LBF10000BC03: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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|LipidBank=DFA7140
|LipidBank=DFA7140
|LipidMaps=LMFA01020172
|LipidMaps=LMFA01020172
|SysName=4-Hexyl Decanoic Acid
|SysName=4-Hexyldecanoic acid
|Common Name=&&4-Hexyl Decanoic Acid&&
|Common Name=&&4-Hexyldecanoic acid&&
|Boiling Point=147-148°C/0.8mmHg [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]
|Boiling Point=147-148°C/0.8mmHg [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]
|Optical=<FONT FACE="Symbol">h</FONT>27/D=1.4450 [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]
|Refractive= eta 27/D=1.4450 [[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]]
|Source=
|Chemical Synthesis=Diethyl (2-hexyloctyl)malonate was heated with ethanolic KOH, and the product was heated after acidification[[Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Yamakawa_T:,J. Pharm. Soc. Jpn.,1950,70,474}}]].
|Metabolism=
}}
}}
{{Lipid/Footer}}

Latest revision as of 09:42, 25 May 2010

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Upper classes: LB LBF



4-Hexyldecanoic acid
LBF10000BC03.png
Structural Information
4-Hexyldecanoic acid
  • 4-Hexyldecanoic acid
Formula C16H32O2
Exact Mass 256.240230268
Average Mass 256.42408
SMILES CCCCCCC(CCCCCC)CCC(O)=O
Physicochemical Information
147-148°C/0.8mmHg Asano_M et al.
η 27/D=1.4450 AsanoMet al.
Diethyl (2-hexyloctyl)malonate was heated with ethanolic KOH, and the product was heated after acidification Asano_M 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. LBF10000BC03 See above. Asano_M et al. 1950