Lacosamide EP Impurity J CAS 100-46-9

Description

Compared with other compounds in its class, the molecular weight of 107.15 g/mol gives Lacosamide EP Impurity J distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Lacosamide EP Impurity J (CAS 100-46-9), a pharmacopoeial impurity reference standard (molecular formula C7H9N, MW 107.15 g/mol) used for the identification and quantification of trace impurities in APIs.

Owing to a nitrile group, an aromatic ring system, Lacosamide EP Impurity J is typically off-white to pale yellow liquid. Its solid-state physicochemical attributes — including a molecular weight of 107.15 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 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 Lacosamide EP Impurity J 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?

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