NOMENCLATURE

Common name metolachlor (BSI, E-ISO, ANSI, WSSA); métolachlore ((m) F-ISO)

IUPAC name 2-chloro-6'-ethyl-N-(2-methoxy-1-methylethyl)aceto-o-toluidide 

Chemical Abstracts name 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide 

CAS RN [51218-45-2]  EEC no. 257-060-8  Development codes CGA 24 705 (Ciba-Geigy) 

PHYSICAL CHEMISTRY

Composition Racemic mixture of (1S)- and (1R)- isomers.  Mol. wt. 283.8  M.f. C₁₅H₂₂ClNO₂  Form Colourless to light tan liquid.  M.p. -62.1 °C  B.p. 100 ºC/0.001 mmHg  V.p. 4.2 mPa (25 ºC) (OECD 104)  K_OW logP = 2.9 (25 ºC)  Henry 2.4 ´ 10^-3 Pa m³ mol^-1 (calc.)  S.g./density 1.12 (20 ºC)  Solubility In water 488 mg/l (25 ºC) (OECD 105). Miscible with benzene, toluene, ethanol, acetone, xylene, hexane, dimethylformamide, ethylene dichloride, cyclohexanone, methanol, octanol, and dichloromethane. Insoluble in ethylene glycol, propylene glycol, and petroleum ether.  Stability Stable up to c. 275 ºC. Hydrolysed by strong alkalis and strong mineral acids. On hydrolysis in buffer (20 ºC), DT₅₀ (calc.) >200 d (2£pH £10).  F.p. 190 °C (1013 mbar) 

APPLICATIONS

Biochemistry Cell division inhibitor. Maize tolerance of chloroacetamides is attributed to rapid detoxification by glutathione transferases.  Mode of action Selective herbicide, absorbed predominantly by the hypocotyls and shoots. Inhibits germination.  Uses Control of annual grasses and some broad-leaved weeds in maize, sorghum, cotton, sugar beet, fodder beet, sugar cane, potatoes, peanuts, soya beans, safflowers, sunflowers, various vegetables, fruit and nut trees, and woody ornamentals. Applied pre-emergence, pre-plant incorporated or early post-emergence at, 1.0-2.5 kg a.i./ha. Often used in combination with broad-leaved herbicides, to extend the spectrum of activity.  Phytotoxicity Well tolerated by most broad-leaved crops, maize, sorghum (safened with fluxofenim or oxabetrinil).  Formulation types EC; FW; GR; SC. 

ANALYSIS

Product analysis by glc with FID (AOAC Methods, 1995, 985.06; CIPAC Handbook, 1988, D, 134). Residues determined by glc with TID or MCD. In drinking water, by gc with FID (AOAC Methods, 1995, 991.07). Details available from Syngenta. 

MAMMALIAN TOXICOLOGY

Oral Acute oral LD₅₀ for rats 2780 mg/kg.  Skin and eye Acute percutaneous LD₅₀ for rats >3170 mg/kg. Mild skin and eye irritant (rabbits). May cause skin sensitisation (guinea pigs).  Inhalation LC₅₀ (4 h) for rats >1.75 mg/l air.  NOEL (90 d) for rats 300 mg/kg diet (c. 15 mg/kg daily), for mice 100 mg/kg diet (c. 100 mg/kg daily), for dogs 300 mg/kg diet (c. 9.7 mg/kg daily).  ADI 0.1 mg/kg b.w.  Water GV 10 mg/l (TDI 3.5 mg/kg b.w.).  Toxicity class WHO (a.i.) III; EPA (formulation) III  EC hazard (R43) 

ECOTOXICOLOGY

Birds Acute oral LD₅₀ for mallard ducks and bobwhite quail >2150 mg/kg. Dietary LC₅₀ (8 d) for bobwhite quail and mallard ducks >10 000 mg/kg.  Fish LC₅₀ (96 h) for rainbow trout 3.9, carp 4.9, bluegill sunfish 10 mg/l.  Daphnia LC₅₀ (48 h) 25 mg/l.  Algae EC₅₀ for Scenedesmus subspicatus 0.1 mg/l.  Bees LD₅₀ (oral and contact) >110 mg/bee.  Worms LC₅₀ (14 d) for earthworms 140 mg/kg soil. 

ENVIRONMENTAL FATE

Animals Rapidly oxidised by rat liver microsomal oxygenases via dechlorination, O-demethylation and side-chain oxidation (J. Agric. Food Chem., 1989, 37, 1088).  Plants In plants, metabolism involves natural product conjugation of the chloroacetyl group, and hydrolysis and sugar conjugation at the ether group. Final metabolites are polar, water-soluble, and non-volatile.  Soil/Environment Major aerobic metabolites are derivatives of oxanilic and sulfonic acids. DT₅₀ in soil c. 20 d (field). K_oc 121-309.