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Parathion-methyl (ISO)
METHYL PARATHION · METACIDE · quinophos · CEKUMETHION · methylparathion (esa,jmaf) · DALF · e601 · a-gro
Identifikatoren & physikalische Daten
| CAS No. | 298-00-0 |
|---|---|
| Summenformel | C8H10NO5PS |
| Durchschnittliche Molmasse | 263,21 g/mol |
| Monoisotopische Masse | 263,00173059 g/mol |
| SMILES | COP(=S)(OC)Oc1ccc([N+](=O)[O-])cc1 |
| InChIKey | RLBIQVVOMOPOHC-UHFFFAOYSA-N |
| PubChem CID | 4130 |
| ChEMBL | CHEMBL346516 |
| ChEBI | CHEBI:38746 |
| EC No. | 206-050-1 |
| DTXSID | DTXSID1020855 |
| Lokaler Name | Parathion-methyl (ISO) |
Chemische & physikalische Eigenschaften
| XLogP | 2,9 |
|---|---|
| Polarare Oberfläche (TPSA) | 106 |
| H-Brücken-Donoren | 0 |
| H-Brücken-Akzeptoren | 6 |
| Frei drehbare Bindungen | 4 |
| Schwere Atome | 16 |
| Formalladung | 0 |
| Komplexität | 279 |
| LogP (Verteilungskoeffizient) | log Kow = 2.862-3 |
| Geruch | Pungent, garlic-like odorOdorless |
| Dichte | 1.358 at 68 °F (EPA, 1998) - Denser than waterwill sink1.358 g/cu cm at 20 °C1.4 g/cm³1.361.358 @ 20°C |
| Color/Form | CrystalsWhite crystalline solidCrystals from cold methanolWhite to tan, crystalline solid or powder [Note: The commercial product in xylene is a tan liquid]Colorless crystals |
| Löslichkeit | less than 1 mg/mL at 73 °F (NTP, 1992)In water, 37.7 mg/L at 20 °CSoluble in organic solventsReadily soluble in common organic solvents, e.g. dichloromethane, toluene >200, hexane 10 to 20 (all in g/L at 20 °C). Sparingly soluble in petroleum ether and some types of mineral oil.Readily soluble in 2-propanol. Hardly soluble in n-hexaneSolubility in water, g/100ml: 0.006Chloroform: Slightly Soluble,Methanol: Slightly Soluble0.005 g/100 mL |
| Flammpunkt | commercial product, containing xylene, has flashpoint of 115F (EPA, 1998)42 °C (Closed cup)46.1°C |
| Siedepunkt | 246 °F at 0.13 mmHg (NTP, 1992)154 °C at 136 Pa289 °F143°C (1.0 mmHg) |
| Decomposition | When heated to decomp it emits very toxic fumes of /nitrogen oxides, phosphorous oxides, and sulfur oxides/.120 °C |
| Schmelzpunkt | 99 to 100 °F (EPA, 1998)35.8 °CMP: 37-38 °C35-38 °C99 °F36°C |
| Dampfdichte | 9.1 (NTP, 1992) - Heavier than airwill sink (Relative to Air) |
| Geruchsschwelle | Odor Threshold Low: 0.0012 [mg/m3]Odor threshold from AIHA0.1328 mg/cu m odor low and high.1.23X10-2 ppm (detection in waterpurity not specified) |
| Dampfdruck | 9.7e-06 mmHg at 68 °F (EPA, 1998)0.0000035 [mmHg]3.5X10-6 mm Hg at 25 °CVapor pressure, Pa at 20 °C: 0.0010.00001 mmHg4.1×10-4 Pa (20 °C) |
| Brechungsindex | nD25 1.5367 |
| Lagerbedingungen | APPROX 4°C |
| Aggregatzustand | solid |
| BRN | 8905814 |
| Henry-Konstante | 5.0×101 mol/(m3Pa) at 25℃, Mackay and Shiu (1981) |
| Stabilität | Stable. Flammable. |
| CAS Datenbank | 298-00-0(CAS DataBase Reference) |
| NIST chemische Informationen | Phosphorothioic acid, o,o-dimethyl-o-p-nitrophenyl ester(298-00-0) |
| EPA chemische Informationen | Methyl parathion (298-00-0) |
Sicherheit & Vorschriften
| GHS-Einstufung | DangerH226: Flammable liquid and vapor [Warning Flammable liquids]H300: Fatal if swallowed [Danger Acute toxicity, oral]H311: Toxic in contact with skin [Danger Acute toxicity, dermal]H330: Fatal if inhaled [Danger Acute toxicity, inhalation]H373 **: May causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure]H400: Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]H410: Very toxic to aquatic life with long lasting effects [Warning Hazardous to the aquatic environment, long-term hazard]P210, P233, P240, P241, P242, P243, P260, P262, P264, P270, P271, P273, P280, P284, P301+P316, P302+P352, P303+P361+P353, P304+P340, P316, P319, P320, P321, P330, P361+P364, P370+P378, P391, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement) |
|---|---|
| Regulatorische Informationen | Hazard Traits - Developmental ToxicityEnvironmental toxNeurotoxicityAuthoritative List - ATSDR NeurotoxicantsCECBP - Priority ChemicalsCWA 303(d)Report - if used as a fragrance or flavor ingredientRegulation (EC) No 1107/2009 (amended)03/166/ECThe 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.) |
| Weitere Sicherheitsinformationen | IMAP assessments - Phosphorothioic acid, O,O-dimethyl O-(4-nitrophenyl) ester: Environment tier I assessmentIMAP assessments - Phosphorothioic acid, O,O-dimethyl O-(4-nitrophenyl) ester: Human health tier I assessment |
| DOT-Kennzeichnung | Poison Flammable Liquid |
| Brandgefahren | Poisonous gases are produced in fire and when heated. Decomposition may lead to sufficient internal pressure to cause the container to rupture violently. Avoid oxidizing materials. Unstable. High temperatures (120F) cause decomposition. (EPA, 1998)Combustible. Liquid formulations containing organic solvents may be flammable. Gives off irritating or toxic fumes (or gases) in a fire. |
| Gesundheitsgefahren | This material is extremely toxicthe probable oral lethal dose is 5-50 mg/kg, or between 7 drops and 1 teaspoonful for a 150-lb. person. Chronic toxicity does not appear to be a major consideration. (EPA, 1998) |
| Gefahrenübersicht | Methyl parathion is an insecticide that does not occur naturally in the environment. Pure methyl parathion exists as white crystals. Impure methyl parathion is a brownish liquid that smells like rotten eggs.Methyl parathion is used to kill insects on farm crops, especially cotton. The EPA now restricts how methyl parathion can be used and appliedonly trained people are allowed to spray it. Methyl parathion can no longer be used on food crops commonly consumed by children.Classified as highly toxic, and most formulations may be used only by certified applicators[EXTOXNET] Allergic contact dermatitis reported in sprayers[Kanerva, p. 1431] 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] |
| DOT-Nummer und Handbuch | 2783 152(solid)3018 152(liquid) |
| Reaktive Gruppe | Nitro, Nitroso, Nitrate, and Nitrite Compounds, OrganicSulfonates, Phosphonates, and Thiophosphonates, Organic |
| EG-Einstufung | Symbol: T+, NR: 5-10-24-26/28-48/22-50/53S: (1/2)-28-36/37-45-60-61 |
| UN-Einstufung | UN Hazard Class: 6.1UN Pack Group: II |
| Special Reports | Toxicology Review: Air Quality Monographs No.73-19 (1973))Toxicology Review: Residue Reviews 46: 1 (1973)Toxicology Review: Economie et Medecine Animales 14 (3): 141 (1973)Toxicology Review: Deutsche Tieraerztliche Wochenschrift 80 (20): 485 (1973)For more Special Reports (Complete) data for METHYL PARATHION (13 total), please visit the HSDB record page. |
| RCRA-Anforderungen | P071As stipulated in 40 CFR 261.33, when methyl parathion, as a commercial chemical product or manufacturing chemical intermediate or an off-specification commercial chemical product or a manufacturing chemical intermediate, becomes a waste, it must be managed according to federal and/or state hazardous waste regulations. Also defined as a hazardous waste is any container or inner liner used to hold this waste or any residue, contaminated soil, water, or other debris resulting from the cleanup of a spill, into water or on dry land, of this waste. Generators of small quantities of this waste may qualify for partial exclusion from hazardous waste regulations (40 CFR 261.5(e)). |
| Brandbekämpfung | Fight fire from maximum distance. Dike fire control water for later disposaldo not scatter the material. Wear special protective clothing.For small fires, use dry chemical, carbon dioxide, water spray, or foam. For large fires, use water spray, fog, or foam. (EPA, 1998)Use water spray, foam, powder, carbon dioxide. |
| Erste-Hilfe-Maßnahmen | Fresh air, rest. Artificial respiration may be needed. Refer for medical attention.Remove contaminated clothes. Rinse and then wash skin with water and soap. Refer for medical attention .First rinse with plenty of water for several minutes (remove contact lenses if easily possible), then refer for medical attention.Induce vomiting (ONLY IN CONSCIOUS PERSONS!). Give a slurry of activated charcoal in water to drink. Refer immediately for medical attention. |
| Erste Hilfe | Note: Parathion-methyl is a cholinesterase inhibitor.Signs and Symptoms of Acute Parathion-Methyl Exposure: Acute exposure to parathion-methyl may produce the following signs and symptoms: pinpoint pupils, blurred vision, headache, dizziness, muscle spasms, and profound weakness. Vomiting, diarrhea, abdominal pain, seizures, and coma may also occur. The heart rate may decrease following oral exposure or increase following dermal exposure. Hypotension (low blood pressure) may occur although hypertension (high blood pressure) is not uncommon. Chest pain may be noted. Respiratory symptoms include dyspnea (shortness of breath), respiratory depression, and respiratory paralysis. Psychosis may occur.Emergency Life-Support Procedures: Acute exposure to parathion-methyl may require decontamination and life support for the victims. Emergency personnel should wear protective clothing appropriate to the type and degree of contamination. Air-purifying or supplied-air respiratory equipment should also be worn, as necessary. Rescue vehicles should carry supplies such as plastic sheeting and disposable plastic bags to assist in preventing spread of contamination.Inhalation Exposure:1. Move victims to fresh air. Emergency personnel should avoid self-exposure to parathion-methyl.2. Evaluate vital signs including pulse and respiratory rate, and note any trauma. If no pulse is detected, provide CPR. If not breathing, provide artificial respiration. If breathing is labored, administer oxygen or other respiratory support.3. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures.4. Transport to a health care facility.Dermal/Eye Exposure:1. Remove victims from exposure. Emergency personnel should avoid self- exposure to parathion-methyl.3. Remove contaminated clothing as soon as possible.4. If eye exposure has occurred, eyes must be flushed with lukewarm water for at least 15 minutes.5. Wash exposed skin areas three times with soap and water.6. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures.7. Transport to a health care facility.Ingestion Exposure:1. Evaluate vital signs including pulse and respiratory rate, and note any trauma. If no pulse is detected, provide CPR. If not breathing, provide artificial respiration. If breathing is labored, administer oxygen or other respiratory support.2. Obtain authorization and/or further instructions from the local hospital for administration of an antidote or performance of other invasive procedures.3. Vomiting may be induced with syrup of Ipecac. If elapsed time since ingestion of parathion-methyl is unknown or suspected to be greater than 30 minutes, do not induce vomiting and proceed to Step(General first aid procedures)Eye: Irrigate immediately - If this chemical contacts the eyes, immediately wash (irrigate) the eyes with large amounts of water, occasionally lifting the lower and upper lids. Get medical attention immediately.Skin: Soap wash immediately - If this chemical contacts the skin, immediately wash the contaminated skin with soap and water. If this chemical penetrates the clothing, immediately remove the clothing, wash the skin with soap and water, and get medical attention promptly.Breathing: Respiratory supportSwallow: Medical attention immediately - If this chemical has been swallowed, get medical attention immediately. |
| Sichere Lagerung | Store in an area without drain or sewer access. Keep in a well-ventilated room. Separated from food and feedstuffs. |
| Expositionsschutz und Persönliche Schutzausrüstung | Biological Exposure Indices (BEI) [ACGIH] - Acetylcholinesterase activity in red blood cells = 70% of individual's baselineButylcholinesterase activity in serum or plasma = 60% of individual's baselineSample at end of shift[TLVs and BEIs] |
| Brandbekämpfungsverfahren | Suitable extinguishing media: Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide. Advice for firefighters: Wear self contained breathing apparatus for fire fighting if necessary.Fire Extinguishing Media: Dry chemical, carbon dioxide for small fires. Water spray or foam for large fires. |
| Lagerbedingungen | Keep container tightly closed in a dry and well-ventilated place.Store in original container, preferably in a locked area, away from children, feed, food. Do not heat above 55 °C. Decomposes rapidly above 100 °C, explosion may be induced. |
| Reinigungsverfahren | Personal precautions, protective equipment and emergency procedures: Wear respiratory protection. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure adequate ventilation. Evacuate personnel to safe areas. Avoid breathing dust. Environmental precautions: Prevent further leakage or spillage if safe to do so. Do not let product enter drains. Discharge into the environment must be avoided. Methods and materials for containment and cleaning up: Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed containers for disposal. |
| Freisetung ohne Brand | Excerpt from ERG Guide 131 [Flammable Liquids - Toxic]:ELIMINATE all ignition sources (no smoking, flares, sparks or flames) from immediate area. All equipment used when handling the product must be grounded. Do not touch or walk through spilled material. Stop leak if you can do it without risk. Prevent entry into waterways, sewers, basements or confined areas. A vapor-suppressing foam may be used to reduce vapors.SMALL SPILL: Absorb with earth, sand or other non-combustible material and transfer to containers for later disposal. Use clean, non-sparking tools to collect absorbed material.LARGE SPILL: Dike far ahead of liquid spill for later disposal. Water spray may reduce vapor, but may not prevent ignition in closed spaces. (ERG, 2024) |
| Entsorgungsverfahren | Generators of waste (equal to or greater than 100 kg/mo) containing this contaminant, EPA hazardous waste number P071, must conform with USEPA regulations in storage, transportation, treatment and disposal of waste.The reduction of methyl parathion with acid and zinc was explored to determine whether this would accelerate degradation of methyl parathion to its less toxic p-aminophenyl deriv and/or produce less toxic breakdown products. Methyl parathion disappearance was followed for 2.5 yr. The acidified powdered zinc treatment at burial proved effective in degrading methyl parathion.The following wastewater treatment technologies have been investigated for methyl parathion: Reverse osmosis.A potential candidate for fluidized bed incineration at a temperature range of 450 to 980 °C and residence times of seconds for liquids and gases, and longer for solids. A potential candidate for rotary kiln incineration at a temperature range of 820 to 1,600 °C and residence times of seconds for liquids and gases, and hours for solids.For more Disposal Methods (Complete) data for METHYL PARATHION (7 total), please visit the HSDB record page. |
| Verschüttetes entsorgen | Personal protection: chemical protection suit including self-contained breathing apparatus. Do NOT let this chemical enter the environment. Sweep spilled substance into covered containers. If appropriate, moisten first to prevent dusting. Carefully collect remainder. Then store and dispose of according to local regulations. |
| Preventive Measures | Based on a study, contaminated denim fabrics should not be laundered in 30 °C (85 °F) temperatureHotter temperatures are more effective to decontaminate work clothing. Although detergents could not be statistically separated, heavy duty liquid detergents appeared to excel in providing higher levels of pesticide removal in water temperatures of 49 °C and 60 °C.Storage, preparation, dispensing (including vending machines), or eating of foods or beverages shall be prohibited in areas where methyl parathion is present. ... Smoking shall be prohibited in areas where methyl parathion is present.All required personal protective clothing and protective equipment shall be provided by the employer and shall be laundered or cleaned daily. ... Personal protective clothing grossly contaminated with methyl parathion shall be decontaminated and laundered separately from other clothing. ... Employees occupationally exposed to methyl parathion shall be required to wash their hands and face with alkaline soap and water before eating, drinking, smoking, and using toilet facilities.It is recommended that clothing (such as denim) contaminated with high concn of methyl parathion be disposed of by burning or burial, as the fabric remains unsafe to the wearer. Fabrics contaminated with lesser methyl parathion concn require a minimum of 3 launderings before biological activity reaches a harmless level. Procedures such as pre-washing and/or multiple washing, appear to be more effective.For more Preventive Measures (Complete) data for METHYL PARATHION (10 total), please visit the HSDB record page. |
| Toxikologische Informationen | CDC-ATSDR Toxicological Profile |
| Körperbelastung | A metabolite of ethyl and methyl parathion (p-nitrophenol) was detected in 2.4% of 6990 urine samples collected from USA persons (12-74 yrs old) between 1976-80(1). 15,904 urine samples from residents of innercity USA homes in seven states which had been illegally treated with methyl parathion for control of cockroaches contained p-nitrophenol at a mean concentration of 75 ug/L, range of <25 to 45,000 ug/L, and a 57% frequency of detection(2). |
| Treatment | If the compound has been ingested, rapid gastric lavage should be performed using 5% sodium bicarbonate. For skin contact, the skin should be washed with soap and water. If the compound has entered the eyes, they should be washed with large quantities of isotonic saline or water. In serious cases, atropine and/or pralidoxime should be administered. Anti-cholinergic drugs work to counteract the effects of excess acetylcholine and reactivate AChE. Atropine can be used as an antidote in conjunction with pralidoxime or other pyridinium oximes (such as trimedoxime or obidoxime), though the use of '-oximes' has been found to be of no benefit, or possibly harmful, in at least two meta-analyses. Atropine is a muscarinic antagonist, and thus blocks the action of acetylcholine peripherally. |
| Wechselwirkungen | Pre-treatment of mice with piperonyl butoxide, the mono-oxygenase inhibitor, before challenge with parathion and methyl parathion led to two-fold potentiation and forty-fold antagonism, respectively. ... Diminution in toxicity of methyl parathion ... must be largely to inhibition of oxon formation. ... When mice were pretreated with diethyl maleate, which depletes hepatic glutathione, methyl parathion toxicity was potentiated four-fold.In mice and rats, pretreatment with cimetidine (75 mg/kg/ip) 30 min prior to methyl parathion administration reduced lethality and delayed the onset of cholinergic signs of toxicity. When cimetidine was administered simultaneously with methyl parathion to mice, neither methyl parathion induced lethality nor cholinergic signs of toxicity were altered. Cimetidine pretreatment failed to decrease parathion induced toxicity in mice.A toxic unit approach was used to test the response addition model for mixtures of pesticides with differing modes of action. Atrazine was tested in binary and ternary combinations with the organochlorine insecticide methoxychlor and organophosphate insecticide methyl-parathion. Atrazine was also tested in binary combinations with additional organophosphates. The toxic unit for atrazine was set slightly below its water solubility limits (toxic unit = 20 ppm), which is well below its 96-hr 50% effective concentration for the fourth instar of the midge, Chironomus tentans. In 96-hr acute toxicity tests using C. tentans, atrazine was found to produce synergistic (greater than additive) toxicity in a binary mixture with methyl-parathion. Less than additive toxicity was found for the combination of atrazine with methoxychlor (likely due to the low toxic unit assigned to atrazine). The ternary combination of atrazine + methyl-parathion + methoxychlor was found to be marginally synergistic. Results of toxicity tests with atrazine in binary combinations with other organophosphates indicate more than additive toxicity for all compounds except mevinophos. Possible hypotheses are presented in an attempt to explain the noted synergistic relationship between atrazine and various organophosphorous insecticides. These results suggest that the response addition model does not always accurately predict mixture toxicity for chemicals with differing modes of action.This study, carried out on the estuarine crab Chasmagnathus granulata, had two main objectives: (i) to correlate inhibition of the cholinesterase activity in the thoracic ganglia caused by a commercial formulation of methyl parathion (O,O-dimethyl-o-p-nitro-phenyl phosphorothionate) with crab mortalityand (ii) to investigate the methyl parathion bioactivation mechanisms. In crabs not pre-exposed to sesamol (3, 4-methylenedioxyphenol), in vivo cholinesterase inhibition showed a dose-related response (ID50 = 0.36 mg/kg, it showed not to be a good tool to establish an effective dose since small amounts of inhibition were correlated to mortalities as high as 50%. Methyl parathion was more toxic to crabs not pre-exposed to sesamol (96 hr LD50 = 0.21 mg/kg pre-exposed to the MFO-inhibitor (96 hr LD50 = 1.02 mg/kg). Pre-exposure to sesamol seems to prevent methyl parathion oxidation, and consequently, its toxicity since the cholinesterase inhibition in crabs pre-exposed to sesamol was lower than that observed in those not pre-exposed to sesamol. In accordance to the idea that the anticholinesterase property of methyl parathion is acquired only after its oxidation, a higher in vitro cholinesterase inhibition induced by chemically oxidized methyl parathion (IC50 = 0.114 uM) in relation to that caused by the fresh methyl parathion (IC50 = 19.2 uM) was observed.For more Interactions (Complete) data for METHYL PARATHION (41 total), please visit the HSDB record page. |
| Zielorgane | Developmental (effects while organs are developing), Hematological (Blood Forming), Neurological (Nervous System)Eyes, skin, respiratory system, central nervous system, cardiovascular system, blood cholinesterase |
| Gesundheitliche Auswirkungen | Acute exposure to cholinesterase inhibitors can cause a cholinergic crisis characterized by severe nausea/vomiting, salivation, sweating, bradycardia, hypotension, collapse, and convulsions. Increasing muscle weakness is a possibility and may result in death if respiratory muscles are involved. Accumulation of ACh at motor nerves causes overstimulation of nicotinic expression at the neuromuscular junction. When this occurs symptoms such as muscle weakness, fatigue, muscle cramps, fasciculation, and paralysis can be seen. When there is an accumulation of ACh at autonomic ganglia this causes overstimulation of nicotinic expression in the sympathetic system. Symptoms associated with this are hypertension, and hypoglycemia. Overstimulation of nicotinic acetylcholine receptors in the central nervous system, due to accumulation of ACh, results in anxiety, headache, convulsions, ataxia, depression of respiration and circulation, tremor, general weakness, and potentially coma. When there is expression of muscarinic overstimulation due to excess acetylcholine at muscarinic acetylcholine receptors symptoms of visual disturbances, tightness in chest, wheezing due to bronchoconstriction, increased bronchial secretions, increased salivation, lacrimation, sweating, peristalsis, and urination can occur. Certain reproductive effects in fertility, growth, and development for males and females have been linked specifically to organophosphate pesticide exposure. Most of the research on reproductive effects has been conducted on farmers working with pesticides and insecticdes in rural areas. In females menstrual cycle disturbances, longer pregnancies, spontaneous abortions, stillbirths, and some developmental effects in offspring have been linked to organophosphate pesticide exposure. Prenatal exposure has been linked to impaired fetal growth and development. Neurotoxic effects have also been linked to poisoning with OP pesticides causing four neurotoxic effects in humans: cholinergi |
| Ökotoxizitätswerte | EC50Species: Simocephalus serrulatus (daphnid) 1st instarConditions: static bioassay, 15 °CConcentration: 0.37 ug/L for 48 hr (95% confidence limit 0.23-0.57 ug/L)Effect: immobilization. /Technical material, 80-99%/Species: Daphnia magna (daphnid) 1st instarConditions: static bioassay, 21 °CConcentration: 0.14 ug/L for 48 hr (95% confidence limit 0.09-0.20 ug/L)LC50Species: Gammarus fasciatus (scud) matureConcentration: 3.8 ug/L for 96 hr (95% confidence limit 2.6-5.5 ug/L) /Technical material, 80-99%/Species: Orconectes nais (crayfish) matureConditions: static bioassay, 15 °C, hard waterConcentration: 15 ug/L for 96 hr /Technical material, 80-99%/For more Ecotoxicity Values (Complete) data for METHYL PARATHION (90 total), please visit the HSDB record page. |
| Umweltverhalten | TERRESTRIAL FATE: Based on a classification scheme(1), Koc values ranging from 366 to 1,516(2,3) indicate that methyl parathion is expected to have moderate to low mobility in soil(SRC). Volatilization of methyl parathion from moist soil surfaces is not expected to be an important fate process(SRC) given a Henry's Law constant of 1.0X10-7 atm-cu m/mole(4). Methyl parathion is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 3.5X10-6 mm Hg at 25 °C(5). Hydrolysis is expected to be an important process in moist soils(SRC), since methyl parathion hydrolyzes in natural water with half-lives ranging from 6.5 to 13 days at 40 °C and pH values less than 8(6). Utilizing loam soils maintained at 10 and 33 kPa soil-water tension, 14C-methyl parathion was approximately 50% mineralized in 28 days(7), indicating that biodegradation is an important environmental fate process in soil(SRC).TERRESTRIAL FATE: Simulated spillage of emulsifiable concentrate and microencapsulated formulations of methyl parathion on soil were studied. Persistence of residues from both formulations spilled as concentration and as simulated drum rinses were followed for up to 45 mo. Spillage of encapsulated formulation resulted in the formation of a solid cake-like deposit on the soil surface. At 45 mo, soil residues had decreased by 64% for emulsifiable concentrate spills, and 68% for the soil beneath the cake. Residue in the cake itself only decr by 31%. Soil residue levels from simulated drum rinses were essentially innocuous by 45 mo for the emulsifiable concentrate and by 1 yr for the microencapsulated material.TERRESTRIAL FATE: 73 acres of alfalfa in Vernal, Utah, were sprayed with an emulsifiable concentrate (EC) containing 6 lb/gal ethyl parathion and 3 lb/gal methyl parathion. The material was applied at 4.15X10-2 gal/acre. Wind conditions were negligible. Samples were taken from the sprayed plot (sites A and B) and from an adjoining non-target pasture (site C). Immediately after treatment, methyl parathion residues averaged 40% of ethyl parathion levels at the 3 sampling stations. Foliar residues of the parent cmpd dissipated rapidly with time. At Site A, the residues dropped below 1.25 mg/kg within 28 hr for methyl parathion. First-order half-life of methyl parathion was 12 hr.AQUATIC FATE: Based on a classification scheme(1), Koc values ranging from 366 to 1,516(2,3) indicate that methyl parathion is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is not expected(4) based upon a Henry's Law constant of 1.0X10-7 atm-cu m/mole(5). According to a classification scheme(6), a BCF range of 8.3 to 959(7,8) suggests bioconcentration in aquatic organisms is low to moderate(SRC). However, methyl parathion is rapidly metabolized in some aquatic organisms(9). Aqueous photolysis half-lives range from 8 to 38 days(10). Hydrolysis is expected to be an important environmental fate process since this compound exhibits half-lives from 6.5 to 13 days at 40 °C in natural waterspH values were less than 8(11). The half-life of methyl parathion in untreated estuarine sediment water studies was 1.2 days (95% confidence limit 0.60-2.0 days). The half-life of methyl parathion in untreated estuarine sediment water studies was 1.2 days (95% confidence limit 0.60-2.0 days)(12). Utilizing a river die-away test using water and sediment cores, methyl parathion had half-lives of 77 to 154 hrs, while in a sterile control the half-life was 367 hrs(13), indicating that biodegradation is 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), methyl parathion, which has a vapor pressure of 3.5X10-6 mm Hg at 25 °C(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase methyl parathion 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 0.3 days(SRC), calculated from its rate constant of 5.9X10-11 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase methyl parathion may be removed from the air by wet and dry deposition(SRC). Methyl parathion absorbs light at wavelengths between 290 and 410 nm(4) and, therefore, may be susceptible to direct photolysis by sunlight(SRC). |
| Lebensmitteluntersuchungswerte | Methyl parathion was detected at concentrations ranging from 0.002 to 0.008 mg/kg in canned food and 0.003 to 0.007 mg/kg in fruit in New Zealand in 1974 and 0.018 to 0.029 mg/kg in leafy vegetables in Canada in 1972(1). In the Total Diet Program (US FDA, 1971-75) methyl parathion was detected in fruits, 0.007 mg/kg and leaf vegetables, trace to 0.010 mg/kg(1). In Market Basket Surveys (US FDA, 1966-69), methyl parathion was detected in leafy and stem vegetables at levels of 0 to >2.00 mg/kg and in root vegetables at levels of 0 to 1.00 mg/kg(1). Results of the FDA Total Diet Studies for fiscal years 1981-82: methyl parathion was detected in 4 of 327 food composites, collected from markets in 27 US cities, at levels ranging from 0.001 to 0.003 ppm, positive detections were in grain and cereal products, leafy vegetables, and root vegetable food groups(2). Methyl parathion was detected in 22 of 6,391 domestic agricultural commodities (celery, oranges, tangerines, alfalfa feed hay, iceburg lettuce, parsley, spinach) and in 67 of 12,044 imported agricultural commodities sampled by the U.S. FDA's Los Angeles District between Oct 1981 to Sept 1986(8). Methyl parathion was detected in peaches-apricots and lettuce in Rome, Italy at concentrations ranging (average) from less than or equal to 3.2 to 4.5 (2.5) ug/kg and less than 3.2 to 18 (3.6) ug/kg, respectively(4). Methyl parathion was detected in fresh carrots in Canada sampled between Jan 1992 and March 1994(5). It was detected in the following imported agricultural commodities in Canada sampled between Jan 1992 and March 1994: fresh apples, fresh grapes, fresh oranges, fresh pears, fresh snowpeas, and fresh tomatoes(5). Methyl parathion was detected in 8 of 234 ready-to-eat foods tested repetitively for 10 years, 1982 to 1991, through the US FDA's Revised Market Basket Survey at an average concentration of 0.0035 ug/g(6). In an FDA survey of domestic and imported pears (tomatoes) conducted between 1992 and 1993, methylMethyl parathion concentrations in seasonal vegetables collected directly from the field in the Agra District, India(1).Table: Average Methyl Parathion Concn (ug/kg) [Table#2930]Methyl parathion in four fresh vegetables from three Chinese agricultural markets(1).Table: Metyl Parathion Concn in ug/g fresh weight [Table#2931]Methyl parathion was detected in 2 of 54 potato samples collected from Egyptian markets between March 1991 and Jan 1992 at concentrations of 0.389 and 0.540 ppm(1). Methyl parathion was detected in 40% of rice, 60% of avocados, 30% of strawberries, and 50% of tomatoes sampled in Mexico(2). Methyl parathion was detected in the following vegetables collected from growers' fields and main selling points in Pakistan between 1988 and 1992 (number of times detected and number of samples, concentration): luffa (turi) (1 of 11, 1.71 mg/kg), cauliflower (1 of 14, 2.5 mg/kg), spinach (1 of 16, 0.15 mg/kg), coriander (1 of 10, 1.5 mg/kg), bitter gourd (1 of 12, 4.0 mg/kg), fenugreek (1 of 8, 0.5 mg/kg), onion (3 of 18, 1.09 to 3.15 m/kg), and Lady's finger (4 of 28, 1.83 to 2.83 mg/kg)(3). Methyl parathion was detected in the following citrus fruits collected from the Valencian Community, Spain, between 1994 and 1995: Clementine 0.2 mg/kg, Navelate orange 0.3 to 0.5 mg/kg, Lanelate orange 0.1 to 1.1 mg/kg, Salustiana orange 0.5 to 3.8, Valencilate orange 0.3 to 0.9, and Star Ruby grapefruit 0.30(4). The compound was detected in citrus fruit in France at concentrations ranging from 0.003 to 1.25 ppm(5). Methyl parathion was detected in 26 of 2223 produce samples (700 vegetables and 1523 fruits) monitored in Sao Paulo City, Brazil, 1994-2001. The 26 positive samples included guava, lettuce, peach, and strawberryrange 0.10-0.41 ug/kg, mean of 0.15 ug/kg(6). |
| Unerwünschte Wirkungen | Other Poison - OrganophosphateSkin Sensitizer - An agent that can induce an allergic reaction in the skin.ACGIH Carcinogen - Not Classifiable. |
| Expositionspfade | The substance can be absorbed into the body by inhalation of its aerosol, through the skin and by ingestion.inhalation, skin absorption, ingestion, skin and/or eye contactOral (L634)inhalation (L634)dermal (L634). |
| Milk Concentrations | Methyl parathion was not detected in samples from tank trucks during the delivery of 3,974 tons Italian raw milk, sampled during delivery times of Oct 2004, Jan 2005, and May 2005detection limit = 1 ug/kg(1). |
| FIFRA-Anforderungen | The following uses of pesticide products containing the active ingredients specified below have been classified for restricted use and are limited to use by or under the direct supervision of a certified applicator.[Table#2927]Tolerances are established for residues of the insecticide methyl parathion, including its metabolites and degradates, in or on the commodities in the table in this paragraph. Compliance with the tolerance levels specified in this paragraph is to be determined by measuring only methyl parathion, O,O-dimethyl O-(4-nitrophenyl) phosphorothioate, in or on the commodity.[Table#2928]While petitions for tolerances for negligible residues are pending and until action is completed on these petitions, interim tolerances are established for residues of the listed pesticide chemicals in or on the following raw agricultural commodities:[Table#2929]... EPA has completed its assessment of the cumulative risks from the organophosphate (OP) class of pesticides as required by the Food Quality Protection Act of 1996. In addition, the individual OPs have also been subject to review through the individual-chemical review process. The Agency's review of individual OPs has resulted in the issuance of Interim Reregistration Eligibility Decisions (IREDs) for 22 OPs /including methyl parathion/, interim Tolerance Reassessment and Risk Management Decisions (TREDs) for 8 OPs, and a Reregistration Eligibility Decision (RED) for one OP, malathion. ... EPA has concluded, after completing its assessment of the cumulative risks associated with exposures to all of the OPs, that: (1) the pesticides covered by the IREDs that were pending the results of the OP cumulative assessment ... are indeed eligible for reregistrationand (2) the pesticide tolerances covered by the IREDs and TREDs that were pending the results of the OP cumulative assessment ... meet the safety standard under Section 408(b)(2) of the FFDCA. Thus, with regard to the OPs, EPA has fulfilled its obligations as to FFDCA tolerance reassessment and FIFRA reregistration, other than product-specific reregistration.For more FIFRA Requirements (Complete) data for METHYL PARATHION (6 total), please visit the HSDB record page. |
| CERCLA-Meldepflichtmengen | Persons in charge of vessels or facilities are required to notify the National Response Center (NRC) immediately, when there is a release of this designated hazardous substance, in an amount equal to or greater than its reportable quantity of 100 lb or 45.5 kg. The toll free number of the NRC is (800) 424-8802. The rule for determining when notification is required is stated in 40 CFR 302.4 (section IV. D.3.b).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. Methyl parathion is an extremely hazardous substance (EHS) subject to reporting requirements when stored in amounts in excess of its threshold planning quantity (TPQ) of 100 or 10,000 lbs. Extremely hazardous substances that are solids are subject to either of two threshold planning quantities ... The lower quantity applies only if the solid exists in powdered form and has a particle size less than 100 micronsor is handled in solution or in molten formor meets the criteria for a National Fire Protection Association (NFPA) rating of 2, 3 or 4 for reactivity. If the solid does not meet any of these criteria, it is subject to the upper ... threshold planning quantity ... . |
| Clean Water Act Anforderungen | Methyl parathion is designated as a hazardous substance under section 311(b)(2)(A) of the Federal Water Pollution Control Act and further regulated by the Clean Water Act Amendments of 1977 and 1978. These regulations apply to discharges of this substance. This designation includes any isomers and hydrates, as well as any solutions and mixtures containing this substance. |
| Landesrichtlinien für Trinkwasser | (AZ) ARIZONA 1.8 ug/L(CA) CALIFORNIA 2 ug/L(FL) FLORIDA 10 ug/L(ME) MAINE 2 ug/L |
| Bundesrichtlinien für Trinkwasser | EPA 1 ug/L |
| Berufliche Expositionsstufe (OEB) | C |
| Arbeitsplatzgrenzwert (OEL) | TWA: 0.2 mg/m3 [skin] |
| Wassergefährdungsklasse (WGK) | 3 |
| UN-Transportnummer | UN 2052/2783/2811 |
| Zollcode | 29201100 |
| RTECS-Nr. | TG0175000 |
| R-Sätze (R) | 5-24-26/28-48/22-50/53-10-67-66-51/53-36-20/22-11-65-38 |
| Toxizität | LD50 in male, female rats (mg/kg): 14, 24 orally67, 67 dermally (Gaines) |
| Gefahrensymbole | T+N,N,T+,Xn,F |
| Sicherheitshinweise (S) | 28-36/37-45-60-61-26-62-16 |
| Gefahrenklasse | 6.1(a) |
| Verpackungsgruppe | II |
| Gefahrstoffdaten | 298-00-0(Hazardous Substances Data) |
Anwendungen & Verwendung
Verwenden
Parathion-methyl is an derivative of Parathion (P192220), an organophosphate insecticide used on cotton, rice and fruit trees.