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Cysteamine hydrochloride

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Identification
Molecular formula
C2H8N2S · HBr
CAS number
300-84-5
IUPAC name
[N'-(2-sulfanylethyl)carbamimidoyl]ammonium;bromide
State
State

At room temperature, this compound is in a solid state. Its solid form is usually stable under normal conditions of storage and handling.

Melting point (Celsius)
134.00
Melting point (Kelvin)
407.15
Boiling point (Celsius)
170.00
Boiling point (Kelvin)
443.15
General information
Molecular weight
127.59g/mol
Molar mass
127.5900g/mol
Density
1.8000g/cm3
Appearence

The compound appears as a white to off-white crystalline solid. It is hygroscopic in nature, meaning it tends to absorb moisture from the air.

Comment on solubility

Solubility of N'-(2-sulfanylethyl)carbamimidoyl]ammonium bromide

The solubility of the compound N'-(2-sulfanylethyl)carbamimidoyl]ammonium bromide can be influenced by a variety of factors, such as temperature, pH, and the presence of solvents. This compound is generally expected to exhibit good solubility in polar solvents, particularly water, due to its ionic nature arising from the ammonium and bromide ions. Here are some key points regarding its solubility:

  • Solvent Type: Polar solvents tend to dissolve ionic compounds effectively.
  • Temperature Effects: Increased temperature often enhances solubility, allowing for more extensive dissolving in a given volume of solvent.
  • pH Influence: The pH level of the solution can impact the protonation state of the compound, further affecting its solubility.
  • Ionic Nature: Compounds containing ammonium and halide ions typically exhibit high solubility in aqueous solutions.

In general, one might say that "the greater the ionic character, the higher the likelihood of solubility in polar solvents." Thus, N'-(2-sulfanylethyl)carbamimidoyl]ammonium bromide is likely to dissolve readily when in contact with water, making it accessible for various chemical applications.

Interesting facts

Interesting Facts about N'-(2-sulfanylethyl)carbamimidoyl;ammonium; bromide

This intriguing compound, commonly known as a thiourea derivative, showcases remarkable properties and applications in various fields of chemistry. Here are some fascinating insights:

  • Unique Structure: The compound features a sulfenyl group that contributes to its reactivity, making it an interesting candidate for organic synthesis and medicinal chemistry.
  • Versatile Applications: It has been explored in the development of pharmaceuticals, agricultural chemicals, and catalytic processes, demonstrating its versatility in real-world applications.
  • Biological Relevance: Derivatives of thiourea compounds, including this one, have shown potential in biological systems, with studies indicating possible benefits in controlling metabolic pathways.
  • Reactivity: The compound can participate in various chemical reactions, including nucleophilic substitution and condensation reactions, highlighting its potential in synthetic organic chemistry.
  • Research Opportunities: Ongoing research continues to unveil new insights about the interactions and applications of this compound, emphasizing the need for exploration in both academic and industrial settings.

In summary, N'-(2-sulfanylethyl)carbamimidoyl;ammonium; bromide stands as a testament to the creativity and complexity found in chemical substances. As scientists continue to investigate its properties and potential, this compound could lead to exciting advancements in multiple scientific domains.