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Methamphetamine and Amphetamine Syntheses Methods Comparison

Jordan Belfort

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why does Al/Hg say only max 100 grams ? you can do that reaction up to 200L a time..... and yield is just 80 percent with correct ratio's, especially if you use nitro as solvent and source of methylamine ofcourse it will mix much better because it DOESNT boil of the methylamine from your reaction as it GENERATES
 

Jordan Belfort

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Mix better because it makes a aezotrope with the oil and methanol
 
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Fernandohatescorn

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Hi for Leckart meth reaction p2p with N-form it says 30-38% yeild is a higher yeilds possible and what percentage?
 

Osmosis Vanderwaal

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No birch reaction? I wonder how synthing an ephedrine precursors to start would compare 🤔
 

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Birch reaction will be later
 

Osmosis Vanderwaal

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18 months ago, I wrote that. I've learned a lot. There's still along way to go, but a birch reaction in the strict sense is our of the range of most drug cooks, and what you see people doing to make meth is more of a "birch-like reaction" or I like to call it the solvated electron, although that's about as big a mis-monoker as saying it's a birch. The lithium/ammoniated nonpolar solvent shouldn't even work, but I've seen it with my own eyes. You guys ever get to this method?
 

jasper

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can you make a video of NaBH4 process not a good chemistry background but really want to learn this method
 

Methodman

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I have a few side questions. What methods make better gear. I dont believe that the end molecule is the same. These p2p. I dont. Know with they are dooing. But the is just not it. Hollow. Pseudo. I would never spent a day sleeping and. Eating. Even the birch was different then ths hypo different then ortho. But there was a. Standard of sorts. This pretty js good for loafing. And jerking off. Any thoughts
 

sumof666

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If u buy "gear" what's on market(and i guessingYou are) think that not more then
20% of your "gear" is the REAL GEAR
Depends from how the dealer usually you'll find probably coffeine, creatine.
Another factor is what acid had been used to create amphetamine salt. Best if its sulfiuric 6 then bioavailability is highest if was used ortofosforic its less aviable for your cells. If would be used citric acid you would be able to use table spoon to feel any kick.
That how I see it
all methods leading to create Afreebase molecule how it been treated and what's been used to dilute your GEAR depends how it workson you .
For me clear amf sulfate works same without influence of method
 

sumof666

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If u buy "gear" what's on market(and i guessingYou are) think that not more then
20% of your "gear" is the REAL GEAR
Depends from how the dealer usually you'll find probably coffeine, creatine.
Another factor is what acid had been used to create amphetamine salt. Best if its sulfiuric 6 then bioavailability is highest if was used ortofosforic its less aviable for your cells. If would be used citric acid you would be able to use table spoon to feel any kick.
That how I see it
all methods leading to create Afreebase molecule how it been treated and what's been used to dilute your GEAR depends how it workson you .
For me clear amf sulfate works same without influence of method
 

Berlin777

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Why all the sources tell different yields for amphetamine synthesis via Leuckart?
 

Chemtrail

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Great post !! Your a gentleman and a scholar!!
 

Osmosis Vanderwaal

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I'd like to see how an electroreduction stacks up here, the fact that there's a lot less chemicals suggests it's cheaper to make, and therefor a better value
 

Chemtrail

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If you were to add LiAlH4 to that "Synthesis Comparison Methods" chart

How will LiAlH4 measure up ??

Or Sodium Cyanoborohydride measure up ??
 

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This synthesis carried out without LiBH4 or NaBH3CN
Because synthesis with these reducing agents are dangerous
 
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Chemtrail

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Dangerous because there cannot be any water H2O none at all?, with these reducing agents
 

GhostChemist

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yes
and for the NaBH3CN, this reagent during long-term storage can generate HCN and subproducts
but this reducing agents very selective in some syntheses
 

Chemtrail

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Thank you

Seems not only dangerous (because of violent reaction with water)

But LiAlH4 and NaBH3CN are expensive too

My labrat thinks NaBH3CN takes a long time 24-48+ hours
and LiAlH4 takes 4-24 hours
For RXN reduction time

Both have really good yeilds
 

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These reducing reagents are apply in different synthesis, as example for the selective reduction of functional groups
 

Chemtrail

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My labrat is jealous of that guy who has "creditentials" within the science community (Sigma-Alrich, Fisher, university and science-related businesses), has permits/licenses and/or identification that allows access to
access to some of these precursors that we (we * as in a bunch of amateur clandestine hobbist druggies that cook drugs in their parents basement, when Momma is not looking lol) dream of ..

My labrat dreams of having a liter of phenylacetone and trying out the various METHods of reducing the ketone

Life is but a dream
 
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