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Each batch is released against an HPLC purity specification, with the exact percentage and chromatogram disclosed on the batch-specific Certificate of Analysis supplied with the order

As described here in the Experimental section in Methods and Results, it has been possible to obtain some estimate of the limiting solubility of niclosamide from nanodrop UV/Vis by evaluating two noisy scans, i.e., one for the blank buffer and one for the niclosamide solution at pH 3.66, where the niclosamide solubility is expected to be its absolute lowest