Cefuroxime Axetil EP Impurity A | CAS 123458-61-7 - 请求报价
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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.
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Cefuroxime Axetil EP Impurity A 用于方法验证
Cefuroxime 对照标准
Cefuroxime Axetil EP Impurity A 用于ANDA申报
Cefuroxime Axetil EP Impurity A 用于强制降解研究
Cefuroxime Axetil EP Impurity A 鉴别标准
Cefuroxime Axetil EP Impurity A 用于DMF申报
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