SU367123A1 - - Google Patents

Info

Publication number

SU367123A1

SU367123A1 SU1608732A SU1608732A SU367123A1 SU 367123 A1 SU367123 A1 SU 367123A1 SU 1608732 A SU1608732 A SU 1608732A SU 1608732 A SU1608732 A SU 1608732A SU 367123 A1 SU367123 A1 SU 367123A1

Authority

SU

USSR - Soviet Union

Prior art keywords

dyes

pyridine

residue

heterocyclic

triethylamine

Prior art date

1971-01-07

Links

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• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
• 239000000975 dye Substances 0.000 description 6
• 238000000034 method Methods 0.000 description 6
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
• 125000000623 heterocyclic group Chemical group 0.000 description 4
• -1 2-benzthiazolyl Chemical group 0.000 description 2
• XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 2
• 238000010438 heat treatment Methods 0.000 description 2
• 239000000203 mixture Substances 0.000 description 2
• 238000002360 preparation method Methods 0.000 description 2
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
• QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
• 229910019142 PO4 Inorganic materials 0.000 description 1
• 102000007620 Pulmonary Surfactant-Associated Protein C Human genes 0.000 description 1
• 108010007125 Pulmonary Surfactant-Associated Protein C Proteins 0.000 description 1
• 230000002378 acidificating effect Effects 0.000 description 1
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
• 238000006243 chemical reaction Methods 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
• 239000000839 emulsion Substances 0.000 description 1
• 238000005755 formation reaction Methods 0.000 description 1
• 125000000524 functional group Chemical group 0.000 description 1
• 125000001183 hydrocarbyl group Chemical group 0.000 description 1
• 230000003993 interaction Effects 0.000 description 1
• 230000003287 optical effect Effects 0.000 description 1
• VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
• VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
• NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
• 239000010452 phosphate Substances 0.000 description 1
• 150000004714 phosphonium salts Chemical class 0.000 description 1
• 239000002244 precipitate Substances 0.000 description 1
• 150000003839 salts Chemical group 0.000 description 1
• 239000004332 silver Substances 0.000 description 1
• 229910052709 silver Inorganic materials 0.000 description 1
• BAZAXWOYCMUHIX-UHFFFAOYSA-M sodium perchlorate Chemical compound [Na+].[O-]Cl(=O)(=O)=O BAZAXWOYCMUHIX-UHFFFAOYSA-M 0.000 description 1
• 229910001488 sodium perchlorate Inorganic materials 0.000 description 1
• 150000003510 tertiary aliphatic amines Chemical class 0.000 description 1
• 150000003512 tertiary amines Chemical class 0.000 description 1
• CMSYDJVRTHCWFP-UHFFFAOYSA-N triphenylphosphane;hydrobromide Chemical compound Br.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 CMSYDJVRTHCWFP-UHFFFAOYSA-N 0.000 description 1
• 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1