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Quinoline Yellow

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Identification
Molecular formula
C27H25ClN2
CAS number
8004-92-0
IUPAC name
2-[2-(2,5-dimethyl-1-phenyl-pyrrol-3-yl)vinyl]-N,N,1-trimethyl-quinolin-1-ium-6-amine;chloride
State
State

At room temperature, Quinoline Yellow is typically found in a solid state. This compound is mainly used in solid form for industrial applications, particularly in dyeing processes due to its intense yellow coloration. It is stable under normal conditions and does not evaporate into gases.

Melting point (Celsius)
168.00
Melting point (Kelvin)
441.15
Boiling point (Celsius)
498.00
Boiling point (Kelvin)
771.15
General information
Molecular weight
401.92g/mol
Molar mass
401.9160g/mol
Density
1.1490g/cm3
Appearence

Quinoline Yellow, in this chloride form, typically appears as a solid crystalline powder. The color is distinctively bright yellow, which is why it's often used in dyes and pigments. The powder can sometimes form clumps and is known for its vibrant hue in solutions.

Comment on solubility

Solubility of 2-[2-(2,5-dimethyl-1-phenyl-pyrrol-3-yl)vinyl]-N,N,1-trimethyl-quinolin-1-ium-6-amine;chloride

This complex organic compound is characterized by its unique structure, and its solubility presents interesting aspects to explore. Generally, the solubility of a compound like this is influenced by several factors:

  • Polarity: The presence of quaternary ammonium groups often enhances solubility in polar solvents, thereby suggesting that this compound may be soluble in water or alcohols.
  • Hydrophilicity: Chloride ions can contribute to higher solubility in aqueous environments due to their ability to interact with water molecules.
  • Organic Solvents: Given the hydrophobic characteristics of the phenyl and pyrrole rings, this compound is likely to exhibit better solubility in organic solvents such as DMSO or ethanol.
  • Temperature Dependency: As with many compounds, solubility can increase with temperature, making higher temperatures advantageous for dissolving this compound in various solvents.

In summary, one could expect
the solubility behavior of this compound to be multifaceted. As with many organic salts, the solubility in aqueous versus organic media is a key consideration, and numerous studies could open up further investigations on this compound's specific solubility profiles.

Interesting facts

Facts about 2-[2-(2,5-dimethyl-1-phenyl-pyrrol-3-yl)vinyl]-N,N,1-trimethyl-quinolin-1-ium-6-amine;chloride

This versatile compound is part of the quaternary ammonium salt family, characterized by its distinctive nitrogen atom connected to four carbon-containing groups. Here are some insightful facts about this unique chemical:

  • Dynamic Structure: The presence of both a quinolinium and a pyrrole unit in its structure imparts interesting electronic and photophysical properties, making this compound valuable in various applications.
  • Fluorescent Properties: With its complex molecular structure, this compound is known to exhibit interesting fluorescence characteristics, which can be harnessed in areas like biological imaging and sensing.
  • Potential in Medicine: The intricate architecture of this compound offers potential in medicinal chemistry, particularly in the development of new pharmaceuticals that target specific biological pathways.
  • Research Applications: Scientists are investigating this compound for its role in organic electronics and as a dye-sensitizer in solar cells, showcasing its versatility even beyond medicinal uses.
  • Stability: The quaternary ammonium structure contributes to its stability in various solvents, which is particularly important in both research and industrial applications.

In summary, 2-[2-(2,5-dimethyl-1-phenyl-pyrrol-3-yl)vinyl]-N,N,1-trimethyl-quinolin-1-ium-6-amine;chloride embodies the intersection of organic chemistry and applied science. Its unique properties and potential for innovative applications continue to spark the curiosity and ingenuity of researchers in the field.

Synonyms
DTXSID90970147