(S)-9-fluoro-3-methyl-10-((2-(methyl(nitroso)amino)ethyl)(nitroso)amino)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid
N,N-Dinitroso Levofloxacin EP Impurity G is a fully characterized chemical compound used as a reference standard of API Levofloxacin. The standard offered is compliant with regulatory guidelines. N,N-Dinitroso Levofloxacin EP Impurity G is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS - NA
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