LBF13101SC01: Difference between revisions

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{{Hierarchy|{{PAGENAME}}}}
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|Melting Point=38-39°C
|Melting Point=38-39°C
|Boiling Point=192°C at 20 mmHg
|Boiling Point=192°C at 20 mmHg
|Solubility=[[Reference:Ahmad_K:Bumpus_FM:Strong_FM:,J. Am. Chem. Soc.,1948,70,3391|{{RelationTable/GetFirstAuthor|Reference:Ahmad_K:Bumpus_FM:Strong_FM:,J. Am. Chem. Soc.,1948,70,3391}}]][[Reference:Chuit_P:Boelsing_F:Hausser_J:Malet_G:,Helv. Chim. Acta,1927,10,113|{{RelationTable/GetFirstAuthor|Reference:Chuit_P:Boelsing_F:Hausser_J:Malet_G:,Helv. Chim. Acta,1927,10,113}}]]
|Solubility=[[Reference:Ahmad_K:Bumpus_FM:Strong_FM:,J. Am. Chem. Soc.,1948,70,3391|{{RelationTable/GetFirstAuthor|Reference:Ahmad_K:Bumpus_FM:Strong_FM:,J. Am. Chem. Soc.,1948,70,3391}}]]<!--0017--><!--0069-->[[Reference:Chuit_P:Boelsing_F:Hausser_J:Malet_G:,Helv. Chim. Acta,1927,10,113|{{RelationTable/GetFirstAuthor|Reference:Chuit_P:Boelsing_F:Hausser_J:Malet_G:,Helv. Chim. Acta,1927,10,113}}]]
|Source=
|Chemical Synthesis=Synthetic by (i) reaction of 1-bromo-10-undecene ethyl malonate and Na and (ii) conversion of 10-undecenoic acid to 11-dodecenoic acid.
|Metabolism=
|Symbol=C13:1
}}
}}
{{Lipid/Footer}}

Latest revision as of 21:00, 14 April 2010

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Upper classes: LB LBF



12-Tridecenoic acid
LBF13101SC01.png
Structural Information
12-Tridecenoic acid
  • 12-Tridecenoic acid
C13:1
Formula C13H24O2
Exact Mass 212.17763001199998
Average Mass 212.32845999999998
SMILES C=CCCCCCCCCCCC(O)=O
Physicochemical Information
38-39°C
192°C at 20 mmHg
AhmadKet al. ChuitPet al.
Synthetic by (i) reaction of 1-bromo-10-undecene ethyl malonate and Na and (ii) conversion of 10-undecenoic acid to 11-dodecenoic acid.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF13101SC01 See above. Ahmad_K et al. 1948
n.a. LBF13101SC01 See above. Chuit_P et al. 1927