- Melting point:
- 1.1838 (rough estimate)
- vapor pressure
- 1.5 x 10-5 Pa (20 °C)
- refractive index
- 1.4790 (estimate)
- storage temp.
- Boiling point:
- 310.7±42.0 °C(Predicted)
- Crystalline Solid
- Water Solubility
- CAS DataBase Reference
- 2032-65-7(CAS DataBase Reference)
- NIST Chemistry Reference
- 4-Methylthio-3,5-xylyl methylcarbamate(2032-65-7)
- EPA Substance Registry System
- Methiocarb (2032-65-7)
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Mercaptodimethur Chemical Properties,Usage,Production
Methiocarb is a colorless crystalline powder.
Insecticide, acaricide and bird repellent.
Insecticide; molluscicide; bird repellent.
Methiocarb is an insecticide, molluscicide and acaricide with contact and stomach action. It is used to control slugs, snails and insects in a wide range of crops. Soil insects are controlled. Methiocarb is also used as a seed-treatment and bird repellent.
ChEBI: A carbamate ester obtained by the formal condensation of the phenolic group of 3,5-dimethyl-4-(methylsulfanyl)phenol with the carboxy group of methylcarbamic acid.
White crystalline powder with a mild odor. Used as an insecticide and immobilizing agent for birds, acaricide and molluscicide.
Mercaptodimethur 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.
As a carbamate insecticide, Mercaptodimethur is a reversible cholinesterase inhibitor and acts on the nervous system. It is classified as very toxic, and the probable oral lethal dose for humans is 50-500 mg/kg or between 1 teaspoon and 1 ounce for a 150 lb. adult.
Highly toxic cholinesterase inhibitor; exhibitsacute, delayed and chronic effects; routesof entry — ingestion, skin absorption andinhalation of vapors; reversible action ofshort duration; toxic symptoms includesalivation, lacrimation, bradycardia, blurredvision, labored breathing, headache, muscle twitching, tremor, and slight paralysis;gastrointestinal effects include nausea, vomiting, abdominal pain, and diarrhea; severepoisoning may lead to convulsions and coma;oral intake of probably 5–10 g may be fatalto adult humans.
LD50 oral (rat): 15–20 mg/kg
LD50 oral (guinea pig): 40 mg/kg
LD50 skin (rat): 350 mg/kg
LD50 skin (wild bird): 100 mg/kg.
When heated to decomposition, Mercaptodimethur emits very toxic fumes of nitrogen and sulfur oxides.
Acaricide, Molluscicide, Insecticide: Used to control slugs and snails, soil insects and spider mites in pome fruit, stone fruit, hops, strawberries, potatoes, beets, maize, vegetables and ornamentals. Also used as seed treatment to control fruit flies on maize and bird repellant on berries and cherries. Methiocarb producers deleted all food uses from their product labels between 1989-92. It is A U.S. EPA restricted Use Pesticide (RUP) except for residential application.
AI3-25726®; ALCO SLUB”M[C]; B 37344®; BAY 5024®; BAY 9026®; BAY 37344®; BAYER 37344®; DCR 736®; DRAZA®; DRAZA G MICROPELLETS®; H 321®; MESUROL®; METHIOCARBE®; OMS- 93®; PBI SLUG GARD®; PROVADA®; SD 9228®; SLUG-GETA®[C]
Methiocarb is an insecticide or molluscicide with a cholinesterase inhibiting effect. A case of contact dermatitis was reported in a carnation grower.
Poison by ingestion, skin contact, and intraperitoneal routes. Used as an insecticide, molluscicide, and bird repellent. When heated to decomposition it emits very toxic fumes of NOx and SOx. See also ESTERS and CARBAMATES.
A potential danger to those involved in the manufacture, formulation, and application of this nonsystemic acaricide and insecticide.
Soil. Methiocarb was oxidized, probably by singlet oxygen, to the corresponding
sulfoxide and trace amounts (<5% yield) of sulfone when sorbed on soil and exposed to
sunlight. The photosensitized oxidation was faster in soils containing the lowest organic
carbon content (Gohre and Miller, 1986).
Plant. On and/or in bean plants, the methylthio group is rapidly oxidized to the sulfoxide and sulfone (Abdel-Wahab et al., 1966) followed by hydrolysis yielding the corresponding thiophenol, methylsulfoxide phenol and methylsulphonyl phenol (Har
Photolytic. When methiocarb in ethanol was irradiated by UV light, only a few unidentified cholinesterase inhibitors were formed (Crosby et al., 1965).
Chemical/Physical. Emits toxic fumes of nitrogen and sulfur oxides when heated to decomposition (Sax and Lewis, 1987).
Methiocarb is oxidised to a sulfoxide and a sulfone in biological media. The resulting two carbamate esters and the parent compound are hydrolysed in soils and plants to the corresponding phenols. Hydroxylation of the N-methyl group on the carbamate function occurs in mammalian preparations in vitro.
UN2757 Carbamate pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required
Methiocarb is unstable in alkaline solution. Its DT50 values at pH 4,7 and 9
(22 °C) are >1 year, 35 days and 6 hours, respectively. Photodegradation
(DT50 6-16 days) contributes to the loss of methiocarb from the environment
River water containing methiocarb was stored in sunlight or artificial light. Samples were taken and analysed by TLC. Methiocarb was rapidly hydrolysed (half-life 3 days) to the phenol (2) which itself degraded (Eichelberger and Lichtenberg, 1971).
In accordance with 40CFR 165 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. Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform to EPA regulations governing storage, transportation, treatment, and waste disposal. Remove material with contaminated soil and place in impervious containers. May be incinerated in a pesticide incinerator at the specified temperature/dwell-time combination. Any liquids, sludges, or solid residues generated should be disposed of in accordance with all applicable federal, state, and local pollution control requirements. If appropriate incineration facilities are not available, material may be buried in a chemical waste landfill. May be amenable to biological treatment at a municipal sewage treatment plant. (Sax/DPIMR).
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2032-65-7, MercaptodimethurRelated Search:
- 3,5-Dimethyl-4-(methylsulfanyl)phenyl methylcarbamate
- 3,5-Dimethyl-4-methylthiophenyl N-methylcarbamate
- 3,5-Xylenol, 4-(methylthio)-, methylcarbamate
- 4-(Methylthio)-3,5-dimethylphenyl methylcarbamate
- 4-Methylmercapto-3,5-dimethylphenyl N-methylcarbamate
- 4-Methylmercapto-3,5-xylyl methylcarbamate
- 3,5-Dimethyl-4-(methylthio)phenol methylcarbamate
- 3,5-DIMETHYL-4-[METHYLTHIO]PHENYL METHYLCARBAMATE
- Methylcarbamic acid 4-(methylthio)-3,5-xylyl ester
- BAYER 37344
- H 321
- METHIOCARB, 1GM, NEAT
- MERCAPTODIMETHUR PESTANAL<TM>
- mercaptodimethur (iso,f,frg)
- methiocarb (bsi,can,nz,esa,iso)
- mercaptodimethur (ISO) methiocarb 3,5-dimethyl-4-methylthiophenyl N-methylcarbamate
- 3,5-dimethyl-4-methylthiophenyl N-methylcarbamate,mercaptodimethur (ISO),methiocarb
- (3,5-dimethyl-4-methylsulfanyl-phenyl) N-methylcarbamate
- (3,5-dimethyl-4-methylsulfanylphenyl) N-methylcarbamate
- N-methylcarbamic acid [3,5-dimethyl-4-(methylthio)phenyl] ester
- Methiocarb 1g [2032-65-7]
- Phenol,3,5-diMethyl-4-(Methylthio)-, 1-(N-MethylcarbaMate)
- Methiocarb Solution, 1000ppm
- Methiocarb Solution, 100ppm
- B 37344
- BAY 37344
- BAY 5024
- BAY 9026
- Borderland black
- Carbamic acid, 3,5-dimethyl-4-methylthiophenyl ester, N-methyl
- Carbamic acid, methyl-, 3,5-dimethyl-4-(methylthio)phenyl ester
- Carbamic acid, methyl-, 4-(methylthio)-3,5-xylyl ester
- Carbamic acid, N-methyl-, 4-(methylthio)-3,5-xylyl ester