This impurity is related to Eprosartan USP RC 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.
Eprosartan USP RC A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(E)-3-(2-Butyl-1H-imidazol-5-yl)-2-(thiophen-2-yl-methyl)acrylic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Eprosartan Molecular Formula: NAC15H18N2O2S
Molecular Weight: 290.4
Storage: Store in a cool, dry place.