Skip to main content

2,4,6-Tribromophenol

ADVERTISEMENT
Identification
Molecular formula
C6H3Br3O
CAS number
118-79-6
IUPAC name
bismuthane;2,4,6-tribromophenol
State
State

At room temperature, 2,4,6-tribromophenol is in a solid state.

Melting point (Celsius)
93.00
Melting point (Kelvin)
366.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
330.81g/mol
Molar mass
330.8140g/mol
Density
2.7630g/cm3
Appearence

2,4,6-Tribromophenol appears as a white crystalline solid with a characteristic phenolic odor.

Comment on solubility

Solubility of Bismuthane and 2,4,6-Tribromophenol

The solubility characteristics of bismuthane (Bismuth or Bismuth(III) hydride) and 2,4,6-tribromophenol, a brominated phenolic compound, present an interesting landscape in terms of their interactions with solvents. Here’s an overview:

Bismuthane (BiH3)

  • Solubility: Bismuthane is known for its low solubility in water.
  • Solvent Interaction: However, it is soluble in non-polar solvents such as benzene or toluene.
  • Behavior in Water: When it comes to aqueous solutions, bismuthane does not dissolve well, which can be attributed to its hydrophobic behavior.

2,4,6-Tribromophenol (C12Br3O)

  • Water Solubility: This compound exhibits moderate solubility in water, making it somewhat accessible for aqueous applications.
  • Organic Solvents: It is more soluble in organic solvents, such as ethanol and acetone, due to its non-polar nature.
  • Applications: Its solubility profile is critical when considering its use in pharmaceutical formulations and chemical syntheses.

In summary, while bismuthane shows a pronounced preference for non-polar environments, 2,4,6-tribromophenol demonstrates versatility with moderate water solubility and enhanced solubility in organic solvents. This duality in solubility plays a significant role in their practical applications and interactions within chemical processes.

Interesting facts

Interesting Facts About Bismuthane; 2,4,6-Tribromophenol

Bismuthane, often referred to in conjunction with its derivative compound 2,4,6-tribromophenol, showcases a remarkable intersection between *organometallic chemistry* and *halogenated phenolic compounds*. Here are some fascinating insights about these substances:

  • Bismuthane: This compound forms a part of the broader group of organobismuth compounds, where bismuth acts similarly to heavy metals like lead and tin. This is interesting since bismuth is known for its low toxicity compared to other heavy elements, making it a safer alternative in various applications.
  • 2,4,6-Tribromophenol: As a *halogenated phenol*, this compound exhibits unique *antimicrobial properties*. Its structure facilitates the disruption of microbial cell walls, making it a popular choice in disinfectants and preservatives.
  • Applications: The combination of these compounds opens avenues for research in areas such as:
    • Medicinal chemistry, where derivatives are explored for potential antibiotic properties.
    • Material science, focusing on the development of flame retardants due to the presence of bromine.
  • Environmental Concerns: The use of halogenated compounds like 2,4,6-tribromophenol raises discussions about environmental impact, particularly regarding *brominated flame retardants* and their persistence in the ecosystem. Awareness and regulatory measures are essential in mitigating these risks.
  • Research Opportunities: The synthesis and study of bismuthane and 2,4,6-tribromophenol are subjects of ongoing research, especially within the context of *green chemistry*. Investigating alternative methods for synthesis that minimize waste and hazardous reagents is a key focus.

In conclusion, both bismuthane and 2,4,6-tribromophenol underline the significant role of chemical compounds in advancing science, while also urging us to consider their implications on health and the environment. As chemists and researchers delve deeper, the potential for innovative applications and sustainable practices continues to unfold.