4-(dimethylamino)butyliminomethanedithiol

Identification

Molecular formula

C₇H₁₆N₂S₂

CAS number

34562-31-7

IUPAC name

4-(dimethylamino)butyliminomethanedithiol

State

At room temperature, 4-(dimethylamino)butyliminomethanedithiol is typically in a liquid state.

Melting point (Celsius)

-2.00

Melting point (Kelvin)

271.15

Boiling point (Celsius)

240.00

Boiling point (Kelvin)

513.15

General information

Molecular weight

191.35g/mol

Molar mass

191.3500g/mol

Density

1.0200g/cm³

Appearence

4-(dimethylamino)butyliminomethanedithiol appears as a pale yellow liquid with a characteristic amine-like odor. The compound may darken upon prolonged exposure to light and air.

Comment on solubility

Solubility of 4-(dimethylamino)butyliminomethanedithiol

The solubility of 4-(dimethylamino)butyliminomethanedithiol can be examined through several factors that influence its behavior in various solvents. Here are some key points to consider:

Polarity: The presence of both dimethylamino and thiol groups contributes to the compound's polar nature, which generally promotes solubility in polar solvents such as water.
Functional Groups: The presence of the aminomethanedithiol component may enhance solubility due to its ability to form hydrogen bonds, which can facilitate interaction with solvent molecules.
pH Sensitivity: The solubility may also vary with changes in pH. Under strongly acidic or basic conditions, protonation or deprotonation of the amine groups can alter the compound’s solubility profile.
Temperature Effects: An increase in temperature usually increases solubility, allowing the compound to dissolve more readily in a suitable solvent.

In summary, while 4-(dimethylamino)butyliminomethanedithiol demonstrates potential solubility in polar solvents due to its functional groups and molecular structure, the extent to which it dissolves can depend on external factors such as pH and temperature. Understanding these variables is essential when considering the practical applications of this compound.

Interesting facts

Interesting Facts about 4-(Dimethylamino)butyliminomethanedithiol

4-(Dimethylamino)butyliminomethanedithiol is a unique compound with intriguing chemical properties and potential applications. Here are some key points that make it noteworthy:

Versatile Applications: This compound is primarily used in the synthesis of various organic molecules. Its functional groups enable it to act as a versatile building block in chemical reactions.
Role as a Ligand: The presence of thiol (-SH) groups suggests that it can act as a ligand in coordination chemistry. Ligands are essential in the formation of metal complexes, which play significant roles in catalysis and materials science.
Biological Interest: Compounds containing thiol groups have been studied for their biological activity. They can participate in redox reactions that are vital for cellular processes, making this compound potentially interesting for biomedical research.
Stability and Reactivity: The imino group (-C=N-) within the structure contributes to the compound's stability while also making it reactive under certain conditions, which is valuable for synthetic chemists seeking to create new materials.
Synthetic Pathways: The synthesis of 4-(dimethylamino)butyliminomethanedithiol often involves multi-step organic reactions, showcasing the creativity and complexity involved in organic chemistry.

In summary, the compound 4-(dimethylamino)butyliminomethanedithiol stands out due to its multifunctionality and the potential it holds in various fields such as chemical synthesis, coordination chemistry, and biochemistry. As scientists continue to explore the intricacies of chemical behavior, compounds like this one can lead to significant advancements in our understanding and application of chemical science.