JP6669871B2 - ヘテロ環酸化性塩基と2−アミノ−5−エチルフェノールカプラーとを含有する染毛用組成物 - Google Patents
ヘテロ環酸化性塩基と2−アミノ−5−エチルフェノールカプラーとを含有する染毛用組成物 Download PDFInfo
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- JP6669871B2 JP6669871B2 JP2018532094A JP2018532094A JP6669871B2 JP 6669871 B2 JP6669871 B2 JP 6669871B2 JP 2018532094 A JP2018532094 A JP 2018532094A JP 2018532094 A JP2018532094 A JP 2018532094A JP 6669871 B2 JP6669871 B2 JP 6669871B2
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- JP
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- Prior art keywords
- group
- pyridin
- amino
- aminopyrazolo
- alkyl
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 140
- 230000001590 oxidative effect Effects 0.000 title claims description 30
- 238000004043 dyeing Methods 0.000 title claims description 23
- 125000000623 heterocyclic group Chemical group 0.000 title claims description 19
- VBCFPAKCBOGUBW-UHFFFAOYSA-N 2-amino-5-ethylphenol Chemical compound CCC1=CC=C(N)C(O)=C1 VBCFPAKCBOGUBW-UHFFFAOYSA-N 0.000 title claims description 14
- -1 C 1 -C 4 alkyl Chemical group 0.000 claims description 68
- 150000003839 salts Chemical class 0.000 claims description 65
- 239000012453 solvate Substances 0.000 claims description 43
- 229910052757 nitrogen Inorganic materials 0.000 claims description 41
- 125000000217 alkyl group Chemical group 0.000 claims description 38
- 239000002585 base Substances 0.000 claims description 36
- 150000001875 compounds Chemical class 0.000 claims description 35
- 239000000835 fiber Substances 0.000 claims description 35
- 239000000126 substance Substances 0.000 claims description 35
- 102000011782 Keratins Human genes 0.000 claims description 33
- 108010076876 Keratins Proteins 0.000 claims description 33
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 33
- 125000003282 alkyl amino group Chemical group 0.000 claims description 31
- 229920006395 saturated elastomer Polymers 0.000 claims description 24
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 20
- 239000003795 chemical substances by application Substances 0.000 claims description 19
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 18
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 17
- CUYKNJBYIJFRCU-UHFFFAOYSA-N 3-aminopyridine Chemical compound NC1=CC=CN=C1 CUYKNJBYIJFRCU-UHFFFAOYSA-N 0.000 claims description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
- 229910052760 oxygen Inorganic materials 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
- 125000002091 cationic group Chemical group 0.000 claims description 14
- 125000005842 heteroatom Chemical group 0.000 claims description 14
- 239000007800 oxidant agent Substances 0.000 claims description 14
- 229910005965 SO 2 Inorganic materials 0.000 claims description 11
- 125000003277 amino group Chemical group 0.000 claims description 11
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 239000001301 oxygen Substances 0.000 claims description 10
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 9
- 229910052717 sulfur Inorganic materials 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 7
- TYUPYVMUQSMZOW-UHFFFAOYSA-N pyrazolo[1,5-a]pyridin-3-amine Chemical compound C1=CC=CC2=C(N)C=NN21 TYUPYVMUQSMZOW-UHFFFAOYSA-N 0.000 claims description 7
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 7
- 125000004434 sulfur atom Chemical group 0.000 claims description 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 6
- AMFYRKOUWBAGHV-UHFFFAOYSA-N 1h-pyrazolo[4,3-b]pyridine Chemical compound C1=CN=C2C=NNC2=C1 AMFYRKOUWBAGHV-UHFFFAOYSA-N 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 4
- 125000005392 carboxamide group Chemical group NC(=O)* 0.000 claims description 4
- 125000005518 carboxamido group Chemical group 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 150000002500 ions Chemical class 0.000 claims description 3
- 125000000565 sulfonamide group Chemical group 0.000 claims description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 claims description 2
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims description 2
- FTVCNCFJNHNLFM-UHFFFAOYSA-N 1-(3-aminopyrazolo[1,5-a]pyridin-2-yl)pyrrolidin-3-ol Chemical compound N=1N2C=CC=CC2=C(N)C=1N1CCC(O)C1 FTVCNCFJNHNLFM-UHFFFAOYSA-N 0.000 claims description 2
- QGUKCZZXLQZORJ-UHFFFAOYSA-N 2-n-(2-pyridin-3-ylethyl)pyrazolo[1,5-a]pyridine-2,3-diamine Chemical compound N=1N2C=CC=CC2=C(N)C=1NCCC1=CC=CN=C1 QGUKCZZXLQZORJ-UHFFFAOYSA-N 0.000 claims description 2
- GRFNBEZIAWKNCO-UHFFFAOYSA-N 3-pyridinol Chemical compound OC1=CC=CN=C1 GRFNBEZIAWKNCO-UHFFFAOYSA-N 0.000 claims description 2
- 150000001721 carbon Chemical class 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 2
- 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 claims description 2
- 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 claims description 2
- 229910052710 silicon Inorganic materials 0.000 claims description 2
- LENLQGBLVGGAMF-UHFFFAOYSA-N tributyl([1,2,4]triazolo[1,5-a]pyridin-6-yl)stannane Chemical compound C1=C([Sn](CCCC)(CCCC)CCCC)C=CC2=NC=NN21 LENLQGBLVGGAMF-UHFFFAOYSA-N 0.000 claims description 2
- 230000003647 oxidation Effects 0.000 claims 2
- 238000007254 oxidation reaction Methods 0.000 claims 2
- SFHYNDMGZXWXBU-LIMNOBDPSA-N 6-amino-2-[[(e)-(3-formylphenyl)methylideneamino]carbamoylamino]-1,3-dioxobenzo[de]isoquinoline-5,8-disulfonic acid Chemical compound O=C1C(C2=3)=CC(S(O)(=O)=O)=CC=3C(N)=C(S(O)(=O)=O)C=C2C(=O)N1NC(=O)N\N=C\C1=CC=CC(C=O)=C1 SFHYNDMGZXWXBU-LIMNOBDPSA-N 0.000 claims 1
- 125000005330 8 membered heterocyclic group Chemical group 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 50
- 239000007788 liquid Substances 0.000 description 26
- 150000002148 esters Chemical class 0.000 description 24
- 239000002253 acid Substances 0.000 description 22
- 125000004432 carbon atom Chemical group C* 0.000 description 19
- 150000001412 amines Chemical class 0.000 description 18
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 15
- 235000014113 dietary fatty acids Nutrition 0.000 description 15
- 239000000194 fatty acid Substances 0.000 description 15
- 229930195729 fatty acid Natural products 0.000 description 15
- 125000003545 alkoxy group Chemical group 0.000 description 14
- 235000001014 amino acid Nutrition 0.000 description 13
- 229940024606 amino acid Drugs 0.000 description 13
- 150000001413 amino acids Chemical class 0.000 description 13
- 150000004665 fatty acids Chemical class 0.000 description 12
- 150000001298 alcohols Chemical class 0.000 description 11
- 239000000975 dye Substances 0.000 description 11
- 229930195733 hydrocarbon Natural products 0.000 description 11
- 150000002430 hydrocarbons Chemical class 0.000 description 11
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 10
- 239000002736 nonionic surfactant Substances 0.000 description 10
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000004040 coloring Methods 0.000 description 9
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 125000000129 anionic group Chemical group 0.000 description 7
- 239000003945 anionic surfactant Substances 0.000 description 7
- 150000003254 radicals Chemical class 0.000 description 7
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 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 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229910052783 alkali metal Inorganic materials 0.000 description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical class NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 5
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 5
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Chemical compound OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 description 5
- 125000002252 acyl group Chemical group 0.000 description 5
- 125000001453 quaternary ammonium group Chemical group 0.000 description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 235000000346 sugar Nutrition 0.000 description 5
- 239000002888 zwitterionic surfactant Substances 0.000 description 5
- 125000006536 (C1-C2)alkoxy group Chemical group 0.000 description 4
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 4
- 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
- OBJQTPFHDSYCLL-UHFFFAOYSA-N 6,7-diamino-2-hydroxy-2,3-dihydro-1h-pyrazolo[1,2-a]pyrazol-5-one Chemical compound C1C(O)CN2C(N)=C(N)C(=O)N21 OBJQTPFHDSYCLL-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical group C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- 229930006000 Sucrose Natural products 0.000 description 4
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 150000001340 alkali metals Chemical class 0.000 description 4
- 150000003863 ammonium salts Chemical group 0.000 description 4
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 4
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 4
- 150000003857 carboxamides Chemical class 0.000 description 4
- 239000003093 cationic surfactant Substances 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XIRNKXNNONJFQO-UHFFFAOYSA-N ethyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC XIRNKXNNONJFQO-UHFFFAOYSA-N 0.000 description 4
- 125000000524 functional group Chemical group 0.000 description 4
- 230000014509 gene expression Effects 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- 229930182478 glucoside Natural products 0.000 description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 4
- 229940055577 oleyl alcohol Drugs 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- 229960004793 sucrose Drugs 0.000 description 4
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 4
- 150000003626 triacylglycerols Chemical class 0.000 description 4
- 235000015112 vegetable and seed oil Nutrition 0.000 description 4
- 239000008158 vegetable oil Substances 0.000 description 4
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 3
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 3
- HWWIVWKTKZAORO-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-ol Chemical compound O1CCNC2=CC(O)=CC=C21 HWWIVWKTKZAORO-UHFFFAOYSA-N 0.000 description 3
- ZLOJSTQJEWRDGU-UHFFFAOYSA-N 6,7-diamino-2,3-dihydro-1h-pyrazolo[1,2-a]pyrazol-5-one Chemical compound C1CCN2C(N)=C(N)C(=O)N21 ZLOJSTQJEWRDGU-UHFFFAOYSA-N 0.000 description 3
- OZQVBSCQQQJYFO-UHFFFAOYSA-N 7,8-dihydropyrazolo[1,2-a]pyridazin-3-one Chemical compound C1CC=CN2C(=O)C=CN21 OZQVBSCQQQJYFO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 3
- SGVYKUFIHHTIFL-UHFFFAOYSA-N Isobutylhexyl Natural products CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004264 Petrolatum Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-O Pyrrolidinium ion Chemical compound C1CC[NH2+]C1 RWRDLPDLKQPQOW-UHFFFAOYSA-O 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 125000005210 alkyl ammonium group Chemical group 0.000 description 3
- 150000008051 alkyl sulfates Chemical class 0.000 description 3
- 235000009697 arginine Nutrition 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 150000008131 glucosides Chemical class 0.000 description 3
- 235000014304 histidine Nutrition 0.000 description 3
- GLUUGHFHXGJENI-UHFFFAOYSA-O hydron piperazine Chemical compound [H+].C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-O 0.000 description 3
- AVAWMINJNRAQFS-UHFFFAOYSA-N n,n-dimethylpyrrolidin-3-amine Chemical compound CN(C)C1CCNC1 AVAWMINJNRAQFS-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 3
- 229940066842 petrolatum Drugs 0.000 description 3
- 235000019271 petrolatum Nutrition 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- NGXSWUFDCSEIOO-UHFFFAOYSA-N pyrrolidin-3-amine Chemical compound NC1CCNC1 NGXSWUFDCSEIOO-UHFFFAOYSA-N 0.000 description 3
- JHHZLHWJQPUNKB-UHFFFAOYSA-N pyrrolidin-3-ol Chemical compound OC1CCNC1 JHHZLHWJQPUNKB-UHFFFAOYSA-N 0.000 description 3
- 229920002545 silicone oil Polymers 0.000 description 3
- 239000005720 sucrose Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- SWSQBOPZIKWTGO-UHFFFAOYSA-N 1,1-dimethylguanidine Chemical compound CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 2
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- YPMOZWCBANATQH-UHFFFAOYSA-N octyl 7-methyloctanoate Chemical compound CCCCCCCCOC(=O)CCCCCC(C)C YPMOZWCBANATQH-UHFFFAOYSA-N 0.000 description 1
- 150000002888 oleic acid derivatives Chemical class 0.000 description 1
- 229920001542 oligosaccharide Polymers 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000012860 organic pigment Substances 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
- 239000002540 palm oil Substances 0.000 description 1
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 1
- 229940101267 panthenol Drugs 0.000 description 1
- 235000020957 pantothenol Nutrition 0.000 description 1
- 239000011619 pantothenol Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 150000004965 peroxy acids Chemical class 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
- 230000002085 persistent effect Effects 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical group [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 150000003017 phosphorus Chemical class 0.000 description 1
- HXEACLLIILLPRG-UHFFFAOYSA-N pipecolic acid Chemical compound OC(=O)C1CCCCN1 HXEACLLIILLPRG-UHFFFAOYSA-N 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
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000003658 preventing hair loss Effects 0.000 description 1
- 150000003139 primary aliphatic amines Chemical class 0.000 description 1
- HVVNJUAVDAZWCB-UHFFFAOYSA-N prolinol Chemical compound OCC1CCCN1 HVVNJUAVDAZWCB-UHFFFAOYSA-N 0.000 description 1
- BPJZKLBPJBMLQG-KWRJMZDGSA-N propanoyl (z,12r)-12-hydroxyoctadec-9-enoate Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(=O)OC(=O)CC BPJZKLBPJBMLQG-KWRJMZDGSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940116422 propylene glycol dicaprate Drugs 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- USPWKWBDZOARPV-UHFFFAOYSA-N pyrazolidine Chemical compound C1CNNC1 USPWKWBDZOARPV-UHFFFAOYSA-N 0.000 description 1
- 125000003072 pyrazolidinyl group Chemical group 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
- MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 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
- 150000003230 pyrimidines Chemical class 0.000 description 1
- JCZPOYAMKJFOLA-UHFFFAOYSA-N pyrrolidine-3,4-diol Chemical compound OC1CNCC1O JCZPOYAMKJFOLA-UHFFFAOYSA-N 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical class C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- UQDJGEHQDNVPGU-UHFFFAOYSA-N serine phosphoethanolamine Chemical compound [NH3+]CCOP([O-])(=O)OCC([NH3+])C([O-])=O UQDJGEHQDNVPGU-UHFFFAOYSA-N 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 229940063673 spermidine Drugs 0.000 description 1
- 229940063675 spermine Drugs 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 229940117986 sulfobetaine Drugs 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 230000035900 sweating Effects 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- 229960003080 taurine Drugs 0.000 description 1
- JKLRIMRKZBSSED-UHFFFAOYSA-N taurocyamine Chemical compound NC(=[NH2+])NCCS([O-])(=O)=O JKLRIMRKZBSSED-UHFFFAOYSA-N 0.000 description 1
- 150000005621 tetraalkylammonium salts Chemical class 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical class CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- BGNWQYFHLCCUTB-MSUUIHNZSA-N tridecyl (z)-docos-13-enoate Chemical compound CCCCCCCCCCCCCOC(=O)CCCCCCCCCCC\C=C/CCCCCCCC BGNWQYFHLCCUTB-MSUUIHNZSA-N 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 229940118576 triisostearyl citrate Drugs 0.000 description 1
- QSFBUDDTFXACIS-UHFFFAOYSA-O trimethyl-[3-(octadecanoylamino)propyl]azanium Chemical class CCCCCCCCCCCCCCCCCC(=O)NCCC[N+](C)(C)C QSFBUDDTFXACIS-UHFFFAOYSA-O 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
- 229940026256 trioctyldodecyl citrate Drugs 0.000 description 1
- APIBROGXENTUGB-ZUQRMPMESA-M triphenyl-[(e)-3-phenylprop-2-enyl]phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C\C=C\C1=CC=CC=C1 APIBROGXENTUGB-ZUQRMPMESA-M 0.000 description 1
- FQAZRHVERGEKOS-UHFFFAOYSA-N tripropan-2-yl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CC(C)OC(=O)CC(O)(C(=O)OC(C)C)CC(=O)OC(C)C FQAZRHVERGEKOS-UHFFFAOYSA-N 0.000 description 1
- BIEMOBPNIWQLMF-UHFFFAOYSA-N tris(2-octyldodecyl) 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCCCCCC(CCCCCCCC)COC(=O)CC(O)(C(=O)OCC(CCCCCCCC)CCCCCCCCCC)CC(=O)OCC(CCCCCCCC)CCCCCCCCCC BIEMOBPNIWQLMF-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-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
- 239000004474 valine Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 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
- 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
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/38—Percompounds, e.g. peracids
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/415—Aminophenols
-
- 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
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
- A61K2800/432—Direct dyes
- A61K2800/4324—Direct dyes in preparations for permanently dyeing the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/88—Two- or multipart kits
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)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Description
(a)少なくとも1種の2−アミノ−5−エチルフェノールカプラー、又はその付加塩若しくは溶媒和物と、
(b)
A1)式(I)のピラゾロピリジン及びその付加塩、その溶媒和物、又はその塩の溶媒和物:
A2)式(II)のピラゾロピリジン酸化性塩基:
Z1及びZ2は、独立に:
・共有単結合;
・以下から選択される二価の基:
・−O(CH2)p−基(pは0〜6の範囲の整数を表す)、
・−NR’6(CH2)q(C6H4)t−基(qは0〜6の範囲の整数を表し、tは0又は1を表し、R’6は水素原子又は任意選択的に1つ以上のヒドロキシル基で置換されていてもよいC1〜C6アルキル基を表す)
を表し;
R’1がメチル基の場合にはZ1は二価の基である−S−、−SO−、又は−SO2−を表していてもよく;
R’1及びR’2は、独立に:
・水素;
・任意選択的に置換されていてもよく任意選択的にO、N、Si、S、SO、及びSO2から選択されるヘテロ原子又は基で中断されていてもよいC1〜C10アルキル基;
・ハロゲン;
・SO3H基;
・任意選択的にN、O、S、SO2及び、−CO−から選択されるヘテロ原子又は基を1つ以上含んでいてもよい、置換又は無置換の、飽和、不飽和、又は芳香族の5〜8員環(環はカチオンであってもよく及び/又はカチオン基で置換されていてもよい);
・基−N+R17R18R19(R17、R18、及びR19は任意選択的に1つ以上のヒドロキシル基で置換されていてもよい直鎖又は分岐のC1〜C5アルキルである);
を表し、Z1、それぞれZ2が共有結合を表す場合には、R’1、それぞれのR’2は、
・任意選択的に置換されていてもよいC1〜C6アルキルカルボニル基;
・−O−CO−R、−CO−O−R、NR−CO−R’、又は−CO−NRR’基(R及びR’は、独立に、水素原子又は任意選択的に置換されていてもよいC1〜C6アルキル基を表す);
も表していてもよく、
R’3、R’4、及びR’5は、同じでも異なっていてもよく、
・水素原子;
・ヒドロキシル基;
・C1〜C6アルコキシ基;
・C1〜C6アルキルチオ基;
・アミノ基;
・モノアルキルアミノ基;
・C1〜C6ジアルキルアミノ基(ここで、アルキル基はこれらが結合している窒素と共に、N、O、S、SO2、及びCOから選択される1つ以上のヘテロ原子又は基を含んでいてもよい、飽和又は不飽和の、芳香族又は非芳香族の、5〜8員のヘテロ環を形成していてもよく、ヘテロ環はカチオンであってもよく及び/又はカチオン基で置換されていてもよい);
・任意選択的に置換されていてもよいC1〜C6アルキルカルボニル基;
・−O−CO−R、−CO−O−R、NR−CO−R’、又は−CO−NRR’の基(R及びR’は上で定義した通りである);
・ハロゲン;
・−NHSO3H基;
・任意選択的に置換されていてもよいC1〜C4アルキル基;
・飽和、不飽和、又は芳香族の、任意選択的に置換されていてもよい炭素を主体とする環;
を表し、
・R’3、R’4、及びR’5は、2つ1組で部分的に飽和又は不飽和の環を形成していてもよく;
Xは式(II)の誘導体の電気陰性度を確保することを可能にするイオン又はイオン性基を表すが;
基R’1及びR’2のうちの少なくとも1つはカチオン基を表すことを条件とする)、並びに
A3)式(III)のジアミノ−N,N−ジヒドロピラゾロン誘導体、及びその付加塩、その溶媒和物、又はその塩の溶媒和物:
R’’3及びR’’4は、同じであっても異なっていてもよく:
・水素原子;
・OR’’5基、NR’’6R’’7基、カルボキシル基、スルホン酸基、カルボキサミド基CONR’’6R’’7、スルホンアミド基SO2NR’’6R’’7、ヘテロアリール、アリール(1つ以上の(C1〜C4)アルキル、ヒドロキシル、C1〜C2アルコキシ、アミノ、又は(ジ)アルキル(C1〜C2)アミノ基で任意選択的に置換されていてもよい)、で構成される群から選択される1つ以上の基で任意選択的に置換されていてもよい、直鎖又は分岐のC1〜C6アルキル基;
・1つ以上の(C1〜C4)アルキル、ヒドロキシル、C1〜C2アルコキシ、アミノ、又は(ジ)アルキル(C1〜C2)アミノで任意選択的に置換されていてもよいアリール基;
・(C1〜C4)アルキル及び(C1〜C2)アルコキシから選択される1つ以上の基で任意選択的に置換されていてもよい5又は6員のヘテロアリール基;
を表し、
・R’’3及びR’’4は、これらが結合している窒素原子と共に5又は7員のヘテロ環を形成していてもよく、その中の炭素原子は任意選択的に置換されていてもよい酸素原子又は窒素原子で置換されていてもよく、
R’’5、R’’6、及びR’’7は、同じであっても異なっていてもよく:
・水素原子;
・ヒドロキシル、C1〜C2アルコキシ、カルボキサミドCONR’’8R’’9、スルホニルSO2R’’8、アリール((C1〜C4)アルキル、ヒドロキシル、C1〜C2アルコキシ、アミノ、又は(ジ)アルキル(C1〜C2)アミノで任意選択的に置換されていてもよい)、アリール((C1〜C4)アルキル、ヒドロキシル、C1〜C2アルコキシ、アミノ、又は(ジ)アルキル(C1〜C2)アミノで任意選択的に置換されていてもよい)、から選択される1つ以上の基で任意選択的に置換されていてもよい、直鎖又は分岐のC1〜C4アルキル基;
を表し、
R’’6、及びR’’7は、同じであっても異なっていてもよく、カルボキサミド基CONR’’8R’’9;スルホニル基SO2R’’8も表していてもよく;
R’’8及びR’’9は、同じであっても異なっていてもよく、水素原子;1つ以上のヒドロキシル又はC1〜C2アルコキシで任意選択的に置換されていてもよい直鎖又は分岐のC1〜C4アルキル基を表し;
R’’1及びR’’2は、これらが結合している窒素原子と共に、ハロゲン原子及びアミノ、(ジ)アルキル(C1〜C4)アミノ、ヒドロキシル、カルボキシル、カルボキサミド、及び(C1〜C2)アルコキシ基、C1〜C4アルキル基(1つ以上のヒドロキシル、アミノ、(ジ)アルキルアミノ、アルコキシ、カルボキシル、又はスルホニル基で任意選択的に置換されていてもよい)で構成される群から選択される1つ以上の基で任意選択的に置換されていてもよい飽和又は不飽和の5〜7員のヘテロ環を形成する)、
から選択される少なくとも1種のピラゾールヘテロ環酸化性塩基と、
を含有する、ケラチン繊維を染色するための組成物である。
本発明の組成物は、1種以上の2−アミノ−5−エチルフェノールカプラーを、遊離形態、又はその付加塩、又はその溶媒和物として含有する。
酸化性塩基A1、A2、及びA3は、水和物、溶媒和物、又は塩の形態であってもよい。
R1、R2、及びR3は、同じであっても異なってもよく、水素又はハロゲン原子;ヒドロキシル基;(C1〜C4)アルキル基;(C1〜C4)アルキルチオ基;(C1〜C4)アルコキシ基;−NHSO3H基;アミノ基;(C1〜C4)アルキルアミノ基;ジ(C1〜C4)アルキルアミノ基(ここで、2つのアルキル基が、これらが結合している窒素原子と共に環(1つ以上の窒素、酸素、又は硫黄原子で中断されていてもよい)を形成していてもよい);上で定義したヘテロ環;スルホンアミド基;カルボニル基;(C1〜C4)アルコキシカルボニル基;カルボキサミド基;又は次式:
・ピラゾロ[1,5−a]ピリジン−3−イルアミン;
・2−アセチルアミノピラゾロ[1,5−a]ピリジン−3−イルアミン;
・2−モルホリン−4−イルピラゾロ[1,5−a]ピリジン−3−イルアミン;
・3−アミノピラゾロ[1,5−a]ピリジン−2−カルボン酸;
・2−メトキシピラゾロ[1,5−a]ピリジン−3−イルアミノ;
・(3−アミノピラゾロ[1,5−a]ピリジン−7−イル)メタノール;
・2−(3−アミノピラゾロ[1,5−a]ピリジン−5−イル)エタノール;
・2−(3−アミノピラゾロ[1,5−a]ピリジン−7−イル)エタノール;
・(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)メタノール;
・3,6−ジアミノピラゾロ[1,5−a]ピリジン;
・3,4−ジアミノピラゾロ[1,5−a]ピリジン;
・ピラゾロ[1,5−a]ピリジン−3,7−ジアミン;
・7−モルホリン−4−イルピラゾロ[1,5−a]ピリジン−3−イルアミン;
・ピラゾロ[1,5−a]ピリジン−3,5−ジアミン;
・5−モルホリン−4−イルピラゾロ[1,5−a]ピリジン−3−イルアミン;
・2−[(3−アミノピラゾロ[1,5−a]ピリジン−5−イル)(2−ヒドロキシエチル)アミノ]エタノール;
・2−[(3−アミノピラゾロ[1,5−a]ピリジン−7−イル)(2−ヒドロキシエチル)アミノ]エタノール;
・3−アミノピラゾロ[1,5−a]ピリジン−5−オール;
・3−アミノピラゾロ[1,5−a]ピリジン−4−オール;
・3−アミノピラゾロ[1,5−a]ピリジン−6−オール;
・3−アミノピラゾロ[1,5−a]ピリジン−7−オール;
・2−メトキシ−6,7−ジメチルピラゾロ[1,5−a]ピリジン−3−アミン;
・2−[(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)オキシ]エタノール;
・4−エチル−2−メトキシ−7−メチルピラゾロ[1,5−a]ピリジン−3−アミン塩酸塩;
・1−(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)ピロリジン−3−オール;
・2,2’−[(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)イミノ]ジエタノール;
・2−[(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)アミノ]エタノール;
・N2−(2−ピリジン−3−イルエチル)ピラゾロ[1,5−a]ピリジン−2,3−ジアミン;
、その付加塩、その溶媒和物、又はその塩の溶媒和物を挙げることができる。
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;
2−アミノ−3−メチルアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−ジメチルアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−エチルアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−イソプロピルアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−(2−ヒドロキシエチル)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;
2−アミノ−3−(2−ヒドロキシプロピル)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;
2−アミノ−3−ビス(2−ヒドロキシエチル)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;
2−アミノ−3−(ピロリジン−1−イル)−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−(3−ヒドロキシピロリジン−1−イル)−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−(ピペリジン−1−イル)−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2,3−ジアミノ−6−ヒドロキシ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2,3−ジアミノ−6−メチル−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2,3−ジアミノ−6−ジメチル−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2,3−ジアミノ−5,6,7,8−テトラヒドロ−1H,6H−ピリダジノ[1,2−a]ピラゾール−1−オン;
2,3−ジアミノ−5,8−ジヒドロ−1H,6H−ピリダジノ[1,2−a]ピラゾール−1−オン;
2,3−ジアミノ−6−ヒドロキシ−6,7−ジヒドロ−5H−ピラゾロ[1,2−a]ピラゾール−1−オン;これらのいくつかは、化学構造により名称を例示するために以下に挙げられている:
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;
2−アミノ−3−エチルアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−イソプロピルアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−(ピロリジン−1−イル)−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2−アミノ−3−(2−ヒドロキシエチル)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;
2−アミノ−3−ジメチルアミノ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
2,3−ジアミノ−5,6,7,8−テトラヒドロ−1H,6H−ピリダジノ[1,2−a]ピラゾール−1−オン;
2,3−ジアミノ−6−ヒドロキシ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オンである。
好ましくは、次の酸化性塩基:
2,3−ジアミノ−6−ヒドロキシ−6,7−ジヒドロ−1H,5H−ピラゾロ[1,2−a]ピラゾール−1−オン;
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;
2,3−ジアミノ−5,6,7,8−テトラヒドロ−1H,6H−ピリダジノ[1,2−a]ピラゾール−1−オン;
及びその付加塩、又はその溶媒和物、又はその塩の溶媒和物である。
本発明の組成物は、他の追加的なカプラー及び酸化性塩基を含有していてもよい。本発明ための使用の2−アミノ−5−エチルフェノール以外のこれらのカプラーの中では、特にメタ−フェニレンジアミン、2−アミノ−5−エチルフェノール以外のメタ−アミノフェノール、メタ−ジフェノール、ナフタレンカプラー、ヘテロ環カプラー、その付加塩、その溶媒和塩、及びその混合物を挙げることができる。
本発明の組成物は、任意選択的には1種以上の界面活性剤も含有していてもよい。
− オキシアルキレン化(C8〜C24)アルキルフェノール;
− 1個又は2個の脂肪鎖を含む、飽和又は不飽和の、直鎖又は分岐の、オキシアルキレン化又はグリセロール化C8〜C40アルコール;
− 飽和又は不飽和の、直鎖又は分岐の、オキシアルキレン化C8〜C30脂肪酸アミド;
− 飽和又は不飽和の、直鎖又は分岐のC8〜C30酸と、ポリエチレングリコールとのエステル;
− 好ましくは、飽和又は不飽和の、直鎖又は分岐のC8〜C30酸と、ソルビトールとのオキシエチレン化エステル;
− 脂肪酸とスクロースとのエステル;
− 任意選択的にオキシアルキレン化(0〜10個のオキシアルキレン単位)されていてもよく、1〜15個のグルコース単位を含む、(C8〜C30)アルキル(ポリ)グルコシド及び(C8〜C30)アルケニル(ポリ)グルコシド、(C8〜C30)アルキル(ポリ)グルコシドエステル;
− 飽和又は不飽和のオキシエチレン化植物油;
− エチレンオキシド及び/又はプロピレンオキシドの縮合物;
− N−(C8〜C30)アルキルグルカミン及びN−(C8〜C30)アシルメチルグルカミン誘導体;
− アルドビオンアミド(aldobionamide);
− アミンオキシド;
− オキシエチレン化及び/又はオキシプロピレン化シリコーン;
− 及びこれらの混合物。
− 1〜100molのエチレンオキシド、好ましくは2〜50、より好ましくは2〜40molのエチレンオキシドを含み、1個又は2個の脂肪鎖を含む、オキシエチレン化C8〜C40アルコール;
− 1〜100、好ましくは2〜50molのエチレンオキシドを含む飽和又は不飽和のオキシエチレン化植物油;
− 任意選択的にオキシアルキレン化(0〜10OE)されていてもよく1〜15個のグルコース単位を含む(C8〜C30)アルキル(ポリ)グルコシド;
− 1〜50molのグリセロール、好ましくは1〜10molのグリセロールを含むモノグリセロール化若しくはポリグリセロール化C8〜C40アルコール;
− 飽和又は不飽和の、直鎖又は分岐の、オキシアルキレン化C8〜C30脂肪酸アミド;
− 飽和又は不飽和の、直鎖又は分岐のC8〜C30の酸とポリエチレングリコールとのエステル;
− 並びにこれらの混合物;
から選択される。
− イミダゾリンの四級アンモニウム塩、例えばRewo社からRewoquat(登録商標) W75という名称で販売;
− ジ−若しくはトリ四級アンモニウム塩、例えばFinetex社から入手可能なFinquat CT−P(Quaternium 89)、及びFinetex社から入手可能なFinquat CT(Quaternium 75);
− ジアシルオキシエチルジメチルアンモニウム、ジアシルオキシエチルヒドロキシエチルメチルアンモニウム、モノアシルオキシエチルジヒドロキシエチルメチルアンモニウム、トリアシルオキシエチルメチルアンモニウム、及びモノアシルオキシエチルヒドロキシエチルジメチルアンモニウム塩などの、少なくとも1つのエステル官能基を含む四級アンモニウム塩(特には塩化物塩又はメチル硫酸塩);
の塩化物塩、並びにこれらの混合物を使用することが特に好ましい。アシル基は、好ましくは14〜18個の炭素原子を含み、より具体的にはパーム油又はひまわり油などの植物油から得られる。化合物が複数のアシル基を含む場合、これらの基は同じであっても異なっていてもよい。
本発明の組成物は、任意選択的には1種以上のアルカリ剤も含有していてもよい。
本発明のある具体的な実施形態によれば、本発明の組成物は、少なくとも1種の化学的酸化剤を含有する。
ある具体的な実施形態によれば、本発明の組成物は、塩の形態の脂肪酸とは異なる1種以上の脂肪性物質を含有する。
本発明のもう1つの主題は、本発明の組成物をケラチン繊維に塗布することを含む、ヒトのケラチン繊維、特には毛髪の染色方法である。
− 上述の式(I)、(II)、又は(III)のうちの少なくとも1種の酸化性塩基と、少なくとも1種の2−アミノ−5−エチルフェノールカプラーと、少なくとも1種のアルカリ剤とを含有する染料組成物;並びに、
− 1種以上の化学的酸化剤を含有する組成物。
本発明のもう1つの主題は、好ましくは少なくとも2つの区画を含む、ケラチン繊維染色用のマルチコンパートメントデバイスであって、本発明の染料組成物(A)を含む少なくとも1つの第1の区画、及び、上述した酸化性組成物(B)を含む少なくとも1つの第2の区画を含む、ケラチン繊維染色用のマルチコンパートメントデバイスである。
a)染色組成物
染色組成物A1及びA2は、その内容が活性物質のg%で下の表に示されている(別段の記載がない限り)成分から調製した。
Claims (12)
- (A)少なくとも1種の2−アミノ−5−エチルフェノールカプラー、又はその付加塩若しくは溶媒和物と、
(B)
A1)式(I)のピラゾロピリジン及びその付加塩、その溶媒和物、又はその塩の溶媒和物:
A2)式(II)のピラゾロピリジン酸化性塩基(oxidation bases):
Z1及びZ2は、独立に:
・共有単結合;
・以下から選択される二価の基:
・−O(CH2)p−基(pは0〜6の範囲の整数を表す);
・−NR’6(CH2)q(C6H4)t−基(qは0〜6の範囲の整数を表し、tは0又は1を表し、R’6は水素原子又は任意選択的に1つ以上のヒドロキシル基で置換されていてもよいC1〜C6アルキル基を表す);
を表し;
R’1がメチル基の場合にはZ1は二価の基である−S−、−SO−、又は−SO2−を表していてもよく;
R’1及びR’2は、独立に:
・水素;
・任意選択的に置換されていてもよく任意選択的にO、N、Si、S、SO、及びSO2から選択されるヘテロ原子又は基で中断されていてもよいC1〜C10アルキル基;
・ハロゲン;
・SO3H基;
・任意選択的にN、O、S、SO2及び、−CO−から選択されるヘテロ原子又は基を1つ以上含んでいてもよい、置換又は無置換の、飽和、不飽和、又は芳香族の5〜8員環(環はカチオンであってもよく及び/又はカチオン基で置換されていてもよい);
・基−N+R19R18R19(R17、R18、及びR19は任意選択的に1つ以上のヒドロキシル基で置換されていてもよい直鎖又は分岐のC1〜C5アルキルである);
を表し、Z1、それぞれZ2が共有結合を表す場合には、R’1、それぞれのR’2は、
・任意選択的に置換されていてもよいC1〜C6アルキルカルボニル基;
・−O−CO−R、−CO−O−R、NR−CO−R’、又は−CO−NRR’ 基(R及びR’は、独立に、水素原子又は任意選択的に置換されていてもよいC1〜C6アルキル基を表す);
も表していてもよく、
R’3、R’4、及びR’5は、同じでも異なっていてもよく、
・水素原子;
・ヒドロキシル基;
・C1〜C6アルコキシ基;
・C1〜C6アルキルチオ基;
・アミノ基;
・モノアルキルアミノ基;
・C1〜C6ジアルキルアミノ基(ここで、アルキル基はこれらが結合している窒素原子と共に、N、O、S、SO2、及びCOから選択される1つ以上のヘテロ原子又は基を含んでいてもよい、飽和又は不飽和の、芳香族又は非芳香族の、5〜8員のヘテロ環を形成していてもよく、ヘテロ環はカチオンであってもよく及び/又はカチオン基で置換されていてもよい);
・任意選択的に置換されていてもよいC1〜C6アルキルカルボニル基;
・−O−CO−R、−CO−O−R、NR−CO−R’、又は−CO−NRR’基(R及びR’は上で定義した通りである);
・ハロゲン
・−NHSO3H基;
・任意選択的に置換されていてもよいC1〜C4アルキル基;
・飽和、不飽和、又は芳香族の、任意選択的に置換されていてもよい炭素を主体とする環;
を表し、
R’3、R’4、及びR’5は、2つ1組で部分的に飽和又は不飽和の環を形成していてもよく;
Xは式(II)の誘導体の電気陰性度を確保することを可能にするイオン又はイオン群を表すが;
基R’1及びR’2のうちの少なくとも1つはカチオン基を表すことを条件とする)
から選択される少なくとも1種のピラゾールヘテロ環酸化性塩基と、
を含有する、ケラチン繊維の染色用組成物。 - 式(I)の化合物が、次の式:
の化合物から選択される、請求項1に記載の組成物。 - 式(I)の3−アミノピラゾロ[1,5−a]ピリジンが、
・ピラゾロ[1,5−a]ピリジン−3−イルアミン;
・2−アセチルアミノピラゾロ[1,5−a]ピリジン−3−イルアミン;
・2−モルホリン−4−イルピラゾロ[1,5−a]ピリジン−3−イルアミン;
・3−アミノピラゾロ[1,5−a]ピリジン−2−カルボン酸;
・2−メトキシピラゾロ[1,5−a]ピリジン−3−イルアミノ;
・(3−アミノピラゾロ[1,5−a]ピリジン−7−イル)メタノール;
・2−(3−アミノピラゾロ[1,5−a]ピリジン−5−イル)エタノール;
・2−(3−アミノピラゾロ[1,5−a]ピリジン−7−イル)エタノール;
・(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)メタノール;
・3,6−ジアミノピラゾロ[1,5−a]ピリジン;
・3,4−ジアミノピラゾロ[1,5−a]ピリジン;
・ピラゾロ[1,5−a]ピリジン−3,7−ジアミン;
・7−モルホリン−4−イルピラゾロ[1,5−a]ピリジン−3−イルアミン;
・ピラゾロ[1,5−a]ピリジン−3,5−ジアミン;
・5−モルホリン−4−イルピラゾロ[1,5−a]ピリジン−3−イルアミン;
・2−[(3−アミノピラゾロ[1,5−a]ピリジン−5−イル)(2−ヒドロキシエチル)アミノ]エタノール;
・2−[(3−アミノピラゾロ[1,5−a]ピリジン−7−イル)(2−ヒドロキシエチル)アミノ]エタノール;
・3−アミノピラゾロ[1,5−a]ピリジン−5−オール;
・3−アミノピラゾロ[1,5−a]ピリジン−4−オール;
・3−アミノピラゾロ[1,5−a]ピリジン−6−オール;
・3−アミノピラゾロ[1,5−a]ピリジン−7−オール;
・2−メトキシ−6,7−ジメチルピラゾロ[1,5−a]ピリジン−3−アミン;
・2−[(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)オキシ]エタノール;
・4−エチル−2−メトキシ−7−メチルピラゾロ[1,5−a]ピリジン−3−アミン塩酸塩;
・1−(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)ピロリジン−3−オール;
・2,2’−[(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)イミノ]ジエタノール;
・2−[(3−アミノピラゾロ[1,5−a]ピリジン−2−イル)アミノ]エタノール;
・N2−(2−ピリジン−3−イルエチル)ピラゾロ[1,5−a]ピリジン−2,3−ジアミン;
及びその付加塩、その溶媒和物、又はその塩の溶媒和物から選択される、請求項1及び2のいずれか1項に記載の組成物。 - 1種以上の界面活性剤を含有する、請求項1〜5のいずれか1項に記載の組成物。
- 1種以上のアルカリ剤を含有する、請求項1〜6のいずれか1項に記載の組成物。
- 酸化性塩基の合計量が、前記ケラチン繊維染色用組成物の総重量に対して、0.0001重量%〜20重量%であり、カプラーの合計量が、前記ケラチン繊維染色用組成物の総重量に対して、0.001重量%〜10重量%の範囲である、請求項1〜7のいずれか1項に記載の組成物。
- 化学的酸化剤を含有する、請求項1〜8のいずれか1項に記載の組成物。
- 請求項1〜9のいずれか1項に記載の組成物をケラチン繊維に塗布することを含む、ケラチン繊維の染色方法。
- ケラチン繊維染色用のマルチコンパートメントデバイスであって、請求項1〜8のいずれか1項に記載の染料組成物を含む少なくとも1つの第1の区画、及び、1種以上の化学的酸化剤を含有する酸化性組成物(B)を含む少なくとも1つの第2の区画を含む、マルチコンパートメントデバイス。
- ケラチン繊維の染色のための、請求項1〜9のいずれか1項に記載の組成物の使用。
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FR1562908A FR3045348B1 (fr) | 2015-12-21 | 2015-12-21 | Composition de coloration des cheveux comprenant une base d'oxydation heterocyclique et un coupleur 2-amino 5-ethyl phenol |
FR1562908 | 2015-12-21 | ||
PCT/EP2016/082011 WO2017108847A1 (en) | 2015-12-21 | 2016-12-20 | Composition for dyeing the hair, comprising a heterocyclic oxidation base and a 2-amino-5-ethylphenol coupler |
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FR3045345B1 (fr) | 2015-12-21 | 2017-12-15 | Oreal | Composition de coloration des cheveux comprenant une base d'oxydation de type para-phenylenediamine et un coupleur 2-amino 5-ethyl phenol |
FR3045379B1 (fr) | 2015-12-21 | 2019-05-24 | L'oreal | Composition de coloration des cheveux comprenant une base d'oxydation, un coupleur 2-amino 5-ethyl phenol et un corps gras |
US10596091B2 (en) * | 2018-05-31 | 2020-03-24 | L'oreal | Hair color-altering compositions |
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JP2019189658A (ja) | 2019-10-31 |
US20180369104A1 (en) | 2018-12-27 |
EP3393445A1 (en) | 2018-10-31 |
BR112018011908B1 (pt) | 2021-07-27 |
JP6957567B2 (ja) | 2021-11-02 |
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