Is this recipe authentic? Please help me.

Discussion in 'Drug Chemistry' started by Alainn_Seona, Dec 26, 2008.

  1. Alainn_Seona

    Alainn_Seona Member

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    Is this an authentic recipe for LSD? A friend told me that it was.....but I am not so sure. Any insight? The exact text given to me is as follows:

    > > Recently I read an article about making Lsd out of bakingsoda, water, cherries, egg whites, red wine, and sugar. I promised my friend i would sell him some, but I lost the recipe. It was in one of these newsgroups, and it got taken off. Please reply!
    > > Can acid be made at home? how?
    > Yes, and it's very simple..
    > First you will need the following ingredients:
    > 2 egg whites
    > 1 oz mixture (3 parts baking soda, 2 parts water)
    > 4 fresh cherries
    > a small amount of red wine (teaspoon)
    > First of all, you'll want to get some good, expensive red wine. The cheap stuff works, but your trips will be crappier and you'll get some nausea.
    > Ok, now that you have your stuff, put the Egg whites and cherries in a large bowl. Start stirring until you get a pinkish mass. Now, Pour in your mixture of baking soda. As you do this you will notice heat building and a small amount of smoke being let off- this is normal. Wait about 10 minutes to cool. Then Pour in the red wine. Immediately after you do this, steam will gather and after afew seconds you will be left with A clear liquid at the bottom of the bowl. This is your acid.
    > Happy tripping.

    You're sick, you know that!? Really twisted!

    The person who asked for the LSD recipe is probably some newbie to drug use who doesn't know much about chemistry. They'll try the above recipe and be in for a really nasty shock.

    So warning to all newbies:

    The above recipe is the well known home-PCP synthesis. Do not try it unless you're ready for a PCP experience. For LSD you need to use only two cherries (not four) and add a small amount (level teaspoon) of sugar prior to the wine.

    If all goes well you should have some pretty mind-blowing acid on your hands (for best results smoke some banadine during the peak... man; what a blast!)

    Hope this clears up some of the irresponsible misinformation spread by Fredeuss.
     
  2. BraveSirRubin

    BraveSirRubin Members

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    Sweet Jesus.
     
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  4. Alainn_Seona

    Alainn_Seona Member

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    That really doesn't answer my question!
    (no offense)
     
  5. Therese Aline

    Therese Aline Slave to the man

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  7. LSDMIKE

    LSDMIKE Member

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    The above recipe is the well known home-PCP synthesis. Do not try it unless you're ready for a PCP experience. For LSD you need to use only two cherries (not four) and add a small amount (level teaspoon) of sugar prior to the wine.

    If all goes well you should have some pretty mind-blowing acid on your hands (for best results smoke some banadine during the peak... man; what a blast!)I know your only fucking but :smilielol5:
     
  8. blitz7341

    blitz7341 Banned

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    BWAHAHAHAHAHAHA i really hope this is a joke.

    here is the real synthesis taken from TIHKAL:

    SYNTHESIS : A solution of 6.7 g KOH in 100 mL H2O, under an inert atmosphere and magnetically stirred, was brought to 75 °C, and 10 g ergotamine tartrate (ET) added. The reaction mixture turned yellow as the ergotamine went into solution over the course of 1 h. The stirring was continued for an additional 3 h. The reaction mixture was cooled to about 10 °C with an external ice bath, and acidified to a pH of about 3.0 by the dropwise addition of 2.5 N H2SO4. White solids started to appear early in the neutralization; approximately 60 mL of sulfuric acid was required. The reaction mixture was cooled overnight, the solids removed by filtration, and the filter cake washed with 10 mL Et2O. The dry solids were transferred to a beaker, suspended in 50 mL 15 % ammonia in anhydrous ethanol, stirred for 1 h, and separated by decantation. This extraction was repeated, and the original decantation and the second extract combined and filtered to remove a few hundred milligrams of unwanted solids. The clear filtrate was stripped of solvent under vacuum, the residual solids dissolved in 50 mL of 1% aqueous ammonia, and this solution was acidified as before with 2.5 N H2SO4. The precipitated solids were removed by filtration and washed with Et2O until free of color. After drying under vacuum to a constant weight, there was obtained 3.5 g of d-lysergic acid hydrate, which should be stored in a dark, sealed container.

    A suspension of 3.15 g d-lysergic acid hydrate and 7.1 g of diethylamine in 150 mL CHCl3 was brought to reflux with stirring. With the external heating removed, there was added 3.4 g POCl3 over the course of 2 min, at a rate sufficient to maintain refluxing conditions. The mixture was held at reflux for an additional 5 min, at which point everything had gone into solution. After returning to room temperature, the solution was added to 200 mL of 1 N NH4OH. The phases were separated, the organic phase dried over anhydrous MgSO4, filtered, and the solvent removed under vacuum. The residue was chromatographed over alumina with elution employing a 3:1 C6H6/CHCl3 mixture, and the collected fraction stripped of solvent under hard vacuum to a constant weight. This free-base solid can be recrystallized from benzene to give white crystals with a melting point of 87-92 °C. IR (in cm-1): 750, 776, 850, 937 and 996, with the carbonyl at 1631. The mass spectrum of the free base has a strong parent peak at mass 323, with sizable fragments at masses of 181, 196, 207 and 221.

    This base was dissolved in warm, dry MeOH, using 4 mL per g of product. There was then added dry d-tartaric acid (0.232 g per g of LSD base), and the clear warm solution treated with Et2O dropwise until the cloudiness did not dispel on continued stirring. This opaqueness set to a fine crystalline suspension (this is achieved more quickly with seeding) and the solution allowed to crystallize overnight in the refrigerator. Ambient light should be severely restricted during these procedures. The product was removed by filtration, washed sparingly with cold methanol, with a cold 1:1 MeOH/Et2O mixture, and then dried to constant weight. The white crystalline product was lysergic acid diethylamide tartrate with two molecules of methanol of crystallization, with a mp of about 200 °C with decomposition, and weighed 3.11 g (66%). Repeated recrystallizations from methanol produced a product that became progressively less soluble, and eventually virtually insoluble, as the purity increased. A totally pure salt, when dry and when shaken in the dark, will emit small flashes of white light.
     
  9. sellekenblour

    sellekenblour Member

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    ..but you forgot the cherries!
     
  10. Alainn_Seona

    Alainn_Seona Member

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    lol i really feel like a newb now
     
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  12. nickers224

    nickers224 Member

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    if it was that easy no one would ever buy lsd from anyone else....
     
  13. nick16

    nick16 Member

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    but you can do that to make pcp correct?
     

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