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Icosadienoic acid

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Identification
Molecular formula
C20H36O2
CAS number
505-69-3
IUPAC name
icosa-11,14-dienoic acid
State
State

At room temperature, icosadienoic acid is in a liquid state. This is consistent with many unsaturated fatty acids that possess one or more double bonds, which lower the melting point and prevent the compound from solidifying at ambient conditions.

Melting point (Celsius)
-5.00
Melting point (Kelvin)
268.15
Boiling point (Celsius)
348.00
Boiling point (Kelvin)
621.15
General information
Molecular weight
308.51g/mol
Molar mass
308.5080g/mol
Density
0.9135g/cm3
Appearence

Icosadienoic acid is a colorless to pale yellow liquid. It is not a solid at room temperature, reflecting its unsaturated fatty acid nature.

Comment on solubility

Solubility of Icos-11,14-dienoic Acid (C20H36O2)

Icos-11,14-dienoic acid is an intriguing compound when it comes to its solubility characteristics. This fatty acid, with a carbon chain length of 20 carbon atoms and two double bonds, presents a unique profile:

  • Solvent Interaction: Icos-11,14-dienoic acid is generally soluble in organic solvents such as ethanol, methanol, and diethyl ether due to its hydrophobic carbon chain.
  • Low Water Solubility: The solubility of this compound in water is quite low, typical for many fatty acids. The long hydrocarbon chain inhibits significant interaction with polar water molecules.
  • Temperature Effect: As with many organic compounds, solubility can be temperature-dependent. Increased temperatures can improve solubility in organic solvents.

In summary, while icosa-11,14-dienoic acid is readily soluble in organic environments, its interaction with water is limited and emphasizes the importance of understanding solvation dynamics in various media. This property can be pivotal for its applications in food science, pharmaceuticals, and various industrial processes.

As always, it’s essential to consider how such solubility properties influence its biological and chemical behavior in practical uses!

Interesting facts

Interesting Facts about Icosa-11,14-Dienoic Acid

Icosa-11,14-dienoic acid, a fascinating compound in the realm of organic chemistry, possesses unique properties that make it a subject of interest for scientists and researchers alike. Here are some intriguing aspects of this compound:

  • Natural Occurrence: Icosa-11,14-dienoic acid is part of the family of fatty acids known as polyunsaturated fatty acids. These types of acids are essential in biological systems and contribute significantly to various metabolic processes.
  • Applications in Nutrition: This compound is often explored for its potential health benefits, particularly its role as a source of essential fatty acids that are crucial for human nutrition and overall health.
  • Potential Therapeutic Uses: Research indicates that fatty acids, like icosa-11,14-dienoic acid, may play a role in alleviating inflammation and improving cardiovascular health. This makes them of high interest in medical studies.
  • Structure and Features: The distinctive structure, with multiple double bonds, gives this compound unique chemical reactivity and flexibility. This allows it to interact with various biological molecules, making it a vital component in cellular processes.
  • Research Opportunities: Current studies are investigating the implications of this acid in pharmaceuticals and dietary supplements, indicating a continuing exploration of its benefits and applications.

In conclusion, icosta-11,14-dienoic acid is an intriguing compound that transcends mere chemical structure, holding important implications in nutrition and potential health benefits. As research continues, it is likely that we will uncover even more about the roles that similar fatty acids play in promoting well-being.

Synonyms
icosa-11,14-dienoic acid
Eicosa-11,14-dienoic acid
Eicosadienoic acid
11,14-Eicosadienoicacid
(11Z,14Z)-eicosadienoic acid
DTXSID101312766
MFCD00673431
CBiol_001980
KBioGR_000046
KBioSS_000046
KBio2_000046
KBio2_002614
KBio2_005182
KBio3_000091
KBio3_000092
XSXIVVZCUAHUJO-UHFFFAOYSA-N
Bio1_000266
Bio1_000755
Bio1_001244
Bio2_000046
Bio2_000526
FAA59838
SY314031
DB-045431
CH3(CH2)4CH=CHCH2CH=CH(CH2)9COOH
CH3(CH2)4-CH=CHCH2CH=CH(CH2)9COOH
Q27165118