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Metformin Hydrochloride

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Identification
Molecular formula
C4H12N5Cl
CAS number
1115-70-4
IUPAC name
[N'-[N'-(4-methoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride
State
State

At room temperature, Metformin hydrochloride is in a solid state. Its stability in solid form makes it a favorable choice for oral medication formulations.

Melting point (Celsius)
223.00
Melting point (Kelvin)
496.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
165.62g/mol
Molar mass
165.6200g/mol
Density
1.5000g/cm3
Appearence

Metformin hydrochloride appears as a white to off-white crystalline powder. This substance is odorless and freely soluble in water, making it easy to handle and process in laboratory or pharmaceutical settings.

Comment on solubility

Solubility of N’-[N’-(4-methoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride

The solubility of N’-[N’-(4-methoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium; chloride can be considered in the context of several important factors:

  • Polarity: This compound is a quaternary ammonium salt, which typically enhances its solubility in polar solvents such as water due to ion-dipole interactions.
  • Temperature: Increased temperature often promotes greater solubility for salts, making this compound more soluble in warmer conditions.
  • pH Levels: Changes in pH can influence the solubility; since this compound has functional groups sensitive to protonation, adjusting the pH may lead to altered solubility profiles.
  • Counterion effects: The presence of chloride ions can support higher solubility because they stabilize the overall structure through ion interactions.

In summary, the solubility of N’-[N’-(4-methoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium; chloride is expected to be moderate to high in aqueous solutions, especially in neutral to basic pH environments. However, the exact solubility can vary based on the specific conditions and concentrations utilized.

Interesting facts

Explore the Wonders of N'-[N'-(4-methoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride

N'-[N'-(4-methoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride is a fascinating compound with unique attributes that make it an intriguing subject of study in chemistry. Here are some compelling facts about this compound:

  • Versatile Applications: This compound is known for its potential in various applications, particularly in the field of organic synthesis and medicinal chemistry. Its unique structure allows it to act as a building block for more complex chemical reactions.
  • Significance of Carbamimidoyl Groups: The presence of carbamimidoyl groups in the structure is noteworthy because they are involved in numerous biological processes. These groups can enhance the compound's ability to interact with biological systems, making it a candidate for drug development.
  • 4-Methoxyphenyl Component: The incorporation of a 4-methoxyphenyl substituent not only contributes to the compound's stability but also can influence its reactivity and solubility. The methoxy group acts as an electron-donating substituent, enhancing the compound's overall electronic properties.
  • Ion Exchange Characteristics: As an ammonium salt, this compound exhibits unique ion exchange properties, which may be explored for applications in catalysis and material science. Ammonium salts often participate in ionic interactions, making them versatile in formulations.

In conclusion, N'-[N'-(4-methoxyphenyl)carbamimidoyl]carbamimidoyl]ammonium;chloride is more than just a chemical entity; it's a gateway to understanding the complexities of chemical interactions and potential therapeutic applications. As research continues to unfold, the importance of such compounds in scientific disciplines cannot be overstated.