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N,N-Dipropyltryptamine

Compound with spectra: 1 NMR, 1 FTIR, and 5 MS (GC)

N,N-Dipropyltryptamine
SpectraBase Compound ID 66r4mCgzcPY
InChI InChI=1S/C16H24N2/c1-3-10-18(11-4-2)12-9-14-13-17-16-8-6-5-7-15(14)16/h5-8,13,17H,3-4,9-12H2,1-2H3
InChIKey BOOQTIHIKDDPRW-UHFFFAOYSA-N
Mol Weight 244.38 g/mol
Molecular Formula C16H24N2
Exact Mass 244.193949 g/mol

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ATR-IR Spectrum
Copyright Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Alltech Associates, Inc., Grace Davison Discovery Sciences
Source of Spectrum Forensic Spectral Research
Catalog Number Free base of 01672

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MS (GC) Spectrum
Copyright Copyright © 2023-2024 Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum H.H.Maurer, M.Meyer, K.Pfleger, A.A. Weber / University of Saarland, D-66424 Homburg Germany
Technique GC/MS

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MS (GC) Spectrum
Copyright Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS

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MS (GC) Spectrum
Copyright Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS

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MS (GC) Spectrum
Copyright Copyright © 2024 DigiLab GmbH and Wiley-VCH GmbH. All Rights Reserved.
Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS

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MS (GC) Spectrum
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum SWG-33-3858-0

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13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
  • INDOLE-N,N-DIPROPYL-TRYPTAMINE
  • N-[2-(1H-Indol-3-yl)ethyl]-N-propylpropan-1-amine
  • DPT
N,N-Dipropyltryptamine hydrochloride
[2-(1H-Indol-3-yl)-ethyl]-[2H(6)]-dipropylamine
INDOLE-N,N-DIBUTYL-TRYPTAMINE
3-(2-Piperidin-1-yl-ethyl)-1H-indole
INDOLE-N-METHYL-N-ETHYL-TRYPTAMINE
N,N-tert-Butylmethyltryptamine
3-(2-[Hydroxy(methyl)amino]ethyl)-1H-indole
N(B),N(B)-Formyl-methyl-tryptamine
N-Heptyltryptamine
N-Decyltryptamine
N-Cyclopropyltryptamine
N-(2-Butyl)tryptamine
Title Journal or Book Year
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 The Analyst 2005
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