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Quinine dichloride

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Identification
Molecular formula
C20H25Cl2N2O
CAS number
549-24-0
IUPAC name
3-[(3-chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)oxy]propyl-dimethyl-ammonium;dichloride
State
State

Quinine dichloride is typically found in a solid state at room temperature, often in the form of crystalline powder. It is stable under normal temperatures and pressures, indicating its resistance to decomposition or reaction in typical ambient conditions.

Melting point (Celsius)
262.00
Melting point (Kelvin)
535.15
Boiling point (Celsius)
391.00
Boiling point (Kelvin)
664.15
General information
Molecular weight
400.91g/mol
Molar mass
400.9050g/mol
Density
1.2400g/cm3
Appearence

Quinine dichloride is typically a solid and appears as a crystalline substance. The crystals are often colorless or white, providing a stark and pure visual characteristic typical of crystalline chemical compounds.

Comment on solubility

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

The solubility of the compound 3-[(3-chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)oxy]propyl-dimethyl-ammonium;dichloride, can be characterized by several factors. Commonly, quaternary ammonium compounds such as this one often exhibit good solubility in polar solvents due to their ionic nature.

Factors Influencing Solubility:

  • Polarity of the Solvent: The compound is likely to dissolve well in polar solvents like water and methanol, largely because of its quaternary ammonium structure, which can interact favorably with the solvent molecules.
  • Ionic Nature: Being a dichloride salt, this compound's solubility is enhanced in aqueous solutions due to ionic dissociation.
  • Temperature: As with many compounds, increased temperature generally enhances solubility, allowing for greater kinetic energy and solubility of the ions.

Overall, while specific solubility data may vary, compounds of this nature are typically highly soluble in polar solvents, making them valuable in many applications, particularly in biochemical contexts where solubility is crucial.

Interesting facts

Interesting Facts about 3-[(3-chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)oxy]propyl-dimethyl-ammonium;dichloride

This compound, with its complex structure and intriguing properties, can be viewed through various scientific lenses. Here's what makes it noteworthy:

  • Pharmacological Potential: The unique cycloheptanoid structure of this compound positions it as a possible candidate in medicinal chemistry. Compounds that contain quinoline derivatives are often investigated for their various biological activities, including antimicrobial and anti-cancer properties.
  • Quaternary Ammonium Compounds: As a quaternary ammonium salt, this compound demonstrates properties that are typical of such salts, including surfactant characteristics. These compounds are known for their ability to interact with biological membranes, which can be crucial for drug delivery systems.
  • Structure-Activity Relationship: The specific arrangement of the chlorinated quinoline and the dimethylammonium moiety may influence its pharmacokinetic and pharmacodynamic profiles. The presence of halogens like chlorine can enhance the compound's lipophilicity and bioavailability, making it a subject of interest for researchers.
  • Potential for Applications: Beyond its medicinal implications, this compound may find use in areas such as materials science or nanotechnology, where its charged nature and amphiphilic properties can help in the formation of nanoparticles or emulsions.

In conclusion, 3-[(3-chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinolin-5-ium-11-yl)oxy]propyl-dimethyl-ammonium;dichloride serves as an example of how complex organic structures have the potential to contribute to advancing scientific knowledge and applications. As researchers delve deeper into its properties and interactions, the vast field of chemical research continues to evolve.

Synonyms
5601-21-8
6H-Cyclohepta(b)quinoline, 3-chloro-11-(3-(dimethylamino)propoxy)-7,8,9,10-tetrahydro-, dihydrochloride
3-Chloro-11-(3-(dimethylamino)propoxy)-7,8,9,10-tetrahydro-6H-cyclohepta(b)quinoline 2HCl