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Names | |
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IUPAC name
Ergosta-5,22-dien-3β-ol
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Systematic IUPAC name
(1R,3aS,3bS,7S,9aR,9bS,11aR)-1-[(2R,3E,4R)-5,6-Dimethylhept-3-en-2-yl]-9a,11a-dimethyl-2,3,3a,3b,4,6,7,8,9,9a,9b,10,11,11a-tetradecahydro-1H-cyclopenta[a]phenanthren-7-ol | |
Other names
brassicasterol
(3β,22E)-ergosta-5,22-dien-3-ol 24β-methylcholesta-5,22-dien-3 beta-ol 24-methyl cholest-5,22-dien-3β-ol | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.006.807 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C28H46O | |
Molar mass | 398.675 g·mol−1 |
Appearance | White solid |
Melting point | 150 to 151 °C (302 to 304 °F; 423 to 424 K) |
Hazards | |
Flash point | Non-flammable |
Related compounds | |
Related Sterols
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cholesterol β-sitosterol campesterol stigmasterol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Brassicasterol (24-methyl cholest-5,22-dien-3β-ol) is a 28-carbon sterol synthesised by several unicellular algae (phytoplankton) and some terrestrial plants, like rape. This compound has frequently been used as a biomarker for the presence of (marine) algal matter in the environment, and is one of the ingredients in stigmasterol-rich plant sterols (Number E499 in the European numbering system). There is some evidence to suggest that it may also be a relevant additional biomarker in Alzheimer's disease.[1]