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Histidine, N-tau-methyl- (2TMS)

 

Replica Mass Spectra of Histidine, N-tau-methyl- (2TMS)

replicalib entry datedetectionmethodspecies
328 August 2012  MassBank GC 2010 Tsujimoto 
405 June 2013  MRI_2013 
219 July 2007 MS-TOFVAR5Reference Substance
3 spectrum(a)
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Spectrum Details

analyteHistidine, N-tau-methyl- (2TMS)
analyte InChIInChI=1S/C13H27N3O2Si2/c1-16-9-11(14-10-16)8-12(15-19(2,3)4)13(17)18-20(5,6)7/h9-10,12,15H,8H2,1-7H3/t12-/m0/s1
analyte mass313.54
chromatogram6018hf_63
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 role 
retention time (sec)644.09
retention index (VAR5 method, n-alkanes C10–C36) 
base peak (m/z)96
maximal intensity745,282
mass-intensity-peaks cardinality305 intensities
minimal m/z45
maximal m/z987
download JCAMP DXSpectrumJcampDx.ashx?id=cdcb48ca-77f4-40d1-82b6-0e58aed5b832
download MSPSpectrumMsp.ashx?id=cdcb48ca-77f4-40d1-82b6-0e58aed5b832

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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