Acid

[MrsDingusus]

hey nubbs
i just happened to remember reading that
recipe a long time ago

never tryed it my self


they also had a resipe for scraping the shit from
the inside of bannana peals in there

funny shit....


but the explosive recipies in there do work...

[Kronix420]

Originally posted by NuBBiN


. My advice is for people to stick with buying from people who know what theyre doing..

But the really hard part is finding those people!

[dirtydingusus]

gawdamn cookies!!!!!!!



that was my post .....not hers!


but my computer seems to want to log me in as her now


fucking cookies!

[XxJWxX]

HappyJ, My bad if I said something about growing, I did not mean that he actually grew, like as in marijuana.

What I meant was, yes he does have a lab, and i've seen it with my own eyes.So dont fucking judge shit over the internet man, thats so stupid and ignorant, I mean........Im sitting here, typing out things that are actually true, I personally know that its true because I did see, but then I come on this website, and I get this bullshit negative response from you? You should think before you say shit like that next time.

Nubbs, yeah it was very expensive. And he was a very very smart guy actually. I dont distinctively remember exactly what ingredients looked like, but he had about 10-15 people come over at seperate times everyday who would buy from him. He made like 150 a day off slangin the acid


Edit: The finished product would be in liquid form. He had hundreds of empty containers (identical to clear eyes/visine containers). He put liquid in there with a syringe and all you had to do, was take off the cap, squirt out maybe the same amount as a tear drop, onto a little piece of paper, and I think it was somewhere to like 100-200 hits of acid per drop. He also had tablets, not sure what it looked like on the inside though. Some were different colors on outside. Once again, none of this is bullshit, im also sure that what he made was in fact LSD, this was a real mature person who would never lie in his life, he was like a perfect christian, except one who did lots and lots and lots of drugs. Actually, I believe hes in college right this second, trying to get his MD. I always knew he'd end up bein a doctor or some shit like that when he got older

[dirtydingusus]

i want some?

[NuBBiN]

when acid is usually made in mass amounts (which is really the only effective way) its in a crystalized form. Its usually later converted into a liquid for blotters and such...so its not grown per se, but in a sense it can be considered something that must be grown, or crystalised...words are so confusing arent they? language is so flawed..when I become ruler of the world, the first thing to do is produce acid for everyone who wants it, then my second job will be to destroy the flawed and conflicting human creation called language...YARHARHAR! (<~~~pirate laugh)

[NuBBiN]

i may be confused, but the guyy who wroe this ACB recipe mentions "I have heard of people taking as much as 1,500-2,000 mics."...that would come out to be 1.5-2mg of acid?...yar she blows! that sounds a little off to me

[dirtydingusus]

158.LSD by The Jolly Roger

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!!)

so it was jolly fucking rodger we can blame for this "recipe"

comeing into existence


has anyone ever accualy tyred this shit?

or what

i mean if we eat a mouthfull of rose wood seeds ?
will we fell like we are triping ?


or will it be like the kids in fla eating angel trupets and dieing?cus they did not know the right amout or which part of the flowwer to eat?


i think when you said "only get it from someone who knows what they are doing"
you where right on
i joke about a lot of shit

but all the acid iv eaten came from someone i knew ....well enuff to trust

and i always picked my own shrooms till i moved out of fla...

[NuBBiN]

yeah the jolly roger is one of the authors of the anarchist cookbook (and most of his recipes are bullshit..even the bomb ones..sad but true..I had my adolescent stint with reading the ACB and trying shit out)..basically his little "acid" recipe is making a whole lot of trouble out of something that is much simpler. morning glory seeds and baby hawaiian wood rose seeds both contain similar acid like amides, rightfully name LSA...its not lsd..and is nowhere near as potent..but yes if you find these seeds and crush them up and mix them in a glass of warm water and send them down the hatch, they will produce a trippy like high that is a mere fraction of the awsomeness of lsd. But first you have to find these seeds that arent treated with chemicals to thwart people from eating them. Then you need to figure out how much you need since everybodys dose is different. Ive tried the morning glory seeds, much more a body/mental buzz than visual trippyness. Plus you have to withstand the severe nausea that comes with eating these seeds, since they have some certain chemicals in the outer membrane that can get you pretty damn sick...basically to someone who has a reliable acid hookup, all of this trouble and nonsense seems pretty pathetic..and you'd probably stand a beter chance at tripping eating some cubensis than trying to make this nasty muck from ghundreds of little wretched tasting seeds

[XxJWxX]

How similar is an acid trip and a shroom trip? Ive done shrooms, no acid though. At the time, I didnt wanna do it. Now i've been thinkin about it for a long time and shit......I wanna fry so bad, but got no cid.

[dirtydingusus]

mushrooms kinda sit down next to you and hang out for awile


and acid grabs ahold of you and drags you along

[XxJWxX]

Is it true that "bad trips" occure on shrooms more frequently then on LSD?

[dirtydingusus]

what do you call a bad trip.....?



one mans hell...






can be anothers utopia!


or even tapiaoka?

[Bstick]

fuck talking about making it lets do some!!!

[MrSmokebigbuds]

Preparatory arrangements:
Starting material may be any lysergic acid derivative, from ergot on rye grain or from culture, or morning glory seeds or from synthetic sources. Preparation #1 uses any amide, or lysergic acid as starting material. Preparations #2 and #3 must start with lysergic acid only, prepared from the amides as follows:

10 g of any lysergic acid amide from various natural sources dissolved in 200 ml of methanolic KOH solution and the methanol removed immediately in vacuo. The residue is treated with 200 ml of an 8% aqueous solution of KOH and the mixture heated on a steam bath for one hour. A stream of nitrogen gas is passed through the flask during heating and the evolved NH3 gas may be titrated is HCl to follow the reaction. The alkaline solution is made neutral to congo red with tartaric acid, filtered, cleaned by extraction with ether, the aqueous solution filtered and evaporated. Digest with MeOH to remove some of the coloured material from the crystals of lysergic acid.

Arrange the lighting in the lab similarly to that of a dark room. Use photographic red and yellow safety lights, as lysergic acid derivatives are decomposed when light is present. Rubber gloves must be worn due to the highly poisonous nature of ergot alkaloids. A hair drier, or, better, a flash evaporator, is necessary to speed up steps where evaporation is necessary.


Preparation #1

Step I. Use Yellow light
Place one volume of powdered ergot alkaloid material in a tiny roundbottom flask and add two volumes of anhydrous hydrazine. An alternate procedure uses a sealed tube in which the reagents are heated at 112 C. The mixture is refluxed (or heated) for 30 minutes. Add 1.5 volumes of H2O and boil 15 minutes. On cooling in the refrigerator, isolysergic acid hydrazide is crystallised.


Step II. Use Red light
Chill all reagents and have ice handy. Dissolve 2.82 g hydrazine rapidly in 100 ml 0.1 N ice-cold HCl using an ice bath to keep the reaction vessel at 0 C. 100 ml ice-cold 0.1 N NaNO2 is added and after 2 to 3 minutes vigorous stirring, 130 ml more HCl is added dropwise with vigorous stirring again in an ice bath. After 5 minutes, neutralise the solution with NaHCO3 saturated sol. and extract with ether. Remove the aqueous solution and try to dissolve the gummy substance in ether. Adjust the ether solution by adding 3 g diethylamine per 300 ml ether extract. Allow to stand in the dark, gradually warming up to 20 C over a period of 24 hours. Evaporate in vacuum and treat as indicated in the purification section for conversion of iso-lysergic amides to lysergic acid amides.


Preparation #2

Step I. Use Yellow light
5.36 g of d-lysergic acid are suspended in 125 ml of acetonitrile and the suspension cooled to about -20 C in a bath of acetone cooled with dry ice. To the suspension is added a cold (-20 C) solution of 8.82 g of trifluoroacetic anhydride in 75 ml of acetonitrile. The mixture is allowed to stand at -20 C for about 1.5 hours during which the suspended material dissolves, and the d-lysergic acid is converted to the mixed anhydride of lysergic and trifluoroacetic acids. The mixed anhydride can be separated in the form of an oil by evaporating the solvent in vacuo at a temperature below 0 C, but this is not necessary. Everything must be kept anhydrous.


Step II. Use Yellow light
The solution of mixed anhydrides in acetonitrile from Step I is added to 150 ml of a second solution of acetonitrile containing 7.6 g of diethylamine. The mixture is held in the dark at room temperature for about 2 hours. The acetonitrile is evaporated in vacuo, leaving a residue of LSD-25 plus other impurities. The residue is dissolved in 150 ml of chloroform and 20 ml of ice water. The chloroform layer is removed and the aqueous layer is extracted with several portions of chloroform. The chloroform portions are combined and in turn washed with four 50 ml portions of ice-cold water. The chloroform solution is then dried over anhydrous Na2SO4 and evaporated in vacuo.


Preparation #3
This procedure gives good yield and is very fast with little iso-lysergic acid being formed (its effect are mildly unpleasant). However, the stoichometry must be exact or yields will drop.


Step I. Use White light
Sulfur trioxide is produced in anhydrous state by carefully decomposing anhydrous ferric sulfate at approximately 480 C. Store under anhydrous conditions.


Step II. Use White light
A carefully dried 22 litre RB flask fitted with an ice bath, condenser, dropping funnel and mechanical stirrer is charged with 10 to 11 litres of dimethylformamide (freshly distilled under reduced pressure). The condenser and dropping funnel are both protected against atmospheric moisture. 2 lb of sulfur trioxide (Sulfan B) are introduced dropwise, very cautiously stirring, during 4 to 5 hours. The temperature is kept at 0-5 C throughout the addition. After the addition is complete, the mixture is stirred for 1-2 hours until some separated, crystalline sulfur trioxide-dimethylformamide complex has dissolved. The reagent is transferred to an air- tight automatic pipette for convenient dispensing, and kept in the cold. Although the reagent, which is colourless, may change from yellow to red, its efficiency remains unimpaired for three to four months in cold storage. An aliquot is dissolved in water and titrated with standard NaOH to a phenolphthalein end point.


Step III. Use Red light
A solution of 7.15 g of d-lysergic acid mono hydrate (25 mmol) and 1.06 g of lithium hydroxide hydrate (25 mmol) in 200 ml of MeOH is prepared. The solvent is distilled on the steam bath under reduced pressure. the residue of glass-like lithium lysergate is dissolved in 400 ml of anhydrous dimethyl formamide. From this solution about 200 ml of the dimethyl formamide is distilled off at 15 ml pressure through a 12 inch helices packed column. the resulting anhydrous solution of lithium lysergate left behind is cooled to 0 C and, with stirring, treated rapidly with 500 ml of SO3-DMF solution (1.00 molar). The mixture is stirred in the cold for 10 minutes and then 9.14 g (125.0 mmol) of diethylamine is added. The stirring and cooling are continued for 10 minutes longer, when 400 ml of water is added to decompose the reaction complex. After mixing thoroughly, 200 ml of saturated aqueous saline solution is added. The amide product is isolated by repeated extraction with 500 ml portions of ethylene dichloride. the combined extract is dried and then concentrated to a syrup under reduced pressure. Do not heat up the syrup during concentration. the LSD may crystallise out, but the crystals and the mother liquor may be chromatographed according to the instructions on purification.


Purification of LSD-25
The material obtained by any of these three preparations may contain both lysergic acid and iso-lysergic acid amides. Preparation #1 contains mostly iso-lysergic diethylamide and must be converted prior to separation. For this material, go to Step II first.


Step I. Use darkroom and follow with a long wave UV
The material is dissolved in a 3:1 mixture of benzene and chloroform. Pack the chromatography column with a slurry of basic alumina in benzene so that a 1 inch column is six inches long. Drain the solvent to the top of the alumina column and carefully add an aliquot of the LSD-solvent solution containing 50 ml of solvent and 1 g LSD. Run this through the column, following the fastest moving fluorescent band. After it has been collected, strip the remaining material from the column by washing with MeOH. Use the UV light sparingly to prevent excessive damage to the compounds. Evaporate the second fraction in vacuo and set aside for Step II. The fraction containing the pure LSD is concentrated in vacuo and the syrup will crystallise slowly. This material may be converted to the tartrate by tartaric acid and the LSD tartrate conveniently crystallised. MP 190-196 C.


Step II. Use Red light
Dissolve the residue derived from the methanol stripping of the column in a minimum amount of alcohol. Add twice that volume of 4 N alcoholic KOH solution and allow the mixture to stand at room temperature for several hours. Neutralise with dilute HCl, make slightly basic with NH4OH and extract with chloroform or ethylene dichloride as in preparations #1 or #2. Evaporate in vacuo and chromatograph as in the previous step.

Note: Lysergic acid compounds are unstable to heat, light and oxygen. In any form it helps to add ascorbic acid as an anti- oxidant, keeping the container tightly closed, light-tight with aluminum foil, and in a refrigerator....thanks...peaces....MrSbb



**NOTE*** THIS IS FOR AN LSD SYNTHESIS