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(24S)-24-ETHYLCHOLEST-5-EN-3-BETA-OL
SpectraBase Compound ID IGx47gjnNPC
InChI InChI=1S/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,19-21,23-27,30H,7-9,11-18H2,1-6H3/t20-,21+,23+,24+,25-,26+,27+,28+,29-/m1/s1
InChIKey KZJWDPNRJALLNS-FBZNIEFRSA-N
Mol Weight 414.7 g/mol
Molecular Formula C29H50O
Exact Mass 414.386166 g/mol
Enantiomer InChIKey KZJWDPNRJALLNS-USLLMGQYSA-N
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum SFA-99-6979-gamma-sitosterol (DOI: 10.1002/jsfa.9986)
Copyright Copyright © 2011-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum Prof. D. Henneberg, MPI f. Kohlenforschung, Muelheim a.d.R., Germany
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum PA-18-295-11
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum PA-28-443-443_34
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SFA-99-6979-.gamma.-sitosterol
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • beta-Sitosterol
  • Sitosterol
  • Stigmasterol
  • Gamma-sitosterol
  • STIGMAST-5-EN-3-OL, (3beta,24S)-
  • STIGMAST-5-EN-3-OL
  • (1S,2R,5S,10S,11S,14R,15R)-14-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltetracyclo[8.7.0.0(2,7).0(11,15)]heptadec-7-en-5-ol
Title Journal or Book Year
Chemical Constituents of Caesalpinia decapetala (Roth) Alston Molecules 2013
A new dihydroxysterol from the marine phytoplankton Diacronema sp. Fitoterapia 2005
The Constituents ofLindera Glauca Journal of the Chinese Chemical Society 2000
New Sterols and Triterpenoids of Ficus pumila Fruit. Chemical and Pharmaceutical Bulletin 1998
Carbon-13 nmr studies on sitosterol biosynthesized from [13C]mevalonates Phytochemistry 1992
24β-Ethylcholest-4-en-3β-ol from the roots of Lawsonia inermis Phytochemistry 1992
Stigmasterols from Typha latifolia Journal of Natural Products 1990
Sterol glucosides from Prunella vulgaris Phytochemistry 1990
13C nuclear magnetic resonance spectra of some C-19-hydroxy, C-5,6 epoxy, C-24 ethyl, and C-19-norsteroids Canadian Journal of Chemistry 1978
Identification of C-24 alkyl epimers of marine sterols by 13C nuclear magnetic resonance spectroscopy Canadian Journal of Chemistry 1978

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