Cookin some LSD

[God v2.0]

if someone says "pwned" one more time i am gonna open up the BIGGEST can of whoop ass that will make the h-bomb test look like god damn beer foam........



damnit that word irritates me!

[God v2.0]

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 H2SO4you 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. 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 i cant find out what Et2O is until free of color. After drying under vacuum to a constant weighta really good food dehydrator can accomplish this step, there was obtained 3.5 g of d-lysergic acid hydrate, which should be stored in a dark, sealed container.

[God v2.0]

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

[da haze meister]

there is NO way you would pull that off.

[Maui Wowie]

Good luck with that stuff...

[WeekenD TokeR]

Look, this thread was kinda stupid in the first place and a lot of stupid things have been said in it. The way I see it, Spicoli fuckin' never has anything positive to say. I've only ever seen him post this 'bigger-stoner-than-thou' bullshit. I remember back when everyone on this site was chilled and peace-loving. If you weren't, you got told and usually either straightened yourself out or left. Now the cannabis.com boards have turned into the hidey hole of wannabe 'net gangsters' and idiots, although I acknowledge the fact that there are still a few traditional, chilled stoners on this forum.

This could probably be considered a negative post and somewhat contradictory, but I'm just tellin' it like it is.

And 'bout this cookin acid shit, the dude never said he was gonna try, he just asked how hard it would be. I think his question has been answered. Quite aggressivley, for that matter.

Peace

[fatweedsack]

yeah

[Eshelmen]

haha i found this

http://www.henriettesherbal.com/arch.../1996/lsd.html

[WeekenD TokeR]

HAHAHAHA! ^^^ Now, that's some funny shit.

[fatweedsack]

dude is that link for real?