Es wird als Herbizid eingesetzt. Environmental Protection Agency has proposed the revocation of all tolerances for residues of terbutryn in or . The European Chemicals Agency (hereinafter “ECHA”) maintains this website ( hereinafter the ECHA website) to enhance public access to . Terbutryn is a General Use Pesticide (GUP). Pesticide properties for terbutryn , including approvals, environmental fate, eco- toxicity and human health issues. It is a triazine compound and is known to inhibit photosynthesis. In the aquatic system terbutryn is very toxic to algae, toxic to fish and medium . Herbicide, an s-triazine that interferes with photosynthesis by . Registered For: Commercial use.
L mcpa present as the potassium salt. Boiling Point : 322. Overview: For the control of seedling broadleaf . FOOD AND AGRICULTURE ORGANIZATION OF THE UNITED NATIONS. You will need Adobe Reader to view some of the files on this page.
This information should not be interpreted without the help of a healthcare provider. If you believe you are experiencing an interaction, contact a . Key issues controlled. Molecular Formula: C10H19N5S, Molecular Weight: 241.
Especially polymer-resin-based renders and paints, used in external thermal . Toxicity was measured by the . It is absorbed by the roots and foliage and acts as an inhibitor of photosynthesis. Sixteen metabolites of terbutryn were isolated from the urine and feces of either rats or a goat given single oral doses of . Notes: Accurate Mass: 241. In both locations, the soil organic matter (SOM) content decreased after clear- ing and cropping. Abstract: An analytical method for the quantification of the herbicides and algaecides diuron, terbuthylazine, and terbutryn in wastewater and soil by.
Biesterfeld offers various formulations. ChEBI Name, terbutryn. Definition, A methylthio-5- triazine that is 2-(methylsulfanyl)-5-triazine substituted by a . Compendium of Pesticide Common Names, including IUPAC and CAS systematic names, molecular formula, structural formula, . Degradation of atrazine was affected to a lesser extent by soil disinfestation.
The used herbicide terbutryn is found to bind via at least two hydrogen bonds to the QB site similar to photosynthetic reaction centers in . A gas chromatographic method for quantitative analysis of terbutryn in crops has been established.