Skip to main content

Apomorphine hydrochloride

ADVERTISEMENT
Identification
Molecular formula
C17H17ClNO2
CAS number
41372-20-7
IUPAC name
(6aR)-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride
State
State

At room temperature, apomorphine hydrochloride is typically found in a solid state in the form of crystalline powder.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.15
Boiling point (Celsius)
272.00
Boiling point (Kelvin)
545.15
General information
Molecular weight
312.81g/mol
Molar mass
312.8140g/mol
Density
1.4300g/cm3
Appearence

Apomorphine hydrochloride typically appears as a pale green crystalline powder that may have a slight discoloration. It can also appear as a colorless to slightly yellow crystalline substance when highly pure. This compound is sensitive to light and air, leading to gradual decomposition which causes a darker color over time.

Comment on solubility

Solubility of (6aR)-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride

The solubility of (6aR)-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride can be complex and is influenced by several factors. Understanding the solubility properties of this compound is essential, especially in applications such as pharmaceuticals and material sciences. Here are some key points regarding its solubility:

  • Polar Solvents: This compound is likely to display higher solubility in polar solvents due to its ionic nature, thanks to the presence of the chloride ion.
  • Nonpolar Solvents: Conversely, solubility in nonpolar solvents may be limited owing to its polycyclic structure that hinders interactions with nonpolar environments.
  • Temperature Influence: It is important to note that solubility can increase with temperature; as the temperature rises, kinetic energy enhances interactions between solute and solvent.
  • pH Dependence: The solubility may also vary with changes in pH, which can affect ionization states and consequently, solubility behavior.

In summary, the solubility of (6aR)-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride is characterized by its dependence on the solvent's polarity, temperature, and pH of the solution. Understanding these factors is crucial for optimizing its usage in various applications.

Interesting facts

Interesting Facts about (6aR)-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride

(6aR)-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride is a fascinating compound with a unique structure and potential applications in various fields. Here are some notable features that highlight its significance:

  • Structural Complexity: This compound features a dibenzoquinoline framework, which is known for its intricate fused ring systems. Such structures often display interesting chemical properties due to their rigid configuration.
  • Biological Relevance: Compounds with the dibenzoquinoline structure have been studied for their biological activities, including potential roles in anticancer therapies and neuroprotective effects. Their interactions with biological molecules make them candidates for drug design.
  • Electron-Deficient Nature: The presence of the quaternary ammonium group (the cationic part of the molecule) contributes to the compound's electron-deficient characteristics, which can enhance its reactivity towards nucleophiles.
  • Chloride Ion Influence: The chloride component can influence the solubility and reactivity of the compound, affecting how it interacts in biological systems or industrial applications.
  • Potential Applications: This molecule may have uses in various areas including:
    • Pharmaceutical development
    • Organic electronics
    • Catalysis

The study of such compounds not only expands our understanding of organic chemistry but also paves the way for innovative solutions to contemporary challenges. The interplay between structure and function in (6aR)-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride exemplifies the beauty and complexity of chemical compounds.

Synonyms
Norapomorphine hydrochloride
20382-69-8
(6aR)-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol;chloride
R-(-)-Norapomorphine Hydrochloride
6a-beta-NORAPORPHINE-10,11-DIOL, HYDROCHLORIDE