Ethyl(3-tert-butyl-1-dimethylcar-bamoyl-1H-1,2,4-triazol-5-ylthio)-acetat

Bezeichnung:Ethyl(3-tert-butyl-1-dimethylcar-bamoyl-1H-1,2,4-triazol-5-ylthio)-acetat

CAS-Nr112143-82-5

Englisch Name:TRIAZAMATE

CBNumberCB9334678

SummenformelC13H22N4O3S

Molgewicht314.4

MOL-Datei112143-82-5.mol

Synonyma

Ethyl(3-tert-butyl-1-dimethylcar-bamoyl-1H-1,2,4-triazol-5-ylthio)-acetat

Ethyl(3-tert-butyl-1-dimethylcar-bamoyl-1H-1,2,4-triazol-5-ylthio)-acetat physikalisch-chemischer Eigenschaften

Schmelzpunkt	60°
Siedepunkt	280°C (rough estimate)
Dichte	1.2357 (rough estimate)
Dampfdruck	1.6 x l0^-4 Pa (25 °C)
Brechungsindex	1.6200 (estimate)
Flammpunkt	189℃
Wasserlöslichkeit	433 mg l^-1(25 °C)
pka	0.48±0.50(Predicted)
BRN	8422595
EPA chemische Informationen	Triazamate (112143-82-5)

Sicherheit

Kennzeichnung gefährlicher	T,N
R-Sätze:	23-25-36-50
S-Sätze:	26-45-61
RIDADR	UN2811 - class 6.1 - PG 2 - EHS - Toxic solids, organic, n.o.s., HI: all
WGK Germany	3
Toxizität	LD50 (14 d) in mice, rats (mg/kg): 61, 50-200 orally; in rats (mg/kg): >5000 dermally (Murray); LC50 (48 h) in daphnia: 0.048 mg/l; (96 h) in bluegill, trout: 1.0, 0.43 mg/l (Murray)

Gefahreninformationscode (GHS)

TRIAZAMATE Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden
Triazamate is used in controlling unpleasant pests.Used in preparation of Thiazole Manganese Zinc compounds and compounds thereof.
Verwenden
Triazamate is used for the control of aphids by foliar application on a wide variety of crops. It is suitable for inclusion in integrated pest management because it is minimally toxic to beneficial insects.
Verwenden
Pesticide.
Definition
ChEBI: A triazole insecticide that is 1H-1,2,4-triazole which is substituted at positions 1, 3, and 5 by N,N-dimethylaminocarbonyl, tert-butyl, and (2-ethoxy-2-oxoethyl)sulfanediyl groups, resp ctively.
Allgemeine Beschreibung
Triazamate is a carbamoyl triazole compound, widely used as an insecticide and its mode of action involves the inhibition of cholinesterase in insect pests.
Stoffwechselwegen
There is only a limited amount of information on the fate of triazamate currently in the public domain. Metabolism in sugar beet and apple has been reported. Animal metabolism studies have been conducted but details are not available. Triazamate is very rapidly metabolised by hydrolysis, decarbamoylation and further metabolism in all biological systems studied (PM).
Degradation
Triazamate is stable under normal conditions and in solution at pH 7 and below. Its DT₅₀ values in buffers are, at pH 5, 7 and 9, 220 days, 49 hours and 1 hour, respectively (PM). Base-catalysed hydrolysis should initially afford triazamate acid (2) by carboxyl ester cleavage (see Scheme 1).
The DTM of triazamate on aqueous photolysis at pH 7 is 301 days (PM)

TRIAZAMATE Upstream-Materialien And Downstream Produkte

Ethyl(3-tert-butyl-1-dimethylcar-bamoyl-1H-1,2,4-triazol-5-ylthio)-acetat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

112143-82-5, TRIAZAMATE Verwandte Suche:

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