Regadenoson Impurity 37 CAS 50427-65-1

Description

The occurrence of Regadenoson Impurity 37 is closely related to a carbohydrate-derived structure in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies Regadenoson Impurity 37 (CAS 50427-65-1), a pharmacopoeial impurity reference standard (molecular formula C5H6O4, MW 130.10 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C5H6O4, Regadenoson Impurity 37 contains a carbohydrate-derived structure; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 130.10 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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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