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O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate

    • Product Name O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate
    • Alias DEMCPT
    • Einecs 252-615-6
    • 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
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    Specifications

    HS Code

    170957

    Chemical_Name O,O-Diethyl-O-(4-Methylcoumarin-7-yl) Phosphorothioate
    CAS_Number 80844-07-1
    Molecular_Formula C14H17O5PS
    Molecular_Weight 328.32
    Appearance White to off-white solid
    Purity ≥98%
    Solubility Soluble in organic solvents such as DMSO, DMF
    Storage_Conditions Store at -20°C in a dry place
    SMILES CCOP(=S)(OCC)OC1=CC2=C(C=CC(=C2)C)C(=O)O1
    InChI InChI=1S/C14H17O5PS/c1-4-18-20(17,19-5-2)21-13-8-10-9-15-14(16)12(10)6-7-11(13)3/h6-9H,4-5H2,1-3H3

    As an accredited O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate 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 1-gram amber glass vial, sealed with a PTFE-lined screw cap, and labeled with full identification.
    Shipping This chemical, O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate, should be shipped in tightly sealed containers, protected from light and moisture. It must be labeled according to hazardous substance transport regulations, and shipped via certified carriers with appropriate documentation and handling precautions to ensure safety and compliance with local and international shipping guidelines.
    Storage O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate should be stored in a tightly sealed container, protected from light and moisture. Store at a cool, dry place, ideally at 2–8°C (refrigerated). Ensure the area is well-ventilated and away from incompatible materials such as strong oxidizing agents. Use appropriate safety measures, including gloves and eye protection, when handling this chemical.
    Application of O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate

    Applications of O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate in Industrial Manufacturing

    As a direct producer of O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate, we supply this compound for several specific downstream sectors. The following application scenarios represent established industrial uses in synthesis, labeling chemistry, agriculture, and analytical technologies. Manufacturers integrate this raw material for its reliable performance in defined processes that require strict compliance and detailed process control.

    1. Fluorescent Tag Label Synthesis for Biochemical Research

    This compound serves as a key intermediate in fluorescent probe design, supporting covalent labeling in biochemical research platforms. End users incorporate it during the synthesis of purpose-built phosphorothioate-linked dyes for nucleic acid and protein analysis. The compound’s unique coupling functionality provides high specificity in custom labeling workflows, with stringent lot traceability maintained for regulated diagnostic kit manufacture.

    Industry compliance standards

    • ISO 13485:2016 for in vitro diagnostic reagent production
    • REACH Regulation (EC) No 1907/2006 for registration
    • Good Manufacturing Practice (GMP) for biochemical intermediates
    • USP <1047> labeling agent controls

    Typical usage ratio

    • 0.1–2.5 mmol per 100 mg target substrate, adjusted to fit degree of labeling and probe sensitivity requirements

    Downstream process integration

    • Introduced during the final coupling step in solid-phase synthesis of oligonucleotide or peptide probes
    • Directly attached at the 3’- or 5’-end of synthesized chains using automated synthesizers

    Final product types

    • Fluorescently tagged DNA/RNA oligonucleotides
    • Labeled peptide conjugates
    • Diagnostic hybridization probes
    • Specialty research kits for molecular biology

    2. Photolabile Protecting Group in Custom Organic Synthesis

    Chemists utilize this molecule as a photolabile protecting group to temporarily mask functional sites during complex organic synthesis, especially in advanced material and pharmaceutical development. The coumarin structure enables controlled deprotection under defined wavelengths, allowing selective chemistry under mild conditions. Adoption into multi-step synthetic routes demands batch-level documentation to support validation and reproducibility for regulated process development.

    Industry compliance standards

    • ICH Q7 GMP guidelines for APIs and intermediates
    • ISO 9001:2015 for process chemical manufacturing
    • FDA 21 CFR Part 211 for controlled manufacturing environments
    • Comprehensive batch records for pharmaceutical intermediates

    Typical usage ratio

    • 0.5–1.5 equivalents per protected group, tailored to functional group chemistry and final yield optimization

    Downstream process integration

    • Added during intermediate steps to mask reactive nucleophiles or alcohols
    • Removed by targeted UV irradiation prior to final product isolation

    Final product types

    • Advanced pharmaceutical intermediates
    • Specialty monomers for polymer chemistry
    • Photo-cleavable linker molecules
    • Analytical reference substances

    3. Marker Compound in Agricultural Pesticide Formulations

    The compound functions as a fluorescent marker within selected agricultural pesticide products for traceability and environmental studies. Manufacturers formulate it alongside active ingredients to track application patterns, runoff, and environmental fate. The marker dose adheres to national residue and environmental regulations. Analytical labs rely on its distinct fluorescence signature for detection in both laboratory and field sampling, ensuring data quality for stewardship programs.

    Industry compliance standards

    • OECD Guideline 501 for chemical traceability
    • FIFRA environmental safety standards
    • ISO 17025 laboratory standards for field residue analysis
    • European Regulation (EC) No 1107/2009 for crop protection product registration

    Typical usage ratio

    • 5–50 mg/kg per formulated pesticide, with volume based on intended detection limit and matrix background

    Downstream process integration

    • Blended during bulk mixing of pesticide concentrate formulation
    • Subjected to homogeneity testing and stability studies prior to packaging

    Final product types

    • Liquid and wettable powder pesticides
    • Agricultural spray concentrates
    • Prepackaged microdose application kits for field trials
    • Environmental tracer packs for regulatory studies

    4. Reference Substrate in Fluorometric Analytical Reagent Production

    This molecule is introduced as a standardized fluorometric reference substrate for quality control in specialty reagent manufacturing. QC laboratories use it for instrument calibration, signal stability checks, and setting baselines in fluorescent detection modules. Downstream integration focuses on lot consistency, photostability, and matrix compatibility checks, especially for companies manufacturing analytical devices or ready-to-use assay kits.

    Industry compliance standards

    • ISO 17034:2016 for reference material producers
    • NIST-traceable calibration protocols
    • ISO/IEC 17025:2017 for analytical laboratory quality
    • USP <857> Spectrophotometry standards

    Typical usage ratio

    • 1–10 µM in calibration standard solutions, determined based on the detection range and sensitivity of the target instrument

    Downstream process integration

    • Sourced during masterbatch preparation for calibration standard kits
    • Aliquoted directly into assay cartridges or bottled reference solutions

    Final product types

    • Reference standard solutions for analytical instrument calibration
    • Fluorescent intensity benchmarking kits
    • Batch QC controls included in research reagent lots
    • Diagnostic fluorescence standard reagents
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    More Introduction

    O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate: Manufacturing Insight and Application

    A Deep Dive Into O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate

    In the landscape of fine chemical production, our team faces constant demands for innovation and reliability. O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate stands out from other organophosphorus compounds. The product didn’t come to the market on a whim; it results from a refining process tuned by years of feedback from experienced scientists and technical staff in both research and applied fields. We see requests come in from university groups, pharmaceutical developers, and specialty labs looking for unique tools that shift away from older solutions that no longer meet rigorous application standards. This compound, built around a coumarin structure, offers a rare blend of photophysical behavior and organophosphorus reactivity.

    We synthesize every batch of O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate in-house. By handling both the coumarin precursor and phosphorylation stages, we control purity at each step. Too many suppliers in the market cut corners. Our approach leaves no room for unexplained impurities or questionable batch variability, because our process chemists take results seriously. Yields matter, but consistent spectroscopic analysis always comes first.

    What Sets This Compound Apart?

    O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate brings together two powerful chemical motifs: the diethyl phosphorothioate group and a methyl-substituted coumarin scaffold. This blend isn’t just for textbook novelty. In fluorescent labeling, photoinitiated reactions, and agricultural chemistry, the coumarin ring serves as a signaling or activatable group, while the organophosphorus side brings reactivity toward nucleophilic attack or esterase-triggered release. Lab teams often demand a single reagent that can operate in both biochemical and photonic regimes. Some compounds land in only one camp, serving either as a probe or as a precursor; this molecule performs both jobs without excessive byproduct formation during installation or cleavage.

    In our facility, product validation runs deeper than matching a supplier spec. Every new lot sees LC-MS, NMR, and UV-vis characterization to ensure the coumarin’s spectral properties remain untouched, and the phosphorus-sulfur bond delivers the expected chemical activity. None of this emerges by simple powder blending or unsupervised batch reactors. Drying, purification, and storage rely on air- and moisture-sensitive protocols, because any step skipped translates to a product our partners cannot trust.

    The Manufacturing Journey

    Industry standards in specialty reagent manufacturing don’t rest on broad promises. As direct producers, raw material traceability tracks back to every barrel and batch. We never outsource key synthesis stages. The O,O-diethyl group is installed using controlled alkylation. The 4-methylcoumarin backbone is synthesized from targeted Pechmann condensation, and coupling demands high precision. Any leftover coumarin or incomplete phosphorylation gets spotted instantly thanks to integrated chromatography and experienced eyes repeatedly inspecting the chromatogram.

    Phosphorothioate chemistry challenges even veteran process engineers. Controlling sulfur-oxygen exchanges in the presence of both aromatic and aliphatic centers requires a blend of traditional Schlenk techniques and modern automated monitoring. We keep a strict handle on temperature, inert gas conditions, and batch timing, not because regulations say so, but because customers return—and stay loyal—only when reproducibility lessons have been learned in the trenches. The final isolation steps, whether via crystallization or column, take place without using bulk solvents that leave traces. Our approach addresses the exacting demands of analytical chemists.

    How Researchers and Industry Use This Compound

    Conversations with collaborators reveal the practical significance of our O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate. Researchers exploit the unique coumarin fluorescence to track, trigger, or control chemical transformations. In biochemical research, the compound’s phosphorothioate entity undergoes enzymatic cleavage under conditions mimicking those found in cells. Such a feature allows for time-resolved monitoring of enzyme activity; the released coumarin fragment glows under standard excitation, a signal that gives quantitative results with minimal background.

    The molecule’s reactivity appeals not just to the scientific imagination, but to the precision required in practical laboratory work. For example, developers of prodrugs or time-release pesticide formulations don’t want random hydrolysis or unwanted side reactions. Competing products often break down indiscriminately, losing activity well before they can reach their target. Our compound resists background hydrolysis, standing up under typical laboratory storage, then responds rapidly to targeted triggers, whether light, enzyme, or chemical nucleophile.

    Because the methyl group at the 4-position on coumarin is retained all through the process, the product provides a unique emission profile—a fingerprint researchers can track without interference from unrelated fluorophores in biological samples. This emission clarity gets mentioned repeatedly by analytical teams who tired of troubleshooting cross-talk with more common blue or green emitting probes.

    Specification and Handling from the Factory Perspective

    Working with O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate every day, operators in our plant learn the nuances of its physical form. The substance arrives as a solid, pale in color, free-flowing thanks to careful crystallization and stagewise drying. Packing lines fill glass or high-density polymer containers under nitrogen, because open atmosphere exposure shortens shelf life and dulls fluorescence. Real-world handling differs from what generic pamphlets describe; the container seals actually matter, and small leaks never go undetected during a final batch inspection.

    Some outsiders dismiss packaging as a trivial step, but only robust barrier films and tight capping keep the molecular structure robust enough for sensitive downstream work. None of our lots ship until stability data confirms two years of reliable storage in typical lab conditions. Our reputation rides on those numbers—if degradation creeps in during routine shipment, both our customers and our R&D team feel the consequences.

    Many suppliers quote melting points or purity by HPLC, then cut communication after the invoice clears. We go further: by providing structure elucidation data alongside spectral charts, every recipient can independently verify that the coumarin and phosphorus signals match what they need for their application. This transparency brings peace of mind to project managers balancing time and money on critical bioassays.

    Choosing O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate Over Other Options

    Competitive offerings appear on procurement lists, but researchers identify shortfalls as soon as the project moves from shelf to bench. Common coumarin or phosphorus-based reagents carry reactive handles, but most cannot bridge the gap to cross-disciplinary research. Some fluoresce in the right window but fail under strong chemical manipulation. Others exhibit the right phosphorus chemistry but introduce byproducts that cloud analytical results.

    O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate leaves fewer variables unaccounted for. Direct feedback from synthetic chemists shows strong conversions when installing this group onto larger molecules. No cryptic protecting group chemistry or special deprotection steps clog reaction planning. This simplicity cuts costs and lab time. Scientists prefer not to keep surprises lurking in chromatography columns; clean conversions and easy detection spare project managers late nights searching for error sources.

    Users working in cellular imaging bring up another recurring difference. Non-specific background fluorescence notoriously plagues experiments that use conventional coumarin esters or phosphate analogues. With our product, the methyl group avoids most of the overlap with endogenous cell fluorescence—a fact evidenced in clearer microscope images and sharper data sets. For agricultural chemical developers, the rate of hydrolytic release trumps background stability, and development teams keep returning to us because the measured half-life in buffered systems matches claims every time.

    Limitations and Pitfalls: Facing Real-World Constraints

    No chemical works everywhere. In our manufacturing records, orders occasionally arrive from teams hoping for performance well beyond what this molecule was built to handle. Harsh basic or oxidative conditions force the phosphorothioate bond to break, especially at temperatures outside standard practice. Our technical liaisons always recommend thorough bench validation before scaling up, so downstream surprises are avoided. The methylcoumarin chromophore won’t survive exposure to aggressive radicals or persistent UV bombardment—something we advise in all application briefings.

    Production itself doesn’t happen in a vacuum. Fluctuations in raw material supply and pricing impact planning. Our on-site teams develop fallback syntheses for the coumarin unit, and maintain backup contracts on reagents like phosphorus trichloride and ethanethiol. This willingness to invest in robust supply chains steers us clear of market shocks, which many resellers and formula aggregators simply can’t do.

    Sometimes storage conditions at the end user site fall short of the recommendations, and this product, like many organophosphorus compounds, pays a price if left unsealed in a humid environment. We monitor such feedback carefully; each incident leads to further improvements in both shipping and labeling.

    Regulatory and Safety Considerations In Context

    Our relationship with chemical authorities goes beyond ticking off paperwork. Direct production means we bear full responsibility for the safe handling and onward use of O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate. We keep Safety Data Sheets updated by reviewing each process update in the plant. The compound doesn’t fall under routine restricted use, but internal handling requires full face and hand protection. Inhalation exposure or direct skin contact is never considered acceptable, so operators receive hands-on training in containment and cleanup. Any waste streams containing the phosphorus core go straight into secured treatment, not regular disposal.

    Regulatory details evolve with advances in analytical detection. We stay tuned in to the latest requirements from regional and global health authorities, and keep our customer base informed on any need-to-know changes affecting transport or downstream application. This attitude beats legal compliance by a margin; it builds trust among buyers relying on real support, not just paperwork.

    Listening to Experience: Customer Success and Industry Trends

    The most illuminating stories about O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate don’t come from sales pitches—they come from repeat customers solving complex problems. Analytical chemists recount stories about data breakthroughs in enzyme kinetics, thanks to this compound’s reliably sharp emission profile. Process engineers in crop science call for ongoing pilot lots to test new controlled-release formulations, because performance rarely lags behind expectation.

    Discussions at technical conferences reveal subtle application tricks: some groups use the compound in flow chemistry modules for rapid screening, commenting that only consistent, low-residue lots allow reliable microfluidic operation. Academic labs have shared accounts of successfully installing this group on peptide backbones, with full quantitation at every step. This is not a result achieved with older, less-selective ester-based coumarins.

    Continuous improvement drives us to keep investing in both equipment upgrades and peer engagement. We never treat a successful project as a final answer. Customers often suggest protocol tweaks or flag detection artifacts, which we integrate and test in our next batch cycle. The feedback loop grows stronger each year, as more teams around the world join the conversation about what makes a chemical tool truly useful.

    Why Manufacture Directly? Lessons From the Factory Floor

    Some may ask why we avoid acting as mere aggregators or resellers. The answer comes from daily experience. Manufacturing O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate in-house means every operator remains accountable for the output, every chemist owns their process, and every single deviation gets traced to its root. The close relationship between equipment, process, and final output keeps our standards higher, protected by institutional knowledge that no distributor can replicate.

    Direct manufacturing hands us a toolbox unavailable to third-party handlers: the ability to modify process parameters, instantly address troubleshooting questions, and produce batch-specific technical data in real time. This model attracts clients who value detailed support in every order. The approach reduces lag, eliminates middlemen distractions, and empowers R&D teams to iterate faster.

    People working on breakthrough projects—whether in molecular diagnostics, agrotech, or drug discovery—share common frustrations with delayed shipments and unclear quality documentation. We’ve seen too many critical timelines slip because a faceless supplier couldn’t answer a simple purity question or provide a reference spectrum. Making every gram ourselves means all those answers live right at our fingertips, ready for direct discussion.

    Outlook: Beyond Today’s Applications

    The journey of O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate in applied research keeps pushing us forward. At the bench, new tricks develop each week. Demand for more photostable or water-soluble analogues motivates our chemistry teams to test alternative protective group strategies and backbone modifications. Customer collaborations drive pilot projects into new domains, such as site-selective protein modification and catalytically triggered imaging sequences.

    As our manufacturing experience deepens, the drive for transparency, reproducibility, and technical engagement doesn’t waver. Every lot of O,O-Diethyl-O-(4-Methylcoumarin-7-Yl) Phosphorothioate leaving our facility is more than a line item. Each batch brings together practical feedback, historical data, and the lived reality of hands-on chemical engineering. The future holds more rigorous standards and broader applications, but one factor endures—a commitment to marrying advanced phosphorus chemistry with the day-to-day needs of the newest and most demanding sectors in science.