Chlorpyrifos 12% + Cypermethrin 1.4% Ulv

Chlorpyrifos 12% + Cypermethrin 1.4% ULV

Chlorpyrifos NOMENCLATURE
Common name chlorpyriphos-éthyl ((m) France); chlorpyriphos ((m) F-ISO, JMAF); chlorpyrifos (BSI, E-ISO, ANSI, ESA, BAN) 
IUPAC name O,O-diethyl O-3,5,6-trichloro-2-pyridyl phosphorothioate
Chemical Abstracts name O,O-diethyl O-(3,5,6-trichloro-2-pyridinyl) phosphorothioate 
CAS RN [2921-88-2] 

Chlorpyrifos APPLICATIONS
Chlorpyrifos Biochemistry Cholinesterase inhibitor.

Chlorpyrifos Mode of action Non-systemic insecticide with contact, stomach, and respiratory action.

Chlorpyrifos Uses Control of Coleoptera, Diptera, Homoptera and Lepidoptera in soil or on foliage in over 100 crops, including pome fruit, stone fruit, citrus fruit, nut crops, strawberries, figs, bananas, vines, vegetables, potatoes, beet, tobacco, soya beans, sunflowers, sweet potatoes, peanuts, rice, cotton, alfalfa, cereals, maize, sorghum, asparagus, glasshouse and outdoor ornamentals, turf, and in forestry. Also used for control of household pests (Blattellidae, Muscidae, Isoptera), mosquitoes (larvae and adults) and in animal houses. Phytotoxicity Non-phytotoxic to most plant species when used as recommended. Poinsettias, azaleas, camellias, and roses may be injured.

Chlorpyrifos Compatibility Incompatible with alkaline materials.

Cypermethrin NOMENCLATURE
Common name  (The ratio of cis- to trans- isomers should be stated.); cyperméthrine ((f) F-ISO); cypermethrin (BSI, E-ISO, ANSI, BAN) 
IUPAC name (RS)-α-cyano-3-phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate Roth: (RS)-α-cyano-3-phenoxybenzyl (1RS)-cis-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
Chemical Abstracts name cyano(3-phenoxyphenyl)methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate 
CAS RN [52315-07-8], formerly [69865-47-0], [86752-99-0] and many other numbers 

Cypermethrin APPLICATIONS
Cypermethrin Biochemistry Acts on the nervous system of the insect, and disturbs the function of neurons by interaction with the sodium channel.

Cypermethrin Mode of action Non-systemic insecticide with contact and stomach action. Also exhibits anti-feeding action. Good residual activity on treated plants.

Cypermethrin Uses Control of a wide range of insects, especially Lepidoptera, but also Coleoptera, Diptera, Hemiptera, and other classes, in fruit (including citrus), vines, vegetables, potatoes, cucurbits, lettuce, capsicums, tomatoes, cereals, maize, soya beans, cotton, coffee, cocoa, rice, pecans, oilseed rape, beet, ornamentals, forestry, etc. Applied at 10-100 g/ha in field crops; 10-50 g/ha in fruit. Control of flies and other insects in animal houses; and mosquitoes, cockroaches, houseflies and other insect pests in public health. Also used as an animal ectoparasiticide.

Cypermethrin Compatibility Incompatible with alkaline materials.






Chlorpyrifos 12% + Cypermethrin 1.4% ULV

Chlorpyrifos NOMENCLATURE
Common name chlorpyriphos-éthyl ((m) France); chlorpyriphos ((m) F-ISO, JMAF); chlorpyrifos (BSI, E-ISO, ANSI, ESA, BAN) 
IUPAC name O,O-diethyl O-3,5,6-trichloro-2-pyridyl phosphorothioate
Chemical Abstracts name O,O-diethyl O-(3,5,6-trichloro-2-pyridinyl) phosphorothioate 
CAS RN [2921-88-2] 

Chlorpyrifos APPLICATIONS
Chlorpyrifos Biochemistry Cholinesterase inhibitor.

Chlorpyrifos Mode of action Non-systemic insecticide with contact, stomach, and respiratory action.

Chlorpyrifos Uses Control of Coleoptera, Diptera, Homoptera and Lepidoptera in soil or on foliage in over 100 crops, including pome fruit, stone fruit, citrus fruit, nut crops, strawberries, figs, bananas, vines, vegetables, potatoes, beet, tobacco, soya beans, sunflowers, sweet potatoes, peanuts, rice, cotton, alfalfa, cereals, maize, sorghum, asparagus, glasshouse and outdoor ornamentals, turf, and in forestry. Also used for control of household pests (Blattellidae, Muscidae, Isoptera), mosquitoes (larvae and adults) and in animal houses. Phytotoxicity Non-phytotoxic to most plant species when used as recommended. Poinsettias, azaleas, camellias, and roses may be injured.

Chlorpyrifos Compatibility Incompatible with alkaline materials.

Cypermethrin NOMENCLATURE
Common name  (The ratio of cis- to trans- isomers should be stated.); cyperméthrine ((f) F-ISO); cypermethrin (BSI, E-ISO, ANSI, BAN) 
IUPAC name (RS)-α-cyano-3-phenoxybenzyl (1RS,3RS;1RS,3SR)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate Roth: (RS)-α-cyano-3-phenoxybenzyl (1RS)-cis-trans-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate
Chemical Abstracts name cyano(3-phenoxyphenyl)methyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropanecarboxylate 
CAS RN [52315-07-8], formerly [69865-47-0], [86752-99-0] and many other numbers 

Cypermethrin APPLICATIONS
Cypermethrin Biochemistry Acts on the nervous system of the insect, and disturbs the function of neurons by interaction with the sodium channel.

Cypermethrin Mode of action Non-systemic insecticide with contact and stomach action. Also exhibits anti-feeding action. Good residual activity on treated plants.

Cypermethrin Uses Control of a wide range of insects, especially Lepidoptera, but also Coleoptera, Diptera, Hemiptera, and other classes, in fruit (including citrus), vines, vegetables, potatoes, cucurbits, lettuce, capsicums, tomatoes, cereals, maize, soya beans, cotton, coffee, cocoa, rice, pecans, oilseed rape, beet, ornamentals, forestry, etc. Applied at 10-100 g/ha in field crops; 10-50 g/ha in fruit. Control of flies and other insects in animal houses; and mosquitoes, cockroaches, houseflies and other insect pests in public health. Also used as an animal ectoparasiticide.

Cypermethrin Compatibility Incompatible with alkaline materials.

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