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

5-Chloro-2-Fluorobenzonitirle

    • Product Name 5-Chloro-2-Fluorobenzonitirle
    • Alias 5-Chloro-2-fluorobenzonitrile
    • Einecs 248-875-7
    • 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
    VTB
    Specifications

    HS Code

    564360

    Productname 5-Chloro-2-Fluorobenzonitrile
    Casnumber 55290-64-7
    Molecularformula C7H3ClFN
    Molecularweight 155.56
    Appearance White to light yellow solid
    Meltingpoint 45-49°C
    Boilingpoint 238-240°C
    Density 1.37 g/cm3 (estimated)
    Purity Typically >98%
    Solubility Slightly soluble in organic solvents
    Storagecondition Store in a cool, dry, well-ventilated area
    Synonyms 5-Chloro-2-fluorobenzenecarbonitrile
    Smiles C1=CC(=C(C=C1Cl)C#N)F
    Refractiveindex 1.537 (estimated)
    Flashpoint 90°C (estimated)

    As an accredited 5-Chloro-2-Fluorobenzonitirle factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100g, tightly sealed with a PTFE-lined cap, labeled with "5-Chloro-2-Fluorobenzonitrile, CAS 57381-49-4" and hazard symbols.
    Shipping 5-Chloro-2-fluorobenzonitrile is shipped in tightly sealed containers to prevent moisture and contamination. It is transported according to chemical safety regulations, often classified as hazardous. Proper labeling, documentation, and handling precautions must be observed. Store in a cool, dry place away from incompatible substances and sources of ignition during transit and storage.
    Storage 5-Chloro-2-fluorobenzonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible substances such as strong acids or bases. Protect from direct sunlight and keep away from heat. Properly label the container and ensure access is limited to trained personnel using appropriate personal protective equipment.
    Application of 5-Chloro-2-Fluorobenzonitirle

    Applications of 5-Chloro-2-Fluorobenzonitrile in Industrial Manufacturing

    As a direct manufacturer of 5-Chloro-2-Fluorobenzonitrile, we focus on downstream industries where this intermediate plays a key role in producing high-value compounds. Below, we outline specific application scenarios spanning pharmaceutical intermediates, agrochemical active ingredient synthesis, performance pigment manufacturing, and advanced material monomer production. Each section details precise standards, formulation ratios, process placement, and types of final products.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    5-Chloro-2-Fluorobenzonitrile serves as a strategic building block in the synthesis routes of certain targeted therapies and anti-infective agents. Leading pharmaceutical manufacturers incorporate this intermediate during multi-step synthetic processes, often as a halogenated aromatic core in the skeleton construction of next-generation drug candidates. The material’s purity and residual profile must consistently meet stringent regulatory audits. Operators typically adjust addition levels during the key condensation or coupling reactions, based on API yield and impurity specifications as verified by validated analytical methods under GMP environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF monographs for intermediates and impurity control
    • Ph. Eur. 2.4.14, 2.4.20 for halogenated compound testing
    • FDA 21 CFR Part 211 (where the site is located in the US)

    Typical usage ratio

    • 0.15–0.30 molar equivalents per mole of target API in the coupling or cyclization stage, with adjustments based on route efficiencies and desired yields

    Downstream process integration

    • Charged in the initial aromatic substitution or coupling step (e.g., palladium-catalyzed cross-coupling) and carried through intermediate crystallization and purification prior to API finishing

    Final product types

    • Anti-viral and anti-infective drug APIs
    • Small molecule kinase inhibitors
    • Specialty intermediates for CNS-active compounds

    2. Agrochemical Active Ingredient Synthesis

    Within the agrochemical sector, multinational crop protection companies utilize this nitrile as a crucial halogenated aromatic moiety for constructing novel herbicidal and insecticidal actives. Compliance with global and local agrochemical substance registration dictates inclusion criteria for traceability, responsibility, and worker safety. Typically, the compound enters during the aromatic nitrile conversion or functional group elaboration steps. The dosage varies with the complexity of the molecular backbone under synthesis, factored by intended field application concentration and productivity constraints.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006 for substance registration
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 for quality management in synthesis

    Typical usage ratio

    • 5–12% by weight in the designated synthetic stage for active ingredient backbone formation; adjusted depending on final molecular target

    Downstream process integration

    • Injected into the aromatic substitution stage; typically forms the core scaffold prior to downstream derivatization and technical-grade purification

    Final product types

    • Pre-emergent and post-emergent herbicide technical concentrates
    • Broad-spectrum insecticidal actives
    • Seed treatment chemicals

    3. Performance Pigment Intermediate

    Advanced pigment manufacturers select halogenated benzonitriles to deliver unique chromophore properties in high-stability colorant offerings. The compound acts as a primary ring structure during pigment core-forming reactions, such as directed azo coupling or phthalocyanine synthesis. Stringent controls for environmental, worker, and end-user safety regulate integration, with dosing determined based on desired shade, lightfastness, and washfastness workloads in final pigment grade. Compliance checkpoints anchor both batch reproducibility and regulatory documentation.

    Industry compliance standards

    • EN 71-3:2019 for toy safety (migration of certain elements)
    • ISO 787/1–24 for pigment testing protocols
    • REACH SVHC candidates list for environmental safety
    • OEKO-TEX Standard 100 (where applicable for textile pigments)

    Typical usage ratio

    • 8–17% by weight within master pigment batch, tailored to desired pigment concentration and shade intensity

    Downstream process integration

    • Inserted at the initial pigment-forming reaction, often via metal-complex or azo-coupling syntheses, followed by milling and formulation

    Final product types

    • High-resistance textile colorants
    • Automotive and industrial coatings pigments
    • Plastisol and polymer coloration masterbatches

    4. Monomer Precursor in High-Performance Polymer Synthesis

    Producers of high-performance specialty polymers incorporate this benzonitrile derivative as a monomer or comonomer during step-growth polymerization. The main application involves fluorinated and chlorinated aromatic backbone integration, enhancing polymer chemical and thermal resistance for engineering applications. The monomer addition ratio and introduction point depend on the target resin’s performance profile, as fine-tuned in the R&D and pilot plant phase. Downstream, compliance covers both workplace safety and final article migration regulation.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (quality and environment for polymer manufacturing)
    • EU Regulation No. 10/2011 for polymeric materials in food contact
    • ASTM D638, D257 for performance polymers
    • TSCA inventory where applicable for US-bound articles

    Typical usage ratio

    • Up to 28 mol% as a comonomer, based on molecular weight target and requirements for halogen incorporation

    Downstream process integration

    • Chemically introduced during the polymer backbone assembly, prior to final condensation and post-synthetic modification or formulation

    Final product types

    • High-barrier polymer films
    • Specialty engineering resin compounds
    • Flame-retardant plastic components for electronics
    Free Quote

    Competitive 5-Chloro-2-Fluorobenzonitirle 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

    Introducing 5-Chloro-2-Fluorobenzonitrile: Focused Experience in Fine Chemical Production

    Understanding the Material and Its Real-World Role

    At our facility, batches of 5-Chloro-2-Fluorobenzonitrile come to life through a synthesis process we have refined over the years. This isn’t a matter of following formulas in a vacuum—the product emerged from countless feedback cycles with customers in the crop science, pigment, and pharmaceutical sectors. Our chemists know firsthand that this particular benzene derivative brings more than just a niche functionality. Its structure, with a chlorine atom on the 5-position and a fluorine on the 2-position of the benzonitrile core, offers a highly selective reactivity profile. This lets formulators introduce it into advanced organic syntheses, especially where precision and yield reliability make a significant difference.

    Unlike more generic benzonitrile derivatives, the inclusion of both a halogen at opposite ends—chlorine at five and fluorine at two—has a marked impact on the electronic characteristics. This specific substitution pattern not only raises the molecule’s resistance to harsh process conditions, it steers downstream functionalization toward cleaner reaction profiles. We have seen time and again that chemists using lesser-substituted variants encounter more byproducts and waste, which translates to difficult purifications and higher costs. 5-Chloro-2-Fluorobenzonitrile, as we produce it, offers a practical answer by letting users streamline key chemical transformations.

    Model, Specifications, and Everyday Details

    Currently, we run multiple scales of this product—multi-kilo lab synthesis and full production-scale campaigns. The usual model specification is defined by purity, water content, and residual solvent analysis. Whether our material heads into an active pharmaceutical intermediate workflow or a specialty colorant process, purity sits above 99% by GC, confirmed every time by in-house QC and cross-checked if a customer needs independent validation. Residual water rarely drifts above 0.2% by Karl Fischer titration. We keep the product dry at every stage from completion through packaging under nitrogen, because trace moisture can disrupt subsequent cross-coupling or cyanation steps.

    The fine, pale solid form flashes a distinctive sharpness—a nod to the material’s chemical rigidity. We don’t press the powder into tablets or pellets, because past experience shows that flowability and dispersibility drop when the texture changes. Customers who ever had to break up lumpy, compacted intermediates know how much time this wastes on an industrial line. Our team runs particle size checks with every campaign, ensuring that clients get a free-flowing product, never a blocky nuisance. Years ago, some tried using impure, off-spec stock and learned the hard way about the downstream headaches—poor solubility, fouling of filtration setups, or even the need to redissolve and reprocess. We learned along with them—it drove us to stick with a process that protects physical and chemical consistency.

    Insights from Daily Production—Why Details Matter

    We get a lot of upstream technical questions. Some want to know what sets our 5-Chloro-2-Fluorobenzonitrile apart from the material found in off-the-shelf catalogs. The simplest answer traces to investment in process robustness. Many producers bring the core benzonitrile to the right substitution pattern through direct halogenation, skipping purification between steps. It’s faster, but that route leaves isomeric impurities and a stubbornly higher level of color bodies, so finished batches often show a faint yellow tint or even early onset of particulate. In contrast, our method leans heavily on intermediate purification and careful chlorination under rigorously controlled temperature envelopes. Admittedly, that costs a little more in energy and solvent—but customers repeatedly tell us the smoother performance pays back tenfold in overall plant efficiency.

    Workers at our plant know exactly how sensitive 5-Chloro-2-Fluorobenzonitrile is to oxygen and ambient moisture, even if it isn’t highly hygroscopic. So, from isolating the intermediate stage to final product transfer, we stick to a low-humidity environment and minimal headspace in drums and containers. Even packaging choices aren't left to chance. Chemists who have opened a batch, expecting reliable behavior, only to discover signs of degradation—these small oversights become expensive lessons. Years ago, we kept a product in ordinary bags and, within weeks, degradation began detectable by spectrometry, forcing us to develop the modified packaging protocols we use today. Since then, shelf life and batch-to-batch consistency have improved measurably. If a customer needs “just-in-time” deliveries, we can pack and ship within hours, bypassing warehouse time and further ensuring the integrity of the product upon arrival.

    End-Use Performance Across the Chemical Industry

    Much of the 5-Chloro-2-Fluorobenzonitrile we ship lands in the hands of pharmaceutical process groups. Here, it serves as a precious intermediate, often en route to complex molecules for crop protection, oncology research, or dye manufacturing. Catalytic cross-coupling and nucleophilic aromatic substitution are the two most common applications we see in practice. The electron-withdrawing effects of both the nitrile and the two halogens create a solid platform for reliable transformations. Formulators working on aniline derivatives or tri-substituted aromatics benefit from decreased byproduct formation—a difference we confirm using spectroscopic analysis on pilot runs.

    In pigment chemistry, the same electronic structure adds value by steering the polycondensation cleanly, which helps pigment manufacturers avoid trace metal impurities. Our larger customers in this sector point out how off-the-shelf equivalents bring discoloration under heat, while our product allows them to deliver extended color stability, which matters for premium coatings and outdoor paints. We regularly receive requests to further cut trace metal content, something we control at the purification stage. This direct involvement in the manufacturing means we’re not guessing or passing on supplier data, but directly monitoring platinum and palladium residues through atomic absorption checks.

    The Subtle Differences Among Benzonitrile Family Members

    Chemists ask about substitution location all the time. 4-Chloro-3-Fluorobenzonitrile has the same empirical formula but behaves completely differently during Suzuki reactions or amidation. The 5-chloro, 2-fluoro arrangement leads to a notably different reactivity—the electronic push-pull means lower rates of side-product formation and less fouling of catalysts downstream. Once a customer ran comparative tests for a high-value intermediate and sent us the LC-MS results: yields for their desired product jumped by nearly 7% when switching to our route, while clean-up time halved. These stories do more to make the case than speculation about theoretical behavior.

    We also see regular confusion with plain 2-fluorobenzonitrile or 5-chlorobenzonitrile. Both are cheaper and easier for untrained operators to prepare, but feedback shows that downstream applications suffer. Control labs often spot more dimers or polymeric byproducts. The dual-substituted structure fills a unique gap—enough deactivation for mild conditions, not so much that reactivity drops off a cliff. We support partners through route selection, sometimes running side-by-side trials with analogues so commercial teams get clear performance data before moving to scale-up. Sometimes, a prospect gets sold on catalog prices and later comes back after wasted effort with impure precursors. Our role is to lay out the results, not just the specs, because ultimately, process reproducibility is where margins are protected.

    Continuous Investment in Process Knowledge

    Chemical manufacturing rarely stands still. Regulations on residual solvents shift. Standards for allowed impurities continue to tighten, especially as global markets change their import rules for pharmaceutical and specialty chemical intermediates. We have spent a lot of time and budget refining not only the molecular synthesis but also the purification, monitoring standards, and documentation so export paperwork and REACH conformity stand up to careful regulatory audits. We respond openly to customer audit teams, demoing our analytical tracks and letting them walk the shop floor to see the extent of our environmental controls.

    Some years ago, a major partner in Europe called for methods to further drive down residual DMF (dimethylformamide) below new guideline levels. It was tempting to argue that the historic process shouldn’t change, but instead, we worked backward through each synthesis stage, from raw chloride source all the way to the crystallization and drying. That change took months of running new pilot processes, but documented gains opened up markets that would have been closed if we stuck to old ways. It’s not just about moving faster—having process ownership means we see exactly where a tweak in vacuum drying or a second re-crystallization pays out in real product consistency.

    Supporting Technical Challenges—What We Have Learned

    End users often tell us where the difficulties arise: long cycle times, tricky reproducibility, suspension settling, or batch variability. Years of feedback and shared failures taught us that customers need support, not lectures. We don’t just drop a drum at the dock and disappear. We collect comments after every delivery. Once, a pharmaceutical group reported slow filtration rates in their downstream step—they traced it to microfine dust in the product. Our team stepped in, analyzed their process, and adjusted the milling stage at our site. The next campaigns produced a coarser, free-flowing material that fit their system, restoring their throughput. These details matter—one small improvement freed up half a day of downtime for a customer whose plant operates on tight timing.

    Solubility problems come up occasionally, especially in cold weather. We keep in touch with end users to track these events, offering technical notes and, if needed, samples with altered particle properties or solvent pre-dissolution to ease their loading steps. Environmental controls in our facility brought these solubility problems down over the years, but we still listen, adjusting shipping or packaging as field needs change.

    Health, Safety, and Compliance Built into the Process

    It’s not enough to talk about chemical purity without acknowledging the full context of health and safety. We maintain closed-system transfer for all toxic precursors and finished product, with fume hood extraction and on-site waste management built into our workflow. The days of open drum filling or bagging outside the production suite are behind us. Our commitment isn’t just regulatory—many of us have families in the communities near our site. What happens here directly affects our own people. Environmental teams at the facility run water, air, and soil checks in real time, rather than just on a compliance schedule. That’s as much for transparency with buyers as it is for our own quality of life.

    Final product batches come with pre-clearance for export to Europe, North America, and Japan, backed up by documentation from our own analytical team. We avoid substitution games—our buyers see the same quality, year after year. Where regulations demand lower impurity levels or tighter control, we adapt both synthesis and documentation, reflecting the realities of the markets we serve.

    Real Differences from Reseller and Distributor Goods

    A common question from new buyers centers on the difference between direct-from-manufacturer material and stock found through third-party channels. The main difference traces back to direct control. We manage every step, from starting raw materials to post-synthetic refining to antioxidant addition and packaging under inert gas. Distributors often work from fluctuating inventories, with less control over storage conditions, and can’t always guarantee traceability; off-flavor, loss of reactivity, and batch degradation are not rare in those supply chains. Our commitment means if something goes wrong, there is a direct point of return—our own lab and customer support, not a maze of phone calls or emails into nowhere.

    Reproducibility, not just chemical purity, comes from real experience. As market volatility rises and supply chain interruptions become more common, that first-hand control gives both us and our customers an edge—less downtime, fewer shipment issues, and a trusted record for audits. Customers with urgent innovations or scale-ups can work directly with our technical team, making tweaks batch-to-batch if needed. We keep feedback loops open, so each round of deliveries builds on the last, improving not only our own standards but those of the industries we serve.

    Looking Ahead—Ongoing Improvements and Collaboration

    Our production line for 5-Chloro-2-Fluorobenzonitrile never really sleeps. We know adjustments will keep coming, whether from regulatory changes or shifts in downstream synthesis. Our chemists and technical support team welcome real input from partners, using every bit of feedback to streamline future campaigns or adapt to new application needs. Whether the next frontier is greener chemistry, advanced analytics, or further impurity control, our approach centers on continuous engagement.

    Looking back at our process evolution, we see improvement driven almost entirely by open dialogue with those who actually use our product. With every iteration, the product leaves our plant a little more suited to its purpose. Customers gain from less rework, more consistent results, and green-light audits—advantages built not just on theory or generic compliance, but years of hands-on manufacturing experience.