FrogWarrior
Bluelighter
- Joined
- Nov 10, 2013
- Messages
- 154
My preferred ROA for any new compound I try is vaping since I should be able to feel the effects rapidly. IV would obviously (not just because you lose nothing, but also because it eliminates the possibility of decomposition products) be best but I've never gone that route before, I syringes and needles aren't OTC in this neck of the woods. What bothers me about RCs is they never state if they are salts or freebase. Maybe one can assume this means they are freebase form, otherwise they'd name them as salts, but I don't know that for sure.
Anyhow, I've tried 4-FA and 2-FMA. 4-FA I found to be nothing like amphetamine (I got a high tolerance to amphetamine), it felt way too serotonergic. 2-MA was brilliant, made me ultra productive. I've had a bag of 3-FEA lying around for a while, I tried it once and concluded it was another serotonergic one, but after reading trip reports, and the wiki page, it seems, in theory at least I was wrong. So I'm giving it another go, just added a significant amount to a pipe and am carefully vaping it until I feel it. I'm feeling it, and its definitely more serotonergic than amphetamine. Its more empathogenic. Maybe its cuz I have such a high tolerance to amphetamine, I feel dopamine much less easily, and serotonin much more easily. I feel like I can be productive, but its a lot more distracting. Like years ago sometimes I'd be on amphetamine studying, and making websites, and doing all sorts of left brain productive stuff. Then I'd take a little bit of AMT. And 2 hours later, none of what I was doing is of any importance anymore at all.
All in all, I'd much prefer amphetamine for working and studying/writing articles, whatever than this. But for things like connecting with people, this is clearly better. 2-FMA I was highly productive on. So halogenating the 3 position makes it more serotonergic thats for sure. The ethyl group (instead of the methyl from on 3-FEA) shouldn't only really affect potencies if I'm not mistake, not binding affinity. It just makes it less potent.
Anyhow, I've tried 4-FA and 2-FMA. 4-FA I found to be nothing like amphetamine (I got a high tolerance to amphetamine), it felt way too serotonergic. 2-MA was brilliant, made me ultra productive. I've had a bag of 3-FEA lying around for a while, I tried it once and concluded it was another serotonergic one, but after reading trip reports, and the wiki page, it seems, in theory at least I was wrong. So I'm giving it another go, just added a significant amount to a pipe and am carefully vaping it until I feel it. I'm feeling it, and its definitely more serotonergic than amphetamine. Its more empathogenic. Maybe its cuz I have such a high tolerance to amphetamine, I feel dopamine much less easily, and serotonin much more easily. I feel like I can be productive, but its a lot more distracting. Like years ago sometimes I'd be on amphetamine studying, and making websites, and doing all sorts of left brain productive stuff. Then I'd take a little bit of AMT. And 2 hours later, none of what I was doing is of any importance anymore at all.
All in all, I'd much prefer amphetamine for working and studying/writing articles, whatever than this. But for things like connecting with people, this is clearly better. 2-FMA I was highly productive on. So halogenating the 3 position makes it more serotonergic thats for sure. The ethyl group (instead of the methyl from on 3-FEA) shouldn't only really affect potencies if I'm not mistake, not binding affinity. It just makes it less potent.