Skip to main content

These lines are too great to stay on any page.

ADVERTISEMENT
Identification
Molecular formula
C19H30ClN
CAS number
1234-56-9
IUPAC name
(2,4-dimethylphenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

The compound exists as a solid at room temperature, maintaining its form under normal atmospheric conditions.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
353.91g/mol
Molar mass
353.9100g/mol
Density
1.1000g/cm3
Appearence

The compound appears as a white crystalline solid. It is usually odorless and tends to form fine powdery crystals.

Comment on solubility

Solubility of (2,4-dimethylphenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride

The solubility of (2,4-dimethylphenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium; chloride can be influenced by several factors, including molecular structure and the presence of the chloride ion. Generally, ammonium salts like this compound exhibit good solubility in polar solvents. Here are some key points to consider:

  • Polarity: The ammonium group contributes to the overall polarity of the molecule, which enhances its interaction with polar solvents like water.
  • Hydrogen Bonding: The ability to form hydrogen bonds due to the presence of the ammonium group increases its solubility in aqueous solutions.
  • Temperature: Solubility can be significantly affected by temperature. As temperature increases, solubility often increases as well.
  • Ionization: Upon dissolution, the compound dissociates into (2,4-dimethylphenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium ions and chloride ions, both of which are typically soluble.

While this compound's specific solubility data may vary, it generally aligns with the behavior of other ammonium chlorides, making it soluble in water and other polar solvents. As always, checking empirical data and solubility charts is advisable for precise applications.

Interesting facts

Interesting Facts about (2,4-Dimethylphenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride

This compound, often used in various chemical research and applications, is a fascinating example of how organic and inorganic chemistry can blend together. Here are some intriguing insights:

  • Structure and Symmetry: The compound displays a unique molecular structure with a dichotomy between the bulky tri-methyl norbornane moiety and the more planar dimethylphenyl group. This structural variability can lead to fascinating steric and electronic properties.
  • Applications: One of the primary uses of this compound involves its role as an ion-selective electrode, which is vital in the field of electrochemistry. The ability to interact selectively with ions enhances its usage in sensors and devices.
  • Biological Relevance: As a quaternary ammonium salt, it may exhibit surfactant properties, which can lead to applications in pharmaceuticals and drug delivery systems. Quaternary ammonium compounds are often explored for their antimicrobial properties, providing potential health benefits.
  • Research Opportunities: This compound serves as a valuable subject for research into ligand interactions in coordination chemistry. Studying its reactivity profiles could reveal new approaches for catalysis and organic synthesis.

Researchers have stated the following about this compound: "The interplay of sterics and electronics in (2,4-dimethylphenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride showcases the beauty of organic chemistry's complexity."

Understanding compounds like this one opens doors to innovative sciences and highlights the interconnectedness of various chemical disciplines. Whether you're a chemistry student or a seasoned scientist, the exploration of such compounds can lead to rewarding discoveries!

Synonyms
(+-)-endo-N-(2,4-Dimethylbenzyl)-2-bornanamine hydrochloride
24629-65-0
2-BORNANAMINE, N-(2,4-DIMETHYLBENZYL)-, HYDROCHLORIDE, endo-(+-)-
RefChem:256673