116-06-3 Usage
Description
Aldicarb is a carbamate pesticide that reversibly inhibits acetylcholinesterase. It is the active ingredient in mixtures used to control insect, mite, and nematode pests in agriculture. Aldicarb has a high acute mammalian toxicity (LD50 = 0.3-0.5 mg/kg) following oral or parenteral administration. Aside from its use as a pesticide, aldicarb has applications as an acetylcholinesterase inhibitor for research purposes.
Chemical Properties
Aldicarb is a noncombustible, white crystalline solid with a slight sulfurous odor.It is not compatible with alkaline materials and is non-corrosive to metals and plastics. It is sparingly soluble in water, but soluble in acetone, xylene, ethyl ether, toluene, and other organic solvents. Aldicarb has been classifi ed as an RUP and hence should only be used by trained and certifi ed workers. Aldicarb is used to control mites, nematodes, and aphids and is applied directly to the soil. It is used widely on cotton, peanut, and soybean crops. In the mid-1980s, there were highly publicized incidents in which misapplication of aldicarb contaminated cucumbers and watermelons and led to adverse effects in people. Aldicarb is metabolized in the liver of mammals fi rst into aldicarb sulfoxide and later into aldicarb sulfone.
Uses
Different sources of media describe the Uses of 116-06-3 differently. You can refer to the following data:
1. Aldicarb is a broad-spectrum, systemic carbamate insecticide used to control nema-todes in soil and a variety of insects and mites on citrus crops, dry beans, grain, sorghum, ornamentals, pecans, peanuts, potatoes, seed alfalfa, soybeans, sugar beets, sugarcane, sweet potatoes, and tobacco.
2. Aldicarb is a soil applied systemic oxime carbamate insecticide
with both contact and oral activities. It controls a broad spectrum of chewing
and sucking insects, mites and nematodes on a wide variety of field,
fruit and vegetables crops such as cotton, citrus, potatoes, sugar beet and
peanuts.
Preparation
Aldicarb is prepared by treating isobutene with nitrosyl chloride, treating the resulting dimeric adduct with sodium methyl sulfide, and converting the resulting oxime to the carbamate with methyl isocyanate. Warning: the dimeric isobutene nitrosochloride is unstable and decomposes explosively at 94 °C. The oxime and end product also decompose vigorously above 140 and 160 °C, respectively.
Definition
ChEBI: The oxime carbamate resulting from the addition of 2-methyl-2-(methylsulfanyl)propanaldoxime to methyl isocyanate. A member of the class of oxime carbamate insecticides, aldicarb is a mixture of E and Z isomers; it is not
nown which isomer is more active.
General Description
White crystals with a slightly sulfurous odor. Commercial formulations are granular Used as an insecticide, acaricide, and nematocide.
Air & Water Reactions
Slightly water soluble.
Reactivity Profile
ALDICARB is a carbamate ester. ALDICARB decomposes at temperatures greater than 212° F. ALDICARB is incompatible with highly alkaline substances. ALDICARB is rapidly converted by oxidizing agents.
Health Hazard
Aldicarb is the most potent of the commercially available carbamate pesticides and is
an unusual source of acute human poisoning. Aldicarb has severe systemic toxicity to
animals and humans. Aldicarb is a cholinesterase inhibitor that prevents the breakdown
of acetylcholine in the synapse. In the case of severe poisoning, the victim dies of
respiratory failure. The primary route of human exposure to aldicarb is consumption
of contaminated food and water from contaminated wells. Occupational exposure to
high levels of aldicarb is due to product handling, and most cases of aldicarb poisoning
occur from loading and application of the pesticide. Aldicarb is extremely toxic both
through the oral and dermal route. Absorption from the gut is rapid and almost complete.
When administered in oil or other organic solvents, aldicarb is absorbed rapidly
through the skin. Its skin toxicity is roughly 1000 times that of other carbamates. In
humans, the onset of symptoms is rapid (15 min to 3 h). Symptoms disappear in 4–12 h.The acute oral LD50 of aldicarb in rats, mice, guinea pigs, and rabbits ranges from 0.5 to
1.5 mg/kg when administered in a liquid or oil form. The toxicities of the dry granules
are distinctly lower (LD50 7.0 mg/kg), though still highly toxic. Aldicarb is a cholinesterase
inhibitor and therefore can result in a variety of symptoms including weakness,
blurred vision, headache, nausea, tearing, sweating, and tremors. At very high concentrations,
aldicarb causes paralysis, respiratory system damage, eventually leading to
the death of the exposed worker.
There is very little evidence of chronic effects from aldicarb exposure. Rats and dogs
fed low doses of aldicarb for 2 years showed no signifi cant adverse effects. One epidemiological
study suggested a possible link between low-level exposure and immunological
abnormalities. The result of this study, however, has been widely disputed. Aldicarb
administered to pregnant rats at very low levels (0.001–0.1 mg/kg/day) depressed AChE
activity more in the fetuses than in the mother. The aldicarb was also retained in the
mother’s body for longer periods than in non-pregnant rats. A three-generation study at
doses of 0.05 and 0.10 mg/kg/day produced no signifi cant toxic effects, and in another
study, a dose of 0.70 mg/kg/day produced no adverse effects. Thus, reproductive effects in
humans are unlikely at expected exposure levels.
Fire Hazard
When heated to decomposition, ALDICARB emits very toxic fumes of nitrogen oxides and sulfur oxides. Incompatible with highly alkaline substances. Unstable in alkali; poor stability at 122F.
Agricultural Uses
Insecticide, Nematicide, Acaricide: A U.S. EPA restricted Use Pesticide (RUP). Not approved for use in EU countries.
Trade name
TEMIC?; TEMIK?; OMS 771?;
TERNIC?; TEMIK 10 G?
Safety Profile
Deadly poison by
ingestion, skin contact, subcutaneous, and
possibly other routes. Human mutation data
reported. Questionable carcinogen. A
powerful systemic poison. In 1985 over 150
people in California exhibited toxic effects
from eating watermelons contaminated with
aldicarb. When heated to decomposition it
emits very toxic fumes of NOx and SOx
Potential Exposure
Exposure to aldicarb and aldicarb sulfoxide and sulfone will occur mainly through the ingestion and contaminated drinking water derived from contaminated ground water as well as contaminated food.
Environmental Fate
Aldicarb and its degradation products are generally very soluble in water and mobile in soil. Adsorption in soil is primarily to organic matter, so leaching is most exten- sive in sandy or sandy loam soils. Aldicarb is very persistent in groundwater, typi- cally degrading to nontoxic products with a half-life between a few weeks to as long as several years. The primary mode of degradation is chemical hydrolysis, with some microbial decay in shallow groundwater. In soils, the primary mode of degradation is oxidation by soil microorganisms and hydrolysis, depending on soil conditions.
Metabolic pathway
In an aqueous buffer solution in the pH range
2.91 ? 5.51, the Cu(II) ion promotes the decomposition
of aldicarb, forming the degradation products 2-methyl-
2-(methylthio)propionitrile and 2-methyl-2-
(methylthio)propanal.
storage
Aldicarb should be kept stored in a dry, cool area, out of reach of children and animals,
and away from food, feedstuffs, fertilizers, and seed.
Shipping
UN2757 Carbamate pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials
Degradation
Aldicarb (1) is susceptible to alkaline hydrolysis. Under basic conditions
(pH 9), aldicarb hydrolysed slowly with a DT50 of approximately 75 days.
Cleavage of the oxime carbamate linkage to yield aldicarb oxime (2) and
the aldicarb nitrile (3) was the primary degradation pathway. Aldicarb
was stable to hydrolysis under acidic (pH 5) and neutral (pH 7) conditions
(Andrawes, 1976a). Aldicarb also degraded in water under photolytic
conditions (xenon lamp) with a DT50 of approximately 4 days (Das, 1990a).
The major photolytic degradation products were aldicarb oxime (2) and
aldicarb nitrile (3) (Andrawes, 1976b).
Incompatibilities
Strong alkalis
Waste Disposal
Do not discharge into drains or sewers. Dispose of waste material as hazardous waste using a licensed disposal contractor to an approved landfill. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Incineration with effluent gas scrubbing is recommended. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposedproperly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.
Check Digit Verification of cas no
The CAS Registry Mumber 116-06-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116-06:
(5*1)+(4*1)+(3*6)+(2*0)+(1*6)=33
33 % 10 = 3
So 116-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O2S/c1-7(2,12-4)5-9-11-6(10)8-3/h5H,1-4H3,(H,8,10)
116-06-3Relevant articles and documents
A convenient method for synthesis of 14C-carbonyl methylcarbamates
Hurst,Dorough
, p. 11 - 16,12,13,14,15 (1978)
-
Alkyl 1-Chloroalkyl Carbonates: Reagents for the Synthesis of Carbamates and Protection of Amino Groups
Barcelo, Gerard,Senet, Jean-Pierre,Sennyey, Gerard,Bensoam, Jean,Loffet, Albert
, p. 627 - 632 (2007/10/02)
The synthesis of 1-chloroalkyl carbonates and their reaction with various type of amines are described.This reaction is useful for the synthesis of carbamate pesticides and for the protection of various amino groups, including amino acids.
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