LBF18113SC01: Difference between revisions

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{{Lipid/Header}}
{{Hierarchy|{{PAGENAME}}}}
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|LipidMaps=LMFA01030065
|LipidMaps=LMFA01030065
|SysName=trans-5-Octadecenoic acid
|SysName=trans-5-Octadecenoic acid
|Common Name=&&5-Octadecylenic acid&&
|Common Name=&&5Z-Octadecenoic acid&&
|Melting Point=43-44°C/47.5°C
|Melting Point=43-44°C/47.5°C
|Solubility=[[Reference:Bagby_MO:Smith_CR_Jr:Mikolajczak_KL:Wolff_IA:,Biochemistry,1962,1,632|{{RelationTable/GetFirstAuthor|Reference:Bagby_MO:Smith_CR_Jr:Mikolajczak_KL:Wolff_IA:,Biochemistry,1962,1,632}}]]
|Solubility=[[Reference:Bagby_MO:Smith_CR_Jr:Mikolajczak_KL:Wolff_IA:,Biochemistry,1962,1,632|{{RelationTable/GetFirstAuthor|Reference:Bagby_MO:Smith_CR_Jr:Mikolajczak_KL:Wolff_IA:,Biochemistry,1962,1,632}}]]<!--0398-->
|Source=
|Chemical Synthesis=Synthetic, by the addition of HI to 5-stearolic acid followed by reduction of the addition product with Zn plus acetic acid.
|Metabolism=
|Symbol=C18:1
}}
}}
{{Lipid/Footer}}

Latest revision as of 08:36, 29 September 2010

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Upper classes: LB LBF



5Z-Octadecenoic acid
LBF18113SC01.png
Structural Information
trans-5-Octadecenoic acid
  • 5Z-Octadecenoic acid
C18:1
Formula C18H34O2
Exact Mass 282.255880332
Average Mass 282.46136
SMILES CCCCCCCCCCCCC=CCCCC(O)=O
Physicochemical Information
43-44°C/47.5°C
Bagby_MO et al.
Synthetic, by the addition of HI to 5-stearolic acid followed by reduction of the addition product with Zn plus acetic acid.
Spectral Information
Mass Spectra
UV Spectra
IR Spectra
NMR Spectra
Other Spectra
Chromatograms
Reported Metabolites, References
Biospecies ID Compound Name Reference Comment
n.a. LBF18113SC01 See above. Bagby_MO et al. 1962