WO2005117816A1 - Kationische chinoxalinthiazolazofarbstoffe enthaltende färbemittel - Google Patents
Kationische chinoxalinthiazolazofarbstoffe enthaltende färbemittel Download PDFInfo
- Publication number
- WO2005117816A1 WO2005117816A1 PCT/EP2005/003506 EP2005003506W WO2005117816A1 WO 2005117816 A1 WO2005117816 A1 WO 2005117816A1 EP 2005003506 W EP2005003506 W EP 2005003506W WO 2005117816 A1 WO2005117816 A1 WO 2005117816A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- anion
- alkyl
- amino
- methyl
- 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
Links
- 0 Cc(cc1)ccc1N(*)* Chemical compound Cc(cc1)ccc1N(*)* 0.000 description 2
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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
-
- 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
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
-
- 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
Definitions
- the present invention relates to certain cationic quinoxalinthiazoleazo dyes for keratin fibers, such as hair, wool or furs.
- oxidation dyes which result from the oxidative coupling of one or more developer components with one or more coupler components
- direct dyes are generally used.
- oxidation-stable, direct dyes can be added to the oxidative system in order to achieve special color effects.
- Direct dyes are incorporated into suitable substrates to be applied to the fiber. This process, commonly known as tinting, is easy to use, extremely mild and is characterized by little damage to the keratin fiber, since no ammonia or peroxide is added.
- the dyes used here have to meet some requirements. For example, they have to be harmless from a toxicological and dermatological point of view and enable the coloring to be achieved in the desired intensity and brilliance.
- the dyeings obtained must also have good lightfastness and resistance to shampoos or hair care products and good rub fastness.
- a combination of different non-oxidative dyes is generally used for a direct, non-oxidative colorant for keratin fibers needed to achieve certain nuances. Since the selection of such dyes, which sufficiently meet the requirements mentioned, is limited, there is still a great need for such dyes.
- the object of the present invention is therefore to provide direct dyes for dyeing keratin fibers, in particular human hair, which meet these requirements.
- cationic quinoxalinthiazoleazo dyes of the general formula (I) can be applied very gently to keratin fibers as direct dyes in colorants without the addition of an oxidizing agent. Since these dyes are stable to oxidizing agents, they can also be used in brightening colorants containing oxidizing agents, for example peroxides.
- the subject of the present invention is therefore
- an oxidative colorant for keratin fibers based on at least one oxidation dye precursor, the agents (a), (b) and (c) being characterized in that they each contain at least one cationic quinoxalinthiazoleazo dye of the general formula (I),
- R1 for a hydrogen atom, an amino group, a Ci-C ⁇ -alkylamino group, a C ⁇ -C 6 - ⁇ /, ⁇ / -dialkylamino group, a C ⁇ -C 6 -alkylcyano group, a hydroxyl group, a nitro group, a methoxymethyl group, a tert - Butyl group, a / so-propyl group, a -C 6 alkyl group, a C 6 alkyloxy group, a C 6 hydroxyalkyl group, a C 6 alkyl carboxylic acid group, a C 1 -C 6 alkyl carboxylic acid ester group, a Ci-C ⁇ -alkylsulfonic acid group, a Ci-C ⁇ -alkylsulfonic acid ester group or a carboxylic acid group (-COOH); R2 represents a group of the general formulas (II) to (VI), (II) (111) (IV)
- R1 ' is equal to a hydrogen atom, an amino group, a C 6 -C 6 -alkylamino group, a C 1 -C 6 - ⁇ /, / V-dialkylamino group, a C 1 -C 6 -alkylcyano group, a hydroxyl group, a nitro group, a methoxymethyl group, one fe / ⁇ -butyl group, a / so-propyl group, a C ⁇ -C 6 alkyl group, a C ⁇ -C 6 alkyloxy group, a Ci-C ⁇ -hydroxyalkyl group, a C ⁇ -C 6 alkylcarboxylic acid group, a C ⁇ -C 6 -alkyl carboxylic acid ester group, a Ci-C ⁇ -alkyl sulfonic acid group, a Ci-C ⁇ -alkyl sulfonic acid ester group or a carboxylic acid group (-COOH); R4 'is
- R6 and R7 independently of one another are hydrogen, an amino group, a C 6 -C 6 -alkylamino group, a C 1 -C 6 -N, N-dialkylamino group, a C 1 -C 6 -N, N- (dihydroxyalkyl) amino group, Fluorine, chlorine, bromine, iodine, a cyano group, a Ci-C ⁇ -alkylcyano group, a methoxymethyl group, a tert-butyl group, an isopropyl group, a Ci-C ⁇ -alkyl group, a C ⁇ -C 6 alkyloxy group, a C ⁇ -C 6 - Hydroxyalkyl group, a Ci-C ß -hydroxy-alkyloxy group, a Ci-C ⁇ -alkylcarboxylic acid group, a CrC ⁇ -alkyl-carboxylic acid ester group, a Ci-C ⁇ -alkylcarboxylic acid amide group
- R3 represents a C 1 -C 6 -alkyl group, a C 2 -C -hydroxyalkyl group or a C -C 6 -polyhydroxyalkyl group; where the alkyl groups can each be branched or linear, and X " ⁇ an anion, preferably a sulfate anion, a phosphate anion, a hydrogen phosphate anion, an oxalate anion, a formate anion, an acetate anion, a citrate anion, a tartrate anion, a malonate anion, a pyruvate anion, an iodide anion represents a chloride anion, a bromide anion or a methyl sulfate anion, with the chloride anion, bromide anion and the methyl sulfate anion being particularly preferred.
- an anion preferably a sulfate anion, a phosphate anion, a hydrogen phosphate anion
- Examples of suitable cationic quinoxalinthiazoleazo dyes of the general formula (I) are: 6-carboxy-2 - ⁇ (E) - [4- (diethylamino) phenyl] azo ⁇ -3-methyl [1,3] thiazolo [4,5 -b] quinoxaline-3-ium-methyl sulfate, 6-carboxy-2 - ((E) - ⁇ 4 - [(2-hydroxyethyl) amino] phenyl ⁇ azo) -3-methyl [1, 3] thiazolo [4, 5-b] quinoxaline-3-ium methyl sulfate, 2 - ((E) - ⁇ 4- [bis (2-hydroxyethyl) amino] phenyl ⁇ azo) -6-carboxy-3-methyl [1,3] thiazolo [ 4,5- b] quinoxalin-3-ium-methyl sulfate, 6-carboxy-2 - ((E) - ⁇ 4 - [
- Preferred compounds of the general formula (I) are 6-carboxy-2 - ⁇ (E) - [4- (diethylamino) phenyl] azo ⁇ -3-methyl [1,3] thiazolo [4,5-b] quinoxalin-3 -ium methyl sulfate, 6-carboxy-2 - ((E) - ⁇ 4 - [(2-hydroxyethyl) amino] phenyl ⁇ azo) -3-methyl [1, 3] thiazolo [4,5-b] quinoxaline- 3-ium methyl sulfate, 2 - ((E) - ⁇ 4- [bis (2- hydroxyethyl) amino] phenyl ⁇ azo) -6-carboxy-3-methyl [1,3] thiazolo [4,5-b] quinoxalin-3-ium-methyl sulfate, 6-carboxy-2 - ((E) - ⁇ 4 - [(2-hydroxyethyl) - (methyl) amino]
- the dye derivatives according to the invention of the general formula (I) can be obtained by standard operations from commercially available or easily manufactured components.
- the colorants according to the invention containing the cationic quinoxalinthiazoleazo dyes of the general formula (I) enable uniform coloring of keratin fibers, in particular human hair, with good stability against light, sweat and shampooing, intensive, brilliant colorations being obtained even under gentle conditions.
- the cationic quinoxalinthiazoleazo dyes of the general formula (I) are preferably present in the colorants according to the invention in a total amount of 0.01 to 10 percent by weight, in particular 0.1 to 8 percent by weight.
- the colorant (a) according to the invention can also include other known direct-dyeing dyes from the group consisting of nitro dyes, azo dyes, athraquinone dyes and triphenylmethane dyes, such as, for example, 1,4-bis [(2-hydroxyethyl) amino] -2-nitrobenzene, 1 - (2-Hydroxyethyl) amino-2-nitro-4- [di (2-hydroxyethyl) amino] benzene, (HC Blue No. 2), 1-Amino-3-methyl-4 - [(2-hydroxyethyl) amino] -6-nitrobenzene, (HC Violet No.
- the abovementioned direct dyes can be present in a total amount of about 0.01 to 4 percent by weight, the total amount of dyes in the colorant according to the invention preferably being about 0.01 to 10 percent by weight, in particular 0.1 to 5 percent by weight.
- the oxidation coloring agent (c) according to the invention which is used with an oxidizing agent (in particular hydrogen peroxide or its
- Addition compounds is mixed, contains in addition to the dyes of the general formula (I) also oxidation dye precursors.
- suitable oxidation dye precursors are as follows
- developer substances 1,4-diamino-benzene (p-phenylenediamine),
- 1,4-diamino-2-methyl-benzene (p-toluenediamine), 1,4-diamino-2,6-dimethyl-benzene, 1,4-diamino ⁇ 3,5-diethyl-benzene, 1,4-diamino -2,5-dimethyl-benzene, 1,4-diamino-2,3-dimethyl-benzene, 2-chloro-1,4-diaminobenzene, 1,4-diamino-2- (thiophene-2-yl) benzene, 1,4-diamino-2- ( thiophene-3-yl) benzene, 1,4-diamino-2- (pyridin-3-yl) benzene, 2,5-diamino-biphenyl, 1,4-diamino-2-methoxymethyl-benzene, 1,4-diamino -2-aminomethylbenzene, 1,4
- Coupler substances N- (3-dimethylaminophenyl) urea, 2,6-diamino-pyridine, 2-amino-4 - [(2-hydroxyethyl) amino] anisole, 2,4-diamino-1- fluoro-5-methyl-benzene, 2,4-diamino-1-methoxy-5-methyl-benzene, 2,4-diamino-1-ethoxy-5-methyl-benzene, 2,4-diamino-1 - (2-hydroxy-ethoxy) -5-methyl-benzene, 2,4-di [(2-hydroxyethyl) amino ] -1,5-dimethoxy-benzene, 2,3-diamino-6-methoxy-pyridine, 3-amino-6-methoxy-2- (methylamino) pyridine, 2,6-diamino-3,5-dimethoxy- pyridine, 3,5-diamino-2,6-dimethoxy
- the total amount of the oxidation dye precursors contained in the colorant (c) according to the invention is about 0.01 to 12 percent by weight, in particular about 0.2 to 6 percent by weight.
- the colorant (a), (b) or (c) according to the invention can furthermore all known and customary additives for such preparations, for example perfume oils, complexing agents, waxes, preservatives, thickeners, antioxidants, alginates, guar gum, hair-care substances such as cationic Contain polymers or lanolin derivatives, or anionic, nonionic, amphoteric or cationic surface-active substances.
- perfume oils for example perfume oils, complexing agents, waxes, preservatives, thickeners, antioxidants, alginates, guar gum, hair-care substances such as cationic Contain polymers or lanolin derivatives, or anionic, nonionic, amphoteric or cationic surface-active substances.
- Amphoteric or nonionic surface-active substances for example betaine surfactants, propoinates and glycinates, such as, for example, cocoamphoglycinates or cocoamphdiglacinates, are preferably ethoxylated surfactants with 1 to 1000 ethylene oxide units, preferably with 1 to 300 ethylene oxide units, such as, for example, glyceride alkoxylates, for example castor oil which is ethoxylated with 25 ethylene oxide units, polyglycolamides, ethoxylated alcohols and ethoxylated fatty alcohols (fatty alcohol alkoxylates) and ethoxylated fatty acid sugar esters, in particular ethoxylated sorbitan fatty acid esters.
- the abovementioned constituents are used in the amounts customary for such purposes, for example the surface-active substances in a concentration of 0.1 to 30 percent by weight, and the care substances in an amount of 0.1 to 5 percent by weight.
- the colorant (a), (b) or (c) according to the invention can, in particular if it is a hair colorant, in the form of a powder or granules which is dissolved in an aqueous or aqueous-alcoholic preparation before use, or else an aqueous or aqueous-alcoholic solution, a cream, a gel, an emulsion or an aerosol foam are present, the hair dye both in the form of a one-component preparation and in the form of a multi-component preparation, for example in the form of a two-component preparation in which the respective dye derivative of the general formulas (I) and (II) is packaged separately from the other constituents and the ready-to-use hair dye is only prepared immediately before use by mixing the two components.
- the colorant (a), (b) or (c) according to the invention generally has a pH of about 2 to 11, preferably about 5 to 10, and in particular a neutral to basic pH of about 7 to 10.
- Suitable acids include the following acids: ⁇ -hydroxycarboxylic acids, such as glycolic acid, lactic acid, tartaric acid, citric acid or malic acid, ascorbic acid, gluconic acid lactone, acetic acid, hydrochloric acid or phosphoric acid, and mixtures of these acids.
- Suitable bases include, in particular, sodium carbonate, sodium hydrogen carbonate, alkanolamines, for example monoethanolamine or triethanolamine, ammonia, aminomethylpropanol and sodium hydroxide and mixtures thereof.
- the colorant according to the invention can be used with one or more oxidizing agents (brightening; oxidizing coloring agent) or without an oxidizing agent (non-oxidative coloring agent).
- the coloring agent according to the invention is generally applied by applying an amount sufficient for hair coloring, depending on the length of the hair about 30 to 120 grams, of the hair coloring agent to the hair, the hair coloring agent at about 15 to 45 degrees Celsius for about 1 to 60 minutes, preferably 5 to 30 minutes, leave to act, then rinse the hair thoroughly with water, if necessary, wash with a shampoo and / or aftertreated with a hair conditioning agent and finally dry.
- the agent is mixed with an oxidizing agent before use.
- the coloring agent described above can furthermore, provided that no oxidizing agents are added to the coloring material, for cosmetic agents contain conventional natural or synthetic polymers or modified polymers of natural origin, whereby a strengthening of the hair is achieved simultaneously with the coloring. Such agents are generally referred to as tinting or color strengthening agents.
- polyvinylpyrrolidone polyvinyl acetate
- polyvinyl alcohol or polyacrylic compounds such as polyacrylic acid or polymethacrylic acid
- basic polymers of esters of polyacrylic acid polymethylacrylic acid and amino alcohols, for example their salts or quaternization products
- polyacrylonitrile compounds and polyvinyl acetate compounds of this type and polyvinyl acetate compounds
- polyvinyl acetate compounds such as polyvinyl pyrrolidone vinyl acetate
- chitosan (deacetylated chitin) or chitosan derivatives for example, can be used as natural polymers or modified natural polymers.
- the aforementioned polymers can be present in the colorant (a) according to the invention in the amounts customary for such agents, in particular in an amount of about 1 to 5 percent by weight.
- the pH of the tinting or color fixing agent according to the invention is preferably about 6 to 9.
- the hair dye with additional setting is used in a known and customary manner by moistening the hair with the setting agent, setting (inserting) the hair for the hairstyle and subsequent drying.
- the colorants (a), (b) and (c) according to the invention enable a uniform, intensive and permanent coloring of keratin fibers (for example human hair, wool or furs) without any noteworthy staining of the skin or scalp, this dyeing surviving five or more hair washes without a noticeable fading of the hair color even in the case of the dye (a).
- keratin fibers for example human hair, wool or furs
- Example 1 Hair dye without oxidizing agent
- the coloring solution is adjusted to a pH of 7 to 10 by adding ammonia.
- the hair is dyed by applying a sufficient amount of the colorant to the hair and rinsing the hair with lukewarm water after a contact time of 30 minutes at 40 ° C. and finally drying it.
- the dyeing results are summarized in Table 1 below.
- Example 2 Hair dye for simultaneous lightening and dyeing (with oxidizing agent)
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- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05716519A EP1761239A1 (de) | 2004-06-04 | 2005-04-04 | Kationische chinoxalinthiazolazofarbstoffe enthaltende färbemittel |
| CA002566879A CA2566879A1 (en) | 2004-06-04 | 2005-04-04 | Cationic quinoxaline thiazole azo dye-containing colorants |
| JP2007513707A JP2008501648A (ja) | 2004-06-04 | 2005-04-04 | カチオン性キノキサリンチアゾールアゾ染料を含有した着色剤 |
| MXPA06013836A MXPA06013836A (es) | 2004-06-04 | 2005-04-04 | Colorantes que contienen tintes zo de quinoxalin tiazol cationicos. |
| US11/569,913 US7500994B2 (en) | 2004-06-04 | 2005-04-04 | Cationic quinoxaline thiazole azo dye-containing colorants |
| AU2005249181A AU2005249181B2 (en) | 2004-06-04 | 2005-04-04 | Cationic quinoxaline thiazole azo dye-containing colorants |
| BRPI0510774-1A BRPI0510774A (pt) | 2004-06-04 | 2005-04-04 | tinturas catiÈnicas dotadas de corante de quinoxalina-tiazol-azo |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004027426A DE102004027426A1 (de) | 2004-06-04 | 2004-06-04 | Kationische Chinoxalinthiazolazofarbstoffe enthaltende Färbemittel |
| DE102004027426.6 | 2004-06-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2005117816A1 true WO2005117816A1 (de) | 2005-12-15 |
Family
ID=34962503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2005/003506 Ceased WO2005117816A1 (de) | 2004-06-04 | 2005-04-04 | Kationische chinoxalinthiazolazofarbstoffe enthaltende färbemittel |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7500994B2 (de) |
| EP (1) | EP1761239A1 (de) |
| JP (1) | JP2008501648A (de) |
| CN (1) | CN1964692A (de) |
| AU (1) | AU2005249181B2 (de) |
| BR (1) | BRPI0510774A (de) |
| CA (1) | CA2566879A1 (de) |
| DE (1) | DE102004027426A1 (de) |
| MX (1) | MXPA06013836A (de) |
| WO (1) | WO2005117816A1 (de) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7977482B2 (en) | 2006-10-23 | 2011-07-12 | The Procter & Gamble Company | Dark coloured azo dyes |
| CN103374020A (zh) * | 2012-04-16 | 2013-10-30 | 南京大学连云港高新技术研究院 | 一类含萘环的噻唑[4,5-b]并喹喔啉类衍生物及其制法 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10029929A1 (de) * | 2000-06-17 | 2001-12-20 | Henkel Kgaa | Mittel zum Färben von keratinhaltigen Faser |
-
2004
- 2004-06-04 DE DE102004027426A patent/DE102004027426A1/de not_active Withdrawn
-
2005
- 2005-04-04 US US11/569,913 patent/US7500994B2/en not_active Expired - Lifetime
- 2005-04-04 EP EP05716519A patent/EP1761239A1/de not_active Withdrawn
- 2005-04-04 JP JP2007513707A patent/JP2008501648A/ja not_active Withdrawn
- 2005-04-04 CA CA002566879A patent/CA2566879A1/en not_active Abandoned
- 2005-04-04 CN CNA2005800182314A patent/CN1964692A/zh active Pending
- 2005-04-04 AU AU2005249181A patent/AU2005249181B2/en not_active Ceased
- 2005-04-04 MX MXPA06013836A patent/MXPA06013836A/es not_active Application Discontinuation
- 2005-04-04 BR BRPI0510774-1A patent/BRPI0510774A/pt not_active IP Right Cessation
- 2005-04-04 WO PCT/EP2005/003506 patent/WO2005117816A1/de not_active Ceased
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10029929A1 (de) * | 2000-06-17 | 2001-12-20 | Henkel Kgaa | Mittel zum Färben von keratinhaltigen Faser |
Non-Patent Citations (2)
| Title |
|---|
| RADULESCU CRISTAINA: "Pharmacodynamic aspects of cationic dyes derivatives of compact condensed systems", REV. CHIM., vol. 54, no. 12, 2003, BUCAREST, pages 965 - 968, XP009048826 * |
| RADULESCU CRISTIANA: "Heteropolysalts of organic bases.", REV. CHIM., vol. 55, no. 4, 2004, BUCAREST, pages 269 - 272, XP009048825 * |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7977482B2 (en) | 2006-10-23 | 2011-07-12 | The Procter & Gamble Company | Dark coloured azo dyes |
| US8152861B2 (en) | 2006-10-23 | 2012-04-10 | The Procter & Gamble Company | Dark coloured azo dyes |
| CN103374020A (zh) * | 2012-04-16 | 2013-10-30 | 南京大学连云港高新技术研究院 | 一类含萘环的噻唑[4,5-b]并喹喔啉类衍生物及其制法 |
| CN103374020B (zh) * | 2012-04-16 | 2016-04-27 | 南京大学连云港高新技术研究院 | 一类含萘环的噻唑[4,5-b]并喹喔啉类衍生物及其制法 |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2005249181A1 (en) | 2005-12-15 |
| CN1964692A (zh) | 2007-05-16 |
| EP1761239A1 (de) | 2007-03-14 |
| BRPI0510774A (pt) | 2007-11-20 |
| MXPA06013836A (es) | 2007-03-01 |
| CA2566879A1 (en) | 2005-12-15 |
| JP2008501648A (ja) | 2008-01-24 |
| DE102004027426A1 (de) | 2005-12-22 |
| AU2005249181B2 (en) | 2008-02-07 |
| US7500994B2 (en) | 2009-03-10 |
| US20080104771A1 (en) | 2008-05-08 |
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