Hexazinone

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Hexazinone
200px
Names
IUPAC name
3-Cyclohexyl-6-dimethylamino-1-methyl-1,3,5-triazine-2,4-dione
Other names
Velpar
Hexazinone
Identifiers
51235-04-2 YesY
ChemSpider 36542 N
Jmol 3D model Interactive image
Interactive image
KEGG C10926 N
PubChem 39965
  • InChI=1S/C12H20N4O2/c1-14(2)10-13-11(17)16(12(18)15(10)3)9-7-5-4-6-8-9/h9H,4-8H2,1-3H3 N
    Key: CAWXEEYDBZRFPE-UHFFFAOYSA-N N
  • InChI=1/C12H20N4O2/c1-14(2)10-13-11(17)16(12(18)15(10)3)9-7-5-4-6-8-9/h9H,4-8H2,1-3H3
    Key: CAWXEEYDBZRFPE-UHFFFAOYAU
  • O=C(N1C2CCCCC2)N=C(N(C)C)N(C)C1=O
  • O=C1/N=C(\N(C(=O)N1C2CCCCC2)C)N(C)C
Properties
C12H20N4O2
Molar mass 252.31
Appearance White crystalline solid
Density 1.25 g/cm3
Melting point 116 °C (241 °F; 389 K)
Soluble
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Hexazinone is an organic compound that is used as a broad spectrum herbicide. It is a colorless solid. It exhibits some solubility in water but is highly soluble in most organic solvents except alkanes. A member of the triazine class herbicides, it is manufactured by DuPont and sold under the trade name Velpar.[1]

It functions by inhibiting photosynthesis and thus is a nonselective herbicide. It is used to control grasses and broadleaf and woody plants. Approximately 33% is used on alfalfa, 31% in forestry, 29% in industrial areas, 4% on rangeland and pastures, and < 2% on sugarcane.[2]

In 1989, hexazinone was deliberately used in an act of vandalism to poison the Treaty Oak in Austin, Texas.

Hexazinone is a pervasive groundwater contaminant, due to its high water solubility.

References

  1. Arnold P. Appleby, Franz Müller, Serge Carpy "Weed Control" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. doi:10.1002/14356007.a28_165
  2. Hexazinone, Herbicide Profile, Pesticide Management Education Program, Cornell University

External links

<templatestyles src="Asbox/styles.css"></templatestyles>