Names | |
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IUPAC name
(9Z,12Z)-9,12-Octadecadienoic acid
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Other names
C18:2 (Lipid numbers)
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.000.428 |
KEGG | |
UNII | |
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Properties | |
C18H32O2 | |
Molar mass | 280.45 g·mol−1 |
Appearance | Colorless oil |
Density | 0.9 g/cm3 |
Melting point | −5 °C (23 °F) −12 °C (10 °F) |
Boiling point | 230 °C (446 °F) at 21 mbar 230 °C (446 °F) at 16 mmHg |
0.139 mg/L | |
Vapor pressure | 16 Torr at 229 °C |
Hazards | |
NFPA 704 | |
Flash point | 112 °C (234 °F) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|
Infobox references | |
Linoleic acid (LA), a carboxylic acid, is a polyunsaturated omega-6 fatty acid, an 18-carbon chain with two double bonds in cis configuration. A shorthand notation like "18:2 (n-6)" or "18:2 cis-9,12" may be used in literature. It typically occurs in nature as a triglyceride ester; free fatty acids are typically low in foods.
Linoleic acid belongs to one of the two families of essential fatty acids, which means that the human body cannot synthesize it from other food components.
The word "linoleic" derived from the Greek word linon (flax). Oleic means "of, relating to, or derived from oil of olive" or "of or relating to oleic acid" because saturating the omega-6 double bond produces oleic acid.
LA is a polyunsaturated fatty acid used in the biosynthesis of arachidonic acid (AA) and thus some prostaglandins, leukotrienes (LTA, LTB, LTC), and thromboxane (TXA). It is found in the lipids of cell membranes. It is abundant in many nuts, fatty seeds (flax seeds, hemp seeds, poppy seeds, sesame seeds, etc.) and their derived vegetable oils; comprising over half (by weight) of poppy seed, safflower, sunflower, corn, and soybean oils.