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Butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]ammonium chloride

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Identification
Molecular formula
C16H26ClNO3
CAS number
728214-70-8
IUPAC name
butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]ammonium;chloride
State
State

This compound is typically a solid at room temperature. Given its structure and molecular weight, it exists as a crystalline solid under standard conditions.

Melting point (Celsius)
186.00
Melting point (Kelvin)
459.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
303.83g/mol
Molar mass
303.8330g/mol
Density
1.1580g/cm3
Appearence

Butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]ammonium chloride often appears as a white to off-white crystalline solid. It can be hygroscopic in nature, meaning it may absorb moisture from the air.

Comment on solubility

Solubility of Butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]ammonium Chloride

The solubility of butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]ammonium chloride can be influenced by several factors, making it quite a fascinating compound to study. Its structure features both hydrophobic (butyl) and hydrophilic (ammonium and ethoxy) components, which grants it unique solubility characteristics.

Factors Affecting Solubility:

  • Polarity: The presence of the ammonium group typically increases the compound's affinity for water, leading to higher solubility in aqueous environments.
  • Hydrophobic Interactions: The butyl group may contribute to lower solubility in polar solvents. Therefore, solubility may be enhanced in organic solvents, particularly those that can interact favorably with hydrophobic moieties.
  • Temperature: In general, increasing temperature can increase solubility, particularly for ionic compounds like this one.
  • pH Levels: Being an ammonium salt, changes in pH could alter its solubility, affecting the ionization of the ammonium group.

In summary, while butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]ammonium chloride is expected to be soluble in water due to its ionic nature, the exact solubility will depend on the specific solvent and environmental conditions. Understanding these interactions can help predict its behavior in various chemical contexts.

Interesting facts

Interesting Facts about Butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]ammonium Chloride

This compound is an intriguing member of the class of ammonium salts known for their role in various biological and industrial applications. Here are some noteworthy points regarding this compound:

  • Biological Relevance: It is often studied for its potential pharmacological properties, particularly its interactions with biological membranes.
  • Synthetic Pathways: The synthesis of this compound involves a unique route that combines dioxin chemistry with quaternary ammonium salt formation, showcasing creative approaches in chemical synthesis.
  • Applications in Material Science: Due to its ionic nature, this compound may be utilized in creating conductive polymers or in surfactant formulations, increasing its utility in material science.
  • Research Potential: The compound's structure suggests it might exhibit interesting reactivity, making it an interesting subject for further research in drug delivery systems.
  • Interdisciplinary Connections: Understanding this compound can bridge multiple disciplines, including organic chemistry, pharmacology, and materials science, leading to innovative applications in various fields.

Overall, the study of butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]ammonium chloride not only highlights its intriguing chemistry but also opens pathways to explore its applications in diverse scientific realms.

Synonyms
Ethomoxane hydrochloride
6038-78-4
M77KGL2QN0
butyl-[(5-ethoxy-2,3-dihydro-1,4-benzodioxin-3-yl)methyl]azanium;chloride
883F HCl
EINECS 227-924-9
UNII-M77KGL2QN0
NSC 106903
dl-8-Ethoxy-2-(n-butylaminomethyl)-1,4-benzodioxane hydrochloride
(+-)-2-(Butylaminomethyl)-8-ethoxy-1,4-benzodioxan hydrochloride
1,4-Benzodioxan-2-methanamine, N-butyl-8-ethoxy-2,3-dihydro-, hydrochloride
1,4-Benzodioxan-2-methanamine, N-butyl-8-ethoxy-2,3-dihydro-, hydrochloride, (+-)-