Ketorolac EP Impurity C

For laboratories conducting meticulous trace-level Ketorolac degradant identification and synthesis-related monitoring, Manasa Life Sciences delivers high-grade Ketorolac EP Impurity D analytical standards. Our high-purity Ketorolac impurity standards ensure absolute accuracy during critical stability testing and batch release protocols. Structurally, the chemical name for this substance is defined as (1RS)-5-Benzoyl-1-methoxy-2,3-dihydro-1H-pyrrolizine-1-carboxylic Acid. It features a unique molecular profile comprising a formula weight of 285.30 g/mol, the distinct molecular formula C₁₆H₁₅NO₄, and it is assigned the registry CAS number 1391053-45-4. We prioritize complete analytical transparency; thus, each batch is comprehensively characterized via state-of-the-art HPLC, LC-MS, NMR, and IR instrumentation. To facilitate seamless alignment with international USP and EP pharmacopeias, our GMP and GDP workflows ensure you receive a pristine substance complete with a transparent CoA and MSDS to satisfy strict USFDA and EMA regulatory audits under the latest ICH guidelines.