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  2. Bisphenol A - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A

    Bisphenol A (BPA) is a chemical compound primarily used in the manufacturing of various plastics.It is a colourless solid which is soluble in most common organic solvents, but has very poor solubility in water.

  3. Epichlorohydrin - Wikipedia

    en.wikipedia.org/wiki/Epichlorohydrin

    Epichlorohydrin (abbreviated ECH) is an organochlorine compound and an epoxide. Despite its name, it is not a halohydrin . It is a colorless liquid with a pungent, garlic-like odor, moderately soluble in water, but miscible with most polar organic solvents . [ 4 ]

  4. Tetrabromobisphenol A - Wikipedia

    en.wikipedia.org/wiki/Tetrabromobisphenol_A

    Further, TBBPA structurally mimics the thyroid hormone thyroxin (T 4) and can bind more strongly to the transport protein transthyretin than T 4 does, likely interfering with normal T 4 activity. TBBPA likely also suppresses immune responses by inhibiting expression of CD25 receptors on T cells , preventing their activation, and by reducing ...

  5. Phenol formaldehyde resin - Wikipedia

    en.wikipedia.org/wiki/Phenol_formaldehyde_resin

    HOC 6 H 4 CH 2 OH + HOC 6 H 5 → (HOC 6 H 4) 2 CH 2 + H 2 O 2 HOC 6 H 4 CH 2 OH → (HOC 6 H 4 CH 2) 2 O + H 2 O. The diphenol (HOC 6 H 4) 2 CH 2 (sometimes called a "dimer") is called bisphenol F, which is an important monomer in the production of epoxy resins. Bisphenol-F can further link generating tri- and tetra-and higher phenol oligomers.

  6. Bisphenol A diglycidyl ether - Wikipedia

    en.wikipedia.org/wiki/Bisphenol_A_diglycidyl_ether

    Bisphenol A diglycidyl ether slowly hydrolyzes to 2,2-bis[4(2,3-dihydroxypropoxy)phenyl)propane (bis-HPPP). Similarly, DGEBA reacts with acrylic acid to give vinyl ester resins . The reaction results in opening of the epoxide ring, generating unsaturated esters at each terminus of the molecule.

  7. Bisphenol - Wikipedia

    en.wikipedia.org/wiki/Bisphenol

    The bisphenols (/ ˈ b ɪ s f ɪ n ɒ l /) are a group of industrial chemical compounds related to diphenylmethane; commonly used in the creation of plastics and epoxy resins. [1] [2] [3] Most are based on two hydroxyphenyl functional groups linked by a methylene bridge.

  8. 4,4'-Biphenol - Wikipedia

    en.wikipedia.org/wiki/4,4'-Biphenol

    The industrial synthesis of 4,4′-biphenol was developed by Allan Hay in the 1960s. [2] [3] As the direct oxidative coupling of phenol gives a mixture of isomers, [4] [5] 4,4′-biphenol is instead prepared from 2,6-di-tert-butylphenol, where para-coupling is the only possibility. [3]

  9. IUPAC polymer nomenclature - Wikipedia

    en.wikipedia.org/wiki/IUPAC_polymer_nomenclature

    A polymer is a substance composed of macromolecules. The latter usually have a range of molar masses (unit g mol −1), the distributions of which are indicated by dispersity (Đ). It is defined as the ratio of the mass-average molar mass (M m) to the number-average molar mass (M n) i.e. Đ = M m /M n. [4]