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2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium dichloride

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Identification
Molecular formula
C36H40N2Cl2
CAS number
37510-23-5
IUPAC name
2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium;dichloride
State
State

At room temperature, it is typically a solid.

Melting point (Celsius)
200.00
Melting point (Kelvin)
473.15
Boiling point (Celsius)
365.20
Boiling point (Kelvin)
638.20
General information
Molecular weight
531.58g/mol
Molar mass
531.5800g/mol
Density
1.3005g/cm3
Appearence

It appears as a colorless or pale yellow crystalline powder.

Comment on solubility

Solubility of 2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium; dichloride

The solubility of the compound 2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium; dichloride can be described as follows:

  • Solubility in Water: Generally, ionic compounds like dichlorides can exhibit varied solubility profiles in water. While the presence of charged groups in the molecular structure suggests potential solubility, the hydrophobic hexadecyl chain could impede complete dissolution.
  • Solubility in Organic Solvents: Given the hydrophobic nature contributed by the long alkyl chain, this compound may have increased solubility in non-polar organic solvents. Compounds with long hydrocarbon tails tend to preferentially solubilize in environments that match their non-polar characteristics.
  • Temperature Dependence: Solubility is often affected by temperature. Increased temperatures can enhance solubility, particularly in organic solvents, due to greater molecular movement.

In conclusion, while ionic character points to potential water solubility, the significant hydrophobic component leads to a more complex solubility profile that may favor organic solvents over aqueous environments. It is essential to consider both the ionic and hydrophobic aspects when predicting the solubility behavior of this compound.

Interesting facts

Interesting Facts about 2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium;dichloride

This fascinating compound, known as 2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium;dichloride, is noteworthy for its structural complexity and potential applications in various fields of research. Here are some compelling aspects that highlight its significance:

  • Quinoline Structure: The presence of isoquinoline moieties provides unique electronic properties that can be exploited in pharmaceutical development, as these compounds often interact with biological targets in intriguing ways.
  • Ion Exchange: As a dichloride salt, it has the capacity for ion exchange, which can be particularly useful in studies related to ionic conductivity and ion transport in biological systems.
  • Antimicrobial Potential: Compounds containing isoquinoline derivatives have demonstrated varying levels of antimicrobial activity. Research continues to explore how this specific compound interacts with microbial agents, opening doors to novel therapeutic strategies.
  • Material Science: Its unique properties might pave the way for innovative advancements in material science, particularly in the development of organic semiconductors and other advanced materials.
  • Fluorescent Properties: Isoquinoline compounds are known for their fluorescence, making this compound a candidate for applications in fluorescent imaging and sensing technologies.
  • Research Opportunities: The dual isoquinoline structure invites extensive research into its mechanisms of action and structure-activity relationships, which could unveil new compounds with improved efficacy.

In summary, 2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium;dichloride captures attention due to its complex structure and potential implications in medicinal chemistry, material sciences, and beyond. Its exploration is likely to reveal further insights into the roles that isoquinoline-based compounds can play in advancing both science and technology.

Synonyms
Hedaquinium chloride
Teoquil chloride
Teoquil
4310-89-8
Cloruro de hedaquinio
Chlorure d'hedaquinium
USAF XR-39
Hedaquinii chloridum
2,2'-Hexadecamethylenebis(isoquinolinium chloride)
BIQ 16
Hedaquinium chloride [INN:BAN]
Hedaquinii chloridum [INN-Latin]
UNII-VKH4J07Q4K
EINECS 224-325-4
Chlorure d'hedaquinium [INN-French]
Cloruro de hedaquinio [INN-Spanish]
VKH4J07Q4K
B1Q 16
Hexadecane-1,16-bis-isoquinolinium chloride
B1Q-16
Isoquinolinium, 2,2'-(1,16-hexadecadecanediyl)bis-, dichloride
HEDAQUINIUM CHLORIDE [INN]
ISOQUINOLINIUM, 2,2'-HEXADECAMETHYLENEBIS-, DICHLORIDE
Hedaquinii chloridum (INN-Latin)
Chlorure d'hedaquinium (INN-French)
Cloruro de hedaquinio (INN-Spanish)
224-325-4
2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium;dichloride
2-(16-isoquinolin-2-ium-2-ylhexadecyl)isoquinolin-2-ium dichloride
SCHEMBL2733777
CHEMBL2106247
DTXSID20962898
KZUZUJNAVUAVOW-UHFFFAOYSA-L
AKOS040748521
NS00047931
Q27291871
2,2'-(Hexadecane-1,16-diyl)di(isoquinolin-2-ium) dichloride
ISOQUINOLINIUM, 2,2'-(1,16-HEXADECANEDIYL)BIS-, CHLORIDE (1:2)