D6128

5α-Cholestan-3β-ol

≥95%

• Synonyme(s) : β-Cholestanol, 3β-Hydroxy-5α-cholestane, Dihydrocholesterol
• Formule empirique (notation de Hill) : C₂₇H₄₈O
• Numéro CAS: 80-97-7
• Poids moléculaire : 388.67
• UNSPSC Code: 12352211
• NACRES: NA.28
• PubChem Substance ID: 24893999
• EC Number: 201-315-8
• Beilstein/REAXYS Number: 2418594
• MDL number: MFCD00066413

Propriétés

• biological source: synthetic (organic)
• Quality Segment: 200
• assay: ≥95%
• form: powder
• shipped in: ambient
• storage temp.: room temp
• SMILES string: CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC[C@H]4C[C@@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
• InChI: 1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20+,21+,22+,23-,24+,25+,26+,27-/m1/s1
• InChI key: QYIXCDOBOSTCEI-QCYZZNICSA-N
• Gene Information: human ... POLA1(5422), TOP2A(7153) ; rat ... Polb(29240)

Description

Application

5α-Cholestan-3β-ol was used as a standard in lipid analysis using HPLC.

Biochem/physiol Actions

5α-Cholestan-3β-ol is derived from cholesterol by the action of intestinal microorganisms. It is known to induce the formation of gall stones in rabbits in the presence of sodium ions.

Informations sur la sécurité

• Classe de stockage: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, type N95 (US)