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Toluene is widely used in the paint, dye, rubber, chemical, glue, printing, and pharmaceutical industries as a solvent. [38] Nail polish, paintbrush cleaners, and stain removers may contain toluene. Manufacturing of explosives (TNT) uses it as well. Toluene is also found in cigarette smoke and car exhaust.
In the petroleum refining and petrochemical industries, the initialism BTX refers to mixtures of benzene, toluene, and the three xylene isomers, all of which are aromatic hydrocarbons. The xylene isomers are distinguished by the designations ortho – (or o –), meta – (or m –), and para – (or p –) as indicated in the adjacent diagram.
Toluene (or methylbenzene) is a common chemical found in chemistry laboratories. An alkylbenzene is a chemical compound that contains a monocyclic aromatic ring attaching to one or more saturated hydrocarbon chains. [ 1 ]
BHT is used as a preservative ingredient in some foods. With this usage BHT maintains freshness or prevents spoilage; it may be used to decrease the rate at which the texture, color, or flavor of food changes. [25] Some food companies have voluntarily eliminated BHT from their products or have announced that they were going to phase it out. [26]
Download as PDF; Printable version ... This page provides supplementary chemical data on toluene. MSDS sheets Structure and properties ... Structure and properties ...
Ethyltoluene is produced by ethylation of toluene: CH 3 C 6 H 5 + C 2 H 4 → CH 3 C 6 H 4 C 2 H 5. Over typical acid catalysts, this process gives a mixture of the 2-, 3-, and 4- isomers. Using a modified zeolite catalyst, the alkylation is shape-selective for the 4- isomer. [1] 4-Ethyltoluene is subjected dehydrogenation to give 4 ...
Structures of the three isomers of tolyl group. In organic chemistry, tolyl groups are functional groups related to toluene. [1] They have the general formula CH 3 C 6 H 4 −R, the change of the relative position of the methyl and the R substituent on the aromatic ring can generate three possible structural isomers 1,2 (ortho), 1,3 (meta), and 1,4 (para).
Ethyltoluenes are prepared by alkylation of toluene with ethylene: CH 3 C 6 H 5 + CH 2 =CH 2 → CH 3 C 6 H 4 CH 2 CH 3. These alkylations are catalyzed by various Lewis acids, such as aluminium trichloride. 3- and 4-Ethyltoluenes are mainly of interest as precursors to methylstyrenes: CH 3 C 6 H 4 CH 2 CH 3 → CH 3 C 6 H 4 CH=CH 2 + H 2