102851-06-9

Fluvalinate is a viscous, yellow oil in appearance. It is very soluble in organic solvents and aromatic hydrocarbons and insoluble in water. Fluvalinate is a synthetic pyrethroid. It is used as a broad-spectrum insecticide against moths, beetles, and other insect pests on cotton, cereal, grape, potato, fruit tree, vegetable and plantation crops, fl eas, and turf and ornamental insects. It is available in emulsifi able concentrates, suspensions, and fl owable formulations. Fluvalinate is a moderately toxic compound in the US EPA toxicity class II. Some formulations may have the capacity to cause corrosion of the eyes. Pesticides containing fl uvalinate must bear the signal word DANGER on the product label. Fluvalinate is classifi ed as an RUP because of its high toxicity to fi sh and aquatic invertebrates.

Exposures to fl uvalinate cause coughing, sneezing, throat irritation, itching, or burning sensations on the arms or face with or without a rash, headache, and nausea. Prolonged period of exposures to pyrethroids cause adverse effects on the CNS, liver, and kidneys. Fluvalinate is slightly toxic to birds.

Pyrethroid insecticide used as a broad spectrum insecticide to control moths, beetles and other pests on cereals, potatoes, fruit trees, vegetables, fleas, cot ton, turf and ornamentals. It is also used to control varroa mites in honey bees. Some applications may be classified as a United States Environmental Protection Agency Restricted Use Pesticide (RUP). Formerly used as an insec ticide. Production discontinued by Sandoz Agro, Inc. Incompatibilities: Corrosive to some metals. Keep away from strong oxidizers and alkaline materials. Decomposes in temperatures above 350℃ releasing toxic vapors of hydrogen chloride, nitrogen oxides, and hydrogen fluoride.

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately.If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions) if breathing has stopped, and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Do not induce vomiting when formulations containing petroleum solvents are ingested. Otherwise, give large quantities of water and induce vomiting. Do not make an unconscious person vomit.

UN2902 Pesticides, liquid, toxic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.

Incineration would be an effective disposal procedure where permitted. If an efficient incinerator is not available, the product should be mixed with large amounts of combustible material and contact with the smoke should be avoided. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers.

Fluvalinate is used to control a wide range of insects and spider mites on fruit trees, vines, vegetables, cereals, cotton, tea, tobacco, ornamentals and other crops. It is also used for parasite control in bee hives.

ChEBI: The (2R) diastereomers of fluvalinate. A synthetic pyrethroid insecticide, it is used to control varroa mites in honey bee colonies.

The information reported below is derived from studies on fluvalinate, the racemic m-valinate (CASRN 69409-94-5). This has been superseded by the D-isomer. Evidence is given below to show that the results derived from fluvalinate are relevant to tau-fluvalinate. The chemical and photochemical degradation of fluvalinate and its degradation in soils have been reported. Information on metabolism in plants, rats, monkeys, cows and chickens is also published. The metabolism of fluvalinate is dominated by hydrolysis followed by oxidation and conjugation of the metabolites. Novel bile acid conjugates are highlighted. All quantitative data reported below are for the lower of usually two doses.

Fluvalinate is readily hydrolysed under basic conditions. Half-lives at pH 5, 7 and 9 were 48,38.5 and 1.1 days, respectively (PM). A value of a few minutes would be expected at pH 12.
The compound is very sensitive to photodegradation. [¹⁴C-trifluoro- methyl]Fluvalinate and [¹⁴C-benzyl]fluvalinateh ave been studied in solution (water and methanol) and as thin films on soils and glass (Quistad and Staiger, 1984). Its half-life in sunlight under these conditions is about 1 day, but in dilute aqueous solution it can be as short as 10 minutes (PM). The only sigruficant product retaining the ester structure (up to 18% yield) was the amide (7). Its formation was non-photochemical and was directly related to the temperature of the system. A minor product which retained both portions of the molecule was the COTelimination product (12). Under aqueous conditions 7 was a minor product and 12 was not detected.
2-Chloro-4-(trifluoromethyl)aniline( 3) was the major product derived from the acid moiety on a thin film on glass and under aqueous conditions (up to 40% and l8%, respectively). On soil surfaces the major products were the amide (7) and the anilino acid, N-(2-chloro-α,α,α-trifluoro-ptolyl)- D-valinate (2), and 35% remained bound. This residue may have arisen via the formation of aniline (3) (which was trapped as a volatile product from the glass surface). The formation of 2 and 7 were considered to be largely non-photochemical because they were also found under dark conditions. The dicarboxylic acid (11) was found as a 1% metabolite on soil surface photolysis.
The 3-phenoxybenzyl (3PB) portion (the alcohol moiety) was seen under all conditions as 3PBA aldehyde (5) and its oxidation product 3PBA (6) (together 40-50% of the applied radioactivity). The cyanohydrin (4) was also detected and this was probably a primary product. Also detected in 341% yields were the formanilide (8), (3-phenoxyphenyl)acetonitrile (9) and the oxamic acid (10). These products are illustrated in Scheme 1.