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| Chlorotoluron Basic information |
| Chlorotoluron Chemical Properties |
Melting point | 148.3° | Boiling point | 367.8±42.0 °C(Predicted) | density | 1.2426 (rough estimate) | refractive index | 1.6000 (estimate) | Fp | 2 °C | storage temp. | APPROX 4°C
| solubility | Chloroform: slightly soluble; Methanol: slightly soluble | pka | 14.43±0.70(Predicted) | form | neat | Water Solubility | 70.43mg/L(20 ºC) | Merck | 13,2191 | BRN | 2647688 | CAS DataBase Reference | 15545-48-9(CAS DataBase Reference) | NIST Chemistry Reference | Chlortoluron(15545-48-9) | EPA Substance Registry System | Chlorotoluron (15545-48-9) |
Hazard Codes | Xn;N,N,Xn,F | Risk Statements | 40-50/53-63-36-20/21/22-11 | Safety Statements | 26-36/37-46-60-61-16 | RIDADR | UN 3077 | WGK Germany | 3 | RTECS | YS7230000 | Hazardous Substances Data | 15545-48-9(Hazardous Substances Data) | Toxicity | rat,LC50,inhalation,1300mg/m3 (1300mg/m3),"Wirksubstanzen der Pflanzenschutz und Schadlingsbekampfungsmittel," Perkow, W., Berlin, Verlag Paul Parey, 1971-1976Vol. -, Pg. -, 1971/1976. |
| Chlorotoluron Usage And Synthesis |
Uses | Herbicide. | Definition | ChEBI: A member of the class of ureas that is N-methyl urea substituted by a 3-chloro-4-methylphenyl group at position 3 and a methyl group at position 1. A herbicide that is non-toxic to honeybees but is moderately toxic to mammals, birds, ea
thworms and most aquatic organisms. | Metabolism | Chlortoluron is rapidly
metabolized in winter wheat. Hydroxylation of the methyl
group on the phenyl ring has been demonstrated as a
detoxification mechanism for chlortoluron resistance in
winter wheat, whereas in the susceptible weed blackgrass
(Alopecurus myosuroides Huds.), the main metabolite is
the mono N-demethylated metabolite (107). In a tolerant
weed, Persian speedwell (Veronica persica Poir.), chlortoluron is rapidly transformed to the nonphytotoxic di-N-demethylated metabolite (107). |
| Chlorotoluron Preparation Products And Raw materials |
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