| Identification | Back Directory | [Name]
Ergostan-3-ol, (3.beta.,5.alpha.,24R)- | [CAS]
474-60-2 | [Synonyms]
Chalinastanol
Dihydrocampesterin
24β-Methylcholestanol
5α-DihydrocaMpesterol
Dihydro-Neospongosterol
(24R)-5α-Ergostan-3β-ol
(3b,5a,24R)-ergostan-3-ol
(3β,5α,24R)-Ergostan-3-ol
5α-Cholestan-24(RS)-Methyl-3β-ol
(3BETA,5ALPHA,24R)-ERGOSTAN-3-OL)
(24R)-24-Methyl-5α-cholestan-3β-ol
Ergostan-3-ol, (3.beta.,5.alpha.,24R)-
5α-Cholestan-20(α/β)-Methyl-3β-ol-25,26,26,26,27,27,27-d7 | [Molecular Formula]
C28H50O | [MDL Number]
MFCD00201592 | [MOL File]
474-60-2.mol | [Molecular Weight]
402.7 |
| Chemical Properties | Back Directory | [Melting point ]
146-147 °C | [Boiling point ]
461.4±13.0 °C(Predicted) | [density ]
0.951±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
Chloroform: slightly soluble | [form ]
A solid | [pka]
15.14±0.70(Predicted) | [color ]
White to off-white |
| Hazard Information | Back Directory | [Uses]
A phytosterol | [Definition]
ChEBI: Campestanol is a 3beta-sterol and a C28-steroid. It derives from a hydride of a 5alpha-campestane. | [Biological Activity]
Campestanol absorption in intestine is similar to th at of cholesterol absorption pathway. Howeverin sitosterolemic homozygotesit is hyperabsorbed from the intestine.''Intestinal absorption of campestanol is lesser compared to cholesterol due to the presence of side chain. Due to the structural similarity with cholesterolcampestanol reduces cholesterol absorption in the intestine and the plasma level of LDL cholesterol. |
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