extraction

I have never extracted DMT before, and whenever I read TEKs, I find myself most hung-up on the evaporation step (if applicable). I wonder how to do it, practically. First of all, I wonder what temperature to have; though that would depend on the non-polar solvent used, so I guess I can just...

So I read the Lazymans Tek and saw that he had gotten 1g out of a Lb of rootbark his first pull which is way to little. Try this. Put 2Kg powdered root bark in bucket, Add three pounds lye and a gallon of water, Stir 3 to 5 min the high amount of lye will cause the water to get extremely hot and...

Is there any limit to how concentrated one could get the acid pulls from MHRB? I suppose the lower the volume, the easiest it should be to actually pull the compounds of interest with non-polar solvent after basifying, but is there a maximum level of thickness/viscosity I should stay clear of?

The most neon yellow DMT I ever extracted. Probably lots of Oligomer going on since I heated the solution to 65C on my hotplate stirring bar. With the knowledge from the thread from Loveall I will not do that again. 26C max heating with silvent solvent on top (that has a boiling point of only 32C.

Main purpose of this TEK is to have emulsion-free procedure which leads from cactus matter to pure white mescaline when followed properly. This TEK is based on this topic describing emulsion-free procedure for initial extraction and adds salting/titration and further purification. So now it can...