Caution: For Laboratory Use Only
This substance is for research and analytical purposes only. Not for human consumption or clinical use.
Eyes: Flush with water for 15 minutes and seek medical attention.
Skin: Wash thoroughly with soap and water; remove contaminated clothing.
Cetirizine EP Impurity E, also known as Ethoxycetirizine, is a specific degradation product or synthetic byproduct associated with the manufacturing of the antihistamine Cetirizine. In the pharmaceutical industry, it serves as a critical reference material for analytical testing, ensuring that final drug products meet the stringent purity requirements set by regulatory bodies like the EDQM.
In the Indian pharmaceutical landscape, which is a global hub for generic drug manufacturing, the demand for high-quality impurity standards is significant. Indian API manufacturers utilize this compound to validate their analytical methods, perform stability studies, and ensure that their Cetirizine production processes effectively minimize impurity levels to comply with international pharmacopeial monographs.
Procurement of this impurity standard requires careful attention to the Certificate of Analysis (CoA) and the specific pharmacopeial grade. Buyers in India should source from reputable suppliers who provide detailed documentation, including NMR and mass spectrometry data, to ensure the integrity of their analytical results during regulatory audits.
Cetirizine 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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Cetirizine 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 for laboratory use only.
Yes, every batch is supplied with a comprehensive CoA including HPLC, NMR, and Mass Spec data.
It is recommended to store at -20°C in a moisture-free environment to maintain stability.
Yes, this product is specifically manufactured to meet European Pharmacopoeia (EP) specifications for impurity E.
Yes, we can provide larger quantities upon request for process development and validation studies.
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