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Dimethylpropranolol-dichloride

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Identification
Molecular formula
C22H32N2O5Cl2
CAS number
119302-37-7
IUPAC name
dimethyl-[3-[(2,3,4-trimethoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)oxy]propyl]ammonium;dichloride
State
State

At room temperature, dimethylpropranolol-dichloride is in a solid crystalline state. The compound is generally stable under normal conditions but should be handled carefully to prevent decomposition.

Melting point (Celsius)
270.00
Melting point (Kelvin)
543.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
422.37g/mol
Molar mass
422.3670g/mol
Density
1.1246g/cm3
Appearence

Dimethylpropranolol-dichloride is typically a white crystalline powder. The compound is hygroscopic, meaning it can absorb moisture from the environment. It is usually supplied in a solid form and should be stored under a desiccator to prevent clumping or degradation due to moisture uptake.

Comment on solubility

Solubility of Dimethyl-[3-[(2,3,4-trimethoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)oxy]propyl]ammonium;dichloride

The solubility of the compound dimethyl-[3-[(2,3,4-trimethoxy-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)oxy]propyl]ammonium;dichloride can be influenced by several factors, primarily due to its complex structure. Here are some key points regarding its solubility:

  • Polarity: This compound contains multiple methoxy groups and a quaternary ammonium group, which may enhance its solubility in polar solvents such as water.
  • Nature of the salt: As a dichloride salt, it is generally more soluble in water compared to its parent free base compound due to the ionic nature of the chloride ions.
  • Solvent considerations: The solubility in organic solvents may vary, and it could be more soluble in methanol or ethanol due to the presence of methoxy groups.
  • pH dependence: The solubility may also change with pH, particularly because quaternary ammonium compounds can interact differently in acid or alkaline conditions.

In summary, the solubility of this compound in aqueous solutions is likely to be relatively high due to its ionic nature and polar functional groups, while its solubility in organic solvents may offer varied results depending on the solvent composition.

Interesting facts

Interesting Facts about Dimethyl-[3-[(2,3,4-trimethoxy-7,8,9,10-tetrahydro-6H-cycloheptabquinolin-5-ium-11-yl)oxy]propyl]ammonium; Dichloride

This compound is a fascinating member of a class of chemicals known for their structural complexity and potential biological applications. The molecule features a unique quaternary ammonium structure with appended methoxy groups, contributing to its chemical behavior and interactions.

Noteworthy Attributes

  • Structural Diversity: The compound contains a quaternary ammonium ion, making it amphiphilic. This property often allows such compounds to interact with biological membranes.
  • Biological Potential: Compounds like this one are studied for their pharmacological effects. The cyclic structure of the quinoline moiety suggests potential for use in medicinal chemistry, especially in antimalarial and anticancer research.
  • Research Interest: Its intricate design, particularly the presence of methoxy groups, may enhance solubility and bioavailability, sparking interest in further pharmaceutical development.

Applications and Research

This compound's unique properties position it as a candidate for various applications:

  • Drug Development: Researchers are exploring the bioactivity of similar compounds to understand their mechanism of action in targeting specific diseases.
  • Material Science: Interestingly, quaternary ammonium compounds are often used as surfactants and can improve the performance of coatings and polymers.

As scientists continue to unravel the complexities and potential of such compounds, it's evident that dimethyl-[3-[(2,3,4-trimethoxy-7,8,9,10-tetrahydro-6H-cycloheptabquinolin-5-ium-11-yl)oxy]propyl]ammonium; dichloride could play a pivotal role in bridging chemistry with therapeutic advancements.

Synonyms
18833-65-3
6H-Cyclohepta(b)quinoline, 11-(3-(dimethylamino)propoxy)-7,8,9,10-tetrahydro-2,3,4-trimethoxy-, dihydrochloride