D6128

5α-Cholestan-3β-ol

≥95%

• Synonym(e): 3β-Hydroxy-5α-cholestan, Dihydrocholesterin
• Empirische Formel (Hill-System): C₂₇H₄₈O
• CAS-Nummer: 80-97-7
• Molekulargewicht: 388.67
• Beilstein: 2418594
• EG-Nummer: 201-315-8
• MDL-Nummer: MFCD00066413
• UNSPSC-Code: 12352211
• PubChem Substanz-ID: 24893999
• NACRES: NA.28

Eigenschaften

• Biologische Quelle: synthetic (organic)
• Qualitätsniveau: 200
• Assay: ≥95%
• Form: powder
• Versandbedingung: ambient
• Lagertemp.: 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
• InChIKey: QYIXCDOBOSTCEI-QCYZZNICSA-N
• Angaben zum Gen: human ... POLA1(5422) , TOP2A(7153) ; rat ... Polb(29240)

Beschreibung

Anwendung

5α-Cholestan-3β-ol was used as a standard in lipid analysis using HPLC.[1][2]

Biochem./physiol. Wirkung

5α-Cholestan-3β-ol is derived from cholesterol by the action of intestinal microorganisms.[3] It is known to induce the formation of gall stones in rabbits in the presence of sodium ions.[4]

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)