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Lactose (1MEOX) (8TMS) MP

 

Replica Mass Spectra of Lactose (1MEOX) (8TMS) MP

replicalib entry datedetectionmethodspecies
122 February 2005 MS-TOFM[STR] 
1628 August 2012  MassBank GC 2010 Tsujimoto 
312 May 2005  M[NIST] 
1828 August 2012  MassBank GC 2010 Ara 
401 November 2001 MS-TOFM[EIGTMS]Reference Substance
519 July 2007 MS-TOFMDN35Reference Substance
1728 August 2012  MassBank GC 2010 Tsujimoto 
622 January 2005 MS-QUADM[ROE] 
719 July 2007 MS-TOFVAR5Reference Substance
801 May 2001 MS-TOFM[EIGTMS]Nicotiana tabacum
18 spectrum(a)
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Spectrum Details

analyteLactose (1MEOX) (8TMS) MP
analyte InChIInChI=1S/C37H89NO11Si8/c1-39-38-26-29(44-52(8,9)10)33(46-54(14,15)16)32(31(45-53(11,12)13)28-41-51(5,6)7)43-37-36(49-57(23,24)25)35(48-56(20,21)22)34(47-55(17,18)19)30(42-37)27-40-50(2,3)4/h26,29-37H,27-28H2,1-25H3/b38-26+
analyte mass948.79
chromatogram3035BB03
citationSchauer N, Steinhauser D, Strelkov S, Schomburg D, Allison G, Moritz T, Lundgren K, Roessner-Tunali U, Forbes MG, Willmitzer L, Fernie AR, Kopka J (2005) FEBS Letters 579, 1332-1337
authorsKopka 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 date01 January 2003
metabolite roleMETB
retention time (sec)2,377.5
retention index (VAR5 method, n-alkanes C10–C36)2,681.58 (predicted, according to Strehmel, N. et.al)
base peak (m/z)204
maximal intensity999
mass-intensity-peaks cardinality224 intensities
minimal m/z41
maximal m/z568
download JCAMP DXSpectrumJcampDx.ashx?id=5a2da9d4-3455-4d7c-b07c-1e95ad183f61
download MSPSpectrumMsp.ashx?id=5a2da9d4-3455-4d7c-b07c-1e95ad183f61

GC-Method

nameM[2]
citationRoessner U, Wagner C, Kopka J, Trethewey RN, Willmitzer L (2000) Plant J 23, 131-142
attributetextdetails
deconvolutionAMDIS, National Institute of Standards and Technology, Gaithersburg, MD, USADIRECTION:Low to High; WIDTH: 20; SUBTRACTION: two; RESOLUTION: low; SENSITIVITY: low; SHAPE: low
derivatizationMEOX; TMSMethoxyamination:60min37°C; Trimethylsilylation:>45min37°C
detectorMS-Quadm/z = 35-600; scans:2/s; MD 800 Thermo-Finnigan, San Jose, CA, USA
extractionmethanol:water (4:1; v/v); 15min70°C 
ion sourceEI70eV
metabolic inactivationcut; liquid nitrogen; -80°C 
partitioningmethanol fraction of a methanol:water:chloroform (approx. 2:2:1, v/v/v) partitioning 
RIALKANEC12, C15, C19, C22, C28, C32, C36
separationGCCOLUMN:5%diphenyl-95%dimethylpolysiloxane (arylene), 30+10m, ID:0.25mm, DF:0.25microm, Rtx-5SilMS Integra-Guard, #NA (Restek, Bad Homburg, Germany); PROGRAM:iso1min70°C, ramp9°C/min, iso5min350°C; FLOW:Helium, 0.6ml/min; INJECTION:1microL, splitless, 230°C; TRANSFER:250°C; IONSOURCE:250°C

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