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HS Code |
648029 |
| Chemical Name | Sodium Edetate |
| Also Known As | Disodium EDTA |
| Cas Number | 139-33-3 |
| Molecular Formula | C10H14N2Na2O8 |
| Molecular Weight | 336.21 g/mol |
| Appearance | White crystalline powder |
| Solubility In Water | Very soluble |
| Ph Range 1 Percent Solution | 4.0 - 6.0 |
| Usage | Chelating agent |
| Storage Conditions | Store in a cool, dry place |
| Melting Point | Approximately 242°C (decomposes) |
| Odor | Odorless |
| Stability | Stable under recommended storage conditions |
As an accredited Sodium Edetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic HDPE drum labeled "Sodium Edetate, 25 kg," with hazard symbols, batch number, and manufacturer details in bold. |
| Shipping | Sodium Edetate, also known as EDTA disodium salt, should be shipped in tightly sealed containers, protected from moisture and contaminants. During transport, ensure containers are clearly labeled and stored in cool, dry conditions. Follow all applicable regulations for chemical shipping and handling to prevent spills, leaks, or accidental exposure. |
| Storage | Sodium Edetate should be stored in a tightly closed container, protected from light and moisture, at a temperature below 25°C. It should be kept in a dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents and acids. Proper labeling and secure storage help prevent contamination or accidental mixing with other chemicals. |
Applications of Sodium Edetate in Industrial ManufacturingSodium Edetate serves key chelation and stabilization roles in industrial production. Below, we detail primary downstream sectors and process-specific usage as integrated by formulators and process engineers in large-scale manufacturing. 1. Pharmaceutical Formulations: Parenteral and Ophthalmic SolutionsPharmaceutical manufacturers rely on this chelating agent to control metal ion-catalyzed degradation and improve product stability in liquid drug formulations. Production teams introduce it during solution compounding for parenteral and ophthalmic preparations, ensuring consistent shelf-life and efficacy by preventing oxidation and discoloration. Only pharmaceutical-grade material, compliant with compendial standards, is used in injectable and eye drop production after qualification through analytical validation within aseptic environments. Industry compliance standards
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2. Food and Beverage Processing: Preservation and Color RetentionFood technologists integrate sodium edetate during the processing of canned vegetables, seafood, and beverages to inhibit oxidative browning and maintain product appearance. Its chelation of iron and copper traces helps preserve color and prevents turbidity in transparent beverages. Food-grade quality is crucial, and all use must strictly follow jurisdictional food additive regulations. Manufacturers use continuous dosing systems or batch addition, optimizing dosage to avoid exceeding allowable daily intake limits and meet label declarations. Industry compliance standards
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3. Personal Care Formulations: Creams, Lotions, and Hair ProductsCosmetic chemists use this ingredient in skincare, haircare, and cream formulations to improve formula stability and minimize color or fragrance degradation. It acts by binding disruptive metal ions introduced either through raw materials or process water. Cosmetic GMP controls and regional ingredient regulations guide the handling and dosing of the chelating agent in both leave-on and rinse-off products. Manufacturer QC teams conduct regular challenge tests for preservative synergy and stability in finished formulations. Industry compliance standards
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4. Water Treatment: Boiler, Cooling, and RO System ConditioningIndustrial water treatment specialists rely on sodium edetate for conditioning feed water and preventing scaling or metal-catalyzed fouling in boilers, cooling circuits, and reverse osmosis (RO) plants. By chelating iron, manganese, and calcium traces, the additive contributes to equipment longevity and reduced maintenance. Dosage and monitoring protocols align with plant-specific water profiles and local environmental discharge regulations. Strict operational records and calibration of dosing pumps ensure industrial system efficiency without regulatory overage. Industry compliance standards
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5. Industrial Cleaning and Detergents: Metal Cleaning and Textile ProcessingDetergent and cleaning chemical manufacturers incorporate sodium edetate in liquid and powder formulations for metal surface cleaning, textile desizing, and bottle washing solutions. The agent’s chelating action enhances removal of scale, rust, and dirt from metals and improves results in hard water conditions. Industrial-scale batches closely regulate content to avoid excessive environmental loading, following both product guidelines and effluent limitations in process plant discharges. Industry compliance standards
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6. Laboratory Diagnostics and Reagents: Sample Collection and Analysis KitsProducers of diagnostic kits and clinical reagents deploy sodium edetate to prevent coagulation and metal ion interference in blood and biological sample tubes, as well as to stabilize sensitive solutions for in vitro testing. Only high-purity analytical grades are used, with cross-validation against assay panels to avoid cross-reactivity or interference. QA teams monitor every incoming and outgoing batch against detailed certificate of analysis and ISO laboratory standards to ensure reliability in clinical and research environments. Industry compliance standards
Typical usage ratio
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Sodium Edetate, widely known by its chemical synonym EDTA-Na2, appears across a host of manufacturing, processing, and laboratory environments. The importance of this product rarely comes from buzzwords or technical jargon. Instead, it's about what years of direct experience have shown: reliability in controlling metal ions, consistency in purification, and practical performance on plant floors where even minor deviations can throw off an entire batch. Our intention in producing Sodium Edetate has always centered on those real-world demands, not just tabulated figures. As a producer, we draw from feedback on production lines, scientific input, and daily troubleshooting to continually refine our approach.
We supply Sodium Edetate as anhydrous, dihydrate, and tetrahydrate forms, with the dihydrate being the most commonly used model in pharmaceutical and food applications. The dihydrate runs with a molecular weight near 372.2, retaining water molecules critical for shelf stability and user handling. Our production lines scale granulation and purity to meet laboratory, food, and industrial requirements. Batch reports frequently show over 99.0% assay, a figure rooted in hands-on process control and actual client demand rather than marketing claims.
Purity does not only mean number of decimals; it reflects control at every step, from sourcing dicyanodiamide and formaldehyde down to the filtration and drying. Our batches regularly show low iron and calcium levels, often less than 10 ppm. These are not arbitrary numbers but reflect realities in the field: in pharmaceutical synthesizing, excess metals cause reaction drift or regulatory headaches. In water treatment, impurities result in persistent fouling or off-odors. We open our batch records to scrutiny by clients—years of practical operation have demonstrated this transparency is more valuable than any certificate on the wall.
Sodium Edetate earns its keep because it solves specialized, persistent problems that other chelating agents miss. In our experience, customers working in clinical diagnostics benefit from the strong metal binding of EDTA-Na2, which minimizes interferences in sensitive blood analysis and histological staining. We’ve seen beverage plants use our technical grade to strip away trace iron and copper, thus preventing both haze formation and unexpected flavor shifts. Each application context shapes our thinking—for example, the food sector prizes not just purity but also batch-to-batch reproducibility, while water softening clients need a product that disperses evenly at scale. Glass manufacturers and pulp mills depend more on fluxing properties and the ability to scavenge calcium and magnesium under high thermal loads. Our recommendations draw on these direct partnerships rather than any one-size-fits-all advice.
Users often ask why Sodium Edetate deserves space on the shelf next to citrates, phosphates, or other chelating agents. The answer lies less in textbook theory, more in observed outcomes. EDTA-Na2’s hexadentate binding means stronger, more complete complexation of transition metals than you get from phosphates or organic acids. In our water analysis lab, samples run cleaner with EDTA than with sodium citrate under identical parameters—for applications demanding trace analysis, this difference is not academic. When compared to EDTA tetrasodium, the disodium version operates with less alkalinity and fewer pH disruptions. Experience tells us that pharmaceutical clients gravitate towards disodium for this reason, since pH drift in buffer solutions leads to regulatory compliance headaches. In food processing, less alkaline products maintain stability and color fidelity in sensitive juice and dairy lines.
Challengers sometimes tout newer complexing agents, but those end up costlier or bring their own side-reactions. Sodium Edetate, refined into either crystalline powder or granular form, dissolves quickly and stores well over months without visible caking or yellowing. Over the years, our storage studies—ranging from humid warehouses in Southern China to northern European logistics centers—have shown consistent, reliable shelf life extending to 24 months with minimal deterioration, provided it’s kept in well-sealed packaging away from strong acids.
Factories consume Sodium Edetate for what it delivers day in and day out: reliable sequestration under a broad range of working temperatures and pressures. We collaborate directly with users to adjust mesh size, flow properties, and trace impurity levels. Drug makers in particular send us requests for tighter control on heavy metal content, especially in excipient grade material. Our QA teams run continuous atomic absorption and titration tests through entire shifts—this tradition of closed-loop feedback loops, between operator and production chemist, ensures adjustments happen before any out-of-spec batch ever leaves the premises.
Pulp and paper clients echo a different set of needs, so we work with them on more economical grades where metal scavenging trumps ultra-high purity. We’ve found that total prevention of pulp yellowing means focusing less on superficial whiteness and more on how EDTA interacts with trace iron and manganese throughout the chlorine-free bleaching steps. By sharing case studies openly, industrial partners gain practical insights rather than sales rhetoric.
Handling Sodium Edetate in the production environment brings practical differences. In our own pilot plants, we’ve found the dihydrate version dissolves faster and leaves behind less residue in mixing tanks compared to the anhydrous model. Staff running automated dosing rarely see clogging or bridge formation, even in high-humidity summer periods. Water treatment operators have fed back to us that granular forms minimize dust exposure and result in less product loss during transfer. These are not coincidental; our engineering teams monitor and adapt granulation patterns, adjust moisture content, and triple-check packaging seals based on hands-on experience.
One lesser discussed challenge comes from packaging sodium edetate at scale. Standard kraft bags often bleed moisture during storage in non-climate-controlled sheds. Years back, we moved to laminate-lined bags and moisture-proof liners. Clients report fewer caking incidents and less reprocessing waste. These packaging improvements come about not by accident, but through repeated collaboration, open complaints, and constant reevaluation of our supply chain partners.
Supplying Sodium Edetate for high-risk uses in infusion solutions, dialysis concentrates, or as an excipient in oral liquid medications brings another layer of rigor. Regulatory agencies expect not only 99% assay but also sub-ppm levels of lead, arsenic, and mercury—gaps in compliance translate into product recalls and trust lost overnight. Our own validation labs have dealt with the practicalities of lot recalls, and from those experiences, we now keep redundant records, preserve retention samples, and provide open channels for on-site audits by pharmaceutical partners. In the world of client audits, nothing replaces concrete paper trails and reproducible batch history.
For clinical labs, sample integrity hinges on repeatable chelation effect. Our routine feedback comes from blood collection tube producers, who confirm that the metal scavenging effect of our EDTA-Na2 prevents premature clotting or erroneous test readings. We’ve had cases where inconsistent batches caused lab delays; the lesson for us was to narrow internal process variability rather than leaning on certificate claims. This willingness to act on user reports builds relationships stronger than any specification alone.
In food and beverage applications, Sodium Edetate plays a critical role in both product stability and appearance. Soft drink formulators and juice producers have encountered metal-catalyzed haze or off-note development well past the point where standard detergents or filtration make a difference. By using our EDTA-Na2, clients consistently reduce shelf-life complaints and minimize surface fouling on filling equipment. Dairy line managers look for our product to prevent separation and maintain flavor over weeks in storage.
A less obvious aspect has been regulatory conformity—not only meeting published tolerances for sodium and calcium, but also confirming lot release for fluoride, nitrate, and potassium, as these can enter unchecked with poorly handled raw inputs. We procure each ingredient batch from vetted vendors, then recheck through our own baseline labs before feedstock moves onto reaction. Traceability remains non-negotiable, since even a single outlier batch can set off large-scale recalls. Over time, this rigorous workflow has enhanced our standing with multinational beverage groups, who visit production lines and see these controls firsthand.
The story of Sodium Edetate in industry is also one of balancing cost and performance. In commodity markets, every fraction of a cent matters. Our plant operations team constantly scrutinizes yield rates, reaction completeness, and energy input during spray drying and milling stages, tracking performance not monthly, but with every batch. This direct connection to the actual chemical synthesis determines not just the specs of the final powder, but its real-world durability in demanding applications.
Across export and domestic sales, fluctuations in input prices do occur—ethylene diamine, formaldehyde, sodium cyanide—yet real expertise means holding the line on delivered cost per kilogram while protecting users from price shocks. This past year, we responded to potassium salt shortages, pivoted sourcing arrangements, and prevented a single missed shipment for long-term clients. It’s the sort of behind-the-scenes adjustment that rarely makes it into brochures but matters most in user experience.
As chemical manufacturers, we bear direct responsibility for waste reduction right at the production source. EDTA receives criticism for environmental persistence, and these concerns lead us to operate closed-loop water circuits and spend on upgraded effluent treatment. Each lot shipment includes a stewardship report detailing not just the chemical’s intended application, but also our actions taken to minimize offsite discharge. Laboratory waste, wash waters, and rinses do not exit untreated; rather, we run them through multiple ion-exchange and microfiltration stages before disposal or return to utility lines. Customers—especially in Europe—ask us for proof; we willingly share quarterly audit results, knowing that regulatory compliance forms only the beginning of our obligation.
Waste minimization does not stop at the factory wall. For lab-scale users, we provide guidance and technical sheets on safe collection and regeneration of EDTA-containing rinse solutions, sharing best practices learned from larger installations. Over the last few years, several industrial partners have adopted on-site recycling of spent chelate solutions—our engineers assist with new technologies such as electrochemical regeneration to help extend the product’s useful lifecycle. Practical tips beat generic advice: we document which metal loads can be recycled, when side-stream treatment makes sense, and how to adapt to shifting discharge permits.
Manufacturing never stands still. Each season introduces new technical or regulatory challenges, and direct user dialogue continuously shapes our approach. In some years, elevated humidity in transit has demanded rapid change in desiccant management; in others, evolving pharmaceutical compendia have forced us to revalidate entire analytical protocols. Production chemists and plant supervisors regularly meet with end users to share process tweaks, troubleshooting lessons, or run joint tests.
Sometimes users identify subtle issues—a slightly slower dissolution rate, an unexpected trace impurity, or altered flowability when switching process tanks. Rather than dismiss these as anomalies, we reproduce conditions, investigate root causes, and refine both upstream and downstream steps. This iterative loop connects factory expertise to real application needs, never assuming that “passing spec” means best possible performance.
The future trajectory of Sodium Edetate runs through deeper partnerships and real transparency. Customers demand not just product declarations, but ongoing access to batch archives, open visits to production runs, and joint problem-solving when surprises arise. Using Sodium Edetate in a world of shifting supply chains or regulatory tightening means flexibility and real technical backup, not promises.
We see our role as more than a seller of commodities—we join in solution-finding when a reaction fails, a filter clogs, or a supplier quality event threatens product flow. Our own in-house technical teams travel for root cause analysis and process audits. Through this cycle of engagement, our knowledge base grows, refining the Sodium Edetate of tomorrow to serve more demanding, nuanced, and safety-focused applications. Years of hands-on operation and close collaboration with clients have proven that credibility stems from results, openness, and a willingness to face challenges together, batch by batch, order by order.