LBF13000BC05: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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|LipidBank=DFA7127
|LipidBank=DFA7127
|LipidMaps=LMFA01020159
|LipidMaps=LMFA01020159
|SysName=9-Methyltridecanoic Acid
|SysName=9-Methyltridecanoic acid
|Common Name=&&9-Methyltridecanoic Acid&&
|Common Name=&&9-Methyltridecanoic acid&&
|Boiling Point=154°C/2mmHg [[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]]
|Boiling Point=154°C/2mmHg [[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]]
|Optical=<FONT FACE="Symbol">h</FONT> 25/D = 1.4462 [[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]]
|Refractive= eta  25/D = 1.4462 [[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]]
|Source=
|Chemical Synthesis=9-Hydroxy-9-methyltridecanitril was warmed with ethanolic KOH. The product was heated with a small amount of iodine at 200°C, followed by hydrogenation with Pt in ethanol[[Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343|{{RelationTable/GetFirstAuthor|Reference:Rapport_H:Baldridge_HD_Jr:,J. Am. Chem. Soc.,1951,73,343}}]].
|Metabolism=
}}
}}
{{Lipid/Footer}}

Latest revision as of 21:00, 14 April 2010

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Upper classes: LB LBF



9-Methyltridecanoic acid
LBF13000BC05.png
Structural Information
9-Methyltridecanoic acid
  • 9-Methyltridecanoic acid
Formula C14H28O2
Exact Mass 228.20893013999998
Average Mass 228.37091999999998
SMILES CCCCC(C)CCCCCCCC(O)=O
Physicochemical Information
154°C/2mmHg Rapport_H et al.
η 25/D = 1.4462 RapportHet al.
9-Hydroxy-9-methyltridecanitril was warmed with ethanolic KOH. The product was heated with a small amount of iodine at 200°C, followed by hydrogenation with Pt in ethanol Rapport_H 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. LBF13000BC05 See above. Rapport_H et al. 1951