ACCESSION: MSBNK-LCSB-LU033604
RECORD_TITLE: Oleyl sarcosine; LC-ESI-QFT; MS2; CE: 60; R=17500; [M+H]+
DATE: 2020.08.19
AUTHORS: Elapavalore, A.; Kondić, T.; Singh, R.; Schymanski, E.
LICENSE: CC BY
COPYRIGHT: Copyright © 2019 by Environmental Cheminformatics, LCSB, University of Luxembourg, Luxembourg
PUBLICATION: Elapavalore, A.; Kondić, T.; et al., Adding Open Spectral Data to MassBank and PubChem Using Open Source Tools to Support Non-Targeted Exposomics of Mixtures (submitted).
PROJECT: ENTACT U.S. Environmental Protection Agency’s Non-Targeted Analysis Collaborative Trial
COMMENT: CONFIDENCE standard compound
COMMENT: INTERNAL_ID 336
COMMENT: DATASET 20200303_ENTACT_RP_MIX505
COMMENT: DATA_PROCESSING MERGING RMBmix ver. 0.2.7
COMMENT: DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0
COMMENT: ORIGINAL_ACQUISITION_NO 11450
COMMENT: ORIGINAL_PRECURSOR_SCAN_NO 11448
COMMENT: RAW_DATA available as MSV000091754 at [DOI:10.25345/C5S46HG75]
CH$NAME: Oleyl sarcosine
CH$NAME: Oleoyl sarcosine
CH$NAME: 2-[methyl-[(Z)-octadec-9-enoyl]amino]acetic acid
CH$COMPOUND_CLASS: N/A; Environmental Standard
CH$FORMULA: C21H39NO3
CH$EXACT_MASS: 353.2930
CH$SMILES: CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CC(O)=O
CH$IUPAC: InChI=1S/C21H39NO3/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20(23)22(2)19-21(24)25/h10-11H,3-9,12-19H2,1-2H3,(H,24,25)/b11-10-
CH$LINK: CAS
110-25-8
CH$LINK: PUBCHEM
CID:6912870
CH$LINK: INCHIKEY
DIOYAVUHUXAUPX-KHPPLWFESA-N
CH$LINK: CHEMSPIDER
5289148
AC$INSTRUMENT: Q Exactive Orbitrap (Thermo Scientific)
AC$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$MASS_SPECTROMETRY: COLLISION_ENERGY 60
AC$MASS_SPECTROMETRY: RESOLUTION 17500
AC$CHROMATOGRAPHY: COLUMN_NAME Acquity BEH C18 1.7um, 2.1x150mm (Waters)
AC$CHROMATOGRAPHY: FLOW_GRADIENT 90/10 at 0-2 min, 0/100 at 15-20 min, 90/10 at 20.1-30 min
AC$CHROMATOGRAPHY: FLOW_RATE 0.20 mL/min
AC$CHROMATOGRAPHY: RETENTION_TIME 21.843 min
AC$CHROMATOGRAPHY: SOLVENT A 0.1% formic acid
AC$CHROMATOGRAPHY: SOLVENT B methanol
MS$FOCUSED_ION: BASE_PEAK 79.0211
MS$FOCUSED_ION: PRECURSOR_M/Z 354.3003
MS$FOCUSED_ION: PRECURSOR_TYPE [M+H]+
MS$FOCUSED_ION: PRECURSOR_INTENSITY 2380361.03125
MS$DATA_PROCESSING: RECALIBRATE loess on assigned fragments and MS1
MS$DATA_PROCESSING: REANALYZE Peaks with additional N2/O included
MS$DATA_PROCESSING: WHOLE RMassBank 2.99.2
PK$SPLASH: splash10-0006-9000000000-ef951e8aa271294b531f
PK$ANNOTATION: m/z tentative_formula formula_count mass error(ppm)
53.0022 C3HO+ 1 53.0022 0.76
53.0386 C4H5+ 1 53.0386 0.46
55.0542 C4H7+ 1 55.0542 0.18
57.0699 C4H9+ 1 57.0699 -0.33
65.0385 C5H5+ 1 65.0386 -0.89
67.0542 C5H7+ 1 67.0542 -0.3
69.0698 C5H9+ 1 69.0699 -0.5
71.0493 C4H7O+ 1 71.0491 1.71
71.0855 C5H11+ 1 71.0855 -0.55
79.0542 C6H7+ 1 79.0542 0.11
81.0699 C6H9+ 1 81.0699 0.31
83.0855 C6H11+ 1 83.0855 -0.21
90.055 C3H8NO2+ 1 90.055 0.39
91.0543 C7H7+ 1 91.0542 0.5
93.0699 C7H9+ 1 93.0699 0.37
95.0493 C6H7O+ 1 95.0491 1.31
95.0855 C7H11+ 1 95.0855 0.09
97.0648 C6H9O+ 1 97.0648 -0.08
97.1012 C7H13+ 1 97.1012 0.23
107.0856 C8H11+ 1 107.0855 0.76
109.1011 C8H13+ 1 109.1012 -0.79
111.0805 C7H11O+ 1 111.0804 0.4
111.1171 C8H15+ 1 111.1168 2.59
121.1012 C9H13+ 1 121.1012 0.18
123.1174 C9H15+ 1 123.1168 4.58
135.1169 C10H15+ 1 135.1168 0.66
149.1327 C11H17+ 1 149.1325 1.66
PK$NUM_PEAK: 27
PK$PEAK: m/z int. rel.int.
53.0022 4991.3 12
53.0386 2861.9 7
55.0542 127735.7 332
57.0699 26655.4 69
65.0385 3154.2 8
67.0542 78754.8 204
69.0698 109002 283
71.0493 2095 5
71.0855 10125.6 26
79.0542 42495.6 110
81.0699 72866.3 189
83.0855 46522.8 121
90.055 383893.3 999
91.0543 8757.4 22
93.0699 48255.1 125
95.0493 3149.7 8
95.0855 44850.1 116
97.0648 11741 30
97.1012 15574.4 40
107.0856 15834.1 41
109.1011 12879.8 33
111.0805 4213.3 10
111.1171 2250.2 5
121.1012 18750 48
123.1174 2487.4 6
135.1169 8463 22
149.1327 2593.8 6
//
