4-(Diethylamino)butyliminomethanedithiol

Identification

Molecular formula

C₉H₁₉N₂S₂

CAS number

107316-88-1

IUPAC name

4-(diethylamino)butyliminomethanedithiol

State

At room temperature, 4-(diethylamino)butyliminomethanedithiol is typically found in a liquid state. It should be stored under inert conditions to prevent degradation.

Melting point (Celsius)

-10.00

Melting point (Kelvin)

263.15

Boiling point (Celsius)

245.00

Boiling point (Kelvin)

518.15

General information

Molecular weight

207.39g/mol

Molar mass

207.3910g/mol

Density

0.9870g/cm³

Appearence

4-(Diethylamino)butyliminomethanedithiol typically appears as a yellow to brown liquid with a characteristic odor. Due to its chemical nature, it may darken upon exposure to air or light.

Comment on solubility

Solubility of 4-(diethylamino)butyliminomethanedithiol

The solubility of 4-(diethylamino)butyliminomethanedithiol is influenced by several factors, including its molecular structure, functional groups, and polarity. Understanding these characteristics can shed light on its solubility behavior:

Polarity: Due to the presence of the diethylamino group, which is polar, this compound tends to exhibit moderate solubility in polar solvents such as water.
Hydrogen Bonding: The thio groups in the structure can form hydrogen bonds, which may enhance solubility in solvents that can engage in hydrogen bonding.
Alkyl Chain: The butyl chain contributes to hydrophobicity, which can control solubility in non-polar solvents.

In summary, 4-(diethylamino)butyliminomethanedithiol is likely to have moderate solubility characteristics, showing better solubility in polar solvents while also being influenced by the hydrophobic nature of its alkyl groups. Understanding the interactions with different solvents is key to predicting its behavior in various applications.

Interesting facts

Interesting Facts about 4-(diethylamino)butyliminomethanedithiol

The compound 4-(diethylamino)butyliminomethanedithiol is a fascinating member of the class of thiol compounds, known for their unique properties and diverse applications. Here are some intriguing aspects of this compound:

Structure and Synthesis: This compound features a distinctive structure that includes both amine and thiol functional groups, which contribute to its reactivity. The synthesis often involves the reaction of various amines with thiol compounds, leading to interesting mechanistic pathways.
Biological Significance: Compounds like 4-(diethylamino)butyliminomethanedithiol may play a role in biological processes. Thiols are known for their antioxidant properties, which are crucial in protecting cells from oxidative stress.
Reactivity: The presence of multiple functional groups makes this compound a versatile building block in organic synthesis. Its ability to act as a donor of electrons or form coordination complexes is of particular interest in coordination chemistry.
Applications: This compound and its derivatives are utilized in various fields, including:
- Pharmaceuticals - as potential drug intermediates.
- Material Science - in the development of polymers and coatings.
- Chemical Research - in studies involving catalysts and reagents.
Safety and Handling: Due to the inclusion of sulfur in its structure, care must be taken when handling this compound. Proper laboratory practices and safety measures are essential to avoid potential hazards.

In summary, 4-(diethylamino)butyliminomethanedithiol is not just a chemical entity; it serves as a vital tool in research and application across numerous scientific disciplines. Its complex structure provides numerous avenues for exploration and innovation.