Description
There are currently no commercial uses of hexachlorobenzene in Australia. Hexachlorobenzene has been used as a pesticide but is no longer registered for this use in Australia. It was also used in the production of fireworks, ammunition, rubber, aluminium, and dyes, and in wood preservation. Hexachlorobenzene was widely used as a pesticide to protect the seeds of onions and sorghum, wheat, and other grains against fungus. Its relevance to the NPI is that it is formed as a by-product during the manufacture of chemicals used as solvents (to dissolve other substances), other chlorine-containing compounds, and pesticides. It is also formed as a by-product in the waste streams of chloralkali and wood-preserving plants, and when burning municipal waste.
Substance details
Substance name: Benzene hexachloro - (HCB)
CASR number: 118-74-1
Molecular formula: C6Cl6 formula weight 284.78
Synonyms: The currently accepted name for this substance is hexachlorobenzene. Synonyms other than benzene hexachloro- include: perchlorobenzene; HCB; hexa c.b.; anticarie; bunt-cure; bunt-no-more; ceku C.B.; no bunt; pentachlorophenyl chloride; no bunt 40; julian's carbon chloride; no bunt 80; sanocide; smut-go; amatin; co-op hexa; granox nm; snieciotox
Physical properties
White needles. Very slightly soluble in water. Slightly soluble in cold alcohol, soluble in benzene, chloroform, ether, carbon disulfide, and boiling alcohol.
Melting Point: 230°C
Boiling Point: 332°C
Specific Gravity: 2.044
Vapour Density: 9.83
1 ppm = 11.6 mg/m3
Chemical properties
Hexachlorobenzene has a very low chemical and biochemical reactivity, and this is reflected in its long persistence in the environment.
Combustible at high temperatures. The substance decomposes on heating, producing toxic fumes. Reacts violently with dimethyl formamide above 65°C.
Further information
The National Pollutant Inventory (NPI) holds data for all sources of benzene hexachloro emissions in Australia.
Description
Safe Work Australia describes HCB as toxic, with a concentration cut-off level of 0.1 % weight/weight.
The heath effects caused by breathing hexachlorobenzene or by getting it on your skin are not known. Porphyria-induced skin disorders have been reported in humans following ingestion of bread prepared from grain containing hexachlorobenzene. There is evidence that hexachlorobenzene is toxic to young children; offspring nursing from hexachlorobenzene exposed mothers are exposed through the milk. Hexachlorobenzene has been found to decrease the survival rates of young children. Therefore, nursing infants of humans may be particularly susceptible due to the transfer of hexachlorobenzene through maternal milk. This has been confirmed by doing experiments in animals. Other animal studies show that eating hexachlorobenzene on a long-term basis can harm the liver, immune system, kidneys, and blood and produce eruptions and pigmentations of the skin. Studies in animals also suggest that eating enough hexachlorobenzene on a long-term basis can lead to cancer of the liver and thyroid. Hexachlorobenzene is generally regarded as a probable carcinogen.
Entering the body
Hexachlorobenzene can enter your body when you eat hexachlorobenzene-contaminated food, breathe hexachlorobenzene particles in the air, and/or when your skin comes in contact with it. Following intake, hexachlorobenzene rapidly spreads to many tissues in the body, especially to fat, probably within a few hours. Most of the hexachlorobenzene leaves your body in the faeces, and smaller amounts are found in the urine. Hexachlorobenzene will remain in your body, especially in fat, for years. A large portion of hexachlorobenzene in fat can be transferred in human milk.
Exposure
You may be exposed to hexachlorobenzene if you live near an industrial site where hexachlorobenzene is used or produced as a by-product, or a waste dump where it has been discarded. At these sites hexachlorobenzene may be carried in the air on dust particles. If you work in an industry that produces the chemical unintentionally as a by-product or uses hexachlorobenzene, you may also be exposed to hexachlorobenzene particles or dust particles that carry hexachlorobenzene and possibly get it on your skin.
Exposure to hexachlorobenzene can occur through eating and drinking foods and liquids, such as milk, other dairy products, meat, and poultry. When this substance is eaten in combination with fat or oil, more of it is taken up by the body than when consumed in drinking water.
Exposure to hexachlorobenzene can also occur through contact with hexachlorobenzene-contaminated soil, dust particles, or industrial releases into the environment.
Because of its low water solubility, hexachlorobenzene is usually not present in drinking water.
Workplace exposure standards
Safe Work Australia sets the workplace exposure standards for airborne contaminants. There are no workplace exposure standards for hexachlorobenzene.
These standards are only appropriate for use in workplaces and are not limited to any specific industry or operation. Make sure you understand how to interpret the standards before you use them.
Drinking water guidelines
There is no guideline for hexachlorobenzene in the Australian Drinking Water Guidelines.
Description
Acute toxic effects may include the death of animals, birds, or fish, and death or low growth rate in plants. Acute effects are seen two to four days after animals or plants come in contact with a toxic chemical substance.
Chronic toxic effects may include shortened lifespan, reproductive problems, lower fertility, and changes in appearance or behaviour.
Entering the environment
Hexachlorobenzene can remain in the environment for a long time, half-life up to 7.5 years. It is only very slightly soluble in water, so most of it will remain in particles on the bottom of lakes and rivers. Hexachlorobenzene adsorbs strongly to soil. High levels can build up in fish, marine mammals, birds, lichens, and animals that eat lichens or fish. It can also build up in wheat, grasses, some vegetables, and other plants.
It has been estimated that about 50% of hexachlorobenzene will eventually end up in terrestrial soil; about 46.75% will end up in aquatic sediments; about 3% will end up in air; and about 0.25% will end up in water.
Where it ends up
Hexachlorobenzene has been detected in environmental samples from around the world, and is recognised as a global pollutant.
Breakdown in soil and groundwater: HCB is a highly persistent compound, with reported field half-lives in the soil environment up to 7.5 years. Evaporation is rapid while it is on soil surfaces, but considerably less so when it is mixed into the soil. HCB is moderately to strongly bound by most soils. Data from testing on hydro-soils indicate that it may be degraded both aerobically and anaerobically. It has low water solubility, and thus is likely to show low mobility in the soil environment. Due to its lengthy persistence, however, even low mobility may result in appreciable travel; therefore, HCB may pose some risk of groundwater contamination. Hexachlorobenzene has been found in well water at low concentrations, up to 5.6 ppb and only in a very small percentage of all of the wells tested.
Breakdown in water: HCB is of low water solubility, so it would most likely reach surface waters via surface run-off by attachment to soil particles. Once in the aquatic environment, it is likely to be short-lived; HCB underwent very rapid, almost complete (that is, less than 5 days) degradation to pentachlorophenol and related compounds in inoculated hydro-soil samples under both aerobic and anaerobic conditions.
Breakdown in vegetation: Breakdown in vegetation appears rapid, with residue levels in grass at approximately 1% of the initial amount after 15 days, and at approximately 0.01% after 19 months.
Breakdown in air: The dominant chemical loss process for gas phase hexachlorobenzene in the troposphere is by reaction with the hydroxyl (OH) radical. Based on this reaction, the atmospheric half-life is calculated to be about 1.4 years. Air to water exchange to (and from) the oceans, and gas-phase hexachlorobenzene and wet and dry deposition of particle-associated hexachlorobenzene, are important.
Environmental guidelines
Australian Water Quality Guidelines for Fresh and Marine Waters: (ANZECC, 1992):
Maximum of 0.007 micrograms/L (i.e. 0.000000007 g/L)
Industry sources
The aerospace industry, sanitary services, and agricultural chemicals manufacturers. Industries involved in the manufacture of solvents, other chlorine-containing compounds, and pesticides, chloralkali and wood-preserving plants, and municipal waste incinerators.
Diffuse sources, and industry sources included in diffuse emissions data
Agricultural runoff, especially from grain applications-because this substance is persistent in the environment, it may be present for years after its use was banned. Sub-threshold facilities, smaller incinerators.
Natural sources
None known.
Transport sources
None known.
Consumer products
Banned from use as a pesticide in Australia. No consumer products should intentionally contain hexachlorobenzene. However, it is a global pollutant and may be found as a contaminant in a variety of foods.
Sources used in preparing this information
- Agency for Toxic Substances and Disease Registry (USA) (accessed, June, 1999)
- Australian and New Zealand Environment and Conservation Council (ANZECC) (1992), Australian Water Quality Guidelines for Fresh and Marine Waters.
- CalEPA Air Resources Board Toxic Air Contaminant Summary (accessed, June, 1999)
- ChemFinder WebServer Project (1995) (accessed, June, 1999)
- Environmental Defense Fund - Summary, Uses, Consumer Products, Rank (industrial, by quantity) (accessed, June, 1999)
- IPCS International Chemical Safety Card (accessed, June 1999)
- Meagher, D (1991), The Macmillan Dictionary of The Australian Environment, Macmillan Education Australia Pty Ltd.
- National Environment Protection Council (1998), National Environment Protection Measure for the National Pollutant Inventory. (accessed, March, 1999)
- New Jersey Health and Safety (accessed, June, 1999)
- Richardson, M (1992), Dictionary of Substances and their Effects, Royal Society of Chemistry, Clays Ltd, England.
- Sittig, M (1991), Handbook of Toxic and Hazardous Chemicals and Carcinogens, 3rd edition, Noyes Publications, USA.
- Technical Advisory Panel (1999), Final Report to the National Environment Protection Council.
- USA EXTOXNET Pesticide Information Profile (accessed, June 1999)
- USA National Toxicology Program Health and Safety Information Sheet (accessed, June 1999)
- US Department of Health and Human Services (1990), NIOSH Pocket Guide to Chemical Hazards, Publication No. 90-117.
- USEPA Health Effects Notebook for Hazardous Air Pollutants (accessed, June, 1999)
- USEPA Integrated Risk Information System Report (accessed, June, 1999)
- USEPA Office of Ground Water and Drinking Water Contaminant Fact Sheet (accessed, June 1999)
- USEPA Toxic Release Inventory Fact Sheet (accessed, June, 1999)
- WorkSafe Australia (accessed, June, 1999)
- Safe Work Australia, Workplace exposure standards for airborne contaminants, accessed June 2021.
- National Health and Medical Research Council (NHMRC), Australian Drinking Water Guidelines (2011) - Updated October 2017, accessed May 2018