Dicamba

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Dicamba[1]
Dicamba.png
Identifiers
CAS number 1918-00-9 YesY
PubChem 10433671
ChemSpider 2922 YesY
UNII SJG3M6RY6H YesY
KEGG C18597 N
ChEBI CHEBI:81856 N
ChEMBL CHEMBL476936 YesY
Jmol-3D images Image 1
Properties
Molecular formula C8H6Cl2O3
Molar mass 221.04 g/mol
Appearance White crystalline solid
Density 1.57
Melting point 114 to 116 °C (237 to 241 °F; 387 to 389 K)
Solubility in water 500 g/L
Solubility in acetone 810 g/L
Solubility in ethanol 922 g/L
Hazards
Flash point 199 °C (390 °F; 472 K)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 N (verify) (what is: YesY/N?)
Infobox references

Dicamba (3,6-dichloro-2-methoxybenzoic acid) is an herbicide. Brand names for formulations of this herbicide include Banvel, Diablo, Oracle and Vanquish. This chemical compound is an organochloride and a derivative of benzoic acid.

Role as herbicide[edit]

Dicamba controls annual and perennial rose weeds in grain crops and highlands, and it is used to control brush and bracken in pastures, as well as legumes and cacti. It kills broadleaf weeds before and after they sprout. In combination with a phenoxy herbicide or with other herbicides, dicamba is used in pastures, range land, and noncrop areas (fence rows, roadways, and wastage) to control weeds. Dicamba is toxic to conifer species but is in general less toxic to grasses.[2]

Dicamba functions by increasing plant growth rate.[2] At sufficient concentrations, the plant outgrows its nutrient supplies and dies.[3]

Resistance[edit]

Some weed species have developed resistance to dicamba. Dicamba resistance in kochia was discovered in 1994 and has not been explained by common modes of resistance such as absorption, translocation, or metabolism.[4]

Genetically modified crops[edit]

The soil bacterium Pseudomonas maltophilia (strain DI-6) converts dicamba to 3,6-dichlorosalicylic acid (3,6-DCSA), which is adsorbed to soil much more strongly than is dicamba but lacks herbicidal activity. Little information is available on the toxicity of this breakdown intermediate. The enzymes responsible for this first breakdown step is a three-component system called dicamba O-demethylase. Monsanto has recently incorporated one component of the three enzymes into the genome of soybean and other broadleaf crop plants, making them resistant to dicamba.[5]

Toxicological effects[edit]

Dicamba does not present unusual handling hazards.[6] It is moderately toxic by ingestion and slightly toxic by inhalation or dermal exposure (oral LD50 in rats: 757 mg/kg body weight, dermal LD50 in rats: >2,000 mg/kg, inhalation LC50 in rats: >200 mg/L).

In a 3-generation study, dicamba did not affect the reproductive capacity of rats. When rabbits were given doses of 0, 0.5, 1, 3, 10, or 20 (mg/kg)/day of technical dicamba from days 6 through 18 of pregnancy, toxic effects on the mothers, slightly reduced fetal body weights, and increased loss of fetuses occurred at the 10 mg/kg dose. U.S. Environmental Protection Agency (EPA) has set the NOAEL for this study at 3 (mg/kg)/day.

In dog tests, some enlargement of liver cells has occurred, but a similar effect has not been shown in humans.[7]

Environmental impact[edit]

Soil[edit]

Dicamba is released directly to the environment by its application as a herbicide for the control of annual broadleaf weeds. It may cause damage to plants as a result of its absorption from the soil by plant roots. Dicamba is mobile in most soils and significant leaching is possible. The adsorption of dicamba to organo-clay soil is influenced by soil pH with the greatest adsorption to soil occurring in acidic soils. Dicamba is moderately persistent in soil. Its reported half-life in soil ranges from 1 to 6 weeks. Dicamba is likely to be more rapidly degraded in soils with high microbial populations, but dissipates more slowly in hardwood forests and wetlands than would be expected from the results of laboratory studies.[citation needed]

At a level of 10 mg/kg in sandy loam soil, dicamba caused a transient decrease in nitrification after two but not three weeks of incubation. The investigator determined that the decrease in nitrification is not substantial and does not suggest the potential for a prolonged impact on microbial activity. In the same study, dicamba did not affect ammonia formation or sulfur oxidation. In a more recent laboratory study, dicamba, at a concentration of 1 mg/kg soil, did not affect urea hydrolysis or nitrification in four soil types.[citation needed]

Water[edit]

Dicamba salts used in some herbicides are highly soluble in water. A recent study conducted by the U.S. Geologic Survey (USGS 1998) found dicamba in 0.11%-0.15% of the ground waters surveyed. The maximum level detected was 0.0025 mg/L. The prevalence of dicamba in groundwater from agricultural areas (0.11%) did not correlate with nonagricultural urban areas (0.35%).

Dicamba was tested for acute toxicity in a variety of aquatic animals. The studies accepted by the U.S. EPA found dicamba acid and DMA salt to be practically nontoxic to aquatic invertebrates. Studies accepted by the U.S. EPA found dicamba acid to be slightly toxic to cold water fish (rainbow trout), and practically nontoxic to warm water fish.

References[edit]

  1. ^ Merck Index, 11th Edition, 3026.
  2. ^ a b 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
  3. ^ http://www.fs.fed.us/r6/nr/fid/pubsweb/dicamba_99.pdf Retrieved 20 May 2010
  4. ^ Cranston, Harwood J.; Kern, Anthony J.; Hackett, Josette L.; Miller, Erica K.; Maxwell, Bruce D.; Dyer, William E. (2001). "Dicamba resistance in kochia". Weed Science 49 (2): 164. doi:10.1614/0043-1745(2001)049[0164:DRIK]2.0.CO;2. 
  5. ^ Behrens, M. R.; Mutlu, N.; Chakraborty, S.; Dumitru, R.; Jiang, W. Z.; Lavallee, B. J.; Herman, P. L.; Clemente, T. E.; Weeks, D. P. (2007). "Dicamba Resistance: Enlarging and Preserving Biotechnology-Based Weed Management Strategies". Science 316 (5828): 1185–8. doi:10.1126/science.1141596. PMID 17525337. 
  6. ^ http://pmep.cce.cornell.edu/profiles/herb-growthreg/dalapon-ethephon/dicamba/herb-prof-dicamba.html. Retrieved 20 May 2010
  7. ^ Pesticide Information Profile - Dicamba, Pesticide Management Education Program, Cornell University.

External links[edit]