| Weight | 228.321 g/mol |
|---|---|
| Formula | C9H16N4OS |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
tebuthiuron (34014-18-1, 35208-55-0)
1-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-1,3- dimethylurea
Score:
#117 in Environmental science
,
#1192 in Biology
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- Degradation of the herbicide tebuthiuron using solar photo-Fenton process and ferric citrate complex at circumneutral pH (Journal of Photochemistry and Photobiology A-chemistry, 2007)
- Multivariate analysis of photo-Fenton degradation of the herbicides tebuthiuron, diuron and 2,4-D (Chemosphere, 2005)
- Heterogeneous photocatalysed reaction of three selected pesticide derivatives, propham, propachlor and tebuthiuron in aqueous suspensions of titanium dioxide (Chemosphere, 2005)
- Effects of picloram and tebuthiuron pellets on sand shinnery oak communities. (Journal of Range Management, 1979)
- A comparative study of the electrochemical oxidation of the herbicide tebuthiuron using boron-doped diamond electrodes. (Chemosphere, 2012)
- Photo-Fenton degradation of the herbicide tebuthiuron under solar irradiation: Iron complexation and initial intermediates (Water Research, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - 1-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-1,3- dimethylurea
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SMILESCC(C)(C)C1=NN=C(S1)N(C)C(=O)NC
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InChIKeyHBPDKDSFLXWOAE-UHFFFAOYSA-N
- Pubchem - tebuthiuron
- Wikipedia - tebuthiuron
Tebuthiuron is a nonselective broad spectrum herbicide of the urea class. It is used in a number of herbicides manufactured by Dow AgroSciences, and is sold under several trade names, depending on the formulation. It is used to control weeds, woody and herbaceous plants, and sugar cane.
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Alternate Names
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Synthesis
Methylaminoformyl chloride
+
5-tert-Butyl-N-methyl-1,3,4-thiadiazol-2-amine
(Schotten-Baumann amide from acid)
Methylboronic acid
+
Reactant
(Chan-Lam coupling reaction)
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