CAS 481-21-0
:5α-Cholestane
Description:
5α-Cholestane, with the CAS number 481-21-0, is a saturated sterol and a derivative of cholesterol. It is characterized by a rigid, multi-ring structure typical of steroid compounds, featuring a total of 27 carbon atoms and a molecular formula of C27H46. This compound is notable for its lack of double bonds, which distinguishes it from its unsaturated counterparts. 5α-Cholestane is typically found in various biological systems and can be derived from the hydrogenation of cholesterol. It is insoluble in water but soluble in organic solvents, reflecting its hydrophobic nature. The compound is often used in biochemical research and as a reference standard in analytical chemistry, particularly in studies involving sterols and lipid metabolism. Its stability and structural integrity make it a valuable substance for understanding the behavior of sterols in biological systems. Additionally, 5α-Cholestane can serve as a biomarker for certain geological and biological processes, contributing to the study of ancient organisms and environmental conditions.
Formula:C27H48
InChI:InChI=1S/C27H48/c1-19(2)9-8-10-20(3)23-14-15-24-22-13-12-21-11-6-7-17-26(21,4)25(22)16-18-27(23,24)5/h19-25H,6-18H2,1-5H3/t20-,21-,22+,23-,24+,25+,26+,27-/m1/s1
InChI key:InChIKey=XIIAYQZJNBULGD-XWLABEFZSA-N
SMILES:C[C@@]12[C@]([C@]3([C@@]([C@]4(C)[C@@](CC3)(CCCC4)[H])(CC1)[H])[H])(CC[C@@]2([C@@H](CCCC(C)C)C)[H])[H]
Synonyms:- (20R)-5α(H),14α(H),17α(H)-Cholestane
- (5Alpha,8Xi,9Xi,14Xi,17Xi,20Xi)-Cholestane
- (5R,8R,9S,10S,13R,14S,17R)-10,13-Dimethyl-17-((R)-6-methylheptan-2-yl)hexadecahydro-1H-cyclopenta[a]phenanthrene
- 28,29,30-Trinorlanostane
- 5-Alpha-Cholestane
- 5A-cholestane
- Cholestan
- Cholestane
- Cholestane, (5α)-
- NSC 224419
- α-Cholestane
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 12 products.
(5-α)-Cholestane
CAS:(5-alpha)-Cholestane analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C27H48Purity:(GC) ≥95%Color and Shape:PowderMolecular weight:372.685α-Cholestane-2,2,3,3,4,4-d6
CAS:Purity:95 atom % DColor and Shape:White SolidMolecular weight:378.715α-Cholestane
CAS:<p>5α-Cholestane belongs to the cholestane steroid class of compounds.</p>Formula:C27H48Purity:99.02% - 99.44%Color and Shape:SolidMolecular weight:372.67α-Cholestane
CAS:Controlled Product<p>Applications α-Cholestane is the trans-decalin homolog of Coprostane.<br>References Ruzicka, et al.: Helv. Chim. Acta, 16, 327 (1933), Yamaga, N., et al.: J. Biochem., 119, 725 (1996), Burkard, I., et al.: J. Lipid Res., 45, 776 (2004), Teng, S., et al.: Br. J. Pharmacol., 151, 367 (2007),<br></p>Formula:C27H48Color and Shape:White To Off-WhiteMolecular weight:372.67α-Cholestane
CAS:Controlled Product<p>a-Cholestane is a fatty acid that is an intermediate in the biosynthesis of cholesterol. It can be found in urine samples as a result of its conversion by the enzyme lecithin:cholesterol acyltransferase (LCAT). LCAT catalyzes the transfer of cholesteryl ester from plasma lipoproteins to the polar head group of phosphatidylcholine, which then becomes lecithin. The LCAT reaction is reversible and is catalyzed by sodium taurocholate. Magnetic resonance spectroscopy can be used to analyze how LCAT affects the surface methodology of a-cholestane.</p>Formula:C27H48Purity:(%) Min. 97%Color and Shape:PowderMolecular weight:372.67 g/mol










