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Maltose (1MEOX) (8TMS) BP

 

Replica Mass Spectra of Maltose (1MEOX) (8TMS) BP

replicalib entry datedetectionmethodspecies
219 January 2005 MS-QUADM[ROE] 
412 June 2003 MS-QuadM[2]Reference Substance
501 November 2001 MS-TOFM[EIGTMS]Standard
622 February 2005 MS-TOFM[STR] 
722 February 2005 MS-TOFM[STR] 
2330 March 2011  Fiehn_GC_2010 
901 December 2003 MS-QuadM[2]Standard
2628 August 2012  MassBank GC 2010 Ara 
2428 August 2012  MassBank GC 2010 Kusano 
1026 November 2004  M[FAME4090]Standard
21 spectrum(a)
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Spectrum Details

analyteMaltose (1MEOX) (8TMS) BP
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-/t29-,30+,31+,32+,33+,34+,35-,36+,37+/m0/s1
analyte mass948.79
chromatogram1215BK05
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 July 2001
metabolite roleMETB
retention time (sec)2,387.76
retention index (VAR5 method, n-alkanes C10–C36)2,754.11 (predicted, according to Strehmel, N. et.al)
base peak (m/z)73
maximal intensity999
mass-intensity-peaks cardinality50 intensities
minimal m/z44
maximal m/z451
download JCAMP DXSpectrumJcampDx.ashx?id=85f4f0d8-317b-455a-90a1-536f0496f859
download MSPSpectrumMsp.ashx?id=85f4f0d8-317b-455a-90a1-536f0496f859

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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