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Acacia confusa

cassss

Rising Star
Hello All đź‘‹
I am just wandering how you extract dmt from acacia confusa I have 2kgs and make the tea with moai but I would like to give extraction a crack
Thanks everyone
 
What's wrong with NMT? I for one quite like Acacia, to me it's much more sacred and mystical than Mimosa (even though Mimosa works fine), there's something special about Acacia Confusa, but i usually do all my work orally. I find NMT to be a much welcome addition to my Tryptaminergic supplementation lol, it's also an endogenously produced compound btw.
 
What's wrong with NMT? I for one quite like Acacia, to me it's much more sacred and mystical than Mimosa (even though Mimosa works fine), there's something special about Acacia Confusa, but i usually do all my work orally. I find NMT to be a much welcome addition to my Tryptaminergic supplementation lol, it's also an endogenously produced compound btw.
It appears that some folks have a tendency to extrapolate their personal preferences as universal truth, or at least to articulate it as such.
 
It appears that some folks have a tendency to extrapolate their personal preferences as universal truth, or at least to articulate it as such.

I just wonder like, is it something with the effects or is it just to do with it being considered an impurity when trying to get pure DMT crystals? Personally for me, for smokeable DMT, i do quite like how cleanly pure white DMT crystals vape, but when i first started out i made a crude freebased extract from both Mimosa, as well as Acacia, using the washing soda and heated 99% iso alcohol thing, and even for being a crude extract, it was nice being able to experience a more "full spectrum" feel from the Mimosa and Acacia. I like both oil and crystals though, i certainly don't mind some oil, i usually go for Changa anyways so it all works out either way lol.
 
I have worked with confusa quite a bit.
I found the best method is to back salt the solvent washes from a regular S2B, defat, rebase and and then perform new solvent washes and freeze precip.
This results in very dry white crystals from confusa.
 
I have worked with confusa quite a bit.
I found the best method is to back salt the solvent washes from a regular S2B, defat, rebase and and then perform new solvent washes and freeze precip.
This results in very dry white crystals from confusa.
Do you think you might be able to explain the extraction process you describe above or provide a link to one that works well. I was just given 500g of acacia confusa and I'd rather not waste much on experimentation. Up until now, I've only ever extracted Mimosa hostilis using STB (using NaOH (lye) + NaCl (table salt)) and Heptane (Bestine) since I'm on the west coast, naphtha is difficult to source inexpensively).
 
Do you think you might be able to explain the extraction process you describe above or provide a link to one that works well. I was just given 500g of acacia confusa and I'd rather not waste much on experimentation. Up until now, I've only ever extracted Mimosa hostilis using STB (using NaOH (lye) + NaCl (table salt)) and Heptane (Bestine) since I'm on the west coast, naphtha is difficult to source inexpensively).
Hi, using ACRB will be broadly similar to your previous extractions, but may produce goo.
 
Acrb extraction, so on my acid wash i can planely see fats/oils on the surface of the acid cook. As a chef we de poulage or skim the fats off. Can I, should I remove this deep red oil?? Keeping it would certainly mess up my crystalization phase??
 
Acrb extraction, so on my acid wash i can planely see fats/oils on the surface of the acid cook. As a chef we de poulage or skim the fats off. Can I, should I remove this deep red oil?? Keeping it would certainly mess up my crystalization phase??
Hi, welcome to the Nexus!

Using naphtha to defat might be more reliable, but it would still be interesting to see the results of simply physically skimming the oil off. If you do, set it to one side to check how it behaves. Be sure to let us know how the exraction goes, and good luck!
 
Thank you for the welcome. I kept it in. I didn't want to risk my yield.
No yield is risked if you keep hold of it in line with the Golden Rule of extracting ;)

All good, either way - you're just more likely to have an oily or gooey product this way.

For future reference, the actives will remain dissolved in the acidic water - oily material is highly unlikely to contain any significant amount of DMT under acidic conditions.
 
I did end up skimming it. So Ill let you know how that goes. I have it separated just for my curiosity. Maybe it will help the over all quality and the stability of the crystals.
 
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