DE238856C - - Google Patents

Info

Publication number

DE238856C

DE238856C DENDAT238856D DE238856DA DE238856C DE 238856 C DE238856 C DE 238856C DE NDAT238856 D DENDAT238856 D DE NDAT238856D DE 238856D A DE238856D A DE 238856DA DE 238856 C DE238856 C DE 238856C

Authority

DE

Germany

Prior art keywords

naphthylamine

acid

aminonaphthol

sulfonic acid

molecule

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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• 239000002253 acid Substances 0.000 claims description 9
• 239000000975 dye Substances 0.000 claims description 7
• 125000000217 alkyl group Chemical group 0.000 claims description 6
• 150000001875 compounds Chemical class 0.000 claims description 4
• JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 claims description 3
• 230000002378 acidificating effect Effects 0.000 claims description 3
• 230000007935 neutral effect Effects 0.000 claims description 3
• 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims 1
• 229920000742 Cotton Polymers 0.000 description 4
• 159000000000 sodium salts Chemical class 0.000 description 3
• 150000003460 sulfonic acids Chemical class 0.000 description 3
• HMNPDEGBVWDHAR-UHFFFAOYSA-N 8-aminonaphthalen-1-ol Chemical compound C1=CC(O)=C2C(N)=CC=CC2=C1 HMNPDEGBVWDHAR-UHFFFAOYSA-N 0.000 description 2
• 150000007513 acids Chemical class 0.000 description 2
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
• 239000000243 solution Substances 0.000 description 2
• -1 ß-naphthylamine sulfonic acids Chemical class 0.000 description 2
• ZYECOAILUNWEAL-NUDFZHEQSA-N (4z)-4-[[2-methoxy-5-(phenylcarbamoyl)phenyl]hydrazinylidene]-n-(3-nitrophenyl)-3-oxonaphthalene-2-carboxamide Chemical compound COC1=CC=C(C(=O)NC=2C=CC=CC=2)C=C1N\N=C(C1=CC=CC=C1C=1)/C(=O)C=1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 ZYECOAILUNWEAL-NUDFZHEQSA-N 0.000 description 1
• 241000947840 Alteromonadales Species 0.000 description 1
• LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
• 239000003929 acidic solution Substances 0.000 description 1
• 125000003277 amino group Chemical group 0.000 description 1
• 125000003118 aryl group Chemical group 0.000 description 1
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
• 239000003086 colorant Substances 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
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
• 230000000717 retained effect Effects 0.000 description 1
• 239000000126 substance Substances 0.000 description 1