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'''''N'',''N''-Diallyltryptamine''' ('''DALT''') is a [[tryptamine]] [[derivative (chemistry)|derivative]]. It has been used as an intermediate in the preparation of [[radiolabeled]] [[diethyltryptamine]].<ref>{{cite journal |author1=Brandt, SD |author2=Tirunarayanapuram, SS |author3=Freeman, S |author4=Dempster, N |author5=Barker, SA |author6=Daley, PF |author7=Cozzi, NV |author8=Martins, CPB | title = Microwave-accelerated synthesis of psychoactive deuterated N,N-dialkylated-[α,α,β,β-d4]-tryptamines | journal = J. Labelled Compd. Radiopharm | date = 2008 | volume = 51 | issue = 14 | pages = 423–429 | doi = 10.1002/jlcr.1557}}</ref>
'''''N'',''N''-Diallyltryptamine''' ('''DALT''') is a [[tryptamine]] [[derivative (chemistry)|derivative]] which has been identified as a new psychoactive substance.<ref>Michely JA, Helfer AG, Brandt SD, Meyer MR, Maurer HH. Metabolism of the new psychoactive substances N,N-diallyltryptamine (DALT) and 5-methoxy-DALT and their detectability in urine by GC-MS, LC-MSn, and LC-HR-MS-MS. ''Anal Bioanal Chem''. 2015 Oct;407(25):7831-42. {{pmid|26297461}} {{doi|10.1007/s00216-015-8955-0}}</ref><ref>Michely JA, Brandt SD, Meyer MR, Maurer HH. Biotransformation and detectability of the new psychoactive substances N,N-diallyltryptamine (DALT) derivatives 5-fluoro-DALT, 7-methyl-DALT, and 5,6-methylenedioxy-DALT in urine using GC-MS, LC-MSn, and LC-HR-MS/MS. ''Anal Bioanal Chem''. 2017 Feb;409(6):1681-1695. {{pmid|27933361}} {{doi|10.1007/s00216-016-0117-5}}</ref> It has been used as an intermediate in the preparation of [[radiolabeled]] [[diethyltryptamine]].<ref>{{cite journal |author1=Brandt, SD |author2=Tirunarayanapuram, SS |author3=Freeman, S |author4=Dempster, N |author5=Barker, SA |author6=Daley, PF |author7=Cozzi, NV |author8=Martins, CPB | title = Microwave-accelerated synthesis of psychoactive deuterated N,N-dialkylated-[α,α,β,β-d4]-tryptamines | journal = J. Labelled Compd. Radiopharm | date = 2008 | volume = 51 | issue = 14 | pages = 423–429 | doi = 10.1002/jlcr.1557}}</ref>


== See also ==
== See also ==

Revision as of 10:03, 8 January 2020

DALT
Clinical data
Routes of
administration
Oral, insufflated, rectal, smoked, IM, IV[citation needed]
ATC code
  • none
Legal status
Legal status
  • DE: NpSG (Industrial and scientific use only)
  • UK: Class A
  • US: Analogue to a Schedule I/II drug (possibly)
  • May be covered under similar Analogue bills in other countries
Identifiers
  • N-Allyl-N-[2-(1H-indol-3-yl)ethyl]prop-2-en-1-amine
CAS Number
PubChem CID
ChemSpider
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H20N2
Molar mass240.34 g/mol g·mol−1
3D model (JSmol)
  • C=CCN(CC=C)CCc2c[nH]c1ccccc12
  • InChI=1S/C16H20N2/c1-3-10-18(11-4-2)12-9-14-13-17-16-8-6-5-7-15(14)16/h3-8,13,17H,1-2,9-12H2 checkY
  • Key:LQEATNFJCMVKAC-UHFFFAOYSA-N checkY
  (verify)

N,N-Diallyltryptamine (DALT) is a tryptamine derivative which has been identified as a new psychoactive substance.[1][2] It has been used as an intermediate in the preparation of radiolabeled diethyltryptamine.[3]

See also

References

  1. ^ Michely JA, Helfer AG, Brandt SD, Meyer MR, Maurer HH. Metabolism of the new psychoactive substances N,N-diallyltryptamine (DALT) and 5-methoxy-DALT and their detectability in urine by GC-MS, LC-MSn, and LC-HR-MS-MS. Anal Bioanal Chem. 2015 Oct;407(25):7831-42. PMID 26297461 doi:10.1007/s00216-015-8955-0
  2. ^ Michely JA, Brandt SD, Meyer MR, Maurer HH. Biotransformation and detectability of the new psychoactive substances N,N-diallyltryptamine (DALT) derivatives 5-fluoro-DALT, 7-methyl-DALT, and 5,6-methylenedioxy-DALT in urine using GC-MS, LC-MSn, and LC-HR-MS/MS. Anal Bioanal Chem. 2017 Feb;409(6):1681-1695. PMID 27933361 doi:10.1007/s00216-016-0117-5
  3. ^ Brandt, SD; Tirunarayanapuram, SS; Freeman, S; Dempster, N; Barker, SA; Daley, PF; Cozzi, NV; Martins, CPB (2008). "Microwave-accelerated synthesis of psychoactive deuterated N,N-dialkylated-[α,α,β,β-d4]-tryptamines". J. Labelled Compd. Radiopharm. 51 (14): 423–429. doi:10.1002/jlcr.1557.