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Revised June 1996
Mevinphos
Trade and Other Names:
Trade names include Apavinphos, CMDP, ENT 22374, Fosdrin, Gesfid,
Meniphos, Menite, Mevinox, Mevinphos, OS-2046, PD5, Phosdrin and
Phosfene.
Regulatory Status:
Mevinphos is a highly toxic compound in EPA toxicity class I. All
emulsifiable and liquid concentrates of mevinphos are classified
as Restricted Use Pesticides (RUPs) by the U.S. Environmental
Protection Agency (EPA), due to their acute oral and dermal
toxicity and residue effects on mammalian, aquatic and bird
species. RUPs may be purchased and used only by certified
applicators. Products containing mevinphos must bear the Signal
Words DANGER - POISON.
Chemical Class:
organophosphate
Introduction:
Mevinphos is an organophosphate insecticide used to control a
broad spectrum of insects, including aphids, grasshoppers,
leafhoppers, cutworms, caterpillars, and many other insects on a
wide range of field, forage, vegetable, and fruit crops. It is
also an acaricide that kills or controls mites and ticks. It acts
quickly both as a contact insecticide, acting through direct
contact with target pests, and as a systemic insecticide which
becomes absorbed by plants on which insects feed. It is available
in concentrate or liquid formulations.
Formulation: It is
available in concentrate and liquid formulations.
Toxicological Effects:
- Acute toxicity: Mevinphos is highly
toxic via the oral route, with reported oral LD50 values
of 3 to 12 mg/kg in rats, and 4 to 18 mg/kg in mice
[2,13]. Via the dermal route it is highly toxic as well,
with reported dermal LD50 values for mevinphos of 4.2
mg/kg in rats, and 40 mg/kg in mice [2,13]. The 1-hour
LC50 for mevinphos in rats is 0.125 mg/L, indicating high
toxicity by inhalation as well [2]. Acute pulmonary
edema, or the filling up of lungs with fluid, and changes
in the structure or function of salivary glands, were
seen in rats that exposed to this concentration for 1
hour. Effects of acute exposure to mevinphos are similar
to those due to exposure to other organophosphates,
except that these may occur at lower doses than with
other organophosphates. Symptoms of acute exposure to
organophosphate or cholinesterase-inhibiting compounds
may include the following: numbness, tingling sensations,
incoordination, headache, dizziness, tremor, nausea,
abdominal cramps, sweating, blurred vision, difficulty
breathing or respiratory depression, and slow heartbeat.
Very high doses may result in unconsciousness,
incontinence, and convulsions or fatality. In humans,
symptoms of poisoning have appeared within as little as
15 minutes to 2 hours after exposure to mevinphos, but
onset of symptoms has been delayed for as long as 2 days
[2]. Several children were made ill by unknowingly
wearing clothing which had been contaminated with
mevinphos. Cholinesterase inhibition resulting from acute
exposure is reversible, but it can persist for 2 to 6
weeks.
- Chronic toxicity: The lowest oral dose
of mevinphos that produced toxic effects (peripheral
nervous system effects) in humans was 690 ug/kg when it
was given intermittently over 28 days [2,8]. Repeated
low-level exposure to mevinphos may cause similar effects
to those observed with acute exposures [2,8]. Severe
symptoms of cholinesterase-inhibition may be produced in
a previously exposed person, whereas symptoms of
cholinesterase-inhibition may not occur in someone who
has not been previously exposed to mevinphos [2,8]. In a
2-year feeding study with rats, no observable effects
occurred at 0.025 mg/kg/day. A similar result was found
in a 2-year feeding study with dogs [8]. No effects on
general health and no poisoning symptoms were seen in a
2-year study with rats fed 4 mg/kg/day, nor in dogs given
dietary doses of 5 mg/kg/day [8]. However, rats were
killed by doses of 20 mg/kg/day mevinphos in their diets
for 13 weeks. Dietary doses of 10 mg/kg/day for 14 weeks
were lethal for dogs [8]. Rats given dietary doses of 10
or 20 mg/kg/day for 13 weeks exhibited degeneration of
the liver, kidneys and cells lining the salivary, tear,
and other glands [13].
- Reproductive effects: In a
three-generation reproduction study with rats, there were
no reproductive effects at 1.2 mg/kg/day [85], indicating
that mevinphos is unlikely to cause reproductive
toxicity.
- Teratogenic effects: No teratogenic
effects were seen in rabbits given doses of 1.0 mg/kg/day
[85], suggesting that this pesticide is not teratogenic.
- Mutagenic effects: No data are currently
available.
- Carcinogenic effects: A 2-year study
with rats fed dietary doses of up to 0.75 mg/kg/day
mevinphos produced no evidence of tumor formation [85].
This evidence suggests that mevinphos is not
carcinogenic.
- Organ toxicity: Target organs affected
by mevinphos include the nervous system, liver, kidneys,
and cells lining the salivary, tear, and other glands.
- Fate in humans and animals: Mevinphos is
rapidly degraded by the liver. Samples taken by autopsy
from a man who had died within 45 minutes of drinking
mevinphos showed the following bodily concentrations of
the compound: 3400 ppm in the stomach wall, 360 ppm in
blood, 240 ppm in the liver, 86 ppm in skeletal muscle,
20 ppm in the kidneys, 8 ppm in urine, and 3 ppm in the
brain [2,8]. In a case of moderate poisoning associated
with occupational exposure to mevinphos, the
concentration of metabolites of mevinphos in the urine
collected during the first 12 hours after onset of
symptoms was 0.4 ppm. The concentration declined rapidly
until 36 hours after onset, and excretion was nearly
complete within 50 hours [2].
Ecological Effects:
- Effects on birds: Mevinphos is highly
toxic to birds. The acute symptoms of mevinphos poisoning
in birds include lack of muscle coordination, curled
toes, salivation, diarrhea, trembling, and wing beating.
Pheasant deaths all occurred 8 to 18 minutes after
treatment; deaths of mallards and grouse occurred 5 to 40
minutes post-treatment [26]. The oral LD50 for mevinphos
is 7.52 mg/kg in chickens, 3 mg/kg in wild bird species,
4.63 mg/kg in female mallards, 1.37 mg/kg in male
pheasants, and 0.75 to 1.50 mg/kg in male grouse. Its
dermal LD50 in ducks is 11 mg/kg [41].
- Effects on aquatic organisms: Mevinphos
is very highly toxic to fish. The 96-hour LC50 for
technical mevinphos is 0.012 mg/L in rainbow trout, and
0.022 mg/L in bluegill sunfish [13]. The 48-hour LC50 for
mevinphos is 0.017 mg/L in rainbow trout; the 24-hour
LC50 is 0.034 mg/L in rainbow trout, 0.041 mg/L in
bluegills, and 0.8 mg/L in mosquito fish [27].
- Effects on other organisms: Mevinphos is
highly toxic to bees, especially when they are exposed to
direct treatment or residues on crops [30].
Environmental Fate:
- Breakdown in soil and groundwater:
Mevinphos is of low persistence in the soil environment,
with reported half-lives of 2 to 3 days [19]. One study
indicated that this material lost its insecticidal
capability in 2 to 4 weeks [85]. It is poorly adsorbed to
soil particles, and thus may be mobile [19]. Its capacity
to contaminate groundwater may be limited by its short
half-life. No harmful effects to soil microorganisms have
been observed from applications of mevinphos formulations
[86].
- Breakdown in water: Mevinphos dissolves
and is readily broken down by water (hydrolyzed), losing
its insecticidal activity within 2 to 4 weeks [31]. In
aqueous solution, mevinphos is hydrolyzed with half-lives
of 1.4 hours at pH 11, 3 days at pH 9, 35 days at pH 7,
and 120 days at pH 6 [8].
- Breakdown in vegetation: When mevinphos
is used as directed, it is not phytotoxic (toxic to
plants). Plants rapidly degrade it to less toxic products
[13]. However, some crops may be sensitive to solvents in
which the active ingredient is formulated, as well as to
excessive dosages [86].
Physical Properties:
- Appearance: Pure mevinphos is a
colorless liquid; technical grade mevinphos is a pale
yellow liquid that has a very mild odor or is odorless
[13].
- Chemical Name:
2-methoxycarbonyl-1-methylvinyl dimethyl phosphate [13]
- CAS Number: 7786-34-7
- Molecular Weight: 224.15
- Water Solubility: >10 mg/L [13];
completely miscible with H2O
- Solubility in Other Solvents: Technical
mevinphos is v.s. in alcohols, ketones, chlorinated
hydrocarbons, aromatic hydrocarbons and most organic
solvents; s.s in aliphatic hydrocarbons and petroleum
ether [13]
- Melting Point: 21 C (E-isomer); 6.9 C
(Z-isomer) [13]
- Vapor Pressure: 17 mPa @ 20 C [13]
- Partition Coefficient: Not Available
- Adsorption Coefficient: 44 [19]
Exposure Guidelines:
- ADI: 0.0015 mg/kg/day [38]
- MCL: Not Available
- RfD: Not Available
- PEL: Not Available
- HA: Not Available
- TLV: 0.092 mg/m3 (8-hour) [47]
Basic Manufacturer:
Amvac Chemical Corp.
4100 E. Washington Blvd.
Los Angeles, CA 90023
- Phone: 213-264-3910
- Emergency: 800-228-5635, ext. 169
References:
References for the information in this PIP can be found in
Reference List Number 5
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.