LBF10000BC02: Difference between revisions

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|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}}]]
|Source=
|Source=
|Chemical Synthesis=It was synthesized from 2-hexyl-2-decenoic acid by hydrogenation with Pt in ethanol[[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}}]];>.
|Chemical Synthesis=It was synthesized from 2-hexyl-2-decenoic acid by hydrogenation with Pt in ethanol[[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}}]].
|Metabolism=
|Metabolism=
}}
}}


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{{Lipid/Footer}}

Revision as of 11:55, 25 November 2009

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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.
It was synthesized from 2-hexyl-2-decenoic acid by hydrogenation with Pt in ethanol Lederer_E et 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