MXPA99004785A - Composition of dyeing for keratinic fibers with a direct cationic coloring and a polyol or ether of pol - Google Patents
Composition of dyeing for keratinic fibers with a direct cationic coloring and a polyol or ether of polInfo
- Publication number
- MXPA99004785A MXPA99004785A MXPA/A/1999/004785A MX9904785A MXPA99004785A MX PA99004785 A MXPA99004785 A MX PA99004785A MX 9904785 A MX9904785 A MX 9904785A MX PA99004785 A MXPA99004785 A MX PA99004785A
- Authority
- MX
- Mexico
- Prior art keywords
- composition
- radical
- dyeing
- polyol
- composition according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 89
- 238000004043 dyeing Methods 0.000 title claims abstract description 66
- 229920005862 polyol Polymers 0.000 title claims abstract description 52
- 150000003077 polyols Chemical class 0.000 title claims abstract description 50
- 239000000835 fiber Substances 0.000 title claims abstract description 36
- 125000002091 cationic group Chemical group 0.000 title claims abstract description 27
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 238000004040 coloring Methods 0.000 title description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 41
- 102000011782 Keratins Human genes 0.000 claims abstract description 29
- 108010076876 Keratins Proteins 0.000 claims abstract description 29
- 210000004209 hair Anatomy 0.000 claims abstract description 24
- 235000011187 glycerol Nutrition 0.000 claims abstract description 20
- 238000000034 method Methods 0.000 claims abstract description 13
- 239000000975 dye Substances 0.000 claims description 31
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims description 21
- 230000003647 oxidation Effects 0.000 claims description 21
- 238000007254 oxidation reaction Methods 0.000 claims description 21
- 239000000982 direct dye Substances 0.000 claims description 20
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 17
- 239000007800 oxidant agent Substances 0.000 claims description 11
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims description 10
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 10
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 8
- 229910052794 bromium Inorganic materials 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 8
- 239000011737 fluorine Substances 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 6
- 125000005842 heteroatom Chemical group 0.000 claims description 6
- 239000011630 iodine Substances 0.000 claims description 6
- 229910052740 iodine Inorganic materials 0.000 claims description 6
- 239000002453 shampoo Substances 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
- 150000008378 aryl ethers Chemical class 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Chemical group 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000005263 alkylenediamine group Chemical group 0.000 claims description 2
- 150000001450 anions Chemical class 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- 150000001555 benzenes Chemical group 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims 3
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- -1 alkyl radical Chemical class 0.000 description 21
- 150000001875 compounds Chemical class 0.000 description 13
- 150000003254 radicals Chemical class 0.000 description 11
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 10
- 239000002585 base Substances 0.000 description 9
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical compound C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 description 3
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 206010001488 Aggression Diseases 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000016571 aggressive behavior Effects 0.000 description 2
- 230000003113 alkalizing effect Effects 0.000 description 2
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N methyl monoether Natural products COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 229940058015 1,3-butylene glycol Drugs 0.000 description 1
- JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- WAEVWDZKMBQDEJ-UHFFFAOYSA-N 2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)COC(C)CO WAEVWDZKMBQDEJ-UHFFFAOYSA-N 0.000 description 1
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
- SXFJDZNJHVPHPH-UHFFFAOYSA-N 3-methylpentane-1,5-diol Chemical compound OCCC(C)CCO SXFJDZNJHVPHPH-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 108010029541 Laccase Proteins 0.000 description 1
- 229930192627 Naphthoquinone Natural products 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 108700020962 Peroxidase Proteins 0.000 description 1
- 102000003992 Peroxidases Human genes 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical class [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 108091007187 Reductases Proteins 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 235000019437 butane-1,3-diol Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229940106189 ceramide Drugs 0.000 description 1
- 150000001783 ceramides Chemical class 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000295 complement effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 229940113120 dipropylene glycol Drugs 0.000 description 1
- 238000009967 direct dyeing Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000002791 naphthoquinones Chemical class 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 235000011118 potassium hydroxide Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000011121 sodium hydroxide Nutrition 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
Abstract
The present invention relates to a dyeing composition for keratin fibers to a dyeing composition for keratin fibers, in particular for human keratin fibers such as hair, comprising, in a medium suitable for dyeing, at least one direct cationic dye of the formula given and characterized in that they also contain at least glycerin and / or a particular polyol and / or particular polyol ether. The invention also relates to the dyeing processes and devices used by the
Description
COMPOSITION OF TIENIDO FOR KERATINIC FIBERS WITH A DIRECT CATIONIC COLORING AND A POLYOL OR A
POLYOL ETHER.
Field of Invention
The invention relates to a dyeing composition for keratin fibers, in particular for human keratin fibers such as hair, comprising, in a medium suitable for dyeing, at least one direct cationic dye of the given formula, and at least glycerol and / or a particular polyol and / or particular polyol ether.
The subject of the invention is also the dyeing methods and devices which use said composition.
Background of the Invention
In the capillary field, two types of coloration can be distinguished.
The first is semi-permanent or temporary coloration, or direct coloring, which resorts to
Ref. 030314 dyes that are able to contribute to the natural coloration of the hair, a more or less pronounced color modification resistant eventually to several shampoos. These dyes are called direct dyes; they can be made with or without oxidizing agent. In the presence of oxidant, the purpose is to obtain a lightening coloration. The lightening coloration is carried out by applying to the hair the extemporaneous mixture of a direct dye and an oxidant and makes it possible, in particular, to obtain by clearing the melanin of the hair, an advantageous effect such as a uniform color in the case of gray hair or highlighting the color in the case of naturally pigmented hair.
The second is the permanent coloration or oxidation coloration. This is carried out with dyes called "oxidation" which comprise oxidation dye precursors and copulators. Oxidation staining precursors, commonly called "oxidation bases", are initially colorless or weakly colored compounds that develop their dyeing power in the hair in the presence of added oxidizing agents at the time of use, leading to the formation of colored compounds and colorants. The formation of these colored compounds and dyes, either by an oxidative condensation of the "oxidation bases" on themselves, or by an oxidative condensation of the "oxidation bases" on modified coloring compounds commonly called "couplers" and generally present in the red compositions used in the oxidation dyeing.
To vary the shades obtained with the indicated oxidation, or enrich them with reflections, it happens that direct dyes are added.
Among the cationic direct dyes available in the field of dyeing of particularly human keratin fibers, the compounds whose structure will be developed in the text that follows are already known; However, these dyes lead to colorations that have still insufficient characteristics, while at the same time in the plane of homogeneity of the color distributed along the fiber ("unisson") (uniformity), it is said then that the coloration is too selective, as in the plane of tenacity, in terms of resistance to the various aggressions that the hair can experience (light, bad weather, shampooing), and in the plane of intensity.
However, after important research carried out on the subject, the applicant firm has now discovered that it is possible to obtain new compositions for the dyeing of keratin fibers capable of carrying colorations that better resist the various aggressions that may be experienced by hairs, more intense and less selective, associating at least glycerin and / or a particular polyol and / or a particular polyol ether with at least one known cationic direct dye of the prior art and of formula (I) defined below.
This discovery forms the basis of the present invention.
Description of the invention
The present invention therefore has as its first object a composition for dyeing keratin fibers and in particular human keratin fibers such as hair, which include in a medium suitable for dyeing, (i) at least one direct cationic dye whose structure corresponds to the following formula (I), characterized in that it also contains (ii) at least glycerin and / or a particular polyol and / or a particular polyol ether.
(i) the cationic direct dye usable according to the present invention is a compound of formula (I) below:
A - N = N - B (I)
in which: symbol A represents a group selected from the following Al a A3 structures:
*?
structures A1 to A3 in which Ri denotes an alkyl radical of C? ~ C, a phenyl radical which can be substituted by an alkyl radical of C? -C or a halogen atom selected from chlorine, bromine, iodine and fluorine; R 2 denotes a C 1 -C 4 alkyl radical or a phenyl radical; R3 and R, identical or different, represent an alkyl radical of C? -C4, a phenyl radical, or, in the case of structure Al, can together form a substituted benzene ring, and in the case of structure A2, they can together form a benzene ring optionally substituted by one or more C?-C4 alkyl radicals, alkoxy
C1-C4, or N02; R3 may also designate a hydrogen atom; Z denotes an oxygen atom, sulfur or a group -NR2; M represents a group -CH, -CR (designating R C 1 -C 4 alkyl), or -NR 5 (X ~) r; K represents a group -CH, -CR (designating R C 1 -C 4 alkyl), or -NR 5 (X ~) r; P represents a group -CH, -CR (r denoting C?-C4 alkyl), or -NRs (X ") r; r designates zero or 1;
R 5 represents a 0"atom, a C 4 -C 4 alkoxy radical, or a C 1 -C 4 alkyl radical, and R 7, identical or different, represent a hydrogen or halogen atom, selected from chlorine, bromine, iodine and fluorine, a C1-C4 alkyl radical, C? -C2 alkoxy, a radical -N02; X? represents an anion preferably selected from chloride, iodide, methyl sulfate, ethyl sulfate, acetate and perchlorate, with the proviso that if R 4 designates a C 1 -C 4 alkyl radical and Z designates a sulfur atom, R 3 does not designate a hydrogen atom;
if R5 designates O ", then r designates zero, if K or P or M designates -N-C1-C4 alkyl X", then
R6 or R7 is different from a hydrogen atom; if K designates -NR5 (X ") r, then M = P = -CH; -CR; if M designates -NR5 (X") r, then K = P = -CH; -CR; if P designates -NR (X ~) r, then K = M and designates - CH or -CR; if Z designates -NR2 and R2 designates a C1-C4 alkyl radical, then at least one of the radicals
Ri, R3 or R4 of A2 is different from a C?-C alkyl radical;
the symbol B represents: - (a) a group of structure Bl following
structure Bl in which, Re represents a hydrogen atom, a halogen atom selected from chlorine, bromine, iodine, and fluorine, an alkyl radical of C? -C, alkoxy of C? -C, a radical OH, -N02, -NHRn, NRi2R? 3, -NHCOalkyl of C? -C4, or form with Rg a ring of 5 or 6 members containing or not one or more heteroatoms selected from nitrogen, oxygen or sulfur; R9 represents a hydrogen atom, a halogen atom selected from chlorine, bromine, iodine and fluorine, an alkyl radical of C?-C4, alkoxy of C? ~C, or forms with Rio or Rn a ring of 5 or 6 members containing or not one or more heteroatoms selected from nitrogen, oxygen or sulfur; Rio represents a hydrogen atom, a radical -OH, a radical -NHRn, a radical -NR? 2R? 3; Rii represents a hydrogen atom, a C 1 -C 4 alkyl radical, a monohydroxyalkyl radical of
C? -C4, C2-C4 polyhydroxyalkyl, a phenyl radical; R12 and 13; identical or different, represent an alkyl radical of C? -C, a monohydroxyalkyl radical of C? ~ C4, polyhydroxyalkyl
C2-C4;
- (b) a 5- or 6-membered nitrogenous heterocyclic group capable of including other heteroatoms and / or carbonylated group and which can be substituted by one or more C 1 -C 4 alkyl, amino or phenyl radicals, and particularly a group of structure B2 following :
structure B2 in which, R 4 and R 15, identical or different, represent a hydrogen atom, a C 1 -C 4 alkyl radical, a phenyl radical,
H3 Y designates the radical -CO or the radical -C =; n = 0 or 1, with, when n designates 1, U designates the radical -CO.
In the structures defined above, the alkyl or C?-C alkoxy group preferably designates methyl, ethyl, butyl, methoxy, ethoxy.
The cationic direct dyes of formula (I) which can be used in the dyeing compositions according to the invention are known compounds and are described, for example, in patent applications FR-2189006, FR-2285851 and FR-2140205 and their certificates of addition.
Among the cationic direct dyes of formula (I) which can be used in the dyeing compositions according to the invention, those of the formula (I) in which the symbol A designates the structure A3 while the symbol B designates the structure Bl or B2 are particularly preferred .
Among these compounds, compounds of structures (I) can be more particularly mentioned? a (I) 77 following:
OR
I. O
CH3SO4"
CH3SO4-
CH3SO4"
CH3SO4- CH3SO4
CH3SO4"CH3SO4- CH3SO4" CH3SO4"
C4H9
0) «
CH3SO4"
CH3SO4 CH,
(!) 76 The cationic direct dye (s) used according to the invention preferably represent from 0.001 to 10% by weight approximately of the total weight of the dyeing composition and even more preferably from 0.005 to 5% by weight approximately of this weight.
(ii) By polyol, for the purposes of the invention, a linear, branched or cyclic, saturated or unsaturated alkyl-type compound which carries at least two OH functions on the alkyl chain and polymers (polyethers) is designated of these polyhydroxy alkyl compounds.
The particular polyols used according to the invention contain at least 4 carbon atoms and can be selected, in particular, from the polyalkanes of C4-Cg as well as polyalkylene glycols such as, more particularly, polyethylene glycols and polypropylene glycols.
Among the C4-Cg polyols, mention may be made in particular of 2-butene-1, -diol, pentane-1, 5-diol, 2,2-dimethyl-propane-1, 3-diol, 3-methyl -pentane-1, 5-diol, pentane-1,2-diol, 2, 2, 4-trimethyl-pentane-1,3-diol, 2-methyl-propane-1,3-diol, hexylene glycol, 1,3-butylene glycol, dipropylene glycol, diethylene glycol, triethylene glycol.
The particular polyol ethers according to the invention are chosen from the C?-C8 aliphatic ethers of C3-Cg polyols and the aromatic Cß-Cß ethers of C2-Cg polyols.
Among the C 1 -C 8 aliphatic ethers of C 3 -Cg polyols, mention may be made in particular of propylene glycol monomethyl ether, propylene glycol monomethyl ether, isopropylene glycol dimethylether, diethylene glycol monomethylether and monomethyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethylether and diethylene glycol dimethylether; among the C6-C8 aromatic ethers of C2-Cg polyols, mention may be made in particular of the monophenylether of ethylene glycol or the monobenzylether of ethylene glycol, the monophenylether of propylene glycol, the monobenzylether of propylene glycol, the monophenylether of diethylene glycol and the monobenzylether of diethylene glycol.
The glycerine and / or the polyol (s) and / or polyol ether (s) described for the purposes of the invention are present in the dyeing composition according to the invention in proportions generally ranging from 0.1 to 40% by weight, and even more particularly from 0.5 to 20% by weight relative to the total weight of the composition.
The appropriate medium for dyeing (or support) is generally constituted by a mixture of water and by at least glycerin and / or a polyol and / or a polyol ether such as defined above. It may also contain one or more organic solvents other than the glycerin and / or the polyols and / or the polyol ether (s) used according to the invention, to solubilize the compounds which are not sufficiently soluble in the medium. As the organic solvent, mention may be made, for example, of C?-C4 alkanols, such as ethanol and isopropanol, as well as aromatic alcohols such as benzyl alcohol, analogous products and mixtures thereof.
The said additional organic solvents can be present in proportions preferably comprised between 0.5 and 40% by weight approximately relative to the total weight of the dyeing composition, and even more preferably between 1 and 20% by weight approximately .
According to the invention, the pH is generally between approximately 2 and 11, and preferably between approximately 5 and approximately 10. It can be adjusted to the desired value by means of acidifying or alkalizing agents usually used in the dyeing of keratin fibers.
Among the acidulating agents, mention may be made, by way of example, of mineral or organic acids such as hydrochloric acid, orthophosphoric acid, sulfuric acid, carboxylic acids such as acetic acid, tartaric acid, citric acid, lactic acid, sulfonic acids.
Among alkalizing agents, mention may be made, by way of example, of ammonia, alkali carbons, alkaline amines such as mono-, di- and triethanolamines as well as their derivatives, sodium or potassium hydroxides and compounds of formula ( II) following:
wherein it is a moiety optionally substituted by a hydroxyl group or a C? -C6 alkyl radical; Rißf 1, Rie and Ri 9 identical or different, represent a hydrogen atom, an alkyl radical of Ci-Ce or hydroxyalkyl of Ci-Cß-
The dye composition according to the invention can contain, in addition to the cationic direct dye (s) defined above, one or more additional direct dyes, which can be chosen, for example, from nitrobenzene dyes, anthraquinone dyes, naphthoquinone dyes, triallylmetanic dyes , zantenic dyes, non-cationic azo dyes.
When it is intended for oxidation dyeing, the dye composition according to the invention contains, in addition to the cationic direct dye (s) and the glycerin and / or the particular polyol and / or the polyol ether defined above, one or more bases of oxidation selected from the oxidation bases conventionally used for oxidation dyeing and among which may be particularly mentioned para-phenylenediamines, bis (phenyl) alkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases.
When used, the oxidation base or bases preferably represent from 0.0005 to 12% by weight approximately of the total weight of the dyeing composition, and even more preferably from 0.005 to 6% by weight approximately of this weight . When it is intended for oxidation dyeing, the dyeing composition according to the invention can also include, in addition to the direct cationic dye and the glycerin and / or the particular polyol and / or the polyol ether defined above as well as the bases of oxidation, one or more copulators in order to modify or enrich with reflections the shades obtained using the direct cationic dye (s) and the oxidation base (s).
The copulators which can be used in the dyeing composition according to the invention can be selected from the couplers conventionally used in oxidation dyeing, among which metaphenyldiamines, eta-aminophenols, meta-diphenols and heterocyclic couplers can be particularly mentioned.
When present, the coupler (s) preferably represent from 0.0001 to 10% by weight approximately of the total weight of the dyeing composition and even more preferably from 0.005 to 5% by weight approximately of this weight. The dyeing composition according to the invention can also include various adjuvants conventionally used in hair dyeing compositions, such as antioxidants, penetrating agents, sequestering agents, perfumes, buffers, dispersing agents, surfactants, smoke-killing agents, ceramides. , preservatives, filtering agents, opacifying agents.
Of course, the person skilled in the art will try to choose this or these possible complementary compounds in such a way that the advantageous properties intrinsically related to the dyeing composition according to the invention are not substantially altered by the addition (s) considered.
The dye composition according to the invention can be presented in various forms, such as in the form of liquids, shampoos, creams, gels, or in any other form suitable for dyeing keratin fibers, and particularly human hair. It can be obtained by extemporaneous mixing of a composition, and also pulverulent, containing the cationic direct dye (s) with a composition containing the glycerin and / or the particular polyol and / or the particular polyol ether.
When the combination of the cationic direct dye and the glycerin and / or the particular polyol and / or the particular polyol ether defined according to the invention is used in a composition intended for oxidation dyeing (one or more oxidation bases are then used in the presence of one or more couplers) or when it is used in a composition intended for the direct lightening dye, then the dyeing composition according to the invention further includes at least one oxidizing agent selected, for example, from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulfates, and enzymes such as peroxidases, laccases, and two-electron oxidase reductases. The use of hydrogen peroxide "or enzymes is particularly preferred.
Another object of the invention is a process for dyeing keratin fibers and in particular human keratin fibers such as hair using the dyeing composition as defined above.
According to a first variant of this dyeing process according to the invention, at least one dyeing composition as defined above is applied to the fibers for a sufficient time to develop the desired dyeing, after which it is rinsed, it is eventually washed with shampoo, it is rinsed again and dried.
The time necessary for the development of the coloration on the keratin fibers is generally between 3 and 60 minutes even more precisely between 5 40 minutes
According to a second variant of this direct dyeing process according to the invention, at least one dyeing composition as defined above is applied to the fibers for a sufficient time to develop the desired dyeing, without final rinsing.
According to a particular embodiment of this dyeing process, and when the dyeing composition according to the invention includes at least one oxidation base and at least one preliminary step consisting of storing separately, on the one hand, a composition (Al ) comprising, in a medium suitable for dyeing, at least one cationic direct dye and at least one glycerin and / or a particular polyol and / or a particular polyol ether such as defined above and at least one oxidation base and, on the other hand, a composition (Bl) that includes, in a medium suitable for dyeing, at least one oxidizing agent, then in proceeding to its mixing at the time of use before applying this mixture on the keratin fibers.
According to another particular embodiment of this dyeing process, and when the dyeing composition according to the invention includes at least one oxidizing agent, the dyeing process includes a preliminary step consisting of storing separately, on the one hand, a composition (A2) comprising, in a medium suitable for dyeing, at least one direct cationic dye and at least glycerin and / or a particular polyol and / or a particular polyol ether such as defined above and, on the other hand, a composition (Bl) which includes, in a medium suitable for the dye, at least one oxidizing agent, then in mixing it at the time of use before applying this mixture on the keratin fibers.
Another object of the invention is a multi-compartment device or dye "kit" or any other conditioning system in several compartments of which a first compartment includes the composition (Al) or (A2) as defined above and a second compartment includes the composition (Bl) as defined above. These devices can be equipped with a means for providing the desired mixture on the hair, such as the devices described in patent FR-2,586,913 in the name of the applicant firm.
The following examples are intended to illustrate the invention without thereby limiting the scope.
EXAMPLES
EXAMPLE 1
The following dye composition was prepared:
Direct cationic dye of formula (I) 2 0.1 g Glycerin 10.0 g
2-amino-2-methyl-propanol ... c.s pH 9
Demineralized water c.s.p 100 g
M.A. *: Active Matter.
The composition indicated above was applied for 30 minutes on wicks of natural gray hair at 90% white. The hair strands were then rinsed, washed with a conventional shampoo and then dried.
They were stained in an intense purple hue.
EXAMPLE 2
The following dye composition was prepared:
Direct cationic dye of formula (I)? Or 0.12 g
Monome ile of propylene glycol 10.0 g
2-amino-2-methyl-propanol ... c.s pH 9
Demineralized water c.s.p 100 g
M.A. *: Active Matter.
The composition indicated above was applied for 30 minutes on wicks of natural gray hair with 90% white. The hair strands were then rinsed, washed with a conventional shampoo, then dried.
They were stained in an intense red tone.
It is noted that in relation to this date, the best method known to the applicant to carry out the aforementioned invention, is that which is clear from the present description of the invention.
Having described the invention as above, the content of the following is claimed as property.
Claims (23)
1. A composition for dyeing keratin fibers and in particular human keratin fibers such as hair, including in a medium suitable for dyeing, (i) at least one direct cationic dye of formula (I) below: A - N = N - B (I) in which: symbol A represents a group selected from the following Al a A3 structures: structures A1 to A3 in which Ri denotes a C 1 -C 4 alkyl radical, a phenyl radical which can be substituted by a C 1 -C 4 alkyl radical or a halogen atom selected from chlorine, bromine, iodine and fluorine; R 2 denotes a C 1 -C 4 alkyl radical or a phenyl radical; R3 and R, which are identical or different, represent a C1-C4 alkyl radical, a phenyl radical, or, in the case of the Al structure, can together form a substituted benzene ring, and in the case of the A2 structure, can together form a benzene ring optionally substituted by one or more alkyl radicals d, and C? -C4, alkoxy C1-C4, or N02; R3 may also designate a hydrogen atom; Z denotes an oxygen atom, sulfur or a group - NR2; M represents a group -CH, -CR (denoting R C 1 -C 4 alkyl), or -NR 5 (X ") r; K represents a group -CH, -CR (denoting R C 1 -C 4 alkyl), or - NR5 (X ") r; P represents a group -CH, -CR (r denoting C?-C 4 alkyl), or -NR 5 (X ") r; r designates zero or 1; R5 represents a 0"atom, an alkoxy radical of C? C4, or a C 1 -C 4 alkyl radical; e and R7 / identical or different, represent a hydrogen or halogen atom, selected from chlorine, bromine, iodine and fluorine, an alkyl radical of C? -C4 alkoxy of C? ~ C2, a radical -N02; X "represents an anion preferably selected from chloride, iodide, methyl sulfate, ethyl sulfate, acetate and perchlorate, with the proviso that if R designates an alkyl radical of Cx-C4 and Z designates an sulfur, R3 does not denote a hydrogen atom, if R5 designates 0", then r designates zero; if K or P or M designates -N-alkyl C? ~ C4 X ", then R6 or R7 is different from a hydrogen atom; if K designates -NR5 (X ~) r, then M = P = -CH; -CR; if M designates -NR5 (X ") r, then K = P = -CH; -CR; if P designates -NR5 (X") r, then K = M and designate - CH or -CR; if Z denotes -NR2 and R2 denotes an alkyl radical of C? ~ C4, then at least one of the radicals Ri, R 3 or R 4 of A2 is different from a C 1 -C 4 alkyl radical; the symbol B represents: - (a) a group of structure Bl following structure Bl in which, Rs represents a hydrogen atom, a halogen atom selected from chlorine, bromine, iodine, and fluorine, an alkyl radical of C? -C, alkoxy of C? -C4, a radical OH, -N02, -NHRU, R? 2Ri3, -NHCOalkyl of C? -C4, or form with Rg a ring of 5 or 6 members containing or not one or more heteroatoms selected from nitrogen, oxygen or sulfur; Rg represents a hydrogen atom, a halogen atom selected from chlorine, bromine, iodine and fluorine, an alkyl radical of C?-C4, alkoxy of C?-C4, or forms with Rio or Rn a ring of 5 or 6 members containing or not one or more heteroatoms selected from nitrogen, oxygen or sulfur; Rio represents a hydrogen atom, a radical -OH, a radical -NHRn, a radical -NR? 2R? 3; R n represents a hydrogen atom, a C 1 -C 4 alkyl radical, a monohydroxyalkyl radical of C1-C4, C2-C4 polyhydroxyalkyl, a phenyl radical; R 12 and Ri 3 / identical or different, represent a C 1 -C 4 alkyl radical, a C 1 -C 4 monohydroxyalkyl radical, polyhydroxyalkyl radical C2-C4; - (b) a 5- or 6-membered heterocyclic nitrogenous group capable of including other heteroatoms and / or carbonylated group and which can be substituted by one or more C?-C4, amino or phenyl alkyl radicals, and particularly a structure group B2 following: structure B2 in which, 14 and i5 identical or different, represent a hydrogen atom, a C 1 -C 4 alkyl radical, a phenyl radical, CH, I 3 Y designates the radical -CO or the radical -C =; n = 0 or 1, with, when n designates 1, U designates the radical -CO, characterized in that said composition also contains: (ii) at least glycerin and / or a polyol containing at least 4 carbon atoms and / or an aliphatic ether of Ci-Cß of C3-Cg polyol and / or a C2-C2 aromatic ether of C2- polyol C9
2. The composition according to claim 1, characterized in that in the formula (I), the C 1 -C 4 alkyl radicals and the C 1 -C 4 alkoxy radicals are methyl, ethyl, butyl, methoxy and ethoxy radicals.
3. The composition according to claim 2, characterized in that the cationic direct dyes respond to the structures (I)? a (I) 7 following: 25 I. O 20 CH3SO4 CH3S04" 25 CH3SO4- CH3SO4- CH3SO4" CH, S04 25 CH3SO4- CH3SO4- I C4H9 twenty 25 (D 49 25 fifteen twenty 25 CH3SO4 ~ 10 fifteen 25 25
4. The composition according to any of the preceding claims, characterized in that the cationic direct dye (s) of formula (I) represent 0.001 to 10% by weight of the total composition.
5. The composition according to claim 4, characterized in that the cationic direct dye (s) of formula (I) represent from 0.005 to 5% by weight of the total weight of the composition.
6. The composition according to any of the preceding claims, characterized in that the glycerin and / or the polyol containing at least 4 carbon atoms and / or the aliphatic ether of Ci-Cß of C3-Cg polyol and / or the aromatic ether of C6 -C8 of C2-C9 polyol represent from 0.1 to 40% by weight of the total weight of the composition.
7. The composition according to claim 6, characterized in that the glycerin and / or the polyol containing at least 4 carbon atoms and / or the aliphatic ether of Ci-Cβ of C3-Cg polyol and / or the aromatic ether of C6-Cs of C2-Cg polyol represent from 0.5 to 20% by weight of the total weight of the composition.
8. The composition according to any of the preceding claims, characterized in that it also contains additional direct dyes.
9. The composition according to any of the preceding claims, characterized in that the medium suitable for the keratin fibers (or support) is constituted by a mixture of water and at least one solvent selected from glycerin and / or polyols and / or ethers of polyols defined in claim 1.
10. The composition according to claim 9, characterized in that the medium further comprises at least one organic solvent.
11. The composition according to any of the preceding claims, characterized in that it has a pH comprised between 2 and 11, and preferably between 5 and 10.
12. The composition according to any of the preceding claims, characterized in that it is intended for oxidation dyeing and because it contains one or more oxidation bases selected from paraphenylenediamines, bis (phenyl) alkylene diamines, para-aminophenols, ortho -aminophenols and heterocyclic bases.
13. The composition according to the rei indication 12, characterized in that the oxidation base (s) represent 0.0005 to 12% by weight of the total weight of the dyeing composition.
14. The composition according to claim 13, characterized in that the oxidation base (s) represent from 0.005 to 6% by weight of the total weight of the dyeing composition.
15. The composition according to any of claims 12 to 14, characterized in that it includes one or more couplers selected from meta-phenyldiamines, meta-aminophenyl, meta-diphenols and heterocyclic couplers.
16. The composition according to claim 15, characterized in that the coupler (s) represent from 0.0001 to 10% by weight of the total weight of the dyeing composition.
17. The composition according to claim 16, characterized in that the coupler (s) represent from 0.005 to 5% by weight of the total weight of the dyeing composition.
18. The composition according to any of the preceding claims, characterized in that it is intended for oxidation dyeing or direct lightening dyeing and because it includes at least one oxidizing agent.
19. A process for dyeing keratin fibers and in particular human keratin fibers such as hair, characterized in that at least one dyeing composition as defined in any of the claims is applied to the fibers | to 11, for a sufficient time to develop the desired coloration, after which it is clarified, it is eventually washed with shampoo, rinsed again and dried.
20. The dyeing process of keratin fibers and in particular of human keratin fibers such as hair, characterized in that at least one dyeing composition as defined in any of claims 1 to 11 is applied to the fibers for a sufficient time to develop the desired coloration, without final rinse.
21. The dyeing process of keratin fibers and in particular of human keratin fibers such as hair, characterized in that it comprises a preliminary step consisting in storing separately, on the one hand, a composition (Al) comprising, in a medium suitable for the dye, at least one direct cationic dye and at least glycerin and / or a polyol and / or a polyol ether as defined in the preceding claims and at least one oxidation base and, on the other hand, a composition (Bl) which includes, in a medium suitable for the dye, at least one oxidizing agent, then in mixing it at the time of use before applying this mixture on the keratin fibers.
22. The dyeing process of keratin fibers and in particular of human keratin fibers such as hair, characterized in that it comprises a preliminary step consisting in storing separately, on the one hand, a composition (A2) comprising, in a suitable medium for the dye, at least one cationic direct dye and at least glycerin and / or a polyol and / or a polyol ether as defined in the preceding claims and at least one oxidation base and, on the other hand, a composition (Bl) which includes, in a suitable medium for the dye, at least one oxidizing agent, then in proceeding to its mixing at the time of use before applying this mixture on the keratin fibers.
23. A multi-compartment dyeing or compartment "kit" device, characterized in that a first compartment includes the composition (Al) or (A2) as defined in claim 21 or 22 and a second compartment includes the composition (Bl) as defined in rei indication 21 or 22.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9806752 | 1998-05-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MXPA99004785A true MXPA99004785A (en) | 2000-08-01 |
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