N&PD Moderators: Skorpio
You should upgrade or use an alternative browser.How can speed come in "base" form
draculic acid69
Bluelighter
F.U.B.A.R.
Bluelight Crew
The fact remains that well made amphetamine sulphate should be a white dry powder with little to no smell. Anything other than that is the result of lazy arse chemists or greedy dealers.draculic acid69
Bluelighter
Correct
The fact remains that well made amphetamine sulphate should be a white dry powder with little to no smell. Anything other than that is the result of lazy arse chemists or greedy dealers.
sekio
Bluelight Crew
draculic acid69
Bluelighter
It still is, just not as bad. From what I hear Amp HCl goes to soup in no time..
-GC
When pure, it's LESS hygroscopic and given the dilution of medical preparations, adequate. For uncut amphetamine, the 50% purity limit applies and even that turns into a paste over a few weeks. I think sulfate is still made because cooks teach cooks but the phosphate is well documented.Deleted member 170540
Bluelight Crew
Melting point depression can lead to a eutectic mixture but will it be crystalline? It depends on the compounds in question but likely not.sekio
Bluelight Crew
raising_da_piggy
Bluelighter
And racemic amphetamine base ( both isomers )
Both parent amps
The racemic one also has no sulphur atom
However , it is possible that it could be differing in the moler ratio that allows for switching up of your stash to prolong a session.raising_da_piggy
Bluelighter
I would be interested to no if one can get a yield of base without distilling ?raising_da_piggy
Bluelighter
sekio
Bluelight Crew
There is zero reason to use amphetamine in base form, though it is intersting to note that it was distributed as base form (absorbed onto a cotton ball) in the Benzedrex inhaler at one time... you'd inhale and it would provide a dose of the volatile amphetamine right to your lungs, where it decongested you! Or you just stuffed the whole cotton into your coffee and had a blast instead.
What are we "getting" amphetamine base from? Sure you can distill it (under vacuum preferably - 80C at 10mmHg), or extract with a variety of solvents (though difluoromethane is a gas at r.t. - boils at like -52C - so you'd need some crazy pressure vessel setup to use that) but that implies you're seperating the base from some mixture of other things.
I would be interested to no if one can get a yield of base without distilling ?
[...]
From my knowledge you I think you could get at amphetamine base via a dichloramethane/difluromethane extraction
If you are trying to convert amphetamine salts of any sort to base, then simply dissolve it in water, then add alkali solution (e.g. sodium carbonate, sodium hydroxide etc) until it all oils out, then extract with whatever nonpolar solvent you have handy, dry over magnesium sulfate (or whatever), then remove the extra nonpolar solvent by distillation.
Unfortunately the end result is a stinky oil that will burn your skin or lips if it touches them, might catch fire if you try to smoke it over a flame, etc. So there is literally no advantage to this.raising_da_piggy
Bluelighter
There is zero reason to use amphetamine in base form, though it is intersting to note that it was distributed as base form (absorbed onto a cotton ball) in the Benzedrex inhaler at one time... you'd inhale and it would provide a dose of the volatile amphetamine right to your lungs, where it decongested you! Or you just stuffed the whole cotton into your coffee and had a blast instead.
What are we "getting" amphetamine base from? Sure you can distill it (under vacuum preferably - 80C at 10mmHg), or extract with a variety of solvents (though difluoromethane is a gas at r.t. - boils at like -52C - so you'd need some crazy pressure vessel setup to use that) but that implies you're seperating the base from some mixture of other things.
If you are trying to convert amphetamine salts of any sort to base, then simply dissolve it in water, then add alkali solution (e.g. sodium carbonate, sodium hydroxide etc) until it all oils out, then extract with whatever nonpolar solvent you have handy, dry over magnesium sulfate (or whatever), then remove the extra nonpolar solvent by distillation.
Unfortunately the end result is a stinky oil that will burn your skin or lips if it touches them, might catch fire if you try to smoke it over a flame, etc. So there is literally no advantage to this.
That's valuable I shall happily take this on board,
I don't like to faulsly profess information particularly that of wich is dangerous . Thank you for your time!