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MassBank Record: MSBNK-LCSB-LU116503

2-(3-Phenylpropyl)pyridine; LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+

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

ACCESSION: MSBNK-LCSB-LU116503
RECORD_TITLE: 2-(3-Phenylpropyl)pyridine; LC-ESI-QFT; MS2; CE: 45; R=17500; [M+H]+
DATE: 2020.08.19
AUTHORS: Elapavalore, A.; Kondić, T.; Singh, R.; Schymanski, E.
LICENSE: CC BY
COPYRIGHT: Copyright © 2019 by Environmental Cheminformatics, LCSB, University of Luxembourg, Luxembourg
PUBLICATION: Elapavalore, A.; Kondić, T.; et al., Adding Open Spectral Data to MassBank and PubChem Using Open Source Tools to Support Non-Targeted Exposomics of Mixtures (submitted).
PROJECT: ENTACT U.S. Environmental Protection Agency’s Non-Targeted Analysis Collaborative Trial
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 1165
COMMENT: DATASET 20200303_ENTACT_RP_MIX508
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 6899
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 6898
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]

CH$NAME: 2-(3-Phenylpropyl)pyridine
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C14H15N
CH$EXACT_MASS: 197.1204
CH$SMILES: C(CC1=CC=CC=C1)CC1=CC=CC=N1
CH$IUPAC: InChI=1S/C14H15N/c1-2-7-13(8-3-1)9-6-11-14-10-4-5-12-15-14/h1-5,7-8,10,12H,6,9,11H2
CH$LINK: CAS 2110-18-1
CH$LINK: PUBCHEM CID:459494
CH$LINK: INCHIKEY JJJPNTQYUJPWGQ-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 404399

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$MASS_SPECTROMETRY: COLLISION_ENERGY 45
AC$MASS_SPECTROMETRY: RESOLUTION 17500
AC$CHROMATOGRAPHY: COLUMN_NAME Acquity BEH C18 1.7um, 2.1x150mm (Waters)
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0-2 min, 0/100 at 15-20 min, 90/10 at 20.1-30 min
AC$CHROMATOGRAPHY: FLOW_RATE 0.20 mL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 13.113 min
AC$CHROMATOGRAPHY: SOLVENT A 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol

MS$FOCUSED_ION: BASE_PEAK 79.0211
MS$FOCUSED_ION: PRECURSOR_M/Z 198.1277
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_INTENSITY 39234020.71875
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 2.99.2

PK$SPLASH: splash10-0002-0900000000-b4e732f226ffd00162ac
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  80.0493 C5H6N+ 1 80.0495 -1.7
  91.0542 C7H7+ 1 91.0542 -0.7
  92.0494 C6H6N+ 1 92.0495 -1.06
  93.0573 C6H7N+ 1 93.0573 -0.54
  94.0651 C6H8N+ 1 94.0651 -0.02
  105.0699 C8H9+ 1 105.0699 -0.02
  106.0651 C7H8N+ 1 106.0651 -0.38
  107.0729 C7H9N+ 1 107.073 -0.2
  118.0651 C8H8N+ 1 118.0651 -0.12
  119.073 C8H9N+ 1 119.073 0.42
  120.0808 C8H10N+ 1 120.0808 -0.06
  196.1126 C14H14N+ 1 196.1121 2.51
  198.1277 C14H16N+ 1 198.1277 -0.31
PK$NUM_PEAK: 13
PK$PEAK: m/z int. rel.int.
  80.0493 34531.2 1
  91.0542 238588.1 9
  92.0494 57180.8 2
  93.0573 579821.1 23
  94.0651 261780.8 10
  105.0699 392163.2 15
  106.0651 1004876.6 40
  107.0729 834094.6 33
  118.0651 39927.3 1
  119.073 25952.5 1
  120.0808 8657073 352
  196.1126 30422.6 1
  198.1277 24545618 999
//

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