Cefalotin EP Impurity A

Impurity profile study of cefalotin sodium by two-​dimensional liquid chromatography-​quadrupole time-​of-​flight mass spectrometry
By Qiu, Ya; Qin, Feng; Wen, Hongliang; Zhao, Jingdan; Liu, Hao; Yang, Meicheng
From Sepu (2015), 33(12), 1314-1319
 
Impurity profiling of cefalotin sodium by MEKC and HPLC
By Liu, Hao; Jia, Zhi-qiang
From Zhongguo Kangshengsu Zazhi (2013), 38(12), 921-927
 
Determination of high molecular weight impurities in cefalotin sodium for injection by HPSEC
By Wang, Chenggang; Zhou, Lichun; Wang, Junqiu
From Zhongguo Yaopin Biaozhun (2010), 11(5), 340-342

 

Cefalotin EP Impurity A is chemically (6R,7R)-3-Methyl-8-oxo-7-[(thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per EP). It is also known as Deacetoxy Cefalotin (EP). Cefalotin EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Cefalotin 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 Cefalotin.

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.