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Fumaric acid, 2-methyl- (2TMS)

 

Replica Mass Spectra of Fumaric acid, 2-methyl- (2TMS)

replicalib entry datedetectionmethodspecies
628 August 2012  MassBank GC 2010 Kusano 
218 December 2004 MS-QuadM[2]Standard
318 December 2004 MS-QuadM[2]Standard
805 June 2013  MRI_2013 
519 July 2007 MS-TOFVAR5Reference Substance
728 August 2012  MassBank GC 2010 Ara 
6 spectrum(a)
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Spectrum Details

analyteFumaric acid, 2-methyl- (2TMS)
analyte InChIInChI=1S/C11H22O4Si2/c1-9(11(13)15-17(5,6)7)8-10(12)14-16(2,3)4/h8H,1-7H3/b9-8+
analyte mass274.46
chromatogram6051hf_42
citation 
authorsBoelling C, Liebig F, Erban A, Kopka J, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
lib entry date19 July 2007
metabolite roleMETB
retention time (sec)391.38
retention index (VAR5 method, n-alkanes C10–C36) 
base peak (m/z)73
maximal intensity976,906
mass-intensity-peaks cardinality264 intensities
minimal m/z45
maximal m/z999
download JCAMP DXSpectrumJcampDx.ashx?id=99ac787e-f005-4b59-aa8b-3b699d59aa9c
download MSPSpectrumMsp.ashx?id=99ac787e-f005-4b59-aa8b-3b699d59aa9c

GC-Method

nameMDN35
citationKopka J, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
attributetextdetails
deconvolutionChromaTOFBASELINE OFFSET: 1; SMOOTHING: 5; PEAK WIDTH: 3s; S/N: 10
derivatizationMEOX; MSTFAMETHOXYAMINATION: 120min at 37°C; TRIMETHYLSILYLATION: 30min at 37°C
detectorMS-TOFm/z = 70-600; scans:20/s;
extractionchloroform:dH2O (2:1; v/v); chloroform (20°C); dH2O (4°C)
ion sourceEI70eV
RIFAME, d6-CholesteroleFAME: C8, C9, C10, C12, C14, C16, C18, C20, C22, C24, C26, C28, C30
separationGCCOLUMN:35%phenyl-65%dimethylpolysiloxane, 30m, ID:0.32mm, DF:0.25µm, MDN-35 (Macherey-Nagel, Düren, Germany); PROGRAM:iso 2min 80°C, ramp 15°C/min, iso 6min 330°C; FLOW:Helium, 2mL/min; INJECTION:1µL, splitless, 230°C; TRANSFER:250°C; IONSOURCE:250°C

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