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Flavin Adenine Dinucleotide Disodium Salt

    • Product Name Flavin Adenine Dinucleotide Disodium Salt
    • Alias FAD
    • Einecs 231-710-0
    • 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
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    Specifications

    HS Code

    366985

    Chemical Name Flavin Adenine Dinucleotide Disodium Salt
    Synonyms FAD disodium salt
    Molecular Formula C27H31N9O15P2Na2
    Molecular Weight 811.51 g/mol
    Cas Number 146-14-5
    Appearance Yellow to orange powder
    Solubility Soluble in water
    Storage Temperature 2-8°C
    Purity Typically ≥95%
    Usage Biochemical research, coenzyme in redox reactions

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

    Packing & Storage
    Packing Flavin Adenine Dinucleotide Disodium Salt, 1g, supplied in a tightly sealed amber glass vial with tamper-evident cap, labeled for laboratory use.
    Shipping Flavin Adenine Dinucleotide Disodium Salt is shipped in tightly sealed containers to protect from moisture, light, and air. It is typically transported at controlled room temperature or refrigerated, depending on manufacturer requirements. The packaging ensures stability during transit and complies with regulations for safe handling of biochemical reagents.
    Storage Flavin Adenine Dinucleotide Disodium Salt should be stored in a tightly sealed container, protected from light and moisture, at -20°C. Avoid repeated freeze-thaw cycles to maintain stability. Use desiccators to prevent exposure to humidity, and keep away from incompatible substances. Proper storage ensures preservation of its biochemical activity and prevents degradation or contamination.
    Application of Flavin Adenine Dinucleotide Disodium Salt

    Applications of Flavin Adenine Dinucleotide Disodium Salt in Industrial Manufacturing

    Flavin adenine dinucleotide disodium salt (FAD-Na₂) serves key roles in biological process manufacturing and industrial biocatalysis. As a supplier, we address diverse sector needs through strict quality control and integration expertise. Below, we outline main commercial-scale application directions with direct relevance to actual production environments.

    1. Pharmaceutical API Production: Cofactor for Enzymatic Synthesis

    Our FAD-Na₂ product supports several API (active pharmaceutical ingredient) syntheses by providing an essential redox cofactor. Biocatalytic steps for chiral amine or alcohol formation, and steroid or antibiotic modifications, require precise FAD concentrations. We support these applications by offering tight in-process quality controls and compatibility documentation, facilitating upstream enzyme formulation as well as in-line downstream processing. Our technical teams also assist with qualification under regulated manufacturing practice.

    Industry compliance standards

    • USP Flavin Adenine Dinucleotide Monographs
    • ICH Q7 GMP for APIs
    • EU GMP Part II for active substance production
    • FDA cGMP 21 CFR Part 211

    Typical usage ratio

    • 0.01–2 mmol/L in enzyme reaction media, adjusted via process optimization according to the enzyme and substrate system

    Downstream process integration

    • Direct addition to biocatalytic reactors during stepwise or continuous fermentation
    • In situ regeneration with associated cofactors during multistep API synthesis
    • In process analytical control for real-time monitoring in cGMP environments

    Final product types

    • Pharmaceutical intermediates (e.g., chiral alcohols, steroids)
    • APIs manufactured via enzymatic transformation (e.g., antibiotics, statins, antiviral agents)

    2. Industrial Enzyme Manufacturing: Flavoenzyme Formulation

    FAD-Na₂ is a required stabilizer and cofactor in production of FAD-dependent flavoenzyme preparations. Commercial-grade catalase, glucose oxidase, and monoamine oxidase formulations use it during fermentation to achieve target activity levels. Using high-purity input enables accurate dosage control during upscaling, ensures batch-to-batch consistency, and supports compliance with food, pharma, and industrial enzyme markets globally.

    Industry compliance standards

    • Food Chemicals Codex (FCC) specifications for enzyme additives
    • EU Regulation 231/2012 (food enzyme purity criteria)
    • ISO 9001/QC management in enzyme production
    • China GB 1886.174 for food additive enzyme preparations

    Typical usage ratio

    • 5–200 mg/L in fermentation broth; optimization based on enzyme type and biomass yield

    Downstream process integration

    • Inoculation into seed culture fermentation media prior to enzyme expression
    • Dosage monitoring during fed-batch processes to adjust for cofactor turnover
    • Quality assurance for final freeze-dried enzyme concentrate or liquid bulk enzyme, documented on batch records

    Final product types

    • Bulk glucose oxidase powder (food processing, diagnostics)
    • Catalase for beverage processing or industrial bleaching
    • Monoamine oxidase for pharmaceutical ingredient modification

    3. Clinical Diagnostic Reagents: Biochemical Assay Kits

    Diagnostic reagent manufacturers employ FAD-Na₂ as an essential electron carrier within in vitro assays for glucose, cholesterol, and amino acid quantification. Our material guarantees high lot-to-lot reproducibility, low bioburden, and explicit traceability, all necessary for regulated medical device reagent manufacturing. We maintain ultra-low contaminant profiles to fit medical/laboratory requirements.

    Industry compliance standards

    • ISO 13485 for medical device reagent manufacture
    • CLSI C62-A1 for clinical chemical reagents
    • FDA 21 CFR 809 (in vitro diagnostic product requirements)
    • IVDR (EU Regulation 2017/746)

    Typical usage ratio

    • 0.2–10 µmol per test kit batch, depending on enzymatic assay and detection sensitivity

    Downstream process integration

    • Weighted addition to pre-mix solution in lyophilized or liquid kit formulations
    • Final QC release based on UV-Vis absorption or HPLC purity profile
    • Validated storage and reconstitution procedures in ready-to-use reagent kits

    Final product types

    • Blood glucose monitoring strips
    • Cholesterol and lactate enzyme kits
    • Clinical bioanalytical lysate preps

    4. Food Biotechnology: Enzymatic Processing Aids

    Food manufacturers utilize FAD-Na₂ to optimize biotransformation processes, such as beverage clarification and flavor compound biosynthesis. Glucose oxidase processes for bread preservation or fruit juice stabilization often specify its controlled input. Our ingredient meets food additive codes for process aids, ensuring traceability for food safety audits and downstream quality declarations.

    Industry compliance standards

    • Codex Alimentarius General Standard for Food Additives (GSFA)
    • US FDA 21 CFR 173.357 (secondary direct food additives for enzyme preparations)
    • EU Regulation 1332/2008 for food enzymes
    • IFS Food/HACCP for supply chain traceability

    Typical usage ratio

    • 1–100 mg/kg in food process enzyme blends, depending on product application and downstream removal efficiency

    Downstream process integration

    • Batch addition during mixing of microbially-produced enzyme cocktails
    • Online monitoring for process control in juice stabilization and dough leavening
    • Accounted for as a processing aid, not present in final retail foods

    Final product types

    • Bakery enzyme blends for bread anti-staling
    • Fruit juice processing enzymes for improved clarity
    • Fermentation-derived aroma enhancement additives

    5. Animal Nutrition and Feed Additives: Enzyme Supplement Formulation

    Manufacturers of animal feed enzyme additives rely on FAD-Na₂ for formulation of oxidative enzyme premixes, especially glucose oxidase for poultry and aquafeed. Consistent supply and particle morphology support reliable large-volume mixing in premix and pelletizing lines. We test for residual solvents and contaminants per feed sector standards to ensure compliance and safety.

    Industry compliance standards

    • EU Regulation (EC) No 1831/2003 on feed additives
    • ISO 22000/FAMI-QS for feed additive production
    • China GB/T 1886.187 for feed enzyme products
    • US AAFCO (Association of American Feed Control Officials) definitions and labeling guidelines

    Typical usage ratio

    • 2–30 mg/kg in enzyme concentrate, adjusted for target feed type and formulation process

    Downstream process integration

    • Incorporated at blend stage with vitamin/mineral premixes before final pelletizing
    • Accuracy verified by in-plant NIR or wet chemistry analysis
    • QA records linked to batch number and supplier traceability program

    Final product types

    • Poultry and livestock enzyme premixes
    • Granulated feed additives for aquaculture
    • Powdered enzyme supplements for silage and ruminant feed
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    Certification & Compliance
    More Introduction

    Flavin Adenine Dinucleotide Disodium Salt: A Manufacturer’s Perspective

    Understanding Flavin Adenine Dinucleotide Disodium Salt (FAD Na2)

    Producing Flavin Adenine Dinucleotide Disodium Salt, with the chemical formula C27H31N9Na2O15P2, calls for both expertise and strict process control. At the plant, we have worked for years to optimize reaction conditions and ensure high purity. FAD Na2 functions as a redox cofactor, making it invaluable for those working on enzymatic reactions, diagnostics, research, and industrial biotechnology. The yellow, water-soluble crystalline powder we deliver can be produced with reliable quality and is ready for immediate application in various fields.

    Production: Real-World Challenges and Commitment to Purity

    Working with FAD Na2 isn't only a question of mixing chemicals. The synthesis process covers several stages, including enzymatic or chemical phosphorylation, careful neutralization, and a series of controlled purification steps. Trace contaminants can compromise the performance of sensitive assays or metabolic studies, so production staff have to check the intermediates, the temperature profiles, and the final filtration steps rigorously.

    Our experience tells us the importance of controlling pH during the synthesis, using high-grade reagents, and performing in-process HPLC analysis for every batch. We’ve seen researchers caught out by inconsistencies in off-the-shelf materials; so in our quality control, we focus heavily on batch-to-batch consistency and maintaining water content within a tight range—typically less than 8%. Moisture can degrade this cofactor rapidly.

    Physical Characteristics and Storage Considerations

    The light, yellow powder form of our FAD Na2 isn’t chosen for looks. This product absorbs moisture from air within minutes, which leads to degradation and loss of potency. From years of storage experience, we insist on vacuum-sealed packaging, low humidity environments, and storage at minus 20°C or below. These measures maintain potency for years. Clients frequently report problems with oxidation from other sources, so we have invested in inert-atmosphere packaging lines. No shortcuts here: every drum is nitrogen-flushed, double-bagged, and sealed.

    Key Specifications: What Sets Quality Batches Apart

    A range of grades exists on the market; some suitable for basic chemical applications and others able to meet the demanding requirements of diagnostic kit manufacturing and cellular research. Our team learned by troubleshooting: purity isn’t the only metric that matters. We analyze for residual nucleotides, pH in aqueous solution, exact sodium content, and UV-Vis absorption spectra. Bioactivity in enzyme assays gives the surest test—a specification sheet doesn’t always reveal whether a batch will deliver in high-sensitivity experiments.

    Seeing failed enzyme reactions in competitive offerings due to small impurity peaks in HPLC or altered UV spectra has pushed us to refine purification. Final lots exit our plant with purity consistently above 98% (HPLC, area %), an absorption maximum at 450 nm, and a minimum 90% recovery in commercial glucose oxidase or other oxidoreductase tests.

    Where FAD Na2 Supports Everyday Research and Industry

    In biochemistry labs, FAD Na2 acts as an electron carrier, essential for redox reactions. Our customers working in university and private research settings add it to enzyme assays for glucose oxidation, fatty acid oxidation, and dehydrogenase reactions. In clinical diagnostics, this molecule is a key reagent for oxidase and dehydrogenase test kits measuring glucose, cholesterol, and other metabolites. Researchers in the food quality sector use it for rapid, enzymatic detection of contaminants as well.

    We see biotech manufacturers using FAD Na2 in the bulk production of recombinant proteins—especially when the target enzyme needs a flavoprotein cofactor. It's a building block in biosensor development that translates biochemical activity directly into electrical signals. Stability during shipment becomes very important here, since sensor calibration depends on the preserved redox activity of the molecule.

    Differences Between FAD Na2 and Other Key Cofactors

    Sometimes we get requests comparing FAD Na2 to NAD+ or FMN. Each cofactor plays a different role. NAD+ interconverts as an electron shuttle in different metabolic pathways, while FMN is a simpler flavin that partners different sets of enzymes. FAD Na2 uniquely provides both adenine and flavin moieties, capable of tougher redox jobs. We always emphasize this difference during technical support calls—using FMN instead of FAD Na2 can completely change reaction outcomes.

    From our production side, preparing FAD Na2 takes more steps and longer purification than NAD+ or FMN. Its molecular size raises solubility and stability challenges, urging precise crystallization and controlled drying. Quality demands are also higher. While FMN can ship with a wider tolerance for impurities without affecting basic lab work, diagnostic kit buyers have zero tolerance for batch inconsistency in FAD Na2. Here, we provide full certificates of analysis, spectral scans, and lot documentation.

    Meeting the Needs of Highly Regulated Industries

    Many of the project teams we work with are producing IVD kits, therapeutics, or nutritional supplements and have regulators or auditors reviewing supply chains. We keep an archive of batch records, cross-reference every incoming and outgoing raw material, and invest in regular method validation. Many years of customer audits have taught us that cutting corners on traceability saves nothing in the long run.

    Our plant uses dedicated equipment for nucleotide and cofactor production, reducing risk of cross-contamination with unrelated organics. Customer feedback led us to introduce lot retention samples, and our documentation system matches each lot to raw material COAs and calibration standards. Stability testing is not a side note: we pull retention samples every few months and check performance in real-world assays.

    Solubility Issues and Solutions in Application

    Dissolving FAD Na2 sometimes creates headaches for research teams. The salt dissolves rapidly in neutral or slightly alkaline water, but hardness in tap water or high ionic strength can result in precipitation or cloudiness. We have worked closely with several clients to troubleshoot: always dissolve in deionized or distilled water, under gentle agitation, to avoid foaming and oxidation. Customers seeking to optimize enzyme reaction rates benefit from dissolving FAD Na2 shortly before use instead of storing solutions, since it slowly degrades even in buffer.

    The challenge of stability in aqueous solution has driven us to develop a line of smaller pack sizes and single-use vials, as well as custom packaging formats for process-scale applications. We also recommend preparing solutions in amber vials or under subdued light, since this cofactor is light sensitive.

    Packaging, Handling, and Delivery: Preventing Avoidable Losses

    We learned early on that the greatest threat to FAD Na2 stability doesn’t always come in the lab, but from shipping and storage. Oxygen, humidity, and temperature swings can quickly shorten shelf life and cause yellowing or diminished activity. Our packaging line uses moisture-proof, light-proof aluminum composite pouches, heat-sealed inside robust fiber drums or insulated boxes. Every lot leaves our plant labeled with production dates, expiry, and storage instructions that help ensure the reagent arrives in the same condition as it left our hands.

    Clients operating in regions with long transit times or high ambient temperatures are offered cold-chain shipping at no surcharge. We maintain stocks in deep-freeze warehouses for rapid call-off, preventing product degradation even if customs clearance delays occur. Professional handling by trained logistics teams who know the product’s sensitivity makes a difference in tight-deadline research work.

    Troubleshooting and Application Support

    Supporting our FAD Na2 goes beyond manufacturing and shipping. Over the years, we have resolved varied field issues: a faint color shift in assay output; unexplained loss of enzymatic activity; or a speck of particulate in a solution vial. Many times, such problems arise from overlooked details—using pipette tips with traces of detergents, relying on expired buffers, or exposing the product to fluorescent lights.

    We field technical questions directly from the end user, not through layers of resellers, so our advice comes from real failures and real solutions. For instance, we have recommended pre-flushing glassware with water, or running background controls to identify batch-specific quirks. Offering lots with custom sodium content or special particle size distributions became standard due to repeated requests from clients using high-pressure systems or microfluidic devices.

    Environmental and Regulatory Considerations

    Sustainability and compliance have become larger priorities in recent years. Waste streams arising in the synthesis of FAD Na2, mostly phosphate and organic residues, are managed in line with local and international requirements. We treat effluent and reclaim solvent wherever practical, not only to meet regulations but also to control costs.

    Clients in the pharmaceutical and food industry often ask about the origin of raw materials, and whether our processes match relevant GMP or ISO norms. Our plant uses only documented, traceable raw nucleotides from certified sources, and our cleaning, allergen management, and cross-contact controls are audited regularly. Regulatory inspections have reinforced our approach: if you leave gaps in documentation or skip validations, downstream recalls and regulatory penalties consume any savings made by cutting steps.

    Quality Assurance through Staff Training and Process Review

    Our plant has faced plenty of learning curves. Years ago, staff rotated between product lines. Errors from unfamiliarity with the unusual texture and sensitivity of FAD Na2 led to rejected batches and rework. Now we run continuous training and regular refresher courses focused only on nucleotide and cofactor production, investing in cross-checks, scheduled audits, and periodic method validation.

    Feedback loops with QA and R&D allow us to flag trends in minor impurities or complaints. Every week, our production group meets with technical and sales support to share findings from the field and update protocols. Direct communication between users, production, and QC bridges the gap between lab data and practical realities.

    Continuous Improvement: Listening to the Field

    Delivering reliable FAD Na2 isn’t just a technical challenge—it’s a process of adapting to new requirements. Clients from research sometimes shift to commercial scale, and with that come demands for larger, sterility-assured batches, or varied pack sizes. We work with end users to incorporate tailored solutions—like low-dust powders for automation, or longer-shelf-life pack formats for extended projects. Each new request leads our technical team to review the production scheme, cross-check interfaces, and sometimes trial new stabilization chemistries.

    Mistakes and surprises along the way have taught us more than any list of “best practices.” It took one high-profile batch failure, many years ago, for us to overhaul our humidity monitoring, and another customer’s failed validation to prompt us to strengthen documentation. These continuous lessons shape every batch we now ship.

    What Matters Most: Building Trust in Every Batch

    The research and diagnostics landscape is evolving quickly. New analytical methods, regulatory standards, and customer expectations surface all the time. In this environment, the core of our work remains simple: making sure each lot of FAD Na2 supports an experiment, a process run, or a diagnostic test without surprises.

    We invest in people, process, and infrastructure so scientists and product developers can focus on innovation instead of troubleshooting. From our perspective as the producer, it’s not the fancy terminology or shiny data sheets that define our FAD Na2—it’s the accumulation of daily diligence, focused improvement, and learning hard lessons side-by-side with our customers.