700122P

campestanol

Avanti Research^™ - A Croda Brand 700122P, powder

• Synonyme(s) : 5α-campestan-3β-ol
• Formule empirique (notation de Hill): C₂₈H₅₀O
• Numéro CAS: 474-60-2
• Poids moléculaire : 402.70
• Code UNSPSC : 12352211
• Nomenclature NACRES : NA.25

Propriétés

• Pureté: >99% (TLC)
• Forme: powder
• Conditionnement: pkg of 1 × 1 mg (700122P-1mg)
• Fabricant/nom de marque: Avanti Research^™ - A Croda Brand 700122P
• Conditions d'expédition: dry ice
• Température de stockage: −20°C
• InChI: 1S/C28H50O/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/h18-26,29H,7-17H2,1-6H3/t19-,20-,21+,22+,23+,24-,25+,26+,27+,28-/m1/s1
• Clé InChI: ARYTXMNEANMLMU-ATEDBJNTSA-N

Description

Description générale

Campestanol has a methyl group at the C-24. It comprises the 10-30% of stanol content in vegetable oil. It is naturally occurring and has similar structure as cholesterol. Campestanol is synthesized by the hydrogenation of campesterol.

Campestanol is a saturated plant stanol.

Actions biochimiques/physiologiques

Campestanol absorption in intestine is similar to that 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.

Conditionnement

5 mL Amber Glass Screw Cap Vial (700122P-1mg)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids