LBF14000BC10: Difference between revisions

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|Optical=<FONT FACE="Symbol">h</FONT>20/D=1.4491 [[Reference:Petrov_AD:Nikishin_GI:Ogibin_IN:Nevolin_FW:Tipisova_TG:,Fette Seifen Anstrichm.,1959,61,940|{{RelationTable/GetFirstAuthor|Reference:Petrov_AD:Nikishin_GI:Ogibin_IN:Nevolin_FW:Tipisova_TG:,Fette Seifen Anstrichm.,1959,61,940}}]]
|Optical=<FONT FACE="Symbol">h</FONT>20/D=1.4491 [[Reference:Petrov_AD:Nikishin_GI:Ogibin_IN:Nevolin_FW:Tipisova_TG:,Fette Seifen Anstrichm.,1959,61,940|{{RelationTable/GetFirstAuthor|Reference:Petrov_AD:Nikishin_GI:Ogibin_IN:Nevolin_FW:Tipisova_TG:,Fette Seifen Anstrichm.,1959,61,940}}]]
|Source=
|Source=
|Chemical Synthesis=Sodium diethylmalonate and 2-bromo-4-methyl tridecane were heated in ethylalcohol and the reaction product was treated with sodium hydroxide. The final product was obtained by vacuum distillation after acidification[[Reference:Petrov_AD:Nikishin_GI:Ogibin_IN:Nevolin_FW:Tipisova_TG:,Fette Seifen Anstrichm.,1959,61,940|{{RelationTable/GetFirstAuthor|Reference:Petrov_AD:Nikishin_GI:Ogibin_IN:Nevolin_FW:Tipisova_TG:,Fette Seifen Anstrichm.,1959,61,940}}]];>.
|Chemical Synthesis=Sodium diethylmalonate and 2-bromo-4-methyl tridecane were heated in ethylalcohol and the reaction product was treated with sodium hydroxide. The final product was obtained by vacuum distillation after acidification[[Reference:Petrov_AD:Nikishin_GI:Ogibin_IN:Nevolin_FW:Tipisova_TG:,Fette Seifen Anstrichm.,1959,61,940|{{RelationTable/GetFirstAuthor|Reference:Petrov_AD:Nikishin_GI:Ogibin_IN:Nevolin_FW:Tipisova_TG:,Fette Seifen Anstrichm.,1959,61,940}}]].
|Metabolism=
|Metabolism=
}}
}}


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{{Lipid/Footer}}

Revision as of 11:55, 25 November 2009

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Upper classes: LB LBF



3,5-Dimethyl Tetradecanoic Acid
LBF14000BC10.png
Structural Information
3,5-Dimethyl Tetradecanoic Acid
  • 3,5-Dimethyl Tetradecanoic Acid
Formula C16H32O2
Exact Mass 256.240230268
Average Mass 256.42408
SMILES CCCCCCCCCC(C)CC(C)CC(O)=O
Physicochemical Information
147-149°C/0.5mmHg Petrov_AD et al.
D20/4=0.8859 Petrov_AD et al.
h20/D=1.4491 Petrov_AD et al.
Sodium diethylmalonate and 2-bromo-4-methyl tridecane were heated in ethylalcohol and the reaction product was treated with sodium hydroxide. The final product was obtained by vacuum distillation after acidification Petrov_AD 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. LBF14000BC10 See above. Petrov_AD et al. 1959