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Estrone, 16alpha-hydroxy- (1MEOX) (2TMS) MP

 

Replica Mass Spectra of Estrone, 16alpha-hydroxy- (1MEOX) (2TMS) MP

replicalib entry datedetectionmethodspecies
119 July 2007 MS-TOFVAR5Reference Substance
1 spectrum(a)
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Spectrum Details

analyteEstrone, 16alpha-hydroxy- (1MEOX) (2TMS) MP
analyte InChIInChI=1S/C25H41NO3Si2/c1-25-14-13-20-19-12-10-18(28-30(3,4)5)15-17(19)9-11-21(20)22(25)16-23(24(25)26-27-2)29-31(6,7)8/h10,12,15,20-23H,9,11,13-14,16H2,1-8H3/b26-24+/t20-,21-,22+,23-,25+/m1/s1
analyte mass459.77
chromatogram6023hf_70
citation 
authorsBoelling C, Liebig F, Erban A, 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 date19 July 2007
metabolite role 
retention time (sec)995.99
retention index (VAR5 method, n-alkanes C10–C36) 
base peak (m/z)73
maximal intensity628,920
mass-intensity-peaks cardinality505 intensities
minimal m/z45
maximal m/z1,000
download JCAMP DXSpectrumJcampDx.ashx?id=03d42e65-b324-409a-960f-8edd0efc001a
download MSPSpectrumMsp.ashx?id=03d42e65-b324-409a-960f-8edd0efc001a

GC-Method

nameMDN35
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
deconvolutionChromaTOFBASELINE OFFSET: 1; SMOOTHING: 5; PEAK WIDTH: 3s; S/N: 10
derivatizationMEOX; MSTFAMETHOXYAMINATION: 120min at 37°C; TRIMETHYLSILYLATION: 30min at 37°C
detectorMS-TOFm/z = 70-600; scans:20/s;
extractionchloroform:dH2O (2:1; v/v); chloroform (20°C); dH2O (4°C)
ion sourceEI70eV
RIFAME, d6-CholesteroleFAME: C8, C9, C10, C12, C14, C16, C18, C20, C22, C24, C26, C28, C30
separationGCCOLUMN:35%phenyl-65%dimethylpolysiloxane, 30m, ID:0.32mm, DF:0.25µm, MDN-35 (Macherey-Nagel, Düren, Germany); PROGRAM:iso 2min 80°C, ramp 15°C/min, iso 6min 330°C; FLOW:Helium, 2mL/min; INJECTION:1µL, splitless, 230°C; TRANSFER:250°C; IONSOURCE:250°C

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