RU99111265A - COMPOSITION FOR DIRECT COLORING KERATIN FIBERS WITH DIRECT CATIONIC DYE AND POLYOL AND / OR SIMPLE POLYOL ETHER - Google Patents
COMPOSITION FOR DIRECT COLORING KERATIN FIBERS WITH DIRECT CATIONIC DYE AND POLYOL AND / OR SIMPLE POLYOL ETHERInfo
- Publication number
- RU99111265A RU99111265A RU99111265/14A RU99111265A RU99111265A RU 99111265 A RU99111265 A RU 99111265A RU 99111265/14 A RU99111265/14 A RU 99111265/14A RU 99111265 A RU99111265 A RU 99111265A RU 99111265 A RU99111265 A RU 99111265A
- Authority
- RU
- Russia
- Prior art keywords
- composition
- direct
- composition according
- polyol
- alkyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims 33
- 229920005862 polyol Polymers 0.000 title claims 14
- 239000000835 fiber Substances 0.000 title claims 13
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title claims 12
- 102000011782 Keratins Human genes 0.000 title claims 10
- 108010076876 Keratins Proteins 0.000 title claims 10
- 150000003077 polyols Chemical class 0.000 title claims 9
- 238000004040 coloring Methods 0.000 title 1
- 239000000975 dye Substances 0.000 claims 15
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims 11
- 125000002091 cationic group Chemical group 0.000 claims 10
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 239000000460 chlorine Substances 0.000 claims 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 230000000875 corresponding Effects 0.000 claims 4
- 238000009967 direct dyeing Methods 0.000 claims 4
- 238000004043 dyeing Methods 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Substances 0.000 claims 4
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 4
- 229910052740 iodine Inorganic materials 0.000 claims 4
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 4
- 239000011630 iodine Substances 0.000 claims 4
- 125000001931 aliphatic group Chemical group 0.000 claims 3
- 125000003277 amino group Chemical group 0.000 claims 3
- 150000001450 anions Chemical class 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 3
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atoms Chemical group N* 0.000 claims 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims 3
- 108020005203 Oxidases Proteins 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000004432 carbon atoms Chemical group C* 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 239000007800 oxidant agent Substances 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- JEVCWSUVFOYBFI-UHFFFAOYSA-N Cyano radical Chemical compound N#[C] JEVCWSUVFOYBFI-UHFFFAOYSA-N 0.000 claims 1
- 108090000854 Oxidoreductases Proteins 0.000 claims 1
- 102000004316 Oxidoreductases Human genes 0.000 claims 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 239000000982 direct dye Substances 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000002453 shampoo Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 238000010186 staining Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 0 Cc1cc(C(*)[N+](*)C2)c2cc1 Chemical compound Cc1cc(C(*)[N+](*)C2)c2cc1 0.000 description 6
Claims (1)
где D обозначает атом азота или группу -СН;
R1 и R2, одинаковые или разные, обозначают атом водорода, радикал С1-С4-алкил, который может быть замещен радикалами CN, ОН или NH2, или вместе с атомом углерода бензольного цикла образуют кислород- или азотсодержащий гетероцикл, который может быть замещен одним или несколькими С1-С4-алкилами, или радикал 4'-аминофенил;
R3 и R3' одинаковые или разные, обозначают атом водорода или галогена, выбранный из хлора, брома, иода и фтора, радикал циано, С1-С4-алкил, С1-С4-алкокси или ацетокси;
X- обозначает анион, преимущественно выбранный из хлорида, метилсульфата и ацетата;
А обозначает группу, выбранную из приведенных ниже структур А1-А18:
где R4 обозначает С1-С4-алкил, который может быть замещен гидроксилом,
R5 обозначает С1-С4-алкокси-радикал при условии, что, когда D обозначает -СН, А обозначает А4 или А13 и R3 не является алкокси-радикалом, то R1 и R2 не могут быть одновременно атомами водорода;
где R6 обозначает атом водорода или С1-С4-алкил;
R7 обозначает атом водорода, радикал алкил, который может быть замещен радикалом -CN или аминогруппой, радикал 4'-аминофенил, или вместе с R6 образует кислород- и/или азотсодержащий гетероцикл, который может быть замещен С1-С4-алкилом;
R8 и R9, одинаковые или разные, обозначают атом водорода или галогена, выбранный из хлора, брома, иода и фтора, радикалы С1-С4-алкил, С1-С4-алкокси или -CN;
Х- обозначает анион, преимущественно выбранный из хлорида, метилсульфата и ацетата;
В обозначает группу, выбранную из приведенных ниже структур B1-B6:
где R1 обозначает С1-С4-алкил;
R11 и R12, одинаковые или разные, обозначают атом водорода или С1-С4-алкил;
где R13 обозначает атом водорода, С1-С4-алкокси, атом галогена, выбранный из хлора, брома, иода и фтора, или аминогруппу;
R14 обозначает атом водорода, С1-С4-алкил или, вместе с атомом углерода бензольного цикла, образует кислород- содержащий и/или замещенный одним или несколькими С1-С4-алкил-радикалами гетероцикл;
R15 обозначает атом водорода или галогена: хлор, бром, иод или фтор;
R16 и R17, одинаковые или разные, обозначают атом водорода или С1-С4-алкил;
D1 и D2, одинаковые или разные, обозначают атом азота или группу -СН;
m = 0 или 1,
при условии, что, когда R13 обозначает незамещенную аминогруппу, тогда D1 и D2 одновременно обозначают группу -СН и m=0;
Х- обозначает анион, преимущественно выбранный из хлорида, метилсульфата и ацетата;
Е обозначает группу, выбранную из приведенных ниже структур Е1-Е8:
где R' обозначает С1-С4-алкил;
когда m = 0 и D1 обозначает атом азота, тогда Е может также обозначать группу, имеющую приведенную ниже структуру E9
где R' обозначает С1-С4-алкил;
причем названная композиция отличается тем, что она также содержит по меньшей мере один полиол или простой алифатический С1-С8-эфир С3-С9-полиола и/или простой ароматический С6-С8-эфир С2-С9-полиола.1. Composition for direct dyeing of keratin fibers, in particular, human keratin fibers such as hair, containing at least one direct cationic dye of the following formulas in the following suitable for dyeing that does not contain oxidases or oxidoreductases; ':
where D denotes a nitrogen atom or a group-CH;
R 1 and R 2 , which are the same or different, denote a hydrogen atom, a C 1 -C 4 -alkyl radical which may be substituted by CN, OH or NH 2 , or together with the carbon atom of the benzene ring form an oxygen or nitrogen-containing heterocycle may be substituted with one or more C 1 -C 4 -alkyls, or the 4'-aminophenyl radical;
R 3 and R 3 'are the same or different, represent a hydrogen or halogen atom selected from chlorine, bromine, iodine and fluorine, a cyano radical, C 1 -C 4 alkyl, C 1 -C 4 alkoxy or acetoxy;
X - denotes an anion predominantly selected from chloride, methyl sulfate and acetate;
And indicates a group selected from the following structures A1-A18:
where R 4 stands With 1 -C 4 -alkyl, which may be substituted by hydroxyl,
R 5 is a C 1 -C 4 -alkoxy radical provided that when D is —CH, A is A4 or A13 and R 3 is not an alkoxy radical, then R 1 and R 2 cannot be hydrogen atoms simultaneously;
where R 6 denotes a hydrogen atom or a C 1 -C 4 -alkyl;
R 7 denotes a hydrogen atom, an alkyl radical, which may be substituted by a -CN radical or an amino group, a 4'-aminophenyl radical, or together with R 6 forms an oxygen- and / or nitrogen-containing heterocycle, which may be substituted with C 1 -C 4 alkyl ;
R 8 and R 9 , which are the same or different, represent a hydrogen or halogen atom selected from chlorine, bromine, iodine and fluorine, C 1 -C 4 -alkyl radicals, C 1 -C 4 -alkoxy or -CN;
X - denotes an anion predominantly selected from chloride, methyl sulfate and acetate;
B stands for a group selected from the structures B 1 -B 6 below:
where R 1 stands With 1 -C 4 -alkyl;
R 11 and R 12 , which are the same or different, represent a hydrogen atom or C 1 -C 4 -alkyl;
where R 13 denotes a hydrogen atom, C 1 -C 4 -alkoxy, a halogen atom selected from chlorine, bromine, iodine and fluorine, or an amino group;
R 14 represents a hydrogen atom, C 1 -C 4 -alkyl or, together with the carbon atom of the benzene ring, forms an oxygen-containing and / or heterocycle substituted by one or more C 1 -C 4 -alkyl radicals;
R 15 denotes a hydrogen or halogen atom: chlorine, bromine, iodine or fluorine;
R 16 and R 17 , which are the same or different, represent a hydrogen atom or C 1 -C 4 -alkyl;
D 1 and D 2 , the same or different, represent a nitrogen atom or a —CH group;
m = 0 or 1,
provided that when R 13 denotes an unsubstituted amino group, then D 1 and D 2 simultaneously denote the group —CH and m = 0;
X - denotes an anion predominantly selected from chloride, methyl sulfate and acetate;
E denotes a group selected from the following structures E1-E8:
where R 'is a C 1 -C 4 -alkyl;
when m = 0 and D 1 denotes a nitrogen atom, then E may also denote a group having the following structure E9
where R 'is a C 1 -C 4 -alkyl;
moreover, the above composition is characterized in that it also contains at least one polyol or a simple aliphatic C 1 -C 8 -ether C 3 -C 9 -polyol and / or a simple aromatic C 6 -C 8 -ether C 2 -C 9 - polyol.
3. Композиция по п.2, отличающаяся тем, что прямые катионные красители соответствуют структурам I 1, I 2, I 4 и I 31.2. The composition according to claim 1, characterized in that the direct cationic dyes of the formula I are selected from the following structures I 1 - I 54:
3. The composition according to claim 2, characterized in that the direct cationic dyes correspond to the structures I 1, I 2, I 4 and I 31.
5. Композиция по п.1, отличающаяся тем, что прямые катионные красители формулы III выбраны из числа соединений, отвечающих приведенным ниже структурам III 1 - III 18:
6. Композиция по п.5, отличающаяся тем, что прямые катионные красители формулы III выбраны из числа соединений, отвечающих структурам III 4, III 5 и III 13.4. The composition according to claim 1, characterized in that the direct cationic dyes of formula II are selected from among the compounds corresponding to the structures II 1 - II 9 below:
5. The composition according to claim 1, characterized in that the direct cationic dyes of the formula III are selected from among the compounds corresponding to the structures III 1 to III 18 below:
6. The composition according to claim 5, characterized in that the direct cationic dyes of formula III are selected from among the compounds corresponding to structures III 4, III 5 and III 13.
8. Композиция по одному из предыдущих пунктов, отличающаяся тем, что прямой катионный краситель или красители формул I, II, III или III' составляют 0,001 - 10% от общей массы композиции.7. The composition according to claim 1, characterized in that the direct cationic dyes of the formula III 'are selected from among the compounds corresponding to the structures III' 1 and III '3 below:
8. Composition according to one of the preceding paragraphs, characterized in that the direct cationic dye or dyes of formulas I, II, III or III 'are 0.001 - 10% of the total weight of the composition.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9806751A FR2779055B1 (en) | 1998-05-28 | 1998-05-28 | DIRECT DYE COMPOSITION FOR KERATINIC FIBERS WITH CATIONIC DIRECT DYE AND POLYOL AND / OR POLYOL ETHER |
FR9806751 | 1998-05-28 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU99111265A true RU99111265A (en) | 2001-03-27 |
RU2166930C2 RU2166930C2 (en) | 2001-05-20 |
Family
ID=9526824
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU99111265/14A RU2166930C2 (en) | 1998-05-28 | 1999-05-27 | Composition for direct coloring of keratin fibers, particularly, man's hair, method of its coloring, packaging of set for coloring composition |
Country Status (18)
Country | Link |
---|---|
US (1) | US6436153B2 (en) |
EP (1) | EP0962219B2 (en) |
JP (1) | JP3814442B2 (en) |
KR (1) | KR100329413B1 (en) |
CN (1) | CN1217648C (en) |
AT (1) | ATE278378T1 (en) |
AU (1) | AU722600B2 (en) |
BR (1) | BR9901829B1 (en) |
CA (1) | CA2273416C (en) |
DE (1) | DE69920801T3 (en) |
ES (1) | ES2230815T5 (en) |
FR (1) | FR2779055B1 (en) |
HU (1) | HUP9901746A3 (en) |
MX (1) | MX221183B (en) |
PL (1) | PL204182B1 (en) |
PT (1) | PT962219E (en) |
RU (1) | RU2166930C2 (en) |
ZA (1) | ZA993199B (en) |
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FR2717383B1 (en) | 1994-03-21 | 1996-04-19 | Oreal | Composition for dyeing oxidation of keratin fibers comprising a derivative of paraphenylenediamine and a cationic or amphoteric substantive polymer and use. |
US5474578A (en) * | 1994-10-03 | 1995-12-12 | Clairol, Inc. | Erasable hair dyeing process |
DE59510392D1 (en) * | 1994-11-03 | 2002-10-31 | Ciba Sc Holding Ag | Cationic imidazole azo dyes |
JP3297056B2 (en) † | 1996-04-25 | 2002-07-02 | ロレアル | Dyeing method of keratin fiber using oxidation dye precursor and powder direct dye |
DE19618595A1 (en) † | 1996-05-09 | 1997-11-13 | Wella Ag | dye |
EP0819422B1 (en) | 1996-07-15 | 1999-10-27 | Kao Corporation | Composition for dyeing of human hair |
FR2757385B1 (en) * | 1996-12-23 | 1999-01-29 | Oreal | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
FR2757387B1 (en) * | 1996-12-23 | 1999-01-29 | Oreal | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
FR2757388B1 (en) * | 1996-12-23 | 1999-11-12 | Oreal | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
FR2757384B1 (en) * | 1996-12-23 | 1999-01-15 | Oreal | KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME |
US6007585A (en) | 1997-10-15 | 1999-12-28 | Avlon Industries, Inc. | Hair brightening system |
-
1998
- 1998-05-28 FR FR9806751A patent/FR2779055B1/en not_active Expired - Lifetime
-
1999
- 1999-05-05 ES ES99401099T patent/ES2230815T5/en not_active Expired - Lifetime
- 1999-05-05 AT AT99401099T patent/ATE278378T1/en active
- 1999-05-05 PT PT99401099T patent/PT962219E/en unknown
- 1999-05-05 EP EP99401099A patent/EP0962219B2/en not_active Expired - Lifetime
- 1999-05-05 DE DE69920801T patent/DE69920801T3/en not_active Expired - Lifetime
- 1999-05-10 ZA ZA9903199A patent/ZA993199B/en unknown
- 1999-05-12 AU AU28082/99A patent/AU722600B2/en not_active Ceased
- 1999-05-21 MX MX9904753A patent/MX221183B/en not_active IP Right Cessation
- 1999-05-25 BR BRPI9901829-2B1A patent/BR9901829B1/en active IP Right Grant
- 1999-05-26 KR KR19990019063A patent/KR100329413B1/en not_active IP Right Cessation
- 1999-05-27 CA CA002273416A patent/CA2273416C/en not_active Expired - Fee Related
- 1999-05-27 PL PL333399A patent/PL204182B1/en not_active IP Right Cessation
- 1999-05-27 HU HU9901746A patent/HUP9901746A3/en unknown
- 1999-05-27 CN CN991092465A patent/CN1217648C/en not_active Expired - Fee Related
- 1999-05-27 RU RU99111265/14A patent/RU2166930C2/en not_active IP Right Cessation
- 1999-05-28 US US09/321,890 patent/US6436153B2/en not_active Expired - Lifetime
- 1999-05-28 JP JP14911399A patent/JP3814442B2/en not_active Expired - Lifetime
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