Anionic direct dye having a tetraalkylammonium counterion, dyeing composition comprising them and method for dyeing keratinous fibres starting from these dyes

Patent metadata

Field	Value
Publication number	US-9968534-B2
Application number	US-201113988153-A
Country	US
Kind code	B2
Filing date	Nov 16, 2011
Priority date	Nov 18, 2010
Publication date	May 15, 2018
Grant date	May 15, 2018

Abstract

The invention relates to the dyeing of human keratinous fibers, in particular the hair, using anionic direct dyes or acid dyes having a tetraalkylammonium counterion of formula (I), with Col (−) m, R 1 , R 2 , R 3 , R 4 , m, and n as defined in the description. A subject-matter of the invention is a dyeing composition comprising an anionic dye of formula (I) and a method for dyeing keratinous fibers, such as the hair, employing the said composition. A subject-matter of the invention is likewise novel dyes of formula (I) and their uses for the coloring of keratinous fibers. This composition makes it possible to obtain a chromatic, powerful and particularly persistent coloring on keratinous fibers.

First claim

The invention claimed is:

1. A method for dyeing human keratinous fibers, said method comprising:
applying to the fibers a composition comprising at least one anionic dye of formula (I)

and optical isomers, geometric isomers, and solvates thereof, wherein in formula (I):
R 1 , R 2 , R 3 and R 4 , which are identical, are chosen from i) linear (C 1 -C 6 )alkyls; and ii) linear (C 2 -C 6 )alkenyls;
it being possible for the alkyl or alkenyl group of the groups of i) and ii) to be interrupted by at least one identical or different heteroatoms chosen from oxygen, sulphur, and N(Rα), wherein Rα is chosen from hydrogen atoms and alkyl groups;
Col (−) m represents the anionic part of the anionic dye comprising at least one sulphonate group and/or at least one carboxylate group,
and wherein m is the anionic charge;
wherein m and n, which are identical or different, represent an integer ranging from 1 to 10;
wherein:
when the anionic part of the anionic dye comprises a sulphonate group or a carboxylate group, then m=n=1;
when the anionic part of the anionic dye comprises anionic groups other than a sulphonate or carboxylate group, the anionic part is combined with at least one cationic counterion, organic, inorganic or R 1 R 2 R 3 R 4 N + , making it possible to achieve electrical neutrality of the formula (I); and
the at least one anionic dye of formula (I) is chosen from the dyes of formulae (II), (II′), (lll), or (III′):
a) diaryl anionic azo dyes of formula (II) or (II′):

wherein in formulae (II) and (II′):
R 7 , R 8 , R 9 , R 10 , R′ 7 , R′ 8 , R′ 9 and R′ 10 , which are identical or different, are chosen from a hydrogen atom or a group chosen from:
alkyl groups;
alkoxy groups or alkylthio groups;
hydroxyl groups or mercapto groups;
nitro groups or nitroso groups;
R ∘ —C(X)—X′—, R ∘ —X′—C(X)—, R ∘ —X′—C(X)—X″—, wherein R ∘ is chosen from a hydrogen atom, alkyl groups, or aryl groups; and X, X′ and X″, which are identical or different, are chosen from oxygen atoms, sulphur atoms, or NR, wherein R is chosen from a hydrogen atom or an alkyl group;
M + (O) 2 S(O − )—, wherein M + is chosen from hydrogen atoms, cationic counterions, or cationic counterions R 1 R 2 R 3 R 4 N + ;
M + (O)CO − —, wherein M + is chosen from hydrogen atoms, cationic counterions, or cationic counterions R 1 R 2 R 3 R 4 N + ;
R″—S(O) 2 —, wherein R″ is chosen from hydrogen atoms, or an alkyl, aryl, (di)(alkyl)amino or aryl(alkyl)amino group;
R″′—S(O) 2 —X′—, wherein R″′ is chosen from an alkyl group or an aryl group which is optionally substituted, and X′ is chosen from oxygen atoms, sulphur atoms, or NR, wherein R is chosen from a hydrogen atom or an alkyl group;
(di)(alkyl)amino groups;
aryl(alkyl)amino, optionally substituted by at least one group chosen from i) nitro; ii) nitroso; iii) M + (O) 2 S(O − )— or iv) alkoxy groups, wherein M + is chosen from hydrogen atoms, cationic counterions, or cationic counterions R 1 R 2 R 3 R 4 N + ;
optionally substituted heteroaryl groups;
cycloalkyl groups;
Ar—N═N—, wherein Ar is an optionally substituted aryl group;
or else two contiguous groups, R 7 with R 8 , R 8 with R 9 , or R 9 with R 10 , together form a fused benzo group A′; and R′ 7 with R′ 8 or R′ 8 with R′ 9 or R′ 9 with R′ 10 together form a fused benzo group B′; with A′ and B′ optionally substituted by one or more groups chosen from i) nitro; ii) nitroso; iii) M + (O) 2 S(O − )—; iv) hydroxyl; v) mercapto; vi) (di)(alkyl)amino; vii) R ∘ —C(X)—X′—; viii) R ∘ —X′—C(X)—; ix) R ∘ —X′—C(X)—X″—; x) Ar—N═N— and xi) aryl(alkyl)amino which is optionally substituted, wherein M + is chosen from hydrogen atoms, cationic counterions, or cationic counterions R 1 R 2 R 3 R 4 N + ;

W is chosen from a sigma σ bond, an oxygen or sulphur atom or a divalent radical i) —NR—, or ii) methylene —C(R a )(R b )—, wherein R a and R b , which are identical or different, are chosen from a hydrogen atom or an aryl group, or else R a and R b form, together with the carbon atom which carries them, a spirocycloalkyl;

with the proviso that the formulae (II) and (II′) comprise at least one sulphonate radical R 1 R 2 R 3 R 4 N + (O) 2 S(O − )— or carboxylate radical R 1 R 2 R 3 R 4 N + (O)C(O − )— on one of the rings A, A′, B, B′ or C; or
b) pyrazolone anionic azo dyes of formulae (III) or (III′):

wherein in formulae (III) and (III′):
R 11 , R 12 and R 13 , which are identical or different, are chosen from a hydrogen atom, a halogen atom, an alkyl group or an M + (O) 2 S(O − )− group, wherein M + is chosen from hydrogen atoms, cationic counterions, or cationic counterions R 1 R 2 R 3 R 4 N + ;
R 14 is chosen from a hydrogen atom, an alkyl group or an M + C(O)O − group, wherein M + is chosen from hydrogen atoms, cationic counterions, or cationic counterions R 1 R 2 R 3 R 4 N + ;
R 15 represents a hydrogen atom;
R 16 represents an oxo group, in which case R′ 16 is absent, or else R 15 with R 16 together form a double bond;
R 17 and R 18 , which are identical or different, are chosen from a hydrogen atom or a group chosen from:
M + (O) 2 S(O − )—, wherein M + is chosen from hydrogen atoms, cationic counterions, or cationic counterions R 1 R 2 R 3 R 4 N + ;
Ar—O—S(O) 2 —, wherein Ar is an optionally substituted aryl group;

R 19 and R 20 , together form either a double bond or an optionally substituted benzo group D′;
R′ 16 , R′ 19 and R′ 20 , which are identical or different, are chosen from a hydrogen atom, an alkyl group, or a hydroxyl group;
R 21 is chosen from a hydrogen atom, an alkyl group, or an alkoxy group;
R a and R b , which are identical or different, are chosen from a hydrogen atom or an aryl group, or else R a and R b form, together with the carbon atom which carries them, a spirocycloalkyl;
Y is chosen from a hydroxyl group or an oxo group;
represents a single bond when Y is an oxo group and represents a double bond when Y represents a hydroxyl group;

with the proviso that the formulae (III) and (III′) comprise at least one sulphonate group R 1 R 2 R 3 R 4 N + (O) 2 S(O − )— on one of the rings D or E or the formulae (III) and (III′) comprise at least one carboxylate group R 1 R 2 R 3 R 4 N + (O)C(O − )—.

2. The method according to claim 1 , wherein R 1 , R 2 , R 3 and R 4 are identical.

3. The method according to claim 1 , wherein R 1 , R 2 , R 3 and R 4 are independently chosen from linear (C 1 -C 6 )alkyl groups.

4. The method according to claim 1 , wherein R 1 , R 2 , R 3 and R 4 are independently chosen from methyl, ethyl, propyl or butyl groups.

5. The method according to claim 1 , wherein m is equal to n.

6. The method according to claim 1 , in which m and n are independently chosen from 1, 2 or 3.

7. The method according to claim 1 , wherein Col (−) m comprises: at least one sulphonate group and at least one aryl or heteroaryl group, wherein the at least one sulphonate group is directly connected to an aryl or heteroaryl group; and optionally at least one anionic group G − , wherein G − , which is identical or different, represents an anionic group chosen from alkoxide O − , thiolate S − , carboxylate or thiocarboxylate C(Q)Q′ − , wherein Q and Q′, which are identical or different, are chosen from oxygen or sulphur atoms.

8. The method according to claim 7 , wherein G − is a carboxylate.

Assignees

• Greaves Andrew
• Oreal

Inventors

• Greaves Andrew

Classifications

• A61Q5/10

  Preparations for permanently dyeing the hair · CPC title

• A61K8/416 Primary

  Quaternary ammonium compounds (A61K8/35 takes precedence) · CPC title

• A61K8/4946

  Imidazoles or their condensed derivatives, e.g. benzimidazoles · CPC title

• A61K8/494

  with more than one nitrogen as the only hetero atom · CPC title

• A61K8/466 Primary

  containing sulfonic acid derivatives; Salts · CPC title