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Ethylidene dichloride

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... [Pg.6]

The gases from the reactor are then cooled and subjected to a caustic wash to remove unreacted hydrogen chloride. This is then followed by a methanol wash to remove water introduced during the caustic wash. A final purification to remove aldehydes and ethylidene dichloride, formed during side reactions, is then carried out by low-temperature fractionation. The resulting pure vinyl chloride is then stored under nitrogen in a stainless steel tank. [Pg.314]

Synonyms CCRIS 224 Chlorinated hydrochloric ether 1,1-Dichlorethane asj/n-Dichloro-ethane Dichloromethylmethane EINECS 200-863-5 Ethylidene chloride Ethylidene dichloride 1,1-Ethylidene dichloride NCI-C04535 RCRA waste number U076 UN 2362. [Pg.410]

Ethylidene Chloride or Ethylidene Dichloride. See Dichlo roe thane in Vol 5 of Encycl, p D1209-R... [Pg.176]

DICHLOROETHANE AND DERIVATIVES Dichloroethane, Ethylene Dichloride or Ethylidene Dichloride, C2H4CI2 mw 98.97. Two isomers are possible ... [Pg.103]

Dichloroethane, as-Dichloroethane, or Ethylidene Dichloride (called 1,1-Dichlor-athan or Athylidenchlorid in Ger),... [Pg.103]

CHLORURE d ETHYLIDENE (FRENCH) CLORURO di ETILIDENE aTALIAN) 1,1-DICHLOORETHAAN (DUTCH) 1,1-DICHLORAETHAN (GERMAN) 1,1-DICLOROETANO (ITALIAN) ETHYLIDENE CHLORIDE ETHYLIDENE DICHLORIDE NCI-C04535 RCRA WASTE NUMBER U076... [Pg.461]

Epoxybutane Ethyl acetate Ethyl acrylate Ethyl benzene Ethyl carbamate Ethyl chloride Ethylene dibromide Ethylene dichloride Ethylene glycol Ethylene imine Ethylene oxide Ethylene thiourea Ethylidene dichloride Fine mineral fibers Formaldehyde Glycol ethers Eleptachlor Elexachlorobenzene Elexachlorobutadiene Elexachlorocyclopentadiene Elexachloroethane Elexamethylene-1,6-diisocyanate Elexamethylphosphoramide Elexane... [Pg.67]

Other acetyl chloride preparations include the reaction of acetic acid and chlorinated ethylenes in the presence of ferric chloride [7705-08-0] (29) a combination of benzyl chloride [100-44-7] and acetic acid at 85% yield (30) conversion of ethylidene dichloride, in 91% yield (31) and decomposition of ethyl acetate [141-78-6] by the action of phosgene [75-44-5], producing also ethyl chloride [75-00-3] (32). The expense of raw material and capital cost of plant probably make this last route prohibitive. Chlorination of acetic acid to monochloroacetic acid [79-11-8] also generates acetyl chloride as a by-product (33). Because acetyl chloride is cosdy to recover, it is usually recycled to be converted into monochloroacetic acid. A salvage method in which the mixture of HC1 and acetyl chloride is scmbbed with H2S04 to form acetyl sulfate has been patented (33). [Pg.82]

ETHYLIDENE CHLORIDE or ETHYLIDENE DICHLORIDE or 1,1-ETHYLIDENE DICHLORIDE (75-34-3) C2H4CI2 Forms explosive mixture with air [explosion limits in air (vol %) 5.6 to 11.4 flash point 10°F/-12°C autoignition temp 856°F/458°C Fire Rating 3], Violent reaction with strong oxidizers, potassium powdered metals alkaline earth (barium, calcium, strontium sometime magnesium is included) and alkali metals (lithium, sodium, potassium, rubidium, cesium, and francium). Contact with strong caustics will cause... [Pg.479]

SYNONYMS ethylidene dichloride, chlorinated hydrochloric ether, ethylidene chloride... [Pg.294]


See other pages where Ethylidene dichloride is mentioned: [Pg.383]    [Pg.198]    [Pg.1486]    [Pg.1486]    [Pg.227]    [Pg.926]    [Pg.176]    [Pg.216]    [Pg.216]    [Pg.609]    [Pg.383]    [Pg.86]    [Pg.559]    [Pg.53]    [Pg.11]    [Pg.176]    [Pg.52]    [Pg.1682]    [Pg.198]    [Pg.176]    [Pg.2404]    [Pg.376]    [Pg.479]    [Pg.200]    [Pg.921]    [Pg.116]    [Pg.2385]    [Pg.2397]    [Pg.110]    [Pg.1002]   
See also in sourсe #XX -- [ Pg.227 ]




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