Specific Applications by Joseph Sherma (Eds.)

By Joseph Sherma (Eds.)

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Analytical columns. 6 mm ID, Part No. 6 mm ID, Catalog No. , 2051 Waukegan Road, Deerfield, Illinois 60015. d. Experimental Procedure for 75 DF and 20 DF Formulations and for Technical Chlorsulfuron i. Preparation of standard solutions. Weigh (±2 mg) 140 mg of chlorsulfuron analytical standard into a 100-ml volumetric flask. 1 mg. 024 M NH 4 OH) and sonicate to dissolve. Allow the flask to return to room temperature then dilute to volume with sample diluent. Pipet 6, 8, and 10 ml of this solution into separate 25-ml volumetric flasks.

121-131 of this series for the residue analysis methods of fenvalerate. REFERENCE Papadopoulou-Mourkidou, E. (1985). Chromatographia 20, 376. 4 Chlorimuron Ethyl R. A. GUINIVAN, W. M. CHANG, AND J. L. PRINCE E. I. Du Pont de Nemours & Company, Inc. Agricultural Products Department Experimental Station Wilmington, Delaware 19898 cc C02C2H5 S02NHCNH(( Cl )) OCH3 Chlorimuron ethyl I. GENERAL A. Empirical Formula CI5HI5N406SC1 B. Alternate Names Classic herbicide contains chlorimuron ethyl (ethy 1, 2-[[[[(4-chloro6-methoxypyrimidin-2-yl) amino] carbonyl] amino] sulfonyl] benzoate as its active ingredient.

54 R. V. SLATES AND M. W. WATSON that are not undersown. Several biennial and some perennial broadleaf weeds are also controlled or suppressed. Chlorsulfuron is absorbed through both roots and foliage and is translocated throughout the plant. In resistant plants, the chlorsulfuron is rapidly detoxified; in suspectible plants, chlorsulfuron inhibits cell division in the growing tips of roots and foliage. Chlorsulfuron toxicity to animals is low. Specific toxicity data are given in Table I. Chlorsulfuron is not carcinogenic, teratogenic, mutagenic, or a reproductive hazard in laboratory tests.

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