Rifapentine impurity 21 CAS 26117-02-2

Description

Compared with other compounds in its class, the molecular weight of 755.80 g/mol gives Rifapentine impurity 21 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Rifapentine impurity 21 (CAS 26117-02-2), a pharmacopoeial impurity reference standard (molecular formula C39H49NO14, MW 755.80 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Rifapentine impurity 21 (C39H49NO14) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 Rifapentine impurity 21 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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