Fluroxypyr

In the wide world of Fluroxypyr, we find a diversity of aspects and approaches that invite us to explore and understand further. From its impact on contemporary society to its relevance in history, Fluroxypyr has been the subject of numerous debates and reflections. In this article, we will delve into the different facets of Fluroxypyr, highlighting its importance and influence in different fields. Through a detailed analysis, we will explore the implications and consequences linked to Fluroxypyr, with the aim of providing a complete and enriching vision of this fascinating topic.

Fluroxypyr
Names
Preferred IUPAC name
acetic acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.126.253 Edit this at Wikidata
UNII
  • InChI=1S/C7H5Cl2FN2O3/c8-3-5(11)4(9)7(12-6(3)10)15-1-2(13)14/h1H2,(H2,11,12)(H,13,14)
    Key: MEFQWPUMEMWTJP-UHFFFAOYSA-N
  • InChI=1/C7H5Cl2FN2O3/c8-3-5(11)4(9)7(12-6(3)10)15-1-2(13)14/h1H2,(H2,11,12)(H,13,14)
    Key: MEFQWPUMEMWTJP-UHFFFAOYAO
  • Fc1nc(OCC(=O)O)c(Cl)c(c1Cl)N
Properties
C7H5Cl2FN2O3
Molar mass 255.03 g·mol−1
Appearance White solid[1]
Density 1,09 g/cm3 (20 °C)[1]
Melting point 232 to 233 °C (450 to 451 °F; 505 to 506 K)[1]
91 mg/L (20 °C)[1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).

Fluroxypyr is an herbicide in the class of synthetic auxins. It is used to control broadleaf weeds and woody brush.[2] It is formulated as the 1-methylheptyl ester (fluroxypyr-MHE).[3]

References

  1. ^ a b c d Record in the GESTIS Substance Database of the Institute for Occupational Safety and Health
  2. ^ "Fluroxypyr: Roadside Vegetation Management Herbicide Fact Sheet" (PDF). Washington State Department of Transportation. February 2006. {{cite journal}}: Cite journal requires |journal= (help)
  3. ^ "Fluroxypyr Human Health and Ecological Risk Assessment" (PDF). USDA Forest Service. June 12, 2009. {{cite journal}}: Cite journal requires |journal= (help)