Hydroxychloroquine EP Impurity F CAS 6281-58-9

Description

Compared with other compounds in its class, the molecular weight of 246.74 g/mol gives Hydroxychloroquine EP Impurity F distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Hydroxychloroquine EP Impurity F (CAS 6281-58-9), a pharmacopoeial impurity reference standard (molecular formula C14H15ClN2, MW 246.74 g/mol) used for the identification and quantification of trace impurities in APIs.

Structurally, Hydroxychloroquine EP Impurity F (C14H15ClN2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 246.74 g/mol, it falls into the medium-molecular-weight range. 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).

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

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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