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docosa-4,15-dien-1-yn-3-ol

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Identification
Molecular formula
C22H36O
CAS number
.37788-22-6
IUPAC name
docosa-4,15-dien-1-yn-3-ol
State
State

At room temperature, docosa-4,15-dien-1-yn-3-ol is a liquid. Due to its relatively low melting point, it remains in liquid form under standard laboratory conditions.

Melting point (Celsius)
-11.20
Melting point (Kelvin)
261.95
Boiling point (Celsius)
215.50
Boiling point (Kelvin)
488.65
General information
Molecular weight
308.53g/mol
Molar mass
308.5320g/mol
Density
0.8456g/cm3
Appearence

Docosa-4,15-dien-1-yn-3-ol is a long-chain unsaturated alcohol. It typically appears as a clear or light yellowish liquid with a slightly oily texture. Being an organic compound, it may emit a faint, characteristic odor.

Comment on solubility

Solubility of Docosa-4,15-dien-1-yn-3-ol

Docosa-4,15-dien-1-yn-3-ol (C22H36O) exhibits unique solubility characteristics primarily due to its long carbon chain and the presence of a hydroxyl group (-OH) that can engage in hydrogen bonding. Here are some key points regarding its solubility:

  • Hydrophobic Nature: The extensive hydrocarbon tail contributes significantly to its hydrophobic properties, making it less soluble in polar solvents like water.
  • Solubility in Organic Solvents: This compound shows good solubility in non-polar solvents such as:
    • Hexane
    • Chloroform
    • Ether
  • Influence of the Hydroxyl Group: The presence of the hydroxyl group enhances solubility in polar environments, but the effect is not enough to counterbalance the hydrophobic characteristics of the long alkyl chain.
  • Practical Considerations: In laboratory applications, consider its solubility profile when preparing solutions or selecting solvents for reactions.

In summary, while docosa-4,15-dien-1-yn-3-ol can dissolve well in organic solvents, its solubility in water remains limited, emphasizing its nonpolar characteristics influenced by its unique structure.

Interesting facts

Interesting Facts About Docosa-4,15-dien-1-yn-3-ol

Docosa-4,15-dien-1-yn-3-ol, a fascinating compound, has garnered interest in various fields of research. Here are some intriguing aspects of this compound that highlight its significance:

  • Structural Complexity: This compound features a unique structural arrangement with multiple functional groups that contribute to its biochemical properties.
  • Biological Role: It is part of the family of polyunsaturated fatty alcohols, which play crucial roles in cellular functions, signaling pathways, and the construction of membranes in biological systems.
  • Potential Health Benefits: Emerging research suggests that docosa-4,15-dien-1-yn-3-ol may have anti-inflammatory properties, making it a subject of interest for therapeutic applications.
  • Source of Interest: This compound is often found in marine organisms, especially in certain types of algae and fish oils, which are known for their health benefits.
  • Research Applications: Chemists and biochemists are exploring its use in developing new pharmaceuticals, nutraceuticals, and functional foods due to its beneficial properties.
  • Sustainability Aspect: The extraction of docosa-4,15-dien-1-yn-3-ol from natural sources promotes the interest in sustainable practices within the industry, especially related to marine resources.

In summary, docosa-4,15-dien-1-yn-3-ol represents a compound with significant implications in health science, sustainability, and biochemistry. Its multi-faceted roles make it a worthwhile subject for ongoing research, especially as the search for natural health solutions continues to expand.

Synonyms
4,15-Docosadien-1-yn-3-ol
139722-81-9
DTXSID60274321