LBF10000BC02: Difference between revisions

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|LipidMaps=LMFA01020166
|LipidMaps=LMFA01020166
|SysName=2-Hexyldecanoic Acid
|SysName=2-Hexyldecanoic Acid
|Boiling Point=140-150°C/0.02mmHg[[Reference:Lederer_E:Portelance_V:Serck-Hanssen_K:,Bull. Soc. Chim. Fr.,1952,,413|{{RelationTable/GetFirstAuthor|Reference:Lederer_E:Portelance_V:Serck-Hanssen_K:,Bull. Soc. Chim. Fr.,1952,,413}}]]
|Common Name=&&2-Hexyldecanoic Acid&&
|Boiling Point=140-150°C/0.02mmHg [[Reference:Lederer_E:Portelance_V:Serck-Hanssen_K:,Bull. Soc. Chim. Fr.,1952,,413|{{RelationTable/GetFirstAuthor|Reference:Lederer_E:Portelance_V:Serck-Hanssen_K:,Bull. Soc. Chim. Fr.,1952,,413}}]]
|Density=D70/4 = 0.8463 [[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 = 0.8463 [[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> 24/D = 1.4432[[Reference:Lederer_E:Portelance_V:Serck-Hanssen_K:,Bull. Soc. Chim. Fr.,1952,,413|{{RelationTable/GetFirstAuthor|Reference:Lederer_E:Portelance_V:Serck-Hanssen_K:,Bull. Soc. Chim. Fr.,1952,,413}}]]
|Optical=<FONT FACE="Symbol">h</FONT> 24/D = 1.4432 [[Reference:Lederer_E:Portelance_V:Serck-Hanssen_K:,Bull. Soc. Chim. Fr.,1952,,413|{{RelationTable/GetFirstAuthor|Reference:Lederer_E:Portelance_V:Serck-Hanssen_K:,Bull. Soc. Chim. Fr.,1952,,413}}]]
}}
}}

Revision as of 07:10, 18 December 2008


Upper classes: LB LBF



2-Hexyldecanoic Acid
LBF10000BC02.png
Structural Information
2-Hexyldecanoic Acid
  • 2-Hexyldecanoic Acid
Formula C16H32O2
Exact Mass 256.240230268
Average Mass 256.42408
SMILES CCCCCCCCC(CCCCCC)C(O)=O
Physicochemical Information
140-150°C/0.02mmHg Lederer_E et al.
D70/4 = 0.8463 MetzgerAet al.
h 24/D = 1.4432 LedererEet al.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF10000BC02 See above. Lederer_E et al. 1952
n.a. LBF10000BC02 See above. Metzger_A et al. 1955