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  2. Tosylamide/formaldehyde resin - Wikipedia

    en.wikipedia.org/wiki/Tosylamide/formaldehyde_resin

    Tosylamide/formaldehyde resin (TSFR) is a polymeric resin used as a plasticizer and secondary film-forming agent in nail polishes. While it was still in use as of 2023, [update] its use has been diminishing in favor of hypoallergenic alternatives, due to the prevalence of reactions causing allergic contact dermatitis of the eyelids , face, and ...

  3. Tosyl group - Wikipedia

    en.wikipedia.org/wiki/Tosyl_group

    Tosyl group (blue) with a generic "R" group attached Tosylate group with a generic "R" group attached. Note the extra oxygen, compared to plain tosyl. In organic chemistry, a toluenesulfonyl group (tosyl group, abbreviated Ts or Tos [nb 1]) is a univalent functional group with the chemical formula −SO 2 −C 6 H 4 −CH 3.

  4. Eyelid dermatitis - Wikipedia

    en.wikipedia.org/wiki/Eyelid_dermatitis

    Eyelid dermatitis is commonly related to atopic dermatitis or allergic contact dermatitis. [1] Volatile substances, tosylamide/formaldehyde resin, epoxy hardeners, insect repellent sprays, and lemon peel oil may be implicated, with many cases of eyelid contact dermatitis being caused by substances transferred by the hands to the eyelids.

  5. These eye masks are like a cold glass of water for your tired ...

    www.aol.com/lifestyle/grace-and-stella-under-eye...

    These eye masks have an impressive almost 30,000 reviews on Amazon and have managed to maintain a 4.3-star rating, too. Nearly 20,000 of those reviews are 5-star ratings. They're effective

  6. List of boiling and freezing information of solvents - Wikipedia

    en.wikipedia.org/wiki/List_of_boiling_and...

    Density (g cm-3) Boiling point (°C) K b (°C⋅kg/mol) Freezing point (°C) K f (°C⋅kg/mol) Data source; Aniline: 184.3 3.69 –5.96 –5.87 K b & K f [1] Lauric acid: 298.9 44 –3.9 Acetic acid: 1.04 117.9 3.14 16.6 –3.90 K b [1] K f [2] Acetone: 0.78 56.2 1.67 –94.8 K b [3] Benzene: 0.87 80.1 2.65 5.5 –5.12 K b & K f [2 ...

  7. Stetter reaction - Wikipedia

    en.wikipedia.org/wiki/Stetter_reaction

    The Stetter reaction is a reaction used in organic chemistry to form carbon-carbon bonds through a 1,4-addition reaction utilizing a nucleophilic catalyst. [1] While the related 1,2-addition reaction, the benzoin condensation, was known since the 1830s, the Stetter reaction was not reported until 1973 by Dr. Hermann Stetter. [2]

  8. The U.S. Food and Drug Administration expanded approval for Johnson & Johnson’s nasal spray, Spravato, to allow it to be used as a standalone treatment for patients with severe depression, the ...

  9. Silicone resin - Wikipedia

    en.wikipedia.org/wiki/Silicone_resin

    Silicone resin with R = CH 3, H or OH. Silicone resins are a type of silicone material which is formed by branched, cage-like oligosiloxanes with the general formula of R n SiX m O y, where R is a non-reactive substituent, usually methyl (Me = −CH 3) or phenyl (Ph = −C 6 H 5), and X is a functional group: hydrogen (−H), hydroxyl (−OH), chlorine (−Cl) or alkoxy (−O −).