| Weight | 229.715 g/mol |
|---|---|
| Formula | C9H16ClN5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
Terbuthylazine (5915-41-3)
Gardoprim · terbythylazine · Click 500 SC
Score:
#110 in Environmental science
,
#1011 in Biology
,
#1124 in Chemistry
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- Selective trace enrichment of chlorotriazine pesticides from natural waters and sediment samples using terbuthylazine molecularly imprinted polymers (Analytical Chemistry, 2000)
- Sorption of the herbicide terbuthylazine in two New Zealand forest soils amended with biosolids and biochars (Journal of Soils and Sediments, 2010)
- Identification of enzymes involved in the metabolism of atrazine, terbuthylazine, ametryne, and terbutryne in human liver microsomes (Chemical Research in Toxicology, 1997)
- In vitro metabolism of atrazine, terbuthylazine, ametryne, and terbutryne in rats, pigs, and humans. (Drug Metabolism and Disposition, 1996)
- MOBILITY AND PERSISTENCE OF THE HERBICIDES ATRAZINE, METOLACHLOR AND TERBUTHYLAZINE IN PLAINFIELD SAND DETERMINED USING FIELD LYSIMETERS (Environmental Toxicology and Chemistry, 1989)
- Fate of diuron and terbuthylazine in soils amended with two-phase olive oil mill waste. (Journal of Agricultural and Food Chemistry, 2007)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Gardoprim
- terbythylazine
- Click 500 SC
- terbutylazine
-
SMILESCCNC1=NC(=NC(=N1)Cl)NC(C)(C)C
-
InChIKeyFZXISNSWEXTPMF-UHFFFAOYSA-N
- Pubchem - Terbuthylazine
- Wikipedia - terbuthylazine
Terbuthylazine is a selective herbicide. Chemically, it is a chlorotriazine; compared with atrazine and simazine, it has a tert-butyl group in place of the isopropyl and ethyl groups, respectively.
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Terbuthylazine
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