1,2,4-Trihydroxyanthraquinone

changed changed 477202730 correct ?? Purpurin powder crop.jpg 1,2,4-trihydroxyanthracene-9,10-dione 200.svg Skeletal formula Purpurin-3D-balls.png Ball-and-stick model 1,2,4-Trihydroxyanthracene-9,10-dione Purpurin, Purpurine, Hydroxylizaric acid correct chemspider correct EBI 8645 6431 correct kegg C10395 1/C14H8O5/c15-8-5-9(16)14(19)11-10(8)12(17)6-3-1-2-4-7(6)13(11)18/h1-5,15-16,19H O=C2c1ccccc1C(=O)c3c2c(O)cc(O)c3O BBNQQADTFFCFGB-UHFFFAOYAW correct EBI 294264 correct chemspider 1S/C14H8O5/c15-8-5-9(16)14(19)11-10(8)12(17)6-3-1-2-4-7(6)13(11)18/h1-5,15-16,19H correct chemspider BBNQQADTFFCFGB-UHFFFAOYSA-N correct CAS 81-54-9 correct FDA L1GT81LS6N 6683 C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)O)O C14H8O5 256.21 g/mol 259 Haynes Haynes, William M. 2016 CRC Handbook of Chemistry and Physics 97th CRC Press 9781498754293 3.530 1,2,4-Trihydroxyanthraquinone, commonly called purpurin, is an anthraquinone. It is a naturally occurring red/yellow dye. It is formally derived from 9,10-anthraquinone by replacement of three hydrogen atoms by hydroxyl (OH) groups. Purpurin is also called verantin, smoke Brown G, hydroxylizaric acid, and C.I. 58205. It is a minor component of the classical lake pigment "madder lake" or Rose Madder. Purpurin is a strong inhibitor of CYP1A1, CYP1A2 and CYP1B1, as well as a weak inhibitor of CYP2A6 and CYP2E1.Eizo Takahashi, Ken-ichi Fujita, Tetsuya Kamataki, Sakae Arimoto-Kobayashi, Keinosuke Okamoto, Tomoe Negishi 31 October 2002 Inhibition of human cytochrome P450 1B1, 1A1 and 1A2 by antigenotoxic compounds, purpurin and alizarin Mutation Research 508 1-2 147-156 12379470 10.1016/s0027-5107(02)00212-9 History Madder root has been used for dying cloth at least since 1500 BC.Madder Root https://web.archive.org/web/20110714160122/http://naturalpigments.com/detail.asp?PRODUCT_ID=455-22B 2011-07-14 catalog entry at Natural Pigments website. Accessed on 2010-01-22. Purpurin and alizarin were isolated from the root by Pierre Robiquet and Colin, two French chemists, in 1826. They were identified as anthracene derivatives by Gräbe and Liebermann in 1868. They also synthesized alizarin from bromoanthraquinone, which, together with the conversion of alizarin into purpurin published previously by M. F. De Lalande, provided the first synthetic route to purpurin.Chemical news and journal of industrial science, Volume 30, Page 207 The positions of the OH groups were determined by Bayer and Caro in 1874–1875. Wahl, Andre; Atack, F. W (1919) The Manufacture Of Organic Dyestuffs. G. Bell And Sons, Limited. Online version accessed on 2010-01-22. Natural occurrence Purpurin occurs in the roots of the madder plant (Rubia tinctorum), together with alizarin (1,2-dihydroxyanthraquinone). The root actually contains colorless glycosides of the dyes. Properties Purpurin is a crystalline solid, that forms orange-red needles melting at 259 C. It becomes red when dissolved in ethanol, and yellow when dissolved with alkalis in boiling water. It is insoluble in hexane but soluble in chloroform, and can be obtained from chloroform as reddish needles. Vankar Padma S. Shanker Rakhi Mahanta Debajit Tiwari S.C. 2008 Ecofriendly sonicator dyeing of cotton with Rubia cordifolia Linn. using biomordant Dyes and Pigments 76 1 207–212 10.1016/j.dyepig.2006.08.023 Unlike alizarin, purpurin is dissolved by boiling in a solution of aluminium sulfate, from which it can be precipitated by acid. This procedure can be used to separate the two dyes.Irving Wetherbee Fay (1919) The chemistry of the coal-tar dyes. Van Nostrand Online version accessed on 2010-01-22. Like many dihydroxy- and trihydroxyanthraquinones, pupurin has a purgative action, although only 1/20 as effective as 1,2,7-trihydroxyanthraquinone (anthrapurpurin).Alister McGuigan, Hugh (1921) An introduction to chemical pharmacology; pharmacodynamics in relation to chemistry. P. Blakiston's son, Philadelphia. Uses Purpurin is a fast dye for cotton printing and forms complexes with various metal ions. It fades faster than alizarin on exposure to sunlight. A study published in Nature journal Scientific Reports suggests that the purpurin could replace cobalt in lithium-ion batteries.Reddy Arava Leela Mohana Nagarajan Subbiah Chumyim Porramate Gowda Sanketh R Pradhan Padmanava Jadhav Swapnil R Dubey Madan John George Ajayan Pulickel M Ajayan Pulickel M 2012 Lithium storage mechanisms in purpurin based organic lithium ion battery electrodes Scientific Reports 10.1038/srep00960 free 2 960 23233879 3518813 2012NatSR...2E.960R Eliminating cobalt would mean eliminating a hazardous material, allow batteries to be produced at room temperature, and lower the cost of recycling batteries. Extracting purpurin from farmed madder is a simple task; alternately, the chemical could be synthesized in a lab.Dying to make greener batteries Chirgwin, Richard 12 December 2012 The Register https://www.theregister.co.uk/2012/12/12/rose_madder_battery_matter/ 12 December 2012 See also Trihydroxyanthraquinone Pierre Robiquet, discoverer of purpurin in 1826 References 30em Category:Anthraquinone dyes Category:Hydroxyquinols Category:Trihydroxyanthraquinones Category:CYP1A1 inhibitors Category:CYP1A2 inhibitors Category:CYP1B1 inhibitors Category:CYP2A6 inhibitors Category:CYP2E1 inhibitors