Method for dyeing keratin material, comprising the use of an organic C1-C6-alkoxy-silane and an alkalising agent

Patent metadata

Field	Value
Publication number	US-11826586-B2
Application number	US-202017631829-A
Country	US
Kind code	B2
Filing date	Jun 8, 2020
Priority date	Aug 1, 2019
Publication date	Nov 28, 2023
Grant date	Nov 28, 2023

Abstract

An object of the present disclosure is a process for coloring keratinous material, in particular human hair. The process includes applying on the keratinous material a first composition (A). The first composition (A) includes (A1) one or more organic C1-C6 alkoxy silanes and/or condensation products thereof, and (A2) at least one colorant compound selected from the group of pigments and/or direct dyes. The process further includes applying a second composition (B) on the keratinous material. The second composition (B) includes (B1) at least one alkalizing agent.

First claim

The invention claimed is:

1. A process of dyeing keratinous material comprising:
treating the keratinous material with
a first composition (A) comprising:
(A1) one or more organic C 1 -C 6 alkoxy silanes and/or condensation products thereof, and
(A2) at least one colorant compound selected from the group consisting of pigments and direct dyes, and
a second composition (B) comprising:
(B1) at least one alkalizing agent.

2. The process according to claim 1 , characterized in that the first composition (A) comprises one or more organic C 1 -C 6 alkoxy silanes (A1) of the formula (S-I) and/or (S-II),
R 1 R 2 N—L—Si(OR 3 ) a (R 4 ) b   (S-I)

where
R 1 , R 2 independently represent a hydrogen atom or a C 1 -C 6 alkyl group,
L is a linear or branched divalent C 1 -C 20 alkylene group,
R 3 , R 4 independently of one another represent a C 1 -C 6 alkyl group,
a, stands for an integer from 1 to 3, and
b stands for the integer 3-a, and
(R 5 O) c (R 6 ) d Si—(A) c -[NR 7 -(A′)] f -[O—(A″)] g -[NR 8 -(A′″)] h -Si(R 6 ′) d ′(OR 5 ′) c ′  (S-II),

where
R5, R5′, R5″, R6, R6′ and R6″ independently represent a C 1 -C 6 alkyl group,
A, A′, A″, A′″ and A″ ″ independently represent a linear or branched divalent C 1 -C 20 alkylene group,
R 7 and R 8 independently represent a hydrogen atom, a C 1 -C 6 alkyl group, a hydroxy C 1 -C 6 alkyl group, a C 2 -C 6 alkenyl group, an amino C 1 -C 6 alkyl group or a group of formula (S-III),
(A″″)—Si(R 6 ″) d ″(OR 5 ″) c ″  (S-III),

c, stands for an integer from 1 to 3,
d stands for the integer 3-c,
c′ stands for an integer from 1 to 3,
d′ stands for the integer 3-c′,
c″ stands for an integer from 1 to 3,
d″ stands for the integer 3-c″,
e stands for 0 or 1,
f stands for 0 or 1,
g stands for 0 or 1,
h stands for 0 or 1,
provided that at least one of e, f, g and h is different from 0, and/or their condensation products.

3. The process according to claim 1 , characterized in that the first composition (A) comprises at least one C 1 -C 6 organic alkoxysilane (A1) of formula (S-1) selected from the group consisting of
(3 aminopropyl)triethoxysilane
(3 aminopropyl)trimethoxysilane
(2 aminoethyl)triethoxysilane
(2 aminoethyl)trimethoxysilane
(3 dimethylaminopropyl)triethoxysilane
(3 dimethylaminopropyl)trimethoxysilane
(2 dimethylaminoethyl)triethoxysilane,
(2 dimethylaminoethyl)trimethoxysilane, and condensation products thereof.

4. The process according to claim 1 , characterized in that the first composition (A) comprises one or more organic C 1 -C 6 alkoxy silanes (A1) of formula (S-IV),
R 9 Si(OR 10 ) k (R 11 ) m   (S-IV),

where
R 9 represents a C 1 -C 12 alkyl group,
R 10 represents a C 1 -C 6 alkyl group,
R 11 represents a C 1 -C 6 alkyl group,
k is an integer from 1 to 3, and
m stands for the integer 3-k,
and condensation products thereof.

5. The process according to claim 1 , characterized in that the first composition (A) comprises at least one C 1 -C 6 organic alkoxysilane (A1) of formula (S-IV) selected from the group consisting of
methyltrimethoxysilane
methyltriethoxysilane
ethyltrimethoxysilane
ethyltriethoxysilane
hexyltrimethoxysilane
hexyltriethoxysilane
octyltrimethoxysilane
octyltriethoxysilane
dodecyltrimethoxysilane,
dodecyltriethoxysilane,
and condensation products thereof.

6. The process according to claim 1 , characterized in that the first composition (A) comprises at least one inorganic pigment (A2) selected from the group consisting of colored metal oxides, metal hydroxides, metal oxide hydrates, silicates, metal sulfides, complex metal cyanides, metal sulfates, bronze pigments, mica- or mica-based colored pigments coated with at least one metal oxide, and metal oxychlorides.

7. The process according to claim 1 , characterized in that the first composition (A) comprises at least one organic pigment (A2) selected from the group consisting of carmine, quinacridone, phthalocyanine, sorghum, blue pigments having the color index numbers Cl 42090, CI 69800, CI 69825, CI 73000, CI 74100, CI 74160, yellow pigments having the color index numbers CI 11680, CI 11710, CI 15985, CI 19140, CI 20040, CI 21100, CI 21108, CI 47000, CI 47005, green pigments with Color Index numbers CI 61565, CI 61570, CI 74260, orange pigments with Color Index numbers CI 11725, CI 15510, CI 45370, CI 71105, red pigments with Color Index numbers CI 12085, CI 12120, CI 12370, CI 12420, CI 12490, CI 14700, CI 15525, CI 15580, CI 15620, CI 15630, CI 15800, CI 15850, CI 15865, CI 15880, CI 17200, CI 26100, CI 45380, CI 45410, CI 58000, CI 73360, CI 73915 and CI 75470.

8. The process according to claim 1 , characterized in that the first composition (A) comprises at least one colored pigment (A2) selected from the group consisting of pigments based on a lamellar substrate platelet, pigments based on a lenticular substrate platelet, and pigments based on a substrate platelet comprising a vacuum-metallized pigment.

9. The process according to claim 1 , characterized in that the first composition (A) comprises at least one cosmetic ingredient selected from the group consisting of hexamethyldisiloxane, octamethyltrisiloxane, decamethyltetrasiloxane, hexamethylcyclotrisiloxane, octamethylcyclotetrasiloxane, and decamethylcyclopentasiloxane.

10. The process according to claim 1 , characterized in that the second composition (B) comprises at least one alkalizing agent (B1) selected from the group consisting of ammonia, C 2 -C 6 alkanolamines, basic amino acids, alkali metal hydroxides, alkaline earth metal hydroxides, alkali metal silicates, alkali metal metasilicates, alkaline earth metal silicates, alkaline earth metal metasilicates, alkali metal carbonates, and alkaline earth metal carbonates.

11. The process according to claim 1 , characterized in that the second composition (B) comprises at least one alkalizing agent (B1) selected from the group consisting of ammonia, 2-aminoethan-l-ol, 3-aminopropan-1-ol, 4-aminobutan-l-ol, 5-aminopentan-l-ol, 1-aminopropan-2-ol, 1-aminobutan-2-ol, 1-aminopentan-2-ol, 1-aminopentan-3-ol, 1- aminopentan-4-ol, 3-amino-2-methylpropan-l-ol, l-amino-2-methylpropan-2-ol, 3- aminopropane-1,2-diol, 2-amino-2-methylpropane-1,3-diol, arginine, lysine, ornithine, histidine, sodium hydroxide,. and potassium hydroxide.

12. The process according claim 1 , characterized in that the second composition (B) contains—based on the total weight of the composition (B)—5.0 to 99.0% by weight of water.

13. The process according to claim 1 , characterized in that the second composition (B) has a pH of from 7.0 to 12.0.

14. The process according to claim 1 , characterized in that the second composition (B) comprises at least one film-forming polymer selected from the group consisting of homopolymers or copolymers of acrylic acid, methacrylic acid, acrylic acid esters, methacrylic acid esters, acrylic acid amides, methacrylic acid amides, vinylpyrrolidone, vinyl alcohol, vinyl acetate, ethylene, propylene, styrene, polyurethanes, polyesters, and polyamides.

15. The process according to claim 1 , comprising the following steps:
(1) applying the first agent (A) to the keratin material,
(2) allowing the agent (A) to act on the keratin material for a period of 1 to 10 minutes,
(3) rinsing the agent (A) out of the keratin material,
(4) applying the agent (B) to the keratin material,
(5) allowing the agent (B) to act on the keratin material for a period of 1 to 10 minutes,
(6) rinsing the agent (B) out of the keratin material.

16. Multicomponent packaging

Assignees

• Henkel Ag & Co Kgaa

Inventors

• Jaiser Phillip
• Lechner Torsten
• Weser Gabriele
• Nowottny Marc
• Mathiaszyk Carsten
• Kriener Caroline
• Schoepgens Juergen
• Kolonko Claudia
• Schumacher Ulrike
• Erkens Udo

Classifications

• A61Q5/065 Primary

  Preparations for temporary colouring the hair, e.g. direct dyes · CPC title

• A61K8/0258 Primary

  Layered structure · CPC title

• A61K8/25

  Silicon; Compounds thereof · CPC title

• A61K8/41

  Amines · CPC title

• A61K8/44

  Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof · CPC title