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Diflubenzuron is an insecticide of the benzoylurea class. [2] It is used in forest management and on field crops [3] to selectively control insect pests, particularly forest tent caterpillar moths, boll weevils, gypsy moths, and other types of moths. [1] It is a widely used larvicide in India for control of mosquito larvae by public health ...
Flufenoxuron is an insecticide that belongs to the benzoylurea chitin synthesis inhibitor group, which also includes diflubenzuron, triflumuron, and lufenuron. [1] Flufenoxuron is a white crystalline powder. It is insoluble in water, is not flammable, and is not an oxidizer.
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The 2024 IRAC poster of insecticide modes of action includes the majority of chemicals listed below. [5] The pesticide manual provides much information on pesticides. [6] [7] Many of the insecticides in the list are not in use.
Toxicity labels [1] viz; red label, yellow label, blue label and green label are mandatory labels employed on pesticide containers in India identifying the level of toxicity (that is, the toxicity class) of the contained pesticide. [1] [2] [3] The schemes follows from the Insecticides Act of 1968 [1] and the Insecticides Rules of 1971.
Dichlorvos (2,2-dichlorovinyl dimethyl phosphate, commonly abbreviated as an DDVP [1]) is an organophosphate widely used as an insecticide to control household pests, in public health, and protecting stored products from insects. The compound has been commercially available since 1961.
Cypermethrin is a broad-spectrum insecticide, which means it kills beneficial insects as well as the targeted insects. [14] Fish are particularly susceptible to cypermethrin, [ 15 ] [ 16 ] but when used as directed, application around residential sites poses little risk to aquatic life. [ 17 ]
Carbaryl is often inexpensively produced by direct reaction of methyl isocyanate with 1-naphthol. [5]C 10 H 7 OH + CH 3 NCO → C 10 H 7 OC(O)NHCH 3. Alternatively, 1-naphthol can be treated with excess phosgene to produce 1-naphthyl chloroformate, which is then converted to carbaryl by reaction with methylamine. [5]