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Glycidyl hexanoate

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Identification
Molecular formula
C9H16O3
CAS number
16230-54-3
IUPAC name
oxiran-2-ylmethyl hexanoate
State
State
Glycidyl hexanoate exists as a liquid at room temperature. This state is typical for many epoxide derivatives with similar structure and molecular weight.
Melting point (Celsius)
-42.00
Melting point (Kelvin)
231.15
Boiling point (Celsius)
243.00
Boiling point (Kelvin)
516.15
General information
Molecular weight
172.21g/mol
Molar mass
172.2120g/mol
Density
0.9850g/cm3
Appearence

Glycidyl hexanoate is typically a colorless liquid. It is known for having a consistent and uniform appearance without any visible impurities under normal conditions.

Comment on solubility

Solubility of Oxiran-2-ylmethyl Hexanoate

Oxiran-2-ylmethyl hexanoate, a compound containing an epoxide functional group, exhibits interesting solubility characteristics that are important for its applications in various chemical processes.

In general, the solubility of oxiran-2-ylmethyl hexanoate can be influenced by several factors:

  • Polarity: The presence of the epoxide group contributes to the polarity of the molecule, enabling it to interact well with water. However, the hexanoate chain also introduces a hydrophobic character, balancing its solubility in polar and non-polar solvents.
  • Solvent Characteristics: Depending on the solvent, oxiran-2-ylmethyl hexanoate can show varying levels of solubility:
    • Highly soluble in polar organic solvents like alcohols or acetone.
    • Moderately soluble in non-polar solvents such as hexane, due to the hydrophobic hexanoate chain.
  • Temperature: Increased temperature often enhances solubility due to increased kinetic energy, allowing the compound to disperse more effectively in solution.

It is also essential to note that the solubility of oxiran-2-ylmethyl hexanoate can impact its reactivity and behavior in formulations, making it a versatile compound in various chemical applications.

In summary, understanding the solubility properties of oxiran-2-ylmethyl hexanoate is crucial for optimizing its use in the industry. As always, the specific conditions must be taken into account to maximize efficacy and utility.

Interesting facts

Exploring Oxiran-2-ylmethyl Hexanoate

Oxiran-2-ylmethyl hexanoate, often referred to as a versatile compound, is renowned in the fields of chemistry and materials science. This compound contains an epoxide ring, which allows it to participate in a variety of reactions. Here are some interesting facts that highlight its significance:

  • Reactivity and Versatility: The epoxide functional group makes oxiran-2-ylmethyl hexanoate reactive, enabling it to be involved in ring-opening reactions. This property is particularly useful in the synthesis of diverse polymers and resins.
  • Applications in Coatings: Due to its chemical structure, this compound is often utilized in the formulation of coatings and adhesives that require durability and resistance to chemical degradation. These applications leverage its unique chemical properties.
  • Biocompatibility: There is ongoing research exploring the biocompatibility of oxiran-2-ylmethyl hexanoate, potentially paving the way for its use in biomedical applications such as drug delivery systems or tissue engineering.
  • Sustainability Potential: As industries pivot towards sustainable practices, the synthesis of this compound using bio-based feedstocks is a subject of interest, offering a greener alternative in materials science.
  • Functionalization: The ability to modify oxiran-2-ylmethyl hexanoate allows chemists to tailor its properties for specific applications, expanding its usability in pharmaceuticals and specialty chemicals.

As a chemist, one might appreciate the elegant complexity of oxiran-2-ylmethyl hexanoate. Its multifaceted nature invites countless possibilities in innovation and application. Scientists often reflect on how such a seemingly simple structure can lead to a vast array of functional materials, embodying the very essence of chemical creativity and exploration.

Synonyms
oxiran-2-ylmethyl hexanoate
Glycidyl hexanoate
17526-74-8
Hexanoic acid oxiranylmethyl ester
(Oxiran-2-yl)methyl hexanoate
Glycidyl ester of hexanoic acid
Hexanoic acid, oxiranylmethyl ester
BRN 1365955
HEXANOIC ACID, 2,3-EPOXYPROPYL ESTER
Hexanoic Acid 2-Oxiranylmethyl Ester; Hexanoic Acid 2,3-Epoxypropyl Ester; Hexanoic Acid Oxiranylmethyl Ester;
starbld0003436
SCHEMBL2318734
DTXSID60938638
LYJNHHFSQGRJFP-UHFFFAOYSA-N
MFCD01723334
HY-W704867
DB-230516
H39551