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1-(2-Methoxyphenyl)-2-Nitroethene

    • Product Name 1-(2-Methoxyphenyl)-2-Nitroethene
    • Alias 2-MeO-β-nitrostyrene
    • Einecs 629-089-4
    • 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

    718991

    Iupac Name 1-(2-Methoxyphenyl)-2-nitroethene
    Molecular Formula C9H9NO3
    Molecular Weight 179.17 g/mol
    Cas Number 32868-80-1
    Appearance Yellow solid
    Melting Point 57-59°C
    Solubility Soluble in organic solvents
    Smiles COC1=CC=CC=C1C=CN(=O)=O
    Inchi InChI=1S/C9H9NO3/c1-13-9-5-3-2-4-8(9)6-7-10(11)12/h2-7H,1H3
    Purity Typically >97%
    Storage Conditions Store at room temperature, dry and dark place

    As an accredited 1-(2-Methoxyphenyl)-2-Nitroethene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 1-(2-Methoxyphenyl)-2-Nitroethene, labeled with hazard symbols and product details.
    Shipping 1-(2-Methoxyphenyl)-2-nitroethene should be shipped in tightly sealed containers, protected from light and moisture. It must be handled according to chemical safety regulations, labeled as a hazardous substance. Transport should comply with local and international regulations, ensuring secure packaging to prevent leakage or accidental release during transit.
    Storage Store **1-(2-Methoxyphenyl)-2-nitroethene** in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing or reducing agents. Protect from direct sunlight, moisture, and heat. Properly label the container and ensure access is limited to trained personnel. Follow all relevant chemical storage regulations and safety guidelines.
    Application of 1-(2-Methoxyphenyl)-2-Nitroethene

    Applications of 1-(2-Methoxyphenyl)-2-Nitroethene in Industrial Manufacturing

    1-(2-Methoxyphenyl)-2-Nitroethene plays an established role as a functional intermediate in several specialized industrial and chemical manufacturing sectors. The following sections outline its core application scenarios, with each focused on real downstream use, integration points, and dedicated compliance standards for formulation and production.

    1. Advanced Organic Synthesis for Pharmaceutical Intermediates

    Pharmaceutical manufacturers use this material as a building block in the synthesis of APIs, especially within the production of certain nitrostyrene derivatives utilized in research and development of CNS-active compounds. Manufacturers introduce the raw material during early-stage condensation reactions, where its reactivity supports targeted downstream modifications. Its incorporation under strict GMP and pharmacopoeial standards ensures traceability and product quality for regulated drug development pipelines.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • U.S. Pharmacopeia (USP) specifications for intermediate purity
    • European Pharmacopeia (Ph. Eur.) substance monographs
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • Entry-level input: 0.8–1.2 molar equivalents based on target molecule design, adjusted for target batch scale and required conversion rates.

    Downstream process integration

    • Introduced during the initial Knoevenagel or Henry condensation reaction step in multi-step syntheses, under controlled solvent and temperature conditions to maximize selectivity for downstream functionalization.

    Final product types

    • Active pharmaceutical ingredient intermediates (API intermediates)
    • Targeted CNS research compounds
    • Custom-synthesized regulated substances for R&D

    2. Fine Chemical Synthesis and Material Science R&D

    In commercial laboratory and industrial R&D, this compound serves as a specialty nitrostyrene for custom synthesis of molecular targets and heterocyclic frameworks. It finds recurring use in the elaboration of novel compounds for organic electronics research and advanced materials, thanks to its reactivity profile and stability under diverse reaction protocols. Chemists select this input where specific nitro-aromatic functionalization is required for further molecule building.

    Industry compliance standards

    • Chemical Manufacturer’s Association (CMA) Responsible Care Management System
    • ISO 9001:2015 (Quality Management Systems)
    • REACH Registration for R&D use above 1 tonne/year
    • GLP guidelines for research chemicals

    Typical usage ratio

    • Variable: 0.5–2.0 parts by weight per reaction batch, calculated from desired final yield and downstream functionalization requirements for each research protocol.

    Downstream process integration

    • Added at the start of target molecule synthesis, typically in a nucleophilic addition or condensation reaction; also used as a precursor for ring-closing reactions to yield structurally complex research materials.

    Final product types

    • Molecular building blocks for organic electronics
    • Custom intermediates for polymer science projects
    • Specialty heterocycles for material testing

    3. Synthesis of Specialty Agrochemical Intermediates

    Chemical manufacturers in the agrochemical sector use this nitrostyrene derivative to construct core intermediates needed for select pre-emergent herbicide and plant growth regulator synthesis. It features in formulating advanced nitroaromatic scaffolds, which are crucial to the biological mode-of-action in regulated agricultural actives. Compliance with agrochemical quality and environmental standards is mandatory, and traceable sourcing data accompany all batches supplied for downstream use.

    Industry compliance standards

    • FAO/WHO Guidelines on Quality Control of Pesticides
    • ISO 17025 for analytical laboratory competence
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • REACH registration for use in chemical plant operations

    Typical usage ratio

    • Intermediate input level: 5–12% by total batch mass, dependent on the synthetic route and required conversion into final agrochemical precursors.

    Downstream process integration

    • Dosed during the α-alkylation or aromatic substitution step of chloronitrostyrene-based synthesis, integrated before catalytic reduction or further derivatization specific to each crop protection active.

    Final product types

    • Herbicide intermediate concentrates
    • Precursors for growth regulator formulations
    • Agrochemical R&D compounds

    4. Manufacture of Performance Dye and Pigment Intermediates

    Producers of high-performance dyes and organic pigments use this compound as a controlled intermediate for the synthesis of azo, nitro, and methoxy-functional colorants. The chemical structure provides an effective starting point for cyclization or reduction steps that yield final dye chromophores, especially where solubility and electronic effects from the methoxy group are required. Stakeholders prioritize compliance with classification and labeling regulations for dyes destined for textiles and plastics.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile safety)
    • GHS/CLP Regulation (EC) No 1272/2008 for pigment labeling
    • ISO 14001 (Environmental Management for chemical manufacturing)
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) recommendations

    Typical usage ratio

    • Feedstock addition: 2–6% by mass, calibrated by the chromophore yield target and specific dyeing or pigment application.

    Downstream process integration

    • Feeds into the Japp-Klingemann or reduction-acylation stage for advanced dye synthesis, where downstream aromatic coupling yields finished pigment molecules for colorant applications.

    Final product types

    • Performance azo dyes
    • Methoxy-functional organic pigments
    • Special effect colorants for plastic and textile sectors
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    Certification & Compliance
    More Introduction

    Introducing 1-(2-Methoxyphenyl)-2-Nitroethene: A Perspective from the Factory Floor

    The Character of a Specialized Intermediate

    Every batch of 1-(2-Methoxyphenyl)-2-Nitroethene we create starts with carefully sourced ortho-anisaldehyde, and this starting point tells the story of its importance. This compound plays a central role in advanced chemical synthesis, particularly where selective reactivity and reliability have no substitute. As a manufacturer, our hands are on every step—the work of our chemists and operators is evident in consistency, color, and purity each time this yellow crystalline solid leaves our plant.

    Purity, Grade, and the Difference Precision Makes

    We define success in this material not just by following a checklist, but by witnessing how researchers and production chemists rely on its profile to build complex molecules. High-purity 1-(2-Methoxyphenyl)-2-Nitroethene, with a melting range typically around 86-89 °C, supports organic transformations where even small impurities can ruin yield or introduce side products. The modest commercial supply of this nitroalkene has always centered on this question: will it enable the next step, or will the customer spend hours troubleshooting expensive reactions?

    Having seen the costs of impurity hands-on—a speck of unreacted aldehyde, a trace of non-aromatic byproducts—our team puts product purification at the heart of manufacturing. We crystallize, wash, and dry. Analytical teams confirm each lot’s spectral data by NMR and IR, ensuring the signature peaks appear where they must. TLC purity consistently approaches 98%+—and this precision leads to the kind of feedback from our customer partners that’s more than numbers: it’s peace of mind on the bench.

    Why 1-(2-Methoxyphenyl)-2-Nitroethene Matters in Real Processes

    Projects that call for 1-(2-Methoxyphenyl)-2-Nitroethene usually require more than a simple aromatic intermediate. The methoxy group on the ortho position and the nitroethylene function combine to deliver highly specific reactivity. Chemists choose this compound because the aryl nitroalkene core offers a controlled entry point for condensation, cyclization, and Michael addition reactions. In synthesis, its electron distribution can steer regioselectivity or help manage stepwise reactivity in building heterocycles or other custom targets.

    We’ve witnessed its use in boutique pharmaceutical development—often early-stage library work where hundreds of analogs get screened for activity. In dye chemistry and electronic materials, the methoxy-activated aryl system gives unique absorbance or conjugation features not found in unsubstituted or para-methoxy analogs. The nitro group brings a balance that’s needed for certain oxidative couplings or reduction-driven transformations.

    Comparing with Common Alternatives

    We see a lot of comparisons to simple β-nitrostyrenes, and some users think any nitro-alkene can fit. That changes fast when side-by-side testing shows the effect the ortho-methoxy group exerts during catalysis, hydrogenation, or condensation. Methyl substitution alone doesn’t deliver the same stabilization or product distribution. Even para-methoxy variants—sometimes more widely available—give noticeably different selectivity or reactivity due to steric hindrance and resonance. Our experience confirms that only the ortho placement, joined with the electron-donating methoxy, provides the reproducibility and the distinctive outcome targeted in fine chemical synthesis.

    Our decades in scale-up have also taught us where limits lie. For certain reactions, competitors selling looser, “lab grade” material ignore the headaches their lack of control brings. Traces of residual solvents, isomeric side-products, or incomplete crystallization create false yields and unexpected chromatography headaches. Our plant invests in repeated recrystallization and solvent-removal steps, taking longer but sidestepping these traps that stall scale progress farther down the line.

    On the Factory Floor: Making, Testing, and Shipping

    In the engine room of production, handling 1-(2-Methoxyphenyl)-2-Nitroethene takes respect and attention. Nitroalkenes require care during filtration and drying—a lesson learned from experience, not theory. Our granulation rigs keep dust levels down; vacuum trays prevent residual moisture that can affect long-term shelf stability. Packing in amber glass, with desiccants, we’re preventing photoisomerization and protecting functionality—a step no distributor sees before it hits their shelf.

    Logistics go hand in hand with manufacturing. Shipments to research users or pilot plants require batch traceability. We stamp every lot with analysis results, capture retention samples, and verify transport stability. Overseas customers see the end result of our process controls: a product that lands with consistent color, crystallinity, and performance.

    Trusted by Specialists Across Industries

    The end-users for 1-(2-Methoxyphenyl)-2-Nitroethene are rarely casual buyers. Research chemists in startups or multinational labs have shared that their real test comes in the reaction flask, not on a datasheet. We’ve learned from direct feedback—which reactions work, which fail due to overlooked contaminants, and which projects get derailed by switching suppliers partway through development.

    Regulatory expectations also play a part, especially as laboratory standards tighten and consumer goods traceability increases. We work proactively with documentation, batch records, and process monitoring—so that when customers need a Certificate of Analysis or confirmation by HPLC, it’s already in place. Our ability to answer these technical requests is anchored in the manufacturing records we build every day, not just the paperwork filled in at the end.

    Value Through Real Manufacturing, Not Resale

    Operating our own reactors, distillation, and crystallization means we aren’t at the mercy of third-party supply swings—not for quality, not for price. The hands-on approach brings its own challenges: plant downtime, equipment wear, bottlenecks during raw material shipment delays. But it also means we can optimize a reaction, reduce by-products, and manage environmentally responsible waste treatment, not just tick regulatory boxes.

    Having weathered demand fluctuations, raw material shortages, and regulatory shifts, we know that the only way to build trust in fine chemicals is through visible control over every step, right up to the final shipment. Those who source only from trading networks or resellers often cut corners unseen by the end user—a risk we neither take nor recommend.

    Handling, Safety, and Shelf Life

    Nitro-alkenes invite respect in handling procedures. We’ve developed our safety protocols by experience and through incident review: all product is handled in well-ventilated, static-protected work areas, and drums or bottles carry both hazard identification and batch tracking. Our shelf-life data, collected over years of shipments and retention sample checks, shows stable performance for up to two years in controlled storage (dry, cool, and dark), but we encourage end users to recheck batch performance when moving to GMP or scale-up.

    Continuous Improvement Based on Feedback

    No production run tells us as much as a customer’s experience. Over the years, chemists and process engineers have shared feedback that guides each improvement—requests for higher purity, different particle size, or alternate solvents for delivery. We respond with trial batches, not guesses, validating changes before full-moving to production scale.

    Our continuous investment in analytical capability helps as well. Routine GC-MS or HPLC doesn’t just check off a box; it lets us spot new impurity patterns, address root causes, and keep improving. We invite open and direct conversation with experienced chemists; their insights, from solubility quirks to crystallization tips, steer us toward more robust and useful lots.

    Environmental Perspective: What Matters in Practice

    Making nitroalkenes calls for close attention to environmental impact. Spent acids, solvents, and washes mean we manage both regulatory compliance and real-world risk. We’ve switched certain process solvents to greener alternatives, not simply to tick a marketing claim but to keep our own workforce safer and reduce the headaches of wastewater disposal. Solvent recovery systems, scrubbers, and closed-transfer lines are not optional—years of environmental audits have shown their value.

    Those who’ve operated reactors through solvent shortages or price spikes appreciate the benefits: lowering emissions, cutting operating costs, and keeping the local community happy. Our neighbors have the right to expect real effort. When authorities visit for inspection, they see documented improvements made not in response to a violation, but embedded in day-to-day operations.

    Beyond Commodity: Supporting Advanced Synthesis

    What turns 1-(2-Methoxyphenyl)-2-Nitroethene from a simple intermediate into a specialty product are its unique roles in research and development. Researchers aiming to build new bioactive molecules, or electronic materials with precisely tuned properties, demand more than a generic source of nitroalkene. Our effort lies not only in making it, but in listening to the ways customers use it.

    By tracking performance in challenging routes—multi-step sequences, late-stage functionalizations, combinatorial approaches—we learn which purity levels or free-flowing properties make a difference. Tinkering with particle size or delivery solvent might seem minor until measured against a chromatogram’s baseline, or the timeline of a discovery project working against patent deadlines. We’ve seen these pressures and adapted our production to match.

    Real Changes on the Line: Innovation Without Gimmicks

    Technical innovation on our site comes from real necessity. Early process routes to this product struggled with selectivity, leading to batches with mixed isomers and hard-to-purify residues. Our chemistry team invested in new reagents, altered mixing orders, and found parameters that speed up conversion without sacrificing yield. Incremental progress matters: switching to different crystallization temperatures, introducing tighter filtration steps, and adjusting pH control based on hands-on measurement, not just published protocol.

    We resist chasing fads or overpromising on “green” credentials we cannot prove. Instead, our progress rests on practical steps—recovering energy, optimizing reaction mass, and treating all process workers as crucial eyes in the system. Their vigilance for off-odors, color changes, or process fluctuations often spots issues automation misses.

    Loyalty Built on Consistent Performance

    Bulk or specialty, buyers return for predictable quality. Some of our long-term partners discovered us by troubleshooting their supply chain; others came when their former supplier let standards slip. We earn trust by delivering the same performance, batch after batch—never relying on clever branding or marketing.

    For synthetic teams under deadline, every day lost to re-purification is money and morale wasted. By focusing on reproducible output and reliable logistics, we help our partners spend their time where it really counts: advancing science, not working around supply failures. The feedback we value most comes not from awards, but from the quiet thank-you message after a successful, hassle-free scale-up.

    Looking Ahead: Supporting Modern Chemistry

    Research needs never stand still. Novel synthetic routes are appearing every year, many using nitroalkenes in new ways or at new scales. Our plant aims to keep pace—by scaling up production, refining analytical methods, and staying ready for custom requirements. Whether a researcher requires just a few grams, or a pilot line projects demand tens of kilos, our team adapts to technical needs on a real foundation.

    Protecting future supply means thinking several steps ahead. We work with reliable raw material partners, invest in spare production capacity, and maintain strong in-house training. This resilience helps our customers sleep at night; whatever changes may come in the research or production landscape, we’re one step removed from the nervous uncertainties of global commodity trading.

    Final Note: For Those Who Value the Real Work of Chemistry

    Every container that leaves our facility reflects more than an inventory count. Over decades, we’ve seen the craft, discipline, and care it takes to make 1-(2-Methoxyphenyl)-2-Nitroethene right and to keep pushing quality forward. Our perspective is grounded in experience—lessons learned from both success and error—and remains focused on supplying researchers and manufacturers who know what real quality means. The details matter, and we welcome those who care enough to insist on them.