FORMOTHION Chemical Properties

Melting point:

25.5℃

Boiling point:

317.8±52.0 °C(Predicted)

Density 

1.361 g/cm³ (20 ºC)

vapor pressure 

1.13 x 10^-4 Pa (20 °C)

refractive index 

1.5541 (589.3 nm 20℃)

Flash point:

25 °C

storage temp. 

2-8°C

pka

-1.79±0.70(Predicted)

Water Solubility 

2600 mg l^-1(24 °C)

form 

solid

BRN 

5942199

CAS DataBase Reference

2540-82-1(CAS DataBase Reference)

EPA Substance Registry System

Formothion (2540-82-1)

Safety Information

Hazard Codes 

Xn

Risk Statements 

21/22-36/38-20/21/22-10

Safety Statements 

36/37-36-26

RIDADR 

3018

WGK Germany 

3

HazardClass 

6.1(b)

PackingGroup 

III

Hazardous Substances Data

2540-82-1(Hazardous Substances Data)

Toxicity

LD50 in rats, rabbits (mg/kg): 350, 410 orally (Liesche)

FORMOTHION Usage And Synthesis

Description

Formothion is a pale yellow liquid or crystalline mass, decomposes on distillation, mp 25–26 ?C, vp 0.113 mPa (20 ?C). It is poorly soluble in water (2.6 g/L at 24 ?C) and miscible with most organic solvents, except aliphatic hydrocarbons. Log Kow = 1.47. Formothion is hydrolyzed in aqueous media to dimethoate (activation) and dimethoate carboxylic acid (degradation): DT₅₀ (23 ?C) at pH 3–9 is less than 1 d.

Chemical Properties

Yellow liquid.Insoluble in water; miscible with common organic solvents.

Chemical Properties

Formothion is an odorless, yellowish viscous oil or crystalline mass.

Uses

Formothion is used to control sucking pests and internally feeding larvae in a variety of crops.

Uses

Acaricide, systemic insecticide.

Definition

ChEBI: Formothion is a dicarboximide.

General Description

Viscous yellow oil or a crystalline mass. Used as an insecticide and acaricide on crops and ornamentals. Not presently produced commercially in the U.S.

Air & Water Reactions

hydrolyzed by water especially under alkaline conditions. [EPA, 1998].

Reactivity Profile

Organophosphates, such as FORMOTHION, 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.

Hazard

Cholinesterase inhibitor.

Health Hazard

FORMOTHION is one of the least toxic systemic organophosphates. FORMOTHION is a compound of low to moderate toxicity. It causes the depression of cholinesterase, leading to accumulation of acetylcholine in the nervous system, which is believed to be responsible for the symptoms.

Fire Hazard

When heated to decomposition, FORMOTHION emits very toxic fumes of nitrogen oxides, phosphorus oxides and sulfur oxides. FORMOTHION is an organophosphorus insecticide. Some of these materials may burn but none of them ignite readily. Container may explode in heat of fire. Fire and runoff from fire control water may produce irritating or poisonous gases. Avoid alkaline pesticides; hydrolyzed by water especially under alkaline conditions.

Agricultural Uses

Insecticide, Acaricide: Formothion is a systemic and contact insecticide used to control spider mites, aphids, psyllids, mealy bugs, whiteflies, jassids, leaf miners, ermine moths, and fruit flies. It is used on tree fruits, vines, olives, hops, cereals, sugar cane, rice. Formothion is available as an emulsifiable concentrate and an ultra-low-volume spray. A U.S. EPA restricted Use Pesticide (RUP). Not approved for use in EU countries

Trade name

AFLIX®; ANTHIO®; ANTIO®; CP 53926®; S 6900®; SAN 244 I®; SAN 6913 I®; SAN 71071®; SPENCER S-6900®; VEL 4284®

Safety Profile

Poison by ingestion, inhalation, sh contact, and intravenous routes. Mutation data reported. When heated to decomposition it emits very toxic fumes of NOx, POx, and SOx. See also ESTERS.

Potential Exposure

Formothion is an insecticide and acar icide for use on crops and ornamentals. Formothion is not currently produced commercially in the U.S.

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Speed in removing material from skinis of extreme importance. Shampoo hair promptly if contaminated. Seek medical attention immediately. If thischemical has been inhaled, remove from exposure, beginrescue breathing (using universal precautions, includingresuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit. Keepvictim quiet and maintain normal body temperature. Effectsmay be delayed; keep victim under observation.

Metabolic pathway

Formothion is broken down in aqueous solution to approximately equal amounts of dimethoate and dimethoate carboxylic acid, the first of which is an activation step and the latter a degradative one. All studies which have investigated the fate of formothion in biological systems have identified these two metabolites but there is evidence that their formation is purely base-catalysed and not enzyme-catalysed. In this respect, the amide group of formothion is much more labile than that of dimethoate since dimethoate carboxylic acid has only been reported in metabolic studies and is not formed by base-catalysed hydrolysis of dimethoate.

storage

Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with thischemical you should be trained on its proper handling andstorage. Store in tightly closed containers in a cool, wellventilated area away from alkaline materials. Wherepossible, automatically pump liquid from drums or otherstorage containers to process containers.

Shipping

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

Degradation

Formothion is hydrolysed by water to dimethoate (2) and dimethoate carboxylic acid (3). Dilute solutions in non-polar organic solvents are stable (PM). El-Oshar and Dauterman (1977) investigated the hydrolysis of [O-¹⁴C-methyl]formothion in 1.0 M phosphate buffer at pH values between 5.5 and 8.0 at 37 °C. The amounts of unchanged formothion and products were assessed after 30 min. At all pH values the amounts of dimethoate (2) and dimethoate carboxylic acid (3) were approximately equal, indicating that the rate of attack by the hydroxyl ion was equal at both carbonyl groups. The rate of hydrolysis was pH dependent with 16.4% hydrolysis at pH 5.5, 65.2% hydrolysis at pH 7.0 and 96.7% hydrolysis at pH 8.0 after 30 min. The route leading to dimethoate carboxylic acid would yield N-methylformamide (4) as the additional product. A suggested route for the base-catalysed hydrolysis of formothion is shown in Scheme 1.

Toxicity evaluation

The acute oral LD₅₀ for rats is 365–500 mg/kg. Inhalation LC50 (4 h) for rats is 3.2 mg/L air. NOEL (2 y) for rats is 80 mg/kg diet (4 mg/kg/d). ADI is 0.02 mg/kg b.w.

Incompatibilities

Strong oxidizers may cause release of toxic phosphorus oxides. Organophosphates, in the pres ence of strong reducing agents such as hydrides, may form highly toxic and flammable phosphine gas. Keep away from alkaline materials.

Waste Disposal

In accordance with 40CFR 165 recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by follow ing package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office.

FORMOTHION(2540-82-1)Related Product Information

• FAMPHUR
• Dimethyl disulfide
• Dimethylphosphorodithioate
• FORMOTHION SOLUTION 100UG/ML IN HEXANE 1ML
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• FORMOTHION SOLUTION 100UG/ML IN ACETONITRILE 1ML
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• O,O-DIMETHYLS-(N-METHYLCARBAMOYLMETHYL)PHOSPHORODITHIOATE
• FORMOTHION