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Testosterone butyrate

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Testosterone butyrate
Clinical data
Routes of
administration		Intramuscular injection
Identifiers
  • [(8R,9S,10R,13S,14S,17S)-10,13-Dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] butanoate
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
ECHA InfoCard100.020.270 Edit this at Wikidata
Chemical and physical data
FormulaC23H34O3
Molar mass358.522 g/mol g·mol−1
3D model (JSmol)
  • CCCC(=O)O[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)C
  • InChI=1S/C23H34O3/c1-4-5-21(25)26-20-9-8-18-17-7-6-15-14-16(24)10-12-22(15,2)19(17)11-13-23(18,20)3/h14,17-20H,4-13H2,1-3H3/t17-,18-,19-,20-,22-,23-/m0/s1
  • Key:OMPTUWYLCDEFSJ-WAUHAFJUSA-N

Testosterone butyrate, or testosterone butanoate, also known as androst-4-en-17β-ol-3-one 17β-butanoate, is a synthetic, steroidal androgen and an androgen ester – specifically, the C17β butanoate ester of testosterone – which was first synthesized in the 1930s and was never marketed.[1][2][3][4] Its ester side-chain length and duration of effect are intermediate between those of testosterone propionate and testosterone valerate.[2]

See also

References

  1. ^ Samuel H. Yalkowsky; Yan He; Parijat Jain (19 April 2016). Handbook of Aqueous Solubility Data, Second Edition. CRC Press. pp. 1288–. ISBN 978-1-4398-0246-5.
  2. ^ a b Ralph Isadore Dorfman; Reginald A. Shipley (1956). Androgens: biochemistry, physiology, and clinical significance. Wiley. p. 119.
  3. ^ Koch, F. C. (1937). "RECENT ADVANCES IN THE FIELD OF ANDROGENS". Cold Spring Harbor Symposia on Quantitative Biology. 5 (0): 34–43. doi:10.1101/SQB.1937.005.01.004. ISSN 0091-7451.
  4. ^ Griffiths, P. J. F.; James, K. C.; Rees, M. (1965). "Crystallographic data for some testosterone esters". Acta Crystallographica. 19 (1): 149–150. doi:10.1107/S0365110X65002918. ISSN 0365-110X.


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