This impurity is related to Sumatriptan EP Impurity B 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.
Sumatriptan EP Impurity B is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:N-Methyl-1-{3-[2-(methylamino)ethyl]-1H-indol-5-yl}methanesulfonamide hydrochloride (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Sumatriptan Molecular Formula: C13H19N3O2S : HCl
Molecular Weight: 281.4 : 36.5
Storage: Store in a cool, dry place.