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Iprodione----------Your Best Choice! Handling Chemicals Ltd.

   
Common Name Iprodione
Chemical Name 3-(3,5-dichlorophenyl)-N-(1-methylethyl)- 2,4-dioxo-1-imidazolidinecarboxamide (CAS)
CAS Number 36734-19-7
Molecular formula C13H13Cl2N3O3
ACTION Contact/locally systemic fungicide.
Structural formula
Description

Appearance: white crystal or powder.
Melting Point:136°C
Vapour Pressure: 0.133 mPa at 25°C.
Stability: Stable in water 13 mg/L at 25°C, soluble in acetone 300 g/l, benzene 200 g/l. Oral LD 50 (Rat)>3,500 mg/kg. Dermal LD 50 (Rabbit) >2,500 mg/kg. Inhatation LC 50 : (1 h.) 0.52 mg/l; (4 h.) 3.3 mg/l.

Specification

Iprodione 95%TC, 97%TC, 50%WP, 25%, 50%SC

 
50WP
95TECH
Contents, %
50.0min
95.0min
Moisture, %
3.0 max
0.8 max
PH value
6.0-8.0
6.0-8.0
Suspensibility, %
80.0 min
-
Fineness(through 44m screen)
99.0 min
-
Non-soluble component in water
-
0.8 max
Wetting time, S
90.0 max
-
Usage Active on a broad spectrum of diseases, Alternaria, Botrytis, Fusarium, Helminthosporium, Monilinia, Rhizoctonia, Sclerotinia, Septoria, etc. Developed in many countries on vine, table grapes, top fruit, stone fruit, almonds, berries, vegetables, ornamentals, flowers, turf, potatoes, oilseed rape, cereals, seed treatment of cereals and vegetables; crops like sugar beets, sunflower, rapeseed, and rice.
Package In 25kg zincified iron or wooden drum with inner plastic bag or packed as required.
Remark  

Note: other sizes and packing available upon request

PHYSICAL CHEMISTRY Iprodione

Composition Tech. is 3 96% pure. Mol. wt. 330.2 M.f. C 13 H 13 Cl 2 N 3 O 3 Form White, odourless, non-hygroscopic crystals or powder. M.p. 134 oC; (tech., 128-128.5 oC) V.p. 5 ' 10 -4 mPa (25 oC) K OW logP = 3.0 (pH 3 and 5) S.g./density 1.00 (20 oC); (tech., 1.434-1.435) Solubility In water 13 mg/l (20 oC). In n -octanol 10, acetonitrile 168, toluene 150, ethyl acetate 225, acetone 342, dichloromethane 450, hexane 0.59 (all in g/l, 20 oC). Stability Relatively stable in acid media, but decomposed in alkaline media. DT 50 1-7 d (pH 7), <1 h (pH 9). Aqueous solutions are degraded by u.v. light, but are relatively stable in simulated sunlight.

APPLICATIONS Iprodione

Mode of action Contact fungicide with protective and curative action. Inhibits germination of spores and growth of fungal mycelium. Uses Control of Botrytis , Monilia , Sclerotinia , Alternaria , Corticium , Fusarium , Helminthosporium , Phoma , Rhizoctonia , Typhula spp., etc. Used mainly on sunflowers, cereals, fruit trees, berry fruit, oilseed rape, rice, cotton, vegetables, and vines as a foliar spray, at 0.5-1.0 kg a.i./ha, and on turf, at 3-12 kg/ha. Can also be used as a post-harvest dip, as a seed treatment, or as a dip or spray at planting. Formulation types DP; EC; FS; SC; SU; WG; WP.

ANALYSIS Iprodione

Product analysis by hplc or glc ( CIPAC Handbook, 1995, G , 98-104; L. Lacroix et al., Anal. Methods Pestic. Plant Growth Regul., 1980, 11, 247). Residues determined by glc with ECD ( idem, ibid. ; Man. Pestic. Residue Anal., 1987, I, 6, S8, S19; Anal. Methods Residues Pestic., 1988, Part I, M1, M12).

MAMMALIAN TOXICOLOGY Iprodione

Reviews FAO/WHO 74, 76 (see part 2 of the Bibliography). Oral Acute oral LD 50 for rats and mice >2000 mg/kg. Skin and eye Acute percutaneous LD 50 for rats and rabbits >2000 mg/kg. Non-irritating to skin and eyes (rabbits). Inhalation LC 50 (4 h) for rats >5.16 mg/l air. NOEL (2 y) for rats 150 mg/kg diet; (1 y) for dogs 18 mg/kg b.w. ADI (JMPR) 0.06 mg/kg b.w. [1995]. Toxicity class WHO (a.i.) III (Table 5); EPA (formulation) IV

ECOTOXICOLOGY Iprodione

Birds Acute oral LD 50 for bobwhite quail >2000, mallard ducks >10 400 mg/kg. Fish LC 50 (96 h) for rainbow trout 4.1, bluegill sunfish 3.7 mg/l. Daphnia LC 50 (48 h) 0.25 mg/l. Algae EC 50 (120 h) for Selenastrum capricornutum 1.9 mg/l. Bees Contact LD 50 >0.4 mg/bee. Worms LC 50 for earthworms >1000 mg/kg soil. Other beneficial spp. Harmless.

ENVIRONMENTAL FATE Iprodione

Animals In rats, ruminants and birds, iprodione is rapidly eliminated. It also undergoes extensive metabolism, by hydrolysis and rearrangement reactions. Plants Metabolism studies in cereals, fruit, leafy and oily crops showed that iprodione is the dominant component of the total residue resulting from foliar application. Soil/Environment Rapidly metabolised in soil, with formation of CO 2 . DT 50 (lab.) 20-80 d; (field) 20-160 d. K oc 373 to 1551. Rate of degradation increases with successive treatments, hence accumulation does not occur.


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