Formothion

HCID 17345CAS 2540-82-1

Basic information

Standard SMILES
COP(=S)(OC)SCC(=O)N(C)C=O
InChIKey
AIKKULXCBHRFOS-UHFFFAOYSA-N
Molecular formula
C6H12NO4PS2
Average molar mass
257.3 g/mol
Monoisotopic mass
256.99453649

Overview

Formothion appears as 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. (EPA, 1998)

Names & identifiers

Preferred name
Formothion
IUPAC
2-dimethoxyphosphinothioylsulfanyl-N-formyl-N-methylacetamide
English name
FORMOTHION
Molecular formula
C6H12NO4PS2
Molecular weight
257.27

Names & synonyms

FORMOTHION2540-82-1AnthioToproseAflixAntioAnthio 25Spencer S-6900Sandoz S-6900Formothion 25 ECAflizOMS-968
Show more names
p1JC7J-38RPP1NUCKSs6900NUCKS1
Afliz [Sandoz]SAN 244 ISAN 6913 ISAN 7107 IVEL 4284ENT 27,257CP 53926S 6900

Database identifiers

CAS
2540-82-1
PubChem CID
17345
DTXSID
DTXSID4041991
ChEMBL
CHEMBL449733
ChEBI
CHEBI:82126
UNII
7O9EWV477R
EC Number
219-818-6
Nikkaji
J3.031G

Properties

Computed structural properties

XLogP
1.5
Topological polar surface area
113 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
6
Rotatable bonds
5
Heavy atoms
14

Experimental & physicochemical properties

Pesticides · 3 items

Acaricides, Insecticides

Active substance -> EU Pesticides database: Not approved

Pesticides -> Organophosphate Insecticides

LogP · 2 items

log Kow = 1.48

1.48

OdorOdorless
Density · 3 items

1.361 at 68 °F (EPA, 1998) - Denser than water; will sink

1.361 at 20 °C

1.361 @ 20°C

Color/Form · 2 items

Yellowish liquid

Viscous pale yellow liquid or crystalline mass

Solubility · 3 items

Completely miscible with common organic solvents, e.g. alcohols, ethers, ketones, chloroform, benzene, toluene, xylene; slightly soluble in hexane; very slightly soluble in ligroin and paraffin oil.

MISCIBLE WITH ... DIETHYL ETHER

In water, 2.6X10+3 mg/L at 24 °C

Physicochemical properties

Melting point
25.5 ℃ · 25.5℃
Boiling point
317.8 · 317.8±52.0 °C(Predicted)
Density
1.361 g/cm3 · 1.361 g/cm3 (20 ºC)
vapor pressure
1.13 x · 1.13 x 10-4 Pa (20 °C)
refractive index
1.5541 · 1.5541 (589.3 nm 20℃)
Flash point
25 °C · 25 °C

Safety & regulation

GHS classification

GHS Classification · 6 items

Warning

H302: Harmful if swallowed [Warning Acute toxicity, oral]

P264, P270, P280, P301+P317, P302+P352, P317, P321, P330, P362+P364, and P501 (click each P-code to see the statement)

Warning

H302 (97.6%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P270, P280, P301+P317, P302+P352, P317, P321, P330, P362+P364, and P501 (click each P-code to see the statement)

Hazard information

Regulatory Information · 2 items

2002/2076

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Other Safety InformationIMAP assessments - Phosphorodithioic acid, S-[2-(formylmethylamino)-2-oxoethyl] O,O-dimethyl ester: Environment tier I assessment
DOT LabelPoison
Fire Hazards · 1 item

When heated to decomposition, it emits very toxic fumes of nitrogen oxides, phosphorus oxides and sulfur oxides. This compound 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. (EPA, 1998)

Health Hazards · 1 item

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. (EPA, 1998)

Hazards Summary · 1 item

Not irritating to rabbit eyes; Effects in high dose animal studies include inhibition of cholinesterase activity, minor histological changes to liver and adrenal glands, functional changes of the liver, and hematological changes; No evidence of skin sensitization, increased tumor incidence, other neurotoxicity, nor developmental or teratogenic toxicity [HSDB] No significant adverse gross or histological changes or increase in tumor frequency observed in two year feeding studies with rats and dogs; [INCHEM JMPR] The average of two baseline respective cholinesterase activity determinations three days apart, with no exposures to enzyme inhibiting pesticides for at least 30 days, is recommended for each worker prior to exposure to cholinesterase inhibitors because of large inter-individual differences in published baseline values. To be established at least once a year. Removal from workplace exposures is recommended until the cholinesterase activity returns to within 20% of baseline. [TLVs and BEIs]

Safety & protection

Fire Fighting · 1 item

This compound is an organophosphorus insecticide. Keep unnecessary people away; isolate hazard area and deny entry. Stay upwind; keep out of low areas. Ventilate closed spaces before entering them. Wear positive pressure breathing apparatus and special protective clothing. Remove and isolate contaminated clothing at the site.

First AidWarning: Effects may be delayed up to 12 hours. Caution is advised.
Exposure Control and Personal Protection · 1 item

Biological Exposure Indices (BEI) [ACGIH] - Acetylcholinesterase activity in red blood cells = 70% of individual's baseline; Butylcholinesterase activity in serum or plasma = 60% of individual's baseline; Sample at end of shift; [TLVs and BEIs]

Fire Fighting Procedures · 2 items

If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped or safely confined. Use water in flooding quantities as fog. Solid streams of water may be ineffective. Cool all affected containers with flooding quantities of water. Apply water from as far a distance as possible. Use "alcohol" foam, carbon dioxide or dry chemical. /Organophosphorus pesticides, liquid, NOS/

Fire Extinguishing: Small fires: dry chemical, carbon dioxide, water spray, or foam. Large fires: water spray, fog, or foam. Move container from fire area if you can do so without risk. Fight fire from maximum distance. Dike fire control water for later disposal; do not scatter material. When heated to decomposition, it emits very toxic fumes off nitrogen oxides, phosphorus oxides and sulfur oxides. This compound is an organophosphorus insecticide. Some of these materials may burn but none of them ignite readily. Fire and runoff from fire control water may produce irritating or poisonous gases. Vapors are heavier than air and will collect in low areas. Containers may explode in fire. Storage containers and parts of containers may rocket great distances, in many directions. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Notify local health and fire officials and pollution control agencies. From a secure, explosion-proof location, use water spray to cool exposed containers. If cooling streams are ineffective (venting sound increases in volume and pitch, tank discolors, or shows any signs of deforming), withdraw immediately to a secure position. If employees are expected to fight fires, they must be trained and equipped in OSHA 1910.156.

Storage Conditions · 4 items

Anthio must be kept in its original labelled container, which should be kept well sealed, and stored in cool, dry and ventilated premises under lock and key. Must be stored at ambient temp not exceeding -15 °C and +30 °C.

Rooms used for storage only should be soundly constructed & fitted with secure locks. Floors should be kept clear & pesticides clearly identified. If repacking is carried out in storage rooms, adequate light should be available; floors should be impervious & sound ... . /Pesticides/

Pesticides containers must be provided with labels indicating the degree of toxicity of the product they contain. The labels must not only give a short description of how to use the prepn, but also state basic precautions to be taken when applying it. /Organophosphorus pesticides/

Pesticides of any degree of toxicity should be transported in containers which are clearly labelled, leak-proof, and not easily damaged. They should never be transported /or stored/ beside, or above any type of food, and all spillages should be immediately reported. /Pesticides/

Cleanup Methods · 4 items

Evacuate and restrict persons not wearing protective equipment from area of spill or leak until cleanup is complete. Remove all ignition sources. Stay upwind; keep out of low areas. Ventilate closed spaces before entering them. Do not touch spilled material; keep leak if you can do so without risk. Use water spray to reduce vapor. Small spills: absorb with sand or other noncombustible absorbent material and place into containers for later disposal. Small dry spills: with clean shovel, place material into clean, dry containers and cover; move containers from spill area. Large spills: dike far ahead of spill for later disposal. It may be necessary to contain and dispose of this chemical as a hazardous waste. If material or contaminated runoff enters waterways, notify downstream users of potentially contaminated waters. Contact your Department of Environmental Protection or your regional office of the federal EPA for specific recommendations. If employees are required to clean-up spills, they must be properly trained and equipped. OSHA 1910.120(q) may be applicable.

Environmental considerations- land spill: Dig a pit, pond, lagoon, holding area to contain liquid or solid material. /SRP: If time permits, pits, ponds, lagoons, soak holes, or holding areas should be sealed with an impermeable flexible membrane liner./ Dike surface flow using soil, sand bags, foamed polyurethane, or foamed concrete. Absorb bulk liquid with fly ash, cement powder, or commercial sorbents. /Organophosphorus pesticides, liquid, NOS/

Environmental considerations- water spill: Use natural barriers or oil spill control booms to limit spill travel. Remove trapped material with suction hoses. /Organophosphorus pesticides, liquid, NOS/

Environmental considerations- air spill: Apply water spray or mist to knock down vapors. /Organophosphorus pesticides, liquid, NOS/

Toxicology

Interactions · 5 items

Formothion was studied, along with 6 other organophosphates, for its interaction with other OP's in rats. There was a slight increase of toxicity when it was combined with dimethoate.

Some phenothiazines may antagonize & some may potentiate the toxic anticholinesterase effects of ... /organophosphorus insecticides/. /Organophosphate cholinesterase inhibitors/

In long term therapy, adrenocorticoids antagonize the antiglaucoma effects of anticholinesterases (incr ocular pressure). ... Anticholinergics antagonize the miotic (antiglaucoma) & other muscarinic effects of anticholinesterases on the autonomic & central nervous systems. Tricyclic antidepressants (anticholinergic effects) antagonize the antiglaucoma (miotic) effects of anticholinesterases in glaucoma. ... Antihistamines with anticholinergic effects antagonize the miotic (antiglaucoma) & CNS effects of anticholinesterases. Anticholinesterases potentiate tranquilizing & behavioral changes induced by antihistamines. The actions of anticholinesterase agents on autonomic effector cells, & to some extent those on CNS, are antagonized by atropine, an antidote of choice. Barbiturates are potentiated by anticholinesterases. ... Dexpanthenol potentiates the effects of anticholinesterases. Fluorophosphate insecticides potentiate the effects of other anticholinesterases. /Anticholinesterases/

Barbiturates are potentiated by anticholinesterases. Although barbiturates may be used cautiously in treating convulsions, extreme care is essential in handling poisonings due to anticholinesterases, particularly organophosphorus pesticides. Echothiophate, a cholinesterase inhibitor used as miotic, potentiates other such inhibitors ... Used for other purposes (additive effects) or possibly synergistic. Those exposed to organophosphate insecticides must take strict precautions. ... Organophosphorus insecticides: additive anticholinesterase effects. Hazardous. Patients on anticholinesterases (even topical, such as eye drops) should avoid areas where organophosphorus insecticides ... recently ... used. /Anticholinesterase/

For more Interactions (Complete) data for FORMOTHION (6 total), please visit the HSDB record page.

Ecotoxicity Values · 5 items

LD50 Pigeon oral 630 mg/kg

LC50 /Cyprinus carpio/ (Carp) = >50 mg/L/96 hr /Conditions of bioassay not specified in source examined/

LC50 /Oncorhynchus mykiss/ (Rainbow trout) 38.3 ppm/96 hr /Conditions of bioassay not specified in source examined/

LD50 /Apis mellifera/ (Bee) oral 1.537 ug/g bw

For more Ecotoxicity Values (Complete) data for FORMOTHION (15 total), please visit the HSDB record page.

Environmental Fate · 5 items

FORMOTHION & DIMETHOATE SHOULD BE CONSIDERED TOGETHER SINCE THEIR SIGNIFICANT RESIDUES APPEAR TO BE IDENTICAL @ HARVEST; THAT IS, EFFECT OF APPLYING DIMETHOATE & FORMOTHION WILL BE ADDITIVE.

TERRESTRIAL FATE: IN LOAMY SOIL HALF-LIFE IS 14 DAYS.

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 150(SRC), determined from a log Kow of 1.48(2) and a regression-derived equation(3), indicates that formothion is expected to have high mobility in soil(SRC). Volatilization of formothion from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.1X10-10 atm-cu m/mole(SRC), derived from its vapor pressure, 8.48X10-7 mm Hg(4), and water solubility, 2,600 mg/L(5). Formothion is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(4). The half-life of formothion in loamy soil is < 1 day, forming dimethoate, and (dimethoxyphosphinthioylthio)acetic acid, which ultimately dissipates(4). A half-life of 14 days in loamy soil(6) suggests biodegradation may be an important environmental fate process in soil(SRC).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 150(SRC), determined from a log Kow of 1.48(2) and a regression-derived equation(3), indicates that formothion is not expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(3) based upon an estimated Henry's Law constant of 1.1X10-10 atm-cu m/mole(SRC), derived from its vapor pressure, 8.48X10-7 mm Hg(4), and water solubility, 2600 mg/L(5). The hydrolysis half-life of formothion is < 1 day in the pH range of 3 to 9 and 23 °C(4). According to a classification scheme(6), an estimated BCF of 3(SRC), from its log Kow(2) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is low(SRC). The rate of decomposition of formothion when exposed to sunlight was 0.014 min-1, corresponding to a half-life of 48 min(8). A half-life of 14 days in soil(9) suggests biodegradation may be an important environmental fate process in water(SRC).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), formothion, which has a vapor pressure of 8.48X10-7 mm Hg at 20 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase formothion is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 4.4 hours(SRC), calculated from its rate constant of 8.8X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase formothion may be removed from the air by wet or dry deposition(SRC).

Food Survey Values · 1 item

Olive trees in Italy were treated with formothion at the recommended application rate (60 g a.i./hectare) and then twice the application rate on November 16 1988(1). Industrial extraction of olive oil was undertaken 53 days postapplication(1). Residues in oil from laboratory pressing ranged from 0.24 mg/kg on day 8 preharvest to <0.01 mg/kg on day 47 preharvest. After 53 days, industrial pressing yielded <0.01 mg/kg formothion residue in oil(1). Formothion was not detected in grapefruit, lemon, orange, apple, pear, apricot, cherries, peach, nectarine, plum, grape, strawberry, blackberry, boysenberry, elderberry, raspberry, rowenberry, bilberry, red current, black current, gooseberry, banana, fig, pomegranate, beetroot, carrot, celeriac, horseradish, parsnip, parsley root, radish, garlic, onion, spring onion, tomato, pepper, eggplant, cucumber, melon, watermelon, squash, sweet corn, broccoli, cauliflower, brussel sprout, white cabbage, red cabbage, spring cabbage, oxheart cabbage, chinese cabbage, kale, lettuce, spinach, chive, dill, marjoram, oregano, parsley, rosemary, thyme, bean, pea, celery, leek, rhubarb, mushroom, sunflower seed, or potato in the 1995-1996 Danish national pesticide monitoring program; however, it was found in mandarin/clementine in 1996(2).

Adverse EffectsOther Poison - Organophosphate
Milk ConcentrationsMany of the organophosphorus insecticides are excreted in the milk ... /Organophosphorus insecticides/

Regulatory information

CERCLA Reportable Quantities · 1 item

Releases of CERCLA hazardous substances are subject to the release reporting requirement of CERCLA section 103, codified at 40 CFR part 302, in addition to the requirements of 40 CFR part 355. Formothion is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 100 lbs.

Safety data

PPE
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
wgk
3
ridadr
3018
Toxicity
LD50 in rats, rabbits (mg/kg): 350, 410 orally (Liesche)
risk_code
21/22-36/38-20/21/22-10
Signal word
Danger

Chemistry & industry

Pharmacology

Mechanism of Action · 5 items

The signs of poisoning due to organophosphorus cmpd are those due to accumulation of acetylcholine & hence overstimulation of parasympathetic nervous system. It is usual to divide them under 3 headings: muscarinic, nicotinic & central. Muscarinic signs ... consist of hypersalivation, lacrimation, sweating & nasal discharge. Miosis, dyspnea, vomiting, diarrhea & frequency of urination ... Nicotinic effects consist of fasciculation of muscles, weakness & paralysis. Central nervous system effects include nervousness, apprehension, ataxia, convulsions & coma. Death is due to resp failure, or sometimes cardiac arrest. There is little difference between signs produced by different organophosphorus compounds, but route of absorption may influence one system more than another. /Organophosphorus cmpd/

Organophosphorus derivatives act by combining with and inactivating the enzyme acetylcholinesterase. ... The inactivation of cholinesterase by cholinesterase inhibitor pesticides allows the accumulation of large amounts of acetylcholine, with resultant widespread effects that may be ... separated into 4 categories: (1) Potentiation of postganglionic parasympathetic activity. ... (2) Persistent depolarization of skeletal muscle ... (3) Initial stimulation following depression of cells of central nervous system ... (4) Variable ganglionic stimulation or blockade ... /Cholinesterase inhibitor pesticides/

The main feature of the toxic mechanism of organophosphorus pesticides is inhibition of the esterase enzyme activity, in particular of cholinesterase, which plays an important physiological part. Organophosphorus pesticides can also indirectly interact with the biochemical receptors of acetylcholine. /Organophosphorus pesticides/

Organophosphates poison insects and humans primarily by phosphorylation of the acetylcholinesterase enzyme at nerve endings. /Organophosphate Cholinesterase-inhibiting pesticides/

For more Mechanism of Action (Complete) data for FORMOTHION (7 total), please visit the HSDB record page.

Biological Half-LifeFollowing oral administration of (14)C-labelled formothion to rats within 24 hr 97% of radioactivity is excreted in urine. With half life of 4 hr it is rapidly broken down, and excreted in form of nontoxic metabolic products.
Metabolism/Metabolites · 5 items

Metabolites include dimethoate, bis(dimethylthiophosphoryl)disulfide and dimethyldithiophosphorylacetic acid...

Hydrolytic attack causes rapid degradation of formothion on bean plants to dimethoate and o,o-dimethyl dithiophosphorylacetic acid. Further breakdown products are methoxon, o,o-dimethyldithiophosphoric acid, and bis(o,o-dimethylthiophosphoryl) disulfide.

Incubation of (14)C-labeled formothion with three subcellular rat liver fractions at 37 °C and pH 7.4 resulted in alteration of all of the formothion within 30 min. The denatured non-enzymatic control gave identical results, indicating that the mechanism for the formation of dimethoate and dimethoate monoacid was not dependent on enzymatic oxidation or reduction reactions. The only metabolites identified were dimethoate and dimethoate monoacid. No dimethoxon was found. Incubation of (14)C-formothion at various pH's at 37 °C resulted in formation of dimethoate and dimethoate monoacid. At an acid pH the rate of formation was much slower than at an alkali pH.

Formothion metabolism in plants has been shown to result in formation of dimethoate and formothion acid (o,o-dimethyl phosphoryl acetic acid). The same transformation of formothion to dimethoate has been observed in animals.

For more Metabolism/Metabolites (Complete) data for FORMOTHION (8 total), please visit the HSDB record page.

MeSH Pharmacological ClassificationPesticides designed to control insects that are harmful to man. The insects may be directly harmful, as those acting as disease vectors, or indirectly harmful, as destroyers of crops, food products, or textile fabrics.
Absorption, Distribution and Excretion · 5 items

Single oral doses of 10 mg/kg body-weight of formothion, labelled with carbon-14 in the carbamoyl group, were administered by stomach tube to male rats. Autoradiographs indicated that the compound was readily absorbed from the stomach. Within 30 minutes after giving the dose, a high level of radioactivity was found in the liver and kidney, although the major activity was still in the stomach. Six hours after administration the activity in the stomach area was low; the main activity then being in the kidneys, with less activity in the liver, intestines, pancreas and thymus. After 24 hours from the time of administration of the dose, distinct radioactivity was found only in the thymus. The urine was the major source of excretion; it contained 98-99% of the radioactivity compared to the feces which had only 1-2%. A total of 51% of the administered radioactivity had been excreted in the urine after 4 hr and 96% after 24 hr. The presence of considerable radioactivity in the bile indicated that there was also excretion of the compound and its metabolites in the bile. However, because so little radioactivity was encountered in the feces nearly all of these compounds must be re-absorbed in the intestine.

Most organophosphate compounds are ... absorbed from skin, conjunctiva, gastrointestinal tract, & lung. /Organophosphate compounds/

The rate of dermal absorption /of organophosphorus pesticides/ may be ... influenced by the solvent used. /Organophosphorus pesticides/

Many of the organophosphorus insecticides are excreted in the milk ... /Organophosphorus insecticides/

For more Absorption, Distribution and Excretion (Complete) data for FORMOTHION (10 total), please visit the HSDB record page.

Uses & manufacturing

Uses · 5 items

Used as acaricide and systemic insecticide; [Merck Index] Not currently commercially produced in the US; Likely discontinued for pesticide use worldwide; [HSDB]

Farming (Pesticides) [Category: Industry]

It is a contact and systemic insecticide and acaricide, effective at 250-500 g ai/ha or at 1.0-1.5 g ai/L, against a wide range of sucking and mining insects such as chewing insects (Cydia pominella and Epilachna beetles) and spider mites. /SRP: Former use in USA/

May be used against spider mites (non-op /non-organophosphate/ resistant strains only), aphids (non-op resistant strains only), psyllids, mealy bugs, armored scales, whiteflies, jassids, thrips, leaf miners, ermine moths, sawflies, fruit flies, olive fly, asparagus fly, mangold fly. /SRP: Former use in USA/

Acaricide, systemic insecticide. /SRP: Former use in USA/

U.S. Production · 2 items

(1972) NOT PRODUCED COMMERCIALLY IN THE US

(1975) NOT PRODUCED COMMERCIALLY IN THE US

Methods of Manufacturing · 4 items

Made by the reaction of 2-chloro-N-formyl-N-methylacetamide with ammonium O,O-dimethyl phosphorodithioate.

Chloroacetyl chloride + N-methylformamide + O,O-dimethyl dithiophosphoric acid (amide formation/ dehydrochlorination).

Formothion is produced by reaction of the sodium salt of O,O-dimethyldithiophosphoric acid with N-methyl N-formyl carbamoylmethyl chloride.

Preparation: Lutz, Schuler, GB 900557 (1962 to Sandoz)

Formulations/Preparations · 5 items

ANTHIO- 25% WT/VOL EMULSIFIABLE CONCENTRATE.

ULV /ultra low volume/; mixed formulations: (formothion +) fenitrothion

Mixtures include: Anthiomix, Sandothion, EC (210 g formothion + 210 g fenitrothion/l)

COMBINATIONS: ANTHIOMIX & SANDOTHION; BASIC PRODUCER

Formothion is available as a 25% and 40% emulsifiable concentrate (ingredients other than formothion undefined).

General Manufacturing Information · 5 items

The WHO Recommended Classification of Pesticides by Hazard identifies Formothion (technical grade) as an active ingredient believed to be obsolete or discontinued for use as a pesticide.

FULL ACTION IS EVIDENT ONE DAY AFTER APPLICATION FOLLOWED BY LONG LASTING EFFECTIVENESS.

ANTHIO 33 INSECTICIDE CANNOT BE DISTILLED WITHOUT DECOMP & IS PRACTICALLY INSOL IN ALIPHATIC HYDROCARBONS.

IT IS INCOMPATIBLE WITH ALKALINE PESTICIDES.

For more General Manufacturing Information (Complete) data for FORMOTHION (10 total), please visit the HSDB record page.

Applications · 4 items

DescriptionFormothion 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.

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

UsesAcaricide, systemic insecticide.

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

Suppliers42 total

Career Henan Chemica Co+86-0371-86658258 +86-13203830695 · [email protected]
湖北威德利化学试剂有限公司181-6332-1995 18062128043 · [email protected]
Hangzhou Go Top Peptide Biotech0571-88211921 · [email protected]
郑州德元凯化工有限公司17837139533 · [email protected]
安耐吉化学&3A(安徽泽升科技有限公司)021-58432009 400-005-6266 · [email protected]

Additional notes

DefinitionChEBI: Formothion is a dicarboximide.

Related reactions

1 records

Linked notes

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