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2,3,5-TRIMETHACARB

2,3,5-TRIMETHACARB
2,3,5-TRIMETHACARB structure
CAS No.
12407-86-2
Chemical Name:
2,3,5-TRIMETHACARB
Synonyms
broot;uc27867;LANDRIN(R);trimethacarb;2,3,5-TRIMETHACARB;trimethylphenylmethylcarbamate;2,3,5-TRIMETHYLPHENYL METHYL CARBAMATE;2,3,5(or3,4,5)-trimethyl-phenomethylcarbamate;Methylcarbamic acid 2(or 4),3,5-trimethylphenyl ester;carbamicacid,methyl-,2,3,5(or3,4,5)-trimethylphenylester
CBNumber:
CB3425785
Molecular Formula:
C11H15NO2
Formula Weight:
193.24
MOL File:
12407-86-2.mol

2,3,5-TRIMETHACARB Properties

Boiling point:
329.46°C (rough estimate)
Density 
1.0945 (rough estimate)
vapor pressure 
6.8 x 10-3 Pa (25 °C)
refractive index 
1.5080 (estimate)
Water Solubility 
>58 mg l-1 (23 °C)
FDA UNII
R97FQQ0N7W
EPA Substance Registry System
Trimethacarb (12407-86-2)
SAFETY
  • Risk and Safety Statements
RIDADR  2757
HazardClass  6.1(b)
PackingGroup  III

2,3,5-TRIMETHACARB Chemical Properties,Uses,Production

Uses

Trimethacarb is an insecticide with primarily stomach action. It is mainly used to control corn root worm larvae in maize but it also controls a wide range of insect and mollusc pests. Trimethacarb acts as a bird and mammal repellent.

Metabolic pathway

The metabolic pathways of trimethacarb in plants, mammals and insects involve mainly oxidation of N-methyl or ring-methyl substituents and conjugation. Some hydroxylation of the phenyl ring and ester hydrolysis occurs. The metabolism of trimethacarb was reviewed by Fukuto (1972), Kuhr and Dorough (1976) and by Schlagbauer and Schlagbauer (1972).

Degradation

Trimethacarb is hydrolysed by strong acids and alkalis but aqueous solutions are stable to light (PM). Trimethacarb was applied to bean leaves and exposed to natural sunlight for 4 days. Both isomers were decomposed more rapidly when exposed to sunlight compared with normal light in the laboratory. The compounds were almost completely decomposed. Major photoproducts resulted from hydroxylation of methyl substituents of the phenyl ring (2 and 3) and of the N-methyl group (5 and 6) (see Schemes 1 and 2). There were few products of hydrolysis (Slade and Casida, 1970; Kuhr and Dorough, 1976).

2,3,5-TRIMETHACARB Preparation Products And Raw materials

Raw materials

Preparation Products


2,3,5-TRIMETHACARB Suppliers

Global( 13)Suppliers
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