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.
Documents
| SDS | |
| COA | |
| Specification | |
| Bulk quote order form | |
| Sample COA |
