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Trichloroethanal

CH2 CCl2- Colourless liquid, b.p. 32°C, manufactured by the dehydrochlorination of trichloroethane. In the presence of light and air, it decomposes with the evolution of HCI, phosgene, and methanal and deposition of some polyvinylidene chloride. Consequently it must be stored away from light and in the presence of dissolved inhibitors (such as phenols and amines). Under the influence of... [Pg.420]

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. ... [Pg.296]

The name D.D.T. is derived from dichlorodiphenylfrichloroethane this is a misnomer since the name represents 27 different compounds. As commonly employed it refers to 2 2-6ts(p-chlorophenyl)-l 1 1-trichloroethane. It is conveniently prepared by the condensation of chlorobenzene and chloral hydrate in the presence of concentrated sulphuric acid ... [Pg.1011]

The principle of headspace sampling is introduced in this experiment using a mixture of methanol, chloroform, 1,2-dichloroethane, 1,1,1-trichloroethane, benzene, toluene, and p-xylene. Directions are given for evaluating the distribution coefficient for the partitioning of a volatile species between the liquid and vapor phase and for its quantitative analysis in the liquid phase. Both packed (OV-101) and capillary (5% phenyl silicone) columns were used. The GG is equipped with a flame ionization detector. [Pg.611]

EMI intermediatesynthesis [COMPOSITE MATERIALS - POLYTffiR-MATREI - THERMOSETS] (Vol 7) 4,4pDichlorodiphenyl-trichloroethane [50-29-3]... [Pg.303]

See other pages where Trichloroethanal is mentioned: [Pg.196]    [Pg.538]    [Pg.538]    [Pg.715]    [Pg.294]    [Pg.294]    [Pg.414]    [Pg.414]    [Pg.462]    [Pg.462]    [Pg.487]    [Pg.487]    [Pg.506]    [Pg.506]    [Pg.512]    [Pg.526]    [Pg.526]    [Pg.577]    [Pg.577]    [Pg.609]    [Pg.609]    [Pg.688]    [Pg.688]    [Pg.1087]    [Pg.1206]    [Pg.1206]    [Pg.100]    [Pg.100]    [Pg.298]    [Pg.298]    [Pg.299]    [Pg.299]    [Pg.112]    [Pg.299]    [Pg.619]    [Pg.1012]    [Pg.1012]    [Pg.1012]    [Pg.1012]    [Pg.1012]    [Pg.1012]    [Pg.1012]    [Pg.1013]    [Pg.375]    [Pg.510]   
See also in sourсe #XX -- [ Pg.250 ]

See also in sourсe #XX -- [ Pg.19 , Pg.145 ]



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1,1,1 -Trichloroethane toxicity

1,1,1 -trichloroethane biotransformation

1,1,1 -trichloroethane conductivity

1,1,1 -trichloroethane ozone depletion

1,1,1 -trichloroethane regulations

1,1,1-Trichloroethane (methyl chloroform

1,1,1-Trichloroethane poisoning

1,1,1-Trichloroethane, manufacture

1,1,1-trichloroethane destruction

1,1,1-trichloroethane photochemical chlorination

1,1,1-trichloroethane, density

1.1.1- Trichloroethane permeation rate

A-trichloroethane

Acetone-trichloroethane-water system

Chlorophenyl)-l 1 1-trichloroethane

Degradation trichloroethane

Dichloro-diphenyl-trichloroethane

Dichlorodiphenyl-trichloroethane

Dichlorodiphenyl-trichloroethane production

F 1,1,1 -Trichloroethane

Halogenated hydrocarbons 1.1.1- trichloroethane

Halothane Trichloroethane

Methoxychlor trichloroethane

Solvent effects 1,1,2-trichloroethane

Solvent, solvents 1,1,1-trichloroethane

System 1,1,2-trichloroethane

THREE-ONE®, 1,1,1-trichloroethane

Trichloroacetaldehyde 2,2,2-trichloroethanal)

Trichloroethane

Trichloroethane

Trichloroethane Epinephrine

Trichloroethane biodegradation

Trichloroethane data

Trichloroethane pyrolysis

Trichloroethane, reaction

Trichloroethane, stainless steel

Trichloroethanes, dehydrochlorination

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