Highly Effective Profenofos + Lambda-Cyhalothrin (20%+1.5% Ec)

Profenofos 20% + Lambda-cyhalothrin 1.5% EC

Profenofos NOMENCLATURE
Common name profenofos (BSI, E-ISO, (m) F-ISO, ANSI, ESA) 
IUPAC name O-4-bromo-2-chlorophenyl O-ethyl S-propyl phosphorothioate
Chemical Abstracts name O-(4-bromo-2-chlorophenyl) O-ethyl S-propyl phosphorothioate 
CAS RN [41198-08-7] 

Profenofos APPLICATIONS
Profenofos Biochemistry Cholinesterase inhibitor. The separate optical isomers, due to the chiral phosphorus atom, show different types of insecticidal activity and ability to inhibit acetylcholinesterase (H. Leader & J. E. Casida, J. Agric. Food Chem., 1982, 30, 546).

Profenofos Mode of action Non-systemic insecticide and acaricide with contact and stomach action. Exhibits a translaminar effect. Has ovicidal properties.

Profenofos Uses Control of insects (particularly Lepidoptera) and mites on cotton, maize, sugar beet, soya beans, potatoes, vegetables, tobacco and other crops, at 250-1000 g/ha.

Profenofos Phytotoxicity Slight reddening of cotton may occur.

Lambda-cyhalothrin NOMENCLATURE
Common name lambda-cyhalothrin (BSI, E-ISO); lambda-cyhalothrine ((f) F-ISO) 
IUPAC name A reaction product comprising equal quantities of (S)-α-cyano-3-phenoxybenzyl (Z)-(1R,3R)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-3-phenoxybenzyl (Z)-(1S,3S)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate Roth: (S)-α-cyano-3-phenoxybenzyl (Z)-(1R)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-3-phenoxybenzyl (Z)-(1S)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate (1:1)
Chemical Abstracts name [1α(S*),3α(Z)]-(±)-cyano(3-phenoxyphenyl)methyl 3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylate 
CAS RN [91465-08-6] 

Lambda-cyhalothrin APPLICATIONS
Lambda-cyhalothrin Biochemistry Acts on the nervous system of insects, and disturbs the function of neurons by interaction with the sodium channel.

Lambda-cyhalothrin Mode of action Non-systemic insecticide with contact and stomach action, and repellent properties. Gives rapid knockdown and long residual activity.

Lambda-cyhalothrin Uses Control of a wide spectrum of insect pests, e.g. aphids, Colorado beetles, thrips, lepidopteran larvae, coleopteran larvae and adults, etc., in cereals, hops, ornamentals, potatoes, vegetables, cotton, and other crops. Provides good control of insect-borne plant viruses, at 2-5 g/ha. Also used for control of insect pests in public health.
  Profenofos 20% + Lambda-cyhalothrin 1.5% EC

Profenofos NOMENCLATURE
Common name profenofos (BSI, E-ISO, (m) F-ISO, ANSI, ESA) 
IUPAC name O-4-bromo-2-chlorophenyl O-ethyl S-propyl phosphorothioate
Chemical Abstracts name O-(4-bromo-2-chlorophenyl) O-ethyl S-propyl phosphorothioate 
CAS RN [41198-08-7] 

Profenofos APPLICATIONS
Profenofos Biochemistry Cholinesterase inhibitor. The separate optical isomers, due to the chiral phosphorus atom, show different types of insecticidal activity and ability to inhibit acetylcholinesterase (H. Leader & J. E. Casida, J. Agric. Food Chem., 1982, 30, 546).

Profenofos Mode of action Non-systemic insecticide and acaricide with contact and stomach action. Exhibits a translaminar effect. Has ovicidal properties.

Profenofos Uses Control of insects (particularly Lepidoptera) and mites on cotton, maize, sugar beet, soya beans, potatoes, vegetables, tobacco and other crops, at 250-1000 g/ha.

Profenofos Phytotoxicity Slight reddening of cotton may occur.

Lambda-cyhalothrin NOMENCLATURE
Common name lambda-cyhalothrin (BSI, E-ISO); lambda-cyhalothrine ((f) F-ISO) 
IUPAC name A reaction product comprising equal quantities of (S)-α-cyano-3-phenoxybenzyl (Z)-(1R,3R)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-3-phenoxybenzyl (Z)-(1S,3S)-3-(2-chloro-3,3,3-trifluoroprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate Roth: (S)-α-cyano-3-phenoxybenzyl (Z)-(1R)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-3-phenoxybenzyl (Z)-(1S)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate (1:1)
Chemical Abstracts name [1α(S*),3α(Z)]-(±)-cyano(3-phenoxyphenyl)methyl 3-(2-chloro-3,3,3-trifluoro-1-propenyl)-2,2-dimethylcyclopropanecarboxylate 
CAS RN [91465-08-6] 

Lambda-cyhalothrin APPLICATIONS
Lambda-cyhalothrin Biochemistry Acts on the nervous system of insects, and disturbs the function of neurons by interaction with the sodium channel.

Lambda-cyhalothrin Mode of action Non-systemic insecticide with contact and stomach action, and repellent properties. Gives rapid knockdown and long residual activity.

Lambda-cyhalothrin Uses Control of a wide spectrum of insect pests, e.g. aphids, Colorado beetles, thrips, lepidopteran larvae, coleopteran larvae and adults, etc., in cereals, hops, ornamentals, potatoes, vegetables, cotton, and other crops. Provides good control of insect-borne plant viruses, at 2-5 g/ha. Also used for control of insect pests in public health.
 

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