Acetochlor

Acetochlor[1]
Names
Preferred IUPAC name
2-Chloro-N-(ethoxymethyl)-N-(2-ethyl-6-methylphenyl)acetamide
Other names
Azetochlor
CP55097
ICIA-5676
Identifiers
CAS Number
  • 34256-82-1 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:2394 checkY
ChEMBL
  • ChEMBL1517425 checkY
ChemSpider
  • 1911 checkY
ECHA InfoCard 100.047.166 Edit this at Wikidata
KEGG
  • C10925 checkY
PubChem CID
  • 1988
UNII
  • 8L08WMO94K checkY
CompTox Dashboard (EPA)
  • DTXSID8023848 Edit this at Wikidata
InChI
  • InChI=1S/C14H20ClNO2/c1-4-12-8-6-7-11(3)14(12)16(10-18-5-2)13(17)9-15/h6-8H,4-5,9-10H2,1-3H3 checkY
    Key: VTNQPKFIQCLBDU-UHFFFAOYSA-N checkY
  • InChI=1/C14H20ClNO2/c1-4-12-8-6-7-11(3)14(12)16(10-18-5-2)13(17)9-15/h6-8H,4-5,9-10H2,1-3H3
    Key: VTNQPKFIQCLBDU-UHFFFAOYAJ
  • ClCC(=O)N(c1c(cccc1CC)C)COCC
Properties
Chemical formula
 C14H20ClNO2
Molar mass 269.77 g·mol−1
Density 1.100 at 30 °C
1.136 at 20 °C
Melting point < 0 °C (32 °F; 273 K)
Solubility in water
 223 ppm
Hazards
Flash point > 100 °C (212 °F; 373 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Acetochlor is an herbicide developed by Monsanto Company and Zeneca. It is a member of the class of herbicides known as chloroacetanilides. Its mode of action is elongase inhibition, and inhibition of geranylgeranyl pyrophosphate (GGPP) cyclization enzymes, part of the gibberellin pathway. It carries high risks of environmental contamination.[2]

Manufacture

Acetochlor is manufactured in two steps from from 2-ethyl-6-methylaniline. A reaction with chloroacetyl chloride gives an anilide which is treated with chloromethyl ethyl ether and sodium hydroxide to form the herbicide.[3]

Uses

In the United States, acetochlor was registered by the EPA as a direct substitute for many herbicides of known concern. The EPA imposed several restrictions and conditions on the use of acetochlor.[4]

It is approved for pre-emergence application or for pre-planting application with soil incorporation, in corn. (maize) at 5 litres / hectare (1835g / hectare of a.i.)[5] It is the main active ingredient in Acenit, Keystone, Guardian, Harness, Relay, Sacemid, Surpass, Top-Hand, Trophy and Winner.

It is used to control weeds in corn, and is particularly useful as a replacement for atrazine in the case of some important weeds.

Safety

Acetochlor has been classified as a probable human carcinogen.[1][4] Acetochlor, as alachlor, can cause nasal turbinate tumors via the generation of a common tissue reactive metabolite that leads to cytotoxicity and regenerative proliferation in the nasal epithelium.[6]

It is a thyroid disruptor.[7][non-primary source needed]

Human health effects from acetochlor at low environmental doses or at biomonitored levels from low environmental exposures are unknown.[8] A case of poisoning with extremely swollen genitals as a symptom was reported after contact.[9]

Ecologic effects

In the United States, acetochlor is the third most frequently detected herbicide in natural waters.[10]

Acetochlor can accelerate metamorphosis in amphibians.[11] It can also affect the development of fish.[11]

See also

References

  1. ^ a b Cornell University Extension Toxicology Network Pesticide Information Profile on Acetochlor
  2. ^ Arregui, M.; Sánchez, D.; Althaus, R.; Scotta, R.; Bertolaccini, I. (2010). "Assessing the risk of pesticide environmental impact in several Argentinian cropping systems with a fuzzy expert indicator". Pest Management Science. 66 (7): 736–740. doi:10.1002/ps.1935. PMID 20232283.
  3. ^ Unger, Thomas A. (31 December 1996). Pesticide Synthesis Handbook. William Andrew. p. 7. ISBN 0815514018.
  4. ^ a b "Acetochlor". EPA. Retrieved 2 April 2010.
  5. ^ "e-phy". agriculture.gouv.fr. Retrieved 17 May 2015.
  6. ^ "Cumulative Risk Assessment for the Chloroacetanilides" (PDF). EPA. 2006-03-29. Retrieved 2 April 2010.
  7. ^ Turque, N.; Palmier, K.; Le Mével, S.; Alliot, C.; Demeneix, B. A. (2005). "A Rapid, Physiologic Protocol for Testing Transcriptional Effects of Thyroid-Disrupting Agents in Premetamorphic Xenopus Tadpoles". Environmental Health Perspectives. 113 (11): 1588–1593. doi:10.1289/ehp.7992. PMC 1310923. PMID 16263516.
  8. ^ "National Report on Human Exposure to Environmental Chemicals". CDC. 11 February 2010. Archived from the original on 5 June 2011. Retrieved 2 April 2010.
  9. ^ Tian, Runhui; Liu, Lingyun; Liang, Zuowen; Guo, Kaimin (2019). "Acetochlor poisoning presenting as acute genital edema: A case report". Urology Case Reports. 22: 47–48. doi:10.1016/j.eucr.2018.10.014. PMC 6214889. PMID 30406020.
  10. ^ Foley, M.; Sigler, V.; Gruden, C. (2008). "A multiphasic characterization of the impact of the herbicide acetochlor on freshwater bacterial communities". The ISME Journal. 2 (1): 56–66. doi:10.1038/ismej.2007.99. PMID 18180747.
  11. ^ a b Li, W.; Zha, J.; Li, Z.; Yang, L.; Wang, Z. (2009). "Effects of exposure to acetochlor on the expression of thyroid hormone related genes in larval and adult rare minnow (Gobiocypris rarus)". Aquatic Toxicology. 94 (2): 87–93. doi:10.1016/j.aquatox.2009.06.002. PMID 19577311.

External links

  • Acetochlor in the Pesticide Properties DataBase (PPDB)
  • U.S. Environmental Protection Agency article on Acetochlor
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