Oxydemeton-methyl

HCID 4618CAS 301-12-2

Grundinformationen

Standard-SMILES
CCS(=O)CCSP(=O)(OC)OC
InChIKey
PMCVMORKVPSKHZ-UHFFFAOYSA-N
Summenformel
C6H15O4PS2
Durchschnittliche Molmasse
246,3 g/mol
Monoisotopische Masse
246,01493759

Überblick

Oxydemeton Methyl can cause female reproductive toxicity and male reproductive toxicity according to The Environmental Protection Agency (EPA).

Namen und Bezeichner

Bevorzugter Name
Oxydemeton-methyl
IUPAC
1-dimethoxyphosphorylsulfanyl-2-ethylsulfinylethane
Lokaler Name
Oxydemeton-methyl
Englischer Name
Oxydemeton-methyl
Summenformel
C6H15O4PS2
Molmasse
246.28

Namen und Synonyme

OXYDEMETON-METHYL301-12-2Demeton-S-methyl sulfoxideOxydemeton methylMetasystox RMetaisosystox sulfoxideMetasystemoxMethyl oxydemeton SOxydemetonmethylAimco systoxMetasystemox RMetasytox R
Weitere Namen anzeigen
r2170B-21097bay21097ent24,964bayer21097NSC 370785aimcosystoxmetasystoxr
MetilmercaptofosoksidMetaisosystoxsulfoxideDemeton-S methyl sulfoxideOxydemeton MOxydemeton-metileIsomethylsystox sulfoxideDemeton-methyl sulphoxideBayer 21097

Datenbank-Bezeichner

CAS
301-12-2
PubChem CID
4618
DTXSID
DTXSID8025541
ChEMBL
CHEMBL1315891
ChEBI
CHEBI:38735
UNII
E2031449YZ
EC Number
206-110-7
Nikkaji
J1.515F

Eigenschaften

Berechnete Struktureigenschaften

XLogP
-0,7
Polarare Oberfläche (TPSA)
97,1 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
6
Frei drehbare Bindungen
7
Schwere Atome
13

Experimentelle und physikochemische Eigenschaften

Pesticides · 5 Einträge

Acaricides, Insecticides

Active substance -> EU Pesticides database: Not approved

Pesticides -> Organophosphate Insecticides

Insecticides

Pesticide (Oxydemeton methyl) -> USDA PDB

LogP · 2 Einträge

log Kow = -0.74 @ 21 °C

-0.74

Density · 2 Einträge

1.289 at 68 °F (NTP, 1992) - Denser than water; will sink

1.289 g/cu cm @ 20 °C

Color/Form · 2 Einträge

Colorless liquid

Yellow oil

Solubility · 3 Einträge

10 to 50 mg/mL at 61 °F (NTP, 1992)

Soluble in common organic solvents except petroleum ether

Completely miscible with water.

Flash Pointless than 71 °F (NTP, 1992)

Physikochemische Eigenschaften

Schmelzpunkt
-20 ℃ · <-20℃
Siedepunkt
106 °C · 106 °C(Press: 0.01 Torr)
Dichte
1.289 g/cm3 · 1.289 g/cm3 (20 ºC)
Dampfdruck
3.8 · 3.8×10-3 Pa (20°C)
Brechungsindex
1.5216 · 1.5216 (589.3 nm 20℃)
storage temp.
0 · 0-6°C

Sicherheit und Regulatorisches

GHS-Klassifizierung

GHS Classification · 6 Einträge

Danger

H301: Toxic if swallowed [Danger Acute toxicity, oral]

P262, P264, P270, P273, P280, P301+P316, P302+P352, P316, P321, P330, P361+P364, P391, P405, and P501 (click each P-code to see the statement)

Danger

H301 (97.6%): Toxic if swallowed [Danger Acute toxicity, oral]

P262, P264, P270, P273, P280, P301+P316, P302+P352, P316, P321, P330, P361+P364, P391, P405, and P501 (click each P-code to see the statement)

Gefahrenhinweise

Regulatory Information · 4 Einträge

Hazard Traits - Developmental Toxicity; Neurotoxicity; Reproductive Toxicity

Commission Regulation (EC) No 451/2000

Oxydemeton-methyl is listed in the dataset of EPA Human Health Benchmarks for Pesticides under the Safe Drinking Water Act (40 eCFR 141)

2007/392

DOT LabelFlammable Liquid Poison
Fire HazardsThis chemical is flammable. (NTP, 1992)
Health Hazards · 1 Eintrag

SYMPTOMS: This compound is a cholinesterase inhibitor. Symptoms from exposure to this compound include anorexia; nausea; vomiting; diarrhea; excessive salivation; pupillary constriction; bronchoconstriction; muscle twitching; convulsions; coma; respiratory failure; pulmonary edema; perspiration; dyspnea; and cyanosis. The effects are cumulative.

Hazards Summary · 1 Eintrag

A cholinesterase inhibitor; Can be absorbed through skin; [CAMEO] A woman who was five months pregnant attempted suicide by ingestion and was hospitalized with symptoms including miosis, respiratory distress, muscular fasciculations, and coma (12 hours after admittance); Blood cholinesterase was reduced by 90%; The remainder of her pregnancy was without incident, and the baby's neurological exams at birth and 8 days later were normal; [HSDB] Occupational exposure less likely to be symptomatic or require hospitalization than exposure to other cholinesterase inhibitors; [Reference #1] 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]

Reactive GroupEsters, Sulfate Esters, Phosphate Esters, Thiophosphate Esters, and Borate Esters

Sicherheit und Schutzausrüstung

Fire FightingFires involving this material can be controlled with a dry chemical, carbon dioxide or Halon extinguisher. (NTP, 1992)
First Aid · 1 Eintrag

EYES: First check the victim for contact lenses and remove if present. Flush victim's eyes with water or normal saline solution for 20 to 30 minutes while simultaneously calling a hospital or poison control center. Do not put any ointments, oils, or medication in the victim's eyes without specific instructions from a physician. IMMEDIATELY transport the victim after flushing eyes to a hospital even if no symptoms (such as redness or irritation) develop.

Exposure Control and Personal Protection · 1 Eintrag

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 Einträge

If material on fire or involved in fire: Do not extinguish fire unless flow can be stopped. 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, dry chemical or carbon dioxide. /Organophosphorus pesticides, liquid, flammable, toxic; Organophosphorus pesticides, liquid, toxic/

If material on fire or involved in fire: Use water in flooding quantities as fog. Extinguish fire using agent suitable for type of surrounding fire. (Material itself does not burn or burns with difficulty.) /Organophosphorus pesticides, solid, toxic/

Storage ConditionsStore in original container, preferably in a locked area, away from children, food, feed.
Cleanup Methods · 3 Einträge

Environmental considerations: Air spill: Apply water spray or mist to knock down vapors. /Organophosphorus pesticides, liquid, flammable, toxic; Organophosphorus pesticides, liquid, toxic; Organophosphorus pesticides, solid, toxic/

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, flammable, toxic; Organophosphorus pesticides, liquid, toxic; Organophosphorus pesticides, solid, toxic/

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, flammable, toxic; Organophosphorus pesticides, liquid, toxic; Organophosphorus pesticides, solid, toxic/

Toxikologische Informationen

Interactions · 1 Eintrag

The effects of vitamin E (alpha-tocopherol) on the rate of lipid peroxidation and lipase activity ln the discrete areas of the brain and spinal cord were studied. Administration of metasystox in two different doses 1.0 and 2.0 mg/kg body weight ip daily for 10 days have shown a dose-related depletion of total lipids cholesterol and esterified fatty acids in the rat cerebral hemisphere, cerebellum brain stem and spinal cord. The rate of lipid peroxidation and lipase activity showed dose-dependent increase in different regions of the CNS. Administration of alpha-tocopherol alone caused significant reduction of lipid peroxidation and lipase activity. When it was admistered simultaneously with metasystox, alpha-tocopherol prevented the metasystox induced increase of lipid peroxidation and lipase activity.

Ecotoxicity Values · 5 Einträge

LD50 ANAS PLATYRHYNCHOS (MALLARD), MALES 4 MO OLD, ORAL 53.9 MG/KG (95% CONFIDENCE LIMIT: 38.9-74.8 MG/KG)

LD50 PHASIANUS COLCHICUS (PHEASANT), MALES 3-4 MO OLD, ORAL 42.4 MG/KG (95% CONFIDENCE LIMIT: 30.6-58.8 MG/KG)

LD50 ALECTORIS CHUKAR MALES & FEMALES, 3-4 MO OLD, ORAL 84.7-157 MG/KG

LD50 PASSER DOMESTICUS,(HOUSE SPARROW) MALES, ORAL 70.8 MG/KG (95% CONFIDENCE LIMIT: 43.4-116 MG/KG)

For more Ecotoxicity Values (Complete) data for OXYDEMETON-METHYL (17 total), please visit the HSDB record page.

Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 9(SRC), determined from a log Kow of -0.74(2) and a regression-derived equation(3), indicates that oxydemeton-methyl is expected to have very high mobility in soil(SRC). Volatilization of oxydemeton-methyl from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 1.6X10-13 atm-cu m/mole(SRC), using a fragment constant estimation method(4). Oxydemeton-methyl is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 2.85X10-5 mm Hg(2). Percent degradation of oxydemeton-methyl after 14 days ranged from 65-99% by various soil microorganisms(5).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 9(SRC), determined from a log Kow of -0.74(2) and a regression-derived equation(3), indicates that oxydemeton-methyl 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 1.6X10-13 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 3.1(SRC), from its log Kow(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is low. At 22 °C the half-lives for hydrolysis of oxydememton-methyl are estimated as 107, 46, and 2 days at pH 4, 7, and 9, respectively(2).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), oxydemeton-methyl, which has a vapor pressure of 2.85X10-5 mm Hg at 20 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase oxydemeton-methyl 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 3.6 hours(SRC), calculated from its rate constant of 1.1X10-10 cu cm/molecule-sec at 25 °C(SRC), that was derived using a structure estimation method(3). Particulate-phase oxydemeton-methyl may be removed from the air by wet and dry deposition(SRC).

Food Survey Values · 1 Eintrag

In the California Department of Food and Agriculture's Priority Pesticide Program in 1989, oxydemeton-methyl was analyzed for in samples of various commodities(2). Residues were found in the following commodities (commodity, samples analyzed, samples with residues): brussel sprouts, 23, 11; cabbage, 32, 3; cauliflower, 22, 2; peppers, 12, 3; chili peppers, 4, 1; and squash (winter or unspecified), 17,1(2). All residues were within tolerance(2). No residues were found in the following commodities (commodity, samples analyzed): string beans, 16; broccoli, 11; cantaloupe, 2; sweet corn, 1; cucumber, 7; honey due, 2; lettuce, 15; summer squash, 1; zucchini, 7(2). No oxydemeton-methyl was detected in 258 vegetable samples analyzed in Ontario-grown vegetables between 1980 and 1985(1). During FDA's regulatory monitoring of domestic and imported adult food eaten by infants and children between FY 1985 and 1991 (10,000 samples), oxydemeton-methyl was only found in 9 out of 2464 samples of domestic apples, maximum residue 0.39 ppm(3). Oxydemeton-methyl was not detected in any of the 27 market baskets of infant foods and adult foods eaten by infants and children during this time period(3). Oxydemeton-methyl was not found in foods studied in the Danish National Pesticide Monitoring Program 1995-1996(4).

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

Regulatorische Informationen

FIFRA Requirements · 3 Einträge

Tolerances are established for residues of the pesticide S-(2-(ethylsulfinyl)-ethyl) O,O-dimethyl phosphorothioate and its cholinesterase-inhibiting metabolites on the following raw agricultural commodities: alfalfa, green; alfalfa, hay, grown for seed; apple; bean, lima; bean, lima, forage; bean, snap, succulent; bean, snap, forage; beet, sugar; beet, sugar, tops; broccoli; Brussels sprouts; cabbage; cattle, fat; cattle, meat byproducts; cattle, meat; cauliflower; clover, forage; clover, hay, grown for seed; clover, seed screenings; corn, forage; corn, fresh, kernel plus cob with husks removed; corn, grain; corn, stover; cotton, undelinted seed; cucumber; eggplant; filbert; goat, fat; goat, meat byproducts; goat, meat; grapefruit; grape; hog, fat; hog, meat byproducts; hog, meat; horse, fat; horse, meat byproducts; horse, meat; lemon; lettuce, head; melon; milk; mint, hay; onion, dry bulb; orange, sweet; pear; pepper; plum, prune, fresh; pumpkin; safflower, seed; sheep, fat; sheep, meat byproducts; sheep, meat; sorghum, forage; sorghum, grain; sorghum milled fractions (except flour); squash, summer; squash, winter; strawberry; turnip; turnip, greens; and walnut.

Tolerances with regional registration, as defined in section 180.1(n), are established for residues of S-(2-(ethyl-sulfinyl)ethyl) O,O-dimethyl phosphorothioate and its cholinesterase-inhibiting metabolites in or on the following raw agricultural commodities: apricot.

As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their future use. Under this pesticide reregistration program, EPA examines health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether they are eligible for reregistration. In addition, all pesticides must meet the new safety standard of the Food Quality Protection Act of 1996. Oxydemeton-methyl is found on List A, which contains most food use pesticides and consists of the 194 chemical cases (or 350 individual active ingredients) for which EPA issued registration standards prior to FIFRA, as amended in 1988. Case No: 0258; Pesticide type: insecticide (acaricide); Case Status: In Pre-Special Review. The pesticide is in or has completed the reregistration process and, meanwhile, is also the subject of an in-depth Special Review.; Active ingredient (AI): Oxydemeton-methyl; Data Call-in (DCI) Date(s): 09/09/92, 04/15/93, 06/12/95, 10/13/95; AI Status: The producers of the pesticide has made commitments to conduct the studies and pay the fees required for reregistration, and are meeting those commitments in a timely manner.

Sicherheitsdaten

wgk
WGK 3
ridadr
3018
RTECS-Nr.
TG1420000
risk_code
24/25-50
Toxizität
LC50 (96-hour) for rainbow trout 4.0 mg/L (Walker, 1964); LC50 (24-hour) for rainbow trout and bluegill sunfish 10 mg/L (Hartley and Kidd, 1987); acute oral LD50 for rats 65–75 mg/kg (Hartley and Kidd, 1987), 30 mg/kg (RTECS, 1985).
hazard_code
T,N

Chemie und Industrie

Pharmakologische Informationen

Mechanism of Action · 1 Eintrag

Organophosphorus insecticides exert their acute effects in both insects and mammals by inhibiting acetylcholinesterase (AChE) in the nervous system with subsequent accumulation of toxic levels of acetylcholine (ACh), which is a neurotransmitter. In many cases, the organophosphorylated enzyme is fairly stable, so that recovery from intoxication may be slow. /Organophosphorus Pesticides/

Biological Half-Life · 2 Einträge

In a dermal absorption study..., radiolabeled /oxydemeton-methyl/ (ODM) (14C-ODM), at a single dose level of 2 mg/kg, was administered dermally or by iv injection to 3 Sprague-Dawley rats/sex/group/time period. ...The plasma half-life of ODM was 2 hr in both males and females following iv administration, and 3 hr in males and 4 hr in females following dermal exposure. For iv administration, the urine half-live was 5-14 hr in males and 2-20 hr females; and for the dermal exposure, 5-10 hr in males and 4-9 hr in females.

Following an oral dose of 5.0 mg/kg /14C-ODM/, tissue radioactivity was evaluated from 2 hr to 10 days post-dosing. The tissue levels of radioactivity paralleled that of the blood. Peak radioactivity in the blood occurred at 1 hr with elimination half-lives of 1.5 hours for the interval of 2-6 hours followed by a longer half-life of approximately 5 days for the interval of 6-24 hours. ...

Metabolism/Metabolites · 3 Einträge

In a metabolism study..., rats were dosed with 14C-1-ethylene-labeled ODM ( 14C-ODM) at a single at dose 1 mg/kg, either iv or orally (po), a single oral dose at 20 mg/kg, or with 14 daily oral doses of unlabeled ODM at 1 mg/kg/day followed by a single oral dose of 14C-ODM at 1 mg/kg. ...The identification of major urinary and fecal metabolites were determined for each treatment group. Analysis of the urinary radioactivity revealed that most of administered 14C-ODM was not metabolized. The respective % for males and females of unmetabolized ODM were 43% and 47% for the 1 mg/kg, iv group; 38% and 47% for the 1 mg/kg, po group; 34% and 55% for the repeat, 1 mg/kg/day, po group; and 59% and 74% for the 20 mg/kg, po group. Two major metabolites and three minor ones were also identified. One major metabolite was identified as 2- (ethylsulfinyl)-1-(methylsulfinyl) ethane, and accounted for 18-21% of the administered dose at 1 mg/kg, iv; 24-25%, at 1 mg/kg, po; 15%, at 15 x 1 mg/kg/day, po; and 5-6%, at 20 mg/kg, po. The second major metabolite was identified as 2-(ethylsulfonyl)-1-(methylsulfinyl) ethane; this metabolite accounted for 11-19% of the administered dose at 1 mg/kg, iv; 16-20%, at 1 mg/kg, po; 12-23%, at 15 x 1 mg/kg/day, po; and 6-19%, at 20 mg/kg, po. One minor metabolite (as a % of the administered dose for both males and females) was identified as ODM sulfone and was present at 1.7-3.4% of the total administered dose at 1 mg/kg, iv; 1.6%, at 1 mg/kg, po; 2.4-2.6%, at 15 x 1 mg/kg/day, po; and 2.6-3.9%, at 20 mg/kg, po. Two other minor metabolites were identified as desmethyl ODM and desmethyl ODM sulfone and were detected only in the 20 mg/kg, po, group at 2.6-3.1% and 1.0-3.1%, respectively. Primary fecal metabolites included unmetabolized ODM (0.2%), ODM sulfide (0.8%) and ODM sulfone (0.2%). The differences in the metabolic profiles suggests that the biotransformation may be saturated at high doses. The results indicate that at 20 mg/kg a marked increase in urinary excretion of unmetabolized parent compound (59-74%) in conjunction with a marked decline in the urinary excretion of metabolites compared to the corresponding values for males and female rats receiving 1 mg/kg (excretion of unmetabolized parent: 34-55%).

Demeton S-methyl sulfoxide is degraded by Pseudomonas putida 1453 by cleavage of thioester bond to form 2-(ethylsulfinyl)ethanethiol, 2-(ethylsulfonyl)ethanethiol and bis(2-(ethylsulfinyl)ethyl)disulfide. Nocardia sp dsm 43252 converts it into bis(2-(ethylsulfonyl)ethyl)disulfide, bis(2-(ethylsulfinyl)ethyl)sulfide, and bis(2-(ethylsulfonyl)ethyl)sulfide. o,o-Dimethylthiophosphoric acid was detected.

Metabolism occurs principally by oxidation, hydrolysis by esterases, and by transfer of portions of the molecule to glutathione. Oxidation of organophosphorus insecticides may result in more or less toxic products. The glutathione transferase reactions produce products, that are, in most cases, of low toxicity. Hydrolytic and transferase reactions affect both thioates and their oxons. /Organophosphorus Pesticides/

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 · 4 Einträge

Following an oral dose of 5.0 mg/kg /14C-ODM/, tissue radioactivity was evaluated from 2 hr to 10 days post-dosing. ...Measurement of tissue radioactivity at 2 hours post-dosing shows that the highest concentration of radioactivity was found in the kidney (4.8 ppm); this is understandable since the urine is the predominant route of elimination. The lowest tissue level was found in the brain (1.7 ppm). Of the other tissues analyzed, concentrations ranged from 2.2 ppm in renal fat to 3.9 ppm in the lung. The remaining tissues (muscle, skin, liver, adrenal gland and testes) concentrations were between 3.0 and 3.6 ppm. After one day the levels of tissue radioactivity were 45-106 times lower that the 2 hr values. By 10 days, residual tissue radioactivity was present and ranged from a low value of 0.00035 ppm in testes to 0.085 ppm in erythrocytes.

In a metabolism study..., rats were dosed with 14C-1-ethylene-labeled ODM ( 14C-ODM) at a single dose 1 mg/kg, either iv or orally (po), a single oral dose at 20 mg/kg, or with 14 daily oral doses of unlabeled ODM at 1 mg/kg/day followed by a single oral dose of 14C-ODM at 1 mg/kg. The results of this study show that 14C-ODM was rapidly absorbed, extensively metabolized, and rapidly excreted. Over a 3-day period, most (90-108%) of the administered dose was excreted. The radioactivity was recovered almost entirely in the urine (89-105% of the administered dose), while feces and expired CO2 accounted for 0.2-2.9% and 0.1% of the administered dose, respectively. There was no indication of bioaccumulation in any tissue or organ. ...The results indicate that at 20 mg/kg a marked increase in urinary excretion of unmetabolized parent compound (59-74%) in conjunction with a marked decline in the urinary excretion of metabolites compared to the corresponding values for males and female rats receiving 1 mg/kg (excretion of unmetabolized parent: 34-55%).

Whole body autoradiography was performed on rats dosed /with 14C-ODM/ iv at 1.0 mg/kg or orally at 10 mg/kg. Following the iv dosing the radioactivity was rapidly distributed throughout the body at 5 min post-dosing. The highest concentrations of radioactivity were found in the kidney, bladder, and accessory genital gland. Lower concentrations were found in the brain, spinal cord, and testes. The concentration in fatty tissues and boney structures were at the limit of detection. Autoradiographs taken 8 hours after the oral dose were found to be essentially the same as with iv administration.

In a dermal absorption study..., radiolabeled ODM (14C-ODM), at a single dose level of 2 mg/kg, was administered dermally or by iv injection to 3 Sprague-Dawley rats/sex/group/time period. Animals were sacrificed 2, 4, 8, 12, 24, 48 and 72 hours or until the radioactivity in urine dropped to 2 times background. For the dermally treated animals, a 12 sq cm area of the application site was removed, washed and counted. For each time period, radioactivity was counted in urine, plasma, the skin, skin solvent wash samples. ...Total recoveries for iv route of administration were 67% for males and 81% for females. For the dermal route of exposure total recoveries were 33% for males and 41% for females. Recoveries of ODM were low, probably due to metabolism and failing to include residual total body counts. Dermal absorption was calculated to be 50.4% for males and 51.8% for females. The dermal absorption rates, as calculated by regression analysis based on mg equivalents of 14C-ODM over time, were 0.15 g/sq cm/hr for males and 0.17 g/sq cm/hr for females.

Verwendung und Herstellung

Uses · 5 Einträge

Used as systemic insecticide and acaricide for cotton, vegetables, fruits, and field crops; [HSDB]

Banned in the EU for use as pesticide for plant protection; [eChemPortal: ESIS] Restricted use pesticide (RUP); [Reference #1]

Farming (Pesticides) [Category: Industry]

For oxydemeton-methyl (USEPA/OPP Pesticide Code: 058702) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

Systemic insecticide, acaricide, effective control by contact and systemic action of many destructive pests that attack certain vegetable, fruit and field crops. Primarily for aphids, mites, thrips, leafhoppers, and other sucking pests.

U.S. Production(1975) No Data
Consumption Patterns · 1 Eintrag

About 30% as an insecticide or acaricide on cotton; about 30% as an insecticide or acaricide on deciduous fruits and nuts; and about 30% as an insecticide or acaricide on vegetables; and about 10% as an insecticide or acaricide on other field crops (1974)

Methods of Manufacturing · 2 Einträge

Oxidation of o,o-dimethyl-s-(2-(ethylthio)ethyl) phosphorothioate

Produced by oxidation of demeton-s-methyl...with hydrogen peroxide (West German patent 947,368) or with chlorine or bromine (West German patent 949,229)...

Formulations/Preparations · 3 Einträge

Metasystox R: Soluble liquid (500 g active ingredient/L)

Croneton MR: Liquid (50 g methyl oxydemeton + 250 g ethiofencarb/L)

Emulsifiable concentrate (250 g active ingredient/L)

Use Classification · 2 Einträge

Insecticides

INSECTICIDES

Anwendungen · 2 Einträge

BeschreibungOxydemeton-methyl, i.e., demeton-S-methyl sulfoxide, is a colorless oil, bp 106 C/0.01 mm Hg, vp 3.8 mPa (20 C). It is miscible with water and soluble in most organic solvents, except petroleum ether. Log Kow = 0.74(21 C). Oxydemeton-methyl is relatively stable in acidic media but hydrolyzed in alkalinemedia;DT50 values (22 C) at pH 4, 7, and 9 are 107, 46, and 2 d, respectively.

VerwendenOxydemeton-methyl is used to control sucking insects on fruit, vines, vegetables, cereals and ornamentals.

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