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Cinnamaldehyde, 3,5-dimethoxy-4-hydroxy-, trans- (1MEOX) (1TMS) MP

 

Replica Mass Spectra of Cinnamaldehyde, 3,5-dimethoxy-4-hydroxy-, trans- (1MEOX) (1TMS) MP

replicalib entry datedetectionmethodspecies
830 March 2011  Fiehn_GC_2010 
928 August 2012  MassBank GC 2010 Tsujimoto 
327 October 2003 MS-QuadM[2]Standard
425 January 2005 MS-TOFM[MOR] 
519 July 2007 MS-TOFVAR5Reference Substance
601 March 2002 MS-QuadM[2]Reference Substance
719 July 2007 MS-TOFMDN35Reference Substance
7 spectrum(a)
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Spectrum Details

analyteCinnamaldehyde, 3,5-dimethoxy-4-hydroxy-, trans- (1MEOX) (1TMS) MP
analyte InChIInChI=1S/C15H23NO4Si/c1-17-13-10-12(8-7-9-16-19-3)11-14(18-2)15(13)20-21(4,5)6/h7-11H,1-6H3/b8-7+,16-9+
analyte mass309.43
chromatogram4157GX22
citation 
authorsLiebig F, Erban A, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany
lib entry date15 March 2005
metabolite roleMETB
retention time (sec)1,328.59
retention index (VAR5 method, n-alkanes C10–C36)2,110.4 (predicted, according to Strehmel, N. et.al)
base peak (m/z)174
maximal intensity999
mass-intensity-peaks cardinality216 intensities
minimal m/z70
maximal m/z329
download JCAMP DXSpectrumJcampDx.ashx?id=45d50f90-964a-426a-b96f-51d2dfafaf7e
download MSPSpectrumMsp.ashx?id=45d50f90-964a-426a-b96f-51d2dfafaf7e

GC-Method

nameM[6]
citationErban A, Schauer N, Fernie AR, Kopka J (2006) In: Weckwerth W (ed): Methods in Molecular Biology Vol., Humana Press Inc., Totowa, USA
attributetextdetails
deconvolutionChromaTOF V1.00 (Pegasus Driver 1.61), LECO, St. Joseph, MI, USAOFFSET:1_SMOOTHING:3_WIDTH:6_SN:>2
derivatizationMEOX; TMSMethoxyamination:90min40°C; Trimethylsilylation:45min40°C
detectorMS-TOFMZ:70-600; SCANS:20/s; Pegasus III TOF-MS; LECO, St. Joseph, MI, 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, C18, C19, C22, C28, C32, C36
separationGCCOLUMN:5%diphenyl-95%dimethylpolysiloxane (arylene), 30+10m, ID:0.25mm, DF:0.25microm, Rtx-5SilMS Integra-Guard, #525560 (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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