Testosterone propionate

• Formula: C₂₂H₃₂O₃
• Molecular weight: 344.4877
• IUPAC Standard InChI: InChI=1S/C22H32O3/c1-4-20(24)25-19-8-7-17-16-6-5-14-13-15(23)9-11-21(14,2)18(16)10-12-22(17,19)3/h13,16-19H,4-12H2,1-3H3/t16?,17?,18?,19-,21?,22?/m1/s1 Copy

  
• IUPAC Standard InChIKey: PDMMFKSKQVNJMI-AZBVOVPMSA-N Copy
• CAS Registry Number: 57-85-2
• Chemical structure:
  This structure is also available as a 2d Mol file
• Stereoisomers:
  • Epitestosterone, propionate
• Other names: Androst-4-en-3-one, 17-(1-oxopropoxy)-, (17β)-; Neo-hombreol; Agovirin; Androlon; Androtest P; Androteston; Anertan; Aquaviron; Bio-testiculina; Enarmon; Enarmon-oil; Homandren (amps); Hormoteston; Masenate; Nasdol; NSC 9166; Okasa-mascul; Orchiol; Orchistin; Oreton; Pantestin; Propiokan; Recthormone testosterone; Solvotest; Sterandryl; Synerone; Telipex; Testaform; Testex; Testodet; Testodrin; Testogen; Testolets; Testonique; Testormol; Testosid; Testosteron propionate; Testosterone-17β-propionate; Testosterone-17-propionate; Testoviron; Testoxyl; Testrex; Tostrin; TP; Uniteston; Androgen; Andronate; Androst-4-en-3-one, 17β-hydroxy-, propionate; Androsteston; Andrusol-P; Homandren; Oreton propionate; Synandrol; Vulvan; 17-(1-Oxopropoxy)androst-4-en-3-one, (17β)-; Orchisterone; Virormone; 3-Oxoandrost-4-en-17-yl propionate, (17β)-; Δ4-androstene-17β-propionate-3-one; 17β-hydroxyandrost-4-en-3-one, propionate; 17β-(Propionyloxy)androst-4-en-3-one; Primotestone; Delta^4-androstene-17beta-propionate-3-one; Androstene-17(beta)-propionate-3-one,delta^8-; 17Beta-hydroxyandrost-4-en-3-one, propionate
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• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • IR Spectrum
  • Mass spectrum (electron ionization)
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: William E. Acree, Jr., James S. Chickos

Enthalpy of fusion

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Regosz, Chmielewska, et al., 1994
Regosz, A.; Chmielewska, A.; Pelplinska, T.; Kowalski, P., Prediction of the solubility of steroid hormones, Pharmazie, 1994, 49, 5, 371. [all data]

Notes

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• Symbols used in this document:
  

  ΔfusH

  Enthalpy of fusion

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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