Osimertinib Impurity 55 CAS 2364486-24-6

Description

Compared with other compounds in its class, the molecular weight of 338.41 g/mol gives Osimertinib Impurity 55 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Osimertinib Impurity 55 (CAS 2364486-24-6), a pharmacopoeial impurity reference standard (molecular formula C22H18N4, MW 338.41 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C22H18N4, Osimertinib Impurity 55 contains a nitrogen-containing heterocyclic scaffold, a nitrile group; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 338.41 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 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 Osimertinib Impurity 55 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

Why CATO?

• ISO 17034 accredited reference material producer (CNAS + ANAB dual accreditation)
• 130,000+ catalog items in stock, COA supplied with every batch
• Worldwide shipping with full export documentation (HS code guidance available)
• Technical support: +86 18665070610 / Nicole.chen@cato-chem.com