JP2006527744A5 - - Google Patents
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- Publication number
- JP2006527744A5 JP2006527744A5 JP2006516303A JP2006516303A JP2006527744A5 JP 2006527744 A5 JP2006527744 A5 JP 2006527744A5 JP 2006516303 A JP2006516303 A JP 2006516303A JP 2006516303 A JP2006516303 A JP 2006516303A JP 2006527744 A5 JP2006527744 A5 JP 2006527744A5
- Authority
- JP
- Japan
- Prior art keywords
- dye
- composition according
- optionally substituted
- group
- cationic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 claims 19
- 125000002091 cationic group Chemical group 0.000 claims 6
- 125000005647 linker group Chemical group 0.000 claims 5
- 102000011782 Keratins Human genes 0.000 claims 3
- 108010076876 Keratins Proteins 0.000 claims 3
- 238000010521 absorption reaction Methods 0.000 claims 3
- 238000004043 dyeing Methods 0.000 claims 3
- 239000000835 fiber Substances 0.000 claims 3
- 125000005842 heteroatoms Chemical group 0.000 claims 3
- 239000007800 oxidant agent Substances 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004429 atoms Chemical group 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 230000000875 corresponding Effects 0.000 claims 2
- 150000002430 hydrocarbons Chemical class 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 230000001590 oxidative Effects 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 1
- DZBUGLKDJFMEHC-UHFFFAOYSA-N Acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 claims 1
- RZVHIXYEVGDQDX-UHFFFAOYSA-N Anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 claims 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M CHEMBL593252 Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims 1
- 229940097275 Indigo Drugs 0.000 claims 1
- 240000007871 Indigofera tinctoria Species 0.000 claims 1
- 235000000177 Indigofera tinctoria Nutrition 0.000 claims 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N Phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims 1
- 229950000688 Phenothiazine Drugs 0.000 claims 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N Xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 150000001450 anions Chemical class 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims 1
- 125000004432 carbon atoms Chemical group C* 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 150000007857 hydrazones Chemical class 0.000 claims 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 claims 1
- 239000002453 shampoo Substances 0.000 claims 1
- GRYBZNLNHVSHPY-UHFFFAOYSA-N sodium;4-hydroxy-5-[(6-oxocyclohexa-2,4-dien-1-ylidene)methylamino]naphthalene-2,7-disulfonic acid Chemical compound [Na+].C=12C(O)=CC(S(O)(=O)=O)=CC2=CC(S(O)(=O)=O)=CC=1NC=C1C=CC=CC1=O GRYBZNLNHVSHPY-UHFFFAOYSA-N 0.000 claims 1
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 125000005649 substituted arylene group Chemical group 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- MHSKRLJMQQNJNC-UHFFFAOYSA-N terephthalamide Chemical group NC(=O)C1=CC=C(C(N)=O)C=C1 MHSKRLJMQQNJNC-UHFFFAOYSA-N 0.000 claims 1
- 0 CN(C)C=CN(C)*N=Nc(cc1)ccc1Nc1nc(NCCOC)nc(Nc(cc2)ccc2Nc(cc2)ccc2N=NC2=[N+]CCN2C)n1 Chemical compound CN(C)C=CN(C)*N=Nc(cc1)ccc1Nc1nc(NCCOC)nc(Nc(cc2)ccc2Nc(cc2)ccc2N=NC2=[N+]CCN2C)n1 0.000 description 1
- CCYLOTMMRSLCAL-HRGRZTPGSA-O C[C@H](C1)/C(/NC(C=C2)=CCC2/N=N/c2[n+](C)cc[n]2C)=C/CC/C(/Nc(cc2)ccc2NC2C=CC(/N=N/c3[n+2]cc[n]3C)=CC2)=N\C1N(CCO)CCO Chemical compound C[C@H](C1)/C(/NC(C=C2)=CCC2/N=N/c2[n+](C)cc[n]2C)=C/CC/C(/Nc(cc2)ccc2NC2C=CC(/N=N/c3[n+2]cc[n]3C)=CC2)=N\C1N(CCO)CCO CCYLOTMMRSLCAL-HRGRZTPGSA-O 0.000 description 1
- UZRAMPDQILKSGI-UHFFFAOYSA-P C[n]1c(/N=N/c(cc2)ccc2Nc(cc2)ccc2Nc2nc(Nc(cc3)ccc3/N=N/c3[n+](C)cc[n]3C)nc(NCCC[n]3cncc3)n2)[nH+]cc1 Chemical compound C[n]1c(/N=N/c(cc2)ccc2Nc(cc2)ccc2Nc2nc(Nc(cc3)ccc3/N=N/c3[n+](C)cc[n]3C)nc(NCCC[n]3cncc3)n2)[nH+]cc1 UZRAMPDQILKSGI-UHFFFAOYSA-P 0.000 description 1
- VUTPQCLYLXXRAM-UHFFFAOYSA-P C[n]1c(NNc(cc2)ccc2Nc(cc2)ccc2Nc2nc(NC(C=C3)=CCC3/N=N/c3[n+](C)cc[n]3C)nc(NCCCCCCO)n2)[nH+]cc1 Chemical compound C[n]1c(NNc(cc2)ccc2Nc(cc2)ccc2Nc2nc(NC(C=C3)=CCC3/N=N/c3[n+](C)cc[n]3C)nc(NCCCCCCO)n2)[nH+]cc1 VUTPQCLYLXXRAM-UHFFFAOYSA-P 0.000 description 1
Claims (19)
に対応する、請求項1から8のいずれか一項に記載の組成物。 The mixed dye has the following formula:
Corresponding to composition according to any one of claims 1 to 8.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0307186A FR2855967B1 (en) | 2003-06-16 | 2003-06-16 | LIGHTENING TINCTORIAL COMPOSITION COMPRISING AT LEAST ONE MIXED CHROMOPHORES CATIONIC DIRECT DYE |
FR03/07186 | 2003-06-16 | ||
PCT/FR2004/001517 WO2004112738A1 (en) | 2003-06-16 | 2004-06-16 | Tinctorial brightener composition containing at least one directly cationic colorant having mixed chromophores |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2006527744A JP2006527744A (en) | 2006-12-07 |
JP2006527744A5 true JP2006527744A5 (en) | 2007-08-02 |
JP4728230B2 JP4728230B2 (en) | 2011-07-20 |
Family
ID=33484445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2006516303A Expired - Fee Related JP4728230B2 (en) | 2003-06-16 | 2004-06-16 | Brightening dyeing composition comprising at least one cationic direct dye having a mixed chromophore |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP1648402A1 (en) |
JP (1) | JP4728230B2 (en) |
KR (1) | KR20060021898A (en) |
CN (1) | CN1835730B (en) |
BR (1) | BRPI0411495A (en) |
FR (1) | FR2855967B1 (en) |
MX (1) | MXPA05013749A (en) |
WO (1) | WO2004112738A1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2895904B1 (en) * | 2006-01-12 | 2008-02-29 | Oreal | USE FOR COLORING WITH THE LIGHTENING EFFECT OF KERATINIC MATERIALS OF A COMPOSITION COMPRISING A CYANINE-LIKE FLUORESCENT DYE |
JP2008105976A (en) * | 2006-10-24 | 2008-05-08 | Shinichiro Isobe | Cosmetic composition |
CN107635537A (en) * | 2015-03-19 | 2018-01-26 | 诺赛尔股份有限公司 | For the composition dyed using cation direct dye to hair |
CN107635538A (en) * | 2015-03-19 | 2018-01-26 | 诺赛尔股份有限公司 | Use the method for direct dyes compound dyed hair |
US9849072B2 (en) | 2015-03-19 | 2017-12-26 | Noxell Corporation | Method of coloring hair with direct dye compounds |
CN107750154A (en) * | 2015-03-19 | 2018-03-02 | 诺赛尔股份有限公司 | For the composition dyed using cation direct dye to hair |
US10034823B2 (en) | 2016-09-16 | 2018-07-31 | Noxell Corporation | Method of coloring hair with washfast blue imidazolium direct dye compounds |
US9918919B1 (en) | 2016-09-16 | 2018-03-20 | Noxell Corporation | Method of coloring hair with washfast yellow imidazolium direct dye compounds |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2215944T3 (en) * | 1994-11-03 | 2004-10-16 | Ciba Specialty Chemicals Holding Inc. | CATIONIC IMIDAZOLAZOIC COLORS. |
FR2773991B1 (en) * | 1998-01-26 | 2000-05-26 | Oreal | USE AS A PROTECTIVE AGENT FOR KERATINIC FIBERS OF HETEROCYCLIC QUATERNARY POLYAMMONIUM POLYMERS AND COSMETIC COMPOSITIONS |
JP2002080332A (en) * | 2000-03-17 | 2002-03-19 | Kao Corp | Hair dye composition |
JP2001261535A (en) * | 2000-03-17 | 2001-09-26 | Kao Corp | Hair dyeing agent composition |
EP1133975B1 (en) * | 2000-03-17 | 2008-02-13 | Kao Corporation | Use of a compound for dyeing hair |
BR0114585A (en) * | 2000-10-12 | 2003-08-26 | Ciba Sc Holding Ag | Cationic Imidazole Azo-Dyes |
FR2822697B1 (en) * | 2001-04-02 | 2003-07-25 | Oreal | NEW DYE COMPOSITION FOR DYEING KERATIN FIBERS COMPRISING A PARTICULAR CATIONIC AZO DYE |
FR2822693B1 (en) * | 2001-04-02 | 2003-06-27 | Oreal | NOVEL TINCTORIAL COMPOSITION FOR DYEING KERATINIC FIBERS COMPRISING A PARTICULAR CATIONIC AZO DYE |
FR2822698B1 (en) * | 2001-04-03 | 2006-04-21 | Oreal | NEW DYE COMPOSITION FOR DYEING KERATIN FIBERS COMPRISING A DICATIONIC MONOAZO DYE |
FR2825625B1 (en) * | 2001-06-12 | 2005-06-17 | Oreal | USE OF DICATIONIC COMPOUNDS IN DYEING OF HUMAN KERATIN FIBERS AND COMPOSITIONS CONTAINING SAME |
EP1404762B1 (en) * | 2001-07-11 | 2009-11-25 | Basf Se | A method of coloring hair using cationic dyes |
-
2003
- 2003-06-16 FR FR0307186A patent/FR2855967B1/en not_active Expired - Fee Related
-
2004
- 2004-06-16 BR BRPI0411495-7A patent/BRPI0411495A/en not_active Application Discontinuation
- 2004-06-16 WO PCT/FR2004/001517 patent/WO2004112738A1/en active Application Filing
- 2004-06-16 KR KR1020057024229A patent/KR20060021898A/en not_active Application Discontinuation
- 2004-06-16 MX MXPA05013749A patent/MXPA05013749A/en active IP Right Grant
- 2004-06-16 JP JP2006516303A patent/JP4728230B2/en not_active Expired - Fee Related
- 2004-06-16 EP EP04767378A patent/EP1648402A1/en not_active Withdrawn
- 2004-06-16 CN CN2004800235158A patent/CN1835730B/en not_active Expired - Fee Related
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