COCAINE GROWING!!!!!!!!

[UpInSmOkE834]

how do u grow cocaine in your closet or sumthin???

[xNoa]

nope

[Dutchmaster]

double nope

[Doobie Snax]

I can't believe u even asked that

[kman]

lmao dumass

[kman]

no offence

[calve]

man, that was even dumber then the time I heard someone ask, "Will you lose it if you don't use it" lol

[endo..jay]

coca needs to be grown in a tropical climate not ur closet maybe if u live in like florida you could get away with it in your back yard

[Dutchmaster]

maybe

[endo..jay]

not to mention making it is no easy task making cocaine hydrochloride (the best form imo) is quite complicated. The pasta is first washed in kerosene. It is then chilled. The kerosene is removed. Gas crystals of crude cocaine are left at the bottom of the tank. Typically, the crystals are dissolved in methyl alcohol. They are then recrystallised and dissolved once more in sulphuric acid. Further washing, oxidation and separation procedures involve potassium permanganate, benzole, and sodium carbonate.

[daZenfmeister]

You sound like you've made this shit before.

[endo..jay]

i have made it a few times its not easy thats why only a few..its not worth the effort unless you yield alot because of the work involved

[Cacophony]

lmao dumass

Coming from someone who can't even spell "dumbass" I sure as hell wouldn't take any offense.

[Dutchmaster]

hahaha i agree

[Juggalotus]

damnit i was going to point out he mispelled it.

[likemclever]

...Ha ha ha....thats funny...

[Day Dreamin Faze]

The reason Columbia is the cocaine capital of the world and why its so pure there is because of the climate and soil the coca plant grows wild.

[smokincowboy86]

it shouldnt be too hard to convert a green house to where it has the right climate. Just get the hortaculture reports about columbia, do a little reserch on the weather, and the just get some plants. but the closet thing is out of the question. Its alot easier for me to grow my plants. i live 20 miles from the nearest town.

[endo..jay]

growing isnt the problem its making cocaine out of it unless u just want to chew on the leaves...the basic formula for cocaine starts by purchasing or making tropinone, converting the tropinone into 2-carbomethoxytropinone (also known as methyl-tropan-3-one-2-carboxylate), reducing this to ecgonine, and changing that to cocaine.

i have done this a few times ;)

[endo..jay]

if anyone is serious about making synthetic coke then i will post my knowledge but its alot to type so unless u ask...

[endo..jay]

i have made everything but LSD mescaline by far was the best cuz u can smoke the peyote as well

[smokincowboy86]

peyote is the shit!!!!! :D

[Doobie Snax]

endo...jay, what's the easiest drug to make? Like a piece of piss. Is there even one?

[endo..jay]

the best and easiest drig to make is codine. in the states opium is legal to grow, illegal to harvest. and from codine you can make heroin if you so chose.
heroin is alittle tricky you need to make codine then morphine then heroin.

[endo..jay]

ok here is the more common way to get codine...opium plants are the best but if u dont have em like me then ur outa luck.

You can extract Codeine, hydrocodone, Oxycodone etc. almost any Rx narcotic with water as because they are soluable in water.
Cold water extraction works well.

Below is an example of a codeine extraction.
The idea behind the following extraction is that
acetaminophen and aspirin (I'll use A/A from now on) are very
_insoluble_ in cold water. Codeine phosphate (the most common
salt of codeine) is very _soluble_ in water including cold water.
The following table explains:

Solubility (31C water) Solubility (21C water)

Aspirin 1g / 100 ml 1g / 300ml

Acetaminophen 1g / 70 ml 1g / 150 ml

Codeine 1g / 2.3 ml 1g / 0.7 ml
Phosphate

So as you can see, both A/A aren't very soluble in 21C
water, so if you cool the water to around 10C, the solubility will
drop even further. That way you can dissolve 20 tablets in 50ml
of hot water, cool the water down to 10C, filter the solution and
end up with the same amount of codeine as the tablets contained
but only a fraction of the original amount of A/A.

[...]

1. Obtain a quantity of tablets containing codeine, check to
see if they contain anything other than codeine, caffeine,
acetaminophen or aspirin. If they do, and you don't know whether
or not it will be a problem, your best bet is not to use them.
Measure out your desired amount of codeine (ex. 64 mg = 8 tablets
* 8mg/tablet). You may want to add 2 extra tablets as it is quite
likely you will lose some codeine in the procedure. As you get
more experience with the procedure you will be able to get
approx. 95% of the codeine extracted.

2. Measure out some nice hot water, use approx. 40ml / 20 tablets
or more if needed. I would suggest you don't go over 50ml for 20
tablets. I don't know if the use of boiling water would destroy
any of the codeine but your best bet is not to use it. Use hot
water but not boiling. Make sure the tablets dissolve completely.
Some dissolve on contact with water while others need some help
dissolving by crushing them. Note : not all of the tablet will
dissolve, there are water-insoluble fillers in the tablet and not
all of the A/A will dissolve either(which is what we want).

3. Place the solution in a cold bath, I just use some ice cubes
in a container of water. Stir the mixture occasionally until the
solution drops to about 15C or lower. You won't need a
thermometer to measure the temperature, just make sure it's
"cold". This will take about 30 min. If you wish to speed this
up, you can use less water to dissolve the tablets, and add ice
chips to cool the mixture faster. Just make sure you don't add
so much ice that you drastically increase the volume of the mixture.

4. Filter the solution using whatever you have. Coffee filters
work well, but lab filters work the best. Just make sure you
don't end up with obvious solids in the filtered solution. This
will take about 1 hr. You may also want to rinse the solids left
over in the filter with some ice-water to extract any remaining
codeine.



Side notes Pretty much anything that CAN be used IV is better if you shoot it. Snorting, on the other hand, in addition to being horrible for your sinuses, is wasteful, and just doesn't work as well. Why? Beats me. I'm only speaking from my own, and many others experience.

Don't use alot of water, use as little as possible. Codeine,hydrocodone, Oxycodone and morphine are all sensitive to heat and light. (Some more than others).
This method will work for oxycodone, but as a side note Percocet and most off-brands contain a relatively small amount of acetaminophen (about 350 mg or so) compared to the oxycodone (5 mg). Since oxycodone is very strong, 2 or 3 percs should have you feeling pretty darn good (as long as you don't have a huge tolerance). As a result, unless you are taking 10 or 15 percs per day, you needn't worry about acetaminophen ingestion.

[endo..jay]

then opnce you have that everything else is easier

Now, make up a caustic solution of about 200ml of water. This is done by slowly adding NaOH to the solution until it has a pH balance of 12 (use cheap pH strips). Then add 30ml of it to the codeine/water mix and then add 50ml of chloroform and shake and allow the heavier solvent to sink to the bottom. Then you must separate off the chloroform layer by using a siphon (use an eyedropper if you need to), then wash the remanding solution again with 30ml of chloroform and once again remove it. Now you must separate all the water from the solvent and I mean every last drop. All of the water must be out, and you can pipette it or use a separator of some kind (like a flask with a tap, so you shut it off when the water gets close to running through). Then evaporate off the chloroform with a pot filled with simmering water in it. Just have a plate sitting on top of the pot and slowly tip in solution and watch white crystalline codeine base appear as the chloroform reduces out by dryness.

Tips: You want white codeine not brown and always use glass; its easier to clean.

Next step producing Morphine from Codeine:
Now, you need to then measure out about 3 grams of pyridine HCL for approximately one and a half grams of codeine and melt it in a long boiling tube (or big test-tube). Then when melted, place in the codeine and it all must dissolve and be able to swish around. Then immediately plug the tube with a tightly rolled paper napkin. It will turn different colors and it will be hard to tell when it's cooked, but let it take about 5 minutes or when the temperature hits around 230 Celsius and then it will be done, and it will stick to the sides of the tube when ready. Then tip all of it into a clean beaker with 100ml of water. Then tip some water back into the now cooler test-tube and rinse all of it out into the beaker. Next add caustic solution drop by drop till you get to pH 14 (take about 3ml of the solution stated above). You will need some pH papers. Now wash the solution with chloroform say 40ml shake well and allow to settle or centrifuge (spin), pipette off the top aqueous layer. Then drop the pH to 9 and shine a light through it; you'll see it thicken with this brown mud like shit. Don't go past 9, add one or two small drops once you hit 9 and filter that crap out. The beat way is to use a vacuum filter with really good filter paper. Now, check the pH you want it to go no lower than 7.5 (using HCL spirits of salts and hydrochloric acid) while it gets to 8pH start rubbing the sides of the beaker with a glass rod or handle of a wooden spoon right in the liquid at the water level rub hard on the beaker glass and morphine will seed in clouds off crystals, then filter them out and dry high above an heating element on a metal spoon (leave the dope on the filter paper and dry it then it is easy to get off it flakes off in chunks).
Note: These crystalline codeine particles can be taken orally (under your tongue for faster results) or mixed in a drink, if you wish not to convert it into heroin.

Now, Converting your Morphine into street quality Heroin (diacetylmorphine)Procedure:
First, place some of your converted morphine into a metal spoon and add acetic anhydride and then cover with a piece of aluminum foil and bake in the oven at around 80 degrees Celsius, for at least 1 hour. Then uncover and turn the oven off. Allow the last of the acetic anhydride to sweat off the substance. Then place the remaining substance in the refrigerator. When the substance is cold, you can move it to a burner (torch lighter) and just heat till you think its at about at least 80 degree's and sniff a couple inches above it. It shouldnt sting your nose, if it does just heat it lightly some more until the smell goes away. Voila! Now the final product is street quality heroin. Ready to either be taken or sold.

[endo..jay]

oh and to the feds reading this my lab is better then yours :p

[robert42]

endo jay u sound cool man ;) u know your shit

hey is peruvian torch powder any good :p ?

[endo..jay]

Trichocereus peruvianus ( perivian torch cactus) mmmmm...it comes from the same family of cacti as san pedro...which has the same properties as peyote

[Dae Styles]

yo endo J.. whats the easiest drug to make covertly, that doesnt really take that long to do.. something i can do in my apt?

[DaBuh]

dont know if anyone posted this but for every 100 pounds of plant material you get 1 pound of coke, its gonna be awful hard to get 100 pounds in a closet

[phoenix]

How difficult is it to make mescaline jay? There is NONE around here at all, I guess because it's hard to make?

[GHoSToKeR]

how do u grow cocaine in your closet or sumthin???
BANNED OR SUMTHIN
:)

[lizka4200]

hey dont bann him...i get a kick out of some of these ridiulous questions ideas suggestions thoughts .........i dont know what to call it

[endo..jay]

One kilo (2.2 lbs) of dried peyote buttons may yield between 10 and 60 grams of pure white needle crystals of mescaline depending on the potency of the plants used. On average the yield is about 20 grams. The usual underground price of a kilo of dried peyote ranges between $125 and $250 (25 to 50 cents per button). From indians in the southwestern USA the price is closer to $50 (10 cents per button). The street price for a gram of pure mescaline is $20 to $30 - if one is lucky enough to find it. One can obtain from a kilo of dried peyote $200 to $1200 worth of mescaline. If San Pedro is employed on may anticipate a yield of 3 to 12 grams of mescaline per kilo of dried cactus. One can legally purchase a kilo of dried San Pedro for $5 to $10 and from it extract $60 to $250 worth of pure mescaline.

[endo..jay]

How difficult is it to make mescaline jay? There is NONE around here at all, I guess because it's hard to make?

its really not that hard all of the items you need you can buy at the store with no worry of government tracking...it takes alittle time but the process is something a monkey with half a brain can do

Grind a kilo of the dried cactus, place this in a large pressure cooker, cover with distilled water, and boil for 30 minutes. Strain the liquids and save them. Return the pulp to the pot, add more water and boil again for 30 minutes. Strain the liquids and combine them with the first strainings. Repeat this process about five times or until the pulp no longer has a bitter taste. Discard the pulp and reduce the volume of the combined strainings by boiling in an open pot. Do not use aluminum ware. When the liquids have been concentrated to the thickness of cream (about one quart), stop the boiling and stir in 400 grams of sodium hydroxide (lye). This makes the mescaline more soluble in benzene and less in water. If a large separatory funnel is available pour the liquids into it and add 1600 ml of benzene. Shake the funnel well for five minutes and let it stand for two hours. If a separatory funnel is not available the process can be carried out in a one gallon jug with a siphon attached.

After standing for 2 hours the water layer will settle to the bottom and the benzene layer will float to the top. Between the two layers will be a thin emulsion layer of mixed water and benzene. Drain off the water and emulsion layers if you are using a separatory funnel or siphon off the benzene layer if you are using the makeshift jug-siphon apparatus. Be certain that neither the water or emulsion layers get into the benzene layer when separating. If any of these layers do get into the benzene during separation pour everything back into the separator, let it stand and repeat the separation more carefully. It is better to leave some benzene layer in the water and emulsion than to get emulsion and water into the benzene. Nothing will be wasted. All of the benzene which contains the mescaline will eventually be salvaged. Sometimes the layers will fail to separate properly. If this is the case immerse the funnel or jug in a deep pot of hot water for two hours. This will break up the emulsion and bring about the separation.

Prepare a solution of 2 parts sulfuric acid and one part water. (never add water to the acid or it will splatter; add the acid a little at a time to the water by pouring it down the inside of the graduate or measuring cup containing the water.) Add 25 drops of the acid solution one drop at a time to the benzene extracts. Stopper the jug and shake well for one minute. Then let stand for five minutes. White streaks of mescaline sulfates should begin to appear in the benzene. If these do not appear, shake the jug more vigorously for two to three minutes and let it settle for five more minutes. I have found that when extracting mescaline from San Pedro it is sometimes necessary to shake the mixture more thoroughly and for a longer time to get the mescaline streaks to form. This is probably because of the lower mescaline content in the plant. This would also apply to any peyote that does not have a high mescaline content. After the streaks appear add 25 more drops of the acid solution in the same manner, shake as before and let settle for ten minutes. More streaks will appear. Add 15 drops of acid, shake and wait 15 minutes for streaks to form. Add 10 drops, shake and wait about 30 minutes. Test the solution with wide range pH paper. It should show that the solution is between pH 7.5 and 8. Allow the mescaline sulfate crystals to completely precipitate. Siphon off as much of the benzene as possible without disturbing the crystals on the bottom of the jug.

The next steps are to salvage any mescaline still in the water and emulsion layer. Combine the benzene siphonings with the water/emulsion layer, shake these well together for 5 minutes and let settle for two hours as before. Carefully remove the benzene layer, treat it again with acid, precipitate the crystals and siphon off the benzene as in the previous steps. Recombine the siphoned benzene with the watery layer and repeat this again and again until no more crystals precipitate. Siphon off as much benzene as possible without drawing crystals through the siphon.

The next step involves removing the remaining benzene from the crystals. There are two methods to choose from. The first is the quickest, but requires ether, which is dangerous and often difficult to procure. Shake up the crystals with the remaining benzene and pour it into a funnel with filter paper. After the benzene has passed through the filter rinse the empty jug with 100 ml of ether to salvage any crystals in the jug and pour the ether over the crystals in the filter. After the ether has passed through the filter repeat the rinsing with another 100 ml of ether. Then let the crystals dry. If ether is not available or you do not wish to use such a highly combustible substance, the precipitate and residual benzene can be poured into a beaker. The jug should be rinsed several more times with a little benzene and added to the beaker so no crystals are left behind. The beaker is then placed in a heat bath until all of the benzene has been evaporated.

The next step is to purify the mescaline sulfate crystals. Dissolve the dry crystals in 200 ml of near-boiling distilled water. Add a pinch of activated charcoal (Norite) and filter while still hot through number 2 filter paper. The hot water which contains the mescaline will pass through the filter. The Norite absorbes impurities from the mescaline. After the liquids have passed through the filter pour a little more hot water over the filter to rinse through any remaining mescaline which may have impregnated the filter paper. Add 10 percent ammonia solution a few drops at a time to the hot filtrates until the solution registers between pH 6.5 and 7. Place a boiling stone in the solution and reduce it's volume to 75 ml by boiling. Remove the boiling stone and allow the solution to cool to room temperature. Place the solution in a freezer or in a refrigerator set to the coldest possible temperature and allow the solution to cool to almost freezing. Tiny white needle-like crystals form around the bottom and sides of the beaker. Break up the crystals with a glass stirring rod while the solution is still ice cold and pour through a filter. Mescaline sulfate is insoluable in near freezing water and will not pass through the filter. Rinse the beaker with fresh ice water and pour this over the filter. The crystals will now be pure white and can be dried under a heat lamp or in an over at 250 degrees F. More mescaline can be salvaged from the water that has passed through the filter by boiling these liquids down to about 20 ml, adding Norite while hot, filtering through number 2 paper as before, chilling the filterate to near freezing as once before, filtering while cold, rinsing with ice water and drying the crystals. This repetition should obtain at least two more grams of mescaline sulfate. If large volume mescaline extraction is being conducted it would be worthwhile to repeat this salvaging procedure several more times.