DE237169C - - Google Patents

Info

Publication number

DE237169C

DE237169C DENDAT237169D DE237169DA DE237169C DE 237169 C DE237169 C DE 237169C DE NDAT237169 D DENDAT237169 D DE NDAT237169D DE 237169D A DE237169D A DE 237169DA DE 237169 C DE237169 C DE 237169C

Authority

DE

Germany

Prior art keywords

parts

molecule

aminoaryl

yellow

acid

Prior art date

1909-06-18

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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• 239000000975 dye Substances 0.000 claims description 12
• 239000002253 acid Substances 0.000 claims description 6
• 150000001875 compounds Chemical class 0.000 claims description 5
• 150000004985 diamines Chemical class 0.000 claims description 3
• LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
• HXSNCIZFPVKYPE-UHFFFAOYSA-N NC=1C(=C(C2=CC=CC=C2C1)O)NC(C1=CC=CC=C1)=O Chemical compound NC=1C(=C(C2=CC=CC=C2C1)O)NC(C1=CC=CC=C1)=O HXSNCIZFPVKYPE-UHFFFAOYSA-N 0.000 claims description 2
• 150000005840 aryl radicals Chemical class 0.000 claims description 2
• HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims description 2
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 2
• PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical class C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 claims description 2
• JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 12
• 239000000243 solution Substances 0.000 description 9
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
• LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 6
• 229920000742 Cotton Polymers 0.000 description 5
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
• 239000000835 fiber Substances 0.000 description 3
• -1 p-aminophenol ethylene ether Chemical class 0.000 description 3
• 235000010288 sodium nitrite Nutrition 0.000 description 3
• 230000015572 biosynthetic process Effects 0.000 description 2
• 238000009967 direct dyeing Methods 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• IDWXQRMUCRXFAK-UHFFFAOYSA-N (2-phenyldiazenylhydrazinyl)benzene Chemical compound C=1C=CC=CC=1N=NNNC1=CC=CC=C1 IDWXQRMUCRXFAK-UHFFFAOYSA-N 0.000 description 1
• DJGYNCWNFYWANE-UHFFFAOYSA-N (3-aminophenyl)-(3-aminophenyl)imino-oxidoazanium Chemical compound NC1=CC=CC(N=[N+]([O-])C=2C=C(N)C=CC=2)=C1 DJGYNCWNFYWANE-UHFFFAOYSA-N 0.000 description 1
• XTTIQGSLJBWVIV-UHFFFAOYSA-N 2-methyl-4-nitroaniline Chemical compound CC1=CC([N+]([O-])=O)=CC=C1N XTTIQGSLJBWVIV-UHFFFAOYSA-N 0.000 description 1
• ICNFHJVPAJKPHW-UHFFFAOYSA-N 4,4'-Thiodianiline Chemical compound C1=CC(N)=CC=C1SC1=CC=C(N)C=C1 ICNFHJVPAJKPHW-UHFFFAOYSA-N 0.000 description 1
• GUJMMWSXMKIWAW-UHFFFAOYSA-N 4-(3-aminophenyl)-5-methylpyrazol-3-one Chemical compound O=C1N=NC(C)=C1C1=CC=CC(N)=C1 GUJMMWSXMKIWAW-UHFFFAOYSA-N 0.000 description 1
• VZTRBZPWPARZGO-UHFFFAOYSA-N 4-(oxiran-2-yl)aniline Chemical compound NC1=CC=C(C2CO2)C=C1 VZTRBZPWPARZGO-UHFFFAOYSA-N 0.000 description 1
• HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-UHFFFAOYSA-N 0.000 description 1
• VVLIWTRLJBSXLR-UHFFFAOYSA-N N-(1,5-diaminocyclohexa-2,4-dien-1-yl)benzamide Chemical compound NC1(CC(=CC=C1)N)NC(C1=CC=CC=C1)=O VVLIWTRLJBSXLR-UHFFFAOYSA-N 0.000 description 1
• 206010039587 Scarlet Fever Diseases 0.000 description 1
• 239000012670 alkaline solution Substances 0.000 description 1
• 125000005001 aminoaryl group Chemical group 0.000 description 1
• 229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
• 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
• 238000001914 filtration Methods 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
• 238000005185 salting out Methods 0.000 description 1
• 150000003839 salts Chemical class 0.000 description 1
• 229910000029 sodium carbonate Inorganic materials 0.000 description 1
• 235000017550 sodium carbonate Nutrition 0.000 description 1
• 238000003756 stirring Methods 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• 239000001043 yellow dye Substances 0.000 description 1