Carprofen EP Impurity B CAS 52263-68-0

Description

Compared with other compounds in its class, the molecular weight of 239.27 g/mol gives Carprofen EP Impurity B distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Carprofen EP Impurity B (CAS 52263-68-0), a pharmacopoeial impurity reference standard (molecular formula C15H13NO2, MW 239.27 g/mol) used for the identification and quantification of trace impurities in APIs.

Carprofen EP Impurity B (C15H13NO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, 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 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).

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

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

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