1,1,3 -trichloropropane

Solubility in water Q20 C Solubility of water in solvent Specific gravity 20/20 C Vapor pressure 20 C Weight per gallon 20 C 

Not more than S% dis-tiUs below 23S C Not less than 95% dis-tiUs below 242 C 

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Carbon tetrachloride Ethylene chloride. Trichloroethylene. Propylene chloride. Ethylene chlorobromide 1 1 2-Trichloroethane Trimethylene chloride Tetrachloroethylene Trimethylene chlorobromide sym. Tetrachloroethane 1 4 Dichlorobutane 1 2 3-Trichloropropane Pentachloroothane. ... 

AU products Usted have flash point (PMCC) > 177°C. The specific gravity at 25°C ranges from 1.27 to 1.31. CAS Registry Number for aU the LPs Usted is [68611-50-7] ie, they are copolymers made from (3) and 1,2,3-trichloropropane, and sodium polysulfide. 

From Allyl Ghloride. The hypochlorination of allyl chloride [107-05-1] gives a mixture of the glycerol dichlorohydrins, 2,3-dichloropropanol and 1,3-dichloropropanol about 7 3 ratio. Because of the poor solubiHty of allyl chloride in water, it is essential to minimize the formation of an organic phase in which direct chlorination of the allyl chloride results in the unwanted by-product 1,2,3-trichloropropane. 

By incorporation of some trihalide to give a branched polymer such as Thiokol ST (about 2% of 1,2,3-trichloropropane is used in this instance). The resultant vulcanisates have lower cold flow and compression set than obtained with Thiokol A. 

By introducing branch points into the polymer chains, for example by incorporating about 2% of 1,2,3,-trichloropropane into the polymerisation recipe, chain extension may proceed in more than two directions and this leads to the formation of networks by chemical cross-links. However, with these structures interchange reactions occur at elevated temperatures and these cause stress relief of stressed parts and in turn a high compression set. 

In contrast, the addition of antimony pentachlonde increases the reactivity of chlorine monofluonde toward 1,2,3-trichloropropane but reduces its selectivity [/3] (equation 12)... 

The degradation of 1,2,3-trichloropropane by Agrobacterium radiobacter strain ADI involves hydrolysis of an intermediate epichlorohydrin (3-chloroprop-l-ene) to the diol (Bosma et al. 1999, 2002). An enzyme from this strain has been modified from the use of epichlorohydrin that is its normal substrate to accept dy-l,2-dichloroethene with the release of chloride and the presumptive formation of glyoxal (Rui et al. 2004). 

Bosma T, J Damborsky, G Stucki, DB Janssen (2002) Biodegradation of 1,2,3-trichloropropane through directed evolution and heterologous expression of a haloalkane dehalogenase gene. Appl Environ Microbiol 68 3582-3587. 

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