Toxic if swallowed
This substance is a potent alkaloid derivative. Handle with extreme caution using appropriate personal protective equipment.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
Atropine EP Impurity A (CAS 500-55-0) is a dehydration product of Atropine. In the pharmaceutical industry, it is strictly monitored as a process-related impurity or degradation product in Atropine sulfate and related anticholinergic drug substances. Its presence is strictly regulated by pharmacopeial standards (EP/USP) to ensure the safety of finished pharmaceutical products.
In the Indian market, this chemical is primarily sourced by pharmaceutical R&D centers, contract research organizations (CROs), and quality control laboratories of major API manufacturers. Given the stringent regulatory environment in India regarding drug purity, high-grade analytical standards are critical for compliance with CDSCO and international export requirements.
Procurement of this material requires careful attention to the Certificate of Analysis (CoA) and the traceability of the reference standard. Buyers should ensure that the supplier provides comprehensive documentation, including NMR, Mass Spectrometry, and HPLC data, to verify the identity and purity of the impurity standard for regulatory submission purposes.
Atropine EP Impurity A 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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Atropine EP Impurity A 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 purposes only.
Yes, every batch is supplied with a comprehensive Certificate of Analysis including HPLC, MS, and NMR data.
It should be shipped in temperature-controlled packaging (cold chain) to maintain stability.
While it is a chemical standard, it is derived from alkaloids; ensure compliance with local narcotic and psychotropic substance regulations if applicable.
Yes, it is specifically designed for use as a reference standard in HPLC method validation for pharmaceutical testing.
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