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5-Cholesten-24α-methyl-3β-ol (30% 24β)

Compound with spectra: 1 NMR, 2 FTIR, 1 Raman, and 2 MS (GC)

5-Cholesten-24α-methyl-3β-ol (30% 24β)
SpectraBase Compound ID 3fQD8kc6yE2
InChI InChI=1S/C28H48O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h9,18-20,22-26,29H,7-8,10-17H2,1-6H3/t19-,20-,22+,23+,24-,25+,26+,27+,28-/m1/s1
InChIKey SGNBVLSWZMBQTH-PODYLUTMSA-N
Mol Weight 400.7 g/mol
Molecular Formula C28H48O
Exact Mass 400.370516 g/mol
Enantiomer InChIKey SGNBVLSWZMBQTH-SNCZQAQVSA-N

View Spectrum of 5-Cholesten-24α-methyl-3β-ol (30% 24β)

MS (GC) Spectrum
Copyright Copyright © 2012-2024 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved.
Source of Spectrum Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences

View Spectrum of 5-Cholesten-24α-methyl-3β-ol (30% 24β)

MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum G4-79-SM34-4

View Spectrum of 5-Cholesten-24α-methyl-3β-ol (30% 24β)

FTIR Spectrum
Copyright Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number C6700-010
Technique KBr1 0.92mg

View Spectrum of 5-Cholesten-24α-methyl-3β-ol (30% 24β)

ATR-IR Spectrum
Copyright Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids
Source of Spectrum Forensic Spectral Research
Catalog Number C6700-010

View Spectrum of 5-Cholesten-24α-methyl-3β-ol (30% 24β)

Raman Spectrum
Copyright Copyright © 2013-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Steraloids Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number C6700-010

View Spectrum of 5-Cholesten-24α-methyl-3β-ol (30% 24β)

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • Campesterol
  • 5-Cholesten-24α-methyl-3β-ol
  • Ergost-5-en-3b-ol
  • 24(R)-methylcholesterol
  • (24R)-24-METHYLCHOLEST-5-EN-3-BETA-OL
  • Ergost-5-en-3-ol
Ergost-5-en-3-ol @
24(R)-methylcholesterol
(8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(1R,4S)-1,4,5-trimethylhexyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
24-METHYL-CHOLESTEROL
(24S)-24-METHYLCHOLEST-5-EN-3-BETA-OL
26,27-Dinorergost-5-en-3-ol, (3.beta.)-
27-Norergost-5-en-3-ol, 25-ethenyl-, (3.beta.,24R,25R)-
27-Norergost-5-en-3-ol, 25-ethenyl-, (3.beta.,25S)-
27-Norergost-5-en-3-ol, 25-ethenyl-, (3.beta.,24R,25S)-
(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(1R,4R)-1-methyl-4-[(1R,2R)-2-methylcyclopropyl]pentyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
24(S)-Hydroxycholesterol
(24S)-Stigmast-5-ene-3.beta.,29-diol
Stigma-5(6)-ene-3.alpha.-ol
14alpha-Sitosterin-5-en-3beta-ol
Title Journal or Book Year
Identification of C-24 alkyl epimers of marine sterols by 13C nuclear magnetic resonance spectroscopy Canadian Journal of Chemistry 1978
Ergost-5-en-3-ol @
(24S)-24-METHYLCHOLEST-5-EN-3-BETA-OL
24(R)-methylcholesterol
(8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(1R,4S)-1,4,5-trimethylhexyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
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