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Butyl Glycidate

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Identification
Molecular formula
C9H14O3
CAS number
926-52-7
IUPAC name
butyl 3-methyloxirane-2-carboxylate
State
State

At room temperature, butyl glycidate is a liquid.

Melting point (Celsius)
-30.00
Melting point (Kelvin)
243.15
Boiling point (Celsius)
229.00
Boiling point (Kelvin)
502.15
General information
Molecular weight
158.19g/mol
Molar mass
158.1890g/mol
Density
1.0321g/cm3
Appearence

Butyl glycidate appears as a colorless liquid. It is clear and often noted for its sweet odor, which is characteristic of esters.

Comment on solubility

Solubility of Butyl 3-Methyloxirane-2-Carboxylate

Butyl 3-methyloxirane-2-carboxylate, a member of the carboxylate esters, exhibits unique solubility characteristics that are essential to its application in various fields. The solubility of this compound can be influenced by several factors:

  • Polarity: The presence of a carboxylic acid group increases polarity, which may enhance solubility in polar solvents.
  • Hydrophobic Alkyl Chain: The butyl group contributes hydrophobic properties, which can hinder solubility in water but improve it in organic solvents.
  • Temperature: Like many chemical compounds, solubility often increases with temperature, allowing for more effective dissolution in liquids.
  • pH Levels: The ionization state of the carboxylate group can vary with pH, affecting solubility in aqueous environments.

Therefore, it is often stated that “the solubility of a substance is a delicate balance between its polar and nonpolar characteristics.” While butyl 3-methyloxirane-2-carboxylate may have limited water solubility, it is more likely to dissolve in organic solvents such as ethanol or acetone. Such solubility behaviors make it a versatile compound in chemical synthesis and product formulation.

Interesting facts

Interesting Facts about Butyl 3-Methyloxirane-2-Carboxylate

Butyl 3-methyloxirane-2-carboxylate is an intriguing compound known for its utility in various chemical applications. Here are some notable aspects:

  • Structure and Reactivity: This compound features a unique oxirane (epoxide) ring, which enhances its reactivity. The presence of the ester functional group plays a significant role in its behavior during chemical reactions.
  • Synthesis: The synthesis of butyl 3-methyloxirane-2-carboxylate often involves the reaction of specific precursors through methods such as O-alkylation, providing a fascinating insight into synthetic organic chemistry.
  • Applications: Due to its reactivity, this compound can serve as a valuable intermediate in the manufacture of polymers, pharmaceuticals, and other organic compounds. Its potential use in material sciences is an area of active research.
  • Biological Activity: Some studies have suggested that compounds with similar structures may exhibit interesting biological properties, paving the way for innovative applications in medicinal chemistry.
  • Environmental Impact: Understanding the behavior of such compounds in the environment is crucial. Researching their degradation pathways helps in evaluating their ecological safety and sustainability.

In conclusion, butyl 3-methyloxirane-2-carboxylate showcases the intricate balance of structure and function in organic chemistry. As a compound with significant potential, it highlights the importance of ongoing research in discovering new applications and understanding its role in various chemical processes.

Synonyms
Butyric acid, 2,3-epoxy-, butyl ester
2,3-Epoxbutyl 2,3-epoxybutyrate
10138-34-8
6J8O32Z8PM
2,3-Epoxybutyric acid, butyl ester
BRN 4970747
2,3-Epoxybutyric acid butyl ester
butyl 3-methyloxirane-2-carboxylate
Oxiranecarboxylic acid, 3-methyl-, butyl ester
UNII-6J8O32Z8PM
SCHEMBL9566682
DTXSID00906098
Q27264994
2-OXIRANECARBOXYLIC ACID, 3-METHYL-, BUTYL ESTER