Skip to main content

Methylammonium chloride

ADVERTISEMENT
Identification
Molecular formula
CH6ClN
CAS number
593-51-1
IUPAC name
carbamimidoyl(methyl)ammonium;chloride
State
State

At room temperature, methylammonium chloride is a solid. It consists of colorless to white crystalline granules or powder.

Melting point (Celsius)
231.00
Melting point (Kelvin)
504.15
Boiling point (Celsius)
271.90
Boiling point (Kelvin)
545.05
General information
Molecular weight
67.52g/mol
Molar mass
67.5180g/mol
Density
1.3130g/cm3
Appearence

Methylammonium chloride appears as a white crystalline solid. These crystals can be quite small and are often granular or powdery in appearance.

Comment on solubility

Solubility of Carbamimidoyl(methyl)ammonium Chloride

Carbamimidoyl(methyl)ammonium chloride, commonly referred to as guanidinium chloride, presents an interesting profile when it comes to solubility. This compound is known for its high solubility in various solvents, which makes it particularly valuable in biochemical applications.

Here are some key points about its solubility:

  • Water Solubility: Guanidinium chloride is highly soluble in water, with a solubility of approximately 1 g per 1.5 mL at room temperature. This characteristic allows it to be easily used in biological and chemical research.
  • Effect of Temperature: The solubility increases with temperature, making it effective for processes requiring higher thermal conditions.
  • Organic Solvents: It also exhibits moderate solubility in certain organic solvents, which can expand its utility in various chemical reactions.
  • Electrolytic Properties: As an electrolyte, it dissociates in solution to form charged species, which can influence the overall properties of the solution, including conductivity.

In summary, the solubility of carbamimidoyl(methyl)ammonium chloride is an essential characteristic that enhances its functionality in various applications, making it indispensable in the realms of biochemistry and molecular biology.

Interesting facts

Interesting Facts about Carbamimidoyl(methyl)ammonium Chloride

Carbamimidoyl(methyl)ammonium chloride is a fascinating compound that showcases the diverse chemistry of ammonium salts. Here are some engaging insights into this unique compound:

  • Structural Composition: This compound features a central carbamimidoyl group (–C(=NH)NH2) that is linked to a methyl group, making it a member of the guanidine family. Its structure can impact its reactivity and interactions with other chemicals.
  • Biological Relevance: Compounds related to carbamimidoyl derivatives are often explored for their roles in biological systems. They can act as intermediates in the synthesis of various bioactive molecules, highlighting the interplay between organic synthesis and biochemistry.
  • Potential Applications: The ammonium chloride moiety can engage in a variety of chemical reactions, making it a valuable ingredient in pharmaceuticals, fertilizers, and other industrial applications. Its ability to donate protons can also make it useful in acid-base chemistry.
  • Research Opportunities: This compound serves as a starting point for researchers exploring supramolecular chemistry and coordination compounds. The unique properties of carbamimidoyl(methyl)ammonium chloride can lead to the development of new materials and catalysts.
  • Historical Context: As a member of the ammonium salt family, its study allows for a deeper understanding of historical chemical advancements, particularly in the formulation of nitrogen-containing compounds, which have been pivotal in agricultural and medicinal chemistry.

In conclusion, carbamimidoyl(methyl)ammonium chloride is more than just a simple compound; it represents a point of convergence between organic synthesis, medicinal chemistry, and agricultural science. As scientists continue to explore its properties and applications, who knows what new discoveries await!

Synonyms
Methylguanidine monohydrochloride
carbamimidoyl(methyl)azanium;chloride
Guanidine, methyl-, monohydrochloride
GUANIDINE, 1-METHYL-, HYDROCHLORIDE