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Mercaptodimethur

Mercaptodimethur Structure
CAS No.
2032-65-7
Chemical Name:
Mercaptodimethur
Synonyms
METHIOCARB;MXMC;Club;OMS93;H 321;Draza;b37344;certan;dcr736;Esurol
CBNumber:
CB1254073
Molecular Formula:
C11H15NO2S
Molecular Weight:
225.31
MOL File:
2032-65-7.mol
MSDS File:
SDS
Modify Date:
2024/6/18 13:26:42

Mercaptodimethur Properties

Melting point 119°C
Density 1.1838 (rough estimate)
vapor pressure 1.5 x 10-5 Pa (20 °C)
refractive index 1.4790 (estimate)
storage temp. 0-6°C
solubility DMF: 20 mg/ml,DMSO: 20 mg/ml,DMSO:PBS (pH 7.2) (1:1): 0.5 mg/ml,Ethanol: 10 mg/ml
form Crystalline Solid
Boiling point 310.7±42.0 °C(Predicted)
pka 12.16±0.46(Predicted)
color White
Water Solubility Insoluble
BRN 1881431
Stability Light Sensitive
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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06,GHS09
Signal word  Danger
Hazard statements  H300-H410
Precautionary statements  P264-P270-P273-P301+P310-P391-P405
Hazard Codes  T;N,N,T
Risk Statements  25-50/53
Safety Statements  22-37-45-60-61
RIDADR  UN 2811/2757
WGK Germany  3
RTECS  FC5775000
HazardClass  6.1(a)
PackingGroup  II
Toxicity LD50 in male, female rats (mg/kg): 70, 60 orally (Gaines)
NFPA 704
0
4 0

Mercaptodimethur price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 36152 Methiocarb PESTANAL?, analytical standard 2032-65-7 100MG ₹4827.95 2022-06-14 Buy
Product number Packaging Price Buy
36152 100MG ₹4827.95 Buy

Mercaptodimethur Chemical Properties,Uses,Production

Description

Methiocarb was originally developed by Bayer as an insecticide. The bird-repellent properties of the compound were quickly recognized, however, and a number of applications for bird damage management followed (42).
Methiocarb is a secondary repellent, and repellency occurs through aversive conditioning, by which birds that feed on treated food become sick and associate either the food or characteristics of the food with the discomfort (21). As a result, affected birds learn to avoid that food item. Often the avoidance response is locationdependent. For example, common ravens (Corvus corax) that learn not to eat eggs at one site will still feed on eggs at a different location (43).

Chemical Properties

Methiocarb is a colorless crystalline powder.

Uses

Insecticide; molluscicide; bird repellent.

Definition

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.

General Description

White crystalline powder with a mild odor. Used as an insecticide and immobilizing agent for birds, acaricide and molluscicide.

Reactivity Profile

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.

Health Hazard

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.

Fire Hazard

When heated to decomposition, Mercaptodimethur emits very toxic fumes of nitrogen and sulfur oxides.

Agricultural Uses

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.

Trade name

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]

Contact allergens

Methiocarb is an insecticide or molluscicide with a cholinesterase inhibiting effect. A case of contact dermatitis was reported in a carnation grower.

Pharmacology

Methiocarb is a carbamate, and its mode of action is via the inhibition of acetylcholinesterase at synapses in the nervous system. Unlike many cholinesterase-inhibiting compounds, however, the effects of methiocarb are rapidly reversible, and the animal experiences only transitory disruption.

Safety Profile

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.

Potential Exposure

A potential danger to those involved in the manufacture, formulation, and application of this nonsystemic acaricide and insecticide.

Environmental Fate

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).

Metabolic pathway

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.

Shipping

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

Waste Disposal

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).

Mercaptodimethur Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 102)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Xiamen AmoyChem Co., Ltd +86-592-6051114 +8618959220845 China 6387 58 Inquiry
Chongqing Chemdad Co., Ltd +86-023-6139-8061 +86-86-13650506873 China 39916 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49392 58 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29824 58 Inquiry
Hebei Mojin Biotechnology Co., Ltd +86 13288715578 +8613288715578 China 12446 58 Inquiry
SIMAGCHEM CORP +86-13806087780 China 17367 58 Inquiry
TargetMol Chemicals Inc. +1-781-999-5354 +1-00000000000 United States 19892 58 Inquiry
LEAP CHEM CO., LTD. +86-852-30606658 China 24738 58 Inquiry
Hebei Guanlang Biotechnology Co., Ltd. +8619930503259 China 18423 58 Inquiry
OMS93 Phenol,3,5-diMethyl-4-(Methylthio)-, 1-(N-MethylcarbaMate) MXMC 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] 3,5-Dimethyl-4-(methylsulfanyl)phenyl methylcarbamate 3,5-dimethyl-4-(methylthio)-phenomethylcarbamate 3,5-dimethyl-4-methylmercaptophenyl-n-methyl-carbamate 3,5-Dimethyl-4-methylthiophenyl N-methylcarbamate 3,5-Dimethyl-4-methyl-thiophenyl-N-carbamat 3,5-dimethyl-4-methylthiophenyln-methylcarbamate 3,5-Xylenol, 4-(methylthio)-, methylcarbamate 4-(Methylthio)-3,5-dimethylphenyl methylcarbamate 4-Methylmercapto-3,5-dimethylphenyl N-methylcarbamate 4-methylmercapto-3,5-dimethylphenyln-methylcarbamate 4-Methylmercapto-3,5-xylyl methylcarbamate 4-methylmercapto-3,5-xylylmethylcarbamate 3,5-Dimethyl-4-(methylthio)phenol methylcarbamate 3,5-DIMETHYL-4-[METHYLTHIO]PHENYL METHYLCARBAMATE Mesurol MESUROL(R) MERCAPTODIMETHUR Methylcarbamic acid 4-(methylthio)-3,5-xylyl ester BAYER 37344 ENT25726 H 321 METHIOCARB, 1GM, NEAT MERCAPTODIMETHUR PESTANAL Metmercapturon[R] mercaptodimethur (iso,f,frg) methiocarb (bsi,can,nz,esa,iso) Methiocarb(Mercaptodimethur) mercaptodimethur (ISO) methiocarb 3,5-dimethyl-4-methylthiophenyl N-methylcarbamate Miechongwei 4-methylthio-3,5-dimethylphenylmethylcarbamate 5-xylenol,4-(methylthio)-methylcarbamate B 37344 b37344 BAY 37344 BAY 5024 BAY 9026 bay37344 bay5024 bay9026 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 carbamicacid,methyl-,3,5-dimethyl-4-(methylthio)phenylester carbamicacid,methyl-,4-(methylthio)-3,5-xylylester carbamicacid,n-methyl-,4-(methylthio)-3,5-xylylester carbamicacid,N-methyl-,4-methylthio-3,5-xylylester certan Club