First i had been blessed by this plant material(acacia confusa)....it s been hard time...
Always ended up with jungle spice...white paste...
Which is powerful in itself but with impurities
Nmt has been the impurity which you have to eject out to be able to crack out the pure dimi....
I m not a chemist but creativity and dmt nexus research got me there ....
What you need :
1/ plant material
2/ acid (i love using acetic acid)
It s sweeter to work with
More easy to handle and SAFE
3/ base ( personal choice is lye aka sodium hydroxide)
4/ naphtha
5/ 2 pipettes
( why i recommend 2 pipettes is because at the final pull you would be using the 2 nd one so tht all the oil /impurities from the previous pull dnt mess with the final one)
Ps: u need more equipments which i did nt mention
Included only the basic so tht i can clearly explain this tek
Procedure:-
1/ u must boil down ur plant material in an acidic ph.....i usually work with ph 3- 4....like 1 bottle of vinegar (5% acetic acid) and 1.5 bottle of water should be an ideal solution to boil it up....i reduce it up to 200 ml...and three times is the magic number to dig most of the magic out the plant material...
Filter off all the plant material....first use thin cloth then use cofee filter too...because the solution is usually really viscous it may hold some of the plant material....cofee filters is the dude...
A small insight about the solution here is tht u converted all the dmt in ur solution into dmt acetate....u became a chemist without even knowing it....
2/ u must now basify ur solution....normally i drop it down to ph 9-10.this convert back the dmt acetate into its freebase form..
A universall indicator is the winner...
3/ prepare an acidic solution in a jar.....use this ratio for vinegar(5% acetuc acid) : 2 parts of water and 1 part vinegar (2:1) ...500 ml would be quite enough...pour 250 ml in two seperate jars ..you ll be using them in awhile....
4/ naphtha pulls.....i usually start with 150ml naphtha....using the same naphtha for each pull..like i said 3 is the magic number....i suspect using the same naphtha reduces the level of impurity highly...
What you have to do is as you pull the first naphtha , insert it in the jar which contain the acidic solution..now you must shake the jar vigorously for like 10 minutes.... What happens actually is all dmt freebase which is in the naphtha pull convert back into dmt acetate....it stays in the acidic solution...and the naphtha can be used back for more pulls... Wash the naphtha in both jars before using back...
5/ re-convert the dmt acetate back to freebase....
After you ve washed all ur naphtha in the acidic solution jars, you are left with 500 ml of acidic solution in which dmt acetate is swimming freely...
You have to basify up this solution back to ph 9-10
What you actually did right here is usually called a reverse defat (mini a/b)
6/ naphtha pulls...USING CLEAN NAPHTHA...
You can now pull the dmt freebase from the basified solution jars using 3 times as magic throughout the experiment....
7/ repeat the reverse defat....
Prepare ur acidic solution in two jars same way u did it at first using same ratio (2:1)
Wash the clean naphtha pull in the jar again ....using the two jars for each pull....
You ll be left once again with an acidic solution which far more cleaner now....
8/ final naphtha pulls......
Collect ur acidic solution from the two jars....
Basify it up to ph 9-10
Pull with 60 ml of naphtha 3 times....
Using CLEAN naphtha and the 2 nd pipette this time
9/ you now have 180 ml of naphtha pull collected in a clean jar....
Unluckily not all the nmt have been seperated till now....
10/ dry ice(solid carbon dioxide)
You should find it in supermarkets or big fridge stores...use cooler bags to handle and store dry ice...because it evaporates really quick and fridge ain t the ideal place to store it...it may frost ur fridge.
Dry ice actually converts all the nmt into nmt carbamate which will drop out of the naphtha pull...
Carefully insert small lumps of dry ice in ur final naphtha pulls...be careful because dry ice will bubble off vigorously in the naphtha jar..when most of the nmt has been converted into its carbamate form...it should drop off the naphtha solution....
But as the dry ice lower the temperature considerably....dmt solid may start dropping too...
The solution is a water bath....
After u have assured tht u ve reacted all the nmt in the solution with dry ice....
U must water bath the jar at a suggested temperature of 40-45 °c...
This should release all the dmt solid trapped in the nmt carbamate...
Let it settle but watch tht ur naphtha solution stays warm because u dnt want to lose dmt yield.....
Then preciously filter off the naphtha from the nmt carbamate using filters.....
U now have a naphtha solutiin which contains only pure magic...
11/ freeze precipitate...
Let ur naphtha solution sit like 24 hr in ur freezer...
After 24 hr take it out of the freezer
Decant off the excess naphtha
Evaporate
And enjoyyyyyyyy
I have forget to mention warm naphtha or use water bath throughout the whole procedure.....i m sorry for my bad english and if i missed something out....
Much love to you all