Moxifloxacin Impurity 100 CAS CATO-C4X-1074100

Description

Compared with other compounds in its class, the molecular weight of 191.66 g/mol gives Moxifloxacin Impurity 100 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

As a process- or degradation-related impurity, Moxifloxacin Impurity 100 (CAS CATO-C4X-1074100, C7H13N3OHCl) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Owing to an amide group, a hydroxyl group, an ether linkage, chlorine substitution, Moxifloxacin Impurity 100 is typically white to off-white crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 191.66 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.

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

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