ACCESSION: MSBNK-LCSB-LU099104
RECORD_TITLE: Terbutylazine; LC-ESI-QFT; MS2; CE: 60; 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 991
COMMENT: DATASET 20200303_ENTACT_RP_MIX502
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 9014
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 9013
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]
CH$NAME: Terbutylazine
CH$NAME: Terbuthylazine
CH$NAME: 2-N-tert-butyl-6-chloro-4-N-ethyl-1,3,5-triazine-2,4-diamine
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C9H16ClN5
CH$EXACT_MASS: 229.1094
CH$SMILES: CCNC1=NC(NC(C)(C)C)=NC(Cl)=N1
CH$IUPAC: InChI=1S/C9H16ClN5/c1-5-11-7-12-6(10)13-8(14-7)15-9(2,3)4/h5H2,1-4H3,(H2,11,12,13,14,15)
CH$LINK: CAS
5915-41-3
CH$LINK: CHEBI
30263
CH$LINK: KEGG
C18810
CH$LINK: PUBCHEM
CID:22206
CH$LINK: INCHIKEY
FZXISNSWEXTPMF-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER
20848
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$MASS_SPECTROMETRY: COLLISION_ENERGY 60
AC$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 17.408 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 230.1167
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_INTENSITY 32464856.34375
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: splash10-00dj-5900000000-879954ff86875d3b2098
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
53.0022 ClH4N+ 1 53.0027 -8.65
57.0699 C4H9+ 1 57.0699 0.45
61.9791 CHClN+ 1 61.9792 -1.26
68.0243 C2H2N3+ 1 68.0243 -0.87
71.0603 C3H7N2+ 1 71.0604 -1.25
79.0057 CH4ClN2+ 1 79.0058 -0.63
90.0105 C3H5ClN+ 1 90.0105 -0.23
96.0556 C4H6N3+ 1 96.0556 -0.31
104.001 C2H3ClN3+ 1 104.001 -0.36
107.037 C3H8ClN2+ 1 107.0371 -0.12
110.0461 C3H4N5+ 1 110.0461 0.01
132.0323 C4H7ClN3+ 2 132.0323 -0.09
138.0774 C5H8N5+ 2 138.0774 -0.2
146.0228 C3H5ClN5+ 1 146.0228 -0.31
172.0388 C5H7ClN5+ 1 172.0384 1.8
174.0541 C5H9ClN5+ 1 174.0541 -0.13
230.1171 C9H17ClN5+ 1 230.1167 1.93
PK$NUM_PEAK: 17
PK$PEAK: m/z int. rel.int.
53.0022 10005.5 1
57.0699 463517.5 62
61.9791 61864.3 8
68.0243 1135901.4 153
71.0603 845345.2 113
79.0057 2842814.5 383
90.0105 117541.8 15
96.0556 3300148.2 444
104.001 1588173.1 214
107.037 16548 2
110.0461 298405.7 40
132.0323 2500653.5 337
138.0774 680547.7 91
146.0228 1799400.1 242
172.0388 13511.8 1
174.0541 7411032 999
230.1171 8465.2 1
//
