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Arachidonic acid 2-hydroxyethyl ester

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Identification
Molecular formula
C22H36O3
CAS number
62341-98-6
IUPAC name
2-hydroxyethyl icosa-5,8,11,14-tetraenoate
State
State

At room temperature, arachidonic acid 2-hydroxyethyl ester is a liquid.

Melting point (Celsius)
-32.00
Melting point (Kelvin)
241.15
Boiling point (Celsius)
324.30
Boiling point (Kelvin)
597.45
General information
Molecular weight
334.52g/mol
Molar mass
334.5150g/mol
Density
0.9075g/cm3
Appearence

Arachidonic acid 2-hydroxyethyl ester is typically a viscous, colorless to pale yellow liquid. It may also be slightly oily in appearance.

Comment on solubility

Solubility of 2-hydroxyethyl icosa-5,8,11,14-tetraenoate (C22H36O3)

2-hydroxyethyl icosa-5,8,11,14-tetraenoate is an interesting compound when it comes to solubility properties. Understanding its solubility is key for various applications, especially in biochemical contexts. Here are some notable points regarding its solubility:

  • Polar and Nonpolar Interactions: The presence of the -OH (hydroxyl) group in the structure suggests that 2-hydroxyethyl icosa-5,8,11,14-tetraenoate could form hydrogen bonds. This makes it more soluble in polar solvents such as water.
  • Ester Characteristics: Being an ester, this compound may exhibit a degree of lipophilicity, thereby increasing its solubility in organic solvents like ethanol or chloroform.
  • Functional Group Influence: Solubility can also be affected by the length and structure of hydrocarbon chains. The long hydrocarbon tail might reduce solubility in polar solvents but enhance solubility in nonpolar solvents.
  • Temperature Effect: As with many organic compounds, solubility can be temperature-dependent. Typically, increasing temperature leads to increased solubility.

In general, while this compound may show some solubility in water due to its polar characteristics, it is likely to exhibit better solubility in organic solvents owing to its overall structure. Understanding these solubility dynamics can provide valuable insights for further chemical formulations and applications in scientific research.

Interesting facts

Interesting Facts about 2-Hydroxyethyl Icosapentaenoate

2-Hydroxyethyl icosa-5,8,11,14-tetraenoate, commonly referred to in discussions involving unsaturated fatty acids, is a fascinating compound primarily found in certain types of oils. Here are some compelling insights:

  • Biological Relevance: This compound is notable for its role in nutrition and cellular function, especially in maintaining lipid balance and promoting cardiovascular health.
  • Unsaturated Characteristics: As a tetraenoic acid, it contains multiple double bonds, which make it an essential part of a balanced diet and are associated with anti-inflammatory properties.
  • Source: Naturally occurring in several fish oils and certain plant oils, 2-hydroxyethyl icosa-5,8,11,14-tetraenoate is a vital component for those seeking to increase their intake of omega fatty acids.
  • Commercial Use: Beyond dietary supplements, this compound is also explored in cosmetic formulations for its potential skin benefits, such as moisture retention and anti-aging properties.
  • Scientific Exploration: Researchers are investigating the therapeutic potentials of compounds like 2-hydroxyethyl icosa-5,8,11,14-tetraenoate in conditions such as arthritis and other inflammatory diseases.

Quote from the Field

As stated in numerous nutrition journals, "The integration of unsaturated fatty acids in our daily diet is not just beneficial—it is necessary for optimal health."

In conclusion, 2-hydroxyethyl icosa-5,8,11,14-tetraenoate exemplifies the intersection of nutrition, biology, and chemistry, showcasing how a single compound can bear significant implications for health and wellness.