((((((R)-1-(6-amino-9H-purin-9-yl)propan-2-yl)oxy)methyl)(((isopropoxycarbonyl)oxy)methoxy)phosphoryl)oxy)methyl diethylcarbamate fumarate
Tenofovir Impurity 13 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.
Tenofovir Impurity 13 for method validation Tenofovir Impurity 13 reference standard Tenofovir Impurity 13 for ANDA filing Tenofovir Impurity 13 for forced degradation studies Tenofovir Impurity 13 identification standard Tenofovir Impurity 13 for DMF filing Tenofovir Impurity 13 HPLC standard Tenofovir Impurity 13 supplier Tenofovir Impurity 13 manufacturer Tenofovir Impurity 13 distributor
