We've Moved! Visit our NEW FORUM to join the latest discussions. This is an archive of our previous conversations...

You can find the login page for the old forum here.
CHATPRIVACYDONATELOGINREGISTER
DMT-Nexus
FAQWIKIHEALTH & SAFETYARTATTITUDEACTIVE TOPICS
12NEXT
Most Clean/Natural DMT Tek Questions Options
 
WaterElf1919
#1 Posted : 9/23/2022 3:53:05 AM

DMT-Nexus member


Posts: 7
Joined: 23-Sep-2022
Last visit: 25-Sep-2022
Location: Earth
Hi guys, I'm new to DMT-Extraction and am seeking the most natural/clean/nontoxic/foodsafe tek aviable which still ideally produces crystals so I can have a nice jar of DMT crystal freebase.


I've seen Vinegar, and D-Limonene Being mentioned, and I am 100% ready to use these chemicals as they are both safe for human consumption.

I don't want to use naptha, etc basically I only want to use foodsafe, edible ingredients.

Vinegar
D-Limonene.... What else?

Can someone please post a tek that matches my specifications? Thanks
 

Live plants. Sustainable, ethically sourced, native American owned.
 
_Trip_
#2 Posted : 9/23/2022 6:20:19 AM

DMT-Nexus member

Senior Member

Posts: 625
Joined: 10-Apr-2021
Last visit: 03-Mar-2024
There's a few options vinegar is fine for an acid cook, you could look at ascorbic acid or citric acid or a number of other natural acids.

D-limo is a good choice for a natural solvent.

As for a base material you can look into food grade caustic soda or food grade calcium hydroxide.

Q21Q21's Vinegar/Lime A/B Extraction Tek is probably what you want to look into.
https://wiki.dmt-nexus.m.../Lime_A/B_Extraction_Tek
Disclaimer: All my posts are of total fiction.

 
WaterElf1919
#3 Posted : 9/23/2022 6:10:33 PM

DMT-Nexus member


Posts: 7
Joined: 23-Sep-2022
Last visit: 25-Sep-2022
Location: Earth
While the Q21Q21 guide look alright, I really want pure white DMT crystals.

I'd rather not smoke DMT-acetate (jimjam dmt) as its harsh to smoke.

I want pure white DMT crystals.. "White N-N-Dimethyltryptamine (DMT) is pure DMT."

Any ideas?

I can get Vinegar, D-Limonene, and Hydrated Lime, etc.
 
fink
#4 Posted : 9/23/2022 7:30:00 PM
DMT-Nexus member


Posts: 575
Joined: 03-May-2020
Last visit: 16-Feb-2024
Out of curiosity, is it the possession and handling of the toxic stuff you want to avoid or the chance of residues in your end product? Because it's relatively simple to avoid contamination especially with a re-x to finish.
I don't know much, but I do know this. With a golden heart comes a rebel fist.
 
WaterElf1919
#5 Posted : 9/23/2022 10:27:35 PM

DMT-Nexus member


Posts: 7
Joined: 23-Sep-2022
Last visit: 25-Sep-2022
Location: Earth
fink wrote:
Out of curiosity, is it the possession and handling of the toxic stuff you want to avoid or the chance of residues in your end product? Because it's relatively simple to avoid contamination especially with a re-x to finish.



Both preferably,

I'm thinknig that naptha for example, may crystalize with the DMT, leading to DMT And Naptha combined crystals.

I'd rather not introduce toxins into the DMT product at all.

I'd prefer to stick to using Vinegar, D-limonene, and Hydrated Lime, and still result in 100% White DMT Crystals, can it be done?
 
dreamer042
#6 Posted : 9/23/2022 10:46:15 PM

Dreamoar

Moderator | Skills: Mostly harmless

Posts: 4711
Joined: 10-Sep-2009
Last visit: 16-Mar-2024
Location: Rocky mountain high
It's a tradeoff, if you want the ultra-pure shiny white crystals you'll need to accept the use of hydrocarbon solvents. If you want 100% food safe materials, you'll need to accept a less aesthetically pleasing result.

You can use USP grade materials if you are concerned about impurities in industrial grade. You can also acquire food grade sodium hydroxide. Just because calcium hydroxide is used in food processing, doesn't mean you'd want to eat a spoonful of it.

Limonine works great but you have to salt the alkaloids out and then deal with the conversion process using acetone or ethanol. Anhydrous acetone will generally give decent crystals, but nothing quite as nice as naphtha. Ethanol will always carry some of the base over due to water content and requires quite a bit of effort to get something of reasonably smokable purity.

I managed to get a smokable crystalline material using lime, ethanol, citric acid, and water in a very long multi-day process that was downright tedious. Still nowhere near as nice as naphtha crystals, but with dedication it can be done. I wouldn't recommend it though.

If you choose to go with the old q21 tek here are a few tips:

- Ditch the vinegar, use a pure crystalline acid like citric, ascorbic, fumaric, etc in some clean water (I prefer distilled, but it's not necessary, tap is fine). You don't need to add a lot of acid to the water, a small spoonful to achieve ph 5-6 is fine for our purposes. If you must use vinegar just put a capful or two into some water don't use it straight.

- You don't need to wait 24 hours between pulls, just mix layers thoroughly for a few minutes and let stand till they separate, repeat this 2-3 times for each pull.

- Don't do the boiling down the vinegar step. The heat conversion works poorly, if at all, boiling vinegar is a terribly stinky and caustic process, and smoking the partially converted acetates is really hard on your lungs. Mix the salts with lime and water, make a paste and let it dry, then pull with acetone or ethanol to get properly freebased material.
Row, row, row your boat, Gently down the stream. Merrily, merrily, merrily, merrily...

Visual diagram for the administration of dimethyltryptamine

Visual diagram for the administration of ayahuasca
 
WaterElf1919
#7 Posted : 9/23/2022 11:02:06 PM

DMT-Nexus member


Posts: 7
Joined: 23-Sep-2022
Last visit: 25-Sep-2022
Location: Earth
dreamer042 wrote:
It's a tradeoff, if you want the ultra-pure shiny white crystals you'll need to accept the use of hydrocarbon solvents. If you want 100% food safe materials, you'll need to accept a less aesthetically pleasing result.

You can use USP grade materials if you are concerned about impurities in industrial grade. You can also acquire food grade sodium hydroxide. Just because calcium hydroxide is used in food processing, doesn't mean you'd want to eat a spoonful of it.

Limonine works great but you have to salt the alkaloids out and then deal with the conversion process using acetone or ethanol. Anhydrous acetone will generally give decent crystals, but nothing quite as nice as naphtha. Ethanol will always carry some of the base over due to water content and requires quite a bit of effort to get something of reasonably smokable purity.

I managed to get a smokable crystalline material using lime, ethanol, citric acid, and water in a very long multi-day process that was downright tedious. Still nowhere near as nice as naphtha crystals, but with dedication it can be done. I wouldn't recommend it though.

If you choose to go with the old q21 tek here are a few tips:

- Ditch the vinegar, use a pure crystalline acid like citric, ascorbic, fumaric, etc in some clean water (I prefer distilled, but it's not necessary, tap is fine). You don't need to add a lot of acid to the water, a small spoonful to achieve ph 5-6 is fine for our purposes. If you must use vinegar just put a capful or two into some water don't use it straight.

- You don't need to wait 24 hours between pulls, just mix layers thoroughly for a few minutes and let stand till they separate, repeat this 2-3 times for each pull.

- Don't do the boiling down the vinegar step. The heat conversion works poorly, if at all, boiling vinegar is a terribly stinky and caustic process, and smoking the partially converted acetates is really hard on your lungs. Mix the salts with lime and water, make a paste and let it dry, then pull with acetone or ethanol to get properly freebased material.


THanks for the detailed reply, how can I ensure that solvents/impurities arn't crystalized along with the DMT-white crystals? Thanks

Also I'm fine with keeping it to foodsafe materials, but is there anyway to get Pure white DMT, instead of jimjam DMT, etc?
 
dreamer042
#8 Posted : 9/24/2022 6:12:16 PM

Dreamoar

Moderator | Skills: Mostly harmless

Posts: 4711
Joined: 10-Sep-2009
Last visit: 16-Mar-2024
Location: Rocky mountain high
There will always be teeny tiny traces of whatever solvent you crystallize the material from present within the crystal matrix. This applies even to supplements and medications extracted/synthesized in professional laboratories and really is not a problem. You breathe far more carcinogens stepping outside and breathing the car exhaust in the morning, or filling up at the gas pump, so there is no reason to have an irrational fear of "toxins" in your product. Just follow any of the teks on the wiki properly and you will get a product that is safe for consumption.
Row, row, row your boat, Gently down the stream. Merrily, merrily, merrily, merrily...

Visual diagram for the administration of dimethyltryptamine

Visual diagram for the administration of ayahuasca
 
idontknow11
#9 Posted : 9/24/2022 6:36:38 PM
DMT-Nexus member


Posts: 6
Joined: 08-Aug-2021
Last visit: 05-Feb-2024
Location: Earth, I think
dreamer042 wrote:
It's a tradeoff, if you want the ultra-pure shiny white crystals you'll need to accept the use of hydrocarbon solvents. If you want 100% food safe materials, you'll need to accept a less aesthetically pleasing result.

You can use USP grade materials if you are concerned about impurities in industrial grade. You can also acquire food grade sodium hydroxide. Just because calcium hydroxide is used in food processing, doesn't mean you'd want to eat a spoonful of it.

Limonine works great but you have to salt the alkaloids out and then deal with the conversion process using acetone or ethanol. Anhydrous acetone will generally give decent crystals, but nothing quite as nice as naphtha. Ethanol will always carry some of the base over due to water content and requires quite a bit of effort to get something of reasonably smokable purity.

I managed to get a smokable crystalline material using lime, ethanol, citric acid, and water in a very long multi-day process that was downright tedious. Still nowhere near as nice as naphtha crystals, but with dedication it can be done. I wouldn't recommend it though.

If you choose to go with the old q21 tek here are a few tips:

- Ditch the vinegar, use a pure crystalline acid like citric, ascorbic, fumaric, etc in some clean water (I prefer distilled, but it's not necessary, tap is fine). You don't need to add a lot of acid to the water, a small spoonful to achieve ph 5-6 is fine for our purposes. If you must use vinegar just put a capful or two into some water don't use it straight.

- You don't need to wait 24 hours between pulls, just mix layers thoroughly for a few minutes and let stand till they separate, repeat this 2-3 times for each pull.

- Don't do the boiling down the vinegar step. The heat conversion works poorly, if at all, boiling vinegar is a terribly stinky and caustic process, and smoking the partially converted acetates is really hard on your lungs. Mix the salts with lime and water, make a paste and let it dry, then pull with acetone or ethanol to get properly freebased material.


You mentioned ditching the vinegar for citric acid. What is the logic behind that? Would it also be preferable when extracting rue alkaloids?
 
dreamer042
#10 Posted : 9/24/2022 6:56:49 PM

Dreamoar

Moderator | Skills: Mostly harmless

Posts: 4711
Joined: 10-Sep-2009
Last visit: 16-Mar-2024
Location: Rocky mountain high
Vinegar leaves a gunky residue when evapped. This isn't really a problem when in solution, but if you are trying to isolate a salt it makes things just that much more difficult.

With rue it stays in solution and my understanding is the acetic acid is imperative to Manske working correctly, I could be wrong on that though. I just know that Manske used acetic acid in the original paper.
Row, row, row your boat, Gently down the stream. Merrily, merrily, merrily, merrily...

Visual diagram for the administration of dimethyltryptamine

Visual diagram for the administration of ayahuasca
 
Voidmatrix
#11 Posted : 9/24/2022 7:28:48 PM

DMT-Nexus member

Welcoming committeeModerator

Posts: 4160
Joined: 01-Oct-2016
Last visit: 21-Apr-2024
Waterelf1919 wrote:
I want pure white DMT crystals.. "White N-N-Dimethyltryptamine (DMT) is pure DMT."


This thread should help you decided if you really need to worry about color when it comes to purity.

One love
What if the "truth" is: the "truth" is indescernible/unknowable/nonexistent? Then the closest we get is through being true to and with ourselves.


Know thyself, nothing in excess, certainty brings insanity- Delphic Maxims

DMT always has something new to show you Twisted Evil

Question everything... including questioning everything... There's so much I could be wrong about and have no idea...
All posts and supposed experiences are from an imaginary interdimensional being. This being has the proclivity and compulsion for delving in depths it shouldn't. Posts should be taken with a grain of salt. 👽
 
WaterElf1919
#12 Posted : 9/25/2022 7:24:01 AM

DMT-Nexus member


Posts: 7
Joined: 23-Sep-2022
Last visit: 25-Sep-2022
Location: Earth
I'm still unsure which tek would be best.

I really am thinking that solvents I use wont be able to fully evaporate out of the crystals of DMT.

I'm also not excited about Red JimJam DMT... I dont want the other MHRB alkaloids, I just want pure DMT..
 
ShadedSelf
#13 Posted : 9/25/2022 3:47:07 PM

DMT-Nexus member


Posts: 256
Joined: 22-Aug-2020
Last visit: 18-Apr-2024
This one seems to be the least toxic in terms of materials, you end up with DMT citrate though.
 
downwardsfromzero
#14 Posted : 9/25/2022 9:11:49 PM

Boundary condition

ModeratorChemical expert

Posts: 8617
Joined: 30-Aug-2008
Last visit: 16-Apr-2024
Location: square root of minus one
WaterElf1919 wrote:
I'm still unsure which tek would be best.

I really am thinking that solvents I use wont be able to fully evaporate out of the crystals of DMT.

I'm also not excited about Red JimJam DMT... I dont want the other MHRB alkaloids, I just want pure DMT..

If you want pure white DMT crystals, whatever method you end up using for the initial extraction can be followed up with a recrystallisation from heptane via freeze precipitation. The heptane - assuming it to be of high purity - will not leave any dangerous residue in the crystals. Remnants will evaporate from the surface of the crystals without trace, notwithstanding the vanishingly small amounts of impurities left over from the initially extracted material. If that appears to be a problem, recrystallise again with fresh heptane.




“There is a way of manipulating matter and energy so as to produce what modern scientists call 'a field of force'. The field acts on the observer and puts him in a privileged position vis-à-vis the universe. From this position he has access to the realities which are ordinarily hidden from us by time and space, matter and energy. This is what we call the Great Work."
― Jacques Bergier, quoting Fulcanelli
 
nitrogenaztec
#15 Posted : 10/2/2022 11:07:51 PM
DMT-Nexus member


Posts: 136
Joined: 27-Sep-2022
Last visit: 03-Apr-2024
Location: Space
Has anyone tried something like this?

https://www.frontiersin....89/fbioe.2020.00356/full

Basically, using enzymes to break down cell walls?? It could replace lye, ideally?

Just a thought?

Heres another idea?

Put water on the powder... leave in a dark area to go totally moldy (lol)... then try to extract the DMT using naptha.

Perhaps the mold would degrade the cell walls?
 
Lil Chizz
#16 Posted : 10/3/2022 2:12:00 AM
DMT-Nexus member


Posts: 10
Joined: 01-Oct-2022
Last visit: 30-Oct-2022
I had perfectly acceptable results from naptha. It was xylene and toulene that I ended up avoiding as I always felt like my results were somewhat sullied by them.
 
downwardsfromzero
#17 Posted : 10/3/2022 11:41:11 PM

Boundary condition

ModeratorChemical expert

Posts: 8617
Joined: 30-Aug-2008
Last visit: 16-Apr-2024
Location: square root of minus one
nitrogenaztec wrote:
Has anyone tried something like this?

https://www.frontiersin....89/fbioe.2020.00356/full

Basically, using enzymes to break down cell walls?? It could replace lye, ideally?

Just a thought?

Heres another idea?

Put water on the powder... leave in a dark area to go totally moldy (lol)... then try to extract the DMT using naptha.

Perhaps the mold would degrade the cell walls?

The clean way to do this would be to purchase fungal cellulase, and hope that the tannins in MHRB don't inactivate the enzyme. To get the tannins out of the way you could try extracting the bark with 40% ethanol at 60°C for three hours, which works for some other kinds of plant material - but at least some of the DMT might then end up in the ethanol. And of course, some cultures regard ethanol as intrinsically impure too.

Trichoderma viride is a robust, common mould that produces cellulase, such that attempts to filter a mouldy rue solution have resulted in the coffee filter dissolving within about 20 minutes. It can get a bit tricky if you're trying to tame wild moulds, you don't want to end up with too much gliotoxin in your brew either.

After using cellulase you'd still need to add some kind of sufficiently strong base in order to be able to extract the DMT into the naphtha. The base converts the DMT to its free base form, as well as breaking down the cell walls in the plant material.

Incidentally, some level of cell wall breakdown can be achieved through a couple of freeze-thaw cycles on moistened plant material.

[EDIT: This has set me thinking though; if DMT is sufficiently soluble in its natural salt form directly into 40% ethanol ("80 proof" vodka to you transatlantic heathens Razz), it may be possible simply to add calcium hydroxide to precipitate the tannins as calcium tannate and be left with a crude solution of DMT freebase in the remaining alcohol. This is most definitely worth trying on the test tube level - and I feel confident enough to say that you might as well use a fairly large test tube.]




“There is a way of manipulating matter and energy so as to produce what modern scientists call 'a field of force'. The field acts on the observer and puts him in a privileged position vis-à-vis the universe. From this position he has access to the realities which are ordinarily hidden from us by time and space, matter and energy. This is what we call the Great Work."
― Jacques Bergier, quoting Fulcanelli
 
nitrogenaztec
#18 Posted : 10/4/2022 11:00:57 AM
DMT-Nexus member


Posts: 136
Joined: 27-Sep-2022
Last visit: 03-Apr-2024
Location: Space
downwardsfromzero wrote:
nitrogenaztec wrote:
Has anyone tried something like this?

https://www.frontiersin....89/fbioe.2020.00356/full

Basically, using enzymes to break down cell walls?? It could replace lye, ideally?

Just a thought?

Heres another idea?

Put water on the powder... leave in a dark area to go totally moldy (lol)... then try to extract the DMT using naptha.

Perhaps the mold would degrade the cell walls?

The clean way to do this would be to purchase fungal cellulase, and hope that the tannins in MHRB don't inactivate the enzyme. To get the tannins out of the way you could try extracting the bark with 40% ethanol at 60°C for three hours, which works for some other kinds of plant material - but at least some of the DMT might then end up in the ethanol. And of course, some cultures regard ethanol as intrinsically impure too.

Trichoderma viride is a robust, common mould that produces cellulase, such that attempts to filter a mouldy rue solution have resulted in the coffee filter dissolving within about 20 minutes. It can get a bit tricky if you're trying to tame wild moulds, you don't want to end up with too much gliotoxin in your brew either.

After using cellulase you'd still need to add some kind of sufficiently strong base in order to be able to extract the DMT into the naphtha. The base converts the DMT to its free base form, as well as breaking down the cell walls in the plant material.

Incidentally, some level of cell wall breakdown can be achieved through a couple of freeze-thaw cycles on moistened plant material.

[EDIT: This has set me thinking though; if DMT is sufficiently soluble in its natural salt form directly into 40% ethanol ("80 proof" vodka to you transatlantic heathens Razz), it may be possible simply to add calcium hydroxide to precipitate the tannins as calcium tannate and be left with a crude solution of DMT freebase in the remaining alcohol. This is most definitely worth trying on the test tube level - and I feel confident enough to say that you might as well use a fairly large test tube.]


Amazingly indepth reply Smile I don't know chemistry well enough to understand everything (or maybe i can understand while reading but wont remember what you are saying? its easier to remember something when you already know the field... more "stuff" for the facts to stick to).

Anyhow its just an idea. Thanks very much for the intelligent reply. It would be cool to see someone try this!

 
Homo Trypens
#19 Posted : 10/4/2022 9:38:59 PM

DMT-Nexus member

Welcoming committeeSenior Member

Posts: 560
Joined: 12-Aug-2018
Last visit: 24-Apr-2024
Location: Earth surface
Hmmm. This ethanol/limestone approach sounds like a fun thing to try!

I think i'll do this with 25g of bark. Maybe next weekend :=)
 
downwardsfromzero
#20 Posted : 10/5/2022 5:33:31 PM

Boundary condition

ModeratorChemical expert

Posts: 8617
Joined: 30-Aug-2008
Last visit: 16-Apr-2024
Location: square root of minus one
Homo Trypens wrote:
Hmmm. This ethanol/limestone approach sounds like a fun thing to try!

I think i'll do this with 25g of bark. Maybe next weekend :=)

Awesome! Be sure to let us know how it goes in a thread of its very own.




“There is a way of manipulating matter and energy so as to produce what modern scientists call 'a field of force'. The field acts on the observer and puts him in a privileged position vis-à-vis the universe. From this position he has access to the realities which are ordinarily hidden from us by time and space, matter and energy. This is what we call the Great Work."
― Jacques Bergier, quoting Fulcanelli
 
12NEXT
 
Users browsing this forum
Guest

DMT-Nexus theme created by The Traveler
This page was generated in 0.043 seconds.