Ketorolac EP Impurity E

Ketorolac EP Impurity E is chemically (1RS)-5-Benzoyl-N-[2-hydroxy-1,1-bis(hydroxymethyl)ethyl]-2,3-dihydro-1H-pyrrolizine-1-carboxamide (as per EP) ; (5-Benzoyl-N-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl)-2,3-dihydro-1H-pyrrolizine-1-carboxamide) (as per USP). It is also known as Ketorolac USP Related Compound A ; Ketorolac Tris Amide Impurity. Ketorolac EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Ketorolac EP Impurity E can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Ketorolac.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.