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Impurities in Ethinylestradiol are identified through comparison with reference standards, spectral analysis, and mass spectrometry to determine their chemical structure and composition.
Stability testing helps monitor impurity levels in Ethinylestradiol formulations during their shelf life to ensure product quality and safety.
Genotoxicity tests help evaluate the potential DNA-damaging effects of impurities in Ethinylestradiol formulations.
Ethinylestradiol impurities are stored at a controlled room temperature, 2-8 °C or according to the Certificate of Analysis (CoA) specifications.
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