Exploring MDPR. To explore a different substance…

Names:
MDPR
N-Propyl-MDA
MDPA
N-Propyl-3,4-methylenedioxyamphetamine
3,4-Methylenedioxy-N-propylamphetamine
IUPAC names:
N-[1-(2H-1,3-Benzodioxol-5-yl)propan-2-yl]propan-1-amine
N-[1-(1,3-Benzodioxol-5-yl)propan-2-yl]propan-1-amine
ID: 118 · Formula: C13H19NO2 · Molecular weight: 221.295
InChI: InChI=1S/C13H19NO2/c1-3-6-14-10(2)7-11-4-5-12-13(8-11)16-9-15-12/h4-5,8,10,14H,3,6-7,9H2,1-2H3

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

Dal Cason, TA. An evaluation of the potential for clandestine manufacture of 3,4-methylenedioxyamphetamine (MDA) analogs and homologs. J. Forensic Sci., 1 May 1990, 35 (3), 675–697. 2.2 MB. https://doi.org/10.1520/JFS12874J

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.

FLEA
MDA
MDAL
MDBU
MDBZ
MDCPM
MDDM
MDE
MDHOET
MDIP
MDMA
MDMEO
MDMEOET
MDOH
MDPL
MDIB
MDTB
MDAM
MDHE
MDOC
MDDEA · MDDE
MDCM
MDBA
MDTFEA
MDMEA
MDMPA
MDMIPA
MDSB
N-Formyl-MDMA
N-Pr-MDPEA
PBDB
DMPA
homo-MDPEA · GAMMA
Safrole
α-Isosafrole
β-Isosafrole
ONE · MDC
MDPPP
5,6-MDAI
6,7-MDAT
α-Me-N-Pr-MDBA
α-MMDBA
MDBZP · Methylenedioxybenzylpiperazine
homo-MDA
homo-MDPR
PrONE · Propylone
MDCPA
499
MDAR
2563
2566
MDEAR
2C-G-3
EBDB · ETHYL-J
F-2
MDIP
METHYL-K
L
314
317
G-2
α-CP-2C-D
DOMAT · DOM-AT
DOVI
4-Isobutoxycathinone
4-Butoxycathinone
homo-MDE
homo-MDDMA
2,3-MMBDB
2,3-EBDB
MDMEA
MMBDB
ED-NDMA
EDEA
DMMCPA
DMMCPA
DMCBA
N-Me-5,8-ADT
N-Pr-ADTN
2765
937
FLEA
MDA
MDAL
MDBU
MDBZ
MDCPM
MDDM
MDE
MDHOET
MDIP
MDMA
MDMEO
MDMEOET
MDOH
MDPL
MDIB
MDTB
MDAM
MDHE
MDOC
MDDEA · MDDE
MDCM
MDBA
MDTFEA
MDMEA
MDMPA
MDMIPA
MDSB
N-Formyl-MDMA
N-Pr-MDPEA
PBDB
DMPA
homo-MDPEA · GAMMA
Safrole
α-Isosafrole
β-Isosafrole
ONE · MDC
MDPPP
5,6-MDAI
6,7-MDAT
α-Me-N-Pr-MDBA
α-MMDBA
MDBZP · Methylenedioxybenzylpiperazine
homo-MDA
homo-MDPR
PrONE · Propylone
MDCPA
499
MDAR
2563
2566
MDEAR
2C-G-3
EBDB · ETHYL-J
F-2
MDIP
METHYL-K
L
314
317
G-2
α-CP-2C-D
DOMAT · DOM-AT
DOVI
4-Isobutoxycathinone
4-Butoxycathinone
homo-MDE
homo-MDDMA
2,3-MMBDB
2,3-EBDB
MDMEA
MMBDB
ED-NDMA
EDEA
DMMCPA
DMMCPA
DMCBA
N-Me-5,8-ADT
N-Pr-ADTN
2765
937
24 February 2018 · Creative Commons BY-NC-SA ·