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Benzamidine hydrochloride

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Identification
Molecular formula
C8H12N3 • HI
CAS number
62583-51-7
IUPAC name
[(N'-benzylcarbamimidoyl)amino]ammonium;iodide
State
State

At room temperature, [(N'-benzylcarbamimidoyl)amino]ammonium;iodide is a solid compound.

Melting point (Celsius)
144.00
Melting point (Kelvin)
417.15
Boiling point (Celsius)
97.20
Boiling point (Kelvin)
370.35
General information
Molecular weight
184.58g/mol
Molar mass
184.5830g/mol
Density
1.7040g/cm3
Appearence

The compound typically appears as a white to off-white crystalline powder. It is usually odorless.

Comment on solubility

Solubility of [(N'-benzylcarbamimidoyl)amino]ammonium iodide

The solubility of [(N'-benzylcarbamimidoyl)amino]ammonium iodide can be intriguing, as it involves both organic and inorganic components. Various factors influence the solubility of this compound, including:

  • Polar Nature: The presence of the iodide ion generally enhances the polarity, allowing for solubility in polar solvents, especially water.
  • Organic Moieties: The benzyl component adds a hydrophobic characteristic, which may limit solubility in highly polar solvents but allows for better solubility in organic solvents.
  • Hydrogen Bonding: The amino groups can engage in hydrogen bonding with solvents, improving solubility in certain cases.

In general, you might expect the compound to exhibit:

  • Moderate solubility in water due to the ionic nature provided by the iodide.
  • Increased solubility in alcohols or other polar organic solvents.

In summary, while solubility may vary based on precise conditions, the characteristics of both its ionic and organic components suggest a fascinating interplay that can be explored in different solvent systems.

Interesting facts

Interesting Facts about [(N'-benzylcarbamimidoyl)amino]ammonium iodide

[(N'-benzylcarbamimidoyl)amino]ammonium iodide is a fascinating chemical compound that has drawn the attention of researchers due to its versatile applications and unique properties. Here are some interesting insights:

  • Versatile Applications: This compound serves as an effective building block in the synthesis of various organic compounds, playing a pivotal role in the development of pharmaceuticals and agrochemicals.
  • Functionality of Organic Iodides: The presence of the iodide ion enhances the reactivity of the compound, making it valuable in nucleophilic substitution reactions, which are crucial in organic synthesis.
  • Research and Development: Scientists are investigating its potential applications in drug delivery systems and its effects on biological mechanisms, paving the way for future therapeutic advances.
  • Catalytic Properties: Lithium salts of related compounds have been studied as catalysts in various chemical reactions, indicating potential applications for [(N'-benzylcarbamimidoyl)amino]ammonium iodide in catalysis.
  • Structure-Activity Relationship: Understanding the structural nuances of this compound aids chemists in predicting its behavior, reactivity, and possible interactions with biological targets.

As a testament to its importance, researchers continually explore the compound's interactions and transformations, emphasizing its potential role in the future of synthetic organic chemistry. The blending of traditional organic frameworks with innovative approaches makes [(N'-benzylcarbamimidoyl)amino]ammonium iodide a subject of ongoing fascination in the chemical community.