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Carbendazim

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Carbendazim[1]
Identifiers
CAS number 10605-21-7 YesY
PubChem 25429
ChemSpider 23741 YesY
UNII H75J14AA89 YesY
KEGG C10897 YesY
ChEMBL CHEMBL70971 YesY
RTECS number DD6500000
Jmol-3D images Image 1
Properties
Molecular formula C9H9N3O2
Molar mass 191.19 g mol−1
Appearance Light gray powder
Melting point

302-307 °C (decomposes)

Solubility in water 8 mg/L
Acidity (pKa) 4.48
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Carbendazim is a widely used broad-spectrum benzimidazole fungicide and a metabolite of benomyl.

The fungicide is used to control plant diseases in cereals and fruit, including citrus, bananas, strawberries, pineapples, and pome.[2] It is also controversially used in Queensland, Australia on macadamia plantations.[3]A 4.7% solution of carbendazim hydrochloride is sold as Eertavas and marketed as a treatment for Dutch elm disease.

Studies have found that high doses of carbendazim cause infertility and destroy the testicles of laboratory animals.[4][5] Carbendazim was included in a biocide ban proposed by the Swedish Chemicals Agency [6] and approved by the European Parliament on January 13, 2009.[7]

[edit] References

  1. ^ Merck Index, 11th Edition, 1794.
  2. ^ Wight, Andrew (14 January 2009). "Two-headed fish mystery deepens". Stock & Land. Archived from the original on 11 January 2012. http://sl.farmonline.com.au/news/nationalrural/agribusiness-and-general/general/twoheaded-fish-mystery-deepens/1406893.aspx?storypage=0. 
  3. ^ Marissa Calligeros (2009-02-02). "Fungicide maker in birth defect storm". Sydney Morning Herald. http://www.smh.com.au/news/environment/fungicide-maker-in-birth-defect-storm/2009/02/02/1233423096718.html. Retrieved 2010-03-21. 
  4. ^ Aire, TA (2005 Aug). "Short-term effects of carbendazim on the gross and microscopic features of the testes of Japanese quails (Coturnix coturnix japonica).". Anatomy and embryology 210 (1): 43-9. PMID 16034611. 
  5. ^ "Carbendazim use banned on fruit crops". ABC. 5 February 2010. http://www.abc.net.au/rural/news/content/201002/s2811428.htm. 
  6. ^ "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. Retrieved 2009-01-14. 
  7. ^ "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. Retrieved 2009-01-14. 

[edit] External links


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