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Cimetidine

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Identification
Molecular formula
C10H16N6S
CAS number
51481-61-9
IUPAC name
2-(2-sulfanylethyl)guanidine
State
State

At room temperature, cimetidine is typically encountered in a solid state. It is usually stable under standard conditions of temperature and pressure.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.00
Boiling point (Celsius)
650.00
Boiling point (Kelvin)
923.00
General information
Molecular weight
252.35g/mol
Molar mass
252.3520g/mol
Density
1.3930g/cm3
Appearence

Cimetidine appears as a crystalline white powder. It is often available in solid form and is known for its crystalline structure that contributes to its stability and reactivity properties in various environments.

Comment on solubility

Solubility of 2-(2-sulfanylethyl)guanidine

The solubility characteristics of the compound 2-(2-sulfanylethyl)guanidine (C10H16N6S) can be quite intriguing due to the presence of functional groups that influence its behavior in various solvents. Here are some key points to consider:

  • Solvent Polarity: 2-(2-sulfanylethyl)guanidine is likely to exhibit higher solubility in polar solvents such as water and alcohols due to its guanidine moiety, which can interact favorably with polar molecules.
  • Hydrophilicity: The presence of the guanidine functional group increases the **hydrophilicity** of the compound, enhancing its ability to dissolve in aqueous solutions.
  • Hydrophobic Regions: Conversely, the hydrocarbon chain may impart some **hydrophobic** characteristics, allowing for solubility in non-polar organic solvents, though to a lesser extent.
  • Temperature Dependency: The solubility of this compound may also be temperature-dependent, potentially increasing in solubility at elevated temperatures as molecular interactions weaken.

In summary, while 2-(2-sulfanylethyl)guanidine is expected to be soluble in polar solvents, its overall solubility is influenced by a delicate balance of its polar and non-polar characteristics. Consideration of the conditions under which solubility is assessed is crucial for understanding its practical applications.

Interesting facts

Interesting Facts About 2-(2-sulfanylethyl)guanidine

2-(2-sulfanylethyl)guanidine is a fascinating compound that captures the attention of both chemists and biochemists alike due to its unique structure and properties. Here are some intriguing aspects:

  • Versatile Applications: This compound has potential uses in pharmaceuticals, particularly in the development of new drugs. Its ability to interact with biological systems opens doors for further exploration in medicinal chemistry.
  • Structural Features: The presence of the guanidine group is significant, as it can act as a strong base and is known for its actions in biological systems, including its role in the regulation of nitric oxide production.
  • Thiol Connections: The sulfanyl group located in the structure enhances its reactivity. Thiols are known for their reducing properties and can act as nucleophiles, making this compound an interesting candidate for various chemical reactions.
  • Research and Development: Ongoing studies focus on the compound's effects on cellular mechanisms. It is observed that compounds containing sulfur often exhibit biological activity, prompting researchers to investigate their pharmacological potential.
  • Interdisciplinary Interest: Chemists, pharmacologists, and materials scientists are all drawn to this compound due to its multifunctional capabilities. Collaborative research efforts often yield innovative solutions to complex problems using guanidine derivatives.

As we advance our understanding of compounds like 2-(2-sulfanylethyl)guanidine, we can unlock new possibilities in drug development and therapeutic applications. It exemplifies the importance of chemical diversity and the impact it has on science and medicine.

Synonyms
2-Mercaptoethylguanidine
1190-74-5
2-(2-sulfanylethyl)guanidine
(2-Mercaptoethyl)guanidine
Guanidine, N-(2-mercaptoethyl)-
S33ZNG2R5Y
2-Guanidinoethanethiol
1-(2-sulfanylethyl)guanidine
N-Guanidylcysteamin [German]
Guanidine, (2-mercaptoethyl)-
MEG
Ethanethiol, 2-guanidino-
UNII-S33ZNG2R5Y
1-(2-Mercaptoethyl)guanidine
N-(2-sulfanylethyl)guanidine
SCHEMBL380025
1-(2-mercapto-ethyl)-guanidine
DTXSID00152290
GAPFINWZKMCSBG-UHFFFAOYSA-N
HSCI1_000282
AKOS006338128
Q27288516