You sure don't seem too forthcoming with posting any evidence to support any of your claims.
Surely the labs sent you some sort of analysis of at least one of your "compounds"? A GC trace? A NMR?
Could you provide the synthesis route used? How about approximate cost and amounts?
Or is there just more excuses?
Why do you have problems discussing the specifics of the compounds with this "shady legality" excuse yet have no problem ordering it from a commercial custom synthesis lab?
I have no problems at all talking at length about the drugs I have synthesized and extracted because (primarily) I'm not a bullshit artist trying to impress anyone unlike you seem to be, and secondarily because without a time machine you couldn't prove I did any of these things. But I provide enough detail that those "in the know" should be able to respect it.
On the other hand, any chemist who knows anything can smell the bullshit from your story a mile away. If you had just stuck with "I'm just a guy who likes playing with Chemdraw" you'd get ten times the respect than this make-believe "I'm the next Sasha Shulgin" act.
Ethyl beats (or tricks) Methyl
Propyl beats Ethyl
Allyl beats Propyl
This is actually the
reverse of how amphetamines are known to behave.
This paper shows the relative activities at DAT for various N-alkylamphetamines.
EC
50 for DA release
Amphetamine: 8.7 ± 1.2 nM
N-methylamphetamine: 24.5 ± 2.1 nM
N-ethylamphetamine: 88.5 ± 9.6 nM
N-propylamphetamine is inactive as a release agent, instead acting as a reuptake inhibitor with IC
50 of 1013 ± 101 nM. (For reference, methylphenidate has an IC
50 of about 20-25 nM)
It also doesn't match
in vivo potencies either:
[ref]
"The potency of these compounds was inversely related to substituent size: amphetamine > N-methyl > N-ethyl > N-propyl > N-butyl"
(Methamphetamine is more potent
in vivo because it is more lipophilic than amphetamine, but more potency cannot really be gained by increasing the N-alkyl group further)
Also, PiHKAL points out that N-allyl-MDA is inactive at 180mg doses.
[ref].
So if anything, N-allylamphetamines would be
exceedingly weak reuptake inhibitors.
I do not believe that your N-allylamphetamines would be active at reasonable doses (sub-100mg).
may have made my thoughts permanently broadcast telepathically. NO LIE.
You understand that making such a statement severely hurts your credibility? If you seriously believe in things like thought broadcasting you are too far gone to provide any sort of reliable statements.
I don't synthesize anything. It doesn't pay anything.
Well, actually, it pays quite well. And to be fair, you would be nothing but a hazard in a lab anyway.