I came here looking for exactly something like this comment. @joseblo How is it that we know that the counterion of the form we are receiving is acetate?
Do we know how the synthesis is purportedly done? Ie, Is it still the original solid phase synthesis using TFA then ion exchange to sub in acetate, or neutralize with NaOH and leave Na… or the hybrid solid/liqiid phase (that I known nothing about other than those words?)
I’m not actually contesting that gray Tirz works for weight, and that the salt in the correct pH solution dissociates to yield the base, but I’m wondering if we’re always receiving the base with the same counter ion or other non-peptide production molecules that might end up in the mix, yet not be visible in HPLC-mass spec purity testing. (Assuming janoshik and the like use HPLC mass spec)
Looking for someone who has looked into this to help me understand, please

I think this is very relevant to @Gr33dyOctopus’ question. Because this could make the soup that we recon a different compound. I am very interested in this because I’m in glps primarily for the less publicized benefits. Also maybe if our subcutaneous pH is not the appropriate pH to free the base, maybe it’s better to buffer the recon…