Enzalutamide Impurity-H, PurCert

PurCert


Properties

Assay Purity >=98%
Density 1.203 g/cm3
Form Solid

Safety Information

Hazard Statement(s) H302-H315-H319-H335
Precautionary Statement  P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
GHS Pictogram
Signal word Warning
Flash point 184 °C
Storage Temp. 2-8°C

Description

Application
Enzalutamide Impurity-H is used in analytical method development HPLCUHPLC method validation stability studies impurity profiling regulatory documentation and routine quality control testing of Enzalutamide pharmaceutical products.

Purpose
The purpose of Enzalutamide Impurity-H is to serve as a reference standard for the identification quantification and control of impurity levels in Enzalutamide active pharmaceutical ingredient (API).

General Description
Enzalutamide Impurity-H is a specified process-related impurity or intermediate associated with the synthesis of the antiandrogen drug Enzalutamide and is characterized during impurity profiling studies to ensure product quality and safety.