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
DMT content per acid cookl? Minimum amount of acid cooks? Options
 
fathomlessness
#1 Posted : 10/11/2016 3:01:11 PM

DMT-Nexus member


Posts: 975
Joined: 24-Jan-2015
Last visit: 28-Feb-2023
I am aware of the wiki saying 2 minimum and 5 maximum

https://wiki.dmt-nexus.m...Q#How_many_acid_cooks.3F

But what are the figures like for the content per acid cook?

for example:

1st cook: 10g

2nd cook: 5g

3rd cook: 2g

4th cook: 1g

5th cook: .5g

I am trying to see if I can get away with just two cooks. This will inevitably save me solvent as a 3rd acid cook would end up producing more liquid that I need to basify and pull from because, IME, you can only reduce so much before emulsions start getting bad (not less than 1/4 IME)
 

Good quality Syrian rue (Peganum harmala) for an incredible price!
 
DansMaTete
#2 Posted : 10/11/2016 4:12:57 PM

[insert something smart/deep here]


Posts: 890
Joined: 20-Oct-2013
Last visit: 27-Apr-2024
Location: Location: just behind but under on the side
The patern is probably more like an acid cook get 80% of alks each time. So for example imagine there is 10g in total:
1st : 8g
2nd : 1.6g
3rd : 0.32g

IME, after 2 pressure cook (2x30min) it's enough but most of the time i process a third just to be sure (with MHRB).

And if it's true the first water pull become to "thick" quickly when you reduce, it's not true with the next ones as they are more dilute. For exemple the third pull can easily be reduced less than 1/10 of it's original volume.

« I love the smell of boiling MHRB in the morning »
 
Jees
#3 Posted : 10/11/2016 7:29:58 PM

DMT-Nexus member


Posts: 4031
Joined: 28-Jun-2012
Last visit: 05-Mar-2024
Powder, pieces, roughly shredded, finely shredded,...
all matters.
 
acacian
#4 Posted : 10/11/2016 9:42:11 PM

DMT-Nexus member


Posts: 2229
Joined: 22-Jul-2011
Last visit: 02-May-2024
Location: in the underbelly of the cosmic womb
with powdered plant material you'll more than likely get the most out in the first cook.. a 2nd is advised. I often don't bother doing a third (but I always add ethanol to my "pulls" so its more efficient)..

with chips 3 is a good idea
 
Psilosopher?
#5 Posted : 10/12/2016 5:11:02 AM

Don't Panic

Senior Member

Posts: 756
Joined: 28-Dec-2014
Last visit: 01-Oct-2022
Location: Everywhen
I don't even do a second acid cook. My yields are consistently near the 2℅ mark using powdered ACRB.

I plan on doing a lot of fiddling with the extraction process once i get a new lab set up.
"A common mistake that people make when trying to design something completely foolproof is to underestimate the ingenuity of complete fools."
 
fathomlessness
#6 Posted : 10/13/2016 3:57:36 AM

DMT-Nexus member


Posts: 975
Joined: 24-Jan-2015
Last visit: 28-Feb-2023
DansMaTete wrote:
The patern is probably more like an acid cook get 80% of alks each time. So for example imagine there is 10g in total:
1st : 8g
2nd : 1.6g
3rd : 0.32g

IME, after 2 pressure cook (2x30min) it's enough but most of the time i process a third just to be sure (with MHRB).

And if it's true the first water pull become to "thick" quickly when you reduce, it's not true with the next ones as they are more dilute. For exemple the third pull can easily be reduced less than 1/10 of it's original volume.



Bodhisativa wrote:
I don't even do a second acid cook. My yields are consistently near the 2℅ mark using powdered ACRB.

I plan on doing a lot of fiddling with the extraction process once i get a new lab set up.


acacian wrote:
with powdered plant material you'll more than likely get the most out in the first cook.. a 2nd is advised. I often don't bother doing a third (but I always add ethanol to my "pulls" so its more efficient)..

with chips 3 is a good idea


Jees wrote:
Powder, pieces, roughly shredded, finely shredded,...
all matters.


How much water are we talking about here though? Enough to stir without any effort at all? Or takes a little bit of effort to stir? (IE. Fill up half the pot with bark, the rest with water?)

P.S. Thanks for the replies Wink

 
fathomlessness
#7 Posted : 10/13/2016 3:59:01 AM

DMT-Nexus member


Posts: 975
Joined: 24-Jan-2015
Last visit: 28-Feb-2023
Jees wrote:
Powder, pieces, roughly shredded, finely shredded,...
all matters.


Yes, mine is always finely/roughly shredded and I have done tests in the past with a second cook still producing lots of DMT. This could be that the first cook didn't have enough water though.
 
fathomlessness
#8 Posted : 10/13/2016 4:00:17 AM

DMT-Nexus member


Posts: 975
Joined: 24-Jan-2015
Last visit: 28-Feb-2023
DansMaTete wrote:

And if it's true the first water pull become to "thick" quickly when you reduce, it's not true with the next ones as they are more dilute. For exemple the third pull can easily be reduced less than 1/10 of it's original volume.



1/10 its volume? If I go under 2/5s of the the original volume I usually run in to emulsion troubles after basification.

Thanks for the clarification of the percentages per cook Thumbs up
 
fathomlessness
#9 Posted : 10/13/2016 4:22:17 AM

DMT-Nexus member


Posts: 975
Joined: 24-Jan-2015
Last visit: 28-Feb-2023
acacian wrote:
but I always add ethanol to my "pulls" so its more efficient)..


What is it really doing? How long are you soaking it for? Are you boiling it with the ethanol or soaking then boiling? Is there actually a substantial difference? What sort of ethanol is this? 100% or should I just dump in some vodka?
 
Psilosopher?
#10 Posted : 10/13/2016 7:10:27 AM

Don't Panic

Senior Member

Posts: 756
Joined: 28-Dec-2014
Last visit: 01-Oct-2022
Location: Everywhen
fathomlessness wrote:
DansMaTete wrote:
The patern is probably more like an acid cook get 80% of alks each time. So for example imagine there is 10g in total:
1st : 8g
2nd : 1.6g
3rd : 0.32g

IME, after 2 pressure cook (2x30min) it's enough but most of the time i process a third just to be sure (with MHRB).

And if it's true the first water pull become to "thick" quickly when you reduce, it's not true with the next ones as they are more dilute. For exemple the third pull can easily be reduced less than 1/10 of it's original volume.



Bodhisativa wrote:
I don't even do a second acid cook. My yields are consistently near the 2℅ mark using powdered ACRB.

I plan on doing a lot of fiddling with the extraction process once i get a new lab set up.


acacian wrote:
with powdered plant material you'll more than likely get the most out in the first cook.. a 2nd is advised. I often don't bother doing a third (but I always add ethanol to my "pulls" so its more efficient)..

with chips 3 is a good idea


Jees wrote:
Powder, pieces, roughly shredded, finely shredded,...
all matters.


How much water are we talking about here though? Enough to stir without any effort at all? Or takes a little bit of effort to stir? (IE. Fill up half the pot with bark, the rest with water?)

P.S. Thanks for the replies Wink



The amount of acid required to react with DMT is actually miniscule compared to the volume required to cook plant material. So the volume should be enough to suspend all of the plant material, and so it can be stirred easily. You could try a minimalists slugde tek, but it's just really messy.

Here's my process in short,

1) Microwave.
2) Acidify.
3) Salinate.
4) Basify.
5) Add solvent and agitate. You can shake, but it takes longer for the emulsion to settle.
6) POUR INTO A LARGE MEASURING CYLINDER (This step makes the pulling soooo much easier, all of the sediment accumulates at the bottom really quick since it's so narrow).
7) Pull.
8 ) Freeze precip or evap, depending on my mood.
"A common mistake that people make when trying to design something completely foolproof is to underestimate the ingenuity of complete fools."
 
acacian
#11 Posted : 10/13/2016 10:12:51 AM

DMT-Nexus member


Posts: 2229
Joined: 22-Jul-2011
Last visit: 02-May-2024
Location: in the underbelly of the cosmic womb
Bodhisativa wrote:


The amount of acid required to react with DMT is actually miniscule compared to the volume required to cook plant material. So the volume should be enough to suspend all of the plant material, and so it can be stirred easily. You could try a minimalists slugde tek, but it's just really messy.


Is there really any volume of acid actually needed for cooking the plant material? my understanding is that dmt as a salt is still soluble in close to neutral water so acid isn't a requirement but more of helping hand.. the plants are generally acidic enough to pretty much get your ph near 5 .. and when you combine that with heat its pretty efficient. I've done extractions without acid a few times with no problem.

[EDIT] Bodhisativa I misread your last post sorry.. didn't realise you were talking about water.
 
Jees
#12 Posted : 10/13/2016 11:36:54 AM

DMT-Nexus member


Posts: 4031
Joined: 28-Jun-2012
Last visit: 05-Mar-2024
acacian wrote:
...Is there really any volume of acid actually needed...
How would we define 'it needs to'? It's not like it doesn't work without unless you have really mineral rich tap water.
I've found for example rue powder cold water extracts better in muriatic acid water pH 1.5 than when tried with just a spoon of citric acid to pH 3 - 4 boiling. So it does matter when we push things this far in lysing cells. Of course this is not the same discussion like between ph 7 and pH 3.

Ayahuasca: Add acid or not?
Acid vs. Non-Acid Brew Experiment: Comparison of Alkaloids Remaining in THP Brewed Caapi
Also, the herbal percolator worked better with acidified water.
I tend to consider mimo and aya quite the same when it comes to boiling the wood.
 
fathomlessness
#13 Posted : 10/13/2016 1:27:17 PM

DMT-Nexus member


Posts: 975
Joined: 24-Jan-2015
Last visit: 28-Feb-2023
Jees wrote:

I've found for example rue powder cold water extracts better in muriatic acid water pH 1.5 than when tried with just a spoon of citric acid to pH 3 - 4 boiling.


I have tried muriatic acid (Hydrochloric acid) with a ph of 1-2 before and got nothing from tested viable bark. Something about low PH destroys the DMT.

I now use white vinegar as I don't want to risk it anymore


Bodhisativa wrote:

The amount of acid required to react with DMT is actually miniscule compared to the volume required to cook plant material. So the volume should be enough to suspend all of the plant material, and so it can be stirred easily. You could try a minimalists slugde tek, but it's just really messy.

Here's my process in short,

1) Microwave.
2) Acidify.
3) Salinate.
4) Basify.
5) Add solvent and agitate. You can shake, but it takes longer for the emulsion to settle.
6) POUR INTO A LARGE MEASURING CYLINDER (This step makes the pulling soooo much easier, all of the sediment accumulates at the bottom really quick since it's so narrow).
7) Pull.
8 ) Freeze precip or evap, depending on my mood.


Ok thanks, that clearing that up for me Thumbs up

Does the microwave actually do anything more than just a standard cook?
 
Jees
#14 Posted : 10/13/2016 8:56:04 PM

DMT-Nexus member


Posts: 4031
Joined: 28-Jun-2012
Last visit: 05-Mar-2024
fathomlessness wrote:
...I have tried muriatic acid (Hydrochloric acid) with a ph of 1-2 before and got nothing from tested viable bark. Something about low PH destroys the DMT....
Did you heat that low pH brew? Some people that have heated theirs report failure.

I would never advocate using such low pH's in general, my note was only illustrative that acid does a job, which is more noticeable in the extremes. The limit where harm is done due too low pH is an unfinished discourse as far as I know of. And I would not be surprised if the cold versus hot/warm makes a difference.

QT's extraction tek (now withdrawn from erowid) suggested to use pH 2 muriatic water. While the tek had a storm of corrections on several points, never was the pH considered harmful for dimitri, it was only considered unnecessarily low to make a tek work OK.
Quote:
...The pH for step 2 is unnecessarily low. While pH 2 won't hurt anything, it's a waste of materials...
Cant find the full tek to see if they boiled or cold water soaked Embarrased
 
acacian
#15 Posted : 10/13/2016 10:41:32 PM

DMT-Nexus member


Posts: 2229
Joined: 22-Jul-2011
Last visit: 02-May-2024
Location: in the underbelly of the cosmic womb
Yeah you are right in that it does have a role to play Jees.. but I think with dmt extraction it is a little overemphasized. If you are boiling your plant material for an hour (x3 as is standard with a/b) then I reckon you'll pull all the alkaloids acid or no acid.. I'm not having a dig at people using acid in their process anyways it was actually a reply to a misread sentence of Bodhisativa's where I thought he was claiming acid to be a "requirement" in extraction.
 
DansMaTete
#16 Posted : 10/14/2016 12:15:03 AM

[insert something smart/deep here]


Posts: 890
Joined: 20-Oct-2013
Last visit: 27-Apr-2024
Location: Location: just behind but under on the side
Shredded MHRB, 2x30min in a PC, no acid, done.



« I love the smell of boiling MHRB in the morning »
 
Psilosopher?
#17 Posted : 10/14/2016 5:11:28 AM

Don't Panic

Senior Member

Posts: 756
Joined: 28-Dec-2014
Last visit: 01-Oct-2022
Location: Everywhen
fathomlessness wrote:
Jees wrote:

I've found for example rue powder cold water extracts better in muriatic acid water pH 1.5 than when tried with just a spoon of citric acid to pH 3 - 4 boiling.


I have tried muriatic acid (Hydrochloric acid) with a ph of 1-2 before and got nothing from tested viable bark. Something about low PH destroys the DMT.

I now use white vinegar as I don't want to risk it anymore


Bodhisativa wrote:

The amount of acid required to react with DMT is actually miniscule compared to the volume required to cook plant material. So the volume should be enough to suspend all of the plant material, and so it can be stirred easily. You could try a minimalists slugde tek, but it's just really messy.

Here's my process in short,

1) Microwave.
2) Acidify.
3) Salinate.
4) Basify.
5) Add solvent and agitate. You can shake, but it takes longer for the emulsion to settle.
6) POUR INTO A LARGE MEASURING CYLINDER (This step makes the pulling soooo much easier, all of the sediment accumulates at the bottom really quick since it's so narrow).
7) Pull.
8 ) Freeze precip or evap, depending on my mood.


Ok thanks, that clearing that up for me Thumbs up

Does the microwave actually do anything more than just a standard cook?


Just some quick calculations:

Assuming 1:1 stoichiometry.

HCl + DMT ---} DMTHCL (can't find the damn arrow keys on this stupid phone.)

Number of moles on 500 mL HCl at pH 3, c = 0.001 M

n = CV

= 0.001 x 0.5

= 0.0005 mol

Number of moles in 1 g of DMT.

n = mass / molar mass

= 1 / 188.269

= 0.005 mol

Therefore, 500 mL of this acid can theoretically dissolve 10g of DMT.


The microwave just aids in cell lysis. I like to be thorough and eliminate all variables between extracts, except the variables i'm testing. That way, i have usable data.
"A common mistake that people make when trying to design something completely foolproof is to underestimate the ingenuity of complete fools."
 
 
Users browsing this forum
Guest

DMT-Nexus theme created by The Traveler
This page was generated in 0.040 seconds.