(S)-(7,8-difluoro-3-methyl-2H-benzo[b][1,4]oxazin-4(3H)-yl)methanesulfonamide
Levofloxacin Impurity 12 is a fully characterized chemical compound used as a reference standard of API Levofloxacin. The standard offered is compliant with regulatory guidelines. Levofloxacin Impurity 12 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 -
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Levofloxacin EP Impurity D (Levofloxacin USP Related Compound F, Defluoro Levofloxacin)
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