(3R,5R,8S,10S,13S,14S)-3-Hydroxy-10,13-dimethyl-3,4,5,6,7,8,10,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(2H)-one CAS 571-49-3

Purity 97%+In StockPharmaceutical Standards
CAS No.571-49-3
Molecular FormulaC19H28O2
Molecular Weight288.42 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3R,5R,8S,10S,13S,14S)-3-Hydroxy-10,13-dimethyl-3,4,5,6,7,8,10,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(2H)-one CAS 571-49-3 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.

CATO supplies (3R,5R,8S,10S,13S,14S)-3-Hydroxy-10,13-dimethyl-3,4,5,6,7,8,10,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(2H)-one (CAS 571-49-3), a certified reference material (molecular formula C19H28O2, MW 288.42 g/mol) for analytical method development and quality control.

Owing to a steroid core, a hydroxyl group, an ether linkage, (3R,5R,8S,10S,13S,14S)-3-Hydroxy-10,13-dimethyl-3,4,5,6,7,8,10,12,13,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthren-17(2H)-one is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 288.42 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 FormulaC19H28O2
Molecular Weight288.42 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1957

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