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Eicosatrienoic acid

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Identification
Molecular formula
C20H34O2
CAS number
506-32-1
IUPAC name
icosa-8,11,14-trienoic acid
State
State

Eicosatrienoic acid is typically found in a liquid state at room temperature due to its long carbon chain and unsaturated nature. This state facilitates its role in biological systems and industrial applications where it can act as an oil or emulsifier.

Melting point (Celsius)
-44.20
Melting point (Kelvin)
229.00
Boiling point (Celsius)
371.15
Boiling point (Kelvin)
644.30
General information
Molecular weight
306.49g/mol
Molar mass
306.5060g/mol
Density
0.9158g/cm3
Appearence

Eicosatrienoic acid is a colorless to pale yellow liquid. This compound, being a polyunsaturated fatty acid, presents a characteristic greasy texture and is hydrophobic, typical of fatty acids.

Comment on solubility

Solubility of Icosa-8,11,14-trienoic Acid

Icosa-8,11,14-trienoic acid, with the chemical formula C20H34O2, exhibits intriguing solubility characteristics that are essential for its applications in various fields. The solubility of this compound can be described as follows:

  • Solvent Type: Icosa-8,11,14-trienoic acid is typically soluble in non-polar or weakly polar organic solvents such as hexane and ethyl acetate.
  • Water Solubility: It is very poorly soluble in water due to its long hydrophobic carbon chain, which does not interact favorably with water molecules.
  • Temperature Effects: Like many organic acids, the solubility may increase with temperature, making it potentially more soluble in heated solvents.

In summary, the solubility of icose-8,11,14-trienoic acid is primarily governed by its molecular structure, with a preference for organic solvents over aqueous solutions. Understanding these solubility properties is vital, especially when considering the compound for practical applications in nutrition or cosmetic formulations.

Interesting facts

Interesting Facts about Icosa-8,11,14-Trienoic Acid

Icosa-8,11,14-trienoic acid, also known as 20:3 n-3, is a fascinating fatty acid that plays a significant role in both human nutrition and biological research. Here are some intriguing aspects of this compound:

  • Structural Uniqueness: The name "icosa" refers to the 20 carbon atoms that make up its backbone, showcasing the importance of carbon chain length in fatty acids. The "trienoic" indicates that it contains three double bonds, which are crucial for its functionality and reactivity.
  • Source: It is primarily found in fish, algae, and seeds, making it a notable component of omega-3 fatty acids. These sources have been associated with numerous health benefits, including cardiovascular health and anti-inflammatory properties.
  • Biological Significance: Fatty acids like icapa-8,11,14-trienoic acid are important for cell membrane integrity and fluidity. They are integral to neural health and have been linked to improved cognitive functions and mood regulation.
  • Metabolic Pathways: In the body, icona-8,11,14-trienoic acid can be converted into eicosanoids, signaling molecules that play a role in inflammatory responses, immune function, and various physiological processes.
  • Research Potential: Due to its potential health benefits and roles within metabolic pathways, icapa-8,11,14-trienoic acid has become a subject of interest in studies aiming to understand the relationship between diet and chronic diseases.

As researchers delve deeper into the properties and effects of this compound, it may hold the key to unlocking new approaches in nutritional science and health enhancements. The intersections of its chemistry with biology illustrate the incredible complexity and interconnectedness of life at the molecular level.

Synonyms
8,11,14-Eicosatrienoic acid
DTXSID70862753
7324-41-6
8,11,14-eicosatrienoic acid, (8Z,11Z,14Z)-
Dihomogammalinolenic Acid
Homo gamma Linolenic Acid
Homo-gamma Linolenic Acid
Dihomo gamma Linolenic Acid
Linolenic Acid, Homo-gamma
8,11,14 Eicosatrienoic Acid
8,11,14-Eicosatrienoic acid (VAN)
CBiol_001986
KBioGR_000006
KBioSS_000006
eicosa-8,11,14 trienoic acid
KBio2_000006
KBio2_002574
KBio2_005142
KBio3_000011
KBio3_000012
DTXCID40811475
HOBAELRKJCKHQD-UHFFFAOYSA-N
Bio1_000272
Bio1_000761
Bio1_001250
Bio2_000006
Bio2_000486
AKOS028109317
DB-044333
NS00082416
CH3(CH2)4CH=CHCH2CH=CHCH2CH=CH(CH2)6COOH
CH3(CH2)4-CH=CHCH2CH=CHCH2CH=CH(CH2)6COOH