JP5456966B2 - 2,3−ジアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン、カップラー、特定の界面活性剤及び酸化剤を含む酸性pHの染料組成物 - Google Patents
2,3−ジアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン、カップラー、特定の界面活性剤及び酸化剤を含む酸性pHの染料組成物 Download PDFInfo
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- JP5456966B2 JP5456966B2 JP2007309392A JP2007309392A JP5456966B2 JP 5456966 B2 JP5456966 B2 JP 5456966B2 JP 2007309392 A JP2007309392 A JP 2007309392A JP 2007309392 A JP2007309392 A JP 2007309392A JP 5456966 B2 JP5456966 B2 JP 5456966B2
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- 239000000203 mixture Substances 0.000 title claims abstract description 90
- 239000007800 oxidant agent Substances 0.000 title claims abstract description 13
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- 239000002253 acid Substances 0.000 title description 5
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- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 12
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 10
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 9
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- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- 229920006395 saturated elastomer Polymers 0.000 claims description 7
- 125000003277 amino group Chemical group 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical group NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 4
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- 102000004316 Oxidoreductases Human genes 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims description 3
- PWJJHLRABLZGCK-UHFFFAOYSA-N 1-bromodec-1-ene Chemical group CCCCCCCCC=CBr PWJJHLRABLZGCK-UHFFFAOYSA-N 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 125000005263 alkylenediamine group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 125000005392 carboxamide group Chemical group NC(=O)* 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 238000010186 staining Methods 0.000 claims description 3
- UEEJHVSXFDXPFK-UHFFFAOYSA-O N-dimethylethanolamine Chemical compound C[NH+](C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-O 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical class OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 2
- 150000003871 sulfonates Chemical class 0.000 claims description 2
- 150000003467 sulfuric acid derivatives Chemical class 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
- 150000005215 alkyl ethers Chemical class 0.000 claims 1
- 125000005526 alkyl sulfate group Chemical group 0.000 claims 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 claims 1
- 150000004965 peroxy acids Chemical class 0.000 claims 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims 1
- 229940117986 sulfobetaine Drugs 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 11
- 239000002453 shampoo Substances 0.000 abstract description 6
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 abstract description 4
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 abstract 2
- HKQMDOQLVUHVGX-UHFFFAOYSA-N 1-bromodecane 2-(dimethylamino)ethanol Chemical compound CN(C)CCO.CCCCCCCCCCBr HKQMDOQLVUHVGX-UHFFFAOYSA-N 0.000 abstract 1
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- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
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- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 description 4
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- 241000158728 Meliaceae Species 0.000 description 4
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- 239000002535 acidifier Substances 0.000 description 4
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- 125000000129 anionic group Chemical group 0.000 description 4
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- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 4
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 3
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- 239000002671 adjuvant Substances 0.000 description 3
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- 229910052801 chlorine Inorganic materials 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 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
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 230000037308 hair color Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
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- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 description 2
- OQEBIHBLFRADNM-UHFFFAOYSA-N 1,4-dideoxy-1,4-imino-d-ribitol Chemical compound OCC1NCC(O)C1O OQEBIHBLFRADNM-UHFFFAOYSA-N 0.000 description 2
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- 239000002270 dispersing agent Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002475 indoles Chemical class 0.000 description 1
- 125000003387 indolinyl group Chemical class N1(CCC2=CC=CC=C12)* 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- HXEACLLIILLPRG-RXMQYKEDSA-N l-pipecolic acid Natural products OC(=O)[C@H]1CCCCN1 HXEACLLIILLPRG-RXMQYKEDSA-N 0.000 description 1
- 150000003893 lactate salts Chemical class 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
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- AVAWMINJNRAQFS-UHFFFAOYSA-N n,n-dimethylpyrrolidin-3-amine Chemical compound CN(C)C1CCNC1 AVAWMINJNRAQFS-UHFFFAOYSA-N 0.000 description 1
- CSHLZYGRAHLJOB-UHFFFAOYSA-N n-(3-aminopyrazolo[1,5-a]pyridin-2-yl)acetamide Chemical compound C1=CC=CC2=C(N)C(NC(=O)C)=NN21 CSHLZYGRAHLJOB-UHFFFAOYSA-N 0.000 description 1
- BKEFUBHXUTWQED-UHFFFAOYSA-N n-(4-amino-3-hydroxyphenyl)acetamide Chemical compound CC(=O)NC1=CC=C(N)C(O)=C1 BKEFUBHXUTWQED-UHFFFAOYSA-N 0.000 description 1
- NGZYRKGJWYJGRS-UHFFFAOYSA-N n-methylpyrrolidin-3-amine Chemical compound CNC1CCNC1 NGZYRKGJWYJGRS-UHFFFAOYSA-N 0.000 description 1
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 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
- 235000021317 phosphate Nutrition 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- HXEACLLIILLPRG-UHFFFAOYSA-N pipecolic acid Chemical compound OC(=O)C1CCCCN1 HXEACLLIILLPRG-UHFFFAOYSA-N 0.000 description 1
- 125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- PRAYXGYYVXRDDW-UHFFFAOYSA-N piperidin-2-ylmethanol Chemical compound OCC1CCCCN1 PRAYXGYYVXRDDW-UHFFFAOYSA-N 0.000 description 1
- BIWOSRSKDCZIFM-UHFFFAOYSA-N piperidin-3-ol Chemical compound OC1CCCNC1 BIWOSRSKDCZIFM-UHFFFAOYSA-N 0.000 description 1
- VUNPWIPIOOMCPT-UHFFFAOYSA-N piperidin-3-ylmethanol Chemical compound OCC1CCCNC1 VUNPWIPIOOMCPT-UHFFFAOYSA-N 0.000 description 1
- HDOWRFHMPULYOA-UHFFFAOYSA-N piperidin-4-ol Chemical compound OC1CCNCC1 HDOWRFHMPULYOA-UHFFFAOYSA-N 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- HVVNJUAVDAZWCB-UHFFFAOYSA-N prolinol Chemical compound OCC1CCCN1 HVVNJUAVDAZWCB-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- TYUPYVMUQSMZOW-UHFFFAOYSA-N pyrazolo[1,5-a]pyridin-3-amine Chemical compound C1=CC=CC2=C(N)C=NN21 TYUPYVMUQSMZOW-UHFFFAOYSA-N 0.000 description 1
- SGIWQNVAHWTFMY-UHFFFAOYSA-N pyrazolo[1,5-a]pyridine-3,4-diamine Chemical compound C1=CC=C(N)C2=C(N)C=NN21 SGIWQNVAHWTFMY-UHFFFAOYSA-N 0.000 description 1
- DIMNHIMUPFMCQG-UHFFFAOYSA-N pyrazolo[1,5-a]pyridine-3,5-diamine Chemical compound C1=CC(N)=CC2=C(N)C=NN21 DIMNHIMUPFMCQG-UHFFFAOYSA-N 0.000 description 1
- HQRFNKWPPWDXOQ-UHFFFAOYSA-N pyrazolo[1,5-a]pyridine-3,6-diamine Chemical compound C1=C(N)C=CC2=C(N)C=NN21 HQRFNKWPPWDXOQ-UHFFFAOYSA-N 0.000 description 1
- AMMRTECEGYRILQ-UHFFFAOYSA-N pyrazolo[1,5-a]pyridine-3,7-diamine Chemical compound NC1=CC=CC2=C(N)C=NN21 AMMRTECEGYRILQ-UHFFFAOYSA-N 0.000 description 1
- LDIJKUBTLZTFRG-UHFFFAOYSA-N pyrazolo[1,5-a]pyrimidine Chemical class N1=CC=CN2N=CC=C21 LDIJKUBTLZTFRG-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 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 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- ILVXOBCQQYKLDS-UHFFFAOYSA-N pyridine N-oxide Chemical compound [O-][N+]1=CC=CC=C1 ILVXOBCQQYKLDS-UHFFFAOYSA-N 0.000 description 1
- MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 description 1
- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 description 1
- CSNFMBGHUOSBFU-UHFFFAOYSA-N pyrimidine-2,4,5-triamine Chemical compound NC1=NC=C(N)C(N)=N1 CSNFMBGHUOSBFU-UHFFFAOYSA-N 0.000 description 1
- SBMSLRMNBSMKQC-UHFFFAOYSA-N pyrrolidin-1-amine Chemical compound NN1CCCC1 SBMSLRMNBSMKQC-UHFFFAOYSA-N 0.000 description 1
- NGXSWUFDCSEIOO-UHFFFAOYSA-N pyrrolidin-3-amine Chemical compound NC1CCNC1 NGXSWUFDCSEIOO-UHFFFAOYSA-N 0.000 description 1
- JHHZLHWJQPUNKB-UHFFFAOYSA-N pyrrolidin-3-ol Chemical compound OC1CCNC1 JHHZLHWJQPUNKB-UHFFFAOYSA-N 0.000 description 1
- JCZPOYAMKJFOLA-UHFFFAOYSA-N pyrrolidine-3,4-diol Chemical compound OC1CNCC1O JCZPOYAMKJFOLA-UHFFFAOYSA-N 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 150000003892 tartrate salts Chemical class 0.000 description 1
- 238000003419 tautomerization reaction Methods 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
- 239000004711 α-olefin 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
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/10—Drugs for disorders of the endocrine system of the posterior pituitary hormones, e.g. oxytocin, ADH
-
- 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
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Endocrinology (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Cosmetics (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Coloring (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Description
・以下の式(I)の2,3-ジアミノ-6,7-ジヒドロ-1H,5H-ピラゾロ[1,2-a]ピラゾール-1-オン及びこの付加塩から選択される少なくとも1つの酸化塩基;
・オキシアルキレン化またはグリセロール化脂肪アルコール、サルフェート型またはスルホネート型アニオン界面活性剤、及びベタイン型両性界面活性剤から選択される少なくとも1つの界面活性剤;並びに
・少なくとも1つの酸化剤;
を含み、組成物のpHが5.5〜7.5の範囲であり、組成物がオキシアルキレン化またはグリセロール化脂肪アルコールを含む場合、それは、3-アミノ-2-メチルアミノ-6-メトキシピリジン;ブロモデカンN,N-ジメチルエタノールアミンで4級化されている1,3-ビス(イソシアナトメチルシクロヘキサン)N,N-ジメチルエタノールアミンとポリオキシエチレンとの縮合から得られる脂肪鎖カチオン性ポリウレタン;エチレンオキシド150または180モルを含むポリエチレングリコール、デシルアルコール、及びメチレンビス(4-シクロヘキシルイソシアネート)の重縮合物;グリセロール2モルでポリグリセロール化されたセテアリルアルコールとグリセロール6モルでポリグリセロール化されたセテアリルアルコールとの混合物;へキシレングリコールのいずれをも含まないという条件を有する、ケラチン繊維の染色用組成物である。
の化合物及びこれらの付加塩から選択される。
の化合物から選択することができる。
の化合物から選択することができる。
Mergital LM2(Cognis)[ラウリルアルコール2 EO]
Ifralan L12(Ifrachem)及びRewopal 12(Goldschmidt)[ラウリルアルコール 12 EO];
Empilan KA 2.5/90FL(Albright & Wilson)及びMergital BL309(Cognis)[デシルアルコール3 EO];
Empilan KA 5/90FL(Albright & Wilson)及びMergital BL589(Cognis)[デシルアルコール5 EO];
Brij 58(Uniqema)及び Simulsol 58(SEPPIC)[セチルアルコール 20 EO];
Eumulgin 05(Cognis)[オレオセチルアルコール 5 EO];
Mergital OC30(Cognis)[オレオセチルアルコール 30 EO];
Brij 72(Uniqema)[ステアリルアルコール 2 EO];
Brij 76(Uniqema)[ステアリルアルコール 10 EO];
Brij 78P(Uniqema)[ステアリルアルコール20 EO];
Brij 700(Uniqema)[ステアリルアルコール 100 EO];
Eumulgin B1(Cognis)[セチルステアリルアルコール 12 EO];
Eumulgin L(Cognis)[セチルアルコール 9 EO 及び 2 PO];
Witconol APM(Goldschmidt)[ミリスチルアルコール 3 PO];
を特に挙げることができる。
の化合物がある。
以下の組成物を調製した。
以下の組成物を調製した。
以下の組成物を調製した。
Claims (15)
- 適切な染色媒体中に、
・以下の式(I)の2,3-ジアミノ-6,7-ジヒドロ-1H,5H-ピラゾロ[1,2-a]ピラゾール-1-オン及びこの付加塩から選択される少なくとも1つの酸化塩基;
・オキシアルキレン化またはグリセロール化脂肪アルコール、サルフェート型アニオン界面活性剤、及びベタイン型両性界面活性剤から選択される少なくとも1つの界面活性剤;並びに
・少なくとも1つの酸化剤;
を含み、組成物のpHが5.5〜7.5の範囲であり、組成物がオキシアルキレン化またはグリセロール化脂肪アルコールを含む場合、それは、3-アミノ-2-メチルアミノ-6-メトキシピリジン;ブロモデカンN,N-ジメチルエタノールアミンで4級化されている1,3-ビス(イソシアナトメチルシクロヘキサン)N,N-ジメチルエタノールアミンとポリオキシエチレンとの縮合から得られる脂肪鎖カチオン性ポリウレタン;エチレンオキシド150または180モルを含むポリエチレングリコール、デシルアルコール、及びメチレンビス(4-シクロヘキシルイソシアネート)の重縮合物;グリセロール2モルでポリグリセロール化されたセテアリルアルコールとグリセロール6モルでポリグリセロール化されたセテアリルアルコールとの混合物;へキシレングリコールのいずれをも含まないという条件を有する、ケラチン繊維の染色用組成物。 - 前記カップラーが、メタ-フェニレンジアミン、メタ-アミノフェノール、メタ-ジフェノール、ナフタレン系カップラー、及び複素環式カップラー、並びにこれらの付加塩から選択される、請求項1に記載の組成物。
- 前記カップラーがメタ-アミノフェノールから選択される、請求項2に記載の組成物。
- 前記メタ-アミノフェノールが、以下の式(II):
の化合物及びこれらの付加塩から選択される、請求項3に記載の組成物。 - 前記R1及びR2が、互いに独立して、水素原子またはモノ-もしくはポリヒドロキシアルキル基を表す、請求項4に記載の組成物。
- 前記カップラーが塩素化メタ-アミノフェノールから選択される、請求項1から5のいずれか一項に記載の組成物。
- 前記オキシアルキレン化脂肪アルコールが、直鎖状または分岐状であり、飽和または不飽和であり、且つ8〜40個の炭素原子、並びに1〜250個のエチレンオキシド基及び/またはプロピレンオキシド基を含む、請求項1から6のいずれか一項に記載の組成物。
- 前記グリセロール化脂肪アルコールが、直鎖状または分岐状であり、飽和または不飽和であり、且つ8〜40個の炭素原子及び1〜30個のグリセロール基を含む、請求項1から7のいずれか一項に記載の組成物。
- 前記サルフェート型アニオン性界面活性剤が、アルキルサルフェート、アルキルアミドサルフェート、アルキルエーテルサルフェート、アルキルアミドエーテルサルフェート、アルキルアリールエーテルサルフェート、またはアルキルエーテルスルホサクシネートのそれぞれの塩から選択され、これらすべての種々の化合物のアルキル基またはアシル基が8〜24個の炭素原子を含み、アリール基がフェニル基またはベンジル基を表し、且つエチレンオキシド基またはプロピレンオキシド基の平均数が2〜50の範囲である、請求項1から8のいずれか一項に記載の組成物。
- 前記ベタイン型両性界面活性剤が、(C8〜C20)アルキルベタイン、スルホベタイン、(C8〜C20)アルキルアミド(C1〜C6)アルキルベタイン、及び(C8〜C20)アルキルアミド(C1〜C6)アルキルスルホベタインから選択される、請求項1から9のいずれか一項に記載の組成物。
- パラ-フェニレンジアミン、ビス(フェニル)アルキレンジアミン、パラ-アミノフェノール、ビス-パラ-アミノフェノール、オルト-アミノフェノール、オルト-フェニレンジアミン、及び2,3-ジアミノ-6,7-ジヒドロ-1H,5H-ピラゾロ[1,2-a]ピラゾール-1-オン以外の複素環式塩基、並びにこれらの付加塩から選択される少なくとも1つの追加の酸化塩基を含む、請求項1から10のいずれか一項に記載の組成物。
- 前記酸化剤が、過酸化水素、過酸化尿素、アルカリ金属臭素酸塩、過酸塩、過酸、及びオキシダーゼ酵素から選択される、請求項1から11のいずれか一項に記載の組成物。
- 所望の着色を発現させるのに十分な時間、請求項1から12のいずれか一項に記載の組成物を繊維に適用し、その後前記繊維をすすぎ、場合によりシャンプーで洗い、再度すすぎ、乾燥させる、ケラチン繊維の染色方法。
- 一方で、適切な染色媒体中に、2,3-ジアミノ-6,7-ジヒドロ-1H,5H-ピラゾロ[1,2-a]ピラゾール-1-オン及びこの付加塩から選択される少なくとも1つの酸化塩基、少なくとも1つのカップラー、並びにオキシアルキレン化またはグリセロール化脂肪アルコール、サルフェート型のアニオン界面活性剤及びベタイン型両性界面活性剤から選択される少なくとも1つの界面活性剤を含む組成物(A)を、他方で、適切な染色媒体中に、少なくとも1つの酸化剤を含む組成物(B)を別々に貯蔵する工程と、次いで、ケラチン繊維に適用する前の使用時にこれらを一緒に混合する工程とを含んだ予備工程を含む、請求項13に記載の方法。
- ケラチン繊維の酸化染色のための、請求項1から12のいずれか一項に記載の組成物の使用。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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FR0655213 | 2006-11-30 | ||
FR0655213A FR2909281B1 (fr) | 2006-11-30 | 2006-11-30 | Composition de coloration de ph acide comprenant la 2,3-diamino-6,7-dihydro-1h, 5h-pyrazolo[1,2-a]pyrazol-1-one, un coupleur, un agent tensio-actif particulier et un agent oxydant |
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JP2008138001A JP2008138001A (ja) | 2008-06-19 |
JP5456966B2 true JP5456966B2 (ja) | 2014-04-02 |
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JP2007309392A Active JP5456966B2 (ja) | 2006-11-30 | 2007-11-29 | 2,3−ジアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン、カップラー、特定の界面活性剤及び酸化剤を含む酸性pHの染料組成物 |
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US (1) | US7651539B2 (ja) |
EP (1) | EP1927376B1 (ja) |
JP (1) | JP5456966B2 (ja) |
KR (1) | KR20080049683A (ja) |
CN (1) | CN101204356A (ja) |
AT (1) | ATE540725T1 (ja) |
BR (1) | BRPI0706237B1 (ja) |
ES (1) | ES2379290T3 (ja) |
FR (1) | FR2909281B1 (ja) |
MX (1) | MX2007015139A (ja) |
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FR2937865B1 (fr) * | 2008-11-06 | 2010-11-12 | Oreal | Composition comprenant la 2,3-diamino-6,7-dihydro-1h,5h-pyrazolo°1,2-a!pyrazol-1-one et le 4,5-diamino 1-(beta-hydroxyethyl) pyrazole a titre de bases d'oxydation |
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BR112022012194A2 (pt) * | 2019-12-20 | 2022-09-06 | Oreal | Dispositivo de múltiplos compartimentos, composição e método para tingir fibras de queratina |
FR3131843A1 (fr) * | 2022-01-20 | 2023-07-21 | L'oreal | Composition de coloration d’oxydation comprenant un tensioactif anionique, un tensioactif amphotere choisi parmi une betaïne et un catalyseur metallique |
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US7485156B2 (en) | 2005-05-31 | 2009-02-03 | L'oreal S.A. | Composition for dyeing keratin fibers, comprising at least one diamino-N,N-dihydropyrazolone derivative, at least one coupler and at least one associative polyurethane polymer |
FR2886138B1 (fr) | 2005-05-31 | 2007-08-10 | Oreal | Composition pour la teinture des fibres keratiniques comprenant un derive de diamino-n,n-dihydro-pyrazalone, un coupleur et un agent tensioactif particulier |
FR2886140B1 (fr) | 2005-05-31 | 2007-08-10 | Oreal | Composition pour la teinture des fibes keratiniques comprenant un derive de diamino-n,n-dihydro-pyrazolone et un derive de l'indole ou de l'indoline |
FR2886137B1 (fr) | 2005-05-31 | 2007-08-10 | Oreal | Composition pour la teinture des fibres keratiniques comprenant un derive de diamino-n,n-dihydro-parazolone, un coupleur et un polymere associatif polyerethane |
US7488356B2 (en) | 2005-05-31 | 2009-02-10 | L'oreal S.A. | Composition for dyeing keratin fibers, comprising at least one diamino-N,N-dihydropyrazolone derivative, at least one coupler, and at least one surfactant |
FR2886132B1 (fr) | 2005-05-31 | 2007-07-20 | Oreal | Composition pour la teinture des fibres keratiniques comprenant un derive de diamino-n,n-dihydro-pyrazolone, un coupleur et un colorant direct heterocyclique |
FR2886141B1 (fr) | 2005-05-31 | 2007-11-30 | Oreal | Composition pour la teinture des fibres keratiniques comprenant un derive de diamino-n,n-dihydro-pyrazolone, un derive de para-aminophenol et un coupleur |
FR2886136B1 (fr) | 2005-05-31 | 2007-08-10 | Oreal | Composition pour la teinture des fibres keratiniques comprenant au moins un derive de diamino-n,n-dihydro- pyrazolone et un colorant d'oxydation cationique |
FR2902323B1 (fr) | 2006-06-20 | 2008-08-08 | Oreal | Procede pour la teinture predictible des fibres keratiniques par application d'une composition contenant un derive diamino-n,n-dihydro-pyrazolone et d'une composition fondamentale ou a reflets dores |
FR2902327B1 (fr) | 2006-06-20 | 2008-08-08 | Oreal | Composition de coloration des fibres keratiniques comprenant la 2,3-diamino-6,7-dihydro-1h,5h-pyrazolo 1,2-a pyrazol-1- one, la para-phenylenediamine ou la para-toluenediamine et un meta-aminophenol substitue |
FR2902328B1 (fr) | 2006-06-20 | 2008-08-08 | Oreal | Composition de coloration des fibres keratiniques comprenant la 2,3-diamino-6,7-dihydro-1h,5h-pyrazolo 1,2-a pyrazol-1- one, le 6-chloro 2-methyl 5-amino phenol et un meta-aminophenol substitue |
FR2909282B1 (fr) | 2006-11-30 | 2009-01-16 | Oreal | Composition de coloration de ph acide comprenant la 2,3-diamino-6,7-dihydro-1h,5h-pyrazolo[1,2-a]pyrazol-1-one, une para-phenylenediamine, un meta-aminophenol et un agent oxydant |
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2006
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2007
- 2007-11-27 AT AT07121663T patent/ATE540725T1/de active
- 2007-11-27 ES ES07121663T patent/ES2379290T3/es active Active
- 2007-11-27 EP EP07121663A patent/EP1927376B1/fr active Active
- 2007-11-29 JP JP2007309392A patent/JP5456966B2/ja active Active
- 2007-11-29 BR BRPI0706237A patent/BRPI0706237B1/pt active IP Right Grant
- 2007-11-29 CN CNA2007103066903A patent/CN101204356A/zh active Pending
- 2007-11-30 MX MX2007015139A patent/MX2007015139A/es active IP Right Grant
- 2007-11-30 RU RU2007144600/15A patent/RU2358714C1/ru not_active IP Right Cessation
- 2007-11-30 US US11/987,450 patent/US7651539B2/en active Active
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KR20080049683A (ko) | 2008-06-04 |
RU2358714C1 (ru) | 2009-06-20 |
JP2008138001A (ja) | 2008-06-19 |
BRPI0706237B1 (pt) | 2015-10-13 |
MX2007015139A (es) | 2008-10-28 |
ATE540725T1 (de) | 2012-01-15 |
CN101204356A (zh) | 2008-06-25 |
US20080163883A1 (en) | 2008-07-10 |
FR2909281B1 (fr) | 2009-01-16 |
EP1927376B1 (fr) | 2012-01-11 |
EP1927376A1 (fr) | 2008-06-04 |
BRPI0706237A2 (pt) | 2008-12-16 |
US7651539B2 (en) | 2010-01-26 |
FR2909281A1 (fr) | 2008-06-06 |
ES2379290T3 (es) | 2012-04-24 |
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