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Ibuprofen

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Identification
Molecular formula
C13H18O2
CAS number
15687-27-1
IUPAC name
3-(1,1-dimethylpropyl)-2-hydroxy-6-methyl-benzoic acid
State
State

At room temperature, ibuprofen is in a solid state.

Melting point (Celsius)
76.00
Melting point (Kelvin)
349.15
Boiling point (Celsius)
157.00
Boiling point (Kelvin)
430.15
General information
Molecular weight
206.28g/mol
Molar mass
206.2830g/mol
Density
1.0360g/cm3
Appearence

Ibuprofen appears as a white crystalline solid. It is commonly available in powdered form or as tablets in commercial preparations for medical use.

Comment on solubility

Solubility of 3-(1,1-dimethylpropyl)-2-hydroxy-6-methyl-benzoic acid

3-(1,1-dimethylpropyl)-2-hydroxy-6-methyl-benzoic acid, typically known in the chemical world as an interesting organic compound, exhibits a particular solubility behavior that can be described as follows:

  • Solvent Compatibility: Due to its hydrophobic alkyl groups, this compound generally shows low solubility in water.
  • Organic Solvents: It is more likely to dissolve in organic solvents such as ethanol, acetone, or dichloromethane.
  • pH Dependence: The presence of the carboxylic acid group suggests that solubility can be affected by the pH of the solution, potentially increasing in basic conditions due to deprotonation.

In summary, the solubility of 3-(1,1-dimethylpropyl)-2-hydroxy-6-methyl-benzoic acid is greatly influenced by the:

  1. The nature of the solvent
  2. The pH level of the solution
  3. The molecular structure that affects interactions with solvent molecules

As a result, understanding its solubility characteristics is crucial for applications and experimentation involving this compound.

Interesting facts

Interesting Facts about 3-(1,1-dimethylpropyl)-2-hydroxy-6-methyl-benzoic acid

3-(1,1-dimethylpropyl)-2-hydroxy-6-methyl-benzoic acid, commonly referred to as a derivative of salicylic acid, is a fascinating compound with various applications and implications in both organic chemistry and industrial use. Below are some engaging insights regarding this compound:

  • Structural Significance: The compound features a benzoic acid core, which is a crucial structure in many naturally occurring substances. The presence of additional functional groups provides unique properties that enhance its versatility.
  • Biological Activity: This compound belongs to a class known for their anti-inflammatory and analgesic properties. The hydroxyl (-OH) group attached to the benzene ring is essential for its biological activity and is a common motif in pharmaceuticals.
  • Synthetic Applications: The synthetic pathways leading to the formation of this compound often involve the use of advanced organic reactions such as esterification and hydrolysis, highlighting the creativity and complexity of organic synthesis.
  • Industrial Relevance: Its derivatives are used in various sectors, including cosmetics and food preservation, due to their stability and effectiveness as preservatives. They help in maintaining product shelf-life and preventing microbial growth.
  • Environmental Impact: As with many organic compounds, understanding the degradation and impact of this compound on the environment is crucial. Research in this area emphasizes the need for sustainable chemical practices.

In summary, 3-(1,1-dimethylpropyl)-2-hydroxy-6-methyl-benzoic acid represents a compelling intersection of medicinal chemistry and industrial utility. Its multifaceted applications and role in natural products continue to inspire research and innovation. As researchers explore new synthetic routes and applications, the potential for this compound within various scientific fields remains vast.

Synonyms
2,6-CRESOTIC ACID, 3-tert-PENTYL-
BRN 2845570
3-tert-Pentyl-2,6-cresotic acid
2-Methyl-5-tert-amylsalicylic acid
20717-19-5
DTXSID40174779
DTXCID7097270
RefChem:248076
SCHEMBL9249361