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HSAB

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Identification
Molecular formula
C10H22N2O2S2
CAS number
64846-91-5
IUPAC name
1,4-bis(2-sulfanylethylamino)butane-2,3-diol
State
State

At room temperature, 1,4-bis(2-sulfanylethylamino)butane-2,3-diol is generally found as a solid.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
252.36g/mol
Molar mass
252.3610g/mol
Density
1.2200g/cm3
Appearence

1,4-bis(2-sulfanylethylamino)butane-2,3-diol typically appears as a crystalline solid. The color may vary from white to a slight off-white hue, reflecting its purity and the presence of any impurities. The compound is known to be quite stable under normal conditions, maintaining its crystalline form.

Comment on solubility

Solubility of 1,4-bis(2-sulfanylethylamino)butane-2,3-diol

The solubility of 1,4-bis(2-sulfanylethylamino)butane-2,3-diol is influenced by several factors, including its structural characteristics and the presence of functional groups. Here are some important considerations:

  • Polarity: This compound features multiple amine groups and hydroxyl groups, which typically increase the polarity of the molecule, enhancing its ability to interact with polar solvents such as water.
  • Sulfhydryl Groups: The presence of sulfhydryl (−SH) groups can also contribute to solubility, as they can form hydrogen bonds.
  • Hydrogen Bonding: The potential for extensive hydrogen bonding due to the hydroxyl (-OH) and amino (-NH2) functionalities can further enhance solubility in aqueous environments.
  • Hydrophobic Interactions: The hydrophobic portions of the molecule may limit solubility in highly polar solvents, indicating a balance between hydrophilic and hydrophobic characteristics.

In conclusion, while 1,4-bis(2-sulfanylethylamino)butane-2,3-diol is expected to exhibit good solubility in polar solvents, the exact solubility can vary based on concentration, temperature, and the presence of other ions or compounds in solution. Understanding these interactions is crucial for its application in various scientific fields.

Interesting facts

Interesting Facts about 1,4-bis(2-sulfanylethylamino)butane-2,3-diol

The compound 1,4-bis(2-sulfanylethylamino)butane-2,3-diol is a fascinating example of a compound with potential applications in pharmaceuticals and biochemistry. Here are some interesting traits that make this compound noteworthy:

  • Structural Complexity: This compound features a unique structure that incorporates both amino and hydroxyl groups, which can be crucial for its reactivity and interaction with biological molecules.
  • Potential Biological Activity: Compounds like this one, with sulfanyl groups, may exhibit interesting biological activities, including antioxidant properties that can protect cells from oxidative stress.
  • Design Versatility: The presence of multiple functional groups offers scientists the ability to modify the compound for specific uses, such as drug development or targeting particular biochemical pathways.
  • Research Applications: It can serve as a valuable model for studying enzyme interactions or cellular processes due to its complexity.
  • Synergistic Effects: The combination of amino groups with sulfanyl moieties can lead to synergistic properties that enhance the compound’s effectiveness in various reactions.

In the words of a renowned chemist, "The beauty of chemistry lies in its intricacies and the potential hidden within complex molecules." Understanding such compounds opens new avenues for innovation in chemistry and medicine.

This compound represents not just a chemical structure, but the promise of scientific discovery and advancement in therapeutic applications.

Synonyms
SCHEMBL4986325