Ah OK, I understand what you are saying now.
That is good information.
I also think I read that the nitromethane route is less "dense" in that one can run larger reactions with the same exotherm. If that makes sense.
Wait, I'm pretty sure I've read that using nitromethane runs hotter than using methylamine, because it is doing two reductions are once. I've never seen that it should run cooler.
It might affect the dosage. I assume the phosphate salt is heavier than the hydrochloride, so you'd likely have. To dose the phosphate higher than the hydrochloride for equivalent effects.
Otherwise, the effects would be the same, the salt doesn't affect the drug's effects.
The leuckart is so simple, but the yields are absolutely garbage.
If people could figure out how to increase yields, this would help the clandestine chemistry community so much.
Apparently magnesium chloride can be used as a catalyst, from what I've gathered online, maybe that will help yields...
I haven't done this, can't prove it works, but from my reading it seems to work. You can order N-methylacetamide from where one orders chemicals, foreign auction sites are good, and hydrolyze it with an acid or base, iirc, into acetic acid and methylamine. It works the same as making methylamine...
From my readings, one can hydrolyzed n methyl formaimed to get methylamine and formic acid, but it is a watched chemical. However, n mehylacetamide, which is somewhat available on foreign auction sites, can also be hydrolyzed into acetic acid and methylamine
Is there any other fent analogues you recommend besides Car F? Just too potent for me to feel safe, no matter the precautions taken.
I've read 3 methyl fentanyl (still too potent for my desires) is good, and alpha methyl fentanyl.
What fentanyl analogues have "legs" aka a longer duration...
Buddy....just look under the video section. It's on there, benzaldehyde to bmk glycidate, just substitute piperonal with benzaldehyde. It's not exactly, you'll have to do some math, but it's the exact same process
I believe mdma, it is the methylene dioxy version of the chemical MAPA, which iirc yields p2p after heating with an acid, not sure of conditions or exact reagents yet. But it should be a precursor for mdma
There is a video on here on making pmk glycidate. If you don't have much access to precursors though, not sure how useful this method will be.
Also, in the end, it's riskier to order precursors like pmk ethyl glycidate, but so much easier, and your risk is in one transaction, not many from...
So this chemical is on on the dea‘s radar, methyl 2-(1,3-benzodioxol-5-yl)-3-oxobutanoate
i am wondering in anyone is producing the ethyl analogue, aka ethyl 2-(1,3-benzodioxol-5-yl)-3-oxobutanoate. I can’t find a cas for this product currently, which to me say no one is making it.
I'm wondering what peoples' opinion on this might be. Fenafnyl and related compounds, and the zene family as a whole are what I'm looking at.
They are both highly potent, but what qualitative differences are there in the experience of either drug?
Also, it seems the highly potent synthetic...
I was just thinking about how the imine is formed before adding sodium borohydride, and I was wondering if this was applicable to amalgam reactions.
Would this even make a difference? Say forming the imine and pouring/dripping that solution into a reaction vessel with a mercury amalgam? Would...
I forgot about the chloro variety! Probably be cheaper than the iodo too. DEA seems pretty slow about changing things, so it seems the best method is to change one chemical at a time, then go to the next, ie the chloro, then the iodo, methyl glycidate to ethyl glycidate, etc.