Dasatinib Impurity 29 CAS CATO-C4X-160729

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Dasatinib Impurity 29.

CATO supplies Dasatinib Impurity 29 (CAS CATO-C4X-160729), a pharmacopoeial impurity reference standard (molecular formula C16H13Cl2N5OS, MW 394.28 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C16H13Cl2N5OS, Dasatinib Impurity 29 contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 394.28 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.

As a certified reference material (CRM), Dasatinib Impurity 29 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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