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Ethyl tricosanoate

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Identification
Molecular formula
C25H50O2
CAS number
30806-19-0
IUPAC name
ethyl tricosanoate
State
State

At room temperature, ethyl tricosanoate is a solid due to its long aliphatic chain which contributes to its waxy nature.

Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
429.80
Boiling point (Kelvin)
702.95
General information
Molecular weight
396.68g/mol
Molar mass
396.6770g/mol
Density
0.8556g/cm3
Appearence

Ethyl tricosanoate is a solid waxy compound that is colorless to pale yellow in appearance. It typically has a consistency and texture characteristic of many long-chain fatty acid esters.

Comment on solubility

Solubility of Ethyl Tricosanoate

Ethyl tricosanoate is an ester formed from the reaction between ethanol and tricosanoic acid, belonging to the class of long-chain fatty acids and their esters. Understanding its solubility is essential for applications in various fields such as biochemistry and food science.

In terms of solubility:

  • Solvent Polarities: Ethyl tricosanoate is a nonpolar compound. This means it is less soluble in polar solvents such as water.
  • Solvent Compatibility: It shows greater solubility in nonpolar organic solvents like hexane, benzene, or chloroform.
  • Temperature Influence: Solubility often increases with temperature; thus, heating nonpolar solvents may enhance the dissolution of ethyl tricosanoate.
  • Intermolecular Forces: The interactions between ethyl tricosanoate molecules and nonpolar solvents are mainly London dispersion forces, which facilitate solubility.

To summarize, while ethyl tricosanoate has limited solubility in polar substances (like water), it is highly soluble in nonpolar solvents, making it suitable for numerous applications in organic chemistry and industrial processes.

Interesting facts

Interesting Facts about Ethyl Tricosanoate

Ethyl tricosanoate, a fascinating ester, is primarily derived from the reaction of tricosanoic acid and ethanol. This compound is gaining interest in various fields due to its unique properties and applications.

Applications in Fragrances and Flavors

Ethyl tricosanoate is often found in products such as:

  • Cosmetics
  • Perfumes
  • Food flavorings

Its pleasant aroma and flavor profile make it a valuable ingredient in the fragrance and food industries, providing a touch of luxury and interest to the products.

Biological Significance

This compound has been studied for:

  • Its role in the chemistry of natural waxes
  • Potential applications in nutrition as a part of dietary fats

In nature, esters like ethyl tricosanoate may contribute to the scent and flavor of various plants and fruits, making them an essential component of the ecosystem.

Chemical Characteristics

As a member of the ester family, ethyl tricosanoate exhibits several intriguing chemical properties:

  • It contributes to the formation of biodiesel when combined with other fatty acids.
  • The stability of its structure makes it less susceptible to rapid degradation compared to other compounds.

Such properties can be particularly relevant in creating sustainable products and maintaining stability in formulations.

Research Opportunities

Scientists are actively exploring various aspects of ethyl tricosanoate, including:

  • Its potential use in controlled drug delivery systems.
  • The impact of its structure on flavor enhancement in food technology.

This compound exemplifies how a simple ester can have multifaceted applications that extend well beyond basic chemical reactions, making it a subject of growing interest in the scientific community.

In summary, ethyl tricosanoate is more than just a compound; it represents a bridge between chemistry and real-world applications, showcasing the beauty of esters in both nature and industry.

Synonyms
ETHYL TRICOSANOATE
18281-07-7
TRICOSANOIC ACID ETHYL ESTER
Tricosanoic acid, ethyl ester
MFCD01074717
Tricosanoic acid-ethyl ester
orb2564146
SCHEMBL28047458
DTXSID10171336
HMS3650A07
Ethyl Tricosanoate, >=99% (GC)
BBL104159
STL557973
AKOS027469848
AS-9579
DB-222259
HY-119491
CS-0068515
NS00096489
SR-01000946757
SR-01000946757-1