It is a nitrosamine impurity that can form during the synthesis, storage, or handling of Bupropion, commonly used in pharmaceuticals.

It is subject to strict guidelines from regulatory bodies like the FDA and EMA to ensure safe levels in medications.

It forms when Bupropion interacts with nitrosating agents, especially under conditions involving heat, moisture, or acidity.

Through the use of appropriate materials, optimized storage conditions, pH control, and routine testing.

Techniques like GC-MS (high sensitivity), LC-MS (accurate measurement), and HPLC-MS (flexible analysis) are employed.

Chemicea provides COA, H-NMR, MASS, HPLC, and TGA reports as standard, with additional reports like CNMR, IR, UV, DEPT, Water content, and CHNS available upon request.

Yes, they meet the standards of USFDA, EMA, ANVISA, TGA, PMDA, and other global health agencies.

N-Nitroso Bupropion is stable for shipping at room temperature, with specific storage requirements detailed in the COA.

Yes, both standard and customized pack sizes are available to meet specific client needs.

Chemicea provides N-Nitroso Bupropion as a reference standard, aiding in method validation, impurity analysis, and regulatory compliance for quality control.