This impurity is related to Letermovir Impurity 10 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.
Letermovir Impurity 10 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:Ethyl (E)-3-(2-((E)-N'-(2-((E)-3-ethoxy-3-oxoprop-1-en-1-yl)-6-fluorophenyl) -4-(3-methoxyphenyl)piperazine-1-carboximidamido)-3-fluorophenyl)acrylateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Letermovir Molecular Formula: C34H36F2N4O5
Molecular Weight: 618.7
Storage: Store in a cool, dry place.