MassBank Record: EA033112



 N'-(2,4-Dimethylphenyl)-N-methylformamidine; LC-ESI-ITFT; MS2; CE: 75%; R=15000; [M+H]+ 
Mass Spectrum
Chemical Structure
Generated by the Chemistry Development Kit (http://github.com/cdk) \n

ACCESSION: EA033112
RECORD_TITLE: N'-(2,4-Dimethylphenyl)-N-methylformamidine; LC-ESI-ITFT; MS2; CE: 75%; R=15000; [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 331

CH$NAME: N'-(2,4-Dimethylphenyl)-N-methylformamidine CH$NAME: Methanimidamide, N-(2,4-dimethylphenyl)-N'-methyl- CH$NAME: N-(2,4-dimethylphenyl)-N'-methyl-formamidine CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C10H14N2 CH$EXACT_MASS: 162.1157 CH$SMILES: C(=NC)Nc1c(cc(cc1)C)C CH$IUPAC: InChI=1S/C10H14N2/c1-8-4-5-10(9(2)6-8)12-7-11-3/h4-7H,1-3H3,(H,11,12) CH$LINK: CAS 33089-74-6 CH$LINK: PUBCHEM CID:36326 CH$LINK: INCHIKEY JIIOLEGNERQDIP-UHFFFAOYSA-N CH$LINK: CHEMSPIDER 33406 CH$LINK: COMPTOX DTXSID1037696
AC$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 75 % (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$CHROMATOGRAPHY: RETENTION_TIME 4.5 min AC$CHROMATOGRAPHY: SOLVENT A water with 0.1% formic acid AC$CHROMATOGRAPHY: SOLVENT B methanol with 0.1% formic acid
MS$FOCUSED_ION: BASE_PEAK 163.1229 MS$FOCUSED_ION: PRECURSOR_M/Z 163.123 MS$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$SPLASH: splash10-0ab9-0900000000-9392e41c0fc0b122f705 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 77.0386 C6H5+ 1 77.0386 0.04 79.0542 C6H7+ 1 79.0542 -0.59 95.0853 C7H11+ 1 95.0855 -2.38 103.0542 C8H7+ 1 103.0542 -0.06 105.0699 C8H9+ 1 105.0699 0.03 106.065 C7H8N+ 1 106.0651 -1.09 107.073 C7H9N+ 1 107.073 0.27 115.0542 C9H7+ 1 115.0542 0.12 117.0573 C8H7N+ 1 117.0573 0.08 120.0808 C8H10N+ 1 120.0808 0.29 121.0885 C8H11N+ 1 121.0886 -0.42 122.0964 C8H12N+ 1 122.0964 0.12 123.0805 C8H11O+ 1 123.0804 0.39 130.0655 C9H8N+ 1 130.0651 3.19 131.0729 C9H9N+ 1 131.073 -0.23 132.0808 C9H10N+ 1 132.0808 -0.12 133.076 C8H9N2+ 1 133.076 -0.19 136.1125 C9H14N+ 1 136.1121 3.48 148.0996 C9H12N2+ 1 148.0995 0.68 163.123 C10H15N2+ 1 163.123 0.22 PK$NUM_PEAK: 20 PK$PEAK: m/z int. rel.int. 77.0386 189320.5 9 79.0542 577799.3 28 95.0853 65962.4 3 103.0542 481039.5 23 105.0699 10560889.5 512 106.065 361421.9 17 107.073 18200091.1 883 115.0542 199581.3 9 117.0573 10355147.6 502 120.0808 1354983.8 65 121.0885 248783.6 12 122.0964 20569472 999 123.0805 136942.2 6 130.0655 94125.4 4 131.0729 363095.8 17 132.0808 11327417.1 550 133.076 882451.6 42 136.1125 59744.5 2 148.0996 66636.2 3 163.123 6517717.7 316 //

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