470-90-6

Amber-colored liquid with a mild chemical odor. Used for control of ticks, flies, lice, and mites on cattle and for blowfly, lice, ked, and itchmite on sheep. Controls fleas and mites on dogs; not used on cats. Applied on organic wastes and breeding places of fly larvae. Also used as a foliage insecticide for potatoes, rice, maize, and sugar cane. Used to control soil insects.

Organophosphates, such as CHLORFENVINFOS(470-90-6), are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

Slightly soluble in water.

A cholinesterase inhibitor.

Acute: cholinesterase inhibitor which affects central nervous system. Severe illness or death possible. Convulsions or coma and death.

Used as a soil insecticide for root maggots, rootworms, and cutworms. Those engaged in the production, formulation, and application of this insecticide.

(Non-Specific--Organophosphorus Pesticide, Liquid, n.o.s.) This material may burn but does not ignite readily. Container may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Avoid iron, steel, and brass. Stable when stored in glass or polyethylene lined containers. Avoid alkaline aqueous solutions.

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. Speed in removing material from skin is of extreme importance. Shampoo hair promptly if contaminated. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) 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. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit. Medical observation is recommended for 24
48 hours after breathing overexposure, as pulmonary edema may be delayed. As first aid for pulmonary edema, a doctor or authorized paramedic may consider administering a drug or other inhalation therapy.

UN3018 Organophosphorus pesticides, liquid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials.

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Strong oxidizers may cause release of toxic phosphorus oxides. Organophosphates, in the presence of strong reducing agents such as hydrides, may form highly toxic and flammable phosphine gas. Keep away from alkaline materials. May be corrosive to metals in the presence of moisture.

Chlorfenvinphos is a nonflammable, yellow oramber liquid with a mild odor. Molecular weight=359.58;Boiling point=110℃at 0.001 mmHg; 168-170℃at0.5 mmHg; Freezing/Melting point=-23-19℃. HazardIdentification (based on NFPA 704 M Rating System):Health 4, Flammability 1, Reactivity 0. Very slightly soluble in water

Chlorfenvinphos is a nonflammable, yellow or amber liquid with a mild odor.

Destruction by alkali hydrolysis or incineration. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

Chlorfenvinphos is used to control soil insects such as root worms on vegetables, bulb flies in wheat and maize and phorid and sciarid flies in mushrooms. It is also used to control Colorado beetles on potatoes, scale insects and mite eggs in citrus and stern borers and hoppers on rice. Other uses are the control of mosquitoes and animal ectoparasites as a sheep and cattle dip.

From 1963 until the early 1990s, chlorfenvinphos was extensively used in veterinary products (dip, dust, and collars) for flea and tick control on pets and domestic animals, and in dairy barns, milk rooms, poultry houses, and other animal buildings. Agriculturally, it was used on potatoes, rice, and maize, and for control of soil insects and nematodes. All uses were canceled in the United States in 1991 and phased out in EU in 2006. Chlorfenvinphos continues to be used in Australia and New Zealand in veterinary products for combating ectoparasites on cattle and sheep.

Insecticide; acaricide.

Chlorfenvinphos is synthesized by the Perkow reaction of triethyl phosphite with 2,4-α,α-tetrachloroacetophenone. Technical product is an E/Z isomer mixture with an E : Z ratio of 1 : 8–9 and an amber liquid, bp 167–170 ?C/0.5 mm Hg, vp 1 mPa (25 ?C), sparingly soluble in water (145 mg/L), and miscible with most common organic solvents such as acetone and aromatic hydrocarbons. Log Kow = 3.85. It is hydrolyzed slowly in slightly alkaline aqueous solutions and rapidly in strongly alkaline solutions; DT₅₀ values are >700 h (pH 1.1, 38 ?C), >400 h (pH 9.1, 38 ?C), and 1.28 h (pH 13, 20 ?C).

The mechanism of toxicity of chlorfenvinphos is related to its binding and inhibition of the serine hydrolase AChE. In the nervous system, AChE hydrolyzes the neurotransmitter acetylcholine, thereby terminating its synaptic action. AChE inhibition increases the availability of acetylcholine at the neural synapse, leading to cholinergic overstimulation, autonomic and neuromuscular dysfunction, and at higher levels, resulting in coma and death. Major metabolites of chlorfenvinphos do not inhibit ChE. Chlorfenvinphos inhibits butyrylcholinesterase which may function as a molecular scavenger for anti-ChE compounds in the blood or substitute for AChE where it is low.
The stress responses to acute exposure of chlorfenvinphos are evidenced in rats by rapidly increased plasma corticosterone concentrations and a prolonged reduced sensitivity to psychostimulants such as amphetamine. These effects were attributed to the hyperactivity of the cholinergic system from ChE inhibition, leading to persistent alterations of the brain cholinergic–dopaminergic balance.
Other potentially more sensitive non-ChE targets that may influence the overall toxicity of chlorfenvinphos include lipid metabolism, oxidative stress, aromatic amino acid transferases, and cytotoxicity. Chlorfenvinphos may act via central noradrenergic mechanisms to induce hypotension by accelerating the noradrenaline turnover in the brain. Chlorfenvinphos induces hepatic CYPs.

Chlorfenvinphos is a chlorovinyl organophosphate insecticide and the commercial material consists of an E/Z isomer mixture with a Z:E ratio of 8-9:1. The Z-isomer is usually the more insecticidal to most species of insect. Metabolism studies have generally used a stereochemical mixture; however, there is evidence that the E-isomer is photoisomerised to the more stable 2-isomer in the field. The breakdown of chlorfenvinphos has been extensively studied in soil, plants and mammals. The major routes of detoxification are by de-ethylation and hydrolysis and are similar in principle to those of related vinyl phosphates. The products of dealkylation and hydrolysis are desethylchlorfenvinphos and 2,2’,4’-trichloroacetophenone plus dimethyl phosphate, respectively. Further metabolism of the chloroacetophenone moiety then leads, via reduction or eventual hydrolysis of the side-chain chlorine substituent, to the formation of 1-(2,4- dichlophenyl)ethane-l,2-diol and 1-(2,4-dichlorophenyl)ethan-1-ol which are conjugated with glucose or glucuronic acid as the ultimate metabolites. Oxidation of the β carbon atom to give 2,4-dichloromandelic acid followed by decarboxylation gives 2,4-dichlorobenzoic acid which is conjugated with glycine in some mammals as the final metabolite. The 2,4dichlorophenyl moiety usually remains intact during metabolism although hydrolysis of ring chlorine has been reported in a soil degradation study. Metabolism studies have been reviewed by Beynon et al. (1973) and by the Pesticide Safety Directorate evaluation on chlorfenvinphos (PSD, 1994).

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with chlorfenvinphos you should be trained on its proper handling andstorage. Should be protected from moisture and stored inglass-lined or polyethylene-lined containers. Keep awayfrom strong bases. Sources of ignition, such as smoking andopen flames, are prohibited where this chemical is used,handled, or stored in a manner that could create a potentialfire or explosion hazard

Chlorfenvinphos is hydrolysed slowly in neutral, acidic and slightly alkaline aqueous solutions but hydrolysed rapidly in strongly alkaline solutions (PM). The E and Z stereoisomers are capable of interconversion by photoisomerisation (Beynon and Wright, 1967).

The toxicity is particularly high to rats (acute oral LD₅₀ 10–40 mg/kg) but is much lower to other mammals (acute oral LD₅₀ for mice 117–200, rabbits 300–1,000, dogs >12, 000 mg/kg). Inhalation LC50 (4 h) for rats is about 0.05 mg/L air. NOEL (2 yr) for rats and dogs is 1 mg/kg diet (0.05 mg/kg/d). ADI is 0.5 μg/kg b.w.
The selective toxicity of chlorfenvinphos to rats is attributed to the poor degradative activity of rat liver microsomal enzymes. In other mammals, liver microsomal mfo catalyzes the detoxification of the insecticide through oxidative deethylation to give 2- chloro-1-(2,4-dichlorophenyl)vinyl hydrogen phosphate. Ultimate metabolites include the glucuronides of 2,4- dichlorophenylethanediol and 1-(2,4-dichlorophenyl)ethanol and N-(2,4-dichlorobenzoyl)glycine. In soils, chlorfenvinphos is gradually decomposed to form α-dichlorophenylethanol, dichloroacetophenone, diethyl hydrogen phosphate, and desethyl chlorfenvinphos.