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Methyl Nitroacetate

    • Product Name Methyl Nitroacetate
    • Alias Nitroacetic acid methyl ester
    • Einecs 221-122-8
    • 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

    185379

    Cas Number 16910-54-6
    Molecular Formula C3H5NO4
    Molecular Weight 119.08
    Appearance Colorless to pale yellow liquid
    Boiling Point 214-215°C
    Melting Point -3°C
    Density 1.394 g/cm3 at 20°C
    Refractive Index 1.444
    Solubility In Water Slightly soluble
    Flash Point 86°C
    Purity Typically ≥98%
    Synonyms Nitroacetic acid methyl ester
    Ec Number 241-090-6

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

    Packing & Storage
    Packing Amber glass bottle, 100 grams, sealed with a screw cap, hazard labels for toxicity and flammability, detailed chemical information provided.
    Shipping Methyl Nitroacetate should be shipped as a hazardous material, classified under UN 2608. It must be securely packed in tightly sealed containers, labeled with appropriate hazard warnings, and protected from heat, moisture, and shock. Follow all relevant regulations (such as IMDG, IATA, and DOT) for transport of toxic and explosive substances.
    Storage Methyl nitroacetate should be stored in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Keep it in tightly sealed containers, protected from direct sunlight and incompatible substances such as strong acids, bases, and reducing agents. Use non-sparking tools during handling, and ensure proper labeling. Store separately from food and oxidizing materials for safety.
    Application of Methyl Nitroacetate

    Applications of Methyl Nitroacetate in Industrial Manufacturing

    Methyl Nitroacetate serves as a critical intermediate in multiple downstream industrial sectors. As a direct manufacturer, we supply material manufactured under strict quality systems to meet precise performance standards in each specialized application. Our product supports efficient synthesis and integration into regulated production workflows across advanced chemical manufacturing domains.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ this material as a building block in heterocyclic and active pharmaceutical ingredient (API) synthesis, especially for anticonvulsants, antibacterial agents, and cardiovascular drugs. It undergoes nucleophilic substitution or condensation in multi-step processes to generate intermediates such as nitroacetophenones and aminonitriles, forming the basis for further transformations in regulated drug manufacturing. Selection of grade and purity aligns strictly with the project’s ICH and pharmacopeial requirements, and process adjustments comply with cGMP constraints at every stage from reaction to purification.

    Industry compliance standards

    • cGMP (Current Good Manufacturing Practices, ICH Q7)
    • USP® and EP pharmacopeial standards (where applicable for downstream APIs)
    • ICH Q3A/B guidelines (Impurity and Residual Solvent Control)

    Typical usage ratio

    • 5 – 25 mol% relative to main substrate, adjusted based on required reaction yield and impurity profile for targeted synthesis route; further purity optimization driven by downstream regulatory synthesis demands

    Downstream process integration

    • Incorporated in stepwise condensation or alkylation during intermediate formation for multi-stage API production; typically charged at the initial reaction or re-dosed by process control based on HPLC monitoring

    Final product types

    • Pharmaceutical intermediates for active ingredients (e.g., nitro compounds, amino acids, substituted phenyl derivatives)
    • Final APIs after subsequent transformations

    2. Agrochemical Active Ingredient Manufacturing

    Crop protection chemistry producers use this compound during the synthesis of pyridine and pyrazole derivatives, as well as specialty herbicide precursors. It acts as a carbon-nitrogen skeleton source during Mannich-type reactions, which are common in the construction of agrochemical leads that must meet pesticide registration standards. Strict batch traceability and compliance with restriction of hazardous substances rules ensure suitability for field crop protection markets.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specifications
    • ISO 9001:2015 Quality Management for agrochemical intermediates
    • REACH Regulation (EC) No 1907/2006 for chemical safety in the EU

    Typical usage ratio

    • 10 – 40% w/w in reactive step, typically as a limiting or excess reagent depending on desired blocking efficiency and downstream functional group tolerance

    Downstream process integration

    • Added during the initial formation of nitroalkyl or nitroaromatic crotonates prior to cyclization and chlorination; monitored by LC-MS to ensure compound integrity for regulatory filings

    Final product types

    • Pre-cursors for selective herbicides (e.g., nitro-triazines, substituted pyrazoles)
    • Intermediates for insecticide and fungicide synthesis

    3. Fine Chemicals and Dyes Manufacturing

    Specialty fine chemical and dye plants require this raw material for high-value pigment synthesis and advanced fluorescent dye intermediates. It provides uniquely functionalized nitroalkyl moieties that enable color tuning and photophysical optimization during the downstream dye condensation and coupling processes. Manufacturing batches require thorough quality documentation and compliance with colorant composition limits according to industrial and consumer goods legislation.

    Industry compliance standards

    • EN 71-3:2019 (Safety of Toys – migration of certain elements, for finished goods)
    • ISO 9001 Quality Management in colorant production
    • Global Textile Standard (GOTS) for dye intermediates when used in textile applications

    Typical usage ratio

    • 15 – 50 mol% in pigment condensation reactions, adjusted for target color intensity and solubility profile required by downstream customers

    Downstream process integration

    • Introduced in the primary colorant precursor formulation or by timed addition into azo-coupling reactions under controlled temperature and pH

    Final product types

    • Nitroaromatic and nitroalkyl based dyes for plastics, textile fibers, and printing inks
    • Photoluminescent and UV-fluorescent fine chemicals

    4. Custom Synthesis for Advanced Materials

    Contract manufacturing organizations and advanced materials labs implement this intermediate in the tailored fabrication of specialty monomers and research-grade polymers, especially in high-performance coatings and functionalized resins. Control over precursor ratios and batch-specific QC enables application in custom synthesis routes where precision substitution and high product purity are mandatory for electronic and performance-critical materials.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management
    • RoHS Directive 2011/65/EU compliance as required in electronics
    • Material Safety Data Sheet (MSDS) documentation for REACH and downstream user communication

    Typical usage ratio

    • 5 – 35 wt% of total monomer or precursor blend, set according to polymer chain design and functional group targeting; adjusted following in-process GC-MS feedback

    Downstream process integration

    • Fed as a primary coreactant in batch or continuous-flow syntheses, typically at monomer charging or initial coupling stage for resin backbone modification

    Final product types

    • Specialty monomers for electronics-grade polymers
    • Chemically-resistant surface coatings and advanced functional resins
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    Certification & Compliance
    More Introduction

    Methyl Nitroacetate: Harnessing Precision in Advanced Chemical Processes

    Our Story With Methyl Nitroacetate

    At our facility, the production of Methyl Nitroacetate represents years of tailored chemical design and practical, problem-solving effort. Several decades ago, few could have imagined that a targeted nitro ester like this one would steadily become a key building block across increasingly complex organic transformations. Over the years we’ve shifted from small-batch synthesis, used mainly in research circles, to highly reproducible, industrial-scale batches that maintain analytic purity batch after batch.

    Many manufacturers encounter challenges in controlling purity, yield, and reproducibility with Methyl Nitroacetate. Handling an active nitro ester can demand extra attention and fine-tuned process control. By investing in better reactor systems and in-line monitoring, we've increased our consistency and reduced the risk of unwanted side products. Such improvements matter because trace byproducts complicate downstream synthesis and waste valuable resources—something anyone in organic synthesis knows slows progress on tight research timetables.

    Product Identity and Specifications

    We prepare Methyl Nitroacetate to strict in-house standards, exceeding 98% HPLC purity. Our batches offer reliable melting points and a defined, clear pale yellow liquid appearance. Reactivity-driven users rely on knowing moisture and residual acid levels are low, so we’ve fine-tuned our purification to keep water content below half a percent and free acid below specified minimums, as verified by regular in-lab titration.

    Each shipment draws from the same controlled reactor runs, using carefully qualified input materials. Small adjustments in the synthesis routine or temperature can swing the ultimate color and odor profile—sometimes subtle changes, but a sure indicator for keen chemists detecting batch-to-batch differences. Our goal centers on producing a reagent that feels the same to every receiving lab or production site, year after year.

    Applications: Real-World Needs and Experiences

    Most buyers of Methyl Nitroacetate push its boundaries in pharmaceutical R&D, especially contract research operations that face broad portfolios of new molecules. We see its usefulness wherever selective nitroalkylation or Michael additions drive synthesis, particularly for compounds requiring clean ester or carboxyl moieties downstream. Examples in our own collaborations have involved β-nitro acids, masked intermediates for anti-infectives, and intermediates in plant protection agents. Sometimes a purchaser will ask for extra drying or slightly adjusted assay requirements—we have incorporated these lessons over the years by constantly revisiting our batch records and test data.

    Its appeal often lies in the way Methyl Nitroacetate allows for controlled carbon–carbon bond formation under milder conditions than classic nitroacetate salts, with less risk of over-alkylation. In one customer’s multi-ton synthesis of a heterocyclic drug candidate, a competitor’s batch introduced undefined side products during a condensation step. After switching to our tighter purity profile, their batch yields increased by nearly ten percent and they cut back extensive re-purification. Such stories motivate us to maintain standards that go beyond what’s typically listed on a commercial data sheet.

    Distinctions From Other Materials

    Every chemist knows that not all nitroacetate esters behave the same. Methyl Nitroacetate often replaces ethyl or t-butyl analogs, mainly because methyl offers lower steric hindrance and a more predictable reactivity profile in nucleophilic substitutions. Compared to the ethyl derivative, the methyl ester cleaves more efficiently in base hydrolysis, helping researchers avoid lingering alkyl fragments that can complicate further transformations or analytic purification.

    During early optimization, many experimenters favor methyl esters for their workhorse properties: ease of formation, manageable volatility during scale-up, and reliable conversion to either acids or derivatives under standard laboratory conditions. Our technical staff fields regular questions from scientists struggling with low-yielding condensations involving bulkier esters or other nitro acid analogues. In one project involving the preparation of custom chiral ligands, a university partner found the reactivity of Methyl Nitroacetate transformed their yield from “barely measurable” to sustainable kilo-scale output. For us, the clear difference always comes from integrating direct feedback and sharing these lessons with both novice and seasoned users.

    The Importance of Raw Material Sourcing

    Securing consistent precursors forms the backbone of reliable Methyl Nitroacetate output. Over time, we’ve built longstanding relationships with raw material suppliers, preferring audited partners and well-documented shipping records. During the high-demand periods following global supply constraints, some vendors struggled to maintain input chemical quality; low-grade nitromethane, for example, can introduce persistent impurity tails that shadow through final product analytics. Based on our own setbacks, we engineered additional intake testing—spot GC checks and frequent supplier audits—to ensure only consistent bulk input reaches our reactor line.

    Our day-to-day work highlights how upstream inconsistencies ripple through to product quality. Some years ago, a minor switch from one supplier’s methylating agent nearly undermined a six-month customer trial, because of subtle contaminant profiles that only showed up under advanced NMR analysis. After quick corrective action, our site team updated qualification protocols so no similar oversight derails future projects. Institutional memory remains critical to avoid repeating known mistakes, and our team maintains a running docket of case studies for regular staff training.

    Handling, Safety, and Environmental Responsible Production

    Methyl Nitroacetate’s nitro group requires respect in storage and transport. We have seen instances—fortunately not at our site—where insufficient venting or reactive incompatibility caused dangerous over-pressures or emission of nitro fumes. Training and equipment, not laminated instructions, determine practical safety outcomes. Keeping stocks cool, dry, and separated from energetic reducing agents or bases forms the core of our day-to-day handling routine.

    On the environmental front, modern chemistry demands accountability. Unlike some larger-volume commodity chemicals, Methyl Nitroacetate seldom appears in unrestricted trade. Our process includes scrubbers and closed transfer systems to minimize any off-gassing, and we recover spent process streams to cut down hazardous waste output. During routine audits, we point to our solvent recycling and closed-loop operations as industry best practices—important, since authorities and nearby communities increasingly monitor even trace atmospheric emissions or hazardous byproducts. By facing these operational realities daily, we build trust with both regulators and our customers.

    Supporting Users Beyond the Bench

    Delivery and batch support stretch far past simple shipping. Our staff spends time on technical calls, working through questions that range from kinetic profiles in new syntheses to shelf-life performance under variable storage. No two facilities handle materials exactly the same way, and we have learned to adjust our fill formats—smaller drums, freeze-sealed ampoules, custom labeling—based on candid feedback and field experience rather than prescriptive “best practices.”

    Several recurring problems crop up in customer workflows. Methyl Nitroacetate occasionally hydrolyzes faster than planned during extended exposure in damp labs or on aging bench stock. To tackle this, we have equipped users with tips for cold-chain storage and on-site stabilization, plus extra analytical checks for early-shelf samples. Many novice chemists see early signs of color change or residue build-up—an artifact of moisture pick-up or prolonged UV exposure. Our customer team shares simple troubleshooting steps that stem from decades of working with this molecule, not just theory.

    Regulatory and Compliance Considerations

    Methyl Nitroacetate's regulated status varies between jurisdictions. We closely track evolving regional requirements in Europe, Asia, and North America. Transport and bulk storage often demand extra paperwork, manifest declarations, and dedicated labeling. At our plant, digital records and integrated safety systems help guarantee that all shipments match both regulatory and end-user compliance lists. Site audits focus not just on documentation but on real working procedures—periodically retraining staff and updating routines as rules shift.

    Recently, several industry groups flagged emerging restrictions on nitro compounds, particularly those with explosive or environmental risk profiles. Our product doesn’t fall under most restricted lists due to its low bulk trade volume, but we monitor legislative changes and maintain open dialogue with both authorities and downstream partners. Several of our major customers, especially in pharmaceuticals, rely on documented chain-of-custody to field regulatory inspections and guarantee fully traceable, auditable synthesis lines. By building these checkpoints into our supply chain, we insulate both ourselves and our customers from sudden regulatory shifts.

    Reliability and Continuous Improvement

    The long-haul of chemical manufacturing constantly tests the boundaries between cost, speed, and quality. We regularly review both in-process yields and final product analytics, benchmarking against leading industry competitors. Out-of-spec batches get immediate cross-team review, and we rely on a combination of analytical fingerprinting and staff team memory to diagnose recurring issues. This hands-on cycle—troubleshooting, root cause analysis, adjustments in purification—refines each synthesis run and trickles into better product for every subsequent batch.

    External feedback, especially from customers running pilot or scale-up studies, directly drives our improvement. Often, performance gaps expose cracks in expected procedure: a longer-than-planned drying cycle or slight shifts in retention times on liquid chromatography. These small but critical observations, shared between bench chemists and plant staff, bring adjustments that circuitry between supplier and user rarely matches. Our own site has seen several process modifications stemming from direct user insight—switching glassware coatings to avoid catalytic decomposition, or tightening up exclusion of light during transfer stages.

    Troubleshooting Process Bottlenecks

    Even with optimal process design, real-world trouble sometimes finds its way into production. One memorable case involved an unexplained color shift in a scheduled reactor run—turning a batch deep orange instead of the expected pale yellow. Early checks showed no change in input materials, and preliminary GC ran clean. Joint troubleshooting uncovered a slow leaching of trace iron from a valve, catalyzing slow decomposition of the product over several hours. Backtracking from the batch records, we swapped material for all transfer lines, solved the problem, and updated our site SOPs to require non-metallic gaskets above certain critical points. These moments underline the need for continuous vigilance, and forensic-level detail at every step.

    Our site workflow leans on early detection and continuous process analytics. Online IR measurements, spot checks using UV-Vis scans, and tight control of reactor temperature slopes help avoid the worst-case loss of an entire batch for preventable reasons. When small process drifts show up—like gradual pH movement in the wash phase or incomplete removal of trace starting material—our lab team steps in fast. That speed and focus results not only from equipment investment, but from a culture of daily improvement and knowledge sharing among technical staff. By maintaining this environment, our users benefit from an uninterrupted supply of quality product.

    Collaboration and Long-Term Commitment

    Each year, we see deeper partnerships with both established pharma customers and emerging specialty research venues. Often, Methyl Nitroacetate starts as a simple catalog order, quickly evolving into a recurring, feedback-rich collaboration. Our technical team hosts regular update meetings with R&D specialists at customer sites, sharing both process updates and any lessons learned from batch experience. Instead of a transactional mindset, we see every contract as an ongoing opportunity to build mutual understanding and technical trust.

    Over the years, certain projects have required custom approaches—like changing solvent systems to minimize cross-contamination risk for a regulated synthesis, or pre-loading specific analytical data with shipments bound for regulatory filings. By remaining open to dialogue, we strengthen both the reliability of our product and the trust customers place in our team’s skill and openness. As both a producer and a working partner, we welcome challenges our users bring us, and in return, share the endless details that can make or break a demanding synthesis run.

    Looking Forward

    Methyl Nitroacetate’s role in advanced chemistry looks sure to evolve further. The molecule’s core strengths—proven reactivity, well-known handling parameters, and compatibility with downstream processing—make it a go-to starting point for R&D and targeted manufacturing. As the field grows more sophisticated and regulations increase, our commitment to collaboration and responsible science only deepens. By continuously refining our synthesis, integrating feedback, and investing in both facilities and people, we support builders and innovators in tomorrow’s chemical landscape.