MassBank Record: SM846301



 Imidacloprid urea; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+ 
Mass Spectrum
Chemical Structure


ACCESSION: SM846301
RECORD_TITLE: Imidacloprid urea; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+
DATE: 2016.12.12
AUTHORS: Krauss M, Schymanski EL, Weidauer C, Schupke H, UFZ and Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2016 UFZ/Eawag
PUBLICATION: Schymanski, EL et al. Critical Assessment of Small Molecule Identification 2016 - Automated Methods. Submitted.
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 8463

CH$NAME: Imidacloprid urea CH$NAME: 1-[(6-chloropyridin-3-yl)methyl]imidazolidin-2-one CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C9H10ClN3O CH$EXACT_MASS: 211.05124 CH$SMILES: c1cc(ncc1CN2CCN=C2O)Cl CH$IUPAC: InChI=1S/C9H10ClN3O/c10-8-2-1-7(5-12-8)6-13-4-3-11-9(13)14/h1-2,5H,3-4,6H2,(H,11,14) CH$LINK: CHEBI 83544 CH$LINK: PUBCHEM CID:15390532 CH$LINK: INCHIKEY ADWTYURAFSWNSU-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 10248201
AC$INSTRUMENT: Q Exactive Plus Orbitrap Thermo Scientific AC$INSTRUMENT_TYPE: LC-ESI-QFT AC$MASS_SPECTROMETRY: MS_TYPE MS2 AC$MASS_SPECTROMETRY: IONIZATION ESI AC$MASS_SPECTROMETRY: ION_MODE POSITIVE AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD AC$MASS_SPECTROMETRY: COLLISION_ENERGY 35 (nominal) AC$MASS_SPECTROMETRY: RESOLUTION 35000 AC$CHROMATOGRAPHY: COLUMN_NAME Kinetex C18 EVO 2.6 um, 2.1x50 mm, precolumn 2.1x5 mm, Phenomenex AC$CHROMATOGRAPHY: FLOW_GRADIENT 95/5 at 0 min, 95/5 at 1 min, 0/100 at 13 min, 0/100 at 24 min AC$CHROMATOGRAPHY: FLOW_RATE 300 uL/min AC$CHROMATOGRAPHY: RETENTION_TIME 5.737 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 203.0925 MS$FOCUSED_ION: PRECURSOR_M/Z 212.0585 MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+ MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1 MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included MS$DATA_PROCESSING: WHOLE RMassBank 2.3.1
PK$SPLASH: splash10-03fr-2980000000-63b3b5a83ecc5a1de517 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 56.0496 C3H6N+ 1 56.0495 2.91 57.0701 C4H9+ 1 57.0699 3.48 65.0387 C5H5+ 1 65.0386 1.21 67.0543 C5H7+ 1 67.0542 1.07 69.0084 C2HN2O+ 1 69.0083 1.27 70.0288 C3H4NO+ 1 70.0287 0.74 71.0605 C3H7N2+ 1 71.0604 1.16 85.0396 C3H5N2O+ 1 85.0396 0.02 86.0349 C2H4N3O+ 1 86.0349 -0.17 90.0338 C6H4N+ 1 90.0338 -0.55 92.0495 C6H6N+ 1 92.0495 0.09 93.0572 C6H7N+ 1 93.0573 -0.58 97.0396 C4H5N2O+ 1 97.0396 -0.78 99.0553 C4H7N2O+ 1 99.0553 -0.23 106.0651 C7H8N+ 1 106.0651 0 107.0604 C6H7N2+ 1 107.0604 -0.04 110.0599 C6H8NO+ 1 110.06 -1.22 114.0105 C5H5ClN+ 2 114.0105 0.09 114.0662 C4H8N3O+ 1 114.0662 -0.16 126.0105 C6H5ClN+ 2 126.0105 -0.12 127.0183 C6H6ClN+ 2 127.0183 -0.6 128.0261 C6H7ClN+ 2 128.0262 -0.23 133.076 C8H9N2+ 1 133.076 -0.43 142.0054 C6H5ClNO+ 1 142.0054 0.03 144.0209 C6H7ClNO+ 1 144.0211 -1.14 156.088 C5H10N5O+ 1 156.088 -0.03 167.0372 C8H8ClN2+ 1 167.0371 1.04 168.0209 C8H7ClNO+ 1 168.0211 -1.19 169.0164 C7H6ClN2O+ 1 169.0163 0.21 169.0526 C8H10ClN2+ 1 169.0527 -0.38 176.0818 C9H10N3O+ 1 176.0818 -0.19 194.048 C9H9ClN3+ 1 194.048 0.45 195.032 C9H8ClN2O+ 1 195.032 0.35 212.0585 C9H11ClN3O+ 1 212.0585 -0.24 PK$NUM_PEAK: 34 PK$PEAK: m/z int. rel.int. 56.0496 410561.8 5 57.0701 86930.6 1 65.0387 195822.8 2 67.0543 77118.7 1 69.0084 106713.3 1 70.0288 257420.8 3 71.0605 315140.3 4 85.0396 374675.2 5 86.0349 648902.2 9 90.0338 212740.2 3 92.0495 593394.3 8 93.0572 498720.6 7 97.0396 271127.8 3 99.0553 14463306 205 106.0651 102305.9 1 107.0604 186643 2 110.0599 245029.4 3 114.0105 937220.6 13 114.0662 372446.9 5 126.0105 9187990 130 127.0183 580935.5 8 128.0261 53646812 762 133.076 459289.5 6 142.0054 161081.4 2 144.0209 160646.1 2 156.088 6777388.5 96 167.0372 88166.8 1 168.0209 81405.9 1 169.0164 223181.4 3 169.0526 622673.8 8 176.0818 951191.9 13 194.048 497259.7 7 195.032 1428422.4 20 212.0585 70316528 999 //