Cefuroxime Axetil EP Impurity C ; Cefuroxime Trichloroacetyl Impurity ; (6R,7R)-7-[[(Z)-(furan-2-yl)(methoxyimino)acetyl]amino]-8-oxo-3-[[[(trichloroacetyl)carbamoyl]oxy]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Cefuroxime EP Impurity D 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 D 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
Related products
Cefuroxime Sodium EP Impurity I (Methoxyiminofurylacetic Acid)
M.F.
M.W. 169.14
CAT# AR-C02187
CAS# 39684-61-2
