You guys are fucking pussies, with like 2 grand i could make a huge batch of LSD and it would sell for massive amounts of money prolly somewhere around 10-12k. here i can translate most of the first paragraph:





SYNTHESIS : A solution of 6.7 g KOH in 100 mL H2O, (mix 6.5grams of Potassium Hydroxide in 100 mL of water) under an inert atmosphere and magnetically stirred, was brought to 75 °C, and 10 g ergotamine tartrate (ET) added Ergotamine is a mold found on rye and other grains, its an alkalai thats poisonous and pretty much makes ya go crazy, called st elmo's fire i believe, this substance is controlled. 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 you add 1 drop at a time of sulfuric acid (be careful with this shit it will eat right through you LITTERALLY) until the pH is 3.0, just use little pH tester strips for a cheap, fairly accurate reading . 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 i think its ethanol. 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 http://en.wikipedia.org/wiki/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, a really good food dehydrator can accomplish this step the residual solids dissolved in 50 mL of 1% aqueous ammonia this is .5 mL of ammonia and 49.5 of water, and this solution was acidified as before with 2.5 N H2SO4 more sulfuric acid baby!. The precipitated solids were removed by filtration and washed with Et2O i cant find out what Et2O is but i think its ethanol can anyone confirm? 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.



its easy
srry about double post
God v2.0 Reviewed by God v2.0 on . Cookin some LSD yeah i have researched how to cook acid and i know its hard and complicated as hell but a small yield can make you trip for days. I was just wondering if anyone here has ever made some and how difficult it was. i figured itd be better if i could hear some personal experience Rating: 5