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MassBank Record: MSBNK-Eawag-EA023210

Norfloxacin; LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+

Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk)

ACCESSION: MSBNK-Eawag-EA023210
RECORD_TITLE: Norfloxacin; LC-ESI-ITFT; MS2; CE: 45%; R=15000; [M+H]+
DATE: 2014.01.14
AUTHORS: Stravs M, Schymanski E, Singer H, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2012 Eawag, Duebendorf, Switzerland
COMMENT: CONFIDENCE standard compound
COMMENT: EAWAG_UCHEM_ID 232

CH$NAME: Norfloxacin
CH$NAME: 1-ethyl-6-fluoro-4-oxo-7-piperazin-1-yl-1,4-dihydroquinoline-3-carboxylic acid
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C16H18FN3O3
CH$EXACT_MASS: 319.1332
CH$SMILES: CCN1C=C(C(O)=O)C(=O)C2=CC(F)=C(C=C12)N3CCNCC3
CH$IUPAC: InChI=1S/C16H18FN3O3/c1-2-19-9-11(16(22)23)15(21)10-7-12(17)14(8-13(10)19)20-5-3-18-4-6-20/h7-9,18H,2-6H2,1H3,(H,22,23)
CH$LINK: CAS 70458-96-7
CH$LINK: KEGG C06687
CH$LINK: PUBCHEM CID:4539
CH$LINK: INCHIKEY OGJPXUAPXNRGGI-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 4380
CH$LINK: COMPTOX DTXSID7037680

AC$INSTRUMENT: LTQ Orbitrap XL Thermo Scientific
AC$INSTRUMENT_TYPE: LC-ESI-ITFT
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE HCD
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 45 % (nominal)
AC$MASS_SPECTROMETRY: RESOLUTION 15000
AC$CHROMATOGRAPHY: COLUMN_NAME XBridge C18 3.5um, 2.1x50mm, Waters
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0 min, 50/50 at 4 min, 5/95 at 17 min, 5/95 at 25 min, 90/10 at 25.1 min, 90/10 at 30 min
AC$CHROMATOGRAPHY: FLOW_RATE 200 ul/min
AC$CHROMATOGRAPHY: RETENTION_TIME 4.4 min
AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid

MS$FOCUSED_ION: BASE_PEAK 320.1415
MS$FOCUSED_ION: PRECURSOR_M/Z 320.1405
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: DEPROFILE Spline
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 1.3.1

PK$SPLASH: splash10-0udi-0059000000-dd2ee816e5228385835d
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  58.0651 C3H8N+ 1 58.0651 -0.96
  70.0652 C4H8N+ 1 70.0651 1.06
  185.0713 C11H9N2O+ 2 185.0709 2.06
  191.0615 C10H8FN2O+ 1 191.0615 0.12
  192.0692 C10H9FN2O+ 1 192.0693 -0.85
  192.0824 C11H11FNO+ 1 192.0819 2.71
  201.1026 C12H13N2O+ 2 201.1022 1.79
  203.0616 C11H8FN2O+ 1 203.0615 0.5
  204.0695 C11H9FN2O+ 1 204.0693 0.72
  205.0773 C11H10FN2O+ 1 205.0772 0.84
  206.0853 C11H11FN2O+ 1 206.085 1.25
  207.0929 C11H12FN2O+ 1 207.0928 0.2
  212.0822 C12H10N3O+ 3 212.0818 1.47
  213.1025 C13H13N2O+ 2 213.1022 1.22
  215.098 C13H12FN2+ 1 215.0979 0.64
  218.0853 C12H11FN2O+ 1 218.085 1.55
  219.093 C12H12FN2O+ 1 219.0928 0.7
  220.1008 C12H13FN2O+ 1 220.1006 0.67
  226.0978 C13H12N3O+ 3 226.0975 1.6
  227.1055 C13H13N3O+ 2 227.1053 0.65
  228.1133 C13H14N3O+ 2 228.1131 0.75
  230.0847 C16H10N2+ 2 230.0838 3.83
  231.0566 C12H8FN2O2+ 1 231.0564 0.77
  231.0929 C13H12FN2O+ 1 231.0928 0.49
  233.1088 C13H14FN2O+ 1 233.1085 1.38
  241.1209 C14H15N3O+ 2 241.121 -0.06
  245.1086 C14H14FN2O+ 1 245.1085 0.5
  247.1118 C13H14FN3O+ 2 247.1115 1
  248.1197 C13H15FN3O+ 2 248.1194 1.22
  254.0925 C14H12N3O2+ 2 254.0924 0.18
  254.1283 C15H16N3O+ 1 254.1288 -1.84
  256.1446 C12H19FN3O2+ 2 256.1456 -3.83
  259.0882 C14H12FN2O2+ 1 259.0877 1.81
  259.1244 C15H16FN2O+ 1 259.1241 1.09
  274.099 C14H13FN3O2+ 2 274.0986 1.24
  274.135 C15H17FN3O+ 1 274.135 0.12
  276.1509 C15H19FN3O+ 1 276.1507 0.92
  282.1237 C16H16N3O2+ 2 282.1237 -0.01
  300.1341 C16H18N3O3+ 1 300.1343 -0.73
  302.1298 C16H17FN3O2+ 1 302.1299 -0.34
  320.1407 C16H19FN3O3+ 1 320.1405 0.7
PK$NUM_PEAK: 41
PK$PEAK: m/z int. rel.int.
  58.0651 8052.8 1
  70.0652 37678.9 4
  185.0713 8775.2 1
  191.0615 10660.8 1
  192.0692 10546.2 1
  192.0824 18890.9 2
  201.1026 15586.7 2
  203.0616 52684.6 6
  204.0695 93580.1 12
  205.0773 207386.1 27
  206.0853 76425.2 10
  207.0929 51565.3 6
  212.0822 10363.1 1
  213.1025 19080.4 2
  215.098 26896.7 3
  218.0853 14018.8 1
  219.093 405505.2 53
  220.1008 23310.8 3
  226.0978 25093.4 3
  227.1055 88729.4 11
  228.1133 77044.3 10
  230.0847 11350.5 1
  231.0566 50455.6 6
  231.0929 22931.4 3
  233.1088 2579328.6 338
  241.1209 15344 2
  245.1086 16087.9 2
  247.1118 21381.4 2
  248.1197 18777.7 2
  254.0925 13078.7 1
  254.1283 17638 2
  256.1446 551232.8 72
  259.0882 29134.8 3
  259.1244 25814.2 3
  274.099 17919.1 2
  274.135 128474.2 16
  276.1509 1770559.7 232
  282.1237 315480.2 41
  300.1341 66377.7 8
  302.1298 7620255.2 999
  320.1407 2623890 343
//

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