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Deciding on a DMT extraction Tek for my first time

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Madhattress said:
Loveall said:
Toluene is less stinky, but I guess you have xylene from Kash's A/B already.

Simply dump a teaspoon of benzoic acid into the xylene. It dissolves and
DMT xtlas precipitate out. BS recommended freezer xtalization.

Essentially it is like a CIELO solvent/acid combo but for DMT.


Benzoic acid is easy to find. It is used in the food and cosmetic industry.
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So after doing a pull with Xylene i would add benzoic acid and then a freezer precipitation or evaporate? And how many pulls should be done at how many ml of xylene for a 50g mhrb extraction?


How much benzoic acid would one use?

Sorry for all the questions just want to understand for if i do this.
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No evaporation. About a teaspoon per quart of xylene/toluene is plenty. It will cloud/crash at room temperature, to fully crash it all put in the freezer per BW (now BS, sorry). However, time alone also helps crash it well at room temp.
 
_Trip_ said:
One thing i forgot to mention, the solvent (Benzine/ naphtha etc) will still hold on to some dmt even at -20c in the freezer. Granted it'll be minimal hence precipitation. However, it wpuld be a good idea to evaporate say 50% before freezing to increase saturation in the benzine this will help extra dmt precipiatate.

Once you have freeze precipiatated the dmt you can evaporate the decantted benzine from the freeze step to recover some dmt (and impurities) or use it on your next extraction as it will be slightly loaded with dmt making the freeze precipiatate yield more next extraction.

Also Norman's tek calls for you to roll the naphtha around I suggest shaking it IMO, however this could create emulsion issues so it becomes a balancing act. Emulsion can still be fixed with a by adding a bit more lye (this is more of an issue with ARB bot MHRB). Downside to adding more lye is the dmt could be more oily/ yellow due to more impurities due to higher pH.
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Okay,that's great information to know. Thanks.

I weighed in my extra yield i got from those two hot pulls and got 200mg.

I am going to attempt one or two more pulls using all the solvent i used for the other pulls. I am going to evaporate all of the liquid down to a small amount and use those to do the last pulls and see if i manage to get anything out.

Some of my pulls i did i think i may have put too much solvent in my jars for the freezer precipitation. So maybe by taking all the liquid/solvent i used for this extraction(from the first pull to the last) i can manage to get more dmt out. I will make sure to have more jars with less solvent in each.

Worth a shot. Lets see..


Here are some photos of the the extra spice i managed to get out thanks to your advise :)
 

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Loveall said:
Madhattress said:
Loveall said:
Toluene is less stinky, but I guess you have xylene from Kash's A/B already.

Simply dump a teaspoon of benzoic acid into the xylene. It dissolves and
DMT xtlas precipitate out. BS recommended freezer xtalization.

Essentially it is like a CIELO solvent/acid combo but for DMT.


Benzoic acid is easy to find. It is used in the food and cosmetic industry.
Click to expand...


So after doing a pull with Xylene i would add benzoic acid and then a freezer precipitation or evaporate? And how many pulls should be done at how many ml of xylene for a 50g mhrb extraction?


How much benzoic acid would one use?

Sorry for all the questions just want to understand for if i do this.
Click to expand...

No evaporation. About a teaspoon per quart of xylene/toluene is plenty. It will cloud/crash at room temperature, to fully crash it all put in the freezer per BW (now BS, sorry). However, time alone also helps crash it well at room temp.
Click to expand...


Okay that is great! So would you use the same amount of xylene to do pulls than is used in the recipe(50ml per 50g mhrb) and would you do multiple pulls as well?
 
Try to shake it this time, but only shake a bit at a time and keep an eye on emulsion, if emulsion occurs let it rest, if it still remains add a little extra lye, give it a quick shake and let it rest again. If the emulsion is still there add a little bit more lye (maybe 3-5 grams at a time for example). If you add way too much lye, the lye will turn the soup into gelatin and the solvent gets trapped.
 
_Trip_ said:
Try to shake it this time, but only shake a bit at a time and keep an eye on emulsion, if emulsion occurs let it rest, if it still remains add a little extra lye, give it a quick shake and let it rest again. If the emulsion is still there add a little bit more lye (maybe 3-5 grams at a time for example). If you add way too much lye, the lye will turn the soup into gelatin and the solvent gets trapped.
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I will make sure to shake it well and be patient with each agitation and pull. This is the last pulls i am going to attempt so I will give it my all in hopes to get some more spice out. Will keep an eye out and see if i need to use the Lye. Would keeping the soup in a hot water bath after shaking also help the emulsion settle?

Thanks so much for all the advise, it has been very informative and so useful for when I do more of my extractions in the future. Learned so much already with my first attempt.
 
Also curious as it is my first time extracting dmt. What do i do with this dmt wax? Do i try and disolve it in solvent and re precipitate? Not even sure how store or use this.
 

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Xylene will get whatever has been missed.

As for the wax. Just put it aside, over a day or couple weeks (sometimes a month or 2) it will solidify and harden. You can smoke it, it'll be safe. It's still DMT just a polymer form.
 
_Trip_ said:
Xylene will get whatever has been missed.

As for the wax. Just put it aside, over a day or couple weeks (sometimes a month or 2) it will solidify and harden. You can smoke it, it'll be safe. It's still DMT just a polymer form.
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Okay cool. Got it:)

After these last pulls i'm going to do the Xylene pull and call it a day. Just need to order my benzoic acid as Loveall has suggested and then I will finish this extraction off.

Just need to ask how much Xylene do I use for that last pull and if i should do multiple pulls as with the Naphtha?

Wow this has been quite the learning curve:d But i love it! thanks again for all the input, I think my next extraction will go much better. I will definitely be doing the Max Ion tek next. I have read through it a couple of times and it seems like a super solid tek and a fun one to do.
 
Sent you a PM before I saw your updates here. Good job! Those xtals are nicely resolved for a first extraction!

Like Trip said, I evap down until the solvent is saturated and pee yellow before freeze precip. But I'm also stewing my soup at 70C before doing my pulls thanks to the hot plate.

Heating your solvent if you are doing a room temp extraction should help you.

To what Trip said, I didn't realize the solvent still held onto DMT past -6C. You said -20C!

If I had, say a medical freezer, what temp should I slowly set it to to maximize precipitation?
 
Toshido said:
To what Trip said, I didn't realize the solvent still held onto DMT past -6C. You said -20C!

If I had, say a medical freezer, what temp should I slowly set it to to maximize precipitation?
Click to expand...

BW's results showed:
Naphtha in the freezer (-20 °C, C6-C7, 60-80 °C)
1,09 g in 1 L
109 mg in 100 ml

It is minimal but it would vary depending on the type of distilled naphtha I would imagine.

I think -20celcius is fine, most freezers will do -20.
 
Toshido said:
Sent you a PM before I saw your updates here. Good job! Those xtals are nicely resolved for a first extraction!

Like Trip said, I evap down until the solvent is saturated and pee yellow before freeze precip. But I'm also stewing my soup at 70C before doing my pulls thanks to the hot plate.

Heating your solvent if you are doing a room temp extraction should help you.

To what Trip said, I didn't realize the solvent still held onto DMT past -6C. You said -20C!

If I had, say a medical freezer, what temp should I slowly set it to to maximize precipitation?
Click to expand...


Hey there! yeah i got you PM. Thanks for the tips anyways:grin:

And thanks! I am pretty happy with my first extraction, it can only go better from here. I will definitely be using a flat pyrex dish with a lid next time :lol: :thumb_up:
 
So those last pulls were very minimal but got a little out. So my total yield this far is around 560mg.


Do you think it is worth doing the Xylene pull after i did so many hot pulls on this soup? (i really was very thorough these last two days with my hot pulls i have done. I shook the shit out of the soups yesterday with my pull i did and this pull was over a couple of hours with around 6 agitations.


Do you think i can safely assume that my bark is on the lower end of % alkaloids contained?

:)
 
_Trip_ said:
Maybe, seems low for MHRB, what's the PH?
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Also feel like it is quite low... Should this tek i used be able to pull it all in theory? Or would a tek such as the Max Ion maybe be more effective?
 
Might be the bark then, worth testing a pull with xylene.

Could be multiple issues, how fine the bark is ground, how effective the acid cook was, how long the lye had to breakdown the bark etc.

Likely you did everything right. Try a max ion of you want. It takes most people multiple extractions to find out what works for them.

(It still could be the bark itself).
 
_Trip_ said:
Might be the bark then, worth testing a pull with xylene.

Could be multiple issues, how fine the bark is ground, how effective the acid cook was, how long the lye had to breakdown the bark etc.

Likely you did everything right. Try a max ion of you want. It takes most people multiple extractions to find out what works for them.

(It still could be the bark itself).
Click to expand...

Yeah i guess ill have to see with the next extraction to really know if it is the bark. I still have 200grams left to extract so hopefully i get better yields and if not then I will have to look elsewhere. Nonetheless, atleast I have done my first DMT extraction and I have learned alot in a short amount of time.

I will do a pull with Xylene and then call it quits on this soup haha.

Thanks Trip for everything. You are a star:thumb_up: :)
 
_Trip_ said:
Might be the bark then, worth testing a pull with xylene.

Could be multiple issues, how fine the bark is ground, how effective the acid cook was, how long the lye had to breakdown the bark etc.

Likely you did everything right. Try a max ion of you want. It takes most people multiple extractions to find out what works for them.

(It still could be the bark itself).
Click to expand...


Just realized,

In Normans tek there is no Acid Cook involved..... it goes straight to making a Lye Solution and letting it sit....

Do you think it would be more worthwhile to look at a tek that does involve a acid cook before bringing the PH up with Lye?
 
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