WO2021121717A1

WO2021121717A1 - Method for dyeing keratin material, comprising the use of an organic c1-c6 alkoxy silane and a dyeing compound and a oligomerester

Info

Publication number: WO2021121717A1
Application number: PCT/EP2020/079169
Authority: WO
Inventors: Rene Krohn; Thomas Hippe; Jessica Brender; Stefan Hoepfner
Original assignee: Henkel Ag & Co. Kgaa
Priority date: 2019-12-16
Filing date: 2020-10-16
Publication date: 2021-06-24
Also published as: DE102019219717A1

Abstract

The invention relates to a method for dyeing keratin material, in particular human hair, according to which the following are used on the keratin material: a first composition (A) which contains: (A1) one or more organic C1-C6-alkoxy-silanes and/or condensation products thereof, and (A2) at least one dyeing compound from the group of pigments and the direct dyes, and a second composition (B) which contains (1B) at least sealing reagent, and optionally a third composition (C) which contains: (C1) at least one care compound (C1) wherein at least one of the compositions (A), (B) and (C) contain at least one oligomerester.

Description

A method for coloring keratin material, comprising the use of an organic C1-C6 alkoxysilane, a coloring compound and an oligomer ester

The present application is in the field of cosmetics and relates to a method for coloring keratinic material, in particular human hair, which comprises the use of two compositions (A) and (B). The composition (A) is a composition which contains at least one organic Ci-C6-alkoxysilane (A1) and at least one coloring compound (A2). The application also describes multi-component packaging units (kit-of-parts) for coloring keratinic material.

The change in the shape and color of keratin fibers, in particular hair, represents an important area of modern cosmetics. The person skilled in the art knows various coloring systems for changing the hair color, depending on the coloring requirements. Oxidation dyes are usually used for permanent, intensive dyeings with good fastness properties and good gray coverage. Such colorants usually contain oxidation dye precursors, so-called developer components and coupler components, which, under the influence of oxidizing agents such as hydrogen peroxide, form the actual dyes with one another. Oxidation dyes are characterized by very long-lasting dyeing results.

If substantive dyes are used, dyes that have already been developed diffuse from the dye into the hair fiber. Compared to oxidative hair coloring, the coloring obtained with substantive dyes is less durable and can be washed out more quickly. Colorations with substantive dyes usually remain on the hair for a period of between 5 and 20 washes.

The use of color pigments is known for short-term color changes on the hair and / or the skin. Color pigments are generally understood to mean insoluble, coloring substances. These are undissolved in the form of small particles in the dye formulation and are only deposited on the outside of the hair fibers and / or the surface of the skin. Therefore, they can usually be removed without leaving any residue by a few washes with detergents containing surfactants. Various products of this type are available on the market under the name of hair mascara.

EP 2168633 B1 deals with the problem of producing long-lasting hair colorations using pigments. The document teaches that when a combination of pigment, organic silicon compound, hydrophobic polymer and a solvent is used, hair can be colored which is particularly resistant to abrasion and / or shampooing. The organic silicon compounds used in EP 2168633 B1 are reactive compounds from the class of alkoxysilanes. These alkoxysilanes hydrolyze in the presence of water at high speed and - depending on the amounts of alkoxysilane and water used in each case - form hydrolysis products and / or condensation products.

If these alkoxysilanes or their hydrolysis or condensation products are used on keratinous material, a film or also a coating is formed on the keratin material, which completely envelops the keratin material and in this way strongly influences the properties of the keratin material. Possible areas of application are, for example, permanent styling or the permanent change in shape of keratin fibers. The keratin fibers are mechanically brought into the desired shape and then fixed in this shape by forming the above-described coating. Another very particularly suitable application is the coloring of keratin material. In the context of this application, the coating or the film is produced in the presence of a coloring compound, for example a pigment. The film colored by the pigment remains on the keratin material or the keratin fibers and results in surprisingly wash-resistant colorations.

A major advantage of the alkoxysilane-based coloring principle is that the high reactivity of this class of compounds enables very fast coating. In this way, good staining results can be achieved after a short application period of just a few minutes. The shorter the exposure times for the hair treatment agent, the greater the comfort for the user. With regard to the durability of the dye, in particular its wash fastness and / or abrasion resistance, there is still room for improvement.

It was the object of the present application to find a method for coloring keratinic material which shows improvements with regard to the color intensity and the fastness properties. In particular, the rubbing fastness should be improved compared to the dyeings that can be achieved with the formulations known from the prior art.

It has surprisingly been found that this object can be achieved in full if the keratin material is colored in a process in which at least two compositions (A) and (B) are applied to the keratin material. Here, the first composition (A) contains at least one organic Ci-C6-alkoxysilane and / or its condensation product and also at least one coloring compound. Optionally, the keratin material can also be treated with a third composition (C). At least one of the compositions (A), (B) and (C) contains an oligomer ester. A first object of the present invention is a method for coloring keratinic material, in particular human hair, in which the keratinic material is used:

- a first composition (A) containing:

(A1) one or more organic Ci-C6-alkoxysilanes and / or their condensation products, and

(A2) at least one coloring compound from the group of pigments and substantive dyes

- a second composition (B) containing:

(B1) a sealing reagent, and

- optionally a third composition (C) which contains

- (C1) at least one care compound, at least one of the compositions (A), (B) and (C) containing at least one oligomer ester.

Such a dyeing process using an oligomer ester surprisingly showed, in addition to intensive dyeing, in particular an improvement in the rubbing fastness of the dyeing.

Treatment of keratinic material

Keratin material or keratin material are to be understood as meaning hair, the skin, the nails (such as fingernails and / or toenails, for example). Furthermore, wool, furs and feathers also fall under the definition of keratinic material.

Keratinic material is preferably understood to mean human hair, human skin and human nails, in particular fingernails and toenails. Keratinic material is very particularly preferably understood to mean human hair.

The term “composition for coloring” is used in the context of this invention for a coloring of the keratin material, in particular the hair, caused by the use of coloring compounds such as thermochromic and photochromic dyes, pigments, mica, substantive dyes. With this coloring, the aforementioned coloring compounds are deposited in a particularly homogeneous and smooth film on the surface of the keratin material or diffuse into the keratin fiber. The film is formed in situ by oligomerization or polymerization of the organic alkoxysilane (s), and by the interaction of the coloring compound and the organic silicon compound and, optionally, further constituents, such as a film-forming polymer.

Organic Ci-C6-alkoxysilanes (A1) and / or their condensation products in the composition (A) The composition (A) is characterized in that it contains one or more organic C 1 -C 6 alkoxysilanes (A1) and / or their condensation products.

The organic Ci-C6-alkoxysilane (s) are organic, non-polymeric silicon compounds which are preferably selected from the group of silanes with one, two or three silicon atoms

Organic silicon compounds, which are alternatively referred to as organosilicon compounds, are compounds that either have a direct silicon-carbon bond (Si-C) or in which the carbon is attached to the silicon via an oxygen, nitrogen or sulfur atom. Atom is linked. The organic silicon compounds according to the invention are preferably compounds which contain one to three silicon atoms. The organic silicon compounds particularly preferably contain one or two silicon atoms.

According to the IUPAC rules, the term silane stands for a group of chemical compounds based on a silicon skeleton and hydrogen. In the case of organic silanes, the hydrogen atoms have been completely or partially replaced by organic groups such as, for example, (substituted) alkyl groups and / or alkoxy groups.

It is characteristic of the Ci-C6-alkoxysilanes that at least one Ci-C6-alkoxy group is bonded directly to a silicon atom. The Ci-C6-alkoxysilanes according to the invention thus comprise at least one structural unit R'R "R" 'Si-0- (Ci-C6-alkyl) where the radicals R', R "and R" 'stand for the three remaining bond valences of the silicon atom .

The Ci-C6 alkoxy group or groups bonded to the silicon atom are very reactive and are hydrolyzed at high speed in the presence of water, the reaction rate also depending, among other things, on the number of hydrolyzable groups per molecule. If the hydrolyzable Ci-C6-alkoxy group is an ethoxy group, the organic silicon compound preferably contains a structural unit R'R "R"'Si-0-CH ₂ -CH3. The radicals R ', R "and R"' again represent the three remaining free valences of the silicon atom.

Even the addition of small amounts of water initially leads to hydrolysis and then to a condensation reaction of the organic alkoxysilanes with one another. For this reason, both the organic alkoxysilanes (A1) and their condensation products can be contained in the composition. A condensation product is understood to mean a product that is formed by the reaction of at least two organic Ci-C6-alkoxysilanes with elimination of water and / or with elimination of a Ci-C6-alkanol.

The condensation products can be, for example, dimers, but also trimers or oligomers, the condensation products being in equilibrium with the monomers.

Depending on the amount of water used or consumed in the hydrolysis, the equilibrium shifts from monomeric Ci-C6-alkoxysilane to condensation product.

In a particularly preferred embodiment, a method is characterized in that the composition (A) contains one or more organic Ci-C6-alkoxysilanes (A1) selected from silanes with one, two or three silicon atoms, the organic silicon compound also comprises one or more basic chemical functions.

This basic group can be, for example, an amino group, an alkylamino group or a dialkylamino group, which is preferably connected to a silicon atom via a linker. The basic group is preferably an amino group, a Ci-C6-alkylamino group or a di (Ci-C6) alkylamino group.

A particularly preferred method is characterized in that the composition (A) contains one or more organic Ci-C6-alkoxysilanes (A1) which are selected from the group of silanes with one, two or three silicon atoms, and where the Ci- C6-alkoxysilanes furthermore comprise one or more basic chemical functions.

Particularly good results could be obtained when Ci-C6-alkoxysilanes of the formula (S-I) and / or (S-II) were used in the process. Since, as already described above, hydrolysis / condensation begins even with traces of moisture, the condensation products of the Ci-C6-alkoxysilanes of the formula (S-I) and / or (S-II) are also included in this embodiment.

In a further very particularly preferred embodiment, a method is characterized in that the first composition (A) contains one or more organic C1-C6 alkoxysilanes (A1) of the formula (S-I) and / or (S-II),

RiR ₂ NL-Si (OR ₃ ) a (R4) b (Sl) where Ri, R2 independently of one another represent a hydrogen atom or a Ci-C6-alkyl group,

L stands for a linear or branched, divalent Ci-C2o-alkylene group,

R3, R4 independently of one another represent a Ci-C6-alkyl group, a, represents an integer from 1 to 3, and b represents the integer 3 - a, and

(R50) c (R6) dSi- (A) e- [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A'”)] _h -Si (R6 ^, ) d (OR5 ^, ) c • (S-II), where

Rs, Rs ·, Rs-, R6, R6 'and R6 “independently represent a Ci-C6-alkyl group,

A, A ‘, A“, A “‘ and A ““ independently of one another represent a linear or branched, divalent Ci-C2o-alkylene group,

R7 and Rs independently of one another for a hydrogen atom, a Ci-C6-alkyl group, a hydroxy-Ci-C6-alkyl group, a C2-C6-alkenyl group, an amino-Ci-C6-alkyl group or a grouping of the formula (S- Ill) stand,

- (A "") - Si (R ₆ ") d" (OR ₅ "(S-Ill),

- c, stands for an integer from 1 to 3,

- d stands for the whole number 3 - c,

- c ‘stands for an integer from 1 to 3,

- d ‘stands for the integer 3 - c‘,

- c "stands for an integer from 1 to 3,

- d "stands for the whole number 3 - c" stands,

- e stands for 0 or 1,

- f stands for 0 or 1,

- g stands for 0 or 1,

- h stands for 0 or 1,

- With the proviso that at least one of the radicals from e, f, g and h is different from 0, and / or their condensation products.

The substituents Ri, R2, R3, R4, Rs, Rs ', Rs ", R6, R6', Re", R7, Rs, L, A, A ', A ", A"' and A "" in the compounds the formula (S1) and (S-II) are explained below by way of example:

Examples of a Ci-C6-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. Preferred examples of a hydroxy-Ci-C6- alkyl groups are a hydroxymethyl, a 2-hydroxyethyl, a 2-hydroxypropyl, a 3-hydroxypropyl, a 4-hydroxybutyl group, a 5-hydroxypentyl and a 6-hydroxyhexyl group; a 2-hydroxyethyl group is particularly preferred. Examples of an amino-Ci-C6-alkyl group are the aminomethyl group, the 2-aminoethyl group and the 3-aminopropyl group. The 2-aminoethyl group is particularly preferred. Examples of a linear divalent Ci-C ₂ o-alkylene group are, for example, the methylene group (-CH ₂ -), the ethylene group (-CH ₂ -CH ₂ -), the propylene group (-CH ₂ -CH ₂ -CH ₂ - ) and the butylene group (-CH ₂ - CH ₂ -CH ₂ -CH ₂ -). The propylene group (-CH ₂ -CH ₂ -CH ₂ -) is particularly preferred. From a chain length of 3 carbon atoms, divalent alkylene groups can also be branched. Examples of branched, divalent C ₃ -C ₂ o-alkylene groups are (-CH ₂ -CH (CH ₃ ) -) and (-CH ₂ -CH (CH ₃ ) -CH ₂ -)

In the organic silicon compounds of the formula (S-l)

RiR ₂ NL-Si (OR ₃ ) a (R4) b (Sl), the radicals Ri and R ₂ independently of one another represent a hydrogen atom or a C1-C6-alkyl group. The radicals Ri and R ₂ are very particularly preferably both a hydrogen atom.

In the middle part of the organic silicon compound is the structural unit or the linker -L- which stands for a linear or branched, divalent Ci-C ₂ o-alkylene group. The divalent Ci-C ₂ o -alkylene group can alternatively also be referred to as a divalent or divalent Ci-C ₂ o-alkylene group, which means that each group -L- can form two bonds.

-L- is preferably a linear, divalent Ci-C ₂ o-alkylene group. With further preference -L- stands for a linear divalent Ci-C6-alkylene group. Particularly preferably -L- stands for a methylene group (-CH ₂ -), an ethylene group (-CH ₂ -CH ₂ -), a propylene group (-CH ₂ -CH ₂ -CH ₂ -) or a butylene group (-CH ₂ - CH ₂ -CH ₂ -CH ₂ -). L very particularly preferably represents a propylene group (—CH ₂ —CH ₂ —CH ₂ -).

The alkoxysilanes of the formula (S-l)

RiR ₂ NL-Si (OR ₃ ) a (R4) b (Sl), each carry the silicon-containing grouping -Si (OR ₃ ) _a (R ₄ ) b at one end In the terminal structural unit -Si (OR3) a (R4) b, the radicals R3 and R4 independently of one another represent a Ci-C6-alkyl group, particularly preferably R3 and R4 independently of one another represent a methyl group or an ethyl group.

Here, a stands for an integer from 1 to 3, and b stands for the integer 3 - a. If a is 3, then b is 0. If a is 2, b is 1. If a is 1, b is 2.

Keratin treatment agents with particularly good properties could be produced if the composition (A) contains at least one organic Ci-C6-alkoxysilane of the formula (S-1) in which the radicals R3, R4 independently of one another represent a methyl group or an ethyl group.

Furthermore, dyeings with the best rub and wash fastness properties could be obtained if the composition (A) contains at least one organic Ci-C6-alkoxysilane of the formula (S-1) in which the radical a stands for the number 3. In this case, the remainder b stands for the number 0.

In a further preferred embodiment, a method is characterized in that the composition (A) contains one or more organic Ci-C6-alkoxysilanes of the formula (S-l), where

- R3, R4 independently of one another represent a methyl group or an ethyl group and

- a stands for the number 3 and

- b stands for the number 0.

In a further preferred embodiment, a method is characterized in that the composition (A) contains at least one or more organic Ci-C6-alkoxysilanes of the formula (S-l),

RiR ₂ NL-Si (OR ₃ ) a (R4) b (Sl), where

- Ri, R2 both stand for a hydrogen atom, and

- L stands for a linear, divalent Ci-C6-alkylene group, preferably for a propylene group (-CH2-CH2-CH2-) or for an ethylene group (-CH2-CH2-),

- R3 stands for an ethyl group or a methyl group,

- R4 represents a methyl group or an ethyl group,

- a stands for the number 3 and

- b stands for the number 0. Organic silicon compounds of the formula (I) which are particularly suitable for solving the problem are

- (3-aminopropyl) triethoxysilane

- (3-aminopropyl) trimethoxysilane

- (2-aminoethyl) triethoxysilane

- (2-aminoethyl) trimethoxysilane

- (3-Dimethylaminopropyl) triethoxysilane

- (3-Dimethylaminopropyl) trimethoxysilane

- (2-Dimethylaminoethyl) triethoxysilane.

- (2-Dimethylaminoethyl) trimethoxysilane and / or

In a further preferred embodiment, a method is characterized in that the first composition (A) contains at least one organic Ci-C6-alkoxysilane (A1) of the formula (S-l) which is selected from the group of

- (3-aminopropyl) triethoxysilane

- (3-aminopropyl) trimethoxysilane

- (2-aminoethyl) triethoxysilane

- (2-aminoethyl) trimethoxysilane

- (3-Dimethylaminopropyl) triethoxysilane

- (3-Dimethylaminopropyl) trimethoxysilane - (2-dimethylaminoethyl) triethoxysilane,

- (2-Dimethylaminoethyl) trimethoxysilane and / or their condensation products.

The aforementioned organic silicon compounds of the formula (I) are commercially available. (3-Aminopropyl) trimethoxysilane can be purchased from Sigma-Aldrich, for example. (3-Aminopropyl) triethoxysilane is also commercially available from Sigma-Aldrich.

In a further embodiment of the method, the composition (A) can also contain one or more organic Ci-C6-alkoxysilanes of the formula (S-II),

(R50) c (R6) dSi- (A) e- [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A'”)] _h -Si (R6 ^, ) d (OR5 ^, ) c • (S-II).

The organosilicon compounds of the formula (S-II) each have the silicon-containing groups (R50) _c (R6) dSi and -Si (R6 ') d' (OR5 ') c at their two ends

In the middle part of the molecule of the formula (S-II) there are the groupings - (A) _e - and - [NR7- (A ')] _f and - [0- (A ”)] _g - and - [NR8- ( A '”)] _h - Here, each of the radicals e, f, g and h can independently represent the number 0 or 1, with the proviso that at least one of the radicals e, f, g and h is different from 0 . In other words, an organic silicon compound of the formula (II) according to the invention contains at least one group from the group consisting of - (A) - and - [NR ₇ - (A ')] - and - [0- (A ”) j- and - [NR ₈ - (A ”')] -

In the two terminal structural _{units (R50) c} (R6) dSi- and - Si (R6 ') d' (OR5 ') c, the radicals R5, R5', R5 "independently of one another represent a Ci-C6-alkyl group. The radicals R6, R6 'and R6 ″ stand independently of one another for a Ci-C6-alkyl group.

Here, c stands for an integer from 1 to 3, and d stands for the integer 3 - c. If c is 3, then d is 0. If c is 2, then d is 1. If c is 1, then d is 2.

Similarly, c ‘stands for an integer from 1 to 3, and d‘ stands for the integer 3 - c ‘. If c ‘stands for the number 3, then d‘ equals 0. If c steht stands for the number 2, then d ‘equals 1. If c ‘stands for the number 1, then d‘ is 2.

Dyeings with the best wash fastness properties could be obtained if the residues c and c 'both stand for the number 3. In this case, d and d 'both stand for the number 0. In a further preferred embodiment, a method is characterized in that the composition (A) contains one or more organic Ci-C6-alkoxysilanes of the formula (S-II),

- R5 and R5 ‘independently represent a methyl group or an ethyl group,

- c and c ‘both stand for the number 3 and

- d and d ‘both stand for the number 0.

If c and c ‘both stand for the number 3 and d and d‘ both stand for the number 0, the organic silicon compounds according to the invention correspond to the formula (S-Ila)

(R50) 3Si- (A) e- [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A'”)] h-Si (OR5 ') 3 (S- Ila).

The radicals e, f, g and h can independently represent the number 0 or 1, at least one radical from e, f, g and h being different from zero. The abbreviations e, f, g and h define which of the groupings - (A) _e - and - [NR7- (A ')] _f - and - [0- (A ”)] _g - and - [ NRs- (A ”')] _h - are located in the central part of the organic silicon compound of the formula (II).

In this context, the presence of certain groups has proven to be particularly advantageous with regard to achieving wash-fast dyeing results. Particularly good results could be obtained when at least two of the radicals e, f, g and h stand for the number 1. Very particularly preferably e and f both stand for the number 1. Furthermore, with very particular preference g and h both stand for the number 0.

If e and f both stand for the number 1 and g and h both stand for the number 0, the organic silicon compounds according to the invention correspond to the formula (S-IIb)

(R50) c (R6) dSi- (A) - [NR7- (A ')] - Si (R6> (0R5') c · (S-Ilb).

The radicals A, A ', A ", A"' and A "" stand independently of one another for a linear or branched, divalent Ci-C2o-alkylene group. The radicals A, A ', A ", A"' and A "" are preferably, independently of one another, a linear, divalent Ci-C2o-alkylene group. The radicals A, A ', A ", A"' and A "" are more preferably, independently of one another, a linear divalent Ci-C6-alkylene group. The divalent Ci-C2o-alkylene group can alternatively be referred to as a divalent or double-bonded Ci-C2o-alkylene group, which means that each grouping A, A ', A ", A"' and A "" can form two bonds.

The radicals A, A ', A ", A"' and A "" are particularly preferably, independently of one another, a methylene group (-CH2-), an ethylene group (-CH2-CH2-), a propylene group (-CH2-CH2-CH2) -) or a butylene group (-CH2-CH2-CH2-CH2-). The radicals A, A ‘, A ″, A ″ and A ″ ″ very particularly preferably stand for a propylene group (-CH2-CH2-CH2-).

If the radical f stands for the number 1, then the organic silicon compound of the invention of the formula (II) contains a structural grouping - [NR7- (A ')] -.

If the radical h stands for the number 1, then the organic silicon compound of the invention of the formula (II) contains a structural grouping - [NR8- (A "’)] -.

The radicals R7 and Rs independently of one another represent a hydrogen atom, a Ci-Ce-alkyl group, a hydroxy-Ci-C6-alkyl group, a C2-C6-alkenyl group, an amino-Ci-C6-alkyl group or a grouping of the Formula (S-Ill)

- (A ““) - Si (R ₆ “) d“ (OR ₅ “) c“ (S-Ill).

The radicals R7 and Rs are very particularly preferably, independently of one another, a hydrogen atom, a methyl group, a 2-hydroxyethyl group, a 2-alkenyl group, a 2-aminoethyl group or a grouping of the formula (S-III).

If the radical f stands for the number 1 and the radical h stands for the number 0, the organic silicon compound contains the grouping [NR7- (A ') j, but not the grouping - [NR8- (A ”')] the radical R7 represents a grouping of the formula (III), then the organic silicon compound comprises 3 reactive silane groups.

In a further preferred embodiment, a method is characterized in that the composition (A) contains one or more organic Ci-C6-alkoxysilanes (A1) of the formula (S-II)

(R50) c (R6) dSi- (A) e- [NR7- (A ')] f- [0- (A ”)] g- [NR8- (A'”)] _h -Si (R6 ^, ) d (OR5 ^, ) c • (II), where

- e and f both stand for the number 1,

- g and h both stand for the number 0,

- A and A 'independently of one another represent a linear, divalent Ci-C6-alkylene group and

- R7 represents a hydrogen atom, a methyl group, a 2-hydroxyethyl group, a 2-alkenyl group, a 2-aminoethyl group or a grouping of the formula (S-III).

In a further preferred embodiment, a method is characterized in that the composition (A) contains one or more organic Ci-C6-alkoxysilanes (A1) of the formula (S-II), where

- e and f both stand for the number 1,

- g and h both stand for the number 0,

- A and A ‘independently of one another represent a methylene group (-CH2-), an ethylene group (-CH2-CH2-) or a propylene group (-CH2-CH2-CH2), and

Organic silicon compounds of the formula (S-II) which are very suitable for achieving the object of the invention are

- 3- (Trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

-N-methyl-3- (trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

-N-methyl-3- (triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

- 2- [bis [3- (trimethoxysilyl) propyl] amino] ethanol

- 2- [bis [3- (triethoxysilyl) propyl] amino] ethanol

- 3- (Trimethoxysilyl) -N, N-bis [3- (trimethoxysilyl) propyl] -1-propanamine - 3- (Triethoxysilyl) -N, N-bis [3- (triethoxysilyl) propyl] -1-propanamine

- N1, N1-bis [3- (trimethoxysilyl) propyl] -1, 2-ethanediamine,

- N1, N1-bis [3- (triethoxysilyl) propyl] -1, 2-ethanediamine,

- N, N-bis [3- (trimethoxysilyl) propyl] -2-propen-1-amine

- N, N-bis [3- (triethoxysilyl) propyl] -2-propen-1-amine

The aforementioned organic silicon compounds of the formula (S-II) are commercially available.

Bis (trimethoxysilylpropyl) amine with the CAS number 82985-35-1 can be purchased from Sigma-Aldrich, for example.

Bis [3- (triethoxysilyl) propyl] amine with the CAS number 13497-18-2 can be purchased from Sigma-Aldrich, for example. N-methyl-3- (trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine is alternatively also referred to as bis (3-trimethoxysilylpropyl) -N-methylamine and can be purchased commercially from Sigma-Aldrich or Fluorochem .

3- (Triethoxysilyl) -N, N-bis [3- (triethoxysilyl) propyl] -1-propanamine with the CAS number 18784-74-2 can be purchased from Fluorochem or Sigma-Aldrich, for example.

In a further preferred embodiment, a method is characterized in that the composition (A) contains one or more organic Ci-C6-alkoxysilanes of the formula (S-II) which are selected from the group of

- 3- (Trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

- N-methyl-3- (trimethoxysilyl) -N- [3- (trimethoxysilyl) propyl] -1-propanamine

- N-methyl-3- (triethoxysilyl) -N- [3- (triethoxysilyl) propyl] -1-propanamine

- 2- [bis [3- (trimethoxysilyl) propyl] amino] ethanol

- 2- [bis [3- (triethoxysilyl) propyl] amino] ethanol

- 3- (Trimethoxysilyl) -N, N-bis [3- (trimethoxysilyl) propyl] -1-propanamine

- 3- (Triethoxysilyl) -N, N-bis [3- (triethoxysilyl) propyl] -1-propanamine

- N1, N1-bis [3- (trimethoxysilyl) propyl] -1, 2-ethanediamine,

- N1, N1-bis [3- (triethoxysilyl) propyl] -1, 2-ethanediamine,

- N, N-bis [3- (trimethoxysilyl) propyl] -2-propene-1-amine and / or

- N, N-bis [3- (triethoxysilyl) propyl] -2-propen-1-amine, and / or their condensation products.

In further dyeing tests it has also been found to be particularly advantageous if at least one organic Ci-C6-alkoxysilane (A1) of the formula (S-IV) was used in the process R ₉ Si (ORio) k (Rn) m (S- IV).

The compounds of the formula (S-IV) are organic silicon compounds which are selected from silanes having one, two or three silicon atoms, the organic silicon compound comprising one or more hydrolyzable groups per molecule.

The alkoxysilane (s) of the formula (S-IV) can also be referred to as silanes of the alkyl-Ci-C6-alkoxysilane type,

RgSi (ORio) k (Rn) m (S-IV), where

- Rg stands for a Ci-Ci2-alkyl group, - R10 stands for a Ci-C6-alkyl group,

- R11 stands for a Ci-C6-alkyl group

- k stands for an integer from 1 to 3, and

- m stands for the integer 3 - k.

In a further embodiment, a particularly preferred method is characterized in that the first composition (A) contains one or more organic C1-C6-

Contains alkoxysilanes (A1) of the formula (S-IV),

R ₉ Si (ORio) k (Rn) m (S-IV), where

Rg stands for a Ci-Ci2-alkyl group,

Rio stands for a Ci-C6-alkyl group,

R11 stands for a Ci-C6-alkyl group, k stands for an integer from 1 to 3, and m stands for the integer 3 - k, and / or their condensation products.

In the organic Ci-C6-alkoxysilanes of the formula (S-IV), the radical Rg stands for a C1-C12-alkyl group. This Ci-Ci2-alkyl group is saturated and can be linear or branched. Rg is preferably a linear Ci-Cs-alkyl group. Rg preferably stands for a methyl group, an ethyl group, an n-propyl group, an n-butyl group, an n-pentyl group, an n-hexyl group, an n-octyl group, an n-dodecyl group or an n-octadecyl group. Rg particularly preferably stands for a methyl group, an ethyl group or an n-hexyl group.

In the Ci-C6-alkoxysilanes of the formula (S-IV), the radical R10 stands for a Ci-C6-alkyl group. R10 particularly preferably represents a methyl group or an ethyl group.

In the Ci-C6-alkoxysilanes of the formula (S-IV), the radical Rn stands for a Ci-C6-alkyl group. Rn particularly preferably represents a methyl group or an ethyl group.

Furthermore, k stands for an integer from 1 to 3, and m stands for the integer 3 - k. If k is 3, then m is 0. If k is 2, then m is 1. If k is 1, m is 2.

Dyeings with the best wash and rub fastness properties could be obtained if the composition (A) contains at least one organic Ci-C6-alkoxysilane (A1) of the formula (S-IV) in which the remainder k stands for the number 3. In this case, the remainder m stands for the number 0. Ci-C6-alkoxysilanes of the formula (S-IV) that are particularly suitable for solving the problem are:

- methyltrimethoxysilane

-

- ethyltrimethoxysilane

- n-propyltrimethoxysilane (also called ans propyltrimethoxysilane)

- n-propyltriethoxysilane (also known as propyltriethoxysilane)

- n-Hexyltrimethoxysilane (also known as hexyltrimethoxysilane)

- n-Hexyltriethoxysilane (also referred to as hexyltriethoxysilane)

- n-Octyltrimethoxysilane (also called octyltrimethoxysilane)

- n-Octyltriethoxysilane (also called octyltriethoxysilane)

- n-Dodecyltrimethoxysilane (also referred to as dodecyltrimethoxysilane) and / or

- n-dodecyltriethoxysilane (also known as dodecyltriethoxysilane)

as well as n-octadecyltrimethoxysilane (also referred to as octadecyltrimethoxysilane) and / or n-octadecyltriethoxysilane (also referred to as dodecyltriethoxysilane).

In a further preferred embodiment, a method is characterized in that the first composition (A) contains at least one organic Ci-C6-alkoxysilane (A1) of the formula (S-IV) which is selected from the group consisting of - methyltrimethoxysilane - methyltriethoxysilane

- ethyltrimethoxysilane

- ethyltriethoxysilane

- propyltrimethoxysilane

- propyltriethoxysilane

- hexyltrimethoxysilane

- hexyltriethoxysilane

- Octyltrimethoxysilane

- octyltriethoxysilane

- dodecyltrimethoxysilane,

- dodecyltriethoxysilane,

- octadecyltrimethoxysilane,

- octadecyltriethoxysilane,

- their mixtures and / or their condensation products.

In a further preferred embodiment, a method is characterized in that the first composition (A) contains at least two structurally different C1-C6-alkoxysilanes.

In a particularly preferred embodiment, a method is characterized in that the first composition (A) contains at least one Ci-C6-alkoxysilane of the formula (I) and at least one Ci-C6-alkoxysilane of the formula (IV).

In a further, very preferred embodiment, a method is characterized in that the first composition (A) contains:

- At least one first Ci-C6-alkoxysilane, which is selected from the group of (3-aminopropyl) trimethoxysilane, (3-aminopropyl) triethoxysilane, (2-aminoethyl) trimethoxysilane, (2- aminoethyl) triethoxysilane, (3-dimethylaminopropyl) trimethoxysilane, (3-dimethylaminopropyl) triethoxysilane, (2-dimethylaminoethyl) trimethoxysilane and (2-dimethylaminoethyl) triethoxysilane, and

- at least one second Ci-C6-alkoxy silane selected from the group consisting methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane. Propyltrimethoxysilane, propyltriethoxysilane, hexyltrimethoxysilane, hexyltriethoxysilane, octyltrimethoxysilane, octyltriethoxysilane, dodecyltrimethoxysilane, dodecyltriethoxysilane, octadecyltrimethoxysilane and octadecyltriethoxysilane.

In a further, very particularly preferred embodiment, a method is characterized in that the first composition (A) contains: - At least one first Ci-C6-alkoxysilane, which comprises (3-aminopropyl) triethoxysilane, and

- at least one second Ci-C6-alkoxy silane, which is selected from the group consisting of methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, hexyltrimethoxysilane, hexyltriethoxysilane, octyltrimethoxysilane, octyltriethoxysilane, dodecyltrimethoxysilane, dodecyltriethoxysilane, octadecyltrimethoxysilane and octadecyltriethoxysilane.

In a further, extremely preferred embodiment, a method is characterized in that the first composition (A) contains:

- At least one first Ci-C6-alkoxysilane, which comprises (3-aminopropyl) triethoxysilane, and

- At least one second Ci-C6-alkoxysilane, which is selected from the group of methyltriethoxysilane, methyltriethoxysilane, ethyltriethoxysilane, hexyltriethoxysilane and octyltriethoxysilane.

The corresponding hydrolysis or condensation products are, for example, the following compounds:

Hydrolysis of Ci-C6-alkoxysilane of the formula (S1) with water (reaction scheme using the example of 3-aminopropyltriethoxysilane):

Depending on the amount of water used, the hydrolysis reaction can also take place several times per Ci-C6-alkoxysilane used:

utt OH Hydrolysis of Ci-C6-alkoxysilane of the formula (S-IV) with water (reaction scheme using the example of methyltrimethoxysilane):

or.

OMe OH

CH ₃ - Si - OMe + 3 H ₂ O CH ₃ - S Ii - OH + 3 MeOH OMe O IH

Possible condensation reactions are for example (shown on the basis of the mixture (3-aminopropyl) triethoxysilane and methyltrimethoxysilane):

and or

In the above exemplary reaction schemes, the condensation to form a dimer is shown in each case, but further condensation to form oligomers with several silane atoms is also possible and also preferred. Both partially hydrolyzed and fully hydrolyzed Ci-C6-alkoxysilanes of the formula (S1) which undergo a condensation with not yet reacted, partially or completely hydrolyzed Ci-C6-alkoxysilanes of the formula (S1) can take part in these condensation reactions. In this case, the Ci-C6-alkoxysilanes of the formula (S1) react with themselves.

In addition, both partially hydrolyzed and fully hydrolyzed Ci-C6-alkoxysilanes of the formula (S1) can also take part in the condensation reactions, which condensation with not yet reacted, partially or completely hydrolyzed Ci-C6-alkoxysilanes of the formula (S-IV) run through. In this case, the Ci-C6-alkoxysilanes of the formula (S-l) react with the Ci-C6-alkoxysilanes of the formula (S-IV).

Furthermore, both partially hydrolyzed and fully hydrolyzed Ci-C6-alkoxysilanes of the formula (S-IV) can also take part in the condensation reactions, which condensation with not yet reacted, partially or completely hydrolyzed Ci-C6-alkoxysilanes of the formula (S- IV) go through. In this case, the Ci-C6-alkoxysilanes of the formula (S-IV) react with themselves.

The composition (A) can contain one or more organic Ci-C6-alkoxysilanes (A1) in various proportions. The person skilled in the art determines this as a function of the desired thickness of the silane coating on the keratin material and of the amount of the keratin material to be treated.

Particularly storage-stable compositions with very good coloring results in use could be obtained if the composition (A) - based on its total weight - one or more organic Ci-C6-alkoxysilanes (A1) and / or the condensation products thereof in a total amount of 30, 0 to 85.0% by weight, preferably from 35.0 to 80.0% by weight, more preferably from 40.0 to 75.0% by weight, even more preferably from 45.0 to 70.0 % By weight and very particularly preferably from 50.0 to 65.0% by weight.

In a further embodiment, a particularly preferred method is characterized in that the first composition (A) - based on the total weight of the composition (A) - one or more organic Ci-C6-alkoxysilanes (A2) and / or the condensation products thereof in one Total amount from 30.0 to 85.0% by weight, preferably from 35.0 to 80.0% by weight, more preferably from 40.0 to 75.0% by weight, even more preferably from 45.0 to 70.0% by weight and very particularly preferably from 50.0 to 65.0% by weight.

Coloring compounds (A2) in the composition (A)

As a second constituent essential to the invention, the composition (A) contains at least one coloring compound (A2) from the group of pigments and substantive dyes. According to the invention, the coloring compound or compounds are selected from the pigments, the substantive dyes, whereby the substantive dyes can also be photochromic dyes and thermochromic dyes.

Composition (A) very particularly preferably contains at least one pigment.

Pigments in the context of the present invention are understood to mean coloring compounds which at 25 ° C. in water have a solubility of less than 0.5 g / L, preferably less than 0.1 g / L, even more preferably less than 0, 05 g / L. The water solubility can for example take place using the method described below: 0.5 g of the pigment is weighed out in a beaker. A stir fry is added. Then one liter of distilled water is added. This mixture is heated to 25 ° C. for one hour while stirring on a magnetic stirrer. If undissolved constituents of the pigment are still visible in the mixture after this period, the solubility of the pigment is below 0.5 g / L. If the pigment-water mixture cannot be assessed visually due to the high intensity of the pigment which may be present in finely dispersed form, the mixture is filtered.

If a proportion of undissolved pigments remains on the filter paper, the solubility of the pigment is below 0.5 g / L.

Suitable color pigments can be of inorganic and / or organic origin.

In a preferred embodiment, an agent is characterized in that it contains at least one coloring compound from the group of inorganic and / or organic pigments.

Preferred color pigments are selected from synthetic or natural inorganic pigments. Inorganic color pigments of natural origin can be made from chalk, ocher, umber, green earth, burnt Terra di Siena or graphite, for example. Furthermore, black pigments such as. B. iron oxide black, colored pigments such. B. ultramarine or iron oxide red and fluorescent or phosphorescent pigments can be used.

Colored metal oxides, hydroxides and oxide hydrates, mixed-phase pigments, sulfur-containing silicates, silicates, metal sulfides, complex metal cyanides, metal sulfates, metal chromates and / or metal molybdates are particularly suitable. Particularly preferred color pigments are black iron oxide (CI 77499), yellow iron oxide (CI 77492), red and brown iron oxide (CI 77491), manganese violet (CI 77742), ultramarines (sodium aluminum sulfosilicates, CI 77007, Pigment Blue 29), Chromium oxide hydrate (CI77289), iron blue (Ferric Ferrocyanide, CI77510) and / or carmine (Cochineal).

Coloring compounds from the group of pigments which are likewise particularly preferred according to the invention are colored pearlescent pigments. These are usually based on mica and / or mica and can be coated with one or more metal oxides. Mica is one of the layered silicates. The most important representatives of these silicates are muscovite, phlogopite, paragonite, biotite, lepidolite and margarite. To produce the pearlescent pigments in conjunction with metal oxides, the mica, predominantly muscovite or phlogopite, is coated with a metal oxide.

As an alternative to natural mica, synthetic mica coated with one or more metal oxide (s) can also be used as a pearlescent pigment. Particularly preferred pearlescent pigments are based on natural or synthetic mica (mica) and are coated with one or more of the aforementioned metal oxides. The color of the respective pigments can be varied by varying the layer thickness of the metal oxide (s).

Likewise preferred pigments based on mica are synthetically produced mica platelets coated with metal oxide, in particular based on synthetic fluorophlogopite (INCI: Synthetic Fluorophlogopite). The synthetic fluorophlogopite platelets are coated, for example, with tin oxide, iron oxide (s) and / or titanium dioxide. The metal oxide layers can also have pigments such as iron (II l) hexacyanidoferrate (l l / l II) or carmine red. Such mica pigments are available, for example, under the name SYNCRYSTAL from Eckart.

In a particularly preferred embodiment, a method is characterized in that the first composition (A) contains at least one inorganic pigment (A2), which is preferably selected from the group of colored metal oxides, metal hydroxides, metal oxide hydrates, silicates, metal sulfides, complex metal cyanides , Metal sulfates, bronze pigments and / or from colored pigments based on mica or mica, which are coated with at least one metal oxide and / or a metal oxychloride.

In a further preferred embodiment, the composition (A) is characterized in that it contains at least one coloring compound (A2) from the group of pigments which is selected from the group of colored metal oxides, metal hydroxides, metal oxide hydrates, silicates, metal sulfides, complex metal cyanides, Metal sulfates, bronze pigments and / or of coloring compounds based on mica or mica, which are coated with at least one metal oxide and / or a metal oxychloride. In a further preferred embodiment, a composition (A) is characterized in that it contains at least one coloring compound (A2) which is selected from pigments based on mica or mica which are mixed with one or more metal oxides from the group consisting of titanium dioxide (CI 77891) , black iron oxide (CI 77499), yellow iron oxide (CI 77492), red and / or brown iron oxide (CI 77491, CI 77499), manganese violet (CI 77742), ultramarines (sodium aluminum sulfosilicates, CI 77007, Pigment Blue 29), chromium oxide hydrate (CI 77289), chromium oxide (CI 77288) and / or iron blue (Ferric Ferrocyanide, CI 77510) are coated.

In a preferred embodiment, a composition (A) is characterized in that it contains at least one coloring compound from the group of inorganic pigments, which is selected from the group consisting of black iron oxide (CI 77499), yellow iron oxide (CI 77492), red Iron oxide (CI 77491) and mixtures thereof.

Yellow iron oxide (or iron oxide yellow) is the name for FeO (OH), in the Color Index under C.I. Pigment Yellow 42 listed.

Red iron oxide (or iron oxide red) is the name for Fe ₂ 03, listed in the Color Index under Cl Pigment Red 101. Depending on the particle size, red iron oxide pigments can be set to have a very yellowish cast (small particle size) to a very bluish cast (coarse particles).

Black iron oxide (or iron oxide black) is listed in the Color Index under Cl Pigment Black 11. Iron oxide black is ferromagnetic. The chemical formula is often given as Fe30 ₄ , in reality there is a mixed crystal of Fe ₂ 03 and FeO with an inverse spinel structure. Additional black pigments are obtained by doping with chromium, copper or manganese.

Brown black iron oxide (or iron oxide brown) usually does not designate a defined pigment, but a mixture of yellow, red and / or black iron oxide.

Iron oxide pigments usually have particle diameters in the range from 2,000 to 4,000 nm. For some application purposes, in particular for cosmetic purposes, it can be advantageous to use iron oxide pigments with significantly smaller particle diameters. For example, hair colorations with iron oxide pigments which have a particle diameter in the range from 100 to 1,000 nm, more preferably 150 nm 700 nm, have better durability and better gray coverage.

Even more preferred is therefore a composition (A) which further comprises a coloring compound from the group of pigments and / or substantive dyes, wherein the coloring compound includes a pigment from the group of iron oxide pigments and wherein the iron oxide pigment has a particle diameter in the range from 100 to 1,000 nm, more preferably 150 nm 700 nm.

Examples of particularly suitable color pigments are commercially available, for example, under the trade names Rona®, Colorona®, Xirona®, Dichrona® and Timiron® from Merck, Ariabel® and Unipure® from Sensient, Prestige® and SynCrystal from Eckart Cosmetic Colors and Sunshine® available from Sunstar.

Particularly preferred pigments with the trade name Colorona® are, for example:

Colorona Copper, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Copper Fine, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Passion Orange, Merck, Mica, CI 77491 (Iran Oxides), Alumina

Colorona Patina Silver, Merck, MICA, CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE)

Colorona RY, Merck, CI 77891 (TITANIUM DIOXIDE), MICA, CI 75470 (CARMINE)

Colorona Oriental Beige, Merck, MICA, CI 77891 (TITANIUM DIOXIDE), CI 77491 (IRON OXIDES) Colorona Dark Blue, Merck, MICA, TITANIUM DIOXIDE, FERRIC FERROCYANIDE Colorona Chameleon, Merck, CI 77491 (IRON OXIDES), MICA

Colorona Aborigine Amber, Merck, MICA, CI 77499 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE)

Colorona Blackstar Blue, Merck, CI 77499 (IRON OXIDES), MICA

Colorona Patagonian Purple, Merck, MICA, CI 77491 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE), CI 77510 (FERRIC FERROCYANIDE)

Colorona Red Brown, Merck, MICA, CI 77491 (IRON OXIDES), CI 77891 (TITANIUM DIOXIDE) Colorona Russet, Merck, CI 77491 (TITANIUM DIOXIDE), MICA, CI 77891 (IRON OXIDES) Colorona Imperial Red, Merck, MICA, TITANIUM DIOXIDE (CI 77891), D&C RED NO. 30 (CI 73360)

Colorona Majestic Green, Merck, CI 77891 (TITANIUM DIOXIDE), MICA, CI 77288 (CHROMIUM OXIDE GREENS)

Colorona Light Blue, Merck, MICA, TITANIUM DIOXIDE (CI 77891), FERRIC FERROCYANIDE (CI 77510)

Colorona Red Gold, Merck, MICA, CI 77891 (TITANIUM DIOXIDE), CI 77491 (IRON OXIDES) Colorona Gold Plus MP 25, Merck, MICA, TITANIUM DIOXIDE (CI 77891), IRON OXIDES (CI 77491)

Colorona Carmine Red, Merck, MICA, TITANIUM DIOXIDE, CARMINE Colorona Blackstar Green, Merck, MICA, CI 77499 (IRON OXIDES)

Colorona Bordeaux, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Bronze, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Bronze Fine, Merck, MICA, CI 77491 (IRON OXIDES) Colorona Fine Gold MP 20, Merck, MICA, CI 77891 (TITANIUM DIOXIDE), CI 77491 (IRON OXIDES)

Colorona Sienna Fine, Merck, CI 77491 (IRON OXIDES), MICA Colorona Sienna, Merck, MICA, CI 77491 (IRON OXIDES)

Colorona Precious Gold, Merck, Mica, CI 77891 (Titanium dioxide), Silica, CI 77491 (Iran oxides), Tin oxide

Colorona Sun Gold Sparkle MP 29, Merck, MICA, TITANIUM DIOXIDE, IRON OXIDES, MICA, CI 77891, CI 77491 (EU)

Colorona Mica Black, Merck, CI 77499 (Iran oxides), Mica, CI 77891 (Titanium dioxide)

Colorona Bright Gold, Merck, Mica, CI 77891 (Titanium dioxide), CI 77491 (Iran oxides)

Colorona Blackstar Gold, Merck, MICA, CI 77499 (IRON OXIDES)

Colorona® SynCopper, Merck, Synthetic Fluorphlogopite (and) Iran Oxides Colorona® SynBronze, Merck, Synthetic Fluorphlogopite (and) Iran Oxides

Other particularly preferred pigments with the trade name Xirona® are, for example:

Xirona® Golden Sky, Merck, Silica, CI 77891 (Titanium Dioxide), Tin Oxide Xirona® Caribbean Blue, Merck, Mica, CI 77891 (Titanium Dioxide), Silica, Tin Oxide Xirona® Kiwi Rose, Merck, Silica, CI 77891 ( Titanium Dioxide), Tin Oxide Xirona® Magic Mauve, Merck, Silica, CI 77891 (Titanium Dioxide), Tin Oxide Xirona® Le Rouge, Merck, Iran Oxides (and) Silica

In addition, particularly preferred pigments with the trade name Unipure® are, for example:

Unipure Red LC 381 EM, Sensient CI 77491 (Iran Oxides), Silica Unipure Black LC 989 EM, Sensient, CI 77499 (Iran Oxides), Silica Unipure Yellow LC 182 EM, Sensient, CI 77492 (Iran Oxides), Silica

Pigments with the trade name Flamenco® are also particularly preferred:

Flamenco® Summit Turquoise T30D, BASF, Titanium Dioxide (and) Mica Flamenco® Super Violet 530Z, BASF, Mica (and) Titanium Dioxide

In a further embodiment, composition (A) can also contain one or more coloring compounds from the group of organic pigments

The organic pigments according to the invention are correspondingly insoluble, organic dyes or color lakes, for example from the group of nitroso, nitro, azo, xanthene, anthraquinone, isoindolinone, isoindoline, quinacridone, perinone, perylene -, diketo- pyrrolopyorrole, indigo, thioindido, dioxazine and / or triarylmethane compounds can be selected.

Particularly suitable organic pigments are, for example, carmine, quinacridone, phthalocyanine, sorghum, blue pigments with the color index numbers CI 42090, CI 69800, CI 69825, CI 73000, CI 74100, CI 74160, yellow pigments with the color index numbers CI 11680 , CI 11710, CI 15985, CI 19140, CI 20040, CI 21100, CI 21108, CI 47000, CI 47005, green pigments with the color index numbers CI 61565, CI 61570, CI 74260, orange pigments with the color index numbers CI 11725 , CI 15510, CI 45370, CI 71105, red pigments with the color index numbers CI 12085, CI 12120, CI 12370, CI 12420, CI 12490, CI 14700, CI 15525, CI 15580, CI 15620, CI 15630, CI 15800, CI 15850, CI 15865, CI 15880, CI 17200, CI 26100, CI 45380, CI 45410, CI 58000, CI 73360, CI 73915 and / or CI 75470.

In a further particularly preferred embodiment, a method is characterized in that the first composition (A) contains at least one organic pigment (A2), which is preferably selected from the group of carmine, quinacridone, phthalocyanine, sorghum, blue pigments with the color index numbers CI 42090, CI 69800, CI 69825, CI 73000, CI 74100, CI 74160, yellow pigments with the color index numbers CI 11680, CI 11710, CI 15985, CI 19140, CI 20040, CI 21100, CI 21108, CI 47000, CI 47005, green pigments with the color index numbers CI 61565, CI 61570, CI 74260, orange pigments with the color index numbers CI 11725, CI 15510, CI 45370, CI 71105, red pigments with the color index numbers CI 12085, CI 12120, CI 12370, CI 12420, CI 12490, CI 14700, CI 15525, CI 15580, CI 15620, CI 15630, CI 15800, CI 15850, CI 15865, CI 15880, CI 17200, CI 26100, CI 45380, CI 45410, CI 58000 , CI 73360, CI 73915 and / or CI 75470.

The organic pigment can also be a colored lacquer. In the context of the invention, the term “colored lacquer” is understood to mean particles which comprise a layer of absorbed dyes, the unit of particles and dye being insoluble under the above-mentioned conditions. The particles can be, for example, inorganic substrates, which can be aluminum, silica, calcium borosilicate, calcium aluminum borosilicate or also aluminum.

For example, the alizarin color varnish can be used as the color varnish.

Because of their excellent light and temperature stability, the use of the aforementioned pigments in the agents according to the invention is particularly preferred. It is also preferred if the pigments used have a certain particle size. This particle size leads on the one hand to a uniform distribution of the pigments in the polymer film formed and on the other hand avoids a rough hair or skin feeling after the application of the cosmetic agent. It is therefore advantageous according to the invention if the at least one pigment has an average particle size D50 of from 1.0 to 50 μm, preferably from 5.0 to 45 μm, more preferably from 10 to 40 μm, in particular from 14 to 30 μm. The mean particle size D50 can be determined using dynamic light scattering (DLS), for example.

Pigments with a specific shape can also have been used to color the keratin material. For example, a pigment based on a lamellar and / or a lenticular substrate platelet can be used. Coloring on the basis of a substrate platelet, which comprises a vacuum metallized pigment (“VMP”), is also possible.

In a further particularly preferred embodiment, a method is characterized in that the first composition (A) contains at least one pigment (A2) selected from the group consisting of the pigments based on a lamellar substrate platelet, the pigments based on a lenticular substrate platelet, and the Pigments based on a substrate platelet, which comprises a vacuum metallized pigment ("VMP").

The substrate platelets of this type have an average thickness of at most 50 nm, preferably less than 30 nm, particularly preferably at most 25 nm, for example at most 20 nm. The average thickness of the substrate platelets is at least 1 nm, preferably at least 2.5 nm, particularly preferably at least 5 nm, for example at least 10 nm. Preferred ranges for the thickness of the substrate platelets are 2.5 to 50 nm, 5 to 50 nm, 10 to 50 nm; 2.5 to 30 nm, 5 to 30 nm, 10 to 30 nm; 2.5 to 25 nm, 5 to 25 nm, 10 to 25 nm, 2.5 to 20 nm, 5 to 20 nm and 10 to 20 nm. Each substrate plate preferably has a thickness that is as uniform as possible.

Due to the small thickness of the substrate platelets, the pigment has a particularly high hiding power.

The substrate platelets have a monolithic structure. In this context, monolithic means consisting of a single closed unit without breaks, layers or inclusions, although changes in structure can occur within the substrate platelets. The substrate platelets are preferably constructed homogeneously, i.e. no concentration gradient occurs within the platelets. In particular, the substrate platelets are not constructed in layers and have no particles or particles distributed therein.

The size of the substrate platelet can be matched to the particular application, in particular the desired effect on the keratinic material. Usually they have Substrate platelets have a mean largest diameter of about 2 to 200 μm, in particular about 5 to 100 μm.

In a preferred embodiment, the aspect ratio, expressed by the ratio of the mean size to the average thickness, is at least 80, preferably at least 200, more preferably at least 500, particularly preferably more than 750. The mean size of the uncoated substrate platelets is understood to be the d50 value of the uncoated substrate platelets. Unless otherwise stated, the d50 value was determined using a Sympatec Helos device with Quixel wet dispersion. To prepare the sample, the sample to be examined was predispersed in isopropanol for a period of 3 minutes.

The substrate platelets can be constructed from any material which can be brought into platelet form.

They can be of natural origin, but also synthetically produced. Materials from which the substrate platelets can be constructed are, for example, metals and metal alloys, metal oxides, preferably aluminum oxide, inorganic compounds and minerals such as mica and (semi) precious stones, as well as plastics. The substrate platelets are preferably constructed from metal (alloys).

Any metal suitable for metallic luster pigments can be considered as the metal. Such metals include iron and steel, as well as all air and water-resistant (semi) metals such as platinum, zinc, chromium, molybdenum and silicon, and their alloys such as aluminum bronze and brass. Preferred metals are aluminum, copper, silver and gold. Preferred substrate platelets are aluminum platelets and brass platelets, with substrate platelets made of aluminum being particularly preferred.

Lamellar substrate platelets are characterized by an irregularly structured edge and are also referred to as "cornflakes" because of their appearance.

Due to their irregular structure, pigments based on lamellar substrate platelets generate a high proportion of scattered light. In addition, the pigments based on lamellar substrate platelets do not completely cover the existing color of a keratinic material and effects analogous to natural graying can be achieved, for example.

Lenticular (= lens-shaped) substrate platelets have an essentially regular round edge and are also known as "silver dollars" due to their appearance designated. Due to their regular structure, pigments based on lenticular substrate platelets predominate in the proportion of reflected light.

Vacuum metallized pigments (VMP) can be obtained, for example, by releasing metals, metal alloys or metal oxides from appropriately coated foils. They are distinguished by a particularly small thickness of the substrate platelets in the range from 5 to 50 nm and by a particularly smooth surface with increased reflectivity. Substrate platelets which comprise a pigment metallized in a vacuum are also referred to in the context of this application as VMP substrate platelets. VMP substrate platelets made of aluminum can be obtained, for example, by releasing aluminum from metallized foils.

The substrate platelets made of metal or metal alloy can be passivated, for example by anodizing (oxide layer) or chromating.

Uncoated lamellar, lenticular and / or VPM substrate platelets, in particular those made of metal or metal alloy, reflect the incident light to a high degree and produce a light-dark flop, but no color impression.

A color impression can be generated, for example, on the basis of optical interference effects. Such pigments can be based on at least once coated substrate platelets. These show interference effects due to the superposition of differently refracted and reflected light rays.

Correspondingly, preferred pigments are pigments based on a coated substrate platelet. The substrate platelet preferably has at least one coating B made of a high-index metal oxide with a coating thickness of at least 50 nm. A further coating A is preferably located between the coating B and the surface of the substrate platelet. If necessary, another coating C, which is different from the layer B below, is located on the layer B.

Suitable materials for the coatings A, B and C are all substances that can be applied permanently and in film form to the substrate platelets and, in the case of the layers A and B, have the required optical properties. In general, a coating of part of the surface of the substrate platelets is sufficient to obtain a pigment with a glossy effect. For example, only the upper and / or lower side of the substrate platelets can be coated, with the side surface (s) being cut out. The entire surface of the optionally passivated substrate platelets, including the side surfaces, is preferably covered by coating B. The substrate platelets are therefore completely from Coating B envelops. This improves the optical properties of the pigment and increases the mechanical and chemical resistance of the pigments. The foregoing also applies to layer A and preferably also to layer C, if any.

Although several coatings A, B and / or C can be present in each case, the coated substrate platelets preferably each have only one coating A, B and, if present, C.

The coating B is made up of at least one high-index metal oxide. Highly refractive materials have a refractive index of at least 1.9, preferably at least 2.0 and particularly preferably at least 2.4. The coating B preferably comprises at least 95% by weight, particularly preferably at least 99% by weight, of high-index metal oxide (s).

The coating B has a thickness of at least 50 nm. The thickness of coating B is preferably not more than 400 nm, particularly preferably at most 300 nm.

High refractive index metal oxides suitable for coating B are preferably selectively light-absorbing (ie colored) metal oxides, such as iron (III) oxide (a- and y-Fe ₂ 03, red), cobalt (II) oxide (blue), chromium (III) oxide (green), titanium (III) oxide (blue, is usually a mixture with titanium oxynitrides and titanium nitrides) and vanadium (V) oxide (orange) and their mixtures. Colorless, high-index oxides such as titanium dioxide and / or zirconium oxide are also suitable.

Coating B can contain a selectively absorbing dye, preferably 0.001 to 5% by weight, particularly preferably 0.01 to 1% by weight, based in each case on the total amount of coating B. Organic and inorganic dyes that are stable in have a metal oxide coating installed.

The coating A preferably has at least one low refractive index metal oxide and / or metal oxide hydrate. Coating A preferably comprises at least 95% by weight, particularly preferably at least 99% by weight, of low-index metal oxide (hydrate). Low refractive index materials have a refractive index of at most 1.8, preferably at most 1.6.

The low refractive index metal oxides which are suitable for coating A include, for example, silicon (di) oxide, silicon oxide hydrate, aluminum oxide, aluminum oxide hydrate, boron oxide, germanium oxide, manganese oxide, magnesium oxide and mixtures thereof, silicon dioxide being preferred. The coating A preferably has a thickness of 1 to 100 nm, particularly preferably 5 to 50 nm, particularly preferably 5 to 20 nm. The distance between the surface of the substrate platelets and the inner surface of coating B is preferably at most 100 nm, particularly preferably at most 50 nm, particularly preferably at most 20 nm Coating B is in the range given above, it can be ensured that the pigments have a high hiding power.

If the pigment based on a substrate flake has only one layer A, it is preferred for the pigment to have a substrate flake made of aluminum and a layer A made of silicon dioxide. If the pigment on the basis of a substrate flake has a layer A and a layer B, it is preferred for the pigment to have a substrate flake made of aluminum, a layer A made of silicon dioxide and a layer B made of iron oxide.

As an alternative to a metal oxide, layer B can comprise a metal particle carrier layer with metal particles applied to the surface of the metal particle carrier layer. In a preferred embodiment, the metal particles directly cover part of the metal particle carrier layer. In this embodiment, the effect pigment has areas in which there are no metal particles, i.e. areas which are not covered with the metal particles.

The metal particle carrier layer comprises a metal layer and / or a metal oxide layer.

If the metal particle carrier layer comprises a metal layer and a metal oxide layer, the arrangement of these layers is not limited.

It is preferred that the metal particle carrier layer comprises at least one metal layer. It is further preferred that the metal layer has an element selected from tin (Sn), palladium (Pd), platinum (Pt) and gold (Au).

The metal layer can be formed, for example, by adding alkali to a metal salt solution containing the metal.

If the metal particle carrier layer contains a metal oxide layer, this preferably does not comprise silicon dioxide. The metal oxide layer preferably contains an oxide of at least one element selected from the group consisting of Mg (magnesium), Sn (tin), Zn (zinc),

Co (cobalt), Ni (nickel), Fe (iron), Zr (zirconium), Ti (titanium) and Ce (cerium). The metal particle carrier layer iii) particularly preferably contains a metal oxide of Sn, Zn, Ti and Ce in the form of a metal oxide layer. The production of the metal particle carrier layer in the form of a metal oxide layer can take place, for example, by hydrolysis of an alkoxide of a metal, which forms the metal of the metal oxide, in a sol-gel process.

The thickness of the metal layer is preferably not more than 30 nm.

The metal particles can comprise at least one element which is selected from the group consisting of aluminum (Al), titanium (Ti), chromium (Cr), iron (Fe), cobalt (Co), nickel (Ni), copper (Cu) , Zinc (Zn), ruthenium (Ru), rhodium (Rh), palladium (Pd), silver (Ag), tin (Sn),

Platinum (Pt), gold (Au) and their alloys. It is particularly preferred that the metal particles have at least one element selected from copper (Cu), nickel (Ni) and silver (Ag).

The average particle diameter of the metal particles is preferably not more than 50 nm, more preferably not more than 30 nm. The distance between the metal particles is preferably not more than 10 nm.

Suitable methods for forming the metal particles are vacuum evaporation, sputtering, chemical vapor deposition (CVD), electroless plating, or the like. Of these methods, electroless plating is particularly preferred.

According to a preferred embodiment, the pigments have a further coating C made of a metal oxide (hydrate), which is different from the coating B below. Suitable metal oxides are, for example, silicon (di) oxide, silicon oxide hydrate, aluminum oxide, aluminum oxide hydrate, zinc oxide, tin oxide, titanium dioxide, zirconium oxide, iron (III) oxide and chromium (III) oxide. Silica is preferred.

The coating C preferably has a thickness of 10 to 500 nm, particularly preferably 50 to 300 nm. By providing the coating C, for example based on T1O2, a better interference can be achieved, with a high hiding power being ensured.

Layers A and C serve in particular as protection against corrosion and also for chemical and physical stabilization. Layers A and C particularly preferably contain silicon dioxide or aluminum oxide, which are applied by the sol-gel process. This method comprises dispersing the uncoated substrate platelets or the substrate platelets already coated with layer A and / or layer B in a solution of a metal alkoxide such as tetraethyl orthosilicate or aluminum triisopropoxide (usually in a solution of organic solvent or a mixture of organic solvent and water with at least 50 wt .-% organic solvent such as a C1 to C4 alcohol), and adding a weak base or acid for hydrolyzing the metal alkoxide, whereby a film of the metal oxide is formed on the surface of the (coated) substrate platelets.

Layer B can be produced, for example, by hydrolytic decomposition of one or more organic metal compounds and / or by precipitation of one or more dissolved metal salts and, if necessary, subsequent aftertreatment (for example conversion of a hydroxide-containing layer that has formed into the oxide layers by annealing).

Although each of the coatings A, B and / or C can be composed of a mixture of two or more metal oxides (hydrate), each of the coatings is preferably composed of a metal oxide (hydrate).

The pigments based on coated lamellar or lenticular substrate platelets or the pigments based on coated VMP substrate platelets preferably have a thickness of 70 to 500 nm, particularly preferably 100 to 400 nm, particularly preferably 150 to 320 nm, for example 180 to 290 nm, on. Due to the small thickness of the substrate platelets, the pigment has a particularly high hiding power. The small thickness of the coated substrate platelets is achieved in particular in that the thickness of the uncoated substrate platelets is small, but also in that the thicknesses of the coatings A and, if present, C are set to the smallest possible value. The thickness of coating B determines the color impression of the pigment.

Pigments based on a substrate platelet comprising artificial mica are also suitable pigments. Particularly preferred are pigments comprising a) a substrate platelet comprising artificial mica, and β) a coating comprising at least one first metal oxide (hydrate) layer comprising T1O2, Sn0 ₂ and / or iron oxide (s).

The adhesion and abrasion resistance of pigments based on coated substrate platelets in the keratinic material can be significantly increased by additionally modifying the outermost layer, depending on the structure, layer A, B or C, with organic compounds such as silanes, phosphoric acid esters, titanates, borates or carboxylic acids becomes. The organic compounds are bound to the surface of the outermost layer A, B or C, preferably containing metal oxide. The outermost layer denotes the layer which is spatially furthest away from the substrate plate. The organic compounds are preferably functional silane compounds which can bond to the layer A, B or C containing metal oxide. These can be either mono- or bifunctional compounds. Examples of bifunctional organic compounds are methacryloxypropenyltrimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3- acryloxypropyltrimethoxysilane, 2-acryloxyethyltrimethoxysilane, 3-methacryloxy propyltriethoxysilane, 3-acryloxypropyltrimethoxysilane, 2-Methacryloxyethyl- triethoxysilane, 2-acryloxyethyltriethoxysilane, 3-methacryloxypropyltris (methox- yethoxy) silane, 3- methacryloxypropyltris (butoxyethoxy) silane, 3-methacryloxypropyltris (propoxy) silane, 3- methacryloxypropyltris (butoxy) silane, 3-acryloxypropyltris (methoxyethoxy) silane, 3-acryloxypropyltris (butoxyethoxy) silane, 3-acryloxypropyltris (butoxy) silane, vinyltrimethoxysilane, vinyltriethoxysilane, vinylethyldichlorosilane, vinylmethyldiacetoxysilane, vinylmethyldiacetylsilane, vinylmethyldiacetoxysilane, vinylmethyldiacetylsilane, vinylmethyldiacetoxysilane, vinylmiethethyldichlorosilane, butoxyethoxy) silane, 3-acryloxypropyltris (butoxyethoxy) silane, vinylmethyldiacetoxysilane, vinylmethyldiacetoxysilane, vinylmethyldiacetoxysilane, vinylmethyldiacetoxysilane, vinylmethyldiacetoxysilane, vinylmethyldiacetoxysilane, butoxyethoxy or phenylallyldichlorosilane. Furthermore, a modification with a monofunctional silane, in particular an alkylsilane or arylsilane, can take place. This has only one functional group which can covalently bind pigments based on coated substrate platelets (ie to the outermost metal oxide-containing layer) or, if not completely covered, to the metal surface. The hydrocarbon residue of the silane faces away from the pigment. Depending on the type and nature of the hydrocarbon radical of the silane, a different degree of hydrophobicity of the pigment is achieved. Examples of such silanes are hexadecyltrimethoxysilane, propyltrimethoxysilane, etc. Pigments based on silicon dioxide-coated aluminum substrate platelets are surface-modified with a monofunctional silane. Octyltrimethoxysilane, octyltriethoxysilane, hecadecyltrimethoxysilane and hecadecyltriethoxysilane are particularly preferred. The changed surface properties / hydrophobization can improve adhesion, abrasion resistance and alignment in the application.

Suitable pigments based on a substrate platelet include, for example, the pigments of the VISIONAIRE series from Eckart.

Pigments based on a lenticular substrate platelet are available, for example, under the name Alegrace® Gorgeous from Schlenk Metallic Pigments GmbH.

Pigments based on a substrate platelet which comprises a vacuum metallized pigment are available, for example, under the name Alegrace® Marvelous or Alegrace® Aurous from Schlenk Metallic Pigments GmbH.

In a further embodiment, a method is characterized in that the composition (A) - based on the total weight of the composition (A) - one or more pigments in a total amount of 0.001 to 20 wt .-%, in particular from 0.05 to 5% by weight.

The compositions (A) can also contain one or more substantive dyes as coloring compounds. Substantive dyes are dyes that are absorbed directly onto the hair and not an oxidative process to develop the color need. Direct dyes are usually nitrophenylenediamines,

Nitroaminophenols, azo dyes, anthraquinones, triary imethane dyes or indophenols.

The substantive dyes for the purposes of the present invention have a solubility in water (760 mmHg) at 25 ° C. of more than 0.5 g / L and are therefore not to be regarded as pigments. The substantive dyes for the purposes of the present invention preferably have a solubility in water (760 mmHg) at 25 ° C. of more than 1.0 g / l. For the purposes of the present invention, the substantive dyes particularly preferably have a solubility in water (760 mmHg) at 25 ° C. of more than 1.5 g / l.

Substantive dyes can be divided into anionic, cationic and nonionic substantive dyes.

In a further preferred embodiment, a composition (A) is characterized in that it contains at least one anionic, cationic and / or nonionic substantive dye as the coloring compound.

In a further preferred embodiment, a method is characterized in that the composition (A) contains at least one coloring compound from the group of anionic, nonionic and / or cationic substantive dyes.

Suitable cationic substantive dyes are, for example, Basic Blue 7, Basic Blue 26, Basic Violet 2 and Basic Violet 14, Basic Yellow 57, Basic Red 76, Basic Blue 16, Basic Blue 347 (Cationic Blue 347 / Dystar), HC Blue No. 16, Basic Blue 99, Basic Brown 16, Basic Brown 17, Basic Yellow 57, Basic Yellow 87, Basic Orange 31, Basic Red 51 Basic Red 76

Nonionic nitro and quinone dyes and neutral azo dyes, for example, can be used as nonionic substantive dyes. Suitable nonionic substantive dyes are those under the international names or trade names HC Yellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, HC Yellow 12, HC Orange 1, Disperse Orange 3, HC Red 1, HC Red 3, HC Red 10, HC Red 11, HC Red 13, HC Red BN, HC Blue 2, HC Blue 11, HC Blue 12, Disperse Blue 3, HC Violet 1, Disperse Violet 1, Disperse Violet 4, Disperse Black 9 known compounds, as well 1,4-diamino-2-nitrobenzene, 2-amino-4-nitrophenol, 1,4-bis- (2-hydroxyethyl) -amino-2-nitrobenzene, 3-nitro-4- (2-hydroxyethyl) -aminophenol, 2- (2- hydroxyethyl) amino-4,6-dinitrophenol, 4 - [(2-hydroxyethyl) amino] -3-nitro-1-methylbenzene, 1-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, 6-nitro-1 , 2,3,4-tetrahydroquinoxaline, 2-hydroxy-1,4-naphthoquinone, picric acid and its salts, 2-amino-6-chloro-4-nitrophenol, 4-ethylamino-3-nitrobenzoic acid and 2-chloro-6-ethylamino-4-nitrophenol. Anionic substantive dyes are also referred to as acid dyes. Acid dyes are understood to mean substantive dyes which have at least one carboxylic acid group (-COOH) and / or one sulfonic acid group (-SO3H). Depending on the pH, the protonated forms (-COOH, -SO3H) of the carboxylic acid or sulfonic acid groups are in equilibrium ^{with their deprotonated forms (-COO-, -S03 _).} The proportion of protonated forms increases with decreasing pH. If substantive dyes are used in the form of their salts, the carboxylic acid groups or sulfonic acid groups are in deprotonated form and are neutralized with corresponding stoichiometric equivalents of cations to maintain electrical neutrality. Acid dyes according to the invention can also be used in the form of their sodium salts and / or their potassium salts.

The acid dyes for the purposes of the present invention have a solubility in water (760 mmHg) at 25 ° C. of more than 0.5 g / L and are therefore not to be regarded as pigments. For the purposes of the present invention, the acid dyes preferably have a solubility in water (760 mmHg) at 25 ° C. of more than 1.0 g / l.

The alkaline earth salts (such as calcium salts and magnesium salts) or aluminum salts of acid dyes often have poorer solubility than the corresponding alkali salts. If the solubility of these salts is below 0.5 g / L (25 ° C, 760 mmHg), they do not fall under the definition of a substantive dye.

An essential feature of acid dyes is their ability to form anionic charges, the carboxylic acid or sulfonic acid groups responsible for this usually being linked to different chromophoric systems. Suitable chromophoric systems are found, for example, in the structures of nitrophenylenediamines, nitroaminophenols, azo dyes, anthraquinone dyes, triarylmethane dyes, xanthene dyes, rhodamine dyes, oxazine dyes and / or indophenol dyes.

One or more compounds from the following group can be selected as particularly suitable acid dyes: Acid Yellow 1 (D&C Yellow 7, Citronin A, Ext. D&C Yellow No. 7, Japan Yellow 403, CI 10316, COLIPA n ° B001), Acid Yellow 3 (COLI PA n °: C 54, D&C Yellow N ° 10, Quinoline Yellow, E104, Food Yellow 13), Acid Yellow 9 (CI 13015), Acid Yellow 17 (CI 18965), Acid Yellow 23 (COLIPA n ° C 29, Covacap Jaune W 1100 (LCW), Sicovit Tartrazine 85 E 102 (BASF), Tartrazine, Food Yellow 4, Japan Yellow 4, FD&C Yellow No. 5), Acid Yellow 36 (CI 13065), Acid Yellow 121 ( CI 18690), Acid Orange 6 (CI 14270), Acid Orange 7 (2-Naphthol orange, Orange II, CI 15510, D&C Orange 4, COLIPA n ° C015), Acid Orange 10 (Cl 16230; Orange G sodium salt), Acid Orange 11 (CI 45370), Acid Orange 15 (CI 50120), Acid Orange 20 (CI 14600), Acid Orange 24 (BROWN 1; CI

20170; KATSU201; nosodiumsalt; Brown No.201; RESORCIN BROWN; ACID ORANGE 24; Japan Brown 201; D&C Brown No.1), Acid Red 14 (C.1.14720), Acid Red 18 (E124, Red 18; CI 16255), Acid Red 27 (E 123, CI 16185, C-Red 46, Echtrot D, FD&C Red Nr.2, Food Red 9, Naphtholred S), Acid Red 33 (Red 33, Fuchsia Red, D&C Red 33, CI 17200), Acid Red 35 (CI C.1.18065), Acid Red 51 (CI 45430, Pyrosin B, Tetraiodfluorescein, Eosin J, lodeosin), Acid Red 52 (CI 45100, Food Red 106, Solar Rhodamine B, Acid Rhodamine B, Red n ° 106 Pontacyl Brilliant Pink), Acid Red 73 (CI CI 27290), Acid Red 87 (Eosin, CI 45380), Acid Red 92 (COLIPA n ° C53, CI 45410), Acid Red 95 (CI 45425, Erythtosine. Simacid Erythrosine Y), Acid Red 184 (CI 15685), Acid Red 195, Acid Violet 43 (Jarocol Violet 43, Ext.D&C Violet n ° 2, Cl 60730, COLIPA n ° C063), Acid Violet 49 (CI 42640), Acid Violet 50 (CI 50325), Acid Blue 1 (Patent Blue, CI 42045), Acid Blue 3 (Patent Blau V, CI 42051), Acid Blue 7 (CI 42080), Acid Blue 104 (CI 42735), Ac id Blue 9 (E 133, Patent Blue AE, Amido Blue AE, Erioglaucin A, CI 42090, C.I. Food Blue 2), Acid Blue 62 (CI 62045), Acid Blue 74 (E 132, CI 73015), Acid Blue 80 (CI 61585), Acid Green 3 (CI 42085, Foodgreenl), Acid Green 5 (CI 42095), Acid Green 9 (C.1.42100), Acid Green 22 (C.1.42170), Acid Green 25 (CI 61570, Japan Green 201, D&C Green No. 5), Acid Green 50 (Brillantsäuregrün BS, Cl 44090, Acid Brilliant Green BS , E 142), Acid Black 1 (Black n ° 401, Naphthalene Black 10B, Amido Black 10B, CI 20 470, COLIPA n ° B15), Acid Black 52 (CI 15711), Food Yellow 8 (CI 14270), Food Blue 5, D&C Yellow 8, D&C Green 5, D&C Orange 10, D&C Orange 11, D&C Red 21, D&C Red 27, D&C Red 33, D&C Violet 2 and / or D&C Brown 1.

The water solubility of the anionic substantive dyes can be determined, for example, in the following way. 0.1 g of the anionic substantive dye are placed in a beaker. A stir bar is added. Then 100 ml of water are added. This mixture is heated to 25 ° C. on a magnetic stirrer while stirring. It is stirred for 60 minutes. The aqueous mixture is then assessed visually. If there are still undissolved residues, the amount of water is increased - for example in steps of 10 ml. Water is added until the amount of dye used has completely dissolved. If the dye-water mixture cannot be assessed visually due to the high intensity of the dye, the mixture is filtered. If a proportion of undissolved dyes remains on the filter paper, the solubility test is repeated with a higher amount of water. If 0.1 g of the anionic substantive dye dissolves in 100 ml of water at 25 ° C., the solubility of the dye is 1.0 g / l.

Acid Yellow 1 is called 8-hydroxy-5,7-dinitro-2-naphthalenesulfonic acid disodium salt and has a solubility in water of at least 40 g / L (25 ° C).

Acid Yellow 3 is a mixture of the sodium salts of mono- and disulfonic acids of 2- (2-quinolyl) -1H-indene-1,3 (2H) -dione and has a water solubility of 20 g / L (25 ° C). Acid Yellow 9 is the disodium salt of 8-hydroxy-5,7-dinitro-2-naphthalenesulfonic acid, its water solubility is above 40 g / L (25 ° C).

Acid Yellow 23 is the trisodium salt of 4,5-dihydro-5-oxo-1- (4-sulfophenyl) -4 - ((4-sulfophenyl) azo) -1H-pyrazole-3-carboxylic acid and works well in water at 25 ° C soluble.

Acid Orange 7 is the sodium salt of 4 - [(2-Hydroxy-1-naphthyl) azo] benzene sulfonate. Its water solubility is more than 7 g / L (25 ° C).

Acid Red 18 is the trinity salt of 7-hydroxy-8 - [(E) - (4-sulfonato-1-naphthyl) -diazenyl)] - 1,3-naphthalenedisulfonate and has a very high solubility in water of more than 20 wt. %.

Acid Red 33 is the diantrium salt of 5-amino-4-hydroxy-3- (phenylazo) -naphthalene-2,7-disulphonate, its water solubility is 2.5 g / L (25 ° C).

Acid Red 92 is the disodium salt of 3,4,5,6-tetrachloro-2- (1,4,5,8-tetrabromo-6-hydroxy-3-oxoxanthen-9-yl) benzoic acid, its water solubility is specified with more than 10 g / L (25 ° C).

Acid Blue 9 is the disodium salt of 2 - ({4- [N-ethyl (3-sulfonatobenzyl] amino] phenyl} {4 - [(N-ethyl (3-sulfonatobenzyl) imino] -2,5-cyclohexadiene-1- ylidene} methyl) benzene sulfonate and has a water solubility of more than 20% by weight (25 ° C).

Furthermore, thermochromic dyes can also be used. Thermochromism includes the property of a material to change its color reversibly or irreversibly depending on the temperature. This can be done both by changing the intensity and / or the wavelength maximum.

Finally, it is also possible to use photochromic dyes. Photochromism includes the property of a material to change its color reversibly or irreversibly depending on the irradiation with light, especially UV light. This can be done both by changing the intensity and / or the wavelength maximum.

In a further embodiment, a method is characterized in that the composition (A) - based on the total weight of the composition (A) - one or more substantive dyes in a total amount of 0.001 to 20 wt .-%, in particular from 0.05 to 5% by weight.

Oligomer esters in the composition (AI

It is essential to the invention that at least one of the compositions (A), (B) and (C) contains at least one oligomer ester. It is also possible for two of the compositions (A), (B) and (C) or all three compositions (A), (B) and (C) each to contain at least one oligomer ester. In a preferred embodiment of the method, composition (A) comprises at least one oligomer ester. Accordingly, a method is particularly preferred in which composition (A) also contains at least one oligomer ester.

Oligomer esters, which are also referred to as oligoesters, are oligomers with ester functions - [- CO-O -] - in their main chain.

Preferred oligomer esters include oligomers of a hydroxylated fatty acid triglyceride and a, preferably saturated, diacid.

Such an oligomer ester is obtained by reacting a hydroxylated fatty acid triglyceride (such as, for example, hydrogenated castor oil) and a, preferably saturated, diacid.

A diacid is understood to mean a hydrocarbon compound which comprises two carboxyl-functional groups - COOH. The diacid can comprise a single diacid or a mixture of multiple diacids.

The oligomer ester can also comprise a mixture of several oligomer esters.

Preferred saturated diacids include, in particular, sebacic acid (or 1,8-decanedicarboxylic acid), succinic acid, adipic acid, azelaic acid, octadecanedioic acid and eicosadicarboxylic acid.

In particular, the oligomer ester can be an oligomer ester whose monomers are represented by the following triglyceride and diacid formulas (I) and (II):

in which

Ri is a saturated or unsaturated, linear or branched alkylene group containing 1 to 18 carbon atoms,

R2 is a saturated or unsaturated, linear or branched alkyl group having 1 to 12 carbon atoms and

X1 is a linear or branched alkylene group, such as, for example, a linear alkylene group - (CH2) _X -, where x can vary from 1 to 30 and in particular from 3 to 15.

When the diacid is sebacic acid, x is 8.

The average degree of oligomerization of the oligomer ester can vary between 3 and 12, more preferably between 4 and 10. Oligomer esters of hydrogenated castor oil and sebacic acid are marketed by CRODA under different names depending on the degree of oligomerization. Such oligomer esters have the INCI name "Hydrogenated Castor Oil / Sebacic Acid Copolymer".

Hydrogenated castor oil contains hydrogenated triricinolein (triglyceride of hydrogenated ricinoleic acid) as its main component. The OH groups at position 12 of two of the hydrogenated ricinoleic acid residues of triricinolein are esterified with a carboxyl group of the diacid.

Accordingly, a method is particularly preferred in which composition (A) further comprises at least one oligomer ester which is selected from the group consisting of oligomer esters of hydrogenated castor oil and sebacic acid.

Preferred oligomer esters are formed from hydrogenated castor oil and sebacic acid and have a degree of oligomerization of about 9.5. Particularly preferred oligomer esters are formed from hydrogenated castor oil and sebacic acid and have a degree of oligomerization of about 4.6.

The commercially available Crodabond® CSA with the INCI name “Hydrogenated Castor Oil / Sebacic Acid Copolymer” in composition (A) is particularly preferred.

Accordingly, a method is particularly preferred in which composition (A) further comprises at least one oligomer ester with the INCI name “Hydrogenated Castor Oil / Sebacic Acid Copolymer”.

The proportion by weight of the at least one oligomer ester in the total weight of the composition (A) is preferably 0.1 to 15% by weight, more preferably 0.1 to 10% by weight and in particular 0.1 to 5% by weight. In a particularly preferred embodiment of the method, composition (A) also contains at least one oligomer ester in an amount of 0.1 to 15% by weight, more preferably 0.1 to 10% by weight and in particular 0.1 to 5% by weight. -%, based on the total weight of the composition (A), wherein the at least one oligomer ester is formed from hydrogenated castor oil and sebacic acid and has a degree of oligomerization of about 4.6.

Other cosmetic ingredients in the composition (AI

In addition, the composition (A) can also contain one or more further cosmetic ingredients.

The cosmetic ingredients which can optionally be used in the composition (A) can be all suitable constituents in order to impart further positive properties to the composition. For example, a solvent, a thickening or film-forming polymer, a surface-active compound from the group of nonionic, cationic, anionic or zwitterionic / amphoteric surfactants, the coloring compounds from the group of pigments, the substantive dyes, the oxidation dye precursors can be used in the composition (A) , the fatty components from the group of C8-C30 fatty alcohols, hydrocarbon compounds, fatty acid esters, the acids and bases belonging to the group of pH regulators, perfumes, preservatives, plant extracts and protein hydrolysates.

The person skilled in the art will select these further substances according to the desired properties of the composition. With regard to further optional components and the amounts of these components used, express reference is made to the relevant manuals known to the person skilled in the art.

In the preparation of the composition (A) the at least one coloring compound (A2) from the group of the pigments and the substantive dyes is preferably used in the form of a pigment suspension comprising the at least one coloring compound (A2) and a liquid carrier medium. The carrier medium is preferably non-aqueous. The carrier medium can for example comprise a silicone oil. Accordingly, the composition (A) can contain the liquid carrier medium in addition to the two ingredients essential to the invention (A1) and (A2).

Water content in the composition (AI

The method is characterized by the application of a first composition (A) to the keratinic material. In the context of the present invention, composition (A) is a ready-to-use composition which, in its present embodiment, can be applied to the keratin materials, in particular to the hair.

In the context of the process, the composition (A) can either be provided in its present form in a container. With the Ci-C6-alkoxysilanes, however, the composition (A) contains very reactive compounds. In order to avoid problems in connection with the storage stability, however, it is particularly preferred to prepare the ready-to-use and reactive composition (A) only shortly before use by mixing two or more storage-stable compositions. For example, the ready-to-use composition (A) can be prepared by mixing a low-water silane blend (A '), which contains the organic Ci-C6-alkoxysilane (s) (A1) in concentrated form, and a water-rich carrier formulation (A ") , which can be a gel, a lotion or a surfactant system, for example.

The ready-to-use composition (A) accordingly preferably has a higher water content, which - based on the total weight of the composition (A) - is in the range from 50.0 to 90.0% by weight, preferably from 55.0 to 90.0% by weight .-%, more preferably 60.0 to 90.0% by weight and particularly preferably 70.0 to 90.0% by weight.

In the context of a further embodiment, a method is characterized in that the composition (A) - based on the total weight of the composition (A) - 50.0 to 90.0% by weight, preferably from 55.0 to 90.0% by weight. -%, more preferably 60.0 to 90.0% by weight and particularly preferably 70.0 to 90.0% by weight of water. pH of the compositions (A)

In further experiments it has been found that the pH values of the composition (A) can have an influence on the color intensities obtained during the dyeing. It was found here that alkaline pH values in particular have an advantageous effect on the dyeing performance that can be achieved in the process.

For this reason, it is preferred that the compositions (A) have a pH of from 7.0 to 12.0, preferably from 7.5 to 11.5, more preferably from 8.0 to 11.0 and very particularly preferably from 8.0 to 10.5.

The pH value can be measured using the usual methods known from the prior art, such as, for example, pH value measurement using glass electrodes using combination electrodes or using pH indicator paper. In a further very particularly preferred embodiment, a method is characterized in that the composition (A) has a pH of from 7.0 to 12.0, preferably from 7.5 to 11.5, more preferably from 8.0 to 11 , 0 and very particularly preferably from 8.0 to 10.5.

Composition (B)

The composition (B) contains a sealing reagent (B1) as an ingredient essential to the invention.

The sealing reagent preferably comprises a compound selected from the group consisting of film-forming polymers, alkalizing agents, acidifying agents, oligomer esters and mixtures thereof.

When composition (A) does not comprise an oligomer ester, composition (B) can comprise an oligomer ester as a sealing reagent (B1).

In a preferred embodiment of the method, composition (B) contains at least one oligomer ester and at least one further compound selected from the group consisting of film-forming polymers, alkalizing agents and acidifying agents as sealing reagent (B1).

If composition (A) and / or composition (C) comprises an oligomer ester, composition (B) preferably contains a compound selected from the group consisting of film-forming polymers, alkalizing agents and acidifying agents as sealing reagent (B1).

Suitable oligomer esters for use in composition (B) include in particular the oligomer esters which have already been described above for use in composition (A). Here, too, it has proven to be particularly advantageous for the rubbing fastness if the at least one oligomer ester is an oligomer ester of hydrogenated castor oil and sebacic acid (INCI: Hydrogenated CastorOil / Sebacic Acid Copolymer) with a degree of oligomerization in the range from 2 to 12, preferably from about 4, 6 includes.

Accordingly, a method is particularly preferred in which composition (B) comprises at least one oligomer ester as sealing reagent (B1), the at least one oligomer ester comprising an oligomer ester of hydrogenated castor oil and sebacic acid (INCI: Hydrogenated Castor Oil / Sebacic Acid Copolymer). Another preferred method is characterized in that the composition (B)

- based on the total weight of the composition (B) - 0.1 to 15% by weight, more preferably from 0.1 to 10% by weight and particularly preferably 0.1 to 5% by weight of an oligomer ester of hydrogenated castor oil and sebacic acid (INCI: Hydrogenated CastorOil / SebacicAcid Copolymer) as sealing reagent (B1).

As an alternative to the at least one oligomer ester or in addition to the at least one oligomer ester, the composition (B) can contain at least one film-forming polymer as sealing reagent (B1).

Polymers are understood to mean macromolecules with a molecular weight of at least 1000 g / mol, preferably of at least 2500 g / mol, particularly preferably of at least 5000 g / mol, which consist of identical, repeating organic units. The polymers of the present invention can be synthetically produced polymers which are produced by polymerizing one type of monomer or by polymerizing different types of monomers which are structurally different from one another. If the polymer is produced by polymerizing one type of monomer, it is called homo-polymer. If structurally different types of monomers are used in the polymerization, the resulting polymer is referred to as a copolymer.

The maximum molecular weight of the polymer depends on the degree of polymerisation (number of polymerised monomers) and the batch size and is also determined by the polymerisation method. For the purposes of the present invention, it is preferred if the maximum molecular weight of the film-forming, hydrophobic polymer is not more than 10 ⁷ g / mol, preferably not more than 10 ⁶ g / mol and particularly preferably not more than 10 ⁵ g / mol.

In the context of the invention, a film-forming polymer is understood to mean a polymer which is capable of forming a film on a substrate, for example on a keratinic material or a keratinous fiber. The formation of a film can be detected, for example, by viewing the keratin material treated with the polymer under a microscope.

In the context of a further preferred embodiment, a method is characterized in that the second composition (B) contains at least one film-forming polymer as sealing reagent (B1).

In a further particularly preferred embodiment, a method is characterized in that the composition (B) contains at least one film-forming polymer, which is preferably selected from the group of homopolymers or copolymers of acrylic acid, of methacrylic acid, of acrylic acid esters, of methacrylic acid esters , of Acrylic acid amides, methacrylic acid amides, vinyl pyrrolidone, vinyl alcohol, vinyl acetate, ethylene, propylene, styrene, polyurethanes, polyesters and / or polyamides.

The film-forming polymers can be hydrophilic or hydrophobic.

In a first embodiment, it can be preferred to use at least one hydrophobic, film-forming polymer as sealing reagent (B1) in composition (B).

A hydrophobic polymer is understood to mean a polymer that has a solubility in water at 25 ° C. (760 mmHg) of less than 1% by weight.

The water solubility of the film-forming, hydrophobic polymer can be determined, for example, in the following way. 1.0 g of the polymer are placed in a beaker. Make up to 100 g with water. A stir bar is added and the mixture is warmed to 25 ° C on a magnetic stirrer while stirring. It is stirred for 60 minutes. The aqueous mixture is then assessed visually. If the polymer-water mixture cannot be assessed visually due to the high turbidity of the mixture, the mixture is filtered. If a proportion of undissolved polymer remains on the filter paper, the solubility of the polymer is less than 1% by weight.

The polymers of the acrylic acid type, the polyurethanes, the polyesters, the polyamides, the polyureas, the cellulose polymers, the nitro-cellulose polymers, the silicone polymers, the polymers of the acrylamide type and the polyisoprenes can be mentioned here in particular .

Particularly suitable film-forming, hydrophobic polymers are, for example, polymers from the group of copolymers of acrylic acid, copolymers of methacrylic acid, homopolymers or copolymers of acrylic acid esters, homopolymers or copolymers of methacrylic acid esters, homopolymers or copolymers of acrylic acid amides, homopolymers or copolymers of methacrylic acid amides, copolymers of vinyl pyrrolidone, copolymers of vinyl alcohol, copolymers of vinyl acetate, homopolymers or copolymers of ethylene, homopolymers or copolymers of propylene, homopolymers or copolymers of styrene, polyurethanes, polyesters and / or the polyamides.

In a further preferred embodiment, a composition (B) is characterized in that it contains at least one film-forming, hydrophobic polymer selected from the group consisting of copolymers of acrylic acid, copolymers of methacrylic acid, homopolymers or copolymers of acrylic acid esters, homopolymers or copolymers of methacrylic acid esters, homopolymers or copolymers of acrylic acid amides, homopolymers or copolymers of methacrylic acid amides, copolymers of vinyl pyrrolidone, copolymers of vinyl alcohol, copolymers of vinyl acetate, homopolymers or copolymers of ethylene, homopolymers or copolymers Propylene, homopolymers or copolymers of styrene, polyurethanes, polyesters and / or polyamides.

In particular, the film-forming hydrophobic polymers which are selected from the group of synthetic polymers, polymers obtainable by free radical polymerization or natural polymers have proven to be particularly suitable for achieving the object of the invention.

Further particularly suitable film-forming hydrophobic polymers can be selected from the homopolymers or copolymers of olefins, such as cycloolefins, butadiene, isoprene or styrene, vinyl ethers, vinyl amides, the esters or amides of (meth) acrylic acid with at least one Ci-C2o-alkyl group, an aryl group or a C2-C10 hydroxyalkyl group.

Further film-forming hydrophobic polymers can be selected from the homo- or copolymers of isooctyl (meth) acrylate, isononyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, lauryl (meth) acrylate), isopentyl (meth) acrylate, n-butyl (meth) acrylate), isobutyl (meth) acrylate, ethyl (meth) acrylate, methyl (meth) acrylate, tert-butyl (meth) acrylate, stearyl (meth) acrylate, hydroxyethyl - (meth) acrylate, 2-hydroxypropyl (methacrylate, 3-hydroxypropyl (meth) acrylate and / or mixtures thereof).

Further film-forming hydrophobic polymers can be selected from the homo- or copolymers of (meth) acrylamide, N-alkyl- (meth) acrylamides, in particular those with C2-C18 alkyl groups, such as, for example, N-ethyl-acrylamide, N-tert-butyl- acrylamide, le N-octyl-crylamide, N-di (C1-C4) alkyl- (meth) acrylamide.

Further preferred anionic copolymers are, for example, copolymers of acrylic acid, methacrylic acid or their Ci-C6-alkyl esters, as sold under the INCI declaration Acrylates Copolymers. A suitable commercial product is, for example Aculyn ^® 33 from Rohm & Haas. However, copolymers of acrylic acid, methacrylic acid or their Ci-C6-alkyl esters and the esters of an ethylenically unsaturated acid and an alkoxylated fatty alcohol are also preferred. Suitable ethylenically unsaturated acids are in particular acrylic acid, methacrylic acid and itaconic acid; suitable alkoxylated fatty alcohols are, in particular, steareth-20 or ceteth-20. On the market most preferred polymers are for example Aculyn _® 22 (Acrylates / Steareth-20 Methacrylate Copolymer), Aculyn _® 28 (Acrylates / Beheneth-25 Methacrylate Copolymer), Structure 2001 _® (Acrylates / steareth-20 itaconate copolymer) Structure 3001 _® (Acrylates / Ceteth-20 Itaconate Copolymer), Structure Plus _® (Acrylates / Aminoacrylates C10-30 Alkyl PEG-20 Itaconate Copolymer), Carbopol® 1342, 1382, Ultrez 20, Ultrez 21 (Acrylates / C10-30 Alkyl Acrylate Crosspolymer ), Synthalen W2000® (Acrylates / Palmeth-25 Acrylate Copolymer) or the Soltex OPT (Acrylates / C 12-22 Alkyl methacrylate Copolymer) sold by Rohme and Haas.

Examples of suitable polymers based on vinyl monomers are the homo- and copolymers of N-vinylpyrrolidone, vinylcaprolactam, vinyl (C1-C6-) alkyl pyrrole, vinyl oxazole, vinyl thiazole and vinyl pyrimidine , of vinylimidazole.

The copolymers octylacrylamide / acrylates / butylaminoethyl methacrylate copolymer, such as is sold commercially by NATIONAL STARCH under the trade names AMPHOMER® or LOVOCRYL® 47, or the copolymers of acrylates / octylacrylamides under the trade names DERMACRYL® are also very particularly suitable LT and DERMACRYL® 79 are sold by NATIONAL STARCH.

Examples of suitable polymers based on olefins are the homo- and copolymers of ethylene, propylene, butene, isoprene and butadiene.

In the context of a further embodiment, the block copolymers which comprise at least one block of styrene or the derivatives of styrene can be used as film-forming hydrophobic polymers. These block copolymers can be copolymers which, in addition to a styrene block, contain one or more other blocks, such as, for example, styrene / ethylene, styrene / ethylene / butylene, styrene / butylene, styrene / isoprene, styrene / butadiene. Corresponding polymers are sold commercially by BASF under the trade name “Luvitol HSB”.

Intense and washfast colorations could be obtained if the composition (B) also contained at least one film-forming polymer as sealing reagent (B1) which was selected from the group of homopolymers and copolymers of acrylic acid, homopolymers and copolymers of methacrylic acid, the Homopolymers and copolymers of acrylic acid esters, homopolymers and copolymers of methacrylic acid esters, homopolymers and copolymers of acrylic acid amides, homopolymers and copolymers of methacrylic acid amides, homopolymers and copolymers of vinyl pyrrolidone, homopolymers and copolymers of vinyl alcohol, homopolymers and Copolymers of vinyl acetate, homopolymers and copolymers of ethylene, of Homopolymers and copolymers of propylene, homopolymers and copolymers of styrene, polyurethanes, polyesters and polyamides.

In a further preferred embodiment, a method is characterized in that the composition (B) contains at least one film-forming polymer as sealing reagent (B1) which is selected from the group of homopolymers and copolymers of acrylic acid, homopolymers and copolymers of methacrylic acid, homopolymers and Copolymers of acrylic acid esters, homopolymers and copolymers of methacrylic acid esters, homopolymers and copolymers of acrylic acid amides, homopolymers and copolymers of methacrylic acid amides, homopolymers and copolymers of vinyl pyrrolidone, homopolymers and copolymers of vinyl alcohol, homopolymers and copolymers of Vinyl acetate, homopolymers and copolymers of ethylene, homopolymers and copolymers of propylene, homopolymers and copolymers of styrene, polyurethanes, polyesters and polyamides.

In a further embodiment, it can be preferred to use at least one hydrophilic, film-forming polymer as sealing reagent (B1) in composition (B).

A hydrophilic polymer is understood to mean a polymer that has a solubility in water at 25 ° C. (760 mmHg) of more than 1% by weight, preferably more than 2% by weight.

The water solubility of the film-forming hydrophilic polymer can be determined, for example, in the following way. 1.0 g of the polymer are placed in a beaker. Make up to 100 g with water. A stir bar is added and the mixture is warmed to 25 ° C on a magnetic stirrer while stirring. It is stirred for 60 minutes. The aqueous mixture is then assessed visually. A completely dissolved polymer appears to be homogeneous under a markoscopy. If the polymer-water mixture cannot be assessed visually due to the high turbidity of the mixture, the mixture is filtered. If no undissolved polymer remains on the filter paper, then the solubility of the polymer is more than 1% by weight.

Nonionic, anionic and cationic polymers can be used as film-forming, hydrophilic polymers.

Suitable film-forming, hydrophilic polymers can, for example, from the group of polyvinylpyrrolidone (co) polymers, polyvinyl alcohol (co) polymers, vinyl acetate (co) polymers, carboxyvinyl (co) polymers, acrylic acid (co) polymers, methacrylic acid (co) polymers, natural gums, polysaccharides and / or acrylamide (co) polymers. Furthermore, it is very particularly preferred to use polyvinylpyrrolidone (PVP) and / or a vinylpyrrolidone-containing copolymer as the film-forming hydrophilic polymer.

In a further very particularly preferred embodiment, a composition (B) is characterized in that it contains at least one film-forming, hydrophilic polymer as sealing reagent (B1), which is selected from the group of polyvinylpyrrolidone (PVP) and the copolymers of polyvinylpyrrolidone.

It is also preferred if the composition (B) contains polyvinylpyrrolidone (PVP) as the film-forming, hydrophilic polymer. Surprisingly, the washfastness of the dyeings which could be obtained with compositions (B) containing PVP was also very good.

Particularly suitable polyvinylpyrrolidones are available for example under the name Luviskol K from BASF SE, in particular Luviskol _® "90 or Luviskol _®" 85 from BASF SE.

The polymer PVP K30, which is sold by the Ashland company (ISP, POI Chemical), can also be used as another polyvinylpyrrolidone (PVP) that is explicitly very particularly suitable. PVP K 30 is a polyvinylpyrrolidone which is very soluble in cold water and has the CAS number 9003-39-8. The molecular weight of PVP K 30 is approx. 40,000 g / mol.

Other particularly suitable polyvinylpyrrolidones are the substances known under the trade names LUVITEC K 17, LUVITEC K 30, LUVITEC K 60, LUVITEC K 80, LUVITEC K 85, LUVITEC K 90 and LUVITEC K 115 and available from BASF.

The use of film-forming hydrophilic polymers from the group of copolymers of polyvinylpyrrolidone has also led to particularly good and rubbing-fast color results.

Especially suitable film-forming, hydrophilic polymers Vinylester vinylpyrrolidone copolymers can be mentioned, as they are sold for example under the trademark Luviskol ^® (BASF) in this context. Luviskol ^® VA 64 and Luviskol ^® VA 73, each vinyl pyrrolidone / vinyl acetate copolymers, are particularly preferred nonionic polymers.

Of the vinylpyrrolidone-containing copolymers, a styrene / VP copolymer and / or a vinylpyrrolidone-vinyl acetate copolymer and / or a VP / DMAPA acrylates copolymer and / or a VP / vinyl caprolactam / DMAPA acrylates copolymer in the composition (B. ) used as sealing reagent (B1). Vinylpyrrolidone-vinyl acetate copolymers are sold under the name Luviskol® VA by BASF SE. A VP / vinyl caprolactam / DMAPA acrylates copolymer is sold by Ashland Inc. under the trade name Aquaflex® SF-40, for example. A VP / DMAPA Acrylates copolymer is sold, for example, under the name Styleze CC-10 by Ashland and is a highly preferred vinylpyrrolidone-containing copolymer.

The copolymers obtained by reacting N-vinylpyrrolidone with at least one further monomer from the group consisting of V-vinylformamide, vinyl acetate, ethylene, propylene, acrylamide, vinylcaprolactam, vinylcaprolactone and / or vinyl alcohol can also be mentioned as further suitable copolymers of polyvinylpyrrolidone .

In a further very particularly preferred embodiment, a composition (B) is characterized in that it contains at least one film-forming, hydrophilic polymer as sealing reagent (B1) which is selected from the group consisting of polyvinylpyrrolidone (PVP), vinylpyrrolidone / vinyl acetate copolymers, vinylpyrrolidone / Styrene copolymers, vinyl pyrrolidone / ethylene copolymers, vinyl pyrrolidone / propylene copolymers, vinyl pyrrolidone / vinyl caprolactam copolymers, vinyl pyrrolidone / vinyl formamide copolymers and / or vinyl pyrrolidone / vinyl alcohol copolymers.

Another suitable copolymer of vinylpyrrolidone is the polymer known under the INCI name maltodextrin / VP copolymer.

It was also possible to obtain intensely colored keratin material, in particular hair, with very good rub fastness properties if a nonionic, film-forming, hydrophilic polymer was used as the film-forming, hydrophilic polymer.

In yet another embodiment, it can be preferred if the composition (B) contain at least one nonionic, film-forming, hydrophilic polymer as sealing reagent (B1).

According to the invention, a nonionic polymer is understood to mean a polymer which in a protic solvent - such as, for example, water - does not carry structural units with permanently cationic or anionic groups under standard conditions which have to be compensated by counterions while maintaining electrical neutrality. Cationic groups include, for example, quaternized ammonium groups but not protonated amines. Anionic groups include, for example, carboxyl and sulfonic acid groups. The compositions (B) which contain, as nonionic, film-forming, hydrophilic polymer, are at least one polymer selected from the group consisting of

- polyvinylpyrrolidone,

- Copolymers of N-vinylpyrrolidone and vinyl esters of carboxylic acids with 2 to 18 carbon atoms, in particular of N-vinylpyrrolidone and vinyl acetate,

- copolymers of N-vinylpyrrolidone and N-vinylimidazole and methacrylamide,

- copolymers of N-vinylpyrrolidone and N-vinylimidazole and acrylamide,

- Copolymers of N-vinylpyrrolidone with N, N-Di (C1 to C4) -alkylamino- (C2 to C4) -alkylacrylamide.

If copolymers of N-vinylpyrrolidone and vinyl acetate are used, it is again preferred if the molar ratio of the structural units contained in the monomer N-vinylpyrrolidone to the structural units in the polymer contained in the monomer vinyl acetate is in the range from 20:80 to 80:20, in particular from 30 to 70 to 60 to 40. Suitable copolymers of vinyl pyrrolidone and vinyl acetate are available, for example, under the trademarks Luviskol® VA 37, Luviskol® VA 55, Luviskol® VA 64 and Luviskol® VA 73 from BASF SE.

Another particularly preferred polymer is selected from the polymers with the INCI name VP / Methacrylamide / Vinyl Imidazole Copolymer, which are available, for example, from BASF SE under the trade name Luviset Clear.

Another very particularly preferred nonionic, film-forming, hydrophilic polymer is a copolymer of N-vinylpyrrolidone and N, N-dimethylaminiopropyl methacrylamide, which, for example, with the INCI name VP / DMAPA Acrylates Copolymer z. B. is sold under the trade name Styleze _® CC 10 by the company ISP.

A cationic polymer is the copolymer of N-vinylpyrrolidone, N-vinylcaprolactam, N- (3-dimethylaminopropyl) methacrylamide and 3- (methacryloylamino) propyl-lauryl-dimethylammonium chloride (INCI name: Polyquaternium-69), which is available, for example, under the trade name AquaStyle ^® 300 (28-32% by weight of active substance in an ethanol-water mixture, molecular weight 350,000) is sold by ISP.

Further suitable film-forming, hydrophilic polymers are, for example

Vinylpyrrolidone-vinylimidazolium methochloride copolymers, as offered under the names Luviquat ^® FC 370, FC 550 and the INCI name Polyquaternium-16 as well as FC 905 and HM 552, Vinylpyrrolidone-vinyl caprolactam-acrylate terpolymers, such as those offered by Acrylsäureestern and acrylamides as the third monomer commercially, for example under the name Aqua Flex ^® SF 40th

Polyquaternium-11 is the reaction product of diethyl sulfate with a copolymer of vinyl pyrrolidone and dimethylaminoethyl methacrylate. Suitable commercial products are available, for example, under the names Dehyquart® CC 11 and Luviquat® PQ 11 PN from BASF SE or Gafquat 440, Gafquat 734, Gafquat 755 or Gafquat 755N from Ashland Inc.

Polyquaternium-46 is the reaction product of vinyl caprolactam and vinyl pyrrolidone with methyl vinyl imidazolium methosulfate and is available, for example, under the name Luviquat® Hold from BASF SE. Polyquaternium-46 is preferably used in an amount of 1 to 5% by weight, based on the total weight of the cosmetic composition. It is very particularly preferred that Polyquaternium-46 is used in combination with a cationic guar compound. It is even highly preferred that Polyquaternium-46 is used in combination with a cationic guar compound and Polyquaternium-11.

Acrylic acid polymers, for example, which can be present in uncrosslinked or crosslinked form, can be used as suitable anionic film-forming, hydrophilic polymers. Corresponding products are sold commercially, for example, under the trade names Carbopol 980, 981, 954, 2984 and 5984 by Lubrizol or also under the names Synthalen M and Synthalen K by 3V Sigma (The Sun Chemicals, Inter Harz).

Examples of suitable film-forming, hydrophilic polymers from the group of natural gums are xanthan gum, gellan gum, carob gum.

Examples of suitable film-forming, hydrophilic polymers from the group of the polysaccharides are hydroxyethyl cellulose, hydroxypropyl cellulose, ethyl cellulose and carboxymethyl cellulose.

Suitable film-forming, hydrophilic polymers from the group of acrylamides are, for example, polymers which are produced starting from monomers of (methyl) acrylamido-C1-C4-alkyl-sulfonic acid or the salts thereof. Corresponding polymers can be selected from the polymers of polyacrylamido methanesulfonic acid, polyacrylamidoethanesulfonic acid, polyacrylamidopropanesulfonic acid, poly-2-acrylamido-2-methylpropanesulfonic acid, poly-2-methylacrylamido-2-methylpropanesulfonic acid and / or poly-2-methylacrylamido-n-butanesulfonic acid. Preferred polymers of the poly (meth) arylamido-C1-C4-alkyl-sulfonic acids are crosslinked and at least 90% neutralized. These polymers can be crosslinked or also uncrosslinked.

Crosslinked and completely or partially neutralized polymers of the poly-2-acrylamido-2-methylpropanesulfonic acid type are known under the INCI names "Ammonium Polyacrylamido-2-methylpropanesulphonate" or "Ammonium Polyacryldimethyltauramide".

Another preferred polymer of this type is the crosslinked poly-2-acrylamido-2methyl-propanesulphonic acid polymer sold by Clamant under the trade name Hostacerin AMPS, which is partially neutralized with ammonia.

In a further explicitly very particularly preferred embodiment, a method is characterized in that the composition (B) contains at least one anionic, film-forming polymer as sealing reagent (B1).

In this context, the best results could be obtained when the composition (B) contains at least one film-forming polymer as sealing reagent (B1) which comprises at least one structural unit of the formula (Pl) and at least one structural unit of the formula (P-II)

in which

M for a hydrogen atom or for ammonium (NH4), sodium, potassium, or magnesium

Calcium stands.

When M stands for a hydrogen atom, the structural unit of the formula (P-1) is based on an acrylic acid unit.

When M stands for an ammonium counterion, the structural unit of the formula (P-1) is based on the ammonium salt of acrylic acid.

When M stands for a sodium counterion, the structural unit of the formula (P-1) is based on the sodium salt of acrylic acid.

If M stands for a potassium counterion, the structural unit of the formula (P-1) is based on the potassium salt of acrylic acid.

If M stands for half an equivalent of a magnesium counterion, the structural unit of the formula (PI) is based on the magnesium salt of acrylic acid. If M stands for half an equivalent of a calcium counterion, the structural unit of the formula (PI) is based on the calcium salt of acrylic acid.

The film-forming polymer or polymers are preferably used in certain quantity ranges in the composition (B). In this context, it has proven to be particularly preferred to solve the problem according to the invention if the composition (B) - based in each case on its total weight - has one or more film-forming polymers as sealing reagent (B1) in a total amount of 0.1 to 18.0 % By weight, preferably from 1.0 to 16.0% by weight, more preferably from 5.0 to 14.5% by weight and very particularly preferably from 8.0 to 12.0% by weight .

In a further preferred embodiment, a method is characterized in that the composition (B) - based on its respective total weight - prefers one or more film-forming polymers as sealing reagent (B1) in a total amount of 0.1 to 18.0% by weight from 1.0 to 16.0% by weight, more preferably from 5.0 to 14.5% by weight and very particularly preferably from 8.0 to 12.0% by weight.

In an alternative embodiment, the sealing reagent (B1) contains an alkalizing agent.

The alkalizing agent is particularly preferably selected from the group consisting of ammonia, C2-C6-alkanolamines, basic amino acids, alkali metal hydroxides and alkaline earth metal hydroxides.

In the context of a further particularly preferred embodiment, a method is characterized in that the composition (B) contains at least one alkalizing agent as sealing reagent (B1) which is selected from the group of ammonia, C2-C6 alkanolamines, basic amino acids, alkali metal hydroxides, alkaline earth metal hydroxides, Alkali metal silicates, alkali metal metasilicates, alkaline earth metal silicates,

Alkaline earth metal metasilicates, alkali metal carbonates and alkaline earth metal carbonates.

It has been found that treatment with a composition (B) which contains ammonia has a particularly good effect on improving the wash fastness and the rub fastness of the dyeings obtained in the process.

In the context of a further very particularly preferred embodiment, a method is characterized in that the composition (B) contains ammonia as the sealing reagent (B1). Good results could also be obtained if the composition (B) contained at least one C2-C6-alkanolamine as sealing reagent (B1).

The alkanolamines which can be used in composition (B) can be selected, for example, from the group of primary amines with a C2-C6-alkyl parent structure which carries at least one hydroxyl group. Preferred alkanolamines are selected from the group formed from 2-aminoethan-1-ol (monoethanolamine), 3-aminopropan-1-ol, 4-aminobutan-1-ol, 5-aminopentan-1-ol, 1-aminopropane -2-ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1-aminopentan-3-ol, 1-aminopentan-4-ol, 3-amino-2-methylpropan-1-ol , 1-amino-2-methylpropan-2-ol, 3-aminopropan-1,2-diol, 2-amino-2-methylpropan-1,3-diol.

In a further preferred embodiment, a method according to the invention is characterized in that the composition (B) contains as sealing reagent (B1) at least one alkalizing agent from the group of alkanolamines, which is preferably selected from the group of 2-aminoethan-1-ol (monoethanolamine) , 3-aminopropan-1-ol, 4-aminobutan-1-ol, 5-aminopentan-1-ol, 1-aminopropan-2-ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1 - aminopentan-3-ol, 1-aminopentan-4-ol, 3-amino-2-methylpropan-1-ol, 1-amino-2-methylpropan-2-ol, 3-aminopropan-1, 2-diol and 2 -Amino-2-methylpropane-1,3-diol.

Good results could also be obtained if the composition (B) contained at least one basic amino acid as sealing reagent (B1).

An amino acid in the context of the invention is an organic compound which, in its structure, contains at least one protonatable amino group and at least one —COOH or one —SO3H group. Preferred amino acids are aminocarboxylic acids, in particular a- (alpha) - aminocarboxylic acids and w-aminocarboxylic acids, with a-aminocarboxylic acids being particularly preferred.

According to the invention, basic amino acids are understood to mean those amino acids which have an isoelectric point p1 of greater than 7.0.

Basic α-aminocarboxylic acids contain at least one asymmetric carbon atom. In the context of the present invention, both possible enantiomers can be used equally as specific compounds or mixtures thereof, in particular as racemates. However, it is particularly advantageous to use the naturally preferred isomer form, usually in the L configuration.

The basic amino acids are preferably selected from the group formed from arginine, lysine, ornithine and histidine, particularly preferably from arginine and lysine. In another In a particularly preferred embodiment, the method is therefore characterized in that the sealing reagent (B1) is an alkalizing agent comprising a basic amino acid from the group of arginine, lysine, ornithine and / or histidine.

In a further preferred embodiment, the method is characterized in that the composition (B) contains as sealing reagent (B1) at least one alkalizing agent from the group of basic amino acids, which is preferably selected from the group of arginine, lysine, ornithine and histidine.

Good results could also be obtained when the composition (B) contains at least one alkali metal hydroxide as sealing reagent (B1). Sodium hydroxide and potassium hydroxide, for example, can be mentioned as very suitable alkali metal hydroxides.

Good results could also be obtained when the composition (B) contained an alkalizing agent comprising at least one alkaline earth metal hydroxide as the sealing reagent (B1). Magnesium hydroxide, calcium hydroxide and barium hydroxide can be mentioned as well-suited alkaline earth metal hydroxides.

Good results could also be obtained if the composition (B) contained at least one alkali metal silicate and / or alkali metal metasilicate as sealing reagent (B1). Suitable alkali metal silicates are, for example, sodium silicate and potassium silicate. Suitable alkali metal metasilicates are, for example, sodium metasilicate and potassium metasilicate.

Good results could also be obtained if the composition (B) contained at least one alkali metal carbonate and / or alkaline earth metal carbonate as sealing reagent (B1). Suitable alkali metal carbonates are, for example, sodium carbonate and potassium carbonate. Suitable alkaline earth metal carbonates are, for example, magnesium carbonate and calcium carbonate.

Within the group of the aforementioned sealing reagent (B1) in the form of an alkalizing agent, ammonia, C2-C6-alkanolamines, basic amino acids and alkali metal hydroxides have proven to be particularly well suited.

In the context of a further particularly preferred embodiment, the method is characterized in that the composition (B) comprises at least one alkalizing agent selected from the group of ammonia, C2-C6-alkanolamines, basic amino acids and alkali metal hydroxides as sealing reagent (B1). In a further particularly preferred embodiment, the method is characterized in that the composition (B) contains as sealing reagent (B1) at least one alkalizing agent selected from the group consisting of ammonia, 2-aminoethan-1-ol, 3-aminopropan-1 -ol, 4-aminobutan-1-ol, 5-aminopentan-1-ol, 1-aminopropan-2-ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1-aminopentan-3-ol , 1-aminopentan-4-ol, 3-amino-2-methylpropan-1-ol, 1-amino-2-methylpropan-2-ol, 3-aminopropan-1,2-diol, 2-amino-2-methylpropane -1, 3-diol, arginine, lysine, ornithine, histidine, sodium hydroxide and potassium hydroxide.

The composition (B) contains the alkalizing agent as sealing reagent (B1) in a cosmetic carrier, preferably in an aqueous cosmetic carrier.

In this context, it has been found to be preferred if the composition (B) - based on the total weight of the composition (B) - 5.0 to 99.0% by weight, preferably 15.0 to 97.0% by weight. %, more preferably 25.0 to 97.0% by weight, even more preferably 35.0 to 97.0% by weight and very particularly preferably 45.0 to 97.0% by weight of water.

In a further embodiment, the method is characterized in that the composition (B) - based on the total weight of the composition (B) - 5.0 to 99.0% by weight, preferably 15.0 to 97.0% by weight , more preferably 25.0 to 97.0% by weight, even more preferably 35.0 to 97.0% by weight and very particularly preferably 45.0 to 97.0% by weight of water.

The alkalizing agents contained in the composition (B) exert an influence on the pH of the composition (B). It was found here that certain alkaline pH values in particular have an advantageous effect on the dyeing performance that can be achieved in the process and the fastness properties of the dyeings.

For this reason, it is preferred that the composition (B), comprising an alkalizing agent as sealing reagent (B1), has a pH of from 7.0 to 12.0, preferably from 7.5 to 11.5, more preferably from 8 .0 to 11.0 and very particularly preferably from 8.5 to 9.5.

The pH value can be measured using the usual methods known from the prior art, such as, for example, pH value measurement using glass electrodes using combination electrodes or using pH indicator paper.

In a further very particularly preferred embodiment, the method is characterized in that the composition (B) contains an alkalizing agent as a sealing reagent (B1) contains and a pH of 7.0 to 12.0, preferably from 7.5 to 11.5, more preferably from 8.0 to 11.0 and very particularly preferably from 8.5 to 9.5 owns.

The pH values in the context of the present invention are pH values that were measured at a temperature of 22 ° C.

In yet another alternative embodiment, the sealing reagent (B1) contains an acidifying agent.

The acidifying agent is particularly preferably selected from the group consisting of inorganic acids, organic acids and mixtures thereof.

Good results could be obtained if the composition (B) contains at least one inorganic acid as sealing reagent (B1). Suitable inorganic acids are, for example, phosphoric acid, sulfuric acid and / or hydrochloric acid, sulfuric acid being particularly preferred.

In a further preferred embodiment, the method is characterized in that the composition (B) contains as sealing reagent (B1) at least one acidifying agent from the group of inorganic acids, which is preferably selected from the group consisting of phosphoric acid, sulfuric acid, hydrochloric acid and mixtures thereof.

In a further, even more preferred embodiment, the method is characterized in that the composition (B) contains sulfuric acid as the sealing reagent (B1).

Good results could also be obtained if the composition (B) contains at least one organic acid as sealing reagent (B1). The organic acid is preferably selected from the group consisting of formic acid, acetic acid, propionic acid, butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, glyceric acid, glyoxylic acid, adipic acid, pimelic acid, propic acid, azelaic acid, Crotonic acid, isocrotonic acid, elaidic acid,

Maleic acid, fumaric acid, muconic acid, citraconic acid, mesaconic acid, camphoric acid, benzoic acid, o, m, p-phthalic acid, naphthoic acid, toluoic acid, hydratropic acid, atropic acid, cinnamic acid, isonicotinic acid, nicotinic acid, bicarbamic acid, 4,4'-dicyano-6,6'-6,6'-dicyano binicotinic acid, 8-carbamoyloctanoic acid, 1, 2,4-pentane tricarboxylic acid, 2-pyrrole carboxylic acid, 1, 2, 4,6,7-naphthalene pentaacetic acid, malonaldehyde, 4-hydroxy-phthalamic acid, 1-pyrazole carboxylic acid, gallic acid or propane tricarboxylic acid, glycolic acid, gluconic acid, Lactic acid, maleic acid, ascorbic acid, malic acid, tartaric acid, citric acid and mixtures thereof.

In a further preferred embodiment, the method is characterized in that the composition (B) contains at least one acidifying agent from the group of organic acids as sealing reagent (B1), the organic acid preferably being selected from the group consisting of formic acid, acetic acid, propionic acid, Butyric acid, isobutyric acid, valeric acid, isovaleric acid, pivalic acid, oxalic acid, malonic acid, succinic acid, glutaric acid, glyceric acid, glyoxylic acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, propiolic acid, crotonic acid, isocrotonic acid, elaidic acid,

In a further, even more preferred embodiment, the method is characterized in that the composition (B) contains acetic acid as the sealing reagent (B1).

Likewise suitable acidifying agents include methanesulfonic acid and / or 1-hydroxyethane-1,1-diphosphonic acid.

Within the group of the aforementioned sealing reagents (B1) in the form of an acidifying agent, sulfuric acid and / or acetic acid have proven to be particularly well suited.

In the context of a further particularly preferred embodiment, the method is characterized in that the composition (B) comprises at least one acidifying agent selected from the group of sulfuric acid, acetic acid and mixtures thereof as sealing reagent (B1).

The composition (B) contains the acidifying agent as sealing reagent (B1) in a cosmetic carrier, preferably in an aqueous cosmetic carrier. The acidifying agents contained in the composition (B) exert an influence on the pH of the composition (B). It was found here that acidic pH values also have an advantageous effect on the dyeing performance that can be achieved in the process and the fastness properties of the dyeings.

For this reason, it is preferred that the composition (B) comprising an acidifying agent as sealing reagent (B1) has a pH of 2.0 to 6.5, preferably from 3.0 to 6.0, more preferably from 4 .0 to 6.0 and very particularly preferably from 4.5 to 5.5.

In a further very particularly preferred embodiment, the method is characterized in that the composition (B) contains an acidifying agent as sealing reagent (B1) and has a pH of 2.0 to 6.5, preferably from 3.0 to 6.0 , more preferably from 4.0 to 6.0 and very particularly preferably from 4.5 to 5.5.

Coloring compounds in the composition (Bf

In the event that the composition (B) furthermore comprises one or more film-forming polymers, it can be preferred that the composition (B) also furthermore comprises at least one coloring compound from the group of pigments and substantive dyes.

All coloring compounds from the group of pigments and substantive dyes which are disclosed as being suitable for use in composition (A) can be used as coloring compounds in the composition (B).

Further cosmetic ingredients in the composition (Bf

In addition, the composition (B) can also contain one or more further cosmetic ingredients.

The cosmetic ingredients which can optionally be used in the composition (B) can be all suitable constituents in order to impart further positive properties to the composition. For example, a solvent, a thickening or film-forming polymer, a surface-active compound can be used in the composition (A) from the group of nonionic, cationic, anionic or zwitterionic / amphoteric surfactants, the oxidation dye precursors, the fatty components from the group of C8-C30 fatty alcohols, the hydrocarbon compounds, fatty acid esters, the acids and bases belonging to the group of pH regulators, that of perfumes , preservatives, plant extracts and protein hydrolysates.

The person skilled in the art will select these further substances according to the desired properties of the compositions. With regard to further optional components and the amounts of these components used, express reference is made to the relevant manuals known to the person skilled in the art.

Composition (C)

The composition (C) can be called an aftertreatment agent. The composition (C) can optionally be used in the process and contains at least one care compound (C1).

In the context of this invention, a care compound (C1) is understood to mean a compound which improves the properties of the coloring obtained by using the compositions (A) and (B) on a keratinic material and / or which the colored keratinic material has desired properties , such as easy combability, soft feel and / or shine, imparts. Improved properties of the coloring include, for example, increased durability of the coloring, improved resistance to shampooing and / or increased resistance to abrasion.

The conditioning compound (C1) may comprise an oligomer ester. If neither composition (A) nor composition (B) comprise an oligomer ester, the method necessarily comprises the use of a composition (C) comprising at least one care compound (C1) comprising an oligomer ester.

In a preferred embodiment of the method, composition (C) comprises at least one oligomer ester as a conditioning compound (C1).

Suitable oligomer esters for use in composition (C) include in particular the oligomer esters which have already been described above for use in compositions (A) and (B). Here, too, it has proven to be particularly advantageous for the rubbing fastness if the at least one oligomer ester is an oligomer ester of hydrogenated castor oil and sebacic acid (INCI: Hydrogenated CastorOil / Sebacic Acid Copolymer) with a degree of oligomerization in the range from 2 to 12, preferably about 4, 6 includes. Accordingly, a method is particularly preferred in which composition (C) comprises at least one oligomer ester, the at least one oligomer ester comprising an oligomer ester of hydrogenated castor oil and sebacic acid (INCI: Hydrogenated CastorOil / Sebacic Acid Copolymer) as the care compound (C1).

Another preferred method is characterized in that the composition (C)

- based on the total weight of the composition (C) - 0.1 to 15% by weight, more preferably from 0.1 to 10% by weight and particularly preferably 0.1 to 5% by weight of an oligomer ester of hydrogenated castor oil and sebacic acid (INCI: Hydrogenated CastorOil / Sebacic Acid Copolymer) as a care compound (C1).

In a further embodiment, a method is preferred in which composition (C) contains at least one oligomer ester as a conditioning compound (C1) and furthermore at least one further conditioning compound (C1).

The composition (C) can, in addition or as an alternative to the at least one oligomer ester, in particular at least one compound selected from the group consisting of cationic surfactants, cationic polymers, amphoteric polymers, nonionic polymers, anionic polymers, plant extracts, protein hydrolyzates, fatty alcohols, silicones, waxes, oligopetides , Vitamins, provitamins, vitamin precursors, betaines, bioquinones, purines (derivatives), taurines (derivatives) and ester oils as a nourishing compound (C1).

The choice of these conditioning compounds will be made by the person skilled in the art according to the desired properties of the composition (C). With regard to further optional components and the amounts of these components used, express reference is made to the relevant manuals known to the person skilled in the art.

Use of compositions (A) and (B) and optionally (C)

The method comprises applying both compositions (A) and (B) to the keratinic material. The two compositions (A) and (B) are two different compositions.

As already described above, it is particularly preferred if the composition (A) is applied to the keratin material first, and then the composition (B) is applied to the keratin material. In the context of a further embodiment, a method comprising the following steps is particularly preferred:

(1) applying the first composition (A) to the keratin material,

(2) allowing the composition (A) to act on the keratin material for a period of 1 to 10 minutes, preferably 1 to 5 minutes,

(3) rinsing the composition (A) from the keratin material,

(4) applying the composition (B) to the keratin material,

(5) allowing the composition (B) to act on the keratin material for a period of 1 to 30 minutes, preferably 1 to 5 minutes,

(6) rinsing the composition (B) from the keratin material.

Rinsing out the keratinous material with water in steps (3) and (6) of the method is understood according to the invention to mean that only water is used for the rinsing process, without any further compositions different from the compositions (A) and (B) would be used.

In a step (1), the composition (A) is first applied to the keratin materials, in particular the human hair.

After application, the composition (A) is allowed to act on the keratin materials. In this context, exposure times of 10 seconds to 10 minutes, preferably from 20 seconds to 5 minutes and very particularly preferably from 30 seconds to 2 minutes on the hair have proven to be particularly advantageous.

In a preferred embodiment of the method, the composition (A) can now be rinsed out of the keratin materials before the composition (B) is applied to the hair in the subsequent step.

In step (4) the composition (B) is now applied to the keratin materials. After application, the composition (B) is now allowed to act on the hair.

Even with a short exposure time for compositions (A) and (B), the process allows dyeings to be produced with particularly good intensity and washfastness. Contact times of from 10 seconds to 10 minutes, preferably from 20 seconds to 5 minutes and very particularly preferably from 30 seconds to 3 minutes on the hair have proven to be particularly advantageous.

In step (6) the composition (B) is then rinsed out of the keratin material with water. Following this, the composition (C) can be applied to the keratinic materials in an aftertreatment step. The composition (C) is also allowed to act on the keratinic materials and then rinsed out again with water.

The positive effects achieved by the composition (C) are particularly long-lasting if the composition (C) is used repeatedly - for example in the course of regular hair washing.

In the context of a further embodiment, a method comprising the following steps in the specified order is very particularly preferred

(1) Application of the composition (A) on the keratinic material,

(2) allowing the composition (A) to act for a period of 10 seconds to 10 minutes, preferably 10 seconds to 5 minutes,

(3) if necessary, rinsing the keratinous material with water,

(4) application of the composition (B) on the keratinic material,

(5) allowing the composition (B) to act for a period of 30 seconds to 30 minutes, preferably from 30 seconds to 10 minutes,

(6) rinsing the keratinous material with water,

(7) application of the composition (C) on the keratinic material,

(8) Allowing the composition (C) to act for a period of time from 10 seconds to 15 minutes, preferably from 30 seconds to 10 minutes, and

(9) Rinsing out the keratinic material with water, the sequence of steps (7), (8) and (9) being carried out at least twice.

(1) Application of the composition (A) on the keratinic material,

(3) if necessary, rinsing the keratinous material with water,

(4) application of the composition (B) on the keratinic material,

(6) rinsing the keratinous material with water,

(7) application of the composition (C) on the keratinic material,

(9) rinsing the keratinous material with water,

(10) application of the composition (C) on the keratinic material, (11) allowing the composition (C) to act for a period of from 10 seconds to 15 minutes, preferably from 30 seconds to 10 minutes, and

(12) Rinsing the keratinous material with water.

In the context of this embodiment, the sequence of steps (1) to (9) takes place within a few hours. There can be a period of a few days between performing steps (9) and (10) to (12).

In the context of a further embodiment, particularly preferred is a method comprising the following steps in the specified order:

(1) applying the first composition (A) to the keratin material,

(3) rinsing the composition (A) from the keratin material,

(4) applying the composition (B) to the keratin material,

(5) allowing the composition (B) to act on the keratin material for a period of 30 seconds to 30 minutes, preferably from 30 seconds to 10 minutes,

(6) rinsing the composition (B) out of the keratin material, and furthermore optionally

(7) application of the composition (C) on the keratinic material,

(9) Rinsing out the keratinic material with water, in which the compositions required, in particular for the dyeing process, are made available in the form of a multi-component packaging unit (kit-of-parts).

A second subject of the present invention is a multi-component packaging unit (kit-of-parts) for coloring keratinous material, comprising a first container with a first composition (A) and a second container with a second composition (B), where at least one of the compositions (A) and (B) contains at least one oligomer ester.

Furthermore, the multi-component packaging unit can also comprise further packaging units, each containing a cosmetic composition. These compositions can in particular contain ingredients which are chemically and / or physically incompatible with ingredients of the composition (A) and / or (B). In particular, the composition (A) contains the alkoxysilanes, a class of highly reactive compounds which, when used, can undergo hydrolysis or oligomerization and / or polymerization.

To avoid premature oligomerization or polymerization, it can be of considerable advantage for the user to prepare the ready-to-use composition (A) only shortly before use.

In a preferred embodiment, therefore, a multi-component packaging unit (kit-of-parts) for coloring keratinous material, packaged separately from one another, comprises a first container with a first composition (A '), comprising one or more organic Ci-C6-alkoxysilanes and / or their Condensation products, a second container with a second composition (A ”), comprising at least one coloring compound from the group of pigments and substantive dyes, and a third container with a third composition (B), comprising a sealing reagent (B1), where at least one of the compositions (A '), (A “) and (B) contains at least one oligomer ester.

The composition (A ”) preferably comprises at least one oligomer ester.

In a further preferred embodiment, a multi-component packaging unit (kit-of-parts) for coloring keratinic material, packaged separately from one another, comprises a first container with a first composition (A '), comprising one or more organic Ci-C6-alkoxysilanes and / or their condensation products , a second container with a second composition (A "), comprising at least one coloring compound from the group of pigments and substantive dyes, a third container with a third composition (A" '), comprising water, and a fourth container with a fourth composition (B), comprising a sealing reagent (B1), wherein at least one of the compositions (A '), (A "), (A"') and (B) contains at least one oligomer ester.

The composition (A ”) preferably comprises at least one oligomer ester. If the method for coloring keratinic material also includes the use of a composition (C) comprises a preferred multi-component packaging unit (kit-of-parts) for coloring keratinic material, comprising a first container with a first composition (A) packaged separately from one another second container with a second composition (B) and a third container with a third composition (C), at least one of the compositions (A), (B) and (C) containing at least one oligomer ester.

Another preferred multicomponent packaging unit (kit-of-parts) for coloring keratinic material comprises a first container with a first composition (A '), packaged separately from one another, comprising one or more organic Ci-C6-alkoxysilanes and / or their condensation products , a second container with a second composition (A ”), comprising at least one coloring compound from the group of pigments and substantive dyes, a third container with a third composition (B), comprising a sealing reagent (B1), a fourth container with a fourth composition (C), comprising at least one care compound (C1), at least one of the compositions (A '), (A ”), (B) and (C) containing at least one oligomer ester.

The composition (A ”) or the composition (C) preferably comprises at least one oligomer ester.

In yet another preferred embodiment, a multi-component packaging unit (kit-of-parts) for coloring keratinic material, packaged separately from one another, comprises a first container with a first composition (A '), comprising one or more organic Ci-C6-alkoxysilanes and / or their condensation products, a second container with a second composition (A "), comprising at least one coloring compound from the group of pigments and substantive dyes, a third container with a third composition (A"'), comprising water, a fourth container with a fourth composition (B) comprising a sealing reagent (B1), and a fifth container with a fifth composition (C) comprising at least one caring compound (C1), wherein at least one of the compositions (A '), (A "), (A"'), (B) and (C) contains at least one oligomer ester.

With regard to the further preferred embodiments of the multi-component packaging units, what has been said about the method applies mutatis mutandis.

Claims

1. A method for coloring keratinic material, in particular human hair, in which the keratinic material is used:

- a first composition (A) containing:

(A2) at least one coloring compound from the group of pigments and substantive dyes,

- a second composition (B) containing:

(B1) a sealing reagent, and optional

- a third composition (C) containing:

(C1) at least one care compound (C1), at least one of the compositions (A), (B) and (C) containing at least one oligomer ester.

2. The method according to claim 1, characterized in that the first composition (A) contains one or more organic Ci-C6-alkoxysilanes (A1) of the formula (S-I) and / or (S-II),

RiR ₂ NL-Si (OR ₃ ) a (R4) b (Sl) where

Ri, R ₂ independently of one another represent a hydrogen atom or a Ci-C6-alkyl group,

L stands for a linear or branched, divalent Ci-C ₂ o-alkylene group,

R ₃ , R4 independently of one another represent a Ci-C6-alkyl group, a, represents an integer from 1 to 3, and b represents the integer 3 - a, and

R5, R5 ‘, R5“, R6, R6 ‘and R6“ independently represent a Ci-C6-alkyl group,

A, A ', A ", A"' and A "" independently represent a linear or branched, divalent Ci-C ₂ o-alkylene group,

R7 and Re independently of one another represent a hydrogen atom, a Ci-C6-alkyl group, a hydroxy-Ci-C6-alkyl group, a C ₂ -C6-alkenyl group, an amino-Ci-C6-alkyl group or a grouping of the formula (S. -Ill) stand, - (A "") - Si (R ₆ ") d" (OR ₅ "(S-Ill),

- c, stands for an integer from 1 to 3,

- d stands for the whole number 3 - c,

- c ‘stands for an integer from 1 to 3,

- d ‘stands for the integer 3 - c‘,

- c "stands for an integer from 1 to 3,

- d "stands for the whole number 3 - c" stands,

- e stands for 0 or 1,

- f stands for 0 or 1,

- g stands for 0 or 1,

- h stands for 0 or 1,

3. The method according to any one of claims 1 to 2, characterized in that the first composition (A) contains at least one organic Ci-C6-alkoxysilane (A1) of the formula (S-l), which is selected from the group

- (3-aminopropyl) triethoxysilane

- (3-aminopropyl) trimethoxysilane

- (2-aminoethyl) triethoxysilane

- (2-aminoethyl) trimethoxysilane

- (3-Dimethylaminopropyl) triethoxysilane

- (3-Dimethylaminopropyl) trimethoxysilane

- (2-dimethylaminoethyl) triethoxysilane,

- (2-Dimethylaminoethyl) trimethoxysilane and / or their condensation products.

4. The method according to any one of claims 1 to 3, characterized in that the first composition (A) contains one or more organic Ci-C6-alkoxysilanes (A1) of the formula (S-IV),

R9Si (ORlo) k (Rll) m (S-IV), where

Rg stands for a Ci-Ci2-alkyl group, Rio stands for a Ci-C6-alkyl group, R11 stands for a Ci-C6-alkyl group k stands for an integer from 1 to 3, and m stands for the integer 3-k, and / or their condensation products.

5. The method according to any one of claims 1 to 4, characterized in that the first composition (A) contains at least one organic Ci-C6-alkoxysilane (A1) of the formula (S-IV) which is selected from the group

- methyltrimethoxysilane

- methyltriethoxysilane

- ethyltrimethoxysilane

- ethyltriethoxysilane

- propyltrimethoxysilane

- propyltriethoxysilane

- hexyltrimethoxysilane

- hexyltriethoxysilane

- Octyltrimethoxysilane

- octyltriethoxysilane

- dodecyltrimethoxysilane,

- dodecyltriethoxysilane,

- octadecyltrimethoxysilane,

- octadecyltriethoxysilane,

- their mixtures and / or their condensation products.

6. The method according to any one of claims 1 to 5, characterized in that the first composition (A) contains at least one inorganic pigment (A2), which is preferably selected from the group of colored metal oxides, metal hydroxides, metal oxide hydrates, silicates, metal sulfides, complexes Metal cyanides, metal sulfates, bronze pigments and / or of colored pigments based on mica or mica, which are coated with at least one metal oxide and / or a metal oxychloride.

7. The method according to any one of claims 1 to 6, characterized in that the first composition (A) contains at least one pigment (A2) selected from the group of pigments based on a lamellar substrate platelet, the pigments based on a lenticular substrate platelet , the pigments based on a substrate platelet comprising a vacuum metallized pigment, and the pigments based on a substrate platelet comprising artificial mica. 8. The method according to any one of claims 1 to 7, characterized in that the second composition (B) further contains at least one pigment selected from the group of pigments based on a lamellar substrate platelet, the pigments based on a lenticular substrate platelet, the Pigments based on a substrate platelet, which comprises a vacuum metallized pigment, and the pigments based on a substrate platelet, which comprises artificial mica.

9. The method according to any one of claims 1 to 8, characterized in that the at least one oligomer ester contains at least one oligomer ester of a hydroxylated fatty acid triglyceride and a, preferably saturated, diacid.

10. The method according to any one of claims 1 to 9, characterized in that the at least one oligomer ester comprises at least one oligomer ester with the INCI name Hydrogenated Castor Oil / Sebacic Acid Copolymer.

11. The method according to any one of claims 1 to 10, characterized in that composition (C) comprises at least one oligomer ester with the INCI name Hydrogenated Castor Oil / Sebacic Acid Copolymer as a care compound (C1).

12. The method according to any one of claims 1 to 11, characterized in that the first composition (A) at least one first pigment (A2), which is selected from the group of colored metal oxides, metal hydroxides, metal oxide hydrates, silicates, metal sulfides, complex metal cyanides, Metal sulfates, bronze pigments and / or colored pigments based on mica or mica coated with at least one metal oxide and / or metal oxychloride, and at least one second pigment (A2) selected from the group of pigments based on a lamellar substrate platelet , the pigments based on a lenticular substrate platelet, the pigments based on a substrate platelet comprising a vacuum metallized pigment, and the pigments based on a substrate platelet comprising artificial mica.

13. Multi-component packaging unit (kit-of-parts) for coloring keratinic material, comprising separately packaged a first container with a first composition (A) comprising (A1) one or more organic Ci-C6-alkoxysilanes and / or their Condensation products, and

(A2) at least one coloring compound from the group of the pigments and the substantive dyes a second container with a second composition (B), comprising (B1) a sealing reagent, and optionally a third container with a third composition (C) comprising (C1) a care compound, at least one of the compositions (A), (B) and (C) containing at least one oligomer ester.

14. Multi-component packaging unit (kit-of-parts) for coloring keratinic material, packaged separately from one another, a first container with a first composition (A '), comprising one or more organic Ci-C6-alkoxysilanes and / or their condensation products, a second container with a second composition (A ”), comprising at least one coloring compound from the group of pigments and substantive dyes, a third container with a third composition (B), comprising a sealing reagent; and optionally a fourth container with a fourth composition (C), comprising (C1) a care compound, at least one of the compositions (A ”), (B) and (C) containing at least one oligomer ester.

15. Multi-component packaging unit (kit-of-parts) for coloring keratinic material, packaged separately from one another, a first container with a first composition (A '), comprising one or more organic Ci-C6-alkoxysilanes and / or their condensation products, a second container with a second composition (A "), comprising at least one coloring compound from the group of pigments and substantive dyes, a third container with a third composition (A" '), comprising water, a fourth container with a fourth composition ( B), comprising (B1) a sealing reagent, and optionally a fifth container with a fifth composition (C), comprising (C1) a care compound wherein at least one of the compositions (A "), (A" '), (B) and (C) contains at least one oligomer ester.