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Ethylene monochloride

Synonyms BRN 1731576 CCRIS 621 Chlorethene Chlorethylene Chloroethene 1-Chloro-ethene Chloroethylene 1-Chloroethylene EINECS 200-831-0 Ethylene monochloride Mono-chloroethene Monochloroethylene MVC RCRA waste number U043 Trovidur UN 1086 VC VCM Vinyl C monomer Vinyl chloride monomer. [Pg.1145]

With hydrogen chloride (hydrogen bromide or hydrogen iodide), to form ethylene monochloride (CH2=CHC1) (monobromide, monoiodide), and 1,1-dichloroethane (ethylidene chloride (CH3CHC12) (dibromide, diiodide)... [Pg.22]

SYNS CHLORETHENE CHLORETHYLENE CHLOROETHENE CHLOROETHYLENE CHLORURE de VINYLE (FRENCH) CLORURO di VINILE (ITALIAN) ETHYLENE MONOCHLORIDE MONOCHLOROETHENE MONOCHLOROETHYL-ENE (DOT) RCRA WASTE NUMBER U043 TROVIDUR VC VCM VINILE (CLORURO di) (ITALIAN) VINYLCHLORID (GERMAN) VINYL CHLORIDE MONOMER VINYL C MONOMER VINYLE (CHLORURE de) (FRENCH) WINYLU CHLOREK (POLISH)... [Pg.1423]

Synonyms Chlorethene Chlorethylene Chlor-oethene Chloroethylene Ethene, chloro- Ethylene monochloride Ethylene, chloro- Monochlor-oethene Monochloroethylene Monovinyl chloride Trovidur VC VCM Vinyl C monomer Vinyl chloride monomer Vinyl chlorine Related Compounds Vinyl bromide (CAS 593-60-2) Vinyl fluoride (CAS 72-02-5) Vinylidene chloride (CAS 75-35-4) 1,2-Dichloroethene (CAS 540-59-0) Elexachlorobutadiene (CAS 87-68-3)... [Pg.2829]

Common Name(s) Chloroethene, Ethylene Monochloride, Monochloroethene, Monochloroethylene, VC, VCM, Vinyl Chloride, Vinyl Chloride Monomer... [Pg.28]

SYNONYMS chloroethene, chloroethylene, chloro-ethene, chloroethylene, ethene, chloro-, ethylene, chloro-, ethylene monochloride, monochloroethane, monochloroethylene... [Pg.379]

Synonyms/Trade Names Chloroethene, Chloroethylene, Ethylene monochloride. Monochloroethene, Monochloroethylene, VC, Vinyl chloride monomer (VCM) ... [Pg.330]

Alternative Names/Abbreviations Vinyi chioride monomer, chioroethene. chloroethylene, ethylene monochloride, VCM... [Pg.257]

CAS-No [75-01-4] chloroethylene ethylene monochloride monochloroethene VC vinyl chloride monomer VINYL CHLORIDE (cylinder) H2C = CHCI... [Pg.918]

Synonyms Chlorethene Chlorethylene Chloroethene Chloroethylene Ethylene monochloride Monochloroethene Monochloroethylene VC VCM Vinyl chloride monomer Classification Vinyl monomer aliphatic organic compd. [Pg.1414]

Ethylene monochloride. See Vinyl chloride 1,8-Ethylene naphthalene. See Acenaphthene Ethylene nitrate. See Ethylene glycol dinitrate Ethylene oxide... [Pg.1726]

Synonyms Chlorethene Chlorethylene Chloroethene Chloroethylene Ethylene monochloride... [Pg.4679]

Numerous organic reactions of sulfur monochloride are of practical and commercial importance. Of particular importance is the reaction of sulfur monochloride with olefins to yield various types of addition products (142). With ethylene, the severe vesicant bis(2-chloroethyl) sulfide [505-60-2] (mustard gas) forms with elemental sulfur and polysulfides (see Chemicals IN war). Propylene reacts similarly ... [Pg.138]

Benzotrichloride with zinc chloride as catalyst reacts with ethylene glycol to form 2-chloroethyl benzoate [7335-25-3] (35). Perchlorotoluene is formed by chlorination with a solution of sulfur monochloride and aluminum chloride in sulfuryl chloride (36). [Pg.59]

Levinstein A process for making mustard gas, (C1CH2CH2)2S, by reacting sulfur monochloride with ethylene ... [Pg.163]

A general strategy for the synthesis of 1,2-dithioles is the addition of two sulfur atoms to the CH = CH-CH- group also, non-ethylenic CH groups should be activated. Elemental sulfur is obviously the best reagent although sulfur monochloride is sometimes used. [Pg.196]

Sulphur monochloride is extensively used in the vulcanisation of caoutchouc at the ordinary temperature by a process discovered by Parkes 9 the chemical reaction appears to involve merely the addition of sulphur chloride to an unsaturated hydrocarbon.10 A similar reaction is involved in the manufacture of mustard gas, diehlorodicthyl-sulphide, from ethylene and sulphur monochloride ... [Pg.80]

Chlorinated Ethers. Ethylene chlorohydrin reacts with sulfuric acid to form f./T-dichloroethyl ether. It is u byproduct of ethylene glycol production. The chlorines on this ether are inert, making it a good solvent. Further chlorination at 20-30 C gives diethyl ether which hydrolyzes to chloroacclaldehyde and ethylene chlorohydrin. Ethylene and sulfur monochloride react to give /J./i -dichlorodiethyl sulfide (mustard gas), which Is a thioelher. [Pg.367]

Myers and Stephen s method, in which a mixture of 75 parts of sulphur dichloride and 25 parts of sulphur monochloride is sprayed in an atmosphere of ethylene. According to the authors, this method permits the rapid and continuous preparation of dichloroethyl sulphide in 93% yield, without over-chlorination. [Pg.219]

Sufficient sulphur monochloride to cover the end of the tube is first placed in the vessel and then ethylene is bubbled in, so arranging the speed of its introduction and the cooling that the temperature of the reaction mixture remains at 30° to 35° C. Meanwhile more sulphur monochloride is added in small portions. Employing 430 kgm. of ethylene, which needs 750 kgm. sulphur chloride, the reaction is completed in about 20 hours. At the end of the reaction the product is siphoned into a settling vessel where the sulphur is removed. [Pg.223]

Guthrie and Niemann, in which diehlorethyl sulfide is formed by the direct action of ethylene gas on sulfur monochloride (see Chart XII), according to the equation ... [Pg.225]

The method of making lewisite was suggested by the analogous method of mustard-gas manufacture used by the Allies. Thus, mustard is formed by the action of ethylene on sulfur monochloride, while lewisite is produced by action of acetylene on araeme trichloride in the pieaenct of aluminum trichloride acting as a catalyst. The dark brown viscid liquid a hich results from this latter reaction is decomposed by treatment with hydrochloric acid at O C. (32 F.), and an oil is obtained which < an be fractionated by distillation in vacuo into three chlor inyl derivatives of arsenic trichloride. These derivatives, which differ from each other only by the successive addition to the arsenic trichloride of one, two, or three molecules of acetylene, are as follows (see Chart Xlll) ... [Pg.228]

All solvents were purified according to the literature methods (6). Sulfur monochloride (Aldrich Chemical Co.) was used as received. Ethylene-propylene-diene terpolymers (Epcar 346 ... [Pg.498]

Okahara and coworkers prepared a number of Ai-alkylamino diols that were not symmetric. They first prepared the monochloride derivative of the oligoethylene glycol by reacting ethylene oxide with 2-chloroethanol in an acidic medium (Kuo et al., 1980). The oligomers were separated by distil-... [Pg.58]

See other pages where Ethylene monochloride is mentioned: [Pg.1486]    [Pg.731]    [Pg.1681]    [Pg.28]    [Pg.76]    [Pg.666]    [Pg.217]    [Pg.1114]    [Pg.1486]    [Pg.731]    [Pg.1681]    [Pg.28]    [Pg.76]    [Pg.666]    [Pg.217]    [Pg.1114]    [Pg.941]    [Pg.389]    [Pg.26]    [Pg.890]    [Pg.58]    [Pg.15]    [Pg.780]    [Pg.842]    [Pg.856]    [Pg.911]    [Pg.890]    [Pg.34]   
See also in sourсe #XX -- [ Pg.731 ]

See also in sourсe #XX -- [ Pg.2 , Pg.22 ]

See also in sourсe #XX -- [ Pg.330 ]



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