ACCESSION: MSBNK-Eawag-EQ302802
RECORD_TITLE: Tiapride; LC-ESI-QFT; MS2; CE: 30; R=35000; [M+H]+
DATE: 2015.08.25
AUTHORS: Beck B, Stravs M, Schymanski E, Singer H, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2015 Eawag, Duebendorf, Switzerland
COMMENT: CONFIDENCE standard compound
COMMENT: EAWAG_UCHEM_ID 3028

CH$NAME: Tiapride
CH$NAME: N-(2-diethylaminoethyl)-2-methoxy-5-methylsulfonyl-benzamide
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C₁₅H₂₄N₂O₄S
CH$EXACT_MASS: 328.14568
CH$SMILES: CCN(CC)CCNC(=O)C1=C(C=CC(=C1)S(=O)(=O)C)OC
CH$IUPAC: InChI=1S/C15H24N2O4S/c1-5-17(6-2)10-9-16-15(18)13-11-12(22(4,19)20)7-8-14(13)21-3/h7-8,11H,5-6,9-10H2,1-4H3,(H,16,18)
CH$LINK: CAS 51012-32-9
CH$LINK: PUBCHEM CID:5467
CH$LINK: INCHIKEY JTVPZMFULRWINT-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 5268
CH$LINK: COMPTOX DTXSID0023664

AC$INSTRUMENT: Q Exactive Orbitrap Thermo Scientific
AC$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$MASS_SPECTROMETRY: COLLISION_ENERGY 30 (nominal)
AC$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 2.6 min
AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid

MS$FOCUSED_ION: BASE_PEAK 329.1529
MS$FOCUSED_ION: PRECURSOR_M/Z 329.153
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: DEPROFILE Spline
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$SPLASH: splash10-0a4i-0091000000-c4544a176e5242fdbb7f
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  74.0964 C4H12N+ 1 74.0964 -0.89
  100.112 C6H14N+ 1 100.1121 -0.46
  212.0376 C9H10NO3S+ 2 212.0376 0.23
  213.0216 C9H9O4S+ 2 213.0216 -0.03
  241.0397 C10H11NO4S+ 1 241.0403 -2.49
  256.0637 C11H14NO4S+ 1 256.0638 -0.53
  329.1528 C15H25N2O4S+ 1 329.153 -0.38
PK$NUM_PEAK: 7
PK$PEAK: m/z int. rel.int.
  74.0964 6986006 27
  100.112 3272021.2 12
  212.0376 1598898 6
  213.0216 4229363.4 16
  241.0397 465677.5 1
  256.0637 254917963.8 999
  329.1528 53451054.9 209
//