Linolelaidic acid: Difference between revisions
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'''Linolelaidic acid''' is a [[trans | {{DISPLAYTITLE:Linolelaidic acid}} | ||
'''Linolelaidic acid''' is a type of [[trans fat]] that is the trans isomer of [[linoleic acid]]. It is a polyunsaturated fatty acid with the chemical formula C<sub>18</sub>H<sub>32</sub>O<sub>2</sub>. Linolelaidic acid is commonly found in partially hydrogenated vegetable oils and is used in the food industry to improve the texture and shelf life of processed foods. | |||
==Structure and Properties== | ==Structure and Properties== | ||
Linolelaidic acid | [[File:Linoelaidic_acid.png|thumb|right|Chemical structure of linolelaidic acid]] | ||
Linolelaidic acid is characterized by its trans double bonds, which differ from the cis configuration found in its counterpart, linoleic acid. This trans configuration results in a more linear structure, which affects the physical properties of the fat, such as its melting point and stability. | |||
==Sources== | ==Sources and Uses== | ||
Linolelaidic acid is | Linolelaidic acid is primarily found in [[partially hydrogenated oils]], which are used in the production of margarine, shortening, and various baked goods. The process of hydrogenation converts some of the cis double bonds in linoleic acid to trans double bonds, forming linolelaidic acid. | ||
==Health | ==Health Implications== | ||
Consumption of trans fats, including linolelaidic acid, has been associated with negative health effects. These include an increased risk of [[cardiovascular disease]], [[inflammation]], and [[insulin resistance]]. As a result, many health organizations recommend limiting the intake of trans fats. | |||
== | ==Biological Role== | ||
In the human body, linolelaidic acid can interfere with the metabolism of essential fatty acids, such as [[arachidonic acid]] and [[eicosapentaenoic acid]]. This interference can disrupt the production of important signaling molecules, such as [[prostaglandins]] and [[leukotrienes]]. | |||
== | ==Regulation and Reduction== | ||
Due to the health risks associated with trans fats, many countries have implemented regulations to reduce their presence in the food supply. This includes mandatory labeling of trans fat content and restrictions on the use of partially hydrogenated oils in food products. | |||
==Related pages== | |||
* [[Linoleic acid]] | |||
* [[Trans fat]] | |||
* [[Hydrogenation]] | |||
* [[Cardiovascular disease]] | |||
[[Category:Fatty acids]] | [[Category:Fatty acids]] | ||
[[Category: | [[Category:Trans fats]] | ||
Latest revision as of 12:05, 15 February 2025
Linolelaidic acid is a type of trans fat that is the trans isomer of linoleic acid. It is a polyunsaturated fatty acid with the chemical formula C18H32O2. Linolelaidic acid is commonly found in partially hydrogenated vegetable oils and is used in the food industry to improve the texture and shelf life of processed foods.
Structure and Properties[edit]

Linolelaidic acid is characterized by its trans double bonds, which differ from the cis configuration found in its counterpart, linoleic acid. This trans configuration results in a more linear structure, which affects the physical properties of the fat, such as its melting point and stability.
Sources and Uses[edit]
Linolelaidic acid is primarily found in partially hydrogenated oils, which are used in the production of margarine, shortening, and various baked goods. The process of hydrogenation converts some of the cis double bonds in linoleic acid to trans double bonds, forming linolelaidic acid.
Health Implications[edit]
Consumption of trans fats, including linolelaidic acid, has been associated with negative health effects. These include an increased risk of cardiovascular disease, inflammation, and insulin resistance. As a result, many health organizations recommend limiting the intake of trans fats.
Biological Role[edit]
In the human body, linolelaidic acid can interfere with the metabolism of essential fatty acids, such as arachidonic acid and eicosapentaenoic acid. This interference can disrupt the production of important signaling molecules, such as prostaglandins and leukotrienes.
Regulation and Reduction[edit]
Due to the health risks associated with trans fats, many countries have implemented regulations to reduce their presence in the food supply. This includes mandatory labeling of trans fat content and restrictions on the use of partially hydrogenated oils in food products.