| |
| Names | |
|---|---|
| Preferred IUPAC name
Methyl (1H-1,3-benzimidazol-2-yl)carbamate | |
| Other names
Mercarzole | |
| Identifiers | |
3D model (JSmol) |
|
| ChEBI | |
| ChEMBL | |
| ChemSpider |
|
| ECHA InfoCard | 100.031.108 
|
| KEGG |
|
PubChem CID |
|
| RTECS number |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| C9H9N3O2 | |
| Molar mass | 191.187 g/mol |
| Appearance | Light gray powder |
| Density | 1.45 g/cm3 |
| Melting point | 302 to 307 °C (576 to 585 °F; 575 to 580 K) (decomposes) |
| 8 mg/L
Disintegration = 302 -305 degree Temperature of disintegration = 1.5 - 2 hrs | |
| Acidity (pKa) | 4.48 |
| Hazards | |
| NIOSH (US health exposure limits): | |
PEL (Permissible) |
Disintegration temp = 302 - 305 degree
Disintegration temp = 1.5 - 2 hrs |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Carbendazim is a fungicide, a member benzimidazole fungicides. It is a metabolite of benomyl.[2]
The fungicide is used to control plant diseases in cereals and fruits, including citrus, bananas, strawberries, macadamia nuts, pineapples, and pomes.[3] A 4.7% solution of carbendazim hydrochloride, sold as Eertavas, is marketed as a treatment for Dutch elm disease.[4]
It is also employed as a casting worm control agent in amenity turf situations such as golf greens, tennis courts etc. and in some countries is licensed for that use only.[5]
High doses of carbendazim cause infertility and destroy the testicles of laboratory animals.[6][7]
Maximum pesticide residue limits (MRLs) for fresh produce in the EU are between 0.1 and 0.7 mg/kg with the exception of loquat, which is 2 mg/kg.[8] The limits for more commonly consumed citrus and pome fruits are between 0.1 and 0.2 mg/kg.
Its use on macadamia plantations has proven controversial in Queensland.[4]
Media related to Carbendazim at Wikimedia Commons
