VERFAHREN ZUR HERSTELLUNG VON 4,5-DINITRO-1,8-DIHYDROXYANTHRACHINON
95-99% pure 4,5-dinitro-1,8-dihydroxyanthraquinone which is essentially free from by-products is obtained by "direct nitration" of 1,8-dihydroxyanthraquinones or 1,8-dimethoxyanthraquinones if the concentrations of acid are chosen such that, when the nitration reaction and, if appropriate,...
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creator | GEHRKE,GUENTER,DR STEINBECK,WERNER,DR |
description | 95-99% pure 4,5-dinitro-1,8-dihydroxyanthraquinone which is essentially free from by-products is obtained by "direct nitration" of 1,8-dihydroxyanthraquinones or 1,8-dimethoxyanthraquinones if the concentrations of acid are chosen such that, when the nitration reaction and, if appropriate, the saponification reaction have ended, an 80-100% strength sulphuric acid is present, or such a sulphuric acid concentration is established by adding water, and the 4,5-dinitro-1,8-dihydroxyanthraquinone which crystallizes out is separated off. |
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STEINBECK,WERNER,DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE2909481A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1980</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>GEHRKE,GUENTER,DR</creatorcontrib><creatorcontrib>STEINBECK,WERNER,DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>GEHRKE,GUENTER,DR</au><au>STEINBECK,WERNER,DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>VERFAHREN ZUR HERSTELLUNG VON 4,5-DINITRO-1,8-DIHYDROXYANTHRACHINON</title><date>1980-09-11</date><risdate>1980</risdate><abstract>95-99% pure 4,5-dinitro-1,8-dihydroxyanthraquinone which is essentially free from by-products is obtained by "direct nitration" of 1,8-dihydroxyanthraquinones or 1,8-dimethoxyanthraquinones if the concentrations of acid are chosen such that, when the nitration reaction and, if appropriate, the saponification reaction have ended, an 80-100% strength sulphuric acid is present, or such a sulphuric acid concentration is established by adding water, and the 4,5-dinitro-1,8-dihydroxyanthraquinone which crystallizes out is separated off.</abstract><edition>3</edition><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | VERFAHREN ZUR HERSTELLUNG VON 4,5-DINITRO-1,8-DIHYDROXYANTHRACHINON |
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