LBF12000BC15: Difference between revisions

No edit summary
No edit summary
 
(14 intermediate revisions by 2 users not shown)
Line 1: Line 1:
{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
{{Hierarchy|{{PAGENAME}}}}


Line 4: Line 6:
|LipidBank=DFA7128
|LipidBank=DFA7128
|LipidMaps=LMFA01020160
|LipidMaps=LMFA01020160
|SysName=6-Ethyldodecanoic Acid
|SysName=6-Ethyldodecanoic acid
|Common Name=&&6-Ethyldodecanoic Acid&&
|Common Name=&&6-Ethyllauric acid&&
|Boiling Point=131-132°C/1mmHg [[Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202}}]]
|Boiling Point=131-132°C/1mmHg [[Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202}}]]
|Source=
|Chemical Synthesis=Barium 6-oxododecanate was treated with ethyl magnesium iodide in ether, then the hydrolysate was heated with iodine at 180°C, followed by hydrogenation with Pt in methyl alcohol[[Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202|{{RelationTable/GetFirstAuthor|Reference:Asano_M:Takahashi_K:Murakami_T:Tsutsumi_Y:Miura_Y:Toyoizumi_Y:,Yakugaku Zasshi,1950,70,202}}]].
|Metabolism=
}}
}}
{{Lipid/Footer}}

Latest revision as of 21:00, 14 April 2010

LipidBank Top
(トップ)
Fatty acid
(脂肪酸)
Glycerolipid
(グリセロ脂質)
Sphingolipid
(スフィンゴ脂質)
Journals
(雑誌一覧)
How to edit
(ページの書き方)


Upper classes: LB LBF



6-Ethyllauric acid
LBF12000BC15.png
Structural Information
6-Ethyldodecanoic acid
  • 6-Ethyllauric acid
Formula C14H28O2
Exact Mass 228.20893013999998
Average Mass 228.37091999999998
SMILES CCCCCCC(CC)CCCCC(O)=O
Physicochemical Information
131-132°C/1mmHg Asano_M et al.
Barium 6-oxododecanate was treated with ethyl magnesium iodide in ether, then the hydrolysate was heated with iodine at 180°C, followed by hydrogenation with Pt in methyl alcohol 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. LBF12000BC15 See above. Asano_M et al. 1950