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Revised June 1996
Chlorothalonil
Trade and Other Names:
Trade names for chlorothalonil include Bravo, Chlorothalonil,
Daconil 2787, Echo, Exotherm Termil, Forturf, Mold-Ex, Nopcocide
N-96, Ole, Pillarich, Repulse, and Tuffcide. The compound can be
found in formulations with many other pesticide compounds.
Regulatory Status:
Chlorothalonil is classified as a General Use Pesticide (GUP) by
the U.S. Environmental Protection Agency. It is classified as
toxicity class II - moderately toxic, due to its potential for
eye irritation. Chlorothalonil containing products have a range
of Signal Words, including WARNING (Bravo 720, 500), CAUTION
(Exotherm Termil), and DANGER (Bravo W-75, Daconil W-75). Each of
these products has a different formulation and product
concentration and thus requires a different Signal Word.
Chemical Class:
chloronitrile
Introduction:
Chlorothalonil is a broad-spectrum organochlorine fungicide used
to control fungi that threaten vegetables, trees, small fruits,
turf, ornamentals, and other agricultural crops. It also controls
fruit rots in cranberry bogs.
Formulation: The
compound can be found in formulations with many other pesticide
compounds.
Toxicological Effects:
- Acute toxicity: Chlorothalonil is
slightly toxic to mammals, but it can cause severe eye
and skin irritation in certain formulations [2]. Very
high doses may cause a loss of muscle coordination, rapid
breathing, nose bleeding, vomiting, hyperactivity, and
death. Dermatitis, vaginal bleeding, bright yellow and/or
bloody urine, and kidney tumors may also occur [17]. The
oral LD50 is greater than 10,000 mg/kg in rats and 6000
mg/kg in mice [9,17]. The acute dermal LD50 in both
albino rabbits and albino rats is 10,000 mg/kg (9,17). In
albino rabbits, 3 mg of chlorothalonil applied to the
eyes caused mild irritation that subsided within 7 days
of exposure [35].
- Chronic toxicity: In a number of tests
of varying lengths of time, rats fed a range of doses of
chlorothalonil generally showed no effects on physical
appearance, behavior, or survival [35]. Skin contact with
chlorothalonil may result in dermatitis or light
sensitivity [35]. Human eye and skin irritation is linked
to chlorothalonil exposure; 14 of 20 workers exposed to
0.5% chlorothalonil in a wood preservative developed
dermatitis. All workers showed swelling and inflammation
of the upper eyelids [35]. Allergic skin responses have
also been noted in farm workers [7].
- Reproductive effects: Administration of
high doses of chlorothalonil to pregnant rabbits through
the stomach during the sensitive period of gestation was
required to induce abortion in 4 of the 9 mothers. This
and other studies suggest that chlorothalonil will not
affect human reproduction at expected exposure levels
[35].
- Teratogenic effects: Long-term studies
indicate that high doses fed to rats caused reduced
weight gains for males and females in each generation
studied [35]. Female rats given high doses of
chlorothalonil through the stomach during the sensitive
period of gestation had normal fetuses, even though that
dose was toxic to the mothers [35]. A study of birth
defects in rabbits showed no effects [36]. Chlorothalonil
is not expected to produce birth defects in humans.
- Mutagenic effects: Mutagenicity studies
on various animals, bacteria, and plants indicate that
chlorothalonil does not cause any genetic changes
[17,35,36]. The compound is not expected to pose
mutagenic risks to humans.
- Carcinogenic effects: Based on evidence
from animal studies, chlorothalonil's carcinogenic
potential is unclear. Male and female rats fed
chlorothalonil daily over a lifetime developed
carcinogenic and benign kidney tumors at the higher doses
[35]. In another study, where mice were fed high daily
doses of chlorothalonil for 2 years, females developed
tumors in the fore-stomach area (attributed to irritation
by the compound) and males developed carcinogenic and
benign kidney tumors [35].
- Organ toxicity: Chronic studies of rats
and dogs fed high dietary levels show that chlorothalonil
is toxic to the kidney. In addition to less urine output,
changes in the kidney included enlargement,
greenish-brown color, and development of small grains
[37].
- Fate in humans and animals:
Chlorothalonil is rapidly excreted, primarily unchanged,
from the body. It is not stored in animal tissues. Rats
and dogs fed very high doses for 2 years eliminated
almost all of the chemical in urine, feces, and expired
air [17,38]. At lower concentrations, chlorothalonil
leaves the body within 24 hours. Residues have not been
found in the tissues or milk of dairy cows fed
chlorothalonil [17].
Ecological Effects:
- Effects on birds: Chlorothalonil is
practically nontoxic to birds. The LD50 in mallard ducks
is 5000 mg/kg [9]. Most avian wildlife are not
significantly affected by this compound [17].
- Effects on aquatic organisms:
Chlorothalonil and its metabolites are highly toxic to
fish, aquatic invertebrates, and marine organisms. Fish,
such as rainbow trout, bluegill, and channel catfish are
noticeably affected even when chlorothalonil levels are
low (less than 1 mg/L). The LC50 is 0.25 mg/L in rainbow
trout, 0.3 mg/L in bluegills, and 0.43 mg/L in channel
catfish [9]. Chlorothalonil does not store in fatty
tissues and is rapidly excreted from the body. Its
bioaccumulation factor is quite low [17].
- Effects on other organisms: The compound
is nontoxic to bees [9].
Environmental Fate:
- Breakdown in soil and groundwater:
Chlorothalonil is moderately persistent. In aerobic
soils, the half-life is from 1 to 3 months. Increased
soil moisture or temperature increases chlorothalonil
degradation. It is not degraded by sunlight on the soil
surface [17]. Chlorothalonil has high binding and low
mobility in silty loam and silty clay loam soils, and has
low binding and moderate mobility in sand [35].
Chlorothalonil was not found in any of 560 groundwater
samples collected from 556 U.S. sites [35].
- Breakdown in water: In very basic water
(pH 9.0), about 65% of the chlorothalonil was degraded
into two major metabolites after 10 weeks. Chlorothalonil
was found in one surface water location in Michigan at
6.5 mg/L [35].
- Breakdown in vegetation:
Chlorothalonil's residues may remain on above-ground
crops at harvest, but will dissipate over time.
Chlorothalonil is a fairly persistent fungicide on
plants, depending on the rate of application. Small
amounts of one metabolite may be found in harvested crops
[37].
Physical Properties:
- Appearance: Chlorothalonil is an
aromatic halogen compound, a member of the chloronitrile
chemical family. It is a grayish to colorless crystalline
solid that is odorless to slightly pungent [9].
- Chemical Name:
tetrachloroisophthalonitrile [9]
- CAS Number: 1897-45-6
- Molecular Weight: 265.92
- Water Solubility: 0.6 mg/L @ 25 C [9]
- Solubility in Other Solvents: acetone
s.s.; dimethyl sulfoxide s.s.; cyclohexanone s.s.;
kerosene i.s.; xylene s.s. [9]
- Melting Point: 250-251 C [9]
- Vapor Pressure: 1.3 mPa @ 40 C [9]
- Partition Coefficient: 437 (calc.): 20.9
[17]
- Adsorption Coefficient: 1380 [14]
Exposure Guidelines:
- ADI: 0.03 mg/kg/day [27]
- MCL: Not Available
- RfD: 0.015 mg/kg/day [8]
- PEL: Not Available
- HA: 0.5 mg/L (longer-term) [35]
- TLV: Not Available
Basic Manufacturer:
Crystal Chemical Inter-America
10303 N.W. Freeway, Suite 512
Houston TX 77083
- Phone: 713-956-6196
- Emergency: Not Available
References:
References for the information in this PIP can be found in
Reference List Number 6
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.