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Methyl p-anisate

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Identification
Molecular formula
C11H14O3
CAS number
6473-91-2
IUPAC name
(4-methoxyphenyl) butanoate
State
State

At room temperature, it is a liquid. This makes it suitable for applications in various chemical processes where a liquid reagent or additive is required.

Melting point (Celsius)
-21.30
Melting point (Kelvin)
251.85
Boiling point (Celsius)
292.00
Boiling point (Kelvin)
565.15
General information
Molecular weight
178.23g/mol
Molar mass
178.2290g/mol
Density
1.0956g/cm3
Appearence

(4-Methoxyphenyl) butanoate is typically a liquid at room temperature. The compound possesses a sweet and floral aroma that resembles that of anise or licorice, lending to its application in perfumery and flavoring. It can also present a color range from colorless to pale yellow, depending on purity and age.

Comment on solubility

Solubility of (4-methoxyphenyl) butanoate

(4-methoxyphenyl) butanoate, a compound with both hydrophilic and hydrophobic characteristics, presents a unique profile in terms of solubility. Understanding its solubility behavior is essential for applications in various fields, particularly in pharmacology and organic synthesis.

Key Solubility Characteristics:

  • Solvent Compatibility: This compound demonstrates moderate solubility in organic solvents such as ethanol and methanol, due to its phenolic group and butanoate moiety.
  • Water Solubility: Its solubility in water is limited. While the methoxy group may offer some hydrogen bonding opportunities, the overall structure is predominantly hydrophobic.
  • Temperature Influence: Solubility may increase with temperature, which is a common trait in many organic compounds, suggesting that higher temperatures could promote dissolution.

For practical applications: when working with (4-methoxyphenyl) butanoate, it is advisable to:

  1. Use non-polar solvents for optimal solubility;
  2. Conduct solubility tests at elevated temperatures to gauge potential increases in solubility;
  3. Be cautious with aqueous applications as solubility is limited.

In conclusion, the solubility of (4-methoxyphenyl) butanoate is primarily influenced by its chemical structure, wherein the balance of hydrophilic and hydrophobic features governs its interaction with various solvents. Understanding these nuances is essential for leveraging its properties in research and industrial applications.

Interesting facts

Interesting Facts about (4-methoxyphenyl) butanoate

(4-methoxyphenyl) butanoate, also known in some contexts as a methoxy derivative of a phenyl ester, offers a compelling case for study due to its unique chemical structure and diverse applications. Here are some engaging insights into this compound:

  • Structural Uniqueness: The presence of a methoxy group on the phenyl ring not only influences the compound's reactivity but also enhances its solubility in organic solvents. This feature provides versatility in both synthetic pathways and practical applications.
  • Applications: Compounds like (4-methoxyphenyl) butanoate are often utilized in the field of organic synthesis, particularly in the production of fragrances, flavor compounds, and pharmaceuticals. This makes it significant for industries aiming to produce complex organic molecules.
  • Biological Activity: Some research studies have indicated that derivatives of butanoates can exhibit biological activity, making them potential candidates for further pharmacological investigations. The methoxy substitution might also play a role in modulating the biological effects of the compound.
  • Aromatic Alterations: The aromatic nature of the phenyl group contributes to different electronic characteristics, which can affect how (4-methoxyphenyl) butanoate interacts with other substances in a chemical reaction or during biological processes.
  • Research Potential: Due to its molecular structure, this compound opens avenues for innovative research. Scientists may explore its role in creating new materials or functionalized nanoparticles, emphasizing the importance of interdisciplinary approaches in chemistry.

In summary, (4-methoxyphenyl) butanoate not only stands out for its chemical characteristics but also for its potential impact across various scientific fields. With ongoing research, this compound may unveil even more exciting opportunities for application and discovery.

Synonyms
(4-methoxyphenyl) butanoate
BUTYRIC ACID, p-METHOXYPHENYL ESTER
14617-95-9
4-Methoxyphenyl butyrate
p-methoxyphenyl n-butyrate
SCHEMBL357271
SCHEMBL4644289
SCHEMBL4644295
DTXSID00163280
Butyric acid, 4-methoxyphenyl ester
AKOS002953752
Butanoic acid,(4-methoxyphenyl)methyl ester