DE19916031A1 - Colorants and uses - Google Patents

Abstract

The present invention relates to means for colouring keratinic fibres which contain 4-amino-2-((diethylamino)methyl)phenol as developing component and 2-methyl-5-aminophenol as coupling component. The inventive means enable brilliant colourings, especially in the orange range, that are characterised by excellent light-fastness and shampooing fastness.

Description

The present invention relates to colorants which, as developer component, 4-amino-2- ((diethylamino) methyl) phenol in combination with 2-methyl-5-aminophenol as Contain coupler component and their use for dyeing keratin fibers.

They play for dyeing keratin fibers, especially human hair so-called oxidation colorants because of their intense colors and good Authenticity properties a preferred role. Such colorants contain oxidation dye precursors, so-called developer components and coupler components. The Developer components form under the influence of oxidizing agents or Atmospheric oxygen among each other or under coupling with one or more couplers components from the actual dyes.

Good oxidation dye precursors are primarily intended to meet the following requirements meet: You must have the desired color shades in the oxidative coupling train sufficient intensity and authenticity. You must also have a good one Possibility to draw on the fiber, especially with human hair no noticeable differences between damaged and newly grown hair may exist (leveling ability). Finally, they should - if as a hair dye for Application coming - do not stain the scalp too much, and above all, they should be in toxicologically and dermatologically harmless.

Primary aromatic amines with a. Are usually used as developer components further, in the para or ortho position, free or substituted hydroxy  or amino group, diaminopyridine derivatives, heterocyclic hydrazones, 4- Aminopyrazole derivatives and 2,4,5,6-tetraaminopyrimidine and its derivatives used.

Special representatives are, for example, p-phenylenediamine, p-toluenediamine, 2,4,5,6-Te traaminopyrimidine, p-aminophenol, N, N-bis- (2-hydroxyethyl) -p-phenylenediamine, 2- (2.5 - Diaminophenyl) ethanol, 2- (2,5-diaminophenoxy) ethanol, 1-phenyl-3-carboxyamido-4- amino-pyrazolon-5, 4-amino-3-methylphenol, 2-aminomethyl-4-aminophenol, 2-Hy droxy-4,5,6-triaminopyrimidine, 2,4-dihydroxy-5,6-diaminopyrimidine, 2,5,6-triamino-4- hydroxypyrimidine and 1,3-N, N'-bis (2'-hydroxyethyl) -N, N'-bis- (4'-aminophenyl) - diamino-propan-2-ol.

As coupler components are usually m-phenylenediamine derivatives, naphthols, Re sorcinol and resorcinol derivatives, pyrazolones and m-aminophenols are used. As Coupler substances are particularly suitable 1-naphthol, 1,5-, 2,7- and 1,7- Dihydroxynaphthalene, m-aminophenol, resorcinol, resorcinol monomethyl ether, m-pheny lendiamine, 1-phenyl-3-methyl-pyrazolon-5, 2,4-dichloro-3-aminophenol, 1,3-bis (2,4-di aminophenoxy) propane, 2-chlororesorcinol, 4-chlororesorcinol, 2-chloro-6-methyl-3-aminophene nol, 2-methylresorcinol, 5-methylresorcinol and 2-methyl-4-chloro-5-aminophenol.

Alone with a developer component or a special coupler / developer combination nation usually does not succeed in creating a natural shade on the hair receive. In practice, therefore, combinations are usually different Developer and / or coupler components used. There is therefore a constant need for new, improved dye combinations. The through the dye combinations achievable colorations should be resistant to light, heat, sweat, friction and the influence of chemical reducing agents, e.g. B. perm fluids. Furthermore should the coloring obtained can be easily removed from the hair again by bleaching can, if it does not meet the individual wishes of the individual and should be undone. Therefore, the task was still new Develop developer-coupler combinations that are expressive, brilliant Color tones, especially in the orange range, can be achieved and also in toxicological ones Are an advance over the state of the art.  

Surprisingly, it has now been found that the developer-coupler combinations 4- Amino-2 - ((diethylamino) methyl) phenol / 2-methyl-5-aminophenol which to such Combined tasks to a high degree.

The present invention therefore relates to agents for dyeing keratin Fibers containing 4-amino-2 - ((diethylamino) methyl) phenol as developer component and 2- Contain methyl-5-aminophenol as a coupler component.

According to the invention, keratin fibers include furs, wool, feathers and in particular understand human hair. Although the colorants of the invention in the first Line is suitable for dyeing keratin fibers, there is in principle one Use contrary to anything else.

The dyeings obtained with the developer / coupler combination according to the invention are characterized by great brilliance as well as high light and shampooing authenticity.

The use of 4-amino-2-aminomethyl derivatives in hair dyes is already in the Literature has been described. For example, DE-A1-35 43 345 is concerned generally with derivatives of 4-amino-2-aminomethylphenols. Furthermore, in the EP A1-857 479 hair dyes have been described which contain 4-amino-2 - ((diethylamino) methyl) - phenol in combination with 5-amino-2-methoxyphenol. This rather vague However, information can be no reference to the with the invention Take combination of achievable effects.

In one embodiment of the present invention, the colorants can still contain further developer components. Preferred according to the invention Developer components are p-phenylenediamine, p-toluenediamine, p-aminophenol, o- Aminophenol, 1- (2'-hydroxyethyl) -2,5-diaminobenzene, N, N-bis (2-hydroxyethyl) -p-phe nylenediamine, 2- (2,5-diaminophenoxy) ethanol, 1-phenyl-3-carboxyamido-4-amino-pyra zolon-5, 4-amino-3-methylphenol, 2,4,5,6-tetraaminopyrimidine, 2-hydroxy-4,5,6- triaminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2,4-dihydroxy-5,6- diaminopyrimidine, 2-dimethylamino-4,5,6-triaminopyrimidine, 2-hydroxy  ethylaminomethyl-4-aminophenol, 4,4'-diaminodiphenylamine, 4-amino-3-fluorophenol, 2-aminomethyl-4-aminophenol, 2-hydroxymethyl-4-aminophenol, bis- (2-hydroxy-5- aminophenyl) methane, 1,4-bis (4-aminophenyl) diazacycloheptane, 1,3-bis (N- (2-hydroxy ethyl) -N (4-aminophenylamino)) - 2-propanol, 4-amino-2- (2-hydroxyethoxy) phenol, 1.10- Bis- (2,5-diaminophenyl) -1,4,7,10-tetraoxadecane and 4,5-diaminopyrazole derivatives EP 0 740 741 or WO 94/08970 such as e.g. B. 4,5-Di-amino-1- (2'-hydroxyethyl) pyrazole.

Particularly preferred developer components are p-phenylenediamine, p-toluenediamine, p-aminophenol, 1- (2'-hydroxyethyl) -2,5-diaminobenzene, 4-amino-3-methylphenol, 2,4,5,6-tetraaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 4-hydroxy-2,5,6-tri aminopyrimidine, 4,5-diamino-1- (2-hydroxyethyl) pyrazole, 2-aminomethyl-4-amino phenol, N, N-bis- (2-hydroxyethyl) -p-phenylenediannine, bis- (2-hydroxy-5-aminophenyl) - methane, 1,10-bis (2,5-diaminophenyl) -1,4,7,10-tetraoxadecane and o-aminophenol.

The agents according to the invention can also be used to shade the attainable colors contain one or more further coupler components. Coupler substances are often aromatic or heterocyclic ring systems, the two reactive groups in meta- Have position. As a rule, m- Phenylenediamine derivatives, naphthols, resorcinol and resorcinol derivatives, pyrazolones and m- Aminophenol derivatives used.

Coupler components preferred according to the invention are:

• M-aminophenol and its derivatives such as 5- (3-hydroxypropylamino) -2- methylphenol, 3-amino-2-chloro-6-methylphenol, 2-hydroxy-4-aminophenoxyethanol, 3-amino-6-methoxy-2-methylaminophenol, 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-dihydroxy-5- (methylamino) benzene, 3- (ethylamino) -4-methylphenol and 2,4-dichloro-3- aminophenol,
• O-aminophenol and its derivatives,
• M-diamino benzene and its derivatives such as 2,4- Diaminophenoxyethanol, 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 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-3,4-diaminopyridine, 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- Hydroxymethyl-1-naphthol, 2-hydroxyethyl-1-naphthol, 1,5-dihydroxynaphthalene, 1,6-dihydroxynaphthalene, 1,7-dihydroxynaphthalene, 1,8-dihydroxynaphthalene, 2,7- Dihydroxynaphthalene 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- Hydroxyindole,
• - Methylenedioxybenzene derivatives such as 3,4-methylenedioxyphenol, 1- Hydroxy-3,4-methylenedioxybenzene, 1-amino-3,4-methylenedioxybenzene and 1- (2'- Hydroxyethyl) amino-3,4-methylenedioxybenzene.

Particularly preferred coupler components in the sense of the invention are 1-naphthol, 1,5-, 2,7- and 1,7-dihydroxynaphthalene, 2-amino-3-hydroxypyridine, 3-amino-2-methylamino- 6-methoxypyridine, resorcinol, 4-chlororesorcinol, 2-methylresorcinol, 2,5-dimethylresorcinol, m- Aminophenol, o-aminophenol and 2-chlororesorcinol.  

The developer and coupler components are usually used in free form. For substances with amino groups, however, it may be preferred to use them in salt form, in particular in the form of the hydrochlorides and sulfates.

The hair colorants according to the invention contain both the developer components and the coupler components are also preferably present in an amount of 0.005 to 20% by weight preferably 0.1 to 5% by weight, based in each case on the entire oxidation colorant. Developer components and coupler components generally become approximate molar amounts used to each other. If the molar use is also useful has proven moderately, is a certain excess of individual oxidation dye precursors 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 be included.

In a preferred embodiment, the hair colorants according to the invention contain for further modification of the color shades in addition to the oxidation dye precursors additionally conventional direct dyes. Direct dyes are common Nitrophenylenediamines, nitroaminophenols, azo dyes, anthraquinones or indophe nole. Preferred direct dyes are those under the international designation HC Yellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, Basic Yellow 57, Disperse Orange 3, HC Red 3, HC Red BN, Basic Red 76, HC Blue 2, HC Blue 12, Disperse Blue 3, Basic Blue 99, HC Violet 1, Disperse Violet 1, Disperse Violet 4, Disperse Black 9, Basic Brown 16 and Basic Brown 17 known compounds and 4-amino-2-nitrodiphenylamine-2'-carboxylic acid, 6-nitro-1,2,3,4-tetrahydroquinoxaline, Hydroxyethyl-2-nitro-toluidine, picraminic acid, 2-amino-6-chloro-4-nitrophenol, 4- Ethylamino-3-nitrobenzoic acid and 2-chloro-6-ethylamino-1-hydroxy-4-nitrobenzene.

The inventive agents according to this embodiment contain the direct dyes preferably in an amount of 0.01 to 20 wt .-%, based on the entire 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, rotten tree bark, sage, blue wood, madder root, catechu, Contain sedre and alkanna root.

Other dye components contained in the colorants according to the invention can also indoles and indolines, and their physiologically tolerable salts. Preferred Examples are 5,6-dihydroxyindole, N-methyl-5,6-dihydroxyindole, N-ethyl-5,6-dihy hydroxy indole, N-propyl-5,6-dihydroxyindole, N-butyl-5,6-dihydroxyindole, 5,6- Dihydroxyindole-2-carboxylic acid, 6-hydroxyindole, 6-aminoindole and 4-aminoindole. Also preferred are 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, 6-hydroxyindoline, 6-aminoindoline and 4-aminoindoline.

It is not necessary that the oxidation dye precursors or the substantive ones Dyes each represent uniform compounds. Rather, in the inventions hair dye according to the invention, due to the manufacturing process for individual dyes, contain minor components in minor amounts to the extent that these do not adversely affect the coloring result or from others Reasons, e.g. B. toxicological, must be excluded.

In a further embodiment of the present invention, the Hair dyes furthermore at least one dye of the reactive type Carbonyl compounds selected from the group of aromatic, heteroaromatic or unsaturated aldehydes or ketones, the dialdehydes or diketones or the acetals, Semi-aminals or imine derivatives of such reactive carbonyl compounds.

Hair dyes of the reactive carbonyl compound type have been known for a long time. Suitable compounds of the aromatic aldehyde type are e.g. B. in the German DE 196 30 274 A1 and DE 196 30 275 A1. Suitable Connections are e.g. B. the 2-hydroxybenzaldehyde, the 4-hydroxy-3-methoxy-benzal dehyd (vanillin) and the 4-hydroxy-3-methoxy-cinnamaldehyde (coniferyl aldehyde).

Suitable compounds of the heteroaromatic aldehyde type are e.g. B. in the German published application DE 197 17 280 A1. Particularly suitable  Dyes are e.g. B. trans-β- (2-furyl) acrolein, 1-methylindole-3-aldehyde, 2- (1,3,3- Trimethyl-2-indolinylidene) acetaldehyde or antipyrin-4-aldehyde. Special products of this type with a pyridinium group are described in German patent application DE 197 45 356.2 described e.g. B. the very suitable 4-formyl-1-methylpyridinium benzenesulfonate and 4-formyl-1-methylquinolinium methane sulfonate or methyl sulfate.

Suitable dyes of the unsaturated aldehyde type are e.g. B. in German Published patent application DE 197 17 224 A1. Suitable for the present invention the glutaconaldehyde in the form of its salts, e.g. B. its alkali or Tetrabutylammoniumsalzes or the 2-chloro-3-hydroxymethylene-1-cyclohexen-1-aldehyde.

Dialdehydes and diketones and their derivatives, which are dyes according to the invention are, for. B. alicyclic and cyclic 1,2- and 1,3-dicarbonyl compounds, such as Isatin, ninhydrin, alloxan, isobarbituric acid, p- and o-quinones, 1,3-indanediones and their Derivatives. Such dyes are found, for. B. in the German patent application DE 43 35 627 A1. Suitable compounds are e.g. B. the malon dialdehyde, preferably in Form of its dimethyl acetal, the 2-nitro-1,3-indanedione or the 2-acetyl-1,3-cyclo hexanedione.

The diketones suitable according to the invention also include cyclic ones Dicarbonyl compounds such as e.g. B. the isatin and its derivatives, as z. B. in the German Offenlegungsschrift DE 44 09 143 A1 are described. According to the invention z. B. the isatinic acid potassium salt, the isatin-5-sulfonic acid potassium salt, the N-allylisatin, 1-piperidinomethylisatin, 1-hydroxymethylisatin and 1- Diethylaminomethylisatin.

Another suitable cyclic dicarbonyl compound is e.g. B. also the dehydro ascorbic acid, its suitability as a hair dye from the German patent application DE 197 45 354.6 is known. Finally, the acetals, imine derivatives and Semi-aminals of the reactive carbonyl compounds mentioned. Such connections are obtained by reacting the carboxyl group with primary alcohols or amines and possibly Obtain water elimination.  

Starting from the unsaturated dialdehydes and diketones, one gets into the Group of the merocyanine and azomethine dyes. Suitable imine derivatives of Glutacondialdehydes are e.g. B. the mono-N-methylaniline derivative of glutaconaldehyde (5- N-methylanilinopentadienal) or the N- (5-anilino-2,4-pentadien-1-ylidene) anilinium chloride. Another suitable vinylogous cyanine dye is 7-dimethylamino-2,4,6- heptatrienylidene dimethylammonium perchlorate. Such connections are called hair dye medium components z. B. from the German patent application DE 197 17 223 A1 known.

Many of the reactive carbonyl compounds mentioned stain fibers containing keratin Expression of different color nuances particularly intensively only in combination with one or several color-enhancing compounds with primary or secondary amino or Hydroxy group, selected from the group of amino acids and peptides, the aromatic amines, phenols, aminophenols and nitrogen-containing heterocycles.

In many cases, deeper (darker) shades are obtained.

Suitable amino acids are e.g. B. the naturally occurring and synthetic Amino acids, e.g. B. arginine, histidine, phenylalanine, dihydroxyphenylalanine, ornithine, Lysine. Suitable peptides are, above all, oligo- and polypeptides, which are sufficient Solubility in water in the preparations according to the invention for keratin reduction exhibit. As examples are e.g. B. glutathione or those in the hydrolysates of collagen, Keratin, elastin, casein, vegetable proteins such as soy protein, wheat gluten or To name almond protein contained oligopeptides.

Suitable aromatic amines and aminophenols are N, N-dimethyl-, N, N-diethyl-, N- (2-hydroxyethyl) -N-ethyl-, N, N-bis- (2-hydroxyethyl) -, N- (2 -Methoxyethyl-), 2-chloro, 2,3-, 2,4- and 2,5-dichloro-p-phenylenediamine, 2,5-dihydroxy-4-morpholinoaniline dihydro bromide, 2-, 3- and 4 -Aminophenol, 2-aminomethyl-4-aminophenol, 2-hydroxymethyl-4-aminophenol, o- and p-phenylenediamine, o- and m-toluenediamine, 2,5-diamino-phenol, -toluene and -phenethol, 4-amino -3-methylphenol, 2- (2,5-diaminophenyl) ethanol, 2,4-diaminophenoxyethanol, 2- (2,5-diaminophenoxy) ethanol, 4-methylamino, 3-amino-4- (2'- hydroxyethyloxy) -, 3,4-methylenediamino- and 3,4-methylenedioxyaniline, 3-amino-2,4-dichloro-, 4-methylamino-, 2-methyl-5-amino-, 3-methyl-4-amino- , 2-methyl-5- (2-hydro xyethylamino) -, 6-methyl-3-amino-2-chloro, 2-methyl-5-amino-4-chloro, 3,4-methylene dioxy-, 5th - (2-Hydroxyethylamino) -4-methoxy-2-methyl- and 4-amino-2-hydroxymethylphenol, 1,3-diamino-2,4-dimethoxybenzene, 2-, 3-, 4-aminobenzoic acid, -phenylacetic acid acid, 2,3-, 2,4-, 2,5-, 3,4-, 3,5-diaminobenzoic acid, 4-, 5-aminosalicylic acid, 3-amino-4-hydroxy-, 4-amino-3- hydroxy-benzoic acid, 2-, 3-, 4-aminobenzenesulfonic acid, 3-amino-4-hydroxybenzenesulfonic acid, 4-amino-3-hydroxynaphthalene-1-sulfonic acid, 6-amino-7-hydroxynaphthalene-2-sulfonic acid, 7-amino- 4-hydroxynaphthalene-2-sulfonic acid, 4-amino-5-hydroxynaphthalene-2,7-disulfonic acid, 3-amino-2-naphthoic acid, 3-aminophthalic acid, 5-aminoisophthalic acid, 1,3,5-, 1,2,4 -Triaminobenzene, 1,2,4,5-tetraaminobenzene, 2,4,5-Triaminophenol, pentaaminobenzene, Hexaaminobenzene, 2,4,6-Triaminoresorcin, 4,5-Diaminobrenzcatechin, 4,6-Diaminopyrogallol, 3,5-Diamino -4-hydroxycatechol, aromatic anilines or phenols with a further aromatic radical, as represented in the formula (I):

in which R ^{1 represents} a hydroxy or an amino group which may be substituted by C _1-4 alkyl, C _1-4 hydroxyalkyl or C _1-4 alkoxyC _1-4 alkyl,
R ² , R ³ , R ⁴ , R ⁵ and their hydrogen, a hydroxy or an amino group, which can be substituted by C _1-4 alkyl, C _1-4 hydroxyalkyl, C _1-4 aminoalkyl or C _{1- 4} -alkoxy-C _1-4 -alkyl group may be substituted, represent a carbon or sulfonic acid group, and
X for a direct bond, a saturated or unsaturated carbon chain with 1 to 4 carbon atoms optionally substituted by hydroxyl groups, a carbonyl, sulfonyl or imino group, an oxygen or sulfur atom, or a group with the formula (II)

Z- (CH ₂ -Y-CH ₂ -Z ') _o (II),

in which Y is a direct bond, a CH ₂ or CHOH group,
Z and Z 'independently of one another are an oxygen atom, an NR ⁷ group in which R ^{7 is} hydrogen, a C _1-4 alkyl or hydroxyC _1-4 alkyl group, the group -O- (CH ₂ ) _p - NH or NH- (CH ₂ ) _{p '} -O, where p and p' are 2 or 3, and
o means a number from 1 to 4,
such as 4,4'-diaminostilbene, 4,4'-diaminostilbene-2,2'-disulfonic acid mono- or di-Na salt, 4,4'-diaminodiphenylmethane, sulfide, sulfoxide, amine, 4 , 4'-diaminodiphenylamine-2-sulfonic acid, 4,4'-diaminobenzophenone, diphenyl ether, 3,3 ', 4,4'-tetraaminodiphenyl, 3,3', 4,4'-tetraamino-benzophenone, 1, 3-bis (2,4-diaminophenoxy) propane, 1,8-bis (2,5-diaminophenoxy) -3,6-dioxaoctane, 1,3-bis (4-aminophenylamino) propane, -2 -propa nol, 1,3-bis- [N- (4-aminophenyl) -2-hydroxyethylamino] -2-propanol, N, N-bis- [2- (4-aminophenoxy) ethyl] methylamine, N -Phenyl-1,4-phenylenediamine.

The aforementioned compounds can be used both in free form and in the form of their physiologically acceptable salts, in particular as salts of inorganic acids, such as salt or sulfuric acid can be used.

Suitable phenols are e.g. B. the 2-, 3- or 4-methoxy, the 3-dimethylamino, 2- (2- Hydroxyethyl) - and 3,4-methylenedioxyphenol, resorcinol and 2-, 4- and 5- Methylresorcinol, the 2- and 4-chlororesorcinol, 2,5-dimethylresorcinol, pyrocatechol, Hydroquinone, pyrogallol, phloroglucin, hydroxyhydroquinone, the 2,4- or 3,4-dihy droxybenzoic or phenylacetic acid, gallic acid, 2,4,6-trihydroxybenzoic acid or the 2,4,5-trihydroxyacetophenone, the 1-naphthol, the 1,5-, 2,3- and 2,7-dihydroxy naphthalene, the 6-dimethylamino-4-hydroxy-2-naphthalenesulfonic acid or the 3,6-dihy droxy-2,7-naphthalenedisulfonic acid.

Suitable nitrogen-containing heterocyclic compounds are e.g. B. 2-, 3-, 4-amino-, 2- Amino-3-hydroxy, 2,6-diamino, 2,5-diamino, 2,3-diamino, 2-dimethylamino-5 - amino, 2-methylamino-3-amino-6-methoxy, 2,3-diamino-6-methoxy, 2,6-dimethoxy 3,5-diamino-, 2,4,5-triamino- and 2,6-dihydroxy-3,4-dimethylpyridine, 2,4-dihydroxy- 5,6-diamino-, 4,5,6-triamino-, 4-hydroxy-2,5,6-triamino-, 2-hydroxy-4,5,6-triamino-, 2,4,5,6-tetraamino-, 2-methylamino-4,5,6-triamino-, 2,4-, 4,5-diamino- and 2-amino-4- methoxy-6-methyl-pyrimidine, 3-amino, 3-amino-5-hydroxy and 3,5-diaminopyrazole,  2-, 3-, 8-aminoquinoline, 4-aminoquininaldine, 2-, 6-aminoonicotinic acid, 5-aminoisoquinoline, 5-, 6-aminoindazole, 5- and 7-amino-benzimidazole and benzothiazole, 2,5-dihydroxy-4- morpholinoaniline and indole and indoline derivatives, such as 4-, 5-, 6- and 7-aminoindole, 5,6- Dihydroxyindole, 5,6-dihydroxyindoline and 4-hydroxyindoline. The aforementioned ver bindings can ver both in free form and in the form of their physiological inert salts, e.g. B. as salts of inorganic acids, such as hydrochloric or sulfuric acid, be used.

These dyeing systems can be further strengthened by suitable nitrogenous ones Heterocycles such as B. piperidine, piperidine-2-, -3- or -4-carboxylic acid, pyridine, 2-, 3- or 4-hydroxypyridine, imidazole, 1-methylimidazole, histidine, pyrrolidine, pyrrolidone, Pyrrolidone-5-carboxylic acid, pyrazole, 1,2,4-triazole, piperazine and their physiological tolerable salts.

Regarding those that can be used in the hair coloring and tinting agents according to the invention Dyes continue to be expressly referred to the monograph Ch. Zviak, The Science of Hair Care, Chapter 7 (pages 248-250; substantive dyes) and Chapter 8, pages 264-267; Oxidation dye precursors), published as Volume 7 of the "Dermato logy "(Ed .: Ch. Culnan and H. Maibach), 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 Federal Association of German Industrial and trading company for pharmaceuticals, health products and personal care tel e.V., Mannheim, referred to.

The oxidation dye can be used to prepare the colorants according to the invention intermediate products are incorporated into a suitable water-containing carrier. Such Carriers are for the purpose of coloring hair z. B. creams, emulsions, gels or even ten foaming solutions containing sid, e.g. B. shampoos, aerosols or other preparations that are suitable for use on hair.

The colorants of the invention can all be for such preparations Known active ingredients, additives and auxiliaries. In many cases, the colorants contain at least one surfactant, in principle both anionic and zwitterionic, am  pholytic, nonionic and cationic surfactants are suitable. In many cases it has but proved to be advantageous, the surfactants from anionic, zwitterionic or select nonionic surfactants.

Suitable anionic surfactants in preparations according to the invention are all anionic surface-active substances suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 10 to 22 carbon atoms. In addition, the molecule can contain glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups. 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 carbon 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 with 10 to 22 C atoms and x = 0 or 1 to 16,
• Acyl sarcosides with 10 to 18 carbon atoms in the acyl group,
• Acyl taurides with 10 to 18 carbon atoms in the acyl group,
• Acyl isethionates with 10 to 18 carbon atoms in the acyl group,
• - Sulfosuccinic acid and dialkyl esters with 8 to 18 carbon atoms in the alkyl group and sulfosuccinic acid mono-alkyl polyoxyethyl ester with 8 to 18 C atoms in the alkyl group and 1 to 6 oxyethyl groups,
• Linear alkanesulfonates with 12 to 18 carbon atoms,
• Linear alpha-olefin sulfonates with 12 to 18 carbon atoms,
• - Alpha-sulfofatty acid methyl esters of fatty acids with 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 with 10 to 18 carbon atoms and x = 0 or 1 to 12,
• Mixtures of surface-active hydroxysulfonates according to DE-A-37 25 030,
• - Sulphated hydroxyalkyl polyethylene and / or hydroxyalkylene propylene glycol ethers according to DE-A-37 23 354,
• - Sulfonates of unsaturated fatty acids with 12 to 24 carbon atoms and 1 to 6 double bin solutions 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 on fatty alcohols with 8 to 22 Represent carbon atoms.

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

Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one -COO ^(-) - or -SO ₃ ^(-) group in the molecule. Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example the cocoalkyl-dimethylammonium glycinate, N-acyl-aminopropy1-N, N-dimethylammonium glycinate, for example the cocoacylaminopropyl-dimethylammonium glycinate, and 2-alkyl -3-carboxymethyl-3-hydroxyethyl-imidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the cocoacylaminoethylhydroxyethylcarboxymethylgly cinat. A preferred zwitterionic surfactant is the fatty acid amide derivative known under the INCI name Cocamidopropyl Betaine.

Ampholytic surfactants are understood to mean those surface-active compounds which, in addition to a C _8-18 -alkyl or -acyl group, contain at least one free amino group and at least one -COOH or -SO ₃ H group in the molecule and are capable of forming internal salts are. Examples of suitable ampholytic surfactants are N-alkylglycine, N-alkylpropionic acid, N-alkylaminobutyric acid, N-alkyliminodipropionic acid, N-hydroxyethyl-N-alkylamidopropylglycine, N-alkyltaurine, N-alkylsarcosine, 2-alkylaminopropionic acid and alkylaminoacetic acid each with about 8 to 18 carbon atoms in the alkyl group. Particularly preferred ampholytic surfactants are the N-coconut alkylaminopropionate, the coconut acylaminoethylaminopropionate and the C _12-18 acylsar cosine.

Nonionic surfactants contain z as hydrophilic groups. B. a polyol group, a poly lyalkylene glycol ether group or a combination of polyol and polyglycol ether group. Such connections are, for example

• - Addition products of 2 to 30 moles of ethylene oxide and / or 0 to 5 moles of propylene oxide linear fatty alcohols with 8 to 22 C atoms, fatty acids with 12 to 22 C atoms and on alkylphenols with 8 to 15 carbon atoms in the alkyl group,
• C _12-22 fatty acid monoesters and diesters of adducts of 1 to 30 mol of ethylene oxide with glycerol,
• C _{8-22 alkyl} mono- and oligoglycosides and their ethoxylated analogs,
• - Addition products of 5 to 60 moles of ethylene oxide with castor oil and hardened rizi nut oil,
• - Addition products of ethylene oxide with sorbitan fatty acid esters
• - Addition products of ethylene oxide with fatty acid alkanolamides.

Examples of those which can be used in the hair treatment compositions according to the invention Cationic surfactants are especially quaternary ammonium compounds. Are preferred Ammonium halides such as alkyltrimethylammonium chlorides, dialkyldimethylammo niumchloride and trialkylmethylammoniumchloride, e.g. B. Cetyltrimethylammo nium chloride, stearyltrimethylammonium chloride, distearyldimethylammonium chloride, Lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetyl methylammonium chloride. Other cationic surfactants that can be used according to the invention represent the quaternized protein hydrolyzates.

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

Alkylamidoamines, especially fatty acid amidoamines, such as that under the name Tego Amid®S 18 available stearylamidopropyldimethylamine, stand out next to one good conditioning effect especially due to its good biodegradability.  

Quaternary ester compounds are also very readily biodegradable "Esterquats", such as the methyl-hydroxyal sold under the trademark Stepantex® kyldialkoyloxyalkyl-ammonium methosulfate and those under the trademark De hyquart® products such as Dehyquart® AU-46.

An example of a quaternary sugar derivative that can be used as a cationic surfactant is provided is the commercial product Glucquat®100, according to INCI nomenclature a "Lauryl Methyl Glu ceth-10 hydroxypropyl dimonium chloride ".

The compounds with alkyl groups used as surfactants can in each case be act uniform substances. However, it is usually preferred in the manufacture these substances from natural vegetable or animal raw materials, so that one Mixtures of substances with different ones depending on the respective raw material Maintains alkyl chain lengths.

In the case of surfactants, the adducts of ethylene and / or propylene oxide with fatty alcohol represent alcohols or derivatives of these addition products, both products with a "normal" homolog distribution as well as those with a narrowed homolog distribution can be used. Under "normal" homolog distribution, Mi understandings of homologues used in the implementation of fatty alcohol and Alkylene oxide using alkali metals, alkali metal hydroxides or alkali receives metal alcoholates as catalysts. Narrowing homolog distributions will be on the other hand, if, for example, hydrotalcites, alkaline earth metal salts of Ether carboxylic acids, alkaline earth metal oxides, hydroxides or alcoholates as catalysts be used. The use of products with a narrow homolog distribution can be preferred.

Furthermore, the hair treatment compositions according to the invention can preferably also have one conditioning agent selected from the group consisting of cationic surfactants, cationic polymers, alkylamidoamines, paraffin oils, vegetable oils and syntheti is formed.  

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

Preferred cationic polymers are, for example

• - Quaternized cellulose derivatives, such as those under the names Celquat © and Po lymer JR® are commercially available. The connections Celquat® H 100, Celquat® L 200 and Polymer JR®400 are preferred quaternized cellulose derivatives.
• - polymeric dimethyldiallylammonium salts and their copolymers with acrylic acid as well as with esters and amides of acrylic acid and methacrylic acid. The one among the Designations Merquat®100 (poly (dimethyldiallylammonium chloride)), Mer quat®550 (dimethyldiallylammonium chloride-acrylamide copolymer) and Merquat® 280 (dimethyldiallylammonium chloride-acrylic acid copolymer) commercially Products available are examples of such cationic polymers.
• - Copolymers of vinyl pyrrolidone with quaternized derivatives of dialkylamino acrylate and methacrylate, such as vinyl quaternized with diethyl sulfate pyrrolidone-dimethylaminomethacrylate copolymers. Such connections are under the names Gafquat®734 and Gafquat®755 are commercially available.
• - Vinylpyrrolidone-methoimidazolinium chloride copolymers, as described under the designation Luviquat® can be offered.
• - 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 lymer main chain.

Cationic polymers of the first four groups are particularly preferred. All polyquaternium-2, polyquaternium-10 and polyquaternium-22 are particularly preferred.

Also suitable as conditioning agents are silicone oils, especially dialkyl and alkylarylsiloxanes such as dimethylpolysiloxane and methylphenylpolysi loxane, and their alkoxylated and quaternized analogues. 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 hydroxyl-amino-modified silicone, which can also be called amodimethicone is drawn), SM-2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil®-Quat 3270 and 3272 (manufacturer: Th. Goldschmidt; diquaternary Polydimethylsiloxanes, Quaternium-80).

Paraffin oils, synthetic, can also be used as conditioning agents prepared oligomeric alkenes and vegetable oils such as jojoba oil, sunflower oil, Orange oil, almond oil, wheat germ oil and peach seed oil.

Suitable hair conditioning compounds are phospholipids, for example wise soy lecithin, egg lecithin and cephaline.

Other active ingredients, auxiliaries and additives are, for example

• Non-ionic polymers such as, for example, vinyl pyrrolidone / vinyl acrylate copolymers, Polyvinyl pyrrolidone and vinyl pyrrolidone / vinyl acetate copolymers and polysiloxanes,
• - zwitterionic and amphoteric polymers such as acrylamidopropyl-tri methyl ammonium chloride / acrylate copolymers and octylacrylamide / methyl methacrylic lat / tert-butylaminoethyl methacrylate / 2-hydroxypropyl methacrylate copolymers,
• Anionic polymers such as 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 / malein acid anhydride copolymers and acrylic acid / ethyl acrylate / N-tert-butyl-acrylamide Terpolymers,
• Thickeners such as agar agar, guar gum, alginates, xanthan gum, gum ara bicum, karaya gum, locust bean gum, linseed gums, dextrans, cellu loose derivatives, e.g. B. methyl cellulose, hydroxyalkyl cellulose and carboxymethylcel lulose, starch fractions and derivatives such as amylose, amylopectin and dextrins, Clays such as B. bentonite or fully synthetic hydrocolloids such. B. polyvinyl alcohol fetch
• Structurants such as glucose and maleic acid,  
• - Protein hydrolyzates, especially elastin, collagen, keratin, milk protein, soy protein and wheat protein hydrolyzates, their condensation products with fatty acids as well as quaternized protein hydrolyzates,
• - perfume oils, dimethyl isosorbide and cyclodextrins,
• - Solubilizers such as ethanol, isopropanol, ethylene glycol, propylene glycol, glycerin and diethylene glycol,
• - anti-dandruff agents such as Piroctone Olamine and Zink Omadine,
• - other substances for adjusting the pH value,
• - Active ingredients such as panthenol, pantothenic acid, allantoin, pyrrolidone carboxylic acids and their salts, plant extracts and vitamins,
• - cholesterol,
• - light stabilizers,
• - consistency enhancers such as sugar esters, polyol esters or polyol alkyl ethers,
• - Fats and waxes such as walrus, beeswax, montan wax, paraffins, fatty alcohols and fatty acid esters,
• - fatty acid alkanolamides,
• Complexing agents such as EDTA, NTA and phosphonic acids,
• - Swelling and penetration substances such as glycerin, propylene glycol monoethyl ether, carbo nates, hydrogen carbonates, guanidines, ureas and primary, secondary and tertiary Phosphates,
• Opacifiers such as latex,
• - pearlescent agents such as ethylene glycol mono- and distearate,
• - blowing agents such as propane-butane mixtures, N ₂ O, dimethyl ether, CO ₂ and air and
• - antioxidants.

The constituents of the water-containing carrier are used to produce the inventive Colorants used in amounts customary for this purpose; e.g. B. become emulsifiers medium in concentrations of 0.5 to 30 wt .-% and thickener in concentration from 0.1 to 25% by weight of the total colorant.

In principle, the oxidative development of the coloring can take place with atmospheric oxygen. However, a chemical oxidizing agent is preferably used, especially when in addition to the coloring, a lightening effect on human hair is desired. As an oxidation  medium come persulfates, chlorites and especially hydrogen peroxide or its arrival storage products on urea, melamine and sodium borate in question. Furthermore it is possible to carry out the oxidation with the help of enzymes. The enzymes can for transferring atmospheric oxygen to the developer component or for reinforcement serve the effect of small amounts of oxidizing agents present. An example of a enzymatic process represents the procedure, the effect of small amounts (e.g. 1% and less, based on the total agent) hydrogen peroxide by peroxidases reinforce.

The preparation of the oxidizing agent is expediently immediately before Hair coloring mixed with the preparation from the oxidation dye precursors. The The resulting ready-to-use hair dye preparation should preferably have a pH in the Range from 6 to 10. The use of hair color is particularly preferred medium in a weakly alkaline environment. The application temperatures can be in egg range between 15 and 40 ° C. After an exposure time of approx. 30 minutes The hair dye is removed from the hair to be dyed by rinsing. The Rinsing with a shampoo is not necessary if a carrier with a high tenside content, e.g. B. a Coloring shampoo was used.

A second object of this invention is the use of the aforementioned means for Dyeing keratin fibers.

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

Embodiments

example 1

After adjusting the pH, the coloring solution was with a commercial 6% Hydrogen peroxide preparation (market product Poly Color Brillance) in a ratio of 1: 1 diluted. The application preparation was applied to a strand of hair (Kerling, natural white) applied. After 30 minutes of exposure at 32 ° C, the lock was rinsed, dried and the dye result obtained visually according to the pocket dictionary of colors (2nd edition, Musterschmidt-Verlag Zürich-Göttingen, 1975).  

The streak was colored red-orange.

In addition, the coloring cream was in a second coloration without the addition of a Oxidizing agent applied to a strand of hair (Kerling, natural white). After 30 min Exposure time at 32 ° C, the tress was rinsed, dried and the resulting dye result determined as described above. The streak was colored pale orange.  

Example 2

After adjusting the pH, the staining solution was with a commercial 6% Hydrogen peroxide preparation (market product Poly Color Brillance) in a ratio of 1: 1 diluted. The application preparation was applied to a strand of hair (Kerling, natural white) applied. After 30 minutes of exposure at 32 ° C, the lock was rinsed, dried and the resulting dye result was determined visually as described above.

The streak was colored violet-brown.  

Example 3

After adjusting the pH, the coloring solution was with a commercial 6% Hydrogen peroxide preparation (market product Poly Color Brillance) in a ratio of 1: 1 diluted. The application preparation was on a strand of hair (Kerling, natural white)  applied. After 30 minutes of exposure at 32 ° C, the lock was rinsed, dried and the resulting dye result was determined visually as described above.

The streak was colored English red.

Example 4

After adjusting the pH, the coloring solution was with a commercial 6% Hydrogen peroxide preparation (market product Poly Color Brillance) in a ratio of 1: 1 diluted. The application preparation was applied to a strand of hair (Kerling, natural white) applied. After 30 minutes of exposure at 32 ° C, the lock was rinsed, dried and the resulting dye result was determined visually as described above.

The streak was dyed Madeira brown.

Claims (7)

1. Agent for dyeing keratin fibers, characterized in that it contains 4-amino-2- ((diethylamino) methyl) phenol as the developer component and 2-methyl-5-amino phenol as the coupler component. 2. Composition according to claim 1, characterized in that it further comprises at least one Developer component selected from the group consisting of p-phenylenediamine, p- Toluenediamine, p-aminophenol, 1- (2'-hydroxyethyl) -2,5-diaminobenzene, 4-amino-3- methylphenol, 2,4,5,6-tetraaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 4- Hydroxy-2,5,6-triaminopyrimidine, 4,5-diamino-1- (2-hydroxyethyl) pyrazole, 2- Aminomethyl-4-aminophenol, N, N-bis- (2-hydroxyethyl) -p-phenylenediamine, bis- (2- hydroxy-5-aminophenyl) methane, 1,10-bis (2,5-diaminophenyl) -1,4,7,10-tetraoxa decane and o-aminophenol, contains. 3. Composition according to one of claims 1 to 2, characterized in that it is at least a further coupler component selected from the group formed by are 1-naphthol, 1,5-, 2,7- and 1,7-dihydroxynaphthalene, 2-amino-3-hydroxypyridine, 3-amino-2-methylamino-6-methoxypyridine, resorcinol, 4-chlororesorcinol, 2-methylresor cin, 2,5-dimethylresorcinol, m-aminophenol, o-aminophenol and 2-chlororesorcinol, contains. 4. Agent according to one of claims 1 to 3, characterized in that developments Oil components in an amount of 0.005 to 20 wt .-%, preferably 0.1 to 5 % By weight, and coupler components in an amount of 0.005 to 20% by weight, preferably wise 0.1 to 5% by weight, based in each case on the entire oxidation coloring agent, are included. 5. Agent according to one of claims 1 to 4, characterized in that at least one direct dye is included. 6. Agent according to one of claims 1 to 5, characterized in that at least one Indole and / or at least one indoline derivative is included. 7. Use of agents according to one of claims 1 to 6 for coloring keratin Fibers.