Laboratory Use Only
This substance is for research and development purposes only. It is not intended for human consumption or clinical use.
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Skin: Wash thoroughly with soap and water.
Apixaban Morpholine Lactum Impurity (CAS 545445-44-1) is a critical reference material utilized in the pharmaceutical industry to ensure the safety and efficacy of Apixaban, a widely prescribed anticoagulant. As a specific degradation or process impurity, it serves as a benchmark for analytical laboratories to monitor the purity profile of active pharmaceutical ingredients (APIs) during synthesis and stability testing.
In the Indian pharmaceutical sector, which serves as a global hub for generic drug manufacturing, this impurity is essential for compliance with stringent regulatory standards set by the CDSCO, USFDA, and EDQM. Indian manufacturers of anticoagulants rely on high-grade reference standards to validate their analytical methods, ensuring that final drug products meet international pharmacopeial requirements for impurity limits.
Procurement of this chemical requires careful attention to the Certificate of Analysis (CoA) and the availability of supporting documentation such as NMR, Mass Spectrometry, and HPLC data. Buyers should source from reputable suppliers who provide stable, well-characterized material, as the accuracy of pharmaceutical quality control depends heavily on the integrity of these reference standards.
Apixaban Morpholine Lactum Impurity 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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Apixaban Morpholine Lactum Impurity 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 research and quality control only.
Yes, every batch is supplied with a comprehensive CoA including HPLC, NMR, and Mass Spectrometry data.
It should be stored in a freezer at -20°C, protected from light and moisture to maintain stability.
Yes, it is specifically designed for use in method development and validation for pharmaceutical impurity testing.
Bulk quantities are available upon request for research institutions and pharmaceutical manufacturers.
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