EP2023766A1 - Dispositif d'application pour utiliser un liquide d'application sur des fibres de kératine - Google Patents

Dispositif d'application pour utiliser un liquide d'application sur des fibres de kératine

Info

Publication number
EP2023766A1
EP2023766A1 EP07729636A EP07729636A EP2023766A1 EP 2023766 A1 EP2023766 A1 EP 2023766A1 EP 07729636 A EP07729636 A EP 07729636A EP 07729636 A EP07729636 A EP 07729636A EP 2023766 A1 EP2023766 A1 EP 2023766A1
Authority
EP
European Patent Office
Prior art keywords
application
amino
application device
container
acid
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP07729636A
Other languages
German (de)
English (en)
Inventor
Anja Reichert
Konstantin Goutsis
Ina Franke
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP2023766A1 publication Critical patent/EP2023766A1/fr
Ceased legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/22—Peroxides; Oxygen; Ozone
    • A—HUMAN NECESSITIES
    • A45—HAND OR TRAVELLING ARTICLES
    • A45D—HAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D19/00—Devices for washing the hair or the scalp; Similar devices for colouring the hair
    • A45D19/0041—Processes for treating the hair of the scalp
    • A45D19/0066—Coloring or bleaching
    • A—HUMAN NECESSITIES
    • A45—HAND OR TRAVELLING ARTICLES
    • A45D—HAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D19/00—Devices for washing the hair or the scalp; Similar devices for colouring the hair
    • A45D19/02—Hand-actuated implements, e.g. hand-actuated spray heads
    • A45D19/026—Hand-actuated implements, e.g. hand-actuated spray heads having brush or comb applicators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/10—Preparations for permanently dyeing the hair
    • A—HUMAN NECESSITIES
    • A45—HAND OR TRAVELLING ARTICLES
    • A45D—HAIRDRESSING OR SHAVING EQUIPMENT; EQUIPMENT FOR COSMETICS OR COSMETIC TREATMENTS, e.g. FOR MANICURING OR PEDICURING
    • A45D2200/00—Details not otherwise provided for in A45D
    • A45D2200/05—Details of containers
    • A45D2200/058—Means for mixing different substances prior to application

Definitions

  • the present invention relates to a special application device for applying an application liquid to keratinic fibers, in particular a liquid dyeing preparation, based on oxidation dye precursors.
  • Human hair as an example of a keratin fiber is treated today in many ways with hair cosmetic preparations. These include, for example, the cleansing of hair with shampoos, the care and regeneration with rinses and cures and the bleaching, dyeing and shaping of the hair with dyes, tinting agents, waving agents and styling preparations. In this case, means for changing or nuancing the color of the head hair play a prominent role.
  • dyeing or tinting agents which contain as coloring component so-called substantive dyes. These are dye molecules that attach directly to the hair and do not require an oxidative process to form the paint. These dyes include, for example, the henna already known from antiquity for coloring body and hair. These dyeings are usually prone to shampooing, so that sometimes after a few washes an undesirable nuance shift or even a visible "discoloration" occurs.
  • oxidation colorants For permanent, intensive dyeings with corresponding fastness properties, so-called oxidation colorants are used. Such colorants usually contain oxidation dye precursors, so-called developer components and coupler components. The developer components form under the influence of oxidizing agents or of atmospheric oxygen with one another or with coupling with one or more coupler components, the actual dyes.
  • the oxidation stains are characterized by excellent, long lasting staining results.
  • a mixture of a larger number of oxidation dye precursors must usually be used; In many cases, direct dyes are still used for shading.
  • the colorants of the three categories described in the form of creams, gels or solutions are usually applied to the fibers with the aid of a brush.
  • dyes that are applied to the fibers as a shampoo formulation or conditioner formulation.
  • DE 199 22 092 A1 describes, for example, a cap-like application device for dyeing hair strands, which is placed on an associated container with hair dye.
  • This application device comprises a plurality of outlet openings for applying the hair dye and adjacent thereto guide prongs, which are drawn during use with combing movements through the hair.
  • bristles are arranged around the outlet opening in order to achieve a more uniform application of the hair dye. Nevertheless, the outlet openings with the bristles do not allow a sufficiently metered application of the hair dye. In particular, an excessive leakage of the hair dye and thus also an unwanted wetting of the scalp can not be effectively excluded. It was therefore an object of the present invention to develop a dyeing system which makes it possible to prepare dyeing agents based on oxidation dye precursors until they are used separately and still allows easy handling by the consumer. In addition, the dyeing properties of the application device should also convince.
  • a first subject of the present invention is therefore an application device for applying an application liquid to keratinic fibers, in particular hair, with at least one container for receiving the application liquid, with an application head which is connected to the at least one container and has a porous application body for applying the Application liquid by sweeping the fibers, wherein the application liquid contains the application liquid at least one oxidation dye precursor and is mixed with an oxidizing agent preparation immediately before use.
  • a first parameter essential to the invention is the use of at least one oxidation dye precursor in the application liquid.
  • oxidation dye precursor summarizes according to the invention developer and Kupperkomponenten.
  • the application liquids according to the invention contain at least one developer component and at least one coupler component. Accordingly, it has proved to be preferred if the application fluid contains at least one developer component.
  • the developer components are usually primary aromatic amines having a further, located in the para or ortho position, free or substituted hydroxy or amino group, diaminopyridine derivatives, heterocyclic hydrazones, 4-aminopyrazolone derivatives and 2,4,5,6-tetraaminopyrimidine and its derivatives ,
  • p-phenylenediamine derivatives of the formula (E1) in which
  • G 1 represents a hydrogen atom, a C 1 - to C 4 alkyl, C 1 - to C 4 - monohydroxyalkyl radical, a C 2 - to C 4 polyhydroxyalkyl radical, a (d- to C 4) alkoxy (C - to C 4 ) -alkyl radical, a 4'-aminophenyl radical or a C 1 to C 4 -alkyl radical which is substituted by a nitrogen-containing group, a phenyl or a 4'-aminophenyl radical;
  • G 2 represents a hydrogen atom, a C 1 - to C 4 alkyl, C 1 - to C 4 - monohydroxyalkyl radical, a C 2 - to C 4 polyhydroxyalkyl radical, a (C 1 - to C 4 J-AIkOXy- ( C 1 - to C 4 ) -alkyl radical or a C 1 - to C 4 -alkyl radical which is substituted by a nitrogen-containing group;
  • G 3 represents a hydrogen atom, a halogen atom such as a chlorine, bromine, iodine or fluorine atom, a C 1 - to C 4 -alkyl radical, a C 1 - to C 4 -monohydroxyalkyl radical, a C 2 - to C 4 - Polyhydroxyalkylrest, a C 1 - to C 4 -hydroxyalkoxy, a C 1 - to C 4 -Acetylaminoalkoxyrest, a C 1 - to C 4 - Mesylaminoalkoxyrest or a C 1 - to C 4 -Carbamoylaminoalkoxyrest;
  • a halogen atom such as a chlorine, bromine, iodine or fluorine atom
  • a C 1 - to C 4 -alkyl radical such as a chlorine, bromine, iodine or fluorine atom
  • G 4 represents a hydrogen atom, a halogen atom or a C 1 - to C 4 -alkyl radical or when G 3 and G 4 are ortho to each other, they may together form a bridging ⁇ , ⁇ -alkylenedioxy group, such as, for example, an ethylenedioxy group.
  • C 1 - to C 4 -alkyl radicals mentioned as substituents in the compounds according to the invention are the groups methyl, ethyl, propyl, isopropyl and butyl. Ethyl and methyl are preferred alkyl radicals.
  • C 1 -C 4 -alkoxy radicals which are preferred according to the invention are, for example, a methoxy or an ethoxy group.
  • a C 1 - to C 4 -hydroxyalkyl group a hydroxymethyl, a 2-hydroxyethyl, a 3-hydroxypropyl or a 4-hydroxybutyl group may be mentioned.
  • a 2-hydroxyethyl group is particularly preferred.
  • a particularly preferred C 2 to C 4 polyhydroxyalkyl group is the 1, 2-dihydroxyethyl group.
  • halogen atoms are according to the invention F, Cl or Br atoms, Cl atoms are very particularly preferred.
  • the other terms used are derived according to the invention from the definitions given here.
  • nitrogen-containing groups of the formula (E1) are in particular the amino groups, C 1 to C 4 monoalkylamino groups, C 1 to C 4 dialkylamino groups, C 1 to C 4 trialkylammonium groups, C 1 to C 4 monohydroxyalkylamino groups, Imidazolinium and ammonium.
  • Particularly preferred p-phenylenediamines of the formula (E1) are selected from p-phenylenediamine, p-toluenediamine, 2-chloro-p-phenylenediamine, 2,3-dimethyl-p-phenylenediamine, 2,6-dimethyl-p-phenylenediamine, 2,6-diethyl-p-phenylenediamine, 2,5-dimethyl-p-phenylenediamine, N, N-dimethyl-p-phenylenediamine, N, N-diethyl-p-phenylenediamine, N, N-dipropyl-p-phenylenediamine, 4-amino-3-methyl- (N, N-diethyl) -aniline, N, N-bis- ( ⁇ -hydroxyethyl) -p-phenylenediamine, 4-N, N- Bis ( ⁇ -hydroxyethyl) amino-2-methylaniline, 4-N, N-bis ( ⁇
  • Very particular preferred p-phenylenediamine derivatives of the formula (E1) according to the invention are p-phenylenediamine, p-toluenediamine, 2- ( ⁇ -hydroxyethyl) -p-phenylenediamine, 2- ( ⁇ , ⁇ -dihydroxyethyl) -p-phenylenediamine and N, N bis (.beta.-hydroxyethyl) -p-phenylenediamine.
  • developer component compounds which contain at least two aromatic nuclei which are substituted by amino and / or hydroxyl groups.
  • binuclear developer components which can be used in the dyeing compositions according to the invention, mention may be made in particular of the compounds corresponding to the following formula (E2) and their physiologically tolerated salts:
  • Z 1 and Z 2 independently of one another represent a hydroxyl or NH 2 -ReSt which is optionally substituted by a C 1 -C 4 -alkyl radical, by a C 1 -C 4 -hydroxyalkyl radical and / or by a bridging Y or which optionally part of a bridging ring system
  • the bridging Y is an alkylene group having 1 to 14 carbon atoms, such as a linear or branched alkylene chain or an alkylene ring, interrupted or terminated by one or more nitrogen-containing groups and / or one or more heteroatoms such as oxygen, sulfur or nitrogen atoms and may optionally be substituted by one or more hydroxyl or C 1 - to C 8 -alkoxy radicals, or a direct bond
  • the bridging Y is an alkylene group having 1 to 14 carbon atoms, such as a linear or branched alkylene chain or an alkylene ring, interrupted or terminated by one or more nitrogen-containing
  • G 5 and G 6 independently of one another represent a hydrogen or halogen atom, a C 1 - to C 4 -alkyl radical, a C 1 - to C 4 -monohydroxyalkyl radical, a C 2 - to C 4 -hydroxyalkyl radical, a C 1 - to C 4 -aminoalkyl radical or a direct compound for bridging Y,
  • G 7 , G 8 , G 9 , G 10 , G 11 and G 12 independently of one another represent a hydrogen atom, a direct bond to the bridge Y or a C 1 - to C 4 -alkyl radical, with the proviso that the compounds of the formula (E2) contain only one bridging Y per molecule.
  • Preferred binuclear developer components of the formula (E2) are in particular: N, N'-bis ( ⁇ -hydroxyethyl) -N, N'-bis (4'-aminophenyl) -1,3-diamino-propan-2-ol, N, N'-bis ( ⁇ -hydroxyethyl) -N, N'-bis (4'-aminophenyl) ethylenediamine, N, N'-bis (4-aminophenyl) tetramethylenediamine, N, N'-bis N, N'-bis (4-aminophenyl) tetramethylenediamine, N, N'-bis (4-methylaminophenyl) tetramethylenediamine, N, N'-diethyl-N, N ' bis (4'-amino-3'-methylphenyl) ethylenediamine, bis (2-hydroxy-5-aminophenyl) methane, N, N'-bis (4'-aminopheny
  • Very particularly preferred binuclear developer components of the formula (E2) are N, N'-bis ( ⁇ -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 and 1, 10-bis (2,5-diaminophenyl) -1, 4,7,10-tetraoxadecane or one of its physiologically acceptable salts.
  • p-aminophenol derivatives of the formula (E3) in which:
  • G 13 represents a hydrogen atom, a halogen atom, a C 1 to C 4 alkyl radical, a C 1 to C 4 monohydroxyalkyl radical, a C 2 to C 4 polyhydroxyalkyl radical, a C 1 to C 4 alkyl group - (C 1 - to C 4 ) -alkyl radical, a C 1 - to C 4 -aminoalkyl radical, a hydroxy- (C 1 -C 4 ) -alkylamino radical, a C 1 - to C 4 -hydroxyalkoxy radical, a C 1 - to C 4 -hydroxyalkyl- (C 1 to C 4 ) -aminoalkyl or a (di-C 1 - to C 4 -alkylamino) - (C 1 to C 4 ) -alkyl, and
  • G 14 is a hydrogen or halogen atom, a C 1 - to C 4 -alkyl radical, a C 1 - to C 4 -monohydroxyalkyl radical, a C 2 - to C 4 -polyhydroxyalkyl radical, a (C 1 - to C 4 ) - Alkoxy (C 1 -C 4 ) -alkyl radical, a C 1 -C 4 -aminoalkyl radical or a C 1 -C 4 -cyanoalkyl radical,
  • G 15 is hydrogen, C 1 - to C 4 alkyl, C 1 - to C 4 - monohydroxyalkyl radical, a C 2 - to C 4 polyhydroxyalkyl radical, a phenyl radical or a benzyl radical, and
  • G 16 is hydrogen or a halogen atom.
  • Preferred p-aminophenols of the formula (E3) are, in particular, p-aminophenol, N-methyl-p-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 2-hydroxymethylamino-4-aminophenol, 4 -Amino-3-hydroxymethylphenol, 4-amino-2- ( ⁇ -hydroxyethoxy) -phenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2-methoxymethyl-phenol, 4-amino -2-aminomethylphenol, 4-amino-2- ( ⁇ -hydroxyethyl-aminomethyl) phenol, 4-amino-2- ( ⁇ , ⁇ -dihydroxyethyl) phenol, 4-amino-2-fluorophenol, 4-amino-2 -chlorophenol, 4-amino-2,6-dichlorophenol, 4-amino-2- (diethyl-aminomethyl) -phenol and their physiological
  • Very particularly preferred compounds of the formula (E3) are p-aminophenol, 4-amino-3-methylphenol, 4-amino-2-aminomethylphenol, 4-amino-2- ( ⁇ , ⁇ -dihydroxyethyl) -phenol and 4-amino 2- (diethylaminomethyl) -phenol.
  • the developer component may be selected from o-aminophenol and its derivatives such as 2-amino-4-methylphenol, 2-amino-5-methylphenol or 2-amino-4-chlorophenol.
  • the developer component may be selected from heterocyclic developer components such as the pyridine, pyrimidine, pyrazole, pyrazole pyrimidine derivatives and their physiologically acceptable salts.
  • Preferred pyridine derivatives are, in particular, the compounds described in the patents GB 1 026 978 and GB 1 153 196, such as 2,5-diamino-pyridine, 2- (4-methoxyphenyl) -amino-3-amino-pyridine, 2,3-diamino-6-methoxy-pyridine, 2- ( ⁇ -methoxyethyl) -amino-3-amino-6-methoxy-pyridine and 3,4-diamino-pyridine.
  • Preferred pyrimidine derivatives are, in particular, the compounds described in German Patent DE 2 359 399, Japanese Laid-Open Patent Publication JP 02019576 A2 or in the published patent application WO 96/15765, such as 2,4,5,6-tetraaminopyrimidine, 4-hydroxy- 2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 2-dimethylamino-4,5,6-triaminopyrimidine, 2,4-dihydroxy-5,6-diaminopyrimidine and 2,5,6- triaminopyrimidine.
  • Preferred pyrazole derivatives are, in particular, the compounds described in patents DE 3 843 892, DE 4 133 957 and patent applications WO 94/08969, WO 94/08970, EP-740 931 and DE 195 43 988, such as 4,5 Diamino-1-methylpyrazole, 4,5-diamino-1- ( ⁇ -hydroxyethyl) pyrazole, 3,4-diaminopyrazole, 4,5-diamino-1- (4'-chlorobenzyl) pyrazole, 4.5- Diamino-1, 3-dimethylpyrazole, 4,5-diamino-3-methyl-1-phenylpyrazole, 4,5-diamino-1-methyl-3-phenylpyrazole, 4-amino-1,3-dimethyl-5-hydrazinopyrazole, 1-Benzyl-4,5-diamino-3-methylpyrazole, 4,5-diamino-3-tert-butyl-1
  • Preferred pyrazolopyrimidine derivatives are, in particular, the derivatives of the pyrazolo [1,5-a] pyrimidine of the following formula (E4) and their tautomeric forms, if a tautomeric equilibrium exists:
  • G 17 , G 18 , G 19 and G 20 independently of one another represent a hydrogen atom, a C 1 - to C 4 -alkyl radical, an aryl radical, a C 1 - to C 4 -hydroxyalkyl radical, a C 2 - to C 4 - Polyhydroxyalkylrest a (C 1 - to C 4 ⁇ AIkOXy- (C 1 - to C 4 ) -alkyl radical, a C 1 - to C 4 - aminoalkyl radical which may optionally be protected by an acetyl-ureide or a sulfonyl radical , a (C 1 - to C 4 ) -alkylamino- (C 1 - to C 4 ) -alkyl radical, a di - [(C 1 - to C 4 ) -alkyl] - (C 1 -C 4 ) -aminoalkyl radical where the dialkyl radicals optionally form a carbon cycle or
  • pyrazolo [1, 5-a] pyrimidines of the above formula (E4) can be prepared as described in the literature by cyclization starting from an aminopyrazole or from hydrazine.
  • coupler components m-phenylenediamine derivatives, naphthols, resorcinol and resorcinol derivatives, pyrazolones and m-aminophenol derivatives are generally used.
  • Suitable coupler substances are in particular 1-naphthol, 1, 5, 2,7- and 1, 7-dihydroxynaphthalene, 5-amino-2-methylphenol, m-aminophenol, resorcinol, resorcinol monomethyl ether, m-phenylenediamine, 1-phenyl-3 methyl pyrazolone-5, 2,4-dichloro-3-aminophenol, 1,3-bis- (2 ', 4'-diaminophenoxy) -propane, 2-chlororesorcinol, 4-chloro-resorcinol, 2-chloro 6-methyl-3-aminophenol, 2-amino-3-hydroxypyridine, 2-methyl resorcinol, 5-methylresorcinol and 2-methyl-4
  • Resorcinol monomethyl ether 2-methylresorcinol, 5-methylresorcinol, 2,5-dimethylresorcinol, 2-
  • Chlororesorcinol 4-chlororesorcinol, pyrogallol and 1,2,4-trihydroxybenzene
  • Pyridine derivatives such as 2,6-dihydroxypyridine, 2-amino-3-hydroxypyridine, 2-amino-5-chloro-3-hydroxypyridine, 3-amino-2-methylamino-6-methoxypyridine, 2,6-dihydroxy-3,4 dimethylpyridine, 2,6-dihydroxy-4-methylpyridine, 2,6-diaminopyridine, 2,3-diamino-6-methoxypyridine and 3,5-diamino-2,6-dimethoxypyridine,
  • Naphthalene derivatives such as 1-naphthol, 2-methyl-1-naphthol, 2-hydroxymethyl-1-naphthol, 2-hydroxyethyl-1-naphthol, 1, 5-dihydroxynaphthalene, 1, 6-dihydroxynaphthalene, 1, 7
  • Morpholine derivatives such as 6-hydroxybenzomorpholine and 6-aminobenzomorpholine,
  • Indole derivatives such as 4-hydroxyindole, 6-hydroxyindole and 7-hydroxyindole,
  • Pyrimidine derivatives such as 4,6-diaminopyrimidine, 4-amino-2,6-dihydroxypyrimidine,
  • Methylenedioxybenzene derivatives such as 1-hydroxy-3,4-methylenedioxybenzene, 1-
  • Coupler components according to the invention are 1-naphthol, 1, 5, 2,7- and 1, 7-dihydroxynaphthalene, 3-aminophenol, 5-amino-2-methylphenol, 2-amino-3-hydroxypyridine, resorcinol, 4-chlororesorcinol , 2-chloro-6-methyl-3-aminophenol, 2-methylresorcinol, 5-methylresorcinol, 2,5-dimethylresorcinol and 2,6-dihydroxy-3,4-dimethylpyridine.
  • the colorants of the invention contain both the developer components and the coupler components preferably in an amount of 0.005 to 20 wt .-%, preferably 0.1 to 5 wt .-%, each based on the total oxidation colorant.
  • developer components and coupler components are generally used in approximately molar amounts to each other.
  • a certain excess of individual oxidation dye precursors is not disadvantageous, so that developer components and coupler components in a molar ratio of 1: 0.5 to 1: 3, in particular 1: 1 to 1: 2 , may be included.
  • a second essential constituent of the application liquid according to the invention is at least one oxidizing agent preparation which is mixed with the dye precursor-containing preparation only immediately before use.
  • the term "immediately before use” preferably means a period of at most 45 minutes before the application liquid is applied to the fibers It is particularly preferred according to the invention to combine the preparations, to thoroughly mix them and directly to the application of the resulting To start application liquid.
  • the preferred oxidizing agents are persulfates, chlorites and, in particular, hydrogen peroxide or its addition products, for example, urea, alkali metal carbonates, melamine and alkali metal borates.
  • the oxidizing agent preparation preferably contains the oxidizing agent (s) in a suitable aqueous, alcoholic or aqueous-alcoholic carrier.
  • suitable aqueous, alcoholic or aqueous-alcoholic carrier are, for example, creams, emulsions, gels or else other preparations which are suitable for mixing with the dye preparation and the subsequent use on the hair.
  • aqueous-alcoholic solutions are to be understood as meaning aqueous solutions containing 3 to 70% by weight of a C 1 -C 4 -alkoxy, in particular ethanol or isopropanol.
  • the agents according to the invention may additionally contain further organic Solvents such as methoxybutanol, benzyl alcohol, ethyl diglycol or 1, 2-propylene glycol. Preference is given to all water-soluble organic solvents.
  • the oxidant preparation is formulated as a powder or as a tablet.
  • tablets are also to be understood as meaning pressed powders according to the invention.
  • percarbamide, percarbonate and perborate are particularly preferred oxidizing agents.
  • the oxidizing agent preparation is formulated as a tablet, it has proven to be particularly preferred if it further contains at least one dissolution accelerator.
  • dissolution accelerator includes gas-evolving components, preformed and trapped gases, disintegrants and mixtures thereof.
  • gas-developing components are used as the dissolution accelerator. Upon contact with water, these components react with each other to form gases in-situ, which create a pressure in the tablet that disintegrates the tablet into smaller particles.
  • suitable acids Preference is given to mono-, di- or trihydric acids having a pK a of from 1.0 to 6.9.
  • Preferred acids are citric, malic, maleic, malonic, itaconic, tartaric, oxalic, glutaric, glutamic, lactic, fumaric, glycolic and mixtures thereof. Particularly preferred is citric acid.
  • the citric acid in particulate form, the particles having a diameter of less than 1000 ⁇ m, in particular less than 700 ⁇ m, very particularly preferably less than 400 ⁇ m.
  • Other alternative suitable acids are the homopolymers or copolymers of acrylic acid, maleic acid, methacrylic acid or itaconic acid having a molecular weight of 2,000 to 200,000. Particularly preferred are homopolymers of acrylic acid and copolymers of acrylic acid and maleic acid.
  • preferred bases are alkali metal silicates, carbonates, bicarbonates and mixtures thereof. Metasilicates, bicarbonates and carbonates are particularly preferred, bicarbonates are most preferred.
  • particulate hydrogencarbonates having a particle diameter of less than 1000 ⁇ m, in particular less than 700 ⁇ m, very particularly preferably less than 400 ⁇ m.
  • Sodium or potassium salts of the above bases are particularly preferred.
  • These gas-evolving components are preferably contained in the tablets according to the invention in an amount of at least 10% by weight, in particular of at least 20% by weight.
  • the gas is preformed or trapped so that upon onset of dissolution of the molded article, gas evolution begins and the further resolution accelerates.
  • suitable gases are air, carbon dioxide, N 2 O, oxygen and / or other non-toxic, non-combustible gases.
  • disintegration auxiliaries so-called shaped body disintegrants
  • dissolution accelerators are incorporated into the moldings as dissolution accelerators in order to shorten the disintegration times.
  • disintegration agent or “disintegration accelerator” is understood as meaning excipients which are suitable for rapid disintegration of moldings in water or gastric juice and for the release of the pharmaceuticals in resorbable form.
  • Swelling disintegration aids are, for example, synthetic polymers such as polyvinylpyrrolidone (PVP) or natural polymers or modified natural substances such as cellulose and starch and their derivatives , Alginates or casein derivatives.
  • PVP polyvinylpyrrolidone
  • natural polymers such as polyvinylpyrrolidone (PVP) or natural polymers or modified natural substances such as cellulose and starch and their derivatives , Alginates or casein derivatives.
  • Disintegrating agents based on cellulose are used as preferred disintegrants in the context of the present invention, so that preferred tablets comprise such cellulose-based disintegrants in amounts of from 0.5 to 50% by weight, preferably from 3 to 30% by weight, based on the total tablet contain.
  • Pure cellulose has the formal gross composition (C 6 H 10 O 5 ) H and is formally a ⁇ -1,4-polyacetal of cellobiose, which in turn is composed of two molecules of glucose.
  • Suitable celluloses consist of about 500 to 5000 glucose units and therefore have average molecular weights of 50,000 to 500,000.
  • Cellulose-based disintegrating agents which can be used in the context of the present invention are also cellulose derivatives obtainable by polymer-analogous reactions of cellulose.
  • Such chemically modified celluloses include, for example, products of esterifications or etherifications in which hydroxy hydrogen atoms have been substituted.
  • Celluloses in which the hydroxy groups have been replaced by functional groups which are not bonded via an oxygen atom can also be used as cellulose derivatives.
  • the group of cellulose derivatives includes, for example, alkali metal celluloses, carboxymethylcellulose (CMC), cellulose esters and ethers, and aminocelluloses.
  • the cellulose derivatives mentioned are preferably not used as the sole cellulosic disintegrating agent but are used in admixture with cellulose.
  • the content of these mixtures of cellulose derivatives is preferably below 50% by weight, particularly preferably below 20% by weight, based on the cellulose-based disintegrating agent.
  • cellulose-based disintegrating agent which is free of cellulose derivatives.
  • the cellulose used as a disintegration aid is preferably not used in finely divided form, but converted into a coarser form, for example granulated or compacted, before it is added to the premixes to be tabletted.
  • the particle sizes of such disintegrating agents are usually above 200 .mu.m, preferably at least 90 wt .-% between 300 and 1600 .mu.m and in particular at least 90 wt .-% between 400 and 1200 microns.
  • the disintegration auxiliaries according to the invention are available commercially for example under the name of Arbocel ® from Rettenmaier.
  • a preferred disintegration assistants for example, Arbocel ® TF-30-HG.
  • microcrystalline cellulose can be used as a further disintegrating agent based on cellulose or as a component of this component.
  • This microcrystalline cellulose is obtained by partial hydrolysis of celluloses under conditions which attack and completely dissolve only the amorphous regions (about 30% of the total cellulose mass) of the celluloses, leaving the crystalline regions (about 70%) intact.
  • Subsequent deaggregation of the microfine celluloses produced by the hydrolysis yields the microcrystalline celluloses which have primary particle sizes of about 5 ⁇ m and can be compacted, for example, into granules having an average particle size of 200 ⁇ m.
  • Suitable microcrystalline cellulose is available commercially for example under the trade name Avicel ®.
  • the accelerated dissolution of the moldings can also be achieved according to the invention by pre-granulation of the further constituents of the tablet.
  • a third essential aspect of the present invention is the nature of the application device.
  • the porous applicator has continuous pores to achieve capillary action.
  • the capillary properties of the application body which is in contact with the application liquid in a wick-like manner, ensure reliable transport of the application liquid out of the at least one container and metered application of the application liquid by sweeping it over the fibers.
  • the application body preferably has a fibrous, sponge, foam, felt or sintered material-like material structure. This material structure causes the desired capillary action of the application body, so that, for example, an unwanted leakage or dripping of the application liquid from the application body is omitted, but at the same time a reliable fluid delivery is ensured by means of the application body.
  • the porous application body can also have a plurality of pin-shaped projections. This increases the effective surface area of the application body and thus improves the order of the application liquid. Accordingly, by means of the coating movement of the applicator body over the keratinic fibers, in particular the hair, a better dyeing result is guaranteed both quantitatively and qualitatively.
  • the application head has a plurality of possibly detachably arranged, comb teeth. These comb teeth are arranged in particular adjacent to the application body.
  • the brushing motion of the entire application head during the application initially provides, by means of the comb teeth, for a disentanglement of the fibers or the hair and thus, above all, for a uniform application of the application liquid.
  • the detachable arrangement of the comb teeth on the application head allows a more versatile use of the application device. It also proves to be advantageous for such an arrangement when the comb teeth protrude from the porous applicator body.
  • a preferred embodiment of the application device is to arrange the comb teeth of the application head in a circle around the application body. Regardless of the respective coating movement direction, the fibers or hair are first unraveled during use in each case before the actual application of the application liquid takes place.
  • the actual application liquid is prepared only immediately before use by mixing the preparation of the oxidizing agent with the preparation containing the dye precursors.
  • correspondingly designed storage and mixing containers are required in the context of the overall device.
  • the suitably designed storage and mixing containers guarantee on the one hand prior to use sufficient storage stability for the individual components of the application liquid and on the other hand ensure appropriate handling of the overall device during use.
  • different variants of the application device are possible. These different variants have in common that immediately before the application, the already mixed preparation of the application liquid is in the container of the device according to the invention.
  • the container is connected to the application head.
  • this container can be ergonomically adapted in its shape to the application process in order to facilitate the handling of the application device for the user.
  • the container can be designed both as a separate application container, in which the ready-mixed preparation of the application liquid is filled before starting the application. Similarly, it is also conceivable that the container serves both as an application container, as well as before application as a mixing container. Mixing container and application container are identical in this variant and form the container. For both design variants is Below a variety of ways described to design such mixing container constructive.
  • the first container contains the oxidizing agent
  • the second container the dye composition
  • the third container serves as a mixing container.
  • Further additional storage containers are possible.
  • To prepare the mixture the desired amount is added from the two storage containers in the mixing container, this closed and, for example, by subsequent shaking of the mixing container, the two components are mixed together.
  • the mixing process can be accelerated by the fact that internals in the mixing vessel when shaking produce a turbulent flow (high Reynolds numbers) and thus improve and accelerate the mixing process.
  • Another embodiment within the scope of the present invention is to provide one or more of the liquid soluble material reservoirs.
  • These soluble storage containers are placed in the mixing container and there dissolved by the respective solvent, preferably a component of the mixture to be prepared.
  • This embodiment has the advantage for the user of never coming into contact with individual components packed in the storage containers during the preparation of the overall preparation.
  • such soluble storage containers are designed as a foil bag.
  • a further variant for producing mixtures according to the invention is the provision of at least two separate containers for storing the respective component, wherein at least one of the containers simultaneously acts as a mixing container.
  • all the above examples of the variant with at least three containers are also conceivable within the scope of the present invention.
  • means which provide pressure equalization between the two containers during the transfer operation.
  • Such means are, for example, arranged within the opening of a reservoir tubes, which can act as a snorkel.
  • one-way valves in the reservoir for pressure equalization are conceivable for such functionalities.
  • closures which only opens upon a triggering command.
  • the user can ensure that the transfer process does not start until the reservoir and mixing container are in the correct position for the mixing process.
  • closures is, for example, a tear-open film which tears open due to an increased internal pressure in the storage container and thus starts the transfer process.
  • the internal pressure in the reservoir can be increased for example by pumping means or by simply squeezing.
  • the storage container for granules, powder or lumpy goods as a blister pack and additionally to provide auxiliaries which allow these blisters to be placed above the opening of the mixing container.
  • the user of such mixing systems simply presses the component contained in the blister through the sealing film into the mixing container.
  • An embodiment of such mixing containers can be, for example, a storage container whose destructible dividing wall can be destroyed by mechanical means mounted on the applicator head and projecting into the container. The destruction takes place in such a case by screwing or placing the applicator head in the application position.
  • Separate devices for destroying the partition are of course conceivable within the scope of the present invention.
  • a fixed partition with a one-way valve.
  • a one-way valve could open, for example, by increasing the internal pressure in one of the two chambers and thus convert the component from one chamber into the other chamber.
  • the increase in internal pressure can be achieved by the flexible design of the entire container and its compression by the user's hand. Also, additional pumping means are quite conceivable.
  • a mixing device with a single container and different chambers separated by partitions, which serve as a reservoir, it may be advantageous to provide an empty mixing chamber in addition to the storage chambers before the start of the mixing process.
  • an element for transferring the components from the individual storage chambers in the mixing chamber may, as already described above embodiments, destructible walls, but also one-way valves in the direction of the mixing chamber.
  • the resulting application liquid is formulated thin liquid.
  • Application fluids which have a viscosity of from 0 to 2000 mPas when mixed with the oxidizer formulation (measured at 22 ° C. in a Brookfield viscometer with spindle 4 and a speed of 4 rpm) have proved to be particularly preferred.
  • a viscosity of 0 to 100 mPas, measured under the conditions mentioned, is particularly preferred according to the invention.
  • a viscosity of 50 to 500 mPas (measured at 20 ° C. (Brookfield viscometer type RV-T, spindle 4 with a rotation speed of 20 rpm) is very particularly preferred according to the invention.
  • the application liquid may contain further components which contribute to the coloring.
  • the application liquid may therefore contain at least one naturally-analogous dye precursor.
  • naturally-analogous dyes such indoles and indolines are preferably used which have at least one hydroxy or amino group, preferably as a substituent on the six-membered ring. These groups may carry further substituents, e.g. Example in the form of etherification or esterification of the hydroxy group or alkylation of the amino group.
  • the colorants contain at least one indole and / or indoline derivative.
  • Particularly suitable precursors of natural-analogous hair dyes are derivatives of 5,6-dihydroxyindoline of the formula (NAV I),
  • G 19 is hydrogen, a C 1 -C 4 -alkyl group or a C 1 -C 4 -hydroxy-alkyl group,
  • G 2O is hydrogen or a -COOH group, where the -COOH group may also be in the form of a salt with a physiologically compatible cation,
  • G 2 i is hydrogen or a C 1 -C 4 -alkyl group
  • G 22 is hydrogen, a C 1 -C 4 -alkyl group or a group -CO-G 24 , in which G 24 is a C 1 -C 4 -alkyl group, and
  • G 23 is one of the groups mentioned under G 22 , and physiologically acceptable salts of these compounds with an organic or inorganic acid.
  • Particularly preferred derivatives of indoline are 5,6-dihydroxyindoline, N-methyl-5,6-dihydroxyindoline, N-ethyl-5,6-dihydroxyindoline, N-propyl-5,6-dihydroxyindoline, N-butyl-5,6 dihydroxyindoline, 5,6-dihydroxyindoline-2-carboxylic acid and 6-hydroxyindoline, 6-aminoindoline and 4-aminoindoline.
  • N-methyl-5,6-dihydroxyindoline N-ethyl-5,6-dihydroxyindoline, N-propyl-5,6-dihydroxyindoline, N-butyl-5,6-dihydroxyindoline and especially 5, 6-Dihydroxyindolin.
  • G 25 is hydrogen, a C 1 -C 4 -alkyl group or a C 1 -C 4 -hydroxyalkyl group,
  • G 26 is hydrogen or a -COOH group, where the -COOH group may also be present as a salt with a physiologically compatible cation,
  • G 27 is hydrogen or a C 1 -C 4 -alkyl group
  • G 28 is hydrogen, a C 1 -C 4 alkyl group or a group -CO-G 30 wherein G 30 represents a C-rC 4 alkyl group, and
  • G 29 is one of the groups mentioned under G 28 , as well as physiologically acceptable salts of these compounds with an organic or inorganic acid.
  • Particularly preferred derivatives of indole are 5,6-dihydroxyindole, N-methyl-5,6-dihydroxyindole, N-ethyl-5,6-dihydroxyindole, N-propyl-5,6-dihydroxyindole, N-butyl-5,6- dihydroxyindole, 5,6-dihydroxyindole-2-carboxylic acid, 6-hydroxyindole, 6-aminoindole and 4-aminoindole.
  • N-methyl-5,6-dihydroxyindole N-ethyl-5,6-dihydroxyindole, N-propyl-5,6-dihydroxyindole, N-butyl-5,6-dihydroxyindole, and especially the 5,6 -Dihydroxyindol.
  • the indoline and indole derivatives can be used in the colorants of the invention both as free bases and in the form of their physiologically acceptable salts with inorganic or organic acids, for.
  • hydrochlorides sulfates and hydrobromides are used.
  • the indole or indoline derivatives are contained therein usually in amounts of 0.05-10 wt .-%, preferably 0.2-5 wt .-%.
  • the amino acid is advantageously an ⁇ -amino acid; Very particularly preferred ⁇ -amino acids are arginine, ornithine, lysine, serine and histidine, in particular arginine.
  • the application liquid may contain at least one substantive dye.
  • Direct dyes are usually nitrophenylenediamines, nitroaminophenols, azo dyes, anthraquinones or indophenols.
  • Preferred substantive dyes are those having the international designations or trade names HC Yellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, HC Yellow 12, Acid Yellow 1, Acid Yellow 10, Acid Yellow 23, Acid Yellow 36, HC Orange 1, Disperse Orange 3, Acid Orange 7, HC Red 1, HC Red 3, HC Red 10, HC Red
  • 1,4-diamino-2-nitrobenzene 2-amino-4-nitrophenol, 1,4-bis ( ⁇ -hydroxyethyl) amino-2-nitrobenzene, 3-nitro-4- ( ⁇ -hydroxyethyl) aminophenol, 2- (2'-hydroxyethyl) amino-4,6-dinitrophenol, 1- (2'-hydroxyethyl) amino-4-methyl-2-nitrobenzene, 1-amino-4- (2'-hydroxyethyl) amino-5 -chloro-2-nitrobenzene, 4-amino-3-nitrophenol, 1- (2'-ureidoethyl) amino-4-nitrobenzene, 4-amino-2-nitrodiphenylamine-2'-carboxylic acid, 6-nitro-1, 2,3,4-tetrahydroquinoxaline, 2-hydroxy-1,4-naphthoquinone, picramic acid and its salts, 2-amino-6-chloro-4-nitrophenol, 4-ethylamino-3-nitrobenzoic acid and 2-
  • the applicator liquids according to the invention may contain a cationic substantive dye.
  • a cationic triphenylmethane dyes such as Basic Blue 7, Basic Blue 26, Basic Violet 2 and Basic Violet 14, b) aromatic systems which are substituted by a quaternary nitrogen group, for example Basic Yellow 57, Basic Red 76, Basic Blue 99, Basic Brown 16 and Basic Brown 17, as well as c) substantive dyes containing a heterocycle having at least one quaternary nitrogen atom, as for example in EP-A2-998 908, to which reference is explicitly made will be mentioned in claims 6 to 11.
  • Preferred cationic substantive dyes of group (c) are in particular the following compounds:
  • the compounds of the formulas (DZ1), (DZ3) and (DZ5) which are also known by the names Basic Yellow 87, Basic Orange 31 and Basic Red 51, are very particularly preferred cationic substantive dyes of group (c).
  • the cationic substantive dyes sold under the trademark Arianor® are also very particularly preferred cationic substantive dyes according to the invention.
  • the agents according to the invention according to this embodiment contain the substantive dyes preferably in an amount of 0.01 to 20 wt .-%, based on the total applicator.
  • preparations of the invention may also naturally occurring dyes such as henna red, henna neutral, henna black, chamomile, sandalwood, black tea, buckthorn bark, sage, bluewood, madder root, Catechu, Sedre and alkano root are included.
  • oxidation dye precursors or the direct dyes it is not necessary for the oxidation dye precursors or the direct dyes to be in each case homogeneous compounds. Rather, in the hair colorants according to the invention, due to the production process for the individual dyes, in minor amounts, further components may be included, as far as they do not adversely affect the dyeing result or for other reasons, e.g. toxicological, must be excluded.
  • the oxidation dye precursors are incorporated in a suitable aqueous, alcoholic or aqueous-alcoholic carrier.
  • suitable aqueous, alcoholic or aqueous-alcoholic carrier are, for example, creams, emulsions, gels or also surfactant-containing foaming solutions, such as, for example, shampoos, or other preparations which are suitable for use on the hair.
  • Particularly preferred according to the invention is a water-containing carrier which contains at least one C 1 -C 4 -alkoxy and at least one further organic solvent. It may be preferred according to the invention, when the water is a proportion of 20 to 60% by weight, preferably from 30 to 50% by weight, the C 1 -C 4 -alcohol contains from 20 to 60% by weight, preferably from 30 to 50% by weight, and the organic solvent accounts for 1 to 30 wt .-%, preferably from 5 to 15 wt .-%, each based on the total application liquid have. In the context of this embodiment, a composition containing water, ethanol and propylene carbonate may be particularly preferred.
  • the application liquid according to the invention is preferably adjusted to a pH of from 5 to 11, in particular from 7.5 to 11, by means of acids and / or alkalizing agents.
  • alkalizing agents are alkali or alkaline earth hydroxides, ammonia or organic amines.
  • the organic amines are preferably selected from the group consisting of monoethanolamine, monoisopropanolamine, 2-amino-2-methyl-propanol, 2-amino-2-methyl-1, 3-propanediol, 2-amino-2-ethyl-1 , 3-propanediol, 2-amino-2-methylbutanol and triethanolamine.
  • monoethanolamine, triethanolamine and 2-amino-2-methyl-propanol and 2-amino-2-methyl-1, 3-propanediol are preferred within the scope of this group.
  • the use of amino acids and / or oligopeptides such as ⁇ -aminocaproic acid as the alkalizing agent is preferred in the context of the present invention.
  • amino acids and oligopeptides whose 2.5% strength by weight solutions have a pH of 9 or greater in water.
  • Such an amino acid is arginine which is preferably used.
  • organic or inorganic acids can be used to adjust the pH.
  • Hydrochloric acid, sulfuric acid and phosphoric acid are to be mentioned in particular as preferred inorganic acids.
  • Preferred organic acids are acetic acid, glycolic acid, citric acid, tartaric acid, lactic acid and malic acid.
  • Malic acid is a particularly preferred acid used.
  • the application liquids according to the invention may contain all known in such preparations active ingredients, additives and excipients. Although it has proved to be preferred, when the application liquids are formulated free of surfactants, the application liquids according to the invention may in another embodiment also contain at least one surfactant, wherein in principle both anionic and zwitterionic, ampholytic, nonionic and cationic surfactants are suitable. In many cases, however, it has proved to be advantageous to select the surfactants from anionic, zwitterionic or nonionic surfactants. Anionic surfactants may be very particularly preferred.
  • Suitable anionic surfactants in preparations according to the invention are all anionic surfactants suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such. Example, a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 10 to 22 C-men men. In addition, glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups may be present in the molecule.
  • anionic surfactants are, in each case in the form of the sodium, potassium and ammonium as well as mono-, di- and trialkanol ammonium salts with 2 or 3 C atoms in the alkanol group, linear fatty acids having 10 to 22 C atoms (Soap),
  • Ethercarbon Acid the formula RO- (CH 2 -CH 2 O) x -CH 2 -COOH, in which R is a linear
  • Alkyl group having 10 to 22 C atoms and x 0 or 1 to 16,
  • Sulfosuccinic acid mono-alkylpolyoxyethyl esters having 8 to 18 C atoms in the alkyl group and 1 to 6 oxyethyl groups, linear alkanesulfonates having 12 to 18 C atoms, linear ⁇ -olefin sulfonates having 12 to 18 C atoms,
  • Alpha-sulfofatty acid methyl esters of fatty acids containing 12 to 18 carbon atoms are especially preferred.
  • Alkyl sulfates and alkyl polyglycol ether sulfates of the formula RO (CH 2 -CH 2 O) x -SO 3 H, in which R is a preferably linear alkyl group having 10 to 18 C atoms and x 0 or 1 to 12,
  • Preferred anionic surfactants are alkyl sulfates, alkyl polyglycol ether sulfates and ether carboxylic acids having 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in the molecule and in particular salts of saturated and in particular unsaturated C 8 -C 22 carboxylic acids, such as oleic acid, stearic acid, isostearic acid and palmitic acid ,
  • Nonionic surfactants contain as hydrophilic group z.
  • Such compounds are, for example Addition products of 2 to 30 moles of ethylene oxide and / or 0 to 5 moles of propylene oxide to linear fatty alcohols having 8 to 22 carbon atoms, to fatty acids having 12 to 22 carbon atoms and on
  • Alkylphenols having 8 to 15 C atoms in the alkyl group having 8 to 15 C atoms in the alkyl group
  • Preferred nonionic surfactants are alkyl polyglycosides of the general formula R 1 O- (Z) x . These connections are identified by the following parameters.
  • the alkyl radical R 1 contains 6 to 22 carbon atoms and may be both linear and branched. Preference is given to primary linear and methyl-branched in the 2-position aliphatic radicals.
  • Such alkyl radicals are, for example, 1-octyl, 1-decyl, 1-lauryl, 1-myristyl, 1-cetyl and 1-stearyl. Particularly preferred are 1-octyl, 1-decyl, 1-lauryl, 1-myristyl.
  • oxo-alcohols compounds with an odd number of carbon atoms in the alkyl chain predominate.
  • the alkyl polyglycosides which can be used according to the invention can contain, for example, only one particular alkyl radical R 1 .
  • these compounds are prepared starting from natural fats and oils or mineral oils.
  • the alkyl radicals R are mixtures corresponding to the starting compounds or corresponding to the particular work-up of these compounds.
  • sugar building block Z it is possible to use any desired mono- or oligosaccharides.
  • sugars with 5 or 6 carbon atoms and the corresponding oligosaccharides are used.
  • Such sugars are, for example, glucose, fructose, galactose, arabinose, ribose, xylose, lyxose, allose, altrose, mannose, gulose, idose, talose and sucrose.
  • Preferred sugar building blocks are glucose, fructose, galactose, arabinose and sucrose; Glucose is particularly preferred.
  • the alkyl polyglycosides which can be used according to the invention contain on average from 1.1 to 5 sugar units. Alkyl polyglycosides having x values of 1.1 to 1.6 are preferred. Very particular preference is given to alkyl glycosides in which x is 1: 1 to 1, 4.
  • the alkyl glycosides can also serve to improve the fixation of fragrance components on the hair.
  • this substance class as a further ingredient of the preparations according to the invention in the event that an action of the perfume oil on the hair which exceeds the duration of the hair treatment is desired.
  • alkoxylated homologs of said alkyl polyglycosides can also be used according to the invention. These homologs may contain on average up to 10 ethylene oxide and / or propylene oxide units per alkyl glycoside unit.
  • zwitterionic surfactants can be used, in particular as cosurfactants.
  • Zwitterionic surfactants are surface-active compounds which carry at least one quaternary ammonium group and at least one -COO * " '- or -SO 3 () group in the molecule
  • Particularly suitable zwitterionic surfactants are the so-called betaines such as N-alkyl-N , N-dimethylammonium glycinates, for example, the cocoalkyl dimethylammonium glycinate, N-acyl-aminopropyl-N, N-dimethylammoniumglycinate, for example Kokosacylaminopropyl- dimethylammoniumglycinat, and 2-alkyl-3-carboxylmethyl-3-hydroxyethyl-imidazoline with 8 each
  • a preferred zwitterionic surfactant is the fatty acid amide derivative known under the INCI name Cocamidopropyl Betaine.
  • ampholytic surfactants are to be understood as meaning those surface-active compounds which, apart from a C 8 -C 20 -alkyl or acyl group in the molecule, contain at least one free amino group and at least one -COOH or -SO 3 H group and which are capable of forming internal salts .
  • suitable ampholytic surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids each having about 8 to 18 C atoms in the alkyl group.
  • Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, coco
  • the cationic surfactants used are, in particular, those of the quaternary ammonium compound type, the esterquats and the amidoamines.
  • Preferred quaternary ammonium compounds are ammonium halides, especially chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides, e.g.
  • cetyltrimethylammonium chloride stearyltrimethylammonium chloride, distearyldimethylammonium chloride, lauryldimethylammonium chloride, lauryldimethylbenzylammonium chloride and tricetylmethylammonium chloride, as well as the imidazolium compounds known under the INCI names Quaternium-27 and Quaternium-83.
  • the long alkyl chains of the above-mentioned surfactants preferably have 10 to 18 carbon atoms.
  • Esterquats are known substances which contain both at least one ester function and at least one quaternary ammonium group as a structural element.
  • Preferred ester quats are quaternized ester salts of fatty acids with triethanolamine, quaternized ester salts of fatty acids with diethanolalkylamines and quaternized ester salts of fatty acids with 1,2-dihydroxypropyldialkylamines.
  • Such products are marketed under the trade names Stepantex® ®, ® and Dehyquart® Armocare® ®.
  • alkylamidoamines are usually prepared by amidation of natural or synthetic fatty acids and fatty acid cuts with dialkylaminoamines.
  • An inventively particularly suitable compound from this group is that available under the name Tegoamid ® S 18 commercially stearamidopropyl dimethylamine.
  • cationic surfactants which can be used according to the invention are the quaternized protein hydrolysates.
  • cationic silicone oils such as, for example, the commercially available products Q2-7224 (manufacturer: Dow Corning, a stabilized trimethylsilylamodimethicone), Dow Corning 929 emulsion (containing a hydroxylamino-modified silicone, also referred to as amodimethicones), SM -2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil ® quat 3270 and 3272 (manufacturer: Th. Goldschmidt; di- quaternary polydimethylsiloxanes, quaternium-80).
  • a suitable cationic surfactant quaternary sugar derivative is the commercial product Glucquat ® 100, according to INCI nomenclature a "lauryl methyl Gluceth-10 Hydroxypropyl Dimonium Chloride".
  • the compounds used as surfactant with alkyl groups may each be uniform substances. However, it is usually preferred to start from the production of these substances from native plant or animal raw materials, so as to obtain substance mixtures with different, depending on the particular raw material alkyl chain lengths.
  • both products with a "normal” homolog distribution and those with a narrow homolog distribution can be used.
  • "normal” homolog distribution are meant mixtures of homologs obtained in the reaction of fatty alcohol and alkylene oxide using alkali metals, alkali metal hydroxides or alkali metal alcoholates as catalysts. Narrowed homolog distributions are obtained when, for example, hydrotalcites, alkaline earth metal salts of ether carboxylic acids, alkaline earth metal oxides, hydroxides or alkoxides are used as catalysts. The use of products with narrow homolog distribution may be preferred.
  • agents used in the process according to the invention may preferably also contain a conditioning agent selected from the group consisting of cationic surfactants, cationic polymers, alkylamidoamines, paraffin oils, vegetable oils and synthetic oils.
  • a conditioning agent selected from the group consisting of cationic surfactants, cationic polymers, alkylamidoamines, paraffin oils, vegetable oils and synthetic oils.
  • Cationic polymers may be preferred as conditioning agents. These are in the
  • Preferred cationic polymers are, for example, quaternized cellulose derivatives, such as are available under the names of Celquat ® and Polymer JR ® commercially.
  • the compounds Celquat ® H 100, Celquat L 200 and Polymer JR ® ® 400 are preferred quaternized cellulose derivatives.
  • Copolymers of vinylpyrrolidone with quaternized derivatives of dialkylaminoacrylate and - methacrylate such as, for example, quaternized with diethyl sulfate, vinylpyrrolidone dimethylaminomethacrylate copolymers such compounds are available under the names Gafquat ® 734 and Gafquat ® 755 commercially.
  • Vinylpyrrolidone-Methoimidazoliniumchlorid copolymers such as those available under the name Luviquat ® , quaternized polyvinyl alcohol and those under the names Polyquaternium 2, Polyquaternium 17, Polyquaternium 18 and
  • Polyquaternium 27 known polymers with quaternary nitrogen atoms in the polymer main chain.
  • cationic polymers of the four first-mentioned groups very particular preference to polyquaternium-2, polyquaternium-10 and polyquaternium-22.
  • conditioning active ingredients are silicone oils, in particular dialkyl and alkylaryl siloxanes, for example dimethylpolysiloxane and methylphenylpolysiloxane, and also their alkoxylated and quaternized analogs.
  • silicones examples include the Dow Corning under the names DC 190, DC 200, DC 344, DC 345 and DC 1401 products sold and the commercial products Q2-7224 (manufacturer: Dow Corning; a stabilized trimethyl silyl amodimethicone), Dow Corning ® 929 emulsion (containing a hydroxylamino-modified silicone which is also known as amodimethicone), SM-2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil ® -Quat 3270 and 3272 (manufacturer: Th Goldschmidt, di-quaternary polydimethylsiloxanes, quaternium-80).
  • Dow Corning a stabilized trimethyl silyl amodimethicone
  • Dow Corning ® 929 emulsion containing a hydroxylamino-modified silicone which is also known as amodimethicone
  • SM-2059 manufactured by General Electric
  • conditioning active ingredients are paraffin oils, synthetically prepared oligomeric alkenes and vegetable oils such as jojoba oil, sunflower oil, orange oil, almond oil, wheat germ oil and peach kernel oil.
  • suitable hair-conditioning compounds are phospholipids, for example soya lecithin, egg lecithin and cephalins.
  • auxiliaries and additives are, for example, nonionic polymers, for example vinylpyrrolidone / vinyl acrylate copolymers,
  • Butylaminoethyl methacrylate ⁇ -hydroxypropyl methacrylate copolymers anionic polymers such as polyacrylic acids, crosslinked polyacrylic acids,
  • Thickeners such as agar-agar, guar gum, alginates, xanthan gum, gum arabic,
  • Derivatives such as amylose, amylopectin and dextrins, clays such. B. bentonite or fully synthetic
  • Hydrocolloids such as e.g. polyvinyl alcohol,
  • Structural agents such as maleic acid and lactic acid, hair conditioning compounds such as phospholipids, for example soya lecithin, egg lecithin and cephalins,
  • Solvents and mediators such as ethanol, isopropanol, ethylene glycol, propylene glycol, glycerol and diethylene glycol, fiber-structure-improving agents, especially mono-, di- and oligosaccharides such as glucose, galactose, fructose, fructose and lactose, quaternized amines such as methyl-1-alkylamidoethyl-2 -alkylimidazolinium methosulfate
  • Anti-dandruff agents such as Piroctone Olamine, Zinc Omadine and Climbazole,
  • Light stabilizers in particular derivatized benzophenones, cinnamic acid derivatives and triazines,
  • Active ingredients such as allantoin, pyrrolidonecarboxylic acids and their salts, and bisabolol,
  • Bodying agents such as sugar esters, polyol esters or polyol alkyl ethers,
  • Fats and waxes such as spermaceti, beeswax, montan wax and paraffins,
  • Swelling and penetration substances such as glycerol, propylene glycol monoethyl ether, carbonates,
  • Opacifiers such as latex, styrene / PVP and styrene / acrylamide copolymers
  • Pearlescing agents such as ethylene glycol mono- and distearate and PEG-3-distearate,
  • Propellants such as propane-butane mixtures, N 2 O, dimethyl ether, CO 2 and air,
  • the constituents of the water-containing carrier are used to prepare the inventive application liquid in amounts customary for this purpose;
  • emulsifiers are used in concentrations of 0.5 to 30 wt .-% and thickening agents in concentrations of 0.1 to 25 wt .-% of the total colorant.
  • the application device 1 shown in FIG. 1 is designed for use with a liquid hair dye. In principle, however, such an application device 1 can also generally serve for the application of any application fluid for keratinic fibers, the application fluid being applied by brushing movements to the fibers.
  • the application device 1 has a container 2 which receives the hair dye or the application liquid and stores it until it is used. For this purpose, it may be useful to provide an absorbent storage element in the interior of the container, which is designed, for example, as a fibrous or sponge-shaped, in order to receive the hair dye or the application liquid.
  • the container 2 has two separate areas inside. In the first, larger area, the application liquid is prepared before the application. In the second, smaller area, the powdery oxidizing agent preparation is formulated before the application. Immediately before the application, the partition wall between the two areas is pierced by an externally actuated mandrel, so that there is a mixing of the two separately assembled components. In this embodiment, the container 2 thus serves the separate packaging, the mixture of the components and also as a storage container during use.
  • FIG. 1 shows the application device 1 in the ready-to-use operating position, ie. H. with open application head 3. Outside the application times, the application head 3 is covered by a cap, not shown, which is attached, for example, to a thread 4 on the container 2. Thus, the application head 3 is sealed from the environment, so that drying of the liquid hair dye is effectively prevented.
  • the applicator body 31 communicates with the liquid hair dye or the application liquid in conjunction to the liquid in the manner of a wick To promote capillary action from the container and to provide for the application to the hair.
  • the porous application body 31 has a material structure with continuous pores in order to achieve the corresponding capillary action.
  • the application body 31 consists in particular of a fibrous, sponge, foam, felt or sintered material-like material. The advantage of such a designed applicator body 31 is not only in the reliable promotion of the hair dye but also in the high fluid absorbency. Namely, the high liquid absorption capability prevents unwanted leakage or dripping of the hair dye from the application device 1.
  • the application body 31 is preferably block-shaped (not shown) or designed with a plurality of pin-shaped projections 32.
  • the embodiment with a plurality of pin-shaped projections 32 increases the effective surface of the application body 31, so that better coloring results are achieved when sweeping the hair.
  • the comb teeth 33 which are likewise formed immediately adjacent to the application body 31 on the application head 3, are used for disentangling the hair during application of the application device 1. This disentangling of the hair results in a more uniform application of the color to the hair.
  • the individual comb teeth 33 are integrally connected to at least one comb element 34 in order to simplify handling and production in general. Furthermore, it makes sense to attach the comb teeth 33 or comb elements 34 releasably to the application head 3, in order to permit an application without comb teeth 33 or comb elements 34, depending on the particular case of use.
  • the comb teeth 33 protrude in the longitudinal direction of the application device 1 with respect to the application body 31 in order to prevent contact of the scalp with the application body 31 or the application fluid, especially in hair applications.
  • the comb teeth 33 are arranged in a circle around the applicator body 31 lying around on the application head 3.
  • the hair is first unraveled during the application of the application device 1, regardless of the respective coating movement direction, before the actual application of the hair dye takes place. This gives improved staining results. 2 application liquids
  • the resulting colorant was mixed with percarbamide in the mixing ratio of colorant: developer 10: 1 immediately before use as described above. Subsequently, the application liquid was applied with the application device according to the invention on the fibers and rinsed after a contact time of 30 minutes.
  • the resulting colorant was mixed with percarbamide in the mixing ratio of colorant: developer 10: 1 immediately before use as described above. Subsequently, the application liquid was applied with the application device according to the invention on the fibers and rinsed after a contact time of 30 minutes.
  • Turpinal ® SL 1-hydroxyethane-1, 1-diphosphonic acid (about 58 - 61%

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Inorganic Chemistry (AREA)
  • Epidemiology (AREA)
  • Birds (AREA)
  • Chemical & Material Sciences (AREA)
  • Emergency Medicine (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)

Abstract

L'objet de la présente demande concerne un dispositif d'application (1) pour utiliser un liquide d'application sur des fibres de kératine comprenant au moins un récipient (2) destiné à recevoir le liquide d'application, une tête d'application (3) qui est reliée à au moins un récipient (2), et comprend un corps d'application poreux (31) pour appliquer le liquide d'application par brossage des fibres, le liquide d'application qui contient au moins un produit semi-fini de colorant d'oxydation étant mélangé aussitôt avant l'utilisation avec un apprêt oxydant.
EP07729636A 2006-06-02 2007-05-30 Dispositif d'application pour utiliser un liquide d'application sur des fibres de kératine Ceased EP2023766A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102006026269A DE102006026269A1 (de) 2006-06-02 2006-06-02 Applikationsvorrichtung zur Anwendung einer Applikationsflüssigkeit auf keratinischen Fasern
PCT/EP2007/055216 WO2007141163A1 (fr) 2006-06-02 2007-05-30 Dispositif d'application pour utiliser un liquide d'application sur des fibres de kératine

Publications (1)

Publication Number Publication Date
EP2023766A1 true EP2023766A1 (fr) 2009-02-18

Family

ID=38565458

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07729636A Ceased EP2023766A1 (fr) 2006-06-02 2007-05-30 Dispositif d'application pour utiliser un liquide d'application sur des fibres de kératine

Country Status (3)

Country Link
EP (1) EP2023766A1 (fr)
DE (1) DE102006026269A1 (fr)
WO (1) WO2007141163A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102019208323A1 (de) * 2019-06-07 2020-12-10 Henkel Ag & Co. Kgaa Haarbehandlungsprodukt mit mehreren Bestandteilen

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050072442A1 (en) * 2002-02-20 2005-04-07 Louis Licari Self-contained hair-coloring system for touch-up, highlighting and less than full treatment applications
US7055528B2 (en) * 2003-03-27 2006-06-06 Alpine Pharmaceuticals Applicator
EP1642563B1 (fr) * 2004-09-24 2019-06-26 Noxell Corporation Méthode de teinture rapide des cheveux

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2007141163A1 *

Also Published As

Publication number Publication date
DE102006026269A1 (de) 2007-12-06
WO2007141163A1 (fr) 2007-12-13

Similar Documents

Publication Publication Date Title
EP1239815B1 (fr) Colorant solide pour fibres de keratine
EP2152226A2 (fr) Colorants d'oxydation destinés à colorer des fibres kératiniques au moyen d'oxygène atmosphérique comme unique agent d'oxydation
DE10120914A1 (de) Pflegende Wirkstoffkombination für Haarfärbemittel
DE102005062830A1 (de) Oxidationsfärbemittel zur Färbung keratinhaltiger Fasern
WO2008022958A2 (fr) Colorant capillaire avec huile et hydrolysat de protéines
DE102004020501A1 (de) Verwendung von Organosilikon-Copolymeren in Haarfärbemitteln
EP1696871B1 (fr) Colorant d'oxydation en tube
DE102005055270A1 (de) Neuer Farbstoffvorproduktkombinationen
EP1789015B1 (fr) Procede pour changer la couleur de fibres keratiniques selon la mode
EP2037871B1 (fr) Colorants d'oxydation pour la coloration de fibres kératiniques avec l'oxygène de l'air comme unique agent oxydant
WO2008012182A2 (fr) Coloration capillaire contenant du beurre de karité
EP2558190B1 (fr) Procédé de fabrication d'un colorant pour fibres keratiniques
EP1453477B1 (fr) Combinaison revelateurs-coupleur contenant du 2,4-dichloro-3-aminophenol
WO2009065632A1 (fr) Colorants par oxydation pour la coloration de fibres kératiniques avec l'oxygène de l'air en tant qu'oxydant exclusif
EP2023766A1 (fr) Dispositif d'application pour utiliser un liquide d'application sur des fibres de kératine
WO2006097167A1 (fr) Agent de coloration sans ammoniac destine a colorer des fibres contenant de la keratine et comprenant de l'oxygene atmospherique utilise comme agent d'oxydation unique
EP2029096A1 (fr) Dispositif d'application pour utiliser un liquide d'application sur des fibres de kératine
EP2026755A2 (fr) Dispositif d'application pour utiliser un liquide d'application sur des fibres de kératine
DE10048733A1 (de) Oxidationsfärbemittel mit 2-Amino-5-methylphenol
DE102005062645A1 (de) Neue Kupplerkomponenten
DE102005025494A1 (de) Mehrstufiges Färbeverfahren für keratinische Fasern
DE102005034146A1 (de) Verfahren und Kit zur oxidativen Färbung keratinischer Fasern
DE102005055268A1 (de) Neue Farbstoffvorproduktkombinationen
DE202004014826U1 (de) Mittel zur Tönung keratinischer Fasern, insbesondere menschlicher Haare

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20081105

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL BA HR MK RS

17Q First examination report despatched

Effective date: 20120612

DAX Request for extension of the european patent (deleted)
REG Reference to a national code

Ref country code: DE

Ref legal event code: R003

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 20121207