General Description
Cream-colored solid.
Reactivity Profile
Aromatic nitro compounds, such as 2-NITROFLUORENE(607-57-8), range from slight to strong oxidizing agents. If mixed with reducing agents, including hydrides, sulfides and nitrides, they may begin a vigorous reaction that culminates in a detonation. The aromatic nitro compounds may explode in the presence of a base such as sodium hydroxide or potassium hydroxide even in the presence of water or organic solvents. The explosive tendencies of aromatic nitro compounds are increased by the presence of multiple nitro groups. Stable under normal conditions. Protect from bases.
Air & Water Reactions
Insoluble in water.
Health Hazard
ACUTE/CHRONIC HAZARDS: Toxic. Hazardous decomposition products. Carcinogen.
Chemical Properties
cream powder
Uses
2-Nitrofluorene is a genotoxic compound and also a biomaker that affects the DNA of living organisms. An environmental pollutant.
Definition
ChEBI: A nitroarene that is fluorene substituted by a nitro group at position 2.
Metabolic pathway
Lung microsomal metabolism of 2-nitrofluorene (NF)
increases in parallel with the accumulation of P-450b
homologous mRNA and microsomal cytochrome P-
450b protein concentration. The formation of the major
metabolite, and potent mutagen, 9-hydroxy-2-
nitrofluorene (9-OHNF) is significantly inhibited by the
addition of polyclonal anti-P-450b-IgG, and by the
addition of the inhibitor, proadifen, to incubations with
lung microsomal protein.
Purification Methods
Crystallise 2-nitrofluorene from aqueous acetic acid or Me2CO (m 158-158.5o, also 160-160.5o). [Beilstein 5 H 628, 5 III 1948.]
