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Tetrabutylammonium chloride

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Identification
Molecular formula
C25H41ClN
CAS number
1112-67-0
IUPAC name
methane;p-tolylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

At room temperature, the compound is typically in a crystalline form and is solid.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.15
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.15
General information
Molecular weight
325.90g/mol
Molar mass
325.8970g/mol
Density
1.0520g/cm3
Appearence

Methane;p-tolylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride appears as a white crystalline solid which is soluble in water and other polar solvents. The compound may have a slight amine-like odor due to the ammonium component.

Comment on solubility

Solubility of p-Tolylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride

The solubility of p-tolylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride can be described as intriguing due to its unique structural characteristics. Here are the key points to consider:

  • Polarity: The ammonium ion contributes to its ionic character, which generally enhances solubility in polar solvents.
  • Solvent Interaction: It is likely to be soluble in water and other polar solvents due to hydrogen bonding capabilities.
  • Hydrophobic Character: The presence of bulky hydrocarbon groups may decrease its solubility in nonpolar solvents.
  • Temperature Effects: Solubility can vary with temperature; elevated temperatures typically improve the solubility of ionic compounds in water.

In conclusion, the solubility of this compound is characterized by the interplay between its ionic nature and the hydrophobic regions derived from its unique structure. As with many ammonium salts, understanding the solvent environment is critical to predicting and explaining its solubility behavior.

Interesting facts

Interesting Facts about p-Tolylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride

p-Tolylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is a fascinating compound that demonstrates the complex interplay between organic chemistry and molecular structure. Here are some captivating insights about this compound:

  • Quaternary Ammonium Salt: This compound belongs to a group known as quaternary ammonium salts, which are noted for their significant roles in biological systems and industrial applications.
  • Chiral Center: The presence of a chiral center makes this compound a subject of interest in stereochemistry, highlighting how different spatial arrangements can influence biochemical interactions.
  • Applications: Compounds like p-tolylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride can be utilized in various fields, including:
    • Pharmaceuticals: Acting as intermediates in drug synthesis.
    • Surface Chemistry: As surfactants to modify surface properties.
    • Catalysis: Playing roles in catalytic processes that enhance reactivity in organic reactions.
  • Interaction with Biological Systems: The ammonium portion of the compound can interact with biological membranes, possibly leading to applications in drug delivery systems.
  • Structural Complexity: The 1,7,7-trimethylnorbornan-2-yl framework provides a unique steric environment, influencing the compound's reactivity and interaction with other molecules.

To encapsulate, p-tolylmethyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is more than just a compound; it embodies a realm of possibilities in science, showcasing how molecular structure governs functionality. As researchers delve into its properties, they may uncover novel applications that bridge chemistry and real-world solutions.

Synonyms
(+-)-endo-N-(p-Methylbenzyl)-2-bornanamine hydrochloride
24652-87-7
2-BORNANAMINE, N-(p-METHYLBENZYL)-, HYDROCHLORIDE, endo-(+-)-
RefChem:256683