This impurity is related to Ampicillin EP Impurity E 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.
Ampicillin EP Impurity E is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2R)-2-[[[(2S,5R,6R)-6-[[(2R)-2-Amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]hept-2-yl]carbonyl]amino]-2-phenylacetic acid ; (R)-2-((2S,5R,6R)-6-((R)-2-Amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxamido)-2-phenylacetic acid (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ampicillin Molecular Formula: C24H26N4O5S
Molecular Weight: 482.6
Storage: Store in a cool, dry place.