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  2. Tetramethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Tetramethylbenzene

    The tetramethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with four methyl groups (–CH 3) as a substituent. [1] Through their different arrangement, they form three structural isomers with the molecular formula C 10 H 14. They also belong to the group of C 4-benzenes.

  3. Durene - Wikipedia

    en.wikipedia.org/wiki/Durene

    Durene, or 1,2,4,5-tetramethylbenzene, is an organic compound with the formula C 6 H 2 (CH 3) 4. It is a colourless solid with a sweet odor. The compound is classified as an alkylbenzene. It is one of three isomers of tetramethylbenzene, the other two being prehnitene (1,2,3,4-tetramethylbenzene) and isodurene (1,2,3,5-tetramethylbenzene ...

  4. C4-Benzenes - Wikipedia

    en.wikipedia.org/wiki/C4-Benzenes

    The C 4-benzenes are a class of organic aromatic compounds which contain a benzene ring and four other carbon atoms. There are three tetramethylbenzenes, six dimethylethylbenzenes, three diethylbenzenes, three isopropylmethylbenzenes, three n-propylmethylbenzenes and four butylbenzenes.

  5. C10H14 - Wikipedia

    en.wikipedia.org/wiki/C10H14

    1,2,4,5-Tetramethylbenzene (durene) 1,3-Dehydroadamantane This page was last edited on 19 January 2020, at 23:37 ...

  6. 3,3',5,5'-Tetramethylbenzidine - Wikipedia

    en.wikipedia.org/wiki/3,3',5,5'-Tetramethylbenzidine

    3,3′,5,5′-Tetramethylbenzidine or TMB is a chromogenic substrate used in staining procedures in immunohistochemistry as well as being a visualising reagent used in enzyme-linked immunosorbent assays (). [1]

  7. Prehnitene - Wikipedia

    en.wikipedia.org/wiki/Prehnitene

    Prehnitene or 1,2,3,4-tetramethylbenzene is an organic compound with the formula C 6 H 2 (CH 3) 4, classified as an aromatic hydrocarbon. It is a flammable colorless liquid which is nearly insoluble in water but soluble in organic solvents.

  8. BTX (chemistry) - Wikipedia

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

    Benzene, toluene, and xylenes can be made by various processes. However, most BTX production is based on the recovery of aromatics derived from the catalytic reforming of naphtha in a petroleum refinery.

  9. Trimethylbenzene - Wikipedia

    en.wikipedia.org/wiki/Trimethylbenzene

    The trimethylbenzenes constitute a group of substances of aromatic hydrocarbons, which structure consists of a benzene ring with three methyl groups (–CH 3) as a substituent. [1] [2] Through their different arrangement, they form three structural isomers with the molecular formula C 9 H 12. They also belong to the group of C 3-benzenes.