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3-Bromo-4-Methoxybenzonitrile

    • Product Name 3-Bromo-4-Methoxybenzonitrile
    • Alias 3-Bromo-4-methoxybenzenecarbonitrile
    • Einecs 843-611-8
    • 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

    661915

    Chemical Name 3-Bromo-4-Methoxybenzonitrile
    Cas Number 85118-06-7
    Molecular Formula C8H6BrNO
    Molecular Weight 212.05
    Appearance White to off-white solid
    Melting Point 76-80°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.57 g/cm³ (approximate)
    Smiles COC1=CC(=CC(=C1)C#N)Br
    Inchi InChI=1S/C8H6BrNO/c1-11-8-3-2-6(4-10)7(9)5-8/h2-3,5H,1H3
    Storage Conditions Store at room temperature, in a dry and ventilated place
    Synonyms 3-Bromo-4-methoxybenzenecarbonitrile
    Pubchem Cid 329085

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

    Packing & Storage
    Packing Glass bottle containing 25 grams, labeled "3-Bromo-4-Methoxybenzonitrile," with hazard symbols and lot number, sealed for laboratory use.
    Shipping 3-Bromo-4-Methoxybenzonitrile is typically shipped in tightly sealed containers to prevent moisture and contamination. It is transported as a hazardous chemical, following regulatory guidelines for labeling, packaging, and documentation. Handle with care, avoiding excessive heat and direct sunlight. Safety data sheets and protective measures are provided to ensure safe delivery.
    Storage **3-Bromo-4-Methoxybenzonitrile** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatibles like strong oxidizers. Protect it from light and moisture. Proper labeling and handling precautions must be followed, and the storage area should be equipped with appropriate spill containment and fire-fighting measures.
    Application of 3-Bromo-4-Methoxybenzonitrile

    Applications of 3-Bromo-4-Methoxybenzonitrile in Industrial Manufacturing

    As an experienced manufacturer specializing in fine chemical intermediates, we recognize the strategic role 3-Bromo-4-Methoxybenzonitrile plays in various advanced industrial processes. Our focus is on real-world applications that meet stringent quality and regulatory demands across specialized chemical production environments. Below, we outline key industrial sectors, established compliance frameworks, precise formulation parameters, production step integration, and downstream end products.

    1. Pharmaceutical Active Ingredient Synthesis

    Major pharmaceutical enterprises rely on this intermediate for targeted synthesis of receptor modulators and central nervous system agents. Its methoxy and nitrile substituents provide crucial handles for regioselective substitution and controlled cyclization during multi-step active pharmaceutical ingredient (API) construction while maintaining molecular integrity. Analytical controls are carried out from initial reaction charging to final purification, as required by regulated environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.)
    • Japanese Pharmacopoeia (JP)

    Typical usage ratio

    • 0.4–1.1 molar equivalents per stage, adjusted according to yield targets and impurity control in stepwise API builds.

    Downstream process integration

    • Charged in route-defining Suzuki, Buchwald-Hartwig, or nucleophilic aromatic substitution during intermediate assembly, followed by purification and quality verification before subsequent transformations.

    Final product types

    • Atypical antipsychotics
    • Selective serotonin receptor antagonists
    • Histamine H1 receptor antagonists under clinical development
    • Small molecule kinase inhibitors

    2. Agrochemical Ingredient Precursor

    Leading crop protection companies incorporate this compound into their research and bulk scale for advanced herbicide and insecticide scaffolds, where bromine reactivity enables formation of functionalized aromatic backbones and methoxy groups enhance selectivity profiles in target biocide actives. Adherence to consistent traceability and impurity monitoring is emphasized throughout process batch records.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • US EPA 40 CFR Part 169
    • China National Standard GB/T 1600 for pesticides
    • FAO/WHO Specifications for Plant Protection Products

    Typical usage ratio

    • 10–25% by molar input depending on route; precise dosage determined by desired substitution degree on final triazine or pyridine rings.

    Downstream process integration

    • Added during aromatic ring functionalization steps, prior to heterocycle closure in pilot and commercial synthesis lines, with inline HPLC verification for bromine and methoxy substitution completeness.

    Final product types

    • Triazine-based systemic herbicides
    • Aromatic nitrile fungicide precursors
    • Nitrogen-containing insecticide actives
    • Seed treatment intermediates

    3. Custom Fluorinated Pharmaceuticals Intermediate

    Specialty biopharmaceutical manufacturers leverage this intermediate to introduce halogenated aromatic building blocks in the assembly of next-generation fluorinated drug candidates. The compound supports transition metal-catalyzed cross-couplings, giving precise substitution patterns required in structure-activity relationship (SAR) studies, and allowing flexible late-stage diversification through selective activation of the bromide site.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • US FDA DMF (Drug Master File) requirements
    • ISO 9001:2015 Quality Management for Fine Chemicals
    • Pharmacopoeial guidelines for residual solvents (USP <467>)

    Typical usage ratio

    • Typically 0.85–1.25 molar equivalent per coupling; further optimized per molecular design and impurity threshold.

    Downstream process integration

    • Utilized in palladium-catalyzed Suzuki-Miyaura or Negishi coupling from pre-dried solvent systems for assembly of fluorinated phenyl segments, followed by chromatographic purification and impurity mapping.

    Final product types

    • Selective fluorinated kinase inhibitors
    • Synthetic anti-viral agent cores
    • Positron emission tomography (PET) tracer analogues
    • NCEs (New Chemical Entities) in late preclinical development

    4. Specialty Dye and Pigment Intermediate

    Established producers in the specialty colorant industry use this intermediate as a key aromatic precursor for synthesizing high-performance azo and anthraquinone dyes. The unique combination of bromine and methoxy functionalization allows for tailored color absorption and molecular stability on technical substrates, supporting high-purity output in niche pigment portfolios for industrial and medical-grade coatings.

    Industry compliance standards

    • EU REACH Registration
    • Oeko-Tex Standard 100 (applicable in textile dyes)
    • ISO 9001 for Quality Management Systems
    • EN 71-3:2019 Safety of Toys – Migration of Certain Elements (for pigment safety in colorant manufacture)

    Typical usage ratio

    • 5–10 mol% as an initial stage component, adjusted in relation to intended chromophore density and desired fastness properties in colorant systems.

    Downstream process integration

    • Fed into aromatic nucleophilic substitution, followed by diazotization and coupling with tailored amine or polyaromatic units during pigment manufacture under solvent-controlled conditions; residual bromide content monitored.

    Final product types

    • Rapid-dispersion azo dyes for synthetic fibers
    • Anthraquinone-based medical imaging pigments
    • High-stability textile colorants
    • Toner electrophotographic pigments
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    Certification & Compliance
    More Introduction

    3-Bromo-4-Methoxybenzonitrile: Precision Matters in Synthesis

    Over the years, we’ve seen the rapid evolution of chemical synthesis hinge on the reliability of specialized building blocks. 3-Bromo-4-Methoxybenzonitrile has become irreplaceable in modern laboratories focused on pharmaceuticals and fine chemicals. Our direct, in-house control over its manufacture means we catch every nuance, every subtle shift in purity or consistency, so chemists and process engineers don’t lose time chasing down batch-to-batch discrepancies. Strong, consistent performance isn’t academic for us; it’s the reason our partners keep coming back with new projects.

    Product Model and Reliable Consistency

    Our product, identified under the trade model BMBCN-083, emerges from a multi-step process we’ve tested and upgraded through years of hard-won experience. Most competitors shuffle between suppliers, which introduces drift in impurity profiles. At our plant, every lot tracks to a controlled route—no detours, no off-spec material. From bromination to methoxylation, each reaction receives close attention from our team: daily monitoring with HPLC, NMR, and wet chemistry, not just automated readouts. We do this because even small deviations can force downstream processes off-track. Consistency creates trust and saves real dollars at scale.

    Our 3-Bromo-4-Methoxybenzonitrile delivers a purity specification above 99.5%, which we validate with side-by-side reference runs using authentic standards, not just theoretical profiles. On request, we support additional checks for water content, residual solvents, and particle size, since filtration and drying rates affect workups in scaled synthesis. The product forms pale crystalline solids that store well when kept dry and cool. Usually, we keep stock sizes from 1 kg up to 100 kg batches, so labs and pilot plants don’t get forced into awkward minimums or waste extra money on oversized containers. Every container comes sealed in moisture-proof packaging, directly filled at the point of synthesis, and the labeling follows up-to-date hazard designations for easy reference in the lab.

    Tackling the Heart of Advanced Chemical Synthesis

    Chemical producers and research chemists value 3-Bromo-4-Methoxybenzonitrile for its flexible role in complex molecule assembly. With its nitrile group anchored to a substituted aromatic ring, this compound is a proven intermediate for both cross-coupling and directed ortho-metalation reactions. Halogenated nitriles like this one, possessing both electronic and steric influences, enable chemists to tune product yields and selectivity in multi-step programs. The methoxy group does more than dress up a structure on paper: it edges reactivity in favored directions and tempers unwanted isomers from forming under basic or transition-metal catalyzed conditions. We've noticed that academic groups stuck with generic 3-bromobenzonitrile often report wider product distributions—simple tweaks in starting material really make all the difference.

    In our client projects, 3-Bromo-4-Methoxybenzonitrile proves its worth especially in the assembly of tailored aromatic scaffolds for new drug candidates. Medicinal chemistry teams relay to us that the bromo substituent at the meta position gives them a reliable anchor for Suzuki, Negishi, and other cross-coupling sequences. The methoxy group at the para site acts as a mask, encouraging selectivity when introducing side chains at specific ring positions. This targeted chemistry lets innovators access analogs that are otherwise out of reach with unsubstituted or differently-substituted benzonitriles. By controlling the feedstock profile, teams can test new drug designs without batch-to-batch headaches. Bench chemists write to us about the drop in purification headaches—less time tweaking silica conditions, fewer side products muddying NMR interpretation.

    Crucial Differences vs. Standard Benzonitriles

    Some might ask what sets this compound apart from ordinary bromo- or methoxybenzonitriles. The answer comes down to how each functional group joins the ring and changes chemical behavior. Regular 3-bromobenzonitrile lacks the electron-donating para methoxy, so it pushes electron density differently through the system. In synthesis, this can lead to lower yields or broader product mixes, with underwhelming selectivity in coupling or substitution reactions. Swapping in a methoxy at the meta position, or leaving out the bromo entirely, cuts off many standard synthetic routes—certain catalysts demand halogen handles for oxidative addition, and some protection strategies rely on well-placed oxygen substituents.

    Our continuous process improvements mean the impurity fingerprint stays lean. Generic alternatives from non-integrated suppliers often show up with residual starting material, inconsistent particle morphology, or higher levels of chlorinated or over-brominated byproducts. Such contaminants don’t just eat into analytical yields; they threaten downstream biological testing where small-molecule registration demands uncontested purity. By running inline analytics for each batch, we built feedback loops that spot and fix problems before product leaves the reactor hall. Quality control here is not just a compliance checkbox—our partner companies rely on repeatable outcomes as a baseline for regulatory submissions and patent filings.

    Applications in Pharmaceuticals and Material Science

    Out in the market, new molecules drive advances in therapies and materials science. 3-Bromo-4-Methoxybenzonitrile features in medicinal chemistry strategies for kinase inhibitors, CNS-active scaffolds, and anti-infectives—its substituent pattern supports the attachment of heteroaryl, alkyl, and biaryl fragments through robust palladium chemistry. We’ve watched research clients develop at least a dozen small-molecule candidates where this building block shortens the synthetic route by one or two steps, either by improving selectivity or by reducing the need for later protecting-group chemistry. It’s not just about saving time: a cleaner route means safer plants, less waste, and fewer surprises at scale-up. For material scientists chasing high-value monomers or functional dyes, this compound’s dual substituents allow precise control over polymer or oligomer properties. Custom electronics, thin-film coatings, and liquid crystals depend on these small choices in molecular design.

    Another practical edge comes from how our product handles scale. Bench scientists and pilot operators take different approaches to solvent choice and work-up. Some prefer traditional aromatic extractions, some depend on greener, high-boiling polar systems. Our crystallization parameters produce a product that redissolves or suspends quickly without unpredictable clumps, which means smoother transitions between small lab runs and kilo-scale processes. We’ve had teams drop us notes about the first time they moved from a 20 g scale to 5 kg and didn’t run into clogging or stuck filtrations—real productivity that avoids unplanned downtime.

    Manufacturing Realities and Everyday Challenges

    Real-life chemistry doesn’t unfold like textbook recipes. Handling 3-Bromo-4-Methoxybenzonitrile safely at scale, we install robust control measures at every equipment juncture. We made a point early on to refine our vent scrubbing for the bromination stage; even minor leaks can threaten worker comfort and trigger local complaints. Careful washing steps during purification keep trace acids and oxidants away from the next synthetic stage. Moisture sometimes creeps in during rainy months—glass-lined reactors with dehumidified feeds make all the difference here, keeping hydrolysis versus desired product under tight control.

    We also realized that not all labs have the same tolerance for residual solvents. Chlorinated solvents can persist in trace amounts if the process isn’t tuned, so we cycle through staged drying and sparging under nitrogen. By taking direct feedback from pilot groups, we've tailored our product finish to get residuals down to levels below 100 ppm. Thanks to in-process analytics, we catch these slips before drums leave the plant. This matters especially for pharmaceutical groups whose downstream steps use sensitive catalysts—ppm-level impurities can poison reactions and drive up costs, usually with no warning until it’s too late. Each batch includes a detailed COA with full impurity data, so engineers don’t fly blind.

    Why Upstream Control Beats Spot Purchasing

    Some procurement teams still shop for their intermediates by price alone, missing the risks that come with sporadic sourcing. In our work, a bad batch from a trader means more than just a slow project: it ripples through regulatory review, clinical supply, and business timelines. Because we stay in direct control, we take responsibility for both raw materials and process tweaks as needed. Our transparency stems from real-time process history, not just paperwork audits. Partners who co-develop intermediates with us plug into this deeper integration, not just for today’s deliveries, but for future projects too. As regulatory demands keep tightening, especially for drug companies, reliable upstream controls shield against failed filings and sudden ingredient bans. We’ve watched regulatory agencies probe source documentation all the way to precursor origins, and only direct production lets us close those records with certainty.

    Safety and Environmental Responsibility

    Handling reagents like bromine at the scale required for tonnage intermediates brings unique challenges. Over the years, we’ve fitted our site with containment systems, high-efficiency particulate scrubbing, and emergency power backups specifically for these synthesis runs. Our waste minimization program grew from both practical and regulatory incentives: solvent recycling, careful bromide containment, and real-time effluent monitoring now sit in the standard operating schedule. That focus pays dividends when customers face end-stage product qualification. Whether it’s nitrosating agent avoidance, RoHS compliance, or REACH pre-registration, our batch histories remain transparent and auditable.

    With regulators and communities demanding cleaner emissions, we installed on-site solvent recovery towers and linked analytical systems that feed right into our inventory audit. We achieved marked cuts in waste stream volume, and periodic third-party checks validate our improvements. This approach isn’t about ticking boxes; it earns us the long-term goodwill of the communities our teams live and work in. For customers, these investments translate to fewer supply chain jitters and fewer doubts about continuity or price shocks related to environmental governance.

    Smart Supply Chain Practices and Customization

    Our years in the business taught us the risks of supply interruptions—raw material swings, global logistics hiccups, or regulatory squeezes. By holding core starting materials on site and maintaining secondary supply options for main precursors, our plant sidesteps the worst volatility. We’ve invested in process automation, but never at the expense of the operator’s judgment. Skilled shift techs review data and sample trends throughout each production run. This hybrid model—machines for efficiency, people for insight—has helped us dodge costly recalls and schedule overruns.

    For research groups or companies running niche programs, we tailor production runs without forcing “special order” premiums or long waits. If a formulation needs a tighter water spec, we adjust drying. If a stability issue pops up on storage trials, we can tweak packaging and documentation straight from the source, not down the distribution chain. Our feedback loop remains short—laboratory, production, and client teams talk directly, cutting red tape and reducing misunderstandings.

    Straightforward Communication and Expert Support

    We don’t separate sales from manufacturing. Engineers and lab managers who reach out for product advice speak directly with chemists and production staff, not distant account handlers. Our technical support isn’t script-driven or lifted from a playbook—we work one-on-one to solve practical challenges, troubleshoot unexpected reactions, or optimize scale-up. New synthetic approaches or novel target molecules? We like hearing about them. This spirit of engaged, down-to-earth collaboration puts our team at the front of the line when academic or pharma groups look for new strategic suppliers.

    We choose to share process knowledge with our partners. People sometimes tell us the learning curve in aromatic halide chemistry is steep—they want to know what snagged others before. We gladly pass along practical advice: optimal solvent selections for coupling, best degassing protocols, and purification shortcuts that work. That transparency builds confidence, especially for groups shifting from bench trials to full-scale pilot plant runs. Bringing years of direct manufacturing under one roof means more than just quicker answers; it means safer scale-up and smoother regulatory filing.

    Looking Ahead: Meeting the Next Wave of Challenges

    As demand grows for more sophisticated chemical building blocks, our focus remains on quality, reliability, and personal accountability. Upstream innovation keeps our synthesis route efficient and our impurity levels low. Downstream integration supports new pharmaceutical, chemical, and materials projects right from the early design phase. By sticking to manufacturing fundamentals—clean inputs, controlled reactions, and unbroken documentation—our batch records hold up to the toughest industry audits.

    We make a point of hearing our customers’ real-world challenges. Market pressures, regulatory shifts, and advances in chemical research drive us to keep getting better. Our role as the direct manufacturer means we adapt quickly to new project needs, improving both process control and supply reliability. As chemists, we know batch failures waste money, eat up time, and slow progress on bigger scientific goals. By putting care and attention behind each step, 3-Bromo-4-Methoxybenzonitrile moves from commodity status to strategic building block, enabling breakthroughs in labs and plants worldwide.

    Each container we ship reflects more than just another chemical unit—it embodies hands-on input from every technician, engineer, and quality manager involved in production. Trust doesn't come from anonymity or outsourcing; it grows from expertise, diligence, and open communication, year after year.