Acid

[XxJWxX]

If any of you know, how do you make LSD (acid)???? I hear people make it at home in their bathtubs and labs, what materials are needed? How is it made? Etc...

Ahem, im not interested in partaking of the act of making any illegal substance, I just wanna know how to do it so that I gain more knowledge

[D9_THC]

I don't deny stealin this from somewhere, and I've never made it myself.... enjoy!

LSD

I think, of all the drugs on the black market today, LSD is the strangest. It is the most recent major drug to come to life in the psychedelic subculture. (Blah blah blah... let's get to the good stuff: How to make it in your kitchen!!)

1) Grind up 150 grams of Morning Glory seeds or baby Hawaiian wood rose seeds.
2) In 130 cc. of petroleum ether, soak the seeds for two days.
3) Filter the solution through a tight screen.
4) Throw away the liquid, and allow the seed mush to dry.
5) For two days allow the mush to soak in 110 cc. of wood alcohol.
6) Filter the solution again, saving the liquid and labeling it "1."
7) Resoak the mush in 110 cc. of wood alcohol for two days.
8) Filter and throw away the mush.
9) Add the liquid from the second soak to the solution labeled "1."
10) Pour the liquid into a cookie tray and allow it to evaporate.
11) When all of the liquid has evaporated, a yellow gum remains. This should be scraped up and put into capsules.

30 grams of Morning Glory seeds = 1 trip
15 Hawaiian wood rose seeds = 1 trip

Many companies, such as Northop-King have been coating their seeds with a toxic chemical, which is poison. Order seeds from a wholesaler, as it is much safer and cheaper. Hawaiian wood rose seeds can be ordered directly from:

Chong's Nursery and Flowers
P.O. Box 2154
Honolulu, Hawaii

LSD DOSAGES
-----------

The basic dosages of acid vary according to what kind of acid is available and what medium of ingestion is used. Chemically, the potency of LSD-25 is measured in micrograms, or mics. If you're chemically minded or making your own acid, then computing the number of micrograms is very important. Usually between 500 and 800 mics is plenty for an 8 hour trip, depending on the quality of the acid, of course. I have heard of people taking as much as 1,500-2,000 mics. This is not only extremely dangerous, it is extremely wasteful.

LSD comes packaged in many different forms. The most common are listed below:

1) The brown spot, or a piece of paper with a dried drop of LSD on it, is always around. Usually one spot equals one trip.
2) Capsuled acid is very tricky, as the cap can be almost any color, size, or potency. Always ask what the acid is cut with, as a lot of acid is cut with either speed or strychnine. Also note dosage.
3) Small white or colored tablets have been known to contain acid, but, as with capsuled acid, it's impossible to tell potency, without asking.

I hope this isn't against the rules.......

[XxJWxX]

Thanks a lot, but is that the only way to make it? You have to have morning glory or hawaiian wood rose?? Or is there anything else

[phunkyphil]

THAT IS NOT AN LSD SYNTHESIS.. and the real instructions are totally illegible unless you have a masters in chemistry, and require stuff that not many people are able to get.. so basically, noone here will be able make any lsd.. sorry


LSA (a different drug, with different effects and side effects than lsd) is a legal hallucinogen found in morning glory and hawiaiian baby woodrose seeds..

http://www.erowid.org/chemicals/lsa/lsa.shtml
http://www.erowid.org/plants/hbw/hbw.shtml
http://www.erowid.org/plants/morning...ng_glory.shtml




misinformation is bad.. when talking about drugs, please KNOW YOUR SHIT, or else you can really fuck people up.

[D9_THC]

Oh... ok...... my bad.

[phunkyphil]

JACS, 78, 3087 (1956). 3-Indolepropionic acid, 94.5 g (0.5 mole) is dissolved in 600 ml of water containing 20 g of NaOH. The solution is mixed with 100 g of Raney Nickle catalyst and hydrogenated at room temp in a steel bomb at about 3,500 psi until the uptake of hydrogen stops (about 20-30 hours). Filter off the catalyst and wash it with a little water to remove the product that is clinging to it. Add 85 ml of concd HCl acid to the filtrate, and cool. If your reduction is incomplete, you will now have unreacted starting material separate, and this must be removed by filtration. Benzoylate the filtrate (the Schotten and Baumann method is preferable), using 210 ml of 12 N NaOH 180 ml of benzoyl chloride. Keep the solution alkaline throughout the benzoylation, and keep the temp below 40°C by cooling. When the benzoyl chloride is fully reacted, the reaction mixture is cooled and acidified with 300 ml of HCl acid. Filter the crude product by filtration, wash with water, and extract with four 1 liter portions of hot water. Separate, and crystallize the resulting syrupy product from a few volumes of methanol. Filter and wash with a little cold methanol to get a little over 100 g that melts at 151-153°. This is l-Benzoyl-3-beta-carboxyethyl-2,3-dihydroindole. This can be purchased to eliminate this step.

1-Benzoyl-5-keto-1,2,2a,3,4,5,-hexahydrobenzindole. 118 g of the above product (1-benzoyl-3-B-carboxyethyl-2,3-dihydroindole) is mixed with 200 ml of pure thionyl chloride. This solution is allowed to stand for 30 min, then it is warmed gently for 15-21 min on a steam bath. Excess thionyl chloride is completely evaporated with the temp maintained between 22-26°C in vacuo. The crude acid chloride is dissolved in dry carbon disulfate. This solution is added, in a thin stream, to a well stirred suspension of 240 g of aluminum chloride in 1750 ml of carbon disulfate in a 5,000 cc flask. Note: this must be done under a fume hood. A complex will separate and bog down the stirring device. Heat this mixture under reflux with stirring for 1 hour. Decompose this mixture by adding 500 g of ice, 250 ml of concd HCl acid, and 500 ml of water, all while good stirring is continued. Cooling of this operation is affected by periodic distillation of the carbon disulfate in vacuo. After the decomposition is complete, any remaining carbon disulfate is removed completely in vacuo, and the product is extracted with 2 liters of benzene. The extract is washed well with 500 ml of 2 N NaOH in three portions, and then with water. Dry (with the usual magnesium sulfate), and evaporate to a small volume in vacuo. Add this small volume to several portions of ether to get the ketone to crystallize (add slowly), and filter, then wash with ether to get 85 g of pure title product, mp: 146-147°C.

1-Benzoyl-4-bromo-5-keto-1,2,2a,3,4,5-hexahydrobenzindole. A solution of the above indole (305 g) in 2,200 ml of glacial acetic acid is warmed to 40°C. While the reaction is illuminated with a 250 watt bulb, 352 g of pyridine hydrobromide perbromide is added in portions, over 5 min with shaking. The solution is then heated to 60° and is held between there and 55°C for 30 min. Treat the mixture with carbon, and evaporate to a small volume in vacuo. The residue is taken up with 2,200 ml of chloroform, and wash this solution with several portions of water, dry as above, and concentrate in vacuo. Crystallize the residue from 2,200 ml of 50% acetic acid and 50% ether to get 270 g of title product that melts at 180.5-181.5°C. Another crop can be obtained from concentrating the fltrates. Yield: 30 g of less pure product.

1-Benzoyl-2,2a,3,4-tetrahydro-4-methyl-2-methyl-1,3-dioxolan-2-yl-methyl-aminobenzindol-5-(1H)one. A solution of the last indole product above (270 g) and 307 g of methylaminoacetone ethylene ketol in 4,500 ml of dry benzene is refluxed for 21 hours under a slow stream of nitrogen. The mixture is cooled and 151 g of methylaminoacetone ethylene ketol hydrobromide is filtered off. The filtrate is washed with ice water, then extracted with 2.5 liters of cold dilute HCl acid containing 150 ml of the concd acid. The acid extracts are immediately added to an excess of ice cold dilute NaOH. Extract with 1 1iter of chloroform, dry over magnesium sulfate, treat with carbon and concentrate by evaporation in vacuo. The residual ketol-ketone is crystallized from acetone to yield 220 g, mp: 135-136°C.








etcetera.. etcetera.. etcetera.....

[KRIMINALELUMENT]

Most acid is nto made 'at home'
Anyone who says they have home made acid doesn't have acid, and I don't know if you should take any of what they're offering as 'home made' acid.
Most of it comes form Northern California, around San Fran.

[NuBBiN]

lol no people dont make acid in their bahttubs or kitchens....alcohol...yes...lsd...no way. Like phunky phil demonstrated, it requires quite a bit of knowledge to make some decent acid. And that recipe that was posted using morning glory or baby hawaiian woodrose seeds doesnt produce acid..it extracts the active Lysergic amides that are similar but much less potent than acid.. that would make LSA...but why go through all that toruble when you can grind up the seeds and eat them on the spot...fuck all the chemical soaking

[XxJWxX]

Actually I have a friend (not mentioning anything else about him) who grows in his bathroom. I know that he has a little lab set in the closet (big closet) where he does make it. I just havent talked to him for almost a year but i've seen inside there and everything, so yeah I guess people do make lsd in there bathrooms

[HappyJ]

You don't grow LSD and I don't believe you for one second that your friend makes LSD. He may be making some kind of chemical slushie that send you tripping but LSD? I doubt it. If he is growing smoething then whatever he is making is probably derived from LSA or something similar.

[phunkyphil]

a dmt extraction from phalaris grass perhaps?

[dirtydingusus]

the recipe dp posted is from the old anarcist cook book


and it is labled "how to make lsd in your kitchen"

and maybe his friend does make the trips....
you dont know wether hes a cemist or not ?

he never said what his friend was growing ....
or that it was part of the prossess




i dont care who is making it i just want some acid!!!!!



please?

[phunkyphil]

unless he has lots of expensive, hard to get equipment hidden in some underground lab under his house, he cant make lsd.

no, you cant make lsd with a chemistry set in your kitchen.

[NuBBiN]

Originally posted by dirtydingusus
the recipe dp posted is from the old anarcist cook book


and it is labled "how to make lsd in your kitchen"

and maybe his friend does make the trips....
you dont know wether hes a cemist or not ?

he never said what his friend was growing ....
or that it was part of the prossess




i dont care who is making it i just want some acid!!!!!



please?

lol well that just goes to further prove peoples point that its all a load of crap, half the stuff in the anarchist's cookbook was bullshit written up that sounded like it would work in theory but was never tested...theoretically yes that recipe might produce a trippy substance, but its not lsd, close, but far from it also. My advice is for people to stick with buying from people who know what theyre doing..

[phunkyphil]

Originally posted by NuBBiN


lol well that just goes to further prove peoples point that its all a load of crap, half the stuff in the anarchist's cookbook was bullshit written up that sounded like it would work in theory

yeah, but im sure the folks at Chong's Nursery and Flowers arent complaining.