Ketorolac EP Impurity D

Accelerate your pharmaceutical quality control timelines with premium Ketorolac EP Impurity C reference standards offered by Manasa Life Sciences. Highly sought-after for robust HPLC method development for Ketorolac impurities, this chemical byproduct is essential for precise validation and forced degradation protocols. Formally designated by its IUPAC chemical name as (1RS)-6-Benzoyl-2,3-dihydro-1H-pyrrolizine-1-carboxylic acid, the compound contains a molecular mass of 255.27 g/mol, fits the empirical formula C₁₅H₁₃NO₃, and carries the identification CAS number 1026936-07-1. Our specialized manufacturing facility delivers this high-grade reference material fully verified through extensive QC evaluation, including HPLC, LC-MS, NMR, and IR spectroscopy. Designed to support clean USFDA and EMA filings under explicit ICH directives, this product is backed by a batch-validated CoA and MSDS and handled through our comprehensive GMP and GDP logistics network.