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|Section2= |Section3= }} 1,3-Dihydroxyanthraquinone, also called purpuroxanthin or xanthopurpurin, is an organic compound with formula that occurs in the plant ''Rubia cordifolia'' (Indian madder).〔 Padma S. Vankar, Rakhi Shanker, Debajit Mahanta and S.C. Tiwari (2008), ''Ecofriendly sonicator dyeing of cotton with ''Rubia cordifolia'' Linn. using biomordant''. Dyes and Pigments, Volume 76, Issue 1, Pages 207-212. 〕 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.〔 Goverdina C. H. Derksen, Harm A. G. Niederländer and Teris A. van Beek (2002), ''Analysis of anthraquinones in ''Rubia tinctorum'' L. by liquid chromatography coupled with diode-array UV and mass spectrometric detection''. Journal of Chromatography A, Volume 978, Issues 1-2, Pages 119-127, 〕 ==Properties== 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.〔 Like many dihydroxy- and trihydroxyanthraquinones, it has a purgative action, although only 1/6 as effective as 1,2,7-trihidroxyanthraquinone (anthrapurpurin).〔 Hugh Alister McGuigan (1921), ''An introduction to chemical pharmacology; pharmacodynamics in relation to chemistry''. P. Blakiston's son, Philadelphia. (Online version ) at archive.org, accessed on 2010-01-30. 〕 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「1,3-Dihydroxyanthraquinone」の詳細全文を読む スポンサード リンク
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