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Uridine 5'-monophosphate (5TMS)

 

Replica Mass Spectra of Uridine 5'-monophosphate (5TMS)

replicalib entry datedetectionmethodspecies
215 March 2005 MS-TOFM[6]Reference Substance
1203 November 2010  Schomburg_GC_2010 
1330 March 2011  Fiehn_GC_2010 
512 May 2005  M[NIST] 
1430 March 2011  Fiehn_GC_2010 
115 March 2005 MS-TOFM[6]Reference Substance
819 July 2007 MS-TOFMDN35Reference Substance
922 February 2005 MS-TOFM[STR] 
8 spectrum(a)
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Spectrum Details

analyteUridine 5'-monophosphate (5TMS)
analyte InChIInChI=1S/C24H53N2O10PSi5/c1-38(2,3)30-17-19-20(33-39(4,5)6)21(34-40(7,8)9)23(31-19)26-16-18(22(27)25-24(26)28)32-37(29,35-41(10,11)12)36-42(13,14)15/h16,19-21,23H,17H2,1-15H3,(H,25,27,28)/t19-,20-,21-,23-/m1/s1
analyte mass701.09
chromatogram6080if_3
citationNA
authorsErban A, Strehmel N, 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 date12 April 2010
metabolite role 
retention time (sec)1,623.19
retention index (VAR5 method, n-alkanes C10–C36)2,838.67 (observed)
base peak (m/z)73
maximal intensity21,223
mass-intensity-peaks cardinality889 intensities
minimal m/z45
maximal m/z1,000
download JCAMP DXSpectrumJcampDx.ashx?id=1572a41f-bcbd-41e1-a72e-c60a22bc0966
download MSPSpectrumMsp.ashx?id=1572a41f-bcbd-41e1-a72e-c60a22bc0966

GC-Method

nameVAR5
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
deconvolutionChromaTOFOFFSET: "just above noise"; SMOOTHING: 20; PEAK WIDTH: 6; S/N: 2
derivatizationMEOX; TMSMETHOXYAMINATION: 90min at 30°C; TRIMETHYLSILYLATION: 30min at 37°C
detectorMS-TOFm/z = 70-600; scans:20/s; Pegasus III TOF mass spectrometer
extractionwater:chloroform (2:1; v/v) 15min at 70°C
gas chromatographAgilent GC 6890 
ion sourceEI70eV
mass spectrometry instrumentPegasus III TOF mass spectrometer 
metabolic inactivationshock-frozen in liquid nitrogen 
RIALKANEC10, C12, C15, C18, C19, C22, C28, C32, C36
separationGCCOLUMN:5%phenyl-95%dimethylpolysiloxane, 30+10m, ID:0.25mm, DF:0.25µm, 5PDM VF-5ms (Varian, Darmstadt, Germany); PROGRAM:iso1min 70°C, ramp 9°C/min, iso 5min 350°C; FLOW:Helium, 0.6mL/min; INJECTION:1µL, splitless, 230°C; TRANSFER:250°C; IONSOURCE:250°C
protocolpropertyvalue
extractionwater chloroform(2:1; v/v) 15min at 70°C
derivatizationderivatisationMETHOXYAMINATION, 90min at 30°C
derivatizationderivatisationTRIMETHYLSILYLATION, 30min at 37°C
separationIon source temperature250°C
separationColumn length30+10m (analytical column + guard column)
separationColumn inner diameter0.25mm
separationTemperature programisotherm 1min 70°C, ramp 9°C/min, isotherm 5min 350°C
ion sourceelectron ionization70eV
detectorLECO instrument modelPegasus III TOF mass spectrometer
detectorhighest observed m/zm/z = 600
detectorlowest observed m/zm/z = 70
detectorsampling frequency20 scans/s
detectormass analyzer typeMS-TOF
deconvolutionmoving average smoothing20
deconvolutionsoftwareChromaTOF
deconvolutionsignal-to-noise ratio2
RIRetention indexdecane
RIRetention indexdodecane
RIRetention indexpentadecane
RIRetention indexoctadecane
RIRetention indexnonadecane
RIRetention indexdocosane
RIRetention indexoctacosane
RIRetention indexdotriacontane
RIRetention indexhexatriacontane
ChromatographyChromatographyAgilent GC 6890

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