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  2. 2,4,6-Tribromophenol - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Tribromophenol

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ?) 2,4,6-Tribromophenol (TBP) is a brominated derivative of phenol. It is used as a fungicide, as a wood preservative, and an intermediate in the preparation of flame retardants.

  3. Bromophenol - Wikipedia

    en.wikipedia.org/wiki/Bromophenol

    Bromophenol. A bromophenol is an organic compound consisting of hydroxyl groups and bromine atoms bonded to a benzene ring. They may be viewed as hydroxyl derivatives of bromobenzene, or as brominated derivatives of phenol. There are five basic types of bromophenols (mono- to pentabromophenol) and 19 different bromophenols in total when ...

  4. Bromine test - Wikipedia

    en.wikipedia.org/wiki/Bromine_test

    The formation of a brominated phenol (i.e. 2,4,6-tribromophenol) or aniline (i.e. 2,4,6-tribromoaniline) in form of a white precipitate indicates that the unknown was a phenol or aniline. The more unsaturated an unknown is, the more bromine it reacts with, and the less coloured the solution will appear.

  5. 2,4,6-Tribromoanisole - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Tribromoanisole

    Infobox references. 2,4,6-Tribromoanisole (TBA) is a chemical compound that is a brominated derivative of anisole. It is one of the chemicals responsible for cork taint. [2] Tribromoanisole is a fungal metabolite of 2,4,6-tribromophenol, which is used as a fungicide. It can be found in minute traces on packaging materials stored in the presence ...

  6. 2,4,6-Tribromoaniline - Wikipedia

    en.wikipedia.org/wiki/2,4,6-tribromoaniline

    2,4,6-Tribromoaniline. Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 2,4,6-Tribromoaniline is a brominated derivative of aniline with the formula C 6 H 4 Br 3 N. It is used in organic synthesis of pharmaceuticals, agrochemicals and fire-extinguishing agents.

  7. CPK coloring - Wikipedia

    en.wikipedia.org/wiki/CPK_coloring

    [4] Column J is the color scheme used by the molecular visualizer Jmol. [9] Column R is the scheme used by Rasmol; when two colors are shown, the second one is valid for versions 2.7.3 and later. [9] [10] Column P consists of the colors in the PubChem database managed by the United States National Institute of Health.

  8. List of reagent testing color charts - Wikipedia

    en.wikipedia.org/wiki/List_of_reagent_testing...

    List of reagent testing color charts. It is advised to check the references for photos of reaction results. [1] Reagent testers might show the colour of the desired substance while not showing a different colour for a more dangerous additive. [2] For this reason it is essential to use multiple different tests to show all adulterants.

  9. CIE 1931 color space - Wikipedia

    en.wikipedia.org/wiki/CIE_1931_color_space

    The resulting normalized color matching functions are then scaled in the r:g:b ratio of 1:4.5907:0.0601 for source luminance and 72.0962:1.3791:1 for source radiance to reproduce the true color matching functions. By proposing that the primaries be standardized, the CIE established an international system of objective color notation.

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