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Revised June 1996
Simazine
Trade and Other Names:
Trade names include Aquazine, Caliber, Cekusan, Cekusima, Framed,
Gesatop, Primatol S, Princep, Simadex, Simanex, Sim-Trol, Tanzine
and Totazine. This compound may also be found in formulations
with other herbicides such as amitrole, paraquat dichloride,
metolachlor, and atrazine.
Regulatory Status:
Simazine is a General Use Pesticide (GUP). It is in EPA toxicity
class IV - practically nontoxic. Products containing simazine
bear the Signal Word CAUTION. In November 1994, the U.S. EPA
began a Special Review of simazine which could result in use
restrictions or even cancellation if data warrant such action.
Chemical Class:
Triazine
Introduction:
Simazine is a selective triazine herbicide. It is used to control
broad-leaved weeds and annual grasses in field, berry fruit,
nuts, vegetable and ornamental crops, turfgrass, orchards, and
vineyards. At higher rates, it is used for nonselective weed
control in industrial areas. Before 1992, simazine was used to
control submerged weeds and algae in large aquariums, farm ponds,
fish hatcheries, swimming pools, ornamental ponds, and cooling
towers. Simazine is available in wettable powder, water
dispersible granule, liquid, and granular formulations. It may be
soil-applied.
Formulation: Simazine
is available in wettable powder, water dispersible granule,
liquid and granular formulations. It may be soil-applied.
Toxicological Effects:
- Acute toxicity: Simazine is slightly to
practically nontoxic. The reported oral LD50 for
technical simazine in rats and mice is >5000 mg/kg
[6,15]; its dermal LD50 is 3100 mg/kg in rats and >
10,000 mg/kg in rabbits [6,15]. The 4-hour inhalation
LC50 in rats is greater than 2 mg/L (6). The formulated
products, in most cases, are less toxic via all routes
[15]. Simazine is nonirritating to the skin and eyes of
rabbits except at high doses [3]. Patch tests on humans
have shown that simazine is not a skin irritant,
fatiguing agent, or sensitizer [3]. However, rashes and
dermatitis from occupational exposure to simazine have
occurred [3]. The triazine herbicides disturb energy
metabolism (thiamin and riboflavin functions). Symptoms
include difficulty in walking, tremor, convulsions,
paralysis, cyanosis, slowed respiration, miosis (pinpoint
pupils), gut pain, diarrhea, and impaired adrenal
function [3]. No cases of poisoning in humans have been
reported from ingestion of simazine [3]. Rats given an
oral dose of 5000 mg/kg exhibited drowsiness and
irregular breathing. In another study, a single oral dose
of 4200 mg/kg produced anorexia, weight loss, and some
deaths in rats within 4 to 10 days [26]. For unknown
reasons, sheep and cattle are especially susceptible to
poisoning by simazine. Doses of 500 mg/kg were fatal in
sheep with death delayed for 5 to 16 days. Symptoms
exhibited by poisoned sheep included lower food intake,
higher water intake, incoordination, tremors, and
weakness, especially in the hindquarters [3].
- Chronic toxicity: Some 90-day feeding
studies showed reduced body weight at 67 to 100 mg/kg/day
[10]. This same effect and kidney toxicity were seen in
rats at doses of 150 mg/kg/day [10]. In 2-year chronic
oral feeding studies in which rats were given daily
dosages of 5 mg/kg/day of simazine in the diet, no gross
or microscopic signs of toxicity were seen [3]. When rats
were given repeated doses of 15 mg/kg/day, some liver
cells degenerated during the first 3 days, but the
condition did not progress. Instead, the liver adapted
and the compound was metabolized [3]. Other effects
observed in test animals include tremors, damage to the
testes, kidneys, liver, and thyroid, disturbances in
sperm production, and gene mutations [10].
- Reproductive effects: No adverse effects
on reproductive capacity or development were observed in
a three-generation study of rats fed 5 mg/kg/day simazine
[10]. High rates of fetotoxicity and decreased birth
weight were noted in the fetuses of pregnant rabbits fed
75 mg/kg/day [26]. Reproductive effects are not likely in
humans under normal circumstances.
- Teratogenic effects: No dose-related
teratogenic effects were observed when rabbits were given
daily doses of 5, 75, or 200 mg/kg for days 7 through 19
of pregnancy [26]. Chronic inhalation of a cumulative
dose of 0.3 mg/L for 8 days in pregnant rats resulted in
no treatment-related developmental abnormalities [10].
Simazine does not appear to be teratogenic.
- Mutagenic effects: Simazine has shown
negative results in a variety of mutagenicity tests on
bacterial cultures [10]. Tests on human lung cell
cultures have produced both positive and negative results
[10]. When injected into adult male fruitflies, simazine
increased the frequency of sex-linked lethal mutations,
but failed to do so when fed to larvae. Other tests for
mutagenicity in fruitflies were negative [3]. It is
likely that simazine is either nonmutagenic or weakly
mutagenic.
- Carcinogenic effects: Simazine was not
tumorigenic in mice at the maximum tolerated dose of 215
mg/kg/day over an 18-month period [10]. In other studies,
doses as low as 5 mg/kg/day produced excess tumors
(thyroid and mammary) in female rats [3,10]. Because of
inconsistencies in the data, it is not possible to
determine simazine's carcinogenic status.
- Organ toxicity: Damage to the testes,
kidneys, liver, and thyroid has been observed in test
animals [3,10].
- Fate in humans and animals: Studies in
rats, goats, and sheep reveal that 60 to 70% of the
ingested dose may be absorbed into the system [10], with
approximately 5 to 10% distributed systemically to
tissues. The remainder is eliminated via urine within 24
hours [6]. Distribution led to detectable levels in red
blood cells (highest), liver, kidney, fat, bone, and
plasma [10]. When a cow was fed 5 ppm for 3 days, no
simazine was found in the cow's milk during the next 3
days. It has been reported that simazine residues were
present in the urine of sheep for up to 12 days after
administration of a single oral dose. The maximum
concentration in the urine occurred from 2 to 6 days
after administration [16].
Ecological Effects:
- Effects on birds: Simazine is
practically nontoxic to birds [6,16]. The reported LD50
values in mallard and Japanese quail are >4600 mg/kg
and 1785 mg/kg, respectively [6]. The acute dietary LD50
values in hens and pigeons are both greater than 5000 ppm
[2]. The 8-day dietary LC50 in bobwhite quail is >5260
ppm and in mallard ducks is >10,000 ppm [6,15].
- Effects on aquatic organisms: Simazine
is slightly to practically nontoxic to aquatic species
[6,15]. The 96-hour LC50 for simazine is >100 mg/L
[46] in rainbow trout, 100 mg/L (wettable powder) in
bluegill sunfish, 0.100 mg/L in fathead minnows [46], as
well as carp [2]. It may be more toxic to Daphia and
stoneflies [46]. A 96-hour LC50 of >3.7 mg/L is
reported in oysters [15].
- Effects on other organisms: While many
mammals may be insensitive to simazine [16], sheep and
cattle are especially sensitive [3]. Simazine is nontoxic
to bees [6,16]. A soil LC50 in earthworms of >1000
mg/kg has been reported [16].
Environmental Fate:
- Breakdown in soil and groundwater:
Simazine is moderately persistent with an average field
half-life of 60 days [20]. Soil half-lives of 28-149 days
have been reported [20]. Residual activity may remain for
a year after application (2 to 4 kg/ha) in high pH soils.
Simazine is moderately to poorly bound to soils [20]. It
does, however, adsorb to clays and mucks. Its low water
solubility, however, makes it less mobile, limiting its
leaching potential [15]. Simazine has little, if any,
lateral movement in soil, but can be washed along with
soil particles in runoff. Simazine is subject to
decomposition by ultraviolet radiation, but this effect
is small under normal field conditions. Loss from
volatilization is also insignificant. In soils, microbial
activity probably accounts for decomposition of a
significant amount of simazine in high pH soils. In lower
pH soils, hydrolysis will occur [15]. Simazine residues
have been detected in groundwater in at least 16 states.
The range was from 0.00002 mg/L to 0.0034 mg/L [23].
- Breakdown in water: The average
half-life of simazine in ponds where it has been applied
is 30 days, with the actual half-life dependent on the
level of algae present, the degree of weed infestation,
and other factors [15]. Simazine may undergo hydrolysis
at lower pH. It does not readily undergo hydrolysis in
water at pH = 7 [15].
- Breakdown in vegetation: Plants absorb
simazine mainly through the roots, with little or no
foliar penetration. From the roots, it is translocated
upward to the stems, leaves, and growing shoots of the
plant [6,15]. It acts to inhibit photosynthesis [6,15].
Resistant plants readily metabolize simazine. Plants that
are sensitive to simazine accumulate it unchanged [6]. It
is possible that livestock or wildlife grazing on these
plants could be poisoned.
Physical Properties:
- Appearance: Simazine is a white or
colorless crystalline solid [6].
- Chemical Name:
6-chloro-N2,N4-diethyl-1,3,5-triazine-2,4-diamine [6]
- CAS Number: 122-34-9
- Molecular Weight: 201.70
- Water Solubility: 5 mg/L @ 20 C [6]
- Solubility in Other Solvents: s. in
methanol, chloroform, and diethyl ether [6]; s.s. in
pentane [6]
- Melting Point: 225-227 C [6]
- Vapor Pressure: 0.000810 mPa @ 20 C [6]
- Partition Coefficient: 1.9600 [6]
- Adsorption Coefficient: 130 [20]
Exposure Guidelines:
- ADI: Not Available
- MCL: 0.004 mg/L [25]
- RfD: 0.005 mg/kg/day [26]
- PEL: Not Available
- HA: Not Available
- TLV: Not Available
Basic Manufacturer:
Ciba-Geigy Corporation
P.O. Box 18300
Greensboro, NC 27419-8300
- Phone: 800-334-9481
- Emergency: 800-888-8372
References:
References for the information in this PIP can be found in
Reference List Number 8
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.