Fenoxaprop-ethyl

Lewis, W.M. (1985). Fenoxaprop-ethyl for smooth crabgrass and goosegrass control in turf. Proc. South. Weed Sci. Soc., 38 104. 

Frumin AL disulfoton Fuji-one isoprothiolane Fuji-grass esprocarb Fuklasin ziram Fumazone DBCP Fundal chlordimeform Fungaflor imazalil Fungazil imazalil Furadan carbofuran Furore fenoxaprop-ethyl Fusarex tecnazene Fusilade fluazifop-butyl... 

Warbax famphur Warbexol famphur Weedazol amitrole Weedex simazine Weedone 2,4,5-T Whip fenoxaprop-ethyl Wypout barban... 

DB dichlorprop diclofop-methyl fenoprop fenoxaprop-ethyl fluazifop-butyl haloxyfop-methyl MCPA... 

C17H360 heptadecanol (mixed primary isomers) 52783-44-5 25.00 0.8272 2 30583 C18H16CIN05 fenoxaprop-ethyl 66441-23-4 25.00 1.3339 2... 

Smith, A.E. 1985. Persistence and transformation of the herbicides 14C Fenoxaprop-ethyl and 14C Fenthiaprop-ethyl in two prairie soils under laboratory and field conditions.. Agric. Food Chem. 33 483-488. 

Fenoxaprop-ethyl (29), formerly on its code number Hoe 33 171, ethyl 2-[4-(6-chloro-2-benzoxaloxy)phenoxy] propionate, was discovered in the laboratories of the Hoechst AG (Bieringer et ai, 1982). 

Graminaceous crops are sensitive to fenoxaprop-ethyl with the exception of wheat and rye. Tolerant broad-leaved crops are clover, cotton, field beans, peas, potatoes, soybean, (Schumacher et al., 1982a, b), sugar beet, sunflower, tobacco, alfalfa and oilseed rape. 

Fenoxaprop-ethyl is absorbed through the leaves and moves in both the xylem and the phloem. The actual site of action is the meristematic tissue of the shoot where it accumulates (Kocher et al., 1982). In plants the compound rapidly degrades to polar products. In soils it is saponified and in 32 days a complete degradation takes place. 

Fenoxaprop-ethyl is weakly toxic to mammals (Bieringer et al., 1982). Acute oral LDso is for rats male 2357, female 2500mg/kg. Subchronic toxicity (90-day feeding study), the no-eflect level for rats is 80 ppm and for dogs 16 ppm. The compound is slightly irritant to rabbit skin and slightly irritant to rabbit eye. It is nonmutagenic in the Ames Test. 

The toxicological properties are also similar to those of fenoxaprop-ethyl. Fenthiaprop-ethyl is about twice as toxic to mammals as fenoxaprop-ethyl (Randte et ai, 1982). 

Moody, R.P. and Ritter, L., 1992, An automated in vitro dermal absorption procedure II. comparative in vivo and in vitro dermal absorption of the herbicide fenoxaprop-ethyl in rats, Toxicol. In Vitro, 6, 53-59. 

When applied alone, safeners generally have Utde visible effects on crop or weed species. This was found, for example, for the safeners fenchlorazole-ethyl and mefenpyr-diethyl [20, 21]. In contrast, fenchlorazole-ethyl exerted an immediate protective effect on wheat and prevented even a transient inhibition of leaf growth by fenoxaprop-ethyl [22). The same was observed subsequently for combinations of mefenpyr-diethyl with fenoxaprop-P-ethyl. 

In the above-mentioned combination, fenoxaprop-ethyl/fenchlorazole-ethyl the racemic form of the herbicide was subsequently replaced by the biologically active... 

Chloro-2-benzoxazoyl) oxy] phenoxy] propanoic acid ethyl ester. See Fenoxaprop-ethyl... 

Ethyl 2-[4-(6-chlorobenzoxazol-2-yloxy) phenoxy] propionate. See Fenoxaprop-ethyl Ethyl 4-chloro-2,3-dihydro-2-oxobenzothiazol-3-yl acetate. See Benazolin-ethyl... 

Fennel fruit. See Fennel (Foeniculum vulgare) Fennel oil Fennel oil, bitter Fennel oil, sweet. See Fennel (Foeniculum vulgare) oil Fennel seed. See Fennel (Foeniculum vulgare) Fennel, sweet, extract. See Fennel (Foeniculum vulgare) extract Fenoxaprop-ethyl CAS 66441-23-4... 

Dalapon 2,4-DB Ethofumesate Fenoxaprop-ethyl Flamprop-isopropyl Isoproturon Linuron MCPA Metazachlor Metoxuron... 

Triphenyl phosphine CisHisSb Triphenylantimony CisHieCINOs Fenoxaprop-ethyl C18H16N2... 

Aryioxyphenoxypropionate Cyhalofop-butyl, diclofop-methyl, fenoxaprop-ethyl, fluazifop-butyl, haloxyfop-methyl... 

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