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MassBank Record: MSBNK-HBM4EU-HB002756

Sulfamethoxazole; ESI-QTOF; MS2; CE: 45eV; R=15000; [M+H]+

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

ACCESSION: MSBNK-HBM4EU-HB002756
RECORD_TITLE: Sulfamethoxazole; ESI-QTOF; MS2; CE: 45eV; R=15000; [M+H]+
DATE: 2020.02.20
AUTHORS: Herbert Oberacher, Institute of Legal Medicine and Core Facility Metabolomics, Medical University of Innsbruck, Innsbruck, Austria
LICENSE: CC0
COPYRIGHT: Copyright (c) 2020 by Institute of Legal Medicine and Core Facility Metabolomics, Medical University of Innsbruck, Innsbruck, Austria
PUBLICATION: Oberacher H, Sasse M, Antignac J-P, Guitton Y, Debrauwer L, Jamin E L, Schulze T, Krauss M, Covaci A, Caballero-Casero N, Rosseau K, Damont A, Fenaille F, Lamoree M, Schymanski E, A European proposal for quality control and quality assurance of tandem mass spectral libraries, Environmental Sciences Europe, https://doi.org/10.1186/s12302-020-00314-9
COMMENT: CONFIDENCE Reference Standard (Level 1)
COMMENT: HBM4EU - science and policy for a healthy future (https://www.hbm4eu.eu)

CH$NAME: Sulfamethoxazole
CH$NAME: 4-Amino-N-(5-methyl-1,2-oxazol-3-yl)benzene-1-sulfonamide
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C10H11N3O3S
CH$EXACT_MASS: 253.0521
CH$SMILES: CC1=CC(NS(=O)(=O)C2=CC=C(N)C=C2)=NO1
CH$IUPAC: InChI=1S/C10H11N3O3S/c1-7-6-10(12-16-7)13-17(14,15)9-4-2-8(11)3-5-9/h2-6H,11H2,1H3,(H,12,13)
CH$LINK: CAS 723-46-6
CH$LINK: COMPTOX DTXSID8026064
CH$LINK: INCHIKEY JLKIGFTWXXRPMT-UHFFFAOYSA-N
CH$LINK: PUBCHEM CID:5329

AC$INSTRUMENT: TripleTOF 5600+SCIEX
AC$INSTRUMENT_TYPE: ESI-QTOF
AC$MASS_SPECTROMETRY: MS_TYPE MS2
AC$MASS_SPECTROMETRY: ION_MODE POSITIVE
AC$MASS_SPECTROMETRY: IONIZATION ESI
AC$MASS_SPECTROMETRY: FRAGMENTATION_MODE CID
AC$MASS_SPECTROMETRY: COLLISION_ENERGY 45 eV
AC$MASS_SPECTROMETRY: RESOLUTION 15000
AC$CHROMATOGRAPHY: FLOW_RATE 20 uL/min
AC$CHROMATOGRAPHY: FLOW_GRADIENT 50/50
AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% acetic acid
AC$CHROMATOGRAPHY: SOLVENT B acetonitrile

MS$FOCUSED_ION: PRECURSOR_M/Z 254.0594
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+

PK$SPLASH: splash10-0a4l-9700000000-4a0ce86127248ad909d7
PK$NUM_PEAK: 71
PK$PEAK: m/z int. rel.int.
  51.0261 0.2 1
  52.0325 0.1 1
  53.0414 2.1 9
  54.0367 0.5 2
  55.0208 0.4 2
  56.0522 0.2 1
  63.0253 0.3 1
  65.0407 89.7 369
  66.0485 2.3 9
  67.0434 0.3 1
  68.0511 0.2 1
  71.0625 0.5 2
  72.0459 1.9 8
  77.0401 0.7 3
  78.0352 0.3 1
  79.043 0.6 2
  80.051 36.5 150
  82.0539 0.1 1
  89.04 0.2 1
  90.0347 0.6 3
  91.0426 0.2 1
  92.0009 0.2 1
  92.0506 205.9 846
  93.0019 0.2 1
  93.0583 37 152
  94.0662 2.3 9
  97.0413 0.4 2
  99.0562 22.1 91
  102.0342 0.3 1
  103.0425 0.4 2
  104.0502 0.6 3
  105.0455 1.2 5
  106.0533 1.1 5
  107.061 9.6 40
  108.0451 243.1 999
  110.0607 0.4 2
  116.0497 0.8 3
  117.0456 0.3 1
  118.0536 1.3 5
  119.061 3.3 14
  120.0686 0.8 3
  121.0766 1.3 5
  122.0053 0.3 1
  127.966 0.2 1
  129.0454 0.7 3
  130.0534 1 4
  131.0607 2.5 10
  132.0685 2.1 8
  133.0638 1.5 6
  134.0718 0.5 2
  135.0125 0.1 1
  140.0177 0.4 2
  142.0536 0.2 1
  143.0611 2.5 10
  144.0566 0.5 2
  145.0639 1.3 5
  146.0717 16.4 68
  147.0794 11.7 48
  148.0873 0.7 3
  149.0173 0.2 1
  156.0118 16.7 69
  159.0018 0.3 1
  159.0795 1.3 5
  160.0873 10 41
  161.0017 1 4
  167.014 0.6 2
  169.029 0.4 2
  172.0515 0.1 1
  173.0588 0.7 3
  175.0202 0.3 1
  176.0283 0.6 2
//

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