Exploring MDBU. To explore a different substance…

Names:
MDBU
N-Butyl-MDA
3,4-Methylenedioxy-N-butylamphetamine
N-Butyl-3,4-methylenedioxyamphetamine
IUPAC names:
N-[1-(2H-1,3-Benzodioxol-5-yl)propan-2-yl]butan-1-amine
N-[1-(1,3-Benzodioxol-5-yl)propan-2-yl]butan-1-amine
102 · C14H21NO2 · 235.322
InChI=1S/C14H21NO2/c1-3-4-7-15-11(2)8-12-5-6-13-14(9-12)17-10-16-13/h5-6,9,11,15H,3-4,7-8,10H2,1-2H3
RDXVRDCQDITVDV-UHFFFAOYSA-N This stereoisomer Any stereoisomer
CCCCNC(Cc1ccc2c(c1)OCO2)C

Braun, U; Shulgin, AT; Braun, G. Centrally active N-substituted analogs of 3,4-methylenedioxyphenylisopropylamine (3,4-methylenedioxyamphetamine). J. Pharm. Sci., 1 Jan 1980, 69 (2), 192–195. 513 kB. https://doi.org/10.1002/jps.2600690220

Braun, U; Shulgin, AT; Braun, G. Prüfung auf zentrale Aktivität und Analgesia von N-substituierten Analogen des Amphetamin-Derivates 3,4-Methylendioxyphenylisopropylamin. Arzneim. Forsch., 1 Jan 1980, 30 (5), 825–830. 1.5 MB.

Noggle, FT; DeRuiter, J; Coker, ST; Clark, CR. Synthesis, identification, and acute toxicity of some N-alkyl derivatives of 3,4-methylenedioxyamphetamine. J. Assoc. Off. Anal. Chem., 1987, 70 (6), 981–986. 1.8 MB.

Shulgin, AT. Basic Pharmacology and Effects. In Hallucinogens. A Forensic Drug Handbook; Laing, R; Siegel, JA, Eds., Academic Press, London, 2003; pp 67–137. 6.3 MB.

2C-G-4
ETHYL-K
F-22
G-3
MDIB
MDTB
MDDEA · MDDE
METHYL-L
F-23
315
316
homo-MDIP
homo-MDPR
N-mor-2-MA
MDMPA
MDMIPA
MDSB
PBDB
IPBDB
N,N-Me-DOMAI
N,N-Me-5,8-ADT
N-Bu-ADTN
2766
DMAL
ATK-0102
10015
10000
Meprylcaine
3,5-DiMeO-PCA
2,5-DMA-NPI
p2-262: MDBU
18 October 2018 · Creative Commons BY-NC-SA ·