700122P
Avanti
campestanol
Avanti Polar Lipids 700122P, powder
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5α-campestan-3β-ol
C28H50O
Recommended Products
Assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 1 mg (700122P-1mg)
manufacturer/tradename
Avanti Polar Lipids 700122P
shipped in
dry ice
storage temp.
−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
InChI key
ARYTXMNEANMLMU-ATEDBJNTSA-N
General description
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.
Biochem/physiol Actions
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.
Packaging
5 mL Amber Glass Screw Cap Vial (700122P-1mg)
Certificates of Analysis (COA)
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Find documentation for the products that you have recently purchased in the Document Library.
Enhancing Extraction Processes in the Food Industry (2016)
SOFW Journal, 149-149 (2002)
Brassinosteroid deficiency due to truncated steroid 5alpha-reductase causes dwarfism in the lk mutant of pea
Plant Physiology, 135(4), 2220-2229 (2004)
Campestanol (24-methyl-5alpha-cholestan-3beta-ol) absorption and distribution in New Zealand white rabbits: effect of dietary sitostanol
Metabolism, Clinical and Experimental, 48(3), 363-368 (1999)
Hyperabsorption and retention of campestanol in a sitosterolemic homozygote: comparison with her mother and three control subjects
Journal of Lipid Research, 41(11), 1883-1889 (2000)
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