Anilazine
From Self-sufficiency
| Anilazine | |
|---|---|
| File:Anilazine.png | |
| 4,6-dichloro-N-(2-chlorophenyl)-1,3,5-triazin-2-amine | |
| Other names Anilazine (Dyrene);
dyrene | |
| style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
| CAS number | 101-05-3 |
| ChemSpider | 7260 |
| SMILES | Script error: No such module "collapsible list". |
| InChI | Script error: No such module "collapsible list". |
| InChI key | IMHBYKMAHXWHRP-UHFFFAOYAQ |
| style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
| Molecular formula | C9H5Cl3N4 |
| Appearance | white to light brown crystals or powder |
| Density | 1.611 g/cm3 |
| style="background: #F8EABA; text-align: center;" colspan="2" | Hazards | |
| Flash point | 232.2 °C |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
| Infobox references | |
Anilazine (ǎ-nǐl-a-zēn) is an organic compound with the chemical formula C9H5Cl3N4. It is a pesticide used on crops. It comes under the category of triazine fungicides. It is used for controlling fungus diseases which attack lawns and turf, cereals, coffee, and a wide variety of vegetables and other crops. It is also used for the control of potato and tomato leafspots.
Toxicity
Oral administration to rats and cats, the most common signs of toxicity were diarrhea and vomiting, respectively. After dermal administration to rabbits, mild skin irritation manifested as edema and erythema was observed. Anilazine was more toxic by intraperitoneal injection than by other routes of administration.[1]
Reference
- ↑ 1
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