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Synthesizing Cisatracurium impurities helps identify and quantify the impurities present in Cisatracurium besylate, a neuromuscular blocking agent used during surgery. It is essential for quality control and ensuring the safety and efficacy of the drug.
The detection and quantification of Cisatracurium impurities typically involve analytical techniques such as high-performance liquid chromatography (HPLC), liquid chromatography-mass spectrometry (LC-MS), etc.
Methanol, DCM (Dichloromethane), or DMSO (Dimethyl sulfoxide) are the solvents used based on the impurity profile of Cisatracurium and its impurities.
Cisatracurium impurities storage is at a controlled room temperature between 2-8 ⁰C. However, impurities such as Cisatracurium Besylate EP Impurity-Q are stored at -20 ⁰C as per the stability of the compound.
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