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Lufenuron 12% + Imidacloprid 19% + Emamectin Ben, Lufenuron + Imidacloprid + Emamectin Benzoate, Lufenuron + Imidacloprid manufacturer / supplier in China, offering Lufenuron 12% + Imidacloprid 19% + Emamectin Benzoate 5% Wdg, Highly Effective Niclosamide (98% Tc), Highly Effective Niclosamide (25% Ec) and so on.

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Lufenuron 12% + Imidacloprid 19% + Emamectin Benzoate 5% Wdg

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Min. Order: 1 kg
Port: Shanghai, China
Production Capacity: 50000 Ton Per Year
Payment Terms: L/C, T/T, D/P
CAS No.: 103055-07-8
Appearance: Granules
Source: Organic Synthesis
Toxicity of High and Low: Low Toxicity of Reagents
Mode: Ingestion
Toxicological Effect: Insect Growth Regulator

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Basic Info

Model NO.: WDG/WG
Formulation Types: Ec
CAS1: 103055-07-8
CAS2: 138261-41-3
CAS3: 155569-91-8
Trademark: Essence
Transport Package: 1g-25kg for Solid Formulations
Specification: FAO, WHO
Origin: China
HS Code: 3808
Lufenuron 12% + Imidacloprid 19% + Emamectin benzoate 5% WDG

Common name lufénuron ((m) F-ISO); lufenuron (BSI, E-ISO, INN) 
IUPAC name (RS)-1-[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]-3-(2,6-difluorobenzoyl)urea
Chemical Abstracts name N-[[[2,5-dichloro-4-(1,1,2,3,3,3-hexafluoropropoxy)phenyl]amino]carbonyl]-2,6-difluorobenzamide 
CAS RN [103055-07-8] 

Lufenuron Biochemistry Chitin synthesis inhibitor, type 0 (Lepidopteran).

Lufenuron Mode of action Acts mostly by ingestion; larvae are unable to moult, and also cease feeding. Also acts transovarially, reducing fecundity and egg hatch.

Lufenuron Uses Insect growth regulator for control of lepidopteran and coleopteran larvae on cotton, maize and vegetables; and rust mites and western flower thrips, at 10-50 g/ha. Also for the prevention and control of flea infestations on pets.

Lufenuron Compatibility Not compatible with pesticides with alkaline reaction (lime sulfur, copper).

Common name imidacloprid (BSI, E-ISO); imidaclopride ((m) F-ISO) 
IUPAC name (E)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine
Chemical Abstracts name (2E)-1-[(6-chloro-3-pyridinyl)methyl]-N-nitro-2-imidazolidinimine 
CAS RN [138261-41-3], formerly [105827-78-9] 

Imidacloprid Biochemistry Acts as an antagonist by binding to postsynaptic nicotinic receptors in the insect central nervous system.

Imidacloprid Mode of action Systemic insecticide with translaminar activity and with contact and stomach action. Readily taken up by the plant and further distributed acropetally, with good root-systemic action.

Imidacloprid Uses Control of sucking insects, including rice-, leaf- and Planthoppers, Aphids, Thrips and Whitefly. Also effective against soil insects, Termites and some species of biting insects, such as Rice water weevil and Colorado beetle. Has no effect on nematodes and spider mites. Used as a seed dressing, as soil treatment and as foliar treatment in different crops, e.g. rice, cotton, cereals, maize, sugar beet, potatoes, vegetables, citrus fruit, pome fruit and stone fruit. Applied at 25-100 g/ha for foliar application, 50-175 g/100 kg seed for most seed treatments, and 350-700 g/100 kg cotton seed. Also used to control Fleas on dogs and cats.

Emamectin benzoate APPLICATIONS

Emamectin benzoate Biochemistry Acts by stimulating the release of γ-aminobutyric acid, an inhibitory neurotransmitter, thus finally activating chloride channels.

Emamectin benzoate Mode of action Non-systemic insecticide which penetrates leaf tissues by translaminar movement. Paralyses the Lepidoptera, which stop feeding within hours of ingestion, and die 2-4 dat.

Emamectin benzoate Uses For control of Lepidoptera on vegetables, brassicas, fruit, maize, tea, grapes and cotton, at up to 16 g/ha, and in pine trees, at 5-25 g/ha. 

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