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Testosterone formate

Clinical data
Other names	Testosterone carboxylate; Testosterone methanoate
Identifiers
IUPAC name phenanthren-17-yl] formate
CAS Number	3129-42-8
PubChem CID	151084
ChemSpider	133166
CompTox Dashboard (EPA)	DTXSID80953328
Chemical and physical data
Formula	C20H28O3
Molar mass	316.441 g·mol
3D model (JSmol)	Interactive image
SMILES C12CC3(1CC2OC=O)CCC4=CC(=O)CC34C
InChI InChI=1S/C20H28O3/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/h11-12,15-18H,3-10H2,1-2H3/t15-,16-,17-,18-,19-,20-/m0/s1 Key:LMUMOFOWZKACOU-RABCQHRBSA-N

Testosterone formate, also known as testosterone carboxylate or testosterone methanoate, as well as androst-4-en-17β-ol-3-one 17β-formate, is a synthetic, steroidal androgen and an androgen ester – specifically, the C17β formate ester of testosterone – which was first synthesized in the 1930s and was never marketed.

See also

• List of androgen esters § Testosterone esters

References

1. Yalkowsky SH, He Y, Jain P (19 April 2016). Handbook of Aqueous Solubility Data, Second Edition. CRC Press. pp. 1233–. ISBN 978-1-4398-0246-5.
2. Blickenstaff RT (2 December 2012). Antitumor Steroids. Academic Press. pp. 76–. ISBN 978-0-323-13916-8.
3. Josephy E, Radt F (1 December 2013). Elsevier's Encyclopaedia of Organic Chemistry: Series III: Carboisocyclic Condensed Compounds. Springer. pp. 3019–. ISBN 978-3-662-25863-7.
4. Koch FC (1937). "Recent Advances in the Field of Androgens". Cold Spring Harbor Symposia on Quantitative Biology. 5: 34–43. doi:10.1101/SQB.1937.005.01.004. ISSN 0091-7451.

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