1,3-Dihydroxyanthraquinone | |
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1,3-dihydroxyanthracene-9,10-dione |
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Other names
Purpuroxanthin; Xanthopurpurin |
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Identifiers | |
CAS number | 518-83-2 |
PubChem | 196978 |
ChemSpider | 170598 |
ChEBI | CHEBI:37502 |
ChEMBL | CHEMBL372711 |
Jmol-3D images | Image 1 |
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Properties | |
Molecular formula | C14H8O4 |
Molar mass | 240.21 g/mol |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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Infobox references |
1,3-Dihydroxyanthraquinone, also called purpuroxanthin or xanthopurpurin is an organic compound with formula C14H8O4 that occurs in the plant Rubia cordifolia (Indian madder).[1] It is one of ten dihydroxyanthraquinone isomers. Its molecular structure can be viewed as being derived from anthraquinone by replacement of two hydrogen atoms (H) by hydroxyl groups (-OH).
Xanthopurpurin occurs in small amounts (as a glycoside) in the root of the common madder plant, Rubia tinctorum, together with alizarin, purpurin and other anthraquinone derivatives.[2]
Xanthopurpurin is insoluble in hexane but soluble in chloroform. It can be obtained from solutions in the latter as reddish crystals that melt at 270–273 °C.[1]
Like many dihydroxy- and trihydroxyanthraquinones, it has a purgative action, although only 1/6 as effective as 1,2,7-trihidroxyanthraquinone (anthrapurpurin).[3]