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The purpose of synthesizing Formoterol impurities is to identify, characterize, and quantify the impurities present in Formoterol drug products. It assesses Formoterol's safety, efficacy, and quality while ensuring compliance with regulatory guidelines.
Formoterol impurities are typically detected and quantified using analytical methods such as high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectrometry (LC-MS).
The polar solvent methanol helps in analyzing Formoterol and its impurities.
Formoterol impurities should be stored at a controlled room temperature between 2-8 ⁰C or as indicated on the Certificate of Analysis (CoA).
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