69ron said:Ok, now you have a bunch of sticky brown impure mescaline. You first wash it with acetone about 2 times. You use about 20 ml of acetone for each wash. With the acetone covering the mescaline, you small the mescaline and much as you can. You want to powderize it in the acetone. Wait for all the particles to settle down and then carefully decant your acetone so that none of the mescaline is decanted with the acetone. Repeat it with 20 ml more acetone.
Cosmo said:I guess SWIM is just paranoid, but being cautious is never a bad thing. Besides SWIM like Bridgesii seems to be more consistent in its content FV has some powdered stuff but its brownish, shit SWIM fresh dried and pulverized Bridgesii was bright green. SWIM never had any luck from pachanoi not sure why. Shit SWIM had no luck with your tek either RON but has a few ideas why that happened. Swim's gonna stay with fresh he knows what he's getting. Plus SWIM is learning to be patience from peeling and drying..a labor of love. No doubt Big Brother is watching one day all things enlightening will be forbidden, then the music will surely die. Thanks for all the input from everyone and when SWIM attempts another extraction he will surely need to tap into your wealth of knowledge some more.
mori said:69ron said:Ok, now you have a bunch of sticky brown impure mescaline. You first wash it with acetone about 2 times. You use about 20 ml of acetone for each wash. With the acetone covering the mescaline, you small the mescaline and much as you can. You want to powderize it in the acetone. Wait for all the particles to settle down and then carefully decant your acetone so that none of the mescaline is decanted with the acetone. Repeat it with 20 ml more acetone.
Hi
I have enjoyed your posts, 69.
This is a great process.. However, I'm having trouble understanding this step of your process. As you implied, its a sticky brown mess. I need you to more clearly define the process of "wash" and define what you mean when you say "small the mescaline".
I imagine the process is add 20ml, and shake, let settle, and decant? Surely with only 20ml added to a gunky mess, this isn't possible?
Also... SWIM foolishly bought a soxhlet setup thinking this the best equip to extract mescaline; only to find bottles, blender and solvents can do the trick lol!
SWIM supposes they'll find more uses for it; SWIM has been wanting one for over ten years..
SWIM is looking forward to trying pure mescaline!
Green is a sign of good health, not a sign of high alkaloid content. Actually, the greener it is usually the lower the alkaloid content is, because these cacti produce more alkaloids when they're NOT doing well.
3 - Pour off the d-limonene through a filter.
4 - Add 25 ml of water with 5 ml of 10% HCl solution to the d-limonene. Mix thoroughly.
PitfromGreece said:Hi Ron,
The whole thing is wonderful, SWIM has pure mescaline, but the yield is somewhat low. Could you explain a little bit more the steps below:
3 - Pour off the d-limonene through a filter.
SWIY just presses the mixture (cactus - limonene) through a coffee press right? SWIM put the limonene through a paper coffee filter also, and maybe some of the mescaline was left there.
4 - Add 25 ml of water with 5 ml of 10% HCl solution to the d-limonene. Mix thoroughly.
SWIM uses a blender to mix thoroughly, the problem is that it takes alot of time for the limonene and HCL solution to really separate. Does SWIY use a blender also or is not necessary?
zeki0 said:Hi ron,
SWIM wanted me to ask these 2 questions:
-What should the final purified mescaline HCL taste like? SWIM tells me that his slightly off-white powder tastes like bitter salt.
-Is it possible that, after cleaning (2x acetone, 1x IPA), the resulting product is anything else other than mesc HCL?
SWIM is finding that his product does not produce the expected effects at doses of 100mg,200mg,300mg.. He suspects that his cactus was not very potent.
SWIM appreciates your work!
69ron said:zeki0 said:Hi ron,
I think you have pure mescaline HCl. I don't think there's any chance of anything else being left after those washes unless a different cactus was used or the tech wasn't followed properly.
Funny you should mention that! Given that this is a fairly high return reaction, SWIM is thinking of performing this operation on a variety of cactus; in particular SWIM picked up a beautiful (and stocky!) Trichocereus Scopulicolus yesterday of about 4.5 foot with a fat diameter of around the size of a side plate (not many lobes on Scop; wide, short and fat lobes). I will be starting a thread for my SWIMs results from this; as soon they receive the d-limonene
Perhaps even an experiment to see if there are any non Trichocereus with mescaline in them. A peyote in the rough so to speak.
I have soo questions regarding d-lemonene. Is it a solvent or a detergent? acid or base? It seems to be sold as everything from fragrence to cleaning gum off shoes as well as pavement cleaner!
Can d-lemonene be stilled to retrieve the other alcoloids? Is there any way of fractioning off each of the results and know whats dropped off as a salt? (EDIT: Yay Column Chromatography!)
Is there any bad reason SWIM can't just reuse the same d-lemonene accross dozens of cactus and have it collect the non Mescaline alcoloids for extraction all at once via evaporation?
A blender is pretty strong and tends to form emulsions. How long is it taking to separate?
Noob said:So swim tried to go ahead and wash with acetone. The acetone dissolved a lot of the dark reddish pigment and ended up looking like thin india ink. There was a black residue that was insoluble in the acetone that stuck to the dish. Swim assumes this is mesc, but why is it black?
Noob said:PLEASE help, somebody. SWIM wants to try the pure mescaline instead of the rough alkaloid extraction with all the other alks.
mori said:Noob, I haven't given this a go yet, i'm still a couple of weeks away from getting the unusual solvent d-lim, but I recommend that you dry the wash solvent off, pulverise the solid, and continue the wash process. I suspect that you used the incorrect intial HCL concentration; and the HCL "extracted extra gunk" as specified in his initial post. Could you clarify which strength of HCL you used, and perhaps the local expert 69 can help you.
Perhaps you could list, in dot form, the procedure you followed? We can't understand whats wrong without that knowledge.