ACCESSION: MSBNK-LCSB-LU025706
RECORD_TITLE: Pymetrozine; 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 257
COMMENT: DATASET 20200303_ENTACT_RP_MIX505
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 2667
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 2665
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]
CH$NAME: Pymetrozine
CH$NAME: 6-methyl-4-[(E)-pyridin-3-ylmethylideneamino]-2,5-dihydro-1,2,4-triazin-3-one
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C10H11N5O
CH$EXACT_MASS: 217.0964
CH$SMILES: CC1=NNC(=O)N(C1)\N=C\C1=CC=CN=C1
CH$IUPAC: InChI=1S/C10H11N5O/c1-8-7-15(10(16)14-13-8)12-6-9-3-2-4-11-5-9/h2-6H,7H2,1H3,(H,14,16)/b12-6+
CH$LINK: CAS
123312-89-0
CH$LINK: CHEBI
39311
CH$LINK: KEGG
C18590
CH$LINK: PUBCHEM
CID:9576037
CH$LINK: INCHIKEY
QHMTXANCGGJZRX-WUXMJOGZSA-N
CH$LINK: CHEMSPIDER
7850487
AC$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$CHROMATOGRAPHY: RETENTION_TIME 5.130 min
AC$CHROMATOGRAPHY: SOLVENT A 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol
MS$FOCUSED_ION: BASE_PEAK 79.0211
MS$FOCUSED_ION: PRECURSOR_M/Z 218.1036
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_INTENSITY 13029940.09375
MS$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$SPLASH: splash10-0a4i-2900000000-f705ea81a1e13fe96777
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
50.0151 C4H2+ 1 50.0151 0.74
51.0229 C4H3+ 1 51.0229 -1.16
52.0182 C3H2N+ 1 52.0182 0.01
53.0386 C4H5+ 1 53.0386 0.1
65.0386 C5H5+ 1 65.0386 0.28
74.0963 C4H12N+ 1 74.0964 -1.62
78.0338 C5H4N+ 1 78.0338 -0.28
79.0416 C5H5N+ 1 79.0417 -0.34
80.0494 C5H6N+ 1 80.0495 -0.54
92.0495 C6H6N+ 1 92.0495 -0.2
93.0573 C6H7N+ 1 93.0573 0.15
96.0444 C5H6NO+ 2 96.0444 -0.24
97.0076 C8H+ 1 97.0073 3.19
98.0348 C3H4N3O+ 1 98.0349 -1.05
103.0291 C6H3N2+ 1 103.0291 -0.06
105.0447 C6H5N2+ 1 105.0447 -0.2
106.0526 C6H6N2+ 1 106.0525 0.2
107.0604 C6H7N2+ 1 107.0604 0.53
111.0315 C3H3N4O+ 1 111.0301 11.84
120.0556 C6H6N3+ 2 120.0556 -0.36
121.0396 C6H5N2O+ 2 121.0396 -0.71
PK$NUM_PEAK: 21
PK$PEAK: m/z int. rel.int.
50.0151 19741 3
51.0229 16158.4 3
52.0182 6028.4 1
53.0386 7477.2 1
65.0386 21555.8 4
74.0963 5352.1 1
78.0338 638096.8 123
79.0416 354196.6 68
80.0494 74884.3 14
92.0495 29006.3 5
93.0573 23673 4
96.0444 283482.4 54
97.0076 21795.2 4
98.0348 20664.5 3
103.0291 16161.6 3
105.0447 5182416 999
106.0526 8162 1
107.0604 12885.7 2
111.0315 344030.3 66
120.0556 7067.2 1
121.0396 55555 10
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