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3-Cyanobenzyl Bromide

    • Product Name 3-Cyanobenzyl Bromide
    • Alias m-Bromomethylbenzonitrile
    • Einecs EINECS 223-154-6
    • 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

    521226

    Chemical Name 3-Cyanobenzyl Bromide
    Cas Number 17194-86-2
    Molecular Formula C8H6BrN
    Molecular Weight 196.05
    Appearance White to off-white crystalline powder
    Melting Point 67-71°C
    Boiling Point 319°C at 760 mmHg
    Density 1.447 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Inchi Key IFDHLPRZHGWIPY-UHFFFAOYSA-N
    Smiles N#CC1=CC=CC(Br)C=C1
    Storage Conditions Store at 2-8°C, protected from light
    Synonyms m-Cyanobenzyl bromide; 3-(Bromomethyl)benzonitrile

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

    Packing & Storage
    Packing A 25-gram amber glass bottle of 3-Cyanobenzyl Bromide, tightly sealed, labeled with hazard symbols, and product details.
    Shipping 3-Cyanobenzyl Bromide is shipped in tightly sealed, chemical-resistant containers, clearly labeled with hazard information. It is classified as a hazardous material and handled according to international shipping regulations. Shipments are protected from moisture, heat, and physical damage, and accompanied by the necessary safety data sheets and documentation during transport.
    Storage 3-Cyanobenzyl bromide should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store it in a cool, dry, and well-ventilated area, preferably in a dedicated corrosives or organics cabinet. Segregate from incompatible substances such as strong bases and oxidizers. Properly label the container, and avoid sources of ignition or strong acids.
    Application of 3-Cyanobenzyl Bromide

    Applications of 3-Cyanobenzyl Bromide in Industrial Manufacturing

    3-Cyanobenzyl Bromide functions as a key intermediate in several highly specialized chemical manufacturing processes. As direct producers of this raw material, we support global B2B partners in sectors where rigorous quality, regulatory traceability, and precise formulation practices are fundamental. Below, we highlight major industrial application scenarios where this compound forms an integral part of complex chemical synthesis workflows, and detail compliance criteria, formulation guidance, process positioning, and representative finished goods.

    1. Pharmaceutical Intermediate Synthesis (Active Pharmaceutical Ingredient Precursors)

    Drug substance manufacturers widely utilize this compound for synthesizing select API precursors, particularly those requiring a meta-cyano-phenyl motif. Medicinal chemistry routes leverage its benzyl bromide functionality to introduce the required aromatic group into early-stage intermediates for antihypertensives and neuroactive compounds. This step typically occurs before subsequent amide formation or cyclization, with rigorous quality control to meet regulatory mandates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopeia Monograph 2.2.46 (Residue on Ignition and Related Substances)
    • 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • Customarily 0.10–0.35 molar equivalents per batch, adjusted by target intermediate yield, reaction pathway, and downstream purification requirements.

    Downstream process integration

    • Charged during nucleophilic aromatic substitution or alkylation following core heterocycle construction and prior to amide coupling. Monitored using in-process HPLC or GC-MS analytical checkpoints during batch reactions.

    Final product types

    • API intermediates for antihypertensive medicines (e.g., sartans)
    • Precursors for select antipsychotic agents
    • Building blocks for central nervous system (CNS) active pharmaceuticals

    2. Agrochemical Synthesis (Herbicide and Pesticide Intermediate)

    Agrochemical formulators incorporate this raw material into production routes for meta-cyano-aryl compounds, utilized as intermediates in herbicide and insecticide active ingredient synthesis. The bromide leaving group allows for straightforward nucleophilic displacement, facilitating subsequent transformation steps in pesticides with intricate aromatic substitution patterns.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management Systems
    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals (EU)

    Typical usage ratio

    • Introduced at 3–7% by weight in pilot-scale syntheses; scaled to 0.15–0.5 molar equivalents in full-scale agrochemical intermediate production, depending on target yield.

    Downstream process integration

    • Blended after initial aromatic ring assembly during the substitution reaction, preceding final amidation or esterification stages; process typically performed in jacketed glass reactors under inert atmosphere.

    Final product types

    • Key intermediates for phenoxy herbicides
    • Cyanobenzyl-based insecticide synthons
    • Building blocks for fungicide compounds requiring meta-cyano substitution

    3. Specialty Dye Ingredient for High-Performance Colorants

    Producers of high-stability, specialty aromatic dyes use this material to prepare advanced dye intermediates with increased photostability and bathochromic shift properties. Aromatic cyanide groups introduced via this reagent provide desired electron-withdrawing effects, contributing to colorfastness under industrial textile processing conditions.

    Industry compliance standards

    • OEKO-TEX Standard 100 – Chemical Safety in Textiles
    • GOTS (Global Organic Textile Standard), section on chemical inputs
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidelines

    Typical usage ratio

    • Applied at 2–5% by weight of total substrate in the arylation step, with exact dose controlled by target shade strength, batch size, and required substrate compatibility.

    Downstream process integration

    • Reacted post-condensation with suitable amine intermediates during diazotization or azo-coupling reactions. Used in closed reactors fitted with pH control and real-time UV-Vis monitoring.

    Final product types

    • High-performance textile dyes for polyester and nylon
    • Special effect dyes for technical fibers and industrial plastics
    • Non-bleeding colorants for automotive interiors and industrial coatings

    4. Advanced Material Monomer and Polymer Intermediate Synthesis

    Manufacturers of advanced materials integrate this material as a functional monomer in the synthesis of specialty polymers, especially where meta-cyano functionality imparts increased thermal resistance or dielectric performance. Its reactivity allows for custom modifications in polymers designed for electronics, membranes, or performance coatings.

    Industry compliance standards

    • IEC 61249-2-21 (Halogen-Free Laminates and Interconnections)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14001 Environmental Management Systems

    Typical usage ratio

    • Usage varies from 1–10% molar fraction depending on polymer chain length, physical property targets, and comonomer reactivity.

    Downstream process integration

    • Loaded at the initial copolymerization or functionalization stage, where it reacts via nucleophilic aromatic substitution with selected diamines or diols, followed by casting and curing operations under inert atmosphere.

    Final product types

    • Halogen-free epoxy laminates for printed circuit boards (PCBs)
    • Thermally stable polyamides for automotive and electronics
    • Functionalized polyesters and specialty copolymers for filtration membranes

    5. Fine and Performance Chemical Intermediate for Liquid Crystals

    High-purity liquid crystal material suppliers employ this compound in custom synthesis streams for meta-substituted aromatic cores. Its precise introduction at early-stage intermediates enables molecular architectures with tunable birefringence, essential for advanced display technologies and technical optics.

    Industry compliance standards

    • JEITA Guidelines for Materials Used in Electronic Displays
    • ISO 9001:2015 (Quality Management for Electronic Chemicals)
    • Environmental, Health, and Safety (EHS) Protocols for Electronic Materials per SEMI S2

    Typical usage ratio

    • Standard application at 0.08–0.25 molar equivalents based on total aryl core content; optimized according to molecular alignment and phase behavior requirements.

    Downstream process integration

    • Introduced in nucleophilic substitution or halide exchange reactions at the initial functional core formation stage, ahead of alkoxy chain installation and final purification by preparative HPLC.

    Final product types

    • Liquid crystal compounds for TFT-LCD and OLED panels
    • Optically active mesogens for advanced displays and sensor arrays
    • Technical intermediates tailored for light modulation applications
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    Certification & Compliance
    More Introduction

    3-Cyanobenzyl Bromide: A Closer Look from the Manufacturer’s Bench

    Our Experience with 3-Cyanobenzyl Bromide

    On the production floor, 3-cyanobenzyl bromide stands out among benzyl halides. Its molecular formula C8H6BrN and CAS number 1714-29-0 track with what research chemists and upstream process engineers expect when dealing with aryl cyanides. As the team that synthesizes and packages this compound, we face the actual day-to-day details that shape purity, safety, and yield. Our best batches show high consistency and can be traced all the way back to the raw materials. We have committed process steps — from charge sequence to agitation speed — dialed in; that doesn’t come from reading datasheets, but from years of hands-on runs and a lot of troubleshooting. Every time we pull a sample off the reactor, analytical testing grounds us in the details that matter for customers working in pharma, agrochemical, and specialty intermediate sectors.

    Manufacturing Nuances: Why This Product Is Different

    3-cyanobenzyl bromide production isn’t just a generic halide swap. Compared to common benzyl bromide, or even 4-cyanobenzyl bromide, the meta positioning of the cyano group changes both reactivity and the process challenge. Starting from the right isomer ensures downstream performance. We synthesize using controlled bromination under specialized temperature profiles, since overtreatment leads to significant byproduct formation and reduction in assay. The cyano group draws electron density, making the bromomethyl group somewhat less reactive than in unsubstituted benzyl bromide. That has practical implications: nucleophilic substitutions show altered rates, and this matters in flows where customers need consistent performance, whether scaling coupling reactions or further functionalizing the ring.

    There is a temptation to treat substitutions on the aromatic ring as minor, but ignoring this can lead to unexpected issues. Some might wonder why meta- over para-cyano. The meta- isomer brings different steric and electronic outcomes, leading to specialty use cases in the synthesis of advanced pharmaceutical intermediates. A shift in isomer will create different final products during downstream synthesis, so for companies seeking a predictable building block for active ingredient development, isomer purity and precise identity make a direct difference. Our product isn’t just chemistry in a bottle; it reflects process rigor and attention on the smallest details, from the filtration and purification stage to the final packing in corrosion-resistant drums.

    Quality Built into Every Batch

    A process-verified batch of 3-cyanobenzyl bromide always looks clean, but that’s not enough. We built in high-resolution GC and NMR analysis to confirm not just the primary peak, but the absence of close-eluting or minutely different contaminants. 3-cyanobenzyl bromide is sensitive to moisture and light, so we cap and store it under nitrogen, in opaque HDPE drums that keep out UV. This process takes more time and effort, but long-term results matter. Labs that use off-the-shelf material with high moisture or low purity usually struggle in downstream reactions — for example, when quaternizing nitrogen heterocycles for drug targets, or during scale-up in pilot plants. Our approach mitigates these pain points so that quality starts at the source.

    End-use applications also call for different concentrations and formats, but we focus on providing the neat liquid at high purity, usually above 98%. If a pharma company requests a particular particle size or dilution, that’s handled with direct process adjustments, not bulk blending after the fact. From personal observation, custom preps need real communication with chemists, not just order takers. Chemical purity is directly tied to synthesis yield, and even minor degradation from light or atmospheric oxygen alters application performance. Companies running exploratory research, scale-up, or ongoing production shouldn’t risk variability, since end cost can eclipse any up-front savings from less-controlled material.

    Application Insights from the Shop Floor

    Talking about theory is easy, but actual demand for 3-cyanobenzyl bromide grew from years of seeing it solve specific synthetic steps that other benzyl halides just couldn’t. The cyano group on the meta position creates a unique synthon for heterocycle formation and aryl-alkyl couplings. Pharmaceutical companies look here for a core intermediate as they assemble complex molecules — for example, when developing drug candidates where substitution pattern determines metabolic fate or potency. Agrochemical researchers see utility for tailored herbicides or growth regulators, since the bromomethyl handles “click” readily yet leaves the cyano untouched through a range of subsequent steps.

    Over time, we saw several market trends repeat: Contract manufacturers wanted larger drum quantities to maintain project flows, while research teams preferred smaller volumes to maintain reactivity and precision. Handling also plays a role; the slightly higher density compared to comparable halides means pumps and metering systems need recalibration to avoid overdosing. We field requests for custom packing, and looking back, the bulk of professional chemists want less packaging friction and more assurance of batch-to-batch consistency. Inefficiency in supply quality — be it through caking, photodegradation, or unknown levels of residual solvent — causes delays further down the chain, so every batch ships after full COA review.

    Some applications require using the compound as a building block for substituted aromatic systems, while others look for the combination of nucleophilic aromatic substitution and the benzylic bromide’s capacity for further derivatization. In specialty chemical manufacturing, unique reactivity profiles open space for more creative synthetic designs. Our technical support staff — hands-on chemists with bench experience — can speak from dozens of real-world case studies, connecting the dots on which small impurity can cause a particular side reaction, or how a certain packing method helps maintain stability over longer transit times.

    Product Integrity: Reactivity and Handling Realities

    From our perspective, product integrity starts at raw materials and runs until the compound lands at the customer’s door. Moisture control, avoidance of strong bases, and protection from light sit at the heart of our process. In the plant, we handle all steps under ventilation, with PPE that goes beyond minimal box-ticking. Small volumes can feel innocuous but the benzylic bromide group confers strong alkylating properties — so each operation receives the same precautions as larger, more regulated aryl bromides. We see many issues arise from improper storage or transfer; once moisture enters, hydrolysis can compromise the reactive bromide, forming benzyl alcohol byproducts and hurting the efficiency at the next synthetic step.

    We often field customer questions about solubility, reactivity toward nucleophiles, and shelf life. This reflects the high degree of planning required further down the line. Even container liners matter: after years of seeing corrosion pitting, we moved away from basic metal containers toward high-density polyethylene with special gaskets. Occupational safety regulators inspect our lines and storage — not just for compliance, but to ensure that teams working with these intermediates can do so without avoidable risk.

    Comparisons with Other Aryl Halides

    Within our catalog, 3-cyanobenzyl bromide sits next to 4-cyanobenzyl bromide, benzyl chloride, and the more common benzyl bromide. Each variant affects downstream chemistry in tangible ways. The meta-cyano introduces both electronic withdrawal and unique spatial factors, so coupling and substitution reactions proceed at different rates compared to the para or ortho isomers. Selectivity during nucleophilic substitution, solubility in organic versus polar solvents, and stability profiles all diverge. This isn’t academic; every gram matters in a plant or high-throughput research facility, and misplaced faith in structural similarity has led to more than one unpleasant surprise.

    Other suppliers might emphasize the availability of “benzyl-type” halides, but process chemists using 3-cyanobenzyl bromide recognize that subtle shifts in electron density alter both the yields and the byproduct profiles in key steps. As one example from our customer feedback, attempts to substitute 4-cyano for 3-cyano in certain pharmacophore construction often led to diminished selectivity, unexpected rearrangement, or outright failure to produce the target molecule. Our process, as a result, places a premium on isomeric precision and clear labeling, making sure chemists get exactly what their synthesis plans call for — and not a generic substitute. From our standpoint, swapping to a less controlled product creates more risk than reward.

    Challenges in Scaling Production

    Scaling from kilo lab to multi-ton lots exposes hidden pitfalls. 3-cyanobenzyl bromide needs careful charge control and heat management, since exotherms from bromination steps can exceed safe operating windows if rushed. Early in development, we replaced old glass-lined reactors after two back-to-back contamination incidents. Nonmetallic contacting parts and a controlled nitrogen sweep now standardize batches, capping oxygen ingress and limiting partial hydrolysis — especially in humid weather. Our scale-up operators double-check all process readings, since even minor deviations in agitation or temperature alter the product profile, producing side compounds or lowering the selectivity that our customers expect.

    We also keep solvent residues tightly controlled, as leftover solvents or trace metallic impurities sneak through without diligent purification. Over multiple batches, we dialed in a final vacuum stripping protocol that preserves yield without raising environmental load. Through process monitoring, we check VOC emissions at multiple points, both to meet standards and to avoid penalties that drive up cost for every stakeholder. Solvent selection now considers waste disposal realities as much as reactivity, since some regulatory environments are tightening restrictions on aromatic solvent use and discharge.

    Our teams learned through repetition that the small details — calibration of holding tanks, careful validation of in-line filters, and regular equipment checks — save more money and time than any last-minute patch job after an off-spec batch. We invest in training operators to recognize subtle cues: discoloration, odor changes, and even slight shifts in viscosity mark early warnings of process drift. Upstream problems compound quickly at scale, so we put process discipline first.

    Safety and Regulatory Compliance

    Working with 3-cyanobenzyl bromide means ongoing engagement with industrial safety practices. As a manufacturer, we align with global safety standards that go well beyond minimum compliance. In our facilities, every batch gets logged and tracked for traceability, supported by updated SDS and hazard communication. While the compound itself is not subject to the most restrictive chemical regulations, it still requires careful handling due to its alkylating properties and potential occupational exposure.

    We invest in sealed, ventilated transfer systems to avoid accidental emissions, and personal monitoring devices capture any airborne bromine or organonitrogen traces. Our operators are enrolled in routine toxicology and exposure checkups, which we set up after learning that repeated low-level exposure, even to trace byproducts, can build up over years. This isn’t just about avoidance of regulatory fines; it speaks to long-term retention and well-being on the production line. Over multiple audits, we have shared incident histories and near-miss data with both our customers and internal teams, leading to better best practices across the board.

    Some jurisdictions have stepped up scrutiny of benzylic bromides, especially as aryl halides land on watchlists for environmental or occupational hazards. We maintain up-to-date records and third-party certification for our processes and provide clear, no-nonsense documentation to customers for their own regulatory submissions or internal reviews. Plant managers, lab coordinators, and safety officers who rely on this material benefit from knowing their supply chain partner is transparent about process and incident data.

    Solving the Most Common Customer Problems

    Based on hundreds of conversations with users, troubles typically start with storage, shelf life, and reactivity consistency. Laboratories running high-value syntheses face stalled reactions or excessive side products if the material absorbs moisture during shipping or waits too long before use. Our solution was to test multiple packing formats, gravitating toward nitrogen-filled, light-blocking containers. Experience showed that even the tightest cap, without inert gas, could let in enough moisture in a humid warehouse to degrade product over a month or so.

    We ran longitudinal stability studies in real-world customer warehouses and spotted degradation pathways. Insights gained prompted us to set clear storage recommendations and work with our logistics partners to shave days off average transit. By building in information exchange with customer process chemists, we adapt pack sizes and shipping frequency, preventing long-term inventory buildup and keeping reactive content high. In many cases, chemists appreciate our openness in batch data and stability info, which helps them plan around sensitive process steps.

    Another key pain point: mismatched reactivity, especially during process scale-up. Researchers often optimize reactions with small flask samples, only to confront unexpected byproducts when running hundreds of liters. Our technical consultations spotlight these “hidden variation” sources. Even packing material can affect trace contaminant profiles, so we share shipping test results with larger customers to avoid friction during critical campaigns. Clear answers, not scripted reassurances, provide peace of mind during urgent project timelines.

    Commitment to Transparency and Ongoing Improvement

    Our teams run regular review cycles on both process efficiency and secondary impacts, including post-market feedback from end-users. Years ago, our chemists realized that incremental gains in handling and purity directly supported customers’ bottom lines — fewer failed batches, less process downtime, and easier regulatory paperwork. We carry out process improvements not only in the core steps but also in how we train plant teams and document QA results. Every time a technical complaint comes back, we kick off a full root-cause investigation, which sometimes leads to small adjustments in purification or filling equipment.

    We believe in open dialogue with both purchasing agents and frontline chemists. This approach has uncovered subtle friction points — for example, how a marginally better drying step translates to higher yields at the customer’s plant, or how reducing particulate content prevented clogged drops during large-volume additions. Our continuous learning culture means our material reflects not only current regulatory expectations but also the realities of practical chemical synthesis. That commitment sets our product apart more than any specification sheet can capture.

    Looking Ahead: Supporting Customers through Chemical Innovation

    The landscape for specialized intermediates like 3-cyanobenzyl bromide keeps evolving, driven by demands for higher purity, easier handling, and greater supply chain transparency. Our decades of experience crafting this and related aryl halides give us a unique vantage point — we understand exactly how small chemistry details ripple outward to impact full-scale industrial processes. By staying engaged with emerging trends in pharma and agrochemical R&D, we proactively adjust processes to meet new environmental and functional demands.

    We invest in employee development, process automation, and open R&D collaboration, so that we can deliver solutions as market needs shift. Where others might offer a catalog list, we see each drum or flask as a partnership — built on communication, technical integrity, and investment in long-term improvement. In a world that increasingly values traceability, quality, and actionable supply information, our commitment to hands-on process control keeps our customers’ operations running efficiently.