Linolenic acid analytical standard

Properties

Related Categories	Alphabetical Index of Analytical Standards, Analytical Standards, Analytical/Chromatography, Applications, Biochemicals and Reagents, Chromatography, Fats (fatty acids, FAMEs, glycerides), Edible Oils, Sterols, Fatty Acids, Fatty Acids and conjugates, Fatty Acyls, Food & Beverage Analysis, Food & Beverage Standards, Free Fatty Acids, Functional Foods, Individual Analytes, L, Lipid Analytical Standards, Lipids, Lipids - FA/FAME/Oils/Sterols, Neats, Nutrition Research, Omega 3 and Omega 6 FAMEs, Omega 6 fatty acids and derivatives, Other Lipid Related Products, Polyunsaturated, Polyunsaturated Fatty Acids (PUFAs) and Omega-3 Fatty Acids, Unsaturated Fatty Acids and Derivatives More...
grade	analytical standard
assay	≥98.5% (GC)
shelf life	(limited shelf life, expiry date on the label)
refractive index	n20/D 1.480(lit.)
	n20/D 1.480
bp	230-232 °C/1 mmHg(lit.)
mp	-11 °C(lit.)
density	0.914 g/mL at 25 °C(lit.)
storage temp.	−20°C

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Description

Biochem/physiol Actions

An ω-3 fatty acid that serves as a precursor to eicosapentaenoic acid (EPA) but not docosahexaenoic acid. Conversion is greater in women than men, and conversely, β-oxidation metabolism is greater in men than women.¹

Price and Availability

Related Papers

1. Conversion of α-linolenic acid to longer-chain polyunsaturated fatty acids in human adults Burdge, G.C., and Calder, P.C. Reprod. Nutr. Dev. 45, 581-597, (2005)

Documents

Certificate of Analysis

FT-IR Condensed Phase

FT-IR Raman

FT-NMR

Pressure-Temperature Nomograph

Safety Information

Personal Protective Equipment	Eyeshields, Gloves
WGK Germany	1
Flash Point(F)	235.4 °F
Flash Point(C)	113 °C

Technical information & documentation associated with this product is available in the Safety & Documentation tab.

Articles

Omega-3 Fatty Acids and Heart Disease

The potential for the prevention and treatment of cardiovascular disease through increased dietary intake of omega-3 (w-3) fish oils is not a recent scientific discovery. A historically important stu...
BioFiles 2007, 2.2, 14.
Keywords: Anti-inflammatory agents, Biochemistry, Cardiovascular, Clinical, Degradations, Esterifications, Immunology, Inflammation, Lipid Metabolism, Metabolism, Metabolites, Nutrition, Oxidations, Transcription

Papers

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1. Conversion of α-linolenic acid to longer-chain polyunsaturated fatty acids in human adults Burdge, G.C., and Calder, P.C. Reprod. Nutr. Dev. 45, 581-597, (2005)

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Rapid modification of the insect elicitor N-linolenoyl-glutamate via a lipoxygenase-mediated mechanism on Nicotiana attenuata leaves. Arjen VanDoorn et al BMC Plant Biol. 10, 164, (2010)

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Interference by naturally occurring fatty acids in a noncellular enzyme-based aromatase bioassay. Marcy J Balunas et al J. Nat. Prod. 69, 700-3, (2006)

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Inhibition of hepatitis C virus replication by peroxidation of arachidonate and restoration by vitamin E. Hua Huang et al Proc. Natl. Acad. Sci. U. S. A. 104, 18666-70, (2007)

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Identification of G protein-coupled receptor 120-selective agonists derived from PPARgamma agonists. Takayoshi Suzuki et al J. Med. Chem. 51, 7640-4, (2008)

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Ganoderic acid DM: anti-androgenic osteoclastogenesis inhibitor. Jie Liu et al Bioorg. Med. Chem. Lett. 19, 2154-7, (2009)

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Activation of PPARgamma by metabolites from the flowers of purple coneflower (Echinacea purpurea). Kathrine B Christensen et al J. Nat. Prod. 72, 933-7, (2009)

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Evaluation of endogenous fatty acid amides and their synthetic analogues as potential anti-inflammatory leads. Hung The Dang et al Bioorg. Med. Chem. 19, 1520-7, (2011)

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Inhibitory effect of novel 5-O-acyl juglones on mammalian DNA polymerase activity, cancer cell growth and inflammatory response. Maruo S, Kuriyama I, et al Bioorg. Med. Chem. 19, 5803-5812, (2011)

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Merck 14,5506

Beil. 2,IV,1781

Aldrich MSDS 1, 1138:D / Corp MSDS 1 (1), 2129:B / FT-IR 1 (1), 502:B / FT-IR 2 (1), 786:C / FT-NMR 1 (1), 785:C / IR-Spectra (3), 294:H / IR-Spectra (2), 265:G / NMR-Reference 2 (1), 437:D / RegBook 1 (1), 551:I / Sigma FT-IR 1 (1), 1417:B / Structure Index 1, 78:D:4 / Vapor Phase 3, 589:A