3,6-Bis(tosyloxy)-α-hyodeoxycholic acid methyl ester CAS 1184-20-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1184-20-9
Molecular FormulaC39H54O8S2
Molecular Weight714.97 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,6-Bis(tosyloxy)-α-hyodeoxycholic acid methyl ester CAS 1184-20-9 chemical structure

Description

Structurally, 3,6-Bis(tosyloxy)-α-hyodeoxycholic acid methyl ester (C39H54O8S2) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system. The molecule exhibits a degree of unsaturation (DBE) of 13.0, corresponding to approximately 13 ring(s) or double-bond equivalent(s). With a molecular weight of 714.97 g/mol, it falls into the high-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

3,6-Bis(tosyloxy)-α-hyodeoxycholic acid methyl ester (CAS 1184-20-9), molecular formula C39H54O8S2 and molecular weight 714.97 g/mol, is a CATO reference standard with documented purity and traceability.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC39H54O8S2
Molecular Weight714.97 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957
Sulfur Atoms2

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