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Aleuritic Acid

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Identification
Molecular formula
C10H12O3
CAS number
548-94-3
IUPAC name
3-ethyl-2-hydroxy-6-methyl-benzoic acid
State
State

At room temperature, aleuritic acid is a solid compound. It typically exists in a crystalline state due to its structured molecular composition.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.00
Boiling point (Celsius)
289.00
Boiling point (Kelvin)
562.00
General information
Molecular weight
166.17g/mol
Molar mass
166.1740g/mol
Density
1.2040g/cm3
Appearence

The compound appears as a white crystalline solid. It has a typical crystalline appearance with a clear to white coloration.

Comment on solubility

Solubility of 3-ethyl-2-hydroxy-6-methyl-benzoic acid

3-ethyl-2-hydroxy-6-methyl-benzoic acid, a member of the benzoic acid family, exhibits interesting solubility characteristics.

Its solubility can be influenced by several factors:

  • Polarity of the Compound: The presence of the hydroxy group (-OH) increases the compound's polarity, making it more soluble in polar solvents such as water.
  • Hydrophobic Interactions: The ethyl and methyl groups contribute hydrophobic properties, which can limit solubility in highly polar environments.
  • pH Levels: As a carboxylic acid, its solubility can significantly increase in alkaline conditions due to deprotonation, leading to the formation of a soluble anion.

In general, one could say:

"The more polar the environment, the greater the solubility of 3-ethyl-2-hydroxy-6-methyl-benzoic acid."

Thus, it tends to be more soluble in organic solvents than in pure water, but still maintains noteworthy solubility in moderate aqueous conditions, particularly when adjusted for pH. This balance between hydrophilicity and hydrophobicity makes it an intriguing compound for both theoretical studies and practical applications.

Interesting facts

Interesting Facts about 3-Ethyl-2-hydroxy-6-methyl-benzoic acid

3-Ethyl-2-hydroxy-6-methyl-benzoic acid, commonly known in scientific circles as an important intermediate in organic chemistry, offers a plethora of fascinating insights regarding its chemical behavior and applications. Here are some noteworthy aspects:

  • Functional Groups: This compound features several functional groups, such as hydroxyl (–OH) and carboxylic acid (–COOH), which significantly influence its reactivity and solubility in various solvents.
  • Synthetic Pathways: Scientists often utilize innovative synthetic pathways to create this compound, enhancing our understanding of electrophilic aromatic substitution reactions. This is crucial for developing new molecules in pharmaceutical research.
  • Applications: Its derivatives are commonly explored for their pharmacological properties, including potential anti-inflammatory and analgesic activities. Researchers frequently investigate such compounds for their therapeutic potentials.
  • Biological Relevance: The presence of the hydroxyl group allows for hydrogen bonding, affecting the compound’s behavior in biological systems, including its interaction with biomolecules.
  • Environmental Chemistry: This acid also plays a role in the study of environmental chemistry, where it may be examined for its degradation pathways and behavior in natural waters.

As emphasized by renowned chemists, "The study of such compounds not only unveils the intricacies of molecules but also opens doors to innovative solutions in drug design and environmental management." The exploration of 3-ethyl-2-hydroxy-6-methyl-benzoic acid is just one of countless examples demonstrating the intersection of chemistry with real-world applications.

Synonyms
2,6-CRESOTIC ACID, 3-ETHYL-
3-Ethyl-2,6-cresotic acid
2-Methyl-5-ethylsalicylic acid
BRN 2834150
20717-15-1
DTXSID80174778
DTXCID8097269
RefChem:248075
SCHEMBL1649463
YZEVAVNJHBUZFP-UHFFFAOYSA-N
ethyl 2-hydroxy-6-methylbenzoic acid