Calcitonin Impurity 9 CAS 28567-37-5

Description

Compared with other compounds in its class, the molecular weight of 502.66 g/mol gives Calcitonin Impurity 9 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Calcitonin Impurity 9 (CAS 28567-37-5), a pharmacopoeial impurity reference standard (molecular formula C38H30O, MW 502.66 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Calcitonin Impurity 9 (C38H30O) is characterized by a hydroxyl group, an ether linkage, a polycyclic aromatic system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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 Calcitonin Impurity 9 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
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• Technical support: +86 18665070610 / Nicole.chen@cato-chem.com