| Weight | 261.119 g/mol |
|---|---|
| Formula | C9H13BrN2O2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
BROMACIL (69484-12-4, 314-40-9)
Hyvar X · bromacil, sodium salt · bromacyl
Score:
#620 in Biology
,
#660 in Chemistry
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- Sigma-Aldrich - BROMACIL26.40 - 49.80 USD
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- Model for uptake of xenobiotics into plants: Validation with bromacil experiments (Environmental Toxicology and Chemistry, 1994)
- Atrazine, Bromacil, and Diuron Resistance in Chlamydomonas A Single Non-Mendelian Genetic Locus Controls the Structure of the Thylakoid Binding Site (Plant Physiology, 1984)
- Studies on removal of metribuzin, bromacil, 2,4-D and atrazine from water by adsorption on high area carbon cloth. (Journal of Hazardous Materials, 2004)
- Analysis of bromacil, diuron and 3,4-dichloroaniline in contaminated well water, using a high-performance liquid chromatographic column-switching procedure (Journal of Chromatography A, 1987)
- Bromacil and diuron herbicides: toxicity, uptake, and elimination in freshwater fish. (Archives of Environmental Contamination and Toxicology, 1987)
- Synthesis and studies with labeled bromacil 2-C14 and terbacil. (Journal of Agricultural and Food Chemistry, 1969)
-
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 - H320: Causes eye irritation
Warning Serious eye damage/eye irritation - Category 2B - H351: Suspected of causing cancer
Warning Carcinogenicity - Category 2 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - Hyvar X
- bromacil, sodium salt
- bromacyl
-
SMILESCCC(C)N1C(=O)C(=C(NC1=O)C)Br
-
InChIKeyCTSLUCNDVMMDHG-UHFFFAOYSA-N
- Pubchem - BROMACIL
- Wikipedia - bromacil
Bromacil is an organic compound with the chemical formula C9H13BrN2O2, commercially available as a herbicide. Bromacil was first registered as a pesticide in the U.S. in 1961.
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