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1-amino-3-methylisothiourea

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Identification
Molecular formula
C2H7N3S
CAS number
5720-37-0
IUPAC name
1-amino-3-methyl-isothiourea
State
State

At room temperature, 1-amino-3-methylisothiourea is in a solid state.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
178.00
Boiling point (Kelvin)
451.15
General information
Molecular weight
103.16g/mol
Molar mass
103.1600g/mol
Density
1.2467g/cm3
Appearence

1-amino-3-methylisothiourea typically appears as a crystalline solid. It is a colorless to white compound, and its solid form is often used in laboratory settings.

Comment on solubility

Solubility of 1-amino-3-methyl-isothiourea

1-amino-3-methyl-isothiourea, with the formula C4H10N2S, exhibits interesting solubility characteristics. Understanding the solubility of this compound can provide insights into its potential applications and behavior in various environments. Here are some key points regarding its solubility:

  • Polar Properties: The presence of amino and thiol functional groups contributes to its polar nature, influencing its solubility in polar solvents.
  • Water Solubility: 1-amino-3-methyl-isothiourea is generally considered soluble in water, primarily due to its ability to form hydrogen bonds with water molecules.
  • Organic Solvents: It may show variable solubility in organic solvents, often being more soluble in those that have similar polar characteristics.

In summary, the solubility of 1-amino-3-methyl-isothiourea is significantly affected by its molecular structure and functional groups, making it an important compound for various chemical reactions, particularly in aqueous environments.

Interesting facts

Interesting Facts about 1-Amino-3-methyl-isothiourea

1-Amino-3-methyl-isothiourea is a fascinating compound that plays a significant role in various biological and chemical research applications. Here are some intriguing aspects of this compound:

  • Chemical Structure: The compound features an isothiourea functional group, which contains a sulfur atom bonded to a carbon atom that is also connected to an amino group. This unique structure allows for interesting reactivity and interaction with other chemical species.
  • Biological Significance: Isothiourea compounds are known to demonstrate important biological activities. They show potential as inhibitors in enzymatic reactions, making them valuable in the development of pharmaceuticals and studying biochemical pathways.
  • Research Applications: Researchers often utilize 1-amino-3-methyl-isothiourea in studies related to nitric oxide synthase. Scientists explore its ability to regulate nitric oxide production, demonstrating its relevance in cardiovascular and neurobiological research.
  • Potential Therapeutic Uses: Due to its properties, this compound may have implications in treating certain diseases where nitric oxide regulation is crucial, including asthma and various cardiovascular conditions.
  • Versatile Reactivity: The presence of both amino and isothiourea functional groups enhances the compound's reactivity, leading to diverse synthetic pathways and facilitating the creation of new derivatives.

In summary, 1-amino-3-methyl-isothiourea is more than just a chemical entity; it embodies potential in medicinal chemistry, offers insights into biological processes, and stands as a testament to the versatility inherent in chemical compounds. As research continues, the true capabilities and applications of this compound are likely to expand, making it an exciting subject of study.