Laboratory Use Only
This substance is intended for R&D and analytical purposes only. Not for human or veterinary use.
Eyes: Flush with water for 15 minutes; seek medical attention.
Skin: Wash thoroughly with soap and water.
Chlortalidone EP Impurity E (CAS 82875-49-8) is a specialized chemical compound utilized primarily within the pharmaceutical research and quality control sectors. It serves as a critical reference material for laboratories performing impurity profiling and stability testing of Chlortalidone, a widely prescribed diuretic medication.
In the Indian pharmaceutical market, this impurity standard is essential for manufacturers adhering to European Pharmacopoeia (EP) guidelines. It enables rigorous quality assurance processes, ensuring that active pharmaceutical ingredients (APIs) meet stringent regulatory standards before they are released for domestic consumption or international export.
Procurement of this chemical requires sourcing from certified suppliers who provide a comprehensive Certificate of Analysis (CoA) and batch-specific documentation. Buyers should prioritize vendors who maintain cold-chain logistics and offer secure, light-protected packaging to ensure the integrity of the reference material upon delivery.
Chlortalidone EP Impurity E 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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Chlortalidone EP Impurity E 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 reference standard intended for laboratory research and quality control only.
Yes, every batch is supplied with a comprehensive CoA including HPLC purity data.
It should be stored in a freezer at -20°C in its original light-protected packaging.
No, it is specifically for analytical testing and validation purposes.
Yes, it is manufactured to meet the specifications required for European Pharmacopoeia compliance testing.
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