O,O-Diethyl-O-1-phenyl-1,2,4-triazol-3-ylthio-phosphat

Bezeichnung:O,O-Diethyl-O-1-phenyl-1,2,4-triazol-3-ylthio-phosphat

CAS-Nr24017-47-8

Englisch Name:Triazophos

CBNumberCB9221130

SummenformelC12H16N3O3PS

Molgewicht313.31

MOL-Datei24017-47-8.mol

Synonyma

Triazophos

O,O-Diethyl-O-1-phenyl-1,2,4-triazol-3-ylthio-phosphat

O,O-Diethyl-O-1-phenyl-1,2,4-triazol-3-ylthio-phosphat physikalisch-chemischer Eigenschaften

Schmelzpunkt	0-5°C
Siedepunkt	260°C
Dichte	1.247
Dampfdruck	3.9×10^-4 Pa (30 °C)
Flammpunkt	25 °C
storage temp.	APPROX 4°C
Löslichkeit	DMSO (Slightly), Methanol (Slightly)
pka	-0.15±0.50(Predicted)
Aggregatzustand	liquid
Wasserlöslichkeit	30-40 mg/L at 20 ºC
BRN	682554
Stabilität	Hygroscopic
NIST chemische Informationen	Triazophos(24017-47-8)
EPA chemische Informationen	Triazophos (24017-47-8)

Sicherheit

Kennzeichnung gefährlicher	T;N,N,T
R-Sätze:	21-23/25-50/53-38-10
S-Sätze:	1/2-36/37-45-60-61
RIDADR	3018
WGK Germany	3
RTECS-Nr.	TF5635000
HazardClass	6.1(a)
PackingGroup	II
HS Code	29339900
Giftige Stoffe Daten	24017-47-8(Hazardous Substances Data)
Toxizität	LD50 in rats (mg/kg): 82 orally, 1100 dermally (Thier); LD50 in rats (mg/kg): 107 i.p.; in rabbits (mg/kg): 280 dermally (Hay)

Gefahreninformationscode (GHS)

Triazophos Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R21:Gesundheitsschädlich bei Berührung mit der Haut.
R23/25:Giftig beim Einatmen und Verschlucken.
R50/53:Sehr giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R38:Reizt die Haut.
R10:Entzündlich.
S-Sätze Betriebsanweisung:
S1/2:Unter Verschluss und für Kinder unzugänglich aufbewahren.
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.
Verwenden
An organophosphorus insecticide.
Verwenden
Triazophos is used to control chewing and sucking insects and mites in a wide range of crops. It is also used to control some nematodes in ornamentals and strawberries.
Verwenden
Pesticide.
Definition
ChEBI: Triazophos is an organic thiophosphate and an organothiophosphate insecticide. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, an acaricide, an agrochemical and a nematicide. It is functionally related to a 1-phenyl-1H-1,2,4-triazol-3-ol.
Allgemeine Beschreibung
Yellowish oil. Used to control insects, mites, and nematodes. Not registered as a pesticide in the U.S.
Reaktivität anzeigen
Organophosphates, such as Triazophos, 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.
Health Hazard
This is an organophosphate pesticide. Triazophos is a cholinesterase inhibitor and acts on the central nervous system. Organic phosphorus insecticides are absorbed by the skin as well as by the respiratory and gastrointestinal tracts.
Brandgefahr
This is an organophosphate pesticide. Some of these materials may burn but none of them ignite readily. Container may explode in heat of fire. Fire may produce irritating or poisonous gases. Degraded by acids and alkalis.
Landwirtschaftliche Anwendung
Insecticide: Triazophos is a broad-spectrum insecticide and acaricide used to control sucking and chewing pests on a variety of crops, including cotton, rice, corn, beets and fruit trees. Not currently registered for use in the U.S. Not approved for use in EU countries . There are more than 30 global suppliers .
Handelsname
HILAZPOPHOS®; HOE 2960 OJ®; HOE 002960®; HOSTATHION®; SUTATHION®
Stoffwechselwegen
The main route of biotransformation of triazophos is degradation to 1- pheny1-3-hydroxy-1,2,4-triazole, probably either via hydrolysis of triazophos oxon or through oxidative cleavage of triazophos itself. The triazole ring of this metabolite is opened to give 1-phenylsemicarbazide and semicarbazide, both of which are conjugated in the rat and also degraded to urea as the main urinary metabolite.
Degradation
Triazophos is stable to light but is hydrolysed by acids and alkalis (PM).

Triazophos Upstream-Materialien And Downstream Produkte

O,O-Diethyl-O-1-phenyl-1,2,4-triazol-3-ylthio-phosphat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

24017-47-8, Triazophos Verwandte Suche:

Send Inquriy