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Menthol methyltransferase

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Identification
Molecular formula
C11H22ClN
CAS number
102-97-6
IUPAC name
methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride
State
State

At room temperature, methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is in a solid state. It is stable under normal conditions and does not readily convert to liquid or gas.

Melting point (Celsius)
186.00
Melting point (Kelvin)
459.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
195.71g/mol
Molar mass
195.7100g/mol
Density
1.0500g/cm3
Appearence

The compound typically appears as a white crystalline solid or powder, often having a very high degree of transparency and purity. Its appearance is consistent with many ionic salts in its class.

Comment on solubility

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

The solubility of methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride can be an intriguing subject due to its unique structural attributes. This compound is an ammonium salt, and typically, ammonium salts are known for their solubility properties. Here are some key points about its solubility:

  • Polar Nature: Being an ammonium compound, it generally exhibits polar characteristics, making it soluble in polar solvents such as water.
  • Hydrogen Bonding: The presence of the ammonium group allows for hydrogen bonding with water, enhancing its solubility.
  • Organic Solvents: It may also dissolve in certain organic solvents, but the degree of solubility can vary based on the solvent's polarity.
  • Ionic Interaction: The chloride ion (Cl-) typically favors high solubility due to its ability to interact well with polar solvents.

Overall, the combination of its chemical structure and the presence of ionic and polar groups suggests that methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride has a good potential for solubility, particularly in aqueous solutions. As with many complex organic compounds, factors such as temperature and concentration also play significant roles in determining the exact solubility behavior.

Interesting facts

Interesting Facts About Methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride

Methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is a fascinating compound that belongs to the class of quaternary ammonium salts. Here are some intriguing insights into its chemistry and applications:

  • Structure and Symmetry: This compound features a unique norbornane framework, characterized by its bridgehead carbon atoms and highly branched substituents. This structural complexity can lead to interesting steric and electronic properties, influencing reactivity and interactions with other molecules.
  • Quaternary Ammonium Benefits: As a quaternary ammonium compound, it holds notable advantages in various fields, such as:
    • Anti-bacterial and anti-fungal properties, making it valuable in healthcare.
    • Application as surfactants in detergents and shampoos, showcasing its versatility.
  • Applications in Science and Industry: The compound is often utilized as a phase transfer catalyst in organic synthesis, allowing for the efficient transfer of reagents between phases. This promotes improved reaction kinetics and can lead to higher yields in synthetic procedures.
  • Research Exploration: The unique configuration of methyl groups and its interaction with other molecules make it an excellent candidate for studies in molecular recognition and host-guest chemistry.

Not only does this compound have a rich chemical profile, but its application potential continues to inspire research and development in both academic and industrial settings. As scientists and chemists delve deeper into its properties, the possibilities for innovation remain vast.

Synonyms
(+-)-endo-N-Methyl-2-bornanamine hydrochloride
22321-23-9
2-BORNANAMINE, N-METHYL-, HYDROCHLORIDE, endo-(+-)-
USP Mecyclamine Related Compound A
MECAMYLAMINE RELATED COMPOUND A (10 MG) (N,1,7,7-TETRAMETHYL BICYCLO [2.2.1] HEPTAN-2-AMINE HYDROCHLORIDE)