Category:
Pharmaceutical Excipients
CAS NO:
/
Standard:
USP,
Capecitabine impurity M is a critical synthetic intermediate and degradation product associated with the production of the oncology drug Capecitabine. It serves as a reference standard for quality control in pharmaceutical manufacturing to ensure purity compliance.
Strictly store under inert atmosphere at controlled temperatures below 25°C. Personnel must utilize appropriate PPE including gloves and respirators due to potential cytotoxicity. Do not use for clinical administration; intended solely for laboratory research and industrial quality assurance.