Ketorolac impurities include synthetic intermediates, degradation products, and structurally related analogs that may arise during manufacturing, formulation, or storage. As a potent NSAID of the pyrrolizine carboxylic acid class, impurity profiling is essential to ensure safety, efficacy, and compliance with ICH guidelines. All impurity compounds are structurally characterized and qualified for toxicological relevance.
We offer pharmacopeial and non-pharmacopeial Ketorolac impurity compounds that conform to European Pharmacopoeia (EP) specifications. These standards support method development, impurity profiling, and stability studies. EP traceable compounds are available upon request and are supplied with validated analytical data including HPLC purity, NMR, and MS characterization.
Our catalog includes a wide range of Ketorolac-related compounds, including positional isomers, hydroxylated metabolites, and synthetic intermediates. These are used in forced degradation studies, impurity identification, and toxicological qualification. All entries are supported by comprehensive analytical documentation and meet international regulatory expectations.
Ketorolac impurity reference standards are supplied with validated analytical data including NMR, MS, and HPLC purity. These compounds are used in pharmaceutical R&D, method validation, and GMP-compliant quality control. EP/USP traceable entries are available upon request. All products are re-tested at regular intervals to ensure consistency and reliability.
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