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Methantheline chloride

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Identification
Molecular formula
C21H26ClNO
CAS number
82-13-7
IUPAC name
2-hydroxyethyl-(1-methyl-2,2-diphenyl-ethyl)ammonium;chloride
State
State

At room temperature, Methantheline chloride is typically found in a solid state.

Melting point (Celsius)
224.00
Melting point (Kelvin)
497.15
Boiling point (Celsius)
996.00
Boiling point (Kelvin)
1 269.15
General information
Molecular weight
379.95g/mol
Molar mass
379.9500g/mol
Density
1.1351g/cm3
Appearence

Methantheline chloride is typically a white to off-white powder. It is highly soluble in water and forms clear solutions when dissolved.

Comment on solubility

Solubility of 2-hydroxyethyl-(1-methyl-2,2-diphenyl-ethyl)ammonium chloride

When evaluating the solubility of 2-hydroxyethyl-(1-methyl-2,2-diphenyl-ethyl)ammonium chloride, several factors come into play due to its unique chemical structure. This compound typically exhibits the following characteristics:

  • Water Solubility: It is likely to be soluble in water because of the presence of the -OH (hydroxyl) group which can engage in hydrogen bonding, enhancing its interaction with water molecules.
  • Polar Solvents: The presence of a quaternary ammonium group in its structure generally increases solubility in polar solvents.
  • Non-Polar Solvents: However, due to its bulky diphenyl structure, solubility in non-polar solvents may be limited, indicating a more complex solubility profile.

In essence, it can be concluded that:

  1. Soluble in water and polar solvents
  2. Limited solubility in non-polar solvents

To summarize, the solubility of 2-hydroxyethyl-(1-methyl-2,2-diphenyl-ethyl)ammonium chloride presents a fascinating interplay between its polar and non-polar components, showcasing the intricacies of solubility in chemical compounds.

Interesting facts

Interesting Facts about 2-Hydroxyethyl-(1-methyl-2,2-diphenyl-ethyl)ammonium Chloride

This compound belongs to a fascinating class of quaternary ammonium salts, which are known for their diverse applications in various fields, from pharmaceuticals to industrial processes. Here are some intriguing aspects of this compound:

  • Quaternization: The presence of a quaternary ammonium group gives this compound unique properties such as enhanced solubility and antimicrobial activity.
  • Structure: The molecule features an ethyl and a diphenyl group, creating a unique steric environment that may impact its reactivity and interactions.
  • Biological Activity: Compounds similar to this one are often studied for their potential therapeutic properties, particularly in treating bacterial infections, due to their ability to disrupt microbial cell membranes.

As science writer John L. F. Cadden aptly put it: "Quaternary ammonium compounds are the unsung heroes of modern chemistry, providing solutions in unsuspected areas." This highlights the importance of this category of compounds in advancing both chemical research and practical applications.

Potential Applications

The compound's unique characteristics suggest a variety of potential applications, such as:

  • Use in antimicrobial agents for disinfectants and hygiene products.
  • Possible incorporation into drug formulations to enhance bioavailability.
  • Role in synthesis pathways for other complex organic compounds.

This compound serves as a perfect example of how the intersection of organic chemistry and practical application can fuel advancements in both science and industry. Its study may lead to groundbreaking discoveries that impact our understanding of chemical interactions and their uses in everyday life.

Synonyms
DPA 307
2-((1-Methyl-2,2-diphenylethyl)amino)ethanol hydrochloride
1,1-Diphenyl-2-(N-beta-hydroxyaethylamino)propanhydrochlorid [German]
ETHANOL, 2-((1-METHYL-2,2-DIPHENYLETHYL)AMINO)-, MONOHYDROCHLORIDE
23164-28-5
1,1-Diphenyl-2-(N-beta-hydroxyaethylamino)propanhydrochlorid
RefChem:340758