It is a nitrosamine impurity that can form during the synthesis, storage, or handling of Ciprofloxacin, a widely used antibiotic.

Regulatory agencies like the FDA and EMA strictly control nitrosamines, including N-Nitroso Ciprofloxacin, due to potential health risks.

It forms when Ciprofloxacin interacts with nitrosating agents, particularly under heat, moisture, or acidic conditions.

By controlling storage conditions, managing pH levels, and routine testing.

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

Chemicea supplies 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 standards required by major agencies like USFDA, EMA, ANVISA, TGA, PMDA, and others.

N-Nitroso Ciprofloxacin is stable for shipping at room temperature, with specific storage guidelines provided in the COA.

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

Chemicea provides N-Nitroso Ciprofloxacin as a reference standard, supporting method validation, impurity analysis, and regulatory compliance.