DE115410C - - Google Patents

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Publication number

DE115410C

DE115410C DENDAT115410D DE115410DA DE115410C DE 115410 C DE115410 C DE 115410C DE NDAT115410 D DENDAT115410 D DE NDAT115410D DE 115410D A DE115410D A DE 115410DA DE 115410 C DE115410 C DE 115410C

Authority

DE

Germany

Prior art keywords

solution

yellow

aldehyde

water

disulfonic acid

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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• 239000000243 solution Substances 0.000 claims description 9
• 150000001299 aldehydes Chemical class 0.000 claims description 7
• NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 claims description 6
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
• UETHPMGVZHBAFB-OWOJBTEDSA-N 4,4'-dinitro-trans-stilbene-2,2'-disulfonic acid Chemical compound OS(=O)(=O)C1=CC([N+]([O-])=O)=CC=C1\C=C\C1=CC=C([N+]([O-])=O)C=C1S(O)(=O)=O UETHPMGVZHBAFB-OWOJBTEDSA-N 0.000 claims description 4
• 239000007800 oxidant agent Substances 0.000 claims description 4
• 230000003647 oxidation Effects 0.000 claims description 4
• 238000007254 oxidation reaction Methods 0.000 claims description 4
• KIHAMCBHCNQCST-UHFFFAOYSA-N 2-formyl-5-nitrobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC([N+]([O-])=O)=CC=C1C=O KIHAMCBHCNQCST-UHFFFAOYSA-N 0.000 claims description 3
• 239000002253 acid Substances 0.000 claims description 3
• OIAFPQXUDHGCPU-UHFFFAOYSA-N 3-(1,2-dinitroso-2-phenylethenyl)benzene-1,2-disulfonic acid Chemical compound N(=O)C(=C(C1=C(C(=CC=C1)S(=O)(=O)O)S(=O)(=O)O)N=O)C1=CC=CC=C1 OIAFPQXUDHGCPU-UHFFFAOYSA-N 0.000 claims description 2
• 238000000034 method Methods 0.000 claims description 2
• 238000003756 stirring Methods 0.000 claims 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 claims description 2
• WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims 4
• 238000006243 chemical reaction Methods 0.000 claims 2
• JGJLWPGRMCADHB-UHFFFAOYSA-N hypobromite Chemical compound Br[O-] JGJLWPGRMCADHB-UHFFFAOYSA-N 0.000 claims 2
• 239000000843 powder Substances 0.000 claims 2
• 238000002360 preparation method Methods 0.000 claims 2
• ACDNGCLBDNWSSF-UHFFFAOYSA-N 2-methyl-5-nitrobenzenesulfonic acid;sodium Chemical compound [Na].CC1=CC=C([N+]([O-])=O)C=C1S(O)(=O)=O ACDNGCLBDNWSSF-UHFFFAOYSA-N 0.000 claims 1
• VWLGQKLHWIVCCZ-UHFFFAOYSA-N 53992-33-9 Chemical compound OS(=O)(=O)CC1=CC=C([N+]([O-])=O)C=C1 VWLGQKLHWIVCCZ-UHFFFAOYSA-N 0.000 claims 1
• 229910019093 NaOCl Inorganic materials 0.000 claims 1
• 239000003929 acidic solution Substances 0.000 claims 1
• 150000007513 acids Chemical class 0.000 claims 1
• -1 aldehyde sulfonic acids Chemical class 0.000 claims 1
• 239000012670 alkaline solution Substances 0.000 claims 1
• HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical class O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims 1
• 230000015572 biosynthetic process Effects 0.000 claims 1
• 238000004040 coloring Methods 0.000 claims 1
• 239000000706 filtrate Substances 0.000 claims 1
• KQPBSBAEBKRAAU-UHFFFAOYSA-N hypochlorous acid;sodium Chemical compound [Na].ClO KQPBSBAEBKRAAU-UHFFFAOYSA-N 0.000 claims 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 claims 1
• 230000003472 neutralizing effect Effects 0.000 claims 1
• 239000012286 potassium permanganate Substances 0.000 claims 1
• 239000000047 product Substances 0.000 claims 1
• 238000005185 salting out Methods 0.000 claims 1
• SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims 1
• 239000007858 starting material Substances 0.000 claims 1
• PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 claims 1
• 239000001043 yellow dye Substances 0.000 claims 1
• LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
• 239000002244 precipitate Substances 0.000 description 3
• 239000007864 aqueous solution Substances 0.000 description 2
• 150000003934 aromatic aldehydes Chemical class 0.000 description 2
• KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
• AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
• CWLGEPSKQDNHIO-JOBJLJCHSA-N (e)-n-[(e)-benzylideneamino]-1-phenylmethanimine Chemical compound C=1C=CC=CC=1/C=N/N=C/C1=CC=CC=C1 CWLGEPSKQDNHIO-JOBJLJCHSA-N 0.000 description 1
• HKMFIGRKKRUXQB-UHFFFAOYSA-N OS(=O)(=O)C1=C(C=O)C=CC=C1[N+]([O-])=O Chemical compound OS(=O)(=O)C1=C(C=O)C=CC=C1[N+]([O-])=O HKMFIGRKKRUXQB-UHFFFAOYSA-N 0.000 description 1
• 241000219492 Quercus Species 0.000 description 1
• XHQYBDSXTDXSHY-UHFFFAOYSA-N Semicarbazide hydrochloride Chemical compound Cl.NNC(N)=O XHQYBDSXTDXSHY-UHFFFAOYSA-N 0.000 description 1
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
• VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
• OTIKYRVPXSEIPV-UHFFFAOYSA-N acetic acid;phenylhydrazine Chemical compound CC(O)=O.NNC1=CC=CC=C1 OTIKYRVPXSEIPV-UHFFFAOYSA-N 0.000 description 1
• BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
• 150000001735 carboxylic acids Chemical class 0.000 description 1
• 238000009833 condensation Methods 0.000 description 1
• 230000005494 condensation Effects 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 239000000975 dye Substances 0.000 description 1
• 238000001914 filtration Methods 0.000 description 1
• ZGCHATBSUIJLRL-UHFFFAOYSA-N hydrazine sulfate Chemical compound NN.OS(O)(=O)=O ZGCHATBSUIJLRL-UHFFFAOYSA-N 0.000 description 1
• 150000007857 hydrazones Chemical class 0.000 description 1
• QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical class ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
• 230000007935 neutral effect Effects 0.000 description 1
• 150000003336 secondary aromatic amines Chemical class 0.000 description 1
• DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 description 1
• 239000001632 sodium acetate Substances 0.000 description 1
• 235000017281 sodium acetate Nutrition 0.000 description 1
• 159000000000 sodium salts Chemical class 0.000 description 1
• 150000003513 tertiary aromatic amines Chemical class 0.000 description 1

Cited By (3)