Sodium Xylene Sulfonate CAS 1300-72-7

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  • Appearance: Colorless liquid
  • Assay: 99. 0%min
  • Stock: In stock
  • Sample: Available
  • Zhishang Chemical: Sodium xylene sulfonate supplement

Basic Info of Sodium Xylene Sulfonate

What is Sodium Xylenesulfonate?

Sodium xylenesulfonate is a water-soluble promoter, a natural compound that enhances the capability of water to liquify various other molecules. Sodium xylenesulfonate is a reduced risk material as well as the risk of adverse health effects connected with work and customer use of the chemical is expected to be low.

Sodium xylenesulfonate can be used in hair shampoos, household and dishwashing detergents, dry cleaners, tough surface area as well as metalworking cleansers, fungicides, adhesives, dyes and also pigments, electroplating, oiling cutting oils, photographic products, inks, textiles, tanning, and so on.

Sodium Xylene Sulfonate Uses

  1. Sodium xylenesulfonate is a water-soluble marketer, which is used to liquify hydrophobic substances and likewise utilized in the research study of liposome system in aqueous service.
  2. Sodium xylenesulfonate service can be used in chemical synthesis.
  3. Sodium xylenesulfonate is a brand-new and also reliable solubilizing conditioner for cleaning products with reduced poisoning.
  4. Sodium xylenesulfonate is made use of in liquid home detergents as well as hair shampoos, degreasing compounds as well as printing Size made use of in textile sector. It is likewise a surfactant in individual treatment products (mainly shampoo) due to the fact that it can be made use of as a clarifier or moistening agent to assist the formula apply even more conveniently.
  5. Sodium xylenesulfonate is also utilized to draw out pentosan and lignin in the paper sector and as an adhesive additive in the natural leather sector.

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Is Sodium Xylene Sulfonate a Surfactant?

Sodium xylenesulfonate is not a genuine surfactant, it can just be a co-solvent: sulfonate is hydrophilic as well as xylyl is lipophilic, but it is not extremely reliable in reducing surface area tension, besides, its molecular chain is as well brief.

Surfactants are substances that decrease the surface area tension (or interfacial stress) in between 2 liquids, in between gases and also fluids, or between fluids and also solids. Surfactants can be utilized as cleaners, moistening representatives, emulsifiers, lathering representatives or dispersants. The term “surfactant” is a mix of surfactants. Reagents that increase surface area stress are essentially “surfactants”, but they are not called surfactants because their role contrasts the typical definition. A typical example of an increase in surface stress is salting out: by adding inorganic salts to an aqueous remedy of a weakly polar material, the compound will speed up. The compound itself may be a surfactant – one of the reasons lots of surfactants are ineffective in seawater. 

Surfactants are generally amphiphilic organic substances, which suggests that they include both hydrophobic teams (their tails) as well as hydrophilic groups (their heads). For that reason, surfactants include both water-insoluble (or oil-soluble) parts and also water-soluble components. When water as well as oil are blended, the interface in between air and also water or in between oil and also water. Water insoluble hydrophobic groups can expand out of the primary liquid stage, into the air or into the oil stage, while water-soluble head groups continue to be in the aqueous stage.
Surfactants are split into ionic surfactants and nonionic surfactants.

Are Sodium Xylene Sulfonate and Sodium p-toluenesulfonate the Very Same Item?

Sodium p-toluenesulfonate comes from sodium xylenesulfonate, yet sodium xylenesulfonate is not always sodium p-toluenesulfonate, the two come from the relationship of inclusion as well as belonging.


  1. Sodium xylenesulfonate – ChemicalBook
  2. Sodium xylene sulfonate – Product Stewardship Summary
  3. Sodium xylenesulfonate – PubChem
  4. “Bubbles, Bubbles, Everywhere, But Not a Drop to Drink”The Lipid Chronicles. 11 November 2011. Archived from the original on 26 April 2012. Retrieved 1 August 2012.

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