Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Methylumbelliferyl Sulfate Potassium Salt

    • Product Name 4-Methylumbelliferyl Sulfate Potassium Salt
    • Alias 4-MUS
    • Einecs 611-971-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    472639

    Product Name 4-Methylumbelliferyl Sulfate Potassium Salt
    Cas Number 66778-35-8
    Molecular Formula C15H13KO7S
    Molecular Weight 376.42 g/mol
    Appearance White to off-white powder
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Synonyms Potassium 4-methylumbelliferyl sulfate
    Application Fluorogenic substrate for sulfatase enzymes
    Excitation Maximum 360 nm
    Emission Maximum 450 nm

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

    Packing & Storage
    Packing The 1-gram quantity of 4-Methylumbelliferyl Sulfate Potassium Salt is provided in a sealed amber glass vial for light protection.
    Shipping 4-Methylumbelliferyl Sulfate Potassium Salt ships in secure, sealed containers to ensure product integrity and prevent contamination. It is typically transported at ambient temperature, unless otherwise specified, and packaged according to standard chemical safety regulations. All shipments comply with local and international hazardous material guidelines for laboratory chemicals.
    Storage 4-Methylumbelliferyl Sulfate Potassium Salt should be stored in a tightly sealed container, protected from light and moisture. Keep at 2–8°C (refrigerated) for maximum stability. Store in a dry, well-ventilated area and avoid exposure to excessive heat or humidity. Ensure that the chemical is clearly labeled and kept away from incompatible substances. Always follow institutional safety guidelines.
    Application of 4-Methylumbelliferyl Sulfate Potassium Salt

    Applications of 4-Methylumbelliferyl Sulfate Potassium Salt in Industrial Manufacturing

    4-Methylumbelliferyl Sulfate Potassium Salt is a specialized chemical intermediate used widely for substrate assays in enzymatic production, quality testing, and biological research. Our manufacturing process certifies compliance with industry standards and guarantees batch-to-batch traceability for demanding downstream applications. Below we outline its principal industrial applications with detailed integration practices, dosage references, and corresponding regulatory frameworks.

    1. Enzymatic Diagnostic Reagents Manufacturing

    This material serves as a fluorogenic substrate for sulfatase enzyme assays in diagnostic reagent manufacturing. When sulfatase interacts with the substrate, it releases a fluorescent product measurable by automated analyzers. This reaction forms the basis of many clinical biochemistry testing kits used for in vitro diagnosis of sulfatase deficiency disorders and lysosomal storage diseases. Manufacturers position this substrate in high-precision quality control protocols, ensuring sensitive, specific detection in reagent formulations supplied to medical laboratories and hospitals.

    Industry compliance standards

    • IVD Directive (IVDD) 98/79/EC and In Vitro Diagnostic Regulation (IVDR) EU 2017/746
    • ISO 13485:2016 (Medical device quality management systems)
    • FDA 21 CFR 820 (Quality System Regulation for medical devices)
    • CLSI Evaluation Protocols (Clinical and Laboratory Standards Institute)

    Typical usage ratio

    • 0.05–0.5 mg per test kit; adjusted according to sensitivity requirements and detection range demanded by enzyme kinetic assays

    Downstream process integration

    • Integrated at QC-formulated assay buffer stage during manufacturing of liquid and lyophilized reagent kits
    • Dispensed under cleanroom conditions with automated filling and freeze-drying equipment

    Final product types

    • Enzyme assay kits for clinical diagnostics
    • Sulfatase activity detection kits
    • Lysosomal storage disorders diagnostic reagents
    • Point-of-care in vitro test kits

    2. Pharmaceutical Quality Control Laboratories

    Pharmaceutical manufacturers use this raw material in standardized in-process and release testing to quantify sulfatase impurities and monitor active enzyme concentrations across production batches. Routine adoption in validated laboratory protocols helps ensure conformance to pharmacopoeial standards and GMP requirements for enzyme- or substrate-containing pharmaceutical products. Laboratory staff calibrate automated microplate readers to the excitation and emission properties of the substrate, supporting high-throughput, low-variance control charts for batch-to-batch consistency.

    Industry compliance standards

    • USP <467>, <1225> (Analytical procedure validation, residual solvents)
    • European Pharmacopoeia (Ph. Eur.) monographs on enzyme preparations
    • ICH Q2(R1) Guidelines for Validation of Analytical Procedures
    • Good Manufacturing Practice (GMP) requirements for APIs and finished pharmaceuticals

    Typical usage ratio

    • Concentration in reaction wells typically 10–100 μM, selected based on enzyme turnover properties and batch assay throughput

    Downstream process integration

    • Employed at the analytical testing step with direct addition to sample microplate wells
    • Integration into automated assay robots and data analysis software

    Final product types

    • Pharmaceutical enzyme bulk APIs
    • Biopharmaceutical vials requiring sulfatase monitoring
    • Stability samples for shelf-life verification
    • Finished drug products containing enzyme preparations

    3. Food Safety and Allergen Detection Testing

    Manufacturers of food diagnostic reagents select this compound as a substrate in fluorescence-based test kits for allergen detection, such as identifying residual sulfated glycoproteins in processed foods. Assays determine minute trace quantities via fluorescence emission, critical for end-product release and regulatory compliance. Kit formulation engineers fine-tune substrate concentrations for each food matrix and optimize buffer compatibility, guaranteeing accurate results in routine quality assurance for food producers and third-party analytical labs.

    Industry compliance standards

    • ISO 22000:2018 (Food safety management systems)
    • Codex Alimentarius methods for allergen testing and contaminants
    • AOAC Official Methods for Foods
    • FDA Food Safety Modernization Act (FSMA) standards

    Typical usage ratio

    • 0.1–1.0 mg per 50 mL sample, adjusted by food matrix complexity and targeted allergen sensitivity in validated test protocols

    Downstream process integration

    • Mixed with buffering agents during food sample extraction and pre-treatment for allergen detection kits
    • Incorporated into portable lateral flow assay devices for on-site testing

    Final product types

    • Allergen detection rapid test strips
    • Multi-analyte microplate food diagnostic kits
    • Testing reagents for contract analytical labs
    • Sampling kits for food manufacturing QA/QC teams

    4. Microbiology Research and Environmental Monitoring

    Industrial and academic research labs use this substrate for routine monitoring of sulfatase-producing microbial populations in environmental samples such as wastewater, sludge, or soils. The high sensitivity of the fluorescence reaction allows rapid profiling of microbial activity, critical for process engineers managing biological treatment reactors. Our manufacturing method delivers batches certified for low background fluorescence, directly supporting trace analysis in environmental workflows and research-grade bioassays.

    Industry compliance standards

    • ISO 17025:2017 (Testing and calibration laboratories)
    • Standard Methods for the Examination of Water and Wastewater (APHA, AWWA, WEF)
    • OECD Guidelines for the Testing of Chemicals, Section 3: Degradation and Accumulation
    • Local EPA and environmental laboratory regulations

    Typical usage ratio

    • Assay concentrations between 25–150 μM, tailored for environmental matrix (e.g., influent, effluent, activated sludge) and analytical protocol sensitivity profiles

    Downstream process integration

    • Added at the substrate incubation stage in 96-well microplate assays or cuvette-based fluorometers
    • Applied during field monitoring with portable fluorescence readers

    Final product types

    • Microbial enzyme test panels for industrial water utilities
    • On-site environmental test kits for sulfatase activity
    • Laboratory-grade environmental sampling reagents
    • Academic teaching kits for microbiology

    5. Bioprocess Development in Industrial Fermentation

    Process development teams in biotechnology and enzyme production industries apply this substrate to profile sulfatase expression in microbial fermentation processes. During scale-up and optimization, online assay systems utilize the substrate to track fermentation performance, enabling feed rate and culture condition adjustments in real-time. Our material specification ensures low impurities for reproducible fluorescence readings in bioreactors operating under stringent quality systems.

    Industry compliance standards

    • ISO 9001:2015 certified quality systems for industrial enzymes
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FAO/WHO Guidelines on enzyme preparations for food processing
    • National patent standards for industrial bioproduction

    Typical usage ratio

    • 25–100 μM working concentration per sample, adjusted based on fermentation broth density, aeration, and expression yield targets

    Downstream process integration

    • Integrated within online or offline sample analysis during upstream bioprocess optimization
    • Added to fermentation supernatant samples for rapid sulfatase activity quantification

    Final product types

    • Industrial-scale sulfatase enzyme preparations
    • Fermentation optimization and monitoring platforms
    • Process validation kits for bioreactor systems
    • Bulk enzyme concentrates for food and feed industries
    Free Quote

    Competitive 4-Methylumbelliferyl Sulfate Potassium Salt prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing 4-Methylumbelliferyl Sulfate Potassium Salt: Manufacturer’s Perspective

    Direct from the Source: Earning Trust through Real Production

    Producing specialty chemicals demands steady vigilance over purity, traceability, and reproducibility. 4-Methylumbelliferyl sulfate potassium salt stands at the intersection of these responsibilities. Over years refining our in-house process for this compound, the main focus has always been consistent batch performance and robust physical chemistry data for routine laboratory use. Laboratories rely on materials that deliver the same results day in and day out, and this product draws its reputation from real feedback at the bench. We do not view activity in a catalog as the finish line; we believe in the accountability that comes from direct manufacturing, where every drum issued tells a story about process care and tight analytical control.

    From Raw Material to Final Product: Internal Quality Gaps Closed

    Raw material selection matters. The 4-methylumbelliferone backbone gets sourced through a tightly defined contract, then subjected to internal staff-run QC screens upon receipt. Unreacted or off-spec feedstocks make their way out of the line immediately, sparing downstream headaches. Our team then reacts this substrate with sulfating agents under close monitoring, repeatedly sampling throughout the process to watch for byproducts or unpredicted intermediates. Mistakes during sulfation can throw off purity, so we devote extra TLC here—temperature, pH, solvent content all get maintained within established performance windows, tightened every year as we study aggregate properties. Any new batch faces a suite of analyses that include HPLC, NMR, and IR. Potassium salt formation, the final step, gets signed off only by experienced staff, since incorrect drying or incomplete neutralization in this phase triggers the biggest purity issues in the scale-up.

    We see a marked difference in finished material quality whenever starting points, temperatures, or titration routines slip. These flats never get past our QC. We deal with real orders from major diagnostic test kit firms and enzyme researchers; one misstep gets noticed, and reputational currency vanishes fast. This pressure drives innovation: we've developed a better final wash protocol for potassium salt formation, and now routinely see nitrogen content below detection limits, translating to reliable shelf life and dissolution.

    Why Purity and Solubility Matter for Practical Lab Use

    4-Methylumbelliferyl sulfate potassium salt often works as a fluorogenic substrate in enzymatic assays, giving off a measurable fluorescence when sulfate is cleaved by sulfatase activity. This transformation sits at the heart of high-throughput diagnostic screening, lysosomal storage disorder research, and environmental sulfatase detection. Any batch inconsistency shows up directly in your assay controls—either as inconsistent background signal, messy kinetics, or complete failure to produce the expected fluorescent shift at the right pH window.

    Unlike resellers, we get calls from lab managers who’ve run into these very issues with discount material from loosely controlled sources. They describe delayed result cycles and lost sample time; worse, they risk questionable diagnosis or project conclusions. In-house analytical data on each lot—fluorescence yield, spectral purity, and water content—forms the backbone of quality here. Most published protocols work off a certain optical density and excitation/emission pair (365/450 nm), so we keep spectral properties documented down to the lot number and retain sample splits for a year post-ship.

    This tight feedback loop with end users has led our R&D to invest in fine-tuning solubility as well. Buffer composition affects substrate delivery; our material comes in a well-dried, free-flowing crystalline powder, carefully tested for caking, agglomeration, and grain size. This physical form gives true ease dissolving at recommended concentrations, both for manual pipetting and automated dispensers. These waypoints cut user troubleshooting, keep experimental plates straightforward, and reduce run-to-run variability.

    Key Distinctions: What Sets Our Production Apart

    Several suppliers repackage bulk chemical from uncertain origins, contributing to grey-market product that often lacks robust documentation, reproducibility data, or defined impurity profiles. Our operation tracks every compound batch to its precursor origins, keeps a running performance log over years, and runs repeat NMR checks on all critical intermediates. One improvement driven by this practice: years ago, we transitioned to a cleaner potassium salt precipitation protocol, eliminating the last traces of sodium—from both the substrate and process buffers—to ensure full compatibility for potassium-specific buffer systems.

    The broader world of fluorogenic enzyme substrates includes 4-methylumbelliferyl-based compounds paired to different leaving groups (phosphate, glucuronide, N-acetyl-β-D-glucosaminide). Each has its uses. Our sulfate salt triggers targeted response for sulfatase work. We do not force a one-size-fits-all solution. Environmental and biomedical fields need different stability, handling, and spectral purity criteria; we have adjusted our drying and packaging process to hit longer shelf lives in less-than-ideal climate control. No extraneous anti-caking agents ever find their way into our product, sidestepping side reactions that have tripped up long-term partners working on ultra-sensitive enzyme assays.

    Feedback from veteran research partners has led us to design packaging options for easy weigh-outs. Both bulk packs for diagnostics production and high-quality vials for life science research get filled directly from qualified lots, not every-commodity intermediate mills. Our labeling system points directly to analytical batch records, making audits or scientific troubleshooting a simple phone call away.

    Beyond Certificates: Real Assurance in Consistency

    Certificates of analysis only tell part of the story. Anyone with a chemical label can issue generic paperwork, but translating batch-to-batch consistency into actionable research results requires tighter integration with the scientific community. We routinely provide third-party laboratory co-validation data on our material’s performance in both classic sulfatase protocols and newer, lower-volume microplate workflows. Several researchers have published validation studies with lot-specific citations to our actual product outputs, demonstrating reproducible reaction kinetics and matching excitation/emission spectra.

    Many common issues traced by customers new to this substrate come back to background noise or incomplete cleavage. We tracked one such incident back to excessive water content in a competitor’s material, causing both hydrolysis during storage and inconsistent substrate concentration in solution. Keeping residual moisture content below 1% for all outgoing vials significantly improved observed shelf life and performance stability in real-world test setups.

    Direct feedback from the field—shared via technical Q&A and raw machine data—drives interventions on our end. This is more than lip service. Decisions around raw material specifications, washing solvents, and packaging design all flow directly from what scientists report about their hands-on experience.

    Comparing Alternatives and Upping the Bar on Transparency

    Some competitors offer the methylumbelliferyl sulfate as sodium or ammonium salts, or even in unspecified forms. These can sometimes compromise buffer compatibility or final assay output sensitivity due to minor counterion interference. Our potassium salt, produced from audited raw streams and always double-checked for ion content, minimizes background interference and matches the needs of standardized phosphate buffer systems in diagnostic kits. Potassium as the counterion has also demonstrated better stability in climatic shelf life studies done alongside central clients.

    A few suppliers ship loosely capped containers that welcome extra moisture absorption, reducing active substrate over time. Our product lands in moisture-barrier containers, each seal checked and inventory rotated by tight date control. We found that receiving damaged packs was the number one complaint among high-throughput screening labs; careful handling and meticulous inventory cycling made a measurable difference to their workflow.

    Another contrast shows up in lot tracking: every outgoing unit of our 4-methylumbelliferyl sulfate potassium salt can be traced directly back to process logs and live batch records. These are kept on-site for immediate reference. For long-term clients facing regulatory audits or project troubleshooting, this level of traceability helps sidestep downtime and accelerates root cause analysis.

    Applications in Diagnostics and Research: End-Use Experience Drives Change

    Diagnostics firms use this substrate for quantifying sulfatase activity in patient samples and quality control for enzyme formulations. Dependable fluorescence shift, minimal background, and full dissolution without sonication—all these qualities go beyond the data sheet to impact clinical workflows. Researchers in environmental science and microbiology also rely on this salt, especially where trace ion contamination derails sensitive microbe profiling.

    Having manufactured at hundreds-of-grams scale, our team sees patterns between production tweaks and field performance. Each time we make even small changes to grinding or packaging protocols, we document performance metrics directly—both in internal use and through trusted external method validation. This approach—testing, iterating, soliciting third-party results—cements reliability in a world where inconsistent enzyme substrate quality slows research, prolongs diagnostics, or, worse, risks patient care.

    Troubleshooting enzyme assays often boils down to substrate quality. High background, poor color/fluorescence, inconsistent cleavage—all trace back to the raw material. In our world, this feedback travels straight from the scientist’s bench to our process optimization team. If a client struggles with a new high-throughput technique using our substrate, we review both the material and their method, aiming for improvements on both ends.

    Meeting Regulatory and Documentation Demands: Beyond Compliance

    Traditional chemical industry compliance asks only for safety sheets and certificates. The new reality—life science, diagnostic manufacturing, biomedical research regulation—requires deeper documentation. We update our technical files not only to meet compliance audits, but also to help scientific buyers present convincing validation packets of their own. Every lot ships with a collapse of raw process data, synthesis route summary, lot-specific chromatographic and spectral traces, and third-party validation summaries (when available). Regulatory inspectors have remarked on this transparency, and several customers have used our documentation packets in their own clinical and quality audits.

    By tracking performance over years, and linking field complaints or outlier results to concrete handling or process events, we offer more than a faceless commodity. This proves critical to clients whose workflows depend on reproducible biochemistry and minimal regulatory friction.

    Improvements over Time: Listening to End-User Labs

    Only years of feedback bring real improvements. In conversation with long-term partners, we learned to avoid particular solvents that left spectrally active trace residues. Switching to cleaner wash protocols cut down on outlier fluorescence values. Pharmacologists pointed out that over-grinding led to static clumping during weigh-outs, which led us to adjust our drying step for less powder cohesion and smoother pours. Diagnostic kit designers pushed us to offer tamper-evident small vials warrantied by microbalance weight checks, so now large and small shipments both receive direct net-weight confirmation. This effort came not from generic customer service policies, but from our daily immersion in client data, test runs, and urgent troubleshooting phone calls.

    We have also taken on direct staff training not only in process chemistry, but also in customer troubleshooting—so callers now speak directly to chemical process engineers, not disconnected sales or logistics staff. This shortens learning cycles on both sides. We see and feel the cost when a batch misses a critical performance mark, since most orders ship with our own brand and engineers’ names directly on the packaging.

    Scientific instrument and equipment advances—such as microplate readers with higher sensitivity or smaller well volume—also press for better raw substrate quality. Smaller errors in substrate concentration now have greater impact. Fielding questions about these advances keeps us alert to evolving standards and new failure modes.

    Not Just a Product, but a Scientific Partnership

    Stepping beyond product specifications or material safety sheets, we invest in a relationship with diagnostics and research circles based on accessible data, open improvement processes, and technical humility. Surprises should show up in new science, not from the bottle labeled with a trusted chemical compound. Each advance in internal process, packaging, or documentation builds on unfiltered client reports, not from bean-counter cost saving or marketing surveys. Our chemical credibility stands both on how the substrate performs at the bench and how rapidly we address any real-world complaint.

    Responding to field needs, we continue to invest in cleaner process intermediates, tighter raw input audits, modernized packaging, and regular review of real-world QA reports. If a problem shows in use, the solution starts on our shop floor the next day.

    Summary: Enduring Commitment to Transparency, Responsiveness, and Laboratory Value

    Manufacturers know that successful research and clinical workflows depend on more than theoretical purity or laboratory calibration. Routine real-world assay performance, documented handling stability, and transparent traceability drive our ongoing investments in the quality of 4-methylumbelliferyl sulfate potassium salt. From the hands-on chemists producing every batch to the final vial on a scientist’s shelf, our process aims at delivering confidence—rooted in measured performance, open documentation, and continuous improvement. In our experience, the true mark of reliability comes not from a binder of certificates, but from long-standing partners who return year after year, sharing new science, identifying fresh challenges, and helping us raise the bar for specialty chemistry in laboratory life.