Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
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Zearalenone

    • Product Name Zearalenone
    • Alias ZEA
    • Einecs 246-262-6
    • 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

    178421

    Cas Number 17924-92-4
    Molecular Formula C18H22O5
    Molecular Weight 318.37 g/mol
    Appearance White to pale yellow crystalline powder
    Melting Point 163-165 °C
    Solubility Soluble in acetone, chloroform, ethyl acetate; slightly soluble in water
    Purity Typically ≥98%
    Storage Temperature 2-8 °C
    Chemical Class Mycotoxin / Resorcylic acid lactone
    Source Produced by Fusarium species fungi
    Iupac Name 2,4-dihydroxy-6-(6-oxo-trans-1-butenyl)benzoic acid lactone
    Synonyms ZEN, F-2 toxin, Zearalenon

    As an accredited Zearalenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Zearalenone, 100 mg, is supplied in a clear, sealed glass vial with a secure cap, inside a labeled protective cardboard box.
    Shipping Zearalenone is shipped as a hazardous laboratory chemical. It should be packaged in tightly sealed containers, protected from light and moisture, and cushioned to prevent breakage. Shipping must comply with local, national, and international regulations for toxic and potentially carcinogenic substances, and should include clear labeling and accompanying safety documentation (SDS).
    Storage Zearalenone should be stored in a tightly sealed container, protected from light, moisture, and air. Keep it at a temperature between 2°C and 8°C (refrigerated), and in a well-ventilated, secure area away from incompatible substances. Ensure storage containers are properly labeled and access is restricted to trained personnel to prevent accidental exposure or contamination.
    Application of Zearalenone

    Applications of Zearalenone in Industrial Manufacturing

    Zearalenone serves as a functional raw material for select regulated sectors within agrochemical, veterinary, and mycotoxin reference industries. Our production adheres strictly to traceability and compliance requirements, supporting customers involved in controlled usage and advanced laboratory processes. The following scenarios outline verified end-use pathways, specifications, and process details to assist formulation and quality professionals in downstream integration.

    1. Mycotoxin Reference Standards for Analytical Laboratories

    Accredited reference material producers and analytical laboratories routinely incorporate zearalenone as a high-purity analytical standard to calibrate testing equipment for mycotoxin monitoring in food and feed safety. The compound enters as part of certified standards production, where consistency and traceability are critical for method validation, interlaboratory comparisons, and regulatory reporting. As a primary calibrant, it enables accurate quantification of naturally occurring contaminants across cereals, oilseeds, and animal feeds, supporting laboratory accreditation and food chain compliance.

    Industry compliance standards

    • ISO 17034: General requirements for the competence of reference material producers
    • ISO/IEC 17025:2017 for laboratory competence
    • EU Regulation No 401/2006: Laying down the methods of sampling and analysis for the official control of mycotoxins
    • AOAC International methods

    Typical usage ratio

    • Reference substances formulated as 10–1000 µg/mL in standard solutions, depending on matrix and instrument calibration needs

    Downstream process integration

    • Weighing and dissolution in solvents for gravimetric preparation
    • Ampoule filling under validated conditions
    • Homogeneity and stability testing in proficiency testing kit production

    Final product types

    • Certified reference standards (CRMs) for mycotoxin analysis
    • Spiking solutions for method development and validation
    • Quality control (QC) kits for laboratory accreditation
    • Proficiency testing (PT) samples for interlaboratory studies

    2. Positive Control in Animal Feed Safety Assessment

    Compound feed manufacturers and animal health research facilities use zearalenone as a positive control during in vitro and in vivo monitoring of mycotoxin detoxification strategies. Its controlled addition validates decontamination processes, supports the development of detoxifying additives, and ensures compliance with legal residue limits. Our deliveries support QA laboratories and R&D centers monitoring extraction efficiency, feed additive efficacy, and legal compliance in finished feeds.

    Industry compliance standards

    • European Commission Regulation (EC) No 574/2011: Maximum levels for certain contaminants in animal feed
    • Good Laboratory Practice (GLP) for feed additive trials
    • Chinese GB 13078-2017: Hygienic standards for compound feed
    • OECD Guidelines for the Testing of Chemicals: Toxicity and efficacy studies

    Typical usage ratio

    • Spiking concentration: 0.1–5 mg/kg in feed material, depending on species and experimental design

    Downstream process integration

    • Premixing into laboratory-scale feed batches prior to additive or detoxification agent application
    • Distribution into test groups for efficacy assessment
    • Sampling and extraction for residue determination

    Final product types

    • Experimental animal feeds for R&D and regulatory trials
    • Feed detoxification testing batches
    • Residue analysis kits used in surveillance programs
    • Standardized mycotoxin-contaminated feed reference materials

    3. Veterinary Toxicology Research Materials

    Veterinary pharmaceutical research institutions rely on zearalenone to investigate the compound’s estrogenic activity and potential health risks in livestock. Controlled formulation and administration within regulated animal trials are essential for toxicodynamics studies and policy guidance. Our batch traceability and purity data support toxicological profiling, biomarker assay work, and risk assessment efforts carried out by universities, contract research organizations, and governmental bodies.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • Directive 2010/63/EU on the protection of animals used for scientific purposes
    • FDA Guidance for Industry #213 (Veterinary Drug Residue Limits)
    • Institutional Animal Care and Use Committee (IACUC) protocols

    Typical usage ratio

    • Dosing range: 0.01–2 mg/kg body weight, depending on species, age, and study design

    Downstream process integration

    • Preparation of dosing solutions or suspensions immediately before administration
    • Oral gavage or feed incorporation for single or repeated dose studies
    • Bioanalysis of blood, tissue, or excreta samples for toxicokinetic profiling

    Final product types

    • Toxicology study reports for regulatory submission
    • Validated analytical methods for screening and diagnostics
    • Preclinical safety assessment dossiers
    • Reference materials for biomarker studies

    4. Mycotoxin Detection System Development (Immunoassay & Instrumental Kits)

    Manufacturers of immunoassay kits and chromatographic testing solutions incorporate zearalenone as a standard antigen or calibrator for the development, validation, and commercial production of rapid test kits and instrumental analysis systems. Our material serves in test batch benchmarking, antibody specificity verification, and matrix calibration for high-throughput screening of grain and feed samples. Product traceability and batch consistency are critical, supporting accurate detection in compliance with export and domestic market surveillance programs.

    Industry compliance standards

    • ISO 13485: Quality management for medical and diagnostic devices (where applicable)
    • Chinese GB/T 5009.209-2016: Determination of zearalenone in foods
    • US FDA BAM Chapter 19: Mycotoxins analysis requirements
    • EN 17269:2019: Performance criteria for mycotoxin screening

    Typical usage ratio

    • Standard concentrations: 1–100 ng/mL in calibration curves depending on assay sensitivity and kit format

    Downstream process integration

    • Inclusion in antigen coating solutions for ELISA plate production
    • Standard preparation for lateral flow and HPLC kit calibration
    • Matrix-matched spiking for performance verification batches

    Final product types

    • ELISA kits for rapid mycotoxin screening
    • Lateral flow (strip) detection devices
    • Instrument calibration kits for HPLC/LC-MS analysis
    • On-site testing kits for food and feed inspection
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    Certification & Compliance
    More Introduction

    Zearalenone: A Field Manufacturer’s Insight

    Looking at Zearalenone from Where We Stand

    Our work with zearalenone begins with a focus on purity and reliability. We’ve seen the difference consistent quality makes in real-world feed and agricultural applications. Zearalenone, which carries the chemical formula C18H22O5, doesn’t often find itself in the spotlight. Our production model for this compound follows robust protocols built up through years of refining our extraction and purification methods. Spectroscopic analysis remains the backbone for us—batch after batch, we reference established standards, always seeking low variability and high recovery. International labs prefer consistent performance. Most of our output offers ≥98% purity, with a familiar appearance: usually white to off-white crystalline powder.

    What Zearalenone Means in Agriculture and Beyond

    As a mycotoxin, zearalenone turns up mostly in cereals and grains. Despite the challenges it brings, its study provides sustained value for animal nutrition research and feed quality control. Each harvest, livestock producers and food safety panels face questions about contamination and safety limits. We produce reference materials and analytical standards, not animal feed additives, keeping the distinction clear. Analytical labs rely on targeted products to calibrate mass spectrometers and chromatographs. The clear specification supports accurate detection of trace residues in a wide range of matrices, from corn and wheat to serum and urine.

    From lab benches to grain elevators, the utility of a pure zearalenone lies in its dependable composition. Without a reliable supplier, test results lose their footing. We share this perspective with food chemists and auditors who oversee safety programs year after year. Our direct involvement in production means we nurse the compound through every stage: extraction, purification, and packaging. We don’t see these steps as mere box-ticking—they form the core of quality monitoring and risk management. Knowing the origin and the traceability chain for each lot means less risk of cross-contamination and sharper analytical confidence.

    Common Forms and Handling Experience

    Most labs choose zearalenone either as a neat crystalline powder or dissolved in acetonitrile or methanol. The neat powder provides the most flexibility, letting customers prepare working solutions according to their protocols. Liquid solutions, on the other hand, can reduce preparation time and minimize error for high-throughput labs. Both types demand careful storage away from heat and light—a discipline we practice ourselves before shipping. Boxes leave our site packed with refrigerant, stashed under controlled temperatures and logged every step of the way. We follow up with stability studies, benchmarking shelf life under variable field and warehouse conditions.

    Meeting Specification Demands with Traceable Production

    Our decades of in-house zearalenone manufacturing make a crucial difference for partners who log every microgram of reference material. When purities deviate or impurities creep in, we spot them early in our control system. Rigorous in-process checks and chromatography data track every lot, tying back to the source material. We do not repackage third-party bulk for relabeling; everything starts with raw agricultural material and ends with a product we’d stand behind in our own quality control lab. For our partners, this means a single-point traceability chain—no guesswork about what’s in the vial or where it’s from.

    There are differences between zearalenone batches available on the market. Some laboratories have reported broad variations in trace contaminant profiles, especially for material sourced through indirect channels. These outliers usually arise from cutting steps in purification or from improper storage along the line. Our own focus involves solvent extraction followed by column chromatography, crystallization, and multiple rounds of filtration—a slow and watchful approach, built to serve food safety labs and agricultural researchers alike.

    Comparing Zearalenone to Other Analytical Standards

    People sometimes ask if our zearalenone comes in the same purity or packaging as aflatoxins, ochratoxins, or fumonisins. The short answer: every compound needs a tailored path to purity and stability. Zearalenone resists moisture, but shows photosensitivity, so our lots ship in amber glass with evidence seals. Particulates, solvent compatibility, and the ability to scale to industrial lots set zearalenone apart from other mycotoxins in everyday handling. The legacy of each batch—purity, crystal habit, stability at room versus chilled temperatures—matters more than superficial packaging similarities.

    Across the industry, some reference standards come as pre-made multi-component mixes. Our focus remains on monocomponent supplies unless a research collaborator requests a custom matrix. In our experience, single-component standards reliably support the calibration of instruments and meet accreditation demands. Researchers who must validate LC-MS/MS or HPLC methods benefit from predictable behavior in extraction and recovery. We keep rigid records on water content, residual solvents, and crystal form, allowing technical staff at partner labs to fine-tune their controls without chasing unknowns.

    Why Internal Manufacturing Trumps Outsourced Supply

    We see clear practical reasons for keeping production under our own roof. Every cycle, we examine yields, impurity profiles, and scalability. Fluctuations in global supply chains rarely shake our output—no surprise shortages or unexplained delays. Our chemists do not rely on certificates from outside brokers; internal proficiency tests and cross-lab validation hold more weight. With zearalenone, risk lurks in loose production standards; we reduce that risk by sticking to the practices that have earned trust across food and safety organizations. Our recurring relationships with industry auditors grew from our willingness to host site visits, share documentation, and open our process to outside review.

    Direct Feedback from Labs Using Zearalenone

    Few things teach as much as direct feedback. In survey after survey, reference labs point to the consistency of our crystallization and the error margins on purity certificates. The feedback loop runs both ways. End users have flagged reduction in false positives when control materials closely match the target analyte. We listened: building a production approach that holds to the same source material and isolation process, batch to batch. Auditors have compared our lots to those from bulk resellers and noticed tighter peak shapes and lower baseline noise on freshly prepared samples. That’s not an accident. We didn’t engineer these advantages overnight; they grew from repeated tweaks to solvent ratios, substrate handling, and cold storage routines.

    Handling Agricultural Demands and Seasonal Challenges

    Manufacturing zearalenone from agricultural raw materials presents seasonal realities. Fungal strains, crop rotations, and harvest cycles all shape the yield and grain quality. During wet years, the initial mycotoxin loads run high, which calls for stricter selection at intake. During dry years, extraction efficiency matters more. Our familiarity with fluctuating field sources helps us forecast challenges well in advance. Unlike traders or overseas consolidators, we hold off on production until intake passes our inbound testing. This practice keeps us nimble as crops shift and regulatory thresholds tighten. If a lot falls short, we reject rather than blend or dilute—a policy that’s paid off in long-term customer trust.

    Longevity and Stability for On-Site Technicians

    On-site chemists and QA managers depend on predictable shelf life. Our studies run up to 24 months, tracking purity drift, photodegradation, and any sign of decompositional change. Reports from the field guide our improvements: field techs tell us where packaging fails, which solvents promote precipitation, and what storage habits extend usability. We act on these reports, gradually improving formulation and packing. All old lots are monitored at intervals to spot outliers and launch corrective actions early. In our experience, the headache of a failed batch in the field costs more than the extra cost of improved packaging. Evidence seals, lot split verification, and double labeling have all been ideas tested and adopted from real feedback.

    Meeting Feed and Safety Regulations

    Global regulators tighten controls year by year. Our own internal bar tips higher than legal limits, keeping to pharma-grade isolation even for materials destined for feed quality labs, not drug makers. Over the decades, we’ve met extra documentation requirements, from identity confirmation down to residual solvent levels. Partners in EU and North American labs require Certificates of Analysis and batch-level traceability. We document parameterized production records to verify each step was carried under controlled conditions. If trace contamination appears, both internal and customer audits can reverse trace each step, from grain intake to final packaging. Regulatory harmonization forces us to keep tight records for each production run, which in turn makes our relationship with industry and academic labs more transparent.

    We monitor science and regulation closely, so our own methods never fall behind. New analytical guidelines or method modifications push us to refine. Sometimes that means an adjustment in our solvent mix, or introducing new HPLC columns. Our approach minimizes disruption to customer workflows—because we build compatibility into every lot. Customers with unique needs rely on that continuity to keep trouble out of their compliance records.

    Optimizing Reference Use in Laboratory Workflows

    Mass spectrometrists, chromatographers, and bioanalytical labs often ask about best practices for using zearalenone standards. Our advice draws on years of technical support and troubleshooting. All standards need calibration routines and secondary checks. Typical dilutions run in the low milligram range, and solvent purity always matters more than the brand of glassware. Any staff turnover gets covered by our ongoing protocol seminars and direct support calls. Our success depends on how well your batch keeps calibration drift in check, not just our claims on a website. Practical knowledge comes from experience—missteps like solvent incompatibility or incorrect light protection waste time; careful planning builds working relationships.

    Our partnerships sometimes involve direct training at customer labs, walking through dilution, handling, and instrument setup step by step. This hands-on strategy started long before webinars were common. It grew out of necessity, as labs struggle with tight timeframes and limited experience with mycotoxin standards. Working together in person, we’ve seen better adoption and fewer costly lab errors.

    Comparing Our Zearalenone Manufacturing to Competing Approaches

    Manufacturers around the globe deliver zearalenone in different forms. Bulk producers send out semi-refined product, often needing additional purification at the customer site. Some brands blend product across multiple origins and repackage without disclosing the histories. In contrast, our focus on single-source, single-process manufacturing carves out a difference in traceability and performance. Our transparency often means more documentation and stricter batch control, but the payoff is fewer return shipments and satisfied regulators.

    Competition sometimes means competing on price, but we do not undercut at the expense of batch purity or shelf life. It might take a bit longer to perfect a batch, or hold a shipment if in-process testing reveals drift. That approach draws on years of seeing what shortcutting causes in the field—disrupted research timelines, regulatory headaches, and lost trust. Our stance is simple: deliver product worth using, with data to back up every claim.

    Day-to-Day Practical Lessons from Zearalenone Production

    As manufacturers, the lessons from everyday production stay with us. Weather can change harvest quality overnight, custom clearance can slow critical reagent shipments, and analytical hardware can drift after months of heavy use. Staying responsive keeps our supply stable. We invest in skilled staff—not just for technical know-how, but because experience heads off problems that only show up under pressure. Unusual impurity tracks, off-color crystals, and shifts in melting point each mean something to a trained eye. That experience never gets captured in standard operating procedures alone.

    Customer relationships keep us learning. Mislabeling, mispacking, or transit delays all show up at a human level. Regular conversations with partner labs have changed how we develop batch control reports and packaging instructions. Practical feedback works better than guesswork—whether it’s a change to a label color or a heat-resistant shipping case for extreme climates. The day-to-day reality means staying curious, never assuming this batch will behave like the last.

    Looking Ahead: The Future of Zearalenone Manufacturing

    With advancements in analytical science, labs need supplies that match demanding detection thresholds. The future means even narrower tolerance bands and more detailed batch documentation. We already see increased calls for isotope-labeled zearalenone, extended stability data, and supply chain tracking down to the original field lot. Our job is to keep adapting—integrating automation without losing the advantages of a practiced team.

    Industry demand for transparency and predictable quality will only grow. More complex feed mixtures, evolving regional regulations, and technological changes in analytical instruments challenge us. Keeping direct lines to our customers and investing in technician skill development remain the backbone of our reliability. We learn from problems, adapt to seasonal cycles, and upgrade equipment not as an afterthought, but as a continual investment in performance. Collaboration with research and industry groups keeps knowledge fresh and maintains trust in the unpredictable landscape of agricultural chemistry.

    After years producing zearalenone for the lab and agricultural community, each batch ties us to the world of crop science, safety testing, and animal nutrition. Our aim is to keep improving the process—finding the right balance between consistency, adaptability, and transparency. The people and equipment behind each gram signal a deeper commitment to quality than any headline or specification ever will.