Omega-6 fatty acid

Omega-6 fatty acids (also referred to as ω-6 fatty acids or n-6 fatty acids) are a family of polyunsaturated fatty acids that have in common a final carbon-carbon double bond in the n-6 position, that is, the sixth bond, counting from the methyl end.[1]

The evening primrose flower (O. biennis) produces an oil containing a high content of γ-linolenic acid, a type of omega-6 fatty acid.

Health effects

The American Heart Association "supports an omega-6 PUFA intake of at least 5% to 10% of energy in the context of other AHA lifestyle and dietary recommendations. To reduce omega-6 PUFA intakes from their current levels would be more likely to increase than to decrease risk for coronary heart disease."[2]

A 2018 review found that an increased intake of omega‐6 fatty acids has been shown to reduce total serum cholesterol and may reduce myocardial infarction (heart attack), but found no significant change in LDL cholesterol and triglycerides.[3] A 2021 review found that omega-6 supplements do not affect the risk of CVD morbidity and mortality.[4]

A 2023 review found that omega-6 polyunsaturated fatty acids are associated with lower risk of high blood pressure.[5] Omega‐6 fatty acids are not associated with atrial fibrillation.[6]

Dietary sources

Dietary sources of omega-6 fatty acids include:[7]

Vegetable oils

Vegetable oils are a major source of omega-6 linoleic acid. Worldwide, more than 100 million metric tons of vegetable oils are extracted annually from palm fruits, soybean seeds, grape seeds, and sunflower seeds, providing more than 32 million metric tons of omega-6 linoleic acid and 4 million metric tons of omega-3 alpha-linolenic acid.[8][9]

Properties of vegetable oils[10][11]
The nutritional values are expressed as percent (%) by mass of total fat.
TypeProcessing
treatment[12]
Saturated
fatty acids
Monounsaturated
fatty acids
Polyunsaturated
fatty acids
Smoke point
Total[10]Oleic
acid
(ω-9)
Total[10]α-Linolenic
acid
(ω-3)
Linoleic
acid
(ω-6)
ω-6:3
ratio
Avocado[13]11.670.652–66
[14]
13.5112.512.5:1250 °C (482 °F)[15]
Brazil nut[16]24.832.731.342.00.141.9419:1208 °C (406 °F)[17]
Canola[18]7.463.361.828.19.118.62:1204 °C (400 °F)[19]
Coconut[20]82.56.361.70.0191.6888:1175 °C (347 °F)[17]
Corn[21]12.927.627.354.715858:1232 °C (450 °F)[19]
Cottonseed[22]25.917.81951.915454:1216 °C (420 °F)[19]
Cottonseed[23]hydrogenated93.61.50.60.20.31.5:1
Flaxseed/linseed[24]9.018.41867.853130.2:1107 °C (225 °F)
Grape seed 10.414.814.3  74.90.1574.7very high216 °C (421 °F)[25]
Hemp seed[26]7.09.09.082.022.054.02.5:1166 °C (330 °F)[27]
High-oleic safflower oil[28]7.575.275.212.8012.8very high212 °C (414 °F)[17]
Olive, Extra Virgin[29]13.873.071.310.50.79.814:1193 °C (380 °F)[17]
Palm[30]49.337.0409.30.29.145.5:1235 °C (455 °F)
Palm[31]hydrogenated88.25.70
Peanut[32]16.257.155.419.90.31819.661.6:1232 °C (450 °F)[19]
Rice bran oil2538.438.436.62.234.4[33]15.6:1232 °C (450 °F)[34]
Sesame[35]14.239.739.341.70.341.3138:1
Soybean[36]15.622.822.657.77517.3:1238 °C (460 °F)[19]
Soybean[37]partially hydrogenated14.943.042.537.62.634.913.4:1
Sunflower[38]8.9963.462.920.70.1620.5128:1227 °C (440 °F)[19]
Walnut oil[39]unrefined9.122.822.263.310.452.95:1160 °C (320 °F)[40]
Comparison of dietary fat composition from a 1995 study

List of omega-6 fatty acids

The chemical structure of linoleic acid, a common omega-6 fatty acid found in many nuts, seeds, and vegetable oils.
Common nameLipid nameChemical name
Linoleic acid (LA)18:2 (n−6)all-cis-9,12-octadecadienoic acid
Gamma-linolenic acid (GLA)18:3 (n−6)all-cis-6,9,12-octadecatrienoic acid
Calendic acid18:3 (n−6)8E,10E,12Z-octadecatrienoic acid
Eicosadienoic acid20:2 (n−6)all-cis-11,14-eicosadienoic acid
Dihomo-gamma-linolenic acid (DGLA)20:3 (n−6)all-cis-8,11,14-eicosatrienoic acid
Arachidonic acid (AA, ARA)20:4 (n−6)all-cis-5,8,11,14-eicosatetraenoic acid
Docosadienoic acid22:2 (n−6)all-cis-13,16-docosadienoic acid
Adrenic acid22:4 (n−6)all-cis-7,10,13,16-docosatetraenoic acid
Osbond acid22:5 (n−6)all-cis-4,7,10,13,16-docosapentaenoic acid
Tetracosatetraenoic acid24:4 (n−6)all-cis-9,12,15,18-tetracosatetraenoic acid
Tetracosapentaenoic acid24:5 (n−6)all-cis-6,9,12,15,18-tetracosapentaenoic acid

The melting point of the fatty acids increases as the number of carbons in the chain increases.[41]

See also

References

Bibliography