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Thiodiglycolic acid

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Identification
Molecular formula
C6H13NO4S2
CAS number
123-93-3
IUPAC name
2,2-bis(2-aminoethylsulfanyl)acetic acid
State
State

This compound is a solid at room temperature, typically existing in a crystalline form.

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
209.33g/mol
Molar mass
209.3300g/mol
Density
1.3710g/cm3
Appearence

2,2-bis(2-aminoethylsulfanyl)acetic acid, commonly known as thiodiglycolic acid, typically appears as white to off-white crystalline powder. It is crystalline in nature and has a characteristic sulfurous odor.

Comment on solubility

Solubility of 2,2-bis(2-aminoethylsulfanyl)acetic acid

When discussing the solubility of 2,2-bis(2-aminoethylsulfanyl)acetic acid (C6H14N2S2O2), it is important to consider several key factors:

  • Polar Nature: Because of the presence of amino groups and a sulfur-containing moiety, this compound exhibits a polar nature, enhancing its interaction with water molecules.
  • Hydrogen Bonding: The amino groups (-NH2) allow for significant hydrogen bonding with solvents, particularly water, which is a major factor that can increase solubility.
  • Sulfhydryl Groups: The sulfanyl (-SH) groups can also participate in hydrogen bonding and may influence solubility in organic solvents, suggesting variable solubility depending on the environment.

In general, 2,2-bis(2-aminoethylsulfanyl)acetic acid is likely to be soluble in water, given its structure that favors solvation through strong intermolecular forces. However, its solubility may be influenced by temperature and pH of the solution, proving that the context significantly affects its behavior.

Overall, understanding the solubility of this compound provides valuable insights into its reactivity and potential applications in various fields. As stated, “solubility is the key to reactivity,” emphasizing the importance of solvation in chemical processes.

Interesting facts

Interesting Facts About 2,2-bis(2-aminoethylsulfanyl)acetic acid

2,2-bis(2-aminoethylsulfanyl)acetic acid, often abbreviated as *BESA*, is a fascinating compound with a variety of applications in both biological and chemical fields. Here are some key highlights:

  • Biochemical Significance: This compound is known for its role as a cysteine derivative, which is crucial in the study of proteins and enzymes. Cysteine plays a critical role in maintaining the structure of proteins through disulfide bonds.
  • Synthetic Utility: BESA serves as a building block in organic synthesis, particularly in the development of novel sulfhydryl-containing compounds, which are important in drug development.
  • Pharmaceutical Potential: Research into BESA suggests that it may have implications in medicinal chemistry, particularly as a potential lead compound for developing therapeutic agents targeting various diseases.
  • Multifunctional Nature: The presence of both amino and thiol groups in its structure allows for versatile reactivity and interactions, making it an excellent candidate for further functionalization.
  • Research Applications: It is often utilized in studies focused on redox biology, where thiols play a pivotal role in cellular processes and signaling pathways.

As scientists continue to explore and understand the intricacies of compounds like 2,2-bis(2-aminoethylsulfanyl)acetic acid, they uncover new avenues in both fundamental research and practical applications. This compound exemplifies the intersection of chemistry and biology, showcasing how a simple molecule can influence complex biological systems.

Synonyms
SCHEMBL10963973