Benomyl
| Names | |
|---|---|
| Preferred IUPAC name 1-(Butylcarbamoyl)-1H-1,3-benzimidazol-2-yl methylcarbamate | |
| Other names Benomyl | |
| Identifiers | |
| 3D model (JSmol) | |
| 825455 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.037.962 | 
| EC Number | 
 | 
| KEGG | |
| PubChem CID | |
| RTECS number | 
 | 
| UNII | |
| UN number | 3077 2757 | 
| CompTox Dashboard (EPA) | |
| 
 | |
| 
 | |
| Properties | |
| C14H18N4O3 | |
| Molar mass | 290.323 g·mol−1 | 
| Appearance | white crystalline solid | 
| Odor | acrid | 
| Melting point | 290 °C (554 °F; 563 K) decomposes | 
| 0.0004% (20 °C) | |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H315, H317, H335, H340, H360, H410 | |
| P203, P261, P264, P271, P272, P273, P280, P302+P352, P304+P340, P316, P317, P318, P319, P321, P332+P317, P333+P317, P362+P364, P391, P403+P233, P405, P501 | |
| Flash point | noncombustible | 
| NIOSH (US health exposure limits): | |
| PEL (Permissible) | TWA 15 mg/m3 (total) TWA 5 mg/m3 (resp) | 
| REL (Recommended) | none | 
| IDLH (Immediate danger) | N.D. | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Benomyl (also marketed as Benlate) is a fungicide introduced in 1968 by DuPont. It is a systemic benzimidazole fungicide that is selectively toxic to microorganisms and invertebrates (especially earthworms), but relatively nontoxic toward mammals.
Due to the prevalence of resistance of parasitic fungi to benomyl, it and similar pesticides are of diminished effectiveness. Nonetheless, it is widely used.