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| | Dehydroepiandrosterone enanthate Basic information |
| Product Name: | Dehydroepiandrosterone enanthate | | Synonyms: | 3b-Hydroxyandrost-5-en-17-one heptanoate;3beta-Heptanoyloxy-5-androsten-17-one;Dehydroepiandrosterone oenanthate;Dhea enanthate;Dhea oenanthate;Einecs 245-970-8;DHEA Enanthate (Prasterone Enanthate);3β-hydroxyandrost-5-en-17-one heptanoate | | CAS: | 23983-43-9 | | MF: | C26H40O3 | | MW: | 400.59 | | EINECS: | 245-970-8 | | Product Categories: | API;steroids | | Mol File: | 23983-43-9.mol |  |
| | Dehydroepiandrosterone enanthate Chemical Properties |
| Melting point | 69-70 °C | | Boiling point | 497.9±45.0 °C(Predicted) | | density | 1.06±0.1 g/cm3(Predicted) |
| | Dehydroepiandrosterone enanthate Usage And Synthesis |
| Originator | Prasterone,Schering | | Uses | Prasterone Enanthate is used in preparation of DHEA enanthates for treating/improving adrenal hormonal balance, immune system function, adipose tissue reduction, skeletal muscle growth, bloating reduction, recovery from training, and increasing strength. | | Manufacturing Process | A mixture of 10.0 g of dehydro-epi-androsterone, 40 ml of pyridine and 20 ml
of oenanthic acid anhydride was warmed for 2 h on a steam bath. About 10
ml of water were added and the mixture was warmed for a further 30 min.
The reaction mixture was then subjected to a steam distillation. The resulting
mixture was extracted with ether and the extract was successively washed
with dilute sodium hydroxide solution, sodium carbonate solution and water.
The solution was dried over sodium sulfate and exaporated. 13.6 g of crude
dehydro-epiandrosterone-3-oenanthate were obtained, melting point 70°-72°C
(recrystallisation from methanol). | | Therapeutic Function | Glucocorticoid |
| | Dehydroepiandrosterone enanthate Preparation Products And Raw materials |
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