very much appreciated. i'll build a statue in your honor in the dmt world
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TEK "TnT tek" - Vodka DMT extraction for oral use TEK (super easy!)
- Thread starter Ambrosaure
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This topic contain a TEK
I just concluded my second test with this first run (using different batches of caapi) and it appears i messed up somewhere as I can barely feel the dmt at a 7g dose (plus 5g 1hour later). The only variation from the tek was that i couldn't figure out how to effectively filter the sludge, so I just decanted the clear liquid. Otherwise I followed it exactly (leaving the MHRB in vodka for 3 days or so). This was using a known strong batch of MHRB. Any thoughts appreciated, thanks.
"Freebase DMT is highly insoluble in water. Because vodka is 60% water, raising the pH actually forces a large portion of the DMT out of the liquid solution, causing it to trap itself in the sludge at the bottom." Don't know if it's true or not, but this may explain it. That sludge is really not filterable...
"Freebase DMT is highly insoluble in water. Because vodka is 60% water, raising the pH actually forces a large portion of the DMT out of the liquid solution, causing it to trap itself in the sludge at the bottom." Don't know if it's true or not, but this may explain it. That sludge is really not filterable...
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I'm guessing that's a LLM ("AI") output. Practical experience shows that DMT freebase is highly soluble in vodka.
How much lime, proportionally, did you use?
ok, cool. I used 115g of lime. The solubility of dmt in vodka wasn't at question, but the pickling lime converts the dmt into freebase which is hydrophobic, and since vodka is largely water there is a repelling force driving it towards the oils, waxes, solids, etc... That's the theory at least, i know nothing about any of this.
Everything looked exactly like the pictures posted by Ambrosaure. I'm assuming you've read through his write up and all is as it should be. it's a remarkably simple tek, so i'm not sure on how/where it could have gone wrong.
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I'm not sure either. The method still counts as experimental, and @Ambrosaure's version is but one iteration of the overall principles. Did you wash your solids with a bit of extra vodka after the first filtration? The strength of partition into nonpolar material hasn't been determined but the following points all apwly:
- there's not much oil/waxy stuff in MHRB anhow;
- the initial vodka pulls would select against oily material to a large extent; and
- DMT FB really is exceedingly soluble in vodka, so partition into that phase seems favourable.
There may be some requirement to take into account the formation of water from the reaction of hydroxide in the lime with the protons from the DMT salt form and any other protonated bases as well as the various tannins. Even so, it will be an absolute maximum of 16/37 of your lime quantity, or about 1840 × 0.027027… = 23 × 8 × 0.27027… = 23 × 2.16216… = 48.3 + (1.15 + 0.23) + 0.046 + 0.0023 + (0.00115 + 0.00023) + … ≈ 49.73 mL water.
The significance of this depends on the volume of vodka used, and was part of the rationale behind freezing the excess water out of the solution aprés lime treatment - even if that stemmed from a failed attempt at freeze precipitation of the DMT. Water is "less soluble" in the detanninised mimosa tincture than the organic components at freezer temperatures, while it was possible to get already purified DMT to crash as an (ethanol rich?) oil from aqueous ethanol at similar temperatures without ice formation being observed.
But that's its own tangent here, stemming from the aforementioned dilution factor - the impact of which depends on the amount of vodka being used.
Is it possible that the caapi was weak, or have you successfully tested it with a less experimental, more reliable DMT source?
Appreciate those thoughts. I used 2 different batches of caapi tincture (first attempt with yellow caapi and the second with black). I'd tested the black one with my changa and it was highly activated to say the very least
I did NOT do a wash on the sediment. I tried to filter it and things got a bit out of hand. Until some tests can be run I think we may want to at least change some of the wording in the tek writeup relating to importance of the final wash. I'd be happy to do another run at it with that in mind this weekend. Do a few washes at the end and be a bit more focused on the sediment layer.
Both attempts used over 10g each and I felt next to nothing besides the caapi. Which is to say, that most of the dmt must have been hiding in the foliage, at least that's how it appears.
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@Transform @blig-blug
So I ran another batch of this. After the initial soak I filtered out the marc using a nut bag followed by a micro mesh for pour over coffee.
Then I introduced the lime, waited for it to separate, decanted the clear yellow layer, ran the grey muck through the same filtration process (nutbag + pour over mesh). I washed the filtered gunk with another round of vodka and filtered all of that. I combined all the filtered liquid and now have a slightly creamy looking coffee solution not at all transparent. If it let it sit for a bit about 1/4 of it turns transparent at the top. All in all I spent a couple hours filtering....
The solution i now have is thicker than the 1 i had prior to stirring in the lime. Which makes me wonder if there is lime in it, of course, binding things up still. Exactly how much needs to get filtered out? I do not think a paper filter would be possible, the mesh barely was. Some insight here would be deeply appreciated. I followed the directions to the letter (which does not properly address the task of filtering). I'm not sure if i've gone overboard with the filtering process due to concerns or if I should do another round of lime and even more filtering. If the latter, what amount of lime makes sense?
I was hoping to test this tomorrow but it may not be ready (or it's already done and I don't know).
So I ran another batch of this. After the initial soak I filtered out the marc using a nut bag followed by a micro mesh for pour over coffee.
Then I introduced the lime, waited for it to separate, decanted the clear yellow layer, ran the grey muck through the same filtration process (nutbag + pour over mesh). I washed the filtered gunk with another round of vodka and filtered all of that. I combined all the filtered liquid and now have a slightly creamy looking coffee solution not at all transparent. If it let it sit for a bit about 1/4 of it turns transparent at the top. All in all I spent a couple hours filtering....
The solution i now have is thicker than the 1 i had prior to stirring in the lime. Which makes me wonder if there is lime in it, of course, binding things up still. Exactly how much needs to get filtered out? I do not think a paper filter would be possible, the mesh barely was. Some insight here would be deeply appreciated. I followed the directions to the letter (which does not properly address the task of filtering). I'm not sure if i've gone overboard with the filtering process due to concerns or if I should do another round of lime and even more filtering. If the latter, what amount of lime makes sense?
I was hoping to test this tomorrow but it may not be ready (or it's already done and I don't know).
Did you dump the lime in all in one go or add it bit by bit?
It's hard to overemphasise the importance of adding the lime in slow increments. Avoiding an excess of lime is paramount to keeping the separation phase as smooth as possible. You may need to use less lime - and if your current process, as it would appear, now has too much lime in it, you may want to consider 'back-titrating' it with a further amount of bark tincture.
There's an ideal end-point where the intense red colour fades to orage-yellow. Allowing a certain amount of reaction time is also desirable on account of the lime's poor solubility.
It is almost certainly necessary to take into account the natural variation between different batches of bark and thus remain vigilant at this experimental stage for signs of anomalous behaviour.
It's hard to overemphasise the importance of adding the lime in slow increments. Avoiding an excess of lime is paramount to keeping the separation phase as smooth as possible. You may need to use less lime - and if your current process, as it would appear, now has too much lime in it, you may want to consider 'back-titrating' it with a further amount of bark tincture.
There's an ideal end-point where the intense red colour fades to orage-yellow. Allowing a certain amount of reaction time is also desirable on account of the lime's poor solubility.
It is almost certainly necessary to take into account the natural variation between different batches of bark and thus remain vigilant at this experimental stage for signs of anomalous behaviour.
This is not a case of user error as far as I can tell, the tek is incomplete and lacking detail. I added the lime extremely slowly and stopped at 100g. If you look at the pictures by the OP, the only possible outcome of filtering the sediment layer is my current status. No worries, i'm just going to abandon this and start working on something else.
edited: i just looked in on it after letting it sit all night and it has gone through a whole other separation phase. There's 5% of sediment on the bottom and 95% clear yellow solution (about 700ml of clear from total of 1250ml). So, that seems like a possible success to me, what do you think?
I gave the solution about 4 hours to separate after stirring in the lime, initially. It might have made more sense to just do a nut bag strain at that time (4 hours in). wash the filtered weirdness with a bit more vodka. add the wash to the rest of the solution, let it sit overnight, decant + then do a major filtering. That will take longer, but with considerably less effort in terms of straining.
edited: i just looked in on it after letting it sit all night and it has gone through a whole other separation phase. There's 5% of sediment on the bottom and 95% clear yellow solution (about 700ml of clear from total of 1250ml). So, that seems like a possible success to me, what do you think?
I gave the solution about 4 hours to separate after stirring in the lime, initially. It might have made more sense to just do a nut bag strain at that time (4 hours in). wash the filtered weirdness with a bit more vodka. add the wash to the rest of the solution, let it sit overnight, decant + then do a major filtering. That will take longer, but with considerably less effort in terms of straining.
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Maybe, as there isn't an "official" write-up yet. Howeer the tek is quite simple, so I'm not sure what detail may be missing.
While stirring?
I think so. I'd let it sit in the fridge for a while if you are worried about it.
I'm unconvinced filtering the sediment instead of decanting (at first) makes sense at all. I decant (running the clean liquid through a filter just in case) and wash the sediment with fresh vodka afterwards, never filtering the sediment. That takes less than half an hour. If you try this tek again, I recommend doing it that way.
indeed. 20g at a time, stirred for 20 seconds
it's looking crystal clear after my filtration steps, so feeling good about it, thanks.
I think the less lime you use the longer separation takes. I was quite careful this time not too add too much (i used 100g compared to last time at 115g) after waiting a 'couple of hours' i had about 100ml of transparent yellow floating on top. After 4 hours I had about 150ml of transparent yellow. If i had left this to settle overnight at this stage I'm guessing my experience would have been more like yours, maybe. But I wasn't sure that I could leave the lime in for that long. Can i?
well, given your experience I can see why you'd be hesitant. But that hasn't been my experience. And, actually, this is exactly what i did on this run. The problem was that the vast majority of what i was working with was sediment and every wash i performed resulted in a coffee milkshake that then needed to go through another separation and filtration. What process were you using to wash?
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Glad to hear that it turned out okay.
Yes, there is no problem at all.
I just added vodka to the sediment, stirred, and waited again for it to decant. It's surprising that in your case it created a kind of emulsion, in my case it separated quite fast. I wonder if it could be related to different particle size of our lime powder or something like that. It's strange, because the first time I actually used calcium oxide (of a very poor quality) that I converted into calcium hydroxide with somewhat uncertain success, so far from a good quality starting point. And yet it still didn't cause any issue.
I haven't measured how much lime I add, but I'm pretty sure during the first stage (not washing) I add much less than 20g at a time. Next time, I'll measure how much it is, but it's probably just a few grams. In my case it always seems to sink very easily.
Clearly more experimentation is needed to understand what variables cause the difference between getting milkshake-like liquid or it decanting easily.
To make sure, is your vodka around 40% alcohol? I know in the US it can legally be higher, and that could explain the differences.
ok, well, next time I will let it separate overnight. I'm guessing that for you the sediment was a relatively small percentage of the solution?
and just a single washing then? I had some very strange looking sediment in that first filtration after adding the lime, possibly calcium tannate
I'm using Mrs Wages Pickling Lime. After my first batch was a dud, i, admittedly, got paranoid about the sediment holding on to the dmt, and likely got carried away with filtering...
ok, will go even slower next time.
yes, i'm diluting 95% Everclear down to 40% - which i guess is technically different than vodka but same strength. my understanding is that a higher percentage alcohol has a risk of leaving lime behind in the solution...
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saturn_salmon
Rising Star
Hello,
I wanted to thank everyone who contributed to this tek, this is great information and very straightforward. This is the first time a home-brew psychedelic has actually worked for me. I tried this method and got the golden liquid as a result:
I noticed these seems to be a bit of a film on the top:
The smell is part vodka, along with another smell I'm not familiar with (I wouldn't call it a sweet smell, kinda has a chemical smell to it). How would you all describe what the smell should be? My concern is that there is calcium hydroxide in there. Am I being overly paranoid?
Here is what I did:
50g mimosa hostilis root bark
500mL of vodka
I put it on a magnetic stirring hot plate at 60C for 5 hours
in the last hour or so, a significant amount of the brew evaporated off leaving me with about 100 mL
I mixed calcium hydroxide into it, I didn't note how much I used but after a couple hours only about 1 or 2 mL of golden liquid had separated. I decided to double the volume by adding more vodka and let it sit for a while and in the mean time I started another batch. After some time, a good amount of liquid separated from the calcium hydroxide and I was able to use a pipette to remove it.
For the second batch, I kept it on the hotplate for 3 hours 45 minutes, and kept the temperature between 45 and 60 C. About 50 to 100 mL evaporated. I filtered with a steel mesh filter followed by coffee filter, leaving me with 300 mL. I didn't add any calcium hydroxide, just left it as the red brew.
I consumed the equivalent of 4g mhrb of the golden extract with 7g Syrian rue. After an hour or two I felt a definite body high but not a full trip. At this point I was nervous about the chemical smell of the vodka dmt extract and wanted to wait to ask you all about it. I drank about 75 mL of my second brew, equivalent to 25g mhrb and took some more Syrian rue.
I had a powerful body high come on, followed by visuals (the things in the room morphing around). I got super nauseated and threw up after about an hour. The peak was very challenging for 2 hours, I had to focus on my breathing and keep myself calm. After that it mellowed out and I sat on my couch for 4 or 5 hours with my cat as I came down.
I don't ever want to consume the raw brew with the tannins again haha, so next time I want to just use the golden extract. Are there any other steps I can take to make sure it is safe to consume?
edit: I just found this link about washing the solvent:
I think I will try this with the sodium carbonate as @Transform suggested
Thanks again to everybody who has contributed to this.
I wanted to thank everyone who contributed to this tek, this is great information and very straightforward. This is the first time a home-brew psychedelic has actually worked for me. I tried this method and got the golden liquid as a result:
I noticed these seems to be a bit of a film on the top:
The smell is part vodka, along with another smell I'm not familiar with (I wouldn't call it a sweet smell, kinda has a chemical smell to it). How would you all describe what the smell should be? My concern is that there is calcium hydroxide in there. Am I being overly paranoid?
Here is what I did:
50g mimosa hostilis root bark
500mL of vodka
I put it on a magnetic stirring hot plate at 60C for 5 hours
in the last hour or so, a significant amount of the brew evaporated off leaving me with about 100 mL
I mixed calcium hydroxide into it, I didn't note how much I used but after a couple hours only about 1 or 2 mL of golden liquid had separated. I decided to double the volume by adding more vodka and let it sit for a while and in the mean time I started another batch. After some time, a good amount of liquid separated from the calcium hydroxide and I was able to use a pipette to remove it.
For the second batch, I kept it on the hotplate for 3 hours 45 minutes, and kept the temperature between 45 and 60 C. About 50 to 100 mL evaporated. I filtered with a steel mesh filter followed by coffee filter, leaving me with 300 mL. I didn't add any calcium hydroxide, just left it as the red brew.
I consumed the equivalent of 4g mhrb of the golden extract with 7g Syrian rue. After an hour or two I felt a definite body high but not a full trip. At this point I was nervous about the chemical smell of the vodka dmt extract and wanted to wait to ask you all about it. I drank about 75 mL of my second brew, equivalent to 25g mhrb and took some more Syrian rue.
I had a powerful body high come on, followed by visuals (the things in the room morphing around). I got super nauseated and threw up after about an hour. The peak was very challenging for 2 hours, I had to focus on my breathing and keep myself calm. After that it mellowed out and I sat on my couch for 4 or 5 hours with my cat as I came down.
I don't ever want to consume the raw brew with the tannins again haha, so next time I want to just use the golden extract. Are there any other steps I can take to make sure it is safe to consume?
edit: I just found this link about washing the solvent:
I think I will try this with the sodium carbonate as @Transform suggested
Thanks again to everybody who has contributed to this.
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i just tested my second batch with a 5 gram dose (+ 50g caapi) and I'm wondering what level of experience i should be expecting at that dose? I would compare it to 3g of mushrooms, i guess, very mild but not nothing. The ayahuasca experiences I'm accustomed to run around 8-10g mushrooms (not that it's directly comparable in that way). So, not sure if i've got a weak batch or if i'm just used to higher doses.
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The other smell is probably DMT. Even if it had calcium hydroxide, you wouldn't notice that by smell, as it doesn't really smell like much.
Your liquid seems fine to me, although it's cloudier than it has been for me. I'd let it sit for a day to see if something decants and it clears out.
That floating layer appeared for me as well. I don't know what it is, but it's a full spectrum extraction and when I sent it to analyze it was shown to be about 70% different plant substances, so I wouldn't worry about that.
Yes, test the pH. If it's excessively high (it will be basic in any case due to the freebase alkaloids in it), you can add some acid (citric, acetic/vinegar...) until it goes down to a more neutral pH.
Another option is to just dissolve your dose in fruit juice, that should be enough acid to neutralize any potential excess calcium hydroxide. Again, you can test the pH.
If you let it sit for a day and nothing decants, it's unlikely to have any calcium hydroxide. When I sent mine to analyze, no calcium hydroxide was found in it.
I think you may be low on harmalas here. 25g MHRB with proper inhibition is so high (unless the MHRB batch is exceptionally weak) so as to be unadvisable IMO. How did you brew your rue tea?
Hard to know, because caapi varies a lot in potency: I've had batches that were just OK at 80g, and batches that were more powerful than that at 40g. With enough MAO inhibition, 5g should be a solid dose, however not nearly as strong as 8-10g mushrooms (assuming you mean 5g MHRB equivalent), at least not in my experience. Maybe next time up your caapi a bit and try a couple more grams of MHRB equivalent.
Good to see some more experience on this thread. I've got the Calcium Hydroxide ready and waiting, just need cheap Vodka and a bit of MHRB.
