MassBank Record: AU111211

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Valsartan; LC-ESI-QTOF; MS2; HILIC; CE: 50 eV; R=35000; [M+H]+
Mass Spectrum
Chemical Structure
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ACCESSION: AU111211
RECORD_TITLE: Valsartan; LC-ESI-QTOF; MS2; HILIC; CE: 50 eV; R=35000; [M+H]+
DATE: 2016.02.26
AUTHORS: Nikiforos Alygizakis, Nikolaos Thomaidis, University of Athens
LICENSE: CC BY
COPYRIGHT: Copyright (C) 2016 Department of Chemistry, University of Athens
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 1112

CH$NAME: Valsartan CH$NAME: (2S)-3-methyl-2-[pentanoyl-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]amino]butanoic acid CH$COMPOUND_CLASS: N/A; Environmental Standard CH$FORMULA: C24H29N5O3 CH$EXACT_MASS: 435.2270398 CH$SMILES: CCCCC(=O)N(CC1=CC=C(C=C1)C1=CC=CC=C1C1=NNN=N1)[C@@H](C(C)C)C(O)=O CH$IUPAC: InChI=1S/C24H29N5O3/c1-4-5-10-21(30)29(22(16(2)3)24(31)32)15-17-11-13-18(14-12-17)19-8-6-7-9-20(19)23-25-27-28-26-23/h6-9,11-14,16,22H,4-5,10,15H2,1-3H3,(H,31,32)(H,25,26,27,28)/t22-/m0/s1 CH$LINK: CAS 137862-53-4 CH$LINK: CHEBI 9927 CH$LINK: PUBCHEM CID:60846 CH$LINK: INCHIKEY ACWBQPMHZXGDFX-QFIPXVFZSA-N CH$LINK: CHEMSPIDER 54833
AC$INSTRUMENT: Bruker maXis Impact AC$INSTRUMENT_TYPE: LC-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$MASS_SPECTROMETRY: COLLISION_ENERGY 50 eV AC$MASS_SPECTROMETRY: RESOLUTION 35000 AC$CHROMATOGRAPHY: COLUMN_NAME ACQUITY UPLC BEH Amide 1.7 um 2.1x100mm, Water AC$CHROMATOGRAPHY: FLOW_GRADIENT 0/100 at 0-2 min, 95/5 at 12 min, 95/5 at 17 min, 0/100 at 17.1, 0/100 at 25 min AC$CHROMATOGRAPHY: FLOW_RATE 200 uL/min AC$CHROMATOGRAPHY: RETENTION_TIME 1.967 min AC$CHROMATOGRAPHY: SOLVENT A Water with 0.01% formic acid and 1mM ammonium formate AC$CHROMATOGRAPHY: SOLVENT B Acetonitrile:Water with 0.01% formic acid and 1mM ammonium formate
MS$FOCUSED_ION: BASE_PEAK 436.2371 MS$FOCUSED_ION: PRECURSOR_M/Z 436.2343 MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+ MS$DATA_PROCESSING: RECALIBRATE identity on assigned fragments and MS1 MS$DATA_PROCESSING: WHOLE RMassBank 1.99.10
PK$SPLASH: splash10-0a4i-0960000000-d6560b000f07587dc077 PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm) 115.0547 C9H7+ 1 115.0542 4.45 129.0455 C8H5N2+ 1 129.0447 6.06 140.0497 C10H6N+ 2 140.0495 1.8 141.0696 C11H9+ 1 141.0699 -2.17 151.0541 C12H7+ 1 151.0542 -0.91 152.0622 C12H8+ 1 152.0621 1.25 153.0703 C12H9+ 1 153.0699 2.79 154.0732 C11[13]CH9+ 1 154.0738 -3.55 163.0545 C13H7+ 1 163.0542 1.89 164.0589 C12[13]CH7+ 1 164.0581 4.87 165.0701 C13H9+ 1 165.0699 1.1 166.0666 C12H8N+ 1 166.0651 8.9 167.0729 C12H9N+ 3 167.073 -0.2 168.07 C11H8N2+ 1 168.0682 11 169.0655 C12H9O+ 2 169.0648 4.44 177.0579 C13H7N+ 2 177.0573 3.37 177.07 C14H9+ 2 177.0699 0.77 178.0781 C14H10+ 2 178.0777 1.97 179.0772 C13[13]CH10+ 1 179.0816 -24.52 180.0816 C13H10N+ 2 180.0808 4.34 181.0657 C13H9O+ 2 181.0648 4.76 181.0843 C8H11N3O2+ 3 181.0846 -1.7 182.0869 C7[13]CH11N3O2+ 1 182.0885 -8.74 190.0659 C14H8N+ 2 190.0651 4.14 191.0717 C14H9N+ 3 191.073 -6.73 192.0693 C13H8N2+ 2 192.0682 5.62 193.0716 C12[13]CH8N2+ 1 193.0721 -2.54 193.0881 C14H11N+ 3 193.0886 -2.34 194.0606 C13H8NO+ 3 194.06 2.83 194.0966 C14H12N+ 3 194.0964 0.66 195.0809 C14H11O+ 3 195.0804 2.17 195.1005 C13[13]CH12N+ 1 195.1003 0.99 196.0764 C13H10NO+ 3 196.0757 3.86 205.0768 C14H9N2+ 3 205.076 3.68 206.0848 C14H10N2+ 3 206.0838 4.45 207.0925 C14H11N2+ 3 207.0917 3.82 208.0765 C14H10NO+ 3 208.0757 3.77 208.0956 C13[13]CH11N2+ 1 208.0956 -0.01 209.0801 C13[13]CH10NO+ 1 209.0796 2.53 209.1074 C14H13N2+ 3 209.1073 0.39 210.092 C14H12NO+ 3 210.0913 2.94 210.1107 C13[13]CH13N2+ 1 210.1112 -2.75 211.0953 C13[13]CH12NO+ 1 211.0952 0.44 235.0908 C15H11N2O+ 3 235.0866 17.71 236.0935 C14[13]CH11N2O+ 1 236.0905 12.56 291.1502 C19H19N2O+ 3 291.1492 3.35 292.155 C18[13]CH19N2O+ 1 292.1531 6.39 PK$NUM_PEAK: 47 PK$PEAK: m/z int. rel.int. 115.0547 2072 5 129.0455 3152 8 140.0497 13356 36 141.0696 2256 6 151.0541 3012 8 152.0622 21340 57 153.0703 65876 177 154.0732 9424 25 163.0545 16124 43 164.0589 3216 8 165.0701 19048 51 166.0666 6960 18 167.0729 9760 26 168.07 3512 9 169.0655 3516 9 177.0579 3736 10 177.07 2332 6 178.0781 78680 212 179.0772 17668 47 180.0816 281048 759 181.0657 6864 18 181.0843 32076 86 182.0869 2808 7 190.0659 158244 427 191.0717 43512 117 192.0693 59768 161 193.0716 10156 27 193.0881 13040 35 194.0606 1940 5 194.0966 13340 36 195.0809 4616 12 195.1005 2096 5 196.0764 9128 24 205.0768 46564 125 206.0848 133152 359 207.0925 369852 999 208.0765 52700 142 208.0956 37264 100 209.0801 8340 22 209.1074 11832 31 210.092 20384 55 210.1107 2312 6 211.0953 3736 10 235.0908 12432 33 236.0935 2576 6 291.1502 11628 31 292.155 2312 6 //