Names | |
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IUPAC name
3-(3,5-Dichlorophenyl)-N-isopropyl-2,4-dioxoimidazolidine-1-carboxamide
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Other names
Glycophene
Promidione |
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Identifiers | |
3D model (Jmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.048.328 |
KEGG | |
PubChem CID
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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 | |
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R-phrases (outdated) | R40, R50/53 |
S-phrases (outdated) | S35, S36/37 |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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what is ?) | (|
Infobox references | |
Iprodione is a hydantoin fungicide and nematicide.
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.
DevGen discovered that iprodione kills nematodes and filed for patent protection for those uses. Iprodione was approved in the Turkish market under the brandname Devguard for use on tomatoes and cucumbers in 2009, was approved in Europe in 2010, and was approved in the US as Enclosure for use in commercial peanut production in May 2010.