| Weight | 342.226 g/mol |
|---|---|
| Formula | C15H17Cl2N3O2 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
PROPICONAZOLE (60207-90-1)
1-((2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-yl)methyl)-1H-1,2,4-triazole
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- Changes in antioxidant metabolism of Vigna unguiculata (L.) Walp. by propiconazole under water deficit stress. (Colloids and Surfaces B: Biointerfaces, 2007)
- Occurrence of azoxystrobin, propiconazole, and selected other fungicides in US streams, 2005-2006 (Water Air and Soil Pollution, 2011)
- Molecular impact of propiconazole on Daphnia magna using a reproduction-related cDNA array (Comparative Biochemistry and Physiology C-toxicology & Pharmacology, 2006)
- Some effects of the fungicide propiconazole on cytochrome P450 and glutathione S-transferase in brown trout (Salmo trutta) (Comparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology, 1999)
- Propiconazole-induced cytochrome P450 gene expression and enzymatic activities in rat and mouse liver (Toxicology Letters, 2005)
- The fungicide propiconazole interferes with embryonic development of the crustacean Daphnia magna (Environmental Toxicology and Chemistry, 2001)
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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 - 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 - 1-((2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-yl)methyl)-1H-1,2,4-triazole
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SMILESCCCC1COC(O1)(CN2C=NC=N2)C3=C(C=C(C=C3)Cl)Cl
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InChIKeySTJLVHWMYQXCPB-UHFFFAOYSA-N
- Pubchem - PROPICONAZOLE
- Wikipedia - propiconazole
Propiconazole is a triazole fungicide, also known as a DMI, or demethylation inhibiting fungicide due to its binding with and inhibiting the 14-alpha demethylase enzyme from demethylating a precursor to ergosterol. Without this demethylation step, the ergosterols are not incorporated into the growing fungal cell membranes, and cellular growth is stopped.
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