Rivaroxaban Impurity 23 CAS 26020-48-4

Description

Compared with other compounds in its class, the molecular weight of 231.48 g/mol gives Rivaroxaban Impurity 23 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Rivaroxaban Impurity 23 (CAS 26020-48-4), a certified reference material (molecular formula C5HCl3O2S, MW 231.48 g/mol) for analytical method development and quality control.

The molecular framework of Rivaroxaban Impurity 23 (C5HCl3O2S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 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.

As a certified reference material (CRM), Rivaroxaban Impurity 23 meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

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