Sodium Dodecyl Sulfate
Sodium dodecyl sulfate is an anionic surfactant with cleaning, emulsification, foaming and other properties. It is widely used in daily chemicals, medicine, food and other fields.

- Definition
- Features
- Applications
- Qualifications
- FAQs
- Case Study
- Online Inquiry

What is Sodium Dodecyl Sulfate?
Sodium dodecyl sulfate is an organic compound with a chemical formula of C12H25SO4Na. It is a white or light yellow powder that is easily soluble in water and insensitive to alkali and hard water. It has cleaning, emulsification and excellent foaming power. It is an anionic surfactant with a biodegradability of >90%.
What are the Features of Sodium Dodecyl Sulfate?

Strong Foaming Property
Foam height ≥180mm, fine and long-lasting foam.

Excellent Emulsification Ability
Significantly reduces oil-water interfacial tension and forms a stable O/W emulsion.

Strong Detergency
Efficient decontamination is achieved by encapsulating grease with micelles.
What are the Applications of Sodium Dodecyl Sulfate?

Personal Care Products
Sodium dodecyl sulfate is used as a foaming agent and surfactant to provide rich foam and cleaning effects.

Industrial Use
Sodium dodecyl sulfate is used in emulsion polymerization and industrial use to control particle size.

Medicine and Scientific Research
Sodium dodecyl sulfate can be used as a detergent for protein electrophoresis, a drug emulsifier, and a cell lysis component.

Special Application
Sodium dodecyl sulfate can also be used as a fire extinguishing foam liquid.
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Question and Answer
Case Study
Growth Studies of Sodium Dodecyl Sulfate Micelles
Quina, Frank H., et al. The Journal of Physical Chemistry 99.46 (1995): 17028-17031.An equation was derived that predicts the size of alkyl sulfate micelles as a function of detergent or added counterion salt concentration. When applied to sodium dodecyl sulfate, the micelles are expected to vary as the 1/4 power of the total common counterion concentration in the aqueous phase, which is in good agreement with recent TRFQ and with measurements using a variety of techniques. The size behavior of other alkyl sulfates is predicted.
Apparent surface tension was determined using a surface tensiometer. Emission measurements were performed on air-equilibrated solutions using a fluorescence spectrometer. Aggregation number was determined using the method of Turro and Yekta.I6 Serial aliquots of a concentrated (0.2 M) stock solution of 9-methylanthracene in spectroscopic quality acetonitrile were added to an aqueous solution containing the emission probe sodium dodecyl sulfate, and the emission intensity after each addition was recorded.
