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  2. 3-Mercaptopropionic acid - Wikipedia

    en.wikipedia.org/wiki/3-Mercaptopropionic_acid

    3-Mercaptopropionic acid (3-MPA) is an organosulfur compound with the formula HSCH 2 CH 2 CO 2 H. It is a bifunctional molecule, containing both carboxylic acid and thiol groups. It is a colorless oil.

  3. Pentaerythritol tetrakis(3-mercaptopropionate) - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol_tetrakis(3...

    Pentaerythritol tetrakis(3-mercaptopropionate) is a common thiol monomer reacted with alkenes in the thiol-ene reaction to form polymeric networks. [3] Being functionalized with four thiol groups, it can react with multifunctional alkenes to form thiol-ene networks.

  4. Shampoo - Wikipedia

    en.wikipedia.org/wiki/Shampoo

    Shampoo lather in hair Bottles of shampoo and lotions manufactured in the early 20th century by the C.L. Hamilton Co. of Washington, D.C., United States. Shampoo (/ ʃ æ m ˈ p uː /) is a hair care product, typically in the form of a viscous liquid, that is formulated to be used for cleaning (scalp) hair.

  5. Polyquaternium - Wikipedia

    en.wikipedia.org/wiki/Polyquaternium

    Copolymer of polyvinyl alcohol and 2,3-epoxypropylamine Polyquaternium-20 Copolymer of polyvinyl octadecyl ether and 2,3-epoxypropylamine Polyquaternium-22 Copolymer of acrylic acid and diallyldimethylammonium Chloride Polyquaternium-24 Quaternary ammonium salt of hydroxyethyl cellulose reacted with a lauryl dimethyl ammonium substituted epoxide.

  6. Can you use micellar water as dry shampoo? Experts weigh in - AOL

    www.aol.com/news/micellar-water-dry-shampoo...

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  7. 3-Mercaptopropionitrile - Wikipedia

    en.wikipedia.org/wiki/3-Mercaptopropionitrile

    3-Mercaptopropionitrile is the organosulfur compound with the formula HSCH 2 CH 2 CN. [1] Containing both thiol and nitrile functional groups , it is a bifunctional compound . A colorless liquid, the compound has found some use as a masked form of thiolate.

  8. Pentaerythritol - Wikipedia

    en.wikipedia.org/wiki/Pentaerythritol

    Pentaerythritol was first reported in 1891 by German chemist Bernhard Tollens and his student P. Wigand. [5] It may be prepared via a base-catalyzed multiple-addition reaction between acetaldehyde and 3 equivalents of formaldehyde to give pentaerythrose (CAS: 3818-32-4), followed by a Cannizzaro reaction with a fourth equivalent of formaldehyde to give the final product plus formate ion.

  9. tert-Butylthiol - Wikipedia

    en.wikipedia.org/wiki/Tert-Butylthiol

    tert-Butylthiol is the main ingredient in many gas odorant blends. [citation needed] It is always utilized as a blend of other compounds, typically dimethyl sulfide, methyl ethyl sulfide, tetrahydrothiophene or other mercaptans such as isopropyl mercaptan, sec-butyl mercaptan and/or n-butyl mercaptan, due to its rather high melting point of −0.5 °C (31.1 °F).