Exploring J. To explore a different substance…

Names:
J · BDB · Benzodioxolylbutanamine · α-Ethyl-3,4-methylenedioxyphenethylamine · 2-Amino-1-(3,4-methylenedioxyphenyl)butane · 1-(1,3-Benzodioxol-5-yl)-2-butanamine
IUPAC names:
1-(2H-1,3-Benzodioxol-5-yl)butan-2-amine
1-(1,3-Benzodioxol-5-yl)butan-2-amine
ID: 94 · Formula: C11H15NO2 · Molecular weight: 193.242
InChI: InChI=1S/C11H15NO2/c1-2-9(12)5-8-3-4-10-11(6-8)14-7-13-10/h3-4,6,9H,2,5,7,12H2,1H3

Trachsel, D. Fluorine in psychedelic phenethylamines. Drug Test. Analysis, 1 Jul 2012, 4 (7-8), 577-590. 1.0 MB. http://dx.doi.org/10.1002/dta.413

Maurer, HH; Kraemer, T; Springer, D; Staack, RF. Chemistry, pharmacology, toxicology, and hepatic metabolism of designer drugs of the amphetamine (Ecstasy), piperazine, and pyrrolidinophenone types. A synopsis. Ther. Drug Monit., 1 Apr 2004, 26 (2), 127–131. 121 kB.

Guy, M; Freeman, S; Alder, JF; Brandt, SD. The Henry reaction: spectroscopic studies of nitrile and hydroxylamine by-products formed during synthesis of psychoactive phenylalkylamines. Cent. Eur. J. Chem., 1 Dec 2008, 6 (4), 526–534. 982 kB. http://dx.doi.org/10.2478/s11532-008-0054-z

Nichols, DE; Hoffman, AJ; Oberlender, RA; Jacob, P; Shulgin, AT. Derivatives of 1-(1,3-benzodioxol-5-yl)-2-butanamine: Representatives of a novel therapeutic class. J. Med. Chem., 1 Jan 1986, 29 (10), 2009–2015. 1.0 MB. http://dx.doi.org/10.1021/jm00160a035

Hardman, HF; Haavik, CO; Seevers, MH. Relationship of the structure of mescaline and seven analogs to toxicity and behavior in five species of laboratory animals. Toxicol. Appl. Pharmacol., 1 Jun 1973, 25 (2), 299–309. 751 kB. http://dx.doi.org/10.1016/S0041-008X(73)80016-X

Nakanishi, K; Miki, A; Zaitsu, K; Kamata, H; Shima, N; Kamata, T; Katagi, M; Tatsuno, M; Tsuchihashi, H; Suzuki, K. Cross-reactivities of various phenethylamine-type designer drugs to immunoassays for amphetamines, with special attention to the evaluation of the one-step urine drug test Instant-View™, and the Emit® assays for use in drug enforcement. Forensic Sci. Int., 10 Apr 2012, 217 (1–3), 174–181. 397 kB. http://dx.doi.org/10.1016/j.forsciint.2011.11.003

Johnson, MP; Hoffman, AJ; Nichols, DE. Effects of the enantiomers of MDA, MDMA and related analogues on [3H]serotonin and [3H]dopamine release from superfused rat brain slices. Eur. J. Pharmacol., 16 Dec 1986, 132 (2–3), 269–276. 559 kB. http://dx.doi.org/10.1016/0014-2999(86)90615-1

EBDB · ETHYL-J
METHYL-J
MMBDB
PBDB
IPBDB
HOBDB
MDA
MDPEA
MDPH
K
L
α-Et-MDA
α-iPr-MDPEA
4C-3a
4C-DMPEA
F2-BDB
DH-α-Et-PEA
ALPHA
homo-MDPEA · GAMMA
Safrole
α-Isosafrole
β-Isosafrole
5,6-MDAI
MDPBP
6,7-MDAT
MDBZP · Methylenedioxybenzylpiperazine
MDCPA
499
MDAR
bk-BDB
2564
2567
MDEAR
MDMA
MDPH
M-ALPHA
7-Me-MDA · EIDA
N,N-Me-MDPEA · Lobivine
PMMA-βk · Methedrone
2-Me-MDA · 2-Methyl-MDA
5-Me-MDA · 5-Methyl-MDA
6-Me-MDA · 6-Methyl-MDA
4-Ethoxycathinone
α-Me-N-Et-MDBA
α,N,N-TMMDBA
α,α,N-TMMDBA
homo-MDA
2-MMA-βk
3-MeOMC · 3-MMA-βk
AcO-MePEA
N,N-Me-2,3-MDPEA
N-Et-2,3-MDPEA
2,3-MDMA
α,α-Me-2,3-MDPEA
2,3-BDB
3,4-DMCPA
N-Et-MDPEA
β,N-Me-MDPEA
EDA
2C-G-1
S-MDMA
R-MDMA
N-Ethyl-N-methylpiperonylamine
2,5-DMAI
2520
2521
2522
1094
1007
EBDB · ETHYL-J
METHYL-J
MMBDB
PBDB
IPBDB
HOBDB
MDA
MDPEA
MDPH
K
L
α-Et-MDA
α-iPr-MDPEA
4C-3a
4C-DMPEA
F2-BDB
DH-α-Et-PEA
ALPHA
homo-MDPEA · GAMMA
Safrole
α-Isosafrole
β-Isosafrole
5,6-MDAI
MDPBP
6,7-MDAT
MDBZP · Methylenedioxybenzylpiperazine
MDCPA
499
MDAR
bk-BDB
2564
2567
MDEAR
MDMA
MDPH
M-ALPHA
7-Me-MDA · EIDA
N,N-Me-MDPEA · Lobivine
PMMA-βk · Methedrone
2-Me-MDA · 2-Methyl-MDA
5-Me-MDA · 5-Methyl-MDA
6-Me-MDA · 6-Methyl-MDA
4-Ethoxycathinone
α-Me-N-Et-MDBA
α,N,N-TMMDBA
α,α,N-TMMDBA
homo-MDA
2-MMA-βk
3-MeOMC · 3-MMA-βk
AcO-MePEA
N,N-Me-2,3-MDPEA
N-Et-2,3-MDPEA
2,3-MDMA
α,α-Me-2,3-MDPEA
2,3-BDB
3,4-DMCPA
N-Et-MDPEA
β,N-Me-MDPEA
EDA
2C-G-1
S-MDMA
R-MDMA
N-Ethyl-N-methylpiperonylamine
2,5-DMAI
2520
2521
2522
1094
1007
19 September 2017 · Creative Commons BY-NC-SA ·