Just reading about you guys acetone washing your RC's.
I've never done it before, but would like to clean some Ket and DCK that I have.
Can anyone please direct me to a good video or guide that shows how to do this?
Much appreciated!
Would it be worth it to wash a gram of some decent ketamine? Not sure about the exact purity but .15 grams seems to get someone with no tolerance pretty fucked up. Don't have much knowledge about how to wash and living space is limited with no access to a private outdoor area. Would you guys...
www.bluelight.org
I've never done any acetone wash, or come across dck, when i did an iso wash on k it was basically dissolve everything in iso then carefully evaporate it off but it can be very dangerous using heat as its so flammable

Or quite lengthy (using air evaporation) but worth it, for the cut i was dealing with anyway (unknown Chinese)
This is the guide i used, i just found it. I used method 1-b.
There is methods for 3 different solvents, but not a method for acetone on there!
........
METHOD 1
In each of 3 small test tubes, I placed 0.5g “K”.
The test tubes were placed in an oven and heated at 75 degrees Celsius for one hour, in order to ensure an anhydrous (water-free) product (water will fuck with our solubilities).
I added 3 solvents – 10ml of a different solvent per tube:
a) anhydrous methanol
b) anhydrous isopropyl alcohol
c) naptha
The tubes were immediately sealed with chemistry-lab grade polymer test-tube stoppers and then quadruple-wrapped in polypropylene, tightly sealed by elastic bands, to ensure they were waterproof and gasproof.
The tubes were then heated gently to their respective boiling points in hot water baths. They were left there for an hour, agitating every 5 minutes, in order to achieve absorption.
Here’s how it should work:
a) Methanol: Ketamine HCl is classified as “freely soluble” in methanol, which means it will dissolve up to 1-10g in each ml of methanol. I can therefore dissolve 10-100g of ketamine in my 10ml tube. Sodium chloride is less soluble, (dissolving at 14g/kg of methanol, which as methanol has a molar mass of approx. 32 and thus weighs 1.42g/ml, which means 1kg of methanol is 704ml, which means 0.25g salt will dissolve in 10ml of methanol).
So, the methanol tube will dissolve both ketamine (well) and sodium chloride (badly). If there’s more than 50% salt by weight in the product, I’d expect to see some not dissolve at room temperature. If we heat the tube, more will dissolve but then return as crystal precipitate at the bottom of the tube once it cools to standard room temperature and pressure.
Methanol also won’t dissolve cuts like talc, so they’ll rest as (probably wet-looking) solids at the bottom of the tube. They should be easily distinguishable in appearance from undissolved salt.
b) Isopropyl alcohol: Ketamine HCl is “soluble” in isopropyl, meaning 10-30ml of isopropyl is needed to dissolve 1g of ketamine. Therefore since there’s only 0.5g of product in the vial, my 10ml of isopropyl should easily dissolve it.
However, sodium chloride is almost totally insoluble in isopropyl (in fact, it’s used to turn < 99% isopropyl into anhydrous isopropyl – just add non-iodized table salt, agitate, let settle, and you’ll get 2 distinct layers, one containing salt+water and the other anhydrous isopropyl). used to “salt” isopropyl to remove water from it, for this very reason).
Therefore, with the isopropyl test we should see all ketamine dissolve and almost all of any salt cut remain undissolved.
c) Naptha: will dissolve ketamine only if it’s ketamine BASE. It will NOT dissolve ketamine hydrochloride. It will also not dissolve sodium chloride.
So if we had pure ketamine HCl, we’d expect:
Tube 1 to be completely clear
Tube 2 to be completely clear
Tube 3 to be unchanged (all crystals at the bottom).
METHOD 2
Dissolve 14g “K” in 100ml anhydrous isopropyl alcohol – covered, 2 hours at room temperature in a stirrer on light agitation. I filtered the solution though medium-flow filter paper under anhydrous conditions using gravity as a drip force (no vacuum or suction). I evaporated the resulting clear liquid in a Teflon pan at just below simmering point of the isopropyl (i.e. around 75 degrees Celsius) until almost gone, then removed from heat, let the remainder airdry for 1 hour, then dessicated in a 60 degree oven for 15 minutes. This is way too fast to result in huge crystals but will result in some crystallization, which I was curious to observe.
The result: a mere 0.6g of little rod-like crystals, which are somewhat like ketamine in appearance but not really. Here are pictures I’ve uploaded to pix.ru – please feel free to visit them via Tor; it’s quite safe:
Edit: the image links dont work.
I can't belive the poor guy only got 0.6g out of 14g



Well i can actually, I've seen 12.5g of 'k' be PURE cut before. Not 1 shard of K involved. It was pure MSG, sourced in UK.
Also seen 25g be pure lidocaine and glue crystals thats right glue, sourced from Germany.
I've also seen 50g of K that contained 33g of GLASS. And loadssss of other fucked up cuts in K over the years ive dabbled in it.
Such greed sickens me.
I hope the guide can help, anyway.
