Parathion (ISO)

Parathion Struktur
56-38-2
CAS-Nr.
56-38-2
Bezeichnung:
Parathion (ISO)
Englisch Name:
Parathion
Synonyma:
DNTP;PARATHION-ETHYL;1605;ETHYL PARATHION;ETHYLPARATHIONE;AAT;Sulphos;e605;PARATION;DNTP MIXTURE
CBNumber:
CB4153452
Summenformel:
C10H14NO5PS
Molgewicht:
291.26
MOL-Datei:
56-38-2.mol

Parathion (ISO) Eigenschaften

Schmelzpunkt:
6.1°C
Siedepunkt:
375°C
Dichte
1.26
Dampfdruck
0.470 at 20 °C, 0.942 at 25 °C, 1.84 at 30 °C, 3.53 at 35 °C, 6.62 at 40 °C, 12.18 at 45 °C (gassaturation method, Spencer et al., 1979)
Brechungsindex
nD25 1.5370
Flammpunkt:
120 °C
storage temp. 
APPROX 4°C
Löslichkeit
2,900 and 2,700 g/kg in petroleum ether and heptane, respectively (Williams, 1951)
Aggregatzustand
liquid
Farbe
Pale-yellow liquid
Wasserlöslichkeit
Slightly soluble
Merck 
13,7105
BRN 
8912188
Henry's Law Constant
8.56 at 25 °C (wetted-wall column, Fendinger and Glotfelty, 1990)
Expositionsgrenzwerte
NIOSH REL: TWA 0.05 mg/m3, IDLH 10 mg/m3; OSHA PEL: TWA 0.1 mg/m3.
Stabilität:
Hygroscopic, Moisture Sensitive
CAS Datenbank
56-38-2(CAS DataBase Reference)
IARC
2B (Vol. 30, Sup 7, 112) 2017
NIST chemische Informationen
Ethyl parathion (o,o-diethyl-o-p-nitrophenylthiophosphate)(56-38-2)
EPA chemische Informationen
Parathion (56-38-2)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher T+;N,N,T+,Xn,F
R-Sätze: 24-26/28-48/25-50/53-67-65-38-11
S-Sätze: 28-36/37-45-60-61-62-16
RIDADR  UN 3278
WGK Germany  3
RTECS-Nr. TF4550000
HazardClass  6.1(a)
PackingGroup  I
HS Code  29201100
Giftige Stoffe Daten 56-38-2(Hazardous Substances Data)
Toxizität LD50 in female, male rats (mg/kg): 3.6, 13 orally; 6.8, 21 dermally (Gaines)
IDLA 10 mg/m3
Bildanzeige (GHS) GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H372 Schädigt bei Hautkontakt und Verschlucken die Organe bei längerer oder wiederholter Exposition. Spezifische Zielorgan-Toxizität (wiederholte Exposition) Kategorie 1 Achtung GHS hazard pictogramssrc="/GHS08.jpg" width="20" height="20" /> P260, P264, P270, P314, P501
H410 Sehr giftig für Wasserorganismen mit langfristiger Wirkung. Langfristig (chronisch) gewässergefährdend Kategorie 1 Warnung GHS hazard pictogramssrc="/GHS09.jpg" width="20" height="20" /> P273, P391, P501
Sicherheit
P262 Nicht in die Augen, auf die Haut oder auf die Kleidung gelangen lassen.
P273 Freisetzung in die Umwelt vermeiden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P314 Bei Unwohlsein ärztlichen Rat einholen / ärztliche Hilfe hinzuziehen.

Parathion (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD

HELLGELBE BIS BRAUNE (TECHNISCHES PRODUKT) FLüSSIGKEIT MIT CHARAKTERISTISCHEM GERUCH.

CHEMISCHE GEFAHREN

Zersetzung beim Erhitzen über 200 °C unter Bildung giftiger Gase mit Kohlenmonoxid, Stickstoffoxiden, Phosphoroxiden und Schwefeloxiden. Reagiert mit starken Oxidationsmitteln. Greift einige Kunststoff-, Gummi- und Beschichtungsarten an.

ARBEITSPLATZGRENZWERTE

TLV: (Einatembare Fraktion und Dampf) 0.05 mg/m? Hautresorption; Krebskategorie A4 (nicht klassifizierbar als krebserzeugend für den Menschen); BEI vorhanden; (ACGIH 2005).
MAK: 0.1 mg/m?(Einatembare Fraktion); Spitzenbegrenzung: überschreitungsfaktor II(8); Hautresorption; Schwangerschaft: Gruppe D; (DFG 2005).

AUFNAHMEWEGE

Aufnahme in den Körper durch Inhalation des Aerosols, über die Haut, durch Verschlucken und über die Augen.

INHALATIONSGEFAHREN

Verdampfung bei 20 °C vernachlässigbar; eine gesundheitsschädliche Partikelkonzentration in der Luft kann jedoch beim Versprühen schnell erreicht werden.

WIRKUNGEN BEI KURZZEITEXPOSITION

WIRKUNGEN BEI KURZZEITEXPOSITION:
Möglich sind Auswirkungen auf das Nervensystem. Führt zu Krämpfen, Atemversagen, Muskelschwäche. Cholinesterasehemmer. Exposition kann zum Tode führen. Die Auswirkungen treten u.U. verzögert ein. ärztliche Beobachtung notwendig.

WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION

Cholinesterasehemmer. Kumulative Wirkung möglich, s. AKUTE GEFAHREN/SYMPTOME.

LECKAGE

Gefahrenbereich verlassen! Fachmann zu Rate ziehen! Ausgelaufene Flüssigkeit möglichst in abdichtbaren Behältern sammeln. Reste mit basischem Stoff behandeln. Reste mit Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen. NICHT in die Umwelt gelangen lassen. Persönliche Schutzausrüstung: Chemikalienschutzanzug mit umgebungsluftunabhängigem Atemschutzgerät.

R-Sätze Betriebsanweisung:

R24:Giftig bei Berührung mit der Haut.
R26/28:Sehr giftig beim Einatmen und Verschlucken.
R48/25:Giftig: Gefahr ernster Gesundheitsschäden bei längerer Exposition durch Verschlucken.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R67:Dämpfe können Schläfrigkeit und Benommenheit verursachen.
R65:Gesundheitsschädlich: kann beim Verschlucken Lungenschäden verursachen.
R38:Reizt die Haut.
R11:Leichtentzündlich.

S-Sätze Betriebsanweisung:

S28:Bei Berührung mit der Haut sofort abwaschen mit viel . . . (vom Hersteller anzugeben).
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S60:Dieses Produkt und sein Behälter sind als gefährlicher Abfall zu entsorgen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
S62:Bei Verschlucken kein Erbrechen herbeiführen. Sofort ärztlichen Rat einholen und Verpackung oder dieses Etikett vorzeigen.

Beschreibung

After exposure to parathion ethyl, one case of a bullous contact dermatitis was reported.

Chemische Eigenschaften

Pure parathion is a pale yellow liquid with a faint odor of garlic, while technical parathion is a deep brown to yellow liquid. It is sparingly soluble in water, but soluble in alcohols, aromatic hydrocarbons, esters, ethers, n-hexane, dichloromethane, 2-propanol, toluene,and ketones. Parathion is one of the most acutely toxic pesticides and the US EPA has classifi ed parathion as an RUP, meaning it should only be handled by qualifi ed, trained, and certifi ed workers. In January 1992, the US EPA announced the cancellation of parathion for all uses on fruit, nut, and vegetable crops. Parathion was used for the control of pests of fruits, nuts, and vegetable crops. The only uses retained are those on alfalfa, barley, corn, cotton, sorghum, soybeans, sunfl owers, and wheat. Further, to reduce exposure of agricultural workers, parathion may only be applied to these crops by commercially certifi ed aerial applicators and treated crops may not be harvested by hand. Parathion is a broad spectrum, organophosphate pesticide used to control many insects and mites.

Physikalische Eigenschaften

Pale yellow to dark brown liquid with a garlic-like odor. Robeck et al. (1965) reported odor threshold concentrations of 3 and 36 ppm for technical and pure grades, respectively.

Verwenden

Parathion is an organophosphate insecticide used on cotton, rice and fruit trees.

Allgemeine Beschreibung

Light-yellow liquid, Parathion turn solid at 6° C, a deadly poison by all routes. Organic phosphate insecticide, acts as an inhibitor of cholinesterase.

Air & Water Reaktionen

Parathion is slightly soluble in water.

Reaktivität anzeigen

Pure parathion is a pale yellow liquid with a faint odour of garlic, while the technical parathion is a deep brown to yellow liquid. It is sparingly soluble in water but soluble in alcohols, aromatic hydrocarbons, esters, ethers, n-hexane, dichloromethane, 2-propanol, toluene, and ketones.
Violent reaction when PARATHION is used as solvent to dissolve endrin. When heated to decomposition Parathion emits very toxic fumes of oxides of sulfur, phosphorus and nitrogen [Lewis, 3rd ed., 1993, p. 984].

Health Hazard

Parathion is highly toxic by all routes of exposure. Parathion, like all organophosphate pesticides, inhibits acetylcholinesterase and alters cholinergic synaptic transmission at neuroeffector junctions (muscarinic effects), at skeletal myoneural junctions, in autonomic ganglia (nicotinic effects), and in the CNS. Exposures to parathion cause symptoms of poisoning that include, but are not limited to, abdominal cramps, vomiting, diarrhea, pinpoint pupils, blurred vision, excessive sweating, salivation and lacrimation, wheezing, excessive tracheobronchial secretions, agitation, seizures, bradycardia or tachycardia, muscle twitching and weakness, and urinary bladder and fecal incontinence. Seizures are much more common in children than in adults. Severe exposures cause loss of consciousness, coma, excessive bronchial secretions, respiratory depression, cardiac irregularity, eventually leading to death. Occupational workers and the general public with health disorders and abnormalities, such as cardiovascular, liver or kidney diseases, glaucoma, or CNS, are at an increased risk of parathion poisoning. Further, high environmental temperatures enhance the severity of parathion poisoning.

Brandgefahr

Combustible material: may burn but does not ignite readily. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.

Landwirtschaftliche Anwendung

Insecticide, Acaricide: The U.S. EPA announced in November, 2000, the cancellation of ethyl parathion immediately on seed corn and the eventual phase out for its use in other pesticide products by the end of 2000. By the end of October, 2003, the U.S. EPA phased out its use to control insects and mites on alfalfa, barley, corn, canola, sorghum, soybeans, sunflowers and wheat. Also used to control nuisance birds. Not listed for use in EU countries. Not registered for use in the U.S. There are 25 global suppliers.

Handelsname

(There are 921 active and canceled/transferred labels registered with the U.S. EPA) ACC 3422®; ALKRON®[C]; ALLERON®; AMERICAN CYANAMID 3422®; APHAMITE®; ARALO®; B 404®; BAY E-605®; BAYER E-605®; BLADAN®; BLADAN F®; COMPOUND 3422®; COROTHION®; CORTHION®; COR-THION®; DANTHION®; DREXEL PARATHION 8E®; E 605®; E 605 F®; ECATOX®; EKATIN WF & WF ULV®; EKATOX®; ETHLON®; ETILON®; FIGHTER®; FOLIDOL®; FOLIDOL E®; FOLIDOL E-605®; FOLIDOL E&E 605®; FOLIDOL OIL®; FOSFERMO®; FOSFERNO®; FOSFEX®; FOSFIVE®; FOSOVA®; FOSTERN®; FOSTOX®; GEARPHOS®; GENITHION®; IDA SEIS-TRES 6-3®; KALPHOS®; KOLODUST®[C]; KYPTHION®; LETHALAIRE G-54®; LIROTHION®; MURFOS®; MURPHOS®; NIRAN®[C]; NIUIF 100®; NITROSTIGMINE®; NOURITHION®; NOVAFOS-M®; OLEOFOS 20®; OLEOPARATHENE®; OLEOPARATHION®; ORTHOPHOS®; PAC®; PACOL®; PARA-KILL®[C]; PARAMAR®; PARA-TOX®[C]; PANTHION®; PARADUST®; PARAPHOS®; PARAWET®; PENNCAP E®; PESTOX PLUS®; PETHION®; PHOSKIL®; PLEOPARAPHENE®; RHODIASOL®; RHODIATOX®; RHODIATROX®; SEIS-TRES 6-3®; SELEPHOS®; SOPRATHION®; STATHION®; SULPHOS®; SUPER RODIATOX®; T-47®; THIOMEX®; THIOPHOS®; THIOPHOS® 3422; TIOFOS®; TOX 47®; TOXOL®; VAPOPHOS®; VITREX®; WOPROPHOS®

Kontakt-Allergie

One case was reported of a bullous contact dermatitis due to ethylparathion.

Sicherheitsprofil

A deadly poison by all routes. Human systemic effects by ingestion: general anesthetic; pulmonary effects; and hdney, ureter, bladder effects, true cholinesterase changes. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental carcinogenic and tumorigenic data. Human mutation data reported. A cholinesterase inhibitor. Parathon, like the other organic phosphorus poisons, acts as an irreversible inhibitor of the enzyme cholinesterase and thus allows the accumulation of large amounts of acetylcholine. When a critical level of cholinesterase depletion is reached, grave symptoms appear. Whether death is actually caused entirely by cholinesterase depletion or by the disturbance of a number of enzymes is not yet known. Recovery is apparently complete if a poisoned animal or human has time to re-form a critical amount of cholinesterase. The organism exposed remains susceptible to relatively low dosages of parathion untd the chohnesterase has regenerated. Small doses at frequent intervals are, therefore, more or less additive. There is no indication that, when recovery from a given exposure is entirely complete, the exposed organism is prejudiced in any way. Combustible when exposed to heat or flame. Violent reaction with endrin. Highly dangerous; shock can shatter the container, releasing the contents A broad spectrum insecticide in agricultural applications. When heated to decomposition it emits highly toxic fumes of NOx, POx, and SOx.

mögliche Exposition

A severely hazardous pesticide formulation. Those exposed include those engaged in manufacture,formulation and application of this broad spectrum insecticide. This material has also been used as a chemical warfare agent.

Carcinogenicity

In an animal bioassay a dose-related increase in the incidence of adrenal cortical adenomas (with a few carcinomas at this site as well) has been observed in one strain of rats in both sexes. The significance of these lesions in aged rats in unclear. Other bioassays in mice and rats had sufficient limitations, such that the IARC deemed them inadequate for evaluation and concluded that there are insufficient data to evaluate the carcinogenicity of parathion for animals and no data for humans.

Stoffwechselwegen

The structure of parathion is similar to those of methyl parathion (the dimethylphosphoryl analogue) and fenitrothion which has a 3-methyl group on the phenyl ring: consequently the environmental fate and pathways for biotransformation are similar. As the first commercial organophosphorus insecticide, many studies have been conducted on its mechanisms of activation and degradation in a very wide range of organisms. The following is necessarily a selection of only some of the results which have been used to illustrate the principles of its metabolism. The principal metabolic routes of degradation in all media are via de-esterification to give O,O-diethyl phosphorothioate and 4-nitrophenol and by de-ethylation to desethylparathion (a less important route). Activation to the toxic anticholinesterase metabolite paraoxon is also a major metabolic route in soil, plants and animals. Paraoxon is also formed photochemically in the environment; however, it is relatively quickly detoxified in animals and plants by esterase and base-catalysed hydrolysis to 4-nitrophenol and diethyl phosphate. A further detoxification mechanism, which is mainly important in the soil, and possibly in plants and in ruminants, is reduction of the 4nitro group to yield aminoparathion. 4-Nitrophenol is conjugated in plants as the glucoside, in insects as the glucoside and/or sulfate ester and in mammals as the glucuronide and the sulfate ester.

Stoffwechsel

The principal degradation routes of parathion in animals, plants, and soil are dearylation and dealkylation to give O,O-diethyl hydrogen phosphorothioate, p-nitrophenol, and desethylparathion. Oxidative desulfuration also occurs to form the active methabolite paraoxon, which is quickly detoxified by hydrolysis. DT50 in soil was 65 d.

Versand/Shipping

UN3278 Organophosphorus compound, liquid, toxic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required, Potential Inhalation Hazard (Special Provision 5).UN2783 Organophosphorus pesticides, solid, toxic, Hazard Class: 6.1; Labels: 6.1-Poisonous materials. UN3018 Organophosphorus pesticides, liquid, toxic, Hazard Class: 6.1; Labels: 6.1- Poisonous materials.

Inkompatibilitäten

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides. Strong oxidizers may cause release of toxic phosphorus oxides. Organophosphates, in the presence of strong reducing agents such as hydrides, may form highly toxic and flammable phosphine gas. Keep away from alkaline materials. Attacks some plastics, rubbers, and coatings. Rapidly hydrolyzed by alkalis.

Waste disposal

Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. In accordance with 40CFR165, follow recommendations for the disposal of pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting your local or federal environmental control agency, or by contacting your regional EPA office. One manufacturer recommends the use of a detergent in a 5% trisodium phosphate solution for parathion disposal and cleanup problems. For parathion disposal in general, however, the recommended method is incineration (816°C, 0.5 second minimum for primary combustion; 1204°C, 1.0 second for secondary combustion) with adequate scrubbing and ash disposal facilities.

Parathion (ISO) Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

56-38-2(Parathion (ISO))Verwandte Suche:


  • phosphorothioicacid,o,o-diethylo-(4-nitrophenyl)ester
  • Strathion
  • Super Rodiatox
  • superrodiatox
  • thiofos
  • thiomex
  • Thiophos
  • Thiophos 3422
  • Thiophos Parathion 4 E.C.
  • thiophos3422
  • Thiophosphate de O,O-diethyle et de O-(4-nitrophenyle)
  • thiophosphatedeo,o-diethyleetdeo-(4-nitrophenyle)
  • thiophosphoricacidO,O’-diethylester
  • thiophosphoricacidO,O’-diethylesterO’’-(4-nitro-phenyl)ester
  • Tiofos
  • TOX 47
  • tox47
  • Vapophos
  • Vitrex
  • phosphorothioicacid,o,o-diethylo-(p-nitrophenyl)ester
  • PhosphorothionicacidO,O-diethyl-O-(4-nitro-phenyl)ester
  • Phosphostigmine
  • Rcra waste number P089
  • rcrawastenumberp089
  • Rhodiasol
  • Rhodiatox
  • Rhodiatrox
  • selephos
  • soprathion
  • soprothion
  • Stabilized ethyl parathion
  • stabilizedethylparathion
  • Stathion
  • deoxynucleoside triphosphate, 10MM Mix
  • deoxynucleoside triphosphate, 2.5MM Mix
  • Parathion standard in chloroforM
  • CleanAmp? dNTP
  • Parathion Solution, 100ppm
  • THIOPHOS(R)
  • SNP(R)
  • O,O-DIETHYL-O-P-NITROPHENYL PHOSPHOROTHIOATE
  • O,O-Diethyl-O-(p-nitrophenyl)thionophosphate
  • O,O-DIETHYL O-(4-NITROPHENYL) PHOSPHOROTHIOATE
  • ORTHOPHOS(R)
  • ACC 3422(R)
  • ALKRON(R)
  • AATP
  • AC 3422
  • ac3422
  • ACC 3422
  • acc3422
  • Alkron
  • Alleron
  • American Cyanamid 3422
  • americancyanamid3422
  • Aphamite
  • Aralo
  • B 404
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