| Identification | Back Directory | [Name]
Dehydroepiandrosterone enanthate | [CAS]
23983-43-9 | [Synonyms]
Dhea enanthate
Dhea oenanthate
Einecs 245-970-8
PRASTERONE ENANTHATE
enanthate 100% natural DHEA
Dehydroepiandrosterone enanthate
Dehydroepiandrosterone oenanthate
PRASTERONE ENANTHATE CAS 23983-43-9
Prasterone Enanthate(DHEA Enanthate)
3beta-Heptanoyloxy-5-androsten-17-one
DHEA Enanthate (Prasterone Enanthate)
5-ANDROSTEN-3-BETA-OL-17-ONE ENANTHATE
3β-hydroxyandrost-5-en-17-one heptanoate
3β-hydroxyandrost-5-en-17-one heptanoate
3b-Hydroxyandrost-5-en-17-one heptanoate
CAS23983-43-9 enanthate 100% natural DHEA
3beta-hydroxyandrost-5-en-17-one heptanoate
Androst-5-en-17-one, 3-[(1-oxoheptyl)oxy]-, (3β)-
Dehydroepiandrosterone enanthate
3b-Hydroxyandrost-5-en-17-one heptanoate
(3S,8R,9S,10R,13S,14S)-10,13-Dimethyl-17-oxo-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl heptanoate | [EINECS(EC#)]
245-970-8 | [Molecular Formula]
C26H40O3 | [MDL Number]
MFCD00271339 | [MOL File]
23983-43-9.mol | [Molecular Weight]
400.59 |
| Hazard Information | Back Directory | [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 |
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BioBioPha Co., Ltd.
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