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4-(Dihydroxyamino)-1,2-benzoquinone

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Identification
Molecular formula
C6H5NO4
CAS number
62451-54-1
IUPAC name
4-(dihydroxyamino)-1,2-benzoquinone
State
State

At room temperature, 4-(dihydroxyamino)-1,2-benzoquinone is typically found as a solid. Its quinone-based structure influences both its color and physical state, contributing to its presence as a vibrant solid form.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.00
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.00
General information
Molecular weight
155.12g/mol
Molar mass
155.1180g/mol
Density
1.6300g/cm3
Appearence

4-(dihydroxyamino)-1,2-benzoquinone appears as an orange to red crystalline powder. It is known for its intense coloration due to the quinone structure, which typically imparts vibrant hues to compounds.

Comment on solubility

Solubility of 4-(Dihydroxyamino)-1,2-benzoquinone (C6H5NO4)

The solubility of 4-(dihydroxyamino)-1,2-benzoquinone can greatly influence its applications in various fields, especially in pharmaceuticals and dyes. Here are some important points regarding its solubility:

  • Polar Characteristics: This compound possesses multiple hydroxyl groups, contributing to its polar nature. Consequently, it is more soluble in polar solvents such as water compared to nonpolar solvents.
  • pH Dependency: The solubility can vary with changes in pH. In acidic conditions, the compound may protonate, altering its solubility profile.
  • Temperature Effects: Like many compounds, increased temperature can generally enhance solubility. Hence, experimentation at different temperatures may yield useful insights on solubility behavior.
  • Dissociation: The extent to which the compound dissociates in solution can also affect solubility, especially at differing concentrations.
  • Complex Formation: It may have the ability to form complexes with metal ions (like iron), which could either increase or decrease solubility depending on the coordination environment.

Overall, understanding the solubility of 4-(dihydroxyamino)-1,2-benzoquinone is essential for its optimal utilization in chemical applications. As with many organic compounds, the interplay between structure, solvent, and environmental conditions can lead to interesting solubility phenomena.

Interesting facts

Interesting Facts about 4-(Dihydroxyamino)-1,2-benzoquinone

4-(Dihydroxyamino)-1,2-benzoquinone is a fascinating compound that holds significant importance in various areas of research, particularly in biochemistry and organic synthesis. Here are some intriguing facts:

  • Biochemical Relevance: This compound is thought to play a role in biological processes, especially in relation to redox reactions. Its structure suggests that it can act as an electron acceptor, which is crucial in metabolic pathways.
  • Antioxidant Properties: Due to its chemical structure, 4-(Dihydroxyamino)-1,2-benzoquinone may exhibit antioxidant activity. Antioxidants are vital in protecting cells from oxidative stress and damage caused by free radicals.
  • Indicator of Environmental Impact: It has been used as a marker for environmental studies, particularly in assessing the impact of pollutants. Its ability to undergo redox reactions makes it a valuable compound in detecting and quantifying certain environmental contaminants.
  • Research Applications: In synthetic organic chemistry, this compound can serve as a versatile intermediate in the synthesis of various organic molecules. Researchers are continually looking at its potential applications in drug design and development.
  • Historical Context: Compounds related to benzoquinones have been studied since the late 19th century. They have been significant in the development of various dyes, pigments, and pharmaceuticals.

Scientists often say, "In chemistry, we seek to understand the materials that build our world," and 4-(Dihydroxyamino)-1,2-benzoquinone exemplifies this pursuit. As research continues, the full potential and applications of this compound are sure to expand, shedding light on its role in both nature and industry.