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Sodium dodecyl aulfate powder is an organic compound with the chemical formula C12H25SO4Na and CAS 151-21-3, white or light yellow powder, easily soluble in water, slightly soluble in ethanol, almost insoluble in chloroform, ether and light petroleum, insensitive to alkali and hard water . It has decontamination, emulsification and excellent foaming power. It is an anionic surfactant that is slightly toxic to the human body, and its biodegradation degree is >90%. It has the characteristics of good emulsification, foaming, water solubility, biodegradability, alkali resistance, hard water resistance, stability in aqueous solution with a wide pH value, easy synthesis, and low price, and has been widely used in Cosmetics, detergents, textiles, papermaking, lubrication, pharmaceuticals, building materials, chemicals, oil extraction and other industries can also be used in basic research on the properties of positive and negative ion surfactant compound systems, micellar catalysis, and molecular orderly assemblies.

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Chemical Formula |
C12H25NaO4S |
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Exact Mass |
288 |
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Molecular Weight |
288 |
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m/z |
288 (100.0%), 289 (13.0%), 290 (4.5%) |
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Elemental Analysis |
C, 49.98; H, 8.74; Na, 7.97; O, 22.19; S, 11.12 |
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Sodium dodecyl aulfate powder (SDS), also known as Sodium Lauryl Sulfate K12, It is a white or light yellow slightly viscous powder, belonging to anionic surfactants. Its molecular structure contains hydrophobic dodecyl chains and hydrophilic sulfate groups, which give it core functions such as emulsification, foaming, permeation, decontamination, and dispersion. As one of the most widely used surfactants in the industrial field, SDS has penetrated into more than 20 industries such as daily chemical, textile, food, medicine, energy, and environmental protection, becoming an indispensable basic raw material for modern industry.
1. Cleaning product system
SDS is a fundamental component in the detergent industry, accounting for 10% -20% of laundry detergent, dishwashing detergent, and dishwashing detergent. Its decontamination mechanism is achieved through micellar action: hydrophobic alkyl chains adsorb oil stains, hydrophilic sulfate groups combine with water to form micelle structures with a diameter of 5-10 nanometers, dispersing oil droplets in water. The emulsification efficiency of SDS for sebum and protein stains is more than three times higher than that of traditional soap bases. In the formula of dishwashing detergent, the combination with sodium citrate can increase the emulsification efficiency of tableware oil by 40%, and the residual amount is less than 0.01ppm.
3. Special cleaning scenarios
The hard water resistance of SDS (tolerance to 500ppm mineralization) makes it outstanding in industrial cleaning:
Metal degreasing: In the cleaning of automotive parts, 0.5% -1% SDS solution can quickly remove oil stains, and the cleaning efficiency is 50% higher than traditional solvents.
Equipment cleaning: In the cleaning of petrochemical pipelines, the alkaline emulsion system formed by the combination of SDS and sodium hydroxide can remove more than 95% of heavy oil scale.
2. Personal care products
In the field of cosmetics, SDS plays multiple roles:
Foaming agent: the concentration of shampoo and shower gel is controlled at 1% -5%, which can produce dense foam with a diameter of 0.1-0.5mm, improving the use experience. Adding 0.5% -2% SDS to toothpaste can not only assist in removing dental plaque, but also disperse active ingredients such as fluoride.
Cleaning agent: SDS in facial cleanser effectively removes oil and dirt from the skin surface by reducing the surface tension to 25-30mN/m. At the same time, when combined with glycerin, it can alleviate dryness.
Moisturizing agent: SDS in skincare products can promote the penetration of ingredients such as vitamin C and hyaluronic acid, and experimental data shows that its transdermal absorption rate is increased by 25% -30%.
The driving force behind the upgrading of the textile industry
1. Pre treatment process
SDS, as a bleaching and dyeing aid, can significantly improve the quality of textiles
Bleach Efficiency Enhancement: In the oxygen bleaching process of cotton fabrics, adding 1-2g/L SDS can increase whiteness by 8-10 degrees and reduce fiber damage.
Dyeing uniformity: In carpet dyeing, the permeability of SDS ensures uniform adsorption of dye molecules, and the color difference Δ E value is controlled within 1.5.
2. Post organizing techniques
SDS plays a key role in textile finishing:
Wool cleaning: A 0.5% -1% SDS solution can remove impurities between the layers of wool scales while maintaining fiber strength, reducing the shrinkage rate by 30%.
Leather softness: In the leather retanning process, the combination of SDS and chrome tanning agents can improve leather softness and increase bending fatigue times by 40%.
Compliance application in the food industry
According to the GB 2760-96 standard, SDS as a food processing aid has strict limits:
Baking products: The maximum usage amount in cakes is 0.5g/kg, which can improve the emulsion stability of batter and increase the volume expansion rate of cakes by 15% -20%.
Beverage industry: Adding 0.1-0.3g/kg SDS to fruit juice beverages can prevent fruit pulp precipitation and extend shelf life by 30%.
Edible oil processing: In the refining of vegetable oil, SDS as a demulsifier can remove more than 90% of phospholipids, significantly improving the transparency of the oil.
1. Pharmaceutical formulation technology
SDS demonstrates multiple values in drug development:
Solubilization effect: By forming a micelle structure, SDS can increase the solubility of poorly soluble drugs (such as aspirin) by 100-1000 times and accelerate the dissolution rate by 50%.
Transdermal absorption: In amlodipine gel, SDS and propylene glycol work together to improve the transdermal absorption efficiency by 50% and the bioavailability by 65%.
Emulsion stability: As the core emulsifier of O/W emulsion, the combination of SDS and glycerol monostearate can optimize the particle size distribution (D50=2.5 μ m) of progesterone cream and increase viscosity stability by 30%.
2. Bioanalytical technology
SDS is irreplaceable in protein research:
SDS-PAGE electrophoresis: 1-2% SDS can denature proteins and uniformly carry negative charges, with a separation accuracy of one thousandth of the molecular weight difference, making it a fundamental tool for proteomics research.
Virus inactivation: 0.1-0.5% SDS can destroy the envelope structure of HIV, influenza virus and other viruses, and is used for disinfection of vaccine production equipment with an inactivation rate of 99.99%.
1. Innovation in energy extraction
SDS achieves technological upgrading in the petroleum industry:
Oil recovery emulsifier: In tertiary oil recovery, SDS can form a stable emulsion, increasing recovery rate by 8% -12% and daily production per well by 3-5 tons.
Mine fire extinguishing: as the core component of foaming agent, SDS based foam liquid can cover the fire source within 30 seconds, and its oxygen isolation efficiency is 40% higher than that of traditional foam, which is suitable for fire extinguishing in confined spaces such as coal mines.
2. Environmental technology innovation
Sodium dodecyl aulfate powder demonstrates new value in pollution control:
Wastewater treatment: Modified zeolite adsorbent (SMZ) combined with SDS achieved a removal rate of 53.1% for hydrate inhibitor (KHI), providing an economic solution for high salt wastewater treatment.
Soil remediation: The combination of SDS and EDTA can activate heavy metals in soil, increasing chelation efficiency by 25% compared to a single reagent and shortening the remediation period by 40%.
3. Preparation of new materials
SDS plays a crucial role in the synthesis of nanomaterials:
Graphene dispersion: As a dispersant, it can improve the uniformity of graphene conductive coatings and reduce the square resistance to below 50 Ω/□.
Quantum dot synthesis: The SDS controlled microreaction environment can reduce the particle size distribution width (PDI) of CdSe quantum dots to below 0.1, and increase the fluorescence quantum yield to 80%.
1. Agricultural technology
SDS achieves increased efficiency in pesticide formulations:
Spray coverage: As an additive, it can reduce the surface tension of the pesticide solution to 22mN/m, reduce the contact angle of the pesticide on the leaf surface to below 15 °, and increase coverage by 35%.
Slow release technology: The microcapsule structure formed by the combination of SDS and chitosan can extend the pesticide release cycle to 30 days and increase the duration of efficacy by three times.
2. 3D printing materials
SDS improves printing performance in photopolymerization resin:
Flattenness: Adding 0.5% -1% SDS can reduce the surface tension of the resin to 28mN/m and the depth of printed layer patterns to below 0.02mm.
Demoulding ability: The release agent formed by the combination of SDS and silicone oil can reduce the peeling force between printed parts and molds to below 0.5N, and increase the yield rate to 98%.

1. Put 9.5mL of glacial acetic acid into a dry reaction bottle in a fume hood, fully cool in an ice bath, add 3.5mL (0.053mol) of chlorosulfonic acid, and mix well. Slowly add 8g (0.043mol) of dodecanol in liquid form or in the form of very fine solid powder to cold acetic acid and chlorosulfonic acid in 5 minutes, and stir for 30 minutes until all the alcohol is dissolved and participates in the reaction. If the alcohol was not completely dissolved, the reaction bottle was taken out from the ice bath, and stirred at room temperature for 10 min. Pour the reaction material into a beaker filled with 30g of crushed ice, add 30mL of n-butanol to the above mixture, and stir for 3min. Slowly add 3mL saturated sodium carbonate aqueous solution under stirring, the solution is alkaline to litmus paper. When the reaction is alkaline, add 10 g of solid anhydrous sodium carbonate and let stand. Pour the upper n-butanol solution from the surface of the water layer into a beaker. Add 20 mL of n-butanol to the water layer, stir well, and separate the n-butanol layer. The n-butanol obtained twice was combined, poured into a separatory funnel to separate the layers, and the water layer was separated. Pour the n-butanol solution into a beaker and evaporate the n-butanol to obtain a white residue which is sodium dodecyl aulfate.

2. Sulfur trioxide method: The reaction device is a vertical reactor. Nitrogen was introduced into the reactor at 32°C through the gas sparge. The nitrogen flow rate is 85.9 L/min. Lauryl alcohol was introduced at 82.7kPa with a flow rate of 58g/min. The liquid sulfur trioxide is passed into the flasher at 124.1 kPa, the flash temperature is maintained at 100°C, and the flow rate of sulfur trioxide is controlled at 0.9072kg/h. Then the sulfated product is rapidly cooled to 50°C, put into the aging device, and left for 10-20 minutes. Finally, put it into the neutralization kettle and neutralize it with alkali. The neutralization temperature is controlled at 50°C, and the liquid product is obtained when the pH value reaches 7-8.5. Spray drying to obtain a solid product.
3. Add 62g of lauryl alcohol into a 250mL four-neck flask equipped with a hydrogen chloride absorption device, a thermometer, an electric stirrer and a dropping funnel, and control the temperature at 25°C. Slowly add 24mL of chlorine through the dropping funnel within 30min under full stirring. For sulfonic acid, the temperature should not exceed 30°C when adding dropwise, pay attention to foaming and prevent the material from overflowing. After adding chlorosulfonic acid, react at 30°C for 2 hours, and absorb the hydrogen chloride gas generated during the reaction with 5% sodium hydroxide solution. After the sulfation is completed, slowly pour the sulfate into a mixture containing 100g of ice and water (ice: water = 2: 1), while fully stirring, and cool the outside with an ice-water bath. Finally, all the reactants in the four-necked flask were washed out with a small amount of water. After uniform dilution, 30% mass fraction of Sodium Dodecyl Aulfate Powder was added dropwise with stirring to neutralize to pH 7-8.5. Then extract with n-butanol and evaporate the n-butanol.
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