Ergosterin
Compound with spectra: 6 NMR, 1 FTIR, and 1 Raman
| SpectraBase Compound ID | CANW8cRIY47 |
|---|---|
| InChI | InChI=1S/C28H44O/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/h7-10,18-20,22,24-26,29H,11-17H2,1-6H3/b8-7+/t19-,20-,22+,24-,25+,26+,27+,28-/m1/s1 |
| InChIKey | DNVPQKQSNYMLRS-NBEWGGKZSA-N |
| Mol Weight | 396.7 g/mol |
| Molecular Formula | C28H44O |
| Exact Mass | 396.339216 g/mol |
| Enantiomer InChIKey | DNVPQKQSNYMLRS-NFGKRQIESA-N |
| Copyright | Copyright © 2014-2025 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | C5600-000 |
| Copyright | Copyright © 2015-2025 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Steraloids Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | C5600-000 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CHCl3:DIOXANE |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C5D5N |
| Copyright | Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- 5,7,22-Cholestatrien-24β-methyl-3β-ol
- Ergosterol
- Provitamin D2
- ERGOSTEROL;(VITAMIN-D-DERIVATIVE)
- ERGOSTEROL;3-BETA-HYDROXYERGOSTA-5,7,22-TRIENE
- ERGOSTA-5,7,22-TRIEN-3-BETA-OL,(ERGOSTEROL)
- ERGOSTEROL;24R-ERGOSTA-5,7,22-TRIEN-3-BETA-OL
(22E)-24-norcholesta-5,7,22-trien-3b-ol
26,27-Dinorergosta-5,7,22-trien-3-ol, (3.beta.,22E)-
Stigmasta-5,7,22-trien-3-ol, (3.beta.)-
27-Norcholesta-5,7,22-trien-3-ol, (3.beta.,22E)-
(3S,9S,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R,3E)-6-methylhepta-3,5-dien-2-yl]-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
Ergosta-5,7,22-triene-3,25,26-triol, (3.beta.,22E)-
(22E)-23-METHYLERGOSTA-5,7,22-TRIEN-3-BETA-OL
ERGOSTA-5,7,22-TRIEN-3-THIOL
5,7,22-Ergostatriene, 3-(methoxymethoxy)-
3-(METHOXYMETHOXY)ERGOSTA-5,7,22-TRIENE
| Title | Journal or Book | Year |
|---|---|---|
| Glycosides of ergosterol derivatives from Hericum erinacens | Phytochemistry | 1991 |
| Effect on ergosterol biosynthesis of a fungicide, SSF-109, in Botrytis cinerea | Phytochemistry | 1990 |
| The occurrence of ergosterol and (22E,24R)-24-ethylcholesta-5,7,22-trien-3β-ol in the unicellular chlorophyte Dunaliellatertiolecta | Canadian Journal of Chemistry | 1979 |
| Identification of C-24 alkyl epimers of marine sterols by 13C nuclear magnetic resonance spectroscopy | Canadian Journal of Chemistry | 1978 |
| 13C n.m.r. spectra of steroids —a survey and commentary | Organic Magnetic Resonance | 1977 |
| Carbon-13 nuclear magnetic resonance spectra of vitamins D and related compounds. | Journal of Nutritional Science and Vitaminology | 1975 |
This compound is available in the following databases:
KnowItAll GC-MS Library
Author: Wiley
The KnowItAll Mass Spectral Library offers a comprehensive collection of mass spectra, including the renowned Wiley Registry, and access to a wide range of compounds including pure organics, drugs, steroids, additives, geochemicals, petrochemicals, biomarkers, and more. Learn more.
Wiley Registry of Mass Spectral Data 2026
Author: Wiley
The foundation library for any analytical laboratory running mass spectrometry, the Wiley Registry provides the broadest coverage available in any mass spectral library Learn more.