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  2. 1-Bromopropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopropane

    Replacing 1-bromopropane with water or acetone-based adhesives is the preferred NIOSH option for controlling occupational exposure, but other options include engineering controls like isolation and ventilation, administrative controls, and PPE that includes respiratory and skin protection.

  3. Bromopropane - Wikipedia

    en.wikipedia.org/wiki/Bromopropane

    Bromopropane is the name of 2 monobrominated propane isomers: 1-Bromopropane (n-propyl bromide) 2-Bromopropane (isopropyl bromide) This page was last edited on 31 ...

  4. Category:Bromoalkanes - Wikipedia

    en.wikipedia.org/wiki/Category:Bromoalkanes

    This page was last edited on 2 December 2021, at 15:41 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. California Proposition 65 list of chemicals - Wikipedia

    en.wikipedia.org/wiki/California_Proposition_65...

    The following is a list of chemicals published as a requirement of Safe Drinking Water and Toxic Enforcement Act of 1986, commonly known as California Proposition 65, that are "known to the state to cause cancer or reproductive toxicity" as of January 3, 2020. [1]

  6. Finkelstein reaction - Wikipedia

    en.wikipedia.org/wiki/Finkelstein_reaction

    1 0.0146 0.00003 64 179 1600 33000 Aromatic Finkelstein reaction. The aromatic chlorides and bromides are not easily substituted by iodide, though they may occur when ...

  7. Dibromopropane - Wikipedia

    en.wikipedia.org/wiki/Dibromopropane

    1,3-Dibromopropane; 1,1-Dibromopropane [Wikidata] 2,2-Dibromopropane This page was last edited on 27 June 2022, at 20:45 (UTC). Text is available under the ...

  8. 1-Bromopentane - Wikipedia

    en.wikipedia.org/wiki/1-Bromopentane

    Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene, which is 1-pentene in the case of 1-bromopentane. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] It is also formed by the reaction of 1-pentanol with hydrogen bromide.

  9. 1-Bromo-3-chloropropane - Wikipedia

    en.wikipedia.org/wiki/1-Bromo-3-chloropropane

    1-Bromo-3-chloropropane is an organohalogen compound with the formula Br(CH 2) 3 Cl. It is a colorless liquid, produced by free-radical addition of hydrogen bromide to allyl chloride. [1] It is used as an alkylating agent to install the –(CH 2) 3 Cl [2] [3] and –(CH 2) 3 – groups. [4] For example, it is a precursor to 4-chlorobutyronitrile.