LBF12000BC14: Difference between revisions

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|LipidBank=DFA7126
|LipidBank=DFA7126
|LipidMaps=LMFA01020158
|LipidMaps=LMFA01020158
|SysName=2-Ethyl-Dodecanoic Acid
|SysName=2-Ethyldodecanoic acid
|Common Name=&&2-Ethyl-Dodecanoic Acid&&
|Common Name=&&2-Ethyllauric acid&&
|Boiling Point=175-180°C/11mmHg [[Reference:Maekawa_E:,Bull. Nagoya Inst. Technol.,1954,6,271|{{RelationTable/GetFirstAuthor|Reference:Maekawa_E:,Bull. Nagoya Inst. Technol.,1954,6,271}}]]
|Boiling Point=175-180°C/11mmHg [[Reference:Maekawa_E:,Bull. Nagoya Inst. Technol.,1954,6,271|{{RelationTable/GetFirstAuthor|Reference:Maekawa_E:,Bull. Nagoya Inst. Technol.,1954,6,271}}]]
|Density=D70/4=0.8535 [[Reference:Metzger_A:Gawalek_G:,J. Prakt. Chem.,1955,2,168|{{RelationTable/GetFirstAuthor|Reference:Metzger_A:Gawalek_G:,J. Prakt. Chem.,1955,2,168}}]]
|Density=D70/4=0.8535 [[Reference:Metzger_A:Gawalek_G:,J. Prakt. Chem.,1955,2,168|{{RelationTable/GetFirstAuthor|Reference:Metzger_A:Gawalek_G:,J. Prakt. Chem.,1955,2,168}}]]
|Optical=<FONT FACE="Symbol">h</FONT>25/D=1.4450(134),<FONT FACE="Symbol">h</FONT>70/D=1.4258 [[Reference:Metzger_A:Gawalek_G:,J. Prakt. Chem.,1955,2,168|{{RelationTable/GetFirstAuthor|Reference:Metzger_A:Gawalek_G:,J. Prakt. Chem.,1955,2,168}}]]
|Refractive= eta 25/D=1.4450(134), eta 70/D=1.4258 [[Reference:Metzger_A:Gawalek_G:,J. Prakt. Chem.,1955,2,168|{{RelationTable/GetFirstAuthor|Reference:Metzger_A:Gawalek_G:,J. Prakt. Chem.,1955,2,168}}]]
|Source=
|Chemical Synthesis=Silver salt of ethyl ethyldecylmalonate was incubated with bromine in carbon tetrachloride.
|Metabolism=
}}
}}


{{Lipid/Footer}}
{{Lipid/Footer}}

Latest revision as of 06:00, 15 April 2010

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Upper classes: LB LBF



2-Ethyllauric acid
Structural Information
2-Ethyldodecanoic acid
  • 2-Ethyllauric acid
Formula C14H28O2
Exact Mass 228.20893013999998
Average Mass 228.37091999999998
SMILES CCCCCCCCCCC(CC)C(O)=O
Physicochemical Information
175-180°C/11mmHg Maekawa_E
D70/4=0.8535 MetzgerAet al.
η 25/D=1.4450(134), η 70/D=1.4258 MetzgerAet al.
Silver salt of ethyl ethyldecylmalonate was incubated with bromine in carbon tetrachloride.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
[hide]Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF12000BC14 See above. Maekawa_E 1954
n.a. LBF12000BC14 See above. Metzger_A et al. 1955