Harmful if swallowed
This substance may cause skin irritation and serious eye irritation. Handle with appropriate laboratory safety gear.
Eyes: Rinse cautiously with water for several minutes.
Skin: Wash with plenty of soap and water.
Azithromycin EP Impurity F (CAS 612069-28-0) is a specific degradation product and process-related impurity of the macrolide antibiotic Azithromycin. In the pharmaceutical industry, it is classified as a critical reference standard required for the validation of analytical methods, particularly High-Performance Liquid Chromatography (HPLC) assays used in quality control laboratories.
In the Indian pharmaceutical sector, which is a global hub for generic drug manufacturing, this impurity is vital for R&D and QC departments. Indian manufacturers of Azithromycin APIs and formulations utilize this standard to perform rigorous impurity profiling, ensuring that their products meet stringent international regulatory requirements, including those set by the EP and USP, for export and domestic distribution.
Procurement of this chemical requires careful attention to the Certificate of Analysis (CoA) and the availability of supporting documentation like NMR, Mass Spectrometry, and IR spectra. Buyers should source from reputable suppliers who provide stable, cold-chain logistics to maintain the integrity of the compound, as it is sensitive to temperature and environmental fluctuations.
Azithromycin EP Impurity F pricing in India depends on grade, order quantity, and delivery location, and it moves with market conditions — so a single fixed price is rarely accurate for a specific requirement.
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Azithromycin EP Impurity F prices in India vary by grade, order quantity and delivery location, and move with market conditions. To get the current price for your requirement, submit an enquiry on Chemical Dekho and receive verified quotes from suppliers and manufacturers within 24 hours.
Yes, this is specifically manufactured to meet European Pharmacopoeia standards for impurity profiling.
Yes, every batch is supplied with a comprehensive CoA including HPLC, NMR, and Mass Spectrometry data.
It is highly recommended to store the product at -20°C in a tightly sealed amber vial to prevent degradation.
Yes, it is intended for use as a reference standard in routine QC testing for Azithromycin API production.
We provide quantities ranging from milligrams for research to larger batches for industrial R&D labs.
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