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(4-aminophenyl)mercury

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Identification
Molecular formula
C6H7HgN
CAS number
100-65-2
IUPAC name
(4-aminophenyl)mercury
State
State

This compound is generally a solid at room temperature.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
307.74g/mol
Molar mass
307.7380g/mol
Density
3.3000g/cm3
Appearence

(4-Aminophenyl)mercury typically appears as a white crystalline solid.

Comment on solubility

Solubility of (4-aminophenyl)mercury

(4-aminophenyl)mercury, with the chemical formula C6H6HgN, exhibits notable solubility characteristics that are important to consider. The solubility of this compound can vary significantly depending on several factors such as:

  • Solvent Type: Generally, (4-aminophenyl)mercury is more soluble in polar solvents such as methanol and dimethyl sulfoxide (DMSO) due to the presence of the amino group, which increases hydrogen bonding capabilities.
  • Temperature: Higher temperatures often enhance the solubility of many organic compounds, and (4-aminophenyl)mercury may follow this trend as well.
  • pH Level: Because it contains an amino group, the solubility can also be affected by the acidity or basicity of the solution, influencing the ionization state of the compound.

In alkaline conditions, (4-aminophenyl)mercury tends to exhibit increased solubility compared to neutral or acidic environments. As a result, it is crucial for researchers to consider these factors during experiments involving this compound.

In summary, understanding the solubility of (4-aminophenyl)mercury not only aids in predicting behavior in various chemical environments but also informs safe handling and application. For those interacting with this compound, "Knowing the solvent is the key to unlocking solubility!"

Interesting facts

Interesting Facts About (4-Aminophenyl)mercury

(4-Aminophenyl)mercury is a fascinating organomercury compound with unique properties and applications. Here are some crucial aspects that make it noteworthy:

  • Structure and Bonding: This compound features a mercury atom bonded to an aromatic ring, specifically a para-aminophenyl group. The presence of the amino group (-NH2) introduces interesting *polar characteristics* that influence the compound's reactivity.
  • Biological Significance: Organomercury compounds like (4-aminophenyl)mercury have raised significant interest in biochemistry. They are studied for their potential effects on biological systems, serving as models to understand mercury's toxicity and its impact on health.
  • Applications in Research: This compound has been instrumental in various research endeavors, particularly in the field of *neuroscience*. It can be used as a tool to study the properties of certain enzymes and protein interactions in biological organisms.
  • Analytical Chemistry: (4-Aminophenyl)mercury is also valued in *analytical chemistry* as a reagent. Its reactivity can aid in the detection and quantification of other compounds, showcasing its versatility in laboratory settings.
  • Caution Required: Due to the toxic nature of mercury, compounds containing mercury should be handled with extreme care. Understanding their chemistry is crucial not only for applications but also for *safety protocols* in chemical laboratories.

In summary, (4-aminophenyl)mercury serves as an intriguing compound that exemplifies the relationship between chemical structure, reactivity, and biological impact. Its study not only contributes to the understanding of *organometallic chemistry* but also prompts discussions about safety in handling toxic substances.

Synonyms
SCHEMBL7153201