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| | PICOLINAFEN Basic information |
| Product Name: | PICOLINAFEN | | Synonyms: | PICOLINAFEN;N-(4-FLUOROPHENYL)-6-[3-(TRIFLUOROMETHYL)PHENOXY]-2-PYRIDINECARBOXAMIDE;N-(4-FLUOROPHENYL)-6-(ALPHA,ALPHA,ALPHA-TRIFLUORO-M-TOLYLOXY)PICOLINAMIDE;n-(4-fluorophenyl)-6-(α,α,α-trifluoro-m-tolyloxy)picolinamide;picolinafen (bsi,iso);N-(4-Fluorophenyl)-6-(α,α,α-trifluoro-m-tolyloxy)picolinamide, N-(4-Fluorophenyl)-6-[3-(trifluoromethyl)phenoxy]-2-pyridinecarboxamide;Picolinafen [iso];Picolinafen Solution,100ppm | | CAS: | 137641-05-5 | | MF: | C19H12F4N2O2 | | MW: | 376.3 | | EINECS: | | | Product Categories: | | | Mol File: | 137641-05-5.mol |  |
| | PICOLINAFEN Chemical Properties |
| Melting point | 107.2-107.6° | | Boiling point | 399.0±42.0 °C(Predicted) | | density | 1.394±0.06 g/cm3(Predicted) | | storage temp. | 0-6°C | | pka | 10.28±0.70(Predicted) | | form | neat | | LogP | 4.367 (est) |
| Hazard Codes | N | | Risk Statements | 50/53 | | Safety Statements | 60-61 | | RIDADR | UN3077 9/PG 3 | | WGK Germany | 2 | | Toxicity | LD50 in rats (mg/kg): >5000 orally; >4000 dermally; LC50 in rats (mg/l): >5.9 by inhalation; LC50 in rainbow trout (96 hr): 0.281 mg/l (White) |
| | PICOLINAFEN Usage And Synthesis |
| Uses | Herbicide. | | Definition | ChEBI: Picolinafen is a pyridinecarboxamide resulting from the formal condensation of the carboxy group of 6-(m-trifluoromethylphenoxy)picolinic acid with the amino group of p-fluoroaniline. A carotenoid biosynthesis inhibitor, it is used as a herbicide for the control of broad-leaved weeds in cereal crops. It has a role as a herbicide, an agrochemical and a carotenoid biosynthesis inhibitor. It is a pyridinecarboxamide, a member of (trifluoromethyl)benzenes, an aromatic ether and a member of monofluorobenzenes. |
| | PICOLINAFEN Preparation Products And Raw materials |
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