5318-76-3

Basic information

• Product Name: 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea dihydrochloride
• Synonyms: 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea dihydrochloride;IMIDOCARBDIHYDROCHLORIDE;IMIDOCARB HCL;Imidocarb Hydrochloride;4A65;Imizocarb;IMidocarb-2HClhydrate (see Data Sheet);Imidocarb dihydrochloride monohydrate
• CAS NO: 5318-76-3
• Molecular Formula: C19H22Cl2N6O
• Molecular Weight: 421.32358
• EINECS: 226-179-7
• Mol File: 5318-76-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 350° (dec)
• Boiling Point: 528.1 °C at 760 mmHg
• Flash Point: 273.2 °C
• Appearance: /
• Vapor Pressure: 1.67E-11mmHg at 25°C
• CAS DataBase Reference: 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea dihydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea dihydrochloride(5318-76-3)
• EPA Substance Registry System: 1,3-bis[3-(4,5-dihydro-1H-imidazol-2-yl)phenyl]urea dihydrochloride(5318-76-3)

Safety Data

• Hazard Codes: Xn
• Statements: 22
• WGK Germany: 3
• Hazardous Substances Data: 5318-76-3(Hazardous Substances Data)

Usage

Uses

Different sources of media describe the Uses of 5318-76-3 differently. You can refer to the following data:
1. Antiprotozoal (Babesia).
2. Imidocarb dihydrochloride, the most effective drug against anaplasmosis, is reported to be curative in a single dosage if given early in the infection during the rise in parasitemia. Multiple doses are required if the animals are treated at a later stage or if a relapse occurs.

InChI:InChI=1/C19H20N6O.2ClH/c26-19(24-15-5-1-3-13(11-15)17-20-7-8-21-17)25-16-6-2-4-14(12-16)18-22-9-10-23-18;;/h1-6,11-12H,7-10H2,(H,20,21)(H,22,23)(H2,24,25,26);2*1H

Upstream product

• 619-24-9 3-nitrobenzonitrile 
• 53104-89-5 2-(3-aminophenyl)-4,5-dihydro-1H-imidazol hydrochloride 
• 503-38-8 trichloromethyl chloroformate 
• 31659-42-4 2-(3-nitrophenyl)-2-imidazoline 

Relevant articles and documents

Preparation method of 2-(3-amino phenyl) imidazoline hydrochloride and imidocarb

The invention relates to the field of chemical engineering and discloses a preparation method of 2-(3-amino phenyl) imidazoline hydrochloride and imidocarb. The preparation method comprises the following steps of: inputting 2-(3-nitryl phenyl) imidazoline, a catalyst and an alcohol-water mixed solution into a reaction kettle, stirring the mixture and raising the temperature to 50-65 DEG C, keeping the temperature and stirring the mixture for 10-20 min to obtain a mixed solution M; dropwise adding formic acid into the solution M, and keeping the temperature to react for 1.5-2.5h to obtain a mixed solution N; cooling the solution N to 40 DEG C below and filtering the solution, and evaporating alcohol to obtain a 2-(3-amino phenyl) imidazoline aqueous solution; dropwise adding hydrochloric acid into the 2-(3-amino phenyl) imidazoline aqueous solution to be neutral; and performing crystallization, suction filtration, pressure reduction and drying to obtain a target product 2-(3-amino phenyl) imidazoline hydrochloride. Compared with catalytic hydrogenation in the prior art, by taking formic acid as a hydrogen donor for transfer hydrogenation, the product purity and yield are of no obvious differences but no safety risks are available, and the preparation method is free of special demand, easy to operate and convenient for production and application.