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About This Item
Empirical Formula (Hill Notation):
C24H38O3
CAS Number:
Molecular Weight:
374.56
UNSPSC Code:
12352211
PubChem Substance ID:
MDL number:
assay
≥98%
SMILES string
C[C@@H](CCC(O)=O)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C
InChI
1S/C24H38O3/c1-15(4-9-22(26)27)19-7-8-20-18-6-5-16-14-17(25)10-12-23(16,2)21(18)11-13-24(19,20)3/h5,15,17-21,25H,4,6-14H2,1-3H3,(H,26,27)
InChI key
HIAJCGFYHIANNA-UHFFFAOYSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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M Tohma et al.
Steroids, 44(1), 47-55 (1984-07-01)
The glycine conjugate of 3 beta-hydroxy-5-cholen-24-oic acid and its sulfate labeled with deuterium at the C-2, -4, and -23 positions were synthesized. A highly sensitive and specific quantitative assay of the bile acid has been developed by selected ion monitoring
L Riello et al.
Journal of pediatric gastroenterology and nutrition, 50(6), 655-660 (2010-04-20)
3beta-Hydroxy-Delta 5-C27-steroid dehydrogenase/isomerase deficiency is a bile acid synthesis defect responsive to primary bile acids. We reviewed its clinical features and response to treatment with a mixture of ursodeoxycholic (UDCA) and chenodeoxycholic acid (CDCA) to titrate the dose of supplements
A Hernanz et al.
Clinica chimica acta; international journal of clinical chemistry, 145(3), 289-296 (1985-02-15)
Fasting bile acids in serum of eight children with the syndrome of hepatic ductular hypoplasia were analyzed by gas chromatography. The children did not receive any kind of treatment during the month before the analysis. Serum concentrations of total bile
Y Yamato et al.
Biology of the neonate, 80(1), 19-25 (2001-07-28)
To elucidate the urinary concentration of total bile acids after birth and the profile of the usual and unusual urinary bile acids, especially 3beta-hydroxy-5-cholen-24-oic acid (Delta(5)-3beta-ol), we measured the concentrations of 13 bile acids in the urine from preterm infants
E Kok et al.
The Journal of biological chemistry, 256(12), 6155-6159 (1981-06-25)
Synthesis of 3 beta-hydroxy-5-[1,2-3H]cholenoic acid has permitted a study of its metabolism in bile-fistula hamsters that received the compound by intravenous infusion. Metabolites in bile were identified by reverse isotope dilution after their complete resolution by high pressure liquid chromatography
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