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4-Methylumbelliferyl Phosphate Disodium Salt

    • Product Name 4-Methylumbelliferyl Phosphate Disodium Salt
    • Alias MUP
    • Einecs 252-730-6
    • 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

    512412

    Name 4-Methylumbelliferyl Phosphate Disodium Salt
    Cas Number 6336-78-9
    Molecular Formula C10H8Na2O6P
    Molecular Weight 320.12 g/mol
    Appearance White to off-white powder
    Solubility Soluble in water
    Storage Temperature -20°C
    Purity Typically ≥98%
    Synonyms 4-MUP, MUP disodium salt
    Lambda Max 360 nm (fluorescence excitation)
    Ec Number 228-934-1
    Application Phosphatase substrate

    As an accredited 4-Methylumbelliferyl Phosphate Disodium Salt factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 100 mg clear glass vial with a screw cap, labeled "4-Methylumbelliferyl Phosphate Disodium Salt."
    Shipping 4-Methylumbelliferyl Phosphate Disodium Salt is shipped in tightly sealed containers, protected from moisture, light, and extreme temperatures. Typically dispatched as a solid, it may require refrigeration or shipment with cold packs based on stability data. All packaging complies with chemical safety and transport regulations to ensure safe delivery.
    Storage **4-Methylumbelliferyl Phosphate Disodium Salt** should be stored tightly sealed in a dry, dark, and well-ventilated area at –20°C, protected from moisture and light. Avoid repeated freeze-thaw cycles. Use appropriate personal protective equipment when handling. Proper storage prevents decomposition and maintains the compound's stability for reliable experimental results. Follow all relevant safety and chemical storage guidelines.
    Application of 4-Methylumbelliferyl Phosphate Disodium Salt

    Applications of 4-Methylumbelliferyl Phosphate Disodium Salt in Industrial Manufacturing

    4-Methylumbelliferyl Phosphate Disodium Salt (MUP) is widely used as an enzymatic substrate in several specialized industrial and laboratory processes. As a direct manufacturer, we ensure consistent quality suitable for demanding downstream formulations and automated production lines. Below, we detail key application segments with precise regulatory, process and integration information.

    1. Clinical Diagnostics – Fluorogenic Enzyme Assays

    In clinical laboratory diagnostics, this raw material forms a core substrate for the fluorometric quantification of phosphatase activities, including alkaline phosphatase in human serum, plasma, and urine. Laboratories incorporate MUP into automated assay panels for disease marker detection. This segment necessitates careful attention to purity, compatibility with high-throughput robotic pipelines, and precise calibration against clinical QC standards.

    Industry compliance standards

    • CLSI (Clinical and Laboratory Standards Institute) guidelines for in vitro diagnostic substrates
    • ISO 15189:2012 for Medical Laboratories
    • FDA 21 CFR 820 (QSR) for diagnostic devices
    • IVDR (EU 2017/746) for in vitro diagnostic medical devices

    Typical usage ratio

    • Assay buffer concentrations between 0.05–1.0 mM, adjusted according to the detection window and enzyme kinetics requirements

    Downstream process integration

    • Formulated into ready-to-use diagnostic reagent kits
    • Dissolution into lyophilized reagent matrices
    • Inclusion in calibrator and control panels for analyzer platforms
    • Direct supply to automated assay cartridge filling stations

    Final product types

    • Clinical chemistry test kits for phosphatase assays
    • Point-of-care diagnostic cartridges
    • Automated analyzer reagents for hospital laboratories
    • Pre-calibrated phosphatase activity standards

    2. Food Safety Testing – Residue Detection Panels

    Food laboratories employ MUP substrates for precise fluorometric detection of phosphatase activity in residue analysis protocols, particularly for verifying pasteurization efficiency in dairy manufacturing. Stringent food safety compliance, reproducible dosing, and compatibility with multiple matrix types are essential for integration into testing automation environments.

    Industry compliance standards

    • ISO 17025 for testing and calibration laboratories
    • AOAC Official Methods of Analysis (phosphatase tests for dairy)
    • EU Regulation 2073/2005 on microbiological criteria for foodstuffs
    • US FDA Grade “A” Pasteurized Milk Ordinance (PMO)

    Typical usage ratio

    • Buffer concentrations typically set in the range of 0.1–0.8 mM, based on matrix interference and instrument sensitivity calibration

    Downstream process integration

    • Direct blending into premixed milk residue test reagents
    • Lyophilized pellets for portable testing kits
    • Incorporation in multi-analyte food screening plates
    • Batch-preparation for automated sample loading systems

    Final product types

    • Dairy pasteurization validation kits
    • Food phosphatase residue test strips
    • Portable field test cartridges
    • High-throughput food screening analyzers

    3. Water and Environmental Testing – Enzymatic Fluorimetric Analysis

    Environmental laboratories leverage MUP for quantifying alkaline phosphatase activities in water quality monitoring and wastewater analysis. This application demands trace impurity data, low fluorescence background, and reliable performance under a diverse range of aquatic matrices typical to regulatory reporting and industrial discharge characterization.

    Industry compliance standards

    • ISO 6878:2004 for phosphate determination in waters
    • United States EPA Standard Methods 4500-P E
    • EN ISO/IEC 17025 for environmental testing laboratories
    • GLP (Good Laboratory Practice) as per OECD guidelines

    Typical usage ratio

    • Assay concentrations between 0.05–0.5 mM, optimized based on ambient phosphate background and sample turbidity

    Downstream process integration

    • Solution blending for chromogenic substrate packs
    • Pre-dosed vials for on-site water analysis
    • Integration into continuous-flow analyzer reagent reservoirs
    • Bulk supply for municipal wastewater monitoring systems

    Final product types

    • Field-test water analysis kits
    • Continuous monitoring reagents for wastewater plants
    • Analytical reagent sets for river and lake surveys
    • Environmental compliance screening panels

    4. Biotechnological Research – Enzyme Kinetics and High-Throughput Screening

    Biotech companies and contract research organizations deploy MUP in the screening and characterization of phosphatase enzyme activity, stability, and inhibition for pharmaceutical and agricultural enzyme discovery. As a sensitive fluorogenic substrate, it requires low-leach packaging, batch consistency, and compatibility with robotic liquid handling in high-throughput workflows.

    Industry compliance standards

    • GLP guidelines for non-clinical laboratory studies
    • ISPE Good Automated Manufacturing Practice (GAMP)
    • EU 2023/607 for in vitro research chemical supply
    • ISO 9001:2015 for quality management systems in R&D

    Typical usage ratio

    • Concentration in assay buffers from 0.01–0.2 mM, adjusted by well volume and signal amplification requirements

    Downstream process integration

    • Dispensing into 96-/384-well microplate formats
    • Ready-mix substrates for robotic pipetting systems
    • Inclusion in high-throughput assay reagent cocktails
    • Bulk supply for custom screening assay manufacture

    Final product types

    • Enzyme assay microplates
    • Robotic screening reagent kits
    • Research-use-only fluorogenic assay panels
    • In vitro enzyme study reference standards

    5. Pharmaceutical Quality Control – Enzyme-Based Contaminant Testing

    Pharmaceutical manufacturers use this substrate for process control and quality assurance steps including monitoring residual phosphatase activity in vaccine and protein biotherapeutic production. Integration into regulated QC environments requires extensive batch traceability, compliance with pharmacopoeial standards, and technical support for validation documentation.

    Industry compliance standards

    • USP <1043>Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • Ph. Eur. 2.6.3 (European Pharmacopoeia enzyme testing)
    • ICH Q7 GMP for active pharmaceutical ingredients
    • PIC/S Guide to Good Manufacturing Practice

    Typical usage ratio

    • Standard addition typically at 0.05–0.3 mM in QC sample buffers, modulated to meet LOD/LOQ validation targets

    Downstream process integration

    • Incorporation into QC kit assembly for process validation
    • Batch-formulation of intermediate test reagents
    • Filling into pre-sterilized vials for GMP-compliant labs
    • Direct use in biomanufacturing environmental control protocols

    Final product types

    • Pharmaceutical process QC kits
    • Vaccine contaminant test reagents
    • GMP-certified protein purification validation panels
    • In-process enzyme monitoring solutions
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    Certification & Compliance
    More Introduction

    4-Methylumbelliferyl Phosphate Disodium Salt: From Bench to Batch

    Introducing a Reliable Substrate for Enzyme Assay Applications

    At our chemical manufacturing facility, every batch of 4-Methylumbelliferyl Phosphate Disodium Salt results from hands-on commitment to quality and application focus. This compound, recognized by its abbreviated name MUP-Na2, consistently supports research and diagnostics with its specificity as a fluorogenic substrate for phosphatase enzymes. Across many years of production, we have fine-tuned our process to deliver a bright, free-flowing powder exhibiting strong purity and lot-to-lot repeatability. It is our direct experience in synthesis and handling that allows us to shed light on what truly matters when working with MUP-Na2.

    Taking a Closer Look: Model and Specifications

    We produce MUP-Na2 with a close eye on both raw material integrity and process control. Each batch undergoes a series of in-process checks to ensure the appearance matches a uniform, pale yellow to white crystalline powder. Water content, spectral properties, melting point, and chromatographic purity all receive thorough scrutiny—not because these metrics simply fill a checklist, but because they directly affect solubility, reactivity, and storage stability in your hands. The final product typically ships at at least 98% purity (HPLC). Each package includes a certificate of analysis for full transparency. The product maintains stability in dark, dry storage at 2-8°C, with our real-time and accelerated stability studies consistently supporting extended shelf life.

    Why Formulation and Handling Matter

    The physical form of MUP-Na2 impacts how it dissolves and responds in your applications. We keep the particle size narrow to support even dissolution in water or buffering solvents. Unlike some higher-hygroscopic competitors on the market, our manufacturing method yields a salt with minimal caking and clumping. Everyone on our production floor knows clumpy product wastes time—whether in a large automated lab or a single benchtop dissolver. Moisture testing receives special attention. Years ago, we noticed how even minor upticks in water content led to diminished shelf stability and occasional discoloration, so we now employ a two-step drying sequence and a low-permeability inner sleeve for every container.

    Applications: Experience from Real-World Labs

    Clients approach us with a range of end uses for MUP-Na2. Its most valuable performance shows in phosphatase assay systems, specifically alkaline phosphatase and acid phosphatase detection. In practice, researchers value the product for its high fluorescence yield: after enzymatic hydrolysis, 4-methylumbelliferone (4-MU) is liberated, fluorescing under UV with a sharp emission maximum. This clarity allows for sensitive quantitation even from low-abundance samples. Environmental water analysis, newborn screening, food quality control, and cell biology workflows rely heavily on the consistency of the substrate signal.

    Typical assays employ concentrations ranging from micromolar to millimolar, often in buffered solutions at physiological pH. Based on customer feedback and comparative testing in our own application lab, we can confirm that the disodium salt dissolves quickly with gentle swirling, making it well-suited to high-throughput microplate and cuvette workflows. In our on-site demonstration lab, side-by-side performance shows signal-to-noise ratios on par with trusted global reference standards, with minimal background fluorescence in blank controls.

    MUP-Na2 Versus Other Fluorogenic Phosphatase Substrates

    For those comparing MUP-Na2 to related enzyme substrates (like p-nitrophenyl phosphate or 6,8-difluoro-4-methylumbelliferyl phosphate), several advantages stand out. MUP-Na2 produces a fluorescent product upon hydrolysis, allowing for much lower detection limits compared to chromogenic options. While p-nitrophenyl phosphate provides colorimetric results, laboratories targeting high sensitivity or small-volume samples nearly always pick MUP due to its cleaner signal and compatibility with standard fluorescence readers. MUP-Na2 supports both endpoint and kinetic assays, with little photobleaching during standard exposure times.

    In a direct comparison with methoxy-substituted analogs, our data reveal narrower excitation and emission bands with lower background interference from common biological matrices. Researchers processing turbid or colored sample types regularly report that MUP-Na2 maintains accuracy even when matrix coloration would mask weaker chromophores. Everyday experience in our own small pilot plant confirms this: our technicians have pulled raw water and nutrient-rich food extracts straight into model assays, seeing the 4-MU signal remain discrete and strong as expected.

    Supporting Science—And Loyalty—Over the Long Term

    Product stability and reproducibility take priority in our operation. Each packaging run receives full traceability, with stability testing drawn from both product retained at our facility and customer feedback on long-term storage observations. Several years back, we reformulated our primary packaging material in response to shipment feedback from humidity-prone regions; the resulting drop in moisture uptake and clump formation exceeded 70%. Labs using automated reconstitution lines saw nearly 100% recovery rates, compared to previous outcomes where clumped substrate went partially unused.

    As manufacturer, we maintain direct collaboration with a range of academic, clinical, and industrial partners. This exchange keeps us sharp to trends and problems in the field. One example: several customers flagged fluorescence drift in stored, pre-diluted substrate solutions. Our internal lab took this head-on, systematically testing buffer systems, storage conditions, and dilution factors. We found the best results with dilution in freshly prepared 50 mM Tris or imidazole buffer at pH 9.0, stored protected from light, and used within a day of preparation. The learning shows how a direct link to both manufacturing and applied science creates value—results we can share with you, not just theoretical numbers.

    Dealing With Batch Variation and Quality Control

    In earlier years, lots of biological substrate chemicals landed in research labs with no guarantee of lot-to-lot consistency. It quickly became clear in our own enzyme evaluation trials that even minor impurities from incomplete synthesis or over-drying alter fluorescence background and assay kinetics. Our QC team now validates each batch using side-by-side enzyme assays referenced against an established internal standard, not just chemical purity alone. This solves the practical issues that crop up in multi-site clinical testing or regulatory science, where one rogue lot creates unnecessary headaches and re-runs. We publish statistical summaries of fluorescence yield for each lot, so researchers can anticipate trivial adjustments rather than wrestling with unexplainable shifts in baseline values.

    Customer Questions—and Realistic Answers

    Questions about MUP-Na2 often move beyond simple “is it pure” or “how should I store it.” We regularly field applications support around assay miniaturization, automated dispensing, spectral interference, and matrix effects. For example, an industrial food test developer reached out, having trouble with high-humidity lab conditions. Together, we mapped out gradual acclimatization steps and best-in-class sealing techniques, which prevented clumping and ensured repeatable pipetting. Beyond that, questions about detecting enzyme kinetics versus endpoint measurements led us to re-test time-course sensitivity, confirming that MUP-Na2 signals remain linear over more measurement cycles than many alternative substrates, based on our own plate reader data.

    By taking every caller seriously—whether academic postdoc or industry QC analyst—we often spot overlooked process details. Not long ago, a clinical lab flagged faint fluorescence in a stored substrate solution. Working through their handling process with them, we identified a trace buffer contaminant from a nonstandard cleaning agent. Resolving cases like this helps all downstream users avoid similar snags. These feedback loops with day-to-day users drive small improvements in our production, packaging, and documentation.

    Why Manufacturing Expertise Matters

    Unlike traders or resellers, we control process conditions from the very first raw material to final fill and packaging. This gives us flexibility to reformulate, troubleshoot, and support specialty requests without delay. Our synthesis and isolation methods sit on decades of study and iterative improvement—not generic procedures scribbled in textbook footnotes. When customer needs shift—or when tighter regulatory scrutiny arrives—we can turn around process validation and quality documentation inside weeks, not months. As regulations and application formats evolve, our technical team directly revises protocols for synthesis, in-process controls, and shelf-life demonstration.

    Hands-on expertise extends to upscaling, waste reduction, and safe handling. Our operators receive direct training from technologists and chemists who work on the core synthetic steps, not just as supervisors but as hands-on participants. This translates into safe, consistent, and reliable manufacturing cycles, minimizing the risk that comes from scaling up delicate fluorogenic chemicals.

    Addressing Environmental and Safety Concerns

    While MUP-Na2 sees applications at very low concentrations, commitment to safety guides every production batch. In past years, we have phased out process solvents with higher environmental impact and improved containment at every isolation step. Our waste collection now routes all organic residues into controlled destruction, avoiding environmental discharge. By selecting sustainable sourcing and renewable utilities where feasible, we do more than just meet compliance.

    Product literature stays consistent, and hazardous substance reviews happen with each process update. For large-volume users with specific waste handling or packaging requests, we routinely provide advice and support to simplify downstream management. Every new employee—lab or plant—carries responsibility for both their safety and the safety of downstream users. We see this not as a slogan, but a direct outcome of caring about the life cycle of every product we make.

    Looking Forward: New Applications and Process Intensification

    Even after years in the field, MUP-Na2 usage continues to expand. Researchers have begun leveraging this substrate not only for phosphatase screening, but as a sensitive probe for emerging diagnostics, including in point-of-care testing platforms and wearable sensor development. As end users request new packaging formats—from single-use aliquots to automation-ready cartridges—we invest in filling and sealing lines that maintain the substrate’s sensitive nature against air and moisture. Our process engineers continue to investigate new isolation and drying techniques to trim batch times and reduce energy use, in order to deliver both updated quality and affordability.

    Conversations with leading academic and industry groups push us toward next-generation substrate design: adding new substituents to tweak spectral properties, or stability enhancement. We don’t limit our insight to our own shop floor—we regularly run collaborative trials with outside labs, sending trial lots or tailored modifications for specific high-throughput or microfluidic settings. The knowledge we gain comes full circle, influencing both future MUP-Na2 supply and providing early feedback on chemical trends in enzyme analytics.

    Supporting Reliable Results Worldwide—Without Intermediaries

    Every shipment of MUP-Na2 leaves our facility backed by our direct expertise. From the initial QC data to field support weeks or months later, we connect with customers as partners in the practical details of science—not as intermediaries or anonymous suppliers. The feedback that returns to our plant floor directly shapes the improvements and innovations you’ll see in each subsequent batch.

    By working hand in hand with researchers, assay developers, and industrial processors, we anticipate problems before they reach the bench. Our goal remains the same as when we produced our first lot: deliver a consistent, stable substrate that helps uncover the details of enzymatic function—batch after batch, project after project. Experience has taught us to never take stability, solubility, or purity for granted, because those details make or break great science.