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Thimerosal

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Identification
Molecular formula
C9H9HgNaO2S
CAS number
54-64-8
IUPAC name
[3-[(3-carboxylato-2,2,3-trimethyl-cyclopentanecarbonyl)amino]-2-methoxy-propyl]mercury(1+);hydron;2-sulfidoacetate
State
State

Thimerosal is typically a solid at room temperature.

Melting point (Celsius)
234.00
Melting point (Kelvin)
507.15
Boiling point (Celsius)
200.00
Boiling point (Kelvin)
473.15
General information
Molecular weight
404.82g/mol
Molar mass
404.8180g/mol
Density
2.4500g/cm3
Appearence

Thimerosal is a powder that is typically white or slightly beige in color. It is crystalline in appearance.

Comment on solubility

Solubility of [3-[(3-carboxylato-2,2,3-trimethyl-cyclopentanecarbonyl)amino]-2-methoxy-propyl]mercury(1+);hydron;2-sulfidoacetate

The solubility of complex compounds like [3-[(3-carboxylato-2,2,3-trimethyl-cyclopentanecarbonyl)amino]-2-methoxy-propyl]mercury(1+];hydron;2-sulfidoacetate can vary significantly based on several factors. Here are some key points to consider:

  • Molecular Structure: The presence of functional groups such as carboxylate and methoxy can enhance solubility by facilitating interactions with water.
  • Polarity: More polar compounds tend to be more soluble in polar solvents like water. This compound's structure suggests it may possess polar characteristics due to its ionic mercury(1+) species and carboxylate groups.
  • pH and Ionic Strength: The solubility of this compound could also depend on the pH of the solution and the ionic strength. Important species such as the hydron can affect these properties.
  • Temperature: Increased temperature usually leads to higher solubility for most salts and organic compounds; however, this may not hold true for all compounds.

In summary, while the solubility of [3-[(3-carboxylato-2,2,3-trimethyl-cyclopentanecarbonyl)amino]-2-methoxy-propyl]mercury(1+];hydron;2-sulfidoacetate may be influenced by its molecular structure and environmental conditions, empirical solubility data should be consulted for precise measurements. Understanding solubility behavior is crucial in chemical applications, especially in biological and environmental contexts.

Interesting facts

Exciting Insights into 3-[(3-carboxylato-2,2,3-trimethyl-cyclopentanecarbonyl)amino]-2-methoxy-propyl]mercury(1+);hydron;2-sulfidoacetate

This complex compound, characterized by its unique structure and functional groups, presents a fascinating study for chemists and students alike. Below are some intriguing aspects:

  • Mercury Interactions: The presence of mercury in this compound highlights its relevance in organometallic chemistry. Mercury compounds are notable for their diverse roles in catalysis and their potential applications in pharmaceuticals.
  • Functional Diversity: The presence of multiple functional groups, including the carboxylato and methoxy groups, enables this compound to participate in various chemical reactions, leading to potential applications in organic synthesis.
  • Biological Relevance: The incorporation of sulfur via sulfidoacetate suggests potential biological activity. Compounds that contain sulfur are essential for many biochemical processes and may offer insights into new medicinal chemistry pathways.
  • Polarity and Solubility: The combination of hydrophobic and hydrophilic components in the molecular structure could affect the compound's overall polarity, influencing its behavior in biological systems and its solubility in various solvents.
  • Structural Complexity: The cyclopentanecarbonyl moiety adds a layer of structural complexity that makes this compound a valuable candidate for the study of molecular interactions and geometric configurations.

Overall, 3-[(3-carboxylato-2,2,3-trimethyl-cyclopentanecarbonyl)amino]-2-methoxy-propyl]mercury(1+);hydron;2-sulfidoacetate serves as a striking example of the intricate relationship between molecular structure and functional properties, offering substantial potential for further research and exploration in various fields of chemistry.

Synonyms
MERCAPTOMERIN
Mercaptomerine
Thiomerin
Mercaptomerina
Mercaptomerinum
20223-84-1
58TLO7I2HN
DTXSID901046256
Mercury, (3-(3-carboxy-2,2,3-trimethylcyclopentanecarboxamido)-2-methoxypropyl)(hydrogen mercaptoacetato)-
DTXCID701505915
3-((3-(((carboxymethyl)sulfanyl)mercurio)-2-methoxypropyl)carbamoyl)-1,2,2-trimethylcyclopentane-1-carboxylic acid
Diucardyn
Diucardyn sodium
Mercaptomerine sodique
RefChem:156556
Sodium mercaptomerin
Thiomerin sodium
[3-[(3-carboxylato-2,2,3-trimethylcyclopentanecarbonyl)amino]-2-methoxypropyl]mercury(1+);hydron;2-sulfidoacetate
Mercaptomerin [INN:BAN]
Mercaptomerine [INN-French]
Mercaptomerinum [INN-Latin]
Mercaptomerina [INN-Spanish]
HSDB 3356
UNII-58TLO7I2HN
N-(gamma-Carboxymethyl-mercapto-mercuri-beta methoxy)propyl camphoramic acid
Mercurate(2-), (3-(((3-carboxylato-2,2,3-trimethylcyclopentyl)carbonyl)amino)-2-methoxypropyl)(mercaptoacetato(2-)-O,S)-, dihydrogen, (T-4)-
SCHEMBL1650120
Mercurate(2-), (3-(((3-carboxylato-2,2,3-trimethylcyclopentyl)carbonyl)amino)-2-methoxypropyl)((mercapto-kappaS)acetato(2-)-kappaO)-, dihydrogen, (T-4)-