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Triethyl Phosphonoacetate

    • Product Name Triethyl Phosphonoacetate
    • Alias TEPA
    • Einecs 210-197-8
    • 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

    317922

    Chemicalname Triethyl Phosphonoacetate
    Casnumber 867-13-0
    Molecularformula C8H17O5P
    Molecularweight 224.19 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 146-148 °C at 8 mmHg
    Density 1.108 g/mL at 25°C
    Refractiveindex n20/D 1.424
    Flashpoint 155 °C
    Solubility Soluble in organic solvents (e.g., ethanol, ether)
    Purity Typically ≥98%

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

    Packing & Storage
    Packing 500 mL Triethyl Phosphonoacetate is packaged in an amber glass bottle with a secure screw cap and hazard labeling.
    Shipping Triethyl Phosphonoacetate is shipped in tightly sealed containers under dry, cool conditions to prevent hydrolysis and degradation. It is transported as a liquid chemical, classified as non-hazardous for air and ground shipping. Proper labeling and safety documentation are included to comply with regulatory standards and ensure safe delivery.
    Storage Triethyl Phosphonoacetate should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and acids. Keep it protected from moisture and direct sunlight. Ideally, store under an inert atmosphere, such as nitrogen or argon, to prevent hydrolysis or degradation. Always follow appropriate chemical safety protocols.
    Application of Triethyl Phosphonoacetate

    Applications of Triethyl Phosphonoacetate in Industrial Manufacturing

    As a dedicated manufacturer of Triethyl Phosphonoacetate, we are committed to supporting advanced industrial applications across key chemical sectors. Below, we outline the main industrial downstream uses where our product has proven, validated value in manufacturing environments, with application details rooted in real-world practice and compliance requirements.

    1. Pharmaceutical Synthesis: Nucleoside Analog Intermediates

    Pharmaceutical manufacturers integrate Triethyl Phosphonoacetate into nucleoside analog API synthesis to achieve high selectivity in C–C bond formation, particularly for advanced antiviral drug intermediates. The compound enters key Horner–Wadsworth–Emmons (HWE) reactions, allowing precise control over α,β-unsaturated ester construction without introducing unwanted side groups, which is critical for downstream GMP validation. Technologists adjust the dosing based on substrate reactivity and targeted yield, ensuring batch consistency and minimizing purification loss in regulated pathways.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapters <823> and relevant monographs
    • European Pharmacopoeia (Ph. Eur.) specifications for intermediates
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals)

    Typical usage ratio

    • 0.8–1.2 molar equivalents per target aldehyde/ketone component, adjusted to ensure full conversion with minimal excess depending on desired conversion efficiency and final yield

    Downstream process integration

    • Charged during the HWE reaction stage after initial substrate activation, followed by product isolation, solvent exchange, and intermediate purification (typically via crystallization or column chromatography)

    Final product types

    • Active pharmaceutical ingredient intermediates, including anti-HIV, anti-hepatitis B/C nucleoside analogs (e.g., tenofovir intermediates, abacavir intermediates)
    • Specialty small molecule drug precursors for continued process into commercial APIs

    2. Agrochemical Active Ingredient Synthesis

    Agrochemical producers utilize Triethyl Phosphonoacetate to synthesize key pyrethroid, herbicide, and insecticide intermediates due to its reliable performance in olefination reactions. The raw material operates within closed batch reactors, where its predictable reactivity profile helps achieve the geometrical selectivity required for downstream biological efficacy. Carefully monitored addition prevents overreaction and allows flexible scale-up, with compliance documentation maintained for regulatory audits and environmental controls.

    Industry compliance standards

    • EPA 40 CFR Part 158 (Data Requirements for Pesticide Registration)
    • ISO 9001:2015 Quality Management for Chemical Synthesis
    • REACH Annex II – Safety Data Sheet (SDS) requirements
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 1.0–1.3 equivalents per halogenated aromatic aldehyde, optimized via lab-scale validation to maximize yield of target E/Z isomers

    Downstream process integration

    • Fed into the Wittig/HWE olefination step of multi-step synthesis, followed by separation of stereo-isomeric intermediates and conversion to final bioactive molecules via subsequent oxidation or hydrolysis reactions

    Final product types

    • Insecticide intermediates for pyrethroid family compounds
    • Precursors for selective herbicide actives
    • Custom intermediates for new crop protection active designs

    3. Functional Materials: Specialty Polymer Additives

    Specialty polymer producers add Triethyl Phosphonoacetate to introduce phosphonate functionalities into polymer backbones, imparting controlled fire-retardant or anti-static properties in engineered plastics and textiles. The ester groups enable precise copolymerization via melt, solution, or emulsion polymerization, depending on the monomer system. The compound’s processing profile and interaction with other phosphorous agents are optimized under close formulation control to meet material property and regulatory guidelines in safety-critical end uses.

    Industry compliance standards

    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • REACH Regulation (EC) No 1907/2006 for polymer additives
    • ISO 9001:2015 Quality Assurance Process Control for Additive Manufacturing
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances) compliance

    Typical usage ratio

    • 1.5–10% by weight relative to monomer feed, depending on the required flame resistance or anti-static property specification; optimized per product line and application

    Downstream process integration

    • Blended with monomer mixture prior to polymerization; incorporation occurs during copolymerization or post-polymerization functionalization, followed by extrusion, molding, or fiber spinning as dictated by end-use requirements

    Final product types

    • Flame-retardant polyester textiles and nonwovens
    • Electrostatic-dissipative engineering polymers
    • Specialty plastic films with regulated phosphonate incorporation

    4. Fine Chemical Building Blocks for Vitamin Synthesis

    Manufacturers of food and nutrition ingredients deploy Triethyl Phosphonoacetate in the chain extension step for critical vitamin intermediates, primarily for vitamins A and E. The reagent allows construction of conjugated polyene or aromatic systems under controlled temperature and catalyst regimes, with usage ratios tailored to batch size and carbon chain elongation profile. Downstream process validation includes impurity profiling in compliance with food-grade standards, ensuring quality traceability through the nutraceutical chain.

    Industry compliance standards

    • FCC (Food Chemical Codex) purity criteria for allowed processing aids
    • GMP+ B2 Feed Safety Assurance (for animal vitamin production)
    • ISO 22000 Food Safety Management System
    • FAO/WHO Codex Alimentarius for Nutritional Additives

    Typical usage ratio

    • 0.6–1.5 equivalents per aldehyde or activated ester group, adjusted by vitamin precursor structure and desired purity of the final product; formulation trials determine minimum effective dose

    Downstream process integration

    • Introduced in the key carbon–carbon bond formation stage during stepwise chain extension transformations, with subsequent work-up ensuring removal of byproducts and excess reagents before crystallization/purification

    Final product types

    • Vitamin A intermediates (e.g., all-trans retinal and related retinoid precursors)
    • Vitamin E (tocopherol) synthesis precursors
    • Fine chemical building blocks for specialty micronutrients

    5. API Intermediate in Anticancer Compound Synthesis

    Producers of advanced oncology APIs employ Triethyl Phosphonoacetate when synthesizing key carbon frameworks for kinase inhibitor and anti-tumor intermediate portfolios. The material’s reliable engagement in regioselective HWE condensation secures the integrity of critical pharmacophores. Strict process validation occurs under cGMP/quality-by-design (QbD) conditions, with comprehensive in-process monitoring to document impurity profiles, batch records, and traceability, as per international regulatory protocols.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • Chinese Pharmacopoeia (ChP) API requirements
    • US FDA DMF (Drug Master File) submission standards
    • EU EudraLex Volume 4 GMP Guidelines for APIs

    Typical usage ratio

    • 0.9–1.1 equivalents per carbonyl precursor, with ratio optimized per synthetic step to minimize residual byproducts and maximize throughput

    Downstream process integration

    • Added at the defined carbon–carbon bond-building stage, then followed by purification into advanced intermediates ahead of final functionalization or cyclization

    Final product types

    • Kinase inhibitor advanced intermediates (e.g., for pyrimidine or quinazoline-core drugs)
    • Oncology lead compound scaffolds ready for final functionalization

    6. Industrial Syntheses of α,β-Unsaturated Esters for Fragrance and Flavor Production

    Manufacturers in fine chemicals for the perfumery and flavor industries rely on Triethyl Phosphonoacetate for specific C–C elongation during custom synthesis of α,β-unsaturated esters essential for aroma profiles. The material facilitates stereoselective formation of double bonds under mild basic conditions, meeting precise olfactory and purity specifications. Process design includes close adjustment of reactant ratios and real-time GC/HPLC monitoring for batch homogeneity, while documentation ensures adherence to food-grade and fragrance regulations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • Food Chemicals Codex (FCC) safety and purity requirements
    • EU Regulation (EC) No 1334/2008 (Flavorings and certain food ingredients with flavoring properties)
    • ISO 9235:2013 for aromatic raw material classification

    Typical usage ratio

    • 1.0–1.5 equivalents per aldehyde, determined by chain length targeted and flavor/fragrance profile specification; small excess can ensure complete reaction for minimal residual aldehyde

    Downstream process integration

    • Added during the controlled HWE or related olefination step, with downstream operations focusing on ester isolation, vacuum distillation, or preparative chromatography to achieve product standardization

    Final product types

    • Custom α,β-unsaturated esters for commercial fragrance bases
    • Flavoring ingredients for food and beverage enrichments (e.g., fruity, floral, and green top notes)
    • Blend components for detergent and personal care perfume formulations
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    Certification & Compliance
    More Introduction

    Triethyl Phosphonoacetate: Reliable Solutions Backed by Real Manufacturing Experience

    Rigorous Manufacturing Standards in Every Batch

    Triethyl phosphonoacetate is not just another phosphonate compound on the market—it represents years of direct production experience and targeted improvements in process control. As the actual manufacturer, every step, from raw material selection to final filtration, reflects a stubborn dedication to consistency. Quality doesn’t start in the finished drum. It begins in nearly obsessive sourcing—finding reliable suppliers for triethyl phosphite and ethyl bromoacetate, using them under tightly controlled temperatures and pressures. We operate in closed reactors equipped with real-time monitoring, running GC analysis throughout each stage. Staff in the plant understand the risks—trace moisture or oxygen leads to side reactions, affecting both purity and yield. That’s not just a chemistry problem; it’s plant downtime and lost resources. After years of fine tuning, we’ve landed on a process that delivers high-purity triethyl phosphonoacetate, generally exceeding 98%, batch after batch.

    The Chemist’s Perspective: Why Purity Changes Outcomes

    Experienced synthetic chemists instantly spot the difference between technical-grade material and the high-purity compound we regularly supply. Small contaminants or residual solvents might sound trivial, but in reality, they slow downstream synthesis, force you through extra purification steps, and bring a headache to every performance test. Our product’s low byproduct content means predictable reactivity in Horner-Wadsworth-Emmons (HWE) reactions. The aldehyde or ketone you pair with triethyl phosphonoacetate responds efficiently, forming the double bond you expect—without surprises from unknown peaks on your NMR.

    Other manufacturers sometimes tolerate a little bit of roughness in the distillation cut, thinking it doesn’t matter. We’ve witnessed how just 1% more impurity can tank a scale-up program. During site audits with customers, the story surfaces: cheap technical-grade product causes variable yields, more column work, more hours wasted. Our operators know the reality—no synthetic chemist would settle for that on a tight deadline, so there is simply no room for corners cut.

    Specifications: What Consistency Really Means

    As the ones who synthesize it, we know every batch is only as good as its GC and NMR profiles. We analyze each lot before release—looking for clarity, a light yellow to colorless liquid, without the haze that signals hydrolysis or oxidation. Refractive index and density remain stable, reflecting the correct molecular balance. The faint ester scent comes as a check on purity—old, oxidized samples smell off, and our team catches that in sensory checks as part of our strict QA protocol.

    Water content sits well below 0.2% for most production runs, thanks to vacuum lines flushed and dried after every cleaning. Phosphonate byproducts barely register. Heavy metals—often a marker for poor reactor hygiene—fall beneath externally required standards, monitored through ICP-OES analysis. These numbers don’t just sit in a report. They’re benchmarks that protect every customer’s synthesis and ensure long-term stability under storage, so chemists can stock up with confidence.

    Real-World Applications in Industrial and Academic Labs

    Triethyl phosphonoacetate found its place first in advanced organic synthesis and remains a staple in our own R&D pilot lines. The main draw lies in the HWE reaction, which chemists leverage to create α,β-unsaturated esters. No textbook replacement captures the versatility or selectivity offered here. We supply contract manufacturers and pharma development teams looking to streamline their workflow—stepwise control, moderate reaction temperatures, high overall yields. Over time, we’ve collaborated with process chemists scaling lactone, pyran, and natural product syntheses from grams to kilograms.

    Universities turn to us during grant-driven programs for developing new medicinal targets. Our product features readily in academic publications when repeatability is a must. Graduate students know the agony of failure tracing back to contaminated starting material. With consistently tested triethyl phosphonoacetate, project timelines meet tight grant deadlines, and results appear cleaner both on paper and in the lab.

    In polymer chemistry, researchers value phosphonate esters for introducing phosphorus into backbone or side-chain modifications, helping tailor flame-retardant properties. Projects in advanced coatings, bioconjugation, and agrochemical synthesis draw heavily from our material, showing just how broadly triethyl phosphonoacetate reaches once purity and reactivity become reliable.

    Differences from Related Phosphonates and Alternatives

    Ask anyone who’s run a parallel synthesis with dimethyl phosphonoacetate or diethyl phosphonoacetate. Triethyl phosphonoacetate stands out every time for its unique combination of reactivity and ease of purification. Its ethyl groups lend less volatility, making it easier to handle in larger glassware or pilot reactors. The more compact methyl esters often carry over through distillation or require more aggressive drying, risking decomposition.

    While dimethyl analogues react slightly faster under basic conditions, they also bring more challenges in post-reaction purification. Triethyl phosphonoacetate’s moderate boiling point—neither too low to evaporate nor so high as to cause bumping—hits a sweet spot. The byproducts and excess reagents strip away more cleanly, resulting in easier workups. Less time spent chasing product through silica or losing yield in rotavap means more productive days in the lab.

    Phosphonate-free olefination reagents exist, like Wittig or Tebbe reagents, but each comes with cost, waste, or compatibility trade-offs. The HWE reaction, powered by triethyl phosphonoacetate, often wins on selectivity and is more tolerant of functional groups. Alkali bases handle our product well, and wise handling avoids harsh decomposition. Our experience says: fewer surprises, fewer reruns, less stress over process variability.

    Process Improvements Driven by Customer Feedback

    History shows product improvement comes directly from listening to end users. One major customer scaled synthesis from 10 kg to 300 kg-per-month using our triethyl phosphonoacetate. Laboratory managers explained where earlier product experienced yellowing after weeks in storage, indicating slow hydrolysis. We took this head-on and worked backwards—installing stricter moisture controls in both storage and shipment, improving both shelf life and usability. Last year, we invested in upgraded filling systems. Exposure to ambient air dropped sharply, and the results showed in reduced peroxide content on shipping samples.

    Customization remains a real advantage of working with an established manufacturer. Whenever a downstream user requires material for an unusual coupling, we can collaborate with their R&D, adjusting cut points or exploring further purification. We treat validation batches as more than box-checking. Each lab gets material that reflects our plant’s peak performance. Many manufacturing partners recount avoiding weeks of troubleshooting simply by switching to our consistent supply. This trust grows from open dialogue—shared analytical data, transparent change management, and prompt issue resolution.

    Handling and Storage: Tips from the Manufacturing Floor

    Working hands-on with triethyl phosphonoacetate means gaining a healthy respect for its sensitivity to air and moisture. Manufacturing crews regularly flush lines and drums with nitrogen. Warehouse staff move fresh batches directly into steel or glass-lined containers, always sealed against humidity. Over the years, plant teams learned the hard way—an unattended open drum picks up enough water overnight to trigger off-spec reactions later, making for expensive rework.

    Labs getting this product should check for tight caps, wear gloves, and keep bottles in a cool, dry place. Field surveys at customer facilities reveal that even small amounts of condensate in dispensing lines speed up hydrolysis or polymerization. Our packaging includes tamper-evident seals and humidity monitors, so nothing escapes attention. Plenty of damage prevention happens beyond paperwork: physical inspections, daily logging, and routine training of every operator dealing with organophosphorus handling.

    Regulatory and Environmental Responsibility

    Our responsibility for triethyl phosphonoacetate goes beyond the manufacturing plant. Every batch aligns with registration requirements on every continent where we ship. Regulatory advisors keep up to date with REACH, TSCA, and other evolving frameworks, making sure that our processes fit the compliance landscape for each customer base. Pre-shipment analysis extends beyond purity—covering residual solvents, elemental impurities, and in some cases, bioaccumulation testing depending on end-use.

    From an environmental angle, we designed our wastewater and solvent recovery systems to limit emissions. Spent solvents from production undergo fractionated distillation and recycling, keeping both site emissions and disposal costs under control. Byproducts go for controlled incineration, meeting local environmental guidelines. Our teams attend yearly seminars on eco-friendly chemical handling and continually reassess every process for improvement—sometimes sparked by a single suggestion on the line.

    On packaging, we shifted to drums and bottles built for clean recyclability. Customers appreciate the ability to send containers back for reconditioning instead of contributing to site waste. Any product recovery from drums returns to our process streams—not landfill. It’s a system built on both bottom-line savings and an ethic of responsible stewardship. Years of working with international clients sharpened our priorities: hazard minimization, regulatory clarity, and support through the entire product lifecycle.

    Supporting Long-Term Research and Scale-Up

    Commercial scale-up isn’t just about meter readings and process charts; it depends on reliability, logistics, and planning. Multiple pharma companies rely on our triethyl phosphonoacetate—from initial feasibility pilots up to multi-hundred-liter campaigns. By keeping close inventory controls and scheduling regular reviews with purchasing teams, delays get cut down. On more than one occasion, we’ve ramped up production at short notice, solving bottlenecks in new drug synthesis. Our logistics team cross-checks shipment routes and storage conditions, reducing transit times and keeping material in optimal condition.

    Customers facing tricky scalability issues have brought samples for us to analyze directly—tracking minute impurities that might build up during larger runs. We don’t keep these findings in the dark. Shared learnings and method improvements go into training manuals and get passed down to every operator on our floor. Shared process reviews with customers identify potential hotspots in storage and dispensing, stopping problems before they snowball at full scale. This draws on years of plant experience—both for our own benefit and that of chemists putting the compound to work.

    Innovation and Continuous Improvement

    New uses for triethyl phosphonoacetate keep emerging, and we adapt alongside them. Collaborations with external research institutes bring feedback from the cutting edge—new ligand synthesis, phosphorus-based flame retardants, even agricultural adjuvants. Our own R&D recently piloted microencapsulation projects, where the reliable reactivity of our phosphonoacetate allows for stable, uniform shell formation in the final product. Feedback from application engineers feeds into the next production change, keeping manufacturing nimble and responsive.

    Engineers reevaluate each year how to cut waste, boost yield, or tighten resource consumption. Recent upgrades include higher-efficiency condensers, reducing solvent use, and modified purification columns that improve both throughput and selectivity. By keeping detailed records of each tweak, we ensure that each innovation sticks—building toward ever better results for end users. If a customer encounters unusual challenges in formulation or incorporation, our team dives into the lab, running parallel tests—not just answering questions, but pushing performance higher.

    Trust Built Through Transparency and Technical Support

    Buyers selecting a phosphonoacetate need more than an MSDS and a purity line on a COA. In our experience, the most productive partnerships come from technical openness. We keep batch records, process diagrams, analytical data, and troubleshooting logs available for review. Early on, we saw how strong technical support builds long-term loyalty. Experienced staff—some with decades on our lines—field support calls, answer technical queries, and assist with troubleshooting on both routine and novel applications.

    Our clients value honest discussions—bad news about a delayed shipment or analytical outlier goes out right away, followed by corrective steps. Many sourcing managers tell us that this reliability means more than a minor price swing elsewhere. When customers face regulatory questions, our compliance staff prepares detailed registration dossiers. When synthesis teams hit roadblocks, we offer real solutions based on manufacturing-level knowledge. This level of engagement shapes the long-standing reputation of our triethyl phosphonoacetate, supported by facts, data, and the living experience accumulated over many years of direct production.

    Conclusion: A Product Shaped by Experience, Ready for the Future

    Every drop of triethyl phosphonoacetate that leaves our plant stands as proof of our belief in quality, responsiveness, and direct accountability. Over years of development, listening to customer concerns, and fixing problems as they arise, we’ve shaped a product that meets real demands—not just as a commodity, but as a foundation of modern synthetic chemistry. We support ambitious new projects and existing workflows, always searching for ways to remove obstacles and raise the bar. Our commitment brings not only purity and reliability, but the kind of partner the industry can trust as research and manufacturing needs shift tomorrow.