Cefuroxime Axetil EP Impurity A | CAS 123458-61-7 - Solicitar cotización

Cefuroxime Axetil EP Impurity A is chemically 1-(Acetyloxy)ethyl (6R,7R)-3-[(carbamoyloxy)methyl]-7-[[(Z)-2-(furan-2-yl)-2-(methoxyimino)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate (as per EP);(1RS,6R,7R)-1-Acetoxyethyl 3-[(carbamoyloxy)methyl]-7-[(Z)-2-(furan-2-yl)-2-(methoxyimino)acetamido]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate (as per USP). It is also known as Cefuroxime Axetil Delta-3-Isomers (USP). Cefuroxime Axetil EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Cefuroxime Axetil EP Impurity A can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Cefuroxime.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.