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Thymol acetate

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Identification
Molecular formula
C12H16O2
CAS number
89-42-9
IUPAC name
(4-hydroxy-5-isopropyl-2-methyl-phenyl) acetate
State
State

At room temperature, thymol acetate is a liquid, highlighting its relatively low melting point and high boiling point compared to many other organic esters.

Melting point (Celsius)
48.50
Melting point (Kelvin)
321.60
Boiling point (Celsius)
237.50
Boiling point (Kelvin)
510.70
General information
Molecular weight
194.24g/mol
Molar mass
194.2430g/mol
Density
0.9997g/cm3
Appearence

Thymol acetate is a colorless to pale yellow liquid with a pleasant, aromatic scent reminiscent of thyme, from which it derives its name. It is usually clear and free from suspended matter.

Comment on solubility

Solubility of (4-hydroxy-5-isopropyl-2-methyl-phenyl) acetate

The solubility of (4-hydroxy-5-isopropyl-2-methyl-phenyl) acetate, with the chemical formula C12H16O2, can be influenced by several factors due to its unique structural characteristics.

Key Points of Solubility

  • Polarity: The presence of both hydroxyl (-OH) and acetate (-COO) groups suggests that this compound may exhibit moderate polarity, enhancing its interactions with polar solvents such as water.
  • Water Solubility: Generally, compounds with larger hydrophobic (non-polar) alkyl groups tend to be less soluble in water. However, the conflicting hydrophilic character of the hydroxyl group can create some solubility under certain conditions.
  • Solvent Effects: This compound may display greater solubility in organic solvents like ethanol, acetone, or chloroform, attracting a favorable affinity due to similar polarity.
  • Temperature Dependence: Enhanced temperature may result in increased solubility, allowing more of the compound to dissolve in a given solvent by breaking intermolecular forces.

In conclusion, while (4-hydroxy-5-isopropyl-2-methyl-phenyl) acetate may not be highly soluble in water, it finds more compatibility within organic solvents, thus presenting intriguing applications in various chemical processes.

Interesting facts

Interesting Facts about (4-hydroxy-5-isopropyl-2-methyl-phenyl) acetate

(4-hydroxy-5-isopropyl-2-methyl-phenyl) acetate, commonly referred to as a derivative of a phenolic compound, provides a fascinating exploration into organic chemistry.

Chemical Structure and Functionality

This compound features a distinctive structure that includes:

  • Phenolic Group: The presence of the hydroxyl (-OH) group on the benzene ring contributes to its reactivity and influence on physical properties.
  • Acetate Moiety: The acetyl group enhances the solubility of the compound in organic solvents, making it advantageous in various chemical applications.
  • Isopropyl Substitution: The isopropyl group not only contributes to steric hindrance but also enhances the compound's overall stability.

Applications

This compound is noteworthy for several reasons:

  • Synthesis: It can serve as an intermediate in organic synthesis, particularly in the development of pharmaceuticals.
  • Fragrance Industry: Compounds with similar structures are often utilized in perfumes and flavorings due to their pleasant scent.
  • Biochemical Research: The phenolic structure is significant in biochemical research, especially relating to antioxidant activity.

Quotes from the Field

As noted by researchers in organic chemistry, “The intricate balance of functional groups within a single molecule can define its versatility and functionality in multiple applications.” This statement resonates particularly well with (4-hydroxy-5-isopropyl-2-methyl-phenyl) acetate, showcasing its relevance.

In summary, (4-hydroxy-5-isopropyl-2-methyl-phenyl) acetate is an intriguing compound distinguished by its unique structural traits and its implications across several fields, including pharmaceutical synthesis, food chemistry, and research. Its study reveals the intricate dance of chemistry that underpins many aspects of our daily lives.