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3,4-Dibromophenol

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Identification
Molecular formula
C6H4Br2O
CAS number
610-97-9
IUPAC name
3,4-dibromophenol
State
State

State at Room Temperature:

3,4-Dibromophenol is typically found in a solid state at room temperature.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
286.50
Boiling point (Kelvin)
559.65
General information
Molecular weight
251.90g/mol
Molar mass
251.9030g/mol
Density
2.2290g/cm3
Appearence

3,4-Dibromophenol appears as a white to light yellow crystalline solid. It has a characteristic phenolic odor. The compound is relatively stable under normal conditions but may darken on prolonged exposure to air and light.

Comment on solubility

Solubility of 3,4-Dibromophenol

3,4-Dibromophenol, with the chemical formula C6H4Br2O, exhibits interesting solubility characteristics in various solvents. This compound is primarily categorized as a **polar organic compound**, affecting its solubility profiles:

  • Water: 3,4-Dibromophenol shows moderate solubility in water. The presence of the hydroxyl (-OH) group contributes to its ability to dissolve, although the bromine substitutions may hinder extensive solvation.
  • Organic Solvents: It is more soluble in organic solvents such as ethanol, acetone, and ether due to the hydrophobic nature of the bromine atoms, which can interact favorably with non-polar environments.
  • Temperature Effects: Like many organic compounds, solubility can increase with temperature. Higher temperatures generally enhance the solubility of 3,4-dibromophenol in both polar and non-polar solvents.

In summary, the solubility of 3,4-dibromophenol is influenced by polarity, hydrogen bonding abilities, and the presence of bromine atoms. Understanding these factors helps in predicting its behavior in various chemical environments, making it essential in applications ranging from synthesis to environmental chemistry.

Interesting facts

Interesting Facts about 3,4-Dibromophenol

3,4-Dibromophenol is an intriguing organic compound that belongs to the class of brominated phenols. This compound is notable not only for its structure but also for its diverse applications and significance in various fields.

Key Features

  • Bromination Reaction: The presence of two bromine atoms in its structure significantly enhances the compound's reactivity. It can undergo various chemical reactions, making it useful in synthetic organic chemistry.
  • Antimicrobial Properties: Studies have shown that 3,4-dibromophenol exhibits antimicrobial activities, which suggests its potential use in formulations aimed at preventing bacterial growth.
  • Environmental Impact: Being a brominated compound, it raises concerns regarding its environmental persistence and potential ecotoxicity. It serves as a reminder of the need for responsible chemical usage.
  • Precursor in Chemical Synthesis: This compound is utilized as a precursor in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.
  • Research Applications: 3,4-Dibromophenol is often used in laboratory research to study the effects of brominated compounds on biological systems.

Significance in Science

As researchers and chemists expand their understanding of dibrominated phenols, compounds like 3,4-dibromophenol illustrate the complex interplay between chemical structure and biological activity. The exploration of its properties provides insights into brominated compounds' broader role in organic chemistry and environmental science. Ultimately, it serves as a reminder of how even simple compounds can have multifaceted implications.


In summary, 3,4-dibromophenol is more than just a chemical formula; it represents a window into the fascinating interactions of organic molecules with biological systems and the environment.

Synonyms
3,4-DIBROMOPHENOL
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