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

Ethyl Nitroacetate

    • Product Name Ethyl Nitroacetate
    • Alias Ethyl 2-nitroacetate
    • Einecs 209-409-5
    • 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

    736752

    Cas Number 532-21-2
    Molecular Formula C4H7NO4
    Molecular Weight 133.10
    Appearance Colorless to pale yellow liquid
    Boiling Point 194-195 °C
    Density 1.297 g/cm³
    Melting Point -29 °C
    Refractive Index 1.428
    Flash Point 83 °C
    Solubility In Water Decomposes

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

    Packing & Storage
    Packing Ethyl Nitroacetate is supplied in a 500 mL amber glass bottle with a secure screw cap, labeled with hazard warnings.
    Shipping Ethyl Nitroacetate should be shipped in tightly sealed containers, protected from light, moisture, and sources of ignition. It must comply with applicable transport regulations for hazardous chemicals, typically classified under UN 2810 (Toxic Liquid, Organic, N.O.S.). Proper labeling, documentation, and handling by trained personnel are required to ensure safe transit.
    Storage Ethyl nitroacetate should be stored in a cool, dry, well-ventilated area away from heat, open flames, and sources of ignition. Keep the container tightly closed and protected from direct sunlight and moisture. Store separately from strong oxidizing agents, reducing agents, acids, and bases. Use appropriate, labeled containers and ensure the storage area has spill containment and proper ventilation to prevent vapor accumulation.
    Application of Ethyl Nitroacetate

    Applications of Ethyl Nitroacetate in Industrial Manufacturing

    Ethyl nitroacetate serves as a critical raw material across multiple fine chemical sectors, driving specialized transformations in pharmaceutical synthesis, agrochemical intermediates, dyestuff manufacturing, and specialty monomer production. As a direct manufacturer, we supply this intermediate to downstream customers who require consistency and tight quality control standards throughout their formulation and large-scale processing.

    1. Pharmaceutical Intermediate Synthesis

    Ethyl nitroacetate is widely used by pharmaceutical producers for the construction of α-nitro and α-amino acid derivatives. It enters as a key step in the synthesis of various non-natural amino acids and heterocyclic scaffolds, particularly those used in complex APIs and advanced intermediates for cardiovascular and central nervous system drugs. Its role as a nucleophilic building block enables regioselective and stereocontrolled ring closures, coupling, or reductive transformations, often under cGMP conditions, with traceability required for regulatory submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monograph requirements for residual solvents and impurities
    • 21 CFR Part 211 (US FDA GMP for Finished Pharmaceuticals)
    • EDQM, Japan PMDA, and WHO Prequalification cross-reference

    Typical usage ratio

    • Formulators typically use ethyl nitroacetate at 0.8–1.5 molar equivalents per targeted linkage, optimizable based on step yield and requirements for downstream purification; deviations depend on substrate reactivity and desired selectivity.

    Downstream process integration

    • Added during amidation or alkylation stages following halogenation or activation of starting material; charged in controlled feeding to manage exotherm and purity during critical API precursor formation under inert atmosphere.

    Final product types

    • Non-natural amino acids for peptide drugs
    • Nitrogen-heterocycle active intermediates
    • API precursors for antihypertensive agents
    • Chiral building blocks for CNS and oncology drug candidates

    2. Agrochemical Intermediate Manufacture

    In the crop protection sector, downstream companies utilize ethyl nitroacetate as an efficient synthon in the preparation of substituted nitroalkanes and derived carbonyl compounds. These serve as key intermediates in the custom manufacture of herbicide and insecticide molecules, particularly those requiring specific substitution at the alpha-carbon or ring closure for selective bioactive profiles. Process lines rely on batch and semi-continuous additions for consistent conversion and robust impurity profiles, essential for field performance and regulatory approval.

    Industry compliance standards

    • FAO/WHO Guidelines for the Quality Control of Pesticides
    • ISO 9001:2015 for agrochemical production
    • REACH Regulation (EC) No 1907/2006 for environmental health safety
    • China GB2763 Maximum Residue Limits in Foods referencing starting material traceability

    Typical usage ratio

    • Standard input dosage is 2–6 weight percent of total batch mass, fine-tuned by the molecular architecture specified in the technical package or formulation protocol for the proprietary agrochemical product line.

    Downstream process integration

    • Introduced in the alkylation or Michael addition phase, often after activation by a base; incorporated before oxidation or reduction steps to generate specific nitroalkyl derivatives needed for targeted bioactivity in pest control agents.

    Final product types

    • Selective herbicide actives
    • Pyridine- and triazine-based insecticide intermediates
    • Fungicide precursors with tailored side chains
    • Fine-tuned adjuvant intermediates

    3. Dyestuff and Pigment Intermediate Production

    Specialty colorant manufacturers employ ethyl nitroacetate for the functionalization of aromatic rings in the synthesis of azo dyes, nitro-containing chromophores, and high-performance pigments. The nitro group and ester functionality enable advanced coupling reactions and rearrangements that yield vivid, high-purity intermediates for vat, disperse, and reactive dye families. Batch quality and input consistency directly impact shade uniformity and color fastness in downstream textile and ink applications.

    Industry compliance standards

    • EN 71-3 Safety of Toys (migration of certain elements, for use in pigment processing)
    • OEKO-TEX® Standard 100 (textile processing chemicals, restricted substances)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals – Manufacturing Restricted Substances List)
    • ISO 14001:2015 (environmental management for dye production)

    Typical usage ratio

    • Added at 1.2–3.0 equivalents relative to amine or coupling partners, depending on the target chromophore structure and process route; adjustments respond to color strength requirement and process validation studies.

    Downstream process integration

    • Charged during electrophilic aromatic substitution or prepared in-situ as a coupling building block; process control focuses on achieving full conversion while minimizing isomeric or byproduct colorants for high batch-to-batch reproducibility.

    Final product types

    • Azo and nitro dye intermediates for textiles
    • Nitroaromatic pigments for paints and printing inks
    • Color bases for high-durability plastics colorants
    • Custom intermediates for hair dye synthesis

    4. Advanced Monomer and Polymer Precursor Manufacturing

    Producers in the specialty polymer segment leverage ethyl nitroacetate for introducing nitro-functionalities into monomers before subsequent polymerization. These engineered monomers impart enhanced reactivity or adhesion to polymers designed for advanced coatings, adhesives, and engineered resins. Control during the derivatization step and purification directly impacts the polymer chain structure, affecting the mechanical and electronic characteristics required in end-use scenarios such as electronics encapsulation and specialty adhesives.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001 for specialty polymer production
    • RoHS Directive 2011/65/EU (for electronic-use polymer applications)
    • UL 94 (V-0, V-1, V-2 flammability standards for electrical polymers)
    • Chemical Control Laws (TSCA, REACH pre-registration for monomers)

    Typical usage ratio

    • Typically applied at 0.5–2.2 molar equivalents per acrylate, methacrylate, or other polymerizable base; process formulation adjusts this based on chain length goals and specific functional density in the finished polymer matrix.

    Downstream process integration

    • Introduced during initial monomer synthesis or as a late-stage functionalizing reagent prior to polymerization; critical for successful post-modification or copolymerization processes requiring uniform nitro group incorporation.

    Final product types

    • Nitro-functionalized monomers for high-performance resins
    • Polymers for electronics component encapsulation
    • Specialty adhesives with improved reactivity
    • Topcoat materials for industrial protection applications
    Free Quote

    Competitive Ethyl Nitroacetate prices that fit your budget—flexible terms and customized quotes for every order.

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

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    Ethyl Nitroacetate: A Manufacturer’s Perspective on Quality and Performance

    Decades in the Lab—Every Batch Tells a Story

    Bringing Ethyl Nitroacetate from raw material to refined product involves more than adherence to procedure—it calls for hands-on diligence at every step. Years in chemical synthesis have shown that true consistency begins in selection of starting materials. Our process relies on pharmaceutical-grade nitromethane and carefully specified ethyl chloroacetate. The differences may look insignificant at first, but subtle variations here can throw off purity, yield, or downstream usability.

    Scale-up from benchwork to branch-wide production often tests resolve and technique. We navigated early hurdles in solvent removal and temperature control—momentary lapses used to cloud our Ether-based workups with by-product. Rigorous in-process monitoring, exhaustive batch testing, and investment in improved glassware gradually lowered error rates and nuisance impurity peaks on the chromatogram. Today, every lot is transparently tracked from raw input to final assay, with multiple checkpoints set at each stage.

    What Sets Our Ethyl Nitroacetate Apart

    Quality is not just a stated specification—it is the sum of what you do every hour in production. We shoot for a minimum content of 99% Ethyl Nitroacetate by GC, buffering shifts in temperature, humidity, and batch size every single morning. Crystalline residue, discoloration, or odd odor signals us long before a certificate is stamped; these are telltale warnings that control parameters need review. By refusing to cut corners on crude material filtration, we keep batch homogeneity tight and avoid headaches in end-use reactions.

    Handling flammable nitro compounds takes experience. Over the years, we implemented strict anti-static protocols, slow-bleed addition rates, and double gassing for venting systems. No shortcut replaces an operator’s habit of “smelling the headspace,” or the routine pass of FTIR before any product goes into major storage. Our lab techs have identified trickling contamination sources like degraded hoses and traced fleeting “off-note” aromas to downstream water lines. Solutions came not from a manual, but from years of troubleshooting and open communication between shifts.

    Ethyl Nitroacetate: Model, Purity, and Character

    We distinguish lots by date-coded batch numbers and digital tracking, though more than a few samples still receive handwritten notes with quirks or observations. Purity of at least 99% GC sets our internal standard, but we’ve learned clarity and color are as critical as a number on a test sheet. Trace water under 0.2% by Karl-Fischer gives users predictable reactivity; excess water led to unexpected product splits in early seasons, costing us entire reactors of material. By drying and testing every liter, we avoid those repeats.

    We supply Ethyl Nitroacetate tailored for medicinal chemistry, advanced intermediates, and specialty synthesis. Our regular customers usually want reliability across multi-kilo batches, so consistency in melting point, color, and solubility go under tight scrutiny. We keep free acid content below trace levels through swift workup and neutralization, which prevents degradation during shipping and storage. Each bottle shows clear, nearly colorless liquid with a faint ester-pungent scent—any deviation, we’re first to notice.

    Differences From Every-Day Intermediates

    Some buyers unfamiliar with Ethyl Nitroacetate mistakenly lump it with simpler esters or nitro compounds. Its unique structure—both a nitro group and an ester group, joined to the same carbon—opens up reaction options no other intermediate offers. We often guide users who previously relied on methyl nitroacetate or chloroacetates: substitutions, alkylations, and Michael additions work differently here, with tighter selectivity and higher yields depending on conditions.

    Changing solvent percentages or reaction temperatures can give unexpected consequences. Years ago, a customer tried running an old methyl nitroacetate protocol—same base, same time, same scale—but ended up with incompletely converted product and emulsified side layers. The feedback spurred us to publish reaction notes, warning about altered rates and phase behaviors. Ethyl Nitroacetate’s balance of boiling point and partitioning lets it handle reactions with less volatility, often giving higher purity separations in organics. Subtle shifts in reactivity set it apart from commodity esters, especially when used for more demanding pharmaceutical or specialty syntheses.

    Everyday Challenges and Solutions in Synthesis

    Every vessel of Ethyl Nitroacetate brings with it tales of optimized procedures and the small crises you can only anticipate by experience. Some batches show misleading clarity but hide minute polymerization triggers—trace acid left over from an incomplete neutralization. Through direct titration of products, we learned to add extra steps for washout and phase separation. If storage tanks sit in high humidity, water slowly creeps in, dropping shelf life and risking hydrolysis. Early iterations relied on basic drum closures—now, stainless full-seal caps and nitrogen blankets hold integrity until the product reaches end-users.

    Solvent residues once threatened product performance, especially if blends of ethyl acetate or toluene were used in the process. After headspace GC validation picked up minuscule cross-contamination, we shifted to single-solvent protocols and run regular purges and equipment validation. Layers of controls seem tiresome, but seasoned operators know they forestall potentially thousands lost to reprocessing or downgraded batches.

    Usage in Modern Synthesis—What Chemists Demand

    Research clients now push for molecules that traditional splits and reductions fail to build efficiently. Ethyl Nitroacetate offers a path to beta-nitro esters, pharmaceutical scaffolds, and chiral building blocks others simply can’t match. Tuning nucleophile or electrophile ratios, or swapping aqueous bases for organics like DBU, transform this “simple” intermediate into a lever for creativity.

    Medicinal chemistry teams tell us direct alkylations and C–C bond-forming reactions work more predictably with our product. Recent customer runs on scale-up batches yielded key intermediates—no need for exotic purification steps, just straightforward filtration, concentration, and clean separation. We keep process notes from these successes close at hand, updating internal guides and informing further scale-ups.

    For those scaling up, our QA team provides on-site or remote troubleshooting. Some users encounter color drift, phase separation, or foam formation—our logs capture root causes and fixes, offering guidance for each tool and reactor difference. We’ve learned where a few minutes of high agitation, or minor delays in precipitation, will make or break yield and purity.

    Comparison with Related Nitro Esters

    Ethyl Nitroacetate delivers performance where others struggle. Some prefer methyl nitroacetate for higher volatility; it comes with handling and stability constraints. Methyl’s reactivity profile often pushes by-product rates higher, especially at elevated temperatures. Isopropyl nitroacetate lags in solubility and increases cost per kilo, as feedstocks are scarcer and purification more involved. Ethyl remains the reliable “sweet spot” for boiling point and working range.

    For nucleophilic substitutions, ethyl’s reactivity produces cleaner reaction streams, while branch-chain analogs need elaborate downstream separation. Benzyl nitroacetate, by contrast, can introduce aryl by-products or require high-pressure hydrogenation for reduction steps. Our product typically sees easier handling, predictable reaction rates, and greater compatibility with aqueous quench and organic purification systems. Customer feedback points to more reliable yields and happier downstream operations.

    Application Notes and Direct Insights From Our Own Floor

    No two reactors run exactly the same way. Over the years, our personnel documented quirks from multi-kilo to pilot production. Fast addition of base in batch nitroacetate syntheses caused sudden foaming and local overheating, costing a full lot. Experience led us to install jacketed cooling, slow titration, and staged additions based on exotherm readings. One-off “fixes” matured into SOPs handed down to every new operator.

    Product destined for high-sensitivity applications—such as peptide synthesis or nucleoside analogs—faces extra controls. We run exhaustive impurity screens, removing trace aldehyde, dioxane, or halide carryovers. Melting point and refractive index are recorded batch by batch; even small drift prompts a full re-test, often days before shipping. We do not accept “almost conforming” lots; troublesome ones are reprocessed or discarded for other use, not handed off with disclaimers.

    Customers working at low-temperature conditions or with sensitive nucleophiles rely on these consistent standards. After a few incidents of unexpected phase splitting, we overhauled separator maintenance, now logging tank empty/clean events. Technicians learned to spot the earliest color change or minor cloudiness as signals to halt lots before they travel farther into the supply chain.

    Supporting Sustainable and Responsible Operations

    Sustainable chemistry forms part of daily work. Ethyl Nitroacetate synthesis involves hazardous reagents and energy-intensive steps, but careful process design cuts waste. Early years saw us scrapping more solvent and venting useful fractions. By introducing closed-loop recoveries and on-site catalyst regeneration, we now reclaim a good portion of “waste” streams, returning solvents and minimizing environmental impact.

    Pressure to cut emissions and improve worker safety drove us to change both process and plant layout. Every operator receives HAZOP training, and every addition involves double-checks by a second shift member. Reactors are never left unmonitored; even at 3am, trained chemists oversee each stage. Emergency protocols are not just bureaucratic—they are lived, rehearsed, and embedded in habits from top floor to the loading dock.

    By sharing line data and “lessons learned,” other manufacturers gain insight into what works and what to avoid. Open exchange is how we closed gaps in risk, operator well-being, and emission control, advancing supply along a path that benefits everyone—from plant workers to end users handling finished products.

    Guidance For the Next Generation

    Younger chemists and processors joining the field soon learn that making Ethyl Nitroacetate is part science, part art. Lab notebooks brimming with data mean little if hands and eyes miss subtle warnings. Mastering the reaction’s character—knowing how even a 1°C shift at reflux, or a drop of extraneous water, can alter outcome—builds better product, safer teams, and repeatable results.

    We welcome direct communication with customers, vendors, and peers. Every note on reactivity, storage, or transportation teaches us something. Learning never stops—batch failures sting, but teach persistence; batch successes pay off in staff confidence, customer reliability, and the deep satisfaction that only a well-made product brings.

    True craftsmanship lies in consistent vigilance: testing, refining, and never assuming a job is “done when conforming.” By honing reliability in every lot of Ethyl Nitroacetate, we support the next wave of chemical innovation and forge partnerships that stretch far beyond a purchase order.