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| Androstenediol Basic information |
| Product Name: | Androstenediol | | Synonyms: | 5-ANDROSTEN-3-BETA, 17-BETA-DIOL;5-ANDROSTENEDIOL;5-ANDROSTENEDIOL, 10,13-DIMETHYL-2,3,4,7,8,9,11,12,14,15,16,17-DODECAHYDRO-1H-CYCLOPENTA[A]PHENANTHRENE-3,17-DIOL;5-androstene-3b,17b-diol;5-ANDROSTENE-3BETA,17BETA-DIOL;ANDROSTENDIOL;ANDROSTENEDIOL, 5-;ANDROSTENEDIOL | | CAS: | 521-17-5 | | MF: | C19H30O2 | | MW: | 290.44 | | EINECS: | 208-306-8 | | Product Categories: | API;Steroids | | Mol File: | 521-17-5.mol |
| Androstenediol Chemical Properties |
| Melting point | 178-182°C | | alpha | -52.2 º (c=0.4,2-propanol) | | Boiling point | 428.4±38.0 °C(Predicted) | | density | 1.12±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 15.01±0.70(Predicted) | | CAS DataBase Reference | 521-17-5(CAS DataBase Reference) |
| Androstenediol Usage And Synthesis |
| Chemical Properties | WHITE CRYSTALLINE POWDER | | Uses | Androstenediol is used for weight training and recovery, and to increase testosterone production and stamina. | | Definition | ChEBI: A 3beta-hydroxy steroid that is 3beta-hydroxyandrost-5-ene carrying an additional hydroxy group at position 17beta. | | Enzyme inhibitor | This sterol (FW = 290.45 g/mol), also referred to simply as androstenediol, is a metabolite of dehydroepiandrosterone (prasterone) isolated independently in the laboratories of Butenandt and Ruzicka, who were awarded the Nobel Prize in Chemistry in 1939. Target(s): glucose-6- phosphate dehydrogenase; steroid 16a-monooxygenase; 17b hydroxysteroid dehydrogenase, also alternative substrate; 17- ketosteroid reductase; estrone sulfotransferase. |
| Androstenediol Preparation Products And Raw materials |
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