Iprodione

Iprodione
Names
IUPAC name
3-(3,5-Dichlorophenyl)-N-isopropyl-2,4-dioxoimidazolidine-1-carboxamide
Other names
Glycophene
Promidione
Identifiers
36734-19-7 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:28909 YesY
ChemSpider 34418 YesY
ECHA InfoCard 100.048.328
KEGG C11208 YesY
PubChem 37517
Properties
C13H13Cl2N3O3
Molar mass 330.16662
Appearance White powder
Melting point 133.4 °C (272.1 °F; 406.5 K)
Boiling point 164.5 °C (328.1 °F; 437.6 K) (decomposes)
12.2 mg/L at 20 °C [1]
Solubility in toluene: 147 g/L; in octanol: 10 g/L
Solubility in acetone 342 g/L
Solubility in hexane 0.59 g/L
Solubility in acetonitrile 168 g/L
Solubility in dichloromethane 450 g/L
Solubility in ethyl acetate 225 g/L
Hazards
Main hazards Limited evidence of carcinogenic effect
R-phrases R40, R50/53
S-phrases S35, S36/37
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Iprodione is a hydantoin fungicide and nematicide.

Application

Iprodion is used on crops affected by Botrytis bunch rot, Brown rot, Sclerotinia and other fungal diseases in plants. It is currently applied in a variety of crops: fruit, vegetables, ornamental trees and scrubs and on lawns. It is a contact fungicide that inhibits the germination of fungal spores and it blocks the growth of the fungal mycelium.

It has been marketed under the brand name "Rovral" and "Chipco green" (both brands of Bayer CropScience). This chemical was developed originally by Rhône-Poulenc Agrochimie (later Aventis CropScience and in 2002 acquired by Bayer). As of 2004 there were no composition patents on iprodione.[1]

DevGen discovered that iprodione kills nematodes and filed for patent protection for those uses.[2] Iprodione was approved in the Turkish market under the brandname Devguard for use on tomatoes and cucumbers in 2009,[3] was approved in Europe in 2010,[4] and was approved in the US as Enclosure for use in commercial peanut production in May 2010.[5]

References

This article is issued from Wikipedia - version of the 8/24/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.