Enzalutamide Impurity-G is used in analytical method development method validation quality control testing stability studies regulatory submissions (such as ANDA filings) and routine pharmaceutical manufacturing to ensure the purity and safety of Enzalutamide.

The purpose of Enzalutamide Impurity-G is to serve as a reference impurity standard for monitoring identifying and controlling impurity levels during the manufacture and quality assessment of Enzalutamide drug substances and products.

Enzalutamide Impurity-G is a process-related impurity of the anti-cancer drug Enzalutamide chemically identified as 2-((3-Fluoro-4-(methylcarbamoyl)phenyl)amino)-2-methylpropanoic acid