Cefalexin EP Impurity E

Determination of ultra-​fined cefalexin by HPLC
By Feng, Xuyun; Kang, Xuliang; Wang, Jiexin; Shao, Lei; Chen, Jianfeng
From Zhongguo Yaoxue Zazhi (Beijing, China) (2008), 43(23), 1833-1834
 
Application of thermogravimetry to the study of thermal decomposition kinetics of cefalexin and its stability
By Zhang, Jian; Chen, Dong-Hua; Yuan, Yu-Hong; Li, Zhao
From Zhongguo Yaoke Daxue Xuebao (2000), 31(2), 94-98
 

Cefalexin EP Impurity E is chemically (6R,7R)-7-[(2,2-Dimethylpropanoyl)amino]-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP). It is also known as 7-ADCA Pivalamide. Cefalexin EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Cefalexin EP Impurity E 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 Cefalexin.

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.