This website uses technical necessary cookies (e.g. session ID) and in addition the Matomo web analytics tool. Matomo enables us to evaluate the use of our website in compliance with GDPR (Directive 95/46/EC). Data Privacy Policy
This banner can be opend with the 'Data Privacy'-button. Your consent to the use of Matomo can be revoked any time. To make that choice, please un-check below.

MassBank MassBank Search Contents Download

MassBank Record: MSBNK-Keio_Univ-KO003506

5-Methoxy-N,N-dimethyltryptamine; LC-ESI-QQ; MS2; CE:50 V; [M+H]+

Mass Spectrum
40.0060.0080.00100.0120.0140.0160.0180.0m/z0.000200.0400.0600.0800.01000Abundance
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-Keio_Univ-KO003506
RECORD_TITLE: 5-Methoxy-N,N-dimethyltryptamine; LC-ESI-QQ; MS2; CE:50 V; [M+H]+
DATE: 2016.01.19 (Created 2007.07.07, modified 2011.05.10)
AUTHORS: Kakazu Y, Horai H, Institute for Advanced Biosciences, Keio Univ.
LICENSE: CC BY-NC-SA
COMMENT: KEIO_ID M103

CH$NAME: 5-Methoxy-N,N-dimethyltryptamine
CH$NAME: Indole, 3-(2-(N,N-dimethylamino)ethyl)-5-methoxy-
CH$COMPOUND_CLASS: N/A
CH$FORMULA: C13H18N2O
CH$EXACT_MASS: 218.14191
CH$SMILES: CN(C)CCC1=CNC2=C1C=C(C=C2)OC
CH$IUPAC: InChI=1S/C13H18N2O/c1-15(2)7-6-10-9-14-13-5-4-11(16-3)8-12(10)13/h4-5,8-9,14H,6-7H2,1-3H3
CH$LINK: CAS 1019-45-0
CH$LINK: KEGG C08309
CH$LINK: NIKKAJI J21.248B
CH$LINK: PUBCHEM SID:10507
CH$LINK: INCHIKEY ZSTKHSQDNIGFLM-UHFFFAOYSA-N
CH$LINK: COMPTOX DTXSID70144324

AC$INSTRUMENT: API3000, Applied Biosystems
AC$INSTRUMENT_TYPE: LC-ESI-QQ
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 50 V

MS$FOCUSED_ION: PRECURSOR_M/Z 219
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+

PK$SPLASH: splash10-0a59-7900000000-995a794ee19726d9dad1
PK$NUM_PEAK: 57
PK$PEAK: m/z int. rel.int.
  40.900 44554.5 1
  42.000 173267.5 2
  43.000 277228.0 2
  44.000 19802.0 1
  46.000 74257.5 1
  55.000 34653.5 1
  56.300 559406.5 5
  58.300 112311993.5 999
  65.000 89109.0 1
  68.900 19802.0 1
  71.800 99010.0 1
  77.000 806931.5 7
  78.000 1272278.5 11
  79.100 252475.5 2
  80.200 133663.5 1
  81.400 34653.5 1
  89.100 361386.5 3
  90.100 603961.0 5
  91.100 3069310.0 27
  101.800 133663.5 1
  103.200 1410892.5 13
  104.100 2173269.5 19
  105.300 4212875.5 37
  106.100 94059.5 1
  107.200 504951.0 4
  108.000 306931.0 3
  114.300 212871.5 2
  115.300 6831690.0 61
  116.200 2089111.0 19
  117.200 4569311.5 41
  118.100 366337.0 3
  119.300 113861.5 1
  121.200 247525.0 2
  126.100 49505.0 1
  127.100 707921.5 6
  128.200 712872.0 6
  129.300 386139.0 3
  130.200 48267375.0 429
  131.200 32559438.5 290
  131.800 1346536.0 12
  133.100 737624.5 7
  133.900 103960.5 1
  140.200 267327.0 2
  141.200 391089.5 3
  142.100 2732676.0 24
  143.100 13737637.5 122
  144.200 752476.0 7
  145.000 123762.5 1
  146.200 143564.5 1
  147.100 480198.5 4
  148.300 108911.0 1
  156.900 54455.5 1
  158.100 3108914.0 28
  159.100 11257437.0 100
  172.000 89109.0 1
  173.300 262376.5 2
  174.200 1009902.0 9
//

Imprint Feedback
system version 2.2.8

Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium

Responsible: Tillmann G. Fischer

Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under the National Research Data Infrastructure – NFDI4Chem – Projektnummer 441958208.

de.NBI logo
EAWAG logo
fnr logo
IPB logo
NORMAN logo
UFZ logo
LCSB logo
HBM4EU logo
nfdi4chem logo