Tolvaptan Impurity 71 CAS CATO-C4X-195571

Description

Compared with other compounds in its class, the molecular weight of 639.57 g/mol gives Tolvaptan Impurity 71 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Tolvaptan Impurity 71 (CAS CATO-C4X-195571), a pharmacopoeial impurity reference standard (molecular formula C36H32Cl2N4O3, MW 639.57 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C36H32Cl2N4O3, Tolvaptan Impurity 71 contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 639.57 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

CATO manufactures Tolvaptan Impurity 71 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