MassBank MassBank Search Contents Download

MassBank Record: MSBNK-Eawag-EQ360604

3,4-Methylenedioxy-N-ethylamphetamine (MDEA); LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+

Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-Eawag-EQ360604
RECORD_TITLE: 3,4-Methylenedioxy-N-ethylamphetamine (MDEA); LC-ESI-QFT; MS2; CE: 60; R=35000; [M+H]+
DATE: 2015.08.25
AUTHORS: Stravs M, Schymanski E, Singer H, Department of Environmental Chemistry, Eawag and Thomaidis N, University of Athens
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2015 Eawag, Duebendorf, Switzerland
COMMENT: CONFIDENCE standard compound
COMMENT: EAWAG_UCHEM_ID 3606

CH$NAME: 3,4-Methylenedioxy-N-ethylamphetamine (MDEA)
CH$NAME: 3,4-methylenedioxyethamphetamine
CH$NAME: 1-(1,3-benzodioxol-5-yl)-N-ethylpropan-2-amine
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C12H17NO2
CH$EXACT_MASS: 207.12593
CH$SMILES: CCNC(C)CC1=CC2=C(C=C1)OCO2
CH$IUPAC: InChI=1S/C12H17NO2/c1-3-13-9(2)6-10-4-5-11-12(7-10)15-8-14-11/h4-5,7,9,13H,3,6,8H2,1-2H3
CH$LINK: CAS 14089-52-2
CH$LINK: PUBCHEM CID:105039
CH$LINK: INCHIKEY PVXVWWANJIWJOO-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 94775
CH$LINK: COMPTOX DTXSID70860971

AC$INSTRUMENT: Q Exactive Plus Orbitrap Thermo Scientific
AC$INSTRUMENT_TYPE: LC-ESI-QFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 60 (nominal)
AC$MASS_SPECTROMETRY: RESOLUTION 35000
AC$CHROMATOGRAPHY: COLUMN_NAME XBridge C18 3.5um, 2.1x50mm, Waters
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0 min, 50/50 at 4 min, 5/95 at 17 min, 5/95 at 25 min, 90/10 at 25.1 min, 90/10 at 30 min
AC$CHROMATOGRAPHY: FLOW_RATE 200 ul/min
AC$CHROMATOGRAPHY: RETENTION_TIME 4.0 min
AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid

MS$FOCUSED_ION: BASE_PEAK 208.1326
MS$FOCUSED_ION: PRECURSOR_M/Z 208.1332
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1
MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included
MS$DATA_PROCESSING: WHOLE RMassBank 1.9.6

PK$SPLASH: splash10-0a5i-0900000000-f70ec61288348785c4d5
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  51.0228 C4H3+ 1 51.0229 -1.5
  53.0385 C4H5+ 1 53.0386 -0.69
  55.0178 C3H3O+ 1 55.0178 -1.11
  65.0384 C5H5+ 1 65.0386 -3.33
  72.0807 C4H10N+ 1 72.0808 -1.61
  77.0383 C6H5+ 1 77.0386 -4.11
  79.0541 C6H7+ 1 79.0542 -1.73
  91.0541 C7H7+ 1 91.0542 -1.72
  93.0334 C6H5O+ 1 93.0335 -0.98
  95.049 C6H7O+ 1 95.0491 -1.49
  103.0541 C8H7+ 1 103.0542 -1.13
  105.0697 C8H9+ 1 105.0699 -1.21
  107.0489 C7H7O+ 1 107.0491 -1.88
  111.044 C6H7O2+ 1 111.0441 -0.68
  115.0541 C9H7+ 1 115.0542 -1.1
  121.0282 C7H5O2+ 1 121.0284 -1.54
  122.0361 C7H6O2+ 1 122.0362 -1.15
  133.0646 C9H9O+ 1 133.0648 -1.14
  135.0438 C8H7O2+ 1 135.0441 -1.67
  145.0646 C10H9O+ 1 145.0648 -1.04
  148.0516 C9H8O2+ 1 148.0519 -1.96
  151.0752 C9H11O2+ 1 151.0754 -1.03
  163.0752 C10H11O2+ 1 163.0754 -1.26
PK$NUM_PEAK: 23
PK$PEAK: m/z int. rel.int.
  51.0228 3366088.5 3
  53.0385 1812414.9 2
  55.0178 21178922 24
  65.0384 2811887 3
  72.0807 107800568 123
  77.0383 9246620 10
  79.0541 62204744 71
  91.0541 4655290.5 5
  93.0334 4275923 4
  95.049 5725347.5 6
  103.0541 40715392 46
  105.0697 874909248 999
  107.0489 2341431.8 2
  111.044 1502220.9 1
  115.0541 7663900.5 8
  121.0282 4274133.5 4
  122.0361 16765651 19
  133.0646 632420096 722
  135.0438 673614016 769
  145.0646 1929235.8 2
  148.0516 2569548 2
  151.0752 13153237 15
  163.0752 265937856 303
//

system version 2.2.6-SNAPSHOT
Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium
de.NBI logo
EAWAG logo
fnr logo
IPB logo
NORMAN logo
UFZ logo
LCSB logo
HBM4EU logo
nfdi4chem logo