| Product Name: | Carbofuran | | Synonyms: | 2,3-dihydro-2,2-dimethyl-7-benzofuranoln-methylc;2,3-dihydro-2,2-dimethyl-7-benzofuranomethylcarbamate;2,3-Dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate;2,3-Dihydro-2,2-dimethyl-7-benzofuranylmethylcarbamate;2,3-Dihydro-2,2-dimethylbenzofuranyl-7-N-methylcarbamate;7-Benzofurano, 2,3-dihydro-2,2-dimethyl, methylcarbamate;7-Benzofuranol, 2,3-dihydro-2,2-dimethyl-, methylcarbamate;7-Benzofuranol,2,3-dihydro-2,2-dimethyl-,methylcarbamate | | CAS: | 1563-66-2 | | MF: | C12H15NO3 | | MW: | 221.25 | | EINECS: | 216-353-0 | | Product Categories: | Insecticides;Pesticides;Pesticides&Metabolites;Amines;Aromatics;Inhibitors;Benzofurans;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks;AcaricidesAlphabetic;C;CA - CGPesticides;CarbamatesMethod Specific;Endocrine Disruptors (Draft);EPA | | Mol File: | 1563-66-2.mol |  |
| | Carbofuran Chemical Properties |
| Melting point | 150-153 °C(lit.) | | Boiling point | 200°C | | density | 1.18 | | vapor pressure | 2 x 10-5 mmHg at 33 °C (quoted, Verschueren, 1983) | | refractive index | 1.5200 (estimate) | | storage temp. | 0-6°C | | solubility | Methylene chloride (>200 g/L), 2-propanol (20–50 g/L) (Worthing and Hance, 1991) | | pka | 12.28±0.46(Predicted) | | form | Powder | | color | White, brown | | Water Solubility | Slightly soluble. 0.07 g/100 mL | | Merck | 13,1813 | | BRN | 1428746 | | Henry's Law Constant | 3.88 (x 10-8 atm?m3/mol)at 30 °C (approximate - calculated from water solubility and vapor pressure) | | Exposure limits | OSHA PEL: TWA 0.1 mg/m3; ACGIH TLV: TWA 0.1 mg/m3. | | LogP | 2.320 | | CAS DataBase Reference | 1563-66-2(CAS DataBase Reference) | | NIST Chemistry Reference | Carbofurane(1563-66-2) | | EPA Substance Registry System | Carbofuran (1563-66-2) |
| | Carbofuran Usage And Synthesis |
| Description | Carbofuran is a broad-spectrum carbamate insecticide and nematocide. It is an odourless, white crystalline solid. On heating, its breakdown can release toxic fumes and irritating or poisonous gases. It is sparingly soluble in water but very soluble in acetone, acetonitrile, benzene, and cyclohexone. The liquid formulations of carbofuran are classified as restricted use pesticides (RUP) because of their acute oral and inhalation toxicity to humans. Granular formulations are also classified as RUP.
In fact, carbofuran was first registered in the United States in 1969 and classified as RUP. Exposure to heat breaks down carbofuran, with the release of toxic fumes. Carbofuran is used for the control of soil-dwelling and foliar-feeding insects. It is also used for the control of aphids, thrips, and nematodes that attack vegetable, ornamental plants, crops of sunflower, potatoes, peanuts, soybeans, sugar cane, cotton, rice, and variety of other crops.
| | Chemical Properties | Carbofuran is a white crystal-like solid. It is slightly soluble in water, is stable under neutral and acidic conditions, but decomposes under alkaline conditions (U.S. EPA,2006a).
| | Uses | Carbofuran is a broad-spectrum N-methyl carbamate sold under the trade name Furadan. First registered in 1969, it is used to control a variety of insect pests on field, fruit, and vegetable crops. Carbofuran is not used in residential settings or food-handling establishments. The chemical is a restricted use pesticide with nearly 1 million pounds of active ingredient almost exclusively used on corn, alfalfa, and potatoes (U.S. EPA, 2006a).
| | Environmental Fate | Carbofuran is highly mobile in soils and can leach into groundwater and enters surface water as runoff. The chemical breaks down though hydrolysis, photodegradation, and moderate bacterial degradation at rates that depend on environmental conditions. Hydrolysis is faster in water with a pH 7, with a half-life ranging from a few hours to 28 days. Carbofuran is stable to hydrolysis in acidic water. Photodegradation is fast in a thin water layer, with a halflife of 6 days. In the top few millimeters of a sandy loam soil, carbofuran degrades in 78 days. Bioconcentration is not expected to occur (U.S. EPA, 2006a). | | References | [1] S. Bretaud, J. -P. Toutant and P. Sagilo, Effects of Carbofuran, Diuron, and Nicosulfuron on Acetylcholinesterase Activity in Goldfish (Carassius auratus), Ecotoxicology and Environmental Safety, 2000, vol. 47, 117-124
[2] Dennis M. Trotter, Robert A. Kent and Michael P. Wong, Aquatic fate and effect of Carbofuran, Critical Reviews in Environmental Control, 1991, vol. 21, 137-176
| | Description | Carbofuran is another systemic insecticidal/nematicidal
carbamate available in granular and liquid formulations.
Because use of carbofuran granules was associated
with bird kills, the U.S. Environmental Protection
Agency (EPA) prohibited the use of carbofuran granules
in 1994. | | Chemical Properties | Carbofuran is a broad-spectrum carbamate insecticide and nematicide. It is an odorless,
white crystalline solid. On heating, it breaks down and can release toxic fumes, and irritating or poisonous gases. It is sparingly soluble in water, but very soluble in acetone,
acetonitrile, benzene, and cyclohexone. The liquid formulations of carbofuran are classifi ed as RUPs because of their acute oral and inhalation toxicity to humans. Granular
formulations are also classifi ed as an RUP. In fact, carbofuran was fi rst registered in the
United States in 1969 and classifi ed as an RUP. Exposure to heat breaks down carbofuran,
with the release of toxic fumes. Carbofuran is used for the control of soil-dwelling and
foliar-feeding insects. It is also used for the control of aphids, thrips, and nematodes that
attack vegetables, ornamental plants, crops of sunfl ower, potatoes, peanuts, soybeans,
sugar cane, cotton, rice, and a variety of other crops | | Uses | Carbofuran is used to control soil-dwelling insect pests and nematodes in a wide range of crops. | | Uses | Broad-spectrum, systemic insecticide, nematocide and acaricide applied in soil to
control soil insects and nematodes or on foliage to control insects and mites. | | Uses | Cholinesterase inhibitor. Use as systemic insecticide, acaricide, nematocide. | | Definition | ChEBI: Carbofuran is a carbamate ester and a member of 1-benzofurans. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, a carbamate insecticide, an EC 3.1.1.8 (cholinesterase) inhibitor, an acaricide, an agrochemical, an avicide and a nematicide. | | General Description | Carbofuran is an odorless white crystalline solid. Contact with skin may burn skin and eyes. When exposed to heat or flames Carbofuran may emit toxic oxides of nitrogen. Carbofuran is toxic by inhalation, skin contact, and/ or ingestion. Carbofuran is used as a pesticide. | | Air & Water Reactions | Slightly soluble in water. | | Reactivity Profile | Carbofuran is a carbamate ester. Carbamates are chemically similar to, but more reactive than amides. Like amides they form polymers such as polyurethane resins. Carbamates are incompatible with strong acids and bases, and especially incompatible with strong reducing agents such as hydrides. Flammable gaseous hydrogen is produced by the combination of active metals or nitrides with carbamates. Strongly oxidizing acids, peroxides, and hydroperoxides are incompatible with carbamates. Carbofuran is unstable in an alkaline media. . | | Health Hazard | The acute oral LD50 of carbofuran to male and female rats is about 8 mg/kg, while the acute dermal LD50 for rats is more than 3000 mg/kg. Carbofuran is mildly irritating to the eyes and skin of rabbits. The acute inhalation toxicity (LC50, 4 h) is 0.075 mg/L for rats. As with other carbamate compounds, carbofuran’s cholinesterase-inhibiting effect is short term and reversible. The symptoms of carbofuran poisoning include, but are not limited to, nausea, vomiting, abdominal cramps, sweating, diarrhea, excessive salivation, weakness, imbalance, blurring of vision, breathing diffi culty, increased blood pressure, and incontinence. Death may result at high doses from respiratory system failure associated with carbofuran exposure. Complete recovery from an acute poisoning by carbofuran, with no long-term health effects, is possible if exposure ceases and the victim has time to regain his or her normal level of cholinesterase and to recover from symptoms. Reports have indicated that risks from exposure to carbofuran are especially high among occupational workers and general public suffering with asthma, diabetes, cardiovascular disease, gastrointestinal or urogenital tracts disturbances. The available studies indicate carbofuran is unlikely to cause reproductive effects in humans at expected exposure levels. Studies indicate carbofuran is not teratogenic. No signifi cant teratogenic effects have been found in the offspring of rats given carbofuran (3 mg/kg/day) on days 5 to 19 of gestation. | | Fire Hazard | May release nitrogen oxides. Containers may explode in heat of fire. Avoid alkalies. Stable under neutral or acid conditions. | | Agricultural Uses | Insecticide, Acaricide, Nematicide: Carbofuran is a broad-spectrum carbamate pesticide that kills insects, mites, and nematodes on contact or after ingestion. It is used against soil and foliar pests of field, fruit, vegetable, and forest crops. Carbofuran, granule form, is banned in the U.S. A U.S. EPA restricted Use Pesticide (RUP). Not approved for use in EU countries. There are 40 global suppliers.. According to the Ecological Incident Investigation System, carbofuran has been responsible for more avian deaths than any other pesticide. | | Trade name | A13-27164®; AU'ULTRAMICIN®; BAY 704143®; BAY 78537®; BRIFUR®; CARBODAN®;
CARBOSIP 5G®; CRISFURAN®; CURETERR®; CHINUFUR®; D 1221®; DIAFURAN®; FMC 10242®; FURACARB®; FURADAN®; FURAN®; FURODAN®; KENFURAN®; KENOFURAN®; NEX®; NIA10242; NIAGARA 10242; NIAGARA NIA-10242; PILLARFURAN®; RAMPART®; YALTOX® | | Contact allergens | It is a pesticide with insecticide properties, of the carbamate
group. It was implicated as a sensitizer in two farmers | | Safety Profile | to decomposition it emits toxic fumes of | | Potential Exposure | A potential danger to those involved
in the manufacture, formulation, and application of this
insecticide, acaricide, and nematocide. | | 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.Effects may be delayed; keep victim under observation. | | Environmental Fate | Carbofuran is soluble in water and is moderately persistent in soil. Its half-life is 30–120 days. It enters surface water as a result of runoff from treated fields and enters groundwater by leaching of treated crops. If released to soil, degradation occurs by chemical hydrolysis and biodegradation. The persistence of carbofuran in the soil increases as the clay and organic matter content of the soil increase, and as the pH and moisture content of soil decrease. Chemical hydrolysis occurs more rapidly in alkaline soil as compared to neutral or acidic soils. Carbofuran is likely to leach to groundwater in soils with low organic content. Volatilization from soil is not expected to be significant, although some evaporation from plants may occur. If released to water, carbofuran degrades by hydrolysis under alkaline conditions and by biodegradation. Aquatic volatilization, adsorption, and bioconcentration are not expected to be important. | | Metabolic pathway | The fate of carbofuran has been investigated in soils, plants, mammals,
birds, fish and insects. Metabolic pathways include hydrolysis, oxidation
(ring and N-methyl hydroxylation) and conjugation. The metabolism of
carbofuran has been extensively reviewed by Schlagbauer and Schlagbauer
(1972) and Kuhr and Dorough (1976). Metabolism in economic
animals was reviewed by Akhtar (1985). Consequently the many primary
publications are not usually cited. | | Metabolism | Carbofuran (1) is degraded by hydrolysis and oxidation
in soil before ultimate mineralization . The
rate of hydrolysis in soils is slightly higher under flooded
than under nonflooded conditions. Products depend on
the soil type and the prevalence of aerobic or anaerobic
conditions, and it was also reported that carbofuran
did not degrade under anaerobic conditions. The products,
3-hydroxycarbofuran (2) and 3-ketocarbofuran (3), have
been isolated from soil extracts after incubation with carbofuran.
The phenol (7) was identified as a major product
in several studies. The products are further degraded and
bound to soil organic matter. Enhanced degradation may
follow repeated applications of carbofuran to soils, and
bacterial cultures capable of rapidly degrading carbofuran
have been obtained from treated soils. | | storage | Carbofuran should be stored in a cool, dry, well-ventilated place, in their original containers only. It should not be kept stored or used near heat, open flame, or hot surfaces | | Shipping | UN2757 Carbamate pesticides, solid, toxic,
Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN
2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1;
Labels: 6.1-Poisonous materials, Technical Name RequiredUN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1;
Labels: 6.1-Poisonous materials, Technical Name Required | | Degradation | Carbofuran (1) is very stable in weakly acidic media and has a DT50 of
<1 year at pH 4 (22°C). It is stable in neutral media but unstable in
basic conditions (PM). Carbofuran was hydrolysed to the phenol (5) with
a half-life of 67 minutes at 37.5 °C at pH 9.5. 3-Ketocarbofuran (3)
and N-hydroxymethylcarbofuran (4) (Scheme 2) were hydrolysed faster
than carbofuran in alkaline solution (Metcalf et al., 1968). Unlabelled
carbofuran was dissolved in water and irradiated by sunlight in India
for 30 days. Samples were extracted and analysed by GC and TLC.
Products were 3-ketocarbofuran (3) and the 4-hydroxycarbofuran phenol
(8). (Raha and Das, 1990). Solid carbofuran was applied to glass plates
and irradiated with fluorescent light or sunlight. 3-Hydroxycarbofuran
(2) was detected after 2 days; 3-ketocarbofuran (3) was not detected
(Metcalf et al., 1968). These pathways are illustrated in Scheme 1. | | Toxicity evaluation | Carbofuran undergoes hydrolytic and oxidative processes
in mammals. In rats, about 72% of the administered
dose was eliminated in the urine within 24 hours
as conjugated metabolites, mainly as conjugates of the 3-
ketocarbofuran phenol (5). The products of metabolism in
plants are 3-hydroxycarbofuran (4) and 3-ketocarbofuran
phenol (5). | | Incompatibilities | Alkaline substances, acid, strong oxidizers, such as perchlorates, peroxides, chlorates, nitrates,
permanganates. | | Waste Disposal | Alkaline hydrolysis is the
recommended mode of disposal. In accordance with
40CFR165, follow recommendations for the disposal of
pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting
your local or federal environmental control agency, or by
contacting your regional EPA office. | | Precautions | During use/handling of carbofuran, workers should wear coveralls or a long-sleeved
uniform, head covering, and chemical protective gloves made of materials such as rubber, neoprene, or nitrile. Occupational workers should know that areas treated with carbofuran are hazardous. The runoff of carbofuran material and the fi re control releases
irritating or poisonous gases. It is advisable that workers should enter storehouses or
carbofuran-treated close spaces with caution |
| | Carbofuran Preparation Products And Raw materials |
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