Skip to main content

Basic Fuchsin

ADVERTISEMENT
Identification
Molecular formula
C20H19ClN3
CAS number
632-99-5
IUPAC name
[4-[bis(4-amino-3-methyl-phenyl)methylene]-2-methyl-cyclohexa-2,5-dien-1-ylidene]ammonium;chloride
State
State

Basic Fuchsin is a solid at room temperature. It is often available as a powder, which can be dissolved in water to form a staining solution.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.00
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.00
General information
Molecular weight
337.85g/mol
Molar mass
337.8530g/mol
Density
1.4450g/cm3
Appearence

Basic Fuchsin appears as a dark green crystalline powder with a metallic sheen. When dissolved in water, it forms a magenta-colored solution, which is used both as a dye and a staining agent in histology and bacteriology.

Comment on solubility

Solubility of [4-[bis(4-amino-3-methyl-phenyl)methylene]-2-methyl-cyclohexa-2,5-dien-1-ylidene]ammonium; chloride

The solubility of [4-[bis(4-amino-3-methyl-phenyl)methylene]-2-methyl-cyclohexa-2,5-dien-1-ylidene]ammonium chloride can be influenced by several factors, primarily due to its complex molecular structure. Here are some key points to consider:

  • Polarity: The presence of both amine and chloride functional groups suggests that this compound may exhibit significant polarity, which often leads to increased solubility in polar solvents such as water.
  • Hydrogen Bonding: The amino groups on the compound can engage in hydrogen bonding with solvent molecules, enhancing solubility.
  • Structure: The bulky aromatic groups may hinder solubility in non-polar solvents due to steric hindrance, making the compound less soluble in organic solvents compared to water.

In conclusion, while the uniqueness of its chemical structure allows for potential solubility in polar solvents, the exact solubility behavior can vary significantly. To sum it up, it’s essential to consider factors like polarity, hydrogen bonding potential, and molecular size when predicting the solubility of this compound in various environments.

Interesting facts

Interesting Facts about [4-[bis(4-amino-3-methyl-phenyl)methylene]-2-methyl-cyclohexa-2,5-dien-1-ylidene]ammonium;chloride

This compound, often referred to in studies involving organic chemistry and medicinal applications, is a fascinating example of complex organic structure with significant implications. Its detailed composition showcases the intricate relationships between different functional groups within a molecular framework.

Structural Highlights

  • Uniqueness of Structure: The presence of a cyclohexa-2,5-dien-1-ylidene moiety combined with bis-substituted amino groups allows for unique reactivity, making it a prime candidate for various synthesis reactions.
  • Ammonium Ion: The ammonium component introduces a positive charge to the molecule, influencing solubility and interactions with other ionic species, which is particularly useful in pharmaceuticals.

Applications and Research

This compound serves as a functional model for multiple studies:

  • Medicinal Chemistry: Compounds like this can act as potential drug candidates, especially in targeted therapy.
  • Organic Synthesis: It can be used as a precursor for synthesizing more complex organic molecules.

Quirkiness of the Compound

Not only is this compound interesting from a chemical standpoint, but it also offers insights into:

  • Properties: The distinct properties stemming from its unique structure can lead to specialized applications in materials science.
  • Research Potential: This compound is poised for further research, which could lead to discoveries in reactive intermediates and catalysts.

In summary, [4-[bis(4-amino-3-methyl-phenyl)methylene]-2-methyl-cyclohexa-2,5-dien-1-ylidene]ammonium;chloride is an exemplary compound reflecting the interplay of structure, reactivity, and potential applications in various scientific fields. Its complex nature not only challenges chemists but also inspires innovative approaches in compound utilization.

Synonyms
neofuchsin
ISO RUBINE
new fuchsin(1+) chloride
New Fuchsin, for microscopy
SCHEMBL342206
SCHEMBL4236473
Magenta III [Magenta (containing C.I. Basic Red 9)]
UNII-A051F48W36
ORDGVBRMUJCHEO-UHFFFAOYSA-M
AKOS000283055
AKOS015916443
N0478
N0873
NS00013506
D91717
[4-[bis(4-amino-3-methylphenyl)methylidene]-2-methylcyclohexa-2,5-dien-1-ylidene]azanium;chloride