Lactofen

Lactofen[1]
Names
IUPAC name
Ethyl O-[5-(2-chloro-α,α,α-trifluoro-p-tolyloxy)-2-nitrobenzoyl]-DL-lactate
Other names
2-Ethoxy-1-methyl-2-oxoethyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate
Identifiers
CAS Number
  • 77501-63-4 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 56077 ☒N
ECHA InfoCard 100.111.278 Edit this at Wikidata
PubChem CID
  • 62276
UNII
  • L44N8UV47O ☒N
CompTox Dashboard (EPA)
  • DTXSID7024160 Edit this at Wikidata
InChI
  • InChI=1S/C19H15ClF3NO7/c1-3-29-17(25)10(2)30-18(26)13-9-12(5-6-15(13)24(27)28)31-16-7-4-11(8-14(16)20)19(21,22)23/h4-10H,3H2,1-2H3 ☒N
    Key: CONWAEURSVPLRM-UHFFFAOYSA-N ☒N
  • InChI=1/C19H15ClF3NO7/c1-3-29-17(25)10(2)30-18(26)13-9-12(5-6-15(13)24(27)28)31-16-7-4-11(8-14(16)20)19(21,22)23/h4-10H,3H2,1-2H3
    Key: CONWAEURSVPLRM-UHFFFAOYAB
  • CCOC(=O)C(C)OC(=O)c1cc(ccc1[N+](=O)[O-])Oc2ccc(cc2Cl)C(F)(F)F
Properties
Chemical formula
 C19H15ClF3NO7
Molar mass 461.77 g·mol−1
Appearance White crystalline solid
Melting point 43.9 to 45.5 °C (111.0 to 113.9 °F; 317.0 to 318.6 K)
Solubility in water
 0.1 mg/L @ 20 degrees C
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
Chemical compound

Lactofen is a complex ester of acifluorfen and is a nitrophenyl ether selective herbicide[2][3] and fungicide.[4][5][6] It is used in postemergence applications to certain crops which are resistant to its action.[2] The name "Lactofen" is approved by the American National Standards Institute and the Weed Science Society of America, and is also approved in China (乳氟禾草灵).

Lactofen is applied as a foliar spray and is commonly used to control broadleaved weeds in soybean, cereals, potatoes and peanuts. It may be combined with oil or fertilizer adjuvants and surfactants. Some formulations include solvents such as xylenes and cumene.[1] It is also used as a fungicide for Sclerotinia white molds on soybean.[4][5][6]

Lactofen is available in solid form or as an emulsifiable concentrate under the trade name COBRA.[1]

Toxicology

Lactofen is slightly to non-toxic to humans when ingested or inhaled. It can cause skin irritation including reddening, swelling and possibly corrosive burns. It is a severe eye irritant and can cause permanent damage to eyes when there is sufficient exposure.[7]

It was found to be practically non-toxic to the species of bird that were studied.[8] Toxicity to fish and other aquatic organisms varied and it was eliminated in fish within fourteen days. It is of low toxicity to bees.[9]

Lactofen has a very low solubility in water and is not expected to contaminate surface waters. It binds tightly to soil and is then broken down in between one and seven days.[8][10]

References

  1. ^ a b c EXTOXNET: Extension Toxicology Network
  2. ^ a b Herbicide Mode-of-Action Summary
  3. ^ SDSU Extension. 2019 South Dakota Pest Management Guide - Soybeans - A guide to managing weeds, insects, and diseases (PDF).
  4. ^ a b "White Mold in Soybeans - Crops". NDSU Agriculture and Extension. Retrieved 2021-07-29.
  5. ^ a b "Applying foliar fungicides for control of white mold in soybeans". Michigan State University Extension. Retrieved 2021-07-29.
  6. ^ a b Kichler, Jeremy (2021-07-19). "Questions of the Week!! 7/19/21 - Colquitt County Ag Report". University of Georgia Extension. Retrieved 2021-07-29.
  7. ^ Valent USA. 1993. Material Safety Data Sheet for Valent Cobra Herbicide. Valent USA Corporation. Walnut Creek, CA.
  8. ^ a b Herbicide Handbook of the Weed Science Society of America. 1989. Sixth edition. Champaign, IL
  9. ^ US Environmental Protection Agency. 1995. File: Lactofen, Integrated Risk Information System (IRIS). National Library of Medicine "Toxline" Database, 4/95.
  10. ^ US Environmental Protection Agency. 1987. Fact Sheet Number 128: Lactofen. Washington, DC.

External links

  • Lactofen in the Pesticide Properties DataBase (PPDB)
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Anilides/anilinesAromatic acidsArsenicals
HPPD inhbitors
OrganophosphorusPhenoxy
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Nitrophenyl ethers
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