(2R,3R,4R,5R)-5-(4-Amino-2-oxopyrimidin-1(2H)-yl)-2-((benzoyloxy)methyl)-4-fluoro-4-methyltetrahydrofuran-3-yl Benzoate
Sofosbuvir Impurity 30 is listed by Simson Pharma as a impurity standards for laboratory research, analytical development and quality-control workflows.
Suitability is method- and purpose-specific. Before use, verify the product name, catalogue number, chemical identifiers, storage requirements and the information reported in the current product or batch documentation. Your laboratory remains responsible for method qualification or validation.
Sofosbuvir Impurity 30 for method validation Sofosbuvir Impurity 30 reference standard Sofosbuvir Impurity 30 for ANDA filing Sofosbuvir Impurity 30 for forced degradation studies Sofosbuvir Impurity 30 identification standard Sofosbuvir Impurity 30 for DMF filing Sofosbuvir Impurity 30 HPLC standard Sofosbuvir Impurity 30 supplier Sofosbuvir Impurity 30 manufacturer Sofosbuvir Impurity 30 distributor
