This impurity is related to Levonorgestrel Hydroxylation 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 Hydroxylation Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(E)-2-ethyl-3-hydroxy-2-(2-(6-methoxy-3,4-dihydronaphthalen-1(2H)-ylidene)ethyl)cyclopentan-1-oneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Levonorgestrel Molecular Formula: C20H26O3
Molecular Weight: 314.4
Storage: Store in a cool, dry place.