BE455830A - - Google Patents

Info

Publication number

BE455830A

BE455830A BE455830DA BE455830A BE 455830 A BE455830 A BE 455830A BE 455830D A BE455830D A BE 455830DA BE 455830 A BE455830 A BE 455830A

Authority

BE

Belgium

Prior art keywords

dyes

acid

good

molecule

amino

Prior art date

Links

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• 239000000975 dye Substances 0.000 description 23
• 239000002253 acid Substances 0.000 description 11
• 230000007935 neutral effect Effects 0.000 description 6
• 238000009736 wetting Methods 0.000 description 6
• 239000000987 azo dye Substances 0.000 description 5
• 150000001875 compounds Chemical class 0.000 description 3
• 150000008049 diazo compounds Chemical class 0.000 description 3
• 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
• 125000001424 substituent group Chemical group 0.000 description 3
• KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
• QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
• 150000007513 acids Chemical class 0.000 description 2
• 239000003086 colorant Substances 0.000 description 2
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 2
• -1 diazole compound Chemical class 0.000 description 2
• 239000000835 fiber Substances 0.000 description 2
• 238000004519 manufacturing process Methods 0.000 description 2
• VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
• 238000000034 method Methods 0.000 description 2
• 230000003381 solubilizing effect Effects 0.000 description 2
• AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 2
• 238000005406 washing Methods 0.000 description 2
• NUMXHEUHHRTBQT-AATRIKPKSA-N 2,4-dimethoxy-1-[(e)-2-nitroethenyl]benzene Chemical compound COC1=CC=C(\C=C\[N+]([O-])=O)C(OC)=C1 NUMXHEUHHRTBQT-AATRIKPKSA-N 0.000 description 1
• WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 description 1
• 241000219498 Alnus glutinosa Species 0.000 description 1
• LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
• OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
• 102000006463 Talin Human genes 0.000 description 1
• 108010083809 Talin Proteins 0.000 description 1
• 230000002378 acidificating effect Effects 0.000 description 1
• 150000001412 amines Chemical class 0.000 description 1
• 125000003277 amino group Chemical group 0.000 description 1
• 229960004909 aminosalicylic acid Drugs 0.000 description 1
• 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
• 150000004982 aromatic amines Chemical group 0.000 description 1
• 239000011324 bead Substances 0.000 description 1
• 239000002775 capsule Substances 0.000 description 1
• 229910052799 carbon Inorganic materials 0.000 description 1
• 230000000295 complement effect Effects 0.000 description 1
• 230000005494 condensation Effects 0.000 description 1
• 238000009833 condensation Methods 0.000 description 1
• 230000027326 copulation Effects 0.000 description 1
• 230000008878 coupling Effects 0.000 description 1
• 238000010168 coupling process Methods 0.000 description 1
• 238000005859 coupling reaction Methods 0.000 description 1
• 238000006193 diazotization reaction Methods 0.000 description 1
• 238000004043 dyeing Methods 0.000 description 1
• 229910052736 halogen Inorganic materials 0.000 description 1
• 150000002367 halogens Chemical class 0.000 description 1
• AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
• 229910017464 nitrogen compound Inorganic materials 0.000 description 1
• 150000002830 nitrogen compounds Chemical class 0.000 description 1
• ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
• 150000002989 phenols Chemical class 0.000 description 1
• 238000003825 pressing Methods 0.000 description 1
• 239000001044 red dye Substances 0.000 description 1
• 150000003839 salts Chemical class 0.000 description 1
• APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
• 238000006277 sulfonation reaction Methods 0.000 description 1
• 150000004961 triphenylmethanes Chemical class 0.000 description 1
• 239000001043 yellow dye Substances 0.000 description 1