So I've read a lot of different teks on the extractions. WTF. Sorry...ok where were we.
Simple a/b, seems simple. But what if we add some logic in the matter. Imagine if you used in the beginning basing a KOH base, already made before the project guys, acidified with sulfuric acid to 7 or 8 maybe 9 here..doesn't matter, re-based with a a softer base lets say ammonium hydroxide..yes it would be more volume of liquid but a finer softer basing..basing is harsh in any a/b...,,then titrate with tartaric acid to p.h. 7 respectively. Let precipitate andand here may be the genius you guys were looking for, after precipitation and dryness, hit with a decolorizing agent solution such as decolorizing carbon or charcoal, filter with vacuum for quickness or just filter..w/e.. and you would have practically pure dmt without any colored impurites. What do you guys think?
Simple a/b, seems simple. But what if we add some logic in the matter. Imagine if you used in the beginning basing a KOH base, already made before the project guys, acidified with sulfuric acid to 7 or 8 maybe 9 here..doesn't matter, re-based with a a softer base lets say ammonium hydroxide..yes it would be more volume of liquid but a finer softer basing..basing is harsh in any a/b...,,then titrate with tartaric acid to p.h. 7 respectively. Let precipitate andand here may be the genius you guys were looking for, after precipitation and dryness, hit with a decolorizing agent solution such as decolorizing carbon or charcoal, filter with vacuum for quickness or just filter..w/e.. and you would have practically pure dmt without any colored impurites. What do you guys think?

