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Cresyl Violet

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Identification
Molecular formula
C28H22N3S2.Cl
CAS number
10510-54-0
IUPAC name
1-ethyl-2-[(1-ethylbenzo[e][1,3]benzothiazol-1-ium-2-yl)methylene]benzo[e][1,3]benzothiazole
State
State

At room temperature, Cresyl Violet is typically a solid in powder form.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.15
Boiling point (Celsius)
297.00
Boiling point (Kelvin)
570.15
General information
Molecular weight
443.57g/mol
Molar mass
443.5680g/mol
Density
1.3300g/cm3
Appearence

Cresyl Violet appears as a dark violet to red powder. When dissolved, it produces a violet solution, which is used commonly in histological stains.

Comment on solubility

Solubility of 1-ethyl-2-[(1-ethylbenzo[e][1,3]benzothiazol-1-ium-2-yl)methylene]benzo[e][1,3]benzothiazole

The solubility of the compound 1-ethyl-2-[(1-ethylbenzo[e][1,3]benzothiazol-1-ium-2-yl)methylene]benzo[e][1,3]benzothiazole is influenced by several fascinating factors:

  • Polarity: The structure of the compound suggests it has regions of both polar and nonpolar character. This differential polarity can affect how well it dissolves in various solvents.
  • Solvent Choice: Typically, compounds with greater aromatic character may have higher solubility in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), or acetone rather than in polar solvents like water.
  • Functional Groups: The presence of the benzothiazole moiety can contribute to solubility in polar organic solvents due to potential interactions with solvents.
  • Temperature Influence: Like many organic compounds, solubility can increase with temperature.

In summary, understanding the solubility of this intricate compound requires consideration of its molecular structure, the nature of available solvents, and practical temperature conditions. As with many compounds of this nature, empirical testing is often necessary to fully comprehend its solubility characteristics. Always bear in mind that “solubility is the key to reactivity!”

Interesting facts

Interesting Facts about 1-Ethyl-2-[(1-ethylbenzo[e][1,3]benzothiazol-1-ium-2-yl)methylene]benzo[e][1,3]benzothiazole

This remarkable compound is a part of the benzothiazole family, which is known for its versatile applications and interesting properties. Here are some fascinating insights:

  • Structure and Function: The compound features a complex structure with multiple aromatic rings, giving it unique electronic properties. The incorporation of the 1-ethylbenzo[e][1,3]benzothiazol-1-ium unit enhances its potential for use in electronic devices, particularly in organic light-emitting diodes (OLEDs).
  • Fluorescent Activity: Compounds like this one are often studied for their luminescent properties. They can fluoresce under ultraviolet light, making them potential candidates for applications in sensors and bioimaging.
  • Biological Relevance: Several benzothiazole derivatives have been investigated for their biological activities, including anti-cancer and anti-bacterial properties. This compound could represent a new avenue in pharmaceutical research.
  • Research and Development: As an area of active study, organic electronics are rapidly evolving. Compounds with such unique structures may pave the way for breakthroughs in energy-efficient technologies and novel materials science.
  • Potential as Dye: Due to their bright colors and robust chemical stability, compounds of this nature are also being explored as dyes in various industries, including textiles and food.

The exploration of 1-ethyl-2-[(1-ethylbenzo[e][1,3]benzothiazol-1-ium-2-yl)methylene]benzo[e][1,3]benzothiazole is promising. As scientists continue to uncover the nuances of its properties, this compound could have significant implications across chemistry, biology, and material science.