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Methacholine chloride

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Identification
Molecular formula
C8H18ClNO2
CAS number
62-51-1
IUPAC name
[3-hydroxy-3-(4-methoxyphenyl)-5-methyl-hex-5-enyl]-dimethyl-ammonium;chloride
State
State
Methacholine chloride is generally in a solid state at room temperature, often handled as a dust or crystal form.
Melting point (Celsius)
131.50
Melting point (Kelvin)
404.65
Boiling point (Celsius)
978.15
Boiling point (Kelvin)
1 251.15
General information
Molecular weight
195.22g/mol
Molar mass
195.2000g/mol
Density
1.0904g/cm3
Appearence

Methacholine chloride is a white, crystalline powder. It typically appears as a solid at room temperature, characterized by its fine crystalline structure.

Comment on solubility

Solubility of [3-hydroxy-3-(4-methoxyphenyl)-5-methyl-hex-5-enyl]-dimethyl-ammonium;chloride

The solubility of the compound [3-hydroxy-3-(4-methoxyphenyl)-5-methyl-hex-5-enyl]-dimethyl-ammonium;chloride is influenced by several key factors:

  • Nature of the Ammonium Ion: Ammonium compounds generally demonstrate high solubility in water.
  • Presence of Hydroxyl Groups: The hydroxyl functional group contributes to the compound's ability to form hydrogen bonds, enhancing solubility in polar solvents.
  • Alkyl Chain Length: The structure includes a long hydrocarbon chain, which can hinder solubility to some extent in non-polar solvents.
  • Methoxy Group: The presence of the methoxy phenyl group may also improve solubility in organic solvents.

In summary, while such a compound may show considerable solubility in aqueous environments due to its ionic nature and functional groups, its overall solubility may vary based on the solvent polarity. As a general rule, compounds with ionic and polar characteristics are expected to be soluble in polar solvents, while non-polar regions may lead to lesser solubility in water. This balance of polar and non-polar characteristics is critical to predicting the solubility behavior of this compound.

Interesting facts

Interesting Facts about [3-Hydroxy-3-(4-methoxyphenyl)-5-methyl-hex-5-enyl]-dimethyl-ammonium; chloride

This unique compound, commonly referred to as a derivative of quaternary ammonium, is notable for its potential applications in various fields of chemistry. Here are some fascinating aspects that might capture the interest of both scientists and students:

  • Quaternary Ammonium Salts: The presence of a quaternary ammonium group implies that this compound may exhibit surfactant properties, making it valuable in formulations ranging from detergents to pharmaceuticals.
  • Biological Activity: Due to its structural complexity, the compound may interact with biological systems in intriguing ways. Researchers are investigating its potential as an antimicrobial agent or a drug candidate due to its unique functional groups.
  • Agrochemical Potential: Some studies suggest that such compounds can have applications in agriculture, potentially enhancing the efficiency of herbicides or pesticides. The 4-methoxyphenyl group may contribute to the compound’s interaction with plant systems.
  • Structure-Activity Relationship (SAR): A key area of study is how modifications to the molecular structure influence its efficacy and safety. Understanding these relationships can play a crucial role in drug design and development.
  • Chloride Role: The chloride part of the compound acts not just as a counterion but could influence solubility and reactivity, impacting how the compound performs in different environments.

As quoted by renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This sentiment underscores the endless possibilities associated with exploring compounds like this one, as ongoing research continues to unravel new applications and benefits.

Overall, while initially, one might not suspect the depth of study surrounding [3-Hydroxy-3-(4-methoxyphenyl)-5-methyl-hex-5-enyl]-dimethyl-ammonium; chloride, its intriguing structure and potential versatility make it a compelling subject for further exploration in both academic and industrial settings.

Synonyms
2238-81-5
Benzyl alcohol, alpha-(2-(dimethylamino)ethyl)-p-methoxy-alpha-(2-methylallyl)-, hydrochloride
alpha-(2-(Dimethylamino)ethyl)-p-methoxy-alpha-(2-methylallyl)benzyl alcohol hydrochloride