(4-bromophenyl)methyl-trimethyl-ammonium

Identification

Molecular formula

C₁₀H₁₅BrN

CAS number

980-26-7

IUPAC name

(4-bromophenyl)methyl-trimethyl-ammonium

State

Solid at room temperature, taking the form of a crystalline powder.

Melting point (Celsius)

112.00

Melting point (Kelvin)

385.15

Boiling point (Celsius)

245.00

Boiling point (Kelvin)

518.15

General information

Molecular weight

258.18g/mol

Molar mass

258.1780g/mol

Density

1.2000g/cm³

Appearence

(4-Bromophenyl)methyl-trimethyl-ammonium typically appears as a white crystalline solid. It may exhibit a slight yellowish tinge depending on purity and environmental conditions.

Comment on solubility

Solubility of (4-bromophenyl)methyl-trimethyl-ammonium

The solubility of (4-bromophenyl)methyl-trimethyl-ammonium can be influenced by several factors, primarily its ionic nature due to the presence of a quaternary ammonium group. Here are some key points regarding its solubility:

Ionic vs. Non-Ionic: As a quaternary ammonium compound, it is typically more soluble in polar solvents due to its ionic characteristics.
Solvent Preference: It is expected to have better solubility in water and other polar solvents compared to non-polar solvents.
Temperature Influence: Higher temperatures generally increase solubility, allowing for greater dissolution in solutions.
Functional Groups: The presence of the bromophenyl group may introduce steric hindrance which can affect solubility, making it less soluble in a highly structured solvent matrix.
Concentration Effects: As with many compounds, increased concentration in a solution could lead to saturation, thus limiting solubility.

In conclusion, the solubility of (4-bromophenyl)methyl-trimethyl-ammonium is significantly affected by its ionic nature and the choice of solvent. It is crucial for applications to consider these factors to ensure effective utilization in various chemical processes.

Interesting facts

Interesting Facts about (4-bromophenyl)methyl-trimethyl-ammonium

(4-bromophenyl)methyl-trimethyl-ammonium is a fascinating quaternary ammonium compound with significant applications in various fields. This compound is characterized by its unique functional groups, rendering it useful in both organic synthesis and industrial processes. Here are some intriguing aspects to explore:

Biological Activity: Quaternary ammonium compounds like (4-bromophenyl)methyl-trimethyl-ammonium are often utilized for their biological properties. They exhibit antimicrobial activity, making them indispensable in the development of disinfectants and antiseptics.
Surfactant Properties: This compound can act as a surfactant due to its amphiphilic nature. Surfactants are crucial in various industries, including pharmaceuticals, cosmetics, and cleaning products.
Charged Species: The positive charge on the nitrogen atom in the trimethylammonium portion enhances its solubility in polar solvents and affects its interaction with biological membranes, which is significant for drug delivery systems.
Stability and Reactivity: The stability of quaternary ammonium salts makes them less prone to hydrolysis compared to their tertiary counterparts, allowing for greater versatility in reactions.
Synthetic Pathways: Scientists often explore multiple synthetic routes to prepare this compound, illustrating the creativity involved in organic synthesis. This includes reactions involving halogenation, alkylation, and ammoniation.

In summary, (4-bromophenyl)methyl-trimethyl-ammonium serves as a key player in not only chemistry but also in practical applications within medicine and industry. The intersection of chemical reactivity and biological activity in compounds like this opens up numerous avenues for research and development.

Synonyms

SCHEMBL10256839