Skip to main content

Thiomersal

ADVERTISEMENT
Identification
Molecular formula
C9H9HgNO2S
CAS number
54-64-8
IUPAC name
chloro-[3-(2,4-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury
State
State

Thiomersal is typically in a solid state at room temperature.

Melting point (Celsius)
232.00
Melting point (Kelvin)
505.15
Boiling point (Celsius)
322.00
Boiling point (Kelvin)
595.15
General information
Molecular weight
404.82g/mol
Molar mass
404.8150g/mol
Density
2.4970g/cm3
Appearence

Thiomersal appears as a white or slightly yellow crystalline powder.

Comment on solubility

Solubility of Chloro-[3-(2,4-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury

The solubility of chloro-[3-(2,4-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury can be quite complex due to its unique molecular structure. Here are some key points to consider:

  • Polar vs. Nonpolar: This compound includes polar functional groups which can influence its solubility in polar solvents, such as water.
  • Mercury Component: The presence of mercury can often lead to lower solubility in aqueous solutions, reflecting metal ion behavior in various solvents.
  • Interactions: The dioxoimidazolidin moiety may enhance interactions with similar polar solvents, potentially increasing the solubility compared to aliphatic compounds.

Overall, the solubility of this compound is influenced by:

  1. The nature of solvents, with *polar solvents* likely offering better solubility.
  2. The *steric effects* of bulky groups which can inhibit close packing in solution.
  3. The *ionic nature* of the chloromercury group which may alter interactions with the solvent.

As a result, while some solubility can be anticipated in appropriate solvents, it is crucial to conduct experimental assessments to determine the exact solubility behavior of chloro-[3-(2,4-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury in various conditions.

Interesting facts

Interesting Facts about Chloro-[3-(2,4-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury

Chloro-[3-(2,4-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury is a fascinating compound that combines the properties of mercury with intriguing organic moieties. Here are some captivating aspects of this compound:

  • Mercury Complex: Being a mercury compound, it exhibits unique reactivity patterns compared to other organometallic compounds, which can lead to various applications in organic synthesis.
  • Biological Interest: The imidazolidinone part of its structure may possess interesting biological activities due to the presence of the dioxo group, potentially influencing its interaction with biological systems.
  • Pharmaceutical Applications: Compounds containing imidazolidinone rings are often investigated in medicinal chemistry for their potential therapeutic effects, such as antimicrobial and anticancer activities.
  • Environmental Impact: As with many mercury-containing compounds, the environmental impact and toxicity of chloro-[3-(2,4-dioxoimidazolidin-1-yl)-2-methoxy-propyl]mercury necessitate careful handling and assessment.

In summary, this compound is a noteworthy member of the organomercury family, bridging the gap between organic chemistry and potential biological applications. Researchers are continually exploring its properties and implications in various fields, from synthetic chemistry to pharmacology. As always, the balance between utility and safety remains a crucial focus when working with mercury compounds.

Synonyms
MERCURY, CHLORO(3-(2,4-DIOXO-1-IMIDAZOLIDINYL)-2-METHOXYPROPYL)-
3367-32-6
1-(3-Chloromercuri-2-methoxy)propylhydantoin
1-(3-Chloromercuri-2-methoxy-1-propyl)-hydantoin
Hydantoin, 1-(3-(chloromercuri)-2-methoxypropyl)-