do what i do, ask people you know. usually someone has a friend of a friend of a friend who sells acid/ any other drug, unless your friends suck

No hookup and $400?

Enjoy your vial of water/RCs.

Dead shows. Seriously, people bring enough acid to Grateful Dead shows to make the whole bay trip. You won't find any on any corner, and if you try to buy $400 of lsd from someone you don't know, you'll probably get ripped off or just get your money taken from you.

The Jam Scene will get you anything. I was at The Allman Brothers Band , Bob weir, and rat dog Concert last week. this is true. but i can say that if you asked any hippie for that type of acid your lookin like a narc.

Actually, it shouldn't be too difficult since you live in northern California. Just look for some hippies and ask if they know where to get some doses.

This is how I get all my acid.

This is how I get all my acid.

Yea I used to do that but the other day I fried so hard and it felt so clean. No bad vibes or anything, Im worried if I buy from hippies it might be 2cb and speed I hear they mix water a minor hallucigen rc and meth so your up all night tripping and you think your on acid I want the bomb shit I want 200 hits for 200 I plan on dosing for the next month, any good tunes I should listen to

200 hits for 200

Good fucking luck. I've never seen L that cheap. You might get it for 6 if you're lucky.

And as was said, you live in Northern California. Go ask some fucking hippies. That's the only people who are gonna have it anyway. You can tell who has the real shit when you meet them.

Yea I used to do that but the other day I fried so hard and it felt so clean. No bad vibes or anything, Im worried if I buy from hippies it might be 2cb and speed I hear they mix water a minor hallucigen rc and meth so your up all night tripping and you think your on acid I want the bomb shit I want 200 hits for 200 I plan on dosing for the next month, any good tunes I should listen to

Listen to the Beatles revolution number nine its is fucking insane, was made for lsd trips

To the kid who said the dealer will take an hour of his time to dose with you, its gona be more like 9 hours of his time, and i do not think that will happen. Even if he has good shit or bad shit \\


But how almost everyone gets there lsd is at psychedelic band concerts/ festivals and what not
Try and score on the 1st day as soon as you get there because if not stored right the shit degrades
Like by the last day of a festival the shit being stored in a hot car ot tent is half as strong as when 1st made

how do you buy acid?

jesus, it isn't that complicated. it just might take a little bit of time/effort

dude i've showed you how fuckin easy it is to buy acid in arcata, what do you expect, someone to come to you? fuckin grow a pair and ask somebody.

also, its the perfect time of the year to find some. this is about the time of year i started asking around my first time, and you know exactly where i got it. its not gonna take any time or effort around here. oh and i've never heard of anybody sellin rc's around here, that shits pretty unheard of here in humboldt.

god damn, after reading your last few threads/posts i see you're the same fuckin moron i remember you as. i could give you all the tips and maybe even help you personally but you still wouldn't fuckin get it.

Find some hippies.

i go to the park in the city of fog

This is exactly what I do when I have some extra cash and want something I usually don't take often. Someone always knows someone who can get it for you. Hasn't failed me yet.

This is exactly what I do when I have some extra cash and want something I usually don't take often. Someone always knows someone who can get it for you. Hasn't failed me yet.

isn't real acid hard to get though. I hear theres only like 15 people in the us that can make it.

isn't real acid hard to get though. I hear theres only like 15 people in the us that can make it.

Don't know where you heard that. Also, you probably mean 15 people that DO make it. Although, I'm willing to bet it's more than 15.

Plenty more than 15 people know how to make it, they just choose not to because of the obvious risks involved.

Don't know where you heard that. Also, you probably mean 15 people that DO make it. Although, I'm willing to bet it's more than 15.

Plenty more than 15 people know how to make it, they just choose not to because of the obvious risks involved.

I know. I hear its one of the hardest drugs to synthezize, plus the DEA watches all the lab equipment you need to even get started. What I took the other day felt like Real acid I had never felt that way before the other times I had tripped, I can recall a few things the first time I dosed everything had waves through it and didn't feel that great but the other night, probably the fith time when I squirted half a vial in my mouth I felt amazing I took it at nine at night the day before and didn't stop tripping hard until around 2 in the afternoon the next day. clocks were popping off the walls and there hands were spinning. what seemed like a mile a minute also I looked at the wall, the album and made connections with the art I felt you could only make on acid. like it was meant to be looked at while tripping. I looked at a white cealing and saw kalediscope patterns running through it bubbling and then I looked in the mirror and saw myself as everyone else saw me I saw all my defects and flaws. then I didn't recognize myself like an ego death or something. the next day I looked up everything

http://en.wikipedia.org/wiki/LSD

and all the effects were exactly what is described.

y. Its unusual psychological effects, which include visuals of colored patterns behind the eyes, a sense of time distorting, crawling geometric patterns, and the loss of the user's sense of identity

also

To a solution of 3-methoxycarbonylindole (7.0g, 40.0mmol) in TFA was added Thallium(III) trifluoroacetate (32.6g, 60.0 mmol) in TFA (140 ml), and the mixture was stirred for 2 hours at r.t. After TFA was evaporated in vacuo, a dark brown oil was obtained. This oil was suspended in 450 ml H2O, and KI (19.9 g, 120.0 mmol) was added to this suspension. The reaction was stirred at r. t. for 2 hours. CH2Cl2:MeOH (95:5, v/v) (300 ml) was added to the reaction mixture and insoluble precipitates were filtered off through a plug of celite. The organic layer was separated and washed with aq. sodium thiosulfate then brine. Removal of the solvent left a brownish solid. Quick purification by a short plug of silica gel afforded a white solid (8.68g) as 4-iodo-indole-3-carboxylic acid methyl ester in 72.1% yield. This material was used directly in the next step. To a solution of 4-iodo-indole-3-carboxylic acid methyl ester (6.02g, 20.0 mmol) in 200 ml methanol was added 200 ml of 40% aq. NaOH. The reaction was refluxed for 1.5 h with stirring. After evaporation of the solvent, the residue was poured into 200 ml water, and extracted with CH2Cl2:MeOH (95:5, v/v; 200 ml x 3). The extract was washed with brine, dried over Na2SO4, and evaporated in vacuo to leave an off-white solid. Purification by chromatography using hexane : ethyl acetate (6:1) afforded a white crystalline solid (3.51g) in 72.3% yield. Understand it? Did you even understand one whole sentance?

that seems so hard to make I can bet most people like me that don't have a hookup are getting some rc and meth or like liquid lsa thats why Im so weary and asking so many questions.

My sister is really nieve like completley but she is going to stanford for something it could be chemistry do you think she could make it, hypothetically.

^ Does she have access to a lab and all the materials needed to make LSD? I'm gonna go ahead and answer that for you and say no.

LSD is serious business, if any ol' chemistry major could make it then maybe idiots like you could actually get LSD.

yea thats why I Think Ive only had it once. And that is why Im saying it seems hard to get.

ib4myboyfriendmakeslsdinabathtub

My boyfriend makes LSD in a bathtub.

But once you start making it, you can make billions of dollars worth easy. The problem is finding buyers.

that shits made out of the stuff under your sink!

Ajax + drain-o + rubbing alcohol + hydrogen peroxide.

Mix well for 30 minutes, and let sit over night.

BAM! LSD.

if you want.......

there IS this shit you can do with bananas,

And peanut shells and dried toothpaste.

jenkem and nutmeg is where it's at though

...

I can't even fit the whole synthesis into one post.

Synthesis of the Precursors for Lysergic Acid Diethylamide

Lysergic Acid Synthesis
This is the easiest way to totally synthesize lysergic acid. There are other ways, but after reviewing other methods, I found this to be superior. It is quite complicated and it takes good modern equipment.

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.

5-Keto-4-N-methyl-N-acetonylamino-1,2,2a,3,4,5-hexahydrobenzindole. 20 g of the above product is dissolved in a mixture of 250 ml of concd HCl acid and 250 ml of water, and the solution is kept under nitrogen for 5 days at 37°. Cool the mixture, treat with carbon, filter, and concentrate the filtrate in vacuo to a small volume. Treat the residue with an excess of sodium bicarbonate, extract with cold chloroform, and remove the chloroform by evaporation in vacuo at room temp. The crude diketone is powdered, slurried with 75 ml of benzene-ether, and filtered. Yield: 9.8 g, mp: 105-107°C.

9-keto-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-(4,3)isoquinoline. 25 g of the above product is mixed with 550 ml of absolute ethanol. Stir this mixture under nitrogen and cool to -15° with an external freezing mixture. Sodium methoxide is added (17 g) and the mixture is stirred for 10 min at -10 to -12°. Cool to -25°, and the product is filtered and washed (while still in the funnel) with cold ethanol and ether. Without exposure to air the crude ketone is immediately slurried with a little ice water and filtered. Wash with ice water, ethanol, then ether (all cold) to yield 16 g of product melting at 145-147°.

4-Acetyl-9-keto-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-4,3-quinoline. 24 g of the last product is added to 80 ml of cold acetic anhydride. The mixture is held at 25° for about 5 min, then thoroughly cooled, filtered, and the product (a solid) washed with ether to yield 20.5 g, mp: 169-170°. A second crop is obtained by concentrating the mother liquor by evaporation.

A mixture of the last product (1.0 g) and 10 g of palladium carbon (5%), in 35 ml of xylene, is heated under reflux for 4 hours. The catalyst is filtered and extracted with hot methanol and chloroform. The combined extract filtrates and the initial filtrate are combined and evaporated in vacuo. The residue is recrystallized from water to give 0.6 g of a monohydrate product that melts at 255-256°. This product is called 4-acetyl-4,5,5a,6-tetrahydro-9-hydroxy-7-methylindolo-(4,3fg)-quinolinium hydroxide betaine.

4-Acetyl-9-hydroxy-7-methyl-4,5,5a,6,7,8,9,10-octahydroindolo-(4,3fg)-quinoline. 1 g of the above betaine in a mixture of 20 ml of ethanol and 5 ml of water, is treated with 0.08 g of sodium borohydride, and this solution is refluxed for 10 min and kept at 25° for 1 hour after the reflux is finished. The solvent is distilled off, and the residue is taken up in a mixture of chloroform and water. The chloroform solution is separated, dried as above, and then the solvent is distilled off. The residue is recrystallized from a nitromethane-ethyl acetate mixture to yield 0.2 g (21%), mp 193-196°. Not only is this a small scale, but it is a poor yield, requiring you to perform it several times to get enough product to perform the next step. When you have more than enough, convert the product into its hydrochloride form by dissolving in dry methanol and precipitating with dry hydrogen chloride.

4-acetyl-9-chloro-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-(4,3fg)-quinoline hydrochloride. 3.1 g of the above product in its hydrochloride form is dissolved in 75 ml of liquid sulfur dioxide contained in a glass lined, high pressure bomb, or autoclave. Thionyl chloride (1.2 ml) is added and the vessel is sealed and kept at 25° for 6 hours. Vent the vessel carefully and remove the mixture. Evaporate the sulfur dioxide while keeping the volume of the solution constant by the slow addition of dry ether. The amorphous chloro hydrochloride is filtered, washed with ether (dry) and dried by evaporating in vacuo to give 3.5 g of product, mp:130-135°.

4-Acetyl-9-cyano-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-(4,3fg)-quinoline. 40 g of dry, powdered sodium cyanide, is added to ice cold liquid hydrogen cyanide and stirred gently with ice bath cooling. Speed up the stirring, continue the cooling, and add 7.5 g of the amorphous product directly above. Continue stirring for 30 min, then the hydrogen cyanide is distilled under enough reduced pressure to keep it coming over the condenser at a temp below 10-12°. The residue is mixed with chloroform and ice water, and the resulting mixture is filtered. The organic layer of the filtrate is separated and the aqueous layer is extracted with two separate portions of chloroform. The combined extracts (this would include the separated chloroform, as usual) are dried over magnesium sulfate, decolorized, and the solvent removed by distillation in vacuo. Crystallize the product in ethyl acetate. Yield: 3.3 g, mp: 173-174°. Recrystallize again for extra purity.

9-Carbomethoxy-7-methyl-4,5,5a,6,6a,7,8,9-octahydroindolo-(4,3fg)-quinoline. 1 g of the last product is mixed with 15 ml of methanol and 0.25 ml of water. With external (ice bath) cooling add 2 ml of concd sulfuric acid slowly. Seal this solution in a high pressure bomb with a glass liner (or in a glass tube taking safety precautions in case of explosion) with a nitrogen atmosphere, and heat at 100° for 23-24 hours. Note: I have seen a big pressure cooker (like gramma cans peas with) work for some of these bomb procedures. I do not recommend it, but here is how to do it right, if you feel you must. Use only the great big heavy duty models, in excellent condition, set the pop off (relief valve) for near maximum position; never, ever tamper or modify this valve to get more pressure. Put the product in a glass beaker, put it in the cooker, flush with nitrogen, heat and stay in a different house during the reaction. Carefully turn off heat, notice or record pressure gauge after time has elapsed. Wait until pressure drops noticeably, bleed off remaining pressure and get product.

Treat the mixture with decolorizing carbon and then evaporate in vacuo to 10 ml. Pour onto a mixture of 30 ml of chloroform, ice, and 10 g of sodium bicarbonate. Separate the chloroform layer, and extract the aqueous phase with three 10 ml portions of chloroform. The combined chloroforms are dried, evaporated to dryness in vacuo, and the product is crystallized from benzene to give 1/2 g of product that melts at 159-160°. You may purify more by recrystallizing from ethyl acetate. This is not very much product. As with the procedure 4 steps back, you will have to perform this step over and over. If you try to double or triple the amounts given, you may get more product, but you will hurt the yield.


Can't even fit the whole synthesis into one post.

dl-Lysergic acid. 3.9 g of the last product is mixed with 78 ml of 1.5% potassium hydroxide solution. Reflux for 30 min under nitrogen. 8.5 g of hydrogen sodium arsonate, and Raney Nickle (16 g wet), that has previously been deactivated by boiling in xylene suspension (see JOC, 455 (1948) to deactivate), is added and the mixture is refluxed and stirred under a nitrogen atmosphere for 20 hours. The solution is treated with carbon, and the crude lysergic acid is precipitated by neutralization to pH 5.6, and then filter it off and wash with water. Yield: 1.04 g. A second crop is obtained in the usual manner (0.15 g). Purify by dissolving in dilute ammonium hydroxide, treat with decolorizing carbon, and reprecipitate with carbon dioxide to get a mp of 242-243°. You may be able to get an analytical or laboratory consultant to make one of these products near the final step, thereby eliminating the need to go through all of the steps as described. This will save you much time, but as these people are highly trained, their time will be costly.


Lysergic Acid Diethylamide from Lysergic Acid:

This is taken from CA, 57, 5979 (1962). It is designed by Hofmann to give 1-methyl-D-lysergic acid, and is modified to give LSD and iso-LSD. Dissolve 0.54 g of lysergic acid in 10 ml of freshly distilled phosphorous oxychloride, stir 0.42 g of powdered, fresh phosphorous pentachloride. Allow to stand at room temp for 2 min, then at 90° for 2 min, then evaporate in vacuo. Extract the residue with hexane to give lysergic acid chloride hydrochloride. To save time you may extract the reaction mixture without evaporating. Add 2.5 g of the hydrochloride to a cooled solution of 7 ml of diethylamine (or analog) in 25 ml of methylene chloride that is cooled to 0° Note This solution is cooled to 0° before the addition. With stirring add 13.75 ml of dry pyridine and stir for 30 min with cooling to keep the temp at 0° or a little below. Warm to room temp and continue the stirring for 90 min. Evaporate in vacuo to get the LSDs. Separate as already described.

"Anybody want some L...S...D?"

"Anybody want some L...S...D?"

Lol, that reminds me. At a music festival once this guy asked my friend if he was looking for doses (he was a drug/festival noob at the time) and he said "What kind?"

The guy's response was "L...S...D..."

Do you not have friends in real life?

Did you know that people know people who know people who sell drugs? It's true.

Did you not know that concerts are usually full of people who do drugs? I'm guessing even if you did you wouldn't know how to go about asking them. All it takes is a cool head and to know NOT to just blurt out "Hey man, can I buy some of your drugs you obviously have?"

It isn't really that hard dude. Common sense goes a long ways. Hit some concerts, bars (if your old enough) or even a college campus (IF you go there). Don't just go walk around a college campus asking for drugs either. That isn't going to help your situation.

well, not everyone knows people who knows people...that they know about anyway. i've met some really square people in college

well, not everyone knows people who knows people...that they know about anyway. i've met some really square people in college

Whether they know it or not, I think everyone knows someone who knows someone who knows someone who is acquainted with someone who knows someone who sells/does drugs.

Lol, that reminds me. At a music festival once this guy asked my friend if he was looking for doses (he was a drug/festival noob at the time) and he said "What kind?"

The guy's response was "L...S...D..."

So...it was good stuff, I take it?

Oh, quite. Two had me frying quite well. Plain white unperfed fluff :)