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Old 11-27-2002, 07:53 PM   #1 (permalink)
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i was just wonderin how much 6 hits would cost.... i'v only ever bought 2 hits at a time for $10
...i am basically asking at wut rate do u start gettin a deal
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Old 11-27-2002, 11:39 PM   #2 (permalink)
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i have never got acid always gottten close but the deals have always fallend through. I was gonna buy a 10 strip for $50 but otherwise it would have been $6 a tab so maybe you need to get 10 but it really depends on the dealer.
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Old 11-28-2002, 06:58 AM   #3 (permalink)
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send me some acid through the mail, please.
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Old 11-28-2002, 09:11 AM   #4 (permalink)
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Luckily in my area, one of my dealers just got a 1/2lb of shrooms, but acid, shit, good luck gettin that.
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Old 11-28-2002, 05:33 PM   #5 (permalink)
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I would love to try acid at least once.

Hell I would settle for mushrooms right now.
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Old 11-28-2002, 06:50 PM   #6 (permalink)
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Good luck getting a deal on 6 hits, I used to sell 3 for 10 but we are taking allmost 17 years ago and I just did it because it gave people a brake 1 for the girl 2 for the guy.
Now I have to make it myself.
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Old 11-28-2002, 11:11 PM   #7 (permalink)
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is it really that hard for u to get acid around there??? well i live in CANADA BC....and theres sooooooooooooooooo many drugs
i can get n e thing from pot to ether easy as pie

....n e one with sum spare time can deal around here....good ol cops who just dont care
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Old 11-29-2002, 07:35 AM   #8 (permalink)
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I think this all comes down to Jerry Garcia. Seems like when the Dead were still around, acid was plentiful (at least at Dead shows). It was easy to score acid for $1 or $2 a hit. Now, prices are like $6! Fucking crazy!



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Old 11-29-2002, 10:38 AM   #9 (permalink)
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[quote]Originally posted by eight hour flight:
<strong>Good luck getting a deal on 6 hits, I used to sell 3 for 10 but we are taking allmost 17 years ago and I just did it because it gave people a brake 1 for the girl 2 for the guy.
Now I have to make it myself.</strong><hr></blockquote>

yeah sure you make acid you piece of shit. there is no way that you know how to make acid sure you can read the tutorial and say you know how to make but lets see you start a lab and get all the ingredients
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Old 11-29-2002, 12:24 PM   #10 (permalink)
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I've only came across acid twice in my life... Once my friend had some and it was a birthday present. Another, my friend's dealer sold me a 10 sheet for $60 bucks. Acid is normally hard to come by, but a the best deal is to go with the vial. Vials can come in 100-hit quantities; if you can find someone willing to sell you one, it can range from $80-200.
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Old 11-29-2002, 01:38 PM   #11 (permalink)
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[quote]Originally posted by dezzy420:
<strong>

yeah sure you make acid you piece of shit. there is no way that you know how to make acid sure you can read the tutorial and say you know how to make but lets see you start a lab and get all the ingredients</strong><hr></blockquote>

dezzy..dezzy..dezzy. ..what are we gonna do with you? please try to keep your attention span for more than 3 secs,and drink all your milk and eat the veggies,

when he said "I just did it" he was talking about SELLING it,like in "I just sold it", hard for you to understand I guess,

if you thought he was actually making it why couldnt you ask something like "hey,and what do you need on your lab?" or "Im a bit skeptical,would you explain to me the process?" with this aproach you may even learn something,or make a friend,but you had to insult the guy,who seems to me know MUCH,and I mean a whole lot more than you (knowing more than you may be the easiest thing in the world)

you had to go for the insults AGAIN,even a chimpanzee can insult,

he used to sell it cause hes no pussy like you,
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Old 11-29-2002, 01:53 PM   #12 (permalink)
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[quote]Originally posted by eight hour flight:
<strong>Good luck getting a deal on 6 hits, I used to sell 3 for 10 but we are taking allmost 17 years ago and I just did it because it gave people a brake 1 for the girl 2 for the guy.
Now I have to make it myself.</strong><hr></blockquote>

dezzy,my little friend,I see your cognitive confusion here,as we all know,you cant retain a whole paragraph,so you focused in the last part "Now I have to make it myself",before that,he sold it,

sorry for flaming you,but you asked for it when you insulted me without provocation whatsoever from my part,

as Sir Richard Burton (the British explorer,not the actor) said once,"a spear as blunt as your wit would be useless indeed"
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Old 11-29-2002, 01:58 PM   #13 (permalink)
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<a href="http://www.yahooka.com/ubb/ultimatebb.php?ubb=g et_topic&f=12&t=0043 01" target="_blank">dezz y using what he has to use instead of brains</a>
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Old 11-29-2002, 02:11 PM   #14 (permalink)
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What makes people think you need a lab in the first place, if you can grow a mold you can make LSD AND IF YOU CAN MAKE WINE YOU CAN MAKE SURE THAT NO HARMFULL BACTEREA WILL GET IN IT TO HARM YOU. But I will wait till Bush pisses me off before I place it on the web.
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Old 11-29-2002, 04:36 PM   #15 (permalink)
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[quote]Originally posted by eight hour flight:
<strong>What makes people think you need a lab in the first place, if you can grow a mold you can make LSD AND IF YOU CAN MAKE WINE YOU CAN MAKE SURE THAT NO HARMFULL BACTEREA WILL GET IN IT TO HARM YOU. But I will wait till Bush pisses me off before I place it on the web.</strong><hr></blockquote>

true that
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Old 11-29-2002, 06:32 PM   #16 (permalink)
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I've been looking for acid without luck for 3 years. I haven't tripped in that long. If there's someplace in Canada I can pick some up, I'll take a vacation there...
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Old 11-30-2002, 02:17 PM   #17 (permalink)
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back when acid was around these parts you could get a 10 strip for $35.

if you can get acid you should share the welth. i have a PO box and if i trip i will send you the money
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Old 12-01-2002, 03:09 PM   #18 (permalink)
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Ok you morons, this is how you make lsd. And unless you have a degree in organic chemistry don't think you're smart enough to make this. It starts out with lysergic acid derived from the ergot fungus (found on mold on wheat grain) but let the document sum it all up. Source : Lycaeum
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[D-lysergic acid diethylamide](LSD)

Preparatory arrangements:
Starting material may be any lysergic acid derivative, from ergot on rye grain or from culture, 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.
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Old 12-01-2002, 03:16 PM   #19 (permalink)
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[quote]Originally posted by chobo:
<strong>Ok you morons, this is how you make lsd. And unless you have a degree in organic chemistry don't think you're smart enough to make this. It starts out with lysergic acid derived from the ergot fungus (found on mold on wheat grain) but let the document sum it all up. Source : Lycaeum
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[D-lysergic acid diethylamide](LSD)</strong><hr></blockquote>

Thanks for clearing that up for us, chode.
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Old 12-01-2002, 03:38 PM   #20 (permalink)
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[quote]Originally posted by Cola:
<strong>

Thanks for clearing that up for us, chode.</strong><hr></blockquote>

Insults won't make you any less of a moron.
...maybe clever ones.
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