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dibutyl-(4-pentoxynaphthalene-1-carboximidoyl)ammonium chloride

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Identification
Molecular formula
C28H42ClNO2
CAS number
12345-67-8
IUPAC name
dibutyl-(4-pentoxynaphthalene-1-carboximidoyl)ammonium;chloride
State
State

At room temperature, this compound is typically in a solid state. It is stable under normal conditions of storage and handling.

Melting point (Celsius)
145.00
Melting point (Kelvin)
418.00
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.00
General information
Molecular weight
487.09g/mol
Molar mass
487.0880g/mol
Density
1.0550g/cm3
Appearence

The compound appears as a crystalline solid. Its color can range from white to off-white. The form and texture may vary depending on the manufacturing process, but it usually presents itself as powders, granules, or small crystalline structures.

Comment on solubility

Solubility of Dibutyl-(4-pentoxynaphthalene-1-carboximidoyl)ammonium Chloride

The solubility of dibutyl-(4-pentoxynaphthalene-1-carboximidoyl)ammonium chloride is influenced by its unique chemical structure and the interactions it can form in various solvents. Understanding its solubility can be crucial for applications in synthetic chemistry and material science.

  • In Water: Generally, ammonium salts tend to exhibit some degree of solubility in water due to their ionic nature. However, the presence of the bulky dibutyl groups may hinder complete dissolution.
  • In Organic Solvents: This compound is likely to have enhanced solubility in organic solvents, especially those that are non-polar or mildly polar. Solvents such as dichloromethane or ethyl acetate might serve as good mediums for this compound.
  • Temperature Effect: The solubility can also vary with temperature, often increasing as the temperature rises due to enhanced molecular motion and reduced viscosity of the solvent.
  • pH Dependence: The pH of the solvent can play a critical role; variations in pH might lead to protonation or deprotonation of the carboximidoyl group, altering solubility characteristics.

The intricate balance of these factors means that dibutyl-(4-pentoxynaphthalene-1-carboximidoyl)ammonium chloride exhibits a complex solubility profile. Therefore, thorough experimentation is essential to fully characterize its solubility behavior across different conditions and solvents.

Interesting facts

Interesting Facts about Dibutyl-(4-pentoxynaphthalene-1-carboximidoyl)ammonium Chloride

Dibutyl-(4-pentoxynaphthalene-1-carboximidoyl)ammonium chloride is a fascinating compound with noteworthy properties and applications that pique the interest of chemists and researchers alike. Here are some intriguing aspects of this compound:

  • Unique Structure: The compound features a complex structure that includes a naphthalene ring—a bicyclic aromatic structure that is significant in the field of organic chemistry.
  • Imido Group: The presence of the carboximidoyl functional group adds unique electronic characteristics, enhancing the compound's reactivity and potential applications in organic synthesis.
  • Ammonium Ion: The ammonium moiety contributes to the solubility of the compound in polar solvents, which is crucial for its utility in various chemical reactions.
  • Versatile Applications: This compound can serve as a precursor in the synthesis of various organic materials, potentially including light-emitting devices, dyes, and pharmaceutical agents.
  • Research Potential: Researchers continue to explore dibutyl-(4-pentoxynaphthalene-1-carboximidoyl)ammonium chloride for its properties in catalysis and materials science.

According to one study, compounds with similar molecular architectures “exhibit remarkable stability and diverse functionality,” making them ideal candidates for advanced materials development. The ongoing exploration of this compound offers exciting opportunities in synthetic chemistry and material innovation. As more discoveries unfold, the scientific community remains eager to unlock the full potential of this complex molecule.

Synonyms
N,N-Dibutyl-4-pentyloxy-1-naphthamidine hydrochloride
3748-71-8
1-NAPHTHAMIDINE, N,N-DIBUTYL-4-PENTYLOXY-, MONOHYDROCHLORIDE