2013 Biological Insecticide Dinotefuran 20%Sc

Specifications
1 formulation 95%TC 20%WP
2 ISO 9001 FAO standard
3 strong product with best quality and competitive price
4 professional Manufacturer
HOT! ! OUR STRONG PRODUCT. ISO 9001
All kinds of specification: 95%TC 20%WP
All kinds of packing: 100ml, 500ml, 1lt, 5lts, 25kgs, 50kgs, 200kgs.
Common Name: Dinotefuran (ISO name)
Chemical Name: (RS)-1-methyl-2-nitro-3-(tetrahydro-3-furylmethyl) guanidine
Melting Point: 107.5° C
Water Solubility: 39.83 g/
Skin Irritation (Technical)
Slightly Irritating
Long Term Health Effects (Technical)
Dinotefuran is not a mutagen, neurotoxin or reproductive toxin.
Control of insect pests such as aphids, whiteflies, thrips, leafhoppers, leafminers, sawflies, mole cricket, white grubs lacebugs,
Ecological Effect
Dinotefuran is highly toxic to honeybees and silkworms.
Dinotefuran is a quick-kill insecticide discovered by researchers at Mitsui Chemicals. A third generation neonicotinoid, dinotefuran was synthesized with acetycholine as the lead compound, making it different from other flea control products currently in use which are
In addition, dinotefuran does not bind to the same insect receptor sites in the nerve synapse as imidacloprid and other neonicotinoids. The binding is permanent causing continuous nerve stimulation and death of the insect. Ingestion is not necessary. Dinotefuran kills by contact.
NOMENCLATURE
Common name dinotefuran (BSI; Pa ISO)
IUPAC name (RS)-1-methyl-2-nitro-3-(tetrahydro-3-furylmethyl)guanidine
Chemical Abstracts name N-methyl-N'-nitro-N''-[(tetrahydro-3-furanyl)methyl]guanidine
CAS RN [165252-70-0] Development codes MTI-446 (Mitsui)
PHYSICAL CHEMISTRY
Mol. Wt. 202.2 M. F. C7H14N4O3 M. P. 94.5-101.5 ° C KOW logP = -0.644 (pH 7) S. G. /density 1.33 Solubility In purified water 54.3? . 3 g/l (20 ° C). PKa No dissociation in range pH 1.4 to 12.3
APPLICATIONS
Biochemistry Agonist of the nicotinic acetylcholine receptor, affecting the synapses in the insect central nervous system. Mode of action Active by ingestion and by contact; Also exhibits root-systemic activity. Uses Controls a range of hemipterous and other pests, at 100-200 g/ha.
MAMMALIAN TOXICOLOGY
Oral Acute oral LD50 for male rats 2804, female rats 2000, male mice 2450, female mice 2275 mg/kg. Skin and eye Acute percutaneous LD50 for male and female rats >2000 mg/kg. Not a skin sensitiser (guinea pigs).
ECOTOXICOLOGY
Birds Acute oral LD50 for mallard ducks 1000, Japanese quail >2000 mg/kg. Fish LC50 (96 h) for carp >1000 ppm; (48 h) for rainbow trout >40 ppm. Daphnia (48 h) 1000 ppm Other aquatic spp. LC50 (48 h) for crayfish 5-10 ppm.