Laboratory Research Use Only
This substance is for R&D purposes only and may cause irritation. Handle with appropriate personal protective equipment.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water.
Alfuzosin EP Impurity E is a specific chemical derivative used primarily as a reference standard in the pharmaceutical industry. As a key impurity associated with Alfuzosin Hydrochloride, an alpha-1 adrenergic blocker used to treat benign prostatic hyperplasia, this compound is critical for manufacturers to monitor and control during the drug synthesis and formulation process.
In the Indian pharmaceutical sector, which serves as a global hub for generic drug manufacturing, the demand for high-quality analytical standards is significant. Indian R&D laboratories and quality control departments utilize this impurity to validate analytical methods, ensuring that final drug products meet stringent international regulatory requirements for purity and safety.
Procurement of this chemical requires sourcing from certified suppliers who provide a Certificate of Analysis (CoA) and analytical data such as NMR and HPLC spectra. Buyers should ensure the material is stored under controlled conditions to maintain its stability and integrity, as it is intended strictly for laboratory and research use, not for human consumption.
Alfuzosin 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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Alfuzosin 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 strictly for laboratory and research purposes.
Yes, every batch is supplied with a comprehensive CoA including HPLC, NMR, and Mass Spectrometry data.
It should be stored in a tightly sealed container at 2-8°C, protected from light and moisture.
Yes, it is specifically designed for use in HPLC method validation and routine impurity monitoring in pharmaceutical QC labs.
It is an EP (European Pharmacopoeia) impurity standard, which is widely accepted and utilized by Indian manufacturers for export-oriented quality control.
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