Exploring MET. To explore a different substance…

Names:
MET · N-Ethyl-N-methyltryptamine
IUPAC name:
N-Ethyl-2-(1H-indol-3-yl)-N-methylethan-1-amine
ID: 5174 · Formula: C13H18N2 · Molecular weight: 202.295
InChI: InChI=1S/C13H18N2/c1-3-15(2)9-8-11-10-14-13-7-5-4-6-12(11)13/h4-7,10,14H,3,8-9H2,1-2H3

Meyers-Riggs, B. N-Alkylated tryptamines. countyourculture, countyourculture: rational exploration of the underground, 10 Mar 2012.

Brandt, SD; Tirunarayanapuram, SS; Freeman, S; Dempster, N; Barker, SA; Daley, PF; Cozzi, NV; Martins, CPB. Microwave-accelerated synthesis of psychoactive deuterated N,N-dialkylated-[α,α,β,β-d4]-tryptamines. J. Labelled Compd. Radiopharm., 1 Nov 2008, 51 (14), 423–429. 169 kB. http://dx.doi.org/10.1002/jlcr.1557

Brandt, SD; Freeman, S; Fleet, IA; Alder, JF. Analytical chemistry of synthetic routes to psychoactive tryptamines. Part III. Characterisation of the Speeter and Anthony route to N,N-dialkylated tryptamines using CI-IT-MS-MS. Analyst, 1 Jan 2005, 130 (9), 1258–1262. 250 kB. http://dx.doi.org/10.1039/b504001a

Brandt, SD; Freeman, S; Fleet, IA; McGagh, P; Alder, JF. Analytical chemistry of synthetic routes to psychoactive tryptamines. Part II. Characterisation of the Speeter and Anthony synthetic route to N,N-dialkylated tryptamines using GC-EI-ITMS, ESI-TQ-MS-MS and NMR. Analyst, 2005, 130 (3), 330–344. 403 kB. http://dx.doi.org/10.1039/b413014f

Brandt, SD; Martins, CP. Analytical methods for psychoactive N,N-dialkylated tryptamines. Trends Anal. Chem., 1 Sep 2010, 29 (8), 858–869. 446 kB. http://dx.doi.org/10.1016/j.trac.2010.04.008 #4

DBT
DET
DIPT
DMT
DPT
EIPT
MBT
MIPT
NET
NMT
T
NIPT
N-HO-NMT
NCPT
PIPT
BIPT
MPT
NPT
NBT
NIBT
NSBT
NTBT
NAT
NHT
DALT
5558
T-NEPOMe
N-Benzyltryptamine
5565
T-NBOMe
DIBT
EPT
MIBT
MSBT
DSBT
N-Formyltryptamine
5601
5602
5603
5604
5605
5606
5607
5608
5609
5610
5611
5612
5613
5614
5615
5616
5617
5618
5619
5620
5621
5622
5623
5624
5625
5626
5627
5628
5629
5630
5631
5632
5633
5634
5635
5636
5637
5638
5639
5640
5641
5642
5643
5645
5646
5647
5648
5649
5650
tert-Butyl N-[2-(1H-indol-3-yl)ethyl]-N-methylglycinate
N2-[2-(1H-Indol-3-yl)ethyl]-N2-methylglycinamide
5653
5654
DAT
DHT
HOT-T
pyr-T
pip-T
mor-T
5073
5074
Gramine
dmpyrrol-T
mepipaz-T
N-Ethylhomotryptamine
Homotryptamine
2-Me-DMT
NIPT
1-Me-DMT
α,N,N-TMT
α-MET
α-PT
NPT
5-Me-DMT
6-Me-DMT
N,N,7-TMT
U-6056 · DMHT
4-Me-α-ET · 4-Me-AET
7-Me-AET
N-Ethylhomotryptamine
DBT
DET
DIPT
DMT
DPT
EIPT
MBT
MIPT
NET
NMT
T
NIPT
N-HO-NMT
NCPT
PIPT
BIPT
MPT
NPT
NBT
NIBT
NSBT
NTBT
NAT
NHT
DALT
5558
T-NEPOMe
N-Benzyltryptamine
5565
T-NBOMe
DIBT
EPT
MIBT
MSBT
DSBT
N-Formyltryptamine
5601
5602
5603
5604
5605
5606
5607
5608
5609
5610
5611
5612
5613
5614
5615
5616
5617
5618
5619
5620
5621
5622
5623
5624
5625
5626
5627
5628
5629
5630
5631
5632
5633
5634
5635
5636
5637
5638
5639
5640
5641
5642
5643
5645
5646
5647
5648
5649
5650
tert-Butyl N-[2-(1H-indol-3-yl)ethyl]-N-methylglycinate
N2-[2-(1H-Indol-3-yl)ethyl]-N2-methylglycinamide
5653
5654
DAT
DHT
HOT-T
pyr-T
pip-T
mor-T
5073
5074
Gramine
dmpyrrol-T
mepipaz-T
N-Ethylhomotryptamine
Homotryptamine
2-Me-DMT
NIPT
1-Me-DMT
α,N,N-TMT
α-MET
α-PT
NPT
5-Me-DMT
6-Me-DMT
N,N,7-TMT
U-6056 · DMHT
4-Me-α-ET · 4-Me-AET
7-Me-AET
N-Ethylhomotryptamine
17 November 2017 · Creative Commons BY-NC-SA ·