This impurity is related to Sotalol 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.
Sotalol EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:N-[4-[2-[(1-Methylethyl)amino]ethyl]phenyl]methanesulfonamide hydrochlorideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Sotalol Molecular Formula: C12H20N2O2S : HCl
Molecular Weight: 256.4 : 36.5
Storage: Store in a cool, dry place.