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MassBank Record: MSBNK-CASMI_2016-SM849302

Ebastin; LC-ESI-QFT; MS2; CE: 35 NCE; R=35000; [M+H]+

Mass Spectrum
Chemical Structure
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ACCESSION: MSBNK-CASMI_2016-SM849302
RECORD_TITLE: Ebastin; 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, E. L.; Ruttkies, C.; Krauss, M.; Brouard, C.; Kind, T.; Dührkop, K.; Allen, F.; Vaniya, A.; Verdegem, D.; Böcker, S.; et al. Critical Assessment of Small Molecule Identification 2016: Automated Methods. Journal of Cheminformatics 2017, 9 (1). DOI:10.1186/s13321-017-0207-1
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 8493

CH$NAME: Ebastin
CH$NAME: 4-(4-benzhydryloxypiperidin-1-yl)-1-(4-tert-butylphenyl)butan-1-one
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C32H39NO2
CH$EXACT_MASS: 469.29808
CH$SMILES: CC(C)(C)C1=CC=C(C=C1)C(=O)CCCN1CCC(CC1)OC(C1=CC=CC=C1)C1=CC=CC=C1
CH$IUPAC: InChI=1S/C32H39NO2/c1-32(2,3)28-18-16-25(17-19-28)30(34)15-10-22-33-23-20-29(21-24-33)35-31(26-11-6-4-7-12-26)27-13-8-5-9-14-27/h4-9,11-14,16-19,29,31H,10,15,20-24H2,1-3H3
CH$LINK: CAS 90729-43-4
CH$LINK: KEGG D01478
CH$LINK: PUBCHEM CID:3191
CH$LINK: INCHIKEY MJJALKDDGIKVBE-UHFFFAOYSA-N
CH$LINK: CHEMSPIDER 3079
CH$LINK: COMPTOX DTXSID6046472

AC$INSTRUMENT: Q Exactive Plus Orbitrap Thermo Scientific
AC$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$MASS_SPECTROMETRY: COLLISION_ENERGY 35 (nominal)
AC$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 11.405 min
AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid

MS$FOCUSED_ION: BASE_PEAK 470.305
MS$FOCUSED_ION: PRECURSOR_M/Z 470.3054
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$SPLASH: splash10-0gi0-0930400000-a3b7001dd8bec489cf92
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
  91.0542 C7H7+ 1 91.0542 0.08
  105.0699 C8H9+ 1 105.0699 0.12
  146.0727 C10H10O+ 1 146.0726 0.59
  152.0621 C12H8+ 1 152.0621 0
  161.0961 C11H13O+ 1 161.0961 -0.02
  165.0699 C13H9+ 1 165.0699 0.37
  166.0778 C13H10+ 1 166.0777 0.39
  167.0855 C13H11+ 1 167.0855 0.14
  169.0647 C12H9O+ 1 169.0648 -0.49
  173.0963 C12H13O+ 1 173.0961 1.11
  188.1196 C13H16O+ 1 188.1196 0.16
  203.1431 C14H19O+ 1 203.143 0.37
  284.2014 C19H26NO+ 1 284.2009 1.74
  302.2116 C19H28NO2+ 1 302.2115 0.44
  470.3057 C32H40NO2+ 1 470.3054 0.66
PK$NUM_PEAK: 15
PK$PEAK: m/z int. rel.int.
  91.0542 479280.5 2
  105.0699 503830.1 2
  146.0727 1541264.6 7
  152.0621 9501873 45
  161.0961 68866760 329
  165.0699 11606901 55
  166.0778 4347992 20
  167.0855 208976768 999
  169.0647 283909 1
  173.0963 363882.5 1
  188.1196 3116539 14
  203.1431 116451264 556
  284.2014 440377.5 2
  302.2116 2872738.5 13
  470.3057 158010496 755
//

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