N-Acetylcysteine ethylester | Solubility of Things

Identification

Molecular formula

C₁₀H₁₇NO₄S₂Na

CAS number

26124-68-5

IUPAC name

sodium;4-(2-acetamidoethyldisulfanyl)butane-1-sulfinate

State

Solid at room temperature (25°C / 77°F).

Melting point (Celsius)

122.00

Melting point (Kelvin)

395.15

Boiling point (Celsius)

195.00

Boiling point (Kelvin)

468.15

General information

Molecular weight

221.33g/mol

Molar mass

221.3290g/mol

Density

1.1850g/cm³

Appearence

The compound appears as a colorless to white crystalline powder, often odorless and with a characteristic bitter taste. It is hygroscopic in nature.

Comment on solubility

Solubility of Sodium 4-(2-Acetamidoethyldisulfanyl)butane-1-sulfinate

Sodium 4-(2-acetamidoethyldisulfanyl)butane-1-sulfinate is a fascinating compound with unique solubility characteristics. Understanding its solubility is crucial for various applications, particularly in biological and chemical processes. Here are some key points:

Solubility in Water: The presence of the sodium ion typically enhances the solubility of this compound in water due to ionic interactions. The polar nature of the acetamido group also contributes to its solubility.
Temperature Effects: Like many salts, solubility may increase with temperature. Hence, it can be beneficial to study its solubility at varying temperatures for optimal applications.
pH Influence: The solubility may be affected by the pH of the solution. A more acidic or alkaline environment can lead to changes in solubility due to the ionization state of the functional groups.
Comparison with Other Compounds: When compared with similar sulfonates or ammonium derivatives, sodium 4-(2-acetamidoethyldisulfanyl)butane-1-sulfinate may exhibit unique solubility properties due to its specific molecular structure.

In conclusion, the solubility of sodium 4-(2-acetamidoethyldisulfanyl)butane-1-sulfinate is influenced by several factors, including ionic character, temperature, and pH. Understanding these aspects can lead to tailored applications in various scientific fields. As the renowned chemist once said, "Solubility is the key to many solutions."

Interesting facts

Exploring Sodium 4-(2-Acetamidoethyldisulfanyl)butane-1-sulfinate

Sodium 4-(2-acetamidoethyldisulfanyl)butane-1-sulfinate is a fascinating compound that has garnered attention in both organic chemistry and medicinal chemistry due to its unique structure and potential applications. Here are some intriguing aspects of this compound:

Structural Complexity: The compound features a ¹butanesulfinate group, which plays a significant role in its reactivity and properties. This unique structure is characterized by the presence of multiple functional groups, making it a candidate for various chemical reactions.
Potential Biochemical Applications: Compounds featuring disulfide bonds, such as the disulfanyl component in this compound, are notable for their roles in biological systems. They often participate in redox reactions and are involved in the stabilization of protein structures.
Influence of Acetamido Group: The acetamido ethyl group adds an amine functionality, which could enhance interaction with biological targets, potentially leading to interesting pharmacological properties. This may make the compound relevant in drug design.
Importance in Synthetic Chemistry: This compound can serve as a precursor or reagent in the synthesis of more complex molecules. Its utilization in various synthetic routes reflects the compound's versatility and importance within chemical research.

In the words of renowned chemist, "Chemistry isn't just about compounds; it's about understanding the intricate dance of electrons and atoms that create life." Sodium 4-(2-acetamidoethyldisulfanyl)butane-1-sulfinate embodies this sentiment by showcasing the elegance of chemical interactions.

In summary, sodium 4-(2-acetamidoethyldisulfanyl)butane-1-sulfinate stands as a testament to the beauty of chemistry, offering a multitude of pathways for exploration and discovery!