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HS Code |
267367 |
| Chemical Name | Sodium Tetradecyl Sulfate |
| Alternative Names | STS, Tetradecyl Sulfate Sodium Salt |
| Chemical Formula | C14H29NaO4S |
| Molar Mass | 332.43 g/mol |
| Appearance | White or off-white powder |
| Solubility In Water | Highly soluble |
| Cas Number | 1191-67-9 |
| Melting Point | 204-207 °C |
| Boiling Point | Decomposes before boiling |
| Usage | Sclerosing agent in medical treatments |
| Ph Of 1 Percent Solution | 7.5–9.5 |
| Storage Conditions | Store in a cool, dry place, away from incompatible substances |
| Odor | Characteristic mild odor |
As an accredited Sodium Tetradecyl Sulfate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100 mL amber glass bottle with a secure cap, labeled “Sodium Tetradecyl Sulfate Solution, 3% w/v,” for laboratory use. |
| Shipping | Sodium Tetradecyl Sulfate should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Handle with care to avoid spills and leaks. Transport must comply with applicable regulations for hazardous chemicals, including proper labeling and documentation. Store upright, in a cool, dry place during transit. |
| Storage | Sodium tetradecyl sulfate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Keep containers clearly labeled and protected from physical damage. Store at room temperature, and ensure spill containment measures are available. Follow all applicable local and national regulations for chemical storage. |
Applications of Sodium Tetradecyl Sulfate in Industrial ManufacturingOur sodium tetradecyl sulfate integrates as a specialty ingredient across select industrial supply chains, delivering controlled functional performance in line with strict global compliance requirements. Below we detail verified downstream manufacturing scenarios where this material forms a critical input, outlining sector-specific standards, process roles, dosage ranges, and end-use product classes based on field expertise and customer formulation data. 1. Pharmaceutical Injection Sclerotherapy AgentsProducers of intravenous sclerosing preparations depend on high-purity sodium tetradecyl sulfate to achieve precise irritation and vein collapse effects during treatment of varicose veins. The ingredient functions as the active sclerosing compound, demanding exacting formulation protocols, validated injection system compatibility, and regulatory data for finished drugs entering regulated markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Topical Dermatological Formulations (Prescription Foams and Solutions)Skin medication manufacturers incorporate sodium tetradecyl sulfate for cutaneous formulations requiring potent surface wetting and local sclerosing action. Product-focused R&D teams specify the material in dermal applications to treat conditions like venous malformations and certain birthmarks. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Industrial Cleaning and Wetting Agent for Precision MetalworkingSpecialty metal processing lines use sodium tetradecyl sulfate as a controlled wetting and emulsifying agent during the degreasing stage of stainless, aluminum, and copper parts manufacturing. Chemical engineers quantify its addition to ensure rapid debris dispersion, minimize surface re-deposition and support corrosion-free outcomes post-cleaning. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Latex and Emulsion Polymerization for Industrial AdhesivesMajor polymer resin manufacturers introduce sodium tetradecyl sulfate as a primary emulsifier in the synthesis of styrene-butadiene and acrylic adhesives. The agent supports uniform micelle formation, critical for target particle size control, polymer chain dispersion, and final bond line consistency in automotive, construction, and packaging adhesives. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Laboratory Diagnostics and In Vitro Medical ConsumablesManufacturers of diagnostic reagent kits formulate sodium tetradecyl sulfate as a cell lysis and protein-denaturing component in sample preparation. Its function is validated for clinical chemistry and hematology devices where reproducible solubilization assures accurate downstream detection and analysis. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Every day in the plant, we work with raw materials that shape practical outcomes instead of just ticking off boxes on a spec sheet. Sodium tetradecyl sulfate (STS) is not a stranger here—its familiar scent, appearance, and handling quirks offer a different perspective compared to similar surfactants. Over the decades, we've produced and refined STS mainly for specialized applications, learning through direct feedback from doctors, researchers, and industry partners rather than trade rumors or untethered marketing. Unlike agents that only promise surface activity, this compound walks the line between just the right degree of hydrophobic and hydrophilic character with a 14-carbon chain that brings its own character to every batch.
Anyone who steps into our finishing area can see the difference between this product and shorter, less selective alkyl sulfates. Every batch starts with a careful alcohol derivation process, where chain length isn’t a guessing game—it’s controlled and monitored. You end up with a fine, white to slightly off-white powder or granule that dissolves smoothly in water, producing a clear to slightly opalescent solution. The model we produce most consistently responds to the pharmaceutical grade, where strict purity standards exceed those found in regular detergents. Our feedstocks and sulfonation lines get cleaned and validated for each run, and we stick to sodium tetradecyl sulfate with minimal unsulfonated residue. Chloride and sulfate content, pH value, and allergen trace screening remain integrated into our QC routines for each shipment.
STS commands notice for therapies that require targeted interaction with biological tissues rather than just broad-based cleansing. In real-world use, the cosmetic and detergent sectors reach for the cheaper, blended alkyl sulfates with shorter carbon chains. They work for general foaming, cleaning, and wetting, but can’t match the performance consistency and biological tolerance that comes from STS. Our customers in the healthcare and pharmaceutical fields, especially manufacturers of sclerotherapy solutions, bring questions about purity, solubility, and trace contaminants, so every run leans toward analytical transparency. The chain length doesn’t just affect foaming and emulsification—it's directly tied to tissue selectivity and irritation potential in medical use. Compared to sodium lauryl sulfate (with a 12-carbon backbone), STS offers different interaction with membranes, which translates into more predictable results and fewer side effects.
Spending time around the reactors means picking up more than data—you get a nose for contamination, a feel for granule texture right before drying, and an instinct for where batches might deviate. Sodium tetradecyl sulfate isn’t just another powder. It flows, but not as freely as sodium lauryl sulfate; it absorbs humidity faster, requiring storage in rooms with positive pressure and low humidity. Any cross-contamination ruins the batch—not a lesson you forget after years of recleaning bins and reworking packaging lines. Even the antistatic methods we use differ from those for shorter or branched-chain analogs. This kind of attention to practical detail rarely finds its way onto sales fliers or trade show banners, but it determines which facilities can truly deliver consistent, reliable material.
Some partners ask why certain lots cost more or process differently than multi-purpose alkyl sulfates. Here, production doesn’t cut corners: average molecular weight, active matter, and residual solvent limits stay within tight windows, batch after batch. High-pressure liquid chromatography (HPLC) and gas chromatography (GC) analyses measure residual alcohols and confirm chain uniformity. Any batch drifting outside the set 98-102 percent active range never leaves the warehouse. Heavy metal analysis and residual organic solvent tests add other layers of control. Compared to commodity surfactants, the stability and minimal impurity levels keep customers coming back. A client working with injectable sclerosing agents doesn’t want surprises—no rogue fats, no off-odors, zero foreign ions above regulatory limits. Our entire approach reflects the real-life stakes involved in medical production.
It’s common for customers to ask about switching from sodium lauryl sulfate (SLS) or sodium decyl sulfate (SDS) to our fourteen-carbon line. These products share the same sulfate ester backbone but diverge sharply at the surface and biological interfaces. STS forms micelles with higher hydrophobicity, which means different wetting patterns and solubilization profiles. You can see it directly in solubility tests with dyes, oils, and biopolymers. In our experience, processing a batch of STS calls for more controlled temperatures, longer dissolution times, and careful monitoring for early gel formation—an issue that rarely crops up with lauryl or decyl analogs. For cleaning formulations needing milder action or lower irritation, the shorter chains do the job. For controlled delivery or sclerosing applications, STS leaves a different footprint, interacting with tissue and cellular membranes in ways that other surfactants simply can’t match.
Our relationship with the medical sector offers decades of perspective on how this compound works beyond the textbook. Sclerotherapy depends on predictable surface activity, low allergenicity, and reliably low levels of organic and inorganic impurities. You quickly learn that slight changes in upstream quality control or alcohol sources can influence the clinical side, even in microgram quantities. An off-odor or slight color change can ruin user confidence and mean the difference between clinical use and chemical waste. Practitioners remind us in direct language about the importance of product consistency—batch deviations matter, and so do metal and organic residuals far below legal limits. These aren’t abstract concerns, and each message from a clinician, pharmacist, or regulatory body triggers another check on our lines.
Environmental responsibility carries weight here. Direct waste reduction starts in the reactor optimization phase, where we minimize byproducts and avoid wasteful intermediate steps. Our wash water circuits run closed-loop, with product and solvent recovery designed into every new line. We moved to more efficient distillation and drying units based on feedback from years of monitoring, not just regulatory mandates. We recognize that STS, while biodegradable with the right effluent control, still requires the right protocols for final treatment and washdown. Local aquatic systems responded well to our reduced-discharge efforts over the last decade, something we verified through independent water sampling and regular audits. Our experience says the cost and inconvenience of proper environmental monitoring pale in comparison to the long-term liability of shortcuts.
Researchers approach us with varied requests—from controlled emulsification for drug delivery microspheres to fine-tuned surface tension reduction for analytical-grade separations. STS’s unique properties fit where generic or mixed-chain surfactants fall short. We work directly with project labs to dial in the micron-level control they need. The compound offers particular value where controlled membrane disruption, selective solubilization, or protein denaturation play central roles. Proteomics labs point to our documentation for purity and trace elements, since small differences in residual metal ions or trace alcohols can foul up entire setups. Experience shows that regulatory approval for new protocols hinges on traceable, consistent input chemicals. Our approaches to validation and lot history grew from direct conversations with research users clarifying what works and what gets in the way.
Sodium tetradecyl sulfate calls for specific treatment every step of the way. We avoid bulk shipping in unlined totes. Instead, lined fiber drums or sealed, moisture-tight bags shield the powder from ambient humidity, which quickly clumps or degrades open storage material. The warehouse runs on low humidity and temperature control, with serialized tracking for every batch. Experience deserves a mention here: early clients taught us that improper transport and decanting made more difference to product acceptance than paperwork or branding. Today, routine inspections back up every shipment and prevent problems before they arise. Storage remains strict—even on the plant floor, partial drums don’t sit exposed for long.
Quality doesn’t exist in a vacuum. Over the years, our documentation requirements changed alongside evolving regulatory and pharmacopoeial lists worldwide. STS headed for clinical use faces more scrutiny, both on-site and from external audit teams. Our process lines use validated cleaning routines and traceability records for each shift and batch, which stands up during audits by pharmaceutical partners. Allergen, heavy metal, and microbial screenings keep up with the latest international expectations. Our plant’s track record for non-conformances and recalls owes a lot to tight enforcement: changes to input chemistry, waste handling, or packaging get validated before routine use. Every shift working with STS means balancing tight control with practical adaptability.
Feedback from long-term users defines success more than shelf-life or a shiny brochure. Mistakes early on showed us that even subtle handling differences—from open-container dosing to environmental conditions in mixing rooms—can affect the end use of sodium tetradecyl sulfate, sometimes in ways even expert users don’t expect. Listen to your customers, especially those in hospitals, labs, and specialty manufacturers. We receive samples and reports that guide product consistency, sometimes pushing us to refine particle size or adjust our drying step for an improved dissolution rate. We openly share updates and recall the few deviations from the past to avoid repetition. True reliability means owning missteps and keeping improvement cyclical, not one-off.
The market landscape for specialty surfactants never stands still. Demand pushes up and down with clinical trends, regulatory shifts, and raw material volatility. The pandemic years showed us exactly how brittle some supply chains are for the right-grade alcohols, processing aids, and skilled labor. Advance planning, dual-sourcing, and investing in backup storage kept our clients supplied when competitors paused deliveries. Even as commodity surfactants fill mass-market needs, producing sodium tetradecyl sulfate with consistent, analytical quality takes more than a stocked warehouse—it takes foresight into external shocks and transparent communication from factory floor to delivery dock.
Challenges remain, such as tightening environmental restrictions, new pharmacopeia monographs, and the need for even finer degrees of traceability. Our experience says that transparency—both upstream and downstream—answers these pressures best. Digital batch codes track all main inputs and receipts. Continued investment in analytical method validation, and regular staff retraining act as brakes against error and lapses, particularly as international standards rise. Layering in automation where it counts (not everywhere) helps with error trapping, but no machine replaces hands-on, experienced staff. Open communication with users guides us to refine specifications for sensitivity, solubility, or purity rather than chasing abstract targets.
Years of handling STS gave us specific, practical knowledge. Routine tasks—like controlling exhaust and humidity during granulation, or triple-checking for allergenic residues—translate into stable supply for workers who need more than an off-the-shelf solution. We don’t just meet labels or paperwork. Each batch leaving our plant stands behind experience and pride in making something that counts. This product reaches clinics, researchers, and formulators who expect not surprises, but certainty. Our team’s day-to-day focus on texture, scent, granularity, and finished packaging keeps each lot truly ready for the next step, wherever the world ships it.