Tranylcypromine - Isotope Labelled Standards

Impurity profiling plays a vital role in enhancing Tranylcypromine preparation processes as it aids in the identification of the root causes of impurity formation. It minimizes impurities and enhances the overall quality of the Tranylcypromine product.

The analysis of impurities in Tranylcypromine presents several challenges, including the need for susceptible analytical methods and the potential variability in impurity levels across different batches.

Process-related impurities in Tranylcypromine are generated during preparation, while product-related contaminants occur due to degradation during the storage or handling of the drug product.

Tranylcypromine Impurities should be stored at a controlled room temperature between 2-8°C or as indicated on the Certificate of Analysis (CoA).