| Weight | 199.257 g/mol |
|---|---|
| Formula | C12H13N3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
Pyrimethanil (53112-28-0)
Score:
#164 in Environmental science
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#2489 in Biology
,
#3107 in Chemistry
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- Enhanced and irreversible sorption of pesticide pyrimethanil by soil amended with biochars (Journal of Environmental Sciences-china, 2010)
- Molecularly imprinted solid-phase extraction method for the high-performance liquid chromatographic analysis of fungicide pyrimethanil in wine (Journal of Chromatography A, 2007)
- Comparative Efficacy of the New Postharvest Fungicides Azoxystrobin, Fludioxonil, and Pyrimethanil for Managing Citrus Green Mold (Plant Disease, 2007)
- Disappearance of Azoxystrobin, Pyrimethanil, Cyprodinil, and Fludioxonil on Tomatoes in a Greenhouse (Journal of Agricultural and Food Chemistry, 2002)
- The effectiveness of pyrimethanil to inhibit germination of Penicillium digitatum and to control citrus green mold after harvest (Postharvest Biology and Technology, 2006)
- Fate of some new fungicides (cyprodinil, fludioxonil, pyrimethanil and tebuconazole from vine to wine (Journal of Agricultural and Food Chemistry, 1997)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H411: Toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 2 - H411: Toxic to aquatic life with long lasting effects
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- Pubchem - Pyrimethanil
- Wikipedia - pyrimethanil
Pyrimethanil is a broad spectrum fungicide often applied to seeds. It inhibits methionine biosynthesis, thus affecting protein formation and subsequent cell division. Pyrimethanil works best on young fungus infestations.
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Pyrimethanil
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