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METOLCARB

  • CasNo:1129-41-5

Product Description

Factory Export Top Purity METOLCARB 1129-41-5 In Stock

  • Molecular Formula: C9H11NO2
  • Molecular Weight: 165.192
  • Appearance/Colour: yellow liquid 
  • Vapor Pressure: 0.000358mmHg at 25°C 
  • Melting Point: 74-77 °C 
  • Refractive Index: 1.5270 (estimate) 
  • Boiling Point: 241.6 °C at 760 mmHg 
  • PKA: 12.38±0.46(Predicted) 
  • Flash Point: 99.9 °C 
  • PSA: 38.33000 
  • Density: 1.085 g/cm3 
  • LogP: 2.10410 

METOLCARB(Cas 1129-41-5) Usage

Preparation

Metolcarb is produced by the reaction between 3- methylphenol and Metolcarb.

Air & Water Reactions

Soluble in water.

Reactivity Profile

METOLCARB 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

High oral and skin toxicity, and moderate inhalation toxicity. (Non-Specific -- Carbamates) Some carbamates appear to be carcinogenic, teratogenic, and/or mutagenic. Carbamates are cholinesterase inhibitors.

Fire Hazard

As for other solid carbamate pesticides, container may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Emits toxic fumes of nitrogen oxides when heated to decomposition. Avoid decomposing heat.

Trade name

DRC 3341?; KUMIAI?; METACRATE?; S 1065?; SOGATOX DUST? 22; TSUMACIDE?; TSUMAUNKA?; VADEN?

Safety Profile

Poison by ingestion and skin contact. Moderately toxic by inhalation. Mutation data reported. When heated to decomposition it emits toxic fumes of NOx. See also CARBAMATES.

Potential Exposure

Metolcarb is an insecticide used for the control of rice leafhoppers, plant-hoppers; codling moth; citrus mealy bug; onion thrips; fruit flies; bollworms and aphids. Not registered as a pesticide in the United States.

Metabolic pathway

The main pathways of metabolism of metolcarb in plants, mammals and insects involve ring-methyl, N-methyl and phenyl-ring hydroxylation and conjugation. Carbamate ester hydrolysis is a minor reaction. Further oxidation of a ring-hydroxymethyl moiety to carboxyl occurs in rats and insects.

Shipping

UN2757 Carbamate pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.

Incompatibilities

Carbamates are incompatible with reducing agents such as hydrides, strong acids, oxidizing acids, peroxides, and bases. Contact with active metals or nitrides cause the release of flammable, and potentially explosive, hydrogen gas. May react violently with bromine, ketones. Incompatible with azo dyes, caustics, ammonia, amines, boranes, hydrazines, strong oxidizers.

Waste Disposal

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. In accordance with 40CFR165, follow 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.

General Description

Colorless crystalline solid. METOLCARB is an insecticide for the control of rice leafhoppers, planthoppers, codling moth, citrus mealybug, onion thrips, fruit flies, bollworms and aphids. Not registered as a pesticide in the U.S.

Agricultural Uses

Insecticide, Acaricide: Metolcarb is an insecticide for the control of rice green leafhoppers, plant-hoppers, codling moth, citrus mealy bug, onion thrips, fruit flies, bollworms and aphids. Not registered for use in the U.S. Not listed for use in EU countries.

InChI:InChI=1/C9H11NO2/c1-7-4-3-5-8(6-7)10(2)9(11)12/h3-6H,1-2H3,(H,11,12)/p-1

1129-41-5 Relevant articles

Fluid insecticidal formulations for treatment of parasitic insect larvae by dermal application

-

, (2008/06/13)

The present invention relates to the use...

Pesticidal composition containing a microencapsulated organo-phosphorus or carbamate in a pyrethroid dispersion

-

, (2008/06/13)

An insecticidal and/or acaricidal and/or...

α-Haloalkyl Haloformates and Related Compounds 1. A Convenient Synthesis of Carbamates via Chloromethyl Carbamates

Patonay, Tamas,Patonay-Peli, Erzsebet,Mogyorodi, Ferenc

, p. 2865 - 2885 (2007/10/02)

The preparation of carbamates under mild...

Pyrazole oxime derivatives and compositions

-

, (2008/06/13)

A pyrazole oxime derivative represented ...

1129-41-5 Process route

phosgene
75-44-5

phosgene

3-methyl-phenol
108-39-4

3-methyl-phenol

metolcarb
1129-41-5

metolcarb

Conditions
Conditions Yield
With methylamine; In toluene;
78%
3-methyl-phenol
108-39-4

3-methyl-phenol

metolcarb
1129-41-5

metolcarb

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: 79.3 percent / Et3 N / CH2 Cl2 / 1.67 h / 5 °C
2: 54 percent / H2 O; hexane / 2 h / Ambient temperature
With triethylamine; In hexane; dichloromethane; water;
In Isopropylbenzene;

1129-41-5 Upstream products

  • 108-39-4
    108-39-4

    3-methyl-phenol

  • 624-83-9
    624-83-9

    methyl isocyanate

  • 132905-78-3
    132905-78-3

    Carbonic acid chloromethyl ester m-tolyl ester

  • 74-89-5
    74-89-5

    methylamine

1129-41-5 Downstream products

  • 39074-23-2
    39074-23-2

    Chloromethyl-methyl-carbamic acid m-tolyl ester

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