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Ursolic acid (2TMS)

 

Replica Mass Spectra of Ursolic acid (2TMS)

replicalib entry datedetectionmethodspecies
101 May 2003 MS-QuadM[2]Newbouldia laevis (P. Beauv.) Seem. ex Bureau
201 May 2003 MS-QuadM[2]Spathodea campanulata P. Beauv.
301 June 2003 MS-QuadM[2]Markhamia acuminata
415 March 2005 MS-TOFM[6]Reference Substance
515 March 2005 MS-TOFM[6]Reference Substance
701 January 2003 MS-QuadM[2]Standard
6 spectrum(a)
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Spectrum Details

analyteUrsolic acid (2TMS)
analyte InChIInChI=1S/C36H64O3Si2/c1-24-16-21-36(31(37)39-41(11,12)13)23-22-34(6)26(30(36)25(24)2)14-15-28-33(5)19-18-29(38-40(8,9)10)32(3,4)27(33)17-20-35(28,34)7/h14,24-25,27-30H,15-23H2,1-13H3/t24-,25+,27+,28-,29+,30+,33+,34-,35-,36+/m1/s1
analyte mass601.06
chromatogram3157BF26
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 June 2003
metabolite roleMETB
retention time (sec)2,967.78
retention index (VAR5 method, n-alkanes C10–C36)3,649.15 (predicted, according to Strehmel, N. et.al)
base peak (m/z)203
maximal intensity999
mass-intensity-peaks cardinality80 intensities
minimal m/z41
maximal m/z586
download JCAMP DXSpectrumJcampDx.ashx?id=33d0c81b-c12c-42eb-848d-f2d57868c38a
download MSPSpectrumMsp.ashx?id=33d0c81b-c12c-42eb-848d-f2d57868c38a

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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