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The FDA's Category 2 designation means the substance may present significant safety risks when used in compounding and is prohibited in compounded medications pending further evaluation
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A change in clarity is generally the most reliable early sign, since a properly reconstituted and well-stored solution should remain visually consistent throughout its usable life
The standard reconstitution workflow for most research peptides using bacteriostatic water is straightforward: allow the lyophilised peptide vial to reach room temperature, add the appropriate volume of bacteriostatic water using a sterile needle and syringe, swirl gently (do not shake vigorously, as this can cause peptide aggregation or degradation), and allow to stand until fully dissolved
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