This impurity is related to Amoxicillin EP Impurity L 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.
Amoxicillin EP Impurity L is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2S,5R,6R)-6-[[(2S,5R,6R)-6-[[(2R)-2-Amino-2-(4-hydroxyphenyl)acetyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carbonyl]amino]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Amoxicillin Molecular Formula: C24H29N5O7S2
Molecular Weight: 563.6
Storage: Store in a cool, dry place.