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

• Formula: C₂₅H₄₈O₂Si₂
• Molecular weight: 436.8184
• IUPAC Standard InChI: InChI=1S/C25H48O2Si2/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/h18-23H,9-17H2,1-8H3/t18-,19+,20-,21-,22-,23-,24-,25-/m1/s1 Copy

  
• IUPAC Standard InChIKey: KBSHKNYEUGMMDQ-ZUHJIWNMSA-N Copy
• CAS Registry Number: 13111-26-7
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  View 3d structure (requires JavaScript / HTML 5)
• Stereoisomers:
  • Androstane-3,17-diol, (3α,5α,17α)-, 2TMS derivative
  • Androstane-3,17-diol, (3α,5α,17β)-, 2TMS derivative
  • Androstane-3,17-diol, (3β,5α,17β)-, 2TMS derivative
  • Androstane-3,17-diol, (3β,5β,17β)-, 2TMS derivative
  • 5-β-Androstan-3-β,17-α-diol, TMS
  • 5α-Androstan-3α,17β-diol, TMS
  • 5α-Androstane-3β,17β-diol,bis-TMS
  • 5β-Androstane-3α,17β-diol,bis-TMS
  • 5β-Androstane-3β,17β-diol,bis-TMS
  • 5A-Androstane-3B,17A-diol, TMS
• Other names: 3α,17β-Bis(trimethylsilyloxy)-5β-androstane; Silane, [[(3α,5β,17β)-androstane-3,17-diyl]bis(oxy)bis[-trimethyl-; Silane, (5β-androstan-3α,17β-ylenedioxy)bis[trimethyl-; 3,17-Bis[(trimethylsilyl)oxy]androstane, (3α,5β,17β)-; 5-β-Androstan-3-α,17-β-diol, bis-TMS; 5β-Androstanediol-3α,17β, bis-TMS; 5beta-Androstan-3alpha,17beta-diol, bis-TMS; 5-β-Androstan-3-α,17-β-diol, TMS; 5B-Androstane-3A,17B-diol, TMS; 5.beta.-Androstane-3.alpha.,17.beta.-diol, bis(trimethylsilyl) ether; Androstanediol (5A-Androstan-3A,17B-diol), TMS; 5B-Androstan-3A,17B-diol, bis-TMS
• Permanent link for this species. Use this link for bookmarking this species for future reference.
• Information on this page:
  • Kovats' RI, non-polar column, isothermal
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Options:
  • Switch to calorie-based units

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.

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]

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]

Notes

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

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
• The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
• Customer support for NIST Standard Reference Data products.