Corticosterone, bis-MO-bis-TMS, anti

• Formula: C₂₉H₅₂N₂O₄Si₂
• Molecular weight: 548.9052
• IUPAC Standard InChI: InChI=1S/C29H52N2O4Si2/c1-28-16-15-21(30-32-3)17-20(28)11-12-22-23-13-14-24(25(31-33-4)19-34-36(5,6)7)29(23,2)18-26(27(22)28)35-37(8,9)10/h17,22-24,26-27H,11-16,18-19H2,1-10H3/t22?,23?,24-,26?,27?,28+,29+/m0/s1 Copy

  
• IUPAC Standard InChIKey: FFEVUTYFVPQKAH-SSYBQPKYSA-N Copy
• Chemical structure:
  This structure is also available as a 2d Mol file
• Stereoisomers:
  • Pregn-4-ene-3,20-dione, 11,21-bis[(trimethylsilyl)oxy]-, bis(O-methyloxime), (11β)-
  • Corticosterone, MO-TMS
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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, custom temperature program

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.

Pereira, Marques, et al., 2001
Pereira, H.M.G.; Marques, M.A.S.; Cardoso, J.N.; Neto, F.R.A., Derivatization study of endogenous and synthetic corticosteroids by gas chromatography mass spectrometry in Recent Advances in Doping Analysis, Schanzer, W.; Geyer, H.; Gotzmann, A.; Mareck-Engelke, U., ed(s)., Sport und Buch Strauss, Koln, 2001, 203-207. [all data]

Notes

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