“ICE” - Crystal Methamphetamine Hydrochloride

GhostChemist

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Introduction

In this work, a water or ethanol-water solutions of methamphetamine hydrochloride are obtained in the first stage. On the next stage, these solutions are crystalized by using of different methods to get methamphetamine hydrochloride (Ice) crystals.

Starting materials:

  • 150 g Racemic methamphetamine hydrochloride
  • 75 ml EtOH 88%
  • 80 ml Acetone
  • 500 ml Water (H2O)

Procedures

Starting methamphetamine hydrochloride. Fig 1
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Methamphetamine hydrochloride dissolved in EtOH. Fig 2
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The obtained solution is filtered through a paper filter. Fig 3
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The filtered solution. Fig 4
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The solution is subjected to freezing at a temperature of -10-(-15)°C for 24-36 hours. Fig 5
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The solution is decanted. Fig 6
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The crystals are filtered using a vacuum filter. Crystals in a warm environment will dissolve in their own mother liquor solution. Fig 7
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Next stage, the crystals are combined again with the mother liquor solution, and 150 ml of water is added. Fig 8
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The resulting solution is filtered through a paper filter. Fig 9
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The filtered solution is evaporated to crystallization at a temperature of 50-70°C over the course of 3 days. This process also prevents the formation of ice crystals. Fig 10
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The fully crystallized solution. Fig 11
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All methamphetamine hydrochloride dissolved in water. Fig 12
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The solution is left in the open air for evaporation and crystallization at room temperature. Crystals began to appear after 1.5 months. Fig 13
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The appearance of the crystallized solution is shown in the Fig 14 and Fig 15.
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Fig 15
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The obtained crystals are carefully transferred onto a vacuum filter and washed with 40 ml of ice-cold anhydrous acetone. Fig 16
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After the first washing, the crystals are additionally washed with another portion of acetone, 40 ml. Fig 17
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The crystals are dried on a vacuum filter. Fig 18
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The crystals resemble transparent plates, reminiscent of ice. Fig 19
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The crystal of the methamphetamine hydrochloride. Fig 20
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Bongani

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1.5 months? Is there no faster way to obtain the crystals?
 

btcboss2022

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What about yield?Thanks.
 

GhostChemist

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50-70% for crystals
the loss of all meth mass after operations not more 1-3%
 
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btcboss2022

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The initial hcl it's racemic one?
Thanks.
 

Akashic

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It doesn’t take that long… depending on solvent/desired consistency, consumable xtals could be achieved in 2 days
1. Acetone wash starting hcl material
2.dry under light warm vacuum <50*c
3.once dry, dissolve hcl powder in dH20 1:1 in grams, ratio can change
4. warm solution and hot filter,
optional* add acetone/ethanol/methanol to filtrate, ratios vary
5. heat solution to 100*+ with care, continue heating until desired saturation is achieved,
6. if available use digital hot plate or better, drop temp to ~75* at the first signs of xtal or thick solution, cover work vessel with filter paper, important to prevent contamination, can also Insulate xtal dishes exterior to aid in slowing the cool down for huge shards. Has to go slow to form thick Columns that are essential to growing bigones 1 to 3 gram +, cooling to quickly forms needles that will never achieve much bulk.
from initial temp drop Do not move xtal dish until its finished. Crucial.
7. Leave leave it be for 1 to 7 day depending on solvent choices
slower the better, don’t be temped look just forget about a few days.
8. Once enough times passed, freeze for 30min, break xtal loose from dish, vacuum filter to dryness. the brief cooling reduces solubility, not trying actually freeze anything, might not be nessary depending on level of dryness, however is more than likely water or solvent mix trapped under the xtal.
If any can be collected, save filtrate for next round, or leave open to evap .
can use vac desiccator, vac funnel, heat gun, vac oven, toaster oven, etc. post xtal drying
9. make sure its dry and free of any residuals, then vacuum seal removing all the air space as possible to preserve and pretreat degradation.
I believe vac sealing also aid the process of forming boulders, undergoes different morphology if left long enough.
as to original post 1.5 months may be optimal to achieve the most stable xtal, however i personally do not know, never having enough product to last that long.

many options and ratios out there, some considered and kept proprietary process, likely the general fundamentals are the same. plain Deionized water is my choice for clean result, just go sparingly so it doesn’t take weeks to xtal
 

hacke8

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Thank you very much for sharing. Although I used the simplest recrystallization, the operation mode of the thread creator is purer.
 

Bongani

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Please share
 
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hacke8

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I used 95% ethanol, added methamphetamine hydrochloride in the boiling state until it was saturated, stopped heating after adding %5 ethanol, and slowly evaporated at room temperature. This crystallization is also very good. There will also be rock lines when the room temperature is low.
 

Bongani

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After how long did the crystals form
 

hacke8

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HenryWeston

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This is a ridiculous crystallisation method. Methanol & anhydrous acetone produces beautiful transparent crystals, and if a little bit of IPA is also used for dissolution you can expect real stunners. A wash with cold anhydrous acetone is good practice and also helps to precipitate more from the mother liquour.
Time til smoke can be 1-24 hrs, sooner if you add more acetone. I’ve never had a mother liquor that colour though, looks like a rough cook & extraction!
 
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hunter12

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Please share the process with methanol and acetone
 

malbona kato

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I’ve never had a mother liquor that colour though, looks like a rough cook & extraction!

Perhaps, you have never exposed your stuff on heat for long time as author does. Albeit, is important step to remove ketone leftovers.
 

Throw-off

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This is for Racemic Methamphetamine HCl right? Not the Dextra isomer?
 

GhostChemist

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yes, d,l-meth
 

hirozaru

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is the method different for racemic and d-meth ? can you explain the differences?
 
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