Skip to main content

[4-[4-[4-(Diethylammonio)butanoyl]fluoranthen-8-yl]-4-oxo-butyl]-diethyl-ammonium dichloride

ADVERTISEMENT
Identification
Molecular formula
C30H42Cl2N2O2
CAS number
.null
IUPAC name
[4-[4-[4-(diethylammonio)butanoyl]fluoranthen-8-yl]-4-oxo-butyl]-diethyl-ammonium;dichloride
State
State

At room temperature, this compound exists as a solid. It is stable under normal conditions, but care should be taken to store it in a cool, dry place to maintain its chemical integrity.

Melting point (Celsius)
141.00
Melting point (Kelvin)
414.00
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.00
General information
Molecular weight
482.48g/mol
Molar mass
482.4800g/mol
Density
1.2600g/cm3
Appearence

The compound appears as a solid at room temperature. It typically forms as a fine powder or crystalline solid with a distinct chemical odor. The appearance can vary from off-white to light yellow, depending on purity and specific formulation.

Comment on solubility

Solubility of 4-[4-[4-(diethylammonio)butanoyl]fluoranthen-8-yl]-4-oxo-butyl]-diethyl-ammonium;dichloride

The solubility of the compound 4-[4-[4-(diethylammonio)butanoyl]fluoranthen-8-yl]-4-oxo-butyl]-diethyl-ammonium;dichloride can be influenced by several factors due to its complex structure and the presence of multiple functional groups.

Key Factors Influencing Solubility:

  • Polarity: The presence of the diethylammonio group increases polarity, which generally enhances solubility in polar solvents such as water.
  • Hydrogen Bonding: This compound may participate in hydrogen bonding due to ammonium functionalities, which can further improve its solubility profile.
  • Electrostatic Interactions: The dichloride ions could facilitate interactions with solvent molecules, promoting solubility in ionic environments.

On the other hand, the overall hydrophobic character related to the fluoranthen moiety may decrease solubility in purely aqueous solutions. Therefore, solubility testing in various solvents including:

  1. Water
  2. Alcohols (e.g., ethanol, methanol)
  3. Dimethyl sulfoxide (DMSO)

is essential for determining the optimal conditions for this compound’s application. In summary, while this compound possesses features that suggest enhanced solubility in polar solvents due to its ammonium and chloride constituents, its overall solubility behavior can be quite complex and requires empirical validation.

Interesting facts

Exploring 4-[4-[4-(diethylammonio)butanoyl]fluoranthen-8-yl]-4-oxo-butyl]-diethyl-ammonium; dichloride

This compound, a sophisticated ionic liquid, showcases the intersection of organic chemistry and materials science. Here are some interesting facets of this intriguing molecule:

  • Dual Functionality: The presence of both diethylammonium and a fluoranthenyl moiety gives this compound unique properties, making it suitable for applications in fields such as organic electronics and photonics.
  • Versatile Applications: Given its ionic liquid nature, this compound may serve as a solvent for chemical reactions or as a medium for the extraction of valuable materials.
  • Stability and Performance: This compound likely exhibits superior thermal and chemical stability, which is vital for enhancing performance in various applications, from electrochemistry to nanotechnology.

Structure and Function

The molecular architecture of this compound is compelling due to:

  • Charge Separation: The dichloride component provides ionic character, which can significantly affect solubility and reactivity.
  • Functional Groups: The butanoyl groups contribute to a range of intermolecular interactions, which may enhance the solvent's properties.
  • Potential for Synthesis: The complexity of this compound opens doors for further synthetic exploration, potentially yielding new derivatives with tailored properties.

In conclusion, 4-[4-[4-(diethylammonio)butanoyl]fluoranthen-8-yl]-4-oxo-butyl]-diethyl-ammonium; dichloride is not just a curious construct of chemical ingenuity but also a bridge to innovative research avenues in modern chemistry. Its multifaceted nature fueled by intriguing structural features and potential applications makes it a unique compound worthy of exploration.

Synonyms
DEAP fluoranthene
27086-86-8
Bis(3-(diethylamino)propyl) 3,9-fluoranthenedicarboxylate dihydrochloride
3,9-Fluoranthenedicarboxylic acid, bis(3-(diethylamino)propyl) ester, hydrochloride
RefChem:336634
3,9-Fluoranthenedicarboxylic acid, bis(3-(diethylamino)propyl) ester, dihydrochloride
3,9-Fluoranthenedicarboxylic acid, bis(3-(diethylamino)propyl) ester, hydrochloride (8CI)
3,9-Fluoranthenedicarboxylic acid , bis(3-(diethylamino)propyl) ester, dihydrochloride
[4-[4-[4-(diethylazaniumyl)butanoyl]fluoranthen-8-yl]-4-oxobutyl]-diethylazanium;dichloride