liquid coke back to powder

smellybelly45

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does anyone know how to turn HCL coke back to powder if dissolved in water with colouring
also how does one extract coke base from water to get HCL
is quality affected
need solution for both
 

gringo0

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Simply dry out the water solution and the product in powder form will be here. During this process flaky shiny fish scale would be lost and you will have dry powder in this part most people put boric acid for that flaky shine and other toxic nonsense for repress to the brick but this is the wrong way
 

peaks

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Can you explain the good way? This i dry last time 60 degrees..
 

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gringo0

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Which type of form is that? Looks yellowish on picture, that could be pasta, base or HCI with dirt from incomplete extraction... Further steps depend on product form
 
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crystalsteal

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how i can wash it? my is also yellow like his its hcl. but i dont want to use aceton becouse of% that i losing with act wash thanks
 

Osmosis Vanderwaal

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The loss of cocaine is very small. Cocaine hclmis "very slightly soluble" in acetone, which mean 1g per 100ml or less. Less if you use quality acetone
 

Osmosis Vanderwaal

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Things yhat make cocaine yellow; benzocaine. Levamisole. Both are actually a pain in the ass but the levamisolemhas a reputation
 

Tovenaar

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You can all get rid off it when your cc is in base… hexane…
 

Osmosis Vanderwaal

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You can't just evaporate the water. You get Karo syrup and it's very hard and expensive to fix
 

gringo0

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What did you suggest in this particular case? If the product is already dissolved in water... Maybe would be an option if the solution level up to alkaline and colect product in base form, dry it and later on convert to slightly acidic to have back originally form
 

Osmosis Vanderwaal

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I tried washing it out with acetone, which was somewhat successful but I took a loss of 30%. A/B extracting it is the day to day solution. Chloroform hexane or diethyl ether could fix it right up
 

Tovenaar

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If you want to get fischscale and gloss back, make to base, dry, dissolve in solvents, adjust ph with hcl 37% to below neutral. Take out crystals, press and dry
 

Osmosis Vanderwaal

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To below neutral is awfully ambiguous. A good chemist is a thorough chemist. Also you make it sound like he is going to drip 37% directly into it, which will ruin it.
 

gringo0

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He is technically right, but here is many thinks in between to be considered...
Alot of parameters should be done correctly and even a little mistake can create "acidic crystals" that can not be acceptable for markets
Crystalization of product requires skill and practice that process at the end done successfully
 

Tovenaar

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You are 100% right.
 

Olaf2

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An incubator would be an advantage in the 60 degree C drying process
 
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