This impurity is related to Levonorgestrel Hydrogenation Impurity 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.
Levonorgestrel Hydrogenation Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:13-ethyl-3-methoxy-7,11,12,13,14,15,16,17-octahydro-6H-cyclopenta[a]phenanthren-17-yl acetateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Levonorgestrel Molecular Formula: C22H28O3
Molecular Weight: 340.5
Storage: Store in a cool, dry place.