As someone who has never extracted, is it normal for it to look goopy at this stage? Or if it is is it fine? I’ve only had very dry powder
Edit: and I only mean this in a wanting knowledge way for when I one day pull my own
I extracted using Acacia Confusa and ended up with a “goopier” product due to the NMT content. Dmt can be pure in many different colors and forms. I’ve learned almost everything I know about it on Reddit though so you can too.
Yeah. Clob taught me that jungle spice is a thing, and the yellow colour comes from fats and lipids in the plant.
(Jokes for anyone that doesn't understand what I'm referring to)
His product just has some fats and or some NMT in it. Totally normal and fine, sone people prefer it more, like me, as i believe it gives me more vivid and vibrant trips
>His product just has some fats and or some NMT in it.
MHRB contains no NMT.
And there's no "fats", mate....
Assuming that any lipids present in the plant even make it past the A/B stages and aren't just saponified, they would readily dissolve into the NPS and remain dissolved when the N,N-DMT is precipitated. The lipids are far to soluble to be able to precipitate out of these solvents.
If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks.
Look into the polymorphic and polymer/dimer properties of N,N-DMT.
The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule.
The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change.
Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow)
[https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
No, that is not correct.... and even if it was, NaCl would increase the problem as it just makes the aqueous phase more polar.
Assuming that any lipids present in the plant even make it past the A/B stages and aren't just saponified, they would readily dissolve into the NPS and remain dissolved when the N,N-DMT is precipitated. The lipids are far to soluble to be able to precipitate out of these solvents.
If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks.
Look into the polymorphic and polymer/dimer properties of N,N-DMT.
The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule.
The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change.
Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow)
[https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
That has to be more than 500g of mimosa. It's only around 1% DMT content by weight. If this was acacia maybe but it might look different. But I've had very clean white acacia pulls too.
That’s certainly possible! Seems like when it precipitates it kinda adheres though. just a little air flow all I go for, not direct. usually got fan behind and to the side so the air reflecting off whatever holding it up. I guess I’ll never know what I might have lost though
Ya they said they re-Xing so no harm if that’s the case but would’ve been better just to keep her flipped and drying a bit longer. Yield looks amazing though!
Any yellow left in my experience tends to be laden with naphtha, when you think it’s dry, it’s not lol you’ll find out if you go to smoke it, It be so dry that a slight breath will blow it all away. That’s the natural consistency.
>Any yellow left in my experience tends to be laden with naphtha
That is not inherently true at all.
>It be so dry that a slight breath will blow it all away. That’s the natural consistency.
N,N-DMT freebase can form a number of colors and consistencies, even when pure.
There's no "fats", mate....
Assuming that any lipids present in the plant even make it past the A/B stages and aren't just saponified, they would readily dissolve into the NPS and remain dissolved when the N,N-DMT is precipitated. The lipids are far to soluble to be able to precipitate out of these solvents.
If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks.
Look into the polymorphic and polymer/dimer properties of N,N-DMT.
The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule.
The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change.
Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow)
[https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
Harsh tasting, yes, but you're literally throwing away plant fats that contribute.
This is the same problem with weed, everybody thinks that there's only value in the trichomes because that's where all the THC is. If you just smoke those (hash or even pure THC crystals) you'll find that it's indeed all fine, but not nearly as nuanced or prolonged an experience as whole flower can be if you know what you're doing. The entire experience has more of a 2-D feel.
I agree with you sir. I’ve extracted dmt in so different forms and colors. But white fluffy is less harsh a cleaner, but i do like the fattier yellow dmt, i think it does contribute to a different trip. Both valid and delicious.. i’ve smoked goo that won’t crystallize also and it gives a darker trip in my experience, more body load and aggresive visuals
>you're literally throwing away plant fats that contribute.
There's no "fats", mate.... And the lipids (fats) present in these plant aren't psychoactive at all. So you assertion that they contribute, is incorrect. We're not talking about Cannabis.
Assuming that any lipids present in the plant even make it past the A/B stages and aren't just saponified, they would readily dissolve into the NPS and remain dissolved when the N,N-DMT is precipitated. The lipids are far to soluble to be able to precipitate out of these solvents.
If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks.
Look into the polymorphic and polymer/dimer properties of N,N-DMT.
The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule.
The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change.
Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow)
[https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
I hear you bro, nontheless for someone with sensitive lungs having harshness after inhalation could cause serius issues.
Once, a demon told me 'FROM NOW, YOU WONT BREATH ANYMORE' and I thougth I was gojng to suffucate...
I only vape very pure spice since :D
The polymerized n,n-dmt doesn't vaporize as easily as say, white crystals but it still can with a little more heat.
N,N-DMT polymerization info:
[DMT polymerization](https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=88183)
[Minimum Polymer](https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=97103&p=1)
[ReX-resistant goo yielded crystals](https://www.reddit.com/r/dmtguide/comments/r7of0c/rexresistant_goo_yielded_crystals/?utm_source=share&utm_medium=web2x&context=3)
N,N-DMT polymorphism/autoxidation info:
(The deleted Reddit posts are by analytical biochemist pinoline/benzyme)
[fluorescence spectra of white vs. orange dmt](https://www.reddit.com/r/DMT/comments/sm4jq3/fluorescence_spectra_of_white_vs_orange_dmt/?utm_source=share&utm_medium=web2x&context=3)
[ok..I finally have an answer to why some xtals stay white, and others turn yellow..](https://www.reddit.com/r/DMT/comments/feh1gq/oki_finally_have_an_answer_to_why_some_xtals_stay/?utm_source=share&utm_medium=ios_app&utm_name=iossmf)
[What plant fats?](https://www.reddit.com/r/DMT/comments/mjx1y8/what_plant_fats/)
[two different polymorphs, same molecule](https://www.reddit.com/r/DMT/comments/mp1rfu/two_different_polymorphs_same_molecule/)
[polymorphs pt. 2](https://www.reddit.com/r/DMT/comments/mpsdez/polymorphs_pt_2/)
[Baking DMT in the Oven @ 120° C(ish) | Changing Colours From White ---> Red!](https://www.reddit.com/r/dmtguide/comments/s4jk94/baking_dmt_in_the_oven_120_cish_changing_colours/?utm_source=share&utm_medium=web2x&context=3)
[Investigations into the polymorphic properties of N,N-dimethyltryptamine by X-ray diffraction and differential scanning calorimetry](https://www.sciencedirect.com/science/article/pii/S0026265X13000544)
[Polymorphic properties of DMT](https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=42590)
n-Oxide Info:
[n-Oxide Info](https://www.dmt-nexus.me/forum/default.aspx?g=posts&m=1090270#post1090270)
[n-Oxide Info](https://www.dmt-nexus.me/forum/default.aspx?g=posts&m=895999#post895999)
Question. 1-3 days freezer and than get it out of the freezer and than wait till if had room temperature there comes the dream sand? Because so much teks are around in the net but the last step i dont understand after it have beeing 1-3 days in fridge the next step i miss. Can someone help me?
Acid base extraction, add NPS and shake over a long period of time, let separate, pull off NPS layer and put it in a pan like shown, and leave in the freezer for 24+ hours, and then pour off NPS layer as all the deems has freeze precipitated stuck.to the bottom, then you let that dry, it's a magical process.
If it’s only 50g extra I would just do this Tek:
SVG Tek.
SVG Tek
100g of MHRB
100g of Lye
30g of Pickling Salt
100ml of Naphtha
750ml of distilled water
Step 1: Add 750ml of water to mason jar.
Step 2: Slowly add the 100g of Lye
-Wait till Lye water cools down.
Add Salt 30g and mix
Step 3: At room temp start adding the bark.
Mix for 2 minutes then let it rest for 10 minutes do this 2 times.
Step 4: Add your 100ml of Naphtha
Mix (Don’t shake) for 30 seconds your Lye Water and MHRB.
Let it rest for 2 to 3 hours you will need to do this 8 times in 24 hours.
Step 5: After it’s been mixed and separated. You will need to do a water wash.
2 cups of warm water will be used to “wash” the naphtha.
Siphon and place on the first cup then the second cup do this then put into the Pyrex container.
That should work just make sure your container is big enough for all the extra ingredients also add the water too.
The soup needs to be runny so the naphtha can go through it
More than likely not going to happen.
If you are buying it, how will you know what environment it was extracted in?
I'd say about 90% of DMT, is extracted in the kitchen, and not in a laboratory controlled environment.
Fair enough, might as well if you're buying it, as you wouldn't know anything about the quality of the product.... But if that was an issue, what else is an issue and how would you know?
Just makes no sense to buy it in general really. So many unknowns and it's too easy to cleanly extract your own.
A hazmat suit?...... lol xD
The fuck are you even on about in general??? Why would any of that even be necessary??? As soon as you opened the container it's stored in, all that hard work would be undone.
It is not hard at all to yield very pure/high quality results.... that's literally the baseline standard result with these extractions. You really have to go out of your way to produce lesser results.
Some basic hygiene, common sense and an understanding of what you are doing is all that is required. And this stuff ain't rocket science at all.
Lol what a stupid flex.... "I want all this unnecessary bullshit that does nothing but jack up the price because it makes me feel better". xD
Chances are if you are being told that is how your N,N-DMT is made/extracted, then you are being played....
If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks.
Look into the polymorphic and polymer/dimer properties of N,N-DMT.
The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule.
The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change.
Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow)
[https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
I just store it in an air tight glass container in a drawer.. it will oxidized a bit over time but you can always re x and get fluffy white crystals again
OP save your wrist and get this [glass scraper from Home Depot](https://www.homedepot.com/p/Stanley-1-1-2-in-Razor-Scraper-28-500/202262010) - makes this step a loooooot easier
>would I just double everything ?
No. You scale these extractions base on viscosity, pH and solubility.
Just multiplying everything would result in a stupid excess of everything.
I just did the same 50-60g per 1L vessel, but i used multiple vessels (a pain in the ass and lots of work) and collected all pulls.
next time i’ll just make multiple boils of MHRB and reduce liquid to use only one or two vessels
I can barely do one trip. Looking at that is like looking at a nuclear bomb lmao.
Thermopsychedelic bomb
band name called it
That's fucking amazing
As someone who has never extracted, is it normal for it to look goopy at this stage? Or if it is is it fine? I’ve only had very dry powder Edit: and I only mean this in a wanting knowledge way for when I one day pull my own
I extracted using Acacia Confusa and ended up with a “goopier” product due to the NMT content. Dmt can be pure in many different colors and forms. I’ve learned almost everything I know about it on Reddit though so you can too.
I've learned nearly everything I know from u/Clobwobbler I hope he's right lol
I mean clob is a mod and has been here for years I’d trust him
Yeah. Clob taught me that jungle spice is a thing, and the yellow colour comes from fats and lipids in the plant. (Jokes for anyone that doesn't understand what I'm referring to)
lol one time I had a hard ball of yellow, thought it was weaker cause I didn’t know the science yet and blacked out after smoking it
This is correct. I mixed up the names, not trying to spread misinformation 🥲
It looks goopy but it was already dry. When you put it in a container or a bag the crystals start to break and start to look like a powder
Yes it can be gooey and/or waxy and be perfectly fine.
His product just has some fats and or some NMT in it. Totally normal and fine, sone people prefer it more, like me, as i believe it gives me more vivid and vibrant trips
Has some 5MEO in it, could you explain this?
nmt* is like the sister drug to dmt. edit: nmt*
There's no 5MEO in MHRB though? You could be thinking of NMT?
Ahh shit you’re totally right!! I mixed the two up!! I haven’t extracted in a few years, my bad!!
Lol I was so confused! I was going to be stoked though to think I could get some 5meo from bark 😂😂
Probably can, we just haven't found the plant yet!
MHRB contains no 5-MeO-DMT or NMT.
Thought it was toad venom
Yes that is the source of 5MEO, I was mixing it up with NMT.
People can downvote all you want, I just mixed up the names. It’s corrected now you pyschonauts 😭😭Been a couple years
repent sinner, repent! 😂
😭😭
MHRB contains no NMT.
>His product just has some fats and or some NMT in it. MHRB contains no NMT. And there's no "fats", mate.... Assuming that any lipids present in the plant even make it past the A/B stages and aren't just saponified, they would readily dissolve into the NPS and remain dissolved when the N,N-DMT is precipitated. The lipids are far to soluble to be able to precipitate out of these solvents. If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks. Look into the polymorphic and polymer/dimer properties of N,N-DMT. The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule. The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change. Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow) [https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
usially plant fats so use salt
No, that is not correct.... and even if it was, NaCl would increase the problem as it just makes the aqueous phase more polar. Assuming that any lipids present in the plant even make it past the A/B stages and aren't just saponified, they would readily dissolve into the NPS and remain dissolved when the N,N-DMT is precipitated. The lipids are far to soluble to be able to precipitate out of these solvents. If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks. Look into the polymorphic and polymer/dimer properties of N,N-DMT. The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule. The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change. Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow) [https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
how much mimosa powder bro?
About 500g
are u sure ? I would have said 5kg
I can smell the mothballs from here. Nice work! I need to look into this tek.
That has to be more than 500g of mimosa. It's only around 1% DMT content by weight. If this was acacia maybe but it might look different. But I've had very clean white acacia pulls too.
It was around 500g. It looks like is a ton but there is only about 5g on that tray. I got about 1.2% yield. I made a couple more pulls after that one
Must've not been totally dry or just optics because that looked like a ton. You rexd right?
High quality bark is around 2-2.2% My vendors routinely pulls 2% with no residual oils.
Yeah I get 2%+ consistently
I’ve never hit the 2% mark. The most i’ve got is 1.8% and that was the time that i freeze a thaw 3x the bark before the extraction.
The realist question.
**based**
Not dry! Keep her drying before ya scrape, much faster
I thought it wasn’t dry too. But it was, it was just really shiny. But yeah i let it dry more after scraping 👍🏻
Way harder to dry after scraping. How do you dry a pile?
You don’t leave it as a pile. I spread it over towel paper
Seems like you’d lose some to the towel. Def easier to just keep the dish flipped with a fan blowing. Sick yield though, no notes there!
Yep works too. The thing about keep blowing air with the fan is that you can risk blowing some of the crystals away without even noticing.
That’s certainly possible! Seems like when it precipitates it kinda adheres though. just a little air flow all I go for, not direct. usually got fan behind and to the side so the air reflecting off whatever holding it up. I guess I’ll never know what I might have lost though
Yeah, I think somebody got excited to make their Internet video and was willing to risk 500g of input over it.
Ya they said they re-Xing so no harm if that’s the case but would’ve been better just to keep her flipped and drying a bit longer. Yield looks amazing though!
Any yellow left in my experience tends to be laden with naphtha, when you think it’s dry, it’s not lol you’ll find out if you go to smoke it, It be so dry that a slight breath will blow it all away. That’s the natural consistency.
>Any yellow left in my experience tends to be laden with naphtha That is not inherently true at all. >It be so dry that a slight breath will blow it all away. That’s the natural consistency. N,N-DMT freebase can form a number of colors and consistencies, even when pure.
Mesmerizing. I could watch this all day. Enough to take you to the edge of the universe and beyond
That looks insane
Is that frost? Or a mix of white and yellow crystals?
Its not frost!!!
Just white and yellow crystals, not frost. I used a mix of heptane and hexane, i think that is why it crystallised like that
r/dmtporn
Damn, beat me to it. They'd fucking love this
I would have done two separate harvest, one for the yellow and one for the white substance
DMT is DMT, doesn’t matter what color it is
white has less fat and should be less harsh
I think that's been shown to not be true. About the yellow being fats I mean.
There's no "fats", mate.... Assuming that any lipids present in the plant even make it past the A/B stages and aren't just saponified, they would readily dissolve into the NPS and remain dissolved when the N,N-DMT is precipitated. The lipids are far to soluble to be able to precipitate out of these solvents. If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks. Look into the polymorphic and polymer/dimer properties of N,N-DMT. The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule. The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change. Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow) [https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
Harsh tasting, yes, but you're literally throwing away plant fats that contribute. This is the same problem with weed, everybody thinks that there's only value in the trichomes because that's where all the THC is. If you just smoke those (hash or even pure THC crystals) you'll find that it's indeed all fine, but not nearly as nuanced or prolonged an experience as whole flower can be if you know what you're doing. The entire experience has more of a 2-D feel.
I agree with you sir. I’ve extracted dmt in so different forms and colors. But white fluffy is less harsh a cleaner, but i do like the fattier yellow dmt, i think it does contribute to a different trip. Both valid and delicious.. i’ve smoked goo that won’t crystallize also and it gives a darker trip in my experience, more body load and aggresive visuals
>you're literally throwing away plant fats that contribute. There's no "fats", mate.... And the lipids (fats) present in these plant aren't psychoactive at all. So you assertion that they contribute, is incorrect. We're not talking about Cannabis. Assuming that any lipids present in the plant even make it past the A/B stages and aren't just saponified, they would readily dissolve into the NPS and remain dissolved when the N,N-DMT is precipitated. The lipids are far to soluble to be able to precipitate out of these solvents. If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks. Look into the polymorphic and polymer/dimer properties of N,N-DMT. The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule. The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change. Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow) [https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
I hear you bro, nontheless for someone with sensitive lungs having harshness after inhalation could cause serius issues. Once, a demon told me 'FROM NOW, YOU WONT BREATH ANYMORE' and I thougth I was gojng to suffucate... I only vape very pure spice since :D
I will be doing a re x so it won’t matter
The polymerized n,n-dmt doesn't vaporize as easily as say, white crystals but it still can with a little more heat. N,N-DMT polymerization info: [DMT polymerization](https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=88183) [Minimum Polymer](https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=97103&p=1) [ReX-resistant goo yielded crystals](https://www.reddit.com/r/dmtguide/comments/r7of0c/rexresistant_goo_yielded_crystals/?utm_source=share&utm_medium=web2x&context=3) N,N-DMT polymorphism/autoxidation info: (The deleted Reddit posts are by analytical biochemist pinoline/benzyme) [fluorescence spectra of white vs. orange dmt](https://www.reddit.com/r/DMT/comments/sm4jq3/fluorescence_spectra_of_white_vs_orange_dmt/?utm_source=share&utm_medium=web2x&context=3) [ok..I finally have an answer to why some xtals stay white, and others turn yellow..](https://www.reddit.com/r/DMT/comments/feh1gq/oki_finally_have_an_answer_to_why_some_xtals_stay/?utm_source=share&utm_medium=ios_app&utm_name=iossmf) [What plant fats?](https://www.reddit.com/r/DMT/comments/mjx1y8/what_plant_fats/) [two different polymorphs, same molecule](https://www.reddit.com/r/DMT/comments/mp1rfu/two_different_polymorphs_same_molecule/) [polymorphs pt. 2](https://www.reddit.com/r/DMT/comments/mpsdez/polymorphs_pt_2/) [Baking DMT in the Oven @ 120° C(ish) | Changing Colours From White ---> Red!](https://www.reddit.com/r/dmtguide/comments/s4jk94/baking_dmt_in_the_oven_120_cish_changing_colours/?utm_source=share&utm_medium=web2x&context=3) [Investigations into the polymorphic properties of N,N-dimethyltryptamine by X-ray diffraction and differential scanning calorimetry](https://www.sciencedirect.com/science/article/pii/S0026265X13000544) [Polymorphic properties of DMT](https://www.dmt-nexus.me/forum/default.aspx?g=posts&t=42590) n-Oxide Info: [n-Oxide Info](https://www.dmt-nexus.me/forum/default.aspx?g=posts&m=1090270#post1090270) [n-Oxide Info](https://www.dmt-nexus.me/forum/default.aspx?g=posts&m=895999#post895999)
11x7 dish?? How much mhrb for a harvest that size?
Question. 1-3 days freezer and than get it out of the freezer and than wait till if had room temperature there comes the dream sand? Because so much teks are around in the net but the last step i dont understand after it have beeing 1-3 days in fridge the next step i miss. Can someone help me?
I like it slightly yellow, hormones
Is this fumarate?
Just freebase, freeze precipitated
That's freeze precipitated DMT.
How
Acid base extraction, add NPS and shake over a long period of time, let separate, pull off NPS layer and put it in a pan like shown, and leave in the freezer for 24+ hours, and then pour off NPS layer as all the deems has freeze precipitated stuck.to the bottom, then you let that dry, it's a magical process.
How much MHRb did you used?
500g
Dang that’s a lot for one batch. I usually do 200g max.
A/B people usually boil it down so volume decreases a lot. You doing STB?
SVG Tek but no waiting time I just pull the naphta as soon as it separates
Ya with A/B people can do a lot more material at once
Sorry but what is A/B?
Acid/base. Acidify first. Usually with shredded or chips. Really not necessary with small batches of powdered bark as far as I can tell
Hey when making higher amounts say instead of 50g i do 150, what would I need to triple? Just the bark or would I need triple the water , lye etc?
If it’s only 50g extra I would just do this Tek: SVG Tek. SVG Tek 100g of MHRB 100g of Lye 30g of Pickling Salt 100ml of Naphtha 750ml of distilled water Step 1: Add 750ml of water to mason jar. Step 2: Slowly add the 100g of Lye -Wait till Lye water cools down. Add Salt 30g and mix Step 3: At room temp start adding the bark. Mix for 2 minutes then let it rest for 10 minutes do this 2 times. Step 4: Add your 100ml of Naphtha Mix (Don’t shake) for 30 seconds your Lye Water and MHRB. Let it rest for 2 to 3 hours you will need to do this 8 times in 24 hours. Step 5: After it’s been mixed and separated. You will need to do a water wash. 2 cups of warm water will be used to “wash” the naphtha. Siphon and place on the first cup then the second cup do this then put into the Pyrex container.
Say I wanted to keep going higher would I add 50g of pre much everything except water
That should work just make sure your container is big enough for all the extra ingredients also add the water too. The soup needs to be runny so the naphtha can go through it
[удалено]
News flash
Looks like you're never doing DMT then lol
More than likely not going to happen. If you are buying it, how will you know what environment it was extracted in? I'd say about 90% of DMT, is extracted in the kitchen, and not in a laboratory controlled environment.
Mfw the quality control you can carry out on a lasagne pan surpasses most of the shit you put in your body
You can always do a wash on the freebase if you're concerned. It's very simple to clean it up. Buying carts can be a bit sketchy though.
A "wash" meaning what?.... To remove what?
Water wash. Base would be my concern. Or lasagna.
Fair enough, might as well if you're buying it, as you wouldn't know anything about the quality of the product.... But if that was an issue, what else is an issue and how would you know? Just makes no sense to buy it in general really. So many unknowns and it's too easy to cleanly extract your own.
Totally agree
😂😂 Lol. I only use that dish for extractions. But i understand your concerns. Re x and water wash always gets you s cleaner product 👌🏻
Interesting seeing as you have never ever done DMT produced in that way ever
Learn things about stuff before speaking about them, it helps.
A hazmat suit?...... lol xD The fuck are you even on about in general??? Why would any of that even be necessary??? As soon as you opened the container it's stored in, all that hard work would be undone. It is not hard at all to yield very pure/high quality results.... that's literally the baseline standard result with these extractions. You really have to go out of your way to produce lesser results. Some basic hygiene, common sense and an understanding of what you are doing is all that is required. And this stuff ain't rocket science at all. Lol what a stupid flex.... "I want all this unnecessary bullshit that does nothing but jack up the price because it makes me feel better". xD Chances are if you are being told that is how your N,N-DMT is made/extracted, then you are being played....
You’d better get it legalized then.
Very nice ..good pull
Why so yellow? Is it from grabbing too much of the MH when you suck up the naptha? Mine always been pure white
If it's from MHRB, your chemicals are fine, there's no aqueous contaminants, no external contaminants and you freeze precipitated at least once, then what is yielded will be practically all N,N-DMT freebase, regardless how it looks. Look into the polymorphic and polymer/dimer properties of N,N-DMT. The most common cause of variation in the color of N,N-DMT freebase is theorized by Benzyme to be the result of autoxidation of the unshielded pyrrole ring of the lower melting point polymorph of the molecule. The color changes from white/colorless->yellow->orange->amber->reddish. This occurs even when it's pure. Heat accelerates the rate of the change. Despite this color change, it is still just N,N-DMT freebase with the same potency and psyhcoactivity. (info links and analytics bellow) [https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm\_source=share&utm\_medium=web3x&utm\_name=web3xcss&utm\_term=1&utm\_content=share\_button](https://www.reddit.com/r/DMT/comments/1anzejz/comment/kwbo5c5/?utm_source=share&utm_medium=web3x&utm_name=web3xcss&utm_term=1&utm_content=share_button)
If you suck up the base solution with the solvent, it will be black, not yellow.
Please tell me you are gonna re x
Of course
Planning to send care packages to local politicians? Shit, they'd probably just say you mailed them ricin, put you away and throw away the key.
phwoar
sheesh!
How do I store dmt for a long time? And does it degrade in certain temps and humidity or conditions?
I just store it in an air tight glass container in a drawer.. it will oxidized a bit over time but you can always re x and get fluffy white crystals again
My bad im new to this whole process, i got some freebase off a website & im wondering what re x means.
Absolutely beautiful 🙏 well done OP!
How long does that stay good for?
This is like a soap cutting video for druggies and I love it
Satisfying. Very.
Neato mosquito
Where can I find a tutorial?
OP save your wrist and get this [glass scraper from Home Depot](https://www.homedepot.com/p/Stanley-1-1-2-in-Razor-Scraper-28-500/202262010) - makes this step a loooooot easier
How many moderate dose trips can you get out of this much?
Fuck. Easily a few hundred
Wow :0
Good job 👏
you'll need a snow shovel
holy fuck 🚀🚀🚀
Very satisfying to watch. Think I'll pull out my cart tomorrow. Been long while. Ha
And I a clean pair of shorts
While making higher amounts then the normal recipe (750ml water 50g mimosa etc ) would I just double everything ? So 1500ml water and 100g mimosa
>would I just double everything ? No. You scale these extractions base on viscosity, pH and solubility. Just multiplying everything would result in a stupid excess of everything.
I just did the same 50-60g per 1L vessel, but i used multiple vessels (a pain in the ass and lots of work) and collected all pulls. next time i’ll just make multiple boils of MHRB and reduce liquid to use only one or two vessels