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Revised June 1996
Bromacil
Trade and Other Names:
Trade names include Borea, Bromax 4G, Bromax 4L, Borocil,
Cynogan, Hyvar X, Hyvar XL, Isocil, Krovar, Rout, Uragan, Urox B,
and Urox HX.
Regulatory Status:
Bromacil is classified by the U. S. Environmental Protection
Agency (EPA) as a General Use Pesticide (GUP). It is in toxicity
class IV - practically nontoxic in dry form, and class II -
moderately toxic in the liquid form. Dry formulations containing
bromacil bear the Signal Word CAUTION. Because of their
irritating effects on skin, eyes, and the respiratory tract,
liquid formulations bear the Signal Word WARNING.
Chemical Class: Not
Available
Introduction:
Bromacil is an herbicide used for brush control on non-cropland
areas. It is especially useful against perennial grasses. It is
also used for selective weed control in pineapple and citrus
crops. It works by interfering with photosynthesis, the process
by which plants use sunlight to produce energy. Bromacil is one
of a group of compounds called uracils. It is sprayed or spread
dry on the soil surface just before, or during, a period of
active weed growth. It is available in granular, liquid, water
soluble liquid, and wettable powder formulations.
Formulation: It is
available in granular, liquid, water soluble liquid, and wettable
powder formulations.
Toxicological Effects:
- Acute toxicity: Liquid formulations of
bromacil are moderately toxic, while dry formulations are
practically non-toxic [8]. The herbicide is irritating to
the skin, eyes, and respiratory tract [68]. When 100
mg/kg of the herbicide was fed to dogs, it caused
vomiting, watering of the mouth, muscular weakness,
excitability, diarrhea, and dilation of the pupils. Rats
that were fed single doses of bromacil experienced
initial weight loss, paleness, exhaustion, and rapid
breathing. Within 4 hours of being given 250 mg/kg, sheep
became bloated and walked with stilted gaits [30].
Bromacil caused mild dermal irritation when it was
applied to the skin of guinea pigs. The LD50 is greater
than 5000 mg/kg in rabbits whose skin is exposed. When
bromacil was administered to the eyes of rabbits, there
was irritation in the conjunctiva (the mucous membrane
lining of the eye), but there was no injury to the cornea
[30]. The inhalation LC50 (4-hour) is greater than 4.8
mg/L air for rats [1]. The oral LD50 for bromacil in rats
is 5200 mg/kg, and in mice is 3040 mg/kg [1,30].
- Chronic toxicity: Enlarged livers were
revealed in autopsies on rats that died after 5 days of
repeated doses of bromacil at 1500 mg/kg/day [30]. Sheep
that died after being given 250 mg/kg/day of bromacil on
4 successive days showed the following: inflammation of
the mucous membrane that lines the stomach and
intestines, congestion and enlargement of the liver,
weakened appearance of the adrenal glands, bleeding of
the heart, and swollen, bleeding lymph nodes [30].
Consumption of bromacil at high levels over a long period
of time has been shown to cause damage to the testes,
liver, and thyroid of laboratory animals [74]. In another
study, female rats fed 62.5 mg/kg/day for 2 years, the
highest dose level, exhibited decreased weight gain. No
other toxic effects were observed [74]. No evidence of
toxicity was detected in dogs fed up to 31.2 mg/kg/day
for 2 years [74]. In an 18-month study in which mice were
given dietary doses of 12.5, 62.5, or 250 mg/kg/day,
changes in the liver and testes were observed at the 62.5
mg/kg/day dosage [74]. Chickens given 500 mg/kg/day
bromacil did show a decrease in weight gain [75].
- Reproductive effects: Bromacil did not
affect the reproduction of rats fed 12.5 mg/kg/day for
three generations [8,74]. This suggests that bromocil
does not cause reproductive effects.
- Teratogenic effects: There was no
evidence of birth defects in the offspring of rats that
were given dietary doses of 12.5 mg/kg/day bromacil, nor
in rabbits that were given 7.5 mg/kg/day on days 8
through 16 of pregnancy [74]. However, toxic effects and
developmental abnormalities of the musculoskeletal system
were seen in the embryos or fetuses of rats which inhaled
very high bromacil doses of 38 mg/L for 2 hours daily,
during days 7 to 14 of pregnancy [22]. Toxic effects and
developmental abnormalities were observed in the fetuses
of pregnant rats repeatedly exposed by inhalation to
bromacil [8]. These data suggest that humans are unlikely
to suffer teratogenic effects from bromacil under normal
circumstances.
- Mutagenic effects: Several mutagenic
screening tests indicate that bromacil is not mutagenic
[74].
- Carcinogenic effects: There is limited
evidence that bromacil causes cancer in animals receiving
high doses over the course of their lifetimes [74]. There
was no evidence of carcinogenicity in rats fed 12.5
mg/kg/day for 2 years of bromacil, but at 62.5 mg/kg/day,
there was at slight increase in hyperplasia of the
thyroid, and one rat developed benign liver tumors
[17,74]. An increased incidence of malignant tumors was
observed in the livers of male mice given 250 mg/kg/day
of bromacil for 78 weeks. No effect on liver tumor
incidence was observed in female mice [74]. Based on
these results, it is not possible to determine bromacil's
carcinogenic potential.
- Organ toxicity: Animal studies have
shown the liver, heart, and lymph nodes to be affected.
- Fate in humans and animals: A number of
studies show that uracils, the class of compounds to
which bromacil belongs, are absorbed into the body from
the gut and excreted primarily in the urine [8,74]. Small
amounts of bromacil were detected in the milk of
lactating cows that were given 5 mg/kg in their food
[30]. No bromacil was found in the urine or feces of
these cows [8].
Ecological Effects:
- Effects on birds: The 8-day dietary oral
LC50 for bromacil is over 10,000 ppm in mallards and
quail [23]. This indicates that it is practically
nontoxic to these species.
- Effects on aquatic organisms: Bromacil
is slightly to practically nontoxic to fish. The 48-hour
LC50 for bromacil in bluegill sunfish is 71 mg/L, in
rainbow trout is 56 75 mg/L, and in carp is 164 mg/L [8].
The 96-hour LC50 in fathead minnows is 182 mg/L [8]. It
is not toxic to aquatic invertebrates [8].
- Effects on other organisms: Bromacil is
not toxic to honeybees [1].
Environmental Fate:
- Breakdown in soil and groundwater:
Bromacil binds, or adsorbs, only slightly to soil
particles, is soluble in water, and is moderately to
highly persistent in soil. Its half-life is about 60
days, but may be as much as 8 months under some
conditions [11]. Soil persistence is correlated to the
organic content of the soil [8,75]. At 18 months after
22.4 kg of bromacil were sprayed on abandoned field
sites, residues of the herbicide were detectable, in
decreasing amounts, in loamy sand, silt loam, silty clay
loam, and light silty clay loam soils. Organic matter
content, cation exchange capacity, total nitrogen, and
soluble salt concentrations were significantly correlated
with residue persistence [8]. Bromacil is expected to
leach quite readily through the soil and contaminate
groundwater. The amount of leaching is dependent on the
soil type and the amount of rainfall or irrigation water.
The potential for bromacil to leach and contaminate
groundwater is greatest in sandy soils. In normal soils,
it can be expected to leach to a depth of 2 to 3 feet
[8]. Tests show that at increased temperatures and long
exposures to sunlight, there is very little loss of
bromacil from dry soil. It does not readily volatilize,
nor does it break down in sunlight [8]. Laboratory
studies show that 5 to 30% of bromacil is lost 6 to 9
weeks after application to the soil, as carbon dioxide
[8].
- Breakdown in water: Bromacil is
estimated to have a 2-month half-life in clean river
water, which is low in sediment [76].
- Breakdown in vegetation: In plants,
bromacil is taken up rapidly by the roots and slightly
absorbed through the leaves [58]. When it is applied at
10 ppm, some types of algae show slowed growth, but most
strains are unaffected [75]. Improper application of
bromacil will destroy shade trees and other desirable
vegetation [76].
Physical Properties:
- Appearance: Bromacil is an odorless,
white crystalline solid [1].
- Chemical Name:
5-bromo-6-methyl-3-(1-methylpropyl)-2,4(1H,3H)pyrimidinidione
[1]
- CAS Number: 314-40-9
- Molecular Weight: 261.10
- Water Solubility: 815 mg/L @ 25 C [1]
- Solubility in Other Solvents: xylene
v.s.; acetone v.s.; acetonitrile v.s.; ethyl alcohol
v.s.; sodium hydroxide v.s. [1]
- Melting Point: 158-159 C [1]
- Vapor Pressure: 0.033 mPa @ 25 C [1]
- Partition Coefficient: Not Available
- Adsorption Coefficient: 32 (acid) [11]
Exposure Guidelines:
- ADI: Not Available
- MCL: Not Available
- RfD: Not Available
- PEL: Not Available
- HA: 0.09 mg/L [74]
- TLV: 10 mg/m3 (8-hour) [17]
Basic Manufacturer:
DuPont Agricultural Products
Walker's Mill, Barley Mill Plaza
P.O. Box 80038
Wilmington, DE 19880-0038
- Phone: 800-441-7515
- Emergency: 800-441-3637
References:
References for the information in this PIP can be found in
Reference List Number 10
DISCLAIMER: The
information in this profile does not in any way replace or
supersede the information on the pesticide product labeling or
other regulatory requirements. Please refer to the pesticide
product labeling.