Maneb

Maneb
Names
	IUPAC name 2-[(Dithiocarboxy)amino]ethyl]carbamodithioato(2-)-kS,kS']manganese
	Other names Manganese ethylene-1,2-bisdithiocarbamate, polymer
Identifiers
CAS Number	12427-38-2 ;
3D model (JSmol)	Interactive image;
ChemSpider	none;
MeSH	Maneb
PubChem CID	3032581;
UNII	K221E12G7T ;
	InChI InChI=1S/C4H8N2S4.Mn/c7-3(8)5-1-2-6-4(9)10;/h1-2H2,(H2,5,7,8)(H2,6,9,10);/q;+2/p-2 Key: YKSNLCVSTHTHJA-UHFFFAOYSA-L;
	SMILES [Mn+]SC(=S)NCCNC(=S)S[Mn]SC(=S)NCCNC(=S)S[Mn]SC(=S)NCCNC(=S)S[Mn]SC(=S)NCCNC(=S)S[Mn]SC(=S)NCCNC(=S)[S-];
Properties
Chemical formula	(C4H6MnN2S4)n
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)
Solubility in water	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]

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]

↑ Arno H. Reidies "Manganese Compounds" Ullmann's Encyclopedia of Chemical Technology 2007; Wiley-VCH, Weinheim. doi:10.1002/14356007.a16_123
↑ "Environmental toxins and Parkinson's disease: what have we learned from pesticide-induced animal models?". Trends Pharmacol. Sci. 30 (9): 475–83. September 2009. 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. http://www.kemi.se/templates/News____5415.aspx.
↑ "MEPs approve pesticides legislation". 2009-01-13. http://www.europarl.europa.eu/news/expert/infopress_page/066-45937-012-01-03-911-20090112IPR45936-12-01-2009-2009-false/default_en.htm.