Caution: Research Use Only
This substance is for laboratory research and analytical use only. Not for human or veterinary consumption.
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Apixaban Chloro Impurity (CAS 2029205-64-7) is a critical analytical reference material utilized in the pharmaceutical industry. It is chemically identified as a chloro-substituted derivative of the anticoagulant drug Apixaban. In the context of pharmaceutical manufacturing, it serves as a vital tool for ensuring the safety and efficacy of the final active pharmaceutical ingredient (API).
In the Indian pharmaceutical sector, this compound is essential for R&D laboratories and quality control departments focused on generic drug manufacturing. As India continues to be a global hub for API production, the demand for high-quality, certified impurity standards has grown significantly to meet stringent international regulatory requirements set by bodies like the USFDA and EDQM.
When procuring this chemical, buyers should prioritize suppliers who provide a comprehensive Certificate of Analysis (CoA) including NMR, Mass Spectrometry, and HPLC data. It is recommended to source from reputable manufacturers who maintain rigorous documentation and offer stable, temperature-controlled shipping to ensure the integrity of the reference material.
Apixaban Chloro 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 Chloro 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 purposes only.
Yes, all our impurity standards are provided with a full CoA including HPLC, NMR, and Mass Spec data.
It is recommended to store the product at -20°C in a dry, dark place to maintain stability.
Yes, it is specifically designed for the development and validation of analytical methods to detect impurities in Apixaban.
It is often referred to as a USP impurity; please verify the specific monograph requirements before purchase.
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