LBF12000BC13: Difference between revisions

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|LipidBank=DFA7125
|LipidBank=DFA7125
|LipidMaps=LMFA01020157
|LipidMaps=LMFA01020157
|SysName= (S)-4-Methyl-Dodecanoic Acid
|SysName=4S-Methyldodecanoic acid
|Common Name=&&(S)-4-Methyl-Dodecanoic Acid&&(S)-4-Methyl-Dodecanoic Acid&&
|Common Name=&&(S)-4-Methyllauric acid&&
|Boiling Point=162-164°C/5.5mmHg [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]]
|Boiling Point=162-164°C/5.5mmHg [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]]
|Density=D25/ =0.888 [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]]
|Density=D25/ =0.888 [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]]
|Refractive=eta25/D=1.4424 [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]]
|Refractive= eta 25/D=1.4424 [[Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857|{{RelationTable/GetFirstAuthor|Reference:Cason_J:Allinger_NL:Allen_CF:,J. Org. Chem.,1953,18,857}}]]
|Source=
|Source=
|Chemical Synthesis=1-Bromo-3-methyl undecane was incubated with potassium cyanide in ethanol, followed by heating in aq. Potassium hydroxide.
|Chemical Synthesis=1-Bromo-3-methyl undecane was incubated with potassium cyanide in ethanol, followed by heating in aq. Potassium hydroxide.

Latest revision as of 06:31, 22 June 2010

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Upper classes: LB LBF



(S)-4-Methyllauric acid
LBF12000BC13.png
Structural Information
4S-Methyldodecanoic acid
  • (S)-4-Methyllauric acid
Formula C13H26O2
Exact Mass 214.19328007599998
Average Mass 214.34433999999996
SMILES CCCCCCCCC(C)CCC(O)=O
Physicochemical Information
162-164°C/5.5mmHg Cason_J et al.
D25/ =0.888 CasonJet al.
η 25/D=1.4424 CasonJet al.
1-Bromo-3-methyl undecane was incubated with potassium cyanide in ethanol, followed by heating in aq. Potassium hydroxide.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF12000BC13 See above. Cason_J et al. 1953