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Cystamine

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Identification
Molecular formula
C8H11NS2
CAS number
51-85-4
IUPAC name
2-(phenyldisulfanyl)ethanamine
State
State

At room temperature, cystamine is generally found in a solid state with a crystalline form.

Melting point (Celsius)
99.00
Melting point (Kelvin)
372.15
Boiling point (Celsius)
91.00
Boiling point (Kelvin)
364.15
General information
Molecular weight
154.26g/mol
Molar mass
154.2550g/mol
Density
1.3443g/cm3
Appearence

Cystamine typically appears as a white crystalline solid. It is often presented as a solid powder that is odorless or has a faint odor characteristic of amines, which can be slightly fishy or ammonia-like.

Comment on solubility

Solubility of 2-(phenyldisulfanyl)ethanamine

The solubility of 2-(phenyldisulfanyl)ethanamine, a compound featuring a disulfide bond, can exhibit unique behavior due to its molecular structure. When evaluating its solubility, consider the following factors:

  • Polarity: The presence of both hydrophobic phenyl groups and a more polar amine functional group makes its solubility in water limited.
  • Solvent Interaction: This compound may be more soluble in non-polar solvents, such as ethers or dichloromethane, due to structural compatibility.
  • Temperature Effects: Like many organic compounds, increasing temperature can enhance solubility by encouraging molecular movement and interaction with the solvent.

As a result, it's safe to say that while 2-(phenyldisulfanyl)ethanamine might not readily dissolve in water, its solubility in organic solvents is expected to be significantly higher. Always remember: the solubility of compounds is influenced by their chemical structure and the nature of the solvent used.

Interesting facts

Interesting Facts About 2-(Phenyldisulfanyl)ethanamine

2-(Phenyldisulfanyl)ethanamine, also known as a compound featuring a unique disulfide linkage, is a fascinating compound within the realm of organic chemistry. Here are some intriguing aspects:

  • Structure and Functionality: The compound consists of an ethanamine backbone with a phenyldisulfanyl substituent. This disulfide group adds a layer of complexity to the molecule, influencing its properties and potential reactivity.
  • Applications in Synthesis: Compounds with disulfide linkages like this one are often explored in synthetic organic chemistry. They can be used in the construction of larger frameworks and could serve as intermediates in various chemical reactions.
  • Biological Significance: Disulfide bonds are critical in many biological systems, particularly in proteins where they help stabilize structures. This compound could potentially be studied for similarities or applications in biological pathways.
  • Potential for Novel Applications: Researchers are continuously investigating compounds containing sulfur for their unique electronic properties and utility in materials science. This compound could be of interest for developing new materials, pharmaceuticals, or catalysts.
  • Safety Considerations: As with many sulfur-containing compounds, it's important to handle this compound with care. Proper safety protocols and disposal methods should be observed when working with such compounds in laboratory settings.

In summary, 2-(phenyldisulfanyl)ethanamine stands as an understated yet intriguing compound, contributing to the extensive field of organic chemistry and offering pathways for future research and applications.

Synonyms
SCHEMBL9655918