Pentyliminomethanedithiol | Solubility of Things

Identification

Molecular formula

C₆H₁₃NS₂

CAS number

35777-21-0

IUPAC name

pentyliminomethanedithiol

State

This compound is a liquid at room temperature.

Melting point (Celsius)

-36.00

Melting point (Kelvin)

237.15

Boiling point (Celsius)

255.00

Boiling point (Kelvin)

528.15

General information

Molecular weight

179.33g/mol

Molar mass

179.3280g/mol

Density

1.0384g/cm³

Appearence

Pentyliminomethanedithiol typically appears as a pale yellow liquid and has a strong, unpleasant odor.

Comment on solubility

Solubility of Pentyliminomethanedithiol

Pentyliminomethanedithiol, with its intriguing molecular structure, showcases diverse solubility properties that can be influenced by various factors. This compound is known to exhibit the following characteristics when it comes to solubility:

Polar Solvents: Pentyliminomethanedithiol is generally more soluble in polar solvents due to the presence of thiol (-SH) groups, which can engage in hydrogen bonding.
Non-Polar Solvents: In non-polar solvents, the solubility may be limited. The longer pentyl chain can enhance solubility in certain non-polar environments, but it is not guaranteed.
Temperature Dependence: Like many compounds, solubility can increase with temperature. Warm solvents can often dissolve more of the compound, making heat an important factor in solubility.
pH Effects: The ionization state of the thiol groups can be affected by pH, thus altering solubility. A change in pH may either increase or decrease solubility depending on the environment.

In summary, the solubility of pentyliminomethanedithiol is a multifaceted topic influenced by factors such as solvent polarity, temperature, and pH. Understanding these aspects is crucial for optimizing its applications in various chemical processes.

Interesting facts

Interesting Facts about Pentyliminomethanedithiol

Pentyliminomethanedithiol is a fascinating compound that has garnered attention for its unique structural characteristics and potential applications in various fields. Here are some engaging insights about this compound:

Structural Diversity: The presence of the iminomethane moiety combined with two thiol groups gives pentyliminomethanedithiol its unique reactivity and bonding capabilities. This makes it a versatile building block in synthetic organic chemistry.
Functional Applications: This compound can be a key player in the synthesis of ligands in coordination chemistry. The thiol groups have a strong affinity for metals, making it useful in creating metal complexes.
Research Potential: Scientists are exploring the use of pentyliminomethanedithiol in areas such as catalysis and drug delivery. The thiol groups can participate in various reactions that can lead to the development of new materials with specific properties.
Natural Interactions: Thiols are known for their role in biological systems. They can participate in enzyme catalysis and are involved in important physiological processes such as protein folding and redox reactions.
Environmental Considerations: As research continues, it becomes essential to evaluate the environmental impacts of compounds like pentyliminomethanedithiol, especially considering the reactivity of thiols and their potential interactions in the ecosystem.

In conclusion, pentyliminomethanedithiol is more than just a chemical compound; it represents the intersection of innovation and application in the field of chemistry. As scientists continue to study its properties and potential uses, this molecule could pave the way for new advancements in materials science and other interdisciplinary areas.