Gentamicin Impurity 13 CAS 49751-51-1

Description

Compared with other compounds in its class, the molecular weight of 321.37 g/mol gives Gentamicin Impurity 13 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Gentamicin Impurity 13 (CAS 49751-51-1), a pharmacopoeial impurity reference standard (molecular formula C13H27N3O6, MW 321.37 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C13H27N3O6, Gentamicin Impurity 13 contains an amide group, a carboxylic acid group, a hydroxyl group, an ether linkage; these features give the compound characteristic functional-group stretching vibrations in infrared spectroscopy. The molecular weight of 321.37 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 Gentamicin Impurity 13 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