Testosterone

• Formula: C₁₉H₂₈O₂
• Molecular weight: 288.4244
• IUPAC Standard InChI: InChI=1S/C19H28O2/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/h11,14-17,21H,3-10H2,1-2H3/t14?,15?,16?,17-,18?,19?/m1/s1 Copy

  
• IUPAC Standard InChIKey: MUMGGOZAMZWBJJ-JZJKZLICSA-N Copy
• CAS Registry Number: 58-22-0
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • Androst-4-en-3-one, 17-hydroxy-, (17α)-
• Other names: Androst-4-en-3-one, 17-hydroxy-, (17β)-; Δ4-Androsten-17β-ol-3-one; Androlin; Andronaq; Andrusol; Cristerona T; Geno-cristaux Gremy; Homosteron; Homosterone; Mertestate; Neotestis; Orquisteron; Perandren; Percutacrine androgenique; Primotest; Primoteston; Sustanon; Sustanone; Teslen; Testandrone; Testiculosterone; Testobase; Testopropon; Testosteroid; Testosteron; Testoviron Schering; Testoviron T; Testrone; Testryl; Virormone; Virosterone; 4-Androsten-17β-ol-3-one; trans-Testosterone; Androst-4-en-17β-ol-3-one; Androst-4-en-3-one, 17β-hydroxy-; Malerone; Malogen, aquaspension injection; Neo-Hombreol F; Oreton; Oreton F; Synandrol F; Testoviron; 17β-Hydroxy-Δ4-androsten-3-one; 17β-Hydroxy-4-androsten-3-one; 17β-Hydroxyandrost-4-en-3-one; 17-Hydroxy-(17β)-androst-4-en-3-one; Cristerone T; Andro 100; Testoderm; Testolin; Testro AQ; 17-Hydroxyandrost-4-en-3-one, (17β)-; 4-Androsten-3-one, 17b-hydroxy-; 17Beta-hydroxyandrost-4-en-3-one; Androst-4-en-3-on-17b-ol; 17β-Testosterone; 4-Androsten-3-one-17β-ol; AndroGel; COL 1621; Intrinsa; Relibra; Striant; Testogel; Testim; component of Di-Genik (Salt/Mix); component of Di-Met (Salt/Mix); component of Duogen (Salt/Mix); component of Mal-O-Fem (Salt/Mix); component of Intrinsa (Salt/Mix); component of Tostrex (Salt/Mix)
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• Information on this page:
  • Phase change data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • IR Spectrum
  • UV/Visible spectrum
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• NIST / TRC Web Thermo Tables, professional edition (thermophysical and thermochemical data)

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Phase change data

Go To: Top, Mass spectrum (electron ionization), Gas Chromatography, References, Notes

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

Data compiled as indicated in comments:
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Enthalpy of fusion

Mass spectrum (electron ionization)

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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

Spectrum

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Additional Data

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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Normal alkane RI, non-polar column, custom temperature program

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References

Go To: Top, Phase change data, Mass spectrum (electron ionization), Gas Chromatography, Notes

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

Grady, Hays, et al., 1973
Grady, L.T.; Hays, S.E.; King, R.H.; Klein, H.R.; Mader, W.J.; Wyatt, D.K.; Zimmere, R.O., Drug purity profiles, J. Pharm. Sci., 1973, 62, 459. [all data]

Wassvik, Holmén, et al., 2006
Wassvik, Carola M.; Holmén, Anders G.; Bergström, Christel A.S.; Zamora, Ismael; Artursson, Per, Contribution of solid-state properties to the aqueous solubility of drugs, European Journal of Pharmaceutical Sciences, 2006, 29, 3-4, 294-305, https://doi.org/10.1016/j.ejps.2006.05.013 . [all data]

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]

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]

Perrigo and Peel, 1981
Perrigo, B.J.; Peel, H.W., The use of retention indices and temperature-programmed gas chromatography in analytical toxicology, J. Chromatogr. Sci., 1981, 19, 5, 219-226, https://doi.org/10.1093/chromsci/19.5.219 . [all data]

Ardrey and Moffat, 1981
Ardrey, R.E.; Moffat, A.C., Gas-liquid chromatographic retention indices of 1318 substances of toxicological interest on SE-30 or OV-1 stationary phase, J. Chromatogr., 1981, 220, 3, 195-252, https://doi.org/10.1016/S0021-9673(00)81925-1 . [all data]

Notes

Go To: Top, Phase change data, Mass spectrum (electron ionization), Gas Chromatography, References

• Symbols used in this document:
  

  Tfus	Fusion (melting) point
  ΔfusH	Enthalpy of fusion

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