Products

2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate

    • Product Name: 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate
    • Alias: DEDMS
    • Einecs: 674-045-5
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    953352

    Productname 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate
    Casnumber 127464-61-1
    Molecularformula C14H22N4O5S
    Molecularweight 358.42 g/mol
    Appearance Yellow to Orange Solid
    Solubility Soluble in water
    Meltingpoint Decomposes above 150°C
    Storagetemperature Store at 2-8°C
    Purity Typically >98%
    Hazardclass Oxidizer, harmful if swallowed
    Synonyms Benzenediazonium, 2,5-diethoxy-4-(4-morpholinyl)-, sulfate
    Application Intermediate for organic synthesis
    Stability Stable when stored under recommended conditions
    Smiles CCOC1=CC(=C(C=C1N2CCOCC2)N=[N+]=[N-])OCC
    Inchikey GILDPQBIMJZBKO-UHFFFAOYSA-N

    As an accredited 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle, 10 grams, tightly sealed, labeled with hazard warnings and product details, stored in protective secondary container.
    Shipping 2,5-Diethoxy-4-(4-Morpholinyl)benzenediazonium sulfate must be shipped as a hazardous material, typically under cool, dry conditions in tightly sealed containers. Packaging must comply with regulations for diazonium salts, which are potentially explosive and sensitive to heat, shock, and friction. Ensure appropriate labeling and documentation during transport. Handle with extreme caution.
    Storage 2,5-Diethoxy-4-(4-Morpholinyl)benzenediazonium sulfate should be stored in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as reducing agents and organic materials. Keep the container tightly closed, protected from moisture, and store under inert atmosphere if possible. Handle with care as diazonium salts can be thermally unstable and potentially explosive when dry.
    Application of 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate

    Applications of 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate in Industrial Manufacturing

    2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate is a specialized diazonium salt used as an intermediate in advanced synthesis across several industrial sectors. Our manufacturing plant supplies this compound to key downstream processes where precise formulation, batch consistency, and regulatory alignment drive demand for high-purity grades tailored to controlled environments.

    1. Synthesis of Advanced Azo Pigments

    In pigment manufacturing, this material serves as the diazonium component for coupling reactions to produce complex azo structures for high-performance colorants. Industrial pigment formulators integrate this compound under controlled pH and temperature to ensure targeted chromophore formation, strict shade reproducibility, and chemical durability, particularly in coatings and inks requiring resistance to light and chemicals.

    Industry compliance standards

    • ISO 18451-1:2019 (Pigments and extenders – Terminology)
    • REACH Regulation (EC) No 1907/2006 Annex XVII for aromatic amines
    • ETAD Guidance for pigment manufacturing and auxiliary chemicals
    • ASTM D3722 for pigment chemical composition

    Typical usage ratio

    • 0.2–1.8 molar equivalents per mol of coupling component
    • Adjustments based on targeted dyestuff yield, batch size, and color intensity

    Downstream process integration

    • Charged into the diazotization reactor under chilled conditions (0–5°C)
    • Immediately coupled with naphthol, acetoacetarylides, or H-acid derivatives in water phase
    • pH controlled by sodium acetate buffer; completion verified via TLC or HPLC
    • By-product removal via filtration and washing, yielding pigment cake for post-treatment

    Final product types

    • Organic azo pigments for automotive coatings
    • Inkjet and flexographic inks
    • Plastisol masterbatches for polymer compounding
    • Color concentrates for industrial paints

    2. Pharmaceutically Active Intermediate Manufacture

    Pharmaceutical synthesis uses this compound as a diazonium source for constructing active pharmaceutical ingredient (API) scaffolds via azo coupling and palladium-catalyzed cross-coupling reactions. The unique substitution pattern allows introduction of electron-donating groups during late-stage functionalization, supporting highly selective syntheses for regulated small-molecule drugs.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredients
    • 21 CFR Part 211 (FDA cGMP – Finished Pharmaceuticals)
    • European Pharmacopoeia monographs for raw materials
    • USP General Chapter <467> (Residual Solvents)

    Typical usage ratio

    • 0.3–0.7 molar equivalents per target coupling partner
    • Dosing adjusted per route development assays for each specific API structure

    Downstream process integration

    • Added to controlled-reactor systems under nitrogen atmosphere to prevent degradation
    • Coupling performed in aqueous or biphasic media, monitored by in-process HPLC
    • Subsequent isolation by extraction, distillation, or preparative chromatography
    • Product advances to further synthetic steps: reduction, hydrolysis, or cyclization

    Final product types

    • Pharmaceutical raw intermediates
    • Final APIs for anti-infective and anticancer agents
    • Pro-drug building blocks with arylazo motifs
    • Diagnostic reagents for clinical chemistry

    3. Advanced Electronic Photoresist Formulations

    The electronic manufacturing sector uses this material as a light-sensitive component for diazonium-based photoresists. The reproducible decomposition and energy release upon UV exposure enable controlled pattern transfer onto silicon wafers. Manufacturers select this raw material for high-resolution lithographic patterning in microchip production lines, where contamination and trace metal levels must remain tightly controlled.

    Industry compliance standards

    • SEMI C80 for electronic grade chemicals
    • IATF 16949 for electronics supply chain traceability
    • JIS K5600 for photoresist quality
    • IEC 61249-2 for material purity in electronic applications

    Typical usage ratio

    • 1.5–5 wt% in photoresist resin matrices
    • Levels adjusted per target film thickness and pattern fidelity requirements

    Downstream process integration

    • Dissolved in solution with cresol novolak resins and organic solvents
    • Casted or spin-coated onto wafer substrates under yellow-light cleanroom conditions
    • UV or deep-UV exposure decomposes diazonium group, forming image areas for etching
    • Post-exposure bake and developer steps remove unexposed areas; QC via SEM analysis

    Final product types

    • Semiconductor photolithography resists
    • Thin-film transistor substrates
    • Liquid-crystal display (LCD) panel interlayers
    • Printed circuit board microvia resists

    4. Synthesis of Analytical Reagents for Water Testing

    Water quality laboratories incorporate this compound as a diazotization reagent in colorimetric detection kits for nitrites and aromatic amines in potable water and industrial effluent analysis. Its high reactivity and specificity yield stable, distinctive chromophores when reacting with sample analytes, enabling reliable detection down to ppb levels.

    Industry compliance standards

    • ISO 17378-2 (Water quality — Nitrite determination — Spectrometric method)
    • EPA Method 354.1 for Standard Methods in Drinking Water
    • EN ISO/IEC 17025:2017 for laboratory chemical testing
    • ASTM D1889 for colorimetric reagent performance

    Typical usage ratio

    • 0.1–0.3 mg per 10 mL test volume
    • Loading determined by method detection limit requirements and color stability

    Downstream process integration

    • Prepared as pre-measured sachets or cartridge additives for analytical test kits
    • Mixed with sample aliquots under controlled conditions; serves as primary diazotizing agent
    • Couples with secondary reagents or color formers to produce quantifiable color response
    • Stability studies performed to verify shelf life in commercial kits

    Final product types

    • Commercial water testing field kits
    • Portable spectrophotometric cuvettes
    • Reagent packs for continuous online water quality monitors
    • Laboratory colorimetric analysis kits

    5. Development of Precursor Intermediates for Liquid Crystal Materials

    The compound acts as a strategic intermediate in the functionalization of aromatic cores used in liquid crystal (LC) material synthesis, supporting downstream production of high-anisotropy, temperature-stable mesogens. Chemical engineers incorporate the diazonium function to introduce complex substituents via azo coupling or Sandmeyer reactions, fine-tuning electro-optical properties critical for advanced display applications.

    Industry compliance standards

    • IEC 62899-201:2022 for electronic display material standards
    • RoHS Directive 2011/65/EU Annex II for electronic-grade substances
    • JIS K7033 for organic intermediate materials for electronics
    • ISO 9001:2015 for production traceability

    Typical usage ratio

    • 0.4–0.9 molar equivalents per aromatic substrate
    • Adjusted to balance reactivity and mesogenic yield in each synthesis batch

    Downstream process integration

    • Charged into batch jacketed reactors for low-temperature diazotization reactions
    • Follow-up azo coupling, halogenation, or etherification to obtain custom intermediate profiles
    • Strict color and phase purity control by differential scanning calorimetry
    • Intermediates forwarded to LC material polymerization or blending stations

    Final product types

    • Twisted nematic display compounds
    • Vertical alignment LC mixtures for high-resolution screens
    • Polymerizable LC monomers
    • Specialty LC mixtures for OLED backplanes

    Free Quote

    Competitive 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615365186327

    Email: admin@ascent-chem.com

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

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

    Certification & Compliance
    More Introduction

    2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate: Experience from the Manufacturer’s Bench

    Understanding Our Own Innovation

    Our team has watched the demand for tailored diazonium salts grow year after year, especially in specialized organic synthesis. In response, we've focused deeply on refining each production aspect of 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate. This compound brings together a diazonium center for coupling versatility with diethoxy and morpholine substitutions that open doors in dye chemistry, sensor technology, and advanced material research.

    Nothing compares to working hands-on with raw materials, witnessing first-hand how minor tweaks in reaction conditions change crystallization or color during final isolation. Every batch reflects that hands-on development, our years of trialing safe energy input, monitoring reaction kinetics, and scaling from pilot volumes to consistent industrial output. We’ve had to learn by producing—not from textbooks, but at the reactor and filtration lines, where detail decides whether a product holds up under a chemist's scrutiny.

    Product Model and Specifications Shaped by Real Production

    For years, labs have specified the need for a diazonium salt with precise electronic and steric characteristics. Our 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate emerged from those requests. We have focused on two primary models: laboratory-scale analytical grade and production-scale process grade.

    The analytical grade exhibits a fine pale yellow to off-white crystalline form, with purity meeting the demands of mechanism studies or high-purity intermediates. We measure each parameters—should any lot stray by more than 0.2% on key impurity classes, we break it down and refine again. In contrast, the process grade can be delivered in larger volumes for developers running pilot polymerizations or bulk dye synthesis, where purity sits above 98% and water content stays predictably under 0.5% by Karl Fischer methods.

    Our standard lot sizes adjust flexibly, thanks to investments in both glass-lined reactors for delicate batches and full stainless plant lines for scale-up. Environmental controls mean our product remains free-flowing and free from clumping that can slow dissolution in reactors, even during humid months. Over the years, we’ve phased out certain older solvents to hit stricter sustainability expectations without jeopardizing the product’s shelf life or consistency during shipment.

    An Eye on Real-World Use Cases

    Diazonium salts have always been tricky—known for heat-sensitivity and reactivity with common solvents. Real chemists in labs employ our 2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate thanks to its distinctive structure. Here, the diethoxy groups at positions 2 and 5 tune electron density on the aromatic ring, steering reactivity in azo-coupling and Sandmeyer reactions with greater selectivity. The morpholine substituent adds both solubility in polar media and a handle for further functionalization—a fact we confirmed by routinely running compatibility trials across various polar and nonpolar solvents before settling on optimal drying and packaging techniques.

    Those working on colorant and dye sciences immediately recognize the difference this substitution pattern delivers. Earlier generation diazonium salts could oxidize or decompose before intended coupling steps. We’ve minimized these issues, honing a shelf-stable form that remains workable under controlled refrigeration for months—this means less downtime in high-throughput labs and more predictable yields for manufacturers printing, dyeing, or developing rapid-assay test strips. We've also validated applications in custom polymer surface modifications. Several universities and start-ups share data where our compound enables grafting unique functional groups onto polymer backbones, supporting advances in smart surfaces and biosensor development.

    What Sets This Diazonium Salt Apart

    Plenty of customers ask us why pick a substituted benzenediazonium salt with diethoxy and morpholinyl groups instead of standard phenyl diazonium derivatives. The answer often surprises: it is not just a matter of cost per mole, but of downstream impact.

    The diethoxy groups create electronic effects on the aromatic core, changing regioselectivity in diazo coupling, particularly with activated and deactivated phenol partners. This grants users higher yield in azo-dye syntheses, evidenced in manufacturing feet where output boost means lower waste and cost per reaction. Our engineers run side-by-side tests every production cycle, measuring not just IR and NMR spectra but reaction conversion and subsequent pigment stability.

    Adding the morpholine ring offers more than enhanced water solubility. In our hands, it brings a smoother handling experience—less static cling, easier weighing on precision balances, and improved dispersibility in reaction media, which translates into cleaner process lines and fewer operational delays. Our quality control team regularly benchmarks flow and compaction properties against a rotating panel of widely used diazonium salts. The morpholinyl group also serves as a backbone for rapid downstream derivatization with targeted nucleophiles, which our materials science collaborators tap into for surface patterning and sensor fabrication.

    Traditional diazonium salts—simple aniline derivatives—ask for more conservative temperature and humidity controls, as minor environmental slips cause unexpected decomposition. Our substituted compound, designed and produced with these practical realities in mind, grants a higher degree of reliability both during transit and on the workbench. Labs tell us that this reliability counts: less risk of hazardous byproducts or lost time chasing down failed reactions.

    Learning Through Scaled Production: Experience in Every Batch

    Working at scale uncovers gaps fast. We still remember a time when small pilot runs would crystallize right on spec, but scaling to 100 kilograms would reveal problems—the slurry would block filters, or tiny impurities would nucleate off-spec particles, leading to poor performance in downstream reactions. These lessons push us to refine and debug our process with every lot, not settle for “close enough.”

    After repeated feedback from both academic researchers and industrial process engineers, we have overhauled our purification flow over the years. Originally, thermal instability limited batch size since spontaneous exotherms could run off the rails. So we focused on incremental cooling with heat-exchange systems, and we now test every production batch for thermal decomposition onset using precise calorimetric techniques. Waste treatment, always an environmental watchpoint in diazonium chemistry, prompted us to redesign solvent recovery lines and push for nearly closed-loop nitrogen handling. This kind of hands-on process vigilance keeps unnecessary escapes out of the workroom air and reduces exposure risk for everyone involved.

    One standout lesson came from our attempts to ship product across the globe through variable weather. We saw caking, minor losses in activity, and even rare container breaches. In response, we invested in triple-sealed packaging with built-in desiccant, based on real shipment failures and feedback from foreign labs. Now our compound holds up during weeks in transit, arriving as workable as it leaves the plant.

    Comparing Against Related Diazotization Products

    Through production volumes and customer feedback, we have learned that not all diazonium salts can swap one-for-one into new research or manufacturing protocols. Many buyers once relied on standard benzenediazonium tetrafluoroborate or chloride, but moved over to our 2,5-Diethoxy-4-(4-Morpholinyl) variant after struggling with solubility problems, poor shelf stability, or inconsistent color yield.

    Sulfate counterions play their part in greater aqueous compatibility and reduce unwanted interference in some downstream couplings, especially compared to chloride or tetrafluoroborate analogs. Our sulfate-based product reflects these user needs—clients working in textile dyeing or surface grafting get higher target yield, while also cutting pre-step purification. These are observations that came directly from partner trial runs and side-by-side conversions—they’re not only theoretical advantages but lived out in daily use.

    We have also faced the challenge of explaining to some customers why this extra functionality justifies the cost. Chemists tuning their protocols for specificity or attempting advanced polymer modifications typically see the difference after running two or three reactions. Cost savings often show up as less downtime, lower rework rates, and fewer failed reaction attempts—not always obvious on a raw materials invoice, but immediately clear once better product throughput lands in their own quarterly numbers.

    Customers occasionally ask about other derivatives featuring similar morpholine or ethoxy substitutions. Experience reminds us that subtle placement and counterion differences translate into major effects on reactivity; our process avoids the harshest acids in diazotization, reducing trace decomposition products often found in lower-grade or hastily-produced alternatives. We engineer for these details not because a brochure says so, but because our process data and repeated in-house trials reinforce that these seemingly small differences can make or break industrial viability.

    Real Challenges and Responses from the Floor

    Processes anchored around diazonium salts face a common basket of operational risks: storage stability, operator safety, batch reproducibility, and waste management. Drawing on our own plant experience, we have learned that one-size-fits-all protocols rarely deliver success. Each new order often prompts a round of in-process analytical checks, with tweaks based on air humidity, local water quality, even packaging supply variability.

    To combat breakdown risks, our technical teams monitor each lot from raw material intake through packaged release, running GC-MS for trace impurity detection and customized colorimetric assays for decomposition markers. Over the years, we've observed that subtle pH drifts during neutralization lead to off-smell, color, or unexpected downstream interferences; adjusting our post-diazotization quenching procedure trimmed our customer complaint rate and improved post-shipment recovery.

    Customers regularly ask for guidance using our product safely and efficiently, especially those unfamiliar with the unique hazards this class presents. We respond not by repeating textbook cautions, but sharing outcome-focused advice: always plan for cooled storage (2–8°C remains best), keep away from reducing agents and strong bases, and weigh out only what will be consumed at once. We’ve seen how minor lapses in these steps lead to both wasted material and unnecessary plant incidents.

    Collaborative Development with Users in Mind

    Much of our progress comes from direct feedback. One example stands out: a research group approached us about scaling up their new dye synthesis for a diagnostic test. Their standard benzenediazonium product decomposed too fast, ruining yield consistency. Through repeated technical exchanges, we helped them switch to our 2,5-Diethoxy-4-(4-Morpholinyl) product, running test batches in our pilot plant under their protocols, carefully sampling and analyzing each stage. The outcome? They doubled their reaction reproducibility and advanced their development timetable.

    On the manufacturing floor, we routinely help customers integrate the product in surface treatments and polymer grafting. The morpholinyl group's chemistry opens up selective surface activation, allowing custom covalent bonding for advanced filtration membranes and sensor substrates. We’ve built datasets together, examining each process variable, optimizing not for our own convenience but for our client’s end-use. Tough feedback sharpens our edge—it tells us which impurity classes hamper utility, and which handling quirks trip up downstream automation. Meeting those challenges takes real-world fixes, not generic recommendations.

    Building for Reliability and Long-Term Trust

    We know labs and manufacturers want results, not surprises. Our on-site quality team stays in close communication with clients, sharing every detail that might impact later steps, either in material traceability or safety planning. Over the years, this close feedback cycle has driven us to overhaul process documentation, provide tailored certificates of analysis, and maintain transparency on any raw material changes.

    Long-term storage, a longstanding pain point, led us to invest in real-time stability testing. Far too many products lose half their activity within a few short months if shipped non-refrigerated or left under poor conditions. Now, periodic stability samples drawn from shipment lots confirm actual shelf-life, not just theoretical timelines. In practice, this means customers receive material with highest certainty about potency and safety.

    Environmental Focus in Modern Diazotization

    Operating in a stricter regulatory climate, we act to stay ahead of environmental standards. Traditional diazotization, if managed poorly, releases nitrous oxides, acid waste, and persistent organic residues. In our own setup, we recapture and neutralize as much as possible. The last few years brought new investments for nitrogen and solvent recovery, allowing bulk cycles to operate with sharply reduced effluent and safer air quality in local communities.

    We have learned through hard experience that cleaner, safer process flow means not only regulatory compliance but added value for end users—who themselves face increasing pressure for greener supply chains. A greener synthesis often results in purer product, fewer batch variabilities, and less hazardous byproduct carryover affecting sensitive downstream chemistries.

    Our Perspective: Value by Experience, Not Hype

    In today’s market, plenty of traders and distributors market chemicals they have never actually handled, storing and repackaging as boxes arrive. In contrast, we know every step of our compound’s journey—from the first weigh-out of starting aniline, through careful diazotization, monitored purification, to custom packaging that protects activity until it reaches the customer’s lab or plant.

    Years of hands-on production push us to solve real-world problems. Real production environments cannot tolerate the wishful thinking of “one product solves all needs.” Effective chemical manufacturing depends on what actually works in context. Our long cycles of pilot testing, exposure to both customer wins and problems, and continued reinvestment in both safe facilities and knowledgeable people have taught us how to read the signals—both good and bad—of a reliable batch.

    2,5-Diethoxy-4-(4-Morpholinyl)Benzenediazonium Sulfate stands out because we devote ourselves to making each lot deliver truly workable results. This approach, rooted in experience, relationships, and full control over each stage, remains the main reason researchers and manufacturing engineers continue to select our product for their innovation pipelines.

    Top