Clopidogrel Impurity 34 CAS 1331383-23-3

Description

Compared with other compounds in its class, the molecular weight of 536.06 g/mol gives Clopidogrel Impurity 34 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Clopidogrel Impurity 34 (CAS 1331383-23-3), a certified reference material (molecular formula C26[13C]H27D3ClNO6S, MW 536.06 g/mol) for analytical method development and quality control.

Owing to deuterium isotope labeling, a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution, Clopidogrel Impurity 34 is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 536.06 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures Clopidogrel Impurity 34 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