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Alkylresorcinol

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Identification
Molecular formula
C8H8O4
CAS number
610-01-1
IUPAC name
2,3-dihydroxy-4-methyl-benzoic acid
State
State

The compound is typically found in a solid state at room temperature.

Melting point (Celsius)
179.50
Melting point (Kelvin)
452.65
Boiling point (Celsius)
442.23
Boiling point (Kelvin)
715.38
General information
Molecular weight
168.15g/mol
Molar mass
168.1510g/mol
Density
1.3605g/cm3
Appearence

2,3-dihydroxy-4-methyl-benzoic acid appears as a crystalline solid. It has a white to off-white color and can form needle-like crystals when observed under a microscope.

Comment on solubility

Solubility of 2,3-Dihydroxy-4-methyl-benzoic Acid

2,3-Dihydroxy-4-methyl-benzoic acid, also known as a derivative of benzoic acid, exhibits noteworthy solubility characteristics. The presence of both hydroxyl (-OH) groups and a carboxylic acid group (-COOH) significantly influences its solubility in various solvents.

Factors contributing to its solubility include:

  • Polar Nature: The -OH and -COOH groups enhance the compound's polarity, enabling it to interact favorably with polar solvents.
  • Hydrogen Bonding: The ability of 2,3-dihydroxy-4-methyl-benzoic acid to form hydrogen bonds with water molecules increases its solubility in aqueous solutions.
  • Temperature Dependency: As is common with many organic acids, solubility may increase with temperature, making it more soluble at elevated temperatures.

In summary, this compound is likely to be:

  1. Soluble in water due to its polar moieties.
  2. More soluble in organic solvents that can engage in hydrogen bonding.
  3. Exhibiting varying solubility at different temperatures, generally increasing with heat.

Overall, the intricate balance of functional groups in 2,3-dihydroxy-4-methyl-benzoic acid plays a pivotal role in its solubility properties, making it a fascinating subject of study for chemists.

Interesting facts

Interesting Facts about 2,3-Dihydroxy-4-methyl-benzoic Acid

2,3-Dihydroxy-4-methyl-benzoic acid, often abbreviated as DHMBA, is a fascinating compound that belongs to the class of benzoic acids. Here are some intriguing aspects of this compound:

  • Biological Relevance: DHMBA is known for its presence in various natural products and has been studied for its potential biological activities, including its role as an antioxidant.
  • Synthetic Versatility: The chemical structure of DHMBA allows for numerous synthetic modifications. This makes it an important intermediate in the synthesis of more complex organic molecules.
  • Pharmaceutical Applications: The compound has been investigated for its possible applications in pharmaceuticals, particularly in developing anti-inflammatory drugs.
  • Research Interest: Due to its unique hydroxyl functional groups, DHMBA is a subject of interest in various fields, including medicinal chemistry and materials science.
  • Natural Sources: This compound has been isolated from certain plants, showcasing its role in the natural world and its potential benefits in human health.

As a scientist or student of chemistry, understanding the properties and behaviors of compounds like 2,3-dihydroxy-4-methyl-benzoic acid enhances our appreciation of organic chemistry's complexity and its interconnectedness with biological systems. The potential applications in medicine and materials further highlight the importance of this compound in both research and practical settings.

Synonyms
2,3-DIHYDROXY-4-METHYLBENZOIC ACID
3929-89-3
o-Pyrocatechuic acid, 4-methyl-
4-Methyl-o-pyrocatechuic acid
6R23QDE5VJ
DTXSID80192533
Benzoic acid, 2,3-dihydroxy-4-methyl-
DTXCID20115024
838-192-0
UNII-6R23QDE5VJ
2,3-dihydroxy-p-toluic acid
SCHEMBL857301
AKOS008119637
DA-17984
2,3-DIHYDROXY-4-METHYLBENZOICACID
CS-0248480
EN300-39965
G27461
Z367679376