Ciprofloxacin Impurity 33 CAS CATO-C4X-136233

Description

Compared with other compounds in its class, the molecular weight of 728.64 g/mol gives Ciprofloxacin Impurity 33 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

As a process- or degradation-related impurity, Ciprofloxacin Impurity 33 (CAS CATO-C4X-136233, C39H40FN3O3PBr) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Ciprofloxacin Impurity 33 (C39H40FN3O3PBr) contains a nitrogen-containing heterocyclic scaffold, an amide group, a phosphonate group, a hydroxyl group, an ether linkage, fluorine/bromine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

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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