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Dying composition comprising a particular disulfide dye and dying method thereof

A disulfide, dyeing method technology, applied in the field of hair dyeing and human keratin fibers, can solve the problems of color discoloration and the like

Inactive Publication Date: 2010-12-08
LOREAL SA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these dyes may undergo color shifting when applied

Method used

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  • Dying composition comprising a particular disulfide dye and dying method thereof
  • Dying composition comprising a particular disulfide dye and dying method thereof
  • Dying composition comprising a particular disulfide dye and dying method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0293]

[0294] A solution consisting of 500 mg cystamine dihydrochloride (2.22 mmol) and 20 ml 0.05M borate buffer (pH 9) was prepared, the buffer adjusted to pH 9 by addition of molar sodium hydroxide. To this solution was added 4.6 grams of reactive blue 44 [Cas 12225-56-8] (60% purity, ie 4.44 mmol). The mixture was stirred at room temperature for 18 hours, and the precipitated dye was filtered and dried. 1.67 g of blue dye (I) were recovered.

Embodiment 2

[0296]

[0297] A solution consisting of 500 mg cystamine dihydrochloride (2.22 mmol) and 20 ml 0.05M borate buffer (pH 9) was prepared, the buffer adjusted to pH 9 by addition of molar sodium hydroxide. To this solution was added 6.23 grams of Active Orange 64 [Cas 61901-80-2] (purity 50%, ie 4.44 mmol). The mixture was stirred at room temperature for 18 hours, and the precipitated dye was filtered and dried. 2.03 g of orange dye (II) were recovered.

Embodiment 3

[0299]

[0300] Basic cystamine (552.2 mg; 3.62 mmol) obtained by addition of sodium hydroxide and extraction with ethyl acetate was dissolved in 2 ml of pentanol using cystamine dihydrochloride. Add a suspension of 2-[(4-methoxyphenyl)diazinyl]-1,3-dimethyl 1H-imidazol-3-ium chloride (2.42 mg; 9.1 mmol) in 80 ml of dichloromethane liquid. The mixture was warmed to 50°C and kept stirring for 1 hour. Concentration in vacuo (removal of dichloromethane) was carried out, 20 ml of water were added and the reaction mixture was maintained at 50° C. for a further hour. The mixture was then cooled and poured into 50 ml of pentanol; a red precipitate appeared, which was filtered, washed with acetone, and dried in vacuo. This gave 1.1 g of a dark red powder having the above structure.

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Abstract

Disclosed herein is a dyeing composition comprising a particular disulphide dye and a method of dyeing human keratin fibers, such as hair, using this composition. This composition makes it possible to obtain particularly fast chromatic colorations.

Description

technical field [0001] The object of the present invention is a dyeing composition containing specific disulfide dyes and a method for dyeing keratin fibres, in particular human keratin fibres, in particular hair, using this composition. Still another object of the invention are novel disulfide dyes. Background technique [0002] It is known to dye keratin fibers, especially human keratin fibers, by direct dyeing. The usual procedure in direct dyeing consists in applying direct dyes, which are colored or coloring molecules having an affinity for these fibers, to spreading them, and then also to rinsing the fibers, on the keratin fibers. [0003] Such direct dyes which are commonly used are, for example, dyes of the benzene-nitro group, anthraquinone dyes, nitropyridines, azo, xanthene, acridine, azine or triarylmethanes. [0004] The dyeings achieved with direct dyes are temporary or semi-permanent, because of the interactive nature of the direct dyes' attachment to the ke...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61K8/49A61Q5/10A61K8/46
CPCC07D251/52A61K2800/94A61K8/494A61Q5/10A61K8/4953A61K8/46A61Q5/065C07D251/50A61K8/4946A61K8/4926
Inventor N·多布雷斯G·热奈因
Owner LOREAL SA