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Thimerosal

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Identification
Molecular formula
C9H9HgNaO2S
CAS number
54-64-8
IUPAC name
sodium;ethylmercury(1+);2-sulfido-1,3-benzoxazole-5-carboxylate
State
State

Thimerosal is a solid at room temperature.

Melting point (Celsius)
234.00
Melting point (Kelvin)
507.15
Boiling point (Celsius)
150.00
Boiling point (Kelvin)
423.15
General information
Molecular weight
404.83g/mol
Molar mass
404.8280g/mol
Density
2.9000g/cm3
Appearence

Thimerosal is an odorless, crystalline white powder.

Comment on solubility

Solubility of Sodium Ethylmercury(1+)-2-sulfido-1,3-benzoxazole-5-carboxylate

The solubility of sodium ethylmercury(1+)-2-sulfido-1,3-benzoxazole-5-carboxylate can be characterized by its unique chemical structure, which influences its interaction with solvents. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is likely soluble in polar solvents due to the presence of ionic characteristics from the sodium and mercury components.
  • Concentration Effects: As with many chemical compounds, solubility can be affected by concentration; higher concentrations may lead to different solubility behaviors.
  • Temperature Influence: Increased temperature often enhances solubility, particularly for compounds with large molecular structures.
  • pH Sensitivity: Changes in pH can also alter solubility, as the carboxylate group may ionize in alkaline conditions, potentially increasing solubility in such environments.
  • Complexation: The presence of sulfido groups and the benzoxazole ring may allow for complexation with certain metal ions, which could further enhance solubility in specific conditions.

In conclusion, understanding the solubility behavior of sodium ethylmercury(1+)-2-sulfido-1,3-benzoxazole-5-carboxylate requires consideration of various factors, emphasizing the interplay between its chemical structure and environmental conditions. As noted, "solubility is not merely a property, but a dynamic characteristic influenced by multiple variables."

Interesting facts

Interesting Facts About Sodium Ethylmercury(1+)-2-Sulfido-1,3-Benzoxazole-5-Carboxylate

Sodium ethylmercury(1+)-2-sulfido-1,3-benzoxazole-5-carboxylate is a fascinating compound that intertwines elements of organic chemistry and biochemistry. Here are some noteworthy aspects of this compound:

  • Mercury Complex: This compound is part of a class known as organomercury compounds, which are characterized by the presence of mercury bonded to organic groups. These compounds have unique properties and uses.
  • Biological Applications: Sodium ethylmercury(1+) is often researched for its potential applications in biological systems, including its interaction with enzymes and proteins. Its structure allows it to participate in chemical reactions that can modify biological activity.
  • Stability and Reactivity: The presence of the ethyl group alongside the mercury contributes to the **stability** and **reactivity** of the compound. This makes it of interest in various chemical syntheses and explorations.
  • Environmental Concerns: With mercury compounds raising ecological concerns, studies on sodium ethylmercury(1+) often emphasize the need to understand its lifecycle and moral implications in research and industrial applications.
  • Unique Functional Groups: The benzoxazole component in this compound introduces significant biochemical characteristics, contributing to its potential pharmacological properties and the ability to act in specific biological systems.

Due to its unique combination of elements and structures, sodium ethylmercury(1+-)2-sulfido-1,3-benzoxazole-5-carboxylate stands as a bridge between chemistry and biology, shedding light on both the benefits and dangers of organomercury compounds. It's a vivid reminder of how intricate and fascinating the world of chemical compounds can be!