Ergostan-3-ol, (3.beta.,5.alpha.,24R)- Chemical Properties

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

Ergostan-3-ol, (3.beta.,5.alpha.,24R)- Usage And Synthesis

Uses

Campestanol can be used as analyte in biological and analytical studies for the determination of 22 natural brassinosteroids in a minute sample of plant tissue by UHPLC-ESI-MS/MS.

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. However, in sitosterolemic homozygotes, it 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 cholesterol, campestanol reduces cholesterol absorption in the intestine and the plasma level of LDL cholesterol.

Ergostan-3-ol, (3.beta.,5.alpha.,24R)-(474-60-2)Related Product Information

• 22(S),23(S)-Homobrassinolide
• Stigmasterol
• Clerosterol
• LUMISTEROL
• CAMPESTEROL 1X1ML CHLOROFORM 100UG/ML
• 9-beta,10-alpha-ergosta-5,7,22-trien-3-beta-ol
• Wood sterols
• EPICHOLESTEROL
• STIGMASTEROL
• Sterol
• Vegetable alcohol
• N/A
• EPICASTASTERONE
• SITOSTANOL, [5,6-3H]
• Ergostan-3-ol, (3.beta.,5.alpha.,24R)-
• Sitostanol-5,6,22,23-D4
• STIGMASTANOL
• 22S,23S-EPICASTASTERONE