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Arachidonoyl glycine

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Identification
Molecular formula
C22H37NO3
CAS number
69110-41-4
IUPAC name
2-(icosa-5,8,11,14-tetraenoylamino)acetic acid
State
State

At room temperature, arachidonoyl glycine is typically in a liquid state due to its relatively low melting point.

Melting point (Celsius)
-8.00
Melting point (Kelvin)
265.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.15
General information
Molecular weight
345.54g/mol
Molar mass
345.5040g/mol
Density
0.9200g/cm3
Appearence

Arachidonoyl glycine is generally appears as a colorless to pale yellow viscous oil.

Comment on solubility

Solubility of 2-(icosa-5,8,11,14-tetraenoylamino)acetic acid

Understanding the solubility of 2-(icosa-5,8,11,14-tetraenoylamino)acetic acid, with the chemical formula C22H37NO3, is essential for its practical applications in various fields, including biochemistry and pharmaceuticals. Here’s an overview of its solubility characteristics:

  • Solvent Compatibility: This compound exhibits varying solubility depending on the solvent. It is generally more soluble in organic solvents such as DMSO (dimethyl sulfoxide) and ethanol, than in water.
  • Hydrophilic vs. Hydrophobic Properties: Due to the presence of the carboxylic acid functional group, the molecule has some hydrophilic characteristics. However, the long hydrocarbon chain confers significant hydrophobic properties, which may limit overall solubility in polar solvents.
  • Temperature Dependence: Like many organic compounds, the solubility of this acid may increase with temperature. Higher temperatures can facilitate the dissolution process, expanding its potential applications.
  • pH Influence: The solubility could also be pH-dependent; being a carboxylic acid, it may ionize at higher pH levels, enhancing its solubility in aqueous solutions.

In conclusion, the solubility of 2-(icosa-5,8,11,14-tetraenoylamino)acetic acid is influenced by its unique structural features, molecular interactions, and environmental conditions. Understanding these aspects enables better utilization of this compound in scientific research and industrial applications.

Interesting facts

Exploring 2-(icosa-5,8,11,14-tetraenoylamino)acetic acid

2-(icosa-5,8,11,14-tetraenoylamino)acetic acid is a fascinating compound with unique properties and potential applications. Here are some interesting facts about this intriguing molecule:

  • Biological Significance: This compound is known for its role in biological systems, particularly in cellular communication and signaling pathways.
  • Structural Complexity: The molecule features an icosa-5,8,11,14-tetraenoyl group, which contributes to its structural complexity and might influence its interaction with biological macromolecules.
  • Research Applications: Scientists are investigating potential uses of this compound in drug design and medicinal chemistry due to its unique functional groups.
  • Potential for Development: With ongoing research, compounds like 2-(icosa-5,8,11,14-tetraenoylamino)acetic acid may lead to the development of new therapies, especially in areas of targeting specific receptors in cells.
  • Functional Versatility: The presence of amino and acetic acid components suggests versatility in chemical reactivity, making it a candidate for various synthetic transformations.

As chemists continue to explore the properties of this compound, it is fascinating to consider its potential implications not only in chemistry but also in fields like pharmacology and materials science.

Synonyms
N-icosa-5,8,11,14-tetraenoylglycine
Bio1_000014
CBiol_001728
KBioGR_000164
KBioSS_000164
2-(icosa-5,8,11,14-tetraenoylamino)acetic acid
KBio2_000164
KBio2_002732
KBio2_005300
KBio3_000327
KBio3_000328
DTXSID60861457
Bio1_000503
Bio1_000992
Bio2_000164
Bio2_000644
JWB90844
icosa-5,8,11,14-tetraenoylamino-acetic acid
Q27164646
2-(1-oxoeicosa-5,8,11,14-tetraenylamino)acetic acid
2-(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenamidoacetic acid