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Contents

   



(Top)
 


1 Health effects  





2 Production  





3 Applications  





4 Regulation  





5 See also  





6 References  





7 External links  














Maneb






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Maneb
Names
IUPAC name

[[2-[(Dithiocarboxy)amino]ethyl]carbamodithioato]](2-)-kS,kS']manganese

Other names

Manganese ethylene-1,2-bisdithiocarbamate, polymer

Identifiers

CAS Number

3D model (JSmol)

ChemSpider
ECHA InfoCard 100.032.400 Edit this at Wikidata
MeSH Maneb

PubChem CID

UNII

CompTox Dashboard (EPA)

  • 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

  • [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
Hazards
GHS labelling:

Pictograms

GHS07: Exclamation markGHS08: Health hazardGHS09: Environmental hazard

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

Maneb is a fungicide and a polymeric complexofmanganese with the ethylene bis(dithiocarbamate) anionic ligand.[1]

Health effects

[edit]

Exposure to Maneb can irritate the eyes, nose, and throat. Prolonged or long-term exposure may interfere with the function of the thyroid.[2]

Production

[edit]

Applications

[edit]

It can be also used to create a toxin-based animal modelofParkinson's disease, usually in primates.[3]

Regulation

[edit]

It was included in a pesticide ban proposed by the Swedish Chemicals Agency [4] and approved by the European Parliament on January 13, 2009.[5]

See also

[edit]

References

[edit]
  1. ^ Arno H. Reidies "Manganese Compounds" Ullmann's Encyclopedia of Chemical Technology 2007; Wiley-VCH, Weinheim. doi:10.1002/14356007.a16_123
  • ^ "MANEB.doc" (PDF).
  • ^ 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. Archived from the original on 2009-01-01. Retrieved 2009-01-14.
  • ^ "MEPs approve pesticides legislation". 2009-01-13. Archived from the original on 2009-01-25. Retrieved 2009-01-14.
  • [edit]
    Retrieved from "https://en.wikipedia.org/w/index.php?title=Maneb&oldid=1229371707"

    Categories: 
    Fungicides
    Manganese(II) compounds
    Polymers
    Dithiocarbamates
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    This page was last edited on 16 June 2024, at 12:42 (UTC).

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