Isavuconazole Impurity 51 CAS CATO-C4X-123651

Description

The occurrence of Isavuconazole Impurity 51 is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies Isavuconazole Impurity 51 (CAS CATO-C4X-123651), a pharmacopoeial impurity reference standard (molecular formula C32H30F2N7O4SCl, MW 682.14 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C32H30F2N7O4SCl, Isavuconazole Impurity 51 contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 682.14 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

CATO manufactures Isavuconazole Impurity 51 under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

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