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Dinitramine

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Identification
Molecular formula
C12H8N4O6
CAS number
29091-05-2
IUPAC name
2,4-dinitro-N-(4-nitrophenyl)aniline
State
State

At room temperature, Dinitramine is a solid. Its crystalline nature contributes to its stable solid state under standard conditions.

Melting point (Celsius)
199.50
Melting point (Kelvin)
472.65
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
303.22g/mol
Molar mass
303.2180g/mol
Density
1.5618g/cm3
Appearence

Dinitramine appears as a bright yellow crystalline solid. It is characterized by its vivid coloration, which is typical of aromatic compounds with multiple nitro groups.

Comment on solubility

Solubility of 2,4-dinitro-N-(4-nitrophenyl)aniline

When examining the solubility of 2,4-dinitro-N-(4-nitrophenyl)aniline, several factors must be considered:

  • Polarity: This compound contains multiple nitro groups, which are known to enhance polarity. However, the presence of the aniline group adds some hydrophobic character.
  • Solvent Interaction: Due to its polar nature, 2,4-dinitro-N-(4-nitrophenyl)aniline is generally more soluble in polar solvents such as water and methanol than in non-polar solvents.
  • Temperature Dependency: Like many organic compounds, solubility can increase with temperature. Thus, heating the solvent may improve the dissolution of this compound.
  • pH Influence: The solubility may also be affected by the pH of the solution. Being an amine, alterations in pH can lead to protonation, affecting solubility.

Overall, it can be stated that while 2,4-dinitro-N-(4-nitrophenyl)aniline exhibits some degree of solubility in polar solvents, its solubility is not exceptionally high, particularly in non-polar media. Proper handling and dissolution conditions are essential for effective usage in any applications.

Interesting facts

Interesting Facts about 2,4-Dinitro-N-(4-Nitrophenyl)aniline

2,4-Dinitro-N-(4-nitrophenyl)aniline, often referred to in the scientific community as a significant synthetic organic compound, is known for its intriguing chemical properties and applications. Here are some fascinating points to consider:

  • Historical Significance: This compound is an important precursor in the synthesis of various azo dyes, which have revolutionized the textile industry since their discovery in the 19th century.
  • Explosive Potential: Its structural characteristics allow it to be utilized in the formulation of certain explosives, making it a compound of interest in the field of materials science and explosives research.
  • Pharmacological Insights: Researchers are continually exploring the pharmacological properties of nitroanilines, like 2,4-dinitro-N-(4-nitrophenyl)aniline, for potential therapeutic applications.
  • Environmental Impact: As nitro compounds, they can pose environmental hazards; thus, understanding their behavior and degradation in various ecosystems is vital.
  • Synthetic Pathways: The synthesis of this compound involves multiple steps, including nitration and amination reactions, showcasing the beauty of organic synthesis.

In summary, 2,4-dinitro-N-(4-nitrophenyl)aniline is not only a versatile compound in synthesis but also a subject of ongoing research in both industrial and environmental applications. Its multifaceted roles underline the importance of understanding chemical compounds in a broader context.

Synonyms
2,4-Dinitro-N-(4-nitrophenyl)aniline
970-76-3
N1-(4-nitrophenyl)-2,4-dinitroaniline
AI3-01555
EINECS 213-536-7
2,4,4'-trinitro diphenylamine
CHEMBL4459184
DTXSID20242662
MQZAHSOZWFOSGD-UHFFFAOYSA-N
AKOS000286060
NS00042494
Benzenamine, 2,4-dinitro-N-(4-nitrophenyl)-