Ozenoxacin Impurity 70 CAS CATO-C4X-279670

Description

Compared with other compounds in its class, the molecular weight of 255.10 g/mol gives Ozenoxacin Impurity 70 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Ozenoxacin Impurity 70 (CAS CATO-C4X-279670) is a certified pharmaceutical impurity reference standard with the molecular formula C11H8Cl2N2O and a molecular weight of 255.10 g/mol.

Ozenoxacin Impurity 70 (C11H8Cl2N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 Ozenoxacin Impurity 70 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

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