Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Fluoronaphthalene

    • Product Name 2-Fluoronaphthalene
    • Alias 2-Fluoronaphthalen
    • Einecs 207-355-2
    • 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
    VTB
    Specifications

    HS Code

    905780

    Cas Number 283-82-1
    Molecular Formula C10H7F
    Molecular Weight 146.16 g/mol
    Iupac Name 2-Fluoronaphthalene
    Synonyms β-Fluoronaphthalene, Naphthalen-2-yl fluoride
    Appearance Colorless liquid
    Boiling Point 242°C
    Melting Point 8°C
    Density 1.156 g/cm³
    Solubility In Water Insoluble
    Flash Point 109°C
    Pubchem Cid 70008
    Smiles FC1=CC2=CC=CC=C2C=C1

    As an accredited 2-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 2-Fluoronaphthalene, tightly sealed with a screw cap, labeled with hazard information and chemical details.
    Shipping 2-Fluoronaphthalene is shipped in tightly sealed containers, away from direct sunlight, heat, and moisture. Proper labeling, including hazard identification, is required. Handle with care as it is flammable and potentially harmful. Follow all relevant shipping regulations, such as DOT and IATA, and provide safety data sheets (SDS) during transport.
    Storage 2-Fluoronaphthalene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and heat. Keep it away from incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. Proper labeling and secondary containment are recommended to avoid accidental spills or exposure. Use appropriate safety precautions when handling.
    Application of 2-Fluoronaphthalene

    Applications of 2-Fluoronaphthalene in Industrial Manufacturing

    2-Fluoronaphthalene serves as a specialized fluorinated aromatic intermediate across multiple downstream sectors, enabling the production of complex molecules in pharmaceuticals, agrochemicals, performance dyes, specialty polymers, and liquid crystal materials. Our material meets stringent quality controls to support advanced synthesis routes and ensure supply chain stability for industrial-scale operations.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies source 2-Fluoronaphthalene for coupling reactions and stepwise synthesis of novel drug molecules, particularly within the development of kinase inhibitors and CNS-active compounds. Its activated fluorine position facilitates downstream functionalization, especially in Suzuki or Buchwald–Hartwig cross-couplings, with stringent attention to impurity profiles and trace metal content at every stage. Manufacturers typically incorporate it during the assembly of the core scaffold in multistep synthesis routes for APIs targeting oncology, neurology, and anti-infective segments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • USP/NF Monograph quality requirements (for downstream APIs)
    • 21 CFR Part 211 cGMP for Finished Pharmaceuticals
    • EDQM Guidance—CEP requirements for EU markets

    Typical usage ratio

    • Ranges from 0.12–0.65 molar equivalents per synthesis batch, adjusted based on the core structure’s substitution needs and reaction yield targets

    Downstream process integration

    • Charged in early-stage heterocycle assembly or during late-stage fluorine introduction via palladium-catalyzed arylation

    Final product types

    • Small-molecule APIs (e.g., anti-cancer drugs, CNS agents)
    • Advanced pharmaceutical intermediates

    2. Agrochemical Active Ingredient Manufacturing

    Producers of herbicides and insecticides implement 2-Fluoronaphthalene as a core building block to synthesize key intermediates in benzoyl-substituted and aryl-aniline agrochemicals. Its unique substitution pattern provides better reactivity for electrophilic aromatic substitution, supporting high selectivity in downstream coupling steps. The presence of the fluorine atom enhances bioactivity and degradation resistance in finished plant protection products.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 25198 guidelines for technical-grade agrochemicals
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EC No. 1907/2006)
    • China GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 0.1–0.35 w/w in the overall agrochemical synthesis, with adjustments for target compound potency and downstream derivatization efficiency

    Downstream process integration

    • Entered into Grignard coupling, Friedel–Crafts acylation, or sequential nitration and reduction reactions in the technical synthesis lines

    Final product types

    • Naphthalene-based herbicides
    • Third-generation fluorinated insecticidal actives
    • Precursor intermediates for fungicides

    3. High-Performance Dye and Pigment Manufacturing

    Specialty dye and pigment producers utilize 2-Fluoronaphthalene to construct high-purity organic dyes for technical textiles, OLED displays, and ink formulations. The fluorinated position supports synthesis of stable chromophore cores that exhibit enhanced photostability and sharp spectral features. This substrate enters direct arylation and diazotization sequences to yield high-performance pigments with defined particle size and dispersibility criteria for precision industrial uses.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management Systems
    • Oeko-Tex Standard 100 for textiles
    • EN 71-3: Safety of Toys (for pigment content)
    • Mokuai Ministry of Environment RoHS compliance (for electronics applications)

    Typical usage ratio

    • 2–7% w/w based on total organic pigment precursor batch, optimized for target color density and purity specifications

    Downstream process integration

    • Loaded into the arylation reactor for controlled coupling with electron-rich aromatics; followed by sulfonation, diazotization, or halogenation as needed for color tuning

    Final product types

    • Fluorinated naphthalene dyes for OLED emissive layers
    • High-performance textile colorants
    • Disperse and acid dyes for digital textile inks

    4. Liquid Crystal Material Formulation

    Material scientists and LCD manufacturers select 2-Fluoronaphthalene as a synthetic intermediate for developing mesogenic units within display-grade liquid crystal compounds. The compound’s rigid planar structure and electron-deficient fluorine incorporation aid in fine-tuning phase transition temperatures and dielectric anisotropy. Companies add this intermediate to ring-extension and etherification routes to produce proprietary liquid crystal mixtures for TN, IPS, and high-resolution display panels.

    Industry compliance standards

    • RoHS Directive 2011/65/EU
    • ISO 9001:2015 for liquid crystal quality systems
    • IEC 62321 determination of certain substances in electrotechnical products
    • JEITA/JEP164 environmental compliance for display materials

    Typical usage ratio

    • 6–15% molar incorporation per mesogen batch, depending on the target nematic or smectic properties of the LC mixture

    Downstream process integration

    • Feeds into nucleophilic aromatic substitution and Grignard synthesis during ring-closure steps; followed by purification and precision blending of LC mixtures

    Final product types

    • Liquid crystal single components (e.g., fluoro-naphthyl derivatives)
    • Custom nematic or smectic LC blends for thin-film transistor (TFT) displays
    • Performance additives for improved switching speed in panel applications

    5. Advanced Polymer Synthesis

    Polymer manufacturers integrate 2-Fluoronaphthalene as a functional monomer for specialty engineering plastics and high-temperature-resistant resins. The aromatic fluorine presence imparts enhanced chemical resistance and dimensional stability, especially useful in polyimide and polyarylene ether ketone (PAEK) systems. The raw material typically undergoes nucleophilic aromatic substitution or condensation polymerization to form copolymers with tailored thermal and mechanical profiles for aerospace and microelectronics markets.

    Industry compliance standards

    • UL 94 flammability requirements
    • ASTM D618–Standard Conditioning Plastics for Testing
    • ISO 10993–Biocompatibility Evaluation (when required for electronic encapsulation)
    • IEC 61249-2-21:2017 halogen-free laminate standards

    Typical usage ratio

    • 2–12 mol% relative to total aromatic monomer content, optimized per end-use thermal and chemical requirements

    Downstream process integration

    • Added during oligomerization or step-growth polymerization alongside diamines or bisphenols; post-polymerization blending and extrusion follow for final material shaping

    Final product types

    • High-performance polyimide and PAEK resins
    • Halogen-resistant laminate materials
    • Microelectronic encapsulants
    Free Quote

    Competitive 2-Fluoronaphthalene prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Fluoronaphthalene: A Closer Look from the Manufacturer’s Perspective

    The Core of 2-Fluoronaphthalene Production

    Walking through the controlled environment of our facility, one gains a real sense of the work required to consistently turn out high-purity 2-Fluoronaphthalene. Handling aromatic hydrocarbons isn’t an ordinary task; it means balancing safety, efficiency, and the intricate chemistry that keeps customers coming back for years. 2-Fluoronaphthalene, known by its CAS number 283-89-2, takes its place in the landscape of specialty fluorinated aromatics because it brings its own unique reactivity to both research and industry-scale processes.

    Our direct involvement with every batch teaches the importance of sticking to purity standards and knowing how various impurities impact downstream processes. In our hands, 2-Fluoronaphthalene typically leaves the reactor as a colorless to slightly yellow crystalline solid, with a melting point in the mid-40s Celsius. Reliable melting point readings have always reflected batch quality, and we closely log spectral data to detect even minor inconsistencies. Shifts in appearance or scent can signal off-spec material, and our experience with naphthalenes enables quick response and containment of any irregularities.

    What Sets 2-Fluoronaphthalene Apart

    In our years manufacturing aromatic fluorides, 2-Fluoronaphthalene stands apart from its relatives due to the site-selective fluorine at the 2-position. Researchers tell us the substitution at this position impacts aromaticity, electron density, and spin, critical attributes for advanced organic synthesis routes. Customers in pharmaceutical intermediates and advanced materials rely on this fine level of control, whether developing building blocks for agrochemicals or pursuing complex organofluorine scaffolds.

    Each molecule’s position matters. For practitioners in organofluorine chemistry, the distinction between 1-Fluoronaphthalene and 2-Fluoronaphthalene isn’t theoretical. During substitution reactions, 2-Fluoronaphthalene’s electronic configuration opens doors to routes not readily accessible from other isomers, particularly during coupling and functionalization steps. We’ve observed colleagues run test reactions side by side with 1-, 2-, and 8-Fluoronaphthalene. Reaction rates and product profiles can diverge greatly, often giving 2-Fluoronaphthalene more flexibility or higher overall yields for certain processes.

    Typical orders come from labs working on nucleophilic aromatic substitution (SNAr), cross-coupling, or even as an intermediate for fluorinated dye production. Solubility in common organic solvents cuts down on processing time. Unlike more chlorinated or brominated naphthalenes, our 2-Fluoronaphthalene presents a balance of reactivity: sufficiently active for broad use but not so aggressive that it complicates handling or storage.

    Specifications from a Practical Standpoint

    Production here means more than hitting a number on a COA. Thoughts go to practical issues—reliability, reproducibility, and the repercussions of mistakes. For 2-Fluoronaphthalene, our in-house standards demand that purity by GC exceeds 99%, with negligible presence of 1-fluoronaphthalene or multi-substituted byproducts. Every batch faces NMR, GC-MS, and melting point checking, but QC rarely ends there. Technical setbacks arise from minute contamination, changes in solvent, or miscalculated temperatures during distillation. Over the years, resolving those issues has led us to tweak parameters and rebuild parts of the synthesis line to avoid carryover between products.

    All our process improvements stem from lab discoveries and customer feedback. Teams in semiconductor research will flag problems far different than those encountered by pharmaceutical customers. Moisture levels, trace metals, and oxygen-sensitive reactions draw out each sector’s priorities. Tuning our processes, right down to the storage vessels, means reducing risk of peroxide formation or air contact. We favor sealed, light-blocking drums or fluoropolymer-lined containers for large shipments—a practice long proven by our minimal return rate over decades.

    Usage Based on Real Experience

    2-Fluoronaphthalene rarely sits on shelves for long. Downstream, much of it participates in Suzuki-Miyaura and other palladium-catalyzed coupling reactions for fluorinated aromatic targets. The reliability of our product’s SNAr characteristics under field-tested conditions stands behind years of customer trust. Academic colleagues leverage the molecular symmetry for ligand design, and more than a few agrochemical companies have modified our formulation protocols to control scale and reaction exotherm on their pilot plants.

    We’ve seen 2-Fluoronaphthalene become a staple in research on liquid crystals and OLED intermediates, owing to the precise location of the fluorine. Our engineers routinely consult with end users about process troubleshooting—one customer shaved hours off purification by switching to our lower-residue packaging, another resolved column fouling by tapping our technical support for post-delivery storage tips.

    From our vantage point, customer inquiries commonly fall into several themes: how the fluorine position affects reactivity, batch-to-batch consistency, and total impurity load. When process chemists push for maximal conversion in scale-up, these questions matter as much as the core purity figure. Handling feedback has sharpened our skill at early-course corrections, avoiding far greater delays or batch rejections down the line.

    Distinctions Between 2-Fluoronaphthalene and Related Compounds

    Chemists handle a range of fluorinated hydrocarbons, but they know the subtle differences in structure greatly determine downstream outcomes. Take 1-Fluoronaphthalene and 2-Fluoronaphthalene: the molecular weight difference vanishes, but functional performance tracks closely with substituent location. Engineers working on polycyclic aromatic frameworks return to 2-Fluoronaphthalene when regioselectivity or coupling-site specificity matters more than brute-force reactivity. Longtime industry partners recall times when switching isomers improved product purity or shortened run time, not by chance but by leveraging molecular symmetry and steric effects.

    In more complex synthesis, 2-Fluoronaphthalene unlocks multi-step sequences incompatible with either the parent naphthalene or different fluoro-naphthalene isomers. For laboratories refining fluorinated monomers or specialty surfactants, it also acts as a key backbone for adding hydrophobic and hydrophilic functions in subsequent reactions. Colleagues developing photovoltaic materials or pharmaceuticals have described marked yield gains using our 2-Fluoronaphthalene over alternatives. In those cases, misplacing a fluorine group adds steps, raises costs, and produces off-target materials.

    Our customers frequently report differences in olfactory thresholds, volatility in solvent, and thermal stability when comparing 2-Fluoronaphthalene to its isomers. Experience has taught us the 2-position fluorine yields manageable vapor pressure at both research and industrial scales, supporting safer transfer and less compound loss, particularly at elevated temperatures. Some projects depend on this relatively tame volatility, especially where open-system transfers or thin-film applications come into play.

    Not everything comes down to molecular property tables. Handling and long-term storage issues often prove more influential over costs than published reactivity studies. Years ago, a polymer manufacturer approached us about inconsistent downstream results. Joint troubleshooting found micro-level contamination from shared equipment between different naphthalene derivatives. Adjusting packaging and scheduling eliminated the issue, reinforcing the importance of single-line manufacturing for specialty grades.

    Attending to Safety, Storage, and Regulatory Needs

    Working with aromatic fluorides calls for close attention to safety and compliance. Inside our plant, every operator receives process-specific training to limit exposure and prevent inadvertent emissions. 2-Fluoronaphthalene’s moderately low vapor pressure means less drift but doesn’t remove the risk of chronic exposure, which drives us to outfitting workspaces with real-time air quality monitoring. We also use fully contained transfer lines and dust extraction hoods, even at the scale where smaller shops might consider them “optional.”

    Long-running experience has shown that routine monitoring and rapid machinery cleaning between runs practically eliminate contamination cross-over, meeting the strict specs required by pharma and electronics applications. Our technical files and retention samples stretch back years, ensuring auditors can verify compliance history anytime.

    Downstream handlers find our packaging approach also reduces accident risk. We’ve invested in tamper-evident seals and anti-static liners, shaped by customer reports about accidental spills during drum or bottle transfer. These improvements emerged from field incidents, not marketing. Beyond the factory, the regulatory regime for aromatic hydrocarbons has tightened continually. Our long view keeps us tuned into both domestic and global chemical regulations concerning shipment, labeling, and personal exposure, and we upgrade technical documentation each time a major rule changes or a customer asks for a new certification.

    Challenges and Steady Progress in Production

    Getting the fluorine onto the naphthalene ring at the right spot forms the backbone of our process—no shortcuts, no guesswork. The actual chemistry of introducing fluorine relies on precise reaction control, preventing over-fluorination or unwanted side reactions. Years ago, our early trials led to low selectivity and high waste, prompting investment in better reactor flow designs and reagent metering. On today’s lines, real-time monitoring correlates purity and yield like never before, cutting both turnaround time and environmental footprint.

    Waste minimization isn’t just compliance—it saves costs, limits downtime, and guarantees neighbors will not raise concerns over emissions. Technical setbacks once shut down production for days due to fouled catalysts or mischarged reagent, but data-driven upgrades and a focus on staff retention made troubleshooting much more efficient. Many on our team have personal investment in the plant, often training their successors in both day-to-day tasks and long-term process improvements. The knowledge stays in-house, not lost to turnover.

    Supporting Innovation Downstream

    Projects using 2-Fluoronaphthalene operate at the intersection of academic research and scalable invention. Several years back, we assisted a medicinal chemist scaling up a bench procedure for a new drug candidate. Initial pilot runs failed to match analytical results from small-scale glassware, puzzling the client and threatening project timelines. Joint batch review, including hands-on time on our reactors, traced the trouble to micro-impurities born from storage vessel incompatibility—something seldom encountered at microgram scale but inescapable across a hundred kilos. After revising container materials and adding a secondary purification loop, their project began hitting projected yields, accelerating clinical milestones.

    Customers don’t only seek technical purity; they rely on manufacturers for logistical problem-solving too. Over the past decade, the uptake of just-in-time delivery and rapid prototyping has meant our warehouse teams and dispatchers now coordinate more tightly than ever with researchers and production chemists. Several have visited our site to co-design custom packaging, ensuring their automation lines never jam with oversized chunks or contaminated deliveries. We make changes fast, sometimes rerouting stock mid-shipment or breaking lots to meet schedule pressures. This comes from a bottom-up understanding that supply chain agility can make or break both our reputation and the progress of our partners’ projects.

    From Small-Scale to Large-Scale: A Shared Journey

    Some may treat their chemical products as simple SKUs with a number attached. We’ve taken a different path, building trust batch by batch, responding to specific performance needs in each new research or manufacturing campaign. Every enhancement to our 2-Fluoronaphthalene production comes from field results, not theoretical modeling. Our focus remains on real-world use, minimizing avoidable risk, and enabling top performers in pharmaceuticals, electronics, and specialty coatings to reach their goals without chemical supply holding them back.

    We approach each customer query as a chance to refine both our product and our process. Scientists working on next-generation OLED materials tell us how trace water content can undermine device longevity. Responding, we improved vacuum drying and policed drum residuals between fills, launching routine shipment-based moisture assays. This feedback also equipped us to serve researchers working on entirely different fields, from liquid crystals to specialty adhesives, many of whom wrestle with similar concerns.

    Continuous Improvement, Grounded in Daily Practice

    Much in chemical manufacturing boils down to everyday discipline and lessons gathered over years rather than singular breakthroughs. Some changes are obvious, like updating a filtration system to extract sub-micron impurities, or adjusting processing lines to avoid cross-contact between analogues. Others unfold quietly over hundreds of batches—such as redefining sampling protocols, or learning from root-cause investigations into minute deviations in spectral lines.

    It’s easy to overlook the daily grind that makes for dependable supply, but customers notice when it falters. Periodic check-ins with top users help flag problems early, whether a drop in product shelf life or a subtle shift in compatibility within complex syntheses. We routinely collaborate with field users on alternatives to traditional halogenated naphthalenes, and frequently point out how subtle changes in reactivity, vapor pressure, or solid form alter reaction mechanics down the line.

    Stronger Connections, Fewer Surprises

    Real partnership with end-users comes from a willingness to tackle out-of-the-ordinary requests. Sometimes a laboratory needs small sample lots with odd specifications. Other times, a multinational group wants hundred-kilo volumes with split deliveries or project-specific QA tracing. No matter the scale, every request tests our process limits. Where possible, we adapt method, form, or shipment to prevent disruption. We’ve found that prompt communication and attention to each scenario often preempts bigger setbacks, such as rework, project delays, or lost opportunity.

    Many years supplying 2-Fluoronaphthalene for such a broad spread of applications—OLED displays, dye synthesis, pharma intermediates, and performance materials—has taught us that the “standard” product really doesn’t fit every user. Recurrent collaboration with clients has sharpened our technical edge, improved packaging, and even influenced production scheduling to serve next-in-line orders faster.

    The Manufacturer’s Perspective—A Shared Goal

    Across our organization, each new order, every inquiry, becomes another data point. We track performance not only in terms of purity and delivery metrics but in the stories that come back to us: batch milestones, successful drug candidates, and quiet upgrades to machine performance. The knowledge we’ve built supporting 2-Fluoronaphthalene production guides our problem-solving, shapes our equipment, and motivates the extra effort needed to meet the evolving needs of the best minds—whether in academic labs, startup incubators, or global corporations.

    We don’t regard 2-Fluoronaphthalene as a commodity; we recognize it as an essential tool for building tomorrow’s materials, medicines, and electronics. Years of working with demanding customers and hands-on troubleshooting have equipped us to answer technical, logistical, or even regulatory questions swiftly. In the future, as both applications and scrutiny around specialty fluorinated aromatics grow, our commitment stands: producing with precision, shipping reliably, and partnering for solutions that matter. Our experience in the fine details of 2-Fluoronaphthalene production gives peace of mind, reduces development uncertainty, and moves projects forward, batch by batch.