Candesartan EP Impurity A Price & Suppliers in India
CAS: 139481-58-6Safety Information
Harmful if swallowed
May cause skin irritation and serious eye irritation. Handle with appropriate laboratory safety equipment.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
AboutCandesartan EP Impurity A
Candesartan EP Impurity A, chemically identified as Candesartan Ethyl Ester, is a critical reference material in the synthesis and quality assurance of the antihypertensive drug Candesartan Cilexetil. It serves as a key marker for monitoring the purity and degradation pathways of the final active pharmaceutical ingredient (API).
In the Indian pharmaceutical landscape, this compound is highly sought after by R&D laboratories and API manufacturing units located in hubs like Hyderabad, Ahmedabad, and Mumbai. It is vital for companies aiming to export finished formulations to regulated markets that require strict adherence to EP and USP monograph specifications.
When procuring this chemical, buyers should prioritize suppliers who provide a comprehensive Certificate of Analysis (CoA) including NMR, Mass Spectrometry, and HPLC data. Given its sensitivity, sourcing from ISO-certified manufacturers or specialized analytical reagent distributors is recommended to ensure batch-to-batch consistency and regulatory traceability.
Applications & Industries
Price in IndiaCandesartan EP Impurity A
Candesartan 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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Frequently Asked Questions
What is the price of Candesartan EP Impurity A in India?
Candesartan 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.
Is this product suitable for HPLC analysis?
Yes, our Analytical Grade is specifically qualified for HPLC and other chromatographic validation methods.
Does it come with a Certificate of Analysis?
Yes, every batch is supplied with a comprehensive CoA including structural verification data.
What is the primary use of this impurity?
It is used as a reference standard to identify and quantify impurities in Candesartan Cilexetil API batches.
Can it be stored at room temperature?
While stable for short periods, long-term storage at 2-8°C is strictly recommended to prevent degradation.
Is this available in bulk for commercial synthesis?
Yes, we offer bulk quantities in HDPE drums for pharmaceutical manufacturing requirements.
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