Details
Stereochemistry | RACEMIC |
Molecular Formula | C18H36O3 |
Molecular Weight | 300.4766 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCC(O)CCCCCCCCC(O)=O
InChI
InChIKey=PAZZVPKITDJCPV-UHFFFAOYSA-N
InChI=1S/C18H36O3/c1-2-3-4-5-8-11-14-17(19)15-12-9-6-7-10-13-16-18(20)21/h17,19H,2-16H2,1H3,(H,20,21)
Approval Year
PubMed
Title | Date | PubMed |
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Fatty acid composition and preservation of the Tyrolean Iceman and other mummies. | 2002 Dec |
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Conversion of fatty acids by Bacillus sphaericus-like organisms. | 2002 Oct |
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Two distinct pathways for the formation of hydroxy FA from linoleic acid by lactic acid bacteria. | 2003 Dec |
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Fluorescein conjugates of 9- and 10-hydroxystearic acids: synthetic strategies, photophysical characterization, and confocal microscopy applications. | 2004 Dec 15 |
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Chemical constituents of cape aloe and their synergistic growth-inhibiting effect on Ehrlich ascites tumor cells. | 2007 May |
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New bioactive fatty acids. | 2008 |
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Adipocere formation via hydrogenation of linoleic acid in a victim kept under dry concealment. | 2008 Mar 5 |
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Production of oxygenated fatty acids from vegetable oils by Flavobacterium sp. strain DS5. | 2009 Oct 1 |
Patents
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143095
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DTXSID901314578
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9561835
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384M5B7IFL
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638-26-6
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2476630
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384M5B7IFL
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79060
Created by
admin on Sat Dec 16 09:41:09 GMT 2023 , Edited by admin on Sat Dec 16 09:41:09 GMT 2023
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SUBSTANCE RECORD