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4-Fluorobenzyl Bromide

    • Product Name 4-Fluorobenzyl Bromide
    • Alias p-Fluorobenzyl bromide
    • Einecs 207-317-7
    • 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

    322245

    Chemical Name 4-Fluorobenzyl Bromide
    Cas Number 459-32-5
    Molecular Formula C7H6BrF
    Molecular Weight 189.03 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 79-80 °C at 14 mmHg
    Density 1.519 g/cm³ at 25 °C
    Melting Point -20 °C
    Refractive Index 1.543
    Flash Point 99 °C
    Synonyms p-Fluorobenzyl bromide, 1-(Bromomethyl)-4-fluorobenzene
    Pubchem Cid 68648

    As an accredited 4-Fluorobenzyl Bromide 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, tightly sealed with a white screw cap; labeled with product name, hazard symbols, and handling instructions.
    Shipping 4-Fluorobenzyl Bromide is shipped in tightly sealed, chemically-resistant containers to prevent leaks and contamination. It is packaged according to international hazardous materials regulations, typically with cushioning and absorbent materials. The shipment includes appropriate labeling and documentation, and is transported by certified carriers specializing in chemical and hazardous goods handling.
    Storage 4-Fluorobenzyl bromide should be stored in a tightly closed container, away from moisture, heat, and direct sunlight, in a cool, dry, and well-ventilated area. It must be kept away from incompatible materials such as strong bases, oxidizers, and reducing agents. Use appropriate secondary containment to prevent leaks and ensure proper labeling according to local chemical safety regulations.
    Application of 4-Fluorobenzyl Bromide

    Applications of 4-Fluorobenzyl Bromide in Industrial Manufacturing

    We specialize in supplying 4-Fluorobenzyl Bromide as an advanced aromatic building block suited for precise integration into specialized chemical synthesis chains. Its fluorinated benzyl structure is essential in targeted downstream manufacturing sectors, where strict regulatory oversight, technical formulation accuracy, and consistent process control are key to commercial product quality and differentiation. Below, we outline its core application scenarios, reflecting verified industrial practice.

    1. Pharmaceutical Intermediates for Active Ingredient Synthesis

    API manufacturers employ 4-Fluorobenzyl Bromide as a critical alkylating agent in multi-step routes to synthesize diverse fluoroaromatic scaffolds, especially for central nervous system (CNS) drugs and anticancer compounds. Its benzylic structure enables reliable substitution reactions, facilitating downstream reactions for bioactive targets while maintaining compliance with regulatory impurity thresholds. We deliver consistent purity tailored for high-performance reactor integration and traceability under global pharmaceutical requirements.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP) substance monographs
    • Drug Master File (DMF) support documentation for regulatory submission
    • EN ISO 9001:2015 Certified Quality Management Systems

    Typical usage ratio

    • Employed at 1.0–2.5 molar equivalents in alkylation or substitution step, relative to nucleophilic reagent; specific ratio determined by API synthetic yield, impurity profile, and scaling factors evaluated in process development.

    Downstream process integration

    • Added as electrophilic intermediate in stagewise batch or continuous reactor operation post-initial fluorination
    • Controlled addition to minimize side reaction formation; in-situ monitoring of halide displacement and conversion

    Final product types

    • Fluorinated API intermediates for CNS, analgesic, or oncology compounds
    • Pilot- and commercial-scale drug substance batches
    • Reference standards for impurity/degradation pathway studies

    2. Agrochemical Intermediate Production

    Leading agrochemical synthesis plants integrate 4-Fluorobenzyl Bromide as a key precursor for the fluorinated side chains required in modern fungicides and herbicides. Its controlled reactivity enables clean coupling reactions and subsequent transformation into active agents, ensuring downstream process reliability and compliance with agricultural regulatory demands for trace-level by-products and residuals.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for pesticide active ingredient development
    • FAO/WHO Food and Agriculture Organization specifications for pesticide ingredients
    • REACH (EC No 1907/2006) substance registration for EU market
    • ISO 9001 Quality Management for plant protection chemical supply chain

    Typical usage ratio

    • Used at 0.8–1.2 mole equivalents per nucleophile in key alkylation or arylation steps, adjusted for product selectivity and downstream activity

    Downstream process integration

    • Dosed during targeted alkylation processes for fluorinated ether or ester linkage formation (often within temperature-controlled reactors)
    • Incorporated pre-purification of intermediates prior to heterocycle assembly or sulfur incorporation

    Final product types

    • Active ingredient intermediates for triazole fungicides
    • Building blocks for new-generation selective herbicides
    • Fluorinated substructures for crop protection R&D

    3. Aroma & Fragrance Ingredient Synthesis

    Fragrance ingredient manufacturers utilize 4-Fluorobenzyl Bromide for the production of fluorinated aromatic notes, enabling the design of novel top and base notes that exhibit controlled volatility and stability under use conditions. The material’s reactivity is managed in accordance with IFRA specifications and strict flavor safety protocols, enabling selective functionalization for downstream esterification or etherification steps without off-odor impact.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • European Regulation (EC) No 1223/2009 on Cosmetic Products
    • ISO 9235: Aromatic Natural Raw Materials - Vocabulary
    • In-house GC–MS purity and contaminant profiling protocols

    Typical usage ratio

    • 0.5–3.0 wt% of reaction batch, ratio fine-tuned for intended functional group conversion and target olfactory threshold in end application

    Downstream process integration

    • Introduced as aromatic alkylating agent in batch ester, ketone, or ether synthesis under monitored conditions
    • Post-synthesis purification (fractional distillation or crystallization) to meet IFRA and end-user purity benchmarks

    Final product types

    • Fluorinated aromatic aldehydes, alcohols, and esters as specialty fragrance ingredients
    • Base notes for perfumery and luxury personal care applications
    • Encapsulated fragrance microcapsules for functional consumer goods

    4. Advanced Polymer and Specialty Monomer Synthesis

    In high-performance polymer manufacturing, 4-Fluorobenzyl Bromide serves as a functional monomer precursor or reactive chain modifier in specialty polymers where selective fluorination imparts improved thermal stability, chemical resistance, and distinct dielectric properties. Process lines maintain stringent batch-to-batch traceability and impurity control to meet polymer industry reliability standards, especially in electronics or medical device materials production.

    Industry compliance standards

    • ISO 9001:2015 for Synthetic Resin and Polymer Additives
    • RoHS Directive 2011/65/EU for electronics-grade polymers
    • UL 94 standard for flame retardance (where required)
    • ASTM D638 for mechanical property evaluation of polymers

    Typical usage ratio

    • 0.1–2.0 mole% relative to total monomer feed; composition customized by chain length, desired thermal properties, and regulatory end-use limits

    Downstream process integration

    • Fed into co-polymerization reactors as reactive comonomer or side group modifier during continuous or staged polymer synthesis
    • Followed by post-polymerization purification, drying, and compounding appropriate to final polymer grade

    Final product types

    • High-performance specialty copolymers for electronics encapsulation
    • Medical device-grade fluorinated polymers
    • Fluorinated resins for coatings and engineered plastics

    5. Fine Chemical Research and Specialty Intermediate Synthesis

    In specialty and custom synthesis laboratories, researchers utilize 4-Fluorobenzyl Bromide for constructing advanced intermediates required in target molecule discovery, functional group mapping, and reaction mechanism elucidation. Its clean reactivity and defined impurity profile allow integration into complex synthesis sequences under controlled conditions subject to analytical verification and compliance with laboratory-scale safety and purity requirements.

    Industry compliance standards

    • ISO/IEC 17025:2017 for laboratory competence in analytical verification
    • OSHA Laboratory Safety Standard 29 CFR 1910.1450 (for US-based labs)
    • REACH EU 1907/2006 Annex XVII (restricted uses/certified supply)
    • GLP (Good Laboratory Practice) for traceable experimental work

    Typical usage ratio

    • 0.5–1.5 equivalents per target functional group on substrate; dosage varies by new molecule structure and yield optimization route

    Downstream process integration

    • Applied in nucleophilic substitution and cross-coupling reactions (e.g., Suzuki, Buchwald) monitored on small scale by TLC, NMR, or LC-MS
    • Purified using chromatographic and crystallization methods for further synthetic steps or mechanistic analysis

    Final product types

    • Reference intermediates for academic or pre-commercial R&D
    • Custom small-molecule markers and labeled compounds (including 19F-labels)
    • Building blocks for chemical biology toolkits
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    Certification & Compliance
    More Introduction

    Introducing 4-Fluorobenzyl Bromide: Manufacturer Perspective on a Key Intermediate

    The Value of 4-Fluorobenzyl Bromide in Modern Chemistry

    4-Fluorobenzyl bromide stands out as a reliable intermediate for building more advanced molecules. Working daily at the reactor bench, I see how a backbone like this finds its way into pharmaceuticals, agrochemicals, and specialty chemicals. In just a few decades, 4-fluorobenzyl bromide shifted from lab oddity to an indispensable toolkit entry, especially for routes where classical benzyl substitutes wouldn’t deliver the properties formulators demanded.

    Developing this compound consistently means understanding more than textbook structures; you deal with fine-tuning batch conditions, controlling moisture, and tracking purity closely to meet what research chemists need. Our direct role in synthesis puts us in a position to explain where each batch matches typical industry spec—pale yellow to colorless liquid, boiling in the 215–218 °C range, handled commonly at 98% or better purity, with minimal di- or tri-halogens and tight control on residual solvents.

    Quality, Reliability, and Physical Properties

    Over time, we have improved the crystallization process to enhance purity at scale. Our protocol avoids extended exposure to air and light thanks to direct transfer into sealed vessels from drying ovens. Sticking to precision temperature controls stops side-reactions at the bromination step—a small detail with big consequences for reactivity downstream.

    Each production run gets analytical validation through both GC and NMR, with IR monitoring for hydrolyzable impurities, since the bromo group on the ring is reactive and can easily hydrolyze in the presence of trace water. Sometimes even trusted suppliers miss the mark here, which frustrates anyone working in a downstream synthesis. Our experience shows that shipping freshly made 4-fluorobenzyl bromide always results in fewer customer complaints, so we prioritize minimal storage time.

    Visually speaking, this product presents as a clear to pale straw liquid at room temperature, moving toward a crystalline form in cooler storage. Some chemists prefer it stored cold, out of light, and under nitrogen. Knowing how customers handle the material shapes our filling and packing. Bottles get purged thoroughly, sealed with PTFE liners, and packaged to minimize oxygen ingress, which helps preserve the clean reactivity profile end-users trust.

    Manufacturing Challenges and Why Purity Matters

    Each year, more clients ask for in-depth process data beyond standard COAs. We stick to open reporting of our actual in-process controls—batch temperatures, pH profiles at each stage, explicit solvent choices—so academic and industrial chemists access more than just numerical specs.

    Trace side-products cause headaches: unpurified 4-fluorobenzyl bromide can produce colored impurities or unpredictable reactivity, especially in palladium-mediated cross-coupling. After several years handling multiple arylbenzyl bromides, we observed 4-fluorobenzyl bromide especially prone to forming benzyl alcohol or dibrominated byproducts if not handled well. Chemists downstream notice the difference. Final API synthesis quality often tracks directly to the cleanness of our bromide precursor.

    Older reports underestimate the cumulative effect trace impurities have in scale-up. On pilot lines, clients describe lower yields or troublesome exotherms linked to micrograms of left-behind byproducts. Our lab team remains in constant dialogue with their R&D to tweak our purification stages, raising thresholds based on the strings of actual HPLC or GC-MS chromatograms. By acting on feedback loops between manufacturing and customer R&D, we move past batch-to-batch unpredictability that plagued the market ten years ago.

    Comparison: 4-Fluorobenzyl Bromide and Its Conventional Counterparts

    Take the standard benzyl bromide—ubiquitous, less tricky to manufacture in bulk, broadly forgiving in terms of impurities. Yet for many synthetics, the fluorinated version opens doors typical benzyls never could. That single fluorine grants extra stability or selectivity in key reactions, and subtle tuning of electronic character changes downstream reactivity significantly. A recurring story in our orders involves customers hitting a wall with basic benzyl bromide and switching to our 4-fluoro version for either increased selectivity in nucleophilic substitutions or superior performance in introducing other functional groups at the benzylic site.

    4-Fluorobenzyl chloride appears on some lists as a cheaper option, but that halide doesn’t offer the same reactivity or the fine-tuned transition-metal compatibility that bromide does. Chloride versions react slower and require harsher conditions, ruling them out for sensitive substrates. In regulated pharmaceutical routes, the cleanliness and tractability of the bromo derivative justify its extra cost. I’ve seen multiple process teams trade up from 4-fluorobenzyl chloride or even traditional benzyl bromide when facing problematic conversions or undesired rearrangements.

    Daily Use Cases in Industry and Research

    Handling requests from drug discovery teams has always provided the clearest window into the true value of this intermediate. Medicinal chemists rely on our batches for the convenience and high conversion rates they need in benzylic alkylation and etherification. Our feedback cycle often begins after a team in-licenses a route bound for IND filings, where available precursors win contracts only if they meet documented process safety and analytical requirements.

    Outside pharmaceuticals, we serve agrochemical startups synthesizing advanced crop protection agents that depend on the electron-rich, fluorinated benzyl moiety. Their needs demand not just high-purity intermediates but timely delivery to meet narrow seasonal development cycles. For these customers, downtime waiting for new batches halts entire field studies. As operators, we rarely get a second chance if the material isn’t right.

    Research scale users benefit from our production whenever their targets demand tailored groups matched to the electronics of a 4-fluorobenzyl unit. Academics pushing new catalysis protocols ask for the tightest impurity profiles. We run tailored lots for unusual requests, for example, customizing solvents for improved crystallinity, or tweaking the isolation step to reduce residual halide levels.

    Handling, Safety, and Regulatory Awareness

    Contact with 4-fluorobenzyl bromide means treating it with respect in our lab and production floor. Our shifts look out for volatile fumes when transferring between vessels, and we always run air monitoring and glove checks. On a busy day, no one wants to stop for remediation, so we check and double-check seals, sample ports, and tank headspace before running the process. We remind our clients to review local handling rules. Several years back, a spill from poorly maintained containers resulted in unnecessary downtime while we cleaned bromine traces out of the ventilation. The lesson stuck: packaging reviewed and fixed for all future shipments.

    From a regulatory angle, we update our substance dossier annually with our latest analytical evidence. Our documentation traces origin all the way to raw materials. Most recipients appreciate getting not only a product spec but a transparent process outline; this transparency supports both local audits and internal process validation. For scale-up runs destined for medical or agricultural products, our team keeps careful chain-of-custody records—every drum, every label logged at dispatch.

    Why Direct Manufacturer Supply Makes a Difference

    Experience in the trenches underscores why chemists and purchasing teams lean towards factory-direct supply. Orders shipped from our plant route directly to the intended destination—no interim repackaging or handling that can degrade sensitive bromoaromatics or introduce uncertainty about storage conditions.

    Some buyers learn the hard way about off-spec or degraded material from repackagers, especially in summer when heat rapidly darkens bromides or stirs up container dust. We manage every batch through a standardized cold-chain transport policy with rapid turnaround. No one on our end benefits from leaving drums in transit—we prefer our materials move from reactor to customer without idle stopover, and we carry the risk until product is received and quality checked by the customer.

    We recognize market competition means end-users have options, but repeat business grows where predictability delivers. Bronzed drums and off-color shippers stick out alongside the pristine bottles shipped within hours of QA release.

    Environmental and Waste Management Commitment

    No chemistry operation these days ignores the challenge of handling hazardous halogenated waste. Runoff from mishandled bromides causes both regulatory and environmental headaches. Over multiple audits, we invested in an on-site incineration system, and our waste bromine now gets recaptured for use in plant sanitation rather than released. Each lot’s byproduct stream passes through neutralization, then secondary analysis before we release any effluent.

    We share updates with our largest clients about stepwise improvements to increase yield with lower waste output. More than regulatory compliance, it reflects the responsibility all manufacturers bear to communities that border chemical production. Within our team, focusing on waste management means everyone stays aware their job impacts more than bottom-line results.

    Continuous Improvement and Exploration of New Applications

    Factory operations, just like the chemistry they support, need continual improvement. Our R&D group reviews each campaign and identifies steps where energy use can shrink and yield edges higher. We currently experiment with process intensification—temperature-controlled microreactors and improved solvent cycles—to reduce both resource consumption and cycle time.

    Customer feedback often uncovers new reaction types that highlight unfamiliar aspects of 4-fluorobenzyl bromide reactivity. One recent request from a biotech group led us to adapt for a cross-coupling route that replaced older, less efficient metal-catalyzed steps. Flexibility in our reaction and purification systems lets us redirect a portion of each production campaign to serve specialized routes with very tight impurity constraints.

    The world of proprietary process chemistry moves rapidly, and although 4-fluorobenzyl bromide has cemented itself as a common intermediate, ongoing dialogue with users—both large industrial and academic—pushes us to revisit legacy assumptions. For example, our latest data shows even trace amounts of 2-fluorobenzyl bromide isomer can skew reaction selectivity. Our plant’s upgraded chromatography detection helps us stay ahead of the specifications curve. Experience underlines that only vigilant analytical controls secure premium outcomes in modern organic synthesis.

    The Path Forward: Building on Real-World Experience

    Not every day’s production is flawless, but our plant ethos focuses on learning from hiccups instead of brushing them aside. Each in-process problem, from scale-up crystallization failures to shipment delays, feeds back into our SOP updating and training cycles. Several years ago, a recurring bottleneck at the solvent swap phase forced a significant investment in real-time monitoring equipment. That investment paid dividends over the following campaigns, cutting both waste and rework by nearly half.

    We see a future where 4-fluorobenzyl bromide’s applications only broaden, especially as synthetic methods move to greener, more selective transformations. Whether your interest lies in traditional SN2 alkylations or novel C–C or C–N couplings, the quality of the benzylic halide remains a non-negotiable input. By anchoring our production strategy in hands-on process oversight and rigorous quality controls, we support the next wave of molecular innovation coming out of both research and industry labs.

    Engagement doesn’t end with batch release or parcel shipment. Our technical staff fields requests for modified lots, process data, application notes, and advice about best storage and handling practices. In our experience, the closer our relationships with customers, the more rapidly we adapt to their evolving chemistry targets.

    Conclusion: Partnering for Better Chemistry

    Decades working at the intersection of plant operations and research support drive home the simple truth: high-quality intermediates shape success rates at every step beyond the plant. The story of 4-fluorobenzyl bromide traces more than a supply chain; it tells how direct dialogue between manufacturer and user creates a feedback loop that leads to better, more reliable chemistry.

    From our vantage point, nothing surpasses the peace of mind that comes from knowing what’s in each drum—supported by real process data and open communication about what makes each batch fit for purpose. As manufacturing partners, our role stretches far beyond the production lot; we see ourselves as extension of our customer’s lab bench, supporting discoveries made possible by materials produced with care, skill, and the right mix of tradition and innovation.