JP2005532444A5 - - Google Patents
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- Publication number
- JP2005532444A5 JP2005532444A5 JP2004518878A JP2004518878A JP2005532444A5 JP 2005532444 A5 JP2005532444 A5 JP 2005532444A5 JP 2004518878 A JP2004518878 A JP 2004518878A JP 2004518878 A JP2004518878 A JP 2004518878A JP 2005532444 A5 JP2005532444 A5 JP 2005532444A5
- Authority
- JP
- Japan
- Prior art keywords
- formazano
- chloride
- group
- pyridinylidene
- formula
- 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.)
- Pending
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- -1 halide ion Chemical group 0.000 claims description 48
- 125000003545 alkoxy group Chemical group 0.000 claims description 14
- 125000003282 alkyl amino group Chemical group 0.000 claims description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 12
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims description 12
- 125000001072 heteroaryl group Chemical group 0.000 claims description 11
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 9
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical group CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 7
- FEWJPZIEWOKRBE-JCYAYHJZSA-L L-tartrate(2-) Chemical group [O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O FEWJPZIEWOKRBE-JCYAYHJZSA-L 0.000 claims description 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-L Oxalate Chemical group [O-]C(=O)C([O-])=O MUBZPKHOEPUJKR-UHFFFAOYSA-L 0.000 claims description 7
- 150000001449 anionic compounds Chemical class 0.000 claims description 7
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical group OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 7
- 229910001412 inorganic anion Inorganic materials 0.000 claims description 7
- 150000002500 ions Chemical class 0.000 claims description 7
- 150000002891 organic anions Chemical class 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 6
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 239000000460 chlorine Substances 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 6
- 125000005191 hydroxyalkylamino group Chemical group 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 5
- 125000001246 bromo group Chemical group Br* 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000002883 imidazolyl group Chemical group 0.000 claims description 3
- 125000002971 oxazolyl group Chemical group 0.000 claims description 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 3
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 3
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 3
- 125000000335 thiazolyl group Chemical group 0.000 claims description 3
- 125000004306 triazinyl group Chemical group 0.000 claims description 3
- 125000001425 triazolyl group Chemical group 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 38
- 229910052757 nitrogen Inorganic materials 0.000 claims 37
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 24
- 150000001875 compounds Chemical class 0.000 claims 17
- 239000000203 mixture Substances 0.000 claims 13
- 102000011782 Keratins Human genes 0.000 claims 10
- 108010076876 Keratins Proteins 0.000 claims 10
- 239000000835 fiber Substances 0.000 claims 10
- 238000000034 method Methods 0.000 claims 9
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 8
- 238000004061 bleaching Methods 0.000 claims 6
- 150000007857 hydrazones Chemical class 0.000 claims 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 6
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 claims 6
- JDIIGWSSTNUWGK-UHFFFAOYSA-N 1h-imidazol-3-ium;chloride Chemical compound [Cl-].[NH2+]1C=CN=C1 JDIIGWSSTNUWGK-UHFFFAOYSA-N 0.000 claims 5
- 238000004043 dyeing Methods 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 239000003638 chemical reducing agent Substances 0.000 claims 4
- 229930195733 hydrocarbon Natural products 0.000 claims 4
- 150000002430 hydrocarbons Chemical class 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 125000004434 sulfur atom Chemical group 0.000 claims 4
- 239000004215 Carbon black (E152) Substances 0.000 claims 3
- 239000000975 dye Substances 0.000 claims 3
- 239000002243 precursor Substances 0.000 claims 3
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 2
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims 2
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- ZTKWLYZCSIGPOU-UHFFFAOYSA-N [Cl-].C(C)[NH+]1NC=CC1 Chemical compound [Cl-].C(C)[NH+]1NC=CC1 ZTKWLYZCSIGPOU-UHFFFAOYSA-N 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims 2
- 239000000982 direct dye Substances 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000000018 nitroso group Chemical group N(=O)* 0.000 claims 2
- 239000007800 oxidant agent Substances 0.000 claims 2
- 230000001590 oxidative effect Effects 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 claims 1
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims 1
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims 1
- LUABANCJXKHLBK-UHFFFAOYSA-N 2,3-dihydro-1h-pyrazole;hydrochloride Chemical compound Cl.C1NNC=C1 LUABANCJXKHLBK-UHFFFAOYSA-N 0.000 claims 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims 1
- LBDQWEZGMHRQSP-UHFFFAOYSA-M 2-methyl-n-(1-methyl-4-pyrrolidin-1-ylpyridin-1-ium-2-yl)imino-n'-[(z)-(1-methyl-4-pyrrolidin-1-ylpyridin-2-ylidene)amino]propanimidamide;chloride Chemical compound [Cl-].C1=C(N2CCCC2)C=CN(C)C1=NN=C(C(C)C)N=NC([N+](=CC=1)C)=CC=1N1CCCC1 LBDQWEZGMHRQSP-UHFFFAOYSA-M 0.000 claims 1
- CSOGPOMWRHPSDN-UHFFFAOYSA-M 2-methyl-n-(1-methylpyridin-1-ium-2-yl)imino-n'-[(e)-(1-methylpyridin-2-ylidene)amino]propanimidamide;chloride Chemical compound [Cl-].C1=CC=CN(C)C1=NN=C(C(C)C)N=NC1=CC=CC=[N+]1C CSOGPOMWRHPSDN-UHFFFAOYSA-M 0.000 claims 1
- WPOZVJTUVDHTRP-UHFFFAOYSA-M 2-methyl-n-(1-methylpyridin-1-ium-4-yl)imino-n'-[(1-methylpyridin-4-ylidene)amino]propanimidamide;chloride Chemical compound [Cl-].C1=CN(C)C=CC1=NN=C(C(C)C)N=NC1=CC=[N+](C)C=C1 WPOZVJTUVDHTRP-UHFFFAOYSA-M 0.000 claims 1
- ZEZRXCKARNTTKP-UHFFFAOYSA-N 3-[(2e)-2-[(e)-1-[[1-(2-carboxyethyl)pyridin-1-ium-2-yl]diazenyl]propylidenehydrazinylidene]pyridin-1-yl]propanoic acid;chloride Chemical compound [Cl-].C1=CC=CN(CCC(O)=O)C1=NN=C(CC)N=NC1=CC=CC=[N+]1CCC(O)=O ZEZRXCKARNTTKP-UHFFFAOYSA-N 0.000 claims 1
- WOTNSXJVWDSCHS-UHFFFAOYSA-N 3-[(2e)-2-[(e)-[1-[[1-(2-carboxyethyl)pyridin-1-ium-2-yl]diazenyl]-2-methylpropylidene]hydrazinylidene]pyridin-1-yl]propanoic acid;chloride Chemical compound [Cl-].C1=CC=CN(CCC(O)=O)C1=NN=C(C(C)C)N=NC1=CC=CC=[N+]1CCC(O)=O WOTNSXJVWDSCHS-UHFFFAOYSA-N 0.000 claims 1
- SSDNHRVIHBEIRA-UHFFFAOYSA-N 3-[(2e)-2-[(e)-[[1-(2-carboxyethyl)pyridin-1-ium-2-yl]diazenyl]methylidenehydrazinylidene]pyridin-1-yl]propanoic acid;chloride Chemical compound [Cl-].OC(=O)CCN1C=CC=CC1=NN=CN=NC1=CC=CC=[N+]1CCC(O)=O SSDNHRVIHBEIRA-UHFFFAOYSA-N 0.000 claims 1
- PCUAIYJAGDUKBZ-UHFFFAOYSA-N 3-[(2e)-2-[(e)-[[[1-(2-carboxyethyl)pyridin-1-ium-2-yl]diazenyl]-phenylmethylidene]hydrazinylidene]pyridin-1-yl]propanoic acid;chloride Chemical compound [Cl-].OC(=O)CCN1C=CC=CC1=NN=C(C=1C=CC=CC=1)N=NC1=CC=CC=[N+]1CCC(O)=O PCUAIYJAGDUKBZ-UHFFFAOYSA-N 0.000 claims 1
- MOWINBDBQSTPTR-UHFFFAOYSA-N 3-[4-[(e)-1-[[1-(2-carboxyethyl)pyridin-1-ium-4-yl]diazenyl]ethylidenehydrazinylidene]pyridin-1-yl]propanoic acid;chloride Chemical compound [Cl-].C1=CN(CCC(O)=O)C=CC1=NN=C(C)N=NC1=CC=[N+](CCC(O)=O)C=C1 MOWINBDBQSTPTR-UHFFFAOYSA-N 0.000 claims 1
- VSCXYHPONOEWAL-UHFFFAOYSA-N 3-[4-[(e)-1-[[1-(2-carboxyethyl)pyridin-1-ium-4-yl]diazenyl]propylidenehydrazinylidene]pyridin-1-yl]propanoic acid;chloride Chemical compound [Cl-].C1=CN(CCC(O)=O)C=CC1=NN=C(CC)N=NC1=CC=[N+](CCC(O)=O)C=C1 VSCXYHPONOEWAL-UHFFFAOYSA-N 0.000 claims 1
- BDLXCTGHXNWJTC-UHFFFAOYSA-N 3-[4-[(e)-[[1-(2-carboxyethyl)pyridin-1-ium-4-yl]diazenyl]methylidenehydrazinylidene]pyridin-1-yl]propanoic acid;chloride Chemical compound [Cl-].C1=CN(CCC(=O)O)C=CC1=NN=CN=NC1=CC=[N+](CCC(O)=O)C=C1 BDLXCTGHXNWJTC-UHFFFAOYSA-N 0.000 claims 1
- QNVSNHSVSAJWMO-UHFFFAOYSA-N 3-[4-[(e)-[[[1-(2-carboxyethyl)pyridin-1-ium-4-yl]diazenyl]-phenylmethylidene]hydrazinylidene]pyridin-1-yl]propanoic acid;chloride Chemical compound [Cl-].C1=CN(CCC(=O)O)C=CC1=NN=C(C=1C=CC=CC=1)N=NC1=CC=[N+](CCC(O)=O)C=C1 QNVSNHSVSAJWMO-UHFFFAOYSA-N 0.000 claims 1
- 229940018563 3-aminophenol Drugs 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- 125000005263 alkylenediamine group Chemical group 0.000 claims 1
- 125000002619 bicyclic group Chemical group 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 239000000118 hair dye Substances 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 229940018564 m-phenylenediamine Drugs 0.000 claims 1
- VPYRTRXGPZFUIP-UHFFFAOYSA-M n-(1-methyl-4-pyrrolidin-1-ylpyridin-1-ium-2-yl)imino-n'-[(z)-(1-methyl-4-pyrrolidin-1-ylpyridin-2-ylidene)amino]benzenecarboximidamide;chloride Chemical compound [Cl-].CN1C=CC(N2CCCC2)=CC1=NN=C(C=1C=CC=CC=1)N=NC([N+](=CC=1)C)=CC=1N1CCCC1 VPYRTRXGPZFUIP-UHFFFAOYSA-M 0.000 claims 1
- KSMLXSUGXCHNNW-UHFFFAOYSA-M n-(1-methyl-4-pyrrolidin-1-ylpyridin-1-ium-2-yl)imino-n'-[(z)-(1-methyl-4-pyrrolidin-1-ylpyridin-2-ylidene)amino]ethanimidamide;chloride Chemical compound [Cl-].C1=C(N2CCCC2)C=CN(C)C1=NN=C(C)N=NC([N+](=CC=1)C)=CC=1N1CCCC1 KSMLXSUGXCHNNW-UHFFFAOYSA-M 0.000 claims 1
- XJNPUACUZFRZAK-UHFFFAOYSA-M n-(1-methyl-4-pyrrolidin-1-ylpyridin-1-ium-2-yl)imino-n'-[(z)-(1-methyl-4-pyrrolidin-1-ylpyridin-2-ylidene)amino]methanimidamide;chloride Chemical compound [Cl-].CN1C=CC(N2CCCC2)=CC1=NN=CN=NC([N+](=CC=1)C)=CC=1N1CCCC1 XJNPUACUZFRZAK-UHFFFAOYSA-M 0.000 claims 1
- KBDJYATYLVSAPW-UHFFFAOYSA-M n-(1-methyl-4-pyrrolidin-1-ylpyridin-1-ium-2-yl)imino-n'-[(z)-(1-methyl-4-pyrrolidin-1-ylpyridin-2-ylidene)amino]propanimidamide;chloride Chemical compound [Cl-].C1=C(N2CCCC2)C=CN(C)C1=NN=C(CC)N=NC([N+](=CC=1)C)=CC=1N1CCCC1 KBDJYATYLVSAPW-UHFFFAOYSA-M 0.000 claims 1
- WQZJTUVNOXNGNK-UHFFFAOYSA-M n-(1-methylpyridin-1-ium-2-yl)imino-n'-[(e)-(1-methylpyridin-2-ylidene)amino]benzenecarboximidamide;chloride Chemical compound [Cl-].CN1C=CC=CC1=NN=C(C=1C=CC=CC=1)N=NC1=CC=CC=[N+]1C WQZJTUVNOXNGNK-UHFFFAOYSA-M 0.000 claims 1
- YELQXDLKRQWSFV-UHFFFAOYSA-M n-(1-methylpyridin-1-ium-2-yl)imino-n'-[(e)-(1-methylpyridin-2-ylidene)amino]ethanimidamide;chloride Chemical compound [Cl-].C/1=CC=CN(C)C\1=N\N=C(/C)\N=N\C1=CC=CC=[N+]1C YELQXDLKRQWSFV-UHFFFAOYSA-M 0.000 claims 1
- WXGVZIJZTVVGBP-UHFFFAOYSA-M n-(1-methylpyridin-1-ium-2-yl)imino-n'-[(e)-(1-methylpyridin-2-ylidene)amino]propanimidamide;chloride Chemical compound [Cl-].C1=CC=CN(C)C1=NN=C(CC)N=NC1=CC=CC=[N+]1C WXGVZIJZTVVGBP-UHFFFAOYSA-M 0.000 claims 1
- XVMGIIRRNHCMDF-UHFFFAOYSA-M n-(1-methylpyridin-1-ium-2-yl)imino-n'-[(z)-(1-methylpyridin-2-ylidene)amino]methanimidamide;chloride Chemical compound [Cl-].CN1C=CC=C\C1=N\N=C\N=N\C1=CC=CC=[N+]1C XVMGIIRRNHCMDF-UHFFFAOYSA-M 0.000 claims 1
- RERLIMPHEDSDSK-UHFFFAOYSA-M n-(1-methylpyridin-1-ium-4-yl)imino-n'-[(1-methylpyridin-4-ylidene)amino]benzenecarboximidamide;chloride Chemical compound [Cl-].C1=CN(C)C=CC1=NN=C(C=1C=CC=CC=1)N=NC1=CC=[N+](C)C=C1 RERLIMPHEDSDSK-UHFFFAOYSA-M 0.000 claims 1
- PVAVJWXLSGCUSV-UHFFFAOYSA-M n-(1-methylpyridin-1-ium-4-yl)imino-n'-[(1-methylpyridin-4-ylidene)amino]ethanimidamide;chloride Chemical compound [Cl-].C1=CN(C)C=CC1=NN=C(C)N=NC1=CC=[N+](C)C=C1 PVAVJWXLSGCUSV-UHFFFAOYSA-M 0.000 claims 1
- WYVRTSODAMAXBT-UHFFFAOYSA-M n-(1-methylpyridin-1-ium-4-yl)imino-n'-[(1-methylpyridin-4-ylidene)amino]methanimidamide;chloride Chemical compound [Cl-].C1=CN(C)C=CC1=NN=CN=NC1=CC=[N+](C)C=C1 WYVRTSODAMAXBT-UHFFFAOYSA-M 0.000 claims 1
- GPSIKQMJBQUFTK-UHFFFAOYSA-M n-(1-methylpyridin-1-ium-4-yl)imino-n'-[(1-methylpyridin-4-ylidene)amino]propanimidamide;chloride Chemical compound [Cl-].C1=CN(C)C=CC1=NN=C(CC)N=NC1=CC=[N+](C)C=C1 GPSIKQMJBQUFTK-UHFFFAOYSA-M 0.000 claims 1
- WPDFSXWXFLDQDK-UHFFFAOYSA-M n-[1-(2-hydroxyethyl)pyridin-1-ium-2-yl]imino-n'-[(e)-[1-(2-hydroxyethyl)pyridin-2-ylidene]amino]ethanimidamide;chloride Chemical compound [Cl-].C/1=CC=CN(CCO)C\1=N\N=C(/C)\N=N\C1=CC=CC=[N+]1CCO WPDFSXWXFLDQDK-UHFFFAOYSA-M 0.000 claims 1
- XUVMIYOSHVNLFY-UHFFFAOYSA-M n-[1-(2-hydroxyethyl)pyridin-1-ium-2-yl]imino-n'-[(e)-[1-(2-hydroxyethyl)pyridin-2-ylidene]amino]propanimidamide;chloride Chemical compound [Cl-].C1=CC=CN(CCO)C1=NN=C(CC)N=NC1=CC=CC=[N+]1CCO XUVMIYOSHVNLFY-UHFFFAOYSA-M 0.000 claims 1
- OXDACPKFKLZGMH-UHFFFAOYSA-M n-[1-(2-hydroxyethyl)pyridin-1-ium-4-yl]imino-n'-[[1-(2-hydroxyethyl)pyridin-4-ylidene]amino]-2-methylpropanimidamide;chloride Chemical compound [Cl-].C1=CN(CCO)C=CC1=NN=C(C(C)C)N=NC1=CC=[N+](CCO)C=C1 OXDACPKFKLZGMH-UHFFFAOYSA-M 0.000 claims 1
- XFRXBDJBJFPZEK-UHFFFAOYSA-M n-[1-(2-hydroxyethyl)pyridin-1-ium-4-yl]imino-n'-[[1-(2-hydroxyethyl)pyridin-4-ylidene]amino]benzenecarboximidamide;chloride Chemical compound [Cl-].C1=CN(CCO)C=CC1=NN=C(C=1C=CC=CC=1)N=NC1=CC=[N+](CCO)C=C1 XFRXBDJBJFPZEK-UHFFFAOYSA-M 0.000 claims 1
- PEKXZBRZDFUTFX-UHFFFAOYSA-M n-[1-(2-hydroxyethyl)pyridin-1-ium-4-yl]imino-n'-[[1-(2-hydroxyethyl)pyridin-4-ylidene]amino]ethanimidamide;chloride Chemical compound [Cl-].C1=CN(CCO)C=CC1=NN=C(C)N=NC1=CC=[N+](CCO)C=C1 PEKXZBRZDFUTFX-UHFFFAOYSA-M 0.000 claims 1
- YNEUXRPQXPSVNA-UHFFFAOYSA-M n-[1-(2-hydroxyethyl)pyridin-1-ium-4-yl]imino-n'-[[1-(2-hydroxyethyl)pyridin-4-ylidene]amino]methanimidamide;chloride Chemical compound [Cl-].C1=CN(CCO)C=CC1=NN=CN=NC1=CC=[N+](CCO)C=C1 YNEUXRPQXPSVNA-UHFFFAOYSA-M 0.000 claims 1
- DFIPEQSVKJXYRP-UHFFFAOYSA-M n-[1-(2-hydroxyethyl)pyridin-1-ium-4-yl]imino-n'-[[1-(2-hydroxyethyl)pyridin-4-ylidene]amino]propanimidamide;chloride Chemical compound [Cl-].C1=CN(CCO)C=CC1=NN=C(CC)N=NC1=CC=[N+](CCO)C=C1 DFIPEQSVKJXYRP-UHFFFAOYSA-M 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 238000005406 washing Methods 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0208494A FR2841901B1 (fr) | 2002-07-05 | 2002-07-05 | Utilisation d'un compose tetraazapentamethinique en tant que colorant direct et nouveaux composes tetraazapentamethiniques |
| PCT/FR2003/002090 WO2004005407A2 (fr) | 2002-07-05 | 2003-07-04 | Composés tétraazapentaméthiniques et leur application pour la teinture des fibres keratiniques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005532444A JP2005532444A (ja) | 2005-10-27 |
| JP2005532444A5 true JP2005532444A5 (enExample) | 2010-10-21 |
Family
ID=29720100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004518878A Pending JP2005532444A (ja) | 2002-07-05 | 2003-07-04 | テトラアザペンタメチン化合物の直接染料としての使用および新規なテトラアザペンタメチン化合物 |
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| EP (1) | EP1378544A3 (enExample) |
| JP (1) | JP2005532444A (enExample) |
| FR (1) | FR2841901B1 (enExample) |
| WO (1) | WO2004005407A2 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2020018327A (ja) | 2018-07-17 | 2020-02-06 | ロレアル | マイクロニードルシート |
| JP7292837B2 (ja) | 2018-08-29 | 2023-06-19 | ロレアル | ケラチン繊維を着色するための方法及び組成物 |
| JP7199936B2 (ja) | 2018-11-27 | 2023-01-06 | ロレアル | ケラチン繊維のための組成物 |
| JP2020169122A (ja) | 2019-03-20 | 2020-10-15 | ロレアル | ケラチン繊維を着色するための方法及びキット |
| FR3097761B1 (fr) | 2019-06-27 | 2021-05-28 | Oreal | Composition comprenant l’acide 12-hydroxystéarique, une amine organique et un corps gras liquide |
| JP2021094146A (ja) | 2019-12-16 | 2021-06-24 | ロレアル | マイクロニードルシートを使用する美容方法 |
| US20230065360A1 (en) | 2019-12-24 | 2023-03-02 | L'oreal | Cosmetic composition comprising a polymer comprising at least one cationic (meth)acrylamide unit, a particular silicone and at least one surfactant |
| FR3113240B1 (fr) | 2020-08-10 | 2024-01-12 | Oreal | Composition comprenant au moins un silicone particulier, au moins un alcane et au moins une teinte directe et/ou au moins un pigment |
| WO2023228870A1 (en) | 2022-05-25 | 2023-11-30 | L'oreal | Composition for coloring keratin fibers |
| FR3137835A1 (fr) | 2022-07-15 | 2024-01-19 | L'oreal | Composition pour la coloration des fibres kératineuses |
| FR3140268A1 (fr) | 2022-09-29 | 2024-04-05 | L'oreal | Processus cosmétique utilisant une particule avec microprotubérance |
| WO2024048429A1 (en) | 2022-08-30 | 2024-03-07 | L'oreal | Cosmetic process using particle with microprotrusion |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE117081C (enExample) | ||||
| DE1222608B (de) * | 1960-10-21 | 1966-08-11 | Kuhlmann Ets | Verfahren zur Herstellung von Farbstoffen der Indazolreihe |
| FR1291555A (fr) * | 1960-10-21 | 1962-04-27 | Cfmc | Nouveaux colorants de la série de l'indazole |
| DD117081A1 (enExample) * | 1974-12-17 | 1975-12-20 | ||
| JPH07186547A (ja) * | 1993-10-21 | 1995-07-25 | Eastman Kodak Co | 光学記録層用色素混合物 |
| US5593872A (en) | 1993-12-10 | 1997-01-14 | Tastemaker | Enzymatic oxidation of alcohols to aldehydes in a continuous reaction system using Candida boidinii |
| FR2741798B1 (fr) * | 1995-12-01 | 1998-01-09 | Oreal | Composition de teinture eclaircissante pour fibres keratiniques comprenant un colorant direct specifique |
| DE19732016A1 (de) * | 1997-07-25 | 1999-01-28 | Henkel Kgaa | Haarfärbemittel |
| DE19809646C2 (de) * | 1998-03-06 | 2003-02-27 | Wella Ag | Oxonolfarbstoffe enthaltende Färbemittel und Verfahren zur Erzeugung von temporären Haarfärbungen |
| FR2780883B1 (fr) * | 1998-07-09 | 2001-04-06 | Oreal | Composition de teinture pour fibres keratiniques avec un colorant direct cationique et un polymere epaississant |
| FR2780880B1 (fr) * | 1998-07-09 | 2001-08-10 | Oreal | Composition de teinture pour fibres keratiniques avec un colorant direct cationique et un polymere epaississant |
| JP2002080332A (ja) * | 2000-03-17 | 2002-03-19 | Kao Corp | 染毛剤組成物 |
| FR2822695B1 (fr) * | 2001-04-02 | 2003-07-25 | Oreal | Nouvelle composition tinctiriale pour la teinture des fibres keratiniques comprenant un colorant azoique cationique particilier |
| FR2822697B1 (fr) * | 2001-04-02 | 2003-07-25 | Oreal | Nouvelle composition tinctoriale pour la teinture des fibres keratiniques comprenant un colorant azoique cationique particulier |
| FR2825702B1 (fr) * | 2001-06-11 | 2003-08-08 | Oreal | Composition pour la teinture des fibres keratiniques comprenant un colorant diazoique diazoique dicationique particulier |
-
2002
- 2002-07-05 FR FR0208494A patent/FR2841901B1/fr not_active Expired - Fee Related
-
2003
- 2003-07-04 JP JP2004518878A patent/JP2005532444A/ja active Pending
- 2003-07-04 WO PCT/FR2003/002090 patent/WO2004005407A2/fr not_active Ceased
- 2003-07-04 EP EP03291678A patent/EP1378544A3/fr not_active Withdrawn
- 2003-07-04 US US10/489,855 patent/US7311736B2/en not_active Expired - Fee Related
-
2007
- 2007-12-11 US US12/000,223 patent/US7399320B2/en not_active Expired - Fee Related
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