JP2006045226A5 - - Google Patents
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- JP2006045226A5 JP2006045226A5 JP2005213262A JP2005213262A JP2006045226A5 JP 2006045226 A5 JP2006045226 A5 JP 2006045226A5 JP 2005213262 A JP2005213262 A JP 2005213262A JP 2005213262 A JP2005213262 A JP 2005213262A JP 2006045226 A5 JP2006045226 A5 JP 2006045226A5
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- JP
- Japan
- Prior art keywords
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- linear
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- same
- 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.)
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- 125000003277 amino group Chemical group 0.000 claims 38
- 150000001875 compounds Chemical class 0.000 claims 33
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 32
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 21
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 16
- 125000000623 heterocyclic group Chemical group 0.000 claims 15
- 125000005842 heteroatom Chemical group 0.000 claims 12
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims 11
- 229910052757 nitrogen Chemical group 0.000 claims 11
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 11
- 125000003118 aryl group Chemical group 0.000 claims 10
- 229920006395 saturated elastomer Polymers 0.000 claims 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- 239000001301 oxygen Substances 0.000 claims 7
- 150000003839 salts Chemical class 0.000 claims 7
- 125000002947 alkylene group Chemical group 0.000 claims 6
- 125000002091 cationic group Chemical group 0.000 claims 6
- 238000004043 dyeing Methods 0.000 claims 6
- 125000005843 halogen group Chemical group 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 5
- 239000000835 fiber Substances 0.000 claims 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 229910052801 chlorine Inorganic materials 0.000 claims 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims 4
- 125000004122 cyclic group Chemical group 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 125000001153 fluoro group Chemical group F* 0.000 claims 4
- 150000002500 ions Chemical class 0.000 claims 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
- 239000004215 Carbon black (E152) Substances 0.000 claims 3
- 102000011782 Keratins Human genes 0.000 claims 3
- 108010076876 Keratins Proteins 0.000 claims 3
- 125000005210 alkyl ammonium group Chemical group 0.000 claims 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims 3
- 229930195733 hydrocarbon Natural products 0.000 claims 3
- 150000002430 hydrocarbons Chemical class 0.000 claims 3
- 239000000203 mixture Substances 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 125000004430 oxygen atom Chemical group O* 0.000 claims 3
- FQUYSHZXSKYCSY-UHFFFAOYSA-N 1,4-diazepane Chemical compound C1CNCCNC1 FQUYSHZXSKYCSY-UHFFFAOYSA-N 0.000 claims 2
- RAXXELZNTBOGNW-UHFFFAOYSA-O Imidazolium Chemical compound C1=C[NH+]=CN1 RAXXELZNTBOGNW-UHFFFAOYSA-O 0.000 claims 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 claims 2
- 150000004985 diamines Chemical class 0.000 claims 2
- QPMLSUSACCOBDK-UHFFFAOYSA-N diazepane Chemical compound C1CCNNCC1 QPMLSUSACCOBDK-UHFFFAOYSA-N 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 239000002904 solvent Substances 0.000 claims 2
- 239000011877 solvent mixture Substances 0.000 claims 2
- BJBUEDPLEOHJGE-UHFFFAOYSA-N (2R,3S)-3-Hydroxy-2-pyrolidinecarboxylic acid Natural products OC1CCNC1C(O)=O BJBUEDPLEOHJGE-UHFFFAOYSA-N 0.000 claims 1
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 claims 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
- FXHRAKUEZPSMLJ-UHFFFAOYSA-N 1-methyl-1,4-diazepane Chemical compound CN1CCCNCC1 FXHRAKUEZPSMLJ-UHFFFAOYSA-N 0.000 claims 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical group C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 1
- IXKNVDAHLCFGCV-UHFFFAOYSA-N 2-(1,4-diazepan-1-yl)ethanol Chemical compound OCCN1CCCNCC1 IXKNVDAHLCFGCV-UHFFFAOYSA-N 0.000 claims 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 238000007126 N-alkylation reaction Methods 0.000 claims 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N Nitrogen dioxide Chemical class O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims 1
- ONIBWKKTOPOVIA-UHFFFAOYSA-N Proline Natural products OC(=O)C1CCCN1 ONIBWKKTOPOVIA-UHFFFAOYSA-N 0.000 claims 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 claims 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 150000001412 amines Chemical group 0.000 claims 1
- -1 amino, hydroxyl Chemical group 0.000 claims 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- AAOVKJBEBIDNHE-UHFFFAOYSA-N diazepam Chemical compound N=1CC(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 AAOVKJBEBIDNHE-UHFFFAOYSA-N 0.000 claims 1
- 238000006193 diazotization reaction Methods 0.000 claims 1
- 239000000982 direct dye Substances 0.000 claims 1
- PMMYEEVYMWASQN-UHFFFAOYSA-N dl-hydroxyproline Natural products OC1C[NH2+]C(C([O-])=O)C1 PMMYEEVYMWASQN-UHFFFAOYSA-N 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 150000004820 halides Chemical class 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- AVAWMINJNRAQFS-UHFFFAOYSA-N n,n-dimethylpyrrolidin-3-amine Chemical compound CN(C)C1CCNC1 AVAWMINJNRAQFS-UHFFFAOYSA-N 0.000 claims 1
- LKPFBGKZCCBZDK-UHFFFAOYSA-N n-hydroxypiperidine Chemical compound ON1CCCCC1 LKPFBGKZCCBZDK-UHFFFAOYSA-N 0.000 claims 1
- HDCCJUCOIKLZNM-UHFFFAOYSA-N n-pyrrolidin-3-ylacetamide Chemical compound CC(=O)NC1CCNC1 HDCCJUCOIKLZNM-UHFFFAOYSA-N 0.000 claims 1
- NTNHDTQXUCWRCJ-UHFFFAOYSA-N n-pyrrolidin-3-ylmethanesulfonamide Chemical compound CS(=O)(=O)NC1CCNC1 NTNHDTQXUCWRCJ-UHFFFAOYSA-N 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
- 150000004885 piperazines Chemical class 0.000 claims 1
- 239000002243 precursor Substances 0.000 claims 1
- 125000001500 prolyl group Chemical group [H]N1C([H])(C(=O)[*])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- NGXSWUFDCSEIOO-UHFFFAOYSA-N pyrrolidin-3-amine Chemical class NC1CCNC1 NGXSWUFDCSEIOO-UHFFFAOYSA-N 0.000 claims 1
- JHHZLHWJQPUNKB-UHFFFAOYSA-N pyrrolidin-3-ol Chemical class OC1CCNC1 JHHZLHWJQPUNKB-UHFFFAOYSA-N 0.000 claims 1
- 150000003235 pyrrolidines Chemical class 0.000 claims 1
- 238000005956 quaternization reaction Methods 0.000 claims 1
- 239000002453 shampoo Substances 0.000 claims 1
- BJBUEDPLEOHJGE-IMJSIDKUSA-N trans-3-hydroxy-L-proline Chemical compound O[C@H]1CC[NH2+][C@@H]1C([O-])=O BJBUEDPLEOHJGE-IMJSIDKUSA-N 0.000 claims 1
- 150000003918 triazines Chemical class 0.000 claims 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0408186A FR2873369B1 (fr) | 2004-07-23 | 2004-07-23 | Monomeres ou dimeres symetriques azoiques cationiques, leur preparation, compositions les comprenant et procede de coloration de fibres keratiniques |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006045226A JP2006045226A (ja) | 2006-02-16 |
| JP2006045226A5 true JP2006045226A5 (https=) | 2008-09-04 |
Family
ID=34948740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2005213262A Withdrawn JP2006045226A (ja) | 2004-07-23 | 2005-07-22 | カチオン性アゾモノマーまたは対称性ダイマー、これらの調製、これを含む組成物 |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP1647550A1 (https=) |
| JP (1) | JP2006045226A (https=) |
| KR (1) | KR100793658B1 (https=) |
| CN (1) | CN1733741A (https=) |
| BR (1) | BRPI0502989A (https=) |
| FR (1) | FR2873369B1 (https=) |
| MX (1) | MXPA05007773A (https=) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009090125A1 (en) | 2008-01-17 | 2009-07-23 | Basf Se | Polymeric hair dyes |
| US20150299468A1 (en) * | 2014-04-22 | 2015-10-22 | Milliken & Company | Organic Colorant Complexes from Reactive Dyes and Articles Containing the Same |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1533642A (fr) | 1966-08-05 | 1968-07-19 | Hysol Corp | Nouvelles compositions conductrices résineuses |
| FR1533643A (fr) * | 1966-08-05 | 1968-07-19 | Durand & Huguenin Ag | Colorants monoazoïques, cationiques, hydrosolubles, leur procédé de préparation et leurs applications |
| FR2096377A1 (en) * | 1970-01-08 | 1972-02-18 | Helene Curtis France | Hair dye - for shampoo - colouring contg a cationic dye and a betainic surfactant |
| DE4320447A1 (de) * | 1993-06-21 | 1994-12-22 | Hoechst Ag | Wasserlösliche faserreaktive Azofarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE4404341A1 (de) * | 1994-02-11 | 1995-08-17 | Hoechst Ag | Wasserlösliche Azoverbindungen, Verfahren zu deren Herstellung und ihre Verwendung als Farbstoffe |
| FR2788432B1 (fr) * | 1999-01-19 | 2003-04-04 | Oreal | Utilisation pour la teinture directe des fibres keratiniques d'une association de deux colorants cationiques |
-
2004
- 2004-07-23 FR FR0408186A patent/FR2873369B1/fr not_active Expired - Fee Related
-
2005
- 2005-07-13 EP EP05291520A patent/EP1647550A1/fr not_active Withdrawn
- 2005-07-21 MX MXPA05007773A patent/MXPA05007773A/es unknown
- 2005-07-22 BR BRPI0502989-9A patent/BRPI0502989A/pt not_active IP Right Cessation
- 2005-07-22 JP JP2005213262A patent/JP2006045226A/ja not_active Withdrawn
- 2005-07-22 KR KR1020050066838A patent/KR100793658B1/ko not_active Expired - Fee Related
- 2005-07-22 CN CNA2005100980636A patent/CN1733741A/zh active Pending
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