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Dinotefuran is a new furanicotinyl insecticide
which represents the third generation of neonicotinoid group. Dinotefuran,
which was developed by Mitsui Chemicals, Inc., was registered in
Japan April 24, 2002 and the registration has been submitted to
the Environment Protection Agency (EPA) in the USA. Dinotefuran
was granted Organophosphorus Alternative and Reduced Risk Status
by the EPA.
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Physical & Chemicals Properties
Code: MTI-446
Common Name: Dinotefuran (ISO name)
Chemical Name: (RS)-1-methyl-2-nitro-3-(tetrahydro-3-furylmethyl)
guanidine
Chemical Structure: 
Melting Point: 107.5° C
Water Solubility: 39.83 g/ |
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Toxicology
Acute Toxicity for Mammalian (Technical)
| Oral (Rat, Mouse) |
LD50 |
≥2,000 mg/kg |
| Dermal (Rat) |
LD50 |
>2,000 mg/kg |
Avian & Aquatic Toxicity
(Technical)
| Japanese quail |
LD50 |
≥2,000 mg/kg |
| Mallard duck |
LD50 |
>997.9 mg/kg/day |
| Carp |
LD50 (96hr) |
>1,000 ppm |
| Daphnia |
LD50 (48hr) |
>1,000 ppm |
Skin Irritation (Technical)
Slightly Irritating
Long Term Health Effects (Technical)
Dinotefuran is not a mutagen, neurotoxin
or reproductive toxin.
Ecological Effect
Dinotefuran is highly toxic to honeybees
and silkworms.
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Environmental Fate (Half-lives)
| Hydrolysis |
Stable |
| Photolysis on Soil |
46 days |
| Aerobic Soil Metabolism |
52 days |
| Field Dissipation |
22 to 68 days |
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Mode of Action
Dinotefuran acts through contact and ingestion and results
in the cessation of feeding within several hours of contact
and death shortly after. Dinotefuran does not inhibit cholinesterase
or interfere with sodium channels. Therefore, its mode of
action is different from those of organophosphate, carbamate,
and pyrethroid compounds. It appears that Dinotefuran acts
as an agonist of insect nicotinic acetylcholine receptors,
but it is postulated that Dinotefuran affects the nicotinic
acetylcholine binding in a mode that differs from other neonicotinoid
insecticides. It is reported that Dinotefuran was highly active
on a certain silverleaf whitefly strain which developed resistance
against imidacloprid.
(larger view)
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Application Method


The information contained in this website
is, to the best of our knowledge, accurate and reliable, but
all suggestions are made without warranty, either express
or implied. The values relevant to properties or the like
of the product stated herein were obtained using field test
specimens prepared at official organizations in some countries
and are not assumed to be identical to values obtained on
the finished product manufactured by our customers and on
our finished product tested by our customers in a different
condition. Nothing herein shall be construed as permission
or as recommendation for uses which infringe valid patents
or as extending a license under valid patents. Because the
conditions and methods of use on the part of our customers
are beyond our control, Mitsui Chemicals, Inc. disclaims any
liability incurred in connection with the use of our products. |
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