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  2. Toluene - Wikipedia

    en.wikipedia.org/wiki/Toluene

    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.

  3. Toluene (data page) - Wikipedia

    en.wikipedia.org/wiki/Toluene_(data_page)

    Download as PDF; Printable version; In other projects ... Structure and properties ... Physical and Chemical Properties of Toluene in chemeo.com

  4. Alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Alkylbenzene

    The simplest member, toluene (or methylbenzene), has the hydrogen atom of the benzene ring replaced by a methyl group. The chemical formula of alkylbenzenes is C n H 2n-6. [2] Safety hazards of toluene. Oftentimes, toluene is used as an organic solvent.

  5. TNT - Wikipedia

    en.wikipedia.org/wiki/TNT

    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.

  6. Tolyl group - Wikipedia

    en.wikipedia.org/wiki/Tolyl_group

    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).

  7. 3-Nitrotoluene - Wikipedia

    en.wikipedia.org/wiki/3-nitrotoluene

    It is made by nitrating toluene by conventional mixed acid (acetyl nitrate doesn't produce it [4]): this reaction mainly affords a 2:1 mixture of 2-nitro and 4-nitro isomers, but after removal of the 2-isomer, the 3-nitrotoluene can be purified by distillation. It is a precursor to toluidine, which is used in producing azo dyes. [3]

  8. BTX (chemistry) - Wikipedia

    en.wikipedia.org/wiki/BTX_(chemistry)

    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.

  9. Butylated hydroxytoluene - Wikipedia

    en.wikipedia.org/wiki/Butylated_hydroxytoluene

    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]