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Ethyl Diazoacetate

    • Product Name Ethyl Diazoacetate
    • Alias EDA
    • Einecs 203-580-9
    • 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

    501470

    Chemicalname Ethyl Diazoacetate
    Casnumber 623-73-4
    Molecularformula C4H6N2O2
    Molarmass 114.10 g/mol
    Appearance Yellow to orange liquid
    Density 1.14 g/cm³
    Boilingpoint 87-90°C at 20 mmHg
    Meltingpoint -20°C
    Solubility Soluble in organic solvents (e.g., ethanol, ether, benzene)
    Refractiveindex 1.431 (20°C)
    Flashpoint 29°C (closed cup)
    Vaporpressure 4 mmHg at 25°C
    Odor Sweet, pleasant odor

    As an accredited Ethyl Diazoacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethyl Diazoacetate is supplied in a 100-gram amber glass bottle, tightly sealed with a PTFE-lined cap and safety labeling.
    Shipping **Ethyl Diazoacetate** should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must be transported as a hazardous material (UN 2987), in accordance with regulations for organic peroxides and toxic substances. Ensure proper labeling and documentation; keep away from incompatible materials and avoid physical shock or rough handling.
    Storage Ethyl diazoacetate should be stored in a tightly sealed container, away from direct sunlight, heat, ignition sources, and moisture. It must be kept in a cool, dry, and well-ventilated area, preferably in a dedicated flammables cabinet. Handle with care, avoiding shock or friction, as it is sensitive and potentially explosive. Store separately from acids, bases, and oxidizing agents.
    Application of Ethyl Diazoacetate

    Applications of Ethyl Diazoacetate in Industrial Manufacturing

    Ethyl diazoacetate serves as a precision reagent in key chemical transformations within pharmaceutical, agrochemical, fine chemical, and materials manufacturing. Our experience as a direct producer allows us to support complex customers’ downstream syntheses with quality-controlled supply, technical guidance, and regulatory alignment specific to each industry segment.

    1. Active Pharmaceutical Ingredient Synthesis

    Pharmaceutical manufacturers employ ethyl diazoacetate as a carbene precursor in one-step and multi-step syntheses of heterocyclic structural motifs. Researchers leverage its reactivity in cyclopropanation, insertion, and esterification reactions to build core intermediates for anti-infective, antineoplastic, and CNS-targeting molecules. Reaction schemes typically require strict stoichiometric control and staged addition at sub-ambient temperatures to maximize selectivity and avoid decomposition, supporting efficient route design from laboratory to commercial scale.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • USP/NF Monograph references for relevant synthesized intermediates
    • 21 CFR Part 211 (Drug Product cGMP)
    • Ph. Eur., JP Pharmacopoeia requirements where applicable

    Typical usage ratio

    • 0.8–1.1 equivalents versus limiting substrate
    • Adjusted based on precursor reactivity, scale-up validation, and impurity profile management

    Downstream process integration

    • Introduced during key cyclopropanation and functionalization steps
    • Monitored under inert conditions with continuous temperature and yield tracking
    • Used in pilot lots prior to Kilo lab and full-scale cGMP campaigns

    Final product types

    • Chiral drug intermediates
    • API building blocks for anti-tumor agents
    • Precursors for CNS-active pharmaceutical compounds

    2. Agrochemical Intermediate Production

    In the agrochemical sector, ethyl diazoacetate is used to synthesize key scaffolds for crop protection agents, including pyrethroid and neonicotinoid precursors. Its application centers on cyclopropanation and α-alkylation reactions under controlled processing to ensure high selectivity and minimize hazardous byproducts. Manufacturing protocols typically include closed-feed dosing and validated waste management to comply with environmental and safety standards through each batch release.

    Industry compliance standards

    • ISO 9001-certified QC protocols for precursor manufacture
    • REACH Registration, Evaluation, Authorisation, and Restriction of Chemicals (EU)
    • EPA Registration Guidelines (40 CFR Parts 150–189, US)
    • GHS Safety Data Sheet and labelling compliance

    Typical usage ratio

    • 0.6–1.2 molar ratio relative to agrochemical key starting material
    • Adjusted per target product yield and endpoint chromatographic profile

    Downstream process integration

    • Fed-batch or semi-continuous addition into reaction vessel containing substrate and catalyst
    • Continuous in-process testing to confirm completion before next synthetic stage
    • Integration with downstream hydrolysis or oxidation steps for tailored intermediate conversion

    Final product types

    • Pyrethroid pesticidal esters
    • Neonicotinoid intermediate structures
    • Herbicide key intermediates (custom synthesis contracts)

    3. Fine Chemical and Specialty Ester Manufacturing

    Specialty ester producers integrate ethyl diazoacetate during the preparation of flavor, fragrance, and engineered ester additives. Manufacturers utilize its controlled reactivity with alcohols and acids to deliver short- and medium-chain esters with tailored functional attributes, maintaining strict batch-to-batch reproducibility for food and non-food-grade outputs. Risk assessments and mitigation for residual diazo-based moieties feature prominently in these applications, enforcing robust clean-in-place and trace residue elimination steps throughout the process.

    Industry compliance standards

    • FSSC 22000 (Food Safety System Certification) where food-contact grades required
    • FCC (Food Chemicals Codex) for final esters applied to consumables
    • IFRA Standards for perfume and cosmetic applications
    • EU Regulation (EC) No 1333/2008 on food additives

    Typical usage ratio

    • 0.5–0.9 molar ratio relative to target alcohol or acid
    • Real ratio depends on required fragrance or flavor intensity, and end-use safety margins

    Downstream process integration

    • Metered dosing into esterification reactor at defined pH control points
    • Automated extraction and distillation for product purification and diazo residue removal
    • QC verification using GC-MS and HPLC per final use certification

    Final product types

    • Food-grade flavoring esters (e.g., ethyl lactate, methyl cyclopropanecarboxylate derivatives)
    • Perfume bases and fragrance enhancers
    • Plasticizer and industrial lubricant precursors

    4. Polymer Modification and Crosslinker Synthesis

    Materials and polymer manufacturers introduce ethyl diazoacetate into modification protocols to generate grafted and crosslinked structures with improved mechanical and surface characteristics. The compound facilitates controlled insertion and functionalization in step-growth and chain-growth polymerizations under anhydrous, nitrogen-flushed conditions, monitored via spectroscopic and rheological assays. Resultant materials deliver enhanced thermal stability, solubility, and adhesion properties for adhesives, coatings, and high-performance films.

    Industry compliance standards

    • ISO 14001 Environmental Management System for process emissions
    • RoHS Directive (Restriction of Hazardous Substances, EU)
    • Relevant section of FDA 21 CFR 175–178 for indirect food contact polymers
    • ASTM D638, ASTM D1002 for mechanical characterization of finished materials

    Typical usage ratio

    • 0.01–0.05 parts per hundred resin (phr) for crosslinking applications
    • Higher ratios up to 0.2 phr for functional modification (experimentally optimized per polymer type)

    Downstream process integration

    • Added during pre-polymer blend or via injection during melt or solution polymerization
    • Mixing and curing under controlled agitation and oxygen exclusion
    • Post-modification purification to remove unreacted diazo components

    Final product types

    • Grafted copolymers for adhesives
    • Functional coatings with tailored reactivity
    • High-barrier films for industrial lamination
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    Certification & Compliance
    More Introduction

    Ethyl Diazoacetate: A Manufacturer’s Perspective on Precision, Reliability, and Ongoing Innovation

    Introduction to Ethyl Diazoacetate: How We Make a Difference

    Ethyl diazoacetate holds a central role in laboratories and manufacturing facilities that demand efficiency and precision in organic synthesis. Every batch our team produces reflects the care, knowledge, and experience we have accumulated over years of refining processes and keeping pace with new technology. Chemists who depend on this compound know exactly why it draws attention—its reactive nature drives versatile transformations that let research, pharmaceutical, and specialty chemical labs solve tough problems quickly. We have seen our customers embark on projects that would stall without reliable access to high-purity reagents. Our approach to manufacturing ethyl diazoacetate always puts real-world lab needs ahead of speculation or cost-cutting, delivering a product that matches the scrutiny of any research journal or FDA inspection.

    Specifications That Matter in Daily Lab Life

    We prepare ethyl diazoacetate with a purity rarely matched outside high-regulation environments. Every lot is characterized by robust GC and NMR analysis, confirming the absence of major side-products or contaminants. We set our practical minimum for purity at 98%, but frequent requests from our pharmaceutical customers have led us to routinely supply upwards of 99%. The familiar yellowish solution shows a consistent density and behavior from container to container. Our customers prefer clear, usable specifications, so we always measure and control water content, acidity, and storage stability using Karl Fischer titration and well-documented accelerated aging studies.

    Practical storage containers, whether ampule or sealed bottle, mitigate decomposition by excluding air and light and are resistant to corrosive effects even during prolonged shipment. Experience has shown us that batch-to-batch consistency saves time, chemicals, and manpower when scaling up from bench to pilot-plant. Feedback from the field has shaped every specification—fluctuating reactivity, unexplained discoloration, or variable foam generation in reactions led to process tweaks and packaging updates.

    From Benchtop to Bulk: Our Production Journey

    We control every step, starting with raw materials. We source the acid chloride precursors only from plants we have audited for traceability and clean handling. Our operational protocol emphasizes strictly regulated temperatures, neutral atmospheres, and real-time process monitoring, avoiding the pitfalls of under- or over-diazotization, two issues that have derailed small-scale labs for years. Waste control—essential for safe diazo chemistry—relies on redundant containment and validated neutralization steps. Our operators use both modern instrumentation and long-standing hands-on checks, since lab data alone sometimes hide subtle early warning signs in the production cycle.

    For shipment, trained staff handle packaging and logistics in line with DG (dangerous goods) regulations on a global scale. We have invested heavily in training for our export staff, knowing that ethyl diazoacetate’s unique hazards pose administrative and safety challenges in transit. Customers in distant facilities rely on this dependability, reporting productive syntheses just days after delivery. Such consistency helps major multinational clients manage their own inventory stress—a lesson we learned firsthand during supply crunches that disrupted countless projects in both Europe and North America.

    Real-World Uses: Not Just for the Standard Textbook Reactions

    Most chemists think of ethyl diazoacetate as a go-to reagent for cyclopropanation through metal-catalyzed reactions or diazo transfer for α-diazoesters, but in our experience, the most innovative uses often arrive through customer calls and project meetings. We have seen teams use it to develop anti-infective agents by leveraging its reactivity in carbene insertion reactions. Agricultural labs have scaled up derivatization to test crop-protective molecules, finding that our high-purity batches make NMR signals clearer during structure elucidation. Peptide and oligonucleotide modification groups report sharper yields in labeling experiments, since impurities from less-controlled sources can drag out purification until material losses hurt results.

    Some research groups specifically search for sources of ethyl diazoacetate that demonstrate stability under refrigeration and lack excess stabilizers that cascade into target molecule contamination. After a client’s feedback, we revised solvent content and ampule design, cutting residual co-solvent peaks and improving product shelf life for those who work in low-temperature storage workflows. Having a direct line of communication with working chemists has continuously shaped not only our updated offerings, but also the way we frame our internal QC.

    Ethyl Diazoacetate Versus Similar Reagents: The Differences in Practice

    Anyone searching for diazo reagents faces a broad selection, from simple diazomethane preparations to more stabilized commercial products like trimethylsilyldiazomethane or sulfonyl azides. In daily synthetic practice, ethyl diazoacetate’s isolation-friendly physical state and moderate volatility have mattered most to our regular clients running multi-step syntheses. Diazomethane’s volatility and toxicity present unique safety hurdles, often requiring on-demand generation in small labs or awkward containment on larger scales. Trimethylsilyldiazomethane carries improved safety over diazomethane but can drag nontrivial silylation byproducts into reaction streams.

    By contrast, ethyl diazoacetate combines controllable reactivity with straightforward handling. Analysts report fewer unexplained side products during workup and isolation; clean aqueous workup delivers esters or alkenes without time-wasting chromatography. We once partnered with a mid-scale pharmaceutical plant which trialed both our product and a competitor’s. The in-process mass balances tracked with our certificate-of-analysis, while the comparison product’s lower stability increased lab downtime from reprocessing. For users needing stable storage, ethyl diazoacetate scores high on shelf life provided it’s kept dry and cold, something which is hard to achieve with many alternative diazo sources.

    From an environmental perspective, established disposal channels already exist for small-scale residues. Our production facility operates continuous air and liquid effluent monitoring, posting results to a secure client portal for clients participating in sustainability audits. Several customers, especially those in green chemistry initiatives, have commended our documented reduction of chlorinated waste by redesigning the workup sequence. Our direct manufacturer status enables us to trial such changes without having to wait for third-party supplier approval cycles, letting us respond quickly to shifts in customer sustainability goals.

    Quality Assurance Built In From Sourcing to Delivery

    Manufacturing guarantees only hold value if customers see them reflected in every shipment. Every campaign begins with raw material screening, where only acid chlorides and ethyl alcohols meeting trace metals and organic purity requirements proceed to synthesis. We document each container’s batch origin, tracking everything through the process with digital logs. Operators, who combine textbook knowledge with real hands-on familiarity, troubleshoot issues that fall between standard test parameters. These could be subtle color changes, unexpected viscosity, or persistent foam that could signal early degradation.

    Final products never leave our facility without comprehensive QC. We don’t just tick off a finished-product spec—our staff investigate batch outliers and consult past runs to catch trends. We routinely run cross-instrument checks, such as confirming IR spectra against GC and titration data to ensure lot-to-lot continuity. Clients have told us this prevents irritating surprises, such as finding their compound didn’t survive long enough for scale-up, or explaining a failed batch to shareholders when up-front warnings would have saved hours and resources.

    Our technical support extends beyond the delivery note. If researchers encounter out-of-spec results during pilot work, we provide actionable troubleshooting—often right from the same chemists responsible for the original production run. This feedback loop ensures changes in customer applications make their way back into future production rounds, constantly closing the gap between stated specifications and real-world results.

    Handling and Practical Safety: Lessons Learned Over Years

    Ethyl diazoacetate, like most diazo compounds, deserves respect. Hands-on training at our plant emphasizes controlled temperatures, protection from direct sunlight, and ventilation systems that keep vapors away from operators. We’ve spent years upgrading storage, investing in temperature alarms and robust secondary containment. Earlier decades brought occasional near-incidents during loading and unloading that pushed us to adopt QR-coded inspection checklists and timer-controlled transfer lines. Service engineers swap field stories about tweaks to remote tank monitoring, all designed to protect both product integrity and personal safety.

    Many customers ask about the fire and explosion risk. Proper education and sealed containment almost always rule out accidental releases, and we encourage site visits and video calls to share effective storage techniques. For overseas clients, safe transport gets priority, with certified DG packaging and full cooperation with airline and sea freight carriers. These moves prevent the hard lessons learned by those who tried to rush shipments without understanding the care required—lost time and damaged trust never make up for a botched delivery.

    Paving the Way for Pharmacological and Agrochemical Breakthroughs

    Ethyl diazoacetate shows up in dozens of published syntheses of marketed and clinical candidate drugs. We collaborate with research chemists aiming for more than textbook transformation—they want robust yields under realistic scale-up conditions, cost-effective repeatability, and minimal regulatory friction. We have participated in confidential joint-development projects where the purity and reliability of this compound allowed medicinal chemists to prove their methods to boards and auditors with confidence. The agility of our process—one we fine-tune based on the actual challenges relayed from these teams—has kept their projects alive in tough regulatory and commercial environments.

    In agriculture, nearly every new herbicide class features at least one diazo-mediated ring construction or insertion. Experience tells us that country-specific regulatory scrutiny often calls for detailed trace metal and residue certificates, and most pilot-scale field operations can't risk contaminated or decomposed starting materials. Our technical liaisons know how to anticipate these questions, having guided numerous projects from initial PO through to the first test batches applied on trial plots.

    Addressing Storage and Logistics: Lessons From the Supply Chain

    Cold chain integrity and clear labeling make the most difference in global shipments. Temperature variation, extended warehouse stops, and security checks all affect the final reagent quality. Our logistics and QA departments have partnered to standardize real-time data logging, so every international shipment includes accessible temperature profiles. Clients report fewer batch failures and storage headaches, because anomalies can be tracked back and explained quickly. During periods of global raw material shortages, we adapted production runs and invested more in advance stockpiling, keeping customers shielded from the worst disruptions. We made the call to prioritize existing loyal customers’ allocations during embargoes or port closures—a decision that strained immediate sales, but saved partnerships over the long haul.

    Customs documentation, especially for diazo materials, remains a tough point worldwide. After seeing clients lose weeks to ambiguous or incomplete papers from middlemen, we now handle all regulatory declarations in-house, including updated UN and IATA codes for each region. Direct manufacturer knowledge plays a pivotal part—a missed declaration can trigger months of seizure, rerouting, and financial loss. We train our team not just on labeling but on the finer points of international regulatory language and risk assessment. This detailed, proactive approach is born out of past headaches, not of marketing slogans.

    Meeting Tomorrow’s Chemistry Demands

    From photoredox catalysis to bioconjugation, each technological advance nudges ethyl diazoacetate into new demands. Our scientists anticipate reaction trends by monitoring pre-publication chemistry and direct input from global customers. Small tweaks, like minimizing trace stabilizers or batch-specific modifications, make a world of difference in academic grants and commercial proposals. Several university consortia have come back to us, reporting smoother adoption of our product lines as they pushed into AI-driven synthesis planning or microreactor platforms. We take every suggestion as a mandate to improve, using every round of feedback to test our real-world impact—not just spreadsheet margins.

    Whether launched in a single project or embedded in a multinational supply network, reliable access to dependable ethyl diazoacetate strengthens the backbone of experimental and production chemistry. The lessons our company has gathered by staying close to customer challenges drive our evolution, keeping our production and quality methods at the sharp edge of scientific development.