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What is the 1,8-Dihydroxyanthraquinone ?
1,8-Dihydroxyanthraquinone is orange-brown or brown powder, while it's Molecular Formula is C14H8O4. 1,8-Dihydroxyanthraquinone can be used:To prepare an inclusion complex with β-cyclodextrin, applicable as a sensor in the estimation of Cu2+?ions in an aqueous solution.As a starting material in the synthesis of 1,4,5,8-tetramethoxyanthracene.As an aromatic scavenger in the modification of lignin, which acts as a corrosion inhibitor for steel.
What is the CAS number for 1,8-Dihydroxyanthraquinone ?
The CAS number of 1,8-Dihydroxyanthraquinone is 117-10-2.
More information of 1,8-Dihydroxyanthraquinone 117-10-2 are:
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Synonyms |
Anthraquinone,1,8-dihydroxy- (8CI);1,8-Dihydroxy-9,10-anthracenedione;1,8-Dihydroxy-9,10-anthraquinone;1,8-Dioxyanthraquinone;Antrapurol;Chrysazin;Danthron;Danthrone;Diaquone;Laxanorm;Laxanthreen; |
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CAS?Number |
117-10-2 |
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Molecular Formula |
C14H8O4 |
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Molecular Weight |
240.215 |
|
Density |
1.541 g/cm3 |
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Melting Point |
191-193 °C |
|
Boiling Point |
452.667 °C at 760 mmHg |
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Flash Point |
241.691 °C |
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HS CODE |
2914.69 |
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PSA |
74.60000 |
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LogP |
1.87320 |
|
Pka |
6.27±0.20(Predicted) |
What is 1,8-Dihydroxyanthraquinone (117-10-2) used for?
Danthron, a natural product, was originally extracted from the roots and rhizome of Polygonaceae plant, also called Da Huang in traditional Chinese herbal medicine. Now it is synthesized in many countries, such as Germany, India, Japan, Poland, the United Kingdom, and the United States. Danthron is reasonably anticipated to be a human carcinogen. Danthron is an anthraquinone that exists at room temperature as a red or orange crystalline powder.It is practically insoluble in water, but soluble in a variety of solvents (acetone, chloroform, diethyl ether, ethanol) and alkaline hydroxide solutions. The stability of danthron is generally good. It is stable under room temperatures and normal pressures.
InChI:InChI=1/C14H8O4/c15-9-5-1-3-7-11(9)14(18)12-8(13(7)17)4-2-6-10(12)16/h1-6,15-16H
Articles related to 1,8-Dihydroxyanthraquinone:
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Article |
Source |
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Oxygenation of Dithranol by complexes of transition elements |
Mueller, Klaus,Duchstein, Hans-Juergen , p. 35 - 38 (1989) |
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REGIOSPECIFIC SYNTHESIS OF QUINIZARIN DERIVATIVES BY CYCLOADDITION |
Cameron, Donald W.,Feutrill, Geoffrey I.,McKay, Peter G. , p. 701 - 702 (1981) |
How to get the best price on 1,8-Dihydroxyanthraquinone?
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