17-β-Methyl-5-α-androstan-3-β,17-α-diol

• Formula: C₂₀H₃₄O₂
• Molecular weight: 306.4828
• IUPAC Standard InChI: InChI=1S/C20H34O2/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/h13-17,21-22H,4-12H2,1-3H3/t13-,14-,15?,16?,17?,18?,19?,20+/m1/s1 Copy

  
• IUPAC Standard InChIKey: QGKQXZFZOIQFBI-PJCKWDJUSA-N Copy
• Chemical structure:
  This structure is also available as a 2d Mol file
• Stereoisomers:
  • Androstane-3,17-diol, 17-methyl-, (3α,5α,17β)-
  • 17-α-Methyl-5-β-androstan-3-β,17-β-diol
  • 17-β-Methyl-5-β-androstan-3-α,17-α-diol
  • 17-β-Methyl-5-β-androstan-3-β,17-α-diol
  • 5A-Androstan-3B,17B-diol, 17A-methyl
  • 17-α-Methyl-5-α-androstan-3-β,17-β-diol
  • 17-α-Methyl-5-β-androstan-3-α,17-β-diol
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• Information on this page:
  • Gas Chromatography
  • References
  • Notes
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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

Normal alkane RI, non-polar column, temperature ramp

View large format table.

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.

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]

Notes

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