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  2. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    Alkyl sulfates if ingested are well-absorbed and are metabolized into a C 3, C 4 or C 5 sulfate and an additional metabolite. The highest irritant of the alkyl sulfates is sodium laurylsulfate, with the threshold before irritation at a concentration of 20%. Surfactants in consumer products are typically mixed, reducing likelihood of irritation.

  3. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  4. Sodium sulfate (data page) - Wikipedia

    en.wikipedia.org/wiki/Sodium_sulfate_(data_page)

    1 Material Safety Data Sheet. ... 5 References. Toggle the table of contents. Sodium sulfate (data page) ... This page provides supplementary chemical data on sodium ...

  5. Solubility table - Wikipedia

    en.wikipedia.org/wiki/Solubility_table

    Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75

  6. Isethionic acid - Wikipedia

    en.wikipedia.org/wiki/Isethionic_acid

    Fatty acid esters of isethionic acid (such as sodium lauroyl isethionate and sodium cocoyl isethionate) are used as biodegradable anionic surfactants. [3] These materials are much milder to skin that other sulfate based surfactants (i.e. sodium lauryl sulfate) [4] making them popular for use in make-up, shampoos and detergent bars including those made by Dove.

  7. α-Olefin sulfonate - Wikipedia

    en.wikipedia.org/wiki/Α-Olefin_Sulfonate

    α-Olefin sulfonates with linear alkenyl radicals from C 12 to C 18 are used as anionic surfactants in various areas of application due to their pronounced foam formation [clarification needed] and foam stability (even with high water hardness), excellent fat-dissolving power and oil dissolving power as well as a favorable ecological profile and low aquatic toxicity and human toxicity.

  8. File:Sodium alkyl sulfates structure.svg - Wikipedia

    en.wikipedia.org/wiki/File:Sodium_alkyl_sulfates...

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  9. Hydroxysultaine - Wikipedia

    en.wikipedia.org/wiki/Hydroxysultaine

    Hydroxysultaine is prepared industrially by the reaction of sodium bisulfite with epichlorohydrin to give the sodium salt (sodium 1-chloro-2-hydroxypropane sulfonate). [1] This is similar to the synthesis of isethionate , which is also used as a 'head-group' in surfactants.