|                                ACETAMIPRID IDENTIFICATION  Common name: Acetamiprid  Other name: Acetamiprid (pa ISO)  Iupac name: (E)-N1-[(6-chloro-3-pyridyl)methyl]-N2-cyano- N1-methylacetamidine  Chemical abstracts name:(E)-N-[(6-chloro-3-pyridyl)methyl]-N′-cyano- N-methylacetamidine  Type:Insecticide for Agriculture  CAS RN:[135410-20-7]    M.F.: C10H11ClN4 S.F.:        Mol Wt:222.7   PHYSICAL CHEMISTRY Form (appearance):       Colourless crystals  M.P.:98.9℃  V.P.:<1×10-3 mPa (25℃) S.G.:1.330 (20℃) Solubility.:   In water 4250 mg/l (25℃). Soluble in acetone, methanol, ethanol, dichloromethane, chloroform, acetonitrile and tetrahydrofuran Stability:   Stable in buffered solutions at pH 4,5,7. Degraded slowly at pH 9 and 45℃. Stable under sunlight Henry:< 5.3×10-8 Pa m3 mol-1(calc) KowlogP:0.80 (25℃)    APPLICATIONFormulation types:FU;GR;EC;WP  Biochemistry:    Agonist of the nicotinic acetylcholine receptor, affecting the synapses in the insect central nervous system  Mode of action:Systemic insecticide with translaminar activity and with contact and stomach action  Uses:Control of Hemiptera, especially aphids, Thysanoptera and Lepidoptera, by soil and foliar application, on a wide range of crops, especially vegetables, fruit and tea. Applied at 75-300 g/ha on vegetables, 100-700 g/ha in orchards   MAMMALIAN TOXICOLOGYOral:Acute oral LD50 for male rats 217, female rats 146, mate mice 198, female mice 184 mg/kg. Skin and eye: Acute percutaneous LD50for male and female rats >2000 mg/kg. Non-irritating to skin and eyes (rabbits); not a skin sensitiser (guinea pigs).  Inhalation:LC50 (4 h) for male and female rats >0.29 mg/l.  Noel:(2 y) for rats 7.1 mg/kg b.w.; (18 mo) for mice 20.3 mg/kg b.w.; (1 y) for dogs 20 mg/kg b.w.  /Other Negative in the Ames test.    ECOTOXICOLOGYBirds:LD50for bobwhite quail 180 mg/k8. LC50 for bobwhite quail >5000 ppm.  Fish:LC50 (24-96 h) for carp >100 mg/l.  Daphnia:LC50 (24 h) >200 mg/l.  Algae:EC50 (72 h) >98.3 mg/l; NOEC (72 h) 98.3 mg/l.    ENVIRONMENTAL FATEPlant:Slowly degraded on or in plants, forming five identified metabolites (H. Saito et al., Proc. 9th IUPAC Intl Congr: Pestic. Chem., London, 1998, 2, 5A-010).  Soil/Environment:DT50 in clay loam 1 d; in light clay 1-2 d. DT50for total residues 15-30 d.          |