Chemical Properties
1,2-Dichlorobenzene (DCB, o-Dichlorobenzene, ODB, Orthodichlorobenzene),
C
6H
4Cl
2, is a colorless to pale yellow liquid with a pleasant aromatic odor. It is a
combustible liquid and can form explosive mixtures with air at or above 151°F.
Combustion and thermal decomposition products include hydrogen chloride gas,
phosgene and chloro-carbons. Its flammable (explosive) limits are as follows:
Lower 2.2%, Upper 9.2%.
Physical properties
Clear, colorless to pale yellow liquid with a pleasant, aromatic, grassy or vegetable-type odor. At
40 °C, the lowest concentration at which an odor was detected was 200 μg/L. At 25 °C, the lowest
concentration at which a taste was detected was 200 μg/L (Young et al., 1996). A detection odor
threshold concentration of 4.2 mg/m
3 (699 ppb
v) was reported by Punter (1983).
Uses
1,2-Dichlorobenzene is used as a solvent; asa fumigant; as an insecticide for termites;as a degreasing agent for metals, wool, andleather; and as a heat transfer medium.
Uses
Solvent for waxes, gums, resins, tars, rubbers, oils, asphalts; insecticide for termites and locust borers; fumigant; deodorizer; removing sulfur from illuminating gas; as degreasing agent for metals, leather, wool; as ingredient of metal polishes; as heat transfer medium; as intermediate in the manufacture of dyes.
Definition
ChEBI: 1,2-dichlorobenzene is a dichlorobenzene carrying chloro substituents at positions 1 and 2. It has a role as a hepatotoxic agent and a metabolite.
Production Methods
1,2-Dichlorobenzene is produced by reacting liquid benzene with gaseous chlorine in the presence of a catalyst at moderate temperature and atmospheric pressure.
Dichlorobenzenes are primarily produced by the chlorination of benzene in the presence of a catalyst (FeCl3 or AlCl3) although there are other possible synthetic routes. The two commercially important isomers are the ortho- and para-dichlorobenzenes.
General Description
A clear colorless liquid with a pleasant odor. Denser than water and insoluble in water. Flash point 150°F. Toxic by inhalation and ingestion. Used to make other chemicals, solvents, fumigants and insecticides and for many other uses.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
1,2-Dichlorobenzene is sensitive to prolonged exposure to light. 1,2-Dichlorobenzene can react vigorously with oxidizers. 1,2-Dichlorobenzene is incompatible with aluminum and aluminum alloys. 1,2-Dichlorobenzene attacks some forms of plastics, rubber and coatings. .
Health Hazard
1,2-Dichlorobenzene exhibits low acute toxi city by inhalation, ingestion, and skin absorp tion. It is more toxic than chlorobenzene.The symptoms are lacrimation, depression ofcentral nervous system, anesthesia, and liverdamage. Lethal concentration in rats for a7-hour exposure period is in the range of800 ppm. The oral LD50 value in rabbits is500 mg/kg. There is no evidence of carcino genicity in animals.
Fire Hazard
Special Hazards of Combustion Products: Poisonous vapors including hydrogen chloride gas, chlorocarbons, chlorine
Flammability and Explosibility
Non flammable
Chemical Reactivity
Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
Safety Profile
Poison by ingestion and
intravenous routes. Moderately toxic by
inhalation and intraperitoneal routes. An
experimental teratogen. Other experimental
reproductive effects. An eye, skin, and
mucous membrane irritant. Causes liver and
hdney injury. Questionable carcinogen.
Mutation data reported. A pesticide.
Flammable when exposed to heat or flame.
Can react vigorously with oxidizing
materials. To fight fire, use water, foam,
CO2, or dry chemical. Slow reaction with
aluminum may lead to explosion during
storage in a sealed aluminum container. When heated to decomposition it emits
toxic fumes of Cl-. See also
CHLOROBENZENE and
CHLORINATED HYDROCARBONS,
AROMATIC.
Potential Exposure
The major uses of o-DCB are as
a process solvent in the manufacturing of toluene diisocyanate and as an intermediate in the synthesis of dyestuffs,
herbicides, and degreasers. p-Dichlorbenzene is used
primarily as a moth repellant, a mildew control agent;
space deodorant; and in insecticides, which accounts for
90% of the total production of this isomer. Information is
not available concerning the production and use of m-DCB.
However, it may occur as a contaminant of o-or p-DCB
formulations. Both o-and p-isomers are produced almost
entirely as by-products during the production of
monochlorobenzene
First aid
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.
storage
Color Code—Red (o-DCB): Flammability Hazard:Store in a flammable liquid storage area or approved cabinet away from ignition sources and corrosive and reactivematerials.
Color Code—Blue (m-DCB): Health Hazard/Poison: Storein a secure poison location.
Color Code—Green (p-DCB): General storage may be used.Prior to working with any DCB you should be trained on itsproper handling and storage. Before entering confined space where this chemical may be present, check to make surethat an explosive concentration does not exist.Dichlorobenzene must be stored to avoid contact withstrong oxidizers, such as permanganates, nitrates, peroxides,chlorates, and perchlorates, hot aluminum or aluminumalloys since violent reactions occur. Store in tightly closedcontainers in a cool, well-ventilated area away from heatand direct light. Sources of ignition, such as smoking andopen flames, are prohibited where dichlorobenzene is used,handled, or stored in a manner that could create a potentialfire or explosion hazard. A regulated, marked area shouldbe established where p-DCB is handled, used, or stored incompliance with OSHA Standard 1910.1045.
Shipping
o-DCB: Requires a shipping label of“POISONOUS/TOXIC MATERIALS.” It falls in HazardClass 6.1 and Packing Group III.m-DCB: Toxic, liquids, organic, n.o.s. requires a shippinglabel of “POISONOUS/TOXIC MATERIALS.” It falls intoHazard Class 6.1 and Packing Group III.Based on regulations, it may be classified as anEnvironmentally hazardous substances, liquid, n.o.s. Underthis classification, it requires a shipping label of “CLASS9.” It falls in Hazard Class 9 and Packing Group III.[20,21]p-DCB: May be classified as an Environmentally hazardous substances, solid, n.o.s. This chemical requires ashipping label of “CLASS 9.” It falls in Hazard Class 9 andPacking Group III.[20,21]
Purification Methods
Contaminants may include the p-isomer and trichlorobenzene [Suslick et al. J Am Chem Soc 106 4522 1984]. It should be shaken with conc or fuming H2SO4, washed with water, dried with CaCl2, and distilled from CaH2 or sodium in a glass-packed column. Low conductivity material (ca 10-10 mhos) has been obtained by refluxing with P2O5, fractionally distilling and passing it through a column packed with silica gel or activated alumina: it is stored in a dry-box under N2 or with activated alumina. [Beilstein 5 IV 654.]
Incompatibilities
1,2-Dichlorobenzene forms hydrogen chloride gas when in the presence of strong oxidizers or chemically active metals like aluminum, or when heated to decomposition (HSDB 2007).
Waste Disposal
Incineration, preferably
after mixing with another combustible fuel. Care must be
exercised to assure complete combustion to prevent
the formation of phosgene. An acid scrubber is necessary
to remove the halo acids produced. Consult with
environmental regulatory agencies for guidance on
acceptable disposal practices. Generators of waste containing
this contaminant (≥100 kg/mo) must conform with EPA
regulations governing storage, transportation, treatment, and
waste disposal
