General Description
DICAMBA(1918-00-9) is a white solid dissolved in a liquid carrier. The carrier is water emulsifiable. The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Since DICAMBA(1918-00-9) is a liquid DICAMBA(1918-00-9) can easily penetrate the soil and contaminate groundwater and nearby streams. DICAMBA(1918-00-9) can cause illness by inhalation, skin absorption and/or ingestion. DICAMBA(1918-00-9) is used as a herbicide.
Reactivity Profile
A halogenated benzoic acid derivative. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acids dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in DICAMBA to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.
Health Hazard
SOLID: Harmful if swallowed.
Fire Hazard
Not flammable.
Uses
Dicamba is mainly used as an herbicide to control weeds, dock,
bracken, and brush. Dicamba is frequently applied with other
herbicides, including atrazine, glyphosate, imazethapyr, ioxynil,
and mecoprop.
Uses
Selective, systemic preemergence and postemergence herbicide used to control both
annual and perennial broad-leaved weeds, chickweed, mayweed and bindweed in cereals
and other related crops.
Definition
ChEBI: A methoxybenzoic acid that is O-methylsalicylic acid substituted by chloro groups at positions 3 and 6.
Agricultural Uses
Herbicide: Used to control annual and perennial broadleaf
weeds in corn, sorghum, small grains, pastures, hay,
rangeland, sugarcane, asparagus, turf, grass-seed crops,
and non-croplands. It can be applied to the leaves or to
the soil. Dicamba controls annual and perennial broadleaf
weeds in grain crops and grasslands, and it is used to control
brush and bracken in pastures. It will kill broadleaf
weeds before and after they sprout. Legumes will be killed
by dicamba. In combination with a phenoxyalkanoic acid
or other herbicide, dicamba is used in pastures, range land,
and non-crop areas such as fence-rows and roadways to
control weeds.
Trade name
BANEX®; BANLEN®; BANVEL®;
BANVEL 4S®; BANVEL 4WS®; BANVEL CST®;
BANVEL HERBICIDE®; BANVEL II HERBICIDE®;
BRUSH BUSTER®; BUSHWHACKER®; CADENCE®;
CASWELL No. 295®; CLARITY®; COMPOUND
B DICAMBA®; DIANATE®; DISTINCT®;
DYVEL®; FALLOWMASTER®; FLOWMASTER®;
GORDON’S TRIGUARD®; GORDON’S TRI-MEC®;
MARKSMAN®; MEDIBEN®; NORTHSTAR®;
SUMMIT®; TARGET®; TRACKER®; TROOPER®;
VANQUISH®; VELSICOL 58-CS-11®; VELSICOL
COMPOUND R®; WEEDMASTER®; YUKON®
Biochem/physiol Actions
Dicamba is a broad leaf growth regulator that mimics plant growth auxins. Dicamba is used as a herbicide and is effective against glyphosate-resistant (GR) giant ragweed.
Pharmacology
Dicamba is highly mobile in soils
and will leach or move upward depending on the flux of
the soil water. Adsorption to soils is generally limited,
although a few studies using acidic kaolinite and muck
soils showed that dicamba was adsorbed to these soils.
Adsorption of dicamba is greatest at low soil pHs and
is minimal at pHs greater than 6.0. Because dicamba is
highly water soluble, it is reasonable to expect that some
loss may occur via soil water runoff from the application
zone. However, studies conducted by Trichelle et al. (44)
showed that such losses were minimal, i.e., less than 5.5%
of applied. The rate of dicamba volatilization is not clear,
although it is likely that it does occur to some extent.
On planchets, approximately 50% of applied dicamba
volatilized over a period of 11 weeks. The significance
of this result is questionable, because in a similar study
using soil, there was no appreciable volatilization (45).
Potential Exposure
AgriculturalChemical; Mutagen. Those involved in manufacture, formulation, and application of this postemergence herbicide. Used to control allual and perennial broad leafweeds in corn, sorghum, small grain pastures, andnoncroplands.
First aid
If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.
Environmental Fate
Biological. In a model ecosystem containing sand, water, plants and biota, dicamba
was slowly transformed to 5-hydroxydicamba (10% after 32 days) which slowly underwent
decarboxylation (Yu et al., 1975).
Soil. Smith (1974) studied the degradation of 14C-ring- and 14C-carboxyl-labeled
dicamba in moist prairie soils at 25°C. After 4 weeks, >50% of the herbicide degraded to
the principal products 3,6-dichlorosalicylic acid and carbon dioxide (Smith, 1974).
The half-lives for dicamba in soil incubated in the laboratory under aerobic conditions
ranged from 0 to 32 days (Altom and Stritzke, 1973; Smith, 1973, 1974; Smith and
Cullimore, 1975). In field soils, the half-lives for dicamba ranged from 6 to 10 days with
an average half-life of 7 days (Scifres and Allen, 1973; Stewart and Gaul, 1977). The
mineralization half-lives for dicamba in soil ranged from 147 to 309 days (Smith, 1974;Smith and Cullimore, 1975). In a Regina heavy clay, the loss of dicamba was rapid.
Approximately 10% of the applied dosage was recovered after 5 weeks. At the end of 5
weeks, approximately 28% was transformed to 3,6-dichlorosalicylic acid and carbon
dioxide (Smith, 1973a).
Groundwater. According to the U.S. EPA (1986) dicamba has a high potential to leach
to groundwater.
Plant. Dicamba is hydrolyzed in wheat and Kentucky bluegrass plants to 5-hydroxy-
2-methoxy-3,6-dichlorobenzoic acid and 3,6-dichlorosalicylic acid at yields of 90 and 5%,
respectively. The remaining 5% was unreacted dicamba (Broadhurst et al., 1966). Dicamba
was absorbed from treated soils, translocated in corn plants and then converted to 3,6-
dichlorosalicylic acid, p-aminobenzoic acid and benzoic acid (Krumzdorf, 1974).
Photolytic. When dicamba on silica gel plates was exposed to UV radiation (λ= 254
nm), it slowly degraded to the 5-hydroxy analog and water solubles (Humburg et al., 1989).
Chemical/Physical. Reacts with alkalies (Hartley and Kidd, 1987), amines and alkali
metals (Worthing and Hance, 1991) forming very water-soluble salts.
When dicamba was heated at 900°C, carbon monoxide, carbon dioxide, chlorine,
hydrochloric acid, oxygen and ammonia were produced (Kennedy et al., 1972, 1972a).
storage
Color Code—Blue: Health Hazard/Poison: Storein a secure poison location. Prior to working with dicamba you should be trained on its proper handling and storage.Store in tightly closed containers in a cool, well-ventilatedarea away from incompatible materials listed above, heat,and water.
Shipping
Benzoic derivative pesticides, solid, toxic, n.o.s.require a label of “POISONOUS/TOXIC MATERIALS.” Itfalls in Hazard Class 6.1
Mode of action
DICAMBA HD 5 is readily absorbed by plants through shoot and root uptake, translocates throughout the plant's system, and
accumulates in areas of active growth. This product interferes with the plant's growth hormones (auxins) resulting in
death of many broadleaf weeds.
Toxicity evaluation
There is very little metabolism of
dicamba in mammals, and most is excreted unchanged
in the urine. For example, rat excreted 96% of ingested
14C-dicamba after 24 hours (46). The acute oral LD50 for
rat is 1707 mg/kg.
Incompatibilities
Incompatible with sulfuric acid, bases,ammonia, aliphatic amines, alkanolamines, isocyanates,alkylene oxides, epichlorohydrin. Dicamba decomposes inheat, producing toxic and corrosive fumes including hydrogen chloride
