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Sodium Edetate

    • Product Name Sodium Edetate
    • Alias edetate-sodium
    • Einecs 200-573-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of Sodium Edetate

    Applications of Sodium Edetate in Industrial Manufacturing

    Sodium 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 Solutions

    Pharmaceutical 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

    • USP-NF (United States Pharmacopeia-National Formulary) Monograph for Edetate Disodium
    • European Pharmacopoeia (Ph. Eur.) 2.2.16, 9.5.5, 11.3.1
    • Japan Pharmacopoeia (JP) monograph
    • GMP (Good Manufacturing Practice) Certification per ICH Q7

    Typical usage ratio

    • 0.005% – 0.02% w/v for parenterals
    • 0.01% – 0.05% for ophthalmic drops
    • Adjusted by formula pH, total volume, and presence of trace metals

    Downstream process integration

    • Dosage during aqueous solution preparation before final filtration
    • Critical role in pre-autoclave stability for terminally sterilized drugs
    • Blending in Class 100/ISO 5 cleanroom compounding suites
    • Documented in batch manufacturing records for regulatory compliance

    Final product types

    • Injectable antibiotics in glass or plastic ampoules
    • IV solutions (electrolyte/infusion bottles)
    • Single-dose and multi-dose ophthalmic eye drops
    • Biologic drug vials requiring metal ion control

    2. Food and Beverage Processing: Preservation and Color Retention

    Food 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

    • FDA 21 CFR 172.135 (Edetate disodium, food additive regulation)
    • EU Commission Regulation (EC) No 1333/2008 on food additives (E386)
    • Codex Alimentarius General Standard for Food Additives (GSFA)
    • HACCP and ISO 22000 food safety management

    Typical usage ratio

    • 50 – 100 mg/kg in canned beans and legumes
    • 25 – 75 mg/kg in bottled soft drinks
    • 60 – 90 mg/kg in processed crabmeat and shellfish
    • Adjusted for product pH, mineral profile, and regulatory maximums

    Downstream process integration

    • Direct addition to brine or syrup prior to can filling
    • Continuous dosing in beverage blending tanks
    • In-line blending with flavor or stabilizer premixes
    • Monitoring of residual levels in final QC before packaging

    Final product types

    • Canned and jarred vegetables (beans, chickpeas, mushrooms)
    • Bottled and canned clear soft drinks
    • Packaged shellfish and crustaceans
    • Pasteurized fruit preserves

    3. Personal Care Formulations: Creams, Lotions, and Hair Products

    Cosmetic 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

    • EU Cosmetics Regulation (EC) No 1223/2009 (Annex III/VI entry)
    • US FDA Voluntary Cosmetic Registration Program (VCRP)
    • ISO 22716:2007 GMP for cosmetics production
    • China NMPA GB/T 29665 Hygienic Standard for Cosmetics

    Typical usage ratio

    • 0.01% – 0.1%, based on total formulation weight
    • Lower end for clear serums, higher for robust emulsions
    • Adjusted for presence of botanicals, pH, packaging type

    Downstream process integration

    • Addition during aqueous phase compounding in main mixing vessel
    • Incorporation before homogenization or emulsification steps
    • QA/QC verification of chelation and preservative activity through stability testing
    • Fully documented in PIF (Product Information File) for regulatory review

    Final product types

    • Face and body creams, daily moisturizers
    • Shampoos and hair conditioners
    • Skin toners and makeup removers
    • Sun protection sprays and lotions

    4. Water Treatment: Boiler, Cooling, and RO System Conditioning

    Industrial 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

    • ANSI/AWWA B200-15 Standard for Water Treatment Chemicals
    • ASME Boiler and Pressure Vessel Code, Section VI
    • EPA guidelines on industrial water discharge (40 CFR Part 423, 432)
    • ISO 9001:2015 Quality Management for plant operations

    Typical usage ratio

    • 0.5 – 10 ppm, calibrated by incoming water mineral content
    • Continuous dosing for high throughput systems
    • Spot dosing for shock treatment during high load periods

    Downstream process integration

    • Injection through metered dosing equipment at feed entry
    • Real-time adjustment based on online water quality sensors
    • Periodic review in routine system maintenance and lab analysis
    • Integration with other water conditioning agents (phosphonates, polyacrylates)

    Final product types

    • Treated steam for HVAC and power generation
    • RO process water for beverage or pharma facilities
    • Circulating water for industrial cooling towers
    • Laboratory and ultrapure water systems

    5. Industrial Cleaning and Detergents: Metal Cleaning and Textile Processing

    Detergent 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

    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • US EPA Design for the Environment (DfE) for cleaning products
    • OECD Guidance on the environmental impact of cleaning agents
    • Safety Data Sheet (SDS) requirements for hazard communication

    Typical usage ratio

    • 0.1% – 0.5% in metal cleaning solutions
    • 0.05% – 0.2% in textile preparation agents
    • Exact ratio based on surface types, wash cycles, and hardness levels

    Downstream process integration

    • Dosing during pre-mixing or final blending with surfactants
    • Quality checks for chelation efficiency and compatibility with other formula components
    • In-plant monitoring for residual content in wash effluent
    • Continuous feed in closed loop industrial bottle washing lines

    Final product types

    • Automotive and industrial metal degreasers
    • Textile desizing and scouring agents
    • Bottle washing concentrates for food and beverage industries
    • Heavy-duty institutional cleaning detergents

    6. Laboratory Diagnostics and Reagents: Sample Collection and Analysis Kits

    Producers 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

    • ISO 13485:2016 for medical devices and diagnostics
    • CLSI GP44-A4 Guidelines for blood collection
    • 21 CFR Part 820 (FDA Quality System Regulation for medical devices)
    • CE-IVD (In Vitro Diagnostic Directive) certification for European markets

    Typical usage ratio

    • Final blood tube concentration: 1.5 – 2.2 mg/mL
    • Clinical buffer and reagent solutions: 0.005% – 0.02%
    • Dosage varies depending on tube fill volume and required analyte preservation

    Downstream process integration

    • Uniform coating or blending into evacuated blood collection tubes
    • Premixing with lyophilized and liquid diagnostic reagent packs
    • Assembly in ISO Class 7 cleanrooms under validated procedures
    • Full traceability in production batch records

    Final product types

    • Vacutainer and blood collection tubes for hematology
    • In vitro diagnostic kits for clinical laboratories
    • Sample stabilization buffers for molecular assays
    • Certified reference solutions for analytical testing
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    Certification & Compliance
    More Introduction

    Sodium Edetate: Meeting the Real Demands of Industry

    Our Perspective as a Sodium Edetate Manufacturer

    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.

    Available Grades and Models

    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.

    Specification Details That Matter on the Floor

    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.

    Product Use: Lessons from Real Industry

    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.

    Practical Differences from Other Chelators and Sodium Salts

    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.

    Key End-User Insights

    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.

    Solubility and Handling Observations

    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.

    Why Pharmaceutical and Clinical Applications Demand More

    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.

    Food and Beverage Insights: Beyond Label Requirements

    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.

    Cost, Performance, and Real-World Durability

    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.

    Environmental Responsibility and Waste Minimization

    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.

    Continuous Improvement Driven by Feedback

    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.

    Moving Forward with an Open Partnership Model

    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.