BE430950A - - Google Patents

Info

Publication number

BE430950A

BE430950A BE430950DA BE430950A BE 430950 A BE430950 A BE 430950A BE 430950D A BE430950D A BE 430950DA BE 430950 A BE430950 A BE 430950A

Authority

BE

Belgium

Prior art keywords

dyes

dye

triarylmethane

groups

contain

Prior art date

Links

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• 239000000975 dye Substances 0.000 claims description 29
• 239000001003 triarylmethane dye Substances 0.000 claims description 3
• CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 2
• 230000002378 acidificating effect Effects 0.000 claims description 2
• 230000015572 biosynthetic process Effects 0.000 claims description 2
• 229910052799 carbon Inorganic materials 0.000 claims description 2
• 238000004519 manufacturing process Methods 0.000 claims description 2
• 230000003381 solubilizing effect Effects 0.000 claims description 2
• 238000006467 substitution reaction Methods 0.000 claims description 2
• 238000000034 method Methods 0.000 claims 2
• CZZZABOKJQXEBO-UHFFFAOYSA-N 2,4-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1 CZZZABOKJQXEBO-UHFFFAOYSA-N 0.000 claims 1
• 125000004432 carbon atom Chemical group C* 0.000 claims 1
• 239000001047 purple dye Substances 0.000 claims 1
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 10
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
• 210000002268 wool Anatomy 0.000 description 6
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
• FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
• 238000009835 boiling Methods 0.000 description 3
• IMPPGHMHELILKG-UHFFFAOYSA-N 4-ethoxyaniline Chemical compound CCOC1=CC=C(N)C=C1 IMPPGHMHELILKG-UHFFFAOYSA-N 0.000 description 2
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
• 238000001816 cooling Methods 0.000 description 2
• 239000013078 crystal Substances 0.000 description 2
• 239000011780 sodium chloride Substances 0.000 description 2
• 238000003756 stirring Methods 0.000 description 2
• CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 description 1
• IQGMRVWUTCYCST-UHFFFAOYSA-N 3-Aminosalicylic acid Chemical compound NC1=CC=CC(C(O)=O)=C1O IQGMRVWUTCYCST-UHFFFAOYSA-N 0.000 description 1
• MLPWLRUWQJVULT-UHFFFAOYSA-N 5-amino-2-hydroxy-3-sulfobenzoic acid Chemical compound NC1=CC(C(O)=O)=C(O)C(S(O)(=O)=O)=C1 MLPWLRUWQJVULT-UHFFFAOYSA-N 0.000 description 1
• 125000003545 alkoxy group Chemical group 0.000 description 1
• 150000001721 carbon Chemical group 0.000 description 1
• 238000006243 chemical reaction Methods 0.000 description 1
• 239000003086 colorant Substances 0.000 description 1
• 238000004043 dyeing Methods 0.000 description 1
• 229910052736 halogen Inorganic materials 0.000 description 1
• 150000002367 halogens Chemical group 0.000 description 1
• KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 description 1
• 229960004963 mesalazine Drugs 0.000 description 1
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
• 239000011541 reaction mixture Substances 0.000 description 1
• 150000003839 salts Chemical class 0.000 description 1
• 125000000542 sulfonic acid group Chemical group 0.000 description 1
• 239000010930 yellow gold Substances 0.000 description 1
• 229910001097 yellow gold Inorganic materials 0.000 description 1