700122P

campestanol

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

• Synonym(e): 5α-campestan-3β-ol
• Empirische Formel (Hill-System): C₂₈H₅₀O
• CAS-Nummer: 474-60-2
• Molekulargewicht: 402.70
• MDL-Nummer: MFCD00201592
• UNSPSC-Code: 12352211
• NACRES: NA.25

Eigenschaften

• Assay: >99% (TLC)
• Form: powder
• Verpackung: pkg of 1 × 1 mg (700122P-1mg)
• Hersteller/Markenname: Avanti Research^™ - A Croda Brand 700122P
• Versandbedingung: dry ice
• Lagertemp.: −20°C
• SMILES String: O[C@@H]1C[C@H]2[C@@]([C@@H]3[C@H]([C@H]4[C@@]([C@H](CC4)[C@@H](CC[C@H](C(C)C)C)C)(CC3)C)CC2)(CC1)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
• InChIKey: ARYTXMNEANMLMU-ATEDBJNTSA-N

Beschreibung

Allgemeine Beschreibung

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. Wirkung

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.

Verpackung

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

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids