O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine

Identification

Molecular formula

C₉H₁₂N₃O

CAS number

Not Assigned

IUPAC name

O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine

State

At room temperature, O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine is typically in a solid state. It appears as a stable crystalline or powdered solid under standard atmospheric conditions.

Melting point (Celsius)

157.80

Melting point (Kelvin)

430.95

Boiling point (Celsius)

223.50

Boiling point (Kelvin)

496.65

General information

Molecular weight

178.21g/mol

Molar mass

178.2100g/mol

Density

1.2640g/cm³

Appearence

The compound is generally found as a crystalline solid, typically appearing as a white or off-white powder. The solid is usually odorless and has a granular structure that can vary depending on the method of synthesis and purification.

Comment on solubility

Solubility of O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine

The solubility of O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine can be influenced by several factors, resulting in intriguing characteristics:

Polarity: Being a hydroxylamine derivative, the compound exhibits polar characteristics that may enhance its solubility in polar solvents, particularly in water.
Hydrogen Bonding: The presence of hydroxyl functional groups allows for strong hydrogen bonding, which boosts its affinity for aqueous environments.
Electrostatic Interactions: The benzimidazolium moiety suggests potential ionic interactions with other solutes, which may help solubilize the compound in ionic liquids or other polar media.
pH Sensitivity: The solubility could be highly pH-dependent, as the protonation states can change under varying pH conditions, altering its solubility profile.

It is essential to note that while the compound may demonstrate good solubility in specific conditions, its overall solubility can vary significantly based on temperature, solvent type, and concentration. As with many organic compounds, understanding these dynamics is key to effectively utilizing O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine in various chemical applications.

Interesting facts

O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine

O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine is a fascinating compound that showcases the intricate relationship between organic chemistry and biological systems. Here are some engaging facts:

Structural Diversity: This compound contains a unique benzimidazole structure, which is known for its versatility and ability to form various derivatives. The inclusion of a hydroxylamine moiety adds to its reactivity profile, allowing for intriguing interactions with other chemical species.
Biological Relevance: Compounds similar to this one have been investigated for their potential as therapeutic agents, particularly in the treatment of various diseases. The ability to modulate biological pathways makes benzimidazole derivatives a promising area of research in medicinal chemistry.
Versatile Reactivity: Hydroxylamines are recognized for their role in organic synthesis, where they can act as both nucleophiles and electrophiles. Their ability to facilitate reactions such as oxidation and reduction is beneficial in creating more complex molecules in laboratory settings.
Research Potential: Current studies are exploring the applications of benzimidazole derivatives in drug development. Their interactions at the molecular level provide insights into how they may function within biological systems, highlighting their significance in pharmaceuticals.

In summary, O-[(3-methyl-1H-benzimidazol-3-ium-2-yl)methyl]hydroxylamine stands at the intersection of chemistry and biology, making it a compound of significant interest for researchers and students alike. Its structural features not only contribute to its chemical properties but also hint at its potential in various practical applications.