| Name | Dehydroepiandrosterone Enanthate |
|---|---|
| Synonyms | 3b-Hydroxyandrost-5-en-17-one heptanoate; CAS23983-43-9 enanthate 100% natural DHEA; 3beta-Heptanoyloxy-5-androsten-17-one; Dehydroepiandrosterone oenanthate; Dhea enanthate; Dhea oenanthate; Einecs 245-970-8; DHEA Enanthate (Prasterone Enanthate) |
| CAS NO | 23983-43-9 |
| EINECS | 245-970-8 |
| Mol File | 23983-43-9.mol |
| Molecular Weight | 400.59 |
| Categories | API;steroids |
| Molecular Formula | C26H40O3 |
| Dehydroepiandrosterone enanthate Chemical Properties | |
|---|---|
| Melting point | 69-70 °C |
| density | 1.06±0.1 g/cm3(Predicted) |
| Boiling point | 477.1±45.0 °C(Predicted) |
| Dehydroepiandrosterone enanthate Usage And Synthesis | |
|---|---|
| Originator | Prasterone,Schering |
| 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 | |
|---|---|
| Raw materials | Sodium hydroxide-->Dehydroepiandrosterone |
| Package method |
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