(6R,7R)-7-((Z)-2-(furan-2-yl)-2-(methoxyimino)acetamido)-3-(hydroxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid;Cefuroxime Sodium Impurity F (EP); Cefuroxime Sodium EP Impurity A;Descarbamoyl Cefuroxime;
Cefuroxime EP Impurity A (Cefuroxime Descarbamoyl) is a fully characterized chemical compound used as a reference standard of API Cefuroxime. The standard offered is compliant with regulatory guidelines. Cefuroxime EP Impurity A (Cefuroxime Descarbamoyl) 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 - 56271-94-4
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