United States Office of Pestidda and Toxic Substances Environmental Protection Office of Pentode Programs (TS-766C) Agency Washington, DC 20460 &EBV Pesticide Fact Sheet Name of Chemical: Reason for Issuance: New Chemical Registration Date ISSUed: January 16, 1986 Fact Sheet Number: DESCRIPTION OF CHEMICAL Generic Name : 2-methyl-2-(methylsulf onyl) propana 1-0- (methyl ami no carbonyl oximel) Common Name: Aidoxycarb Trade Name: Standak Other Names: Sulfocarb, Aldicarb sulfone EPA Shaughnessy Code: 110801 Chemical Abstracts Service (CAS) Number: 1646-88-4 Year of Initial Registration: 1986 Pesticide Type: Insecticide/Nematicide Chemical Family: Carbamate U.S. Producer: Union Carbide Agricultural Products Co., Inc. No other producer at this time USE PATTERNS AND FORMULATIONS Application Sites; Containerized honey locust trees (Commercial Use Only) to control honey locust gall midge Type of Formulations; Insecticide/fertilizer spike; registered to International Spike, Inc. Method of Application; Spike is inserted into soil in container Application Rate; One or more spikes of 1% active ingredient per container, depending on size of container or plant. Usual Carriers; Formulation is a pressed mixture of aldoxycarb and fertilizer chemicals. ------- 2 3. SCIENCE FINDINGS Summary Science Statement Technical aidoxycarb has high mammalian acute toxicity. It has not been shown to cause oncogenic, mutagenic, teratogenic, delayed rieurotoxin or reproduction effects. Aldoxycarb is a known degradate/metabolite of aldicarb produced by the oxidation of the thio—moiety. Sufficient data are available to characterize aldoxycarb from an environmental fate and ecological standpoint. Aldoxycarb is extremely toxic to wildlife. Use precautions are being imposed to reduce potential hazards. Although aldoxycarb has the potential to contaminate groundwater under certain environmental conditions, the proposed containerized plant use will preclude any measurable contamination. A tolerance assessment is not needed because the registered use pattern is for an ornamental plant. There are no data gaps. Chemical Characteristics of Technical Aldoxycarb Physical State Crystalline powder at 20°C Color: White Odor: Slightly sulfurous Melting Point: 140—142° C Vapor Pressure: 9 x l05 mm Hg at 25° C Density: 1.35 g/cm 3 at 200 C ph: 3—6 Toxicology Characteristics of Technical Aldoxycarb Acute oral: 21.4 mg/kg, Toxicity Category I Acute dermal: 1000 mg/kg, Toxicity Category II Primary Dermal Irritation: No irritation, Toxicity Category III Primary Eye Irritation: No irritation, Toxicity Category IV Acute Inhalation: 0.209 mg/i, Toxicity Category II. ------- 3 Neurotoxicity: Not an acute delayed neurotoxic agent at doses up to 250 mg/kg (highest dose tested (HDT)). Oncogenicity: Two studies, rat and mouse. Both are acceptable and are negative for oncogenic effects up to 9.6 mg/kg/day (HDT). Teratogenicity: Two teratology studies, rat and rabbit have been evaluated to deter-mine the teratogenic potential of aldoxycarb. Both studies were negative for teratogenic effects at levels up to 9.6 mg/kg (HDT). Reproduction/3—generatiofl: No effects on reproduction at levels up to 9.6 mg/kg (HDT). Metabolism: The metabolism of aldoxycarb is adequately under- stood. It is metabolized by hydrolysis of the carbamate ester to form the oxime. Other reactions of the oxime occur. Mutagenicity: Adequate studies are available to demonstrate aldoxycarb is not a mutagen. Physiological and Biochemical Behavioral Characteristics Mechanism of pesticidal Action: A systemic insecticide/nemati— cide which causes reversible carbamylation of the acetocholine- sterase enzyme of tissues, allowing accumulation of acetyl— choline at cholinergic neuroeffector junctions (muscarinic effects) and at skeletal muscle myoneural junctions and in autonomic ganglia (nicotinic effects). The central nervous system is also impaired. Symptoms of poisoning include: headache, dizziness, weakness, ataxia, pinpoint pupils, blurred or dark vision, muscle twitching, nausea, vomiting, diarrhea, convulsions and death. The onset of these symptoms is rapid and their severity depends on the dose. The immediate cause of death is usually respiratory failure. Metabolism and persistence in Plants and Animals : Acceptable studies have been submitted which show aldoxycarb is metabolized in plants and animals by hydrolysis of the carbamate ester- to form the oxime. Further reactions of the oxime yield aldoxycarb aldehyde, aldoxycarb alcohol, aldoxycarb acid and aldoxycarb nitrile. The oxime and alcohol metabolites are easily conjugatd to form water soluble glycosides, sulfates, and other compounds. ------- 4 Environmental_Characteristics In soil and water, aldoxycarb is very stable under acidic conditions, stable at neutral conditions and very unstable to hydrolysis at alkaline conditions. It is rapidly hydrolyzed to sulfocarb oxime which in turn rapidly degrades to methane sultoriic acid and 2—hydroxy isobutryraldehyde oxime. Aldoxycarb is rapidly degraded to a variety of materials under both aerobic and anerobic conditions. In certain soils, such as those with a sandy loam texture, it has a half—life of 2—4 weeks. Aldoxycarb is mobile in certain soil types and does have the potential to contaminate groundwater under certain situations. Soil types of high sand content and organic matter will promote leaching of parent and degradation products, which are of lower toxicity than that of the parent compound. However, it is believed the containerized ornamental plant use will not result in groundwater contamination because of the fact that application is made to soils in containers. Ecological Effects of Technical Aldoxycarb Avian oral: Mallard duck — 33.5 mg/kg Aviar. dietary: Waterfowl species (Mallard duck) — >10,000 ppm Upland game species (Bobwhite quail) — 5,706 ppm Freshwater fish: Coldwater species (rainbow trout) — 42.0 ppm Warmwater species (bluegill sunfish) — 53.0 ppm Acute Freshwater Invertebrates: Daphriia — 0.176 ppb Precautionary language would be required for outdoor terrestrial use for hazards to wildlife. 4. SUMMARY OF REGULATORY POSITION AND RATIONALE The Agency has determined to register aldoxycarb for container- ized ornamental plants because, adequate studies are available to assess the toxicological and environmental characteristics of aldoxycarb and its potential effects to humans from this use. The Agency concludes from this studies that this use pattern will not pose any unreasonable adverse effects to humans or the environment. None of the criteria for unreasonable adverse effects listed in section 162.11(a) of Title 40 of the U.S. Code of Federal Regulations have been met or exceeded for this use. 5. SUMMARY OF MAJOR DATA GAPS There are no data gaps. ------- 5 6. CONTACT PERSON AT EPA Jay S. Ellenberger Product Manager (12) Insecticide—Rodenticide Branch Registration Division (TS—767C) Office of Pesticide Programs, Environmental Protection Agency, 401 M St., S.W. Washington, D.C. 20460. Office location and telephone number: Rm. 202, Crystal Mall Bldg. 2 1921 Jefferson Davis Highway, Arlington, VA 22202, (703) 557—2386. DISCLAIMER: The information presented in this Chemical Information Fact Sheet is for informational purposes only and may not be use to fulfill data requirements for pesticide registration and reregistration. ------- |