2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol

Identification

Molecular formula

C₅H₁₀N₂S₄

CAS number

1069-54-1

IUPAC name

2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol

State

At room temperature, it remains in a liquid state, characterized by its oily appearance and pungent smell due to the presence of thiol groups.

Melting point (Celsius)

-35.00

Melting point (Kelvin)

238.15

Boiling point (Celsius)

113.00

Boiling point (Kelvin)

386.15

General information

Molecular weight

176.33g/mol

Molar mass

176.3300g/mol

Density

1.3300g/cm³

Appearence

The compound appears as a colorless to pale yellow liquid. It is typically clear and oily in texture with a characteristic sulfuric odor, common to thiol-containing compounds.

Comment on solubility

Solubility of 2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol

The solubility of 2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol is an important aspect to consider, especially regarding its potential applications and interactions in various chemical environments. Here are some key points regarding its solubility:

General Solubility: This compound is expected to have modest solubility in polar solvents due to the presence of multiple thiol (-SH) groups, which can engage in hydrogen bonding.
Aqueous Solubility: It is likely to be more soluble in water compared to non-polar solvents owing to its polar nature.
pH Dependence: The solubility can significantly vary with changes in pH levels, as the ionization of thiol groups may be affected.
Temperature Influence: Increased temperature typically enhances solubility, potentially making this compound more soluble at elevated temperatures.

In conclusion, the solubility characteristics of 2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol highlight its potential utility in various formulations and applications, but further experimental data may be required for specific solubility benchmarks.

Interesting facts

Discovering 2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol

2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol is a fascinating compound that belongs to the family of dithiols, which are characterized by the presence of two thiol (–SH) groups. Here are some intriguing insights into this compound that highlight its significance in chemistry:

Biological Relevance: Compounds containing thiol groups play a crucial role in biological processes. They are key in protein function and enzyme activity due to their ability to form disulfide bonds, which stabilize protein structures.
Versatile Reactivity: The presence of both amine and thiol functional groups means that 2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol can participate in a variety of chemical reactions, making it an excellent candidate for synthetic applications in organic chemistry.
Potential Applications: This compound has potential uses in the development of pharmaceutical agents. The thiol groups can act as reducing agents or as ligands in metal complexes, which are often used in medicinal chemistry.
Material Science: Its unique structure may also lend itself to applications in material science, particularly in creating materials with specific chemical properties, such as enhanced conductivity or stability.

In the words of a noted chemist, “The beauty of chemical compounds lies not just in their structures but in the myriad of possibilities they present.” The discovery and study of compounds like 2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol serve as a testament to this notion, opening doors to new research and innovative solutions in various fields.

In summary, 2-[bis(sulfanyl)methyleneamino]propyliminomethanedithiol is more than just a complex molecule; it is a bridge to understanding essential biochemical processes and driving advancements in science. Its unique properties make it a compound worthy of attention and further exploration.