about
Gas chromatography with tandem differential mobility spectrometry of fatty acid alkyl esters and the selective detection of methyl linolenate in biodiesels by dual-stage ion filtering.Classification of biodiesel and fuel blends using gas chromatography - differential mobility spectrometry with cluster analysis and isolation of C18:3 me by dual ion filtering.Autoxidation and yellowing of methyl linolenate.Evaluation of phytochemicals from medicinal plants of Myrtaceae family on virulence factor production by Pseudomonas aeruginosa.Discrimination among geometrical isomers of alpha-linolenic acid methyl ester using low energy electron ionization mass spectrometry.Determination of the composition of fatty acid mixtures using GC x FI-MS: a comprehensive two-dimensional separation approach.Metabolism and lipogenic effects of the cyclic monomers of methyl linolenate in the rat.Effect of quercetin and genistein on copper- and iron-induced lipid peroxidation in methyl linolenate.Comparative methyl linoleate and methyl linolenate oxidation in the presence of bovine serum albumin at several lipid/protein ratios.Two new fatty acids esters were detected in ginseng stems by the application of azoxystrobin and the increasing of antioxidant enzyme activity and ginsenosides content.Impact of lipid physical state on the oxidation of methyl linolenate in oil-in-water emulsions.Mutagenicity tests of lipid oxidation products in Salmonella typhimurium: monohydroperoxides and secondary oxidation products of methyl linoleate and methyl linolenate.Benchmark Calculations for Bond Dissociation Enthalpies of Unsaturated Methyl Esters and the Bond Dissociation Enthalpies of Methyl LinolenateChemical composition of volatile and fixed oils from ofSalvia argenteaL. (Lamiaceae) growing wild in SicilyThe identification of the allylic nitrite and nitro derivatives of methyl linoleate and methyl linolenate by negative chemical ionization mass spectroscopy.Thermal decomposition of methyl linoleate and methyl linolenate hydroperoxides analyzed by capillary gas chromatographyAnalysis of autoxidized fats by gas chromatography-mass spectrometry: X. Volatile thermal decomposition products of methyl linolenate dimers
P921
Q33466254-9E4A0673-55A7-4FC4-B584-5F71900F0D7CQ33468021-4B71FEEE-23CE-4D8B-B512-214B61C11336Q35584475-1430128C-E840-4F73-86AB-AC0B1E5E43C1Q40293873-0687190C-AD98-4D0E-816E-E8D7DD8E242DQ43599256-E592DE90-2494-4555-9413-641212C2C14AQ43866687-3893FD3C-0C9E-4915-9679-D01A802BC7A1Q44344276-06F17D74-332F-413D-A33A-F43ED9DFB546Q44585679-5A2AFAB4-7F2D-47F2-AFE0-173B0011CAD4Q44713773-6C344108-B6A4-484D-8B5B-77388029E651Q46450825-7B55B353-17A5-4018-90D1-C8C8BD0A61B3Q46815897-197640D0-E5F9-42B3-90BC-7E0FEBC12684Q50204745-0DFC58AA-46B8-4181-915F-2FE22118481EQ57401883-086D6041-BAAF-4744-9728-29C53885E11EQ58612604-7009816A-3296-466C-8344-14FC14A91923Q64889437-3BAF6F15-D780-4600-ADF3-95DBA96BD451Q68076443-6ADB0C7D-DF63-41CD-A77E-5A2A3C80195AQ88117628-3AFE6B9F-9531-44B7-9AB5-93F5E8D2F9EC
P921
description
chemesch Verbindung
@lb
chemical compound
@en
chemical compound
@en-ca
chemical compound
@en-gb
chemická sloučenina
@cs
chemická zlúčenina
@sk
chemiese verbinding
@af
chemische Verbindung
@de
chemische Verbindung
@de-ch
chemische verbinding
@nl
name
methyl linolenate
@en
type
label
methyl linolenate
@en
prefLabel
methyl linolenate
@en
P6689
P592
P661
P662
P683
P2017
CC/C=C\C/C=C\C/C=C\CCCCCCCC(=O)OC
P2067
P231
P232
P233
CCC=CCC=CCC=CCCCCCCCC(=O)OC
P234
1S/C19H32O2/c1-3-4-5-6-7-8-9-1 ...... 2-18H2,1-2H3/b5-4-,8-7-,11-10-
P235
DVWSXZIHSUZZKJ-YSTUJMKBSA-N
P2566
100.005.549
P274
P3073
P3117
DTXSID5041560
P4964
splash10-055f-9100000000-b4672589fefe1c9de76b
splash10-0a7m-9300000000-75b4a3d615bd452aa011
P592
CHEMBL1172198
P652
0S1NS923K6