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1,3,6,8-Tetranitropyrene

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Identification
Molecular formula
C16H6N4O8
CAS number
75321-20-9
IUPAC name
1,3,6,8-tetranitropyrene
State
State
At room temperature, 1,3,6,8-tetranitropyrene is a solid.
Melting point (Celsius)
231.00
Melting point (Kelvin)
504.15
Boiling point (Celsius)
635.00
Boiling point (Kelvin)
908.15
General information
Molecular weight
370.23g/mol
Molar mass
370.2280g/mol
Density
1.8650g/cm3
Appearence

1,3,6,8-Tetranitropyrene appears as a yellow crystalline solid. It is often researched in scientific contexts due to its derivation from the pyrene structure, which contributes to its aromatic and planar nature. As a nitro derivative, it possesses distinctive yellow color typically associated with aromatic nitro compounds.

Comment on solubility

Solubility of 1,3,6,8-Tetranitropyrene

1,3,6,8-Tetranitropyrene, a notable compound in the family of nitroaromatic compounds, exhibits *limited solubility* in water, making it a challenging substance in several applications. Here are some key points regarding its solubility:

  • Water Solubility: It is sparingly soluble in water due to its hydrophobic pyrene structure, causing it to readily separate from aqueous solutions.
  • Organic Solvents: This compound has a significantly higher solubility in organic solvents such as acetone, ethyl acetate, and benzene, which can be attributed to favorable interactions with non-polar environments.
  • Toxicity Concerns: Despite its low aqueous solubility, the compound can still pose risks in the environment, leading to potential bioaccumulation in aquatic organisms.
  • Environmental Impact: Its insolubility in water makes it prone to sedimentation rather than dissolution and transport in aquatic ecosystems.

In summary, the *limited water solubility* of 1,3,6,8-tetranitropyrene significantly influences its behavior in both laboratory and environmental settings, highlighting the importance of understanding solubility when working with such complex compounds.

Interesting facts

Interesting Facts about 1,3,6,8-Tetranitropyrene

1,3,6,8-tetranitropyrene is an intriguing compound with a rich history and significant implications in various fields. Here are some fascinating details about this aromatic nitro compound:

  • Explosive Properties: This compound is known for its potential as a high-energy material. Its unique structure contributes to a high degree of stability while also allowing it to release a substantial amount of energy upon detonation.
  • Applications in Military: Due to its explosive properties, 1,3,6,8-tetranitropyrene is primarily used in military explosives and propellants. Researchers continue to study its efficacy and safety in various applications.
  • Environmental Concerns: As a nitroaromatic compound, it presents challenges related to environmental pollution. The persistence of such compounds in the environment raises red flags for toxicity, leading to closer regulatory scrutiny.
  • Synthesis and Challenges: The synthesis of this compound involves complex chemical reactions and careful handling. The process can be hazardous, requiring precise control over conditions to avoid unwanted side reactions.
  • Research Significance: 1,3,6,8-tetranitropyrene serves as a subject of interest in both chemical research and materials science. Its behavior can help scientists understand the underlying principles of explosive chemistry and its interaction with various materials.

In summary, 1,3,6,8-tetranitropyrene embodies a balance of utility and risk, making it a significant compound in both scientific studies and practical applications. Its explosive potential, coupled with environmental considerations, continues to inspire research and innovation in the field of chemistry.

Synonyms
1,3,6,8-TETRANITROPYRENE
Pyrene, 1,3,6,8-tetranitro-
28767-61-5
XT7XK9XXR8
NSC 156560
BRN 2315192
NSC-156560
DTXSID6075223
4-05-00-02471 (Beilstein Handbook Reference)
RefChem:177477
DTXCID0037867
684-180-1
C16H6N4O8
NSC156560
UNII-XT7XK9XXR8
1,3,6,8-Tetranitro-pyrene
CHEMBL354712
SCHEMBL28477123