Caution: For Laboratory Use Only
This substance is for research and analytical purposes only. It may be harmful if swallowed, inhaled, or absorbed through the skin.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
Bumetanide EP Impurity D (CAS 153012-65-8) is a specific chemical derivative utilized as a reference standard in the pharmaceutical industry. It serves as a critical marker for monitoring the synthesis and stability of Bumetanide, a potent loop diuretic used in the treatment of edema associated with congestive heart failure and renal impairment.
In the Indian pharmaceutical landscape, this impurity is essential for R&D laboratories and quality control departments of API manufacturers. As India continues to strengthen its position as a global hub for generic drug manufacturing, the demand for high-quality, certified reference standards to comply with European Pharmacopoeia (EP) guidelines has grown significantly.
Procurement of this chemical requires careful attention to analytical documentation, including Certificate of Analysis (CoA) and HPLC chromatograms. Buyers should source from reputable suppliers who provide stable, cold-chain-compliant shipping to ensure the integrity of the reference material upon arrival at the facility.
Bumetanide EP Impurity D 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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Bumetanide EP Impurity D 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 product is manufactured to meet the specifications defined for Bumetanide Impurity D in the European Pharmacopoeia.
Each shipment includes a Certificate of Analysis (CoA), HPLC report, and MSDS.
It should be transported in temperature-controlled packaging (2-8°C) to prevent degradation.
This is an analytical reference standard and is not intended for direct clinical or therapeutic use.
Lead times vary by supplier; however, most analytical standards are available ex-stock or within 1-2 weeks.
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