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  2. Hydrogen bromide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_bromide

    Hydrogen bromide is the inorganic compound with the formula HBr. It is a hydrogen halide consisting of hydrogen and bromine. A colorless gas, it dissolves in water, forming hydrobromic acid , which is saturated at 68.85% HBr by weight at room temperature.

  3. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  4. Bromide - Wikipedia

    en.wikipedia.org/wiki/Bromide

    The classic case is sodium bromide, which fully dissociates in water: NaBr → Na + + Br −. Hydrogen bromide, which is a diatomic molecule, takes on salt-like properties upon contact with water to give an ionic solution called hydrobromic acid. The process is often described simplistically as involving formation of the hydronium salt of bromide:

  5. Tetralin - Wikipedia

    en.wikipedia.org/wiki/Tetralin

    Safety data sheet (SDS) JT Baker MSDS: Except where otherwise noted, ... It is also used for the laboratory synthesis of hydrogen bromide: C 10 H 12 + 4 Br 2 → C 10 ...

  6. Hydrobromic acid - Wikipedia

    en.wikipedia.org/wiki/Hydrobromic_acid

    Hydrobromic acid is an aqueous solution of hydrogen bromide.It is a strong acid formed by dissolving the diatomic molecule hydrogen bromide (HBr) in water. "Constant boiling" hydrobromic acid is an aqueous solution that distills at 124.3 °C (255.7 °F) and contains 47.6% HBr by mass, which is 8.77 mol/L. Hydrobromic acid is one of the strongest mineral acids known.

  7. 1,2-Dibromoethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Dibromoethane

    1,2-Dibromoethane has wider applications in the preparation of other organic compounds including those carrying modified diazocine rings [9] and vinyl bromide that is a precursor to some fire retardants. [4] In organic synthesis, 1,2-dibromoethane is used to brominate carbanions and to activate magnesium for certain Grignard reagents.