700122P

campestanol

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

• Sinónimos: 5α-campestan-3β-ol
• Fórmula empírica (notación de Hill): C₂₈H₅₀O
• Número de CAS: 474-60-2
• Peso molecular: 402.70
• Número MDL: MFCD00201592
• Código UNSPSC: 12352211
• NACRES: NA.25

Propiedades

• Ensayo: >99% (TLC)
• Formulario: powder
• envase: pkg of 1 × 1 mg (700122P-1mg)
• fabricante / nombre comercial: Avanti Research^™ - A Croda Brand 700122P
• Condiciones de envío: dry ice
• temp. de almacenamiento: −20°C
• cadena SMILES: 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
• Clave InChI: ARYTXMNEANMLMU-ATEDBJNTSA-N

Descripción

Descripción general

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.

Acciones bioquímicas o fisiológicas

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.

Envase

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

Información legal

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids