Chlorobromomethane is a clear, colorless topale yellow liquid with a chloroform-like odor. Odor threshold=400 ppm. Molecular weight=129.39; Specific gravity (H2O:1)=1.93; Boiling point=68.3℃; Freezing/Melting point=2 88℃; Vapor pressure=115 mmHg at20℃. Hazard Identification (based on NFPA 704 M RatingSystem): Health 2, Flammability 0, Reactivity 0. Insolublein water.
Chlorobromomethane is a clear, colorless, to
pale-yellow liquid with a chloroform-like odor
white to light yellow crystal powder
Clear, colorless liquid with a sweet, chloroform-like odor
Bromochloromethane is used primarily as an extinguishing agent due to its oxygen-depleting properties.
ChEBI: A one-carbon compound substituted by a chloro and a bromo group.
A clear colorless liquid with a sweet chloroform-like odor. Denser than water (density 1.991 g / cm3) and insoluble in water. Hence sinks in water. Boiling point 68°C. Vapors may cause illness if inhaled. Nonflammable. When exposed to high temperatures may emit toxic fumes. Used as a fire extinguishing agent.
Bromochloromethane is sensitive to light (may discolor). Incompatible with strong bases and strong oxidizing agents. Also incompatible with active metals, calcium, aluminum, magnesium, zinc and their alloys. Attacks some forms of plastics, rubber and coatings. .
Toxic by ingestion. Vapors may cause dizziness or suffocation. Exposure in an enclosed area may be very harmful. Contact may irritate or burn skin and eyes. Fire may produce irritating and/or toxic gases. Runoff from fire control or dilution water may cause pollution.
Some of these materials may burn, but none ignite readily. Most vapors are heavier than air. Air/vapor mixtures may explode when ignited. Container may explode in heat of fire.
Mildly toxic by
ingestion and inhalation. Mutation data
reported. This material has a narcotic action
of moderate intensity, although of
prolonged duration. Animals exposed for
several weeks to 1000 pprn had blood
bromide levels as high as 350 mgl100 g.
Therefore, until further data are available, it
should be considered at least as toxic as carbon tetrachloride and more than minimal
exposure to its vapors should be avoided.
Dangerous; when heated to decomposition
it emits highly toxic fumes of Brand Cl-.
See also BROMIDES and
CHLORINATED HYDROCARBONS,
ALIPHATIC.
This compound is used in brominated
flame retardants; a fire-extinguishing agent; and in organic
synthesis
If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin,remove contaminated clothing and wash immediately withsoap and water. Seek medical attention immediately. If thischemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, includingresuscitation mask) if breathing has stopped and CPR if heartaction has stopped. Transfer promptly to a medical facility.When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Donot make an unconscious person vomit. Medical observationis recommended for 24-48 h after breathing overexposure,as pulmonary edema may be delayed. As first aid for pulmonary edema, a doctor or authorized paramedic may consideradministering a corticosteroid spray.
The U.S. EPA classification is D
(not classifiable as to human carcinogenicity). Bromochloromethane
is structurally similar to dichloromethane (methylene
chloride), which is classified B2 (probable human
carcinogen). The classification is based on the lack of data
regarding the carcinogenicity of bromochloromethane in
humans or animals; however, there are data indicative of
genotoxic effects and structural relationships to halogenated
methanes classified as B2 (probable human carcinogens).
No MCLGs or MCLs have been proposed, however, a DWEL of 0.5
mg/L was recommended (U.S. EPA, 2000).
Naturally formed by algal biological processes (Orkin et al., 1997) and is a disinfection
byproduct in public water treatment systems.
Biological. When bromochloromethane (5 and 10 mg/L) was statically incubated in the dark at
25 °C with yeast extract and settled domestic wastewater inoculum for 7 d, 100% biodegradation
with rapid adaptation was observed (Tabak et al., 1981).
Photolytic. The following rate constants were reported for the reaction of bromochloromethane
and OH radicals as measured by both flash photolysis resonance fluorescence and discharge flow
electron paramagnetic resonance techniques (x 10-13 cm3/molecule?sec): 0.91 at 4 °C, 1.11–1.13 at
25 °C, 1.32–1.34 at 40 °C, 1.55–1.58 at 57 °C, 1.76–1.90 at 76 °C, 2.10–2.26 at 97 °C (Orkin et
al., 1997).
Chemical/Physical. Although no products were identified, the estimated hydrolysis half-life in
water at 25 °C and pH 7 is 44 yr (Mabey and Mill, 1978). Bromochloromethane reacts with
bisulfide ion (HS-), produced by microbial reduction of sulfate, forming 1,3,5-trithiane and
dithiomethane. Estimated reaction rate constants at 25 and 35 °C were 7.29 x 10-5 and 2.42 x 10-
4/M?sec, respectively (Roberts et al., 1992).
Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling andstorage. Chlorobromomethane must be stored to avoid contact with chemically active metals, since violent reactionsoccur. Store in tightly closed containers in a cool, wellventilated area away from heat.
UN1887 Bromochloromethane, Hazard Class:
6.1; Labels: 6.1-Poisonous materials.
Incompatible with strong oxidizers (possible explosion), reducing agents, bases, carbonates, furyl alcohol, chemically active metals, such as calcium; base metals
in the presence of moisture, powdered aluminum; zinc, magnesium. Liquid attacks some plastics, rubber, and coatings.
Incinerate together with flammable solvent in furnace equipped with afterburner and
alkali scrubber.
