Chemistry:Testosterone butyrate
From HandWiki
Short description: Chemical compound
![]() | |
Clinical data | |
---|---|
Routes of administration | Intramuscular injection |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
Chemical and physical data | |
Formula | C23H34O3 |
Molar mass | 358.522 g·mol−1 |
3D model (JSmol) | |
| |
|
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]
Medication | Form | Major brand names | Duration |
---|---|---|---|
Testosterone | Aqueous suspension | Andronaq, Sterotate, Virosterone | 2–3 days |
Testosterone propionate | Oil solution | Androteston, Perandren, Testoviron | 3–4 days |
Testosterone phenylpropionate | Oil solution | Testolent | 8 days |
Testosterone isobutyrate | Aqueous suspension | Agovirin Depot, Perandren M | 14 days |
Mixed testosterone estersa | Oil solution | Triolandren | 10–20 days |
Mixed testosterone estersb | Oil solution | Testosid Depot | 14–20 days |
Testosterone enanthate | Oil solution | Delatestryl | 14–20 days |
Testosterone cypionate | Oil solution | Depovirin | 14–20 days |
Mixed testosterone estersc | Oil solution | Sustanon 250 | 28 days |
Testosterone undecanoate | Oil solution | Aveed, Nebido | 100 days |
Testosterone buciclated | Aqueous suspension | 20 Aet-1, CDB-1781e | 90–120 days |
Nandrolone phenylpropionate | Oil solution | Durabolin | 10 days |
Nandrolone decanoate | Oil solution | Deca Durabolin | 21 days |
Methandriol | Aqueous suspension | Notandron, Protandren | 8 days |
Methandriol bisenanthoyl acetate | Oil solution | Notandron Depot | 16 days |
Metenolone acetate | Oil solution | Primobolan | 3 days |
Metenolone enanthate | Oil solution | Primobolan Depot | 14 days |
Note: All are via i.m. injection. Footnotes: a = TP, TV, and TUe. b = TP and TKL. c = TP, TPP, TiCa, and TD. d = Studied but never marketed. e = Developmental code names. Sources: See template. |
See also
References
- ↑ Handbook of Aqueous Solubility Data (Second ed.). CRC Press. 19 April 2016. pp. 1288–. ISBN 978-1-4398-0246-5. https://books.google.com/books?id=cfFzJFthLCIC&pg=PA1288.
- ↑ 2.0 2.1 Androgens: biochemistry, physiology, and clinical significance. Wiley. 1956. p. 119. https://archive.org/details/in.ernet.dli.2015.548094.
- ↑ "Recent advances in the field of androgens.". Cold Spring Harbor Symposia on Quantitative Biology (Cold Spring Harbor Laboratory Press) 5: 34–43. January 1937. doi:10.1101/SQB.1937.005.01.004.
- ↑ "Crystallographic data for some testosterone esters". Acta Crystallographica 19 (1): 149–150. 1965. doi:10.1107/S0365110X65002918. ISSN 0365-110X. Bibcode: 1965AcCry..19..149G.
![]() | Original source: https://en.wikipedia.org/wiki/Testosterone butyrate.
Read more |