L2626
Methyl linolenate
≥99% (GC)
Synonym(s):
Linolenic acid methyl ester, Methyl cis,cis,cis-9,12,15-octadecatrienoate
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CN¥4,919.26
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100 μL
CN¥4,919.26
About This Item
Linear Formula:
CH3(CH2CH=CH)3(CH2)7COOCH3
CAS Number:
Molecular Weight:
292.46
Beilstein:
1728194
EC Number:
MDL number:
UNSPSC Code:
12352211
PubChem Substance ID:
NACRES:
NA.25
Recommended Products
biological source
plant
Quality Level
Assay
≥99% (GC)
form
liquid
refractive index
n20/D 1.470 (lit.)
bp
182 °C/3 mmHg (lit.)
density
0.895 g/mL at 25 °C (lit.)
functional group
ester
lipid type
unsaturated FAs
shipped in
ambient
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1 of 4
This Item | 442475 | 51968 | B1760 |
|---|---|---|---|
| assay 98% | assay - | assay - | assay ≥96% (HPLC) |
| Quality Level 100 | Quality Level 200 | Quality Level 300 | Quality Level 200 |
| form crystals | form - | form - | form solid |
| mp 177-180 °C (lit.) | mp 177-180 °C (lit.) | mp 177-180 °C (lit.) | mp 177-180 °C (lit.) |
![苯并[e]芘 98%](/deepweb/assets/sigmaaldrich/product/structures/162/859/cd1f8e1f-2539-4f36-be04-8bad9d301215/640/cd1f8e1f-2539-4f36-be04-8bad9d301215.png)
![苯并[a]芘 certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland](/deepweb/assets/sigmaaldrich/product/structures/253/820/be96d879-1811-46c0-8f11-612019691c2d/640/be96d879-1811-46c0-8f11-612019691c2d.png)
Application
- Exogenous Jasmonic Acid Alleviates Blast Resistance Reduction Caused by LOX3 Knockout in Rice.: The research explores the role of jasmonic acid, associated with methyl linolenate, in enhancing blast resistance in rice. The findings show that external application of jasmonic acid can compensate for the resistance loss due to LOX3 knockout, providing insights into plant disease management strategies (Su et al., 2023).
- Effects of (13)C isotope-labeled allelochemicals on the growth of the invasive plant Alternanthera philoxeroides.: This study uses (13)C-labeled methyl linolenate to trace allelochemical effects on invasive plant species. The results indicate a significant impact on plant growth, suggesting potential applications in controlling invasive species (Hua et al., 2023).
Biochem/physiol Actions
Methyl linolenate, a polyunsaturated fattly acid (PUFA), is used in studies on the mechanisms and prevention of oxidation/peroxidation of unsaturated fatty acids. Methyl linolenate is being studied as a possible skin whitening agent with anti-melanogenesis activity.
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113.0 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Kevin Huvaere et al.
The journal of physical chemistry. B, 114(16), 5583-5593 (2010-04-10)
Triplet-excited riboflavin ((3)RF*) was found by laser flash photolysis to be quenched by polyunsaturated fatty acid methyl esters in tert-butanol/water (7:3, v/v) in a second-order reaction with k approximately 3.0 x 10(5) L mol(-1) s(-1) at 25 degrees C for
Rosario Zamora et al.
Journal of agricultural and food chemistry, 51(16), 4661-4667 (2004-01-07)
The oxidation of methyl linoleate (LMe) and methyl linolenate (LnMe) in the presence of bovine serum albumin (BSA) in the dark at 60 degrees C was studied to analyze the role of the type of fatty acid and the protein/lipid
William Y Boadi et al.
Journal of applied toxicology : JAT, 23(5), 363-369 (2003-09-17)
The single and combined effects of two abundant flavonoids, namely quercetin and genistein, were investigated according to their ability to inhibit the oxidation of methyl linolenate via Fenton's pathway. Antioxidative activity was determined by oxidizing methyl linolenate suspended in a
Saori Okuda et al.
Journal of agricultural and food chemistry, 53(24), 9624-9628 (2005-11-24)
The purpose of this research was to examine the influence of the physical state of lipids on iron-promoted oxidation of methyl linolenate in octadecane oil-in-water emulsions. Octadecane and methyl linolenate oil-in-water emulsions were prepared that contained droplets having the octadecane
Philippe Lesot et al.
Analytical chemistry, 80(8), 2963-2972 (2008-03-11)
The quantitative determination of isotopic (2H/1H)i ratios at natural abundance using the SNIF-NMR protocol is a well-known method for understanding the enzymatic biosynthesis of metabolites. However, this approach is not always successful for analyzing large solutes and, specifically, is inadequate
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