化合物详情
CAS55290-64-7
分子式C6H10O4S2
分子量210.271 g/mol
非危品
Physical Description | Dimethipin appears as colorless crystals with a mild odor. Used as a defoliant.
科学粮草官-词典编辑部,修订于:2026-07-06

Toxicity
ToxicityEPA Ecotoxicity
Pesticide Ecotoxicity Data from EPA: 30
Fate Summary
ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), dimethipin, which has a measured vapor pressure of 3.8X10-7 mm Hg at 25 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase dimethipin is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals and ozone(SRC); the half-lives for these reactions in air are estimated to be about 3.0 and 3.7 hours, respectively(3,SRC). Particulate-phase dimethipin may be physically removed from the air by wet and dry deposition(SRC).
Soil Adsorption / Mobility
A Koc of 3.3 was determined in clay (%organic matter 4.8, pH 5.9)(1,3). According to a recommended classification scheme(2), the measured Koc of dimethipin suggests it is expected to have very high mobility in soil(SRC).
Environmental Bioconcentration
An estimated BCF of 0.44 was calculated for dimethipin(SRC), using a measured log Kow of -0.17(1) and a recommended regression-derived equation(2). According to a classification scheme(3), this BCF suggests that bioconcentration in aquatic organisms is low(SRC).
Volatilization from Water / Soil
The Henry's Law constant for dimethipin is 1.7X10-8 atm-cu m/mole(1). This value indicates that dimethipin will be essentially nonvolatile from water surfaces(2,SRC). Volatilization from wet and dry soil surfaces is not expected based on dimethipin's measured Henry's Law constant(1) and vapor pressure of 3.8X10-7 mm Hg, respectively(2).
Environmental Abiotic Degradation
The rate constant for the vapor-phase reaction of dimethipin with photochemically-produced hydroxyl radicals has been estimated as 1.3X10-10 cu cm/molecule-sec at 25 °C(SRC) using a structure estimation method(1,SRC). This corresponds to an atmospheric half-life of about 3.0 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(1,SRC). The rate constant for the vapor phase reaction with ozone has been estimated as 7.4X10-17 cu cm/molecule-sec at 25 °C(1). This corresponds to an atmospheric half-life of about 3.7 hours at an average ambient ozone concentration of 7X10+11 molecules/cu cm(1,SRC). Stability of dimethipin to light is greater than or equal to 7 days at 25 °C(2). In aqueous solution, dimethipin is degraded(2); rate and method of degradation were not speci...
Artificial Pollution Sources
Dimethipin's production and use as a defoliant and seed desiccant(1,2) will result in its release to the environment(SRC).
Probable Routes of Human Exposure
Occupational exposure to dimethipin may occur through inhalation of dust particles and dermal contact with this defoliant/desiccant during or after its application or at workplaces where dimethipin is produced or used. (SRC)
Environmental Fate / Exposure Summary
Dimethipin will be released to the environment from its production and use as a defoliant and seed desiccant. If released to air, a measured vapor pressure of 3.8X10-7 mm Hg at 25 °C indicates that dimethipin will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase dimethipin will be degraded in the atmosphere by reaction with ozone and photochemically-produced hydroxyl radicals; the half-lives for these reactions have been estimated as 3.7 and 3.0 hours, respectively. Particulate-phase dimethipin may be physically removed from the atmosphere by wet and dry deposition. If released to soil, a measured Koc of 3.3 indicates that dimethipin will have very high mobility. Volatilization from wet and dry soil surfaces is not expected based on this compound's H...
Target Organs
Hepatic
Toxicity Data
LC50 (rat) > 1,200 mg/m3
Adverse Effects
Occupational hepatotoxin - Secondary hepatotoxins: the potential for toxic effect in the occupational setting is based on cases of poisoning by human ingestion or animal experimentation.
RAIS Toxicity Values
Oral Chronic Reference Dose Reference: OPP
Non-Human Toxicity Values
LD50 Rat oral 1,660 mg/kg /Harvade/
Non-Human Toxicity Excerpts
Extreme eye irritant, not a dermal irritant (rabbits). Weak sensitizer (guinea pigs).
1 or Cancer Risk Level 1E-06
Fraction of Contaminant Absorbed Dermally from Soil: 0.1
Evidence for Carcinogenicity
CLASSIFICATION: C; possible human carcinogen. BASIS FOR CLASSIFICATION: Classification is based on an elevated combined incidence of pulmonary adenomas/carcinomas in male, but not in female, CD-1 mice. A rat study is undergoing further evaluation. HUMAN CARCINOGENICITY DATA: None. ANIMAL CARCINOGENICITY DATA: Limited.
Hazard Quotient Level 3 or Cancer Risk Level 1E-04
Fraction of Contaminant Absorbed Dermally from Soil: 0.1





