KR20010022885A - 산화 베이스로서 피라졸로-[1,5-a]-피리미딘 및 피리딘 커플러를 함유하는 염색용 조성물, 및 염색 방법 - Google Patents
산화 베이스로서 피라졸로-[1,5-a]-피리미딘 및 피리딘 커플러를 함유하는 염색용 조성물, 및 염색 방법 Download PDFInfo
- Publication number
- KR20010022885A KR20010022885A KR1020007001489A KR20007001489A KR20010022885A KR 20010022885 A KR20010022885 A KR 20010022885A KR 1020007001489 A KR1020007001489 A KR 1020007001489A KR 20007001489 A KR20007001489 A KR 20007001489A KR 20010022885 A KR20010022885 A KR 20010022885A
- Authority
- KR
- South Korea
- Prior art keywords
- amino
- pyrimidine
- alkyl
- composition
- dyeing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 65
- 238000004043 dyeing Methods 0.000 title claims abstract description 56
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title claims abstract description 30
- LDIJKUBTLZTFRG-UHFFFAOYSA-N pyrazolo[1,5-a]pyrimidine Chemical compound N1=CC=CN2N=CC=C21 LDIJKUBTLZTFRG-UHFFFAOYSA-N 0.000 title claims abstract description 28
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims abstract description 10
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 title claims description 10
- 239000007822 coupling agent Substances 0.000 title 1
- 230000001590 oxidative effect Effects 0.000 claims abstract description 29
- 239000000835 fiber Substances 0.000 claims abstract description 24
- 102000011782 Keratins Human genes 0.000 claims abstract description 21
- 108010076876 Keratins Proteins 0.000 claims abstract description 21
- -1 (C 1 -C 4 ) alkyl radical Chemical class 0.000 claims description 55
- 150000003839 salts Chemical class 0.000 claims description 21
- 239000002253 acid Substances 0.000 claims description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- 239000002585 base Substances 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 10
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 9
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 8
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 8
- 239000007800 oxidant agent Substances 0.000 claims description 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 6
- 125000003282 alkyl amino group Chemical group 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 230000002255 enzymatic effect Effects 0.000 claims description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical group Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 4
- 150000005840 aryl radicals Chemical class 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 235000012054 meals Nutrition 0.000 claims description 4
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- BMTSZVZQNMNPCT-UHFFFAOYSA-N 2-aminopyridin-3-ol Chemical compound NC1=NC=CC=C1O BMTSZVZQNMNPCT-UHFFFAOYSA-N 0.000 claims description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 3
- MRQOOXQWSNRMAM-UHFFFAOYSA-N 2,5-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine Chemical compound NC1=CC(C)=NC2=C(N)C(C)=NN21 MRQOOXQWSNRMAM-UHFFFAOYSA-N 0.000 claims description 2
- BXBOXUNPNIJELB-UHFFFAOYSA-N 2,6-dimethoxypyridine-3,5-diamine Chemical compound COC1=NC(OC)=C(N)C=C1N BXBOXUNPNIJELB-UHFFFAOYSA-N 0.000 claims description 2
- VFFKUMJVZWLOQM-UHFFFAOYSA-N 2,6-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine Chemical compound NC1=C(C)C=NC2=C(N)C(C)=NN21 VFFKUMJVZWLOQM-UHFFFAOYSA-N 0.000 claims description 2
- LGZOJZFHAJJLCF-UHFFFAOYSA-N 2,7-dimethylpyrazolo[1,5-a]pyrimidine-3,5-diamine Chemical compound CC1=CC(N)=NC2=C(N)C(C)=NN21 LGZOJZFHAJJLCF-UHFFFAOYSA-N 0.000 claims description 2
- RPTFEYVETOJOPF-UHFFFAOYSA-N 2-(3,4-diamino-6-methoxypyridin-2-yl)ethanol Chemical compound COC1=CC(N)=C(N)C(CCO)=N1 RPTFEYVETOJOPF-UHFFFAOYSA-N 0.000 claims description 2
- OIAATOHBNVCLJY-UHFFFAOYSA-N 2-[(3-amino-5-methylpyrazolo[1,5-a]pyrimidin-7-yl)amino]ethanol Chemical compound N1=C(C)C=C(NCCO)N2N=CC(N)=C21 OIAATOHBNVCLJY-UHFFFAOYSA-N 0.000 claims description 2
- ATBJHESGXAEWOU-UHFFFAOYSA-N 2-[(3-aminopyrazolo[1,5-a]pyrimidin-7-yl)-(2-hydroxyethyl)amino]ethanol Chemical compound OCCN(CCO)C1=CC=NC2=C(N)C=NN21 ATBJHESGXAEWOU-UHFFFAOYSA-N 0.000 claims description 2
- RHIPXPBQVGXJNL-UHFFFAOYSA-N 2-[(3-aminopyrazolo[1,5-a]pyrimidin-7-yl)amino]ethanol Chemical compound OCCNC1=CC=NC2=C(N)C=NN21 RHIPXPBQVGXJNL-UHFFFAOYSA-N 0.000 claims description 2
- ZQLZWNDBBQUIEY-UHFFFAOYSA-N 2-[(7-aminopyrazolo[1,5-a]pyrimidin-3-yl)-(2-hydroxyethyl)amino]ethanol Chemical compound NC1=CC=NC2=C(N(CCO)CCO)C=NN12 ZQLZWNDBBQUIEY-UHFFFAOYSA-N 0.000 claims description 2
- HARBPHQCTIDSBX-UHFFFAOYSA-N 2-[(7-aminopyrazolo[1,5-a]pyrimidin-3-yl)amino]ethanol Chemical compound NC1=CC=NC2=C(NCCO)C=NN12 HARBPHQCTIDSBX-UHFFFAOYSA-N 0.000 claims description 2
- FJLWSRYKQCJGGK-UHFFFAOYSA-N 2-[3,5-diamino-6-(2-hydroxyethoxy)pyridin-2-yl]oxyethanol Chemical compound NC1=CC(N)=C(OCCO)N=C1OCCO FJLWSRYKQCJGGK-UHFFFAOYSA-N 0.000 claims description 2
- MWXUGXZKBKIMKB-UHFFFAOYSA-N 2-methylpyrazolo[1,5-a]pyrimidine-3,7-diamine Chemical compound NC1=CC=NC2=C(N)C(C)=NN21 MWXUGXZKBKIMKB-UHFFFAOYSA-N 0.000 claims description 2
- OBOSXEWFRARQPU-UHFFFAOYSA-N 2-n,2-n-dimethylpyridine-2,5-diamine Chemical compound CN(C)C1=CC=C(N)C=N1 OBOSXEWFRARQPU-UHFFFAOYSA-N 0.000 claims description 2
- BGMAIXRJQFTHIH-UHFFFAOYSA-N 3-amino-4H-pyrazolo[1,5-a]pyrimidin-5-one Chemical compound C1=CC(O)=NC2=C(N)C=NN21 BGMAIXRJQFTHIH-UHFFFAOYSA-N 0.000 claims description 2
- DMBUAGDHNUPLRA-UHFFFAOYSA-N 5,6-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine Chemical compound NC1=C(C)C(C)=NC2=C(N)C=NN21 DMBUAGDHNUPLRA-UHFFFAOYSA-N 0.000 claims description 2
- VNECCGPOXBLLOG-UHFFFAOYSA-N 5-amino-2,6-dimethoxypyridin-3-ol Chemical compound COC1=NC(OC)=C(O)C=C1N VNECCGPOXBLLOG-UHFFFAOYSA-N 0.000 claims description 2
- AJGLCXBDYCEVIE-UHFFFAOYSA-N 5-chloro-3-hydroxy-1h-pyridin-2-one Chemical compound OC1=CC(Cl)=CN=C1O AJGLCXBDYCEVIE-UHFFFAOYSA-N 0.000 claims description 2
- KIEGFAYDOKCBOK-UHFFFAOYSA-N 6-hydroxy-4,5-dimethyl-1h-pyridin-2-one Chemical compound CC1=CC(=O)NC(O)=C1C KIEGFAYDOKCBOK-UHFFFAOYSA-N 0.000 claims description 2
- ATCBPVDYYNJHSG-UHFFFAOYSA-N 6-methoxy-2-n-methylpyridine-2,3-diamine Chemical compound CNC1=NC(OC)=CC=C1N ATCBPVDYYNJHSG-UHFFFAOYSA-N 0.000 claims description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 claims description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 claims description 2
- RVWZJQLGEUQYMT-UHFFFAOYSA-N N1=C(C)C=C(O)N2N=CC(N)=C21 Chemical compound N1=C(C)C=C(O)N2N=CC(N)=C21 RVWZJQLGEUQYMT-UHFFFAOYSA-N 0.000 claims description 2
- PKACFTKQQUDJDA-UHFFFAOYSA-N OC1=CC=NC2=C(N)C=NN21 Chemical compound OC1=CC=NC2=C(N)C=NN21 PKACFTKQQUDJDA-UHFFFAOYSA-N 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims description 2
- 125000002843 carboxylic acid group Chemical group 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 239000011630 iodine Substances 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 150000004965 peroxy acids Chemical class 0.000 claims description 2
- FFNJDUZBKSGSIV-UHFFFAOYSA-N pyrazolo[1,5-a]pyrimidine-3,5-diamine Chemical compound C1=CC(N)=NC2=C(N)C=NN21 FFNJDUZBKSGSIV-UHFFFAOYSA-N 0.000 claims description 2
- PNFZIEOWPDFJBH-UHFFFAOYSA-N pyrazolo[1,5-a]pyrimidine-3,7-diamine Chemical compound NC1=CC=NC2=C(N)C=NN21 PNFZIEOWPDFJBH-UHFFFAOYSA-N 0.000 claims description 2
- VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 claims description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 2
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- 229940095064 tartrate Drugs 0.000 claims description 2
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 claims description 2
- 239000000975 dye Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 235000019441 ethanol Nutrition 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 240000000249 Morus alba Species 0.000 description 3
- 235000008708 Morus alba Nutrition 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-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
- 238000004040 coloring Methods 0.000 description 3
- 230000035900 sweating Effects 0.000 description 3
- FNXIURBJYHTJHO-UHFFFAOYSA-N 1h-pyrazolo[4,3-d]pyrimidine-3,7-diamine Chemical compound N1=CN=C2C(N)=NNC2=C1N FNXIURBJYHTJHO-UHFFFAOYSA-N 0.000 description 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-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
- 239000002535 acidifier Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000002932 luster Substances 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229960003330 pentetic acid Drugs 0.000 description 2
- 230000019612 pigmentation Effects 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 2
- 229940001584 sodium metabisulfite Drugs 0.000 description 2
- 235000010262 sodium metabisulphite Nutrition 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 1
- JJHVYGVVMBYCMQ-UHFFFAOYSA-N 6-hydroxy-4-methyl-1h-pyridin-2-one Chemical compound CC=1C=C(O)NC(=O)C=1 JJHVYGVVMBYCMQ-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 229920002907 Guar gum Polymers 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 compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 229940106189 ceramide Drugs 0.000 description 1
- 150000001783 ceramides Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000000665 guar gum Substances 0.000 description 1
- 229960002154 guar gum Drugs 0.000 description 1
- 235000010417 guar gum Nutrition 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 238000005691 oxidative coupling reaction Methods 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Description
실시예 | 1 | 2 | 3 |
3,7-디아미노피라졸로피리미딘·2HCl(화학식 Ⅰ 의 산화 베이스) | 0.666 | 0.666 | 0.666 |
2-아미노-3-히드록시피리딘 (화학식 Ⅱ 의 커플러) | 0.333 | - | - |
2,6-디아미노피리딘 (화학식 Ⅱ 의 커플러) | - | 0.333 | - |
3,5-디아미노-2-(γ-히드록시프로필옥시에틸옥시)피리딘·2HCl(화학식 Ⅱ 의 커플러) | - | - | 0.858 |
일반 염색 매개물 No.1 | (*) | (*) | (*) |
탈이온수 qs | 100 g | 100 g | 100 g |
실시예 | 염색 pH | 수득한 색조 |
1 | 10 ±0.2 | 진주광택을 지닌 적회색 |
2 | 10 ±0.2 | 짙은 적자색 |
3 | 10 ±0.2 | 짙은 적자색 |
실시예 | 4 | 5 | 6 |
3,7-디아미노피라졸로피리미딘·2HCl(화학식 Ⅰ 의 산화 베이스) | 0.666 | 0.666 | 0.666 |
2,6-디히드록시-4-메틸피리딘 (화학식 Ⅱ 의 커플러) | 0.345 | - | - |
2,6-디히드록시-3,4-디메틸피리딘 (화학식 Ⅱ 의 커플러) | - | 0.417 | - |
3,5-디아미노-2-(β,γ-디히드록시프로필옥시)피리딘·2HCl(화학식 Ⅱ 의 커플러) | - | - | 0.816 |
일반 염색 매개물 No.2 | (**) | (**) | (**) |
탈이온수 qs | 100 g | 100 g | 100 g |
실시예 | 염색 pH | 수득한 색조 |
4 | 5.7 ±0.2 | 진주광택을 지닌 적회색 |
5 | 5.7 ±0.2 | 진주광택 |
6 | 5.7 ±0.2 | 짙은 적자색 |
Claims (11)
- 염색에 적합한 매질 내에 하기 화학식 Ⅰ 의 피라졸로[1,5-a]피리미딘 및 이의 산 또는 염기 부가염으로부터 선택된 하나 이상의 산화 베이스, 및 화학식 Ⅱ 의 피리딘 및 이의 산 부가염으로부터 선택된 하나 이상의 커플러를 함유하며, 화학식 Ⅰ 및/또는 화학식 Ⅱ 의 화합물의 산화를 일으킬 수 있는 어떠한 효소계도 존재하지 않는 것을 특징으로 하는 케라틴 섬유, 특히 모발과 같은 인간 케라틴 섬유의 산화 염색용 조성물:[화학식 Ⅰ]{식 중,- R1, R2, R3및 R4는 동일 또는 상이하며, 수소원자, (C1-C4)알킬 라디칼, 아릴 라디칼, 히드록시(C1-C4)알킬 라디칼, 폴리히드록시(C2-C4)알킬 라디칼, (C1-C4)알콕시(C1-C4)알킬 라디칼, 아미노(C1-C4)알킬 라디칼 (아민은 아세틸, 우레이도 또는 술포닐로 보호될 수 있다), (C1-C4)알킬아미노(C1-C4)알킬 라디칼, 디[(C1-C4)알킬]아미노(C1-C4)알킬 라디칼 (디알킬은 5- 또는 6-원 지방족 또는 헤테로시클릭 고리를 형성할 수 있다), 히드록시(C1-C4)알킬아미노(C1-C4)알킬 라디칼 또는 디[히드록시(C1-C4)알킬]아미노(C1-C4)알킬 라디칼을 나타내며;- X 라디칼은 동일 또는 상이하며, 수소원자, (C1-C4)알킬 라디칼, 아릴 라디칼, 히드록시(C1-C4)알킬 라디칼, 폴리히드록시(C2-C4)알킬 라디칼, 아미노(C1-C4)알킬 라디칼, (C1-C4)알킬아미노(C1-C4)알킬 라디칼, 디[(C1-C4)알킬]아미노(C1-C4)알킬 라디칼 (디알킬은 5- 또는 6-원 지방족 또는 헤테로시클릭 고리를 형성할 수 있다), 히드록시(C1-C4)알킬아미노(C1-C4)알킬 라디칼, 디[히드록시(C1-C4)알킬]아미노(C1-C4)알킬 라디칼, 아미노 라디칼, (C1-C4)알킬아미노 라디칼, 디[(C1-C4)알킬]아미노 라디칼, 할로겐원자, 카르복실산기 또는 술폰산기를 나타내며;- i 는 0, 1, 2 또는 3 이며;- p 는 0 또는 1 이며;- q 는 0 또는 1 이며;- n 은 0 또는 1 이며;단,- p + q 는 0 이 아니고;- (ⅱ) p + q 가 2 이면, n 은 0 이며, NR1R2및 NR3R4기는 (2,3), (5,6), (6,7), (3,5) 또는 (3,7) 위치에 있고;- (ⅲ) p + q 가 1 이면, n 은 1 이며, NR1R2(또는 NR3R4) 및 OH 기는 (2,3), (5,6), (6,7), (3,5) 또는 (3,7) 위치에 있다},[화학식 Ⅱ]{식 중,- R5는 수소원자 또는 히드록실, 아미노, (C1-C4)알콕시, 모노- 또는 디(C1-C4)알킬아미노, 모노히드록시(C1-C4)알킬아미노, 폴리히드록시(C2-C4)알킬아미노, 모노히드록시(C1-C4)알콕시, 폴리히드록시(C2-C4)알콕시 또는 모노히드록시(C1-C4)알콕시(C1-C4)알콕시 라디칼을 나타내며;- R6은 수소원자 또는 히드록실, 아미노 또는 (C1-C4)알킬 라디칼을 나타내며;- R7은 수소원자 또는 (C1-C4)알킬 라디칼을 나타내며;- R8은 수소원자 또는 염소, 브롬, 요오드 또는 불소와 같은 할로겐원자, 또는 아미노 라디칼을 나타내며;- R9는 수소원자 또는 히드록실, 아미노, (C1-C4)알콕시, 모노히드록시(C1-C4)알콕시 또는 폴리히드록시(C2-C4)알콕시 라디칼을 나타내며;- R5내지 R9라디칼 중 둘 이상은 수소원자가 아니다}.
- 제 1 항에 있어서, 화학식 Ⅰ 의 피라졸로[1,5-a]피리미딘이 하기 및 이의 산 또는 염기 부가염으로부터 선택되는 것을 특징으로 하는 조성물:- 피라졸로[1,5-a]피리미딘-3,7-디아민,- 2-메틸피라졸로[1,5-a]피리미딘-3,7-디아민,- 2,5-디메틸피라졸로[1,5-a]피리미딘-3,7-디아민,- 피라졸로[1,5-a]피리미딘-3,5-디아민,- 2,7-디메틸피라졸로[1,5-a]피리미딘-3,5-디아민,- 3-아미노피라졸로[1,5-a]피리미딘-7-올,- 3-아미노-5-메틸피라졸로[1,5-a]피리미딘-7-올,- 3-아미노피라졸로[1,5-a]피리미딘-5-올,- 2-(3-아미노피라졸로[1,5-a]피리미딘-7-일아미노)에탄올,- 3-아미노-7-(β-히드록시에틸아미노)-5-메틸피라졸로[1,5-a]피리미딘,- 2-(7-아미노피라졸로[1,5-a]피리미딘-3-일아미노)에탄올,- 2-[(3-아미노피라졸로[1,5-a]피리미딘-7-일)(2-히드록시에틸)아미노]에탄올,- 2-[(7-아미노피라졸로[1,5-a]피리미딘-3-일)(2-히드록시에틸)아미노]에탄올,- 5,6-디메틸피라졸로[1,5-a]피리미딘-3,7-디아민,- 2,6-디메틸피라졸로[1,5-a]피리미딘-3,7-디아민,- 2,5,N-7,N-7-테트라메틸피라졸로[1,5-a]피리미딘-3,7-디아민.
- 제 1 항 또는 제 2 항에 있어서, 화학식 Ⅱ 의 피리딘이 하기 및 이의 산 부가염으로부터 선택되는 것을 특징으로 하는 조성물:- 2,6-디히드록시-3,4-디메틸피리딘,- 5-클로로-2,3-디히드록시피리딘,- 3,5-디아미노-2,6-디메톡시피리딘,- 3-아미노-2-(β-히드록시에틸)아미노-6-메톡시피리딘,- 2,6-비스(β-히드록시에틸옥시)-3,5-디아미노피리딘,- 3-아미노-5-히드록시-2,6-디메톡시피리딘,- 3-아미노-2-메틸아미노-6-메톡시피리딘,- 2-아미노-3-히드록시피리딘,- 2-디메틸아미노-5-아미노피리딘,- 2,6-디아미노피리딘,- 3,5-디아미노-2-(β,γ-디히드록시프로필옥시)피리딘,- 3,5-디아미노-2-(γ-히드록시프로필옥시에틸옥시)피리딘.
- 제 1 항 내지 제 3 항 중 어느 한 항에 있어서, 산 부가염이 히드로클로라이드, 히드로브로마이드, 술페이트, 시트레이트, 숙시네이트, 타르트레이트, 락테이트 및 아세테이트로부터 선택되며, 염기 부가염이 수산화나트륨, 수산화칼륨, 수성 암모니아 또는 아민으로 수득된 것들로부터 선택되는 것을 특징으로 하는 조성물.
- 제 1 항 내지 제 4 항 중 어느 한 항에 있어서, 화학식 Ⅰ 의 피라졸로[1,5-a]피리미딘(들) 및/또는 이들의 산 또는 염기 부가염(들)이 염색 조성물 총 중량에 대해 0.0005 내지 12 중량% 를 나타내는 것을 특징으로 하는 조성물.
- 제 5 항에 있어서, 화학식 Ⅰ 의 피라졸로[1,5-a]피리미딘(들) 및/또는 이들의 산 또는 염기 부가염(들)이 염색 조성물 총 중량에 대해 0.005 내지 6 중량% 를 나타내는 것을 특징으로 하는 조성물.
- 제 1 항 내지 제 6 항 중 어느 한 항에 있어서, 화학식 Ⅱ 의 피리딘(들) 및/또는 이들의 산 부가염(들)이 염색 조성물 총 중량에 대해 0.0001 내지 10 중량% 를 나타내는 것을 특징으로 하는 조성물.
- 제 7 항에 있어서, 화학식 Ⅱ 의 피리딘(들) 및/또는 이들의 산 부가염(들)이 염색 조성물 총 중량에 대해 0.005 내지 5 중량% 를 나타내는 것을 특징으로 하는 조성물.
- 케라틴 섬유, 특히 모발과 같은 인간의 케라틴 섬유의 산화 염색 방법으로서, 제 1 항 내지 제 8 항 중 어느 한 항에 정의된 하나 이상의 염색용 조성물을 상기 섬유에 적용하고, 사용시 염색용 조성물에 첨가되거나, 동시에 또는 연속적으로 적용되는 산화 조성물에 존재하는 비효소적 산화제를 사용하여, 산성, 중성 또는 알칼리성 pH 에서 발색시키는 것을 특징으로 하는 방법.
- 제 9 항에 있어서, 산화제가 과산화수소, 과산화수소 요소, 알칼리금속 브로메이트, 과산 및 과염으로부터 선택되는 것을 특징으로 하는 방법.
- 제 1 항 내지 제 8 항 중 어느 한 항에 정의된 염색용 조성물을 포함하는 제 1 구획, 및 비효소적 산화제를 함유하는 산화 조성물을 포함하는 제 2 구획의 수 개의 구획을 갖는 염색 다중 구획 장치 또는 키트.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR98/07797 | 1998-06-19 | ||
FR9807797A FR2779952B1 (fr) | 1998-06-19 | 1998-06-19 | Composition tinctoriale contenant une pyrazolo-[1,5-a]- pyrimidine a titre de base d'oxydation et un coupleur pyridinique, et procedes de teinture |
PCT/FR1999/001294 WO1999066894A1 (fr) | 1998-06-19 | 1999-06-02 | COMPOSITION TINCTORIALE CONTENANT UNE PYRAZOLO-[1,5-a]-PYRIMIDINE A TITRE DE BASE D'OXYDATION ET UN COUPLEUR PYRIDINIQUE, ET PROCEDES DE TEINTURE |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20010022885A true KR20010022885A (ko) | 2001-03-26 |
KR100364310B1 KR100364310B1 (ko) | 2002-12-11 |
Family
ID=9527632
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020007001489A Expired - Fee Related KR100364310B1 (ko) | 1998-06-19 | 1999-06-02 | 산화 베이스로서 피라졸로-[1,5-a]-피리미딘 및 피리딘커플러를 함유하는 염색용 조성물, 및 염색 방법 |
Country Status (18)
Country | Link |
---|---|
US (1) | US6692540B1 (ko) |
EP (1) | EP1030648B1 (ko) |
JP (1) | JP2002518610A (ko) |
KR (1) | KR100364310B1 (ko) |
CN (1) | CN1149065C (ko) |
AR (1) | AR019326A1 (ko) |
AT (1) | ATE255401T1 (ko) |
AU (1) | AU4044499A (ko) |
BR (1) | BR9906542A (ko) |
CA (1) | CA2301076A1 (ko) |
DE (1) | DE69913307T2 (ko) |
ES (1) | ES2212559T3 (ko) |
FR (1) | FR2779952B1 (ko) |
HU (1) | HUP0003487A3 (ko) |
PL (1) | PL338699A1 (ko) |
PT (1) | PT1030648E (ko) |
RU (1) | RU2193390C2 (ko) |
WO (1) | WO1999066894A1 (ko) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2831056B1 (fr) * | 2001-10-24 | 2004-05-28 | Oreal | Composition tinctoriale comprenant le 1-n-(b-hydroxyethyl) 4-hydroxy indole a titre de premier coupleur ; procedes de teinture |
FR2832148B1 (fr) * | 2001-11-14 | 2004-05-21 | Oreal | Nouvelles bases d'oxydation 2,5-diaminopyridine utiles pour la teinture des fibres keratiniques |
FR2845280B1 (fr) * | 2002-10-04 | 2006-06-02 | Oreal | Nouveaux coupleurs 6-alcoxy-2,3-diaminopyridine dont le radical amino en position 2 est un radical amino disubstitue et utilisation de ces coupleurs pour la teinture des fibres keratiniques |
US7044987B2 (en) | 2002-10-04 | 2006-05-16 | L'oreal S.A. | 6-alkoxy-2,3-diaminopyridine couplers in which the amino radical in position 2 is a monosubstituted amino radical, and use of these couplers for dyeing keratin fibres |
US7238211B2 (en) | 2002-10-04 | 2007-07-03 | L'oreal S.A. | 6-alkoxy-2,3-diaminopyridine couplers in which the amino radical in position 2 is a disubstituted amino radical, and use of these couplers for dyeing keratin fibres |
FR2845281B1 (fr) * | 2002-10-04 | 2006-05-05 | Oreal | Composition tinctoriale comprenant au moins une base d'oxydation pyrazolopyrimidine et au moins un coupleur 6-alcoxy 2,3-diaminopyridimine |
FR2845283B1 (fr) * | 2002-10-04 | 2006-05-05 | Oreal | Composition tinctoriale comprenant au moins une base d'oxydation heterocyclique et au moins un coupleur 2,3-diaminopyridine substitue |
EP1586302A1 (fr) * | 2004-04-05 | 2005-10-19 | L'oreal | Composition tinctoriale comprenant au moins une base d'oxydation pyrazolopyrimidine et au moins un coupleur 6-alcoxy-2,3-diaminopyridine |
US10329298B2 (en) | 2016-08-31 | 2019-06-25 | Agios Pharmaceuticals, Inc. | Inhibitors of cellular metabolic processes |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
LU71015A1 (ko) * | 1974-09-27 | 1976-08-19 | ||
DE3115643A1 (de) * | 1981-04-18 | 1982-12-16 | Henkel Kgaa | "verwendung von dihydroxypyridinen als kupplerkomponente in oxidationsharrfarbstoffen und haarfaerbemittel" |
DE3132885A1 (de) * | 1981-08-20 | 1983-03-03 | Wella Ag | Mittel und verfahren zur faerbung von haaren |
DE3148651A1 (de) * | 1981-12-09 | 1983-07-21 | Henkel Kgaa | "haarfaerbemittel, enthaltend 5-halo-2,3-pyridindiole als kupplerkomponente" |
DE3442128A1 (de) * | 1984-11-17 | 1986-05-22 | Wella Ag | Neue 3-amino-5-hydroxypyridinderivate und diese verbindungen enthaltende haarfaerbemittel |
DE3530732A1 (de) * | 1985-08-28 | 1987-03-12 | Wella Ag | Mittel und verfahren zur faerbung von haaren mit 2,6-diamino-pyridinderivaten |
FR2586913B1 (fr) | 1985-09-10 | 1990-08-03 | Oreal | Procede pour former in situ une composition constituee de deux parties conditionnees separement et ensemble distributeur pour la mise en oeuvre de ce procede |
DE3917304A1 (de) * | 1989-05-27 | 1990-11-29 | Wella Ag | Oxidationshaarfaerbemittel |
DE3942357A1 (de) * | 1989-12-21 | 1991-06-27 | Boehringer Mannheim Gmbh | 3-aminopyrazolo-heterocyclen, deren verwendung zur bestimmung von wasserstoffperoxid, wasserstoffperoxid-bildenden systemen, peroxidase, peroxidatisch wirksamen substanzen oder von elektronenreichen aromatischen verbindungen, entsprechende bestimmungsverfahren und hierfuer geeignete mittel |
US5082467A (en) * | 1990-02-08 | 1992-01-21 | Kao Corporation | Dye composition for keratinous fibers |
DE4029324A1 (de) * | 1990-09-15 | 1992-03-19 | Henkel Kgaa | Haarfaerbemittel |
DE4133957A1 (de) * | 1991-10-14 | 1993-04-15 | Wella Ag | Haarfaerbemittel mit einem gehalt an aminopyrazolderivaten sowie neue pyrazolderivate |
JPH0678313B2 (ja) * | 1992-03-06 | 1994-10-05 | 花王株式会社 | 2−アルコキシ−3,5−ジアミノピリジン誘導体、その塩及びこれを含有する角質繊維染色剤組成物 |
FR2698266B1 (fr) | 1992-11-20 | 1995-02-24 | Oreal | Utilisation du 4-hydroxy- ou 4-aminobenzimidazole ou de leurs dérivés comme coupleurs dans des compositions tinctoriales d'oxydation, compositions et procédés de mise en Óoeuvre. |
FR2707489B1 (fr) | 1993-07-13 | 1995-09-22 | Oreal | Composition de teinture d'oxydation des fibres kératiniques comprenant un para-aminophénol, le 2-méthyl 5-aminophénol et une paraphénylènediamine et/ou une bis-phénylalkylènediamine. |
FR2746309B1 (fr) * | 1996-03-22 | 1998-04-17 | Oreal | Composition de teinture des fibres keratiniques contenant des pyrazolopyrimidineoxo ; leur utilisation pour la teinture comme coupleurs, procedes de teinture |
FR2750048B1 (fr) * | 1996-06-21 | 1998-08-14 | Oreal | Compositions de teinture des fibres keratiniques contenant des derives pyrazolo-(1, 5-a)-pyrimidine, procede de teinture, nouveaux derives pyrazolo-(1, 5-a)-pyrimidine et leur procede de preparation |
FR2763241B1 (fr) | 1997-05-13 | 1999-07-02 | Oreal | Composition de teinture des fibres keratiniques comprenant une pyrazolin-4,5-dione et une amine primaire aromatique |
FR2763841B1 (fr) | 1997-06-03 | 2000-02-11 | Oreal | Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition |
FR2771631B1 (fr) * | 1997-12-03 | 2001-02-02 | Oreal | Compositions de teinture des fibres keratiniques contenant des 3-amino pyrazolo-[1,5-a]-pyrimidines, procede de teinture, nouvelles 3-amino pyrazolo- [1,5-a]-pyrimidines et leur procede de preparation |
-
1998
- 1998-06-19 FR FR9807797A patent/FR2779952B1/fr not_active Expired - Fee Related
-
1999
- 1999-06-02 JP JP2000555580A patent/JP2002518610A/ja active Pending
- 1999-06-02 US US09/485,914 patent/US6692540B1/en not_active Expired - Fee Related
- 1999-06-02 RU RU2000106525/14A patent/RU2193390C2/ru not_active IP Right Cessation
- 1999-06-02 WO PCT/FR1999/001294 patent/WO1999066894A1/fr not_active Application Discontinuation
- 1999-06-02 DE DE69913307T patent/DE69913307T2/de not_active Expired - Fee Related
- 1999-06-02 HU HU0003487A patent/HUP0003487A3/hu unknown
- 1999-06-02 KR KR1020007001489A patent/KR100364310B1/ko not_active Expired - Fee Related
- 1999-06-02 ES ES99923653T patent/ES2212559T3/es not_active Expired - Lifetime
- 1999-06-02 CN CNB998013854A patent/CN1149065C/zh not_active Expired - Fee Related
- 1999-06-02 CA CA002301076A patent/CA2301076A1/fr not_active Abandoned
- 1999-06-02 PL PL99338699A patent/PL338699A1/xx not_active Application Discontinuation
- 1999-06-02 BR BRPI9906542-8A patent/BR9906542A/pt not_active IP Right Cessation
- 1999-06-02 PT PT99923653T patent/PT1030648E/pt unknown
- 1999-06-02 AT AT99923653T patent/ATE255401T1/de not_active IP Right Cessation
- 1999-06-02 AU AU40444/99A patent/AU4044499A/en not_active Abandoned
- 1999-06-02 EP EP99923653A patent/EP1030648B1/fr not_active Expired - Lifetime
- 1999-06-17 AR ARP990102906A patent/AR019326A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
FR2779952A1 (fr) | 1999-12-24 |
CN1275071A (zh) | 2000-11-29 |
EP1030648A1 (fr) | 2000-08-30 |
HUP0003487A3 (en) | 2004-01-28 |
US6692540B1 (en) | 2004-02-17 |
PL338699A1 (en) | 2000-11-20 |
AR019326A1 (es) | 2002-02-13 |
DE69913307T2 (de) | 2004-09-16 |
BR9906542A (pt) | 2007-05-29 |
RU2193390C2 (ru) | 2002-11-27 |
ATE255401T1 (de) | 2003-12-15 |
KR100364310B1 (ko) | 2002-12-11 |
HUP0003487A2 (hu) | 2001-02-28 |
WO1999066894A1 (fr) | 1999-12-29 |
AU4044499A (en) | 2000-01-10 |
FR2779952B1 (fr) | 2000-08-04 |
EP1030648B1 (fr) | 2003-12-03 |
PT1030648E (pt) | 2004-04-30 |
CA2301076A1 (fr) | 1999-12-29 |
ES2212559T3 (es) | 2004-07-16 |
DE69913307D1 (de) | 2004-01-15 |
JP2002518610A (ja) | 2002-06-25 |
CN1149065C (zh) | 2004-05-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6797013B1 (en) | Oxidation dyeing composition for keratinous fibres containing a 3-aminopyridine azo derivative and dyeing method using said composition | |
US6395042B1 (en) | Composition for the oxidation dyeing of keratin fibers and dyeing process using this composition | |
US5980585A (en) | Compositions for dyeing keratinous fibers comprising imidazopyridine derivatives and process | |
KR20010022961A (ko) | 케라틴 섬유의 산화 염색용 조성물 및 이를 사용한 염색 방법 | |
ES2255175T3 (es) | Composicion para el teñido por oxidacion de las fibras queratinicas que comprende 2-cloro 6-metil 3-aminofenol y dos bases de oxidacion, y procedimiento de teñido. | |
JP2000309517A (ja) | ケラチン繊維の酸化染色用組成物及びこの組成物を使用する染色方法 | |
KR100336672B1 (ko) | 케라틴 섬유용 산화 염색 조성물 및 상기 조성물을 사용한 염색 방법 | |
KR100364310B1 (ko) | 산화 베이스로서 피라졸로-[1,5-a]-피리미딘 및 피리딘커플러를 함유하는 염색용 조성물, 및 염색 방법 | |
JP3307607B2 (ja) | ケラチン繊維染色用組成物及びそれを用いた染色方法 | |
US6277156B1 (en) | Oxidation dyeing composition for keratin fibres comprising 2-chloro-6-methyl-3-aminophenol and an oxidation base, and dyeing method | |
AU730767B2 (en) | Composition for the oxidation dyeing of keratin fibres and dyeing process using this composition | |
KR20000069232A (ko) | 케라틴 섬유용 산화 염색 조성물 | |
KR20010022886A (ko) | 산화 베이스로서의 피라졸로[1,5-a]피리미딘 및 나프탈렌 커플러를 함유하는 염색 조성물, 및 염색 방법 | |
JP3451096B2 (ja) | ケラチン繊維の酸化染色用組成物と該組成物を使用する染色方法 | |
JP2000309516A (ja) | 酸化ベースとして単環式のポリアミノピリミジンとピラゾロ[1,5−a]ピリミジン、及びカップラーを含有する染色用組成物及び染色方法 | |
KR20010022960A (ko) | 케라틴 섬유의 산화 염색용 조성물 및 이를 사용한 염색 방법 | |
CZ2000383A3 (cs) | Barvící prostředek obsahující pyrazolo[l,5- ajpyrimidin jako oxidační bázi a naftalenové spojovací činidlo a způsob barvení | |
CZ440999A3 (cs) | Prostředek pro oxidativní barvení keratinových vláken a způsob barvení používající tento prostředek | |
CZ426799A3 (cs) | Prostředek pro oxidační barvení keratinových vláken a postup barvení za použití tohoto prostředku | |
CZ2000382A3 (cs) | Prostředek pro oxidační barvení keratinových vláken a způsob barvení používající tento prostředek |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A201 | Request for examination | ||
PA0105 | International application |
Patent event date: 20000214 Patent event code: PA01051R01D Comment text: International Patent Application |
|
PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 20000214 Comment text: Request for Examination of Application |
|
PG1501 | Laying open of application | ||
E902 | Notification of reason for refusal | ||
PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 20020130 Patent event code: PE09021S01D |
|
E701 | Decision to grant or registration of patent right | ||
PE0701 | Decision of registration |
Patent event code: PE07011S01D Comment text: Decision to Grant Registration Patent event date: 20020923 |
|
GRNT | Written decision to grant | ||
PR0701 | Registration of establishment |
Comment text: Registration of Establishment Patent event date: 20021128 Patent event code: PR07011E01D |
|
PR1002 | Payment of registration fee |
Payment date: 20021128 End annual number: 3 Start annual number: 1 |
|
PG1601 | Publication of registration | ||
LAPS | Lapse due to unpaid annual fee | ||
PC1903 | Unpaid annual fee |