Jump to content

Fluroxypyr

From Wikipedia, the free encyclopedia
Fluroxypyr
Names
Preferred IUPAC name
[(4-Amino-3,5-dichloro-6-fluoropyridin-2-yl)oxy]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 [77 °F], 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]

[edit]

References

[edit]
  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)
pFad - Phonifier reborn

Pfad - The Proxy pFad of © 2024 Garber Painting. All rights reserved.

Note: This service is not intended for secure transactions such as banking, social media, email, or purchasing. Use at your own risk. We assume no liability whatsoever for broken pages.


Alternative Proxies:

Alternative Proxy

pFad Proxy

pFad v3 Proxy

pFad v4 Proxy