This impurity is related to Erlotinib EP Impurity G 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.
Erlotinib EP Impurity G is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:4-Chloro-6-(2-chloroethoxy)-7-(2-methoxyethoxy)quinazolineCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Erlotinib Molecular Formula: C13H14Cl2N2O3
Molecular Weight: 317.2
Storage: Store in a cool, dry place.