4-(5-((2-Chloroethyl)(2-((2,3-dihydroxypropyl)thio)ethyl)amino)-1-methyl-1H-benzo(d)imidazol-2-yl)butanoic acid
Bendamustine Impurity 17 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.
Bendamustine Impurity 17 for method validation Bendamustine Impurity 17 reference standard Bendamustine Impurity 17 for ANDA filing Bendamustine Impurity 17 for forced degradation studies Bendamustine Impurity 17 identification standard Bendamustine Impurity 17 for DMF filing Bendamustine Impurity 17 HPLC standard Bendamustine Impurity 17 supplier Bendamustine Impurity 17 manufacturer Bendamustine Impurity 17 distributor
