Skip to main content

Cysteamine thiocarboxamide

ADVERTISEMENT
Identification
Molecular formula
C3H8N2S2
CAS number
556-58-5
IUPAC name
2-aminoethylsulfanylmethanimidothioic acid
State
State

At room temperature, Cysteamine thiocarboxamide is typically a solid. It is known to absorb moisture from the air due to its hygroscopic nature.

Melting point (Celsius)
70.00
Melting point (Kelvin)
343.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
122.15g/mol
Molar mass
122.2020g/mol
Density
1.1730g/cm3
Appearence

This compound typically appears as a colorless to pale yellow solid or crystalline powder. It is hygroscopic and may have a slight amine-like odor.

Comment on solubility

Solubility of 2-aminoethylsulfanylmethanimidothioic Acid

The solubility of 2-aminoethylsulfanylmethanimidothioic acid can be influenced by various factors, including its molecular structure and the presence of functional groups. This compound is characterized by the presence of amino and thio groups, which often enhance its interaction with polar solvents. As a result, the solubility profile can typically be described with the following points:

  • Polar Solvents: 2-aminoethylsulfanylmethanimidothioic acid is expected to be highly soluble in polar solvents such as water due to its hydrophilic groups.
  • Nonpolar Solvents: The solubility in nonpolar solvents may be significantly lower, owing to the lack of favorable interactions.
  • Temperature Dependence: An increase in temperature may enhance solubility as increased kinetic energy facilitates the dissolution process.

Moreover, the compound's ionic nature when ionized can further affect solubility, leading to higher solubility in aqueous environments. As with many other compounds, assessing the pH of the solution can also be critical, as changes can influence the ionization state of the compound, thus affecting its solubility. In conclusion, while 2-aminoethylsulfanylmethanimidothioic acid may exhibit significant solubility in water and other polar solvents, its behavior in various environments and under different conditions warrants further investigation.

Interesting facts

Exploring 2-Aminoethylsulfanylmethanimidothioic Acid

2-Aminoethylsulfanylmethanimidothioic acid, commonly known as a derivative of thioic acids, presents a fascinating area of study within the realm of organic chemistry. This compound showcases a unique structural composition that influences its chemical properties and applications. Here are some interesting highlights:

  • Bioactive Potential: The presence of the amino (-NH2) and thio (-S-) groups suggests potential bioactivity, making it a candidate for further research in pharmaceutical applications.
  • Synthetic Versatility: 2-aminoethylsulfanylmethanimidothioic acid can serve as a useful building block in organic synthesis due to its functional groups, allowing chemists to construct a variety of complex molecules.
  • Mechanistic Insights: Studying the reactivity patterns of this compound can yield insights into nucleophilic substitutions and redox reactions, which are fundamental to understanding more complex biochemical pathways.
  • Research Applications: Its unique structure can be explored for potential applications in drug formulation, particularly in areas targeting cellular pathways, due to its ability to interact with biological systems effectively.
  • Thioimide Chemistry: Being a thioamide, the compound offers intriguing properties distinctive from conventional amides, showcasing the importance of sulfur in organic chemistry.

As scientists delve deeper into the properties and applications of 2-aminoethylsulfanylmethanimidothioic acid, its role could expand significantly within medicinal chemistry and materials science. The exploration of such compounds continues to highlight the rich tapestry of possibilities that organic chemistry unfolds.