(3S,5S,6S,8R,9S,1R,13S,14S,17S)-1,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,6,17-triol CAS 49644-04-4

Purity 97%+In StockPharmaceutical Standards
CAS No.49644-04-4
Molecular FormulaC19H32O3
Molecular Weight308.46 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3S,5S,6S,8R,9S,1R,13S,14S,17S)-1,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,6,17-triol CAS 49644-04-4 chemical structure

Description

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.

(3S,5S,6S,8R,9S,1R,13S,14S,17S)-1,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,6,17-triol (CAS 49644-04-4) is a high-purity analytical reference standard with the molecular formula C19H32O3 and a molecular weight of 308.46 g/mol.

The molecular framework of (3S,5S,6S,8R,9S,1R,13S,14S,17S)-1,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,6,17-triol (C19H32O3) is characterized by a steroid core, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

Physical & Chemical Properties

Molecular FormulaC19H32O3
Molecular Weight308.46 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1971

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