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Names

5-MeO-DBT
5-Methoxy-N,N-dibutyltryptamine

IUPAC name

N-Butyl-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]butan-1-amine

ID 5462 · Formula C₁₉H₃₀N₂O · Molecular weight 302.454

Tags Tryptamine

InChI InChI=1S/C19H30N2O/c1-4-6-11-21(12-7-5-2)13-10-16-15-20-19-9-8-17(22-3)14-18(16)19/h8-9,14-15,20H,4-7,10-13H2,1-3H3

InChI Key WVGCRISHWANOTO-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES CCCCN(CCc1c[nH]c2c1cc(OC)cc2)CCCC

ChemSpider 30798625
PubChem 53485365
Wikidata Q82637002
Wikipedia 5-MeO-DBT
Wikipedia, see also List of substituted tryptamines
Project Response 5-MeO-DBT (2212-20)
aipsin.com N,N-Bu-5-MeO-T (Iss. 9, Sep 2020: III-60)
aipsin.com N,N-Bu-5-MeO-T (Iss. 7, Jul 2020: V-11)

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. https://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, 21 Feb 2005, 130 (3), 330–344. 403 kB. https://doi.org/10.1039/b413014f

Brandt, SD; Martins, CPB. Analytical methods for psychoactive N,N-dialkylated tryptamines. Trends Anal. Chem., 1 Sep 2010, 29 (8), 858–869. 446 kB. https://doi.org/10.1016/j.trac.2010.04.008 #38

5-MeO-DIBT · 5-Methoxy-N,N-diisobutyltryptamine

5-Nonyloxy-T · 5-Nonyloxytryptamine

5-Pentyloxy-N,N-diethyltryptamine · 5-Pentyloxy-DET

5-MeO-DSBT · 5-Methoxy-N,N-di-sec-butyltryptamine

7 Dec 2019 · · Isomer Design