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(9-ethylcarbazol-3-yl)ammonium chloride

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Identification
Molecular formula
C14H15ClN2
CAS number
401608-67-7
IUPAC name
(9-ethylcarbazol-3-yl)ammonium;chloride
State
State
At room temperature, this compound is typically in a solid state with a crystalline structure.
Melting point (Celsius)
193.00
Melting point (Kelvin)
466.15
Boiling point (Celsius)
307.00
Boiling point (Kelvin)
580.15
General information
Molecular weight
262.76g/mol
Molar mass
262.7600g/mol
Density
1.2500g/cm3
Appearence

The compound typically appears as a crystalline solid, often white or off-white in color. The crystalline structure may exhibit a degree of glossiness under light.

Comment on solubility

Solubility of (9-ethylcarbazol-3-yl)ammonium Chloride

The solubility of (9-ethylcarbazol-3-yl)ammonium chloride can be described as follows:

  • Water Solubility: This compound tends to be soluble in water due to its ionic nature, particularly as it contains the ammonium group which is hydrophilic.
  • Solvent Interaction: Polar solvents are more likely to dissolve (9-ethylcarbazol-3-yl)ammonium chloride effectively compared to non-polar solvents.
  • Concentration Effects: Its solubility may vary significantly with concentration levels, demonstrating higher solubility at lower concentrations.
  • Temperature Dependency: As is common with many salts, an increase in temperature can enhance solubility.

In summary, due to the presence of both the ammonium ion and the chloride ion, (9-ethylcarbazol-3-yl)ammonium chloride showcases a good degree of solubility in aqueous environments, making it a versatile compound across various applications in chemical science.

Interesting facts

Interesting Facts about (9-ethylcarbazol-3-yl)ammonium;chloride

(9-ethylcarbazol-3-yl)ammonium;chloride is a fascinating compound in the realm of organic and medicinal chemistry. Below are some interesting aspects that highlight its significance:

  • Versatile Applications: This compound is widely studied for its potential applications in organic electronics, particularly in light-emitting diodes (OLEDs) and solar cells due to its unique electronic properties.
  • Structure and Function: It’s derived from carbazole, a polycyclic aromatic compound that serves as a core structure in many organic materials. The ethyl substituent at the ninth position introduces interesting steric and electronic effects that can be exploited in various chemical reactions.
  • Biological Interest: The presence of the ammonium group suggests potential for interactive biological activities, making it a candidate for further research in pharmacology. Compounds like this are often investigated for their ability to modulate biological systems.
  • Research and Development: Scientists are keen to study the photophysical properties of (9-ethylcarbazol-3-yl)ammonium;chloride. Its reactivity and stability under different conditions can lead to the development of innovative materials.

In summary, (9-ethylcarbazol-3-yl)ammonium;chloride is not just another compound; it stands at the intersection of physics and chemistry, driving forward advancements in technology and health.

Synonyms
(9-ethylcarbazol-3-yl)azanium;chloride
NS00081776
(9-Ethyl-9H-carbazol-3-yl)ammonium chloride