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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.
Structure and properties ... Physical and Chemical Properties of Toluene in chemeo.com This page was last edited on 12 April 2023, at 11:55 (UTC). ...
DNT is hydrogenated to produce 2,4-toluenediamine, which in turn is phosgenated to give toluene diisocyanate. In this way, about 1.4 billion kilograms are produced annually, as of the years 1999–2000. [6] Other uses include the explosives industry. It is not used by itself as an explosive, but some of the production is converted to TNT.
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 ...
The resulting DBT/H18-DBT mixture has a notable hydrogen storage capacity of 6.2wt%, is minimally toxic, and high thermal stability with ignition temperature at 450°C. [ 17 ] [ 3 ] [ 21 ] While the storage capacity is 6.2 wt% and the energy density is 1.9 kWh/L, considering the de-hydrogenation limitation the storage capacity is 6.0 wt% and ...
It is mainly used to manufacture toluene diisocyanate, which is a key raw material in polyurethane chemistry. [4] It is still the starting material used when non-phosgene methods of production of toluene diisocyanate are used. [5] [6] It is also a degradation product of polyurethane materials produced using toluene diisocyanate.
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).
TNT is occasionally used as a reagent in chemical synthesis, but it is best known as an explosive material with convenient handling properties. The explosive yield of TNT is considered to be the standard comparative convention of bombs and asteroid impacts. In chemistry, TNT is used to generate charge transfer salts.