EP3226975A1

EP3226975A1 - Oxidizing colorant

Info

Publication number: EP3226975A1
Application number: EP15785145.2A
Authority: EP
Inventors: Torsten LECHNER; Aileen WAGNER
Original assignee: Henkel AG and Co KGaA
Current assignee: Henkel AG and Co KGaA
Priority date: 2014-12-03
Filing date: 2015-10-28
Publication date: 2017-10-11
Also published as: DE102014224804A1; US10251821B2; WO2016087130A1; US20170266086A1

Abstract

The subject matter of the present invention is a composition for the oxidative hair treatment containing - 50 - 96 wt % water, - 0.5 - 20 wt % hydrogen peroxide, at least one linear saturated 1-alkanol with 12 - 30 carbon atoms in a total volume of 2.7 - 6 wt %, at least one polyethylene glycol ether of a linear saturated C12-C22 alkanol with 15 - 20 ethylene oxide units in the molecule in a total volume of 0.3 - 1 wt %, at least one anionic surfactant in a total volume of 0.3 - 1 wt %, at least one cellulose ether in a total volume of 0.1 - 0.5 wt % and at least one oil in a total volume of 0.1 - 0.5 wt %, wherein all indicated volumes relate to the weight of the composition. A composition of this type is highly suitable as an oxidant for powdered color preparations, containing oxidizing coloring intermediates and also pigments, which do not permanently change the color of the fibers, as well as, optionally, containing solid inorganic alkalizing agents, as well as, optionally, ammonium salts, like ammonium chloride and ammonium sulphate, in particular with respect to the application properties of the application mixture, like dispersion stability and dripping characteristics or stay on the hair.

Description

"Oxidation dyes"

The present application relates to compositions which are suitable as oxidizing agents for pulverulent dyeing preparations, wherein the pulverulent dyeing preparations oxidation dye precursors and beyond pigments which do not permanently change the color of the fibers and optionally solid inorganic alkalizing and optionally further ammonium salts, such as Ammonium chloride and ammonium sulfate, and with which the application properties of the application mixture, such as dispersion stability and dripping behavior of the mixture or the whereabouts of the mixture on the hair, improve.

Another object of the present application relates to means for dyeing keratinous fibers, which can be prepared from two separate compositions by mixing the two compositions, wherein one of the two compositions, an oxidative composition according to the first subject of the application and the second composition is a powdery Dyeing preparation which contains at least one oxidation dye precursor and at least one pigment which does not permanently change the color of the fibers. A further subject matter of the present application relates to a kit for an oxidation colorant for the permanent dyeing of keratinic fibers, comprising a powdery dye preparation and an aqueous hydrogen peroxide preparation, wherein the hydrogen peroxide preparation is optimized in such a way that the ready-to-use mixture of powder and hydrogen peroxide preparation is a viscous paste which forms Apply well to the fibers to be dyed and remain there for 10 to 60 minutes during the period of use, without prematurely dripping off the hair in large quantities.

A further subject matter of the present application relates to a process for the oxidative color change of keratinous fiber, wherein the ready-to-use colorant is prepared by mixing the components of the aforementioned kit before use.

For the color change of human hair, the expert knows various methods. In general, for the dyeing of human hair either direct dyes or oxidation dyes are used which are formed by oxidative coupling of one or more developer components with each other or with one or more coupler components. Coupler and developer components are also referred to as oxidation dye precursors. The colors obtained with oxidation colors are usually referred to as permanent or semi-permanent colorations.

As oxidizing agent, these agents usually contain hydrogen peroxide. Since hydrogen peroxide is only insufficiently stable on storage in the alkaline pH range, oxidative colorants usually consist of two components which are mixed together immediately before use. The one component contains hydrogen peroxide in aqueous solution or emulsion, this composition for stabilizing the hydrogen peroxide an acidic pH in the range from 3 to 5.5. The second component contains the dye precursors and one or more alkalizing agents in an amount such that the application mixture of both components has a pH in the range of 8 to 11. In addition, there are also dyeing kits and dyeing methods in which the application mixture of both components has a pH in the range of about 6 to 7.9; However, the staining results of these so-called "acidic" stains often do not reach the quality achieved with alkaline application blends.

Usually, the colorant component is present as an emulsion, gel of about 20 to 85 wt .-%. However, there are also dyeing kits in which the colorant component is in powder form. The advantage of these powders is that the oxidation dye precursors are solid and undissolved and therefore do not have to be stabilized to the same extent as premature oxidation, such as dyeing emulsions or dyeing gels. Also, the production of dyeing powder is less expensive technically and economically cheaper than the production of dyeing emulsions and gels.

Powdered oxidation dye precursors may clump on prolonged storage, which makes it difficult to prepare a homogeneous application mixture of the powder and the aqueous oxidizing agent preparation. Therefore, the dye powders are usually added to a trickle or anti-caking agent, which itself is not water-soluble, such as silica. In addition, there are dyeing sets with dye powders and oxidizing agent preparations in the market, the dye containing powder insoluble pigments, which roughly reproduce the color impression of the obtained permanent hair color. For oxidative hair dyeing, the dye powder is mixed with an aqueous oxidizer formulation, for example in a bottle or shaker, and the resulting cream-form application mixture is applied to the hair to be dyed, where it remains for a residence time of 5 to 60 minutes before being rinsed off becomes. These products may suffer from the disadvantage that the application mixture, which is a dispersion of the insoluble powder constituents in the aqueous oxidizing agent preparation, separates into solid and liquid components before the recommended exposure time, thereby losing viscosity and dripping off the hair.

The object of the present invention was therefore to provide an improved oxidizing agent preparation for oxidative colorants of dye powders and oxidizing agents, with which stable powder dispersions can be produced which have sufficient viscosity throughout the contact time and remain on the hair without dripping off.

It has surprisingly been found that aqueous hydrogen peroxide preparations containing at least one fatty alcohol, one or more certain fatty alcohol ethoxylates, at least one anionic surfactant, at least one cellulose ether, each in selected amount ranges, and small amounts of at least one oil solve the task in a very good manner.

A first subject of the present invention is therefore an oxidation composition for oxidative hair treatment containing

- 50 - 96 wt .-% water,

0.5-20% by weight hydrogen peroxide, at least one linear saturated 1-alkanol having 12-30 carbon atoms in a total amount of 2.7-6 wt.%,

at least one polyethylene glycol ether of a linear saturated C 12 -C 22 -alkanol having 15-30 ethylene oxide units in the molecule in a total amount of 0.3-1% by weight,

at least one anionic surfactant in a total amount of 0.3-1% by weight,

at least one cellulose ether in a total amount of 0, 1 - 0.5 wt .-% and

at least one oil in a total amount of 0.1-0.5% by weight,

all amounts are based on the weight of the oxidation composition.

The oxidation composition according to the invention contains, in each case based on their weight, 50-96% by weight, preferably 70-93% by weight, particularly preferably 80-90% by weight of water.

The oxidation composition of the invention contains, in each case based on their weight, 0.5 to 20 wt .-%, preferably 1 to 12 wt .-%, particularly preferably 3 to 6 wt .-% hydrogen peroxide.

The oxidation composition according to the invention contains, in each case by weight, at least one linear saturated 1-alkanol having 12-30 carbon atoms in a total amount of 2.7-6% by weight, preferably in a total amount of 3-5.5% by weight. %, more preferably in a total amount of 3.5 - 4.5 wt .-%.

Preferably, the at least one linear saturated 1-alkanol having 12-30 carbon atoms selected from myristyl alcohol, cetyl alcohol, stearyl alcohol, arachidyl alcohol, and behenyl and from mixtures of these alkanols, preferably from cetyl alcohol, stearyl alcohol and cetyl alcohol / stearyl alcohol mixtures. Preferred oxidation compositions according to the invention contain, in each case by weight, a cetyl alcohol / stearyl alcohol mixture in a total amount of 2.7-6% by weight, preferably in a total amount of 3-5.5% by weight, more preferably in one Total amount of 3.5 - 4.5 wt .-%.

The oxidation composition according to the invention contains, in each case by weight, at least one polyethylene glycol ether of a linear saturated C 12 -C 22 -alkanol having 15-30 ethylene oxide units in the molecule in a total amount of 0.3-1% by weight, preferably 0.4-0, 8 wt .-%, particularly preferably 0.5 to 0.7 wt .-%.

Preferably, the at least one polyethylene glycol ether is selected from polyethylene glycol ethers of lauryl alcohol, myristyl alcohol and cetyl alcohol, each having 15-30 ethylene oxide units in the molecule, more preferably selected from laureth-23.

Particularly preferred oxidation compositions according to the invention contain, based on their weight, at least one polyethylene glycol ether of lauryl alcohol, myristyl alcohol or cetyl alcohol, each having 15-30 ethylene oxide units in the molecule, in a total amount of 0.3-1% by weight, preferably 0.4. 0.8 wt .-%, particularly preferably 0.5 to 0.7 wt .-%. Extremely preferred oxidation compositions according to the invention contain, in each case based on their weight, Laureth-23 in a total amount of 0.3 to 1 wt .-%, preferably 0.4 to 0.8 wt .-%, particularly preferably 0.5 to 0.7 wt .-%.

The oxidation composition of the invention comprises, in each case based on their weight, at least one anionic surfactant in a total amount of 0.3 to 1 wt .-%, preferably 0.4 to 0.8 wt .-%, particularly preferably 0.5 to 0.7 wt .-%.

The at least one anionic surfactant is preferably selected from the sodium salts of fatty alcohol sulfates, preferably selected from sodium cetyl sulfate, sodium stearyl sulfate and sodium cetyl / stearyl sulfate mixtures.

Particularly preferred oxidation compositions according to the invention comprise, in each case based on their weight, at least one anionic surfactant selected from the sodium salts of fatty alcohol sulfates, preferably selected from sodium cetyl sulfate, sodium stearyl sulfate and sodium cetyl / stearyl sulfate mixtures, in a total amount of 0.3-1 wt. %, preferably 0.4 to 0.8 wt .-%, particularly preferably 0.5 to 0.7 wt .-%.

The oxidation composition according to the invention contains, in each case based on its weight, at least one cellulose ether in a total amount of 0.1-0.5% by weight, preferably 0.2-0.4% by weight, particularly preferably 0.25-0 , 3% by weight.

The at least one cellulose ether is preferably selected from hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, methylhydroxyethylcellulose and mixtures thereof, more preferably selected from hydroxyethylcellulose.

Particularly preferred oxidation compositions according to the invention comprise, in each case based on their weight, at least one cellulose ether selected from hydroxyethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, methylhydroxyethylcellulose and mixtures thereof, more preferably selected from hydroxyethylcellulose, in a total amount of 0.1-0.5% by weight, preferably 0.2-0.4% by weight, more preferably 0.25-0.3% by weight.

The oxidation composition of the invention contains, in each case based on their weight, at least one oil in a total amount of 0, 1 to 0.5 wt .-%, preferably 0.2 to 0.4 wt .-%.

According to the invention preferred oils are selected from natural and synthetic hydrocarbons, particularly preferably of paraffin oils, CI8-C3o-isoparaffins, especially isoeicosane, polyisobutenes and polydecenes, for example, under the designation Emery ^® 3004, 3006, 3010 or under the name Ethylflo ^® from Albemarle or Nexbase ^® 2004G from Nestle are available, further selected from C8-Ci6-isoparaffins, in particular isododecane, isododecane, isotetradecane, and isohexadecane and mixtures thereof, as well as 1, 3-di- (2-ethylhexyl) -cyclohexane (obtainable, for. B. under the trade name Cetiol ^® S from BASF).

Further oils preferred according to the invention are selected from the benzoic acid esters of linear or branched C 8-22 alkanols. Particularly preferred are benzoic C12-C15 alkyl esters, z. B. available as a commercial product Finsolv® TN, isostearyl benzoate, z. B. available as a commercial product Finsolv® SB, ethylhexyl benzoate, z. B. available as a commercial product Finsolv® EB, and benzoic acid octyldocecylester, z. B. available as a commercial product Finsolv® BOD.

Further oils preferred according to the invention are selected from fatty alcohols having 6 to 30 carbon atoms, which are unsaturated or branched and saturated or branched and unsaturated. The branched alcohols are also often referred to as Guerbet alcohols, since they are obtainable by the Guerbet reaction. Preferred alcohol oils are 2-hexyldecanol (Eutanol® G 16), 2-octyldodecanol (Eutanol® G), 2-ethylhexyl alcohol and isostearyl alcohol.

Further preferred oils are selected from mixtures of Guerbet alcohols and Guerbet alcohol esters, e.g. the commercial product Cetiol® PGL (2-hexyldecanol and 2-hexyldecyl laurate).

Further inventively preferred cosmetic oils are selected from the triglycerides (= triple esters of glycerol) of linear or branched, saturated or unsaturated, optionally hydroxylated C8-30 fatty acids. Particularly preferred may be the use of natural oils, e.g. Amaranth seed oil, apricot kernel oil, argan oil, avocado oil, babassu oil, cottonseed oil, borage seed oil, camelina oil, thistle oil, peanut oil, pomegranate seed oil, grapefruit seed oil, hemp oil, hazelnut oil, elderberry seed oil, currant seed oil, jojoba oil, linseed oil, macadamia nut oil, corn oil, almond oil, marula oil, evening primrose oil, olive oil, palm oil, Palm kernel oil, Brazil nut oil, pecan nut oil, peach kernel oil rapeseed oil, castor oil, sea buckthorn pulp oil, sea buckthorn kernel oil, sesame oil, soybean oil, sunflower oil, grapeseed oil, walnut oil, wild rose oil, wheat germ oil, and the liquid portions of coconut oil and the like. But are also synthetic triglyceride oils, in particular Capric / Caprylic triglycerides, z. As the commercial products Myritol® 318, Myritol® 331 (BASF) or Miglyol® 812 (Hüls) with unbranched fatty acid residues and glyceryl triisostearin with branched fatty acid residues.

Further cosmetic oils which are particularly preferred according to the invention are selected from the dicarboxylic acid esters of linear or branched C 2 -C 10 -alkanols, in particular diisopropyl adipate, di-n-butyl adipate, di- (2-ethylhexyl) adipate, dioctyl adipate, diethyl / di-n- butyl / dioctyl sebacate, diisopropyl sebacate, dioctyl malate, dioctyl maleate, dicaprylyl maleate, diisooctyl succinate, di-2-ethylhexyl succinate and di (2-hexyldecyl) succinate.

Further cosmetic oils which are particularly preferred according to the invention are selected from the esters of linear or branched saturated or unsaturated fatty alcohols having 2 to 30 carbon atoms with linear or branched saturated or unsaturated fatty acids having 2 to 30 carbon atoms which may be hydroxylated. These include 2-hexyldecyl stearate (Eutanol ^® G 16 S), 2-hexyldecyl laurate, isodecyl neopentanoate, isononyl isononanoate, 2-ethylhexyl palmitate (Cegesoft ^® C 24) and 2-ethylhexyl stearate (Cetiol ^® 868). Also preferred are isopropyl myristate, isopropyl palmitate, isopropyl stearate, isopropyl isostearate, isopropyl oleate, isooctyl stearate, isononyl stearate, isocetyl stearate, isononyl isononanoate, isotridecyl isononanoate, cetearyl isononanoate, 2-ethylhexyl laurate, 2-ethylhexyl isostearate, 2-ethylhexyl cocoate, 2-octyldodecyl palmitate, butyloctanoic acid 2-butyloctanoate , Diisotridecyl acetate, n-butyl stearate, n-hexyl laurate, n-decyl oleate, oleyl oleate, oleyl erucate, erucyl oleate, erucyl erucate, ethylene glycol dioleate and ethylene glycol dipalmitate. Further inventively preferred cosmetic oils are selected from the addition products of 1 to 5 propylene oxide units of mono- or polyhydric Cs-22 alkanols, such as octanol, decanol, decanediol, lauryl alcohol, myristyl alcohol and stearyl alcohol, eg. B. PPG-2 myristyl ether and PPG-3 myristyl ether (Witconol APM ^®).

Further cosmetic oils preferred according to the invention are selected from the adducts of at least 6 ethylene oxide and / or propylene oxide units with monohydric or polyhydric C 3-22 alkanols, such as glycerol, butanol, butanediol, myristyl alcohol and stearyl alcohol, which may be esterified if desired, z. As PPG-14 butyl ether (Ucon Fluid ^® AP), PPG-9-butyl ether (Breox B25 ^®), PPG-10 butanediol (Macol ^® 57), PPG-15 stearyl ether (Arlamol ^® E), and Glycereth-7 -diisononanoate.

Further cosmetic oils preferred according to the invention are selected from the C 8 -C 22 -fatty alcohol esters of monohydric or polyhydric C 2 -C 7 -hydroxycarboxylic acids, in particular the esters of glycolic acid, lactic acid, malic acid, tartaric acid, citric acid and salicylic acid. Such esters based on linear Cw / is alkanols, eg. B. Ci2-Ci5-alkyl lactate, and of branched in the 2-position C 12/13 alkanols are under the trademark Cosmacol ^® from the company Nordmann, Rassmann GmbH & Co, Hamburg, refer, in particular the commercial products Cosmacol ^® ESI, Cosmacol ^® EMI and Cosmacol ^® ETI.

Further inventively preferred cosmetic oils are selected from the symmetrical, asymmetric or cyclic esters of carbonic acid with C3-22-alkanols, C3-22-alkanediols or C3-22-alkanetriols, eg. B. dicaprylyl carbonate (Cetiol ^® CC) or the esters according to the teaching of DE 19756454 A1, in particular glycerol carbonate.

Other cosmetic oils which may be preferred according to the invention are selected from the esters of dimers of unsaturated C 12-22 fatty acids (dimer fatty acids) with monovalent linear, branched or cyclic C 2 -C 6 alkanols or with polyfunctional linear or branched C 2 -C 6 alkanols.

Other cosmetic oils which are suitable according to the invention are selected from the silicone oils to which z. As dialkyl and alkylaryl, such as cyclopentasiloxane, cyclohexane siloxane, dimethylpolysiloxane and methylphenylpolysiloxane, but also hexamethyldisiloxane, octamethyltrisiloxane and decamethyltetrasiloxane include. Preferred may be volatile silicone oils, which may be cyclic, such as. For example, octamethylcyclotetrasiloxane, decamethylcyclopentasiloxane and dodecamethylcyclohexasiloxane and mixtures thereof, as described for. B. in the commercial products DC 244, 245, 344 and 345 of Dow Corning. Also suitable are volatile linear silicone oils, in particular hexamethyldisiloxane (L2), octamethyltrisiloxane (L3), decamethyltetrasiloxane (L4) and any mixtures of two and three of L2, L3 and / or l_4, preferably mixtures such as those described for. In the commercial products DC 2-1 184, Dow ^Corning® 200 (0.65 cSt) and Dow ^Corning® 200 (1.5 cSt) from Dow Corning. Preferred nonvolatile silicone oils are selected from higher molecular weight linear dimethylpolysiloxanes, commercially available e.g. Dow ^Corning® 190, Dow ^Corning® 200 fluid having kinematic viscosities (25 ° C) in the range of 5 to 100 cSt, preferably 5 to 50 cSt, or even 5 to 10 cSt, and Dimethylpolysiloxane with a kinematic viscosity (25 ° C) of about 350 cSt.

It may be extraordinarily preferred according to the invention to use mixtures of the abovementioned oils.

Preferred oxidation compositions according to the invention are characterized in that the cosmetic oil is selected from natural and synthetic hydrocarbons, more preferably from paraffin oils, Ci8-C3o-isoparaffins, in particular isoeicosane, polyisobutenes and polydecenes, C8-Ci6-isoparaffins, and 1, 3-di- (2-ethylhexyl) -cyclohexane; the benzoic acid esters of linear or branched Cs-22 alkanols; Fatty alcohols having 6 to 30 carbon atoms which are unsaturated or branched and saturated or branched and unsaturated; Triglycerides of linear or branched, saturated or unsaturated, optionally hydroxylated Csso fatty acids, in particular natural oils; the dicarboxylic acid esters of linear or branched C 2 -C 10 alkanols; the esters of linear or branched saturated or unsaturated fatty alcohols having from 2 to 30 carbon atoms with linear or branched saturated or unsaturated fatty acids having from 2 to 30 carbon atoms which may be hydroxylated; the addition products of 1 to 5 propylene oxide units of mono- or polyhydric Cs-22 alkanols; the addition products of at least 6 ethylene oxide and / or propylene oxide units to mono- or polyfunctional 03-22-alkanols; the C8-C22 fatty alcohol esters of monovalent or polyvalent C2-C7 hydroxycarboxylic acids; the symmetric, unsymmetrical or cyclic esters of carbonic acid with C3-22 alkanols, C3-22 alkane diols or C3-22 alkane triols; the esters of dimers of unsaturated C 12 -C 22 -fatty acids (dimer fatty acids) with monovalent linear, branched or cyclic C 2 -C 6 -alkanols or with polyfunctional linear or branched C 2 -C 6 -alkanols; Silicone oils and mixtures of the aforementioned substances.

The oxidation composition according to the invention preferably has a viscosity in the range of 1000-6000 mPas, particularly preferably 1500-3500 mPas, in each case measured at 22 ° C. in the Brookfield viscometer type RV-T with spindle LV-1 or with spindle RV-1 and a speed of 30 revolutions / minute.

To stabilize the oxidizing agent during storage, it is particularly preferred if the oxidation composition according to the invention has an acidic pH, in particular a pH in the range from 2.5 to 5.5, preferably from 3.0 to 5.0. Preferred acidifying agents are edible acids, such as, for example, citric acid, acetic acid, malic acid or tartaric acid, and also dilute mineral acids, in particular phosphoric acid.

To stabilize the oxidizing agent in the oxidation composition according to the invention, it is preferred to use so-called complexing agents. Complexing agents are substances that can complex metal ions. Preferred complexing agents are so-called chelate complexing agents, ie substances which form cyclic compounds with metal ions, a single ligand occupying more than one coordination site on a central atom. The number of bound ligands depends on the coordination number of the central ion. Customary and preferred chelating agents in the context of the present invention are, for example, polyoxycarboxylic acids, polyamines, Ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA) and Hydroxyethandiphosphon- acids or their alkali metal salts. Compounds which are preferred according to the invention are phosphonates, preferably hydroxyalkane or aminoalkane phosphonates and, in particular, 1-hydroxyethane-1, 1-diphosphonate (HEDP) or its di- or tetrasodium salt and / or ethylenediamine tetramethylene phosphonate (EDTMP) or its hexasodium salt and / or diethylene triamine pentamethylenephosphine - phonate (DTPMP) or its hepta- or octasodium salt. Also dipicolinic acid is preferably used according to the invention as a complexing agent. Agents containing a combination of an EDTA salt and HEDP and dipicolinic acid are particularly preferred according to the invention.

Further preferred oxidation compositions according to the invention are composed as follows, all quantities being based on the weight of the oxidation composition:

- 50 - 96 wt .-% water,

0.5-20% by weight hydrogen peroxide,

at least one linear saturated 1-alkanol having 12-30 carbon atoms in a total amount of 2.7-6 wt.%,

at least one anionic surfactant in a total amount of 0.3-1% by weight,

at least one cellulose ether in a total amount of 0, 1 - 0.5 wt .-% and at least one oil in a total amount of 0.1 - 0.5 wt .-%,

from 3 to 5.5% by weight of cetearyl alcohol,

0.3-1% by weight of laureth-23,

0.3-1% by weight of sodium cetearyl sulfate,

0.1 - 0.5 wt .-% hydroxyethyl cellulose are included;

80-96% by weight of water,

0.5-20% by weight hydrogen peroxide,

at least one anionic surfactant in a total amount of 0.3-1% by weight,

wherein 3.5-4.5% by weight of cetearyl alcohol,

0.4 to 0.8% by weight of laureth-23,

0.3-1% by weight of sodium cetyl sulfate,

0.1 - 0.5 wt .-% hydroxyethyl cellulose are included; 80-96% by weight of water,

0.5-20% by weight hydrogen peroxide,

at least one anionic surfactant in a total amount of 0.3-1% by weight,

wherein 3.5-4.5% by weight of cetearyl alcohol,

0.4 to 0.8% by weight of laureth-23,

0.3-1% by weight of sodium stearylsulfate,

0.1 - 0.5 wt .-% hydroxyethyl cellulose are included;

80-96% by weight of water,

0.5-20% by weight hydrogen peroxide,

at least one anionic surfactant in a total amount of 0.3-1% by weight,

wherein 3.5-4.5% by weight of cetearyl alcohol,

0.4 to 0.8% by weight of laureth-23,

0.3-1% by weight of sodium stearylsulfate,

0.1-0.5% by weight of hydroxypropylcellulose,

- 50 - 96 wt .-% water,

0.5-20% by weight hydrogen peroxide,

at least one anionic surfactant in a total amount of 0.3-1% by weight,

from 3 to 5.5% by weight of cetearyl alcohol, 0.3-1% by weight of laureth-23,

0.3-1% by weight of sodium cetearyl sulfate,

0.1 - 0.5 wt .-% hydroxyethyl cellulose are included and

the composition has a pH in the range of 2.5 to 5.5 and a viscosity in the range of 1000-6000 mPas, preferably 1500-3500 mPas.

A further subject of the present application is a kit for the oxidative color change of keratinic fibers, containing two separate compositions, wherein one of the two compositions is an oxidation composition as described above containing

- 50 - 96 wt .-% water,

0.5-20% by weight hydrogen peroxide,

at least one anionic surfactant in a total amount of 0.3-1% by weight,

wherein all quantities are based on the weight of the oxidation composition, and the second composition is a powdery dyeing preparation which contains at least one oxidation dyestuff precursor and at least one pigment which does not permanently change the color of the fibers.

With regard to further preferred embodiments of the kit according to the invention, what has been said regarding the oxidation composition according to the invention applies mutatis mutandis.

A further subject of the present application is a process for the oxidative color change of keratinic fibers, which is characterized by the following process steps:

Providing an oxidation composition containing

- 50 - 96 wt .-% water,

0.5-20% by weight hydrogen peroxide,

at least one anionic surfactant in a total amount of 0.3-1% by weight,

at least one cellulose ether in a total amount of 0, 1 - 0.5 wt .-% and at least one oil in a total amount of 0.1 - 0.5 wt .-%, wherein all amounts are based on the weight of the oxidation composition, and providing a powdery dyeing preparation containing at least one oxidation dye precursor and at least one pigment not permanently changing the color of the fibers, preparing a mixture of the aforementioned oxidation composition and the aforementioned powdery dyeing preparation, preferably in a weight ratio from oxidation composition to powdered dyeing preparation from 6 to 12, more preferably from 8 to 1 1 and most preferably from 9 to 10,

immediately afterwards the ready-to-use agent is distributed on the fibers,

Leaving the agent on the fibers for a period of 1 to 60 minutes, then rinsing the remaining agent from the fibers and possibly drying the hair.

The method according to the invention comprises mixing the liquid oxidation composition with a powdery dyeing preparation which contains at least one oxidation dye precursor and at least one pigment which does not permanently change the color of the fibers. The mixing of the two components is preferably carried out in a resealable container.

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

According to the invention, keratinic or keratin-containing fibers are to be understood as meaning wool, furs, feathers and, in particular, human hair. The dyeing and / or lightening process according to the invention can in principle but also for use on other natural fibers such. As cotton, jute, sisal, linen, silk or modified natural fibers, such as regenerated cellulose, nitro, alkyl or hydroxyalkyl or acetyl cellulose can be used.

A pulverulent dyeing preparation which contains at least one oxidation dye precursor and at least one pigment which does not permanently change the color of the fibers constitutes, in addition to the oxidation composition according to the invention, the second essential part of the kit according to the invention and the process according to the invention.

According to the invention, the term "pulverulent" is to be understood as meaning a solid, free-flowing dosage form of individual particles, in which the individual particles have grain sizes in the range of 0.1 μm to a maximum of 1 mm , Granulating or pelletizing, or be adjusted by the addition of certain excipients in their particle size of the requirements of the means, for example, to allow a better dispersion of the dyeing preparation.

Powdery dyeing formulations which are preferred according to the invention have a bulk density in the range from 300 to 600 g / l (grams / liter), preferably from 400 to 550 g / l, particularly preferably from 450 to 500 g / l. The determination of the bulk density is preferably carried out according to the currently valid DIN standard.

As a first essential ingredient, the powdery dyeing preparation used in the invention contains at least one oxidation dye precursor, preferably from one or more a plurality of developer components and optionally one or more coupler components is selected.

Preferably, at least one oxidation dye precursor is present in a total amount of 0.01-80 wt%, preferably 0.1-60 wt%, more preferably 0.5-45 wt%, most preferably 0.7 - 30 wt .-%, each based on the weight of the powdered dyeing preparation containing.

It may be preferred according to the invention to select as developer component at least one compound from the group formed from p-phenylenediamine, p-toluenediamine, 2- (2-hydroxyethyl) -p-phenylenediamine, 2- (1,2-dihydroxyethyl) - p-phenylenediamine, N, N-bis (2-hydroxy-ethyl) -p-phenylenediamine, N- (4-amino-3-methylphenyl) -N- [3- (1 H -imidazol-1-yl) -propyl ] amine, N, N'-bis (2-hydroxyethyl) -N, N'-bis (4-aminophenyl) -1, 3-diamino-propan-2-ol, bis (2-hydroxy-5- aminophenyl) methane, 1, 3-bis- (2,5-diaminophenoxy) -propan-2-ol, N, N'-bis (4-aminophenyl) -1, 4-diazacycloheptane, 1, 10 Bis- (2,5-diaminophenyl) -1, 4,7,10-tetraoxadecane, p-aminophenol, 4-amino-3-methylphenol, 4-amino-2-aminomethylphenol, 4-amino-2- ( 1, 2-dihydroxyethyl) phenol, 4-amino-2- (diethylaminomethyl) phenol, 4,5-diamino-1- (2-hydroxyethyl) pyrazole, 2,4,5,6-tetraaminopyrimidine, 4-hydroxyphenyl xy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine and their physiologically acceptable salts.

Preferably, at least one developer component is in a total amount of 0.01-80 wt .-%, preferably from 0.1 to 60 wt .-%, particularly preferably from 0.5 to 45 wt .-%, most preferably from 0.7 - 30 wt .-%, each based on the weight of the powdered dyeing preparation containing.

Coupler components do not form a significant color within the framework of the oxidative dyeing alone, but always require the presence of developer components. Therefore, it is preferred according to the invention that at least one coupler component is additionally used when using at least one developer component.

Preferred coupler components according to the invention are selected from 3-aminophenol, 5-amino-2-methylphenol, N-cyclopentyl-3-aminophenol, 3-amino-2-chloro-6-methylphenol, 2-hydroxy-4-amino-nophenoxyethanol, 2 6-Dimethyl-3-aminophenol, 3-trifluoroacetylamino-2-chloro-6-methylphenol, 5-amino-4-chloro-2-methylphenol, 5-amino-4-methoxy-2-methylphenol, 5- (2-hydroxyethyl ) amino-2-methylphenol, 3- (diethylamino) phenol, N-cyclopentyl-3-aminophenol, 1, 3-dihydroxy-5- (methylamino) benzene, 3-ethylamino-4-methylphenol, 2,4-dichloro 3-aminophenol, 2- (2,4-diaminophenoxy) ethanol, 1, 3-bis (2,4-diaminophenoxy) propane, 1-methoxy-2-amino-4- (2-hydroxyethylamino) benzene, 1,3-bis (2,4-diaminophenyl) propane, 2,6-bis (2'-hydroxyethylamino) -1-methylbenzene, 2 - ({3 - [(2-hydroxyethyl) amino] -4 -methoxy-5-methylphenyl} amino) ethanol, 2 - ({3 - [(2-hydroxyethyl) amino] -2-methoxy-5-methylphenyl} amino) ethanol, 2 - ({3 - [(2-hydroxyethyl) amino] -4,5-dimethylphenyl} amino) ethanol, 2- [3-morpholin-4-yl-phenyl) -amino] -ethanol, 3-amino-4- ( 2-methoxyethoxy) -5-methylphenylamine, 1-amino-3-bis- (2-hydroxyethyl) aminobenzene, resorcinol, resorcinol monomethyl ether, 2-methylresorcinol, 5-methylresorcinol, 2,5-dimethylresorcinol, 2-chlororesorcinol, 4- Chlororesorcinol, pyrogallol, 1, 2,4-trihydroxybenzene, 2,6-dihydroxypyridine, 2-amino-3-hydroxypyridine, 2-amino-5-chloro-3-hydroxypyridine, 3 Amino-2-methylamino-6-methoxypyridine, 2,6-dihydroxy-3,4-dimethylpyridine, 2,6-dihydroxy-4-methylpyridine, 2,6-diaminopyridine, 2,3-diamino-6-methoxypyridine, 3, 5-diamino-2,6-dimethoxypyridine, 2,6-dihydroxy-3,4-dimethylpyridine, 3,4-diaminopyridine, 2- (2-methoxyethyl) amino-3-amino-6-methoxypyridine, 2- 4'-methoxyphenyl) amino-3-aminopyridine, 1-naphthol, 2-methyl-1-naphthol, 2-hydroxymethyl-1-naphthol, 2-hydroxyethyl-1-naphthol, 1, 3-dihydroxynaphthalene, 1, 5-dihydroxy - naphthalene, 1, 6-dihydroxynaphthalene, 1, 7-dihydroxynaphthalene, 1, 8-dihydroxynaphthalene, 2,7-dihydroxynaphthalene, 2,3-dihydroxynaphthalene, 4-hydroxyindole, 6-hydroxyindole, 7-hydroxyindole, 4-hydroxyindoline , 6-hydroxyindoline, 7-hydroxyindoline, 4,6-diaminopyrimidine, 4-amino-2,6-dihydroxy-pyrimidine, 2,4-diamino-6-hydroxypyrimidine, 2,4,6-trihydroxypyrimidine, 2-amino-4 -methylpyrimidine, 2-amino-4-hydroxy-6-methylpyrimidine and 4,6-dihydroxy-2-methylpyrimidine or mixtures of these compounds or their physiologically tolerated salts.

Preferably, at least one coupler component in a total amount of 0.01- 60 wt .-%, preferably from 0.1 to 40 wt .-%, particularly preferably from 0.5 to 30 wt .-%, most preferably from 0.7 - 25 wt .-%, each based on the weight of the powdered dyeing preparation containing.

In this case, developer components and coupler components are generally used in approximately equimolar amounts relative to one another. Although the equimolar use has proven to be expedient, a certain excess of individual oxidation dye precursors is not detrimental, so that developer components and coupler components in a molar ratio of 1: 0.5 to 1: 3, in particular 1: 1 to 1: 2 , may be included.

Kits preferred according to the invention for the oxidative color change of keratinic fibers are characterized in that the above-mentioned preferred or inventive preferred oxidation composition and powdered dye preparation in a weight ratio of oxidation composition to powdered dyeing preparation of 6 to 12, more preferably from 8 to 1 1 and exceptionally preferred from 9 to 10, are included.

Kits according to the invention for the oxidative color change of keratinic fibers are characterized in that the above-mentioned inventive or inventively preferred oxidation composition and the aforementioned pulverulent dyeing preparation in a weight ratio of oxidation composition to powdered dyeing preparation from 6 to 12, particularly preferably from 8 to 1 1 and most preferably from 9 to 10, wherein the kit does not contain other components which are added to the ready-to-use coloring mixture while components for pre- or post-treatment of the keratinic fibers, for example conditioners or shampoos, may be included in the kit. Further preferred kits according to the invention for the oxidative color change of keratinic fibers are characterized in that they are prepared from an abovementioned inventive or inventively preferred oxidation composition and an abovementioned pulverulent dyeing composition. preparation in a weight ratio of oxidation composition to pulverulent coloring preparation of 6 to 12, more preferably from 8 to 1 1 and most preferably from 9 to 10 consist.

Preferred processes for the oxidative color change of keratinic fibers according to the invention are characterized in that the above-mentioned pulverulent dyeing preparation in the weight ratio of oxidation composition to powdered dyeing preparation of 6 to 12, more preferably from 8 to 1 1 and exceptionally preferably from 9 to 10, mixed together become.

Preferably, at least one developer component is present in a total amount of 0.001-15% by weight, preferably 0.01-10% by weight, more preferably 0.1-8% by weight, most preferably 0.5-4 Wt .-%, each based on the weight of the mixture of powdered dyeing preparation and inventive oxidation composition.

Also preferred is at least one coupler component in a total amount of 0.001-15 wt .-%, preferably from 0.01 to 10 wt .-%, particularly preferably from 0, 1-8 wt .-%, most preferably from 0.5 4 wt .-%, each based on the weight of the mixture of powdered dyeing preparation and inventive oxidation composition.

Also preferred is at least one oxidation dye precursor in a total amount of 0.002 to 30 wt .-%, preferably from 0.02 to 20 wt .-%, particularly preferably from 0.2 to 16 wt .-%, most preferably from 1, 0 - 8 wt .-%, each based on the weight of the mixture of powdered dyeing preparation and inventive oxidation composition.

As a second essential ingredient, the pulverulent dyeing preparation used according to the invention contains at least one pigment which does not change the color of the fibers permanently and not semi-permanently. For the purposes of the present applications, this means that the coloring of the hair fibers during the process according to the invention is not caused by the pigments in the powdered dyeing composition and that any color impression of the keratin fibers caused by the pigments is not fast to washing and after a single rinsing of the hair For example, when rinsing at the end of the process according to the invention, lost again, that is not permanent and not semi-permanent. In contrast, permanent staining is an oxidative staining of the keratin fibers in which the oxidation dye precursors penetrate the hair and in the fiber react with the oxidant to form oligomeric dye molecules that remain in the fiber due to their size and high fastness Rinsing and washing operations, mechanical abrasion and light have. Semi-permanent within the meaning of the present application are dyeings with so-called substantive dyes; These include cationic direct dyes, anionic direct dyes and nouns direct dyes. The coloring of the keratinic fibers by the oxidation dye precursors contained in the dyeing preparation is neither influenced nor impaired by the pigments which do not permanently color.

The non-permanent or semi-permanent coloring pigments have essentially the task of increasing the optical attractiveness of the powdered dyeing preparation for the user. Another essential task of the non-permanent or semi-permanent coloring pigments is to give the powdered dyeing preparation in about the color obtained by the inventive method and with the kit according to the invention on the keratinic fiber.

Suitable pigments for the process according to the invention can be selected from all keratinic fibers suitable for cosmetic use that are not permanently or semi-permanently coloring pigments. Preferred are so-called effect and / or pearlescent pigments, which may be of organic and / or inorganic origin.

Due to their excellent light, weather and / or temperature resistance, the use of inorganic pigments is particularly preferred in the process according to the invention.

The preferred volume-average particle size of the - preferably inorganic - pigments is 0.1 μιη - 1 mm, more preferably from 0.5 μιη - 120 μιη and extraordinarily 10 μιη - 80 μιη. Preferred non-permanent or semi-permanent coloring pigments are selected from inorganic pigments which may be of natural origin. Inorganic color pigments of natural origin can be prepared, for example, from chalk, ocher, umber, green earth, baked Terra di Siena or graphite.

Furthermore, as inorganic color pigments white pigments such. As titanium dioxide or zinc oxide, black pigments, such as. B. iron oxide black, colored pigments, such as. As ultramarine or iron oxide red, and fluorescent or Phosphoreszenzpigmente be used, preferably at least one pigment is a colored, non-white pigment. Particularly suitable are metal oxides, hydroxides and oxide hydrates, mixed phase pigments, sulfur-containing silicates, metal sulfides, complex metal cyanides, metal sulfates, chromates and / or molybdate. Particularly preferred color pigments are titanium dioxide (Cl 77891), black iron oxide (Cl 77499), yellow iron oxide (Cl 77492), red and brown iron oxide (Cl 77491), manganese violet (Cl 77742), ultramarines (sodium aluminum sulfosilicates, Cl 77007, Pigment Blue 29), chromium oxide hydrate (CI77289), iron blue (Ferric Ferrocyanide, CI77510) and / or Carmine (Cochineal).

Suitable effect pigments are preferably understood as meaning metallic effect pigments, such as, for example, bronze pigments.

Further inventively preferred non-permanent or semi-permanent coloring pigments are the so-called pearlescent pigments. These usually consist of mica flakes (mica) which are coated with one or more metal oxides or metal oxychlorides, such as bismuth oxychloride, this layer (s) being optionally doped with further metal salts or metal oxides. Natural mica-based and natural mica / metal oxide-based pearlescent pigments are preferred according to the invention. Mica belongs to the layer 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, mica particles, predominantly muscovite or phlogopite, are coated with at least one metal oxide.

As an alternative to natural mica, it is also possible to use synthetic mica coated with one or more metal oxide (s) as pearlescent pigment. Such suitable pearlescent pigments based on synthetic mica are described in the publication WO 2005/065632, to which reference is expressly made.

Particularly preferred pearlescent pigments are based on natural or synthetic mica (mica) and are coated with one or more metal oxides.

The color of the respective pigments can be varied by varying the layer thickness of the metal oxide (s). Examples of particularly suitable pearlescent pigments commercially, for example under the trade names Rona ^®, Colorona® ^®, Dichrona® ^® and Timiron ^® from Merck, ariable ^® by the company Sensient, Prestige ^® by the company Eckart Cosmetic Colors and Sunshine ^® from Sunstar available.

In a preferred embodiment, the pulverulent dyeing composition contains as non (semi-) permanent coloring pigment at least one inorganic dyeing, effect and / or pearlescent pigment, which is preferably selected from metal oxides, metal hydroxides, metal oxide hydrates, sulfur-containing silicates, metal sulfides, complex metal cyanides, metal sulfates , Bronze pigments and / or pigments based on mica, which are coated with at least one metal oxide and / or a metal oxychloride.

In a particularly preferred embodiment, the pulverulent dyeing composition contains as non (semi-) permanently coloring pigment at least one inorganic dye and / or pearlescent pigment selected from titanium dioxide (Cl 77891), black iron oxide (Cl 77499), yellow iron oxide (Cl 77492), red and / or brown iron oxide (Cl 77491), manganese violet (Cl 77742), ultramarines (sodium aiuminiumsulfosilicates, Cl 77007, Pigment Blue 29), chromium oxide hydrate (Cl 77289), iron blue (Ferric Ferrocyanide, Cl 77510) and / or from mica pigments coated with one or more metal oxides.

Particular preference is given to pulverulent dyeing formulations which contain one or more mica pigments which are reacted with titanium dioxide (Cl 77891), black iron oxide (Cl 77499), red and / or brown iron oxide (Cl 77491) and / or ultramarines (sodium aiuminiumsulfosilicates, Cl 77007, Pigment Blue 29) are coated.

In a preferred embodiment of the process according to the invention or of the kit according to the invention, the pulverulent dyeing preparation, based on the weight of the powdery dyeing preparation, contains at least one pigment which does not change the color of the fibers permanently or semi-permanently in a total amount of 1-40% by weight .-%, preferably 3 to 30 wt .-%, particularly preferably 5 to 25 wt .-% and in particular 7.5 to 20 wt .-%.

In a further particularly preferred embodiment of the process according to the invention or the kit according to the invention, the pulverulent dyeing preparation contains, in each case based on the Weight of the powdered dye preparation:

at least one oxidation dye precursor in a total amount of 0.01-80 wt .-%, preferably from 0, 1-60 wt .-%, particularly preferably from 0.5 to 45 wt .-%, most preferably from 0.7 to 30 Wt .-%, and

at least one pigment which does not change the color of the fibers permanently or semi-permanently in a total amount of 1 to 40% by weight, preferably 3 to 30% by weight, more preferably 5 to 25% by weight and in particular 7.5 to 20% by weight.

In a further particularly preferred embodiment of the process according to the invention or of the kit according to the invention, the pulverulent dyeing preparation contains, in each case based on the weight of the pulverulent dyeing preparation:

at least one developer component in a total amount of 0.01-80 wt .-%, preferably from 0, 1-60 wt .-%, particularly preferably from 0.5 to 45 wt .-%, most preferably from 0.7

- 30 wt .-%, and

at least one coupler component in a total amount of 0.01-60 wt .-%, preferably from 0.1 to 40 wt .-%, particularly preferably from 0.5 to 30 wt .-%, most preferably from 0.7 to 25 Wt .-%, and

In a further preferred embodiment of the process according to the invention or the kit according to the invention, the pulverulent dyeing preparation contains at least one solid inorganic alkalizing agent. These are to be understood as meaning, according to the invention, in particular in an aqueous medium, alkaline salts or silicates. Solid inorganic alkalizing agents useful in the present invention are preferably selected from the group consisting of sodium hydroxide, potassium hydroxide, calcium hydroxide, magnesium hydroxide, magnesium carbonate hydroxide, barium hydroxide, sodium phosphate, potassium phosphate, sodium silicate, sodium metasilicate, potassium silicate, potassium metasilicate, ammonium carbonate, sodium carbonate, potassium carbonate and magnesium carbonate , as well as mixtures of these alkalizing agents. Particularly preferred alkalizing agents are sodium silicate, sodium metasilicate and magnesium carbonate hydroxide, as well as Mixtures thereof, exceptionally preferred are mixtures of sodium metasilicate and magnesium carbonyl hydroxide. The at least solid inorganic alkalizing agent is preferably in a total amount of 10 - 60 wt .-%, particularly preferably 20 - 50 wt .-%, most preferably 25 - 40 wt .-%, each based on the weight of the powdered dyeing preparation. Since the inventive and inventively preferred oxidation compositions, the dyeing process according to the invention and the kits of the invention to a mixture of oxidation composition and powdered dyeing preparation in a weight ratio of oxidation composition to powdered dyeing preparation of 6 to 12, more preferably from 8 to 1 1 and exceptionally from 9 to 10 are optimized, the total amount of solid inorganic alkalizing agent must be selected so that the mixture, ie the ready-to-use colorant, an alkaline pH, preferably a pH of 8 to 1 1, 5, more preferably a pH of 8.5 to 11, most preferably has a pH of 9.0 to 10.5.

To reduce the formation of dust and to improve the flowability of the powdery dyeing preparation, it may be advantageous to add an oil component to the dyeing preparation. In principle, all cosmetic oils are suitable for this purpose, which have already been mentioned as being suitable for the oxidation compositions according to the invention and preferred according to the invention. Paraffin oil, hydrogenated homopolymers of 1-decene having a degree of polymerization n of 3 to 9 (with the INCI name Polydecene) and ester oils, such as isopropyl myristate, isononyl isononanoate and 2-ethylhexyl stearate, have proven to be particularly suitable for the addition to the pulverulent dyeing preparation.

A further embodiment of the first subject of the invention is therefore characterized in that the dyeing preparation additionally contains at least one oil, which is preferably selected from paraffin oil, hydrogenated homopolymers of 1-decene with a degree of polymerization n of 3 to 9 and ester oils and mixtures thereof.

Particularly preferred is at least one oil, which is preferably selected from paraffin oil, hydrogenated homopolymers of 1-decene having a degree of polymerization n of 3 to 9 and ester oils, in a total amount of 0.01 to 5 wt .-%, in particular of 0.05 to 3 wt .-% and especially from 0.08 to 2.0 wt .-%, each based on the weight of the powdered dyeing preparation.

Extraordinary preference is given to paraffin oil in an amount of from 0.01 to 5% by weight, in particular from 0.05 to 3% by weight and in particular from 0.08 to 1.0% by weight, based in each case on the weight of powdery dye preparation.

In a further preferred embodiment of the method or the kit of the invention, the pulverulent dyeing preparation contains at least one ammonium compound selected from ammonium chloride, ammonium carbonate, ammonium bicarbonate, ammonium sulfate and / or ammonium carbamate and mixtures of these compounds, preferably ammonium chloride, in a total amount of 1 to 50 wt. -%, more preferably from 5 to 40 Wt .-% and in particular from 15 to 35 wt .-%, each based on the weight of the powdered dyeing preparation.

Further embodiments of the oxidation composition, the kit and the dyeing method according to the invention are characterized in that neither the oxidation composition nor the pulverulent dyeing preparation contains a polymer which is substituted by at least two C 8 -C 30 -alkyl groups. Such polymers, which are preferably associative thickeners, have proved in certain cases unfavorable for the dripping properties of the ready-to-use colorant.

With regard to further preferred embodiments of the kit according to the invention, mutatis mutandis, the statements concerning the inventive and inventively preferred oxidation compositions as well as the comments made on the pulverulent dyeing formulations used according to the invention apply.

With regard to further preferred embodiments of the process according to the invention, mutatis mutandis, the statements concerning the inventive and inventively preferred oxidation compositions and the statements made with respect to the pulverulent dyeing formulations used according to the invention apply.

The ready-for-use colorant of the method according to the invention is preferably prepared by combining the inventive or preferred oxidation composition according to the invention with a powdery dyeing preparation used in a resealable container and subsequent mixing.

In the subsequent process step, the ready-to-use colorant is distributed on the keratinic fibers. In the process of dyeing human hair, the ready-to-use agent is distributed directly on the hair of the user. Preferably, the distribution is done manually. For this purpose, the user removes the ready-to-use agent the mixing container, preferably the resealable container, by ladling or pouring on the hand and subsequent distribution and preferably incorporation of the agent on the head hair. Preference is given to the direct contact between ready colorant and the hands by the use of suitable gloves, such as disposable gloves, for example made of latex avoided.

Subsequently, the ready-to-use colorant remains on the fibers to be treated for a period of 1 to 60 minutes. Preferably, the period is in the range of 10 to 45 minutes, more preferably 20 to 30 minutes.

The application temperatures can range between 15 and 40 ° C. Optionally, a higher or more precisely defined temperature can also be set by external heat sources during the retention time of the agent on the fibers. It is particularly preferable to support the color change by physical measures. Methods according to the invention in which the application is assisted by the action of heat, IR and / or UV radiation during the exposure time may be preferred. After the end of the exposure time, the ready-to-use colorant or the remaining colorant is removed in the last process step by rinsing off the fibers to be treated. For this purpose, the fibers are rinsed with water and / or an aqueous surfactant preparation. Usually for this purpose 20 ° C to 40 ° C warm water or an appropriately tempered aqueous surfactant preparation is used. Optionally, this may be followed by further treatment steps, such as the application of a leave-on or rinse-off conditioner, another dyeing step, for example, the coloring or lightening of highlights, a hair deformation and / or the drying of the hair.

Examples

The following preparations were prepared. Table 1 contains examples of powdered dyeing formulations; Table 2 contains an example of an oxidation composition according to the invention. Unless stated otherwise, the amounts given are in% by weight, in each case based on the weight of the individual composition.

1) Powdery Dye Preparations (Table 1)

Commodities I II III IV V VI

Sodium metasilicate FE

22,73 22,73 22,73 22,73 22,73 22,73 anhydrous

Magnesium carbonate hydroxide 9, 15 9,15 13,77 9,10 9,10 1 1, 40

Perfume 0.60 0.60 0.60 0.60 0.60 0.60

Paraffin Liquidum 1, 65 1, 65 1, 65 1, 65 1, 65 1, 65 p-toluenediamine Sulfate 17.60 14.3 1, 50 4.79 3.56 1, 97

Resorcinol 5.73 4.91 1, 25 1, 57 0.99 0.22

3-aminophenol 2.40 1, 85 0.65 0.37 0.30 0.06

2,4-Diaminophenoxyethanol

1, 53 0.76 2.40

2HCl

4,5-diamino-1- (2-

5.10

hydroxyethyl) pyrazole sulfate

2-methylresorcinol 0.20 0.17 0.18

2-Amino-3-hydroxypyride in 0.34

2,7-Dihydroxynaphthalene 0.27

4-chlororesorcinol 0.43 0.48

Ariabel ^® Blue 4.50

Prestige ^® Fire Red 4.50

Colorona® ^® Blackstar Gold 13.60 1 1 40 1 1 40

Colorona® ^® Mica Black 13.60 Colorona® ^® Precious Gold 9.10

Timiron ^® Diamond MP 149 4,50 4,50 4,50 4,50 4,50 4,50

Ammonium chloride ad 100

Color of powdered dark red black brown brown gold dyeing brown violet

2) Oxidation Composition According to the Invention (Table 2)

3) List of raw materials used

Ariable ^® Blue (INCI name: Cl 77007 (ultramarine S) Silicic acid aluminum sodium salt, sulfurized, Pigment Blue 29), Sensient; Prestige ^® Fire Red (INCI name: Mica, CI 77491 (Iron Oxides)), Eckart Cosmetic Colors; Colorona ^® Black Star Gold (INCI name: Mica, Cl 77499 (Iron Oxides), Merck; Colorona ^® Mica Black (INCI name: Cl 77499 (Iron Oxides) Mica, Cl 77891 (Titanium oxides)), Merck; Colorona ^® Precious gold (INCI name: Mica, Cl 77891 (Titanium oxides), silica, Cl 77499 (Iron Oxides), SnO), Merck; Timiron ^® Diamond MP 149 (INCI name: Mica, Cl 77891 (Titanium oxides)), Merck ,

4) colorations

1 1 g of the powdered color change preparation I or 1 1 g of the powdered color change preparation VI were each mixed with 100 g of the oxidation composition of the invention in a resealable mixing container by vigorous, continuous shaking (40 times) with each other.

The ready-to-use product from preparation I was dyed black, while the ready-to-use product from preparation VI was dyed golden. The products were each from the Taken with the hollow hand and evenly distributed on two identical strands of hair (alkino).

The respective ready-to-use agent remained on the hair strands for a period of 30 min at room temperature (20 ° C.).

The remaining agents were then each rinsed with lukewarm water (25 ° C) from the hair strands for about 2 minutes, and the strands were dried with a towel. Uniform, durable and glossy colors of high color intensity and color were obtained. The hair tress dyed from Preparation I had a black color. The strand of hair dyed from preparation VI had a golden blonde color.

Claims

claims

An oxidation composition for oxidative hair treatment containing

- 50 - 96 wt .-% water,

0.5 to 20% by weight of hydrogen peroxide,

at least one polyethylene glycol ether of a linear saturated C 12 -C 22 -alkanol having 15-30 ethylene oxide units in the molecule in a total amount of 0.3-1% by weight, at least one anionic surfactant in a total amount of 0.3-1% by weight,

at least one cellulose ether in a total amount of 0, 1 - 0.5 wt .-% and at least one oil in a total amount of 0, 1 - 0.5 wt .-%,

all amounts are based on the weight of the oxidation composition.

2. Composition according to claim 1, characterized in that the at least one linear saturated 1-alkanol having 12-30 carbon atoms is selected from myristyl alcohol, cetyl alcohol, stearyl alcohol, arachidyl alcohol, and behenyl alcohol and mixtures of these alkanols, preferably from cetyl alcohol, stearyl alcohol and cetyl alcohol / Stearyl alcohol mixtures.

3. The composition according to any one of claims 1 or 2, characterized in that the at least one polyethylene glycol ether is selected from polyethylene glycol ethers of lauryl alcohol, myristyl alcohol and cetyl alcohol, each having 15 - 30 ethylene oxide units in the molecule.

4. The composition according to any one of claims 1 to 3, characterized in that the at least one polyethylene glycol ether is selected from laureth-23rd

5. Composition according to one of claims 1 to 4, characterized in that the at least one anionic surfactant is selected from the sodium salts of fatty alcohol sulfates, preferably selected from sodium cetyl sulfate, sodium stearyl sulfate and sodium cetyl / stearyl sulfate mixtures.

6. A composition according to any one of claims 1 to 5, characterized in that the at least one cellulose ether is selected from hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropylmethyl cellulose, methyl hydroxyethyl cellulose and mixtures thereof, preferably selected from hydroxyethyl cellulose.

7. A composition according to any one of claims 1 to 6, characterized in that the at least one oil is selected from selected from natural and synthetic hydrocarbons, more preferably from paraffin oils, Ci8-C3o-isoparaffins, in particular isoeicosane, polyisobutenes and polydecenes, C8- Ci6 isoparaffins, as well as 1, 3-di (2-ethylhexyl) cyclohexane; the benzoic acid esters of linear or branched Cs-22 alkanols; Fatty alcohols having 6 to 30 carbon atoms which are unsaturated or branched and saturated or branched and unsaturated; Triglycerides of linear or branched, saturated or unsaturated, optionally hydroxylated Csso fatty acids, in particular natural oils; the dicarboxylic acid esters of linear or branched C 2 -C 10 -alkanols; the esters of linear or branched saturated or unsaturated fatty alcohols having from 2 to 30 carbon atoms with linear or branched saturated or unsaturated fatty acids having from 2 to 30 carbon atoms which may be hydroxylated; the addition products of 1 to 5 propylene oxide units of mono- or polyhydric Cs-22 alkanols; the addition products of at least 6 ethylene oxide and / or propylene oxide units of mono- or polyhydric C3-22 alkanols; the C8-C22 fatty alcohol esters of monovalent or polyvalent C2-C7 hydroxycarboxylic acids; the symmetric, unsymmetrical or cyclic esters of carbonic acid with C3-22 alkanols, C3-22 alkane diols or C3-22 alkane triols; the esters of dimers of unsaturated C 12 -C 22 fatty acids (dimer fatty acids) with monovalent linear, branched or cyclic C 2 -C 6 alkanols or with polyvalent linear or branched C 2 -C 6 alkanols; Silicone oils and mixtures of the aforementioned substances.

8. Kit for oxidative color change keratinischer fibers, containing two separate compositions, wherein

one of the two compositions is an oxidation composition according to any one of claims 1-7 and

the second composition is a powdered dyeing composition containing at least one oxidation dye precursor and at least one pigment that does not permanently or semi-permanently alter the color of the fibers.

9. Kit for the oxidative color change of keratinic fibers according to claim 8, characterized in that the powdery dyeing preparation further contains at least one solid inorganic alkalizing agent, which is preferably selected from the group consisting of sodium hydroxide, potassium hydroxide, calcium hydroxide, magnesium hydroxide, magnesium carbonate hydroxide, barium hydroxide , Sodium phosphate, potassium phosphate, sodium silicate, sodium metasilicate, potassium silicate, potassium metasilicate, ammonium carbonate, sodium carbonate, potassium carbonate and magnesium carbonate, and mixtures of these alkalizing agents, more preferably selected from sodium silicate, sodium metasilicate and magnesium carbonate hydroxide and mixtures thereof, most preferably selected from mixtures of sodium metasilicate and magnesium carbonate hydroxide, in one Total amount of 10 - 60 wt .-%, particularly preferably 20 - 50 wt .-%, most preferably 25 - 40 wt .-%, each based on the weight of the powdered dyeing composition contains.

10. Kit for the oxidative color change of keratinic fibers according to any one of claims 8 or 9, characterized in that neither the oxidation composition nor the powdered dyeing preparation contain a polymer which is substituted with at least two C8 - C30 alkyl groups.

1 kit for the oxidative color change of keratinic fibers according to any one of claims 8 to 10, characterized in that at least one ammonium compound selected from ammonium chloride, ammonium carbonate, ammonium bicarbonate, ammonium sulfate and / or ammonium carbamate and mixtures of these compounds, preferably ammonium chloride, in a total amount of 1 to 50 wt .-%, particularly preferably from 5 to 40 wt .-% and in particular from 15 to 35 wt .-%, in each case based on the weight of the powdery dyeing preparation, is contained.

Kit for the oxidative color change of keratinic fibers according to any one of claims 8 to 1 1, characterized in that the oxidation composition according to any one of claims 1-7 has a pH in the range of 2.5 to 5.5 and a viscosity in the range of 1000 to 6000 mPas, preferably 1500 to 3500 mPas.

13. A process for the oxidative color change of keratinic fibers, characterized by the following process steps:

Providing an oxidation composition containing

- 50 - 96 wt .-% water,

0.5 to 20% by weight of hydrogen peroxide,

at least one polyethylene glycol ether of a linear saturated C 12 -C 22 -alkanol having 15-30 ethylene oxide units in the molecule in a total amount of 0.3-1 wt.

%

at least one anionic surfactant in a total amount of 0.3-1% by weight,

all quantities are based on the weight of the oxidation composition, and

Provision of a pulverulent dyeing preparation which comprises at least one oxidation dye precursor and at least one color which does not permanently change the color of the fibers Contains pigment,

Preparation of a mixture of the abovementioned oxidation composition and the abovementioned pulverulent dyeing preparation, preferably in a weight ratio of

Oxidizing composition to powdered dyeing preparation of 6 to 12, more preferably from 8 to 1 1 and most preferably from 9 to 10,

immediately afterwards the ready-to-use agent is distributed on the fibers,

Leaving the agent on the fibers for a period of 1 to 60 minutes, then

Rinsing out the remaining agent from the fibers and possibly drying the hair.

14. A process for the oxidative color change of keratinic fibers according to claim 13, characterized in that an oxidation composition according to any one of claims 2-7, which has a pH in the range of 2.5 to 5.5 and a viscosity in the range of 1000 to 6000 mPas, preferably 1500 to 3500 mPas, and a powdered dyeing preparation according to any one of claims 8 - 1 1 are used.

15. A process for the oxidative color change of keratinic fibers according to claim 13 or 14, characterized in that the mixture of oxidation composition and pulverulent dyeing preparation has a pH of 8 to 1 1, 5, particularly preferably a pH of 8.5 to 1 1 , most preferably has a pH of 9.0 to 10.5.