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D-Glucose-6-Phosphate Disodium Salt

    • Product Name D-Glucose-6-Phosphate Disodium Salt
    • Alias G6P
    • Einecs 248-278-5
    • 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

    448879

    Product Name D-Glucose-6-Phosphate Disodium Salt
    Synonyms Glucose-6-phosphate disodium salt, G6P Na2
    Chemical Formula C6H11Na2O9P
    Molecular Weight 306.10 g/mol
    Cas Number 3671-99-6
    Appearance White to off-white powder
    Solubility Soluble in water
    Storage Temperature 2-8°C
    Purity Typically ≥98%
    Empa Number EMPA 10036
    Ph Value 6.5 - 7.5 (50 mg/mL in H2O)
    Use Biochemical research, enzyme substrate

    As an accredited D-Glucose-6-Phosphate Disodium Salt factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing D-Glucose-6-Phosphate Disodium Salt is supplied in a sealed amber glass bottle, labeled, containing 25 grams of fine white powder.
    Shipping D-Glucose-6-Phosphate Disodium Salt is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be stored and transported at controlled room temperature. Appropriate labeling and handling precautions are followed to ensure safety and compliance with relevant chemical transport regulations. Avoid exposure to extreme temperatures and direct sunlight.
    Storage D-Glucose-6-Phosphate Disodium Salt should be stored tightly sealed in a cool, dry place, protected from light and moisture. Recommended storage temperature is at 2–8°C (refrigerated). Avoid exposure to air and contaminants. Properly label and store the chemical in its original container, away from incompatible substances. Ensure that storage complies with safety and regulatory guidelines for laboratory chemicals.
    Application of D-Glucose-6-Phosphate Disodium Salt

    Applications of D-Glucose-6-Phosphate Disodium Salt in Industrial Manufacturing

    D-Glucose-6-Phosphate Disodium Salt serves as a vital biochemical intermediate in bio-industrial fermentation, pharmaceutical synthesis, in vitro diagnostic reagent formulations, medical research kits, and specialized food ingredient applications. As a direct manufacturer, we ensure strict quality and supply consistency to meet the demands of advanced industrial customers worldwide.

    1. Biotechnological Fermentation and Cell Culture Media

    In industrial-scale fermentation, D-Glucose-6-Phosphate Disodium Salt functions as an essential energy source and metabolic regulator for microbial and mammalian cell culture production systems. It enters glycolytic pathways directly, supporting high-efficiency biosynthesis for products such as recombinant proteins and therapeutic enzymes. Controlled dosing prevents excessive acidification and allows for precise modulation of cell growth and productivity, especially during glucose-limited fed-batch or perfusion processes. Manufacturers in vaccine, antibody, and biopharma intermediate production rely on highly pure imports with consistent solubility and endotoxin profiles to maintain batch reproducibility and meet regulatory submissions.

    Industry compliance standards

    • Ph. Eur. 10.0 standards (cell culture media reagents)
    • USP <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • OECD/ICH Q5A (Viral safety in biopharmaceuticals)
    • 21 CFR Part 211 (cGMP for finished pharmaceuticals)

    Typical usage ratio

    • Generally 0.2–1.5 g/L as a feed supplement in multiple-stage media depending on cell density and metabolic rate
    • Adjustment based on real-time glucose/lactate monitoring and downstream product yield targets

    Downstream process integration

    • Dissolve into feed streams for bioreactors or seed train expansion steps
    • Applied as a controlled supplement in glucose-managed fed-batch strategies
    • Utilized in high-density culture protocols for increased target protein concentrations

    Final product types

    • Recombinant antibodies (IgG, IgM)
    • Vaccine antigens (viral protein subunits)
    • Therapeutic enzymes (glucocerebrosidase, Pegloticase)
    • Cell-culture derived diagnostics and culture-adapted virus seeds

    2. In Vitro Diagnostic Reagent Manufacturing

    Diagnostic kit producers utilize D-Glucose-6-Phosphate Disodium Salt as a key substrate in enzyme-coupled assays, particularly for glucose-6-phosphate dehydrogenase (G6PD), hexokinase, and NADPH cycle reactions. The material requires high assay-grade purity (<0.5% heavy metals, minimal microbial contamination) for reliable colorimetric and spectrophotometric measurements. Reagent stability is critical for shelf life and clinical accuracy. Strict batch records, traceable lot documentation, and compliance with IVD manufacturing standards ensure analyte sensitivity and specificity for use in clinical biochemistry laboratories and point-of-care devices.

    Industry compliance standards

    • IVDR (EU) 2017/746 for in vitro diagnostic medical devices
    • ISO 13485:2016 (QMS for medical device manufacturers)
    • CLSI C24-A3 (Clinical laboratory reagent quality control)
    • 21 CFR 820 Subpart C (IVD design controls)

    Typical usage ratio

    • Substrate concentrations typically 1–10 mM in test kit formulations
    • Exact mass per vial depends on targeted working range and kit calibration protocol

    Downstream process integration

    • Direct addition into buffer matrices for ready-to-use reagent preparation
    • Lyophilized or liquid reagent blends for automated analyzer cartridges
    • Sequential incorporation in stepwise enzyme-coupled reaction platforms

    Final product types

    • Blood glucose monitoring kits (hexokinase method)
    • G6PD activity test strips
    • Biochemistry panel assay sets
    • Research-use-only enzyme diagnostic kits

    3. Pharmaceutical API Synthesis (Intermediates)

    Pharmaceutical firms employ D-Glucose-6-Phosphate Disodium Salt as an intermediate during multistep active pharmaceutical ingredient synthesis, especially for nucleotide analogues, metabolic disorder treatments, and cofactor-enriched parenteral formulations. High purity with strict heavy metal and bioburden limits is mandatory. Producers must qualify all raw material lots via validated analytical methods to avoid cross-contamination. Documentation for Drug Master Files (DMFs) and repeated supply audits ensure traceability from procurement to downstream hydrochloride or riboflavin ester derivatives. Particle size and hydration state determine suitability for solid-phase or liquid process routes.

    Industry compliance standards

    • USP-NF monograph (when applicable for intermediates)
    • ICH Q3A/B (Impurities in new drug substances/products)
    • EU GMP Annex 8 (API supply chain traceability)
    • FDA Guidance for Industry: Drug Master Files

    Typical usage ratio

    • Feedstock concentration varies 0.05–0.25 mol/mol relative to nucleobase or amino alcohol reactant
    • Dose rate adjusted for process yield and impurity thresholds in specific synthesis routes

    Downstream process integration

    • Introduced during phosphorylation or glycosylation reaction stages
    • Mixed in aqueous-organic slurries for batch or flow chemistry setups
    • Filtered prior to coupling reactions to remove residual particulates

    Final product types

    • NADP/NADPH cofactor precursors
    • Phosphate prodrug intermediates
    • Liver glycogen metabolism disorder APIs
    • Rare disease treatment compounds

    4. Nutraceutical and Medical Food Ingredient Formulation

    Medical food manufacturers incorporate D-Glucose-6-Phosphate Disodium Salt in controlled-release oral and parenteral nutrition blends designed for specific patient populations, such as individuals with glycogen storage disease or inherited metabolic deficiencies. The ingredient provides bioavailable glucose-6-phosphate for rapid replenishment of cellular energy stores, reducing the metabolic burden on impaired pathways. Blending protocol requires allergen-free, non-GMO raw material with cGMP-level traceability. Finished formula development involves pilot-scale compounding to validate nutrient stability, caloric accuracy, and sensory acceptability for clinical settings.

    Industry compliance standards

    • FDA 21 CFR Part 104 (Nutritional Quality Guidelines for Foods)
    • EU Regulation (EU) No 2016/128 (Food for Special Medical Purposes)
    • FSSC 22000 (Food Safety System Certification)
    • ISO 22000:2018 (Food safety management)

    Typical usage ratio

    • Added at 0.5–4% w/w in nutrient powders or 2–12 g per serving in clinical oral solutions
    • Concentration adjusted on basis of end-use energy release profile and patient tolerance study results

    Downstream process integration

    • Pre-mixed in low-humidity blending rooms to prevent caking and preserve flowability
    • Homogenized into single-serve sachets or liquid fill forms with micronutrient premixes
    • Sterile filtration for ready-to-administer parenteral or enteral products

    Final product types

    • Medical food blends for metabolic management
    • Specialized oral rehydration powders
    • Nutritional supplements for clinical nutrition
    • Hospital-use energy management solutions
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    Certification & Compliance
    More Introduction

    D-Glucose-6-Phosphate Disodium Salt: Our Take as the Manufacturer

    Understanding the Role of D-Glucose-6-Phosphate Disodium Salt

    In our daily grind here in the plant, few products see as much hands-on attention as D-Glucose-6-Phosphate Disodium Salt. On the surface, it looks like just another powder, but over the years we’ve seen firsthand how this compound shapes critical processes in research, diagnostics, and industrial biotechnology. Unlike standard glucose, this salt merges the pathways of biochemistry and practical application, delivering more than just a source of sugar. It acts as a direct precursor for a number of metabolic steps, and its disodium form means it behaves reliably in a wide range of solutions—a quality that sets it apart for many customers.

    From Raw Materials to Reliable Output

    We start with quality raw D-glucose. The modification process involves controlled phosphorylation using carefully selected reagents. The result must consistently offer the right solubility and chemical identity, which we check batch after batch using rigorous in-house analytics. Over the years, the feedback we get from regulars in diagnostics and enzymology labs has helped us fine-tune drying conditions, purity benchmarks, and packaging options. Moisture control is tricky: too much, the salt cakes and loses flow; too little, and static builds. Every step shows up in the final granule size, which influences how fast it dissolves and how consistently it interacts with enzymes in actual assays. That’s not something that happens by accident, especially at industrial scale.

    Model and Specifications: Why They Matter in Practical Terms

    We produce several models, tailored by grade and intended usage. Some demand analytical purity for enzyme assays or clinical chemistry; others call for technical grades used in fermentation or bulk synthesis. The main difference boils down to the level of trace metals, organic impurities, and residual moisture content. Tight control lets us offer our top-selling variant at over 98% purity by HPLC, based on feedback from university labs running sensitive dehydrogenase experiments. Others opt for a slightly lower grade, saving cost on industrial-scale runs where fraction-of-a-percent differences don’t impact yield.

    Years ago, we had trouble with cross-contamination during production changeover, especially in lines switching from sodium to potassium salts. That drove us to develop stricter cleaning routines and exclusive equipment. These adjustments, while costly upfront, cut down on unpredictable test results and call-backs, something our users appreciate when scale-up timelines are tight. We add a check for heavy metals below 5 ppm, and always test for endotoxins, even in non-pharma batches, because no one wants surprise interference when running cell-based assays.

    Where D-Glucose-6-Phosphate Disodium Salt Fits into the Real World

    You see this salt most often on the bench in research labs exploring glycolysis or pentose phosphate pathways. We’ve noticed routine orders from cell metabolism groups, usually buying our highest grade for spectrophotometric enzyme activity kits. Others employ it in fermentation boosters or as a biochemical standard for calibration curves. We get the occasional call from the food industry, chasing novel uses in flavor or preservation, though these uses are more limited compared to classic buffers or sweeteners.

    On the analytical side, assay manufacturers mix our salt into ready-to-use kits for blood glucose diagnostics. Having walked dozens of customers through troubleshooting enzyme kinetics, we’ve learned the value of a consistently behaving substrate with well-defined solubility and zero unexplained color. In high-throughput settings, even a small inconsistency in granulation or residual phosphate makes the difference between reliable data and wasted batches. Our team has stressed that point during every customer visit, making purity and reproducibility a recurring theme.

    The Chemistry Behind the Salt

    As straightforward as the name sounds, D-Glucose-6-Phosphate Disodium Salt packs plenty of chemistry into a single molecule. It bears a glucose backbone, phosphorylated at the 6-carbon, capped with two sodium ions to ensure electrical neutrality and easy handling. Compared to regular glucose, it’s less hygroscopic, which means it stores better and tolerates quick weighing without clumping up. Our technical staff always points out that the disodium variant maintains a stable pH in solution, which customers love when working with sensitive enzyme cocktails.

    Phosphorylation brings its own challenges, though. The tendency of phosphates to react with residual metals or trace contaminants means every run needs fresh solvents and careful monitoring of glassware and plasticware. Even minor missteps, like using untreated water or reusing containers, show up as impurities in later tests. We learned early that batch-to-batch consistency relies on paying close attention long before the salt ever reaches final filtration.

    Distinctions from Other Similar Compounds

    D-Glucose-6-Phosphate exists in other forms, including monopotassium, monocalcium, and free acid. The disodium salt stands out for its rapid dissolution in water, low chelation liability, and predictable performance across pH 6-8. Unlike monopotassium salts, which can skew buffer systems and require extra adjustment, our product avoids introducing excess potassium ions—which sometimes interfere in sodium-based enzyme systems. Years ago, a major client tipped us off to unexpected inhibitory effects when switching from sodium to potassium buffer; since then, we’ve always verified ion compatibility for specialty grades.

    Different salt types also influence storage life. The disodium variety holds up better against humidity pickup—a big advantage for users in tropical climates, or those lacking dedicated climate control in their storerooms. Free acid forms, impressive on paper, often need stabilizers and fast application before they break down; our disodium formulation gives users a more forgiving window. Listening to researchers complain about “mystery degradation” in overseas shipments steered us toward thick, moisture-barrier pouches and deliberate warehouse airflow, decisions that improved shelf life by months.

    Supporting Innovation with the Right Ingredients

    Much of the research momentum in metabolism and diagnostics builds on the availability of consistent, high-purity substrates. D-Glucose-6-Phosphate Disodium Salt has become a backbone standard for those exploring pathways involving hexokinase, glucose-6-phosphate dehydrogenase, and other enzymes central to modern biology. Without a trustworthy starting material, assay control becomes a roll of the dice. From our own batch logs, we’ve fielded requests for sub-ppm impurity limits and custom screening protocols because even the smallest unknown component can stymie a cell culture run or mask the true result of a metabolic assay.

    Keeping pace requires more than holding to certificates of analysis. We field real-world questions: “Will your latest lot dissolve in saline as fast as the last one?” or “Did you tweak the drying cycle last quarter?” Our response relies on frequent in-process checks and customer-facing tech support, because an out-of-spec batch isn’t just a hassle for us—it can derail a funding round or clinical study for the end user. Over time, that lived experience built the company’s reputation as a behind-the-scenes fixer, the supplier that not only understands chemical structures but also knows how a missed trace contaminant can jam up an entire month’s worth of work.

    The Practicalities of Packaging and Transport

    Big buyers come in with logistics concerns, especially those sending shipments abroad or needing to restock multiple sites. D-Glucose-6-Phosphate Disodium Salt travels best in high-barrier, low-permeability bags, heat-sealed to guard against moisture migration. Open bins or thin plastic liners won’t cut it—turnover tests in our own storerooms showed early on that cheap packaging led to rapid caking and, in bad cases, false-negative results in colorimetric tests. We went back and swapped packaging suppliers to improve multilayer bags, and started double-bagging for shipments leaving the region. That proved worth the investment: customers dealing with tropical or monsoon climates rarely talk about clumping or loss of solubility anymore.

    Large-volume buyers sometimes need drums, but we push for smaller units if turnover is slow. Few things waste more product than a half-used barrel left open too long. Staff training on resealing, humidity control, and stock rotation make a real difference—many of our partners report fewer rejected lots when following these basic procedures. It’s not glamorous, but it keeps standards high across the whole supply chain.

    Meeting Regulatory and Analytical Expectations

    Research-grade D-Glucose-6-Phosphate Disodium Salt faces tight scrutiny, especially in applications intersecting with clinical trials or published analytical methods. Our batches ship with full traceability to each synthesis run, so users running ISO or GLP labs don’t get caught without the right certificates. Many pharma and biotech clients want to know not only the assay result, but also the nitty-gritty: microbial counts, heavy metal traces, and exact moisture numbers, all checked right before dispatch. We’ve had our own QC team tune mass spectrometry protocols to flag even trace degradants, cutting down complaints about “off” lots that disrupt test kits and downstream processes.

    Documentation matters just as much as product homogeneity. The best batches come with tight paperwork, proving every step was followed, every variable monitored, and every anomaly explained or quarantined. This expectation, honed through numerous audits and unscheduled spot-checks, keeps our internal procedures sharp and our staff invested in ongoing improvement. In some ways, the experience of recovering a batch redirected to “hold” after an outlier test pushes us further than any outside regulations. That sense of responsibility travels with every unit we pack and ship.

    Feedback Loops and Product Refinement

    Few improvements spring wholly from novel invention. Most gains come from open dialogue with regular users, audit teams, and in-house technical staff who spot patterns in complaints and requests. One example involves solubility challenges: several university clients, using automated pipetting robots, reported clogging and settling in high-throughput well plates. We ran extra particle-size analyses, found a small fraction of overgrown crystallites, and adjusted our grind cycle—solving the problem in time for their next semester run.

    In another case, demand from contract manufacturers led to tighter controls on sodium ion content. They found minute drifts in sodium levels tipped the balance in multienzyme preparations, especially for those scaling up to pilot production. Based on their shared batch data, we reviewed dosing procedures and tweaked calibration of our addition equipment, shaving down lot-to-lot drift.

    We also get requests for customization, though these take time to validate. One trend involves blending D-Glucose-6-Phosphate Disodium Salt into premixes for veterinary diagnostics, sparing end users from individual weighing and reducing error. Coordinating with customers, we help them troubleshoot stability and reactivity issues that pop up when combining multiple actives into a single sachet.

    The Ongoing Role of D-Glucose-6-Phosphate Disodium Salt

    Each week, we see how this product reflects broader trends in diagnostics, research, and production. Enzyme kinetics studies continue to expand, and every incremental assay improvement trickles down to people working in core labs, food testing, or point-of-care diagnostics. Our team anticipates more requests for higher purity, smaller batch sizes, or dynamic packaging as priorities evolve. In the last year, the upswing in remote learning and decentralized trials pushed increased sales to university departments with small, repeat orders and a demand for extra documentation.

    Operational agility on the manufacturing side stays essential. Raw input quality fluctuates, as suppliers deal with swings in agricultural availability and market price. Our purchasing, production, and QC arms meet regularly to calibrate lots, anticipating seasonal changes in supply chain reliability. Cross-functional cooperation—a fancy term in some industries—is a living reality in ours. Everyone from operators to engineers to sales and regulatory staff needs a unified sense of the task at hand. Any lapse ripples outward and can show up three months later on a customer’s bench.

    Risks and Troubleshooting on the Manufacturing Floor

    No process runs perfectly. Process drift remains an ever-present threat. Careless handling or unexpected contamination in the phosphate addition step still shows up in our process deviation logs every so often. A burst of humidity or an undetected crack in a process line can tip an entire batch out of spec. Open communication, process transparency, and quick recall systems protect both our bottom line and the trust of those relying on our material. Our willingness to pull or retest inventory has built loyalty among buyers who can’t afford uncertainty.

    On a technical level, analytical instrumentation shapes everyday troubleshooting. Whenever a performing batch lands at 97% where 98% is required, or shows a shadow peak on the chromatogram, root cause analysis follows. We track every formulation deviation, mill setting shift, and batch sample mishap. Sometimes user-side problems drive improvement too: we’ve developed a dedicated Q&A channel, connecting technical experts directly with customers to resolve issues or answer specific use questions, ensuring that issues don’t languish in automated queues. These strategies mean more predictable outcomes—for us and for the scientists depending on sharp assay results.

    Looking Forward: The Next Chapter

    In the course of working with D-Glucose-6-Phosphate Disodium Salt, patterns emerge. Users increasingly lean on us to deliver not just a reliable raw material, but also clear data, understandable instructions, and responsive technical support. Researchers racing to deadline, engineers scaling up processes, and analysts troubleshooting results all need a supplier who listens as closely as they manufacture. Our participation in industry forums and user workshops brings new ideas and uncovers pockets of demand we might have missed.

    We expect market demand to shift further toward granular documentation, traceability, and flexible supply options. New research into enzyme function, diagnostics miniaturization, and bio-manufacturing puts pressure on us to deliver both purity and convenience. By keeping our ear to the ground—hearing what works and where pain points crop up—we hope to stay not just a vendor, but an actual partner in scientific advancement. The story of D-Glucose-6-Phosphate Disodium Salt, at its core, becomes a record not simply of what we make, but how we adapt, troubleshoot, and support, every day.