17α-Methyltestosterone

• Formula: C₂₀H₃₀O₂
• Molecular weight: 302.4510
• IUPAC Standard InChI: InChI=1S/C20H30O2/c1-18-9-6-14(21)12-13(18)4-5-15-16(18)7-10-19(2)17(15)8-11-20(19,3)22/h12,15-17,22H,4-11H2,1-3H3/t15?,16?,17?,18?,19?,20-/m1/s1 Copy

  
• IUPAC Standard InChIKey: GCKMFJBGXUYNAG-NSDIEPNESA-N Copy
• CAS Registry Number: 58-18-4
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • Androsten-17-(beta)-ol-3-one, 17(alpha)-methyl-delta^4-
  • 17-epi-Methyltestosterone
• Other names: Testosterone, 17-methyl-; Methyltestosterone; 17-Methyltestosterone; Androst-4-en-3-one, 17-hydroxy-17-methyl-, (17β)-; Androst-4-en-3-one, 17β-hydroxy-17-methyl-; Andrometh; Androsan; Androsten; Anertan; Anertan, tablets; Dumogran; Glosso-Sterandryl; Homandren; Hormale; M.T.Mucorettes; Malestrone; Malogen; Masenone; Mastestona; Mesterone; Metandren; Metrone; Neo-Hombreol-M; Nu-man; Oreton Methyl; Oreton-M; Steronyl; Synandrets; Synandrotabs; Testhormone; Testora; Testoviron; 17α-Methyl-3-oxo-4-androsten-17β-ol; 17-Methyltestosteron; Metestone; Nabolin; Neo-Homobreol (M); Oraviron; Syndren; Testred; 4-Androstene-17α-methyl-17β-ol-3-one; 17-β-Hydroxy-17-methylandrost-4-en-3-one; NSC-9701; 17β-Hydroxy-17α-methylandrost-4-en-3-one; Android; Orchisterone-M; Perandren; 17α-methyl-Δ4-androsten-17β-ol-3-one; Androst-4-en-3-on-17β-ol, 17α-methyl; 17-Hydroxy-17-methyl-3-keto-androstene-4; Androst-4-ene-17α-methyl-17β-ol-3-one; CDB 110; RU 24400; U 2842; Testovis Depot; Androst-4-en-3-on-17B-ol, 17A-methyl; 17(Alpha)-methyl-delta^4-androsten-17-(beta)-ol-3-one
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• Information on this page:
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
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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

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

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Normal alkane RI, non-polar column, temperature ramp

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

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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.

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]

Schänzer, Opfermann, et al., 1992
Schänzer, W.; Opfermann, G.; Donike, M., 17-Epimerization of 17α-methyl anabolic steroids in humans: metabolism and synthesis of 17α-hydroxy-17β-methyl steroids, Steroids, 1992, 57, 11, 537-550, https://doi.org/10.1016/0039-128X(92)90023-3 . [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

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