Dichloroethane, organic solvents

Dichloroethane [75-34-3] CH CHCl, ethylidene chloride, ethylidene dichloride, is a colorless Hquid with an ethereal odor. It is miscible with most organic solvents and all chloriaated solvents. It is employed as a solvent, but its largest iadustrial use is as an iatermediate ia the production of... 

Dichloroethane [107-06-2] ethylene chloride, ethylene dichloride, CH2CICH2CI, is a colorless, volatile Hquid with a pleasant odor, stable at ordinary temperatures. It is miscible with other chlorinated solvents and soluble in common organic solvents as well as having high solvency for fats, greases, and waxes. It is most commonly used in the production of vinyl chloride monomer. 

This approach allowed us also to determine the difference in the surface potentials between mutually saturated water and an organic solvent namely, nitrobenzene, nitroethane and 1,2-dichloroethane, and isobutyl methyl ketone (IBMK). The qualitative data show a very strong influence of the added organic solvent on the surface potential of water, while the presence of water in the nonaqueous phase has practically no... 

Most of the liquid-liquid interfaces that have been studied involve water and an organic solvent such as nitrobenzene or 1,2-dichloroethane (1,2-DCE). Although these systems form stable interfaces, the solubility of one solvent in the other is usually quite high. For example, the solubility of water in 1,2-DCE is 0.11 M, and that of 1,2-DCE in water is 0.09 M. So each of the two liquid components is a fairly concentrated solution of one solvent in the other. It is therefore unlikely that the interface is sharp on a molecular level. We rather expect an extended region with a thickness of the order of a few solvent diameters, over which the concentrations of the two solvents change rapidly (see Fig. 12.1). The lower the solubility of one solvent in the other, the thinner this interfacial region should be. These expectations are supported by the indication that the dipole potentials at these interfaces seem to be small, at least near the pzc, but spectroscopic information is lacking at present. 

By the example of 34 different alkynes, it was convincingly demonstrated that the product of the treatment of [PtCLJ with CO at 40-110 °C is a very powerful alkyne hydration catalyst some of the reactions are shown on Scheme 9.7 [25], The best medium for this transformation is THF containing 5 % H2O. The reaction can also be performed in a water-organic solvent two-phase system (e.g. with 1,2-dichloroethane), however in this case addition of a tetralkylammonium salt, such as Aliquat 336, is required to facilitate mass transfer between the phases. After the reaction with CO, the major part of platinum is present as H2[ Pt3(CO)6 n], but the catalytic effect was assigned to a putative mononuclear Pt-hydride, [PtHCl(CO)2], presumably formed from the cluster and some HCl (supplied by the reduction of [PtCU]). The hydration of terminal acetylenes follows Markovnikov s mle leading exclusively to aldehyde-free ketones. 

Pu reported the synthesis of axially chiral-conjugated polymer 82 bearing a chiral binaphthyl moiety in the main chain by the cross-coupling polymerization of chiral bifunctional boronic acid 80 with dibromide 81 (Equation (39)). The polymer is soluble in common organic solvents, such as THE, benzene, toluene, pyridine, chlorobenzene, dichloromethane, chloroform, and 1,2-dichloroethane. The polymer composed of racemic 80 was also synthesized, and the difference of characteristics was examined. Optically active polymer 82 was shown to enhance fluorescence quantum yield up to = 0.8 compared with the racemic 82 ( = 0.5). Morphologies of the optically active and racemic polymers were also compared with a systematic atomic-force microscopy (AEM). 

Similar but even more pronounced anionic effects were observed with liquid membranes based on ionophore 80 and exhaustively purified organic solvents (nitrobenzene or 1,2-dichloroethane) but no polymer matrix. The use of such membranes allows to minimize the concentration of ionic impurities that could take the role of anionic sites. For a membrane with ionophore 80, the SHG response... 

Initially, kinetic resolutions of 2-(trimethylsilyl)-5-[l -(2, 2, 2 -trifluoro-l -hydroxy-ethyl)]furan with a wide variety of lipases and vinyl alkanoates were examined in 1,2-dichloroethane. On the basis of these results, the system consisting of an enzyme (Novozym 435, Candida antarctica, Novo Nordisk Co. Ltd.) and vinyl propionate was sufficient to obtain optical pure alcohol and ester with a high -value. Moderate effect on the optical purity was observed on changing the organic solvents. Obviously, Novozym 435-CH2ClCH2Cl system is the most convenient practical system for obtaining the optically pure alcohol and the ester on the basis of comparison of the reaction time and the -value. 

Most of the side reactions have already been discussed in Section 26.1.3.3. (dediazoniation in organic solvents). Chlorinated aliphatic solvents, such as 1,2-dichloroethane and dichloro-methane, lead to an extensive formation of chloroaromatics, and aromatic solvents, even halogenated examples, can be arylated to some extent by arenediazonium tetrafluoroborates (vide supra). For example, during dediazoniation of benzenediazonium tetrafluoroborate in toluene, chlorobenzene, bromobenzene or anisole, 3-5 % of substituted biphenyls Ph-C6H4-X (X = Me, Cl, Br, OMe) are formed together with 0.5-0.8% of fluorobiphenyls.5 Fluorobiphenyls are formed through an ionic pathway (only 2- and 4-isomers are formed) whereas chlorobiphenyls result from a radical process (X = Cl, 2-/3-/4-isomer 26 47 27).243... 

Nitroglycerine is readily dissolved in most organic solvents and itself behaves as a good solvent. Thus, it is completely miscible in all proportions at room temperature with the following liquids methyl alcohol, ethyl acetate, anhydrous acetic add, benzene, toluene, xylenes, phenol, nitrobenzene, nitrotoluenes, pyridine, chloroform, dichloroethane, dichloroethylene, and the like. 

The viscosity behavior of poly[(a-carboxymethyl)ethyl isocyanide] may be studied in neutral organic solvents. The concentration dependence of its reduced specific viscosity in 1,2-dichloroethane is shown in Fig. 11. A linear dependence indicates that the coefficients of higher concentration terms of the usual virial equations are negligibly small—a case which should be found with molecules, such as stiff rods, that give few intermolecular entanglements in dilute solution. 

In the traditional process, the dried and ground paprika is extracted by organic solvents (such as hexane, acetone, benzene, methylene chloride, or dichloroethane) which have low boiling points. These traditional processes have several disadvantages. Most organic solvents like benzene and the chlorinated solvents are toxic, and government food regulations dictate... 

POMs form by a self-assembly process, typically in an acidic aqueous solution and can be isolated as powder or crystals with counter-cations. Appropriate selection of counter-cations can control the solubility of POMs in various reaction media. For homogeneous system, alkylammonium cations, generally TBA, are selected as counter-cations of POM anions for the dissolution in organic solvents such as acetonitrile, DMF, DMSO and 1,2-dichloroethane. POMs with metal counter-cations such asNa +, K+,Rb+,Cs + and Ag + are not soluble in common organic solvents. 

It should be noted that mixtures of isomers are involved in many cases of organic solvents e.g., mixed xylene isomers, mixed cis- and trans-decalin, mixed 1,1- and 1,2-dichloroethane, or mixed cresols, without obvious detrimental effects on the particular application attempted. However, in the following it is assumed that definite single substances are to be dealt with. 

Organic solvents, which induce CYP2E1, are comprised of a few broad chemical classes, including hydrocarbons such as benzene and toluene, halogenated aliphatic compounds such as carbon tetrachloride and dichloroethane, aliphatic alcohols such as ethanol, and hydroxyethers such as 2-methoxyethanol. Industrial solvents are frequently mixtures of several compounds. The most frequent solvent-associated toxicity occurs from occupational exposure. A number of organic solvents have been examined for their effects on the immune system, and the requirement for their bioactivation to produce immunotoxicity has been well established. 

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