MassBank Record: EA103803



 4-Formylaminoantipyrine; LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: EA103803
RECORD_TITLE: 4-Formylaminoantipyrine; LC-ESI-ITFT; MS2; CE: 30%; R=7500; [M+H]+
DATE: 2014.01.14
AUTHORS: Stravs MDepartment of Environmental Chemistry, Eawag, Schymanski EDepartment of Environmental Chemistry, Eawag, Singer HDepartment of Environmental Chemistry, Eawag, Department of Environmental Chemistry, Eawag
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2012 Eawag, Duebendorf, Switzerland
COMMENT: CONFIDENCE standard compound
COMMENT: EAWAG_UCHEM_ID 1038

CH$NAME: 4-Formylaminoantipyrine CH$NAME: N-(1,5-dimethyl-3-oxidanylidene-2-phenyl-pyrazol-4-yl)methanamide CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C12H13N3O2 CH$EXACT_MASS: 231.1008 CH$SMILES: O=C2C(\NC=O)=C(\C)N(C)N2c1ccccc1 CH$IUPAC: InChI=1S/C12H13N3O2/c1-9-11(13-8-16)12(17)15(14(9)2)10-6-4-3-5-7-10/h3-8H,1-2H3,(H,13,16) CH$LINK: CAS 1672-58-8 CH$LINK: PUBCHEM CID:72666 CH$LINK: INCHIKEY WSJBSKRPKADYRQ-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 65525
AC$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 30 % (nominal) AC$MASS_SPECTROMETRY: RESOLUTION 7500 AC$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$CHROMATOGRAPHY: RETENTION_TIME 3.7 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 232.1088 MS$FOCUSED_ION: PRECURSOR_M/Z 232.1081 MS$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$SPLASH: splash10-01q9-0090000000-5e87d5f9e5f61ac4154f PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 56.0494 C3H6N+ 1 56.0495 -1.71 77.0384 C6H5+ 1 77.0386 -2.03 83.0604 C4H7N2+ 1 83.0604 -0.06 85.076 C4H9N2+ 1 85.076 -0.64 94.0652 C6H8N+ 1 94.0651 0.58 104.0494 C7H6N+ 1 104.0495 -0.44 111.0553 C5H7N2O+ 1 111.0553 -0.26 145.0762 C9H9N2+ 1 145.076 1.21 146.0603 C9H8NO+ 1 146.06 1.78 159.0916 C10H11N2+ 1 159.0917 -0.53 173.0711 C10H9N2O+ 1 173.0709 0.76 187.0865 C11H11N2O+ 1 187.0866 -0.64 189.0899 C10H11N3O+ 1 189.0897 1.3 204.1131 C11H14N3O+ 1 204.1131 0.01 214.0975 C12H12N3O+ 1 214.0975 0.19 232.1082 C12H14N3O2+ 1 232.1081 0.55 PK$NUM_PEAK: 16 PK$PEAK: m/z int. rel.int. 56.0494 198267.7 53 77.0384 22914.3 6 83.0604 410692.7 111 85.076 50048.8 13 94.0652 56357 15 104.0494 263641.9 71 111.0553 21310.1 5 145.0762 22911 6 146.0603 16420.1 4 159.0916 180290.6 49 173.0711 60934.5 16 187.0865 225836.3 61 189.0899 41109.5 11 204.1131 1654070.7 449 214.0975 2228952.9 606 232.1082 3673725 999 //