TRIAZAMATE
Synonym(s):Ethyl (3-tert-butyl-1-dimethylcarbamoyl-1H-1,2,4-triazol-5-ylthio)acetate;Ethyl 2-{{1-[(dimethylamino)carbonyl]-3-(1,1-dimethylethyl)-1H-1,2,4-triazol-5-yl}thio}acetate
- CAS NO.:112143-82-5
- Empirical Formula: C13H22N4O3S
- Molecular Weight: 314.4
- MDL number: MFCD01632354
- SAFETY DATA SHEET (SDS)
- Update Date: 2023-04-23 13:52:06
What is TRIAZAMATE?
The Uses of TRIAZAMATE
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.
The Uses of TRIAZAMATE
Pesticide.
The Uses of TRIAZAMATE
Triazamate is used in controlling unpleasant pests.Used in preparation of Thiazole Manganese Zinc compounds and compounds thereof.
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.
General Description
Triazamate is a carbamoyl triazole compound, widely used as an insecticide and its mode of action involves the inhibition of cholinesterase in insect pests.
Metabolic pathway
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)
Properties of TRIAZAMATE
Melting point: | 60° |
Boiling point: | 280°C (rough estimate) |
Density | 1.2357 (rough estimate) |
vapor pressure | 1.6 x l0-4 Pa (25 °C) |
refractive index | 1.6200 (estimate) |
Flash point: | 189℃ |
pka | 0.48±0.50(Predicted) |
form | neat |
Water Solubility | 433 mg l-1(25 °C) |
BRN | 8422595 |
EPA Substance Registry System | Triazamate (112143-82-5) |
Safety information for TRIAZAMATE
Signal word | Danger |
Pictogram(s) |
Skull and Crossbones Acute Toxicity GHS06 Environment GHS09 |
GHS Hazard Statements |
H301:Acute toxicity,oral H319:Serious eye damage/eye irritation H330:Acute toxicity,inhalation H400:Hazardous to the aquatic environment, acute hazard |
Precautionary Statement Codes |
P273:Avoid release to the environment. P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing. |
Computed Descriptors for TRIAZAMATE
New Products
ALUMINIUM IODIDE 100 GM BUFFER CAPSULE PH 7.0 - 10 CAP BUFFER SOLUTION PH 9.5 (BORATE) EZEE BLUE GEL STAINER BORAX CARMINE (GRENACHERS ALCOHOLIC) POTASSIUM IODATE - IODIDE SOLN 0.1 N Dabigatran Acyl-O3-D-Glucuronide Trifluoroacetic Acid Salt Isofolic Acid Dabigatran 2-O-acylglucuronide metabolite Dabigatran Acyl-?-D- glucuronide Trifluroacetic Acid Erythromycin EP Impurity A Desloratidine Related Compound ARelated products of tetrahydrofuran
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