Caution: For Laboratory Use Only
This substance is for R&D use only. Not for human or veterinary consumption. Handle with standard laboratory precautions.
Eyes: Flush eyes with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
Atenolol EP Impurity I, also known as Desmethyl Atenolol, is a specific degradation product or synthetic byproduct associated with the manufacturing of the beta-blocker Atenolol. In the pharmaceutical industry, it serves as a critical reference material for analytical testing, ensuring that final drug products meet stringent safety and purity profiles mandated by regulatory bodies.
In the Indian pharmaceutical market, this chemical is primarily procured by Quality Control (QC) laboratories, Contract Research Organizations (CROs), and API manufacturing units. With India being a global hub for generic drug production, the demand for high-quality, certified reference standards is significant to maintain international export standards and domestic regulatory compliance.
Procurement of this impurity requires careful attention to the Certificate of Analysis (CoA) and the availability of supporting documentation such as HPLC, NMR, and Mass Spectrometry data. Buyers should ensure that the supplier provides a stable, well-characterized product, as the integrity of analytical results depends heavily on the purity and traceability of the reference standard.
Atenolol EP Impurity I 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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Atenolol EP Impurity I 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.
Yes, this is manufactured to meet the specifications outlined in the European Pharmacopoeia for Atenolol Impurity I.
Yes, every shipment includes a comprehensive CoA detailing HPLC purity, NMR, and Mass Spec data.
No, this is an analytical reference standard intended for laboratory testing and validation, not for use as an ingredient in drug formulation.
It should be stored immediately at 2-8°C, or at -20°C for extended shelf life, away from direct sunlight.
Yes, we can provide larger quantities for research and development purposes upon request.
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