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Quinacrine dihydrochloride

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Identification
Molecular formula
C23H30Cl2N4O
CAS number
69-05-6
IUPAC name
[4-carboxy-7-(diethylammonio)-4-(1-naphthyl)heptyl]-diethyl-ammonium;dichloride
State
State

At room temperature, Quinacrine dihydrochloride is typically in a solid state. It is stable under normal conditions and is stored as a powder due to its crystalline nature. The compound is handled in solid form for most applications.

Melting point (Celsius)
239.00
Melting point (Kelvin)
512.15
Boiling point (Celsius)
363.00
Boiling point (Kelvin)
636.15
General information
Molecular weight
505.43g/mol
Molar mass
505.4290g/mol
Density
1.1205g/cm3
Appearence

Quinacrine dihydrochloride typically appears as a bright yellow crystalline powder. It is known for its vivid color, which is a characteristic feature of many dyes and related chemical compounds. The powder is often used in solutions, where it imparts a strong yellow coloration.

Comment on solubility

Solubility of [4-carboxy-7-(diethylammonio)-4-(1-naphthyl)heptyl]-diethyl-ammonium;dichloride

The solubility of the compound [4-carboxy-7-(diethylammonio)-4-(1-naphthyl)heptyl]-diethyl-ammonium;dichloride is influenced by several key factors:

  • Ionic Nature: Being a quaternary ammonium salt, this compound exhibits ionic characteristics which typically enhance solubility in polar solvents such as water.
  • Hydrophilic Functional Groups: The presence of the carboxylic acid group (-COOH) contributes to its solubility by allowing hydrogen bonding and interaction with water molecules.
  • Molecular Structure: The aliphatic hydrocarbon segments may exhibit hydrophobic behavior, potentially reducing overall solubility but can be countered by the positively charged diethylammonio groups.
  • Effect of Counterions: The dichloride counterion can enhance solubility since chlorides are generally soluble in water.

Overall, one can anticipate that the compound will demonstrate a fair degree of solubility in polar solvents, while demonstrating lower solubility in non-polar solvents. It is essential to conduct specific solubility experiments under various conditions to gain precise insights into its solubility characteristics.

Interesting facts

Interesting Facts about [4-carboxy-7-(diethylammonio)-4-(1-naphthyl)heptyl]-diethyl-ammonium;dichloride

This fascinating compound belongs to the class of ammonium salts and is notable for its unique structure and potential applications in various scientific fields. Below are some engaging facts about this compound:

  • Complex Structure: The compound features a complex arrangement, including a carboxyl group and a naphthyl moiety, which contribute to its intriguing chemical behavior.
  • Charge Dynamics: As an ammonium salt, it carries a positive charge due to the diethylammonio groups, impacting its interactions with other ions and molecules.
  • Biological Relevance: Compounds with similar structures have been explored for their potential roles in medicinal chemistry, particularly in developing pharmaceuticals that target specific biological pathways.
  • Solvent Interactions: Its unique functional groups may facilitate interactions with different solvents, leading to interesting solvation effects that are valuable for researchers.
  • Application in Research: Scientists are particularly interested in its influence on membrane potentials and ion transport, which has implications for studying cellular processes.

Overall, [4-carboxy-7-(diethylammonio)-4-(1-naphthyl)heptyl]-diethyl-ammonium;dichloride serves as an exemplary case of how the elaborate architecture of chemical compounds can pave the way for discovery in both fundamental and applied sciences.

Synonyms
1-Naphthaleneacetic acid, alpha,alpha-bis(3-(diethylamino)propyl)-, dihydrochloride
6394-75-8
alpha,alpha-Bis(3-(diethylamino)propyl)-1-naphthaleneacetic acid dihydrochloride