Why would you think I'd be interested in that?
Ghislain
Why would you think I'd be interested in that?
Ghislain
So dmt extractions,
well its not at all as difficuld as it seems, its just a basic acid base extraction, not allot of time is needed to make it at all, my i stress that this article is for educational purposes only as dmt is ilegal in most of the world,
swim takes about 100gr of source material, using MHRB will be best as it contains a good amount,it is put in a pot, and vinagar and water 50/50 is added , about 1.5L this is simmerd for 4 hours,
the solution is filterd and the process repeated 1 time, this will give about 3L of solution,
slowy the slolution is simmerd of, untill swim has about 1L of liquid,
a concentrated solution of NaoH is made and added to bring the ph up to 14, (yes it needs to be this high) when this is done it will from white strance and it will become soja souce color black, the solution is set on a heat source (electric) so it will meantain hot during the rest of the extraction.
some naptha is warmed up in a hot water bath, make it as hot as swim can, then add it to the solution about 200ml and slowly mix the stuff by slowly shaking the pot, swim must make sure the naphta will be in contact with all of the solution. seperate the naptha from the solution after 30min then repeat 4x increasing the time the naptha sits in there by 15min etch time,
the naptha is all collected having about 800ml of naptha, then distill of the naptha until swim has about 50/100ml left, take it out and but it in a glas wide neked jar, and let it cool, it will become white when cooled, swim must put this in the freezer as cold as swim can get and then let it sit for 12-24hrs, after that swim cancollect wonderful white crystals by shaking the jar and then filtering it through filter paper drying the the jar and and whats in the filter paper, yeilds are between 1.5-2%
the resulting crystals can be recrystalized using IPA, to get rid of excess naptha,
be sure to distill the naptha before use, and be sure not to use open fire, thats it..
kind regards
###dmt is hyperspace fuel###
Last edited by Wigwamman; 03-11-2016 at 01:03 PM.
Question for any that can answer: In almost all the basifying steps I've read here and The Nexus, everyone seems to use NaOH. My question is, has anyone used or tried potassium carbonate or other such alternatives to see if its the same? Likewise, I've read that one can use any acid of their choice, though acetic is the go-to, supposedly citric, phosphoric, and hydrochloric as well as others work with the same proficiency; has anyone hypothetically () experimented to find out for sure, and if so is it still the same basic premise? (and thus less to do with the actual reagents and more to do with the general nature of the solvent structuring of acid/base, polar/non-polar etc)
~Seth-Ra
Kyrie eleison.
I would imagine it is a case of what has worked safe and well in the past Seth.
I don't think it takes a particular acid or base, but acetic acid is recommended in all the texts I have seen so far, as is NaoH for the base. The reason, I believe, is that this is the healthiest option, but that belief has no academic basis.
If handled carefully, none of the acid or base ends up in the final product anyway.
I think gentle mixing is the order of the day, because the materials used are not far from those used to make soap, and I believe that is what happens if vigorous mixing is applied; I could be totally wrong
Good luck with your search.
Ghislain
Thank you for the response Ghislain.![]()
Well I theoretically have plenty of acetic acid and lye on hand, so I'd not deviate from the known process and waste materials experimenting on the first few run throughs.
If someone were to end up, after the first pull of an A/B extraction process, with a white, almost semen-like gum, would that just need to be acid dissolved again, and defatted, basified and re-extracted?
I read where one said it just needed to be dried, powdered fine, and continued to dry - but I'd imagine one would want to just re-extract and de-fat it. (I assume it would be a fat-content problem from the plant, which theoretically would be acacia confusa; as there's more info and recommended de-fatting for mimosa but not as much intel on the acacia hence the uncertainty of whether de-fatting was even necessary.)
Gentle mixing is indeed the name of the game.
~Seth-Ra
Kyrie eleison.
So....
Xylene and fumeric acid ey....
The future of DmT extraction ey....
If at first you don't succeed....
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