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Crystal Violet

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Identification
Molecular formula
C25H30N3Cl
CAS number
548-62-9
IUPAC name
4-[(4-amino-3-methyl-phenyl)-(4-imino-3-methyl-cyclohexa-2,5-dien-1-ylidene)methyl]-2-methyl-aniline
State
State

At room temperature, Crystal Violet is typically in a solid state. It is widely found in powder form, which can be solubilized in water to form a solution for various applications including biological staining and as a pH indicator.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.00
Boiling point (Celsius)
583.00
Boiling point (Kelvin)
856.00
General information
Molecular weight
407.98g/mol
Molar mass
407.9790g/mol
Density
1.1900g/cm3
Appearence

Crystal Violet appears as a green powder with a metallic luster. When dissolved in water, it forms a purple or violet solution. It's commonly used as a dye and is known for its bright, vivid coloration. The solid material is prone to air oxidation, causing it to darken when exposed to air over time.

Comment on solubility

Solubility of 4-[(4-amino-3-methyl-phenyl)-(4-imino-3-methyl-cyclohexa-2,5-dien-1-ylidene)methyl]-2-methyl-aniline

The solubility of 4-[(4-amino-3-methyl-phenyl)-(4-imino-3-methyl-cyclohexa-2,5-dien-1-ylidene)methyl]-2-methyl-aniline is influenced by its intricate molecular structure and functional groups. Here are some key points to consider:

  • Polarity: This compound contains both amino and imino groups, which can interact favorably with polar solvents, enhancing its solubility in polar environments.
  • Hydrophobic Regions: The presence of the phenyl and cyclohexadiene groups introduces hydrophobic characteristics that may limit solubility in highly polar solvents.
  • Solvent Interaction: Generally, compounds of this nature tend to be more soluble in organic solvents like dimethyl sulfoxide (DMSO) and methanol, rather than in water.
  • Effect of pH: The solubility can vary significantly with changes in pH, especially due to the amino group's ability to either accept or donate protons, thereby impacting the overall charge of the molecule.

In summary, while 4-[(4-amino-3-methyl-phenyl)-(4-imino-3-methyl-cyclohexa-2,5-dien-1-ylidene)methyl]-2-methyl-aniline exhibits a tendency towards solubility in certain solvents, its solubility profile remains a complex interplay of structural features and environmental factors.

Interesting facts

Interesting Facts about 4-[(4-amino-3-methyl-phenyl)-(4-imino-3-methyl-cyclohexa-2,5-dien-1-ylidene)methyl]-2-methyl-aniline

This complex organic compound is a fascinating member of the aniline family, known for its diverse applications in the field of chemistry and material science. It boasts a unique structure that combines elements of both aromatic and aliphatic compounds, making it a subject of interest for researchers focused on molecular interactions and synthetic pathways.

Key Highlights:

  • Diverse Applications: The compound is often studied for potential use in dye synthesis, pharmaceuticals, and advanced materials, showcasing the versatility of aniline derivatives.
  • Structural Intricacies: With multiple functional groups, this compound presents an opportunity for chemists to explore unique reactivity patterns and molecular behavior.
  • Biological Relevance: Compounds related to this structure have been investigated for their biological activity, particularly in pharmacology where derivatives may show promising therapeutic effects.
  • Photochemical Properties: Researchers have shown interest in the photochemical characteristics of such compounds, particularly in light-absorbing materials and their potential role in solar energy applications.

In an era of advancing technology, this compound stands out not just for its chemical significance but also for its implications in developing new materials and pharmaceuticals. As the chemist Marie Curie once said, "Nothing in life is to be feared, it is only to be understood." This is particularly true in the exploration of 4-[(4-amino-3-methyl-phenyl)-(4-imino-3-methyl-cyclohexa-2,5-dien-1-ylidene)methyl]-2-methyl-aniline, where understanding its properties can lead to groundbreaking advancements.

Synonyms
new fuchsin free base
25739-74-6
CHEBI:87672
4-[(4-amino-3-methylphenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]-2-methylaniline
4,4'-((4-Imino-3-methylcyclohexa-2,5-dien-1-ylidene)methylene)bis(2-methylaniline)
4,4'-[(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methylene]bis(2-methylaniline)
Zsorubin
New fuchsine (free base)
SCHEMBL8947530
CHEMBL2007831
DTXSID60863133
NCI60_042204
CS-0369908
AE-641/05021062
Q27159819
4-[(4-amino-3-methylphenyl)(4-imino-3-methyl-2,5-cyclohexadien-1-ylidene)methyl]-2-methylphenylamine