ACCESSION: MSBNK-LCSB-LU020106
RECORD_TITLE: 4-Methoxyaniline; LC-ESI-QFT; MS2; CE: 90; 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 201
COMMENT: DATASET 20200303_ENTACT_RP_MIX501
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 2033
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 2031
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 90
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$CHROMATOGRAPHY: RETENTION_TIME 3.937 min
AC$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$FOCUSED_ION: PRECURSOR_INTENSITY 5471485
MS$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$SPLASH: splash10-0006-9100000000-ea88c91caaad4b09dd9d
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
51.023 C4H3+ 1 51.0229 0.88
53.0386 C4H5+ 1 53.0386 0
54.0464 C4H6+ 1 54.0464 -0.4
55.0178 C3H3O+ 1 55.0178 -0.43
63.0229 C5H3+ 1 63.0229 -1.14
64.0307 C5H4+ 1 64.0308 -1.19
65.0385 C5H5+ 1 65.0386 -0.75
66.0463 C5H6+ 1 66.0464 -1.26
67.0541 C5H7+ 1 67.0542 -1.74
68.0494 C4H6N+ 1 68.0495 -1.15
77.0385 C6H5+ 1 77.0386 -1.15
79.0542 C6H7+ 1 79.0542 -0.67
80.0494 C5H6N+ 1 80.0495 -0.73
81.0573 C5H7N+ 1 81.0573 -0.48
82.0413 C5H6O+ 1 82.0413 0.08
92.0257 C6H4O+ 1 92.0257 -0.06
92.0494 C6H6N+ 1 92.0495 -0.62
93.0573 C6H7N+ 1 93.0573 -0.27
94.0651 C6H8N+ 1 94.0651 -0.01
95.0491 C6H7O+ 1 95.0491 -0.64
96.0443 C5H6NO+ 1 96.0444 -1.2
97.0647 C6H9O+ 1 97.0648 -0.86
107.0492 C7H7O+ 1 107.0491 0.37
108.0443 C6H6NO+ 1 108.0444 -0.69
108.0567 C7H8O+ 1 108.057 -2.56
109.0522 C6H7NO+ 1 109.0522 -0.37
110.06 C6H8NO+ 1 110.06 -0.04
123.0678 C7H9NO+ 1 123.0679 -0.35
124.0757 C7H10NO+ 1 124.0757 -0.19
PK$NUM_PEAK: 29
PK$PEAK: m/z int. rel.int.
51.023 3559 1
53.0386 114719 57
54.0464 19973.9 10
55.0178 7858.1 3
63.0229 36948.9 18
64.0307 35914.1 18
65.0385 286264.5 143
66.0463 74246.4 37
67.0541 7797.5 3
68.0494 5354.6 2
77.0385 71063.2 35
79.0542 29672.3 14
80.0494 313972.3 157
81.0573 687079.1 344
82.0413 5672.2 2
92.0257 570562.4 286
92.0494 360194.5 180
93.0573 1989631.8 999
94.0651 20162.1 10
95.0491 337938.3 169
96.0443 21387.5 10
97.0647 6066.3 3
107.0492 4384.6 2
108.0443 146456.1 73
108.0567 10082.7 5
109.0522 433560.2 217
110.06 33249.9 16
123.0678 53595.5 26
124.0757 138087.8 69
//
