MassBank MassBank Search Contents Download

MassBank Record: MSBNK-BAFG-CSL2311109091

Norfloxacin; LC-ESI-QTOF; MS2; 60 V

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

ACCESSION: MSBNK-BAFG-CSL2311109091
RECORD_TITLE: Norfloxacin; LC-ESI-QTOF; MS2; 60 V
DATE: 2023.11.10
AUTHORS: Kevin S. Jewell; Björn Ehlig; Arne Wick
LICENSE: dl-de/by-2-0
COPYRIGHT: Copyright 2023 Federal Institute of Hydrology, Koblenz, Germany
COMMENT: CONFIDENCE Reference Standard (Level 1)
COMMENT: Chromatography method: dx.doi.org/10.1016/j.chroma.2015.11.014
COMMENT: Acquisition method: 10.1002/rcm.8541

CH$NAME: Norfloxacin
CH$COMPOUND_CLASS: Antimicrobial; Pharmaceutical
CH$FORMULA: C16H18FN3O3
CH$EXACT_MASS: 319.1332
CH$SMILES: CCN1C=C(C(=O)C2=CC(=C(C=C21)N3CCNCC3)F)C(=O)O
CH$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: INCHIKEY OGJPXUAPXNRGGI-UHFFFAOYSA-N

AC$INSTRUMENT: TripleTOF 5600 SCIEX
AC$INSTRUMENT_TYPE: LC-ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 60
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$CHROMATOGRAPHY: COLUMN_NAME Zorbax Eclipse Plus C18 2.1 mm x 150 mm, 3.5 um, Agilent
AC$CHROMATOGRAPHY: COLUMN_TEMPERATURE 40 °C
AC$CHROMATOGRAPHY: FLOW_GRADIENT 0 min min 98% A, 1 min 98% A, 2 min 80% A, 16.5 min 2% A, 22 min 2% A, 22.1 min 98% A, 27 min 98% A
AC$CHROMATOGRAPHY: FLOW_RATE 0.3 mL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 5.167 min
AC$CHROMATOGRAPHY: SOLVENT A: Water 0.1% Formic acid, B: Acetonitrile 0.1% Formic acid

MS$FOCUSED_ION: PRECURSOR_M/Z 320.1405
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$DATA_PROCESSING: COMMENT Export with Spectra 1.9.12 MsBackendMassbank 1.7.4
MS$DATA_PROCESSING: WHOLE RMassBank 2.3.1

PK$SPLASH: splash10-0f8i-0960000000-2601729f9d17430794fa
PK$NUM_PEAK: 68
PK$PEAK: m/z int. rel.int.
  116.0493 0.7 31
  128.0514 0.8 36
  130.0653 0.6 27
  133.0344 0.4 18
  134.0394 1.3 59
  135.0487 0.8 36
  136.056 1.4 63
  143.0728 0.6 27
  148.0547 4.5 205
  149.061 0.5 22
  154.0563 0.4 18
  155.0624 0.9 41
  156.0689 1.2 54
  157.0742 0.6 27
  158.0691 0.4 18
  160.0558 0.6 27
  161.0245 0.5 22
  161.0589 2.4 109
  162.0336 1.4 63
  162.0621 0.9 41
  163.0423 0.7 31
  163.0663 1.2 54
  164.0487 0.9 41
  169.0756 0.9 41
  170.0753 0.7 31
  171.0952 0.4 18
  173.0506 0.6 27
  174.0588 1.5 68
  175.0645 2.4 109
  176.0502 0.5 22
  176.0748 5.7 260
  177.0606 0.5 22
  177.085 0.6 27
  183.0866 0.7 31
  185.0684 0.9 41
  186.0645 0.4 18
  187.0302 0.9 41
  187.0688 0.7 31
  188.0372 1.9 86
  188.0726 0.8 36
  189.052 0.8 36
  189.0815 12.5 570
  191.0619 1.4 63
  196.0856 0.8 36
  197.0662 0.4 18
  197.0971 1 45
  198.067 0.6 27
  198.0975 0.8 36
  203.0618 6.9 314
  203.0965 1.5 68
  204.0672 0.7 31
  204.1043 4.4 200
  205.0749 2 91
  210.1042 0.6 27
  211.1154 0.5 22
  212.0818 0.4 18
  215.0294 0.6 27
  217.0318 0.7 31
  217.0811 0.5 22
  218.0844 0.5 22
  225.0834 0.4 18
  231.055 21.9 999
  233.1022 0.6 27
  245.0645 0.6 27
  252.0816 0.4 18
  254.0908 1.7 77
  282.1172 0.8 36
  302.1368 0.9 41
//

Imprint Feedback
system version 2.2.8

Copyright © 2006 MassBank Project; 2011 NORMAN Association; 2021 MassBank Consortium

Responsible: Tillmann G. Fischer

Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under the National Research Data Infrastructure – NFDI4Chem – Projektnummer 441958208.

de.NBI logo
EAWAG logo
fnr logo
IPB logo
NORMAN logo
UFZ logo
LCSB logo
HBM4EU logo
nfdi4chem logo