EP3223789A1

EP3223789A1 - Agents for dyeing keratin fibres, containing at least one cationic azo dye with two heterocyclic groups

Info

Publication number: EP3223789A1
Application number: EP15780859.3A
Authority: EP
Inventors: Antje Gebert-Schwarzwälder; Ralph Nemitz; Astrid Kroos
Original assignee: Henkel AG and Co KGaA
Current assignee: Henkel AG and Co KGaA
Priority date: 2014-11-25
Filing date: 2015-10-14
Publication date: 2017-10-04
Also published as: WO2016083014A1; DE102014223934A1

Abstract

The invention relates to agents for dyeing keratin fibres, in particular human hair, containing, in a cosmetic carrier (a) at least one direct dye of formula (I), wherein Het 1 represents a non-saturated, cationic heterocycle and Het 2 represents a saturated, uncharged heterocycle.

Description

"Agent for changing the color of keratinic fibers containing at least one cationic azo dye having two heterocyclic groups"

The present invention relates to color-changing agents of keratinic fibers, in particular human hair, containing (a) at least one cationic azo dye having two heterocyclic groups.

For the dyeing of keratinic fibers, either direct dyes or oxidation dyes are generally used. Although intensive dyeings with good fastness properties can be obtained with oxidation dyes, the development of the color is generally carried out under the influence of oxidizing agents such. H2O2, which in some cases can result in damage to the fiber. Furthermore, some oxidation dye precursors or certain mixtures of oxidation dye precursors may have a sensitizing effect on persons with sensitive skin. Direct dyes are applied under gentler conditions. Their disadvantage lies in the fact that the dyeings often have only insufficient fastness properties.

Depending on the desired color result, the expert uses substantive dyes of different classes of dyes. The direct dyes known from the prior art include, for example, the class of nitro dyes, the anthraquinone dyes, the azo dyes, the triarylmethane dyes or the methine dyes. All of these classes of dyes should meet a specific requirement profile for use in the cosmetics sector. Thus, direct dyes should provide an intensive dyeing result and have the best possible fastness properties. Due to environmental influences, the color result obtained with substantive dyes should be influenced as little as possible, i. For example, the dyes should have good fastness to washing, lightfastness and rubfastness. Also, chemical influences that the keratinic fibers may be exposed to after the dyeing process (such as perms) should change the color result as little as possible.

In order to achieve lightening at the same time as dyeing, the direct dyes should if possible also be compatible with the usual oxidizing agents used in bleaching processes (such as hydrogen peroxide and / or persulfates).

For the strong lightening of dark hair not only hydrogen peroxide alone, but a combination of hydrogen peroxide and persulfates (eg ammonium persulfate, potassium persulfate and / or sodium persulfate) is used. If, therefore, dark hair is lightened in one step and dyed at the same time in a bright shade, the use of a mixture of hydrogen peroxide, persulfates and a direct dye is advantageous. Although many intensive coloring direct dyes are known to those skilled in the dyeing of hair, but he knows only a very limited range of dyes that the strong oxidative conditions, such as a Mixture of the above oxidizing agents represents survive without decomposition. In addition, the oxidation-stable dyes known from the prior art have serious disadvantages with regard to their other fastness properties.

For the simultaneous dyeing and strong whitening of hair there is thus still a need for dyes with high stability to strong oxidizing agents. Even under these extreme conditions of use, these dyes should not lose their positive fastness and dyeing properties.

It has been found that luminous and intense colorations can be produced in particular with cationic substantive dyes. Cationic dyes are often characterized by a particularly high affinity for keratin fibers, which can be attributed to the interactions of the positive charges of the dyes with negatively charged structural components of the keratinic fibers. Therefore, it is often possible to achieve particularly intensive dyeings with cationic dyes.

For example, the representatives Basic Orange 31 (alternative name: 2 - [(4-aminophenyl) azo] -1,3-dimethyl-1H-imidazolium chlorides, CAS No. 97404-02, which are well-known from the prior art are cationic azo dyes 9) and Basic Red 51 (alternative name: 2 - [((4-dimethylamino) phenyl) azo] -1,3-dimethyl-1H-imidazolium chloride, CAS No. 77061-58-6).

Both dyes stain keratin fibers with outstanding color intensity in orange to red shades. There is still a need for substantive blue dyes which are optimally compatible with these two dyes.

The object of the present application is therefore to provide colorants for keratinic fibers, in particular human hair, which have good performance properties in terms of color depth and fastness properties, in particular light fastness, rubfastness and wash fastness, as well as perspiration and cold wave fastness. In the case of simultaneous use with oxidation dyes and / or oxidants, the direct dyes should have high stability to hydrogen peroxide and other oxidizing agents and not lose their positive fastness and dyeing properties. In addition, as bright and intense colors as possible should be achieved.

In addition, the aforementioned dyes should also be particularly well compatible with the cationic azo dyes Basic Orange 31 and Basic Red 51.

It has now been found that the use of a cationic azo dye of formula (I) whose structure is characterized by the presence of two heterocyclic moieties in cosmetic color-change agents on keratinic fibers results in particularly intense and bright colorations.

The dyes of the general formula (I) have proven to be particularly stable to oxidants, in particular stable to a combination of hydrogen peroxide and persulfates. A first object of the present invention is a means for color-changing keratinic fibers, in particular human hair, contained in a cosmetic carrier

(a) at least one substantive dye of the formula (I)

(L)

in which

Het 1 represents one of the structures (II), (I II), (IV), (V), (VI) or (VII),

R 1, R 2 independently of one another represent a hydrogen atom, a C 1 -C 6 -alkyl group

Halogen atom from the group chlorine, bromine, fluorine or iodine, for a Ci -Ce-

Alkoxy group or stand for a nitro group,

R 3, R 6 independently of one another are a C 1 -C 6 -alkyl group, a C 2 -C 6 -alkenyl group or a hydroxy-C 2 -C 6 -alkyl group,

R4, R5 independently represent a hydrogen atom, a Ci-Ce-alkyl group, a

Alkoxy group or stand for a nitro group,

Het 2 represents one of the structures (VI II), (IX), (X) (XI), (XII) or (XIII),

R 7 is a hydrogen atom or a C 1 -C 6 -alkyl group,

X- for a physiologically acceptable anion, preferably for an anion from the

Group chloride, bromide, iodide, methyl sulfate, methyl sulfonate, p-toluenesulfonate, acetate, hydrogen sulfate, 2 sulfate or 2 Tetrachlorozinkat, stands.

Keratinic fibers, keratin-containing fibers or keratin fibers are understood to mean furs, wool, feathers and, in particular, human hair. Although the compositions according to the invention are primarily suitable for whitening keratin fibers, in principle there is nothing to prevent their use in other fields as well.

The term "color change of keratin fibers" as used in the invention encompasses any form of color change of the fibers, including in particular color changes encompassed by the terms tinting, bleaching, matting, oxidative dyeing, semi-permanent dyeing, permanent dyeing and temporary dyeing Coloring bleaching is understood to mean the simultaneous lightening and coloring of the keratinic fibers which can be achieved by the simultaneous use of oxidizing agent and dye in the staining modifying agent.

The agents according to the invention contain the substantive dyes of the formula (I) in a cosmetic vehicle. This cosmetic carrier is preferably aqueous, alcoholic or aqueous-alcoholic. For the purpose of hair treatment, such carriers are for example creams, emulsions, gels or surfactant-containing foaming solutions, such as shampoos, foam aerosols or other preparations which are suitable for use on the hair. But it is also possible to provide for storage a powdery or tablet-like formulation. This is then mixed before use in an aqueous solvent or with organic solvents or with mixtures of water and organic solvents to obtain the application mixture. For the purposes of the invention, an aqueous carrier contains at least 40% by weight, in particular at least 50% by weight, of water. In the context of the present invention, aqueous-alcoholic carriers are water-containing compositions containing from 3 to 70% by weight. a Ci -C4-alcohol, in particular ethanol or isopropanol to understand. The compositions according to the invention may additionally contain other organic solvents, for example 4-methoxybutanol, ethyl diglycol, 1,2-propylene glycol, n-propanol, n-butanol, n-butylene glycol, glycerol, diethylene glycol monoethyl ether and diethylene glycol mono-n-butyl ether, contain. Preference is given to all water-soluble organic solvents. Preferred agents according to the invention are characterized in that they additionally comprise a non-aqueous solvent, preferred agents according to the invention containing the solvent in a concentration of 0.1 to 30% by weight, preferably in a concentration of 1 to 20% by weight, very particularly preferably in a concentration of 2 to 10 wt .-%, each based on the agent.

As essential ingredient (a) the agents according to the invention contain at least one substantive dye of the formula (I).

The substituents R 1 to R 7 of the compounds of the formula (I) are described below by way of example: Examples of a C 1 -C 6 -alkyl group are the groups methyl, ethyl, propyl, isopropyl, n-butyl, s-butyl and t-butyl, n- Pentyl and n-hexyl. Propyl, ethyl and methyl are preferred alkyl radicals. Examples of a C2-C6 alkenyl group are vinyl, allyl, but-2-enyl, but-3-enyl and isobutenyl, preferred C2-C6 alkenyl radicals are vinyl and allyl. Halogen atoms are selected from the group chlorine, bromine, fluorine and / or iodine, in which case chlorine and bromine are particularly preferred. Exemplary of a Ci-Ce alkoxy group, the methoxy, the ethoxy and the propoxy group can be mentioned. A nitro group is a grouping -NO2 to understand.

Each substantive dye of the formula (I) has a cationic, heterocyclic end group Het 1. Het 1 is an unsaturated heterocycle with a positive charge that is neutralized by the physiologically compatible counterion X-. Het 1 represents a grouping from the group of formulas (II) to (VII)

Formula (II) represents a cationic thiazolium end group.

Formula (II I) represents a cationic imidazolium end group.

Formula (IV) represents a cationic, 1,2,4-triazolium end group.

Formula (V) represents a cationic 1, 3,4-thiadiazolium end group.

Formula (VI) represents a cationic 1, 2,4-thiadiazolium end group.

Formula (VII) represents a cationic pyrazolium end group.

In the formulas (I I) to (VII), a position is in each case marked with an asterisk which indicates the point of attachment of the heterocyclic end group Het 1 with the azo group in the formula (I).

By selecting the end group Het 1, the absorption spectrum of the dye and thus also the coloration of the dye can be influenced.

If intensive dyeings in the blue-violet range and especially in the blue range are desired, it is advantageous if Het 1 stands for a heterocyclic end group of the formula (II).

On the other hand, if it is desired to obtain brilliant colorations in the red region, it is preferable if Het 1 is selected from the heterocyclic end groups of the formulas (III) or (IV).

In addition, with dyes of the formula (I) in which Het 1 is a group selected from the formulas (II), (III) or (IV), it is possible to produce particularly pure and luminous hues. For this reason, it is particularly preferred if the agent (a) according to the invention contains at least one substantive dye of the general formula (I) in which

Het1 stand

In a particularly preferred embodiment, an agent according to the invention is characterized in that it contains (a) at least one substantive dye of the general formula (I) in which

Het1 represents one of the structures (II), (II I) or (IV)

In the formula (I), the radicals R1 and R2 indicate the substituents on the phenyl ring of the substantive dye. Here, R 1 and R 2 independently of one another can be a hydrogen atom, a C 1 -C 6 -alkyl group, a halogen atom from the group consisting of chlorine, bromine, fluorine or iodine, a C 1 -C 6 -alkoxy group or a nitro group.

Particularly intensive colorations are obtained when R 1 and R 2 independently of one another represent a hydrogen atom or a C 1 -C 6 -alkyl group, more preferably a hydrogen atom or a methyl group.

R1. R 2 independently of one another represent a hydrogen atom or a C 1 -C 6 -alkyl group, preferably a hydrogen atom or a methyl group.

The heterocyclic group Het1 is selected from one of the structures of the formulas (I I) to (VII), these heterocyclic groups carrying the radicals R3, R4, R5 and / or R6.

The radicals R3 and R6 are each positioned on a nitrogen atom of the heterocycle and may independently of one another be a Ci-Ce-alkyl group, a C2-Ce-alkenyl group or a hydroxy-C2-Ce-alkyl group.

The radicals R4 and R5 are each located on a carbon atom of the heterocyclic end groups of the formulas (II) to (VII). R4 and R5 independently of one another represent a hydrogen atom, a C 1 -C 6 -alkyl group, a halogen atom from the group consisting of chlorine, bromine, fluorine or iodine, a C 1 -C 6 -alkoxy group or a nitro group.

It is preferred if R 3 and R 6 independently of one another are a C 1 -C 6 -alkyl group, in particular a methyl group or an ethyl group.

R3, R6 independently of one another are a C 1 -C 6 -alkyl group, preferably a methyl group or an ethyl group. Furthermore, the dyes of the formula (I) according to the invention for the production of attractive and intense color shades are particularly suitable when R4 and R5 are independently a hydrogen atom or a Ci-Ce-alkyl group, in particular a hydrogen atom or a methyl group.

R4, R5 independently of one another represent a hydrogen atom or a C 1 -C 6 -alkyl group, preferably a hydrogen atom or a methyl group.

In summary, a composition according to the invention in a further particularly preferred embodiment is characterized in that it contains (a) at least one substantive dye of the general formula (I) in which

R 3, R 6 independently of one another are a C 1 -C 6 -alkyl group, preferably a methyl group or an ethyl group, and

The direct-acting dyes of the formula (I) according to the invention are characterized by the presence of a second heterocycle Het 2. Het 2 is a saturated, uncharged heterocyclic system. Het 2 represents one of the structures of formulas (VI II) to (XII I).

In the formulas (VIII) to (XII I), in each case a position is marked with an asterisk which indicates the point of attachment of the saturated heterocyclic end group with the phenyl ring in formula (I). The structure of the formula (VII I) is a morpholinyl group linked via the N atom.

The structure of formula (IX) is a piperidinyl group linked via the N atom. The structure of formula (X) is a pyrrolidinyl group linked via the N atom. The structure of the formula (XI) is an azepine group linked via the N atom (alternative name: 1-azacycloheptyl group). The structure of formula (XII) is a thiomorpholinyl group linked via the N atom.

The structure of formula (XIII) is a piperazinyl group linked via an N atom. The Piperazinylendgruppe of formula (XIII) further carries the radical R7, which may be a hydrogen atom or a Ci-Ce-alkyl group. Preferably, R7 is a hydrogen atom or a methyl group.

A central object of the present invention was to find dyes with high stability to the usually employed in the bleaching of keratin fibers oxidizing agents (hydrogen peroxide + persulfates). The finding of correspondingly stable dyes allows the simultaneous strong lightening and coloring of keratinic fibers.

In the course of the work leading to this invention it has been found that the oxidation stability of a cationic dye can be improved by the choice of a suitable heterocyclic group Het 2 over an analogous open-chain cationic dye.

The reason for this surprisingly increased oxidation stability could - without being bound to this theory - be the spatial geometry of the dye, since the nitrogen atom is forced by the presence of the heterocycle in a rigid ring system.

The spatial orientation of this ring system may prevent the attack of the oxidant (i.e., the nucleophilic attack, e.g., a hydroxide anion HOO, is hindered by the steric orientation of the ring).

It is particularly preferred in this context if the heterocycle Het 2 stands for one of the structures (VIII), (IX) or (X).

Het 2 represents one of the structures (VI II), (IX) or (X).

In a further preferred embodiment, an agent according to the invention is also characterized in that it contains (a) at least one substantive dye of the general formula (I) in which

Het 2 stands for the structure (XIII)

in which

R7 represents a hydrogen atom or a methyl group.

The dyes of the formula (I) according to the invention are cationic azo dyes which are positively charged. The positive charge is in each case neutralized by the anionic counterion X (of the structural units (II) to (VII)). Here, the cationic organic part is responsible for the coloring of the keratin fibers. The counterion X serves only to preserve the electron neutrality, so that the exact nature of the counterions X does not play a significant role in achieving the desired color result. Since the dyes are used in cosmetic color change agents, the counterion must be physiologically compatible. Physiologically acceptable in this context means suitable for use in the cosmetic (i.e., for use on human hair and human skin). The counterion X is a physiologically acceptable anion, which is preferably selected from the group chloride, bromide, iodide, methyl sulfate, methyl sulfonate, p-toluenesulfonate, acetate, hydrogen sulfate, Vz sulfate or Vz Tetrachlorozinkat.

Chloride is understood as meaning an anion Cl ^" , bromide is understood as meaning an anion Br, and iodide is understood to mean an anion J-." Methylsulfate is understood to mean an anion H3COSO4.

Under methylsulfonate, an anion is ^"understood. Among p-toluenesulfonate anion H3C is (CeH4) ^S03" H3CSO3 understood. By acetate is meant an anion H3CCOO-. By hydrogen sulfate is meant an anion HSO4 ^" .

Vz sulphate is understood to be one-half equivalent of the doubly negatively charged anion SO4 ^{2 "} .Vz tetrachlorozincate is understood to be half the equivalent of the doubly negatively charged anion ZnCU ^2" .

In a further preferred embodiment, an agent for color-changing keratinic fibers is characterized in that it comprises at least one compound of the general formula (I) which is selected from

-Methyl 2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazole-3-ium

Salts of 3-methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazole-3

Salts of 3-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

Salts of 3-ethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

Salts of 3-ethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazole-3

Ethyl 2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

holin-4-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

Salts of 3,5-dimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

- Salts of 3,5-dimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-5-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts des3-ethyl-5-methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1, 3-thiazol-3-ium

- Salts of 3-ethyl-5-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3,4-dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1, 3-thiazol-3-ium ] diazene-1-yl} -1,3-thiazole-3

- Salts of 3,4-dimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-4-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-4-methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-4-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of the 1, 3-dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium -yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

enyl] diazene-1-yl} -1H-imidazole-3-ium

rpholin-4-yl) phenyl] diazene-1-yl} -1H-imidazole-3-ium

-yl) phenyl] diazen-1-yl} -1H-imidazol-3-iumyl] diazen-1-yl} -1H-imidazole-3-ium

nyl] diazene-1-yl} -1H-imidazole-3-ium

-yl) phenyl] diazene-1-yl} -1 H -imidazol-3-ium enyl] diazen-1-yl} -1 H -imidazol-3-ium-yl) -phenyl] diazene-1-yl} -1 H-imidazol-3- ^'l) phenyl] diazen-1-yl} -1 H-imidazol-3-IUMS

- Salts of the 1, 3-diethyl-5-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

Salts of 1,3,4-trimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1H-imidazole-3

Salts of 1,3,4-trimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3,4-trimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

lin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-diethyl-4-methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-imidazol-3-ium

1) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,4-dimethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1H-1, 2,4-triazole-4-ium

Salts of 1,4-dimethyl-5- {2- [4- (piperdin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium

Salts of 1,4-dimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium olin-4-yl) phenyl] diazene-1-yl} -1 H-1, 2,4-triazole-4-ium

-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazole-4-ium

enyl] diazene-1-yl} -1H-1, 2,4-triazole-4-ium

Salts of 1,3,4-trimethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1 H-1, 2,4-triazole-4-ium

®

- Salts of the 1, 3,4-trimethyl-5- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4-ium

/ -yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazol-4-ium enyl] diazen-1-yl} -1 H-1,2,4-triazole-4-ium-phenyl ] diazene-1-yl} -1 H-1, 2,4-triazole-4-ium I) phenyl] diazene-1-yl} -1 H-1, 2,4-triazole-4-ium

-yl} -3-methyl-1,3-thiazole-3-ium

- Salts of 3-methyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

Salts of 3-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

1 -yl) phenyl] diazene-1-yl} -3-ethyl-1,3-thiazole-3-ium

Salts of 3-ethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

Salts of 3-ethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

nyl] diazen-1-yl-3,5-dimethyl-1,3-thiazole-3-ium

Salts of 3,5-dimethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

Salts of 3,5-dimethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazole-3

-yl) phenyl] diazen-1-yl} -1, 3-thiazole-3-ium

- Salts of 3-ethyl-5-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazene-1-yl} -3,4-dimethyl-1,3-thiazole-3-ium Salts of 3,4-dimethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazole-3

Salts of 3,4-dimethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium iazen-1-yl} -3- ethyl 4-methyl-1,3-thiazole-3-ium

- Salts of 3-ethyl-4-methyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

Salts of 3-ethyl-4-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1,3-dimethyl-1H-1,3-imidazol-3-ium yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

nyl] diazene-1-yl} -1H-imidazole-3-ium

yl] diazene-1-yl} -1,3-diethyl-1H-1,3-imidazol-3-iumene-1-yl-1-yl-1-yl-1-imidazol-3-ium

-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

en-1-yl-1, 3,5-trimethyl-1H-1,3-imidazol-3-ium

Salts of the 1, 3,5-trimethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

Salts of the 1, 3,5-trimethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

3-diethyl-5-methyl-1H-1,3-imidazole-3-ium

Salts of 1,3-diethyl-5-methyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

Salts of 1,3-diethyl-5-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

3,4-trimethyl-1H-1,3-imidazole-3-ium

- Salts of the 1, 3,4-trimethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3,4-trimethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

diethyl-4-methyl-1H-1,3-imidazole-3-ium

- Salts of the 1, 3-diethyl-4-methyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazol-3-ium

henyl] diazene-1-yl} -1H-imidazole-3

Salts of the 5- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1, 4-dimethyl-1H-1, 2,4-triazole-4-ium

Salts of 1,4-dimethyl-5- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium

Salts of 1,4-dimethyl-5- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium enyl] diazen-1-yl} -1, 4-diethyl-1H-1, 2,4-triazol-4-iumphenyl] diazene-1-yl} -1H-1,2,4-triazole-4 -iums

-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazole-4-ium

en-1-yl-1, 3,4-trimethyl-1H-1, 2,4-triazole-4-ium

Salts of 1,3,4-trimethyl-5- {2- [4- (thiomorpholin-4-yl) phenyl] diazene-1-yl} -1H-1, 2,4-triazole-4

Salts of 1,3,4-trimethyl-5- {2- [4- (piperazin-1-yl) phenyl] diazene-1-yl} -1H-1,2,4-triazole-4-ium diethyl-3-methyl-1H-1, 2,4-triazole-4-ium

Salts of the 1, 4-diethyl-3-methyl-5- {2- [4- (thiomorpholin-4-yl) phenyl] diazene-1-yl} -1H-1, 2,4-triazole-4 IUMS

henyl] diazene-1-yl} -1H-1, 2,4-triazole-4- ^'

The aforementioned compounds are cationic dyes wherein the organic cation is neutralized by the anion X-. The anions X- are each a physiologically tolerable anion, preferably from the group consisting of chloride, bromide, iodide, methylsulfate, methylsulfonate, p-toluenesulfonate, acetate, hydrogensulfate, sulfate or tetrachlorozincate.

Explicitly very particularly preferred according to the invention are agents for dyeing keratinic fibers which contain at least one dye (a) of the formula (I) which is selected from the group consisting of

3-Methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium chloride

3-Methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium bromide

3-Methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium p-toluenesulfonate 3-methyl-2- {2- [ 4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium methylsulfate 3-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene -1-yl} -1, 3-thiazol-3-ium ^_1/2 sulfate

3-Methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium Vz tetrachlorozincate

^■ 3-Methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium chloride

^■ 3-Methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium bromide

^■ 3-Methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium p-toluenesulfonate

^■ 3-Methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium methyl sulfate

^■ 3-Methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1, 3-thiazol-3-ium ^_1/2 sulfate

^■ 3-Methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium Vz tetrachlorozincate

3-Methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium chloride

3-Methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium bromide

3-Methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium p-toluenesulfonate 3-methyl-2- {2- [ 4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium methylsulfate 3-methyl-2- {2- [4- (pyrrolidin-1-yl) -phenyl] diazene -1-yl} -1, 3-thiazol-3-ium ^_1/2 sulfate

3-Methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium Vz tetrachlorozincate

- 1, 3-Dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazol-3-ium chloride

- 1, 3-Dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1H-imidazole-3-ium bromide

- 1, 3-dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1 H -imidazol-3-ium p-toluenesulfonate

- 1, 3-Dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1H-imidazole-3-ium methyl sulfate

- 1, 3-Dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazol-3-ium Vz sulfate

- 1, 3-dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazol-3-ium Vz tetrachlorozincate

1, 3-dimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1 ^■ yl} -1 H-imidazol-3- to chloride

1, 3-dimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1 ^■ yl} -1 H-imidazol-3- to bromide

1, 3-dimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1 ^■ yl} -1 H-imidazol-3 to p-toluenesulfonate, 1, 3-dimethyl-2- { 2- [4- (piperidin-1-yl) phenyl] diazen-1 ^■ yl} -1 H-imidazol-3-sulfate to give methyl 1, 3-dimethyl-2- {2- [4- (piperidin-1-yl ) phenyl] diazen-1 ^■ yl} -1 H-imidazol-3 by ^_1/2 sulfate

en-1 ^■ yl} -1H-imidazole-3-tetrachlorozincate

1, 3-dimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1 ^■ yl} -1 H-imidazol-3-ium chloride

1, 3-dimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1 ^■ yl} -1 H-imidazol-3-ium bromide

1, 3-dimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1 ^■ yl} -1 H-imidazol-3-ium p-toluenesulfonate, 1, 3-dimethyl-2- { 2- [4- (pyrrolidin-1-yl) phenyl] diazene-1 ^■ yl} -1H-imidazole-3-ium methylsulfate - 1, 3-dimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1 H-imidazol-3-ium ^_1/2 sulfate

-1 -yl} -1H-imidazole-3-ium Vi tetrachlorozincate

- 1, 4-Dimethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1H-1, 2,4-tnazole-4-ium chloride

- 1, 4-Dimethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazole-4-ium bromide

- 1, 4-Dimethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1H-1, 2,4-triazole-4-ium p-toluenesulfonate - 1 , 4-Dimethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1 H-1, 2,4-triazole-4-ium methylsulfate-1, 4-dimethyl -5- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazol-4-ium ^_1/2 sulfate

n-1-yl-1H-1, 2,4-triazole-4-ium Vi tetrachlorozincate

- 1, 4-Dimethyl-5- {2- [4- (piperdin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium chloride

- 1, 4-Dimethyl-5- {2- [4- (piperdin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium bromide

- 1, 4-Dimethyl-5- {2- [4- (piperdin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazol-4-ium p-toluenesulfonate

- 1, 4-Dimethyl-5- {2- [4- (piperdin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium methyl sulfate

- 1, 4-dimethyl-5- {2- [4- (piperdine-1-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazol-4-ium ^_1/2 sulfate

- 1, 4-Dimethyl-5- {2- [4- (piperdin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium Vi tetrachlorozincate

- 1, 4-Dimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1H-1, 2,4-triazole-4-ium chloride

- 1, 4-Dimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1H-1,2,4-triazole-4-ium bromide

- 1, 4-Dimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1H-1,2,4-triazole-4-ium p-toluenesulfonate

- 1, 4-Dimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1H-1, 2,4-triazole-4-ium methyl sulfate - 1, 4-dimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazol-4-ium ^_1/2 sulfate - 1,4-Dimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1H-1,2,4-triazole-4-ium Vz tetrachlorozincate The compositions according to the invention for Color change of keratinic fibers preferably contain the substantive dye or dyes of the formula (I) in a total amount of from 0.01 to 4.5% by weight, preferably from 0.05 to 2.8% by weight, more preferably from 0 , 1 to 2.2 wt .-% and particularly preferably from 0.2 to 1, 2 wt .-%. The amount by weight in this case refers to the total amount of all compounds of the formula (I) contained in the middle, which is related to the total weight of the agent in relation.

In a further preferred embodiment, an agent for dyeing keratinic fibers according to the invention is therefore characterized in that it contains, based on the total weight of the agent, one or more substantive dyes (a) of the formula (I) in a total amount of from 0.01 to 4 , 5 wt .-%, preferably from 0.05 to 2.8 wt .-%, more preferably from 0.1 to 2.2 wt .-% and particularly preferably from 0.2 to 1, 2 wt .-% contains.

The dyes of the general formula (I) can be prepared, for example, by the following method:

Thus, for example, the educt 2-aminothiazole can be converted in concentrated sulfuric acid with nitrosyl sulfuric acid into the diazonium ion:

The reactive diazonium ion then undergoes an azo coupling reaction with a heterocyclic aniline derivative (here N-phenylmorpholine):

The 4-phenylmorpholine which can be used as starting material in the azo coupling reaction is commercially available, for example, from Acros or Aldrich.

Finally, the neutral dimer dye formed in the azo coupling reaction can be double quaternized with quaternizing agents. The quaternization reaction is preferably in one polar aprotic solvents (such as DMSO, DMF etc.). Suitable quaternizing agents are, for example, dimethyl sulfate, methyl bromide or p-toluenesulfonate.

In a particularly preferred embodiment, the agents according to the invention additionally contain at least one surfactant. It has been found that very intense color results could be obtained in particular if the agents according to the invention additionally contained at least one anionic surfactant (b).

Surfactants are amphiphilic (bifunctional) compounds which consist of at least one hydrophobic and at least one hydrophilic moiety. The hydrophobic moiety is preferably a hydrocarbon chain of 8-24 carbon atoms, which may be saturated or unsaturated, linear or branched. With particular preference, this alkyl chain is linear.

For anionic surfactants, the hydrophilic moiety comprises a negatively charged hydrophilic moiety. The negatively charged hydrophilic head group may be, for example, a carboxylic acid group bwz. the salt of a carboxylic acid group, a sulfonic acid group or the salt of the sulfonic acid group, a sulfuric acid ester group or the salt thereof, a phosphonic acid group or the salt of the phosphonic acid group, or a Phosphorsäureestergration or the salt thereof.

The cosmetic agent according to the invention usually comprises an aqueous carrier. In aqueous solution, the abovementioned hydrophilic head groups of the anionic surfactant-such as, for example, the carboxylic acid and the salts of the carboxylic acids-are in an equilibrium whose position is determined by the pH of the agent. If, for example, a fatty acid is used as the anionic surfactant, then a small proportion of the fatty acid is present in aqueous solution in the form of the protonated fatty acid, whereas the major part of the fatty acid is deprotonated in aqueous solution and converted in this way into the salt of the fatty acid. For this reason, the definition of an anionic surfactant also includes a surfactant with a - still protonated - acid group.

An anionic surfactant (b) for the purposes of the present invention contains no cationic groups, ie zwitterionic surfactants are not included in the definition of an anionic surfactant. Anionic surfactants according to the invention are accordingly characterized by the presence of a water-solubilizing, anionic group such as. As a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group having about 8 to 30 carbon atoms. In addition, in the molecule, glycol or

Polyglycol ether groups, ester, ether and amide groups and hydroxyl groups may be included. Typical examples of anionic surfactants are alkylbenzenesulfonates, alkanesulfonates, olefinsulfonates, alkyl ether sulfonates, glycerol ether sulfonates, α-methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, fatty alcohol ether sulfates, glycerol ether sulfates, hydroxy mixed ether sulfates, monoglyceride (ether) sulfates, fatty acid amide (ether) sulfates, mono- and dialkyl sulfosuccinates, mono- and Dialkyl sulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosinates, fatty acid taurides, acyl lactylates, acyl tartrates, acyl glutamates, acyl aspartates, alkyl oligoglucoside sulfates, protein fatty acid condensates (especially wheat-based vegetable products) and alkyl (ether) phosphates. If the anionic surfactants contain polyglycol ether chains, these may have a conventional, but preferably a narrow homolog distribution.

Examples of anionic surfactants according to the invention are, in each case in the form of the sodium, potassium and ammonium as well as the mono-, di- and trialkanolammonium salts having 2 to 4 C atoms in the alkanol group,

linear and branched fatty acids with 8 to 30 carbon atoms (soaps),

Ether carboxylic acids of the formula R-O- (CH 2 -CH 2 O) x-CH 2 -COOH, in which R is a linear alkyl group having 8 to 30 C atoms and x = 0 or 1 to 16,

Acylsarcosides having 8 to 24 carbon atoms in the acyl group,

Acyltaurides having 8 to 24 carbon atoms in the acyl group,

Acyl isethionates having 8 to 24 carbon atoms in the acyl group, which are accessible by esterification of fatty acids with the sodium salt of 2-hydroxyethane-sulfonic acid (isethionic acid). If you for this esterification fatty acids with 8 to 24 carbon atoms, ie z. As lauric, myristic, palmititic or stearic or technical fatty acid fractions, eg. If, for example, the C 12-18 fatty acid fraction obtainable from coconut fatty acid is used, the C 12 -C 12 acyl isethionates which are preferably suitable according to the invention are obtained,

Sulfobernsteinsäuremono- and dialkyl esters having 8 to 24 carbon atoms in the alkyl group and sulfosuccinic monoalkylpolyoxyethylester having 8 to 24 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups. Sulfosuccinic acid mono- and dialkyl esters can be prepared by reacting maleic anhydride with a fatty alcohol having 8-24 carbon atoms to form the maleic monoester of the fatty alcohol and further reacting with sodium sulfite to form the sulfosuccinic acid ester. Particularly suitable sulfosuccinic acid esters are derived from fatty alcohol fractions containing 12-18 C Atoms off, as z. B. from coconut fatty acid or Kokosfettsäuremethylester are accessible by hydrogenation,

linear alkanesulfonates having 8 to 24 C atoms,

linear alpha-olefin sulfonates having 8 to 24 C atoms,

Alpha-sulfofatty acid methyl esters of fatty acids having 8 to 30 carbon atoms,

Alkyl sulfates and alkyl polyglycol ether sulfates of formula R-0 _(CH2 -CH20 -OS0 ₃ H, = in which R is a preferably linear alkyl group having 8 to 30 carbon atoms and x is 0 or 1 to 12,

Hydroxysulfonates essentially corresponding to at least one of the following two formulas or mixtures thereof and salts thereof,

CH ₃ - (CH 2 -CHOH- (CH 2) _P - (CH-SO ₃ M) - (CH 2 -CH 2 -O- (CnH 2nO -H, and / or

-S0 ₃ M -0 _2n O -H where in both formulas y and z = 0 or integers from 1 to 18, p = 0, 1 or 2 and the sum (y + z + p) is a number from 12 to 18 , x = 0 or a number from 1 to 30 and n is an integer from 2 to 4 and M is H or alkali metal, in particular sodium, potassium, lithium, alkaline earth metal, in particular magnesium, calcium, zinc and / or an ammonium ion, which may optionally be substituted, in particular mono-, di-, tri- or tetraammonium ions having C1 to C4 alkyl, alkenyl or aryl radicals,

sulfated hydroxyalkylpolyethylene and / or hydroxyalkylene glycol ethers of the formula R ¹ - 3M) -CHR ³ - (OCHR) n-OR ² with R ¹ , a linear alkyl radical having 1 to 24 C atoms, R ^{2 is} a linear or branched, saturated alkyl radical with 1 to 24 C atoms, R ^{3 is} hydrogen or a linear alkyl radical having 1 to 24 C atoms, R ^{4 is} hydrogen or a methyl radical and M is hydrogen, ammonium, alkylammonium, alkanolammonium, in which the alkyl and alkanol radicals are each 1 having up to 4 carbon atoms, a metal atom selected from lithium, sodium, potassium, calcium or magnesium or and n is a number in the range of 0 are to 12, and further the total number of carbon atoms 2 contained in R ¹ and R ³ to 44,

Sulfonates of unsaturated fatty acids having 8 to 24 carbon atoms and 1 to 6 double bonds,

Esters of tartaric acid and citric acid with alcohols which are adducts of about 2-15 molecules of ethylene oxide and / or propylene oxide with fatty alcohols containing 8 to 22 carbon atoms, alkyl and / or alkenyl ether phosphates of the formula

R ¹ (OCH) _n -O- (PO-OX) -OR ² ,

in the R ^{1 is} preferred for an aliphatic hydrocarbon radical having 8 to 30 carbon atoms, R ^{2 is} hydrogen, a radical (CH ₂ CH ₂ 0 or X, n for numbers from 1 to 10 and X is hydrogen, an alkali or alkaline earth metal or NR ³ R ⁴ R ⁵ R ⁶ , where R ³ to R ⁶ independently of one another represent hydrogen or a bis-hydrocarbon radical,

sulfated fatty acid alkylene glycol esters of the formula RCO (AlkO in the RCO-- for a linear or branched, aliphatic, saturated and / or unsaturated acyl radical having 6 to 22 C atoms, Alk for CH 2 CH 2, CHCH 3 CH 2 and / or CH 2 CHCH 3, n for numbers from 0.5 to 5 and M for a metal such as alkali metal, in particular sodium, potassium, lithium, alkaline earth metal, in particular magnesium, calcium, zinc, or ammonium ion, such as ⁺ NR ³ R ⁴ R ⁵ R ⁶ , where R ³ to R ^{6 are} independently hydrogen or a C1 to C4 - hydrocarbon radical,

Monoglyceride sulfates and monoglyceride ether sulfates of the formula

R ⁸ OC- (OCH 2 CH 2) x -OCH 2 - [CHO (CH 2 CH 2 O) yH] -CH 2 O (CH 2 CH 2 O) z -SO ₃ X,

in which R ⁸ CO is a linear or branched acyl radical having 6 to 22 carbon atoms, x, y and z are in total 0 or numbers of 1 to 30, preferably 2 to 10, and X is an alkali or alkaline earth metal. Typical examples of monoglyceride (ether) sulfates suitable for the purposes of the invention are the reaction products of lauric acid monoglyceride, coconut fatty acid monoglyceride, palmitic acid monoglyceride, stearic acid monoglyceride, oleic acid monoglyceride and tallow fatty acid monoglyceride and their ethylene oxide adducts with sulfur trioxide or chlorosulfonic acid in the form of their sodium salts. Preferably monoglyceride sulfates are used, in which R ⁸ CO is a linear acyl radical having 8 to 18 carbon atoms,

Amide ether carboxylic acids, R ¹ -CO-NR ² -CH ² CH ² -O- (CH ² CH ² O) _n CH ² COOM, wherein R ^{1 is} a straight-chain or branched alkyl or alkenyl radical having a number of carbon atoms in the chain of 2 to 30, n is an integer from 1 to 20 and R ² is hydrogen, methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl or iso-butyl and M is hydrogen or a metal such as alkali metal, especially sodium , Potassium, lithium, alkaline earth metal, in particular magnesium, calcium, zinc, or an ammonium ion, such as ⁺ NR ³ R ⁴ R ⁵ R ⁶ , where R ³ to R ⁶ are each independently hydrogen or a C ¹ to C ⁴ hydrocarbon radical. Such products are obtainable, for example, by the company Chem Y under the product name Akypo ^®, and acyl glutamates of the formula XOOC-CH2CH2CH (C (NH) OR) -COOX, in which RCO is a linear or branched acyl group containing 6 to 22 carbon atoms and 0 and / or 1, 2 or 3 double bonds and X is hydrogen, an alkali and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium.

The treatment of keratinic fibers with agents containing (a) at least one direct-acting dye of formula (I) and (b) at least one anionic surfactant resulted in particularly intense colorations in attractive nuances. It has surprisingly been found that the color absorption capacity could be further optimized by using one or more special anionic surfactants. Particularly intense blue colorations were obtained when the dyes (a) of the formula (I) with at least one anionic surfactant (b) from the group

linear and branched fatty acids having 8 to 30 C atoms, Ether carboxylic acids of the formula R-O- (CH 2 -CH 2 O) x-CH 2 -COOH, in which R is a linear alkyl group having 8 to 30 C atoms and x = 0 or 1 to 16,

Acylsarcosides having 8 to 24 carbon atoms in the acyl group,

Acyltaurides having 8 to 24 carbon atoms in the acyl group,

- Amidethercarbonsäuren, R ¹ -CO-NR ² -CH ² CH ² -O- (CH ² CH ² O) ₂ COOM, with R ¹ as a straight-chain or branched alkyl or alkenyl radical having a number of carbon atoms in the chain of 2 to 30, n is a an integer from 1 to 20 and R ² is hydrogen, a methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl or iso-butyl radical and M is hydrogen or a metal such as alkali metal, in particular sodium, potassium, lithium, alkaline earth metal, in particular magnesium, calcium, zinc, or an ammonium ion, such as ⁺ NR ³ R ⁴ R ⁵ R ⁶ , where R ³ to R ⁶ independently of one another represent hydrogen or a C ¹ to C ⁴ hydrocarbon radical. Such products are obtainable, for example by the company Chem Y under the product name Akypo ^®, and

Acylglutamates of the formula XOOC-CH 2 CH 2 CH (C (NH) OR) -COOX in which RCO is a linear or branched acyl radical having 6 to 22 carbon atoms and 0 and / or 1, 2 or 3 double bonds and X is hydrogen, an alkali metal and / or alkaline earth metal, ammonium, alkylammonium, alkanolammonium or glucammonium.

In a particularly preferred embodiment, an agent according to the invention is therefore characterized in that it contains (b) at least one anionic surfactant which is selected from the linear and branched fatty acids having 8 to 30 C atoms,

- Ethercarbonsäuren the formula R-0- (CH2-CH20) x-CH2-COOM, in the

R is a linear alkyl group having 8 to 30 carbon atoms,

x is an integer from 0 to 16,

M is hydrogen or a metal such as alkali metal, in particular sodium, potassium, lithium, alkaline earth metal, in particular magnesium, calcium, zinc, or an ammonium ion (NH 4 ⁺ ),

Acylsarcosides having 8 to 24 carbon atoms in the acyl group,

Acyl taurides having 8 to 24 carbon atoms in the acyl group,

Acylisethionatne having 8 to 24 carbon atoms in the acyl group, which are accessible by esterification of C8-C24 fatty acids with the sodium salt of 2-hydroxyethane-sulfonic acid (isethionic acid), - Amidethercarbonsäuren, R ¹ -CO-NR ² -CH ² CH ² -O- (CH ² CH ² O) _y CH ² COOM, wherein

R ^{1 is} a C ² -C 30 -alkyl group,

y is an integer from 1 to 20,

R ^{2 is} hydrogen, methyl, ethyl, propyl, isopropyl, n-butyl, t-butyl or iso-butyl, and

M represents hydrogen or a metal such as an alkali metal, in particular sodium, potassium, lithium, an alkaline earth metal, in particular Vz magnesium, Vz calcium, Vz zinc, or an ammonium ion (NH4 ⁺ ).

A particularly good paint absorption capability could be observed if at least one ether carboxylic acid of the formula R-O- (CH 2 -CH 2 O) -CH 2 -COOH or its salt was used as the anionic surfactant (b). The use of - optionally ethoxylated - ether carboxylic acids is therefore explicitly very particularly preferred.

In an explicitly very particularly preferred embodiment, an agent according to the invention is therefore characterized in that at least one anionic surfactant (b) contains from the group of the ether carboxylic acids of the formula (B1)

R-O- (CH 2 -CH 2 O) x-CH 2 -COOM (B1),

in which

R is a linear alkyl group having 8 to 30 carbon atoms,

x is an integer from 0 to 16,

M represents hydrogen or a metal such as an alkali metal, in particular sodium, potassium, lithium, an alkaline earth metal, in particular Vz magnesium, Vz calcium, Vz zinc, or an ammonium ion (NH4 ⁺ ). Furthermore, x is particularly preferably the numbers 5, 6 or 7.

In a further very particularly preferred embodiment, an agent according to the invention is therefore characterized in that the anionic surfactant (b) comprises at least one ether carboxylic acid of the formula (B1)

R-O- (CH 2 -CH 2 O) x-CH 2 -COOM (B1),

in which

R is a linear alkyl group having 8 to 30 carbon atoms,

x is the integer from 5 to 1, in particular the numbers 5, 6 or 7,

M is hydrogen or a metal such as an alkali metal, especially sodium, potassium, lithium

Alkaline earth metal, in particular Vz magnesium, Vz calcium, Vz zinc, or an ammonium ion (NH4 ⁺ ) stands.

The very particularly preferred anionic surfactants of the formula (B1) are obtainable, for example, under the trade name

- Akypo Soft 45 HP from Kao (sodium laureth-6 carboxylate)

- Akypo Soft 45 NV from Kao (sodium laureth-5 carboxylate) Akao RLM 100 NV from Kao (sodium laureth-1 1 carboxylate)

The agents according to the invention for dyeing keratinic fibers preferably contain one or more anionic surfactants (b) in a total amount of from 0.05 to 4.5% by weight, preferably from 0.1 to 2.1% by weight, more preferably from 0.15 to 1, 8 wt .-% and most preferably from 0.2 to 0.9 wt .-%. The data in% by weight are based on the total amount of all anionic surfactants (b) which are related to the total amount of the colorant.

In a further particularly preferred embodiment, an agent for dyeing keratinic fibers according to the invention is therefore characterized in that it contains, based on the total weight of the composition, one or more anionic surfactants (b) in a total amount of 0.05 to 9.5 wt. %, preferably from 0.1 to 3.1 wt .-%, more preferably from 0.15 to 2.5 wt .-% and most preferably from 0.2 to 0.9 wt .-%.

As described above, it has been found that by varying the anionic surfactant (s) (b) the color absorption capacity of the substantive dyes of the formula (I) can be influenced.

In general, the paint lift can be improved by using at least one anionic surfactant. The use of at least one - optionally ethoxylated - ether carboxylic acid and / or its salt, as described in formula (B1), has proved to be particularly advantageous in this context. In this regard, it was observed that the keratin fibers could be dyed in especially intense shades, especially when the ether carboxylic acid (s) and / or its salts were included as the main anionic surfactant in the composition of the invention.

In other words, the dyeing results were particularly intense when the inventive compositions contained one or more ether carboxylic acids of the formula (B1), and, moreover, if all other anionic surfactants used were only present in minor amounts. The use of the ether carboxylic acid (s) of the formula (B1) as the main surfactant can be quantified by specifying a weight ratio which contains the total amount of anionic surfactants of the formula (B1) present in the total amount of all anionic surfactants (b) present in the composition Relation sets.

In a further particularly preferred embodiment, an agent for dyeing keratinic fibers according to the invention is therefore characterized in that the weight ratio of all the anionic surfactants of the formula (B1) present in the composition to the total amount of the anionic surfactants present in the composition is 0.5, is preferably 0.6, more preferably 0.75, and most preferably 0.9,

wherein the anionic surfactants of the formula (B1) are the following surfactants

R-O- (CH 2 -CH 2 O) x-CH 2 -COOM (B1),

With

R is a linear alkyl group having 8 to 30 C atoms,

x is an integer from 0 to 16, M is hydrogen or a metal such as alkali metal, in particular sodium, potassium, lithium, alkaline earth metal, in particular magnesium, calcium, zinc, or an ammonium ion (NH4 ⁺ ).

Example: An agent for coloring keratinic fibers contains:

(a) 1, 0 g - 3-Methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium methyl sulfate

(b) 0.23 g of sodium laureth-6-carboxylate (B1) and

(b) 0.10 g of sodium laureth sulfate (2 EO)

The weight ratio of all of the average anionic surfactants of formula (B1) to the total amount of anionic surfactants present in the composition is [0.23 / (0.23 + 0.1)] = 0.69

Example: An agent for coloring keratinic fibers contains:

(a) 0.5 g of 3-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium methyl sulfate

(b) 0.23 g of sodium laureth-6-carboxylate (B1) and

no further anionic surfactants

The weight ratio of all of the anionic surfactants of the formula (B1) present in the average to the total amount of the anionic surfactants present in the composition is [.23 / .23] = 1.0

Furthermore, the compositions according to the invention may also contain one or more cationic surfactants. Cationic surfactants are understood to mean surfactants, ie surface-active compounds, each having one or more positive charges. Cationic surfactants contain only positive charges. Usually, these surfactants are composed of a hydrophobic part and a hydrophilic head group, wherein the hydrophobic part usually consists of a hydrocarbon skeleton (eg consisting of one or two linear or branched alkyl chains), and the positive charge (s) are located in the hydrophilic head group. Cationic surfactants adsorb at interfaces and aggregate in aqueous solution above the critical micelle concentration to positively charged micelles.

Examples of cationic surfactants are

Quaternary ammonium compounds which can carry as hydrophobic radicals one or two alkyl chains with a chain length of 8 to 28 carbon atoms

quaternary phosphonium salts substituted with one or more alkyl chains having a chain length of 8 to 28 C atoms or

tertiary sulfonium salts.

Further, the cationic charge may also be in the form of an onium structure as part of a heterocyclic ring (e.g., an imidazolium ring or a pyridinium ring).

In addition to the functional unit carrying the cationic charge, the cationic surfactant may also contain other uncharged functional groups, such as is the case with esterquats. Suitable cationic surfactants of this type are, for example, physiologically tolerable salts of N, N, N-trimethyl-1-hexadecanaminium, in particular N, N, N-trimethyl-1-hexadecanaminium chloride, which is also sold under the trade name Dehyquart A-CA.

Another suitable cationic surfactant is a physiologically acceptable salt of dimethyl distearyldimethylammonium, more preferably dimethyl distearylammonium chloride.

Other cationic surfactants can be selected from the group of cationic imidazolium compounds.

The composition according to the invention may contain the cationic surfactant (s) in a total amount of from 0.1 to 4.8% by weight, preferably from 0.2 to 2.4% by weight, more preferably from 0.3 to 1.8 Wt .-% - based on the total weight of the composition - included.

Agents suitable according to the invention can furthermore be characterized in that they additionally comprise at least one zwitterionic surfactant. Suitable zwitterionic surfactants are betaines, N-alkyl-N, N-dimethylammonium glycinates, N-acylaminopropyl-N, N-dimethylammonium glycinates, and 2-alkyl-3-carboxymethyl-3-hydroxyethyl-imidazolines. A preferred zwitterionic surfactant is known by the INCI name Cocamidopropyl Betaine.

Agents suitable according to the invention are characterized in that the agent additionally contains at least one amphoteric surfactant. Preferred amphoteric surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids. Particularly preferred amphoteric surfactants are N-cocoalkylaminopropionate, cocoacylaminoethylaminopropionate and C 12 -C 18 -acylsarcosine.

Furthermore, it has proven to be advantageous if the agents contain other, nonionic surfactants. Preferred nonionic surfactants are alkylpolyglycosides and alkylene oxide addition products to fatty alcohols and fatty acids with in each case 2 to 30 mol of ethylene oxide per mole of fatty alcohol or fatty acid. Preparations having excellent properties are also obtained if they contain fatty acid esters of ethoxylated glycerol as nonionic surfactants.

The nonionic, zwitterionic or amphoteric surfactants are used in proportions of from 0.1 to 45% by weight, preferably from 1 to 30% by weight and very particularly preferably from 1 to 15% by weight, based on the total amount of ready-to-use agents.

In a further preferred embodiment, the agents according to the invention additionally comprise at least one further substantive dye in addition to the compound of the formula (I). By combining with other cationic substantive dyes, the achievable range of nuances can be extended, and the dyeing properties can be further improved.

Direct dyes can be subdivided into anionic, cationic and nonionic substantive dyes. The substantive dyes are preferably selected from the cationic substantive dyes, since these are well compatible with the dyes of general formula (I).

In a further particularly preferred embodiment, an agent according to the invention is characterized in that it additionally contains at least one further cationic substantive dye which is different from the dyes of the formula (I).

One or more dyes from the group Basic Yellow 87, Basic Orange 31, Basic Red 51, Basic Violet 2 and Cationic Blue 347 have proven to be particularly compatible.

The dyes of the formula (I) with the cationic azo dyes Basic Orange 31 and Basic Red 51 are particularly well compatible. By combining a dye of the formula (I) with Basic Orange 31 and / or Basice Red 51, nuances can be produced in the entire color spectrum-apart from purely yellow shades.

In a further particularly preferred embodiment, an agent according to the invention is characterized in that it additionally contains Basic Orange 31 and / or Basic Red 51.

However, the composition according to the invention may additionally contain at least one nonionic substantive dye. This can be selected from the group HC Yellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, HC Yellow 12, HC Orange 1, Disperse Orange 3, HC Red 1, HC Red 3, HC Red 7, HC Red 10 , HC Red 1, HC Red 13, HC Red BN, HC Blue 2, HC Blue 1 1, HC Blue 12, Disperse Blue 3, HC Violet 1, Disperse Violet 1, Disperse Violet 4, Disperse Black 9, 1, 4 Diamino-2-nitrobenzene, 2-amino-4-nitrophenol, 1,4-bis (2-hydroxyethyl) amino-2-nitrobenzene, 3-nitro-4- (2-hydroxyethyl) aminophenol, 2- (2-hydroxyethyl) amino-4,6-dinitrophenol, 4 - [(2-hydroxyethyl) amino] -3-nitro-1-methylbenzene, 1-amino-4- (2-hydroxyethyl) amino-5-chloro-2 nitrobenzene, 4-amino-3-nitrophenol, 1- (2'-ureidoethyl) amino-4-nitrobenzene, 2 - [(4-amino-2-nitrophenyl) amino] benzoic acid, 4 - [(3

Hydroxypropyl) amino] -3-nitrophenol, 4-nitro-o-phenylenediamine, 6-nitro-1,2,3,4-tetrahydroquinoxaline, 2-hydroxy-1,4-naphthoquinone, picramic acid and its salts, 2-amino 6-chloro-4-nitrophenol, 4-ethyl-amino-3-nitrobenzoic acid and 2-chloro-6-ethylamino-4-nitrophenol.

In addition, anionic direct dyes may also be present, which are available under the international names or trade names Acid Yellow 1, Yellow 10, Acid Yellow 23, Acid Yellow 36, Acid Orange 7, Acid Red 33, Acid Red 52, Pigment Red 57: 1, Acid Blue 7, Acid Green 50, Acid Violet 43, Acid Black 1, Acid Black 52, Bromophenol Blue and Tetrabromophenol Blue are known. The agents according to the invention can furthermore also be used together with oxidation dyes. Such oxidation colorants additionally contain at least one oxidation dye precursor, preferably at least one developer-type oxidation dye precursor and at least one coupler-type oxidation dye precursor. Particularly suitable developer-type oxidation dye precursors are selected from at least one compound from the group formed from p-phenylenediamine, p-toluenediamine, 2- (2-hydroxyethyl) -p-phenylenediamine, 2- (1,2-dihydroxyethyl ) -p-phenylenediamine, N, N-bis- (2-hydroxyethyl) -p-phenylenediamine, 2-methoxymethyl-p- phenylenediamine, N- (4-amino-3-methylphenyl) -N- [3- (1 H -imidazol-1-yl) propyl] amine, N, N'-bis (2-hydroxyethyl) -N, N ' bis (4-aminophenyl) -1, 3-diamino-propan-2-ol, bis (2-hydroxy-5-aminophenyl) -methane, 1, 3-bis (2,5-diaminophenoxy) propane 2-ol, N, N'-bis (4-aminophenyl) -1, 4-diazacycloheptane, 1, 10-bis (2,5-diaminophenyl) -1, 4,7,10-tetraoxadecane, p-aminophenol , 4-amino-3-methylphenol, 4-amino-2-aminomethylphenol, 4-amino-2- (1, 2-dihydroxyethyl) phenol, 4-amino-2- (diethylaminomethyl) phenol, 4,5-diamino 1- (2-hydroxyethyl) pyrazole, 2,4,5,6-tetraaminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 2,3-diamino-6 , 7-dihydro-1H, 5H-pyrazolo [1, 2-a] pyrazole-1 -one and their physiologically acceptable salts.

Particularly suitable coupler-type oxidation dye precursors are selected from the group formed from 3-aminophenol, 5-amino-2-methylphenol, 3-amino-2-chloro-6-methylphenol, 2-hydroxy-4-aminophenoxyethanol, 5 Amino-4-chloro-2-methylphenol, 5- (2-hydroxyethyl) amino-2-methylphenol, 2,4-dichloro-3-aminophenol, 2-aminophenol, 3-phenylenediamine, 2- (2,4-diaminophenoxy ) ethanol, 1, 3-bis (2,4-diaminophenoxy) propane, 1-methoxy-2-amino-4- (2-hydroxyethylamino) benzene, 1, 3-bis (2,4-diaminophenyl) propane, 2, 6-Bis (2'-hydroxyethylamino) -1-methylbenzene, 2 - ({3 - [(2-hydroxyethyl) amino] -4-methoxy-5-methylphenyl} amino) ethanol, 2 - ({3 - [(2 - hydroxyethyl) amino] -2-methoxy-5-methylphenyl} amino) ethanol, 2- ({3 - [(2-hydroxyethyl) amino] -4,5-dimethylphenyl} amino) ethanol, 2- [3-morpholine 4-ylphenyl) amino] ethanol, 3-amino-4- (2-methoxyethoxy) -5-methylphenylamine, 1-amino-3-bis (2-hydroxyethyl) aminobenzene, resorcinol, 2-methylresorcinol, 4-chlororesorcinol , 1, 2,4-trihydroxybenzene, 2-amino-3-hydroxypyridine, 3-A mino-2-methylamino-6-methoxypyridine, 2,6-dihydroxy-3,4-dimethylpyridine, 3,5-diamino-2,6-dimethoxypyridine, 1-phenyl-3-methylpyrazol-5-one, 1-naphthol, 1, 5-dihydroxynaphthalene, 2,7-dihydroxynaphthalene, 1, 7-dihydroxynaphthalene, 1, 8-dihydroxynaphthalene, 4-hydroxyindole, 6-hydroxyindole, 7-hydroxyindole, 4-hydroxyindoline, 6-hydroxyindoline, 7-hydroxyindoline or mixtures thereof Compounds or their physiologically acceptable salts.

The additional substantive dyes, developer components and coupler components are preferably used in a proportion of 0.0001 to 5.0 wt .-%, preferably 0.001 to 3.5 wt .-%, each based on the ready-to-use agent. In this case, developer components and coupler components are generally used in approximately molar amounts to each other. Although the molar use has proven to be expedient, a certain excess of individual oxidation dye precursors is not disadvantageous, so that developer components and coupler components in a molar ratio of 1: 0.5 to 1: 3, in particular 1: 1 to 1: 2 , can stand.

If the dyeing is carried out with the substantive dyes of the formula (I) according to the invention and an oxidative lightening of the keratin fibers in one step, the agents according to the invention additionally comprise an oxidizing agent, preferably hydrogen peroxide and / or one of its solid addition products of organic or inorganic compounds. In a preferred embodiment, hydrogen peroxide itself is used as the aqueous solution. The concentration of a hydrogen peroxide solution in the composition according to the invention is determined on the one hand by the legal requirements and on the other hand by the desired effect; preferably 6 to 12 wt .-% solutions are used in water. According to preferred application-ready means of the first subject of the invention are characterized in that, based on the total weight of the ready-to-use agent, 0.5 to 20 wt .-%, preferably 1 to 12.5 wt .-%, particularly preferably 2.5 to 10 Wt .-% and in particular 3 to 6 wt .-% hydrogen peroxide, each based on the total weight of the composition.

In a further particularly preferred embodiment, an agent according to the invention is characterized in that, based on the total weight of the composition, it is 0.5 to 12.5% by weight, preferably 2.5 to 10% by weight and in particular 3 to 6 Wt .-% hydrogen peroxide.

To achieve enhanced whitening and bleaching action, the composition may further contain at least one peroxo salt. Suitable peroxo salts are inorganic peroxo compounds, preferably selected from the group formed from ammonium peroxodisulfate, alkali metal peroxodisulfates, ammonium peroxomonosulfate, alkali metal peroxomonosulfates, alkali metal peroxodiphosphates and alkaline earth metal peroxides. Particularly preferred are peroxodisulfates, in particular ammonium peroxodisulfate, potassium peroxodisulfate and sodium peroxodisulfate.

In a further particularly preferred embodiment, an agent according to the invention is characterized in that it additionally contains at least one persulfate from the group consisting of ammonium peroxodisulfate, potassium peroxodisulfate and sodium peroxodisulfate.

The persulfates are each in an amount of 0.5 to 20 wt .-%, preferably 1 to 12.5 wt .-%, particularly preferably 2.5 to 10 wt .-% and in particular 3 to 6 wt .-%, based on the total weight of the ready-to-use agent, contained in the agent according to the invention.

In a further particularly preferred embodiment, an agent according to the invention is characterized in that it contains at least one persulfate from the group consisting of ammonium peroxodisulfate, potassium peroxodisulfate and sodium peroxodisulfate.

Ammonium peroxodisulphate (or ammonium persulphate) is a compound of the formula (ΝΗ ΘΣΟΘ) which is a compound of the formula K2S2O8 which is a compound of the formula K2S2O8 Sodium peroxodisulphate (or sodium persulphate) is a compound of the formula Formula Na2S20s.

In a further particularly preferred embodiment, an agent according to the invention is characterized in that it contains, based on the total weight of the agent, one or more persulfates from the group consisting of ammonium peroxodisulfate, potassium peroxodisulfate and sodium peroxodisulfate in a total amount of 0.5 to 20% by weight, preferably from 1, 0 to 12.5 wt .-%, more preferably from 2.5 to 10 wt .-% and particularly preferably from 3.0 to 6.0 wt .-%.

The direct-acting dyes of the general formula (I) according to the invention have themselves proved to be particularly stable to certain mixtures of ammonium peroxodisulfate, potassium peroxodisulfate and sodium peroxodisulfate.

In a further particularly preferred embodiment, an agent according to the invention is characterized in that it contains, based on the total weight of the agent,

- 0.2 to 13.5 wt .-%, preferably 0.5 to 1, 5 wt .-%, ammonium peroxodisulfate

- 0.5 to 4.5 wt .-%, preferably 1, 5 to 2.5 wt .-%, potassium peroxodisulfate and

- 0.2 to 1, 8 wt .-%, preferably 0.4 to 0.8 wt .-%, sodium peroxodisulfate.

The dyeing and / or matting agent may contain further bleaching power boosters to enhance the bleaching effect, such as, for example, tetraacetylethylenediamine (TAED), 1,5-diacetyl-2,4-dioxo-hexahydro-1,3,5-triazine (DADHT), Tetraacetylglycoluril (TAGU), N-nonanoylsuccinimide (NOSI), n-nonanoyl or isononanoyloxybenzenesulfonate (n- or i-NOBS), phthalic anhydride, triacetin, ethylene glycol diacetate and 2,5-diacetoxy-2,5-dihydrofuran and carbonate salts or bicarbonate salts in particular ammonium bicarbonate, ammonium carbonate, sodium bicarbonate, disodium carbonate, potassium bicarbonate, dipotassium carbonate and calcium carbonate, and nitrogen-containing, heterocyclic bleach boosters, such as 4-acetyl-1-methylpyridinium p-toluenesulfonate, 2-acetyl-1-methylpyridinium p-toluenesulfonate, and N- Methyl 3,4-dihydroisoquinolinium p-toluenesulfonate.

To further increase the lightening, at least one SiC> 2 compound, such as silicic acid or silicates, in particular water glasses, may additionally be added to the composition according to the invention. It may be preferred according to the invention, the SiC> 2 compounds in amounts of 0.05 wt .-% to 15 wt .-%, particularly preferably in amounts of 0.15 wt .-% to 10 wt .-% and very particularly preferably in amounts of from 0.2% by weight to 5% by weight, based in each case on the anhydrous composition according to the invention. The quantities given in each case the content of SiC> 2 compounds (without their water content) in the funds again.

The colorants may further contain additional active ingredients, auxiliaries and additives in order to improve the dyeing performance and to adjust further desired properties of the agents.

Preferably, the colorants are provided as a liquid preparation and the agents therefore optionally additionally added a further surfactant, said surfactants depending on the field of application as surfactants or as emulsifiers: They are preferably selected from anionic, zwitterionic, amphoteric and nonionic surfactants and emulsifiers ,

The colorants of the invention may contain other auxiliaries and additives. Thus, it has proved to be advantageous if the agent contains at least one thickener. With regard to these thickeners, there are no fundamental restrictions. Both organic and purely inorganic thickening agents can be used.

Suitable thickeners are anionic synthetic polymers;

cationic, synthetic polymers;

naturally occurring thickeners such as nonionic guar gums, scleroglucan gums or xanthan gums, gum arabic, ghatti gum, karaya gum, gum tragacanth, carrageenan gum, agar, locust bean gum, pectins, alginates, starch fractions and derivatives such as amylose, Amylopectin and dextrins, as well as cellulose derivatives such as methylcellulose, carboxyalkylcelluloses and hydroxyalkylcelluloses;

nonionic, fully synthetic polymers, such as polyvinyl alcohol or polyvinylpyrrolidinone; as well as inorganic thickening agents, in particular phyllosilicates such as, for example, bentonite, especially smectites, such as montmorillonite or hectorite.

Dyeing processes on keratin fibers usually take place in an alkaline medium. However, in order to preserve the keratin fibers as well as the skin as much as possible, the setting of too high a pH value is not desirable. Therefore, it is preferred if the pH of the ready-to-use agent is between 7 and 11, in particular between 8 and 10.5. For the purposes of the present invention, the pH values are pH values which were measured at a temperature of 22 ° C.

The alkalizing agents which can be used in accordance with the invention for adjusting the preferred pH can be selected from the group consisting of ammonia, alkanolamines, basic amino acids and inorganic alkalizing agents such as (earth) alkali metal hydroxides, (earth) alkali metal metasilicates, (alkaline) alkaline metal phosphates and (Alkaline) alkali metal hydrogen phosphates. Preferred inorganic alkalizing agents are magnesium carbonate, sodium hydroxide, potassium hydroxide, sodium silicate and sodium metasilicate. Organic alkalizing agents which can be used according to the invention are preferably selected from monoethanolamine, 2-amino-2-methylpropanol and triethanolamine. The basic amino acids which can be used as alkalizing agents according to the invention are preferably selected from the group formed from arginine, lysine, ornithine and histidine, more preferably arginine. However, it has been found in the context of the investigations on the present invention that further preferred agents according to the invention are characterized in that they additionally contain an organic alkalizing agent. An embodiment of the first subject of the invention is characterized in that the agent additionally contains at least one alkalizing agent which is selected from the group consisting of ammonia, alkanolamines and basic amino acids, in particular ammonia, monoethanolamine and arginine or its compatible salts.

Furthermore, it has proved to be advantageous if the colorants, in particular if they additionally contain hydrogen peroxide, contain at least one stabilizer or complexing agent. Particularly preferred stabilizers are phenacetin, alkali benzoates (sodium benzoate) and salicylic acid. Furthermore, all complexing agents of the prior art can be used. According to the invention preferred Complexing agents are nitrogen-containing polycarboxylic acids, in particular EDTA and EDDS, and phosphonates, in particular 1-hydroxyethane-1, 1-diphosphonate (HEDP) and / or ethylenediaminetetramethylenephosphonate (EDTMP) and / or diethylenetriaminepentamethylenephosphonate (DTPMP) or their sodium salts.

Furthermore, the agents according to the invention may contain other active ingredients, auxiliaries and additives, for example nonionic polymers such as, for example, vinylpyrrolidinone / vinyl acrylate copolymers, polyvinylpyrrolidinone, vinylpyrrolidinone / vinyl acetate copolymers, polyethylene glycols and polysiloxanes; additional silicones, such as volatile or nonvolatile, straight-chain, branched or cyclic, crosslinked or uncrosslinked polyalkylsiloxanes (such as dimethicones or cyclomethicones), polyarylsiloxanes and / or polyalkylarylsiloxanes, in particular polysiloxanes with organofunctional groups, such as substituted or unsubstituted amines (amodimethicones), carboxyl, Alkoxy and / or hydroxyl groups (dimethicone copolyols), linear polysiloxane (A) polyoxyalkylene (B) block copolymers, grafted silicone polymers; cationic polymers such as quaternized cellulose ethers, quaternary group polysiloxanes, dimethyldiallylammonium chloride polymers, acrylamide-dimethyldiallyl ammonium chloride copolymers, diethyl sulfate quaternized dimethylaminoethylmethacrylate-vinylpyrrolidinone copolymers, vinylpyrrolidinone-imidazolinium methochloride copolymers, and quaternized polyvinyl alcohol; zwitterionic and amphoteric polymers; anionic polymers such as polyacrylic acids or crosslinked polyacrylic acids; Structurants such as glucose, maleic acid and lactic acid, hair conditioning compounds such as phospholipids, for example, lecithin and cephalins; Perfume oils, dimethylisosorbide and cyclodextrins; fiber structure improving agents, in particular mono-, di- and oligosaccharides such as glucose, galactose, fructose, fructose and lactose; Dyes for staining the agent; Anti-dandruff agents such as Piroctone Olamine, Zinc Omadine and Climbazole; Amino acids and oligopeptides; Protein hydrolysates on animal and / or vegetable basis, as well as in the form of their fatty acid condensation products or optionally anionically or cationically modified derivatives; vegetable oils; Sunscreens and UV blockers; Active ingredients such as panthenol, pantothenic acid, pantolactone, allantoin, pyrrolidinonecarboxylic acids and their salts, and bisabolol; Polyphenols, in particular hydroxycinnamic acids, 6,7-dihydroxycoumarins, hydroxybenzoic acids, catechins, tannins, leucoanthocyanidins, anthocyanidins, flavanones, flavones and flavonols; Ceramides or pseudoceramides; Vitamins, provitamins and vitamin precursors; Plant extracts; Fats and waxes such as fatty alcohols, beeswax, montan wax and paraffins; Swelling and penetrating substances such as glycerol, propylene glycol monoethyl ether, carbonates, hydrogen carbonates, 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 and propellants such as propane-butane mixtures, N2O, dimethyl ether, CO2 and air. The choice of these other substances will be made by those skilled in the art according to the desired properties of the agents. With regard to further optional components and the amounts of these components used, reference is expressly made to the relevant manuals known to the person skilled in the art. The additional active ingredients and auxiliaries are preferably used in the agents according to the invention in amounts of from 0.0001 to 25% by weight, in particular from 0.0005 to 15% by weight, based on the total weight of the application mixture.

The means of the first subject of the invention can be used in processes for changing the color of keratinic fibers, as in dyeing processes, but in particular also in processes for the simultaneous bleaching and dyeing of human hair.

The agents according to the invention can be formulated as single-component agents or as multicomponent agents, such as two-component agents or three-component agents, and used accordingly. Separation into multicomponent systems is particularly suitable where incompatibilities of the ingredients are to be expected or feared; the agent to be used in such systems is manufactured by the consumer just prior to use by mixing the component. The agent according to the invention for the color change of keratinic fibers is always understood to mean the ready-to-use agent.

If the agent according to the invention is made available to the user in the form of a one-component agent, then the ready-to-use agent need not first be prepared, but can be taken directly from the container in which it was made up and applied to the keratinic fibers.

Bleaching agents, however, are usually two-component products in which an oxidizing agent-containing component (A1) shortly before application with an (alkalizing) agent

(A2) and this ready-mix mixture is applied to the hair.

In this case, the agent according to the invention is the ready-to-use agent which was prepared shortly before use by mixing (A1) and (A2).

Here, the substantive dyes of the general formula (I) in the component (A1) (i.e., together with the oxidizing agent) or in the component (A2) (together with the

Alkalizing agent) are made up.

It is also possible and in accordance with the invention if the ready-to-use agent is prepared by mixing three components shortly before application to the human hair

- The component (A1) at least one substantive dye of the general formula (I) and at least one alkalizing agent

Component (A2) contains at least one first oxidizing agent (for example hydrogen peroxide) and

- Component (A3) contains at least one second oxidizing agent (eg one or more peroxodisulfate salts). During the exposure time of the agents on the fiber, it may be advantageous to assist the dyeing, color changing or matting process by supplying heat. The heat supply can be done by an external heat source, such as warm air of a hot air blower, as well as, especially in a hair lightening on the living subjects, by the body temperature of the subject. In the latter case, the treated batch is usually covered with a hood. An exposure phase at room temperature is also according to the invention. In particular, the temperature during the exposure time between 20 ° C and 40 ° C, in particular between 25 ° C and 38 ° C. After the end of the exposure time, the remaining dyeing preparation is rinsed with water or a cleaning agent from the hair. As a cleaning agent can be used in particular commercial shampoo, in particular then can be dispensed with the detergent and the rinsing can be done with water when the brightening agent has a strong surfactant-containing carrier.

With regard to further preferred embodiments of the use and method according to the invention, what has been said about the agents according to the invention applies mutatis mutandis.

Examples

Direct adduct 1: 3-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazol-3-ium methylsulfate

DZ 1 (inventive) mino) phenyl] diazen-1-yl} -1, 3-thiazol-3-ium methyl sulfate

DZ 2 (comparison)

Dyeing

1 . Determination of oxidation stability

The following color creams were prepared (all data in% by weight, active substance)

The direct dyes DZ1 and DZ2 were each pre-dissolved in a little water and mixed with the remaining formulation ingredients.

The following developer emulsion was prepared (total amount 36 g) Developers emulsion

Sodium hydroxide 0.2

Etidronic acid 0.5

Sodium laureth sulfate 07

Acrylate Compolymer 4.3

Hydrogen peroxide (50% solution) 8.0

Water 22.0 g

5 the following bleaching powder prepared (total 13.6 g)

Developers emulsion

Ammonium persulfate 1, 8

Potassium sulphate 5.8

Sodium persulfate 2.1

Sodium silicate 3.8

Disodium EDTA 0.1

Each of the color creams E and V1 was mixed in a weight ratio of 1: 1: 1 with the developer emulsion and with the bleaching powder.

colorations

Each 1, 8 g of the dyeing cream were applied to an approximately 6 cm long strand of human hair (Kerling Euronaturhaar, 80% gray) and left there for 30 minutes at 30 ° C. After completion of the exposure time, the hair was rinsed, washed with a conventional shampoo and then dried. After drying, the color and intensity of the streaks were visually evaluated under the daylight lamp.

Color intensity: + = bad +++ = medium +++++ = very good

2. Determination of the color intensity

The following coloring creams were prepared (all data in% by weight, active substance)

E2 E3

Cetearyl Alcohol 1, 0 1, 0 (C16 / C18-fatty alcohol)

Coconut Alcohol

1, 0 1, 0

(C12 / C18-fatty alcohol)

Methylparaben 0.1 0.1

Propylparaben 0.1 0.1

Cocoamidopropyl betaine (zwitterionic surfactant) 1, 0 -

Sodium laureth-5 carboxylate (anionic surfactant) - 1, 0

DZ 1 (according to the invention) 0.5 0.5

Ammonium sulfate 1, 0 1, 0

Water ad 100 ad 100

The first five components were melted together. This melt was emulsified with hot water, then the dye dissolved in propylene glycol was added and the ammonium sulfate solution added. The indicated pH was adjusted with ammonia, then made up to 100 g with water.

colorations

Color intensity: + = bad +++ = medium +++++ = very good

Claims

claims

Agent for the color change of keratinic fibers, in particular human hair, contained in a cosmetic carrier

(a) at least one substantive dye of the formula (I)

(I)

in which

Het 1 represents one of the structures (II), (III), (IV), (V), (VI) or (VII),

R 1, R 2 independently of one another represent a hydrogen atom, a C 1 -C 6 -alkyl group, a halogen atom from the group consisting of chlorine, bromine, fluorine or iodine, for a

Ce alkoxy group or stand for a nitro group,

R3, R6 independently of one another represent a C 1 -C 6 -alkyl group, a C 2 -C 6 -alkyl group

Alkenyl group or a hydroxy-C 2 -C 6 -alkyl group,

R4, R5 independently of one another represent a hydrogen atom, a C 1 -C 6 -alkyl group, a halogen atom from the group consisting of chlorine, bromine, fluorine or iodine,

Ce alkoxy group or stand for a nitro group,

Het 2 represents one of the structures (VIII), (IX), (X) (XI), (XII) or (XII I),

R 7 is a hydrogen atom or a C 1 -C 6 -alkyl group,

X- for a physiologically acceptable anion, preferably for an anion from the

Group chloride, bromide, iodide, methyl sulfate, methyl sulfonate, p-toluenesulfonate, acetate, hydrogen sulfate, 2 sulfate or 2 Tetrachlorozinkat stands.

2. Composition according to claim 1, characterized in that it contains (a) at least one substantive dye of the general formula (I) in which

Het1 represents one of the structures (II), (III) or (IV)

3. Composition according to one of claims 1 to 2, characterized in that it contains (a) at least one substantive dye of the general formula (I), in the

R 1, R 2 independently of one another represent a hydrogen atom or a C 1 -C 6 -alkyl group, preferably a hydrogen atom or a methyl group.

4. Composition according to one of claims 1 to 3, characterized in that it contains (a) at least one substantive dye of the general formula (I), in which

R3, R6 independently of one another for a Ci-Ce-alkyl group, preferably for a

Methyl group or for an ethyl group, stand and

5. Composition according to one of claims 1 to 4, characterized in that it contains (a) at least one substantive dye of the general formula (I), in the

Het 2 represents one of the structures (VIII), (IX) or (X).

6. Composition according to one of claims 1 to 5, characterized in that it contains (a) at least one substantive dye of the general formula (I) which is selected from

- Salts of 3-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1, 3-thiazol-3-ium

- Salts of 3-methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3,5-dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3,5-dimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-5-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

- Salts of 3-ethyl-5-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

- Salts of 3,4-dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1, 3-thiazol-3-ium

- Salts of 3,4-dimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-4-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazene-1-yl} -1,3-thiazole-3-ium

- Salts of 3-ethyl-4-methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazene-1-yl} -1,3-thiazole-3-ium

- Salts of 3-ethyl-4-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

- Salts of the 1, 3-dimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-dimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-dimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-diethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium - Salts of the 1, 3-diethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-diethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-imidazol-3-ium

- Salts of the 1, 3,5-trimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3,5-trimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,3,5-trimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-diethyl-5-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,3-diethyl-5-methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-diethyl-5-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-imidazol-3-ium

- Salts of the 1, 3,4-trimethyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3,4-trimethyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,3,4-trimethyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-diethyl-4-methyl-2- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,3-diethyl-4-methyl-2- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,3-diethyl-4-methyl-2- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,4-dimethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4-ium

- Salts of 1,4-dimethyl-5- {2- [4- (piperdin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium

- Salts of 1,4-dimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium

- Salts of the 1,4-diethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium

- Salts of 1,4-diethyl-5- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium - Salts of the 1, 4-diethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4-ium

- Salts of the 1, 3,4-trimethyl-5- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4-ium

- Salts of the 1, 3,4-trimethyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazole-4-ium

- Salts 1, 4-diethyl-3-methyl-5- {2- [4- (morpholin-4-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazole-4-iums

Salts of the 1, 4-diethyl-3-methyl-5- {2- [4- (piperidin-1-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4- IUMS

Salts of 1,4-diethyl-3-methyl-5- {2- [4- (pyrrolidin-1-yl) phenyl] diazene-1-yl} -1H-1, 2,4-triazole-4 IUMS

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -3-methyl-1,3-thiazol-3-ium

- Salts of 3-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -3-ethyl-1,3-thiazol-3-ium

- Salts of 3-ethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 3-ethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -3,5-dimethyl-1,3-thiazol-3-ium

- Salts of 3,5-dimethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

- Salts of 3,5-dimethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -3-ethyl-5-methyl-1,3-thiazole-3-ium

- Salts of 3-ethyl-5-methyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

- Salts of 3-ethyl-5-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -3,4-dimethyl-1,3-thiazol-3-ium

- Salts of 3,4-dimethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium

- Salts of 3,4-dimethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1,3-thiazol-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -3-ethyl-4-methyl-1,3-thiazol-3-ium

- Salts of 3-ethyl-4-methyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1,3-thiazole-3-ium - Salts of 3-ethyl-4-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1, 3-thiazole-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1,3-dimethyl-1H-1,3-imidazole-3-ium

- Salts of 1,3-dimethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-dimethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1,3-diethyl-1H-1,3-imidazol-3-ium

- Salts of 1, 3-diethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3-diethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-imidazol-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1,3,5-trimethyl-1H-1,3-imidazole-3-ium

- Salts of the 1, 3,5-trimethyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of the 1, 3,5-trimethyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1,3-diethyl-5-methyl-1H-1,3-imidazole-3-ium

- Salts of the 1, 3-diethyl-5-methyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,3-diethyl-5-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1,3,4-trimethyl-1H-1,3-imidazole-3-ium

- Salts of 2- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1,3-diethyl-4-methyl-1H-1,3-imidazole-3-ium

- Salts of the 1, 3-diethyl-4-methyl-2- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 1,3-diethyl-4-methyl-2- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-imidazole-3-ium

- Salts of 5- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1, 4-dimethyl-1H-1, 2,4-triazole-4-ium - Salts of 1,4-dimethyl-5- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-1,2,4-triazole-4-ium

- Salts of 1,4-dimethyl-5- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4-ium

- Salts of 5- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1, 4-diethyl-1H-1, 2,4-triazole-4-ium

- Salts of the 1, 4-diethyl-5- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazole-4-ium

- Salts of the 1, 4-diethyl-5- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4-ium

- Salts of the 5- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1, 3,4-trimethyl-1H-1, 2,4-triazole-4-ium

- Salts of the 1, 3,4-trimethyl-5- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4-ium

- Salts of the 1, 3,4-trimethyl-5- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4-ium

Salts of the 5- {2- [4- (azepan-1-yl) phenyl] diazen-1-yl} -1, 4-diethyl-3-methyl-1H-1, 2,4-triazole-4 IUMS

Salts of the 1, 4-diethyl-3-methyl-5- {2- [4- (thiomorpholin-4-yl) phenyl] diazen-1-yl} -1 H-1, 2,4-triazole-4 iums and / or

Salts of 1,4-diethyl-3-methyl-5- {2- [4- (piperazin-1-yl) phenyl] diazen-1-yl} -1H-1, 2,4-triazole-4- IUMS.

Composition according to one of claims 1 to 6, characterized in that it - based on the total weight of the composition - one or more substantive dyes (a) of the formula (I) in a total amount of 0.01 to 4.5 wt .-% , preferably from 0.05 to 2.8% by weight, more preferably from 0.1 to 2.2% by weight and particularly preferably from 0.2 to 1.2% by weight.

Agent according to one of claims 1 to 7, characterized in that it contains (b) at least one anionic surfactant selected from among

- linear and branched fatty acids with 8 to 30 carbon atoms,

- Ethercarbonsäuren the formula R-0- (CH ₂ -CH ₂ 0) x-CH ₂ -COOM, in the

R is a linear alkyl group having 8 to 30 carbon atoms,

x is an integer from 0 to 16,

M represents hydrogen or a metal such as an alkali metal, in particular sodium, potassium, lithium, an alkaline earth metal, in particular Vz magnesium, Vz calcium, Vz zinc, or an ammonium ion (NH4 ⁺ ), Acylsarcosides having 8 to 24 C atoms in the acyl group,

Acyltaurides having 8 to 24 C atoms in the acyl group,

Acyl isethionates having 8 to 24 carbon atoms in the acyl group, which are accessible by esterification of Ce-C24 fatty acids with the sodium salt of 2-hydroxyethane-sulfonic acid (isethionic acid),

Amide ether carboxylic acids, R ¹ -CO-NR ² -CH ² CH ² -O- (CH ² CH ² O) _y CH ² COOM, where R ^{1 is} a C ² -C 30 -alkyl group,

y is an integer from 1 to 20,

M is hydrogen or a metal such as an alkali metal, especially sodium, potassium,

Lithium, an alkaline earth metal, in particular Vz magnesium, Vz calcium, Vz zinc, or an ammonium ion (NH4 ⁺ ) stands.

9. Composition according to one of claims 1 to 8, characterized in that at least one anionic surfactant (b) from the group of ether carboxylic acids of the formula (B1)

R-O- (CH 2 -CH 2 O) x-CH 2 -COOM (B1),

in which

R is a linear alkyl group having 8 to 30 carbon atoms,

x is an integer from 0 to 16,

M is hydrogen or a metal such as alkali metal, especially sodium, potassium,

10. Composition according to one of claims 1 to 9, characterized in that it - based on the total weight of the composition - one or more anionic surfactants (b) in a total amount of 0.05 to 9.5 wt .-%, preferably from 0.1 to 3.1 wt .-%, more preferably from 0.15 to 2.5 wt .-% and most preferably from 0.2 to 0.9 wt .-%.

1 1. Composition according to one of claims 1 to 10, characterized in that the weight ratio of all anionic surfactants of the formula (B1) contained in the average to the total amount of the anionic surfactants present in the middle at a value of 0.5, preferably of 0.6, on is preferably 0.75 and particularly preferably 0.9, wherein the anionic surfactants of the formula (B1) are the following surfactants

R-O- (CH 2 -CH 2 O) x-CH 2 -COOM (B1),

With

R is a linear alkyl group having 8 to 30 C atoms, x is an integer from 0 to 16,

M is hydrogen or a metal such as an alkali metal, in particular sodium, potassium, lithium, an alkaline earth metal, in particular Vz magnesium, Vz calcium, Vz zinc, or an ammonium ion (NH4 ⁺ ).

12. Composition according to one of claims 1 to 1 1, characterized in that it - based on the total weight of the composition - 0.5 to 12.5 wt .-%, preferably 2.5 to 10 wt .-% and in particular 4 , 0 to 9.0 wt .-% hydrogen peroxide.

13. Composition according to one of claims 1 to 12, characterized in that it contains at least one persulfate from the group ammonium peroxodisulfate, potassium peroxodisulfate and sodium peroxodisulfate.

14. Composition according to one of claims 1 to 13, characterized in that - based on the total weight of the agent -

- 0.2 to 13.5 wt .-%, preferably 0.5 to 1, 5 wt .-%, ammonium peroxodisulfate

- 0.2 to 1, 8 wt .-%, preferably 0.4 to 0.8 wt .-%, sodium peroxodisulfate.