Fenitrothion (ISO) Chemische Eigenschaften,Einsatz,Produktion Methoden
ERSCHEINUNGSBILD
BRAUNE BIS GELBE FLüSSIGKEIT MIT CHARAKTERISTISCHEM GERUCH.
CHEMISCHE GEFAHREN
Zersetzung beim Erhitzen oder Verbrennen unter Bildung giftiger Rauche mit Stickstoffoxiden, Phosphoroxiden und Schwefeloxiden.
ARBEITSPLATZGRENZWERTE
TLV nicht festgelegt (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).
AUFNAHMEWEGE
Aufnahme in den Körper durch Inhalation des Aerosols, über die Haut und durch Verschlucken.
INHALATIONSGEFAHREN
Nur ungenügende Angaben vorhanden über die Geschwindigkeit, mit der eine gesundheitsschädliche Konzentration in der Luft beim Verdampfen bei 20°C erreicht wird.
WIRKUNGEN BEI KURZZEITEXPOSITION
WIRKUNGEN BEI KURZZEITEXPOSITION: Die Substanz reizt die Augen und die Haut. Möglich sind Auswirkungen auf das Nervensystem mit nachfolgenden Krämpfen, Atemversagen und Tod. Cholinesterasehemmer. Die Auswirkungen treten u.U. verzögert ein. ärztliche Beobachtung notwendig.
WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION
Cholinesterasehemmer. Kumulative Wirkung möglich (s. AKUTE GEFAHREN/SYMPTOME).
LECKAGE
Ausgelaufene Flüssigkeit möglichst in abdichtbaren Behältern sammeln. Reste mit Sand oder inertem Absorptionsmittel aufnehmen und an einen sicheren Ort bringen. NICHT in die Kanalisation spülen. Persönliche Schutzausrüstung: Chemikalienschutzanzug mit umgebungsluftunabhängigem Atemschutzgerät.
R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R23:Giftig beim Einatmen.
R21/22:Gesundheitsschädlich bei Berührung mit der Haut und beim Verschlucken.
R67:Dämpfe können Schläfrigkeit und Benommenheit verursachen.
R65:Gesundheitsschädlich: kann beim Verschlucken Lungenschäden verursachen.
R38:Reizt die Haut.
R11:Leichtentzündlich.
S-Sätze Betriebsanweisung:
S2:Darf nicht in die Hände von Kindern gelangen.
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.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S62:Bei Verschlucken kein Erbrechen herbeiführen. Sofort ärztlichen Rat einholen und Verpackung oder dieses Etikett vorzeigen.
Chemische Eigenschaften
Pure fenitrothion is a yellowish brown liquid with an unpleasant odor. It is insoluble in water, but readily soluble in common organic solvents, such as acetone, alcohol, benzene, chlorinated hydrocarbons, dichloromethane, 2-propanol, toluene, in ethers, methanol, and xylene. It decomposes explosively. Fenitrothion is a contact insecticide and a selective acaricide of low ovicidal properties. Fenitrothion is effective against a wide range of pests, namely, penetrating, chewing, and sucking insect pests (coffee leaf-miners, locusts, rice stem borers, wheat bugs, fl our beetles, grain beetles, grain weevils) on cereals, cotton, orchard fruits, rice, vegetables, and forests. It may also be used as a fl y, mosquito, and cockroach residual contact spray for farms and public health programs. Fenitrothion is also effective against household insects and all nuisance insects. WHO confi rmed its effectiveness as a vector control agent for malaria. It is extensively used in other countries, including Japan, where parathion has been banned. Occupational workers are exposed to fenitrothion during mixing, loading/transportation, and fi eld applications.
Verwenden
Fenitrothion is used to control sucking, chewing and boring
insects in cereals, soft fruit, tropical fruit, vines, sugar cane, vegetables,
turf and forestry. It is also used as a public health insecticide for the
control of flies, cockroaches and mosquitoes. Other uses are for the control
of stored product pests and locusts.
Definition
ChEBI: An organic thiophosphate that is O,O-dimethyl O-phenyl phosphorothioate substituted by a methyl group at position 3 and a nitro group at position 4.
Allgemeine Beschreibung
Brownish-yellow oil. Used as a selective acaricide and a contact and stomach insecticide against chewing and sucking insects on rice, orchard fruits, vegetables, cereals, cotton and forest. Also used against flies, mosquitoes, and cockroaches.
Reaktivität anzeigen
Organophosphates, such as Fenitrothion, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.
Hazard
Cholinesterase inhibitor, use may be
restricted.
Health Hazard
Fenitrothion is an organophosphate insecticide. It is a highly toxic cholinesterase inhibitor, that acts on the nervous system. Does not cause delayed neurotoxicity and contact produces little irritation.
Brandgefahr
When heated to decomposition, Fenitrothion emits very toxic fumes of oxides of nitrogen, phosphorus and sulfur. Decomposition at 212-284F produces a mixture of organophosphorus polymers. Unstable in alkaline media. Stable for 2 years if stored at 68-77F. Do not store above 104F.
Handelsname
ACCOTHION®; ACEOTHION®; AGRIA
1050®; AGRIYA 1050®; AGROTHION®; AMERICAN
CYANAMID CL-47,300®; ARBOGAL®; BAY 41831®;
BAYER 41831®; BAYER S 5660®; CEKUTROTHION®;
CL 47300®; CP47114®; CYFEN®; CYTEL®;
CYTEN®; DICATHION®; DICOFEN®; DYBAR®;
EI 47300®; FALITHION®; FENITEX®; FENITOX®;
FENSTAN®; FOLETHION®; FOLITHION®; H-35-F
87 (BVM)®; 8057HC®; KALEIT®; KEEN SUPERKILL
ANT AND ROACH EXTERMINATOR®; KILLGERM
TETRACIDE INSECTICIDAL SPRAY®; KOTION®;
MEP (PESTICIDE)®; METATHION®; METATHIONE®;
METATION®; MICROMITE®; MONSANTO CP
47114®; NITROPHOS®; NOVATHION®; NUVAND®;
NUVANOL®; OLEOSUMIFENE®; OMS 43®;
OVADOFOS®; PENNWALT C-4852; PESTROY®; S
112A®; S 5660®; SMT®; SUMITHION®[C]; TURBAIR
GRAIN STORAGE INSECTICIDE®; VERTHION®
Sicherheitsprofil
Poison by ingestion,
inhalation, intravenous, and intraperitoneal
routes. Moderately toxic by skin contact,
intratracheal, and subcutaneous routes.
Human systemic effects: coma, diarrhea,
dyspnea, gastrointestinal changes,
hypermodtty, nausea or vomiting,
respiratory depression. Mutation data
reported. When heated to decomposition it
emits very toxic fumes of NOx, POx, and
sox
mögliche Exposition
A potential danger to those involved
in the manufacture, formulation, and application of this
insecticide. It is a selective acaricide; and a contact and
stomach insecticide. Used to control chewing and sucking
insects on rice, orchard fruit; vegetables, cereals, cotton,
and in forests. Also protects against flies, mosquitoes, and
cockroaches
Stoffwechselwegen
Fenitrothion is a non-systemic insecticide, the biotransformations and
environmental fate of which have been intensively studied and reviewed.
Metabolism has been studied in mammals (including humans), birds,
fish, crustacea, molluscs, insects, algae, plants and soil. The major routes
of biotransformation involve desulfuration to the oxon analogue
(fenitrooxon) and hydrolysis to give dimethyl phosphate, O,O-dimethyl
phosphorothioate and 3-methyl-4-nitrophenol. Demethylation to give
desmethylfenitrothion and its decomposition products, reduction of
the nitro group and oxidation of the ring methyl group also
occur. Demethylation via glutathione-S-methyl transferases in the liver
is a particularly important mechanism in mammals. Reduction of
the nitro group to an amino group is important in anaerobic soils
and ruminants but this has also been shown to occur in rats, rabbits
and humans where it is presumably carried out by bacteria in the gut.
Oxidation of the 3-methyl group to hydroxymethyl and carboxylate
has been shown to be a degradative route in birds. The major routes of
phase II metabolism involve conjugation of 3-methyl-4-nitrophenol to the
glucoside in plants and insects, to the sulfate ester in birds and the sulfate
ester and glucuronide in mammals.
Stoffwechsel
The main biotransformation routes involve oxidative
desulfuration to the oxon and dearylation to give
dimethyl hydrogen phosphate, O,O-dimethyl hydrogen
phosphorothioate and 3-methyl-4-nitrophenol. Demethylation
dependent on glutathion-S-alkyl transferase is particularly
important in mammals.Oxidation of the 3-methyl
group to hydroxymethyl and then carboxyl group is also
a degradative route. Reduction of the nitro group to an
amino group occurs in anaerobic soils and ruminants. The
DT
50 in soils under upland and submerged conditions were
12–28 and 4–20 d, respectively.
Versand/Shipping
UN3017 Organophosphorus pesticides, liquid,
toxic, flammable, flash point not ,23C, Hazard class: 6.1;
Labels: 6.1-Poisonous materials, 3-Flammable liquid.
UN2810 Toxic liquids, organic, n.o.s., Hazard Class: 6.1;
Labels: 6.1-Poisonous materials, Technical Name Required
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
Waste disposal
Incineration (for large
amounts); alkaline hydrolysis and landfill (for small
amounts). 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.
Fenitrothion (ISO) Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
