Canagliflozin Impurity 30 CAS 1358581-37-9

Description

The occurrence of Canagliflozin Impurity 30 is closely related to a flavonoid core, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies Canagliflozin Impurity 30 (CAS 1358581-37-9), a pharmacopoeial impurity reference standard (molecular formula C25H27FO6S, MW 474.54 g/mol) used for the identification and quantification of trace impurities in APIs.

Owing to a flavonoid core, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution, Canagliflozin Impurity 30 is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 474.54 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

As a certified reference material (CRM), Canagliflozin Impurity 30 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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