Colorless crystals. Vapor pressure 29 mPa (25°C). Partition coefficient KOWlgP=4.34, Henry's constant 5.16 Pa- m3/mol (calculated value). Solubility in water 1.8mg/L(25℃);Solubility in other solvents(25℃,kg/kg):Acetone9.1,Dichloromethane7.1,Methanol0.98,Xylene4.6,Chlorobenzene5.6.Hydrolyzed by DT5080d(pH 5~9,35℃). Flash point 46.7°C.
ChEBI: Tridiphane is a dichlorobenzene.
Tridiphane is commercially synthesised through a multi-step organic process that centres on constructing its oxirane (epoxide) ring and attaching the two key substituents: a 3,5-dichlorophenyl group and a 2,2,2-trichloroethyl group. The production typically begins with the preparation of the appropriate halogenated aromatic and aliphatic precursors, which are then coupled through nucleophilic substitution or halogenation reactions. The final step involves epoxidation to form the oxirane ring, yielding the active tridiphane molecule.
Enzyme inhibitor - inhibits meristematic activity
Moderately toxic by ingestion andskin contact. An experimental teratogen. Experimentalreproductive effects. When heated to decomposition itemits toxic fumes of Clí.
Poison by ingestion andintraperitoneal routes. Moderately toxic by intraduodenalroute. When heated to decomposition it emits toxic fumesof NOx.
