Iprodione

Base Information

• Chemical Name: Iprodione
• CAS No.: 36734-19-7
• Deprecated CAS: 61840-50-4
• Molecular Formula: C13H13Cl2N3O3
• Molecular Weight: 330.171
• Hs Code.: 29332900
• European Community (EC) Number: 253-178-9
• UNII: S3AYV2A6EU
• DSSTox Substance ID: DTXSID3024154
• Nikkaji Number: J3.500I
• Wikipedia: Iprodione
• Wikidata: Q411542
• Metabolomics Workbench ID: 45107
• ChEMBL ID: CHEMBL1862887
• Mol file: 36734-19-7.mol

Synonyms:1-isopropylcarbamoyl-3-(3,5-dichlorophenyl)hydantoin;glycophen anphor;IPCDPH;iprodione;Rovral;Rovrol

Chemical Property of Iprodione

Chemical Property:

• Appearance/Colour: Colorless, odorless crystal
• Vapor Pressure: 5 x 10-7 Pa (25 °C)
• Melting Point: 130-134 °C(lit.)
• Refractive Index: 1.575
• PKA: 9.19±0.20(Predicted)
• Flash Point: 2 °C
• PSA: 69.72000
• Density: 1.464 g/cm³
• LogP: 3.27380
• Storage Temp.: APPROX 4°C
• Water Solubility.: 0.0013 g/100 mL
• XLogP3: 3.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 329.0333967
• Heavy Atom Count: 21
• Complexity: 448

Purity/Quality:

99.9% ^*data from raw suppliers

Iprodione ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn,N,F
• Hazard Codes: Xn,N,F
• Statements: 40-50/53-36-20/21/22-11
• Safety Statements: 36/37-60-61-36-26-16

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Fungicides
• Canonical SMILES: CC(C)NC(=O)N1CC(=O)N(C1=O)C2=CC(=CC(=C2)Cl)Cl
• Uses: Fungicide. 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.

Technology Process of Iprodione

There total 5 articles about Iprodione which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 92.3%

3-(3',5'-Dichlorophenyl)imidazolidine-2,4-dione (27387-87-7) + Isopropyl isocyanate (1795-48-8) → Iprodione (36734-19-7,61840-50-4)

Guidance literature:

In water;

Reference yield: 92.0%

→ Iprodione (36734-19-7,61840-50-4)

Guidance literature:

Reference yield: 91.0%

3-(3,5-dichloro-phenyl)-ureidoacetic acid (62584-33-2) + Isopropyl isocyanate (1795-48-8) → Iprodione (36734-19-7,61840-50-4)

Guidance literature:

With hydrogenchloride; triethylamine; In chlorobenzene;

upstream raw materials:

3-(isopropylcarbamoyl)-5-(3,5-dichlorophenyl)hydantoic acid

3-(3,5-dichloro-phenyl)-ureidoacetic acid

Isopropyl isocyanate

3-(3',5'-Dichlorophenyl)imidazolidine-2,4-dione

Downstream raw materials:

3-(3,5-dichloro-phenyl)-ureidoacetic acid

isopropylamine

3,5-Dichloroaniline

3-(3',5'-Dichlorophenyl)imidazolidine-2,4-dione

Refernces

• 1、 -. "Broadcast carriers for pesticides and their use". . . Retrieved 2008/06/13.
• 2、 -. "Fungicidal composition for seed dressing". . . Retrieved 2008/06/13.