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Uric acid (4TMS)

 

Replica Mass Spectra of Uric acid (4TMS)

replicalib entry datedetectionmethodspecies
928 August 2012  MassBank GC 2010 Tsujimoto 
101 November 2001 MS-QuadM[2]Standard
201 May 2001 MS-TOFM[EIGTMS]Standard Addition
830 March 2011  Fiehn_GC_2010 
1005 June 2013  MRI_2013 
319 July 2007 MS-TOFVAR5Reference Substance
401 August 2002 MS-QuadM[2]Lotus japonicus (Regel) K. Larsen
512 May 2005  M[NIST] 
601 December 2003 MS-QuadM[2]Standard
9 spectrum(a)
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Spectrum Details

analyteUric acid (4TMS)
analyte InChIInChI=1S/C17H36N4O3Si4/c1-25(2,3)18-13-14(19(16(18)23)26(4,5)6)20(27(7,8)9)17(24)21(15(13)22)28(10,11)12/h1-12H3
analyte mass456.84
chromatogramNA(_49)
citation 
authorsRoessner-Tunali U, Forbes MG, University of Melbourne, School of Botany, 3010 Victoria, Australia
lib entry date19 January 2005
metabolite roleMETB
retention time (sec) 
retention index (VAR5 method, n-alkanes C10–C36)2,090.76 (predicted, according to Strehmel, N. et.al)
base peak (m/z)441
maximal intensity999
mass-intensity-peaks cardinality275 intensities
minimal m/z70
maximal m/z463
download JCAMP DXSpectrumJcampDx.ashx?id=3f53a9a8-c5ed-4e39-b875-feb77e20953a
download MSPSpectrumMsp.ashx?id=3f53a9a8-c5ed-4e39-b875-feb77e20953a

GC-Method

nameM[ROE]
citationU. Roessner, J. Patterson, M. Forbes, G. Fincher, P. Langridge, A. Bacic, Plant Physiology 142 (2006) 1087
attributetextdetails
deconvolutionXcalibur program 
derivatizationMEOX; MSTFAMETHOXYAMINATION: 120min at 37°C; SILYLATION: 30min at 37°C
detectorMS-QUADm/z = 70-600; scans:2/s; DSQ quadrupole mass spectrometer
extractionmethanol:chloroform 
ion sourceEI70eV
RIALKANEC12, C15, C19, C22, C28, C32, C36
separationGCCOLUMN:5%diphenyl-95%dimethylpolysiloxane, 30+10m, ID:0.25mm, DF:0.25µm, VF-5MS (Varian, Darmstadt, Germany); PROGRAM:injection at 70°C, ramp 1°C/min to 76°C, ramp 6°C/min to 330°C, iso at 330°C for 10min; FLOW:Helium, 1mL/min; INJECTION:1µL, splitless, 230°C; TRANSFER:280°C; IONSOURCE:250°C

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