The purely imaginary method described below does work, but it works really really slow. SWIM's FOAF was able to extract ~100mg freebase alkaloids from 10g of MHRB. This method does not discriminate between the alkaloids that are extracted (j.spice, d., d-Noxide etc etc), this is however a subject of discussion.
The tek:
1) dissolve 5g of citric acid per 100ml acetone
2) take the shredded/powdered bark and cover it with enough citric acid acetone. Incubate in a warm place, gently agitating every so often. After 2-3 hours, filter off the citric-acid saturated acetone extract and set aside (this solution should have acquired the dark reddish colour of MHRB). Repeat 2 more times.
3) saturate acetone with fumaric acid. Acetone can hold ~20mg/ml fumaric acid if let for a day or so to completely dissolve.
4) Add the fumaric acid-saturated acetone in the citric acid-saturated acetone MHRB extract. One cannot put too much.
5) Set it aside and wait for 2-3 days. One should see a yellowish precipitate on the bottom.
NOTE: In step 2 one is making an acetone extraction and at the same time converting the alkaloids their citrate salt. After addition of the fumaric acid-saturated acetone in step 4, there is an interconversion of alkaloid-citrate to alkaloid-fumarate salt, like:
dmt-citrate + fumaric acid <-> dmt-fumarate + citric acid
citric acid has a pKa of 3.13, while fumaric acid's pka is 3.43. Fumaric acid is a weaker acid and thus in the above reaction one should have most of the dmt as a citrate salt and just a tiny amount as a fumarate salt. dmt-fumarate however is totally insoluble in acetone (while dmt-citrate is perfectly soluble), and it precipitates as soon as it forms. The insolubility of dmt-fumarate acts therefore as a "sink" and given time all of the dmt-citrate will eventually convert to dmt-fumarate and precipitate out.
6) wash the precipitated fumarate salts with acetone, then take them out and let them dry.
7) dissolve the alkaloid-fumarate salts in 5ml of tap water, then and then add saturated sodium carbonate to make the solution basic. The alkaloids will be freebased and the solution will become milky. In 3 days they will precipitate out forming nice needle-like crystal in the basic solution. At this stage, one can filter the solution (nasty procedure since the crystals tend to be sticky and waxy) and retrieve any left alkaloids by dissolving them in acetone.
8 ) Let the crystals dry, wash them with acetone (it removes any traces of sodium corbonate which is totally insoluble in acetone), evaporate the acetone and enjoy the product.
For the FOAF of SWIM 30mg were for a good STRONG experience.
Infundibulum wrote:Hold this tek back for a bit; SWIM's FOAF is trying a better version that might have much much better results.
But if SWIY wants to try it as it is, better do it witha 10-20g just to get a feeling for it before jumping to bigger amounts.
SWIM's FOAF does not like this tek that much, it does work however, and it needs some improvements.
so was this better version ever made? anyone tried to research this further? is this tek viable without lab grade products? what are the yelds?
swim is delighted with this tek, the idea of not using lye or strong solvents pleases swims elves a lot!
even if this gets kinda expensive with such a high acetone use, swim is really tempted to try this out!
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