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Dimethindene

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Identification
Molecular formula
C18H24ClNO
CAS number
3614-69-5
IUPAC name
2-[bis(2,6-dimethylphenyl)methoxy]ethyl-dimethyl-ammonium;chloride
State
State

At room temperature, Dimethindene maleate is in a solid state.

Melting point (Celsius)
146.00
Melting point (Kelvin)
418.15
Boiling point (Celsius)
124.00
Boiling point (Kelvin)
397.15
General information
Molecular weight
540.14g/mol
Molar mass
540.1440g/mol
Density
1.1000g/cm3
Appearence

Dimethindene maleate is typically found as a white or almost white crystalline powder.

Comment on solubility

Solubility of 2-[bis(2,6-dimethylphenyl)methoxy]ethyl-dimethyl-ammonium;chloride

The solubility of 2-[bis(2,6-dimethylphenyl)methoxy]ethyl-dimethyl-ammonium;chloride presents a fascinating study of how organic compounds behave in various solvents. Understanding its solubility is crucial for applications in chemical processes and formulations. Here are some key points to consider:

  • Polar Nature: Given the presence of a quaternary ammonium group, this compound is likely to exhibit moderate to good solubility in polar solvents such as water.
  • Organic Solvents: It may also dissolve well in organic solvents like ethanol and methanol due to its hydrophobic phenyl rings.
  • Solubility Variation: The solubility can vary significantly with temperature and concentration, making it essential to perform solubility tests under specific conditions for accurate data.

In summary, the solubility of this compound is influenced by both its molecular structure and the nature of the solvent used. As a general rule, **polar solvents** enhance solubility for **ionic** and **polar** compounds, while **non-polar solvents** would be less effective. Therefore, thorough investigations are often necessary to gain a complete understanding of its behavior in different environments.

Interesting facts

Interesting Facts about 2-[bis(2,6-dimethylphenyl)methoxy]ethyl-dimethyl-ammonium Chloride

This fascinating compound is a quaternary ammonium compound, which plays a significant role in various applications due to its surfactant properties. Here are some engaging insights:

  • Chemical Structure: The compound features a unique structure characterized by a nitrogen atom bonded to four organic groups, making it a typical example of quaternary ammonium compounds. The presence of 2-dimethylphenyl groups adds aromatic stability and hydrophobic properties.
  • Functionality: This compound is often used as a surfactant, which makes it crucial in formulations ranging from cleaning products to industrial applications. Its ability to reduce surface tension enhances its effectiveness in emulsifying and dispersing agents.
  • Biological Activity: Compounds like this one have been studied for their potential antibacterial and antifungal activities. They interact with microbial cell membranes, altering their permeability and leading to cell death.
  • Environmental Impact: The use of these compounds is subject to scrutiny due to their persistence in the environment. Researchers are continually investigating ways to enhance their biodegradability while maintaining efficacy.
  • Versatility: Applications for 2-[bis(2,6-dimethylphenyl)methoxy]ethyl-dimethyl-ammonium chloride extend beyond cleaning products; it can also be found in pharmaceuticals, personal care products, and as a biocide, showcasing its diversity in chemical utility.
  • Research and Development: Ongoing studies aim to optimize the synthesis of this compound for improved performance and safety in consumer products. Innovations in this area could lead to eco-friendlier alternatives to more traditional surfactants.

In summary, 2-[bis(2,6-dimethylphenyl)methoxy]ethyl-dimethyl-ammonium chloride stands as a prime example of the intricate balance between chemistry and application, underscoring the importance of these compounds in our daily lives and industries.

Synonyms
BS 5933
beta-Dimethylaminoethyl 2,6,2',6'-tetramethylbenzhydryl ether hydrochloride
N,N-Dimethyl-2-(di-2,6-xylylmethoxy)ethylamine hydrochloride
ETHYLAMINE, N,N-DIMETHYL-2-(DI-2,6-XYLYLMETHOXY)-, HYDROCHLORIDE
18539-34-9