Fluometuron

Fluometuron
Names
Preferred IUPAC name
N,N-Dimethyl-N′-[3-(trifluoromethyl)phenyl]urea
Other names
1,1-Dimethyl-3-[3-(trifluoromethyl)phenyl]urea; 1,1-Dimethyl-3-(α,α,α-trifluoro-m-tolyl)-urea; 3-(3-Trifluoromethylphenyl)-1,1-dimethylurea; 3-(m-Trifluoromethylphenyl)-1,1-dimethylurea; C 2059; Ciba 2059; Cotoran; Cotoran 85DF; Fluomethuron; Lanex; N-(3-Trifluoromethylphenyl)-N′,N′-Dimethylurea; N-(m-Trifluoromethylphenyl)-N′,N′-Dimethylurea; Pakhtaran
Identifiers
  • 2164-17-2 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:82012
ChemSpider
  • 15702
ECHA InfoCard 100.016.819
  • 16562
UNII
  • 296378G1S8 checkY
  • DTXSID8020628
  • InChI=1S/C10H11F3N2O/c1-15(2)9(16)14-8-5-3-4-7(6-8)10(11,12)13/h3-6H,1-2H3,(H,14,16)
  • O=C(Nc1cc(ccc1)C(F)(F)F)N(C)C
Properties
C10H11F3N2O
Molar mass 232.206 g·mol−1
Density 1.39 g/cm3[1]
Melting point 163 to 164 °C (325 to 327 °F; 436 to 437 K)[1]
90 ppm (0.0105%) at 20 °C[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Fluometuron is an herbicide. In the United States it was approved for use on cotton and sugarcane crops in 1974, but since 1986 is only approved for use on cotton.[2]

Fluometron's herbicide resistance class is Group C, (Australia), C2 (global), Group 7, (numeric, i.e. Group 5, due to a merger). It is photosynthesis inhibitor.[3]

References

  1. ^ a b c Fluometuron, Pesticide Information Profile
  2. ^ Reregistration Eligibility Decision (RED) for Fluometuron, US Environmental Protection Agency
  3. ^ "Classification of Herbicides According to Site of Action". Retrieved 19 July 2025.
  • Fluometuron in the Pesticide Properties DataBase (PPDB)
Retrieved from "https://en.wikipedia.org/w/index.php?title=Fluometuron&oldid=1325128787"