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Powder vs Tea vs Resin vs Acetate vs Hcl Options
 
Virola78
#21 Posted : 6/22/2010 10:35:30 PM

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endlessness wrote:
Virola78 wrote:
Got all the chems i need. And also got the SP cactus cuttings: 10x 25-30cm from the plaza.
Some cuttings look different in color, from freshgreen to blueish. Also shape was different, ribs, grooves etc.
Clearly taken from different motherplants. As expected of course.

endlessness wrote:
Virola, unless you made the dried cactus from the same fresh cactus species that you are gonna extract, then you cant really compare yields because its two different sources of alkaloids....


So i have treated the cuttings separate. Resulting in 10 piles of strips of green flesh (without skin). (Damn that took me allot of time) Then i have taken half (weight) of each pile and put those together in a pot. To make a tea -> Phlux- tek.

The other half of each pile is drying outside in the shadow -> 69ron tek

Very happy



cant wait for the results!! what are you gonna salt out with in ron's tek, hcl or vinegar? If you have both, maybe do a side-by-side on that too, half the limo pulls with hcl and half with acetate Very happy

(hehe I know its a lot of work, whatever you do test is very nice to know! )


Im going to salt all the xylene from the 69ron tek with vinegar. Havent got enough material for comparison 69ron mesc-HCl vs 69ron mesc-acetate...
The loss would be too much possibly leaving me to little product to do serious quality testing (i tend to play it safe, slowly up the dose..)

Too bad i havent got kilo's SP laying around Confused
Maybe later when i can find some more reliable and usuable data on the use of LED lighting to grow them myself. Havent been succesful a that so far.
Long term project...pfff


“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 

Good quality Syrian rue (Peganum harmala) for an incredible price!
 
Virola78
#22 Posted : 6/22/2010 10:36:30 PM

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obliguhl wrote:
Better dry them quick. The catch mold after 3-4 days.


Tomorow i will put them in the sun then.

“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
69ron
#23 Posted : 6/23/2010 11:37:31 AM

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Dagger wrote:
"69ron" wrote:
For health reasons, SWIM has stopped using the HCl because you cannot easily get food grade hydrochloric acid.

Purify it. Just pour the hcl in one small bowl, then put an equal size bowl with pure water in the other. Put both inside a big airtight container. Let it stay for a few weeks. When you open it again, pure hcl should have migrated over to the pure water. It would be half strength of the original hcl bowl if there is equal amounts of water.

Look here:
Youtube - The Home Scientist 007 - Purify hydrochloric acid


HCl is actually just a gas that happens to like being in water. That's an interesting way to purify it. I'm glad I read this post. This is really good information.

I'll have to try that out. It's a very simple test.

Is there any gas other than HCl in pool grade HCl that might migrate over to the clean water? Or is this pretty much a sure fire way of purifying HCl? For sure this gets rid all non-gases present.

I think this would make HCl suitable for use. Only a gas would migrate over, and such a gas would always evaporate off of your final product, so it would be of little concern.

Thanks for posting that Dagger. That's valuable info!
You may remember me as 69Ron. I was suspended years ago for selling bunk products under false pretenses. I try to sneak back from time to time under different names, but unfortunately, the moderators of the DMT-Nexus are infinitely smarter than I am.

If you see me at the waterpark, please say hello. I'll be the delusional 50 something in the American flag Speedo, oiling up his monster guns while responding to imaginary requests for selfies from invisible teenage girls.
 
Virola78
#24 Posted : 6/23/2010 12:29:34 PM

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w0mbat wrote:
Hey guys -

This seems like an easy way to make reagent grade HCl from Technical grade HCl: http://www.youtube.com/watch?v=jv1Ms6Subg4 (you are gonna kick yourselves after seeing this) I have not tried it yet but it seems like it could work & yield a relatively "clean" form of HCl.

Another way of making pure(?) HCl, using technical grade sulfuric acid and sea salt: http://www.youtube.com/watch?v=RIbqd8ssNsw

HCl can also be produced using NaHSO4, salt, and heat. NaHSO4 can be bought food-grade online, making this approach seem like a pretty safe one. It just requires a test tube that can be sealed off so the HCl gas from the reaction of NaHSO4 and NaCl can be bubble up through water in another test tube. Link: http://www.youtube.com/watch?v=2mWbeieqx3s


cough

“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
Virola78
#25 Posted : 6/29/2010 2:49:48 PM

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Well im having issues with the Phlux- tek.

The tea clogged the coffeefilter, so i used some water to get it through. Now im trying to bring the tea back (again) to a volume i can handle (about 400ml), but again there is allot of solids forming. These solids will prob clog my sep funnel. Any advice?
Im thinking of just evapping it and having a go at the resin.. hope the heat hasnt done much damage.. Confused

The 69ron tek is much easier so far. Doing a fourth pull at the moment. After that i will just have to wait for all the HCl and water to evap.
(yea i decided to use lab grade HCl 2% solution instead of vinegar)

“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
obliguhl
#26 Posted : 6/29/2010 6:00:38 PM

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What about some old cloths? You could probaly squeeze the water through.
 
Virola78
#27 Posted : 7/1/2010 1:54:48 PM

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obliguhl wrote:
What about some old cloths? You could probaly squeeze the water through.


thx dude
but cloth wont filter out the tiny particles. A coffeefilter will do, but then i ill have to use more water again, to keep gravity going. And then i will have to reduce the tea again, and thats when there will be solids forming again Confused

At the moment i am looking in my resin evap dish. The solids are forming a beautiful fingerprintlike pattern on the bottom.
I will be happy with this i have. Guess its the way things go for me. Im still learning Smile

Btw there are some nice crystals forming in the 69ron tek evap dishes. Looks promising.
“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
w0mbat
#28 Posted : 7/3/2010 3:16:25 AM

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Virola - SWIM has found that your problem is a common one, and that fine particles even get through double- and quadruple-layered filters of muslin fabric. Try letting your acidic tea sit in the fridge overnight. Solids should settle on the bottom by morning. Carefully remove the top 3/4 of the liquid layer and filter it through a coffee filter again, it should go through easier this time.

To the remaining 1/4 of your tea, add more distilled water or vinegar, let it sit overnight, and then remove the top 3/4 or so of the water layer again. Repeat once more and you should have all of the active material without any of the plant gunk. Reduce the volume again and you should be good to go on to the next phase of your tech.

benzyme wrote:

i'm tellin ya, one day i'll interface a mass spec and uv-vis spectrophotometer to a modular synthesizer

 
Virola78
#29 Posted : 7/10/2010 12:24:45 PM

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w0mbat wrote:
Virola - SWIM has found that your problem is a common one, and that fine particles even get through double- and quadruple-layered filters of muslin fabric. Try letting your acidic tea sit in the fridge overnight. Solids should settle on the bottom by morning. Carefully remove the top 3/4 of the liquid layer and filter it through a coffee filter again, it should go through easier this time.

To the remaining 1/4 of your tea, add more distilled water or vinegar, let it sit overnight, and then remove the top 3/4 or so of the water layer again. Repeat once more and you should have all of the active material without any of the plant gunk. Reduce the volume again and you should be good to go on to the next phase of your tech.



Ok thanks for the tips. But this is too much work imo (so far).
Maybe i will do it again later, to see if this 'tea tek' can give me a cleaner crude product to start with.

Some silly cat tried a bit of the mescaline-HCl of the 69ron tek. The cat now realizes mescaline really needs to be fairly pure to have full effect. The cat begins to understand now what people mean when they say that the other alkaloids 'overshadow' or 'numb' the true mescaline experience.

Also the cat so far concludes for himself (for his 'way of lab'Pleased that mesc-HCl washed with acetone then IPA, is much cleaner than previous mesc-acetate washed with MEK.

There needs to be done more experimenting Very happy


“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
w0mbat
#30 Posted : 7/10/2010 1:43:16 PM

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Virola78 wrote:
w0mbat wrote:
Virola - SWIM has found that your problem is a common one, and that fine particles even get through double- and quadruple-layered filters of muslin fabric. Try letting your acidic tea sit in the fridge overnight. Solids should settle on the bottom by morning. Carefully remove the top 3/4 of the liquid layer and filter it through a coffee filter again, it should go through easier this time.

To the remaining 1/4 of your tea, add more distilled water or vinegar, let it sit overnight, and then remove the top 3/4 or so of the water layer again. Repeat once more and you should have all of the active material without any of the plant gunk. Reduce the volume again and you should be good to go on to the next phase of your tech.



Ok thanks for the tips. But this is too much work imo (so far).
Maybe i will do it again later, to see if this 'tea tek' can give me a cleaner crude product to start with.



I agree, it takes forever. That's why SWIM has switched to STB with lye-water. Lye is probably the best thing there is for breaking down cactus mucilage anyways...
benzyme wrote:

i'm tellin ya, one day i'll interface a mass spec and uv-vis spectrophotometer to a modular synthesizer

 
Virola78
#31 Posted : 7/10/2010 2:14:28 PM

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w0mbat wrote:
...I agree, it takes forever. That's why SWIM has switched to STB with lye-water. Lye is probably the best thing there is for breaking down cactus mucilage anyways...


There is no mucilage when using the 69ron tek, using lime instead of lye
and if the cactus powder* is mixed thoroughly with the lime powder before slowly mixing in the water, then the NP (xylene was used) can later be very easily separated from this cactus-lime-water-mix
use a big jar (1,5L) and just pour off the NP, see picture

* green flesh only, without skin. cut into strips, left to dry, powderized by coffeegrinder



some 50ml of the original 300ml xylene will remain in the mix after the first pull. so after the first pull there is 250ml xylene to salt.
the remaining 50ml be retrieved from the mix by using a coffeepress after the last pull.

nothing new here really
but i was wondering why to use lye and figured it was because of the 'mucilage'?

“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
jbark
#32 Posted : 7/10/2010 3:49:35 PM

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I should maybe start another thread to ask this, but here goes: is it really worth all the trouble to get pure mescaline? The resin I have is quite strong and very enjoyable, so i can't help wonder what the principle differences would be effectwise between this and a purer product...

Cheers,
JBArk
JBArk is a Mandelthought; a non-fiction character in a drama of his own design he calls "LIFE" who partakes in consciousness expanding activities and substances; he should in no way be confused with SWIM, who is an eminently data-mineable and prolific character who has somehow convinced himself the target he wears on his forehead is actually a shield.
 
Virola78
#33 Posted : 7/10/2010 4:41:23 PM

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jbark wrote:
I should maybe start another thread to ask this, but here goes: is it really worth all the trouble to get pure mescaline? The resin I have is quite strong and very enjoyable, so i can't help wonder what the principle differences would be effectwise between this and a purer product...

Cheers,
JBArk


^ there is some resin too, made from the same batch of cactus material.
But it was not tried in full dosis. so no comparisons yet.
maybe other animals have seriously compared?

Atm some tripperhappy cat is very excited about the purified mesc-HCl.
He did another (=3rd) IPA wash (which did not take on/off colour) and will be trying ~400mg soon
Very happy

hopefully no dissapointing surprises.
full dose should sufficiently eliminate 'misinterpretation of effect of other alkaloids' or perhaps (euforic) placebo effects.

“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
w0mbat
#34 Posted : 7/10/2010 7:05:46 PM

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Virola78 wrote:

Atm some tripperhappy cat is very excited about the purified mesc-HCl.
He did another (=3rd) IPA wash (which did not take on/off colour) and will be trying ~400mg soon
Very happy



What does the final product look like? Using ron's lime technique, SWIM ended up with a waxy, somewhat sticky, grayish-white product after washing with IPA. It looked almost like mescaline acetate, only whiter and a little less goey. The lye-water STB technique he is now using has produced regular crystals.

Edit: I should say that the salting was done with ~3% HCl, not with vinegar.
benzyme wrote:

i'm tellin ya, one day i'll interface a mass spec and uv-vis spectrophotometer to a modular synthesizer

 
Virola78
#35 Posted : 7/10/2010 9:17:26 PM

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w0mbat wrote:
Virola78 wrote:

Atm some tripperhappy cat is very excited about the purified mesc-HCl.
He did another (=3rd) IPA wash (which did not take on/off colour) and will be trying ~400mg soon
Very happy



What does the final product look like? Using ron's lime technique, SWIM ended up with a waxy, somewhat sticky, grayish-white product after washing with IPA. It looked almost like mescaline acetate, only whiter and a little less goey. The lye-water STB technique he is now using has produced regular crystals.


What?
i dont think mescaline acetate should be washed with IPA. the acetate should be washed with MEK, as far as i have understood.

Anyways, the 69ron tek using dried, powderized, green flesh without skin, lime, water, xylene, HCl 2%, 99% acetone washx2, 99% IPA washx3, will yield some off white free flowing powder. And it is very potent Shocked Shocked Shocked

OMFG you have no idea what i just experienced
i had no idea

“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
69ron
#36 Posted : 7/10/2010 9:41:55 PM

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Virola78 wrote:
Also the cat so far concludes for himself (for his 'way of lab'Pleased that mesc-HCl washed with acetone then IPA, is much cleaner than previous mesc-acetate washed with MEK.


This is true. The MEK wash for mescaline acetate doesn’t work nearly as well as an IPA wash for mescaline HCl. For this reason, until a better cleanup method is found for mescaline acetate, if you want pure mescaline you need to go with mescaline HCl.

Nearly 99% pure mescaline HCl can be obtained from mescaline HCl by washing with acetone and then IPA. The purity was verified by another member on this forum a while back.

Keep in mind that you can make mescaline HCl from mescaline acetate by simply pouring HCl onto mescaline acetate and evaporating it. It’s very simple. This works because HCl is a strong acid and acetic acid is a weak acid.
You may remember me as 69Ron. I was suspended years ago for selling bunk products under false pretenses. I try to sneak back from time to time under different names, but unfortunately, the moderators of the DMT-Nexus are infinitely smarter than I am.

If you see me at the waterpark, please say hello. I'll be the delusional 50 something in the American flag Speedo, oiling up his monster guns while responding to imaginary requests for selfies from invisible teenage girls.
 
69ron
#37 Posted : 7/10/2010 9:44:26 PM

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Virola78 wrote:
i dont think mescaline acetate should be washed with IPA. the acetate should be washed with MEK, as far as i have understood.


IPA was the first thing tried to wash mescaline acetate and it didn’t work. IPA completely dissolves mescaline acetate. So does acetone.
You may remember me as 69Ron. I was suspended years ago for selling bunk products under false pretenses. I try to sneak back from time to time under different names, but unfortunately, the moderators of the DMT-Nexus are infinitely smarter than I am.

If you see me at the waterpark, please say hello. I'll be the delusional 50 something in the American flag Speedo, oiling up his monster guns while responding to imaginary requests for selfies from invisible teenage girls.
 
Virola78
#38 Posted : 7/10/2010 10:45:25 PM

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69ron wrote:
Virola78 wrote:
i dont think mescaline acetate should be washed with IPA. the acetate should be washed with MEK, as far as i have understood.


IPA was the first thing tried to wash mescaline acetate and it didn’t work. IPA completely dissolves mescaline acetate. So does acetone.


Seriously dude, ty.

“The most important thing in illness is never to lose heart.” -Nikolai Lenin

I know that you believe you understand what you think I said, but I'm not sure you realize that what you heard is not what I meant.
 
endlessness
#39 Posted : 7/10/2010 10:51:41 PM

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but maybe w0mbat was talking about mescaline hcl (notice the quote in his post), so maybe he used ron's tek but salted with hcl?

otherwise indeed you guys are right and he shouldnt wash mesc acetate with IPA / acetone as it will dissolve it
 
w0mbat
#40 Posted : 7/11/2010 12:34:47 AM

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endlessness wrote:
but maybe w0mbat was talking about mescaline hcl (notice the quote in his post), so maybe he used ron's tek but salted with hcl?

otherwise indeed you guys are right and he shouldnt wash mesc acetate with IPA / acetone as it will dissolve it


Yes, precisely - I salted with HCl. Sorry for the confusion.

The final product I am left with looks sort of like vanilla ice cream. IPA washes did not get rid of whatever was giving it that consistency.
benzyme wrote:

i'm tellin ya, one day i'll interface a mass spec and uv-vis spectrophotometer to a modular synthesizer

 
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