Maneb
 | |
| Names | |
|---|---|
| IUPAC name
[[2-[(dithiocarboxy)amino]ethyl]carbamodithioato]](2-)-kS,kS']manganese | |
| Other names
Manganese ethylene-1,2-bisdithiocarbamate, polymer | |
| Identifiers | |
12427-38-2  | |
| 3D model (Jmol) | Interactive image |
| ECHA InfoCard | 100.032.400 |
| MeSH | Maneb |
| PubChem | 3032581 |
| |
| |
| Properties | |
| (C4H6MnN2S4)n | |
| Molar mass | 265,31 g·mol−1 |
| Appearance | Yellow to brown colored crystalline solid |
| Density | 1.92 g/cm3 |
| Melting point | 192 to 204 °C (378 to 399 °F; 465 to 477 K) (decomposes) |
| 160 mg/L | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is ?) | |
| Infobox references | |
Maneb is a fungicide and a polymeric complex of manganese with the ethylene bis(dithiocarbamate) anionic ligand.[1]
Applications
It can be also used to create a toxin-based animal model of Parkinson's disease, usually in primates.[2]
Regulation
It was included in a pesticide ban proposed by the Swedish Chemicals Agency [3] and approved by the European Parliament on January 13, 2009.[4]
References
- ↑ Arno H. Reidies "Manganese Compounds" Ullmann's Encyclopedia of Chemical Technology 2007; Wiley-VCH, Weinheim. doi:10.1002/14356007.a16_123
- ↑ Cicchetti F, Drouin-Ouellet J, Gross RE (September 2009). "Environmental toxins and Parkinson's disease: what have we learned from pesticide-induced animal models?". Trends Pharmacol. Sci. 30 (9): 475–83. doi:10.1016/j.tips.2009.06.005. PMID 19729209.
- ↑ "Interpretation of criteria for approval of active substances in the proposed EU plant protection regulation". Swedish Chemicals Agency (KemI). 2008-09-23. Retrieved 2009-01-14.
- ↑ "MEPs approve pesticides legislation". 2009-01-13. Retrieved 2009-01-14.
External links
- Maneb in the Pesticide Properties DataBase (PPDB)
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