Landiolol Impurity 59 CAS CATO-C4X-262159

Description

Compared with other compounds in its class, the molecular weight of 462.41 g/mol gives Landiolol Impurity 59 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Landiolol Impurity 59 (CAS CATO-C4X-262159), a pharmacopoeial impurity reference standard (molecular formula C15H14N2O11S2, MW 462.41 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C15H14N2O11S2, Landiolol Impurity 59 contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 462.41 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).

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 Landiolol Impurity 59 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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