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Metformin Hydrochloride

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Identification
Molecular formula
C4H12ClN5
CAS number
1115-70-4
IUPAC name
carbamimidoyl-[N'-[4-(methylcarbamoyl)phenyl]carbamimidoyl]ammonium;chloride
State
State

At room temperature, Metformin hydrochloride is a solid.

Melting point (Celsius)
233.00
Melting point (Kelvin)
506.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
165.62g/mol
Molar mass
165.6240g/mol
Density
1.2900g/cm3
Appearence

Metformin hydrochloride appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of Carbamimidoyl-[N'-[4-(methylcarbamoyl)phenyl]carbamimidoyl]ammonium Chloride

The solubility of carbamimidoyl-[N'-[4-(methylcarbamoyl)phenyl]carbamimidoyl]ammonium chloride (often referred to as its common name) can be influenced by various factors such as temperature, solvent polarity, and pH.

Key Points About Its Solubility:

  • General Behavior: This compound is likely to be soluble in polar solvents such as water due to the presence of ammonium groups which can engage in hydrogen bonding with water molecules.
  • Temperature Dependency: It is observed that most organic salts increase in solubility with rising temperatures; thus, heating the solvent may enhance solubility.
  • Effect of pH: The solubility may also be affected by the pH of the solution, as the ionization state of the ammonium ion can change with acidity or basicity.
  • Comparison to Similar Compounds: Comparing to other ammonium salts, one could expect moderate to high solubility in aqueous solutions.

In conclusion, while specific numerical values for solubility may vary, it is reasonable to state that carbamimidoyl-[N'-[4-(methylcarbamoyl)phenyl]carbamimidoyl]ammonium chloride has a favorable solubility profile due to its ionic nature and molecular structure. This property can be further harnessed in various applications, both in research and industry.

Interesting facts

Interesting Facts about Carbamimidoyl-[N'-[4-(methylcarbamoyl)phenyl]carbamimidoyl]ammonium; Chloride

This fascinating compound belongs to the class of carbamimidoyl derivatives, which are notable for their intriguing chemical behavior and potential applications. Here are some key points that illustrate the importance and interest surrounding this compound:

  • Structural Complexity: The compound features a unique design characterized by multiple carbamimidoyl and methylcarbamoyl groups, which contributes to its complexity and highly reactive nature.
  • Pharmaceutical Potential: Compounds with similar structures are frequently investigated for their biological activities and can serve as lead compounds in drug discovery, notably in the fields of cancer therapy and antimicrobial treatments.
  • Dual Identity: Being amphiphilic in nature, this compound can interact with both hydrophilic and hydrophobic environments, making it a candidate for various applications including drug delivery systems.
  • Research Interest: Scientists are delving into the reliable synthesis and characterization of such compounds, focusing on optimization methods to enhance their efficacy and reduce side effects.
  • Analytical Techniques: The study of such complex compounds typically employs a range of modern analytical techniques, including NMR spectroscopy, mass spectrometry, and chromatography for detailed structural elucidation.

As with many compound innovations, the continuous experimentation and evaluation of carbamimidoyl derivatives could lead to groundbreaking products that significantly impact healthcare and materials science. The exploration of its unique properties is a vibrant area of research, contributing not only to theoretical knowledge but also practical advancements in chemistry.

Synonyms
BENZAMIDE, p-(3-AMIDINOGUANIDINO)-N-METHYL-, MONOHYDROCHLORIDE
p-(3-Amidinoguanidino)-N-methylbenzamide monohydrochloride
4751-82-0
DTXSID70197173
DTXCID80119664