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Dinoseb

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Identification
Molecular formula
C12H10N2O5
CAS number
88-85-7
IUPAC name
2,6-dinitro-4-phenyl-phenol
State
State

At room temperature, Dinoseb is a solid.

Melting point (Celsius)
40.50
Melting point (Kelvin)
313.65
Boiling point (Celsius)
375.00
Boiling point (Kelvin)
648.15
General information
Molecular weight
240.21g/mol
Molar mass
240.2050g/mol
Density
1.5250g/cm3
Appearence

Dinoseb appears as orange crystals, flaky or powdery in texture. It has a characteristic odor that can be somewhat strong and pungent.

Comment on solubility

Solubility of 2,6-Dinitro-4-phenyl-phenol

The solubility of 2,6-dinitro-4-phenyl-phenol is an interesting characteristic that can be influenced by various factors. Here are some key points to consider:

  • Solvent Compatibility: This compound typically shows better solubility in organic solvents such as acetone and ethanol, rather than in polar solvents like water.
  • Hydrophobic Nature: Due to the presence of multiple nitro groups and a phenyl ring, the compound exhibits a degree of hydrophobicity, which can limit solubility in aqueous environments.
  • Temperature Influence: As with many organic compounds, solubility may increase with temperature, allowing for better dissolution in organic solvents.
  • pH Sensitivity: The solubility may also be influenced by the pH of the solution, due to potential deprotonation of the hydroxyl group under basic conditions, which could enhance solubility.

In summary, while 2,6-dinitro-4-phenyl-phenol is not highly soluble in water, it finds compatibility with various organic solvents, rendering it suitable for certain applications in industrial and laboratory settings. As noted in chemical literature, "the solubility of a compound is as much about understanding its chemical structure as it is about its physical environment."

Interesting facts

Interesting Facts about 2,6-Dinitro-4-phenyl-phenol

2,6-Dinitro-4-phenyl-phenol, often referred to in scientific literature for its unique properties, is an intriguing compound with several noteworthy aspects:

  • Structure and Composition: This compound features a complex arrangement that includes two nitro groups and a phenyl group attached to a central phenolic structure. These substitutions significantly influence its chemical reactivity and stability.
  • Reactivity: The presence of the nitro groups contributes to the compound's electrophilic character, making it a valuable reagent in various organic synthesis applications. It can participate in numerous chemical reactions such as electrophilic aromatic substitution.
  • Applications: 2,6-Dinitro-4-phenyl-phenol is used in the development of dyes and pigments due to its vibrant color properties. Its unique structure allows it to be utilized in the synthesis of more complex molecules in pharmaceutical and agrochemical industries.
  • Toxicity Considerations: Like many nitro-derivatives, this compound requires careful handling. Understanding the potential hazards and toxicity is crucial for researchers working with it.
  • Research Opportunities: Ongoing research into compounds like 2,6-dinitro-4-phenyl-phenol aims to explore their mechanism of action and develop new applications, particularly in materials science and medicinal chemistry.

As a chemistry student or scientist, delving into the intricacies of this compound can enhance your understanding of both organic synthesis and the broader implications of chemical safety and application. Exploring its unique properties can lead to exciting discoveries!

Synonyms
4-Hydroxy-3,5-dinitrobiphenyl
4097-53-4
2,6-dinitro-4-phenylphenol
3,5-Dinitro-4-biphenylol
4-BIPHENYLOL, 3,5-DINITRO-
MLS002695315
524YYF9P6Q
NSC-95700
SMR001561221
3,5-DINITRO-BIPHENYL-4-OL
CCRIS 5770
NSC 95700
BRN 1996271
NSC95700
3,5-dinitrobiphenyl-4-ol
NCIOpen2_005794
UNII-524YYF9P6Q
4-06-00-04615 (Beilstein Handbook Reference)
cid_20043
2,6-dinitro-4-phenyl-phenol
SCHEMBL5707253
CHEMBL1716414
BDBM91395
DTXSID10193972
HMS3079C13
3,5-Dinitro[1,1'-biphenyl]-4-ol
AKOS025122365
[1,1'-Biphenyl]-4-ol, 3,5-dinitro-