ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
化工社オープンプロジェクト:[email protected]AIアクセス:llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.7.8
  1. ホーム
  2. /化合物

チオりん酸O,O-ジエチルO-(5-フェニル-3-イソオキサゾリル)

Isoxathion

HCID 29307
ノート反応
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
18854-01-8
標準SMILES
CCOP(=S)(OCC)Oc1cc(-c2ccccc2)on1
InChIKey
SDMSCIWHRZJSRN-UHFFFAOYSA-N
分子式
C13H16NO4PS
平均分子量
313.31 g/mol
単同位体質量
313.05376616

概要

Isoxathion is an organic thiophosphate that is O,O-diethyl hydrogen phosphorothioate in which the hydrogen of the hydroxy group is replaced by a 5-phenyl-1,2-oxazol-3-yl group. It has a role as an agrochemical and an EC 3.1.1.7 (acetylcholinesterase) inhibitor. It is an organothiophosphate insecticide and an organic thiophosphate. It is functionally related to a 5-phenylisoxazol-3-ol.

名称と識別子

優先名称
Isoxathion
IUPAC
diethoxy-[(5-phenyl-1,2-oxazol-3-yl)oxy]-sulfanylidene-λ5-phosphane
現地名
チオりん酸O,O-ジエチルO-(5-フェニル-3-イソオキサゾリル)
英語名
Isoxathion
分子式
C13H16NO4PS
分子量
313.31

名称と別名

ISOXATHION18854-01-8KarphosIsoxathion [ISO:BSI]SI-6711O,O-Diethyl O-(5-phenyl-3-isoxazolyl) phosphorothioateIsoxathion [BSI:JMAF:ISO]O,O-Diethyl O-5-phenylisoxazol-3-ylphosphorothioateDTXSID0042080IRA3YFG6CXHSDB 6692O,O-Diethyl O-(3-(5-phenyl)-1,2-isoxazolyl)phosphorothionate
名称をさらに表示
カルホスイソキサチオンチオりん酸O,O-ジエチル-O-(5-フェニル-3-イソオキサゾリル)チオりん酸O,O-ジエチルO-(5-フェニル-3-イソオキサゾリル)イソキサチオン標準品イソキサチオン標準液O,O-ジエチルO-(5-フェニル-3-イソオキサゾリル)ホスホロチオアートジエチル-(5-フェニル-3-イソキサゾリル)-チオホスフェイトチオりん酸O,O-ジエチル-O-(5-フェニル-3-イソオキサゾリル) (別名 イソキサチオン)チオりん酸O, O-ジエチル-O-(5-フェニル-3-イソオキサゾリル) (別名イソキサチオン)イソキサチオン標準物質イソキサンチオンネキリトン・KO,O-ジエチル O-5-フェニル-1,2-オキサゾール-3-イル ホスホロチオアートネキリガード・KO,O-ジエチル-O-(5-フェニル-3-イソキサゾリル)ホスホロチオエート標準品チオりん酸O,O-ジエチル-O-(5-フェニル-3-イソオキサゾ リル)e-48

物性

構造計算による物性

XLogP
4.2
極性表面積
85.8 Ų
水素結合供与体数
0
水素結合受容体数
6
回転可能結合数
7
重原子数
20
形式電荷
0
複雑度
328

実験および物理化学的性質

Pesticides · 3 件

Insecticides

Active substance -> EU Pesticides database: Not approved

Pesticides -> Organophosphate Insecticides

LogP · 2 件

log Kow = 3.73

4.58

Odor...An ester-like odor.
Color/FormYellowish liquid
Solubility · 2 件

Readily soluble in organic solvents.

In water, 1.9 mg/l @ 25 °C

Boiling Point160 °C/0.15 mmHg
Decomposition · 2 件

Decomposes at 160 °C.

When heated to decomposition it emits very toxic fumes of /nitrogen, phosphorous and sulfur oxides/.

Vapor Pressure0.00000222 [mmHg]
Physical DescriptionYellowish liquid; [HSDB]
Stability/Shelf LifeUnstable to alkalis.
Collision Cross Section180.8 Ų [M+Na]+ [CCS Type: DT; Buffer gas: N2; Ionization: ESI+; Dataset: TOXCAST; Source Identifier: DTXSID0042080]

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 6 件

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+H311 (100%): Toxic if swallowed or in contact with skin [Danger Acute toxicity, oral; acute toxicity, dermal]

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)

危険有害性情報

Regulatory Information2002/2076
Hazards Summary · 1 件

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 Emergency Guidelines · 5 件

/GUIDE 131: FLAMMABLE LIQUIDS-TOXIC/ Health: TOXIC; may be fatal if inhaled, ingested or absorbed through skin. Inhalation or contact with some of these materials will irritate or burn skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution. /Organophosphorus pesticide, liquid, flammable, poisonous; Organophosphorus pesticide, liquid, flammable, toxic; Organophosphorus pesticide, liquid, poisonous, flammable; Organophosphorus pesticide, liquid, toxic, flammable/

/GUIDE 131: FLAMMABLE LIQUIDS-TOXIC/ Fire or Explosion: HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion and poison hazard indoors, outdoors or in sewers. Those substances designated with a "P" may polymerize explosively when heated or involved in a fire. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water. /Organophosphorus pesticide, liquid, flammable, poisonous; Organophosphorus pesticide, liquid, flammable, toxic; Organophosphorus pesticide, liquid, poisonous, flammable; Organophosphorus pesticide, liquid, toxic, flammable/

化学と産業

薬理情報

Mechanism of Action · 2 件

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/

The first essential step in the initiation of the delayed neuropathic effect of an organophosphate is phosphorylation of a target protein in the nervous system. The protein has esteratic enzyme activity. The phosphorylation, which was originally studied radiochemically, can be monitored conveniently as progressive inhibition of the activity of this enzyme, which is now referred to as Neuropathy Target Esterase (NTE or Neurotoxic Esterase)... . The second, and equally essential, step is the transformation of the phosphorylated NTE to a modified form: one of the remaining ester bonds of the inhibitor molecule attached to the NTE active site undergoes a biochemical cleavage leaving an ionized acidic residue bound to the protein: this residue is negatively charged and the reaction is referred to as "aging". Both inhibition and aging of inhibited NTE are essential to initiate neuropathy, but the role of the negative charge in the initiation of axonal degeneration is not known. The process of "aging" of inhibited NTE has some analogy with the better-known "aging" of inhibited AChE. However, the analogy does not last above the level of enzyme inhibition. Acute toxicity arises directly from the loss of catalytic activity of AChE, leading to accumulation of excess physiological substrate. Mere loss of catalytic activity of NTE (without aging) does not initiate neuropathy. There is no evidence of a deleterious accumulation of a physiological substrate for NTE or lack of hydrolysis products after inhibition in vivo, and the effect of the negative charge may be focused on some quite separate process. /Organophosphorus Pesticides/

Metabolism/Metabolites · 2 件

...Rats were given 30 mg/kg isoxathion and subjected to whole body autoradiography 1 and 24 hours after dosing. ...At least 11 radioactive metabolites were detected. Four of these were identified: 3-hydroxy-5-phenylisoxazole, hippuric-acid, 3-(beta-D-glucopyranuronosyloxy)-5-phenylisoxazole, and 5-phenyl-3-isoxazolyl-sulfate.

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. In general, phosphorothioates are not directly toxic but require oxidative metabolism to the proximal toxin. The glutathione transferase reactions produce products, that are, in most cases, of low toxicity. Hydrolytic and transferase reactions affect both the thioates and their oxons. /Organophosphorus Pesticides/

関連反応

0 件
反応記録を作成

現在のフィルター条件では反応記録がありません。

化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
HSDB6692
HSDB-6692
Isoxathion 0.1
ISOXATHION STANDARD
Propargite Impurity 8
EINECS 242-624-8BRN 1222135Phosphorothioic acid, O,O-diethyl O-(5-phenyl-3-isoxazolyl) esterISOXATHION [ISO]ISOXATHION [HSDB]DTXCID8022080CHEBI:34801O,O-diethyl O-(5-phenylisoxazol-3-yl) thiophosphate

データベース識別子

CAS
18854-01-8
PubChem CID
29307
DTXSID
DTXSID0042080
ChEMBL
CHEMBL3182191
ChEBI
CHEBI:34801
UNII
IRA3YFG6CX
EC Number
242-624-8
Nikkaji
J3.456H
Other Experimental Properties · 2 件

Decomposes at 160 °C

When heated to decomposition it emits very toxic fumes of NOx, POx, and SOx.

物理化学的性質

融点
25 ℃ · <25℃
沸点
160 °C · 160°C (rough estimate)
比重(密度)
1.48 g/ml · 1.48 g/ml
蒸気圧
-4 Pa · -4 Pa (25 °C)
貯蔵温度
0 · 0-6°C
溶解性
クロロホルム(微量)、メタノール(微量)
水溶解度
1.9 mg · 1.9 mg l-1 (25 °C)
酸解離定数(Pka)
-6.17 · -6.17±0.28(Predicted)
外見
液体
色
無色~淡黄色
比重
1.48 · 1.48
BRN
1222135 · 1222135
Henry's Law Constant
1.6 · 1.6×102 mol/(m3Pa) at 25℃, HSDB (2015)
EPAの化学物質情報
Isoxathion (18854-01-8)

/GUIDE 131: FLAMMABLE LIQUIDS-TOXIC/ Public Safety: CALL Emergency Response Telephone Number ... . As an immediate precautionary measure, isolate spill or leak area for at least 50 meters (150 feet) in all directions. Keep unauthorized personnel away. Stay upwind. Keep out of low areas. Ventilate closed spaces before entering. /Organophosphorus pesticide, liquid, flammable, poisonous; Organophosphorus pesticide, liquid, flammable, toxic; Organophosphorus pesticide, liquid, poisonous, flammable; Organophosphorus pesticide, liquid, toxic, flammable/

/GUIDE 131: FLAMMABLE LIQUIDS-TOXIC/ Protective Clothing: Wear positive pressure self-contained breathing apparatus (SCBA). Wear chemical protective clothing that is specifically recommended by the manufacturer. It may provide little or no thermal protection. Structural firefighters' protective clothing provides limited protection in fire situations ONLY; it is not effective in spill situations where direct contact with the substance is possible. /Organophosphorus pesticide, liquid, flammable, poisonous; Organophosphorus pesticide, liquid, flammable, toxic; Organophosphorus pesticide, liquid, poisonous, flammable; Organophosphorus pesticide, liquid, toxic, flammable/

For more DOT Emergency Guidelines (Complete) data for ISOXATHION (16 total), please visit the HSDB record page.

DOT Hazard Classification · 2 件

Isoxathion

Severe marine pollutant

Hazard Classes and Categories · 5 件

Acute Tox. 3 (100%)

Acute toxicity - category 3

Acute toxicity (Oral) - Category 3

Acute toxicity (Oral) - Category 3

Acute Tox. 3 *

Standard Transportation Number · 6 件

49 216 74; Organophosphorus pesticide, liquid, not otherwise specified (compounds and preparations) (insecticides, other than agricultural, NEC)

49 216 75; Organophosphorus pesticide, liquid, not otherwise specified (compounds and preparations) (agricultural insecticides, NEC, liquid)

49 105 44; Organophosphorus pesticide, liquid, not otherwise specified (compounds and preparations) (insecticides, other than agricultural, NEC)

49 105 45; Organophosphorus pesticide, liquid, not otherwise specified (compounds and preparations) (agricultural insecticides, NEC, liquid)

49 216 76; Organophosphorus pesticide, solid, not otherwise specified (compounds and preparations) (insecticides, other than agricultural, NEC)

49 216 77; Organophosphorus pesticide, solid, not otherwise specified (compounds and preparations) (agricultural insecticides, NEC, other than liquid)

Shipment Methods and Regulations · 4 件

Severe marine pollutant

No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that person is registered in conformance ... and the hazardous material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by ... /the hazardous materials regulations (49 CFR 171-177)./

The International Air Transport Association (IATA) Dangerous Goods Regulations are published by the IATA Dangerous Goods Board pursuant to IATA Resolutions 618 and 619 and constitute a manual of industry carrier regulations to be followed by all IATA Member airlines when transporting hazardous materials.

The International Maritime Dangerous Goods Code lays down basic principles for transporting hazardous chemicals. Detailed recommendations for individual substances and a number of recommendations for good practice are included in the classes dealing with such substances. A general index of technical names has also been compiled. This index should always be consulted when attempting to locate the appropriate procedures to be used when shipping any substance or article.

Shipping Name/ Number DOT/UN/NA/IMO · 5 件

UN 3018; Organophosphorus pesticides, liquid, toxic, not otherwise specified

UN 3017; Organophosphorus pesticides, liquid, toxic, flammable, not otherwise specified, flashpoint between 23 °C and 61 °C

UN 2783; Organophosphorus pesticides, solid, toxic, not otherwise specified

UN 2784; Organophosphorus pesticides, liquid, flammable, toxic, not otherwise specified, flashpoint less than 23 °C

For more Shipping Name/ Number DOT/UN/NA/IMO (Complete) data for ISOXATHION (6 total), please visit the HSDB record page.

安全と保護具

Exposure Control and Personal Protection · 1 件

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 件

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/

Cleanup Methods · 3 件

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/

Disposal Methods · 1 件

SRP: The most favorable course of action is to use an alternative chemical product with less inherent propensity for occupational exposure or environmental contamination. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material's impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations.

Preventive Measures · 5 件

If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. /Organophosphorus pesticides, solid, toxic

If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. Build dikes to contain flow as necessary. Attempt to stop leak if without undue personnel hazard. Use water spray to knock-down vapors. /Organophosphorus pesticides, liquid, toxic/

If material not on fire and not involved in fire: Keep sparks, flames, and other sources of ignition away. Keep material out of water sources and sewers. Build dikes to contain flow as necessary. Use water spray to knock-down vapors. /Organophosphorus pesticides, liquid, flammable, toxic/

Personnel protection: Avoid breathing dusts, and fumes from burning material. Keep upwind. Avoid bodily contact with the material. Do not handle broken packages unless wearing appropriate personal protective equipment. Wash away any material which may have contacted the body with copious amounts of water or soap and water. /Organophosphorus pesticides, solid, toxic/

For more Preventive Measures (Complete) data for ISOXATHION (8 total), please visit the HSDB record page.

毒性情報

Interactions · 1 件

Because different classes of enzymes may be inhibited, the effects of organophosphorus pesticide poisoning may be complex and potentially at least could involve interactions with drugs as well as with other pesticides or chemicals. Potentiation may also involve solvents or other components of formulated pesticides. Certain drugs such a phenothiazines, antihistamines, CNS depressants, barbiturates, xanthines (theophylline), aminoglycosides and parasympathomimetic agents are to be avoided because of increased toxicity. /Organophosphorus pesticides/

Ecotoxicity Values · 5 件

LC50 Cyprinus carpio 2.1 mg/l/48 hr /Conditions of bioassay not specified/

LD50 Chicken oral 21,600 ug/kg

LC50 Daphnia pulex 0.0052 mg/L/3 hr /Conditions of bioassay not specified/

LC50 Bufo bufo japonicus (Toad; 25-35 days, 0.34 g tadpole) 5,100 ug/L/72 hr; 12,000 ug/L/24 hr; 5,300 ug/L/48 hr; 5,100 ug/L/96 hr; static /Formulated product/

For more Ecotoxicity Values (Complete) data for ISOXATHION (6 total), please visit the HSDB record page.

Environmental Fate · 3 件

TERRESTRIAL FATE: Based on a classification scheme(1), a Koc value of 14,568(2) indicates that isoxathion is expected to be immobile in soil(SRC). Volatilization of isoxathion from moist soil surfaces is not expected to be an important fate process(SRC) given an estimated Henry's Law constant of 6.1X10-8 atm-cu m/mole(SRC), using a fragment constant estimation method(3). Isoxathion is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 2.2X10-6 mm Hg(SRC), determined from a fragment constant method(4). Isoxathion has been shown to biodegrade in soil with the major metabolic pathway being via the formation of 3-hydroxy-5-phenylisoxazole to 5-phenyl-4-oxazolin-2-one, benzoylacetamide and benzoic acid(5).

AQUATIC FATE: Based on a classification scheme(1), a Koc value of 14,568(2) indicates that isoxathion is 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 6.1X10-8 atm-cu m/mole(SRC), developed using a fragment constant estimation method(4). According to a classification scheme(5), an estimated BCF of 150(SRC), from its log Kow of 3.73(6) and a regression-derived equation(7), suggests the potential for bioconcentration in aquatic organisms is high(SRC). However, aquatic organisms readily metabolize this class of compounds(8) and organophosphates can be altered chemically(9) once released into the environment. Aqueous photolytic half-lives of 12-18 days have been reported, with the addition of humic acids increasing the rate of photolysis by up to 25%(10). Percent biodegradation of isoxathion from three ponds near Nagoya City, Japan ranged from 0-31% after four days of incubation; compared to aniline (biodegradation rate as high as 86%), this compound was classified as not expected to biodegrade rapidly(11).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), isoxathion, which has an estimated vapor pressure of 2.2X10-6 mm Hg at 25 °C(SRC), determined from a fragment constant method(2), will exist in both the vapor and particulate phases in the ambient atmosphere. Vapor-phase isoxathion 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 hrs(SRC), calculated from its rate constant of 1.2X10-10 cu cm/molecule-sec at 25 °C(SRC) that was derived using a structure estimation method(3). Particulate-phase isoxathion may be removed from the air by wet and dry deposition(SRC).

Adverse EffectsOther Poison - Organophosphate
Milk ConcentrationsMany of the organophosphorus insecticides are excreted in the milk ... /Organophosphorus insecticides/
Effluent ConcentrationsIsoxathion, 200-4,300 g applied at a rate of 0.50 g/sq m, was not detected in drainage samples from 24 Japanese golf courses, monitored from 1994 to 1996; detection limit less than 0.001 mg/l(1).
Medical Surveillance · 3 件

Measurement of whole blood-AChE is the most widely adopted method for monitoring the effects of occupational exposure to organophosphorus insecticides. Physiological variations in blood ChE levels occur in a healthy person and are seen among a population. It has been estimated that the coefficient of variation for AChE activity in samples from an individual is 8-11%, and that a decrease of 23% below pre-exposure level may, therefore, be considered significant. If the average of several pre-exposure values were available, then a decrease of 17% would be significant. It has been recommended that, if measured activity is reduced by 30% or more of the pre-exposure value, AChE measurements should be repeated at appropriate intervals to confirm the results. Depressions of AChE or ChE in excess of 20-25% are considered diagnostic of exposure but not, necessarily, indicative of hazard. Depressions of 30-50% or more are considered indicators for removal of an exposed individual from further contact with pesticides until levels return to normal. /Organophosphorus Pesticides/

...Organophosphorus pesticides may undergo hydrolysis in vivo to yield substituted phosphoric acids that are subsequently excreted in urine. Advances in gas chromatography and combined gas chromatography/mass spectrometry (GC/MS) have made it possible to analyse the urine of exposed persons for the presence of appropriate metabolites. It is usually necessary to preserve the sample by the addition of chloroform, to concentrate or extract the metabolite(s), and to convert them to suitably-volatile derivatives that can be detected by GC. Obviously, access to a well-equipped analytical laboratory, capable of the quick processing of samples, is a necessary factor if monitoring by urine analysis is proposed. However, in some cases, simpler and sensitive colorimetric tests are available for screening the urine of exposed persons. Thus, 4-nitrophenol can be measured directly in the urine of workers exposed to parathion. Consideration of the concentration of metabolite(s) in the urine can be helpful in determining patterns of exposure, and these concentrations can be calibrated against the effects on AChE for a particular pesticide. However, the time-course and peak of excretion of metabolites appears to vary according to dose, so that serial sampling and analyses of urine are desirable. Levels of metabolite alone cannot be considered a guide to hazard. This is obvious when it is realized that pesticides that have very different toxicities may yield identical acidic metabolites. Thus, the level of metabolites in urine, after exposure to sufficient amounts of the very toxic parathion-methyl to depress blood-AChE to 50%, will be much lower than that of the identical metabolites, following exposure to the related fenitrothion, which is about 40 times less toxic. /Organophosphorus Pesticides/

SRP: Workers should undergo an annual medical exam. Contraindications for work with organophosporous pesticides are organic diseases of the CNS, mental disorders and epilepsy, and pronounced endocrine disorders. Blood cholinesterase, both plasma and RBC, must be determined before work starts. In the event of prolonged work periods, this activity should be determined at intervals of 3-4 days. Persons exhibiting a fall in cholinesterase activity of 25% or more must be transferred to other work where they are not exposed until cholinesterase activity is restored. /Organophosphorous pesticides/

Soil Adsorption/Mobility · 1 件

The Koc of isoxathion in turf grass soil is 14,568(1). According to a classification scheme(2), this estimated Koc value suggests that isoxathion is expected to be immobile in soil. Rf (retention factor) values for isoxathion were reported as 0.63, 0.50, and 0.62, using three Japanese soils - Hiratsuka (sandy loam, 69.8% sand, 19.6% silt, 10.6% clay, 3.2% organic matter, pH 5.9), Tanashi (loam, 60.5% sand, 30.2% silt, 9.3% clay, 8.4% organic matter, pH 6.0), and Yasu (sandy loam, 56.6% sand, 29.9% silt, 1.56% clay, 1.8% organic matter, pH 4.9), respectively(3).

Atmospheric Concentrations · 2 件

URBAN/SUBURBAN: Air samples from Kitayushu City, Japan during 21-22 July 1991 and 23-24 April, 1992 were tested for isoxathion; concentrations of 0.63 ng/cu m and not detected (detection limit = 0.2 ng/cu m), respectively, were reported(1).

SOURCE DOMINATED: Isoxathion was detected, not quantified in air samples collected from golf courses in the Kanagawa Prefecture, Japan; levels were higher in daytime(1).

Human Toxicity Excerpts · 5 件

/SIGNS AND SYMPTOMS/ Signs and symptoms of acute intoxication by organophosphorus insecticides include muscarinic, nicotinic, and central nervous system (CNS) manifestations. Symptoms may develop rapidly, or there may be a delay of several hours after exposure before they become evident. The delay tends to be longer in the case of more lipophilic compounds, which also require metabolic activation. Symptoms may increase in severity for more than one day and may last for several days. In severe cases, respiratory failure is a dominant effect. /Organophosphorus Pesticides/

/SIGNS AND SYMPTOMS/ Although many epidemiological studies have been carried out, few controlled studies on man have been reported. It is generally recognized that there are behavioural and psychic changes during overt clinical poisoning by organophosphorus insecticides and that these may take several months to regress. However, there is no information to suggest that effects occur at exposure levels that do not either alter ChE levels or produce physical symptoms. ...Much /of the work on different aspects of behavior as affected by organophasphates/ was based on generalized complaints from workers occupationally exposed to many agricultural chemicals (and probably also to automobile fuels and lubricants and to alcohol). In summary, ...in human subjects sufficiently exposed to organophosphates to depress plasma- or erythrocyte-ChEs, some or all of the following behavioral variables might be impaired. In cognition: vigilance, information processing and psychomotor speed, and memory; in speech: both performance and perception; in psychic state: increased tendencies to depression, anxiety, and irritability; and in EEG records: a tendency to faster frequencies and higher voltages. /Organophosphorus Pesticides/

/SIGNS AND SYMPTOMS/ Respiratory and ocular symptoms are expected to appear first after exposure to airborne organophosphorus pesticides. /Organophosphorus pesticides/

/SIGNS AND SYMPTOMS/ The clinical picture of organophosphorus intoxication results from accumulation of ACh at nerve endings. ...The symptoms can be summarized in three groups as follows: (a) Muscarinic manifestations- increased bronchial secretion, excessive sweating, salivation, and lachrymation; pinpoint pupils, bronchoconstriction, abdominal cramps (vomiting and diarrhea); and bradycardia. (b) Nicotinic manifestations- fasciculation of fine muscles and, in more severe cases, of diaphragm and respiratory muscles; and tachycardia. (c) Central nervous system manifestations- headache, dizziness, restlessness, and anxiety; mental confusion, convulsions, and coma; and depression of the respiratory centre. All these symptoms can occur in different combinations and can vary in time of onset, sequence, and duration, depending on the chemical, dose, and route of exposure. Mild poisoning might include muscarinic and nicotinic signs only. Severe cases always show central nervous system involvement; the clinical picture is dominated by respiratory failure, sometimes leading to pulmonary edema, due to the combination of the above-mentioned symptoms. /Organophosphorus Pesticides/

Artificial Pollution SourcesIsoxathion's former production may have resulted in its release to the environment through various waste streams; it's use as an insecticide(1) may have resulted in its direct release to the environment(SRC).
Environmental Biodegradation · 2 件

AEROBIC: Half-lives in turf grass soil and other soils of 5 and 15-40 days, respectively, have been reported for isoxathion(1). Isoxathion was added to fresh water inoculums from three ponds near Nagoya City, Japan and using the Handai biodegradation test method(2). Biodegradation rates were measured at different times over the years were as follows: Ara-ike (irrigation reservoir), June 1991 thru October 1992, 6-23% after 4-day incubation; Makinoga-oke (located in a park near a residential area and a golf course), July 1990 thru April 1991, 0-31% after 4-day incubation; Tatsuga-ike (boating pond in a park), July 1989-March 1992, 14-22% after 4-day incubation(2). In comparison to aniline which exhibited a biodegradation rate as high as 86%, this compound is not expected to biodegrade rapidly(2).

30 ppm of 14C-labeled isoxathion was incubated in 50 g of three Japanese soils - Hiratsuka (sandy loam, 69.8% sand, 19.6% silt, 10.6% clay, 3.2% organic matter, pH 5.9), Tanashi (loam, 60.5% sand, 30.2% silt, 9.3% clay, 8.4% organic matter, pH 6.0), and Yasu (sandy loam, 56.6% sand, 29.9% silt, 1.56% clay, 1.8% organic matter, pH 4.9). Soils were maintained at 60% field capacity for non-flooded conditions and at 150% field capacity for flooded conditions. %14C-isoxathion recovered from non-flooded Hiratsuka soil was 75, 51, and 32 after 20, 40, and 60 days, respectively, initial half-life = 44 days; % recovered from flooded Hiratsuka soil - 46, 14, and 5, respectively, initial half-life = 18 days. %14C-isoxathion recovered from non-flooded Tanashi soil was 69, 17, and 10 after 10, 30, and 45 days, respectively, initial half-life = 19 days). %14C-isoxathion recovered from non-flooded Yasu soil was 80 and 47 after 10 and 20 days, respectively, initial half-life = 31 days(1). The major metabolic pathway is via the formation of 3-hydroxy-5-phenylisoxazole to 5-phenyl-4-oxazolin-2-one, benzoylacetamide and benzoic acid(1).

安全データ

wgk
3
ridadr
3018
PRTR法
第1種指定化学物質
hs_code
29349990
risk_code
24/25-50/53
安衛法
57,57-2
消防法
危-4-1-II
hazard_code
T,N
safety_code
28-36/37-45-60-61
hazard_class
6.1(b)
packing_group
III
毒劇物取締法
III
環境リスク評価
イソキサチオン(18854-01-8)
有毒物質データの
18854-01-8(Hazardous Substances Data)
Absorption, Distribution and Excretion · 1 件

Male Wistar-rats were dosed orally with 20 mg/kg carbon-14 labeled isoxathion. Urine, feces, and expired air were collected for up to 24 hours after dosing and assayed for carbon-14. Selected animals were killed between 30 min and 24 hr after dosing and the tissue distribution of carbon-14 activity was determined. Urine and feces samples were analyzed for metabolites. Rats were given 30 mg/kg isoxathion and subjected to whole body autoradiography 1 and 24 hours after dosing. Radiolabel was rapidly excreted mainly in the urine, 82.5% being eliminated in the first 24 hr. Cumulative excretion of carbon-14 amounted to 85% in the urine and 14% in the feces. Only negligible amounts of radiolabel were excreted in expired gases. Tissue carbon-14 activity was maximal 30 min after dosing, the largest amounts occurring in the liver, kidney, and blood. Only negligible amounts of tissue radioactivity were found after 24 hr. Autoradiography showed that initially the highest radioactivity occurred in the gastrointestinal contents. Large amounts were observed in the liver and kidney. After 24 hours, significant radioactivity occurred only in the intestinal contents.

用途と製造

Uses · 6 件

Used as contact and stomach insecticide for fruits, tea, tobacco, ornamentals, rice, sugarcane, vegetables, turf, and trees; [HSDB]

No longer registered as a pesticide for use in the US; [HSDB] Banned in the EU for use as pesticide for plant protection; [eChemPortal: ESIS]

Farming (Pesticides) [Category: Industry]

For isoxathion (USEPA/OPP Pesticide Code: 057802) there are 0 labels match. /SRP: Not registered for current 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./

Control of scale insects, aphids, hoppers, beetles, and caterpillars on citrus fruit, tea, tobacco, garden trees, rice, sugarcane, and vegetables. /Former use/

Insecticide with contact and stomach action. ...Effective against Aphididae, Coccidae, Diaspididae and Margarodidae (at 500-1000 g/ha) in cabbages, citrus and ornamentals; also against Agromyzidae, Cicadellidae, Delphacidae, Ephydridae and Pyralidae (at 600-900 g/ha) in paddy rice; against Coleoptera (at 1.2 kg/ha) in turf and trees; against Noctuidae and Pieridae (at 500-1000 g/ha) in pome fruit, citrus fruit and vegetables. /Former use/

Formulations/Preparations · 2 件

Tradename: 'Karphos' (Sankyo)

Tech. is >93%.

General Manufacturing InformationThe WHO Recommended Classification of Pesticides by Hazard identifies Isoxathion (technical grade) as Class IB: highly hazardous; Main Use: insecticide.
応用分野 · 6 件

解説イソキサチオン (C13H16NO4PS) とは、殺虫剤に分類されネキリムシやケムシ類、カイガラムシなど害虫から農作物を守る用途で使用される農薬の成分です。 有機リン系の農薬で、農薬の作用機構による分類ではアセチルコリンエステラーゼ阻害のグループ (1B) に分類されます。イソキサチオンを含む農薬が害虫の体内に取り込まれると、中枢神経系に存在するコリンエステラーゼと結合することによって、その活性が低下します。興奮性神経伝達物質の1種であるアセチルコリンが分解できなくなり、神経細胞間にアセチルコリンが蓄積して、正常な神経伝達機能が阻害されることが殺虫効果となると考えられています。 また、農薬が散布された葉や果実を経口し効果のでる食毒作用と、直接農薬がかかり効果のでる接触毒作用の2つの作用効果が確認されているため、より多くの害虫に効くことが特徴です。安全性については、毒物及び劇物取締法で、劇物に指定されています。 哺乳動物の体内に蓄積しにくいことが確認されています。飲み込んだり吸入すると有害、眼刺激、長期または反復ばく露による神経系障害、ならびに水生生物への強毒性が指摘されています。 アメリカやヨーロッパ同様に日本国内においても、食品に残留する基準値が設定されています。

用途イソキサチオン試験用標準品。

用途農薬(殺虫剤) (NITE CHRIP)

説明Isoxathion is a pale yellow liquid, bp 160 C/0.15 mm Hg, vp

使用Isoxathion is used to control sucking pests, leaf miners and some chewing pests in a variety of fruit, vegetables and ornamental plants.

使用用途イソキサチオンの使用用途は、害虫の防除です。ネキリムシやケムシ類、カイガラムシ、ハエ類、ヨトウムシなど幅広い害虫に登録があり使用ができます。 イソキサチオンを含む農薬の使用方法は大きく分けて2つあります。 1. 農作物に散布する 1つ目は、イソキサチオンを成分とする殺虫剤を、水に希釈して散布する方法です。この方法は害虫の発生初期に使用する場合が多いです。 また、野菜類やミカン、花き類、樹木のカイガラムシやケムシ類、アワノメイガ、ハエ類など多くの農作物と害虫に登録があり、使用できることが特徴になります。 2. 土壌に散布する 2つ目は、イソキサチオンを成分とする殺虫剤を、土壌に散布する方法です。この方法は種の播種時や苗などの定植前に土壌散布または散布した農薬を土壌に混和して使用します。 野菜類のネキリムシやコガネムシ類、タネバエなど地下部を加害する害虫に対して高い効果があります。

サプライヤー38 社

湖北威德利化学试剂有限公司186-02735115 18062128043 · [email protected]
河南赢创生物科技有限公司16650615803 · [email protected]
陕西缔都新材料有限公司029-63373950 17392216152 · [email protected]
VladaChem GmbH+49-7246-3082843 +86-18411632868 · [email protected]
梯希爱(上海)化工贸易有限公司021-61109150 · [email protected]
上海相辉医药科技有限公司13761987713; 13761987713 · [email protected]
上海艾梯西生物科技有限公司18721763493 · [email protected]
BOC Sciences1-631-485-4226; 16314854226 · [email protected]
上海毕楷科技有限公司18516304666 · [email protected]
四川库利南科技有限公司400-1166-196 18981987031 · [email protected]
艾科试剂4008-755-333 18080918076 · [email protected]
南京生利德生物科技有限公司025-57798810 18652991625 · [email protected]
上海将来实业股份有限公司400-0066400 13621662912 · [email protected]
上海将来实业股份有限公司021-61552785 · [email protected]
天津阿尔塔科技有限公司022-65378550-8551 · [email protected]
天津阿尔塔科技有限公司022-6537-8550 15522853686 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
艾吉析科技(上海)有限公司17717235263 17717235263 · [email protected]
湖北万业众诚化学试剂有限责任公司18671296875 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
山东西亚化学有限公司4009903999 13395398332 · [email protected]
南京罗迈美生物科技有限公司[email protected]
山东小野化学股份有限公司0539-6362799 20)
Shanghai Acmec Biochemical Technology Co., Ltd.+86-18621343501 · [email protected]
Shaanxi Didu New Materials Co. Ltd+86-86-17392712779 +86-13289823923 · [email protected]
深圳市丽晶生化科技有限公司0755-85201366 18938635012 · [email protected]
深圳聚合生化科技有限公司+86-400-002-6226 13028896684 · [email protected]
爆牛贸易重庆有限公司+86-023-6139-8061 +86-86-13650506873 · [email protected]
XIAMEN AMITY INDUSTRY AND TRADE CO., LTD.+8618950047208 · [email protected]
SHANGHAI KEAN TECHNOLOGY CO., LTD.+8613817748580 · [email protected]
SUZHOU SENFEIDA CHEMICAL CO.,LTD+86-0512-83500002 +86-15195660023 · [email protected]
上海安谱实验科技股份有限公司18502138905 · [email protected]
上海杰股生物科技有限公司021-51698675 · [email protected]
南京枫景晴生物科技有限公司15062262630 · [email protected]
DAYANG CHEM (HANGZHOU) CO.,LTD+86-88938639 +86-17705817739 · [email protected]
TargetMol中国(陶术生物)15002134094 · [email protected]
Hefei TNJ Chemical Industry Co.,Ltd.+86-0551-65418671 +86-189 4982 3763 · [email protected]
亚索试剂400-873-6778 18660992876 · [email protected]

補足説明

定義ChEBI: An organic thiophosphate that is O,O-diethyl hydrogen phosphorothioate in which the hydrogen of the hydroxy group is replaced by a 5-phenyl-1,2-oxazol-3-yl group.

For more Human Toxicity Excerpts (Complete) data for ISOXATHION (8 total), please visit the HSDB record page.