Levocarnitine impurity 29 Ammonium Salt CAS 41363-39-7 (free acid)

Description

CATO manufactures Levocarnitine impurity 29 Ammonium Salt 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.

CATO supplies Levocarnitine impurity 29 Ammonium Salt (CAS 41363-39-7 (free acid)), a pharmacopoeial impurity reference standard (molecular formula C7H6NO4SH4N, MW 218.23 g/mol) used for the identification and quantification of trace impurities in APIs.

Levocarnitine impurity 29 Ammonium Salt (C7H6NO4SH4N) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

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