new mdma just dropped

1. 2024-10-18 at 10:57 PM UTC

   #1
   xy0 Houston [scull my yellowish-beige sinhalese]
   https://m.youtube.com/watch?v=i43mLFsw6SM
   "
   First reaction https://pubs.acs.org/doi/10.1021/ja1033777
   Bisulfite adduct general procedure used
   Second reaction general procedure used
   Literature about fluorinated derivatives with different procedure (from aldehyde):
   https://onlinelibrary.wiley.com/doi/10.1002/cbdv.200690035
   These fluorinated derivatives are fully legal in most countries, but always check local regulations. The product in this video is legal in my jurisdiction. For educational and documentation purposes only, not a tutorial."
2. 2024-10-18 at 11 PM UTC

   #2
   

   RisiR † 29 Autism

   Originally posted by xy0 These fluorinated derivatives are fully legal in most countries

   
   I assume they are far more potent with a longer half-life than regular MDMA, though. Is that how fluorinated amphetamines work? I think so. Be careful.
3. 2024-10-18 at 11:08 PM UTC

   #3
   

   the man who put it in my hood Black Hole [miraculously counterclaim my golf]
   question mark?
   https://en.wikipedia.org/wiki/DFMDA
4. 2024-10-18 at 11:13 PM UTC

   #4
   

   RisiR † 29 Autism

   Originally posted by the man who put it in my hood question mark?
   https://en.wikipedia.org/wiki/DFMDA

   
   https://en.m.wikipedia.org/wiki/4-Fluoromethamphetamine
   
   Other amps have quite a few fluoro derivates. 4fa, 4fma, 2fma etc. But I assume you know this. They have been around forever.
5. 2024-10-18 at 11:18 PM UTC

   #5
   xy0 Houston [scull my yellowish-beige sinhalese]
   we used to get 4fmc when we couldn't get 4mmc. i guess i just never saw this (or this new SeDMA).
6. 2024-10-18 at 11:18 PM UTC

   #6
   

   the man who put it in my hood Black Hole [miraculously counterclaim my golf]
   I think this is the same paper as the one from the YT vid it seems to originate from 2006
   
   Synthesis of Fluoro Analogues of 3,4-(Methylenedioxy)amphetamine
   (MDA) and Its Derivatives
   by Daniel Trachsel*a ), Marcel Hadornb ), and Franz Baumbergerb )
   CHEMISTRY & BIODIVERSITY ± Vol. 3 (2006)
   https://citeseerx.ist.psu.edu/document?repid=rep1&type=pdf&doi=820d672ead44ebea16bdd50b67b74393b4d0c8d4