with the proviso that

• The sum of p + q is not equal to 0,
• if p + q equals 2, n has the value 0, and the groups NG ¹⁷ G ¹⁸ and NG ¹⁹ G ²⁰ occupy the positions (2, 3); (5, 6); (6, 7); (3,5) or (3,7);
• if p + q is 1, n is 1, and the groups NG ¹⁷ G ¹⁸ (or NG ¹⁹ G ²⁰ ) and the group OH occupy the positions (2, 3); (5, 6); (6, 7); (3, 5) or (3,7);

The substituents used in formula (IV) are according to the invention analogous to the above Executions defined.

When the pyrazolo [1,5-a] pyrimidine of the above formula (IV) contains a hydroxy group at one of the 2, 5 or 7 positions of the ring system, there is a tautomeric equilibrium, for example as shown in the scheme:

Among the pyrazolo [1,5-a] -pyrimidines of the above formula (IV) can be called in particular special:

• - pyrazole [1,5-a] pyrimidine-3,7-diamine;
• 2,5-dimethylpyrazolo [1,5-a] pyrimidine-3,7-diamine;
• - pyrazole (1,5-a] pyrimidine-3,5-diamine;
• 2,7-dimethylpyrazolo [1,5-a] -pyrimidine-3,5-diamine;
• 3-amino-pyrazolo [1,5-a] -pyrimidin-7-ol;
• 3-amino-pyrazolo [1,5-a] -pyrimidin-5-ol;
• - 2- (3-amino-pyrazolo [1,5-a] -pyrimidin-7-ylamino) -ethanol;
• - 2- (7-amino-pyrazolo [1,5-a] -pyrimidin-3-ylamino) -ethanol;
• - 2 - [(3-amino-pyrazolo [1,5-a) -pyrimidin-7-yl) - (2-hydroxy-ethyl) -amino] -ethanol;
• - 2 - [(7-amino-pyrazolo [1,5-a] -pyrimidin-3-yl) - (2-hydroxy-ethyl) -amino] -ethanol;
• 5,6-dimethylpyrazolo [1,5-a] pyrimidine-3,7-diamine;
• 2,6-dimethylpyrazolo [1,5-a] pyrimidine-3,7-diamine;
• 2,5, N7, N7-tetramethylpyrazolo [1,5-a] -pyrimidine-3,7-diamine;

and their physiologically acceptable salts and their tautomeric forms when a tau Tomeric equilibrium is present.

The pyrazolo [1,5-a] -pyrimidines of the above formula (IV) can be used as in the literature described by cyclization starting from an aminopyrazole or hydrazine getting produced.

As coupler components usually m-phenylenediamine derivatives, naphthols, Re sorcin and resorcinol derivatives, pyrazolones and m-aminophenol derivatives. When Coupler substances are in particular 1-naphthol, 1,5-, 2,7- and 1,7-dihydroxy naphthalene, 5-amino-2-methylphenol, m-aminophenol, resorcinol, resorcinomonomethyl ether, m-phenylenediamine, 1-phenyl-3-methyl-pyrazolone-5, 2,4-dichloro-3-aminophenol, 1,3-bis- (2,4-diaminophenoxy) -propane, 2-chloro-resorcinol, 4-chloro-resorcinol, 2-chloro-6- methyl-3-aminophenol, 2-amino-3-hydroxypyridine, 2-methylresorcinol, 5-methylresorcinol and 2-methyl-4-chloro-5-aminophenol.

Coupler components preferred according to the invention are:

• M-aminophenol and its derivatives such as, for example, 5-amino-2-methylphenol, 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- (diethylamino) phenol, N-cyclopentyl-3-aminophenol, 1,3-dihy droxy-5- (methylamino) -benzene, 3- (ethylamino) -4-methylphenol and 2,4-dichloro-3- aminophenol,
• O-aminophenol and its derivatives,
• - M-diaminobenzene and its derivatives such as 2,4-diaminophenoxy ethanol, 1,3-bis- (2,4-diaminophenoxy) -propane, 1-methoxy-2-amino-4- (2'-hydroxy ethylamino) benzene, 1,3-bis- (2,4-diaminophenyl) -propane, 2,6-bis- (2-hydroxyethyl amino) -1-methylbenzene and 1-amino-3-bis (2'-hydroxyethyl) aminobenzene,
• - o-diaminobenzene and its derivatives such as 3,4-diaminobenzoic acid and 2,3-diamino-1-methylbenzene,  
• Di- or trihydroxybenzene derivatives such as resorcinol, Resorcinol monomethyl ether, 2-methylresorcinol, 5-methylresorcinol, 2,5-dimethylresorcinol, 2-chlororesorcinol, 4-chlororesorcinol, pyrogallol and 1,2,4-trihydroxybenzene,
• Pyridine derivatives such as 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 and 3,5-diamino-2,6-dimethoxypyridine,
• - Naphthalene derivatives such as 1-naphthol, 2-methyl-1-naphthol, 2-hydroxy methyl-1-naphthol, 2-hydroxyethyl-1-naphthol, 1,5-dihydroxynaphthalene, 1,6-dihy droxynaphthalene, 1,7-dihydroxynaphthalene, 1,8-dihydroxynaphthalene, 2,7-dihydroxy naphthalene and 2,3-dihydroxynaphthalene,
• - Morpholine derivatives such as 6-hydroxybenzomorpholine and 6-amino benzomorpholine,
• Quinoxaline derivatives such as 6-methyl-1,2,3,4-tetrahydroquinoxaline,
• Pyrazole derivatives such as 1-phenyl-3-methylpyrazol-5-one,
• - Indole derivatives such as 4-hydroxyindole, 6-hydroxyindole and 7-hydroxy indole,
• - Pyrimidinderivate, such as 4,6-diaminopyrimidine, 4-amino-2,6-dihydroxy pyrimidine, 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, or
• - Methylendioxybenzolderivate such as 1-hydroxy-3,4-methylenedioxyben zol, 1-amino-3,4-methylenedioxybenzene and 1- (2'-hydroxyethyl) amino-3,4-methylene dioxybenzene.

Particularly preferred coupler components are 1-naphthol, 1,5-, 2,7- and 1,7-dihy droxynaphthalene, 3-aminophenol, 5-amino-2-methylphenol, 2-amino-3-hydroxypyridine, Resorcinol, 4-chlororesorcinol, 2-chloro-6-methyl-3-aminophenol, 2-methylresorcinol, 5-methylresorcinol, 2,5-dimethylresorcinol and 2,6-dihydroxy-3,4-dimethylpyridine.

It is not necessary that the oxidation dye precursors or the substantive Dyes each represent uniform compounds. Rather, in the inventions Hair colorants according to the invention, due to the production process for the individual  Dyes, in minor amounts still contain other components, as far as these do not adversely affect the staining result or for other reasons, z. As toxicological, must be excluded.

With regard to the hair dyeing and tinting compositions according to the invention can be used Dyes is still expressly referred to the monograph Ch. Zviak, The Science of Hair Care, chapter 7 (pages 248-250, direct dyes) and chapter 8, pages 264-267; Oxidation dye precursors), published as volume 7 of the series "Dermato logy "(ed .: Ch., Culnan and H. Maibach), published by Marcel Dekker Inc., New York, Basel, 1986, as well as the "European Inventory of Cosmetic Raw Materials", published by the European Community, available in disk form from the Bundesverband Deutscher Industrial and commercial enterprise for pharmaceuticals, health products and personal care tel e. V., Mannheim.

The oxidation dye precursors are preferred in the agents according to the invention Amounts from 0.01 to 20 wt .-%, preferably 0.5 to 5 wt .-%, each based on the entire medium, included.

As precursors of naturally-analogous dyes such indoles and indolines are preferred set, the at least one hydroxy or amino group, preferably as a substituent on Six-ring, exhibit. These groups may carry further substituents, e.g. B. in shape an etherification or esterification of the hydroxy group or an alkylation of the amino group.

Particularly suitable precursors of naturally-analogous hair dyes are derivatives of 5,6-dihydroxyindoline of the formula (Va),

in the independently of each other

• R ¹ is hydrogen, a C ₁ -C ₄ -alkyl group or a C ₁ -C ₄ -hydroxy-alkyl group,
• R ² is hydrogen or a -COOH group, where the -COOH group may also be present as a salt with a physiologically compatible cation,
• R ³ is hydrogen or a C ₁ -C ₄ -alkyl group,
• R ⁴ is hydrogen, a C ₁ -C ₄ -alkyl group or a group -CO-R ⁶ , in which R ⁶ is a C ₁ -C ₄ -alkyl group, and
• R ⁵ is one of the groups mentioned under R ⁴ ,
  and physiologically acceptable salts of these compounds with an organic or inorganic acid.

Particularly preferred derivatives of indoline are the 5,6-dihydroxyindoline, N-methyl-5,6- dihydroxyindoline, N-ethyl-5,6-dihydroxyindoline, N-propyl-5,6-dihydroxyindoline, N-butyl-5,6-dihydroxyindoline, 5,6-dihydroxyindoline-2-carboxylic acid and 6-hydroxy indoline, 6-aminoindoline and 4-aminoindoline.

Particularly noteworthy within this group are N-methyl-5,6-dihydroxyindoline, N-ethyl-5,6-dihydroxyindoline, N-propyl-5,6-dihydroxyindoline, N-butyl-5,6-dihydroxy indoline and in particular 5,6-dihydroxyindoline.

Also suitable as precursors of naturally-analogous hair dyes are derivatives of the 5,6-dihydroxyindole of the formula (Vb),

in the independently of each other

• R ¹ is hydrogen, a C ₁ -C ₄ -alkyl group or a C ₁ -C ₄ -hydroxyalkyl group,
• R ² is hydrogen or a -COOH group, where the -COOH group may also be present as a salt with a physiologically compatible cation,
• R ³ is hydrogen or a C ₁ -C ₄ -alkyl group,
• R ⁴ is hydrogen, a C ₁ -C ₄ -alkyl group or a group -CO-R ⁶ , in which R ⁶ is a C ₁ -C ₄ -alkyl group, and
• R ⁵ is one of the groups mentioned under R ⁴ ,
• - As well as physiologically acceptable salts of these compounds with an organic or inorganic acid.

Particularly preferred derivatives of indole are 5,6-dihydroxyindole, N-methyl-5,6-dihy droxyindole, N-ethyl-5,6-dihydroxyindole, N-propyl-5,6-dihydroxyindole, N-butyl-5,6-dihy droxyindole, 5,6-dihydroxyindole-2-carboxylic acid, 6-hydroxyindole, 6-aminoindole and 4- Aminoindole.

Within this group, N-methyl-5,6-dihydroxyindole, N-ethyl-5,6- dihydroxyindole, N-propyl-5,6-dihydroxyindole, N-butyl-5,6-dihydroxyindole and especially in particular the 5,6-dihydroxyindole.

The indoline and indole derivatives can in the Ver used as both free bases and in the form of their physiolo gically compatible salts with inorganic or organic acids, eg. B. the hydrochlo ride, the sulfates and hydrobromides used. The indole or indoline derivatives are in these usually in amounts of 0.05-10 wt .-%, preferably 0.2-5 wt .-% contain.

In a further embodiment, it may be preferred according to the invention, the indoline or indole derivative in hair dyes in combination with at least one amino acid or an oligopeptide. The amino acid is advantageously an α-Ami is nitric acid; most preferred α-amino acids are arginine, ornithine, lysine and Histidine, especially arginine.

In addition to the dye precursors, the colorants according to the invention can be further Nuancierung substantive dyes included. These are usually selected from Nitrophenylenediamines, nitroaminophenols, azo dyes, anthraquinones or indophe nole. Preferred substantive dyes are those under the international name or trade names HC Yellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, Basic Yellow 57, HC Orange 1, Disperse Orange 3, HC Red 1, HC Red 3, HC Red 13, HC Red  BN, Basic Red 76, HC Blue 2, HC Blue 12, Disperse Blue 3, Basic Blue 7, Basic Blue 26, Basic Blue 99, HC Violet 1, Disperse Violet 1, Disperse Violet 4, Basic Violet 2, Basic Violet 14, Acid Violet 43, Disperse Black 9, Acid Black 52, Basic Brown 16 and Basic Brown 17 known compounds and 1,4-bis (β-hydroxyethyl) amino-2-nitrobenzene, 3-nitro-4- (β-hydroxyethyl) aminophenol, 4-amino-2-nitrodiphenylamine-2'-carboxylic acid, 6-nitro-1,2,3,4-tetrahydroquinoxaline, 2-hydroxy-1,4-naphthoquinone, hydroxyethyl-2- nitro-toluidine, picramic acid, 2-amino-6-chloro-4-nitrophenol, 4-ethylamino-3-nitroben benzoic acid and 2-chloro-6-ethylamino-1-hydroxy-4-nitrobenzene. The invention Agents according to this embodiment preferably contain the substantive dyes in an amount of 0.01 to 20 wt .-%, based on the total colorant.

Furthermore, the preparations according to the invention can also occur in nature Dyes such as henna red, henna neutral, henna black, chamomile flower, Sandalwood, black tea, buckthorn bark, sage, bluewood, madder root, catechu, Sedre and alcano root included.

In addition to the oxidase system according to the invention, the inventive dyeing also other enzymes, such as laccases, other phenol-oxidizing Enzymes, such as ascorbate oxidase or bilirubin oxidase, peroxidases or contain oxidases with their respective substrates. Preferred oxidases are at For example, choline oxidase, glucose oxidase, alcohol oxidase, pyruvate oxidase, Oxalate oxidase, cholesterol oxidase, uricase, lactate oxidase, xanthine oxidase, pyra nose oxidase, glycerol oxidase and galactose oxidase. In the context of this off Guidance form particularly preferred are agents which, in addition to the phenol-oxidizing enzyme also uricase, glucose oxidase and / or xanthine oxidase and their respective Contain substrates.

For the preparation of the colorants of the invention, the dye precursors in a suitable water-containing carrier can be incorporated. For the purpose of hair coloring advertising are such carrier z. As creams, emulsions, gels or surfactant-containing mende solutions, eg. As shampoos, foam aerosols or other preparations for the Application on the hair are suitable.  

The colorants of the invention may further be all for such preparations be knew active ingredients, additives and excipients included. In many cases, the colorants contain at least one surfactant, wherein in principle both anionic and zwitterionic, am phytic, nonionic and cationic surfactants are suitable. The expert can a possible influence of the various surfactants on the activity of erfindungsge If necessary, check the enzyme system by simple preliminary tests.

In a preferred embodiment of the present invention is in the means for Coloring keratinous fibers a combination of anionic and nonionic Ten siden or a combination of anionic and amphoteric surfactants used. However, it has proved in individual cases to be advantageous, the surfactants from amphoteric or Select nonionic surfactants, since these are usually the inventive dye influence the process less.

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 alkyl group having about 10 to 22 carbon atoms. In addition, glycol or poly glycol ether groups, ester, ether and amide groups and hydroxyl groups can be contained 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 with 2 or 3 C atoms in the alkanol group,

• - linear fatty acids with 10 to 22 carbon atoms (soaps),
• Ether carboxylic acids of the formula RO- (CH ₂ -CH ₂ O) _x -CH ₂ -COOH, in which R is a linear alkyl group having 10 to 22 C atoms and x = 0 or 1 to 16,
• Acylsarcosides having 10 to 18 C atoms in the acyl group,
• Acyltaurides having 10 to 18 C atoms in the acyl group,
• Acyl isethionates having 10 to 18 C atoms in the acyl group,
• - Sulfobernsteinsäuremono- and -dialkylester having 8 to 18 carbon atoms in the alkyl group and sulfosuccinic acid mono-alkylpolyoxyethylester having 8 to 18 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups,
• Linear alkanesulfonates having 12 to 18 C atoms,  
• - linear alpha-olefin sulfonates having 12 to 18 C atoms,
• Alpha-sulfofatty acid methyl esters of fatty acids containing 12 to 18 carbon atoms,
• Alkyl sulfates and alkyl polyglycol ether sulfates of the formula RO (CH ₂ -CH ₂ O) _x -SO ₃ H, in which R is a preferably linear alkyl group having 10 to 18 C atoms and x = 0 or 1 to 12,
• Mixtures of surface-active hydroxysulfonates according to DE-A-37 25 030,
• - Sulfated Hydroxyalkylpolyethylen- and / or Hydroxyalkylenpropylenglykolether according to DE-A-37 23 354,
• - Sulfonates of unsaturated fatty acids with 12 to 24 carbon atoms and 1 to 6 doublebin according to DE-A-39 26 344,
• - esters of tartaric acid and citric acid with alcohols, the addition products of about 2-15 molecules of ethylene oxide and / or propylene oxide with fatty alcohols having 8 to 22 Represent C atoms.

Preferred anionic surfactants are alkyl sulfates, Alkylpolyglykolethersulfate and ether carboxylic acids having 10 to 18 carbon atoms in the alkyl group and up to 12 Glykolethergrup groups in the molecule and in particular salts of saturated and especially unsaturated C ₈ -C ₂₂ carboxylic acids, such as oleic acid, stearic acid, isostearic acid and palmitic acid.

Nonionic surfactants contain as hydrophilic group z. As a polyol group, a Po lyalkylenglykolethergruppe or a combination of polyol and polyglycol ether group. Such compounds are, for example

• - Addition products of 2 to 30 moles of ethylene oxide and / or 0 to 5 moles of propylene oxide to linear fatty alcohols containing 8 to 22 carbon atoms, to fatty acids containing 12 to 22 carbon atoms Atoms and alkylphenols having 8 to 15 C atoms in the alkyl group,
• C ₁₂ -C ₂₂ -fatty acid mono- and diesters of addition products of 1 to 30 mol of ethylene oxide with glycerol,
• C ₈ -C ₂₂ alkyl mono- and oligoglycosides and their ethoxylated analogs, and
• - Addition products of 5 to 60 moles of ethylene oxide with castor oil and hydrogenated Ri zinusöl.

Preferred nonionic surfactants are alkyl polyglycosides of the general formula R ¹ O- (Z) _X. These compounds are available, for example, under the trade name Plantacare® from Henkel and are characterized by the following parameters.

The alkyl radical R ¹ contains 6 to 22 carbon atoms and may be both linear and branched ver. Preference is given to primary linear and methyl-branched in the 2-position aliphati cal radicals. Such alkyl radicals are, for example, 1-octyl, 1-decyl, 1-lauryl, 1-myristyl, 1-cetyl and 1-stearyl. Particularly preferred are 1-octyl, 1-decyl, 1-lauryl, 1-myristyl. When so-called "oxo-alcohols" are used as starting materials, compounds with an odd number of carbon atoms in the alkyl chain predominate.

The alkyl polyglycosides which can be used according to the invention can contain, for example, only one particular alkyl radical R ¹ . Usually, however, these compounds are made starting from natural fats and oils or mineral oils. In this case, the alkyl radicals R are mixtures corresponding to the starting compounds or corresponding to the particular work-up of these compounds.

Particular preference is given to those alkylpolyglycosides in which R ¹

• consisting essentially of C ₈ and C ₁₀ -alkyl groups,
• essentially of C ₁₂ and C ₁₄ alkyl groups,
• - Essentially from C ₈ - to C ₁₆ alkyl groups or
• - Consists essentially of C ₁₂ - to C ₁₆ -alkyl groups.

As sugar building block Z it is possible to use any desired mono- or oligosaccharides. Usually, sugars with 5 or 6 carbon atoms and the corresponding Used oligosaccharides. Such sugars are, for example, glucose, fructose, galac tose, 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 1.6 are preferred. All particularly preferred are alkyl glycosides in which x is 1.1 to 1.4.  

The alkyl glycosides can also serve, in addition to their surfactant effect, the fixation to improve fragrance components on the hair. The person skilled in the art will therefore be that on the duration of the hair treatment beyond the effect of the perfume oil on the hair is desired, preferably to this class of substance as further ingredient resort to the preparations of the invention. An invention particularly preferred alkyl glucoside is the commercial product Plantacare® 12000G.

The alkoxylated homologs of said alkylpolyglycosides can also be invented be used according to. These homologs can average up to 10 ethylene contain oxide and / or propylene oxide per alkyl glycoside unit.

Furthermore, especially as co-surfactants, zwitterionic surfactants who used the. As zwitterionic surfactants are those surface-active compounds designated net, which carry in the molecule at least one quaternary ammonium group and at least one - COO ^(-) - or -SO ₃ ^(-) group. 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-dimethylammoniumglycinate, for example cocoacylaminopropyldimethylammonium glycinate , and 2-alkyl-3-carboxy-methyl-3-hydroxyethyl-imidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the Kokosacylaminoethylhydroxyethyl carboxymethylglycinat. A preferred zwitterionic surfactant is the fatty acid amide derivative known by the INCI name Cocamidopropyl Betaine.

Also particularly suitable as co-surfactants are ampholytic surfactants. Under on pholytic surfactants are those surface-active compounds understood that in addition to a C ₈ -C ₁₈ alkyl or acyl group in the molecule at least one free amino group and at least one -COOH or -SO ₃ H group and capable of forming inner salts are. Examples of suitable ampholytic 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 18 C-Ato men in the alkyl group. Particularly preferred ampholytic surfactants are N-coco alkylaminopropionate, Kokosacylaminoethylaminopropionat and C _12-18 -Acylsarco sin.

According to the invention as cationic surfactants in particular those of the type of quar ammonium compounds, esterquats and amidoamines.

Preferred quaternary ammonium compounds are ammonium halides, in particular These are chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethyl ammonium chlorides and trialkylmethylammonium chlorides, e.g. B. cetyltrimethylammo ammonium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride, Lauryldimethylammonium chloride, Lauryldimethylbenzylammoniumchlorid and tricetyl methylammonium chloride, as well as those under the INCI names Quaternium-27 and Quaternium-83 known imidazolium compounds. The long alkyl chains of the above surfactants mentioned preferably have 10 to 18 carbon atoms.

Esterquats are known substances which contain at least one ester radio tion and 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 esters salts of fatty acids with 1,2-dihydroxypropyldialkylamines. Such products are included For example, under the trademarks Stepantex®, Dehyquart® and Armocare® distributed. The products Armocare® VGH-70, an N, N-bis (2-palmitoyloxy ethyl) dimethyl ammonium chloride, and Dehyquart® F-75 and Dehyquart® AU-35 Examples of such esterquats.

The Alkylamidoamine are usually by amidation natural or synthetic fatty acids and fatty acid sections prepared with dialkylaminoamines. An inventor According to the invention, particularly suitable compound from this group of substances provides that the name Tegoamid® S 18 commercially available Stearamidopropyl-dimethylamine represents.

Further cationic surfactants which can be used according to the invention are the quaternized Protein hydrolysates.

Likewise suitable according to the invention are cationic silicone oils, such as those described in US Pat Commercially available products Q2-7224 (manufacturer: Dow Corning, a stabilized trimethylsilylamodimethicone),  Dow Corning 929 emulsion (containing a hydroxylamino-mo modified silicone, also referred to as amodimethicone), SM-2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil® Quat 3270 and 3272 (Manufacturer: Th. Goldschmidt; diquaternary polydimethylsiloxanes, quaternium-80).

An example of a cationic surfactant employable quaternary sugar derivative the commercial product Glucquat®100, according to INCI nomenclature a "Lauryl Methyl Glu ceth-10 hydroxypropyl dimonium chlorides ".

The compounds used as surfactant with alkyl groups may be in each case act uniform substances. However, it is usually preferred in the production These substances are based on native plant or animal raw materials, so that one Substance mixtures with different, depending on the particular raw material alkyl chain lengths receives.

For the surfactants, the adducts of ethylene and / or propylene oxide to fat Alcohols or derivatives of these addition products may represent both products with a "normal" homolog distribution as well as those with a narrow homologue genverteilung be used. Under "normal" homolog distribution are thereby Mixtures of homologues understood in the reaction of fatty alcohol and Alkylene oxide using alkali metals, alkali metal hydroxides or alkali obtained metal alkoxides as catalysts. Narrow homolog distributions become when, for example, hydrotalcites, alkaline earth metal salts of ethercar bonsäuren, alkaline earth metal oxides, hydroxides or alcoholates used as catalysts become. The use of products with restricted homolog distribution can be be preferred.

Furthermore, the agents according to the invention preferably contain at least one alkali sierungsmittel. Preferred alkalizing agents are ammonia, monoethanolamine, Sodium hydroxide, potassium hydroxide, isopropylamine, isopropanolamine, 2-amino-2 methylpropan-1-ol and especially arginine, lysine and histidine.  

Furthermore, the colorants of the invention can preferably still a konditio active ingredient selected from the group consisting of cationic surfactants, katio niche polymers, alkylamidoamines, paraffin oils, vegetable oils and synthetic Oils is formed, contained. With regard to the cationic surfactants, see the above referenced.

Cationic polymers may be preferred as conditioning agents. These are in usually polymers containing a quaternary nitrogen atom, for example in the form of an Am monium group.

Preferred cationic polymers are, for example

• - Quaternized cellulose derivatives, as they are known under the names Celquat® and Po lymer JR® are commercially available. The compounds Celquat® H 100, Celquat® L 200 and Polymer JR®400 are preferred quaternized cellulose derivatives.
• - Dimethyldiallylammoniumsalze polymeric and their copolymers with acrylic acid so such as esters and amides of acrylic acid and methacrylic acid. The under the designation Merquat®100 (poly (dimethyldiallylammonium chloride)), Merquat®550 (Dimethyldiallylammonium chloride-acrylamide copolymer) and Merquat® 280 (Dimethyldiallylammonium chloride-acrylic acid copolymer commercially available Products are examples of such cationic polymers.
• - Copolymers of vinylpyrrolidone with quaternized derivatives of dialkylamino acrylates and methacrylates such as vinyl quaternized with diethyl sulfate pyrrolidone-dimethylaminoethyl methacrylate copolymers. Such compounds are under the names Gafquat®734 and Gafquat®755 commercially available.
• - Vinylpyrrolidone-Methoimidazoliniumchlorid copolymers, as described under the name Luviquat®.
• - Quaternized polyvinyl alcohol

as well as those under the designations

• - Polyquaternium 2,
• - Polyquaternium 17,
• - Polyquaternium 18 and
• - Polyquaternium 27 known polymers with quaternary nitrogen atoms in the Po lymerhauptkette.

Particularly preferred are cationic polymers of the first four groups as well Polyquaternium-2, most preferred are Polyquaternium-2, Polyquaternium-10 and Polyquaternium-22. Among the compounds known as Polyquaternium-2 in particular the commercial product Mirapol®A-15 is preferred.

Further suitable conditioning agents are silicone oils, in particular dialkyl and alkylarylsiloxanes such as dimethylpolysiloxane and methylphenylpolysi loxan, as well as their alkoxylated and quaternized analogs. Examples of such silicones are those of Dow Corning under the designations DC 190, DC 200, DC 344, DC 345 and DC 1401 distributed products as well as the commercial products Q2-7224 (manufacturer: Dow Corning; a stabilized trimethylsilylamodimethicone), Dow Corning® 929 emulsion (containing a hydroxylamino-modified silicone, which may also be described as amodimethicones characterized), SM-2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil® Quat 3270 and 3272 (manufactured by Th. Goldschmidt; diquaternary Polydi methylsiloxanes, quaternium-80).

Also usable as conditioning agents are paraffin oils, synthetically herge introduced oligomeric alkenes as well as vegetable oils such as jojoba oil, sunflower oil, orange oil, Almond oil, wheat germ oil and peach kernel oil.

Likewise suitable hair conditioning compounds are phospholipids, for example soy lecithin, egg lecithin and cephaline.

Furthermore, the preparations used according to the invention preferably contain min at least one oil component.

Oil components which are suitable according to the invention are in principle all water-insoluble oils and fatty substances and their mixtures with solid paraffins and waxes. When According to the invention, those substances whose solubility in water is insoluble in water are defined Water at 20 ° C is less than 0.1 wt .-%. The melting point of the individual oil or fat components is preferably below about 40 ° C. Oil and fat comp at room temperature, d. H. are liquid below 25 ° C, can invent According to the invention, be particularly preferred. When using multiple oil and grease components  as well as possibly solid paraffins and waxes, however, it is generally also sufficient when the mixture of oil and fat components and possibly paraffins and waxes these conditions are sufficient.

A preferred group of oil components are vegetable oils. Examples of such Oils are sunflower oil, olive oil, soybean oil, rapeseed oil, almond oil, jojoba oil, orange oil, Wheat germ oil, peach kernel oil and the liquid portions of coconut oil.

However, other triglyceride oils are also suitable, such as the liquid components of beef tallow as well as synthetic triglyceride oils.

Another, particularly preferred group according to the invention as an oil component Barer compounds are liquid paraffin oils and synthetic hydrocarbons as well Di-n-alkyl ethers having a total of between 12 and 36 carbon atoms, in particular 12 to 24 carbon atoms Atoms, such as di-n-octyl ether, di-n-decyl ether, di-n-nonyl ether, di-n- undecyl ether, di-n-dodecyl ether, n-hexyl n-octyl ether, n-octyl-n-decyl ether, n-decyl-n- undecyl ether, n-undecyl-n-dodecyl ether and n-hexyl-n-undecyl ether, and di-tert-butyl ether, di-iso-pentyl ether, di-3-ethyldecyl ether, tert-butyl-n-octyl ether, iso-pentyl-n- octyl ether and 2-methylpentyl-n-octyl ether. The available as commercial products Verbin 1,3-di- (2-ethyl-hexyl) -cyclohexane (Cetiol® S) and di-n-octyl ether (Cetiol® OE) may be preferred.

Also usable according to the invention oil components are fatty acid and fatty alcohol ester. The monoesters of the fatty acids with alcohols having 3 to 24 C atoms are preferred. This substance group is the product of the esterification of fatty acids with 6 to 24 C atoms, such as, for example, caproic acid, caprylic acid, 2-ethylhexanoic acid, Capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitolein 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 as well as their technical mixtures, the z. B. in the pressure splitting of natural Fats and oils, in the oxidation of aldehydes from Roelen's oxosynthesis or the dimerization of unsaturated fatty acids incurred with alcohols such as Isopropyl alcohol, caproic alcohol, caprylic alcohol, 2-ethylhexyl alcohol, capric alcohol,  Lauryl alcohol, isotridecyl alcohol, myristyl alcohol, cetyl alcohol, palmitoleyl alcohol, Stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, Li nolyl alcohol, linolenyl alcohol, elaeostearyl alcohol, arachyl alcohol, gadoleyl alcohol, Behenyl alcohol, erucyl alcohol and brassidyl alcohol and their technical mixtures, the z. As in the high pressure hydrogenation of technical methyl esters based on fats and oils or aldehydes from Roelen's oxosynthesis and as a monomer fraction incurred in the dimerization of unsaturated fatty alcohols. According to the invention preferred are isopropyl myristate, C16-18 alkyl isononanoate (Cetiol® SN), Stearic acid 2-ethylhexyl ester (Cetiol® 868), cetyl oleate, glycerol tricaprylate, coconut fat alcohol caprinate / caprylate and n-butyl stearate.

Furthermore, dicarboxylic acid esters such as di-n-butyl adipate, di (2-ethylhexyl) adipate, Di (2-ethylhexyl) succinate and di-isotridecyl acelate, and diol esters such as ethylene glycol dioleate, ethylene glycol diisotridecanoate, propylene glycol di (2-ethylhexanoate), Propy glycol di-isostearate, propylene glycol di-pelargonate, butanediol di-isostearate and Neopentyl glycol di-capylate is oil component usable in the invention, as well complex esters such. B. the diacetyl-glycerol monostearate.

Finally, fatty alcohols containing 8 to 22 carbon atoms may also be used according to the invention kende oil components are used. The fatty alcohols can be saturated or unge saturates and be linear or branched. Applicable in the context of the invention are, for example Decanol, octanol, octenol, dodecenol, decenol, octadienol, dodecadienol, Decadienol, oleyl alcohol, eruca alcohol, ricinoleic alcohol, stearyl alcohol, isostearyl alcohol, Cetyl alcohol, lauryl alcohol, myristyl alcohol, arachidyl alcohol, capryl alcohol, caprin alcohol, linoleyl alcohol, linolenyl alcohol and behenyl alcohol, and their Guerbet alcohols, and these listings are given by way of example and not by way of limitation should. However, the fatty alcohols are derived from preferably natural fatty acids, wherein usually characterized by recovery from the esters of fatty acids by reduction can be done. Also usable according to the invention are those fatty alcohols cuts caused by the reduction of naturally occurring triglycerides such as beef tallow, Palm oil, peanut oil, rapeseed oil, cottonseed oil, soybean oil, sunflower oil and linseed oil or from their transesterification products with corresponding alcohols resulting fatty acid esters produced, and thus represent a mixture of different fatty alcohols.  

The oil components are preferably in Menden from 0.05 to 10 wt .-%, in particular from 0.1 to 2 wt .-% used in the colorants of the invention.

In a preferred embodiment of the present invention is formed in Auflö solution of the colorants in water a gel. For this purpose, the dye thickener such as agar-agar, guar gum, alginates, xanthan gum, gum arabic, karaya gum, Locust bean gum, linseed gums, dextrans, cellulose derivatives, e.g. Methyl cellulose, hydroxyalkylcellulose and carboxymethylcellulose, starch fractions and De such as amylose, amylopectin and dextrins, clays such. B. bentonite or vollsynthe tables hydrocolloids such. B. polyvinyl alcohol added. Particularly preferred Verdic are xanthans, alginates and highly substituted carboxymethylcelluloses.

Other active ingredients, auxiliaries and additives are, for example

• Zwitterionic and amphoteric polymers such as acrylamidopropyl tri methylammonium chloride / acrylate copolymers and octylacrylamide / methyl methacrylate lat / tert-butylaminoethyl methacrylate / 2-hydroxypropyl methacrylate copolymers,
• Anionic polymers such as, for example, polyacrylic acids, crosslinked polyacrylic acids, Vinyl acetate / crotonic acid copolymers, vinyl pyrrolidone / vinyl acrylate copolymers, Vinyl acetate / butyl maleate / isobornyl acrylate copolymers, methyl vinyl ether / maleic acid Anhydride copolymers and acrylic acid / ethyl acrylate / N-tert-butyl acrylamide terpo mers,
• - structurants such as maleic acid and lactic acid,
• Protein hydrolysates, in particular elastin, collagen, keratin, silk, milk protein , Soy protein and wheat protein hydrolysates, their condensation products with Fatty acids and quaternized protein hydrolysates,
• Perfume oils, dimethylisosorbide and cyclodextrins,
• Solvents and mediators such as ethanol, isopropanol, ethylene glycol, propylene glycol, glycerol and diethylene glycol,
• - Fiber structure improving agents, in particular mono-, di- and oligosaccharides such as glucose, galactose, fructose, fructose and lactose,
• Quaternized amines such as methyl-1-alkylamidoethyl-2-alkylimidazolinium methosulfate
• Defoamers like silicones,  
• Dyes for staining the agent,
• Anti-dandruff agents such as Piroctone Olamine, Zinc Omadine and Climbazole,
• - Sunscreens, in particular derivatized benzophenones, cinnamic acid derivatives and triazines,
• - Substances for adjusting the pH, such as conventional acids, in particular special edible acids and bases,
• - active substances such as allantoin, pyrrolidonecarboxylic acids and their salts, and bisabolol,
• Vitamins, provitamins and vitamin precursors, in particular those of groups A, B ₃ , B ₅ , B ₆ , C, E, F and H,
• - Plant extracts such as the extracts of green tea, oak bark, stinging nettle, Hama melis, hops, chamomile, burdock root, horsetail, hawthorn, lime blossom, Almond, aloe vera, spruce needle, horse chestnut, sandalwood, juniper, coconut, Mango, Apricot, Lime, Wheat, Kiwi, Melon, Orange, Grapefruit, Sage, Ros Marin, Birch, Mallow, Meadowfoam, Quendel, Yarrow, Thyme, Melissa, Hominy, coltsfoot, marshmallow, meristem, ginseng and ginger root,
• - cholesterol,
• Bodying agents such as sugar esters, polyol esters or polyol alkyl ethers,
• - fats and waxes such as spermaceti, beeswax, montan wax and paraffins,
• - fatty acid,
• Complexing agents such as EDTA, NTA, β-alaninediacetic acid and phosphonic acids,
• - Swelling and penetration substances such as glycerol, propylene glycol monoethyl ether, Carbo nate, bicarbonates, guanidines, ureas and primary, secondary and tertiary phosphates,
• Opacifiers such as latex, styrene / PVP and styrene / acrylamide copolymers
• Pearlescing agents such as ethylene glycol mono- and distearate and PEG-3-distearate,
• - pigments,
• Stabilizer for hydrogen peroxide and other oxidizing agents,
• Propellants such as propane-butane mixtures, N ₂ O, dimethyl ether, CO ₂ and air,
• - antioxidants.

Regarding further optional components as well as the amounts of this com components is expressly referred to the relevant manuals known to those skilled in the art,  z. B. Kh. Schrader, bases and formulations of cosmetics, 2nd edition, Hüthig book Verlag, Heidelberg, 1989, referenced.

Conveniently, the enzyme preparation immediately before the hair coloring with the Preparation mixed from the dye precursors. The pH of the users preparation is preferably between 5 and 11, in particular between 5.5 and 10.5, most preferably between 6 and 9. The application temperatures can ei in In the range between 15 and 40 ° C, temperatures between 20 and 35 ° C are particularly preferred according to the invention. After a contact time of approx. 30 minutes the hair dye is removed by rinsing the hair to be dyed. The after Washing with a shampoo is unnecessary if a strong surfactant-containing carrier, eg. B. a Dyeing shampoo, was used.

In a further embodiment of the present invention, it may be preferred that Formulate enzyme preparation free of antioxidants and / or complexing agents, since these can block the action of the enzymes.

A second object of the present invention is a method of coloring keratinic fibers in which a composition according to the invention is applied to the fibers is rinsed off and after a contact time again.

A third object of the present invention is the use of a phenol oxidizing enzyme which can be obtained from fungi of the genus Acremonium, for coloring keratinous fibers, in particular human hair.

The following embodiments are intended to explain the subject invention in more detail.  

embodiments 1. Application recipes

All quantities in the following formulations are, unless otherwise stated, Weight.

Colorant A

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 ¹ 0.4 Plantacare® 1200 ² 3.0 Dehyton® K ³ 2.5 ammonium sulfate 0.5 Natrosol® 250 HR ⁴ 1.0 4-Amino-2 - ((diethylamino) methyl) phenol dihydrochloride 2.67 2-amino-3-hydroxypyridine 1.1 Ammonia (25% in water) ad pH 8.5 water ad 100 ¹ cetylstearyl alcohol with approx. 20 EO units (INCI name: Ceteareth-20) (Cognis) @ ² C _12-16 -fatty alcohol-1,4-glucoside (about 50% active ingredient; INCI name: lauryl glucoside) (Cognis) @ ³ fatty acid amide with betaine structure (about 30% active ingredient, INCI name: Cocamidopropyl Betaine) (Henkel) @ ⁴ hydroxyethylcellulose (Hercules)

Colorant B

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-Amino-2-aminomethyl-phenol-dihydrochloride 0,002 2-amino-3-hydroxypyridine 0,004 3-methyl-4-aminophenol 0,007 1,3-bis (2 ', 4'-diaminophenoxy) -propantetrahydrochlorid 0.0005 p-toluenediamine sulphate 0.06 resorcinol 0.01 3-Amino-2,4-dichlorphenolhydrochlorid 0,008 3-Aminopherol 0,002 4-chlororesorcinol 0.01 arginine 1.0 Monoethynolamin ad pH 8.5 water ad 100

Colorant C

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-amino-2-chlorophenol 0.8 2-amino-3-hydroxypyridine 0.1 3-methyl-4-aminophenol 0.3 5-amino-2-methylphenol 0.07 resorcinol 0.2 3-aminophenol 0.2 1- (2'-hydroxyethyl) -2,5-diaminobenzene sulfate 0.7 4-methyl 0.1 5,6-dihydroxyindole 0.05 Monoethanolamine ad pH 8.5 water ad 100

Dye D

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-aminophenol 0.49 4-amino-3-methylphenol 0.55 2-amino-3-hydroxypyridine 1.0 p-toluenediamine sulphate 0.2 6-hydroxyindole 0.1 5 - ((2'-hydroxyethyl) amino) -2-methylphenol 0.1 1,2,3,4-tetrahydro-6-nitroquinoxaline 0.05 HC Yellow 5 ⁵ 0.03 HC Red 1 ⁶ 0.02 sodium hydroxide ad pH 8.0 water ad 100 ⁵ 2 - ((2'-amino-4'-nitrophenyl) amino) ethanol @ ⁶ 4-amino-2-nitrodiphenylamine

Colorant E

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-Amino-2-aminomethyl-phenol-dihydrochloride 2.0 2-methylamino-3-amino-6-methoxypyridine 2.25 arginine ad pH 7.5 water ad 100

Colorant F

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-Amino-2-aminomethyl-phenol-dihydrochloride 0,017 2-methylamino-3-amino-6-methoxypyridine 0,002 1- (2'-hydroxyethyl) -2,5-diamiuobenzol sulfate 0.03 1-naphthol 0.02 2-methyl 0.0006 lysine ad pH 8.5 water ad 100

Colorant G

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-Amino-2 - ((diethylamino) methyl) phenol dihydrochloride 0.1 2-methylamino-3-amino-6-methoxypyridine 0,002 3-methyl-4-aminophenol 0.07 2,4,5,6-tetra-sulfate 1.0 p-toluenediamine sulphate 1.1 3-aminophenol 0,006 resorcinol 0.11 2-methyl 0.54 2,7-dihydroxynaphthalene 0.032 2-amino-3-hydroxypyridine 0.4 4-amino-2-nitro-diphenylamine-2'-carboxylic acid 0.1 Ammonia, (25% in water) ad pH 8.5 water ad 100

Colorant H

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-amino-2-chlorophenol dihydrochloride 1.0 2-methylamino-3-amino-6-methoxypyridine 1.7 2-amino-4-nitro-6-chlorophenol 0.05 HC Red BN ⁷ 0.2 5,6-Dihydroxyindolin hydrobromide 0.1 Ammonia (25% in water) ad pH 8.5 water ad 100 ⁷ 4- (3'-hydroxypropyl) amino-3-nitrophenol (Clariant)

Colorant I

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-Amino-2 - ((diethylamino) methyl) phenol dihydrochloride 1.25 4-Amino-2-aminomethyl-phenol-dihydrochloride 1.0 5-amino-2-methyl-phenol 1.23 2-amino-2-methylpropan-1-ol ad pH 8.0 water ad 100

Colorant J

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-Amino-2 - ((diethylamino) methyl) phenol dihydrochloride 0.5 Bis- (2-hydroxy-5-aminophenyl) methane 0.4 5-amino-2-methylphenol 0.55 p-toluenediamine sulphate 0.3 p-Phenylenediamine dihydrochloride 0.2 resorcinol 0.07 2,7-dihydroxynaphthalene 0.09 2-methyl 0.07 o-aminophenol 0.03 5,6-Dihydroxyindolin hydrobromide 0.05 Ammonia (25% in water) ad pH 9.0 water ad 100

Colorant K

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 ammonium sulfate 0.5 Natrosol® 250 HR 1.07 4-Amino-2-aminomethyl-phenol-dihydrochloride 0.02 5-amino-2-methylphenol 0.03 3-methyl-4-aminophenol 0.01 2,4,5,6-tetra-sulfate 0.8 p-toluenediamine sulphate 0.09 3-aminophenol 0,004 resorcinol 0.04 2-methyl 0.22 2,7-dihydroxynaphthalene 0.3 4-amino-2-nitro-diphenylamine-2'-carboxylic acid 0.15 1,2,3,4-tetrahydro-6-nitroquinoxaline 0.25 Ammonia (25% in water) ad pH 8.5 water ad 100

Colorant L

Fatty alcohol mixture C ₁₂ -C ₁₈ 5.25 Eumulgin® B2 0.4 Plantacare® 1200 3.0 Dehyton® K 2.5 sodium 0.1 ammonium sulfate 0.5 Natrosol® 250 HR 1.0 4-Amino-2-aminomethyl-phenol-dihydrochloride 1.06 4-aminophenol 0.55 5-amino-2-methylphenol 0.74 4-hydroxyindole 0.1 1,3-bis (2 ', 4'-diaminophenoxy) -propantetrahydrochlorid 0.3 2-methylamino-3-amino-6-methoxy-pyridine dihydrochloride 0.1 Ammonia (25% in water) ad pH 8.5 water ad 100

Colorant M

Hydrenol®D ⁸ 8.0 C12-C18 fatty alcohol 2.0 Akypo Soft® 45 NV ⁹ 10.0 Eumulgin® B1 ¹⁰ 0.5 Eumulgin® B2 0.5 5-amino-2-methylphenol 0.02 3-Amino-2-chloro-6-methylphenol 0.36 Bis (2,4-diaminophenoxy) propane tetrahydrochloride 0.0002 3-methyl-4-aminophenol 0.02 4-Amino-2-aminomethyl-phenol-dihydrochloride 0.40 p-toluenediamine sulphate 0.34 N, N-bis (2-hydroxyethyl) -p-phenylenediamine sulfate 0.48 resorcinol 0.33 m-aminophenol 0.0011 2-amino-3-hydroxypyridine 0.009 ammonium chloride 0.3 Ammonia (25% in water) ad pH 8.5 water ad 100 ⁸ C _16-18 fatty alcohol (INCI name: Cetearyl alcohol) (Cognis) @ ⁹ C _12-14 fatty alcohol-4,5-EO-acetic acid sodium salt (21% active ingredient in water, INCI name: sodium laureth-6 carboxylate) (KAO) @ ¹⁰ cetyl stearyl alcohol + 12 EO (INCI name: Ceteareth-12) (Cognis)

Colorant N

Hydrenol®D 8.0 C12-C18 fatty alcohol 2.0 Akypo Soft® 45 NV 10.0 Eumulgin® B1 0.5 Eumulgin® B2 0.5 m-aminophenol 0.005 3-amino-2-methylamino-6-methoxypyridinhydrochlorid 0,002 2-amino-3-hydroxypyridine 0.24 2,7-dihydroxynaphthalene 0.02 2-methyl 0.6 p-toluenediamine sulphate 0.73 resorcinol 0.13 2,6-dihydroxy-3,4-dimethyl-pyridine 0.1 2,4,5,6-tetra 1.3 5-amino-2-methylphenol 0.03 5- (β-hydroxyethyl) amino-2-methylphenol 0.3 2-nitro-4-aminodiphenylamine-2'-carboxylic acid 0.1 ammonium chloride 0.4 perfume oil 0.2 Ammonia (25% in water) ad pH 8.5 water ad 100

Colorant O

Hydrenol® D 8.0 C12-C18 fatty alcohol 2.0 Akypo Soft® 45 NV 10.0 Eumulgin® B1 0.5 Eumulgin® B2 0.5 2-methyl 0.48 p-toluenediamine sulphate 0.6 1- (2'-hydroxyethyl) -2,5-diaminobenzene 0.6 resorcinol 0.21 2,6-dihydroxy-3,4-dimethyl-pyridine 0.66 2,4,5,6-tetra 3.0 3-methyl-4-aminophenol 0.16 3-Amino-2-chloro-6-methyl-phenol 0.11 5-amino-2-methylphenol 0.03 1.5 Diyhdroxynaphthalin 0,002 ammonium chloride 0.2 Mirapol®A-15 ¹¹ 1.5 perfume oil 0.2 histidine ad pH 8.5 water ad 100 ¹¹ polymeric quaternary ammonium salt (about 64% active ingredient, INCI name: Polyquaternium-2) (RHONE-POULENC)

Colorant P

Hydrenol®D 5.0 C12-C18 fatty alcohol 2.0 Texapon® NSO ¹² 3.0 ammonium sulfate 0.5 5-amino-2-methylphenol 0.56 3-methyl-4-aminophenol 0,055 p-toluenediamine sulphate 0.65 resorcinol 0.14 4-aminophenol hydrochloride 0.6 4-amino-2-nitro-diphenylamino-2'-carboxylic acid 0.05 6-nitro-1,2,3,4-tetrahydroquinoxalin 0.1 Ammonia (25% in water) ad pH 8.0 water ad 100 ₁₂ sodium salt of lauryl ether sulfate (about 27% active ingredient, INCI name: Sodium Laureth Sulfate) (Cognis)

Colorant Q

Hydrenol®D 5.0 C12-C18 fatty alcohol 2.0 Texapon®NSO 3.0 ammonium sulfate 0.5 Bis (2,4-diaminophenoxy) propane tetrahydrochloride 0,003 p-toluenediamine sulphate 0.033 resorcinol 0.0055 4-aminophenol hydrochloride 0,014 2-amino-3-hydroxypyridine 0.0035 arginine 1.0 Ammonia (25% in water) ad pH 7.0 water ad 100

For coloration, in each case 1 part of the above-described colorants with 0.1 part an enzyme preparation mixed. The enzyme preparation contains, based on the Protein amount, 0.3 wt .-% enzyme obtained from fungi of the genus Acremonium murorum.

This application preparation is applied to the fibers to be dyed, there for 30 Leave minutes and then rinsed out.

Claims (16)

1. An agent for dyeing keratinous fibers containing in a cosmetically acceptable carrier at least one dye precursor, characterized in that it contains at least one phenol-oxidizing enzyme, which can be obtained from fungi of the genus Acremonium contains. 2. Composition according to claim 1, characterized in that the enzyme is purified. 3. Composition according to one of claims 1 or 2, characterized in that the enzyme can be obtained from Acremonium murorum. 4. Composition according to claim 3, characterized in that the enzyme from Acremonium murorum var. murorum with CBS approval number 157.72 can. 5. Composition according to one of claims 1 or 2, characterized in that the enzyme can be obtained from Acremonium obclavatum. 6. Composition according to one of claims 1 to 5, characterized in that it as a color contains at least one developer component. 7. Composition according to one of claims 1 to 6, characterized in that it as a color contains at least one indole and / or indoline derivative. 8. Composition according to one of claims 1 to 7, characterized in that it at least contains a coupler component. 9. Composition according to one of claims 1 to 8, characterized in that it continues contains at least one substantive dye. 10. Composition according to one of claims 1 to 9, characterized in that it continues contains at least one surfactant. 11. Composition according to claim 10, characterized in that it is a nonionic or a contains amphoteric surfactant.   12. Composition according to one of claims 10 or 11, characterized in that it has a A surfactant combination of at least one anionic surfactant with at least one contains amphoteric surfactant and / or with at least one nonionic surfactant. 13. Composition according to one of claims 1 to 12, characterized in that it is an alkali contains sierungsmittel. 14. Composition according to one of claims 1 to 13, characterized in that it is a contains cationic polymer. 15. A process for dyeing keratinic fibers, characterized in that an agent according to one of claims 1 to 14 is applied to the fibers and after a Exposure time is rinsed off again. 16. Use of a phenol oxidizing enzyme derived from fungi of the genus Acremonium can be obtained for oxidative staining of keratinic fibers.