4-hydroxy-2,5-dimethyl-3,4-diphenylcyclopent-2-en-1-one CAS 5423-06-3

Purity 97%+In StockPharmaceutical Standards
CAS No.5423-06-3
Molecular FormulaC19H18O2
Molecular Weight278.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-hydroxy-2,5-dimethyl-3,4-diphenylcyclopent-2-en-1-one CAS 5423-06-3 chemical structure

Description

CATO supplies 4-hydroxy-2,5-dimethyl-3,4-diphenylcyclopent-2-en-1-one (CAS 5423-06-3), a certified reference material (molecular formula C19H18O2, MW 278.35 g/mol) for analytical method development and quality control.

4-hydroxy-2,5-dimethyl-3,4-diphenylcyclopent-2-en-1-one (C19H18O2) contains a steroid core, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

CATO manufactures 4-hydroxy-2,5-dimethyl-3,4-diphenylcyclopent-2-en-1-one under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC19H18O2
Molecular Weight278.35 g/mol
AppearancePale yellow to 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958

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