Dinitrobenzene exists in three isomers (o-, m-,and p-); the meta form is the most widely used. All arewhite to yellow crystalline solids having a characteristicodor. Molecular weight= 168.12; Boiling point = (o-)318℃; (m-) 300℃; (p-) 299℃; (mixed) 305℃; Freezing/Melting point = (o-) 117118℃; (m-) 90℃; (p-)173174℃; (mixed) 7585℃; Flash point = (o-, m-,and p-) 149150℃. NFPA 704 M Hazard Identification(ortho-): Health 3, Flammability 1, Reactivity 4. Solubilityin water is poor for o-, m-, and mixed isomers; none forp-isomer.
light yellow-brown powder
1,2-Dinitrobenzene was used as internal standard for analysis of the explosives, TNT, RDX, and tetryl in sea water by vapor phase chromatography with the nickel-63 electron capture detector.
ChEBI: 1,2-dinitrobenzene is a dinitrobenzene.
Colorless to yellow solid. Sinks and slowly mixes with water.
All three isomers have similar properties and may react vigorously with oxidizing materials. Their reaction with nitric acid (nitration) will lead to a mixture of trinitrobenzenes possessing high-explosive properties [Urbanski, 1967, vol. 3, p. 290]. If heat and reaction conditions of the nitration are not controlled, detonation comparable to TNT may occur [Anon., J. R. Inst. Chem., 1960, 84, p. 451]. Mixture of 1,3-dinitrobenzene with tetranitromethane was found highly explosive [Urbanski, 1964, vol. 1, 592]. 1,2-dinitrobenzene is a severe explosion hazard when shocked or exposed to heat or flame. When heated to decomposition all dinitrobenzens emit toxic fumes of nitrogen oxides [Sax, 9th ed., 1996, p. 1374].
INHALATION, INGESTION, OR SKIN ABSORPTION: Headache, vertigo and vomiting followed by exhaustion, numbness of the legs, staggering and collapse. Intense methemoglobinenia may lead to asphyxia severe enough to injure the CNS. EYES: Irritation. SKIN: Stains skin yellow.
Suspected carcinogen.
Poison by inhalation and ingestion.
Moderately toxic by sktn contact. Can cause
liver, kidney, and central nervous system
injury. Combustible when exposed to heat
or flame; can react vigorously with oxidzing
materials. A severe explosion hazard when
shocked or exposed to heat or flame. It is
used in bursting charges and to fiu artillery
shells. Mixtures with nitric acid are highly
explosive. To fight fire, use water, Co2, dry
chemical. Dangerous; when heated to
decomposition it emits highly toxic fumes of
NO, and explodes. See also mand pDINITROBENZENE and NITRO
COMPOUNDS of AROMATIC
HYDROCARBONS.
Compound Description (m-isomer):Mutagen; Reproductive Effector; Human Data; PrimaryIrritant; (o- and p-isomers) Mutagen. Dinitrobenzenes areused in the synthesis of dyestuffs, dyestuff intermediates,and explosives; in celluloid production.
If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.Effects may be delayed; medical observation isrecommended.Note to physician: Treat for methemoglobinemia.Spectrophotometry may be required for precise determination of levels of methemoglobinemia in urine.
Biological. Under anaerobic and aerobic conditions using a sewage inoculum, 1,2-dinitrobenzene degraded to nitroaniline (Hallas and Alexander, 1983).
Photolytic. Low et al. (1991) reported that the nitro-containing compounds (e.g., 2,4-
dinitrophenol) undergo degradation by UV light in the presence of titanium dioxide yielding
ammonium, carbonate, and nitrate ions. By analogy, 1,2-dinitrobenzene should degrade forming
identical ions.
Chemical/Physical. Releases toxic nitrogen oxides when heated to decomposition (Sax and
Lewis, 1987). 1,2-Dinitrobenzene will not hydrolyze in water (Kollig, 1993).
(1) Color Code—Yellow Stripe: Reactivity Hazard;Store separately in an area isolated from flammables, combustibles, or other yellow-coded materials. (2) Color Code—Blue: Health Hazard/Poison: Store in a secure poison location. Prior to working with dinitrobenzene you should betrained on its proper handling and storage. Dinitrobenzenemust be stored to avoid contact with strong oxidizers (suchas chloride, bromine, chlorine dioxide, nitrates, and permanganates), since violent reactions occur. Contact with causticsand chemically active metals (such as tin and zinc) mayevolve heat, causing a buildup in pressure. Store in tightlyclosed containers in a cool, well-ventilated area away fromshock or heat, which may cause this chemical to explode.Storage outdoors or in explosion-proof areas is preferred.Sources of ignition, such as smoking and open flames, areprohibited where dinitrobenzene is handled, used, or stored.Metal containers used in the transfer of 5 gallons or more ofdinitrobenzene should be grounded and bonded. Drums mustbe equipped with self-closing valves, pressure vacuum bungs,and flame arresters. Use only nonsparking tools and equipment, especially when opening and closing containers ofdinitrobenzene. Wherever dinitrobenzene is used, handled,manufactured, or stored, use explosion-proof electrical equipment and fittings
Dinitrobenzenes all require a “POISONOUS/TOXIC MATERIALS” label. They fall in Hazard Class 6.1and Packing Group II.
Crystallise it from EtOH. [Beilstein 5 IV 738.]
