Weight | 214.294 g/mol |
---|---|
Formula | C8H14N4OS |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
METRIBUZIN (21087-64-9)
Sencor · Lexone · Zenkor
Score:
#1238 in Biology
,
#1425 in Chemistry
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- Comparative sensitivity of five species of macrophytes and six species of algae to atrazine, metribuzin, alachlor, and metolachlor (Environmental Toxicology and Chemistry, 1998)
- Measurement and simulation of the movement and degradation of atrazine and metribuzin in a fallow soil (Pesticide Science, 1982)
- Effect of soil amendments on sorption and mobility of metribuzin in soils (Chemosphere, 2007)
- The Influence of Straw Mulch on the Soil Reception and Persistence of Metribuzin (Weed Science, 1982)
- The influence of soil properties on the rates of degradation of metamitron, metazachlor and metribuzin (Pesticide Science, 1987)
- Metribuzin metabolism in tomato: Isolation and identification of N-glucoside conjugates (Pesticide Biochemistry and Physiology, 1983)
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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 - Sencor
- Lexone
- Zenkor
- 4-amino-6-tert-butyl- 3-(methylthio)-s-triazin-5-(4H)-one
- Bay 94,337
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SMILESCC(C)(C)C1=NN=C(N(C1=O)N)SC
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InChIKeyFOXFZRUHNHCZPX-UHFFFAOYSA-N
- Pubchem - METRIBUZIN
- Wikipedia - metribuzin
Metribuzin (4-amino-6-tert-butyl-3-(methylthio)-as-triazin-5(4H)-one) is an herbicide used both pre- and post-emergence in crops including soy bean, potatoes, tomatoes and sugar cane. It acts by inhibiting photosynthesis by disrupting photosystem II. It is widely used in agriculture and has been found to contaminate groundwater.
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