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1-Bromo-4-Fluoronaphthalene

    • Product Name 1-Bromo-4-Fluoronaphthalene
    • Alias 1-bromo-4-fluoro-naphthalene
    • Einecs 629-001-6
    • 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

    158861

    Chemical Name 1-Bromo-4-Fluoronaphthalene
    Molecular Formula C10H6BrF
    Molecular Weight 225.06 g/mol
    Cas Number 321-93-7
    Appearance Colorless to light yellow liquid
    Boiling Point 280-282 °C
    Density 1.578 g/cm3
    Refractive Index 1.624
    Purity Typically >98%
    Smiles Brc1cccc2ccc(F)cc12
    Pubchem Cid 117969
    Flash Point 126 °C
    Solubility Insoluble in water, soluble in organic solvents
    Storage Conditions Store at room temperature, tightly sealed

    As an accredited 1-Bromo-4-Fluoronaphthalene 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 of 1-Bromo-4-Fluoronaphthalene, sealed with a red screw cap and labeled with safety information.
    Shipping 1-Bromo-4-Fluoronaphthalene is typically shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material due to its chemical properties. Shipping must comply with local, national, and international regulations, including proper labeling, packaging, and transportation by licensed carriers experienced in handling chemicals.
    Storage Store 1-Bromo-4-Fluoronaphthalene in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, protected from direct sunlight and sources of ignition. Clearly label the container and ensure appropriate chemical safety measures are in place, including secondary containment and restricted access to authorized personnel.
    Application of 1-Bromo-4-Fluoronaphthalene

    Applications of 1-Bromo-4-Fluoronaphthalene in Industrial Manufacturing

    We supply 1-Bromo-4-Fluoronaphthalene as a high-purity intermediate to pharmaceutical, agrochemical, dye, and electronic materials industries. The following industrial scenarios illustrate established downstream applications supported by real market demand, regulatory standards, and technical process integration using this specialized compound.

    1. Pharmaceutical Intermediate Synthesis

    This material serves as a key scaffold in the multi-step synthesis of specialty heterocyclic compounds for advanced pharmaceutical active ingredients, especially those requiring fluorinated aromatic structures for enhanced metabolic stability and bioavailability. Medicinal chemistry teams incorporate it at early or mid-stages for constructing complex drug candidates, with downstream manufacturers focusing on fluorine-substituted APIs targeting central nervous system or oncology therapies.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) Chapter <795>, <1078>
    • European Pharmacopoeia (Ph. Eur.)
    • Safety evaluations per REACH and TSCA for industrial intermediates

    Typical usage ratio

    • Employ in 1–8 mol% of total synthetic mass, with precise ratio adjusted based on target yield and stage-of-synthesis route requirements. Batch size and target molecule substitution govern loading.

    Downstream process integration

    • Most downstream users introduce via palladium- or copper-catalyzed coupling (e.g., Suzuki, Buchwald–Hartwig) after initial halogen exchange or direct nucleophilic substitution protocols. Handling with dry solvents and inert atmosphere requirements is standard.

    Final product types

    • Fluoro-naphthylamine building blocks
    • Central nervous system API intermediates
    • Oncology-targeted small-molecule drug leads
    • Late-stage intermediates for branded pharmaceutical R&D

    2. Agrochemical Synthesis (Herbicides and Fungicides)

    Major agrochemical manufacturers source this compound for specific substitution patterns in the development of next-generation herbicides and fungicides, where the unique naphthalene skeleton and fluorine atom improve environmental stability and biological selectivity. Used mainly in the preparation of intermediates required for patent-protected, bioactive molecules, its functionality streamlines the design of active agro-ingredients with regulated residue profiles.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 Quality Management
    • Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market (Europe)

    Typical usage ratio

    • Incorporate between 0.5–3.5 mol% based on downstream target compound structure and total batch mass; actual loading referenced against final biological activity goals and process scalability evaluations.

    Downstream process integration

    • Add intermediate to nucleophilic aromatic substitution or electrophilic metal-catalyzed coupling stages, allowing introduction of crop-specific functional groups with precise regioselectivity in formulation labs and pilot plants.

    Final product types

    • Fluorinated herbicidal intermediates
    • Systemic fungicide cores (e.g., naphthalene-carboxamides)
    • Specialty pesticide actives with custom residue profiles
    • Pre-commercial samples for biological field trials

    3. Advanced Dye and Pigment Synthesis

    Dye and pigment makers utilize 1-Bromo-4-Fluoronaphthalene in specialty synthesis programs aiming for high-performance coloration, particularly in high-end textile and plastics coloration where photostability and color strength are determined by selective halogenated naphthalene inclusion. The compound enables extended conjugation and targeted fluorination strategies, used only where high color fastness and thermal stability must be achieved for demanding applications such as automotive plastics or fiber-reactive textile dyes.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile dyes, input level)
    • EN 71-3 Safety of Toys (pigments for plastic coloration)
    • ISO 9001:2015, Quality Management Systems
    • EU REACH Annex XIV/XVII (hazardous substance control)

    Typical usage ratio

    • Loaded typically at 1–7 mol% in step-growth dye precursor mixtures; percent adjusted based on desired hue intensity, solubility in substrate, and customer-specific lightfastness tests.

    Downstream process integration

    • Feed directly into azo coupling or condensation reactions during masterbatch pigment production; high-temperature or solvent-based processing lines require staged material addition for uniform product performance.

    Final product types

    • High-fastness textile dyes (e.g., fiber-reactive naphthalene dyes)
    • Specialty organic pigments for plastics
    • UV-resistant coatings colorants
    • Custom pigment dispersions for inkjet inks

    4. OLED and Electronic Material Intermediates

    Producers of organic electronics introduce this molecule in the early development of naphthalene-based electron transport layers and light-emitting compounds for organic light-emitting diodes (OLED) and related organic semiconductors. The fluorinated naphthalene motif elevates charge mobility and device stability, and selection of this intermediate forms part of the design of high-performance aromatic building blocks for optoelectronic device materials.

    Industry compliance standards

    • IEC 62341-1-1: OLED Displays – Performance Testing
    • RoHS Directive 2011/65/EU (EU Restriction of Hazardous Substances)
    • ISO 14001:2015 Environmental Management
    • JIS C 62741 for Japanese OLED materials

    Typical usage ratio

    • Integrated at 0.8–4 mol% in organic synthesis sequences; loading depends on targeted optical and electrical properties specified by downstream device engineers and customer QC protocols for batch uniformity.

    Downstream process integration

    • Introduced via solution-phase or solid-phase coupling chemistry to form naphthalene-based monomers, which are then polymerized or further functionalized for electrode/injection/host layers in device assembly lines.

    Final product types

    • Naphthalene-based hole or electron transport materials
    • Organic light-emitting diode (OLED) intermediates
    • Semi-conducting polymers for flexible displays
    • Photoresist materials for advanced photolithography
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    Certification & Compliance
    More Introduction

    1-Bromo-4-Fluoronaphthalene: Making a Difference Where Precision Counts

    Bringing 1-Bromo-4-Fluoronaphthalene to Industry—Our Perspective

    Our facility has been focused on the synthesis and purification of naphthalene derivatives for over two decades. Through this experience, certain compounds stand out—not just for their rarity, but for the kind of reliability and quality that separates “good enough” chemistry from truly precise results. 1-Bromo-4-Fluoronaphthalene (CAS No. 573-12-8), which we label as Model BFNA-400 for internal tracking, sits firmly in that category. It is not merely another halogenated aromatic; it plays a crucial part in a growing branch of advanced material development and pharmaceutical research because of its dual functionalization.

    On our shop floors, the attention to detail during every batch of this compound goes beyond box-checking. Each step of production, from initial naphthalene ring selection to the control of temperature and halogen introduction, answers to precise standards. This is critical because users—often R&D teams trying to build new OLED emitters, crop protection agents, or synthesize pharmaceutical intermediates—count on a product that will not introduce “ghost peaks” or impurities into their work. Impurities, even at ppm levels, tend to affect step yields and muddy analytical profiles. Consistency here becomes a direct contributor to real-world innovation and commercially viable scale-up.

    Why Industry Demands This Compound

    The structure of 1-Bromo-4-Fluoronaphthalene offers separate points for cross-coupling and functional group manipulations. Its bromine atom unlocks Suzuki, Stille, and Heck couplings with high selectivity, while the fluorine atom’s presence enables specific substitutions and influences the bioavailability or electronic behavior of the resulting molecule. In our own collaborations with electronics manufacturers, researchers consistently prefer the 1-bromo-4-fluoro variant over mono-halogenated naphthalenes, especially when they want better control of regiochemistry in downstream synthesis. The compound finds a solid footing in areas like OLED intermediates, specialty dyes, and active pharmaceutical ingredient (API) development because of this flexibility.

    We notice repeat demand from the fine chemicals sector, where the additional fluorine atom allows tuning of electron distribution on the naphthalene ring—a subtlety that often means the difference between a target compound performing as modeled or stalling in the test phase. Even as analysts focus on new halogenated frameworks, our customers report that switching from simple 1-bromonaphthalene to this difunctionalized version cuts down on the number of synthetic steps and, occasionally, overall raw material costs.

    What Sets Our 1-Bromo-4-Fluoronaphthalene Apart

    The majority of chemical suppliers out there rely on bulk halogenation and simple chromatography to produce 1-Bromo-4-Fluoronaphthalene. Our plant approaches this differently, investing in higher-purity bromine and fluorinating agents, and running additional controls to ensure single-isomer selectivity. We run the compound through multi-stage purification: prep-scale GC and HPLC verification ensures that each keg or drum delivers under 0.2% total impurities by area. End-users, particularly in pharmaceutical labs, share that this eliminates the need for costly pre-processing and helps maintain reproducibility of their own reactions. In the early 2010s, we caught on to the trend for lower-metal content in naphthalene intermediates, and our current product falls well within stringent global standards for palladium, copper, and iron residues.

    Shipping and handling practices reflect the compound’s sensitivity, especially since the bromo and fluoro moieties can cause reactivity with certain packaging. Our containers use fluoropolymer linings and moisture guards. During a critical shipment for a U.S. agrochemical client, this protocol prevented cross-contamination that would have ruined weeks of downstream research. Our investment in packaging paid off in both customer satisfaction and actual product performance.

    Differences That Shape Outcomes

    1-Bromo-4-Fluoronaphthalene does not behave the same way as its close relatives like 1-bromonaphthalene or 1-fluoronaphthalene. We have compared these compounds side by side in various carbon coupling, nucleophilic substitution, and electrophilic aromatic reaction trials. The presence of both a bromine and a fluorine atom at specified ortho/para positions provides more options for downstream modification. Chemists get a compound resilient to harsh conditions that remains reactive enough for precise transformations. Sometimes our partners in OLED research require tightly controlled emission properties in their final product. They see measurable improvements—higher color purity and operational lifespan—when starting their synthesis from our 1-Bromo-4-Fluoronaphthalene versus single-halide naphthalene sources.

    Pharmaceutical researchers give us feedback that the difunctionalized nature accelerates their lead compound optimization. By using a single intermediate with two activation sites, they limit the number of protection and deprotection steps and cut timelines, especially during route scouting stages. If they started with 1-bromonaphthalene, they would spend extra time and budget on post-modification or ring activation strategies.

    How Model BFNA-400 Supports Advanced Applications

    The demand for next-generation materials like high-definition OLED screens, efficient dye-sensitized solar cells, and new herbicide candidates places pressure on chemical suppliers to keep up with rising purity and low impurity requirements. 1-Bromo-4-Fluoronaphthalene, produced to meet ≥99% GC purity, consistently meets or exceeds these expectations, even as specs from end-users narrow year by year. Our own plant data and third-party batch analyses reinforce this compound’s suitability for regulated and semi-regulated sectors.

    We have seen this product open doors on many occasions—our advanced ceramics customers developed brighter phosphors; pigment manufacturers enhanced pigment fastness in specialty inks; pharmaceutical partners progressed candidate molecules into preclinical trials faster using intermediates synthesized from this material. There simply aren’t many other building blocks that support such a range while meeting demanding impurity control.

    Nuances in Sourcing and Handling

    Raw material sourcing influences every aspect of the finished product. We only accept precursors from verified suppliers managing their own halogen separation and ring isomerization protocols. When a single precursor shipment failed our NMR fingerprint check, we halted batch processing straightaway, even though it meant missing an order deadline. Such decisions protect our customers’ timelines long term. No matter what supply chain fluctuations look like, this approach builds confidence in every lot we send out.

    Handling a dual-halide aromatic brings additional challenges compared to simpler naphthalene derivatives. The process team spends significant effort mitigating moisture ingress and controlling exothermic stages during bromination and fluorination. Our doors are always open for customer site audits, and we frequently host technical teams from partner companies. Showcasing our safety, documentation, and process oversight first-hand gives users a sense of the integrity baked into every batch.

    Lessons Learned From Industry Feedback

    Direct feedback from material scientists and process chemists led us to improve our process controls for this material even further. For example, one customer was using our product as a precursor in a high-value API, but discovered that trace iron contamination was causing colored byproducts during a late-stage step. Through trace analytics and retooling of our own cleaning protocols and filtration systems, we were able to reduce metal contaminants from <10 ppm to under 2 ppm. This update moved the needle for several users with similar requirements.

    We have also learned that batch consistency means more than just purity: isomer ratio, trace solvent levels, and particle size all influence downstream performance, particularly in scale-up situations. Some clients in dye-sensitized applications need sub-100 ppm water content to avoid hydrolysis or color instability. Responsive changes to our in-process drying cycles and packaging methods addressed this need without raising the overall cost per kilogram.

    Sustainability and Future Trends

    The broader chemical sector’s push for sustainable production and safe handling has changed how we approach synthesis pathways. Halogen reagents, particularly bromine and fluorine sources, require rigorous containment and waste stream monitoring. Our plant has invested in closed-loop halogen recovery and in-plant absorption systems; by recapturing halide gases, we keep emissions well under legal limits and drastically cut raw material consumption. Last year alone, our process redesign helped us reclaim nearly 80% of spent halides and prevented their release into the surrounding environment.

    We participate in industry-wide initiatives to develop safer halogenation catalysts and greener solvents, in part because the well-being of our own operators matters. By shifting to lower-toxicity base fluids in post-reaction washes and recycling solvent streams whenever feasible, we have minimized off-site waste shipments and ensured a safer workspace for our team. These efforts translate into a more reliable and responsible source product for customers facing growing regulatory and sustainability expectations.

    Comparisons to Competing Products

    Some buyers seek to compare 1-Bromo-4-Fluoronaphthalene to other halogenated naphthalenes or to products sourced from catalog houses. Through our own evaluations and user reports, a few key points emerge. Mono-halogenated products lack the dual-point reactivity of this material and often require additional synthetic steps, reducing the efficiency of multi-step target preparations. Meanwhile, lower-graded or commodity-sourced material tends to introduce trace contaminants due to broader process tolerances. End-users often discover that such small differences balloon in importance during high-throughput or regulated work.

    Our clients choosing between different halogen positions on the aromatic core frequently observe better yield and selectivity in cross-coupling reactions using the 1-bromo-4-fluoro configuration. We have run proprietary reaction series to optimize ligand/catalyst pairs for this substrate, and the results consistently lead to cleaner workups and easier purification compared to counterparts like 2-bromo-6-fluoronaphthalene or even 1,4-dibromonaphthalene. Because our product’s structure delivers optimal reactivity balance—not overly activated, but not so inert as to resist desired transformations—chemists can scale up with fewer surprises and less need for process troubleshooting.

    As a Manufacturer—Why These Details Matter

    Clients rarely see the floor meetings, the night shift corrections, or the pre-dawn quality control samples that drive each batch toward specification. Behind every tote shipped, teams at our plant challenge themselves to think through not just the composition, but the context of use. If an OLED chemist needs a sharper emission profile, our variable-purity runs and low-metal options offer a meaningful difference. For pharmaceutical teams chasing tight impurity control, our robust documentation and transparent analytics help fulfill regulatory submissions without a scramble. This all traces back to the choices made in synthesis planning, purification, and logistical coordination.

    End applications are moving beyond traditional sectors; each year we field new technical questions from battery manufacturers, material science teams, and advanced polymer researchers. The push for finer control, lower detection limits, and scalable performance in demanding environments means every upstream detail matters. Most of the time, success starts with an intermediate that “just works”—one that respects the dollars, days, and discipline invested by downstream partners. 1-Bromo-4-Fluoronaphthalene shines here not only for its chemical advantages but for the trust it continues to build batch after batch.

    Parting Words from the Production Floor

    Where some might see a commodity, operators, chemists, and engineers at our plant recognize the role 1-Bromo-4-Fluoronaphthalene plays in technological progress. Achieving sharp specifications and maintaining supply consistency demands commitment. Customers come to us because shortcuts create new headaches: stray isomers fouling catalysts, reactive contaminants triggering safety reviews, or shipments stalled on paperwork glitches. Through a combination of disciplined process control and an openness to direct customer input, we have positioned this compound as a dependable and innovative building block.

    As markets progress, we see growing expectations for safety, sustainability, and technical reliability—not just minimum specs on a page. For those shaping the next wave of electronics, therapeutics, or specialty chemicals, the quality of every intermediate matters as much as the tools and teams building with them. We are proud to produce a material that not only meets these standards, but aspires to raise them with each batch we make.