An agricultural fungicide and seed treatment agent.
Chlorobenzenes are organic compounds consisting of a benzene ring substituted with one or more chlorine atoms, used as solvents, refrigerants, and intermediates in the production of other chemicals, but with limited use due to environmental and health concerns.
Hydrocarbon compounds with one or more of the hydrogens replaced by CHLORINE.
Chemicals that kill or inhibit the growth of fungi in agricultural applications, on wood, plastics, or other materials, in swimming pools, etc.
Industrial products consisting of a mixture of chlorinated biphenyl congeners and isomers. These compounds are highly lipophilic and tend to accumulate in fat stores of animals. Many of these compounds are considered toxic and potential environmental pollutants.
An organochlorine pesticide, it is the ethylene metabolite of DDT.
An enzyme that catalyzes the decarboxylation of UROPORPHYRINOGEN III to coproporphyrinogen III by the conversion of four acetate groups to four methyl groups. It is the fifth enzyme in the 8-enzyme biosynthetic pathway of HEME. Several forms of cutaneous PORPHYRIAS are results of this enzyme deficiency as in PORPHYRIA CUTANEA TARDA; and HEPATOERYTHROPOIETIC PORPHYRIA.
Substances or energies, for example heat or light, which when introduced into the air, water, or land threaten life or health of individuals or ECOSYSTEMS.
A highly poisonous organochlorine insecticide. The EPA has cancelled registrations of pesticides containing this compound with the exception of its use through subsurface ground insertion for termite control and the dipping of roots or tops of non-food plants. (From Merck Index, 11th ed)
An oxidation product of HEPTACHLOR formed by many plants and animals, including humans, after exposure to HEPTACHLOR. It has been shown to remain in soil treated with HEPTACHLOR for over fifteen years and is toxic to animals and humans. (From ATSDR Public Heath Statement, April 1989)
An insecticide and herbicide that has also been used as a wood preservative. Pentachlorphenol is a widespread environmental pollutant. Both chronic and acute pentachlorophenol poisoning are medical concerns. The range of its biological actions is still being actively explored, but it is clearly a potent enzyme inhibitor and has been used as such as an experimental tool.
A diverse group of metabolic diseases characterized by errors in the biosynthetic pathway of HEME in the LIVER, the BONE MARROW, or both. They are classified by the deficiency of specific enzymes, the tissue site of enzyme defect, or the clinical features that include neurological (acute) or cutaneous (skin lesions). Porphyrias can be hereditary or acquired as a result of toxicity to the hepatic or erythropoietic marrow tissues.
An organochlorine insecticide that has been used as a pediculicide and a scabicide. It has been shown to cause cancer.
A group of compounds containing the porphin structure, four pyrrole rings connected by methine bridges in a cyclic configuration to which a variety of side chains are attached. The nature of the side chain is indicated by a prefix, as uroporphyrin, hematoporphyrin, etc. The porphyrins, in combination with iron, form the heme component in biologically significant compounds such as hemoglobin and myoglobin.
Pesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics.
Chemicals used to destroy pests of any sort. The concept includes fungicides (FUNGICIDES, INDUSTRIAL); INSECTICIDES; RODENTICIDES; etc.
A polychlorinated pesticide that is resistant to destruction by light and oxidation. Its unusual stability has resulted in difficulties in residue removal from water, soil, and foodstuffs. This substance may reasonably be anticipated to be a carcinogen: Fourth Annual Report on Carcinogens (NTP-85-002, 1985). (From Merck Index, 11th ed)
Halogenated hydrocarbons refer to organic compounds containing carbon and hydrogen atoms, where one or more hydrogen atoms are replaced by halogens such as fluorine, chlorine, bromine, or iodine.
Colorless reduced precursors of porphyrins in which the pyrrole rings are linked by methylene (-CH2-) bridges.
The exposure to potentially harmful chemical, physical, or biological agents in the environment or to environmental factors that may include ionizing radiation, pathogenic organisms, or toxic chemicals.
Pesticides or their breakdown products remaining in the environment following their normal use or accidental contamination.

Intestinal T lymphocytes of different rat strains in immunotoxicity. (1/108)

In order to study the intestinal mucosal immune cells, with emphasis on single T lymphocytes, an inventory was made of single and organized lymphocytes in the epithelium and lamina propria of the small intestines of untreated Wistar, Fischer 344, and Lewis rats. The single and organized lymphocytes were examined microscopically. In addition, the single lymphocytes in the epithelium (IEL) and lamina propria (LPL) were analyzed by flow cytometry. Next, the use of flow cytometry analysis was explored to detect changes in the IEL T-lymphocyte population in subacute oral studies with the immunomodulating agents azathioprine and hexachlorobenzene. Untreated random-bred Wistar rats exhibited a large interindividual variability in IEL composition, while the variability was small in inbred Fischer 344 and Lewis rats. The explorative study with the 2 model immunomodulating compounds demonstrated that hexachlorobenzene increased the number of intraepithelial T lymphocytes with CD8+ phenotype at the cost of T cells with CD4+ phenotype in Lewis rats. Azathioprine did not induce distinct effects on the percentages of IEL. The data indicate that the intraepithelial lymphocytes in the intestines are a potential target for orally administered immunomodulating compounds and should therefore receive more attention in toxicologic pathology studies.  (+info)

Environmental exposure to hexachlorobenzene (HCB) and risk of female breast cancer in Connecticut. (2/108)

Earlier studies have provided inconclusive results relating hexachlorobenzene (HCB), an organochlorine fungicide, to female breast cancer risk. The current study, with a total of 304 breast cancer cases and 186 controls recruited in Connecticut between 1994 and 1997, examined the association by directly comparing breast adipose tissue levels of HCB between incident breast cancer cases and noncancer controls. The cases and controls were patients who had breast biopsies or surgery at the Yale-New Haven Hospital (New Haven, CT) and histologically diagnosed either as breast cancer or benign breast disease. Information on major known or suspected risk factors for breast cancer was obtained through in-person interview by trained interviewers. No significant difference in mean breast adipose tissue levels of HCB was observed between breast cancer patients (21.0 ppb) and controls (19.1 ppb) in this large case-control study. The risk also did not vary significantly by menopausal status, estrogen or progesterone receptor status of the breast cancer cases, breast cancer histology, stage of diagnosis, or type of benign breast disease. Among parous women who reported ever breast feeding, an odds ratio (OR) of 0.5 [95% confidence interval (CI), 0.2-1.4] was observed when the highest quartile was compared with the lowest quartile. However, no association was observed among parous women who reported never breast feeding (OR = 0.7; 95% CI, 0.3-1.7 for the fourth quartile). For nulliparous women, the adjusted OR was 2.1 (95% CI, 0.5-8.8) for the third tertile when compared with the lowest based on few subjects. Therefore, our study does not support a positive association between environmental exposure to HCB and risk of breast cancer.  (+info)

Organochlorine in the serum of inhabitants living near an electrochemical factory. (3/108)

OBJECTIVES: To measure the impact of occupational and lifestyle factors on concentrations of organochlorine compounds in a general population sample living near an electrochemical factory with a high airborne concentration of hexachlorobenzene (HCB). METHODS: Serum samples from 608 people (328 selected from a random sample) were collected in 1994. Information on lifestyles, occupation, and medical condition was obtained by questionnaire. RESULTS: HCB and polychlorinated biphenyls (PCBs) were detected in all samples (means 36.7 ng/ml and 4.3 ng/ml respectively), followed by dichlorodiphenyl dichloroethane (DDE) and beta-hexachlorocyclohexane (beta-HCH), found in 98.7% and 87.3% of the samples respectively (means 4.6 ng/ml and 2.5 ng/ml, respectively). Concentrations of HCB were the highest ever reported. Occupation in the factory was the main determinant of the variation in concentrations of HCB (regression coefficients 1.52 (SEM 0.14) in 1n (HCB) for workers in the production department, and 2.13 (0.23) for workers in maintenance department) and explained the highest concentrations of HCB found in men of middle age. In retired workers, concentrations of HCB declined with time since retirement. The PCBs, dichlorodiphenyl trichloroethane (DDT), and beta-HCH were independent of the occupation and concentrations were similar to those found in other populations. Concentrations of beta-HCH and DDE in the whole population, and HCB among non-workers, were higher in women than in men. Concentrations of all measured organochlorine compounds increased with age and body mass index. Consumption of locally caught fish was an independent determinant of HCB and PCB concentrations. CONCLUSIONS: This population incorporated HCB directly through occupation in the electrochemical factory, by airborne pollution, and consumption of locally caught fish. Concentrations of other common organochlorine compounds were not higher than expected. Environmental exposures to these compounds deserve attention due to their persistence and potential health effects.  (+info)

The role of the immune system in hexachlorobenzene-induced toxicity. (4/108)

Hexachlorobenzene (HCB) is a persistent environmental pollutant. The toxicity of HCB has been extensively studied after an accidental human poisoning in Turkey and more recently it has been shown that HCB has immunotoxic properties in laboratory animals and probably also in man. Oral exposure of rats to HCB showed stimulatory effects on spleen and lymph node weights and histology, increased serum IgM levels, and an enhancement of several parameters of immune function. Moreover, more recent studies indicate that HCB-induced effects in the rat may be related to autoimmunity. In Wistar rats exposed to HCB, IgM antibodies against several autoantigens were elevated; in the Lewis rat, HCB differently modulated two experimental models of autoimmune disease. Oral exposure of rats to HCB induces skin and lung pathology in the rat. Recently several studies have been conducted to investigate whether these skin and lung lesions can be related to HCB-induced immunomodulation, and these studies will be discussed in this review. HCB-induced skin and lung lesions probably have a different etiology; pronounced strain differences and correlation of skin lesions with immune parameters suggest a specific involvement of the immune system in HCB-induced skin lesions. The induction of lung lesions by HCB was thymus independent. Thymus-dependent T cells were not likely to be required for the induction of skin lesions, although T cells enhanced the rate of induction and the progression of the skin lesions. No deposition of autoantibodies was observed in nonlesional or lesional skin of HCB-treated rats. Therefore, we concluded that it is unlikely that the mechanism by which most allergic or autoimmunogenic chemicals work, i.e., by binding to macromolecules of the body and subsequent T- and B-cell activation, is involved in the HCB-induced immunopathology in the rat. Such a thymus-independent immunopathology is remarkable, as HCB strongly modulates T-cell-mediated immune parameters. This points at a very complex mechanism and possible involvement of multiple factors in the immunopathology of HCB.  (+info)

Comparative hepatocarcinogenicity of hexachlorobenzene, pentachlorobenzene, 1,2,4,5-tetrachlorobenzene, and 1,4-dichlorobenzene: application of a medium-term liver focus bioassay and molecular and cellular indices. (5/108)

Of the twelve different chlorobenzene isomers, a thorough evaluation of carcinogenicity has only been assessed on monochlorobenzene, 1,2-, and 1,4-dichlorobenzene, and hexachlorobenzene. In the studies presented here, we measured the ability of 1,4-dichlorobenzene (DCB), 1,2,4,5-tetrachlorobenzene (TeCB), pentachlorobenzene (PeCB), and hexachlorobenzene (HCB) to promote glutathione S-transferase pi (GSTP1-1) positive preneoplastic foci formation in rat liver, following diethylnitrosamine (DEN) initiation. The results from these studies show that TeCB, PeCB, and HCB all promote the formation of GSTP1-1 positive foci and that DCB does not. The numbers and area of foci were greatest following HCB promotion, and TeCB and PeCB were approximately equal in their promoting ability. Levels of hepatic CYP1A2, CYP2B1/2, non-focal GSTP1-1, and c-fos were measured in response to treatment with the 4 chlorobenzene isomers, as were reduced glutathione (GSH) and oxidized glutathione (GSSG) levels. Results from these studies show that induction of CYP1A2 and CYP2B1/2 have correlation with both the presence and degree of GSTP1-1 foci promotion by the 4 chlorobenzenes. Alterations in GSH and GSSG levels were similar in PeCB- and TeCB-treated animals in that GSSG levels were significantly decreased, whereas HCB and DCB did not have this effect, although HCB treatment led to a significant increase in GSH levels. We conclude that induction of CYP1A2 or CYP2B1/2 by chlorobenzene isomers may indicate promotional ability, and that this property might be exploited to predict the hepatocarcinogenicity of other chlorobenzene isomers.  (+info)

Susceptibility to infections and immune status in Inuit infants exposed to organochlorines. (6/108)

We investigated whether organochlorine exposure is associated with the incidence of infectious diseases in Inuit infants from Nunavik (Arctic Quebec, Canada). We compiled the number of infectious disease episodes during the first year of life for 98 breast-fed and 73 bottle-fed infants. Concentrations of organochlorines were measured in early breast milk samples and used as surrogates to prenatal exposure levels. Immune system parameters were determined in venous blood samples collected from infants at 3, 7, and 12 months of age. Otitis media was the most frequent disease, with 80. 0% of breast-fed and 81.3% of bottle-fed infants experiencing at least one episode during the first year of life. During the second follow-up period, the risk of otitis media increased with prenatal exposure to p,p'-DDE, hexachlorobenzene, and dieldrin. The relative risk (RR) for 4- to 7-month-old infants in the highest tertile of p, p'-DDE exposure as compared to infants in the lowest tertile was 1. 87 [95% confidence interval (CI), 1.07-3.26]. The RR of otitis media over the entire first year of life also increased with prenatal exposure to p,p'-DDE (RR, 1.52; CI, 1.05-2.22) and hexachlorobenzene (RR, 1.49; CI, 1.10-2.03). Furthermore, the RR of recurrent otitis media ( [Greater/equal to] 3 episodes) increased with prenatal exposure to these compounds. No clinically relevant differences were noted between breast-fed and bottle-fed infants with regard to immunologic parameters, and prenatal organochlorine exposure was not associated with immunologic parameters. We conclude that prenatal organochlorine exposure could be a risk factor for acute otitis media in Inuit infants.  (+info)

Serum concentrations of hexachlorobenzene in family members of workers in an electrochemical factory. (7/108)

OBJECTIVES: This study analyzed the effect of living in the same household with a worker employed in an electrochemical factory on the hexachlorobenzene (HCB) concentrations of serum in the general population of Flix, Spain. METHODS: A total of 608 subjects from the general population (response rate 42%) completed a questionnaire about residence, occupation, life-styles, and medical history and provided blood samples. Among them, 412 had never worked in the electrochemical factory. Information about the occupation of the family members was completed, and the subjects were classified with the degree of relationship with the worker having been taken into account. A multiple linear regression analysis was conducted to model HCB serum for nonfactory workers. RESULTS: Having a spouse who worked in the factory was associated with elevated HCB concentrations in serum. The adjusted relative increases were 1.28 (P=0.0004) and 1.23 (P=0.0022) times the corresponding value of people not living with workers of the factory, respectively for spouses of current and past workers. Relatives other than spouses did not show any increase. CONCLUSIONS: The results of this study suggest that, among nonworkers, living with a worker of the electrochemical factory in Flix is associated with an increase in concentrations of HCB in blood. These findings may suggest a source of exposure to HCB that has thus far not been studied and that could be important in populations not occupationally exposed to organochlorines.  (+info)

Excretion of hexachlorobenzene and metabolites in feces in a highly exposed human population. (8/108)

A set of 53 individuals from a population highly exposed to airborne hexachlorobenzene (HCB) were selected to study the elimination kinetics of this chemical in humans. The volunteers provided blood, 24-hr urine, and feces samples for analysis of HCB and metabolites. The serum HCB concentrations ranged from 2.4 to 1,485 ng/mL (mean +/- SD, 124 +/- 278), confirming that this human population has the highest HCB blood levels ever reported. All analyzed feces samples contained unchanged HCB (range, 11-3,025 ng/g dry weight; mean +/- SD, 395 +/- 629). The HCB concentration in feces strongly correlated with HCB in serum (r = 0.85; p < 0.001), suggesting an equilibrium in feces/serum that is compatible with a main pulmonary entrance of the chemical and low intestinal excretion of nonabsorbed foodborne HCB. The equilibrium is also compatible with a nonbiliary passive transfer of the chemical to the intestinal lumen. Two HCB main metabolites, pentachlorophenol (PCP) and pentachlorobenzenethiol (PCBT), were detected in 51% and 54% of feces samples, respectively. All urine samples contained PCP and PCBT, confirming the conclusions of a previous study [Environ Health Perspect 105:78-83 (1997)]. The comparison between feces and urine showed that whereas daily urinary elimination of metabolites may account for 3% of total HCB in blood, intestinal excretion of unchanged HCB may account for about 6%, thus showing the importance of metabolism in the overall elimination of HCB. The elimination of HCB and metabolites by both routes, however, appears to be very small (< 0.05%/day) as compared to the estimated HCB adipose depots. Features of HCB kinetics that we present in this study, i.e., nonsaturated intestinal elimination of HCB and excretion in feces and urine of inert glutathione derivatives, may explain, in part, the absence of porphyria cutanea in this human population heavily exposed to HCB.  (+info)

Hexachlorobenzene (HCB) is not typically included in standard medical textbooks or resources as it's more of a environmental and industrial chemical. However, I can provide you with an definition from a toxicological perspective:

Hexachlorobenzene (C6Cl6) is an organic compound that consists of a benzene ring with six chlorine atoms attached to it. It is a persistent organic pollutant, which means it does not break down easily and can accumulate in the environment and living organisms. HCB has been used as a pesticide, fungicide, and chemical intermediate in various industrial processes. Exposure to this compound can lead to several health issues, including skin lesions, damage to the nervous system, and impaired immune function. It's also considered a possible human carcinogen by some agencies. Long-term environmental exposure to HCB is of particular concern due to its bioaccumulation in the food chain and potential adverse effects on human health and the environment.

Chlorobenzenes are a group of chemical compounds that consist of a benzene ring (a cyclic structure with six carbon atoms in a hexagonal arrangement) substituted with one or more chlorine atoms. They have the general formula C6H5Clx, where x represents the number of chlorine atoms attached to the benzene ring.

Chlorobenzenes are widely used as industrial solvents, fumigants, and intermediates in the production of other chemicals. Some common examples of chlorobenzenes include monochlorobenzene (C6H5Cl), dichlorobenzenes (C6H4Cl2), trichlorobenzenes (C6H3Cl3), and tetrachlorobenzenes (C6H2Cl4).

Exposure to chlorobenzenes can occur through inhalation, skin contact, or ingestion. They are known to be toxic and can cause a range of health effects, including irritation of the eyes, skin, and respiratory tract, headaches, dizziness, nausea, and vomiting. Long-term exposure has been linked to liver and kidney damage, neurological effects, and an increased risk of cancer.

It is important to handle chlorobenzenes with care and follow appropriate safety precautions to minimize exposure. If you suspect that you have been exposed to chlorobenzenes, seek medical attention immediately.

Chlorinated hydrocarbons are a group of organic compounds that contain carbon (C), hydrogen (H), and chlorine (Cl) atoms. These chemicals are formed by replacing one or more hydrogen atoms in a hydrocarbon molecule with chlorine atoms. The properties of chlorinated hydrocarbons can vary widely, depending on the number and arrangement of chlorine and hydrogen atoms in the molecule.

Chlorinated hydrocarbons have been widely used in various industrial applications, including as solvents, refrigerants, pesticides, and chemical intermediates. Some well-known examples of chlorinated hydrocarbons are:

1. Methylene chloride (dichloromethane) - a colorless liquid with a mild sweet odor, used as a solvent in various industrial applications, including the production of pharmaceuticals and photographic films.
2. Chloroform - a heavy, volatile, and sweet-smelling liquid, used as an anesthetic in the past but now mainly used in chemical synthesis.
3. Carbon tetrachloride - a colorless, heavy, and nonflammable liquid with a mildly sweet odor, once widely used as a solvent and fire extinguishing agent but now largely phased out due to its ozone-depleting properties.
4. Vinyl chloride - a flammable, colorless gas, used primarily in the production of polyvinyl chloride (PVC) plastic and other synthetic materials.
5. Polychlorinated biphenyls (PCBs) - a group of highly stable and persistent organic compounds that were widely used as coolants and insulating fluids in electrical equipment but are now banned due to their toxicity and environmental persistence.

Exposure to chlorinated hydrocarbons can occur through inhalation, skin contact, or ingestion, depending on the specific compound and its physical state. Some chlorinated hydrocarbons have been linked to various health effects, including liver and kidney damage, neurological disorders, reproductive issues, and cancer. Therefore, proper handling, use, and disposal of these chemicals are essential to minimize potential health risks.

Industrial fungicides are antimicrobial agents used to prevent, destroy, or inhibit the growth of fungi and their spores in industrial settings. These can include uses in manufacturing processes, packaging materials, textiles, paints, and other industrial products. They work by interfering with the cellular structure or metabolic processes of fungi, thereby preventing their growth or reproduction. Examples of industrial fungicides include:

* Sodium hypochlorite (bleach)
* Formaldehyde
* Glutaraldehyde
* Quaternary ammonium compounds
* Peracetic acid
* Chlorhexidine
* Iodophors

It's important to note that some of these fungicides can be harmful or toxic to humans and other organisms, so they must be used with caution and in accordance with safety guidelines.

Polychlorinated biphenyls (PCBs) are a group of man-made organic chemicals consisting of 209 individual compounds, known as congeners. The congeners are formed by the combination of two benzene rings with varying numbers and positions of chlorine atoms.

PCBs were widely used in electrical equipment, such as transformers and capacitors, due to their non-flammability, chemical stability, and insulating properties. They were also used in other applications, including coolants and lubricants, plasticizers, pigments, and copy oils. Although PCBs were banned in many countries in the 1970s and 1980s due to their toxicity and environmental persistence, they still pose significant health and environmental concerns because of their continued presence in the environment and in products manufactured before the ban.

PCBs are known to have various adverse health effects on humans and animals, including cancer, immune system suppression, reproductive and developmental toxicity, and endocrine disruption. They can also cause neurological damage and learning and memory impairment in both human and animal populations. PCBs are highly persistent in the environment and can accumulate in the food chain, leading to higher concentrations in animals at the top of the food chain, including humans.

Dichlorodiphenyl dichloroethylene (DDE) is a chemical compound that is formed as a byproduct when dichlorodiphenyltrichloroethane (DDT) is metabolized or breaks down in the environment. DDE is an organochlorine pesticide and is similar in structure to DDT, with two phenyl rings and two chlorine atoms attached to a central ethylene molecule.

DDE is highly stable and does not break down easily in the environment, which means that it can persist for many years and accumulate in the food chain. It is lipophilic, meaning that it tends to accumulate in fatty tissues, and bioaccumulates in animals that are higher up in the food chain.

DDE has been shown to have toxic effects on both wildlife and humans. It can disrupt hormone systems, particularly those related to reproduction, and has been linked to reproductive problems in birds and other animals. In humans, exposure to DDE has been associated with increased risk of certain cancers, developmental delays in children, and other health problems.

DDE is no longer used as a pesticide in many countries, but it can still be found in the environment due to its persistence and ability to accumulate in the food chain. People can be exposed to DDE through contaminated food, water, or air, as well as through contact with soil or dust that contains DDE.

Uroporphyrinogen decarboxylase is a vital enzyme in the biosynthetic pathway of heme, which is a crucial component of hemoglobin in red blood cells. This enzyme is responsible for catalyzing the decarboxylation of uroporphyrinogen III, a colorless porphyrinogen, to produce coproporphyrinogen III, a brownish-red porphyrinogen.

The reaction involves the sequential removal of four carboxyl groups from the four acetic acid side chains of uroporphyrinogen III, resulting in the formation of coproporphyrinogen III. This enzyme's activity is critical for the normal biosynthesis of heme, and any defects or deficiencies in its function can lead to various porphyrias, a group of metabolic disorders characterized by the accumulation of porphyrins and their precursors in the body.

The gene responsible for encoding uroporphyrinogen decarboxylase is UROD, located on chromosome 1p34.1. Mutations in this gene can lead to a deficiency in the enzyme's activity, causing an autosomal recessive disorder known as congenital erythropoietic porphyria (CEP), also referred to as Günther's disease. This condition is characterized by severe photosensitivity, hemolytic anemia, and scarring or thickening of the skin.

Environmental pollutants are defined as any substances or energy (such as noise, heat, or light) that are present in the environment and can cause harm or discomfort to humans or other living organisms, or damage the natural ecosystems. These pollutants can come from a variety of sources, including industrial processes, transportation, agriculture, and household activities. They can be in the form of gases, liquids, solids, or radioactive materials, and can contaminate air, water, and soil. Examples include heavy metals, pesticides, volatile organic compounds (VOCs), particulate matter, and greenhouse gases.

It is important to note that the impact of environmental pollutants on human health and the environment can be acute (short-term) or chronic (long-term) and it depends on the type, concentration, duration and frequency of exposure. Some common effects of environmental pollutants include respiratory problems, cancer, neurological disorders, reproductive issues, and developmental delays in children.

It is important to monitor, control and reduce the emissions of these pollutants through regulations, technology advancements, and sustainable practices to protect human health and the environment.

Chlordane is a man-made chlorinated hydrocarbon compound that was widely used as a pesticide, particularly for termite control, from the 1940s until it was banned in the United States in 1988 due to its toxicity and persistence in the environment. It is a colorless or light brown liquid with a mild, aromatic odor.

Chlordane is an extremely toxic compound to insects and has been shown to have negative effects on human health as well. Exposure to chlordane can cause a range of adverse health effects, including neurological damage, liver toxicity, and an increased risk of cancer. It is classified as a probable human carcinogen by the International Agency for Research on Cancer (IARC) and the United States Environmental Protection Agency (EPA).

Chlordane is highly persistent in the environment and can accumulate in the food chain, posing a particular risk to wildlife and humans who consume contaminated food or water. It can also volatilize from soil and water into the air, where it can be transported long distances and contribute to air pollution. As a result, chlordane continues to pose a significant environmental and health hazard, even though its use has been banned for several decades.

Heptachlor epoxide is a metabolite and environmental breakdown product of heptachlor, which is a chlorinated hydrocarbon insecticide. It is an organochlorine compound that was widely used in the past for agricultural and residential pest control purposes, including termite treatments and crop protection.

Heptachlor epoxide is formed through the oxidation of heptachlor by various biological and environmental processes. It is more stable and persistent in the environment compared to heptachlor, making it a significant contaminant in soil, water, and air. Heptachlor epoxide has been classified as a probable human carcinogen by the International Agency for Research on Cancer (IARC) and the United States Environmental Protection Agency (EPA). It can accumulate in the fatty tissues of living organisms, including humans, and poses potential risks to human health and the environment.

Pentachlorophenol is not primarily a medical term, but rather a chemical compound with some uses and applications in the medical field. Medically, it's important to understand what pentachlorophenol is due to its potential health implications.

Pentachlorophenol (PCP) is an organochlorine compound that has been widely used as a pesticide, wood preservative, and disinfectant. Its chemical formula is C6HCl5O. It is a white crystalline solid with a distinct, somewhat unpleasant odor. In the environment, pentachlorophenol can be found in soil, water, and air as well as in various organisms, including humans.

Pentachlorophenol has been associated with several potential health risks. It is classified as a probable human carcinogen by the International Agency for Research on Cancer (IARC) and as a possible human carcinogen by the United States Environmental Protection Agency (EPA). Exposure to pentachlorophenol can occur through inhalation, skin contact, or ingestion. Potential health effects include irritation of the skin, eyes, and respiratory tract; damage to the liver and kidneys; neurological issues; and reproductive problems.

In a medical context, pentachlorophenol might be relevant in cases where individuals have been exposed to this compound through occupational or environmental sources. Medical professionals may need to assess potential health risks, diagnose related health issues, and provide appropriate treatment.

Porphyrias are a group of rare genetic disorders that affect the production of heme, a component in hemoglobin that carries oxygen in the blood. The diseases are caused by mutations in the genes involved in the production of heme, leading to the buildup of porphyrins or their precursors in the body. These substances can be toxic and can cause various symptoms depending on the specific type of porphyria. Symptoms may include abdominal pain, neurological problems, and skin issues. Porphyrias are typically divided into two categories: acute porphyrias, which affect the nervous system, and cutaneous porphyrias, which primarily affect the skin.

Lindane is defined in medical terms as an agricultural and pharmaceutical compound that contains thegamma-isomer of hexachlorocyclohexane (γ-HCH). It has been used as a topical treatment for scabies and lice infestations, although its use is now limited due to concerns about toxicity and environmental persistence. Lindane works by disrupting the nervous system of insects, leading to paralysis and death. However, it can also have similar effects on mammals, including humans, at high doses or with prolonged exposure. Therefore, its use is restricted and alternatives are recommended for the treatment of scabies and lice.

Porphyrins are complex organic compounds that contain four pyrrole rings joined together by methine bridges (=CH-). They play a crucial role in the biochemistry of many organisms, as they form the core structure of various heme proteins and other metalloproteins. Some examples of these proteins include hemoglobin, myoglobin, cytochromes, and catalases, which are involved in essential processes such as oxygen transport, electron transfer, and oxidative metabolism.

In the human body, porphyrins are synthesized through a series of enzymatic reactions known as the heme biosynthesis pathway. Disruptions in this pathway can lead to an accumulation of porphyrins or their precursors, resulting in various medical conditions called porphyrias. These disorders can manifest as neurological symptoms, skin lesions, and gastrointestinal issues, depending on the specific type of porphyria and the site of enzyme deficiency.

It is important to note that while porphyrins are essential for life, their accumulation in excessive amounts or at inappropriate locations can result in pathological conditions. Therefore, understanding the regulation and function of porphyrin metabolism is crucial for diagnosing and managing porphyrias and other related disorders.

Insecticides are substances or mixtures of substances intended for preventing, destroying, or mitigating any pest, including insects, arachnids, or other related pests. They can be chemical or biological agents that disrupt the growth, development, or behavior of these organisms, leading to their death or incapacitation. Insecticides are widely used in agriculture, public health, and residential settings for pest control. However, they must be used with caution due to potential risks to non-target organisms and the environment.

Pesticides are substances or mixtures of substances intended for preventing, destroying, or repelling pests. Pests can be insects, rodents, fungi, weeds, or other organisms that can cause damage to crops, animals, or humans and their living conditions. The term "pesticide" includes all of the following: insecticides, herbicides, fungicides, rodenticides, bactericides, and various other substances used to control pests.

It is important to note that while pesticides are designed to be toxic to the target pests, they can also pose risks to non-target organisms, including humans, if not used properly. Therefore, it is essential to follow all label instructions and safety precautions when handling and applying pesticides.

DDT (dichlorodiphenyltrichloroethane) is a synthetic insecticide that was widely used in the mid-20th century to control agricultural pests and vector-borne diseases such as malaria. It belongs to a class of chemicals called organochlorines, which are known for their persistence in the environment and potential for bioaccumulation in the food chain.

DDT was first synthesized in 1874, but its insecticidal properties were not discovered until 1939. Its use as an insecticide became widespread during World War II, when it was used to control typhus and malaria-carrying lice and mosquitoes among troops. After the war, DDT was widely adopted for agricultural and public health purposes.

However, concerns about the environmental and human health effects of DDT led to its ban or severe restriction in many countries starting in the 1970s. The United States banned the use of DDT for most purposes in 1972, and the Stockholm Convention on Persistent Organic Pollutants (POPs) prohibited its production and use globally in 2004, except in cases where there is a risk of vector-borne diseases.

DDT has been linked to several health problems, including reproductive effects, developmental toxicity, neurotoxicity, and endocrine disruption. It is also highly persistent in the environment, with a half-life of up to 15 years in soil and up to 30 years in water. This means that DDT can accumulate in the food chain, posing risks to wildlife and humans who consume contaminated food or water.

In summary, DDT is a synthetic insecticide that was widely used in the mid-20th century but has been banned or restricted in many countries due to its environmental and health effects. It belongs to a class of chemicals called organochlorines, which are known for their persistence in the environment and potential for bioaccumulation in the food chain. DDT has been linked to several health problems, including reproductive effects, developmental toxicity, neurotoxicity, and endocrine disruption.

Halogenated hydrocarbons are organic compounds containing carbon (C), hydrogen (H), and one or more halogens, such as fluorine (F), chlorine (Cl), bromine (Br), or iodine (I). These compounds are formed when halogens replace one or more hydrogen atoms in a hydrocarbon molecule.

Halogenated hydrocarbons can be further categorized into two groups:

1. Halogenated aliphatic hydrocarbons: These include alkanes, alkenes, and alkynes with halogen atoms replacing hydrogen atoms. Examples include chloroform (trichloromethane, CHCl3), methylene chloride (dichloromethane, CH2Cl2), and trichloroethylene (C2HCl3).
2. Halogenated aromatic hydrocarbons: These consist of aromatic rings, such as benzene, with halogen atoms attached. Examples include chlorobenzene (C6H5Cl), bromobenzene (C6H5Br), and polyhalogenated biphenyls like polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs).

Halogenated hydrocarbons have various industrial applications, including use as solvents, refrigerants, fire extinguishing agents, and intermediates in chemical synthesis. However, some of these compounds can be toxic, environmentally persistent, and bioaccumulative, posing potential health and environmental risks.

Porphyrinogens are organic compounds that are the precursors to porphyrins, which are ring-shaped molecules found in many important biological molecules such as hemoglobin and cytochromes. Porphyrinogens are themselves derived from the condensation of four pyrrole molecules, and they undergo further reactions to form porphyrins.

In particular, porphyrinogens are intermediates in the biosynthesis of heme, which is a complex organic ring-shaped molecule that contains iron and plays a critical role in oxygen transport and storage in the body. Abnormalities in heme biosynthesis can lead to various medical conditions known as porphyrias, which are characterized by the accumulation of porphyrinogens and other intermediates in this pathway. These conditions can cause a range of symptoms, including neurological problems, skin sensitivity to light, and abdominal pain.

Environmental exposure refers to the contact of an individual with any chemical, physical, or biological agent in the environment that can cause a harmful effect on health. These exposures can occur through various pathways such as inhalation, ingestion, or skin contact. Examples of environmental exposures include air pollution, water contamination, occupational chemicals, and allergens. The duration and level of exposure, as well as the susceptibility of the individual, can all contribute to the risk of developing an adverse health effect.

Pesticide residues refer to the remaining pesticide chemicals, including their metabolites and degradation products, that are present in or on food commodities or environmental samples after a pesticide application has ended. These residues can result from agricultural use, such as spraying crops to control pests, or from non-agricultural uses, like treating buildings for termite control.

Regulatory agencies establish maximum residue limits (MRLs) to ensure that the levels of pesticide residues in food and feed are below those that may pose a risk to human health. Monitoring programs are in place to check compliance with these MRLs, and enforcement actions can be taken if violations occur.

It's important to note that not all pesticide residues are harmful, as some pesticides degrade into harmless compounds over time or leave behind residues below levels of concern for human health. However, long-term exposure to even low levels of certain pesticide residues may still pose a risk and should be avoided when possible.

Neurological changes have been reported in rodents exposed to hexachlorobenzene. Hexachlorobenzene may cause embryolethality ... Hexachlorobenzene has a half life in the soil of between 3 and 6 years. Risk of bioaccumulation in an aquatic species is high. ... Hexachlorobenzene is an animal carcinogen and is considered to be a probable human carcinogen. After its introduction as a ... Hexachlorobenzene has been made on a laboratory scale since the 1890s, by the electrophilic aromatic substitution reaction of ...
Vorozhtsov, N. N., Jr.; Platonov, V. E.; Yakobson, G. G. (1963). "Preparation of hexafluorobenzene from hexachlorobenzene". ...
... is itself a metabolite of hexachlorobenzene and is found in the urine and the excretions of animals ... Koss, G.; Koransky, W.; Steinbach, K. (June 1976). "Studies on the toxicology of hexachlorobenzene: II. Identification and ... Kulka, Marshall (1959). "Reaction of Hexachlorobenzene with Mercaptides". J. Org. Chem. 24 (4): 235-237. doi:10.1021/ ... Pentachlorobenzenethiol can be obtained from hexachlorobenzene. Pentachlorobenzenethiol is a combustible gray solid with an ...
p. 2. Thompson, Leo E.; Nicholas Megalos; David Osborne (Feb 27 - Mar 2, 2000). Hexachlorobenzene Destruction With the Geomelt ...
... hexachlorobenzene, and nickel compounds. Many teratogens exert specific effects on the fetus by epigenetic mechanisms. While ...
DDT (dichlorodiphenyltrichloroethane) Hexachlorobenzene (HCB) PCBs (polychlorinated biphenyls) Toxaphene Monomethylmercury. ...
The company also produced arsenic trichloride, thionyl chloride, and hexachlorobenzene. Hooker expanded into plastics ...
Caesium chloride treated with titanium(II) chloride and hexachlorobenzene produces crystalline CsTi2Cl7. In these structures ...
Lonsdale, K. (1931). "An X-Ray Analysis of the Structure of Hexachlorobenzene, Using the Fourier Method". Proceedings of the ...
She was the first to use Fourier spectral methods while solving the structure of hexachlorobenzene in 1931. During her career ... Lonsdale, K. (1931). "An X-Ray Analysis of the Structure of Hexachlorobenzene, Using the Fourier Method". Proceedings of the ... In addition to discovering the structure of benzene and hexachlorobenzene, Lonsdale worked on the synthesis of diamonds. She ...
... and hexachlorobenzene (HCB) in rats". Environmental Research. 10 (3): 384-389. Bibcode:1975ER.....10..384I. doi:10.1016/0013- ...
Toxins that have been studied in conjunction with olestra treatment include dioxins, hexachlorobenzene, and polychlorinated ... and olestra on tissue distribution of hexachlorobenzene". American Journal of Physiology. Gastrointestinal and Liver Physiology ...
Hydrocarbons are also a major concern such has PCBs (polychlorinated biphenyls) and HCB (hexachlorobenzene). These are said to ...
Some of these pollutants are DDT, aldrin, chlordane, dieldrin, endrin, heptachlor, hexachlorobenzene, and toxaphene. With these ...
One example of a ductile molecular solid, that can be bent 180°, is hexachlorobenzene (HCB). In this example the π-π ... Examples of molecular solids that halogen bond are hexachlorobenzene and a cocrystal of bromine 1,4-dioxane. For the second ...
... of hepatic microsomal enzyme activity produced by administration of pure hexachlorobiphenyl isomers and hexachlorobenzene". ...
Picloram in Agent White and Super-Orange was contaminated by hexachlorobenzene (HCB) a dioxin-like carcinogen.[citation needed ...
Some pesticides, including aldrin, chlordane, DDT, dieldrin, endrin, heptachlor, hexachlorobenzene, mirex and toxaphene, are ... Hexachlorobenzene, Mirex, Toxaphene, Polychlorinated Biphenyls, Dioxins and Furans Archived 26 September 2007 at the Wayback ...
... and hexachlorobenzene. DDT and hexachlorobenzene are associated with decreased semen quality, while PCBs are associated with ...
... hexachlorobenzene, and ash. Highly toxic dioxins, produced in small amounts in almost all burning processes, can be produced in ...
These chemicals have been known to produce extremely toxic byproducts, including dioxins and hexachlorobenzenes. Exposure to ...
A side product of the synthesis of PCNB is hexachlorobenzene (HCB), which is considered as hazardous as PCNB. 5 Cl2 + C6H5NO2 ...
Common chlorothalonil synthesis procedures frequently result in contamination of it with small amounts of hexachlorobenzene ( ... Technical grade chlorothalonil contains traces of dioxins and hexachlorobenzene, a persistent organic pollutant banned under ...
Hexachlorobenzene (HCB) was first introduced in 1945-59 to treat seeds because it can kill fungi on food crops. HCB-treated ...
To control termites that attack dead material, hexachlorobenzene, also known as benzene hexachloride-BCH, can be applied to the ...
... with an efficiency comparable to decachlorobutane and hexachlorobenzene (BHC). Unlike the latter, it is somewhat volatile and ...
Two chemicals, hexachlorobenzene and polychlorinated biphenyls, were listed in both categories A and C. Currently, five ...
Several PBTs are emitted by the pulp and paper industry at measurable levels, including lead, hexachlorobenzene (HCB), dioxins ... hexachlorobenzene (HCB) and polycyclic aromatic hydrocarbons (PAH). In addition, the Toxics Release Inventory (TRI) is a ...
For example, the levels of PCBs, hexachlorobenzene, and lindane measured in water, lichens, and tree bark have been shown to be ...
... hexachlorobenzene, mirex, and toxaphene. The EPA has determined that lifetime exposure to 0.01 milligrams per liter of ...
Neurological changes have been reported in rodents exposed to hexachlorobenzene. Hexachlorobenzene may cause embryolethality ... Hexachlorobenzene has a half life in the soil of between 3 and 6 years. Risk of bioaccumulation in an aquatic species is high. ... Hexachlorobenzene is an animal carcinogen and is considered to be a probable human carcinogen. After its introduction as a ... Hexachlorobenzene has been made on a laboratory scale since the 1890s, by the electrophilic aromatic substitution reaction of ...
Hexachlorobenzene has been found in at least 84 of the 1,430 National Priorities List sites identified by the Environmental ... Exposure to hexachlorobenzene occurs primarily from eating low levels in contaminated food. The main health effect from eating ... What happens to hexachlorobenzene when it enters the environment?. *Hexachlorobenzene is very slow to breakdown in air and is ... What is hexachlorobenzene?. Hexachlorobenzene is a fungicide that was used in the United States until 1984. It has not been ...
2642 Hexachlorobenzene (Previous) (Back) (Next) Geometry predicted using PM7. # Species Formula 2632 Pentachlorophenol. HC6OCl5 ... SHIFT=20 PM7 Hexachlorobenzene H=-8.6 HR=C&P1970 C 0.00000000 +0 0.0000000 +0 0.0000000 +0 0 0 0 C 1.39279866 +1 0.0000000 +0 ...
EPTIS helps you find a suitable proficiency testing (PT) scheme for your laboratory.
Association between serum concentrations of hexachlorobenzene and polychlorobiphenyls with thyroid hormone and liver enzymes in ... Association between serum concentrations of hexachlorobenzene and polychlorobiphenyls with thyroid hormone and liver enzymes in ...
We examined the relation between serum levels of the pesticides heptachlor epoxide (HCE), hexachlorobenzene (HCB), and β- ... Maternal pregnancy serum level of heptachlor epoxide, hexachlorobenzene, and β-hexachlorocyclohexane and risk of cryptorchidism ... hexachlorobenzene, and β-hexachlorocyclohexane and risk of cryptorchidism in offspring. Environmental Research, 105(3), 364-369 ...
Hexachlorobenzene (HCB) , Pentachlorobenzene (PeCB) , DDT , Polychlorinated dibenzodioxins (PCDDs) and polychlorinated ...
Hexachlorobenzene. Contributor(s): Newhook, R , Dormer, W , World Health Organization , International Programme for Chemical ... Hexachlorobenzene -- toxicity -- adverse effects , Environmental exposure , Chemical Toxicology and CarcinogenicityNLM ...
Australia is the stolen lands of Aboriginal & Torres Strait Islander people and sovereignty of these lands was never ceded. We pay respect to Elders, past and present, and acknowledge the pivotal role that Aboriginal & Torres Strait Islander people continue to play within the Australian community. All content produced for australianmap.net is licensed ...
The recent events in Sydney indicate a route of communication to the public from the scientists should be developed. This may reduce the "scare" from the press and shield the fishing industry from impacts produced by false or inaccurate media reporting.[1]. However the two studies that were the basis for media stories were reported accurately and did not overstate the results. The first study, which triggered the media attention, was the 1987 Malabar Bioaccumulation Study. The results of this study are shown in Table 1 & 2. The Sydney Morning Herald reported the results as follows: ...
Hexachlorobenzene (HCB) Listed under Annex A and Annex C. First introduced in 1945 to treat seeds, HCB kills fungi that affect ...
Hexachlorobenzene. CAS No. 118-74-1. serum or plasma. Mirex. CAS No. 2385-85-5. serum or plasma. ...
EU - EU Publishes Hexachlorobenzene Requirement in Persistent Organic Pollutants Regulation. The EU has published a limit for ... hexachlorobenzene under the Persistent Organic Pollutants Regulation. This new law will become effective on December 13, 2022. ...
Hexachlorobenzene. 0.13. 63. L74. 87-68-3. Hexachlorobutadiene. 0.50. 64. L75. 67-72-1. Hexachloroethane. 3.00. ...
HEXACHLOROBENZENE 11 HALOGENATED AROMATICS. 9 PHENOL COMPOUNDS 9 DDE 10 ANIONIC DETERGENTS. 9 ...
A pick up service is provided by the Department of Environmental Health & Safety. Waste material should be placed into glass, metal, or plastic containers and kept closed. Segregate waste by hazard classes. Collect halogenated waste separate from nonhalogenated waste.. ...
Hexachlorobenzene episode in Turkey. Biomed Environ Sci. 1989 Mar. 2(1):36-43. [QxMD MEDLINE Link]. ... developed porphyria due to the ingestion of hexachlorobenzene (HCB), a fungicide that was added to wheat seedlings. [6] ...
Dehalorespiration with hexachlorobenzene and pentachlorobenzene by Dehalococcoides sp. strain CBDB1. Arch. Microbiol. 180 (6), ... Dehalorespiration with hexachlorobenzene and pentachlorobenzene by Dehalococcoides sp. strain CBDB1. Author. Jayachandran, G.; ... strain CBDB1 used hexachlorobenzene and pentachlorobenzene as electron acceptors in an energy-conserving process with hydrogen ... strain CBDB1 with hexachlorobenzene or pentachlorobenzene as electron acceptors failed if these compounds were provided as ...
Hexachlorobenzene episode in Turkey. Biomed Environ Sci. 1989 Mar. 2(1):36-43. [QxMD MEDLINE Link]. ... developed porphyria due to the ingestion of hexachlorobenzene (HCB), a fungicide that was added to wheat seedlings. [6] ...
Hexachlorobenzene. 2000 µg/mL. CAS #: 118-74-1 * Hexachlorocyclopentadiene. 2000 µg/mL. CAS #: 77-47-4 ...
Hexachlorobenzene, Hexachloro-1,3-butadiene, n-Hexane, Manganese sulfate, Methylene chloride, Methyl ethyl ketone, ...
Hexachlorobenzene. -. -. -. -. 5. -. 6. Red Gum. 14. 9. 9. 3. -. -. -. Mg/Al (-60 mesh). -. -. -. -. 12. 12. 11. ...
Effect of Alpha-lipoic acid amide on hexachlorobenzene porphyria. Biochem Mol Biol Int 1999;47:815-23. View abstract. ...
Hexachlorobenzene 1500-15000 μg/kg. Hexachlorobutadiene 1500-15000 μg/kg. Hexachloroethane 1500-15000 μg/kg. ...
... hexachlorobenzene [HCB]), and chlorine, all generated as byproducts during magnesium production at the U.S. Magnesium plant in ... hexachlorobenzene [HCB]); and chlorine existed for workers at U.S. Magnesium. Recommendations for controlling workplace ...
hexachlorobenzene. 213. hexachloroethane. 0. hydroquinone +. 978. iron(III) nitrilotriacetate. 76. lead chromate. 1. ...
Ambient aquatic life water quality criteria for hexachlorobenzene : draft.. 1988. 49. Ambient aquatic life water quality ...
Beyond Pesticides, November 5, 2018) As you know, the stakes in this midterm election are high. Many races are too close to call and will be decided by voter turnout. As we have read, our vote will make a difference!. The stakes are high. People and the environment are being poisoned. Pollinators are disappearing. Waterways are being contaminated. Biodiversity is threatened. Children -especially farmworker children-are suffering brain damage, and pesticide exposure is linked to the increase in ADHD and autism. Pesticide exposure is implicated in cancer, Parkinsons disease, reproductive dysfunction, diabetes, learning disabilities, and more.. We need people in elected positions - from local officials to national offices - who will listen to constituents who know the need for protection from pesticides and understand the urgent need to adopt of organic practices. Learn about your candidates and vote!. What more we can do. Take someone with you to the polls. Offer assistance to your neighbors who ...
  • We examined the relation between serum levels of the pesticides heptachlor epoxide (HCE), hexachlorobenzene (HCB), and β-hexachlorocyclohexane (β-HCCH) in pregnant women, and the occurrence of cryptorchidism in their sons. (eur.nl)
  • The International Agency for Research on Cancer (IARC) says that hexachlorobenzene is possibly carcinogenic to humans. (cdc.gov)
  • The EU has published a limit for hexachlorobenzene under the Persistent Organic Pollutants Regulation. (intertek.com)
  • 1-800-232-4636 concentrations of hexachlorobenzene. (cdc.gov)
  • Hexachlorobenzene is a fungicide that was used in the United States until 1984. (cdc.gov)
  • [ 4 ] During the period 1955-1959, approximately 4000 people in southeast Anatolia (Turkey) developed porphyria due to the ingestion of hexachlorobenzene (HCB), a fungicide that was added to wheat seedlings. (medscape.com)
  • Exposure to hexachlorobenzene occurs mainly from eating low levels in contaminated food. (cdc.gov)
  • The requesters asked NIOSH to assess employee exposures to chlorinated hydrocarbons (CHCs), including chlorinated dibenzo-p-dioxins (PCDDs), chlorinated dibenzofurans (PCDFs), and polychlorinated biphenyls (PCBs), certain pesticides (e.g., hexachlorobenzene [HCB]), and chlorine, all generated as byproducts during magnesium production at the U.S. Magnesium plant in Rowley, Utah. (cdc.gov)
  • Australians use the term 'intractable wastes' to describe their stockpile of discarded organochlorines such as PCBs, hexachlorobenzene, dioxin and pesticides. (newscientist.com)
  • Hexachlorobenzene, or perchlorobenzene, is an organochloride with the molecular formula C6Cl6. (wikipedia.org)
  • Dehalorespiration with hexachlorobenzene and pentachlorobenzene by Dehalococcoides sp. (ufz.de)
  • strain CBDB1 used hexachlorobenzene and pentachlorobenzene as electron acceptors in an energy-conserving process with hydrogen as electron donor. (ufz.de)
  • strain CBDB1 with hexachlorobenzene or pentachlorobenzene as electron acceptors failed if these compounds were provided as solutions in hexadecane. (ufz.de)
  • strain CBDB1 was able to grow with hexachlorobenzene or pentachlorobenzene when added in crystalline form directly to cultures. (ufz.de)
  • The final end-products of hexachlorobenzene and pentachlorobenzene dechlorination were 1,3,5-trichlorobenzene, 1,3- and 1,4-dichlorobenzene, which were formed in a ratio of about 3:2:5. (ufz.de)
  • To our knowledge, this is the first report describing reductive dechlorination of hexachlorobenzene and pentachlorobenzene via dehalorespiration by a pure bacterial culture. (ufz.de)
  • When heated to decomposition, hexachlorobenzene emits highly toxic fumes of hydrochloric acid, other chlorinated compounds (such as phosgene), carbon monoxide, and carbon dioxide. (wikipedia.org)
  • Hexachlorobenzene is a stable, white, crystalline chlorinated hydrocarbon. (wikipedia.org)
  • Hexachlorobenzene is a white crystalline solid that does not occur naturally in the environment. (cdc.gov)
  • Since then, Harvard researchers reported a link between persistent pollutants, like hexachlorobenzene, and diabetes in their Nurses' Health Study. (nutritionfacts.org)
  • In a U.S. supermarket survey, salmon and sardines were most heavily tainted with hexachlorobenzene, with salmon "the most contaminated food" of all-especially farmed salmon, perhaps "the greatest, source of dietary [pollutants]," averaging nearly ten times the PCB load of wild-caught salmon. (nutritionfacts.org)
  • Hexachlorobenzene may cause embryolethality and teratogenic effects. (wikipedia.org)
  • Hexachlorobenzene in tissues, body for general population is ingestion of food, hexachlorobenzene in air is poorly fluids, and feces can be used as including fish caught in contaminated absorbed through the lungs and that biomarker for hexachlorobenzene areas. (cdc.gov)
  • Animal carcinogenicity data for hexachlorobenzene show increased incidences of liver, kidney (renal tubular tumours) and thyroid cancers. (wikipedia.org)
  • Liver disease is the main adverse health effect caused by high levels of exposure to hexachlorobenzene. (cdc.gov)
  • Studies in animals suggest that eating food with hexachlorobenzene for a long time can cause cancer of the liver, kidney, and thyroid. (cdc.gov)
  • An MRL of 0.008 mg/kg/day has been hexachlorobenzene as reasonably combustion of municipal waste. (cdc.gov)
  • Hexachlorobenzene (HCB) is an organochloride. (beis.gov.uk)
  • Hexachlorobenzene has a half life in the soil of between 3 and 6 years. (wikipedia.org)
  • Hexachlorobenzene sticks strongly to soil and can be slowly degraded by microorganisms. (cdc.gov)
  • Half the hexachlorobenzene in soil will disappear in 3-6 years. (cdc.gov)
  • Alvarez L, Hernandez S, Martinez-de-Mena R, Kolliker-Frers R, Obregon M, Kleiman de Pisarev D (2005) The role of type I and type II 5′ deiodinases on hexachlorobenzene-induced alteration of the hormonal thyroid status. (springer.com)
  • Human and animal studies have demonstrated that hexachlorobenzene crosses the placenta to accumulate in foetal tissues and is transferred in breast milk. (wikipedia.org)
  • Much lower exposures can occur from drinking water and breathing air contaminated with hexachlorobenzene. (cdc.gov)
  • Hexachlorobenzene breaks down slowly in air. (cdc.gov)
  • Hexachlorobenzene has been found in at least 113 of the 1,699 National Priorities List sites identified by the Environmental Protection Agency (EPA). (cdc.gov)
  • Where is hexachlorobenzene found? (nutritionfacts.org)
  • In FLEHS II, geometric mean concentrations (with 95 % confidence interval (CI)) of 307 (277-341) and 36.5 ng L −1 (34.0-39.2) were found for p,p ′-dichlorophenyldichloroethylene ( p,p ′-DDE) and hexachlorobenzene (HCB). (springer.com)
  • There is no strong evidence that hexachlorobenzene causes cancer in people. (cdc.gov)
  • No acute-, intermediate- or chronic hexachlorobenzene causes cancer in is formed as a waste product during the duration inhalation MRLs were derived people. (cdc.gov)
  • Hexachlorobenzene is a white crystal ine the general population. (cdc.gov)
  • Infants and young children appeared to be especially sensitive to the effects of very high levels of hexachlorobenzene in the Turkish bread poisoning epidemic during the 1950s. (cdc.gov)
  • Half of the hexachlorobenzene detected in surface water will disappear in 3-6 years. (cdc.gov)
  • Because hexachlorobenzene accumulates in body fat (including breast tissue) where it can remain for long periods, long-term exposure can result in a build-up of hexachlorobenzene in the body. (cdc.gov)
  • This fact sheet answers the most frequently asked health questions (FAQs) about hexachlorobenzene. (cdc.gov)
  • How can hexachlorobenzene affect my health? (cdc.gov)
  • Hexachlorobenzene is highly bioaccumulated by animals that live in hexachlorobenzene-contaminated water. (cdc.gov)
  • Details for: Hexachlorobenzene. (who.int)
  • Hexachlorobenzene is very slow to breakdown in air and is subject to long-range transport in the atmosphere. (cdc.gov)