Dihydrotestosterone formate
Clinical data
Other namesAndrostanolone formate; Stanolone formate; 5α-Dihydrotestosterone 17β-formate; 17β‐(Formyloxy)‐5α‐androstane‐3‐one
Routes of
administration		Intramuscular injection
Identifiers
  • [(5S,8R,9S,10S,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl] formate
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC20H30O3
Molar mass318.457 g·mol−1
3D model (JSmol)
  • C[C@]12CCC(=O)C[C@@H]1CC[C@@H]3[C@@H]2CC[C@]4([C@H]3CC[C@@H]4OC=O)C
  • InChI=1S/C20H30O3/c1-19-9-7-14(22)11-13(19)3-4-15-16-5-6-18(23-12-21)20(16,2)10-8-17(15)19/h12-13,15-18H,3-11H2,1-2H3/t13-,15-,16-,17-,18-,19-,20-/m0/s1
  • Key:ZQSXNBHXKJQHBH-VHUDCFPWSA-N

Dihydrotestosterone formate, also known as androstanolone formate or stanolone formate, as well as 5α-dihydrotestosterone 17β-formate,[1] is a synthetic androgen and anabolic steroid and a dihydrotestosterone ester that was never marketed.[2][3]

See also

References

  1. ↑ Yalkowsky SH (26 March 2003). Handbook of Aqueous Solubility Data. CRC Press. pp. 1166–. ISBN 978-0-203-49039-6.
  2. ↑ Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 640–. ISBN 978-1-4757-2085-3.
  3. ↑ Morton IK, Hall JM (6 December 2012). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 261–. ISBN 978-94-011-4439-1.


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