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3,4-Dimethoxy-B-Nitrostyrene

    • Product Name 3,4-Dimethoxy-B-Nitrostyrene
    • Alias DMBNS
    • Einecs 221-729-8
    • 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
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    Specifications

    HS Code

    572719

    Chemical Name 3,4-Dimethoxy-B-Nitrostyrene
    Molecular Formula C10H11NO4
    Molecular Weight 209.20 g/mol
    Appearance Yellow crystalline solid
    Melting Point 96-99 °C
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Cas Number 22928-18-3
    Structure B-nitrostyrene core with methoxy groups at the 3 and 4 positions of the benzene ring
    Smiles COC1=CC(=C(C=C1OC)C=C[N+](=O)[O-])

    As an accredited 3,4-Dimethoxy-B-Nitrostyrene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 10 grams of 3,4-Dimethoxy-B-Nitrostyrene, sealed in an amber glass vial with a tamper-evident cap.
    Shipping 3,4-Dimethoxy-B-Nitrostyrene is shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. The packaging complies with regulations for hazardous materials, protecting the chemical from light, heat, and moisture during transit. Proper labeling ensures safe handling, and shipping is typically via ground or air freight with appropriate documentation.
    Storage 3,4-Dimethoxy-β-nitrostyrene should be stored in a tightly sealed container, away from direct sunlight, heat sources, and incompatible materials such as strong acids, bases, and oxidizing agents. Store in a cool, dry, well-ventilated area, ideally at room temperature or lower. Proper labeling and secure storage are essential to prevent accidental exposure or contamination.
    Application of 3,4-Dimethoxy-B-Nitrostyrene

    Applications of 3,4-Dimethoxy-B-Nitrostyrene in Industrial Manufacturing

    3,4-Dimethoxy-B-Nitrostyrene serves as a key intermediate in specialized fine chemical and pharmaceutical synthesis. Its well-defined reactivity and functional group compatibility make it essential for downstream transformations in high-value manufacturing environments. Below, we detail its precise applications in recognized industrial contexts with a focus on regulatory adherence, processing parameters, integration steps, and finished product outcomes.

    1. Pharmaceutical Intermediates for CNS-Active Compound Synthesis

    This intermediate contributes to targeted steps in the synthesis of CNS-active molecules, especially phenethylamine and tryptamine derivatives. The nitrostyrene moiety undergoes further reduction or substitution, and the dimethoxy pattern allows for structural elaboration in medicinal chemistry programs. Production lines following cGMP protocols rely on this compound for its reliable core structure to introduce pharmacophores with consistent purity standards required for regulatory submission batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia General Monograph 2034
    • USP General Chapter <797> for preparation of sterile drug products

    Typical usage ratio

    • Applied at 0.1–0.4 molar equivalents relative to parent amine; ratio adjusted during process development according to target molecule yield and impurity profile

    Downstream process integration

    • Introduced during nitrostyrene condensation with benzaldehyde analogs; reduced via catalytic hydrogenation or chemical reduction prior to subsequent substitution steps; batch-wise or flow synthesis integration based on project scale

    Final product types

    • API intermediates for CNS agents (e.g., psychoactive phenethylamines and analogs)
    • N-substituted phenethylamine library compounds for preclinical screening

    2. Building Block in Agrochemical Development

    In crop protection R&D, this compound enables the creation of aromatic nitro intermediates for insecticide and fungicide models. Its electron-rich aromatic ring and nitro group allow for subsequent modifications required for structure-activity relationship optimization. Chemical engineers use this intermediate for pilot-scale batches that advance into field study candidates while meeting regulatory expectations for purity and traceability.

    Industry compliance standards

    • FAO/WHO Guidelines on Good Manufacturing Practice for Pesticide Manufacturing
    • OECD Series on Pesticides – Test Guidelines for Product Chemistry
    • ISO 9001:2015 Quality Management Systems in Agrochemical Manufacturing

    Typical usage ratio

    • Added at 5–15% w/w of the core formulation batch; scaled depending on downstream derivatization sequence and target bioactivity

    Downstream process integration

    • Enters at the aromatic nitration or reduction stage within multistep synthesis; combined with other aromatic building blocks or halogenation agents for derivatization, ahead of formulation into technical concentrate

    Final product types

    • Intermediates for new generation insecticides
    • Prototype fungicides for premarket registration

    3. Dye and Pigment Intermediate for Specialty Colorant Manufacturing

    The compound acts as a precursor for nitroaromatic dyes, especially those requiring ortho- and para-substituted methoxy groups for bathochromic shifts. Formulators leverage this molecule to introduce electron-donating effects that yield high-tint value pigments. Manufacturing employs close control of reaction conditions to achieve color purity and meets standards for industrial coloring agents used in plastics, coatings, and inks.

    Industry compliance standards

    • REACH (EC 1907/2006) for registration and use in colorants
    • ETAD Position Paper on Impurities in Colorants
    • ASTM D5206 for industrial dye quality control

    Typical usage ratio

    • Employed at 1–8% mass fraction in the dye precursor stage; amount adjusted based on required chromophore loading and desired absorption properties

    Downstream process integration

    • Supplied at the diazotization or coupling reaction stage for dye construction; processed under temperature and catalyst control with subsequent isolation and milling

    Final product types

    • Nitro-methoxy azo dyes for plastics and synthetic fibers
    • Special effect pigments for printable ink concentrates

    4. Intermediate for Specialty Organic Synthesis in Research and Pilot-Scale Plants

    Synthetic chemists and contract manufacturing organizations access the nitrostyrene for constructing complex organic scaffolds in medicinal and material chemistry. Its reactivity profile supports Michael additions and further substitutive elaboration. The controlled production environment ensures minimal batch-to-batch variability, supporting demanding analytical and process validation requirements in first-in-human or advanced material projects.

    Industry compliance standards

    • ISO 17025: Testing and Calibration Laboratories Requirements
    • RoHS Directive (where applicable for electronics-related development)
    • EU Regulation 2023/2006 on Good Manufacturing Practice for Materials Intended for Contact with Food (for food-safe materials R&D)

    Typical usage ratio

    • Introduced at 0.05–0.5 molar equivalents depending on target scaffold complexity and pathway selectivity

    Downstream process integration

    • Applied in initial carbon–carbon bond forming step via Knoevenagel or Michael addition; input point determined by retrosynthetic analysis and functional group compatibility; also used in tele- and continuous-flow microreactor development settings

    Final product types

    • Advanced synthetic intermediates for custom project needs
    • Reference compounds for analytical standards
    • Specialty monomers for high-performance material evaluation
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    Certification & Compliance
    More Introduction

    3,4-Dimethoxy-B-Nitrostyrene: A Manufacturer’s Perspective

    Getting to the Core of 3,4-Dimethoxy-B-Nitrostyrene Production

    Many years on the plant floor and in the lab teach a manufacturer to look closely at what sets certain chemicals apart in the industry. 3,4-Dimethoxy-B-Nitrostyrene stands out among the aryl nitroalkenes for good reason. Known to many by its chemical formula C10H11NO4, this compound draws attention primarily within research, specialty synthesis, and niche intermediate needs. The process relies on careful control at every turn, from sourcing simple starting materials to fine-tuning crystallization and maintaining purity. It’s never just a catalog number here—every batch brings a fresh set of challenges and a record of practical learning.

    Sourcing pure p-anisaldehyde and nitromethane consistently makes a difference in finished quality. On the plant floor, the work shifts depending on the lot—room temperature, air quality, and humidity can shift yields by a few percent without warning. We see the biggest improvements in product clarity and downstream performance when meticulous attention goes into solvent distillation and temperature control during the initial condensation. Even filtration methods cannot be left to chance: slower filtration often delivers a purer solid, while pressure filtration helps scale production for larger runs. A genuine understanding of what our partners expect from this compound guides every small adaptation.

    Honest Details on Specifications and Quality

    We are not pushing paper here; each shipment represents time and labor spent to achieve straightforward quality. Customers rarely see the hours logged in walking the line between yield and purity. On average, finished product from our reactors boasts purity above 97% by GC-MS, with strict screening for trace solvents and by-products. Color and odor often speak louder than paperwork. Bright yellow-orange crystals, lacking in musty or sharp odors, tell a seasoned technician more about the run than any certificate.

    Exact melting points on incoming and outgoing samples form the cornerstone of our internal QC. For this nitrostyrene, those points usually fall between 129–131°C. Deviations spark investigation on the spot. Each batch needs to stand up not only to analytical scrutiny but to the actual demands of synthetic chemists relying on consistency from shipment to shipment.

    Drying and final packaging turn out to be as important as reactor performance. Slight residual moisture can cause aggregation or degrade the active nitro double bond. Sealed polyethylene or glass containers, inerted headspace, and shipment in climate-controlled trucks mitigate these risks. Bin labels and batch identification tie back to a traceable record—anyone in our production team can backtrack eight years in the ledger should a question arise.

    Distinct Characteristics: How 3,4-Dimethoxy-B-Nitrostyrene Stands Out

    Not every nitrostyrene delivers the same results in applied settings. The addition of methoxy groups at the 3 and 4 positions of the aromatic ring creates a compound with specific reactivity that direct competitors do not provide. Researchers and process chemists using this molecule typically point to increased electron donation from the methoxy substituents. This feature modulates both the aromatic ring and the nitroalkene function, giving a reactivity profile distinct from unsubstituted or mono-methoxy analogs.

    In organic synthesis, reactivity difference becomes practical, not theoretical. Workflows involving cyclizations, reductive aminations, or various heterocyclic constructions benefit from the adjustment in electron density brought by these two groups. Chemists relying on other beta-nitrostyrenes without the 3,4-dimethoxy substitution often wrestle with sluggish reaction rates or unpredictable side product formation. We hear from both large research institutions and small entrepreneurial labs about the reduction in step count when moving from plain beta-nitrostyrene to our double-methoxy variant.

    Even in terms of color and texture at the bench, the product feels different in the hand. The crystals form with a tight uniform appearance—no dusty fine particulates or clumpy masses. This matters during storage, weighing, and blending with other solid reagents. Handling differences may not show up in brochures, but for our customers, daily workflow and staff time mean real money and safety.

    Common Applications: Beyond the Textbook

    Surveys and direct calls reveal that 3,4-Dimethoxy-B-Nitrostyrene finds most use in research and pilot-scale routes targeting bioactive compound development. Medicinal chemistry teams focus on its role as a versatile intermediate in building substituted phenethylamines and related analogs. The reasons have less to do with broad textbook coverage than recent trends in exploring CNS-active structures—structures where methoxy substitution often correlates with differentiated binding profiles and, occasionally, better in vivo properties.

    Outside strict medical research, we have seen notable uptake in material science experimentation, where this compound serves as a precursor to substituted aryl polymers. Anecdotal feedback highlights improved UV stability or resistance to degradation in certain copolymer blends. A subset of customers incorporates the molecule into specialty dyes and photoactive materials, largely due to the stability imparted by the double methoxy configuration.

    We listen for unexpected successes too—a recent stretch saw strong demand from a lab working on new ionic liquids. Their chemists reported that the methoxy pattern on the aryl ring led to better solubility and tuneable viscosity in their proprietary applications. Examples like these underscore the adaptability possible when manufacturers and end users hold an open dialogue.

    Examining the Synthesis: Factory Lessons and Small Fixes

    Lessons from previous syntheses influence every new run at scale. Early on, we dealt with inconsistent yields and occasional darkening of product—signals of overreaction or trace contamination from nitromethane. Our process chemists found that precise pH control during aqueous work-up cut down on tarring and increased usable product recovery. Instead of defaulting to broad filtration or generic solvent washes, focused process development makes a difference in long-term efficiency.

    Choosing equipment turned into a real-world test of adaptability. Basic glass reactors with overhead stirring suffice at small volumes. For commercial runs, though, jacketed stainless steel reactors with direct solvent recovery outpace batch glassware in both cost and sustainability. Aggressive cleaning protocols and valve maintenance have become non-negotiable. Sloppy attention here leads to order delays and frustrated clients.

    Scrupulous record-keeping and staff training keep mistakes from compounding. New technicians tend to underestimate just how easily a wrong addition or temperature surge can ruin product quality. Documented process deviations give us hard data to drive skills development. In truth, our best innovations rarely appear in published procedures but in the work our team does behind closed doors to make each run a little safer, cheaper, and more reliable.

    Challenges: Supply Chain, Environmental, and Regulatory Realities

    No manufacturer can ignore challenges that stretch beyond the laboratory walls. Sourcing high-purity precursors brings its own risks. Disruptions in nitromethane or anisaldehyde shipments, for example, can choke production for weeks. During global supply shocks, every supplier and customer feels the strain. Stockpiling large inventories or dual-sourcing sometimes solves the short-term crunch, yet these come with higher costs or added management complexity.

    Environmental scrutiny on the use and disposal of nitroaromatic compounds pushes our team to invest in upgraded scrubbers, better solvent recycling, and emissions monitoring. The drive for greener chemistry shapes R&D focus. Experimentation with alternative solvents and milder reaction conditions consumes dozens of pilot runs each year. The ultimate balance—cost, safety, and reduced impact—remains a moving target, but each small gain matters.

    Regulatory expectations increase year on year. Auditors from local and international agencies regularly examine batch records, waste manifests, and staff safety procedures. As experienced manufacturers, we document process changes, worker training logs, and incident reports rigorously. Our partners depend on complete transparency—not just for traceability, but for protecting their own certifications and license to operate.

    Market Feedback and Continuous Improvement

    Not all feedback comes in writing. Troubled calls at odd hours, rushed sample requests, or returned lots with tiny product loss can reveal more about market shifts than any trend report. Our R&D and operations teams meet monthly, going over both the problems and the quiet runs that signal things working well. We track customer comments not only on quality, but on shipping speed, technical support, and adaptability for new projects.

    Common requests for custom particle size, non-standard packaging, or certifications prompt in-house investments. For example, after several customers shared issues with moisture absorption in large drums, our packaging workflow shifted to smaller, tamper-evident units with improved seals. Field-driven improvements like container upgrades or split shipments deliver real results in end-user labs trying to maximize shelf life and minimize handling risk.

    Partnership with trusted freight companies ensures critical shipments face reduced delay or spoilage, especially as unpredictable weather and tighter transport rules make “on-time delivery” harder to guarantee season to season. Implementing more robust barcoding and scanning further reduces the chance of order mis-picks—a sore spot for many manufacturers during rapid growth.

    Comparing 3,4-Dimethoxy-B-Nitrostyrene to Its Relatives

    A practical distinction develops when putting this compound side by side with alternatives. Unsubstituted beta-nitrostyrene remains easier and cheaper to produce, but trade-offs show up fast during complex syntheses: slower reactions, harder separation of side products, and more frequent purification steps. 2,5-Dimethoxy and 3,5-dimethoxy substitutions widen the product portfolio but usually deliver changed reactivity and, often, more expensive starting materials with less predictable demand.

    Users shifting from mono-methoxy to the 3,4-dimethoxy form cite real improvements. The dual methoxy pattern leads to higher conversion rates during aromatic substitution and smoother downstream reductions. Internal side-by-side trials on reduction to the corresponding amine intermediate showed greater selectivity and less tar formation, especially under milder conditions. This translates to less solvent use, fewer hours in purification, and a safer process overall.

    Some products in the same chemical family come as dense powders or sticky solids, which frustrate those working with them in gloveboxes or automated powder feeders. With 3,4-dimethoxy-B-nitrostyrene, the crisp crystal structure and reduced tendency for caking help line workers save both time and frustration, and they cut down on waste during transfer and weighing.

    Solubility differences catch many first-time users off guard. In some organic solvents, this compound dissolves faster and forms clearer solutions at lower temperatures—the influence of the electron-donating groups again showing up in a subtle, practical manner. Chemists scaling reactions from milligrams to kilograms notice the saved hours and improved process window.

    Building Reliability in the Supply Chain

    Keeping relationships strong with both old clients and newcomers requires more than a well-written spec sheet. Real trust builds through steady, aboveboard communication and a willingness to acknowledge and fix weaknesses. For this nitrostyrene—still a specialty product—production volumes rarely get close to commodity scale. That means small delays or hiccups carry outsized risk for those depending on “just in time” stock.

    We operate with buffer inventories built from several years of data, not guesswork. For recurring orders, advance scheduling and early shipment reservation reduce last-minute chaos. Of equal importance, open lines with regulatory agencies, technical consultants, and logistics providers help prevent compliance or customs issues from stalling delivery.

    Stable supply ultimately comes from investing ahead of surges in demand. In the last year alone, we expanded reactor capacity and wrung out more throughput per shift to anticipate both regular orders and sudden one-off purchases tied to new grant awards or research pivots. Each expansion draws from the lessons and setbacks accumulated across decades on the factory floor.

    Turning Raw Materials Into Lasting Value

    For those of us who design, manufacture, and deliver chemicals like 3,4-dimethoxy-B-nitrostyrene, success relies on more than clean glassware or well-run reactors. It stems from listening to the quiet frustrations and practical hopes of those further down the supply chain. Every incremental change in efficiency, safety, or communication reflects a mix of tradition and innovation forged over time.

    Some customers seek out performance at any price. Most value reliability and openness. For many products—especially those destined for regulated or life sciences sectors—the margins for error narrow each year. History teaches that cutting corners, sacrificing purity, or hiding inconvenient truths never works out. Our best batches come from the hands and attention of those who take pride in the process and stand behind each shipment.

    The story of each drum or bag of 3,4-dimethoxy-B-nitrostyrene shipped from our plant contains years of accumulated skill—sometimes hard-won and always evolving. Keeping an open ear to changing needs and a keen eye on what makes a difference in the field allow us to create products that solve more than just chemical equations. That’s the steady foundation from which we’ll keep building, one batch at a time.