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Iprodione

Iprodione Structure
CAS No.
36734-19-7
Chemical Name:
Iprodione
Synonyms
IPRODION;3-(3,5-dichlorophenyl)-1-iso-propylcarbamoylhydantion;3-(3,5-Dichlorophenyl)-N-(1-methylethyl)-2,4-dioxo-1-imidazolidinecarboxamide;KIDAN;ROVER;anfor;rovrol;ROVRAL;330.16;fa2071
CBNumber:
CB7131064
Molecular Formula:
C13H13Cl2N3O3
Molecular Weight:
330.17
MOL File:
36734-19-7.mol
MSDS File:
SDS
Modify Date:
2024/7/24 17:31:20

Iprodione Properties

Melting point 130-134 °C(lit.)
Density 1.6223 (rough estimate)
vapor pressure 5 x 10-7 Pa (25 °C)
refractive index 1.6140 (estimate)
Flash point 2 °C
storage temp. Sealed in dry,Room Temperature
solubility DMSO: 100 mg/mL (302.87 mM)
form Solid
pka 9.19±0.20(Predicted)
color White to off-white
Water Solubility 0.0013 g/100 mL
Merck 13,5096
BRN 895003
LogP 3.000
CAS DataBase Reference 36734-19-7(CAS DataBase Reference)
NIST Chemistry Reference Iprodione(36734-19-7)
EPA Substance Registry System Iprodione (36734-19-7)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS08,GHS09
Signal word  Warning
Hazard statements  H351-H410
Precautionary statements  P202-P273-P280-P308+P313-P391-P405
Hazard Codes  Xn,N,F
Risk Statements  40-50/53-36-20/21/22-11
Safety Statements  36/37-60-61-36-26-16
RIDADR  UN 3077 9/PG 3
WGK Germany  3
RTECS  NI8870000
HS Code  29332900
Toxicity LD50 in mice, rats (g/kg): 4, 3.5 orally (Lacroix, 1980)

Iprodione price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 559792 [3-(3,5-Dichlorophenyl)-2,4-dioxoimidazolidinyl]-N-(methylethyl)carboxamide 97% 36734-19-7 25G ₹31479.1 2022-06-14 Buy
Sigma-Aldrich(India) 36132 Iprodione PESTANAL?, analytical standard 36734-19-7 100MG ₹6051.18 2022-06-14 Buy
Product number Packaging Price Buy
559792 25G ₹31479.1 Buy
36132 100MG ₹6051.18 Buy

Iprodione Chemical Properties,Uses,Production

Uses

Iprodione is a non-systemic fungicide that exhibits both protectant and eradicant activities against the spores and mycelium of a number of parasitic fungi. It is effective against Alternaria, Botrytis, Corticium, Fusarium, Helminthosporium, Monilinia, Phoma, Pleiochaeta, Rhizoctonia and Sclerotinia, etc. in nut crops, fruit trees (stone and pome fruit), vines, berries, vegetables, cereals, oilseed rape, cotton and ornamentals. Iprodione also controls various summer and winter turf diseases.

Definition

ChEBI: An imidazolidine-2,4-dione in which the nitrogen at position 1 is substituted by an N-(isopropyl)carboxamide group while that at position 3 is substituted by a 3,5-dichlorophenyl group. A contact fungicide, it blocks the growth of the fu gal mycelium and inhibits the germination of fungal spores. It is used on fruit and vegetable crops affected by various fungal diseases. It is also used as a nematicide.

Production Methods

The synthesis uses 3,5-dichloroaniline which is coupled with glycine and phosgene. The urea substructure is formed by reaction with isopropylamine and phosgene. Many fungicide mixtures with Iprodione are on the market.

Safety Profile

Moderately toxic by ingestion. When heated to decomposition it emits very toxic fumes of NOx and Cl-.

Environmental Fate

Soil. Readily degrades in soil (half-life 20 to 160 days) releasing carbon dioxide 3,5dichloroaniline (Walker, 1987) and (Hartley and Kidd, 1987; Worthing and Hance, 1991). The rate of degradation increases with repeated applications of this fungicide. In a clay loam, the half-life was 1 week. After the second and third applications, the half-lives were 5 and 2 days, respectively (Walker et al., 1986).
Plant. Translocation and uptake by potato plants were reported (Cayley and Hide, 1980). Iprodione is rapidly metabolized in plants to 3,5-dichloroaniline (Cayley and Hide, 1980; Hartley and Kidd, 1987).
Chemical/Physical. In an aqueous solution at pH 8.7, iprodione hydrolyzed to N-(3,5dichloroanilinocarbonyl)-N-(isopropylaminocarbonyl)glycine (Belafdal et al., 1986). At pH 8.7, complete hydrolysis occurred after 14 hours (Cayley and Hide, 1980).
Gomez et al. (1982) studied the pyrolysis of iprodione in an helium atmosphere at 400–1,000°C. Decomposition began at 300°C producing isopropyl isocyanate and 3-(3,5dichlorophenyl)hydantoin. Above 600°C, the hydantoin ring began to decompose forming the following products: 3-chloroaniline, 3,5-dichloroaniline, chlorinated benzenes and benzonitrile. From 800 to 1,000°C, the hydantoin ring was completed destroyed whichled to the formation of aryl isocyanates, anilines and the corresponding diarylureas, namely 3-(3,5-dichlorophenyl)urea and 1-(3-chlorophenyl)-3-(3,5-dichlorophenyl)urea (Gomez et al., 1982).

Metabolic pathway

The opening and rearrangement of the dioxoimidazolidine ring is the initial and major degradation/metabolic reaction for iprodione. Iprodione degrades in soil via cleavage of the dioxoimidazolidine-carboxamide linkage, followed by ring opening to yield 3,5-dichloroaniline and CO2. In plants and animals, primary degradation reactions include N-dealkylation of the isopropyl moiety, ring opening and aryl hydroxylation (Scheme 1).

Iprodione Preparation Products And Raw materials

Global( 266)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
Pharma Affiliates 172-5066494 Haryana, India 6761 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
Qingdao Trust Agri Chemical Co.,Ltd +8613573296305 China 267 58 Inquiry
Henan Bao Enluo International TradeCo.,LTD +86-17331933971 +86-17331933971 China 2503 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21669 55 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29897 58 Inquiry
Xiamen AmoyChem Co., Ltd +86-592-6051114 +8618959220845 China 6387 58 Inquiry
Chongqing Chemdad Co., Ltd +86-023-6139-8061 +86-86-13650506873 China 39916 58 Inquiry
CONIER CHEM AND PHARMA LIMITED +8618523575427 China 49391 58 Inquiry
3-(3,5-dichlorophenyl)-N-iso-propyl-2,4-dioxo-1-imidazoline carboxamide [3-(3,5-Dichlorophenyl)-2,4-dioxoiMidazolidinyl]-N-(Methylethyl)carboxaMide standard solution 3-(3,5-Dichlorophenyl)-n-Isopropyl-2,4-dioxo-1-Imidazolidinecarboximide Iprodione 100mg [36734-19-7] [3-(3,5-Dichlorophenyl)-2,4-dioxoimidazolidinyl]-N-(methylethyl)carboxamide,Iprodione rop500f Roval dust Roval flo Roval green Roval WP Rovral flo rovrol Rp 26019 rp26019 Turbair roval [3-(3,5-Dichlorophenyl)-2,5-dioxoiMidazolidinyl]-N-(Methylethyl)carboxaMide standard solution IPRODIONE METABOLITE IPRODIONE GLYCOPHENE CHIPCO 26019 KIDAN LABOTEST-BB LT00134860 1-ISO-PROPYLCARBAMOYL-3-(3,5-DICHLOROPHENYL)HYDANTOIN [3-(3,5-DICHLOROPHENYL)-2,4-DIOXOIMIDAZOLIDINYL]-N-(METHYLETHYL)CARBOXAMIDE PROTURF ROVER ROVRAL ROVRAL(R) VERISAN ’rovral’hn 1-Imidazolidinecarboxamide, 3-(3,5-dichlorophenyl)-N-(1-methylethyl)-2,4-dioxo- 1-Imidazolidinecarboxamide,3-(3,5-dichlorophenyl)-N-(1-methylethyl)-2,4-dioxo- 26019rp 3-(3,5-dichlorophenyl)hydantoin-1-carboxylicacidisopropylamide 3-(3,5-dichlorophenyl)-n-(1-methylethyl)-2,4-dioxo-1-imidazolidinecarboxamid 3-(3,5-dichlorophenyl)-n-(1-methylethyl)-2,4-dioxo-1-imidazolinecarboxamide 3-(3,5-Dichlorophenyl)-N-isopropyl-2,4-dioxo-1-imidazolidinecarboxamide 3-(3,5-dichlorophenyl)-n-isopropyl-2,4-dioxo-1-imidazolidinecarboximide(acn) 3-(3,5-dichlorophenyl)-n-isopropyl-2,4-dioxoimidazolidine-1-carboxamide 330.16 anfor c13-h13-cl2-n3-o3 CDA roval FA 2071 fa2071 Glycophen Iprodial lea2043 Lfa 2043 lfa2043 MRC 910 mrc910 NRC 910 nrc910 prodione Promidione ROP 500 F VIROVAL