Talk:3-Methylfentanyl

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Comments

Concerning the quote:

and is currently a problematic drug of abuse in Scandinavian and Eastern European countries such as Finland[7] and Estonia.[8]

I have done a quick search and cannot fint any evidence of this being true in the case of Scandinavia. Secondly, Finland is not a part of Scandinavia. I believe this should be edited. --TheBlurstOfTimes (talk) 13:45, 27 March 2012 (UTC)[reply]

This page needs a section, perhaps under chemical weapons, on long term effects

Just as radiation victims get monitored, the >700 Moscow survivors/exposure victims should be monitored for effects. This page should have a section for the long term. 143.232.210.150 (talk) 18:01, 12 June 2012 (UTC)[reply]

Isomers

There are 4 isomers each with a different actions. The more potent isomers haver a lower duration of action. I think that's worth adding because it helps students while not adding anything og value to clandestime chemists. The 3-methyl-4-piperidone exists as a tautomer i.e. you cannot obtain a single isomer without partial crystalization - and that isn't going to hallen. — Preceding unsigned comment added by 81.99.74.135 (talk) 14:00, 14 April 2017 (UTC)[reply]

3,3 Dimethyl

In the related propiram and phenapromide classes, the 3,3-dimethyl piperidine analogues are more potent than the 3-monomethyl analogues. If you overlay them, you can see why. I think it's safe to make this point because NOBODY is going to make these classes when considering cost and complexity. I think it's somewhere in my patents database BUT they had to make the precursor and the clandestine 'cooks' are nowhere near sophisticated enough to tackle the demanding synthesis. In fact, I sent a list of 624 precursors to the Met so I presume this is already covered (I put a lot of time tying to cover them all). — Preceding unsigned comment added by 81.99.74.135 (talk) 16:14, 28 May 2017 (UTC)[reply]