Substance

ID:351801

Names and Identifiers
IUPAC Traditional name
(1S,2R,5S,11R,14R,15R)-14-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadeca-7,9-dien-5-ol
IUPAC name
(1S,2R,5S,11R,14R,15R)-14-[(2R,5R)-5,6-dimethylhept-3-en-2-yl]-2,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadeca-7,9-dien-5-ol
Synonyms
5,7,22-Ergostatrien-3β-ol(3β)-麦角-5,7,22-三烯甘油-3-醇3β-羟基-5,7,22-麦角三烯3β-Hydroxy-5,7,22-ergostatriene维生素原 D2Provitamin D2麦角固醇Ergosterol
Registration numbers
EC Number
CAS Number
Beilstein Number
MDL Number
PubChem SID
Properties
Safety Information
RID/ADR
UN 2811 6.1/PG 2
MSDS Link
UN Number
2811
Personal Protective Equipment
Eyeshields, Faceshields, full-face particle respirator type N100 (US), Gloves, respirator cartridge type N100 (US), type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
German water hazard class
3
Storage Temperature
2-8°C
Hazard Class
6.1
Packing Group
2
GHS Hazard statements
H413
Physical Property
Melting Point
160-163 °C
156-158 °C(lit.)
Optical Rotation
[α]20/D -120±10°, c = 1% in chloroform
Product Information
Impurities
~3% water
Purity
≥95.0% (HPLC)
Empirical Formula (Hill Notation)
C28H44O
Molecule Details
Biochem/physiol Actions
Ergosterol is a biological precursor of Vitamin D2 found in cell membranes of fungi and some protists such as trypanosomes. Ergosterol may be used to study the function of anti-fungal drugs such as Amphotericin B and its analogues and to study the ergosterol biosynthesis pathway within various fungi.
Molecular Spectra
No Data Available
Click here to submit data
References
No Data Available
Click here to submit data