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Methylparabens

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Identification
Molecular formula
C10H12O4
CAS number
54963-21-8
IUPAC name
2,3-dihydroxy-4-isopropyl-benzoic acid
State
State

At room temperature, the compound is typically in a solid state.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.00
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.00
General information
Molecular weight
211.21g/mol
Molar mass
211.2280g/mol
Density
1.3190g/cm3
Appearence

2,3-Dihydroxy-4-isopropyl-benzoic acid typically appears as an off-white to pale yellow crystalline solid. It is known for its tendency to form small, needle-like crystals.

Comment on solubility

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

2,3-Dihydroxy-4-isopropyl-benzoic acid, with its unique structure, exhibits notable solubility characteristics that are essential for its applications. Understanding the solubility of this compound involves several key factors:

  • Polar Functional Groups: The presence of hydroxyl groups (-OH) significantly enhances its solubility in polar solvents, especially water. These groups can form hydrogen bonds, which facilitate solvent interaction.
  • Hydrophobic Regions: The isopropyl group contributes to the hydrophobic nature of the compound, which can lead to decreased solubility in non-polar solvents.
  • pH Dependence: As a carboxylic acid, the solubility of 2,3-dihydroxy-4-isopropyl-benzoic acid may vary with pH. At lower pH levels, it exists primarily in its protonated form, which may affect solubility.
  • Temperature Effects: Solubility can also be influenced by temperature. Typically, an increase in temperature enhances solubility for most solutes, including this compound.

In summary, the solubility of 2,3-dihydroxy-4-isopropyl-benzoic acid is not a straightforward matter but depends on various interplaying factors. Its dual character as both a polar and non-polar entity makes it an intriguing subject for further research and application.

Interesting facts

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

2,3-Dihydroxy-4-isopropyl-benzoic acid, also known as IBU (Ibuprofen's structural isomer), is a fascinating compound in the world of organic chemistry. This compound showcases a unique combination of functional groups that contribute to its interesting chemical behavior and potential applications. Here are some noteworthy aspects:

  • Versatile Chemical Properties: The presence of hydroxyl (-OH) groups lends it significant polarity, making it more reactive in various organic reactions compared to its non-hydroxylated counterparts.
  • Biochemical Relevance: As a derivative of benzoic acid, this compound may hold potential in pharmaceutical research, especially in the study of anti-inflammatory properties similar to those exhibited by ibuprofen.
  • Applications in Synthesis: Owing to its structure, 2,3-dihydroxy-4-isopropyl-benzoic acid can serve as a valuable intermediate in the synthesis of more complex organic molecules, enabling scientists to design novel compounds.
  • Studying Isomerism: The exploration of such compounds can deepen one's understanding of stereochemistry, particularly how different functional groups can influence the biological activity and reactivity of a compound.

Moreover, research into this compound can lead to insights into metabolic pathways of similar molecules in the human body, enriching our comprehension of drug mechanisms and enhancing therapeutic efficacy.

Overall, 2,3-dihydroxy-4-isopropyl-benzoic acid not only fascinates with its structure but also opens doors to numerous applications in chemistry and medicine!

Synonyms
2,3-dihydroxy-p-cumic acid
2,3-DIHYDROXY-4-(1-METHYLETHYL)BENZOIC ACID
4-isopropyl-o-Pyrocatechuic acid
2,3-dihydroxy-4-(propan-2-yl)benzoic acid
2,3-dihydroxy-4-isopropylbenzoic acid
2,3-dihydroxy-4-propan-2-ylbenzoic acid
C06580
SCHEMBL2934039
CHEBI:16725
DTXSID70941138
Q27102045