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Cocaine (Le Junk) Making Freebase Cocaine... The Correct Procedure!

The correct method for making 100% pure freebase cocaine is to dissolve 1 gram of adulterated cocaine in 40 ml.s of water in either a large glass beaker or glass mason jar. Whatever you decide on, just make sure it's glass.

If any remains undissolved, it's not cocaine, so we need to get it out of there before wasting any time on that crap. Therefore, if any does remain undissolved, simply filter it into a seperate glass container via a standard round cofee filter and plastic funnel. Once all of the liquid has drained thru, add 20 more ml.s of water thru the same filter to gather any cocaine water than may have permiated the filter paper. Our final objective is to have a total of 60 ml.s of water per every one gram of cocaine. In other words, if all of your original cocaine dissolved completely in the original 40 ml.s, then simply add 20 more ml.s of fresh water to that and move on........

In a seperate beaker or shotglass, add 20 ml.s of 10% ammonia (Ace Hardware brand) to 20 ml.s of distilled water. Stir thoroughly. Your ammonia must be unscented and contain absolutely nothing but ammonia and water. It's extremely difficult to find, and the only place I could find it was Ace Hardware. I know this because I first looked at Home Depot, Menards, Lowes, all grocery stores and pharmacies. I'm just saving you the trouble, so go to Ace Hardware. The tall thin white bottle will say "Ammonia 10%". That's the one you'll be needing......

Now this next part is EXTREMELY IMPORTANT! Using a glass eye dropper, slowly add exactly 1 ml. of the ammonia solution to the dissolved cocaine water. A cloudy bright white precipitate will form with each and every drop. Between each 1 ml. added, stir for 2-3 minutes each time. Now, there's a HUGE reason for doing it this slowly, so don't just go and percipitate all of the freebase out in one big shot, okay? With each 1 ml. of the ammonia soln., stir for 2-3 minutes each time, preferably with a glass stir rod. Try extremely hard to not touch any part of the glass container with the stir rod while stirring. You'll understand why later. After about 4-5 ml.s and 2-3 minutes between each ml. added, an extremely nasty and unpleasant looking goo will start to form on your stir rod. This is not cocaine freebase, but instead one of the easier forming bases like amphetamine etc. Continue slowly adding the 1 ml. of ammonia soln. and keep checking the stir rod after the 3 minute stirring period. The goo will continue to grow on the stir rod as all of the other freebases other than cocaine continue to precipitate out first. After awhile, you'll finally start seeing the final base, cocaine, start forming on the stir rod as a bleach white, rock hard substance. Once this happens, pour the entire contents of the water/cocaine mixture into another fresh glass beaker or mason jar, because all that is left to form now will be the last and final base, cocaine! In addition, now clean off the goo from the stir rod containing all the other bases, or junk, and make sure it's clean for the last and final stage of the process.

Continue adding the ammonia soln. to the cocaine/water mixture until no more white percipitate forms with the addition of more ammonia soln. Once all of the 100% pure cocaine freebase is completely done precipitating, pour the contents into a filter and let drain thoroughly. One drained, open the filter and pour the freebase into a glass beaker with a small amount (20 ml.s per gram) of plain fresh water in it. Stir completely to completely rinse off all of the ammonia soln. and then once again pour into a filter. Once drained and while still in the filter, pour a little more fresh water over the now pure cocaine freebase to wash away any final traces of ammonia.

Remove the filter paper containing the pure cocaine freebase and place the filter paper still containing the freebase inside between a few paper towels, press firmly on the clump portion to absorb any additional moisture and then while still in the filter paper, blow dry until dry to the touch. Carefully open over a ceramic plate and let all of the freebase fall out onto it. Let air dry for as long as it takes to become completely dry (especially if your planning on reconverting it back to 100% pure cocaine hydrochloride). This could be as long as overnight.

Make sure you weigh your adulterated coke beforehand, and then once again after the pure freebase dries. Do your calculation to determine the EXACT purity of the crap you were originally sold. Call your dealer and tell him to fuck off that it's only 26%, and then find a new dealer.

Now, either smoke an entirely different freebase than anything you've ever smoked before, or turn the freebase back into your very first batch of nearly pure cocaine hydrochloride. Enjoy!

Using the bi-carb method is an absolute ghetto method way of making cocaine/amphetamine/ephedrine/psuedoephedrine freebase mix, nothing more. There should never be heat involved in the making of cocaine freebase.

I'll attach a picture of the final product when performed with this exact method after recrystallizing it into 100% pure cocaine hydrochloride. Now tell me that ain't one sweet ass lookin' pile of blow!

Le Junk...at your service
I realize this is a very old post but hope maybe some smart person can help me out here.

I am interested to try it. I cannot find 10% Ammonia. What are my options? I'm sure it's in this thread somewhere but I have not come across it yet. It seems like 28% is available around could I just do some diluting and turn it in to 10%? 1 part 28% and add .64 part extra water? That might be the math. Can anyone confirm this?

Also, if anyone can help me out here too it would be great.

What would happen if I just used 28% without dilution? or what if I just used the normal household 4-5% at the grocery store.
 
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Yes, you can. Or just use less. I keep adding one drop at a time, stirring vigourously in between drops, until the white milky freebase ceases to precipitate out of solution. You’ll also be able to smell when there’s excess ammonia as it has a very strong odour, and if there’s excess then all of the cocaine has been converted, assuming you’ve been stirring thoroughly. Make sure to wash your freebase in doubled up coffee filters with at least three rinses of distilled water to get rid of the ammonia etc.
All I get is flakes of white in the water after stirring and adding ammonia slowly nothing hard forms
 
Yes I got the same thing. All the "silt" settled at the bottom of the glass. It was fluffy, I've tried everything, microwaving it, heating it just before the boiling point and it hardens, I've filtered this fluff and tried that.

Anyone have advice?
 
All I get is flakes of white in the water after stirring and adding ammonia slowly nothing hard forms
Try the microwave for 20 seconds at a time, really important to not let it boil but youll you'll see a circular puck form with a hole in the middle. Take it out, rinse a few times, let dry and it turns out decent
 
All I get is flakes of white in the water after stirring and adding ammonia slowly nothing hard forms
That’s freebase cocaine - it’s just in very small pieces which is why it doesn’t seem hard. If you want big hard pieces you can dissolve it in a small amount of acetone and evaporate the acetone. What’s left will be essentially re-crystallised.

I prefer smoking the fine powder/flakes as I find they vaporise much more quickly and don’t require as much heat. It’s a lot easier to get big hits. But you have to be sure to use the right type of pipe/pipe set up when vaping fine powder.
 
I also want to add that the hot method is much more efficient (because of polar versus non-polar and solubility) but also that much more dangerous. Of the 3 methods, this cold method is the safest and nearly efficient enough to make it worth it.
What is the hot ether method? I've always been a little infatuated with trying to make the best freebase and comparing the many methods. I always hear of ether method and Richard Pryor lighting himself on fire but never see it (albeit for obvious reasons.) Cocaine and freebase aren't the drugs I like or use and I don't sell anything so I'm not sure why I constantly read about it and try these methods. It does seem to have the most buzz compared to washing/purifying/basing anything else.

Also the first time I tried the Ammonia method I got a huge pancake shaped mound out of 1 gram. I dried and packed it but it was way to big. I tried cooking it down with distilled water (or maybe some of the filtered out mix, I cant remember,) on a hot plate and it looked more accurate and the reduced to a more appropriate amount (like 0.3) but still seemed off. I think the pH might had gotten to around 10 by strips and less by meter. So Im wondering if I didnt get it high enough or I didnt "wash" the yo before starting. Any insight would be appreciated.
Thanks
 
What is the hot ether method? I've always been a little infatuated with trying to make the best freebase and comparing the many methods. I always hear of ether method and Richard Pryor lighting himself on fire but never see it (albeit for obvious reasons.) Cocaine and freebase aren't the drugs I like or use and I don't sell anything so I'm not sure why I constantly read about it and try these methods. It does seem to have the most buzz compared to washing/purifying/basing anything else.

Also the first time I tried the Ammonia method I got a huge pancake shaped mound out of 1 gram. I dried and packed it but it was way to big. I tried cooking it down with distilled water (or maybe some of the filtered out mix, I cant remember,) on a hot plate and it looked more accurate and the reduced to a more appropriate amount (like 0.3) but still seemed off. I think the pH might had gotten to around 10 by strips and less by meter. So Im wondering if I didnt get it high enough or I didnt "wash" the yo before starting. Any insight would be appreciated.
Thanks
There is not hot ether method. Ether (or any nonpolar solvent) can be used with aqueous ammonia (or any strong base) for extra purification/without the need for rinsing the freebase, but it’s not easy for most people to get so not generally advised, as well as having fumes that can get you drunk, are quite volatile etc.

I don’t get what you mean by ‘way too big’? Sounds like you must have vaporised some of the freebase when trying to ‘cook it down’ with water - which does nothing by the way, totally pointless. Not washing it isn’t that big a deal. You don’t need any heat with the ammonia method so that’s not it. pH was high enough, so that’s not it either.
 
There is not hot ether method. Ether (or any nonpolar solvent) can be used with aqueous ammonia (or any strong base) for extra purification/without the need for rinsing the freebase, but it’s not easy for most people to get so not generally advised, as well as having fumes that can get you drunk, are quite volatile etc.

I don’t get what you mean by ‘way too big’? Sounds like you must have vaporized some of the freebase when trying to ‘cook it down’ with water - which does nothing by the way, totally pointless. Not washing it isn’t that big a deal. You don’t need any heat with the ammonia method so that’s not it. pH was high enough, so that’s not it either.
"Hot" ether is just how I saw it referred to in the earlier post on this thread
"Way too Big" as in after starting with a g of unwashed coke, i filtered out ammonia water and had what looked like 2g. I didn't weigh it but it was the size of a name brand prescription bottle cap, about 1.75" diameter round by .5" I assumed cuts based out too or something. I was going to check back in online or go back to adding ammonia but after doing some other activities i had the idea to throw it water and melt it down. That resulted in a harder more pop corn looking product but still not all the right product.
If i thought Id get a response so quick i would've waited but I'm still going to try again. Thanks for that btw.
 
I’m pretty sure that’s just because the cocaine hcl you had was in a much more dense form and the ammonia method makes very fluffy freebase cocaine that takes up a lot more space. It’s very easy to misgauge amount by eye, especially when you change the structure from more crystallised to less.

Once again, there’s no way to melt it down with water. The only way to do that is by using acetone or a nonpolar solvent to re-crystallise.
 
To melt down the freebase I mean. That's interesting though, its fluffy freebase...
I dumped out the contents of the beaker into a filter and had a bunch of wet clumps I guess it was.
So I wrapped it in the filter and some paper towels, following some drying method I read.
After it compacted into the solid clump, and was somewhat dry I put it in a beaker of distilled water to rinse.
It was then I went rogue and turned on the heat to try and melt it. I monitored the temp but probably didn't cool it quick enough. as it condensed and hardened into the smaller amount.

I also did the initial process with a magnetic stirrer which lowest speed stated 100rpm on the ordering page and matching the tek but I believe it was faster than that. It really whipped it up. I stopped about every 0.5ml to check pH and status. I also went extremely slow (not really on purpose I just have no concept of time anymore nd maybe was slightly sedated.)

So points to fix next time: Please add anything you think
1. stick to stirring by hand with glass stirrer
2. wash with anhydrous acetone prior
3. Just let it dry longer and dont just vaporize the end product for nothing.

Do you mean recrystallize back to HCL form or just kind of washing the base form?
 
You already had freebase - there was no point in putting it in water and heating it. Zero.

No, I mean re-crystallise it in freebase form.
I always had experience cooking down crack and it was always better. I thought it removed excess sodium bic iarb. In this case I thought it might melt it down to an oil and I could condense it and burn off anything unwanted...?
 
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