ACCESSION: MSBNK-LCSB-LU014605
RECORD_TITLE: 4-Methoxyaniline; LC-ESI-QFT; MS2; CE: 75; 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 146
COMMENT: DATASET 20200303_ENTACT_RP_MIX500
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 2038
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 2036
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]
CH$NAME: 4-Methoxyaniline
CH$NAME: p-Anisidine
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C7H9NO
CH$EXACT_MASS: 123.0684
CH$SMILES: COC1=CC=C(N)C=C1
CH$IUPAC: InChI=1S/C7H9NO/c1-9-7-4-2-6(8)3-5-7/h2-5H,8H2,1H3
CH$LINK: CAS
104-94-9
CH$LINK: CHEBI
82388
CH$LINK: KEGG
C19326
CH$LINK: PUBCHEM
CID:7732
CH$LINK: INCHIKEY
BHAAPTBBJKJZER-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER
13869414
AC$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 75
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$CHROMATOGRAPHY: RETENTION_TIME 3.938 min
AC$CHROMATOGRAPHY: SOLVENT A 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol
MS$FOCUSED_ION: BASE_PEAK 79.0211
MS$FOCUSED_ION: PRECURSOR_M/Z 124.0757
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_INTENSITY 5932913.953125
MS$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$SPLASH: splash10-0006-9200000000-2f77a141f5cb27290f0e
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
50.0152 C4H2+ 1 50.0151 1.58
53.0386 C4H5+ 1 53.0386 1.3
55.0179 C3H3O+ 1 55.0178 0.52
63.023 C5H3+ 1 63.0229 0.48
64.0307 C5H4+ 1 64.0308 -1.26
65.0385 C5H5+ 1 65.0386 -0.42
66.0464 C5H6+ 1 66.0464 -0.41
67.0543 C5H7+ 1 67.0542 0.4
68.0495 C4H6N+ 1 68.0495 0.11
77.0384 C6H5+ 1 77.0386 -1.73
78.0338 C5H4N+ 1 78.0338 -0.67
78.0465 C6H6+ 1 78.0464 1.74
79.0542 C6H7+ 1 79.0542 -0.83
80.0495 C5H6N+ 1 80.0495 -0.31
81.0573 C5H7N+ 1 81.0573 -0.24
82.0413 C5H6O+ 1 82.0413 0.28
92.0257 C6H4O+ 1 92.0257 0.47
92.0495 C6H6N+ 1 92.0495 0.16
93.0573 C6H7N+ 1 93.0573 0.27
94.0651 C6H8N+ 1 94.0651 0.13
95.0491 C6H7O+ 1 95.0491 0.05
96.0443 C5H6NO+ 1 96.0444 -0.45
96.0808 C6H10N+ 1 96.0808 0.57
97.0648 C6H9O+ 1 97.0648 0.19
107.0492 C7H7O+ 1 107.0491 0.31
108.0444 C6H6NO+ 1 108.0444 -0.05
108.0569 C7H8O+ 1 108.057 -0.29
109.0522 C6H7NO+ 1 109.0522 0.26
110.0601 C6H8NO+ 1 110.06 0.16
123.0679 C7H9NO+ 1 123.0679 0.07
124.0757 C7H10NO+ 1 124.0757 0.22
PK$NUM_PEAK: 31
PK$PEAK: m/z int. rel.int.
50.0152 4032.5 2
53.0386 67293.8 36
55.0179 5785.9 3
63.023 9057.2 4
64.0307 9486.9 5
65.0385 175928.7 96
66.0464 28590.8 15
67.0543 7689.2 4
68.0495 5192.9 2
77.0384 24254.3 13
78.0338 2826.6 1
78.0465 2304.5 1
79.0542 35433.7 19
80.0495 133640.4 73
81.0573 476216.9 261
82.0413 3247.4 1
92.0257 276445.8 151
92.0495 534502.8 293
93.0573 1818408 999
94.0651 28928.6 15
95.0491 234672.1 128
96.0443 28316.1 15
96.0808 3026 1
97.0648 12917.5 7
107.0492 6748.5 3
108.0444 71061.9 39
108.0569 4142.8 2
109.0522 544566.9 299
110.0601 48986 26
123.0679 70286.4 38
124.0757 443212.4 243
//
