Bromacil

Bromacil
Names
IUPAC name
5-bromo-3-(butan-2-yl)-6-methylpyrimidine-2,4(1H,3H)-dione or 5-bromo-3-sec-butyl-6-methyluracil
Other names
Bromazil, Borea, Bromax 4G, Cynogan, Uragan, 5-Bromo-6-methyl-3-(1-methylpropyl)uracil
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.005.679 Edit this at Wikidata
EC Number
  • 206-245-1
KEGG
RTECS number
  • YQ9100000
UNII
  • InChI=1S/C9H13BrN2O2/c1-4-5(2)12-8(13)7(10)6(3)11-9(12)14/h5H,4H2,1-3H3,(H,11,14) checkY
    Key: CTSLUCNDVMMDHG-UHFFFAOYSA-N checkY
  • InChI=1/C9H13BrN2O2/c1-4-5(2)12-8(13)7(10)6(3)11-9(12)14/h5H,4H2,1-3H3,(H,11,14)
    Key: CTSLUCNDVMMDHG-UHFFFAOYAA
  • O=C1C(\Br)=C(/NC(=O)N1C(CC)C)C
Properties
C9H13BrN2O2
Molar mass 261.1157
Appearance Odorless, colorless to white, crystalline solid
Density 1.46 g/cm3
Melting point 157.5 to 160 °C (315.5 to 320.0 °F; 430.6 to 433.1 K) sublimes[1]
Boiling point none - sublimes[1]
0.08% (25°C)[1]
Hazards
GHS labelling:
GHS07: Exclamation markGHS09: Environmental hazard
Warning
H302, H315, H319, H335, H410
P261, P264, P270, P271, P273, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P391, P403+P233, P405, P501
NIOSH (US health exposure limits):
PEL (Permissible)
 none[1]
REL (Recommended)
 TWA 1 ppm (10 mg/m3)[1]
IDLH (Immediate danger)
 N.D.[1]
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 ?)

Bromacil is an organic compound with the chemical formula C9H13BrN2O2, commercially available as a herbicide. Bromacil was first registered as a pesticide in the U.S. in 1961,[2] and by 1974 1,017,000 pounds (461,000 kg) was used annually in the US, largely by government and industry.[3] It is used for brush control on non-cropland areas.[4] It works by interfering with photosynthesis by entering the plant through the root zone and moving throughout the plant.[5] Bromacil is one of a group of compounds called substituted uracils. These materials are broad spectrum herbicides used for nonselective weed and brush control on non-croplands, as well as for selective weed control on a limited number of crops, such as citrus fruit and pineapple.[4] Bromacil is also found to be excellent at controlling perennial grasses.

Safety

There are quite a few safety precautions that should be taken when dealing with Bromacil. Dry formulations containing bromacil must bear the word "Caution" and liquid formulas must signal "Warning."[4] Care should be exercised when spraying Bromacil on plants because it will also stop the photosynthesis of the adjacent non-target plants, therefore killing them. Bromacil should never be used in residential or recreation areas for risk of exposure. Bromacil is slightly toxic if individuals accidentally eat or touch residues and practically nontoxic if inhaled. Bromacil is a mild eye irritant and a very slight skin irritant. It is not a skin sensitizer.[6] In studies using laboratory animals, bromacil is slightly toxic by the oral, dermal, and inhalation routes and has been placed in Toxicity Category IV (the lowest of four categories) for these effects.[2] This herbicide should be stored in a cool, dry place and after any handling a thorough hand-washing is advised.

In regards to occupational exposure, the National Institute for Occupational Safety and Health has recommended workers handing bromacil not exceed an exposure of 1 ppm (10 mg/m3) over an eight-hour time-weighted average.[7]

Facts

Bromacil (40%) is combined with the active ingredient diuron in the herbicide Krovar, which is used by companies such as the Washington State Department of Transportation (WSDOT). It is in a group of chemicals that are absorbed through the gut and excreted primarily in the urine. The half-life of bromacil in soils is about 60 days, but as long as 8 months in some conditions.[6] Bromacil is available in granular, liquid, water-soluble liquid, and wettable powder formulations.[4] Because bromacil is a possible human carcinogen and systemic toxicity may result from intermediate exposure (one week to several months), U.S. Environmental Protection Agency (EPA) assessed risk to workers using several major exposure scenarios. Bromacil is stable to hydrolysis under normal environmental conditions.[2]

Applications

Bromacil is applied mainly by sprayers including boom, hand-held, knapsack, compressed air, tank-type, and power sprayers. Bromacil is also applied using aerosol, shaker, or sprinkler cans. Solid forms of bromacil are spread using granule applicators and spreaders. In the United States, application using aircraft is allowed only for Special Local Need registrations to control vegetation on the Department of Defense's Yakima Firing Center in the state of Washington.[2]

References

  1. ^ a b c d e f NIOSH Pocket Guide to Chemical Hazards. "#0063". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ a b c d United States Environmental Protection Agency. "Bromacil". 1996, p.1-11. Accessed October 9, 2012
  3. ^ "Pesticide Usage Survey of Agricultural, Governmental, and Industrial Sectors in the United States, 1974". epa.gov. EPA. 1977.
  4. ^ a b c d Cornell University. “Bromacil”. 1993, p. 1. Accessed October 9, 2012
  5. ^ USDOE-Bonneville Power Administration. 2000, p.1-9. Accessed October 9, 2012
  6. ^ a b Washington State Department of Transportation. “Bromacil”. 2006, p.1-4. Accessed October 9, 2012
  7. ^ Centers for Disease Control and Prevention (4 April 2011). "Bromacil". NIOSH Pocket Guide to Chemical Hazards. Retrieved 13 November 2013.