Linoleamide DEA

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Identification

Molecular formula
C20H37NO2
CAS Number
1336-21-6
IUPAC Name
N-(2-hydroxyethyl)octadeca-9,12-dienamide
Molecular Weight
311.53g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
0.9220g/cm3
Synonyms
Linoleoylethanolamide
Interesting facts

Interesting Facts about N-(2-hydroxyethyl)octadeca-9,12-dienamide

N-(2-hydroxyethyl)octadeca-9,12-dienamide, a fascinating compound often encountered in organic synthesis and materials science, presents a variety of intriguing characteristics that make it a subject of interest for chemists and biochemists alike. Here are some notable points:

  • Versatile Applications: This compound is utilized in numerous applications, ranging from cosmetics and personal care products to potential uses in drug formulation due to its unique properties.
  • Amide Bond: The presence of an amide functional group signifies its potential reactivity and stability in biological systems, making it useful in medicinal chemistry.
  • Hydroxyethyl Group: The hydroxyethyl moiety enhances solubility and provides the compound with hydrophilic characteristics, which can lead to interesting interactions in aqueous environments.
  • Unsaturation: The presence of double bonds in the long carbon chain not only affects its physical properties but also contributes to the compound's reactivity, presenting opportunities for further transformations.

Researchers are particularly drawn to compounds like N-(2-hydroxyethyl)octadeca-9,12-dienamide for their ability to mimic natural substances, paving the way for innovations in sustainable chemistry and green materials. As highlighted in a recent study, “Compounds featuring the hydroxyethyl moiety can greatly influence biological activity and interaction with cellular systems." By exploring the chemistry behind this compound, scientists continue to uncover vital insights that bridge the gap between synthetic chemistry and practical applications.

In summary, N-(2-hydroxyethyl)octadeca-9,12-dienamide represents a compelling subject of study, merging synthetic capability with biological relevance, which is essential for advancing both academic research and industrial innovation.

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