30125-63-4

Basic information

• Product Name: TERBUTHYLAZINE-DESETHYL
• Synonyms: TERBUTHYLAZIN-DESETHYL;TERBUTHYLAZINE-DESETHYL;DESETHYLTERBUTHYLAZINE;DESETHYLTERBUTYLAZINE;2-AMINO-4-TERT-BUTYLAMINO-6-CHLORO-1,3,5-TRIAZINE;TERBUTHYLAZIN-DESETHYL PESTANAL 250 MG;Deethylterbuthylazine;2-Amino-4-tert-butylamino-6-chloro-1,3,5-triazine, Desethylterbutylazine
• CAS NO: 30125-63-4
• Molecular Formula: C₇H₁₂ClN₅
• Molecular Weight: 201.66
• Mol File: 30125-63-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 386.8°Cat760mmHg
• Flash Point: 100 °C
• Appearance: /
• Density: 1.323g/cm³
• Vapor Pressure: 3.44E-06mmHg at 25°C
• Refractive Index: 1.614
• PKA: 3.92±0.10(Predicted)
• BRN: 514392
• CAS DataBase Reference: TERBUTHYLAZINE-DESETHYL(CAS DataBase Reference)
• NIST Chemistry Reference: TERBUTHYLAZINE-DESETHYL(30125-63-4)
• EPA Substance Registry System: TERBUTHYLAZINE-DESETHYL(30125-63-4)

Safety Data

• Hazard Codes: Xi
• Statements: 43
• Safety Statements: 36/37
• WGK Germany: 3
• Hazardous Substances Data: 30125-63-4(Hazardous Substances Data)

Usage

Definition

ChEBI: A diamino-1,3,5-triazine that is 1,3,5-triazine-2,4-diamine substituted by a tert-butyl group at the amino nitrogen and a chloro group at position 6. It is metabolite of the herbicide terbutylazine.

General Description

Terbuthylazin-desethyl is a triazine herbicide used for the control and elimination of weeds.

InChI:InChI=1/C7H12ClN5/c1-7(2,3)13-6-11-4(8)10-5(9)12-6/h1-3H3,(H3,9,10,11,12,13)

Upstream product

• 5915-41-3 terbuthylazine 

Relevant articles and documents

Photosensitized degradation of terbuthylazine in water

We investigated the photodegradation of terbuthylazine, an s-triazine herbicide, in the presence of hydrogen peroxide (H2O2), titanium dioxide (TiO2), acetone or humic substances. In the presence of H2O2 and UV light, the degradation of terbuthylazine quickly leads to the formation of ammeline. The degradation pathway consists of dealkylation reactions giving 2-chloro-4,6-diamino-1,3,5-triazine, and then ammeline through hydroxylation. Irradiation of terbuthylazine with simulated solar light in the presence of titanium dioxide gives also dealkylation products in the first stage of degradation. Acetone at 1% (v/v) produces a 7-fold enhancement of the degradation rate. In the presence of humic substances, different results were obtained, depending on the origin of the substances tested. The humic acids isolated from a soil accelerate the degradation speed, whereas the fulvic acids from a small stream reduce it.