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  2. Hydrotrope - Wikipedia

    en.wikipedia.org/wiki/Hydrotrope

    The chemical structure of the conventional Neuberg's hydrotropic salts (proto-type, sodium benzoate) consists generally of two essential parts, an anionic group and a hydrophobic aromatic ring or ring system. The anionic group is involved in bringing about high aqueous solubility, which is a prerequisite for a hydrotropic substance.

  3. Sodium nonanoyloxybenzenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_nonanoyloxybenzenes...

    Sodium nonanoyloxybenzenesulfonate (NOBS) is an important component of laundry detergents and bleaches. It is known as a bleach activator for active oxygen sources, allowing formulas containing hydrogen peroxide releasing chemicals (specifically sodium perborate , sodium percarbonate , sodium perphosphate , sodium persulfate , and urea peroxide ...

  4. File:Sodium xylene sulfonate.svg - Wikipedia

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

    This file contains additional information, probably added from the digital camera or scanner used to create or digitize it. If the file has been modified from its original state, some details may not fully reflect the modified file.

  5. Sulfonate - Wikipedia

    en.wikipedia.org/wiki/Sulfonate

    The sulfonate ion. In organosulfur chemistry, a sulfonate is a salt, anion or ester of a sulfonic acid. Its formula is R−S(=O) 2 −O −, containing the functional group −S(=O) 2 −O −, where R is typically an organyl group, amino group or a halogen atom. Sulfonates are the conjugate bases of sulfonic acids.

  6. Sodium benzenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_benzenesulfonate

    Sodium benzenesulfonate is an organic compound with the formula C 6 H 5 SO 3 Na. It is white, water-soluble solid, It is produced by the neutralization benzenesulfonic acid with sodium hydroxide. It is also a common ingredient in some detergents. The compound typically crystallizes from water as the monohydrate. [1]

  7. Xylene - Wikipedia

    en.wikipedia.org/wiki/Xylene

    The physical properties of the isomers of xylene differ slightly. The melting point ranges from −47.87 °C (−54.17 °F) (m-xylene) to 13.26 °C (55.87 °F) (p-xylene)—as usual, the para isomer's melting point is much higher because it packs more readily in the crystal structure. The boiling point for each isomer is around 140 °C (284 °F).

  8. Organosulfate - Wikipedia

    en.wikipedia.org/wiki/Organosulfate

    Sodium laurylsulfate tested on Uronema parduczi, a protozoan, was found to have the lowest effect value with the 20 h-EC5 being 0.75 milligrams per litre (2.7 × 10 −8 lb/cu in). Chronic exposure tests with C 12 to C 18 with the invertebrate Ceriodaphnia dubia found the highest toxicity is with C 14 ( NOEC was 0.045 mg/L).

  9. Sulfone - Wikipedia

    en.wikipedia.org/wiki/Sulfone

    The structure of a sulfone Dimethyl sulfone, an example of a sulfone. In organic chemistry, a sulfone is a organosulfur compound containing a sulfonyl (R−S(=O) 2 −R’) functional group attached to two carbon atoms.