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Chemical Identification
Common Name
Fenoxycarb
中文通用名
苯氧威
IUPAC
ethyl 2-(4-phenoxyphenoxy)ethylcarbamate
CAS
ethyl [2-(4-phenoxyphenoxy)ethyl]carbamate
CAS No.
79127-80-3,72490-01-8
Molecular Formula
C17H19NO4
Molecular Structure
Category
Activity
Fenoxycarb is an insect growth regulator active by contact and ingestion. It also has some ovicidal activity. The product controls larval stages (in particular last instars) of Lepidoptera and certain hemipteran species. The company recommends one or two applications per season depending on pest pressure. Fenoxycarb should not be used during blooming periods.
CropUse
CropUses:
fruits, turf, amenity areas, ornamentals, vines

Fruit

75-200 g ai/ha; 25-300 g ai/hl

Vines

135-270 g ai/ha

Stone fruit

7.5-15 g ai/hl

Premix
FENOXYCARB+PERMETHRIN
Fenoxycarb+beta-cypermethrin
Baits, water dispersible granule, wettable powder. 
Premix Parters: difenoconazole; fenpropimorph; fenpropimorph prochloraz; prochloraz; propiconazole; propiconazole tebuconazole; tebuconazole;
Physical Properties
Molecular weight:301.3; Physical form:Colourless to white crystals. Density:1.23 (20 °C) ( OECD 109); Melting point:53-54 °C ( OECD 102); Flash point:c. 224 °C; Vapour pressure:8.67 ×10-4 mPa (25 °C) ( OECD 104); Henry constant:3.3 × 10-5 Pa m3 mol-1 ( calc.); Partition coefficient(n-octanol and water):logP = 4.07 (25 °C) ( OECD 107); Solubility:In water 7.9 mg/l ( pH 7.55-7.84, 25 °C). In ethanol 510, acetone 770, toluene 630, n-hexane 5.3, n-octanol 130 (all in g/l).; Stability:Stable to light. Stable to hydrolysis in aqueous solutions at pH 3, 7, and 9 at 50 °C.;
Toxicology
Oral:Acute oral LD50 for rats >10 000 mg/ kg. Percutaneous:Acute percutaneous LD50 for rats >2000 mg/ kg (occlusive). Non-irritating and non-sensitising to skin (maximisation test); not an eye irritant. Inhalation: LC50 for rats >4400 mg/m3 air. Phytotoxicity:Some varieties of pears, vines, citrus fruit and ornamentals may be injured.
Environmental Profile
Ecotoxicology: 
Algae: EC50 (96 h) for Scenedesmus subspicatus 1.10 mg/l.Bees:Non-toxic to bees; oral LC50 (24 h) >1000 ppm.Birds:Acute oral LD50 for Japanese quail >7000 mg/kg. LC50 (8 d) for bobwhite quail >25 000 ppm.Daphnia: LC50 (48 h) 0.4 mg/l.Fish: LC50 (96 h) for carp 10.3, rainbow trout 1.6 mg/l.Worms: LC50 (14 d) for earthworms 850 mg/ kg soil.Other beneficial spp.:Under field conditions, fenoxycarb (formulated as 'Insegar 25 WP') is safe to predators such as Phytoseiidae, to endoparasitic Hymenoptera species, to certain predators such as predatory bugs, and it is semi-selective on certain predators such as coccinel 

Environmental fate: 
Animals:In rats, the major metabolic path is ring hydroxylation to form ethyl [2-[p-(p-hydroxyphenoxy)phenoxy]ethyl]carbamate.Soil:Low mobility in soil, no bioaccumulation. Relatively fast degradation in soil and water: DT50 1.7-2.5 months (lab.), few to 31 days (field).Plant:Rapidly degraded in plants.WATER SOLUBILITY: 6 ppm
Transport Information
Signal Word:CAUTION; Hazard Class:III(Slightly hazardous)

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