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Pesticides >> Insecticides>> Fenbutatin Oxide

Fenbutatin Oxide 55%SC


Fenbutatin Oxide

Common name Fenbutatin Oxide (BSI, E-ISO, JMAF); fenbutatin-oxyde ((m) F-ISO)
IUPAC name bis[tris(2-methyl-2-phenylpropyl)tin] oxide
Chemical Abstracts name hexakis(2-methyl-2-phenylpropyl)distannoxane
Other names hexakis CAS RN [13356-08-6] EEC no. 236-407-7 Development codes SD 14 114 (Shell) Official codes ENT 27 738

Fenbutatin Oxide APPLICATIONS
Mode of action Non-systemic acaricide with contact and stomach action. Uses Control of all motile stages of a wide range of phytophagous mites on pome fruit, stone fruit, citrus fruit, soft fruit, vines, bananas, cucurbits, ornamentals, and glasshouse crops. Gives long residual control. Phytotoxicity Phytotoxic to tangerines, tangelos, and some varieties of grapefruit. Otherwise, non-phytotoxic when used as directed. Formulation types SC; WP. Selected tradenames: 'Osadan' (Japan only) (BASF); 'Torque' (BASF); 'Vendex' (Du Pont, BASF)

'Torq' (Fargro) mixtures: 'Mitedown' (+ polynactins) (Eikou Kasei)

Product analysis by potentiometric non-aqueous titrimetry (CIPAC Handbook, 1988, D, 77). Residues determined by glc with ECD or FPD of suitable derivative (Anal. Methods Pestic. Plant Growth Regul., 1978, 10, 139; Methodensammlung Rückstandsanal. Pflanzenschutzmitteln, 1987, S24; M. Sano et al., J. Assoc. Off. Anal. Chem., 1979. 62, 764). Details available from BASF.

Reviews FAO/WHO 65, 67 (see part 2 of the Bibliography). Oral Acute oral LD50 for rats 2631, mice 1450, dogs >1500 mg/kg. Skin and eye Acute percutaneous LD50 for rabbits >2000, rats >1000 mg/kg. Irritating to skin and severely irritating to eyes. Inhalation LC50 0.23 mg a.i. (as dust)/l. NOEL (2 y) for rats 100 mg/kg diet, for dogs 15 mg/kg daily. ADI (JMPR) 0.03 mg/kg b.w. [1992]. Toxicity class WHO (a.i.) III (Table 5); EPA (formulation) III EC hazard T+; R26| Xi; R36/38| N; R50, R53

Birds Dietary LC50 (8 d) for bobwhite quail 5065 mg/kg diet. Fish LC50 (48 h) for rainbow trout 0.27 mg a.i./l (as WP formulation). Daphnia LC50 (24 h) 0.05-0.08 mg/l. Bees Acute oral LD50 >0.1 mg/bee. Other beneficial spp. No adverse effects to a wide range of predatory and parasitic arthropods.

Soil/Environment In soil, it is metabolised to dihydroxy-bis(2-methyl-2-phenylpropyl)stannane and 2-methyl-2-phenylpropyl stannonic acid, presumably ultimately forming tin oxide/hydroxide. In tests in commercial use, there was minimal movement of Fenbutatin Oxide or its metabolites out of the top 30 cm of soil (A. Gray et al., Pestic. Sci., 43, 295-302 (1995))

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