Piroxicam EP Impurity L(Meloxicam EP Impurity F) CAS 118854-48-1

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Piroxicam EP Impurity L(Meloxicam EP Impurity F).

CATO supplies Piroxicam EP Impurity L(Meloxicam EP Impurity F) (CAS 118854-48-1), a pharmacopoeial impurity reference standard (molecular formula C13H15NO5S, MW 297.33 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Piroxicam EP Impurity L(Meloxicam EP Impurity F) (C13H15NO5S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone 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. 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), Piroxicam EP Impurity L(Meloxicam EP Impurity F) 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

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