Benzo[j]fluoranthene is a polycyclic aromatic hydrocarbon (PAH) characterized by its fused aromatic rings, specifically consisting of five fused benzene rings. It is a colorless to pale yellow solid at room temperature and is known for its hydrophobic nature, making it poorly soluble in water but soluble in organic solvents. This compound is primarily formed through the incomplete combustion of organic materials, such as fossil fuels and biomass. Benzo[j]fluoranthene is recognized for its potential carcinogenic properties, as it can be metabolized into reactive intermediates that may interact with cellular macromolecules, leading to DNA damage. Its presence is often monitored in environmental studies due to its persistence in the environment and its association with air and soil pollution. In terms of physical properties, it has a relatively high melting point and boiling point compared to many other organic compounds, reflecting its stable aromatic structure. Safety measures should be taken when handling this substance, as it poses health risks upon exposure.

Benzo[j]fluoranthene

205-82-3: Benzo[j]fluoranthene is a polycyclic aromatic hydrocarbon (PAH) characterized by its fused aromatic rings, specifically consisting of five fused benzene rings. It is a colorless to pale yellow solid at room temperature and is known for its hydrophobic nature, making it poorly soluble in water but soluble in organic solvents. This compound is primarily formed through the incomplete combustion of organic materials, such as fossil fuels and biomass. Benzo[j]fluoranthene is recognized for its potential carcinogenic properties, as it can be metabolized into reactive intermediates that may interact with cellular macromolecules, leading to DNA damage. Its presence is often monitored in environmental studies due to its persistence in the environment and its association with air and soil pollution. In terms of physical properties, it has a relatively high melting point and boiling point compared to many other organic compounds, reflecting its stable aromatic structure. Safety measures should be taken when handling this substance, as it poses health risks upon exposure.

Benzo(J)fluoranthene is a polycyclic aromatic hydrocarbon that has been shown to have tumorigenic and genotoxic effects in CD-1 mice. It binds to the dna in the nucleus of liver cells, leading to cancer. Benzo(J)fluoranthene has also been shown to cause autophagy, which is a process by which cells break down their own components for energy in response to starvation or other stress. This compound was found to induce synchronous fluorescence with a fluorescence detector and can be used as a fluorescent probe for DNA binding activity.

CAS 205-82-3

Benzo[j]fluoranthene

Benzo(J)fluoranthene

Ref: 3D-FB180101