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.[1] It is naturally occurring and has similar structure as cholesterol.[2] Campestanol is synthesized by the hydrogenation of campesterol.[3]

Campestanol is a saturated[4] plant stanol.

Acciones bioquímicas o fisiológicas

Campestanol absorption in intestine is similar to that of cholesterol absorption pathway.[2] However, in sitosterolemic homozygotes, it is hyperabsorbed from the intestine.[1]

Intestinal absorption of campestanol is lesser compared to cholesterol due to the presence of side chain.[5] Due to the structural similarity with cholesterol, campestanol reduces cholesterol absorption in the intestine and the plasma level of LDL cholesterol.[4]

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