Stanolone

• Formula: C₁₉H₃₀O₂
• Molecular weight: 290.4403
• IUPAC Standard InChI: InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12,14-17,21H,3-11H2,1-2H3/t12-,14?,15?,16?,17-,18?,19?/m1/s1 Copy

  
• IUPAC Standard InChIKey: NVKAWKQGWWIWPM-FLGGQZOGSA-N Copy
• CAS Registry Number: 521-18-6
• Chemical structure:
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• Other names: Androstan-3-one, 17-hydroxy-, (5α,17β)-; 5α-Androstan-3-one, 17β-hydroxy-; Anaboleen; Anabolex; Androlone; Cristerona MB; Neodrol; Proteina; Protona; Stanaprol; Stanorone; Testosterone, dihydro-; 17β-Hydroxy-3-androstanone; 4-Dihydrotestosterone; 4,5α-Dihydrotestosterone; 5α-Dihydrotestosterone; 5α,17β-Hydroxyandrostan-3-one; 5α-Androstan-17β-ol-3-one; 5-α-Androstanolone; Dihydrotestosterone; Andractim; Androstanolone; DHT; 17-β-Hydroxy-5-α-androstan-3-one; (5α,17β)-17-Hydroxy-androstan-3-one; 17beta-Hydroxy-5alpha-androstan-3-one; (+)-Androstan-17β-ol-3-one; Androstan-17β-ol-3-one; LG 152; NSC 10972; 17-Hydroxyandrostan-3-one, (5α,17β)-; 5B-Androstan-3-on-17B-ol; 5A-Androstan-3-on-17B-ol
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• Information on this page:
  • Phase change data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • 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: Eugene S. Domalski and Elizabeth D. Hearing

Enthalpy of phase transition

Gas Chromatography

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Kovats' RI, non-polar column, isothermal

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Van Den Dool and Kratz RI, non-polar column, temperature ramp

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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.

Masse, de Maury, et al., 1989
Masse, J.; de Maury, G.; Chauvet, A.; Terol, A., Thermoanalytical study of some steroids. V. Adrostanolone, Thermochim. Acta, 1989, 149, 1-14. [all data]

Quilliam and Westmore, 1978
Quilliam, M.A.; Westmore, J.B., Sterically crowded trialkylsilyl derivatives for chromatography and mass spectrometry of biologically-important compounds, Anal. Chem., 1978, 50, 1, 59-68, https://doi.org/10.1021/ac50023a020 . [all data]

Brooks, Thawley, et al., 1971
Brooks, C.J.W.; Thawley, A.R.; Rocher, P.; Middleditch, B.S.; Anthony, G.M.; Stillwell, W.G., Characterization of Steroidal Drug Metabolites by Combined Gas Chromatography-Mass Spectrometry, J. Chromatogr. Sci., 1971, 9, 1, 35-43, https://doi.org/10.1093/chromsci/9.1.35 . [all data]

Tretyakov, 2014
Tretyakov, K.V., Retention Data. NIST Mass Spectrometry Data Center., NIST Mass Spectrometry Data Center, 2014. [all data]

Notes

Go To: Top, Phase change data, Gas Chromatography, References

• Symbols used in this document:
  

  ΔHtrs

  Enthalpy of phase transition

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