Anhui Liwei Chemical Co., Limited
Products

4-[(E)-2-Nitroethenyl]Phenol


    • Product Name 4-[(E)-2-Nitroethenyl]Phenol
    • Alias 4-Hydroxy-β-nitrostyrene
    • Einecs 'EINECS 223-949-8'
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    769836

    Iupac Name 4-[(E)-2-Nitroethenyl]phenol
    Molecular Formula C8H7NO3
    Molar Mass 165.15 g/mol
    Cas Number 4448-61-3
    Appearance Yellow to orange solid
    Melting Point 137-139°C
    Solubility In Water Slightly soluble
    Boiling Point No data available (decomposes)
    Density No data available
    Pubchem Cid 2724108
    Smiles C1=CC(=CC=C1C=CC([N+](=O)[O-])=O)O
    Inchi InChI=1S/C8H7NO3/c10-8-4-2-7(3-5-8)1-6-9(11)12/h1-6,10H/b6-1+
    Synonyms 4-Hydroxy-β-nitrostyrene; 4-Hydroxy-2-nitrostyrene
    Refractive Index No data available
    Pka No data available

    As an accredited 4-[(E)-2-Nitroethenyl]Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "4-[(E)-2-Nitroethenyl]Phenol," 25g, hazard and handling icons, tamper-evident seal, chemical supplier branding.
    Shipping 4-[(E)-2-Nitroethenyl]Phenol is shipped in tightly sealed containers to prevent moisture and light exposure. It is classified as a hazardous material and must comply with relevant transportation regulations. Proper labeling, documentation, and use of compatible packing materials are required to ensure safe transit and prevent leaks or contamination.
    Storage 4-[(E)-2-Nitroethenyl]phenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and bases. Ensure proper labeling and avoid exposure to moisture. Store under conditions that minimize the risk of decomposition or dangerous reactions. Use appropriate personal protective equipment when handling.
    Free Quote

    Competitive 4-[(E)-2-Nitroethenyl]Phenol prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615380400285 or mail to sales2@liwei-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615380400285

    Email: sales2@liwei-chem.com

    Get Free Quote of Anhui Liwei Chemical Co., Limited

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

    Certification & Compliance
    More Introduction

    4-[(E)-2-Nitroethenyl]Phenol: Focused Solutions from Direct Manufacturing

    Authentic Quality, Practical Value

    Years at the core of chemical synthesis have taught us clarity: chemists want honest molecules, reliable performance, and no surprises. 4-[(E)-2-Nitroethenyl]phenol is one of those key intermediates that keeps surfacing in advanced laboratories as well as production lines. Our batches follow single-lot synthesis under tightly regulated conditions, based on well-documented industrial standards. Every lot leaves our floor with full assay documentation by HPLC and NMR, so users don’t have to second-guess the quality or source.

    We work with material at genuine commercial scale, not just pilot manufacturing or kilo-labs. This difference isn’t about marketing: it impacts every customer who cares about repeatable outcomes in multi-step syntheses or scale-up projects. Our specification for 4-[(E)-2-Nitroethenyl]phenol includes limits on isomeric impurities well below the typical literature margin. Residual solvents get held to the lowest ppm range, and the melting range stays consistent batch to batch. Even after years of large-volume shipping, we keep to a strict moisture limit, essential for customers planning Grignard or reductive coupling transformations.

    Every industry can boast about "high purity," but direct experience tells us that downstream reactions respond to the real-world impurity profile—not numbers on a generic certificate. Our 4-[(E)-2-Nitroethenyl]phenol supports transformations that depend on the nitroalkene’s E-geometry, especially for researchers driving conjugation or cross-coupling without endless byproduct issues. Anyone who has run a Michael addition or a vinylogous substitution with a poorly defined nitrostyrene knows the hours lost to purification—so we keep control over the stereochemistry and provide impurity specifics for each dispatch, not just generic data sheets.

    Why Use 4-[(E)-2-Nitroethenyl]Phenol?

    Synthetic chemists recognize 4-[(E)-2-Nitroethenyl]phenol as a true workhorse in the lab. The combination of a nitrovinyl moiety and a phenolic group shapes selectivity and reactivity in a way that’s hard to replace. Customers commonly target heterocycle construction or the development of tailored intermediates for pharmaceuticals and advanced agrochemicals, and many rely on the vinyl nitro motif as a flexible handle for further transformations. For aromatic substitution or fine-tuned functionalization, the para-phenolic group brings enhanced reactivity—something model compounds can’t always predict until tested at bench scale.

    From the manufacturing angle, we’ve watched smaller players struggle to keep both the E-stereochemistry and phenolic hydroxyl group intact during workup and storage. Our process skips excess thermal input and tightens up pH controls on workup to avoid forming dimers or tars. In forty-kilogram glass-lined reactors, this translates into fewer headaches on receipt for R&D teams who don’t want variability. The feedback from our customers—often researchers or scale-up managers—drives our focus here: batch reproducibility, low trace metal content, and genuine E/N isomer control define the daily grind that gets real projects to completion.

    In terms of safety and storage, we disable the most common failure: product decomposition from ambient light or above-ambient humidity. We use nitrogen-purged, dark amber bottles or lined drums for all primary packaging. This move protects the sensitive nitroalkene double bond, extending the material’s shelf stability several months longer compared to clear-glass equivalents. No matter whether a client is purchasing for a major synthesis campaign or a proof-of-concept experiment, they get material that performs as expected, with straightforward handling and minimal extra precautions beyond standard nitro-aromatic practice.

    Differences That Matter in Practice

    Across several decades synthesizing advanced nitro compounds, we have witnessed subtle material differences play out across full reaction cascades. Some competitors target only the bulk commodity tier: broader specs, less rigorous impurity controls, and essentially an "off the shelf" mindset. Our method was shaped by firsthand experience helping clients salt out low-yielding intermediates, strip away stray solvents, or hunt down sources of batch failure. With 4-[(E)-2-Nitroethenyl]phenol, the highest value sits not only in the main assay number but in the way minor impurities are handled. Residual aldehydes, typically overlooked, have hampered clean condensation reactions at more than one customer site. Our team routinely tracks aldehydic byproducts down to low ppm, reflecting real-world needs, not margin-driven shortcuts.

    Almost no two projects use this intermediate in the same way, and our feedback loop with customers confirms that. Recent runs aimed at complex oxazole synthesis required matched melting ranges and careful control of residual phenol, while another campaign—targeting intermediates for novel crop protection—called attention to the need for minimal trace acids and photostable packaging. Each application made us re-examine practical details, not abstract promises.

    It’s easy for traders or resellers to import this compound by the drum and slap on a fresh label, but their "maximum purity" claims rarely translate to predictable performance in specialized chemistry. Direct manufacturing creates opportunities to pre-test each lot for its practical fit in coupling reactions, Michael additions, or further arylation steps. We routinely run small pilot transformations on-site to screen for unexpected byproducts or reactivity shifts; the result is tighter feedback between bench and plant, so each batch outperforms run-of-the-mill commodity stock.

    Our post-reaction quenching stage has eliminated trace metallic residues—well below industry averages and tighter than USP dictates for related nitrobenzenes. This difference ripples through to those developing APIs or high-purity coatings, where even minor drag from metallic contaminants can trigger downstream regulatory flags. We engage with analytical teams to adjust our filtration specs and review our GC/MS run data for patterns over multiple lots, pushing past just automated certificate outputs. Workers in scale-up know that these small improvements change project timelines.

    Applications: From Fine Chemicals to Advanced Synthesis

    By design, 4-[(E)-2-Nitroethenyl]phenol fits a wide suite of advanced applications, especially where selectivity matters more than brute force quantity. In academic and industrial labs, this compound often underpins the construction of bioactive scaffolds, linkable cores for molecular probes, and starting points for combinatorial libraries. Our customers drive much of the innovation—pharma teams screen new analogs built around the phenolic nitroalkene, while materials scientists push for more resilient, cross-linkable aromatic intermediates.

    We support teams exploring the mechanistic chemistry of nitroalkene conjugate additions, as well as those implementing newer catalytic couplings. Small changes in the impurity or isomer profile can steer entire outcomes, so our batches aim to keep refreshingly simple analytics and documentation. These factors speed up preliminary structure-activity relationship (SAR) studies and help customers avoid wasted time de-tangling unexpected TLC spots or project delays tied to non-reproducible starting materials.

    Each year we see more demand from labs synthesizing frameworks for specialty dyes, semiconductors, or optoelectronic materials. Here, even sub-percent levels of common phenolic byproducts or tars can disrupt film formation or colorfastness. We work directly with formulators to adapt our isolation methods, moving beyond standard protocols that treat purity as a simple pass/fail. The history of each batch tells a story of small adjustments, documentable results, and practical lessons learned from the lab bench—not just theoretical best practices.

    One Compound, Many Journeys: Customization in Practice

    With years of direct manufacturing and feedback from global R&D, we understand that standard one-size-fits-all production doesn't quite cut it for 4-[(E)-2-Nitroethenyl]phenol. Real projects ask for real flexibility. For example, a customer scaling up a new anti-infective route needed lower sodium content to sidestep byproduct formation in a subsequent oxidation; another requested ultra-low peroxide readings for planned photochemistry. We support these by customizing phase separation, filtration, and packaging—bearing in mind both the molecular structure and user workflow.

    Experience suggests "custom synthesis" doesn’t work if plant schedules slip or if QA becomes a bottleneck. That’s why our technical and operations teams keep open communication. Engineers, operators, and quality experts collaborate before the first kilogram leaves the facility, checking both the crude reaction and the isolated product for all off-spec signals. In past projects where a specific impurity or scale-up challenge emerged late, we adapted the manufacturing route—sometimes slowing down, sometimes changing solvent ratios—rather than shipping compromised product.

    Global logistics remain a continuing concern, especially when handling sensitive or high-value batches. We use chemical-resistant liners, triple-sealed containers, and lot-level tracking to deliver product tight against temperature or humidity swings. At bulk scale, we adapt documentation to each receiving site’s needs—not just a language translation but practical batch notes and observations, so the lessons from our plant floor carry through to the teams using the material on the other end.

    Proven Partnerships: Working Through the Hurdles

    The manufacturing history of 4-[(E)-2-Nitroethenyl]phenol is littered with learning moments. Early on, we misjudged the risks of trace formaldehyde buildup from aldehyde scavenging steps; only after a handful of returns—and a few sleepless nights—did we adapt purification to virtually eliminate this risk. Now, we include GC traces on known aldehydes, abundantly shared with customers who care about downstream toxicity or odor profile.

    On another occasion, a customer flagged issues with orange discoloration during long-term storage. Our engineering team narrowed this down to photolysis of the nitroalkene double bond, so now we standardize all post-quench handling under red-light workspaces and dark storage, and instruct warehouse teams to ship exclusively in controlled-light transports. These hard-won lessons shape everything from our batch record-keeping to our packaging choices.

    Direct engagement with end-users sharpens our edge. During one collaborative campaign for a research hospital, a need arose for extended-release drug intermediate work. Through direct QC-to-QA feedback, we were able to tweak both crystallization temperature and buffering agents in the last isolation step. This hands-on approach often leads to further process improvements, helping both us and the client hit tighter impurity and moisture numbers. Partnerships like these build resilience in the supply chain when projects pivot or regulatory needs shift fast.

    Regulatory Readiness, Documentation, and Traceability

    As regulatory requirements keep tightening across pharmaceutical and specialty chemical sectors, we took proactive steps to align both our documentation and purification routes with customer needs. Our 4-[(E)-2-Nitroethenyl]phenol leaves the plant with a full batch record, traceable analytical runs, impurity profile printouts, and real QA signoff. This isn’t just a paperwork exercise—it streamlines customer audits, shortens qualification timeframes, and removes the hand-waving common in third-party distribution chains.

    Regulatory teams can access actual batch samples and full analytical packages. Chromatograms and NMR data are available for review, supporting customers facing tightening raw material declarations or new compliance barriers. By managing the synthetic route and isolation ourselves, we head off the most common causes of regulatory headaches: mystery peaks, incomplete impurity tracking, or incomplete history of reprocessing. Our team responds daily to requests for supplementary documentation or advice on international compliance quirks, adding genuine value beyond the product barcode.

    Continuous Improvement: The Heart of Real Production

    We didn’t reach our current standards by clinging to a fixed SOP. Years of feedback, customer complaints, and internal troubleshooting shaped the production route for this phenolic nitroalkene. Close listening to teams running scale-ups or screening for new drug leads prompted us to re-examine everything—chilling lines, solvent charge rates, workflows, and even drying temperatures. Every process tweak aims at cheaper, cleaner, or faster output without losing the control that makes complex syntheses successful.

    New automation in in-line monitoring keeps each reactor’s profile traceable in real time, so hazard points or out-of-spec signals get caught before they reach the isolation step. Our older processes relied on post-reaction sampling or crude batch pooling, but over the last five years we’ve implemented digital tracking and in situ reading to catch early trends, like accumulation of micro-impurities across long runs. Meeting the needs of customers in highly regulated sectors raised the bar, and we keep pace with ongoing reviews and training.

    Open feedback always makes us sharper. Sometimes it leads us to lower waste or environmental impact on the back end, sometimes it just drives incremental purity gains that pass right on to the next order. Direct manufacturing keeps knowledge—and responsibility—inside our own doors, not spread across half a dozen subcontractors. Those investing their careers in complex chemistry deserve tools that reflect the same commitment.

    What Real-World Manufacturing Means for You

    In a landscape crowded with resellers, redistributors, and brokers, direct-from-manufacturer 4-[(E)-2-Nitroethenyl]phenol brings clarity. Experienced chemists recognize the value in real material consistency, batch traceability, and honest process descriptions. Our approach to this molecule sets us apart not through empty technical jargon or overloaded datasheets, but in the working details that matter: reproducibility, impurity control, packaging engineered for sensitivity, and a feedback-driven history of real-world improvement.

    Every specification isn’t just a number, but a promise rooted in decades of hands-on experience, tested by both success and mistakes. For those who rely on 4-[(E)-2-Nitroethenyl]phenol—whether pursuing further functionalization, heterocycle formation, pharmaceutical intermediates, or advanced materials—our manufacturing focus translates to less wasted time, more predictable results, and a direct relationship between the person who makes the molecule and the person who transforms it.