Weight | 336.826 g/mol |
---|---|
Formula | C19H17ClN4 |
Hydrogen Acceptors | 4 |
Hydrogen Donors | 0 |
Aromatic Rings | 3 |
Rotatable Bonds | 6 |
Fenbuconazole (119611-00-6, 114369-43-6)
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- Baseline Sensitivities of Fungal Pathogens of Fruit and Foliage of Citrus to Azoxystrobin, Pyraclostrobin, and Fenbuconazole (Plant Disease, 2005)
- The effect of fenbuconazole on cell proliferation and enzyme induction in the liver of female CD1 mice (Toxicology and Applied Pharmacology, 2006)
- Simultaneous enantioselective determination of fenbuconazole and its main metabolites in soil and water by chiral liquid chromatography/tandem mass spectrometry (Journal of Chromatography A, 2011)
- Residue analysis and degradation studies of fenbuconazole and myclobutanil in strawberry by chiral high-performance liquid chromatography-tandem mass spectrometry. (Journal of Agricultural and Food Chemistry, 2011)
- Environmental behavior of the chiral triazole fungicide fenbuconazole and its chiral metabolites: enantioselective transformation and degradation in soils. (Environmental Science & Technology, 2012)
- Determination of genotoxic effects of chlorfenvinphos and fenbuconazole in Allium cepa root cells by mitotic activity, chromosome aberration, DNA content, and comet assay (Pesticide Biochemistry and Physiology, 2012)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H351: Suspected of causing cancer
Warning Carcinogenicity - Category 2 - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 - H400: Very toxic to aquatic life
Warning Hazardous to the aquatic environment, acute hazard - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 -
SMILESC1=CC=C(C=C1)C(CCC2=CC=C(C=C2)Cl)(CN3C=NC=N3)C#N
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InChIKeyRQDJADAKIFFEKQ-UHFFFAOYSA-N
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