This impurity is related to Cefazolin EP Impurity A is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Cefazolin EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(6R,7R)-7-Amino-3-[[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanyl]methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid ; (6R,7R)-7-Amino-3-[(5-methyl-1,3,4-thiadiazol-2-ylthio)methyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cefazolin Molecular Formula: C11H12N4O3S3
Molecular Weight: 344.4
Storage: Store in a cool, dry place.