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  2. Oxindole - Wikipedia

    en.wikipedia.org/wiki/Oxindole

    Oxindole (2-indolone) is an aromatic heterocyclic organic compound with the formula C 6 H 4 CH 2 C(O)NH. It has a bicyclic structure, consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing ring. Oxindole is a modified indoline with a substituted carbonyl at the second position of the 5-member indoline ring ...

  3. Sodium thiosulfate - Wikipedia

    en.wikipedia.org/wiki/Sodium_thiosulfate

    The relevant reaction is akin to the iodine reaction: thiosulfate reduces the hypochlorite (the active ingredient in bleach) and in so doing becomes oxidized to sulfate. The complete reaction is: 4 NaClO + Na 2 S 2 O 3 + 2 NaOH → 4 NaCl + 2 Na 2 SO 4 + H 2 O. Similarly, sodium thiosulfate reacts with bromine, removing the free bromine from ...

  4. Sodium hypochlorite - Wikipedia

    en.wikipedia.org/wiki/Sodium_hypochlorite

    Sodium hypochlorite solutions, such as liquid bleach, will release toxic chlorine gas when mixed with an acid, such as hydrochloric acid or vinegar. A 2008 study indicated that sodium hypochlorite and organic chemicals (e.g., surfactants, fragrances) contained in several household cleaning products can react to generate chlorinated organic ...

  5. 4-Hexylresorcinol - Wikipedia

    en.wikipedia.org/wiki/4-Hexylresorcinol

    4-Hexylresorcinol is an organic compound with local anaesthetic, antiseptic, and anthelmintic properties. [2]As an antiseptic, it is marketed as S.T.37 by Numark Laboratories, Inc. (in a 0.1% solution) for oral pain relief and as a topical antiseptic.

  6. Benzethonium chloride - Wikipedia

    en.wikipedia.org/wiki/Benzethonium_chloride

    The US Food and Drug Administration (FDA) specifies that the safe and effective concentrations for benzethonium chloride are 0.1-0.2% in first aid products. [2] Aqueous solutions of benzethonium chloride are not absorbed through the skin. It is not approved in the US and Europe for use as a food additive.

  7. Ammonia solution - Wikipedia

    en.wikipedia.org/wiki/Ammonia_solution

    At 15.6 °C (60.1 °F), the density of a saturated solution is 0.88 g/ml; it contains 35.6% ammonia by mass, 308 grams of ammonia per litre of solution, and has a molarity of approximately 18 mol/L. At higher temperatures, the molarity of the saturated solution decreases and the density increases. [ 8 ]

  8. Peracetic acid - Wikipedia

    en.wikipedia.org/wiki/Peracetic_acid

    As an alternative, acetyl chloride and acetic anhydride can be used to generate a solution of the acid with lower water content. Peracetic acid is generated in situ by some laundry detergents . This is achieved by the action of bleach activators , such as tetraacetylethylenediamine and sodium nonanoyloxybenzenesulfonate , upon hydrogen peroxide ...

  9. Trisodium phosphate - Wikipedia

    en.wikipedia.org/wiki/Trisodium_phosphate

    Trisodium phosphate was at one time extensively used in formulations for a variety of consumer-grade soaps and detergents, and the most common use for trisodium phosphate has been in cleaning agents. The pH of a 1% solution is 12 (i.e., very basic ), and the solution is sufficiently alkaline to saponify grease and oils.