Laboratory Use Only
This substance is for research and analytical purposes only. Not for human consumption or clinical use.
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Azilsartan Ethyl Impurity (CAS 1403474-70-3) is a specific chemical derivative utilized as a reference standard in the pharmaceutical sector. It is chemically identified as the ethyl ester form of the active pharmaceutical ingredient Azilsartan, a potent angiotensin II receptor blocker used in hypertension treatment.
In the Indian pharmaceutical landscape, this compound is essential for R&D laboratories and quality control departments. It is primarily used to identify and quantify potential impurities during the synthesis and stability testing of Azilsartan-based formulations, ensuring that final drug products meet stringent regulatory requirements set by the CDSCO and international bodies.
Procurement of this impurity requires careful attention to purity certificates and analytical documentation. Buyers should source from reputable suppliers who provide a comprehensive Certificate of Analysis (CoA) including NMR, Mass Spectrometry, and HPLC data to verify the structural integrity and purity of the batch.
Azilsartan Ethyl Impurity 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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Azilsartan Ethyl Impurity 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.
No, this is an analytical impurity standard intended strictly for laboratory research and quality control.
We provide a Certificate of Analysis (CoA), HPLC chromatogram, and MSDS with every shipment.
It is recommended to store this at -20°C in a dry, dark place to maintain stability.
Yes, it is specifically designed for use as a reference marker in HPLC method validation.
Bulk quantities are available upon request for process development, subject to lead time.
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