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114-26-1 Mosquito Killer Insecticide Beta-Cypermethrin 1% Propoxur 0.7% HN

114-26-1 Mosquito Killer Insecticide Beta-Cypermethrin 1% Propoxur 0.7% HN

Brand Name : MOLOTUS

Model Number : Beta-Cypermethrin 1%+Propoxur 0.7% HN

Certification : ISO

Place of Origin : CHINA

MOQ : Negotiable

Price : Negotiable

Payment Terms : L/C, T/T, Western Union

Delivery Time : 20-25 days

Packaging Details : 20L, 10L, 5L, 1l, 500ML, 250ML,100ML as client's demand

Active ingredient : Beta-Cypermethrin+ propoxur

Formulation : 1.7% HN

Usage Area : Pest Control In Warehouse, Dump Areas, Drainage Ditch And Other Closed Area Or Area Difficult To Spray

Target : Cockroaches, Mosquitoes, Flies And Other Pests

M.F. : 52315-07-8

Classification : Thermal Fogging Agent

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114-26-1 Mosquito Killer Insecticide Beta-Cypermethrin 1% Propoxur 0.7% HN


Quick details


Product name

Propoxur + Beta-Cypermethrin 1.7%HN

Active Ingredient

Beta-Cypermethrin 1%+Propoxur 0.7%

Hazard Classification

Minor Toxicity

Control Spectrum

It Offers Pest Control In Warehouse, Dump Areas, Drainage Ditch And Other Closed Area Or Area Difficult To Spray For Control Of Cockroaches, Mosquitoes, Flies And Other Pests. The Product Could Also Be Used For Control Of Foodstuff, Tobacco And Other Store Pests.

Features

Not Dilution In Used,It Burned To Form Fogs For A Long Term Residual In Spatial And Diffusion By Hot Fogging Machine.

Application Instructions

Thermal Fogging Insecticide Applied By Professional Equipments And No Needing To Dilute. For Further Information, Please Check The Direction And Label.

Packaging

As client's demand

Control objects

NOMENCLATURE

Common name propoxur (BSI, E-ISO, F-ISO, ESA); PHC (JMAF); arprocarb* (former BSI name)

IUPAC name 2-isopropoxyphenyl methylcarbamate

Chemical Abstracts name 2-(1-methylethoxy)phenyl methylcarbamate

CAS RN [114-26-1] EEC no. 204-043-8


PHYSICAL CHEMISTRY

Mol. wt. 209.2 M.f. C11H15NO3 Form Colourless crystals; (tech., white to cream-coloured crystals). M.p. 90 ºC (crystal form I), 87.5 ºC (crystal form II, unstable) B.p. Decomposes on distillation V.p. 1.3 mPa (20 ºC); 2.8 mPa (25 ºC) KOW logP = 1.56 Henry 1.5 ´ 10-4 Pa m3 mol-1 (20 °C) S.g./density 1.17 (20 ºC) Solubility In water 1.75 g/l (20 ºC). Soluble in most organic solvents, e.g. isopropanol >200, toluene 94, hexane 1.3 (all in g/l, 20 ºC). Stability Stable in water at pH 7. Hydrolysed by strong alkali; DT50 (22 ºC) 1 y (pH 4), 93 d (pH 7), 30 h (pH 9); DT50 (20 ºC) 40 min (pH 10). Direct photodegradation is not a major contributor to the overall elimination of propoxur from the environment (DT50 5-10 d); indirect photodecomposition (addition of humic acid) is more rapid (DT50 88 h).


APPLICATIONS

Biochemistry Cholinesterase inhibitor. Mode of action Non-systemic insecticide with contact and stomach action. Gives rapid knockdown, and has long residual activity. Uses Control of cockroaches, flies, fleas, mosquitoes, bugs, ants, millipedes and other insect pests in food storage areas, houses, animal houses, etc. Control of sucking and chewing insects (including aphids) in fruit, vegetables, ornamentals, vines, maize, alfalfa, soya beans, cotton, sugar cane, rice, cocoa, forestry, etc.; also against migratory locusts and grasshoppers. Phytotoxicity Chrysanthemums, carnations, and hydrangeas may be injured at higher dose rates. Blossom thinning may occur on fruit trees. Formulation types AE; DP; EC; FU; GR; RB; SL; UL; WP; Oilspray. Compatibility Mixtures with alkaline substances are not stable.



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