This impurity is related to Atenolol EP Impurity I 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.
Atenolol EP Impurity I is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:2-(4-(3-(Ethylamino)-2-hydroxypropoxy)phenyl)acetamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Atenolol Molecular Formula: C13H20N2O3
Molecular Weight: 252.3
Storage: Store in a cool, dry place.