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(4-Formylphenyl)trimethylammonium chloride

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Identification
Molecular formula
C10H14NO
CAS number
464926-03-4
IUPAC name
(4-formylphenyl)-trimethyl-ammonium
State
State

At room temperature, (4-formylphenyl)trimethylammonium chloride is typically in a solid state.

Melting point (Celsius)
244.00
Melting point (Kelvin)
517.00
Boiling point (Celsius)
280.00
Boiling point (Kelvin)
553.00
General information
Molecular weight
181.24g/mol
Molar mass
181.2430g/mol
Density
1.2400g/cm3
Appearence

The compound typically appears as a white to off-white crystalline solid. The crystals are usually colorless to pale yellow, depending on the purity and any possible impurities. The compound is hygroscopic and may absorb moisture from the air, affecting its overall appearance.

Comment on solubility

Solubility of (4-formylphenyl)-trimethyl-ammonium

The solubility of (4-formylphenyl)-trimethyl-ammonium can be influenced by several factors, making it an interesting compound to study.

  • Polarity: The presence of a trimethylammonium group makes the compound polar, which typically enhances its solubility in polar solvents such as water and alcohols.
  • Hydrogen Bonding: The formyl group may participate in hydrogen bonding, promoting interactions with solvent molecules and further increasing solubility.
  • Concentration: Solubility can vary significantly with concentration; it’s important to consider that (4-formylphenyl)-trimethyl-ammonium might have different solubility limits under different conditions.

As a result, the solubility can be summarized as follows:

  1. Likely soluble in polar solvents.
  2. Possible limited solubility in non-polar solvents.
  3. Concentration-dependent behavior not to be overlooked.

In practical applications, it is often recommended to conduct a solubility test in the desired solvent to determine the exact solubility limits under specific conditions. This can be crucial for ensuring effectiveness in chemical reactions or formulations.

Interesting facts

Interesting Facts about (4-formylphenyl)-trimethyl-ammonium

(4-formylphenyl)-trimethyl-ammonium, commonly known in scientific literature, presents a fascinating study in organic chemistry and its applications. This compound features a quaternary ammonium structure, characterized by its positive charge, which influences its reactivity and interaction with other molecules.

Unique Properties and Uses

  • Quaternary Ammonium Compound: The presence of the nitrogen atom bonded to three methyl groups as well as a phenyl ring derived from 4-formylphenol imbues this compound with unique physicochemical properties. Quaternary ammonium salts are known for their surfactant and antimicrobial potential.
  • Versatile Reactions: This compound can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, making it a useful building block in organic synthesis.
  • Biological Relevance: Certain derivatives of quaternary ammonium compounds exhibit significant biological activity, including antimicrobial, antifungal, and antiviral properties. Researchers are investigating their efficacy in pharmaceutical applications.
  • Ligand Potential: The trimethylammonium moiety can serve as a ligand in coordination chemistry, facilitating the formation of complexes with transition metals, which can be useful in catalysis.

Scientific Insights

As a scientist studying (4-formylphenyl)-trimethyl-ammonium, one could appreciate the balance it strikes between organic and inorganic chemistry. The fusion of an organic framework with a cationic center allows for diverse applications, from material science to medicinal chemistry. In the words of chemist and educator Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This sentiment perfectly encapsulates the innovative spirit behind exploring compounds like (4-formylphenyl)-trimethyl-ammonium.

In conclusion, the study of (4-formylphenyl)-trimethyl-ammonium not only illustrates the intricacies of molecular design but also highlights the potential for real-world applications, making it a compound worth delving into for any chemistry enthusiast.

Synonyms
(4-formylphenyl)-trimethyl-azanium
Benzenaminium, 4-formyl-N,N,N-trimethyl-, iodide
CBDivE_014091
SCHEMBL2780476
4-formyl-N,N,N-trimethylanilinium
ALBB-029028
STL036438
AKOS002663349