Androst-5-ene-3,17-diol, (3β,17α)-, 2TMS derivative

• Formula: C₂₅H₄₆O₂Si₂
• Molecular weight: 434.8025
• IUPAC Standard InChI: InChI=1S/C25H46O2Si2/c1-24-15-13-19(26-28(3,4)5)17-18(24)9-10-20-21-11-12-23(27-29(6,7)8)25(21,2)16-14-22(20)24/h9,19-23H,10-17H2,1-8H3/t19-,20-,21-,22-,23+,24-,25-/m1/s1 Copy

  
• IUPAC Standard InChIKey: YXSPGYZGGCSNLG-UYJXDEQJSA-N Copy
• CAS Registry Number: 13111-27-8
• 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-5-ene-3β,17β-diol, 2TMS derivative
  • Androst-5-en-3β,17α-diol, TMS
  • Androst-5-en-3β,17β-diol, TMS
  • 5-Androsten-3-α,17-β-diol, TMS
  • 5-Androsten-3,17-diol, TMS
  • Androstenediol (Androst-5-en-3B,17B-diol), TMS
• Other names: 3β,17α-Bis(trimethylsiloxy)androst-5-ene; Silane, [[(3β,17α)-androst-5-ene-3,17-diyl]bis(oxy)]bis[trimethyl-; Silane, (androst-5-en-3β,17α-ylenedioxy)bis[trimethyl-; Bis(trimethylsilyl) derivative of 5-Androstene-3β,17α-diol; 3,17-Bis[(trimethylsilyl)oxy]androst-5-ene, (3β,17α)-; 5-Androsten-3-β,17-α-diol, bis-TMS; Androst-5-en-3β,17α-diol, di-TMS; Androst-5-en-3B,17A-diol, TMS; 5-Androsten-3-β,17-α-diol, TMS; Epitestosterone precursor (Androst-5-en-3B,17A-diol), TMS
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• Information on this page:
  • Kovats' RI, non-polar column, isothermal
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Kovats' RI, non-polar column, isothermal

Go To: Top, References, Notes

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

References

Go To: Top, Kovats' RI, non-polar column, isothermal, Notes

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

Smith, Joannou, et al., 1978
Smith, A.G.; Joannou, G.E.; Mák, M.; Uwajima, T.; Terada, O.; Brooks, C.J.W., Oxidation of 3β-hydroxyandrostenes by the 3β-hydroxysteroid oxidase (cholesterol oxidase) from Brevibacterium sterolicum prior to their analysis by gas-liquid chromatography-mass spectrometry, J. Chromatogr., 1978, 152, 2, 467-474, https://doi.org/10.1016/S0021-9673(00)85083-9 . [all data]

Berthou, Picart, et al., 1976
Berthou, F.; Picart, D.; Bardou, L.; Floch, H.H., Separation of C₁₉ and C₂₁ dihydroxysteroids by open-hole tubular glass columns and lipophilic gel chromatography, J. Chromatogr., 1976, 118, 2, 135-155, https://doi.org/10.1016/S0021-9673(00)81203-0 . [all data]

Notes

Go To: Top, Kovats' RI, non-polar column, isothermal, References

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