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Methylglyoxal bis(guanylhydrazone)

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Identification
Molecular formula
C9H14N8
CAS number
1068-19-9
IUPAC name
1-(diaminomethylene)-2-[4-(N-guanidino-C-methyl-carbonimidoyl)phenyl]guanidine
State
State

At room temperature, methylglyoxal bis(guanylhydrazone) is typically found in a solid state. It is relatively stable under normal conditions.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.00
Boiling point (Celsius)
525.00
Boiling point (Kelvin)
798.00
General information
Molecular weight
210.24g/mol
Molar mass
210.2390g/mol
Density
1.2700g/cm3
Appearence

Methylglyoxal bis(guanylhydrazone) typically appears as a white to off-white crystalline solid. It is often found in laboratories in powdered form.

Comment on solubility

Solubility of 1-(diaminomethylene)-2-[4-(N-guanidino-C-methyl-carbonimidoyl)phenyl]guanidine

The solubility of the compound 1-(diaminomethylene)-2-[4-(N-guanidino-C-methyl-carbonimidoyl)phenyl]guanidine can be quite complex. Generally, the solubility of such organic compounds is influenced by several factors:

  • Polarity: Compounds with polar functional groups tend to dissolve better in polar solvents, while non-polar groups favor non-polar solvents.
  • Temperature: As the temperature increases, solubility can increase for many compounds, although some may precipitate out as temperature changes.
  • pH: The solubility of guanidine derivatives is often pH-dependent, with changes in acidity influencing the ionization of functional groups. Higher pH levels may enhance solubility due to an increase in the ionization of basic groups.
  • Hydrogen Bonding: The ability to form hydrogen bonds with the solvent can significantly increase solubility. Compounds containing amino groups, like this one, often engage in hydrogen bonding.

In summary, while specific quantitative solubility data may be lacking, the presence of multiple functional groups in this guanidine derivative suggests it may exhibit moderate to high solubility in polar solvents such as water or ethanol, particularly when conditions favor ionization. Therefore, the solubility profile of this compound deserves further exploration under varying conditions to fully understand its behavior.

Interesting facts

Interesting Facts About 1-(Diaminomethylene)-2-[4-(N-guanidino-C-methyl-carbonimidoyl)phenyl]guanidine

This complex compound is notable for its involvement in the field of medicinal chemistry, particularly in its application as a potential therapeutic agent. Here are some intriguing aspects that highlight its significance:

  • Pharmacological Potential: The compound exhibits characteristics that make it a candidate for developing pharmaceuticals, especially in treating various conditions related to the cardiovascular system and metabolic disorders.
  • Structural Sophistication: The intricate design of its structure showcases the versatility of guanidine derivatives in medicinal chemistry. The presence of multiple functional groups, such as guanidino and carbonimidoyl, enhances its reactivity and potential interactions with biological targets.
  • Target Mechanism: Compounds like this one can act on specific enzyme systems, potentially modulating biological pathways. Understanding its mechanism can provide valuable insights into drug design and efficacy.
  • Research Applications: Ongoing studies investigate its utility not only in pharmacology but also in biochemical research, offering avenues for exploring cellular mechanisms and protein interactions.
  • Historical Context: Guanidine-derived compounds have a rich history in medicinal chemistry, furthering our understanding of biological systems and leading to the development of various therapeutic agents.

As research continues and new technologies emerge, the future of 1-(diaminomethylene)-2-[4-(N-guanidino-C-methyl-carbonimidoyl)phenyl]guanidine appears promising, paving the way for novel treatments and deeper scientific understanding.