Alvimopan - Isotope Labelled Standards

Analyzing impurities in Alvimopan is critical to ensure drug safety and effectiveness. The impurities can affect drug quality, stability, and safety reducing its efficacy or causing harm to patients. Analyzing impurities can help identify their sources, enabling manufacturers to control their formation.

Manufacturers can take various steps to control impurity levels in Alvimopan, including using high-quality starting materials, optimizing reaction conditions, implementing effective purification techniques, and monitoring impurity levels throughout the manufacturing process.

Methanol is a solvent used in analyzing many impurities in Alvimopan.

Alvimopan impurities are stored at a controlled room temperature between 2-8 °C or as indicated on the Certificate of Analysis (CoA).