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Revised June 1996
Quizalofop-p-ethyl
Trade and Other Names:
Trade and other names of products containing quizalofop-p-ethyl
include Assure II, Copilot, Pilot Super, Sheriff, Targa D+, and
Targa Super Quizalofop. The compound may be found in formulations
with other herbicides such as benazolin and clopyralid (trade
name Benazalox).
Regulatory Status:
The compound is a General Use Pesticide (GUP). Quizalofop-p-ethyl
is a slightly toxic compound in EPA toxicity class III. End-use
products are required to have the Signal Word CAUTION on their
labels.
Chemical Class: phenoxy
compound
Introduction:
Quizalofop-p-ethyl is a selective, postemergence phenoxy
herbicide. It is used to control annual and perennial grass weeds
in potatoes, soybeans, sugar beets, peanuts, vegetables, cotton
and flax, as well as other crops.
Quizalofop-p and quizalofop-p-ethyl should not be confused
with quizalofop or quizalofop ethyl. The latter two compounds are
distinctly different from the former two. The material in this
profile refers only to the technical compound quizalofop-p-ethyl
unless otherwise stated.
Formulation: Not
Available
Toxicological Effects:
- Acute toxicity: Quizalofop-p-ethyl is
slightly toxic by oral exposure. The reported oral LD50
values of the compound are 1210 to 1670 mg/kg in male
rats, and 1182 to 1480 mg/kg in female rats [5,6]. Mice
are only slightly less susceptible to the compound.
Quizalofop-p-ethyl has reported LD50 values of 1753 to
2350 mg/kg in male mice and 1805 to 2360 mg/kg in female
mice [5.6]. For the formulated product Assure, the
reported oral LD50 values are 6600 mg/kg in male rats and
5700 in female rats [5]. Exposure of the skin of rabbits
to the compound indicated that the compound is only
slightly toxic by this route as well. The acute
percutaneous (absorbed through the skin) LD50 for
quizalofop-p-ethyl in mice, rats, and rabbits is greater
than 2000 mg/kg [6]. For the formulated product Assure,
the reported dermal LD50 in rabbits is greater than 5000
mg/kg [5]. Quizalofop-p-ethyl is slightly to practically
nontoxic via inhalation, both in technical form and
formulation. Reported 4-hour inhalation LC50s values are
5.8 mg/L for technical quizalofop-p-ethyl and 75 mg/L for
Assure in rats [5]. Quizalofop-p-ethyl is nonirritating
to the skin and only slightly irritating to the eyes in
rabbits [5]. It is nonsensitizing to the skin of guinea
pigs. The Assure formulation, however, is severely
irritating to rabbit eyes [5].
- Chronic toxicity: In a 1-year feeding
study on dogs, doses of up to 10 mg/kg/day (the highest
dose tested in that study) caused no observed effects
[31]. In a 90-day feeding study in rats, doses of 6.4
mg/kg/day and higher produced liver lesions and increased
liver weight [31]. In a 2-year study of rats, doses of 5
mg/kg/day produced no observed effects [31].
- Reproductive effects: Data from
reproductive studies indicated only decreased body weight
gains, and did not report findings of impaired
reproductive function in test animals [31]. A 6-month
study in dogs found atrophy of the semeniferous tubles at
doses of 2.5 mg/kg/day, but was unclear whether this was
extensive enough to result in impaired reproductive
function [31]. These data are insufficient to draw
conclusions regarding the likely reproductive effects of
quizalofop-p-ethyl in animals, but suggest that effects
on human reproduction are unlikely under normal
circumstances.
- Teratogenic effects: In a
two-generational study in rats, doses of 2.5 mg/kg/day
and higher produced increased liver weights in offspring
[31]. No teratogenic effects were observed in another
study in rats at doses of up to 300 mg/kg/day (the
highest doses tested) over an unspecified period,
although maternal decreases in body weight, food
consumption, and corpora lutea were observed at doses of
100 mg/kg/day [31]. These data suggest that teratogenic
or developmental effects are unlikely in humans.
- Mutagenic effects: The results of many
assays for mutagenicity and genotoxicity of
quizalofop-p-ethyl show no mutagenic or genotoxic
activity. Quizalofop-p-ethyl was not found to be
mutagenic in the Ames assay, either with or without
metabolic activation, nor was mutagenic activity seen in
Chinese hamster ovary cell culture tests [6]. Assays for
chromosome structural aberrations and alterations in DNA
damage repair capacity were also negative [5].
- Carcinogenic effects: In an 18-month
carcinogenicity study on mice, increased liver weights,
changes in blood chemistry, and some changes in liver
tissue structure were detected, but no carcinogenic or
tumor-causing activity was reported [8]. This study
suggests that this compound is not carcinogenic.
- Organ toxicity: Available data show that
the target organ in test animals has consistently been
the liver in rats and dogs [8]. It is possible that
testes may be a target organ in some species; e.g., dogs
[7].
- Fate in humans and animals: Quizalofop-p
appears to be rapidly broken down in mammals. More than
90% of a single oral dose is eliminated in urine within 3
days [6].
Ecological Effects:
- Effects on birds: Quizalofop-p-ethyl is
practically nontoxic to birds. The reported 8-day feeding
(dietary) LC50 is greater than 5000 ppm in bobwhite quail
and mallard ducks. The reported LD50 for
quizalofop-p-ethyl is greater than 2000 mg/kg in mallard
ducks [5].
- Effects on aquatic organisms:
Quizalofop-p-ethyl is highly to very highly toxic to
fish. Reported 96-hour LC50 values are 10.7 mg/L in
rainbow trout and 0.46 to 2.8 mg/L in bluegill sunfish
[5].
- Effects on other organisms:
Quizalofop-p-ethyl is practically nontoxic to bees, with
a 48-hour contact LD50 of greater than 100 mg/bee [7].
Environmental Fate:
- Breakdown in soil and groundwater:
Quizalofop-p-ethyl is moderately persistent in soils,
with a reported half-life of 60 days [5,6]. It may be
more rapidly broken down in soil with high microbial
activity [5]. It is moderately to strongly sorbed to
soils [5], and studies indicate very low soil mobility
[5]. It should not leach significantly into water.
- Breakdown in water: No data are
currently available.
- Breakdown in vegetation: No data are
available regarding the breakdown of the compound;
however, it is absorbed from the leaf surface and
translocated throughout the plant. It accumulates in the
active growing regions of stems and roots [5].
Physical Properties:
- Appearance: The compound is a pale brown
crystal [6].
- Chemical Name:
(R)-2-[4-(6-chloroquinoxalin-2-yloxy)phenoxy]propionic
acid [6]
- CAS Number: 100646-51-3
- Molecular Weight: 372.80
- Water Solubility: 0.4 mg/L @ 20 C [6]
- Solubility in Other Solvents: s. in
hexane; v.s. in acetone, ethanol, and xylene [6]
- Melting Point: 76-77 C [6]
- Vapor Pressure: 0.000011 mPa @ 20 C [6]
- Partition Coefficient: Not Available
- Adsorption Coefficient: 510 [5]
Exposure Guidelines:
- ADI: Not Available
- MCL: Not Available
- RfD: Not Available
- PEL: Not Available
- HA: Not Available
- TLV: Not Available
Basic Manufacturer:
Zeneca Agricultural Products
1800 Concord Pike
Wilmington, DE 19897
- Phone: 800-759-4500
- Emergency: 800-759-2500
References:
References for the information in this PIP can be found in
Reference List Number 7
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.