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3-Fluoro-4-Aminobenzonitrile

    • Product Name 3-Fluoro-4-Aminobenzonitrile
    • Alias 3-Fluoro-4-cyanoaniline
    • Einecs 629-204-7
    • 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

    380527

    Chemical Name 3-Fluoro-4-Aminobenzonitrile
    Cas Number 51310-24-6
    Molecular Formula C7H5FN2
    Molecular Weight 136.13
    Appearance Light yellow to brown solid
    Melting Point 93-96°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms 3-Fluoro-4-cyananiline
    Smiles C1=CC(=C(C=C1N)C#N)F
    Inchi InChI=1S/C7H5FN2/c8-6-2-1-5(10)7(3-6)4-9/h1-3H,10H2

    As an accredited 3-Fluoro-4-Aminobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging consists of a sealed amber glass bottle containing 25 grams of 3-Fluoro-4-Aminobenzonitrile, labeled with safety and handling information.
    Shipping 3-Fluoro-4-aminobenzonitrile is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material, so transport complies with local, national, and international regulations. Appropriate labeling and documentation are provided, and shipping is typically through licensed couriers specializing in chemical transport.
    Storage 3-Fluoro-4-Aminobenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at room temperature and ensure proper labeling. Handle under a fume hood and avoid prolonged exposure to skin or inhalation of dust.
    Application of 3-Fluoro-4-Aminobenzonitrile

    Applications of 3-Fluoro-4-Aminobenzonitrile in Industrial Manufacturing

    3-Fluoro-4-Aminobenzonitrile serves as a key intermediate in the synthesis of several high-value specialty chemicals adopted in regulated industrial segments. The following application scenarios reflect established downstream uses in line with industry-specific compliance, practical formulation details, distinct process roles, and actual finished goods production across global chemical markets.

    1. Agrochemical Active Ingredient Synthesis

    This compound enters agrochemical manufacturing chains as a core building block for constructing fluorinated and aminated herbicide molecules. Producers employ it in advanced stage synthesis, enabling crucial substitution patterns for target selectivity in crop protection agents. Its inclusion directly influences downstream hydrolysis, coupling, and ring closure steps, defining the structure-activity relationship required for modern agricultural formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • US EPA Registration Requirements for Pesticide Active Ingredients
    • China GB/T 1604-2001 General Rules for Agricultural Chemicals

    Typical usage ratio

    • Ranges from 5% to 18% (w/w) of total synthetic intermediates depending on the target molecule’s substitution profile; adjusted based on desired agrochemical selectivity and final active ingredient purity requirements.

    Downstream process integration

    • Direct nucleophilic substitution at the fluorine-bearing ring or cyclization in the penultimate step of the synthetic route, preceding formulation into wettable powders or liquid concentrates.

    Final product types

    • Herbicide active ingredients (e.g., fluorinated pyridine-type selectives)
    • Insecticides with aminonitrile functional groups

    2. Pharmaceutical Intermediate for Anticancer Agents

    Drug manufacturers source this material for assembling molecular scaffolds in several small-molecule oncology therapies. Its unique fluorine and amino functional groups enable critical positions for structure-based drug design, especially in synthesis routes for kinase inhibitors and targeted heterocyclic APIs. High purity and trace impurity profiles influence qualification in GMP-compliant pharmaceutical processes.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapters <1000>–<1100> for Intermediates
    • European Pharmacopoeia (Ph. Eur.) Monographs
    • US FDA cGMP 21 CFR Parts 210/211

    Typical usage ratio

    • 6% to 15% (w/w) in stepwise molecular assembly; specific loading tuned by synthetic yield targets and impurity control within the API process.

    Downstream process integration

    • Benzonitrile condensation and Buchwald coupling as a late-stage intermediate, directly linking into final heterocycle ring construction or functionalization prior to salt formation and purification.

    Final product types

    • Small-molecule anticancer APIs (e.g., pyridine/pyrimidine kinase inhibitors)
    • Synthetic intermediates in proprietary pharmaceutical pipelines

    3. Dye and Pigment Intermediate Production

    Colorant manufacturers integrate this ingredient to synthesize high-performance and specialty dyes used in plastics, textiles, and digital printing. The compound’s electron-withdrawing fluorine enhances lightfastness and chemical stability, while the cyano and amino functionalities facilitate unique azo and anthraquinone dye structures sought for demanding coloration applications.

    Industry compliance standards

    • Oeko-Tex Standard 100 for Restricted Substances in Dye Manufacturing
    • EU REACH Regulation (EC) No 1907/2006 for Chemical Registration
    • ISO 105 Series for Dye Fastness Testing
    • ZDHC Manufacturing Restricted Substances List (MRSL)

    Typical usage ratio

    • 3% to 10% of the total mass in the diazotization and amination step; efficiency depends on the target chromophore’s molecular weight and substitution complexity.

    Downstream process integration

    • Entry at diazotization as a coupling partner or as a precursor in the nucleophilic aromatic substitution, prior to sulfonation and crystallization.

    Final product types

    • Acid dyes for textile printing
    • Disperse dyes for polyester fibers
    • Specialty pigments for inkjet and plastics

    4. Synthesis of Specialty Electronic Chemicals

    Semiconductor materials businesses use this raw material to produce functional organic molecules employed in display technologies, OLED emitters, and specialty resins. The fluorine atom improves electronic properties such as charge mobility, while the amino and cyano groups provide anchoring points for subsequent modification, essential in constructing high-purity materials for demanding microelectronic environments.

    Industry compliance standards

    • IEC 61249-2-21 for Base Materials in Printed Circuit Boards
    • RoHS Directive (EU) 2015/863 for Electrical and Electronic Equipment
    • JEITA ET-7304 Standards for Organic Semiconducting Materials
    • ISO 9001:2015 for Quality Management

    Typical usage ratio

    • 1% to 6% (w/w) in monomer or oligomer precursor feed mixtures; exact dosing varies by the targeted electronic property and process yield.

    Downstream process integration

    • Core reactant in base resin polymerization, followed by advanced purification and thin-film deposition by spin coating, printing, or vapor-phase processing.

    Final product types

    • OLED emitter materials and charge transport layers
    • Photoresists for advanced lithography
    • Functional polymers for flexible electronic components

    5. Raw Material for Fluorinated Building Blocks in Fine Chemicals

    Producers in the fine and specialty chemicals sector utilize this compound to construct complex fluorinated intermediates required in research and proprietary synthesis routes. Its molecular structure enables further derivatization, including hydrazinolysis, cross-coupling, and Grignard reactions, facilitating the creation of libraries for advanced development projects and final products where precise functionalization is critical.

    Industry compliance standards

    • Custom synthesis to ISO 9001:2015 and ISO 14001:2015
    • REACH Registration as per (EC) No 1907/2006 for new substances
    • Internal company-specific analytical quality standards
    • Compliance with Transport and Hazard Communication (GHS, DOT)

    Typical usage ratio

    • Adjustable from 2% to 12% based on the precursor scale, reaction pathway, and specific project requirements in pilot or commercial scale syntheses.

    Downstream process integration

    • Multiple steps: initial building block for Grignard or Suzuki couplings, introduced at the functionalization or diversification step of custom molecule development.

    Final product types

    • Substituted benzonitriles and aminopyridines used in R&D
    • Custom fluorinated intermediates for contract research organizations (CROs)
    • Specialty reagents for laboratory and industrial scale-up
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    Certification & Compliance
    More Introduction

    3-Fluoro-4-Aminobenzonitrile: Refining Chemical Building Blocks with Precision

    Introducing a Key Intermediate

    Every batch of 3-Fluoro-4-Aminobenzonitrile that leaves our facility stands as a reflection of the technical attention and care built through years of manufacturing experience. In the fine chemicals sector, consistency and exceptional purity aren’t just promises—they’re benchmarks that chemists at our site uphold batch after batch. Our product, known throughout our teams as 3F4ABN, sits in a category of advanced aromatic intermediates that shape new innovations in life sciences and performance materials.

    We focus our operations around the exact needs of chemists who make therapeutics, dyes, imaging agents, and electronic materials. 3-Fluoro-4-Aminobenzonitrile (chemical formula C7H5FN2, CAS 367-26-4) captures a unique intersection: it combines an electron-withdrawing nitrile with a fluorinated aromatic ring and an amine group, all in a single small molecule. Lab researchers in the pharmaceutical and agrochemical fields recognize this motif for its ability to impart bioactivity, improve metabolic profiles, and modulate polarity in molecules they design.

    From Production Floor to Purity Benchmarks

    Years of process refinement have taught us the details that matter most. The synthesis of 3F4ABN proceeds through carefully controlled aromatic substitution and purification steps. Control over temperature gradients, pH, and the purity of fluorinated feedstocks all matter. From the sound of the agitators to the precise addition of reagents, everything revolves around maintaining color, odor, melting point, and impurity thresholds within narrow targets. Our finished product typically arrives as a pale powder, free-flowing and easy to handle, usually with a purity reaching beyond 99%.

    Impurities in this molecule often arise from incomplete reactions or uncontrolled hydrolysis during amino introduction. Early on, we encountered variability tied to moisture levels and the quality of sodium fluoride. By deploying strict in-line moisture sensors and doubling down on vacuum handling during packaging, we saw degradation rates fall and shelf lives extend by several months. We keep analytical labs just steps from our reactors to give our team immediate feedback—not just for regulatory compliance, but to catch subtle shifts batch-to-batch that can hint at process drift. No outside spec results get blended or reprocessed; outliers never reach the packing line.

    Why Fluorine Matters

    Adding a fluorine at the 3-position on the benzene ring sets this molecule apart from other aminobenzonitriles. Protein binding, metabolic stability, and electronic effects of this specific substitution draw attention from chemists who engineer new drug candidates or molecular probes. The difference isn’t academic: compounds based on fluorinated aromatics often pass through biological membranes more predictably, resist oxidative degradation, and offer higher selectivity in binding assays.

    Fluorination also makes the ring more resistant to unwanted side reactions. Without the 3-fluoro group, other aminobenzonitriles tend to display higher reactivity toward certain nucleophiles or in oxidative environments. Our product’s shelf stability outperforms non-fluorinated analogs in many storage and transit tests, reducing waste in both distribution logistics and end-use formulations. We’ve seen pharmaceutical partners who switched from common benzonitrile analogs to our 3F4ABN reduce byproduct formation in downstream amide couplings, translating to fewer column purifications and less solvent usage per kilo of API.

    Handling and Application Experience

    Despite the small volume of each commercial order—sometimes as little as a few kilograms—each lot gets meticulous handling. Our team stores and ships 3-Fluoro-4-Aminobenzonitrile under dry nitrogen. Once, a customer received a shipment that picked up ambient moisture during a storm, compromising their analytical results. We immediately traced the root cause, improved our container sealing, and implemented extra desiccant packing. Since then, customer complaints about caking or discoloration have dropped to nearly zero.

    Over the years, our product has been incorporated in custom syntheses for kinase inhibitors, PET radiotracer precursors, and several dyes used in OLED display manufacturing. Not all routes need this specific substitution, but whenever a molecular design calls for high polarity contrast or selective bioavailability, requests for 3F4ABN increase. We have seen researchers use it as a starting material for building more complex scaffolds—adding carbon chains or coupling the amine group to protected acids. The electron-withdrawing effect of both the -CN and -F groups gives room for selective transformations under mild conditions, minimizing side product headaches. That’s hard to engineer into less-specialized analogs.

    Comparisons with Similar Intermediates

    Aminobenzonitriles come in many substitution patterns. We used to make a broad suite: ortho, para, di-substituted variants with just nitro, amino, halogen, or nothing at all on the ring. Over time, feedback kept circling back to the performance and reliability of 3-Fluoro-4-Aminobenzonitrile. The meta-fluoro group lends extra chemical resilience; even under strong bases or oxidants, product losses run much lower compared to non-fluorinated or ortho-fluorinated versions.

    One key difference: para-amino benzonitriles tend to display symmetry that makes downstream substitution less controlled. By placing the amino at 4 and the fluoro at 3, chemists achieve differentiation—unlocking regioselective coupling opportunities. The result is greater freedom in designing next-generation drug or pigment candidates. For dye makers, the impact shows up as enhanced photostability; for pharmaceutical teams, it translates into more distinct structure-activity relationships during lead optimization.

    Some receiving plants opt for 3-chloro-4-aminobenzonitrile, or even unsubstituted 4-aminobenzonitrile, for their cost advantage. From years of working with formulation partners, we observe that those options frequently introduce new stability or reactivity quirks—sometimes fouling reactors or introducing hard-to-remove byproducts. We don’t simply chase cost per kilo. The fluorinated variant commands a premium, and customers with challenging synthetic routes routinely find added value through cleaner reactions and more predictable yields. Less spent on purification and rework often makes up the difference.

    Feedback Loop: R&D and Manufacturing Learnings

    Continuous improvement anchors our process philosophy. No process survives unchanged through several years without adaptation. Advances in fluorination chemistry, cleaner solvents, and new solid-phase extraction systems allowed us to slash impurity footprints and improve throughput. Our R&D teams and plant operators collaborate to root out bottlenecks and sources of variability. At times, it’s as simple as adjusting column packing techniques; other times, we introduce new filtration steps.

    Sometimes, direct operator observation surpasses sensors and charts. One worker noticed a faint off-odor coming from a still. Investigation led us to replace a gasket grade even though it met all supplier certifications, since its trace outgassing interacted with the product at high temperature. This attention to detail ensures that what you receive arrives in optimal condition, batch after batch. Customer trust only grows when technical feedback gets acted on; we share these stories because transparency grows partnerships grounded in real results.

    Safety Isn't an Afterthought

    Aromatic nitriles don’t tolerate shortcuts. Handling powdered intermediates with both amino and nitrile groups calls for disciplined air and dust controls. Our team spends significant training hours on spill response, PPE, and first-aid techniques. Exposure limits, ventilation checks, and vacuum filtration protocols anchor our daily routine. While the chemical itself holds low volatility and resists microbial degradation, the dust can irritate skin and mucous membranes. We place a premium on containment and fast cleanup. No one leaves the floor without decontaminating boots and coveralls, minimizing cross-contamination in all shared spaces.

    We update our safety protocols with every regulatory guideline change. New data about chronic exposure, environmental loading, or waste treatment routes doesn’t gather dust in our compliance office. Instead, we work side-by-side with the customer’s EHS teams to provide both production and disposal insights, helping end-users meet and beat local and national environmental regulations. The more technical exchange there is, the less costly reactive problem solving becomes down the road.

    Meeting Batch and Scale-Up Demands

    Formulation and process scale-up challenge both the supplier’s engineering and the customer’s R&D. Our reactors scale flexibly between pilot runs and commercial tonnage, keeping quality systems consistent regardless of order size. For one pharmaceutical partner, we transitioned from five-kilo batches for preclinical studies to multi-ton volumes supporting global registration. The biggest hurdle: maintaining analytically identical product lots, even as total run times and sampling frequency shifted. Advanced process controls provide non-stop analytical checks, nipping deviations in the bud before any lot leaves the plant.

    As regulations tighten and custom syntheses require new traceability standards, we invested in digital batch tracking and real-time impurity fingerprinting. This isn’t just for show—customers sometimes trace subtle shifts in product reactivity back to impurity profiles invisible to traditional titration or melting point analysis. We make sure every lot ships with a full dossier: NMR, HPLC chromatograms, IR scans, residual solvent results. The worldwide regulatory landscape doesn’t wait, and we don’t expect our clients to compromise or chase paperwork just to get their next experiment or launch out the door.

    Tackling Industry Challenges and Future Trends

    Demand for fluorinated aromatics continues to climb. Drug pipelines lean on small, highly functionalized molecules that call for intricate substituent placement—fluoro, amino, nitrile, and more. At the same time, regulatory scrutiny grows around waste streams and sustainability practices in specialty chemical manufacturing. For us, the challenge means two things: keep pushing downstream purification yields higher to minimize solvent waste, and work with supply partners who demonstrate real stewardship in production and fluorination chemistry. A “green” supply chain isn’t just a buzzword; solvent recycling and minimized liquid effluent are real metrics customers demand.

    We’re also seeing more interest in customized particle size and polymorph control, especially from formulators who care about dissolution and compacting in solid dosage forms. Our process engineers worked with a handful of these customers to design new milling and sieving protocols, delivering materials that meet not only chemical, but also physical requirements. Requests range from sub-100 micron powders for rapid dissolution to coarser grades that resist static caking during high-speed transfer.

    Real-World Success, One Batch at a Time

    A case stands out where a Japanese partner faced persistent clogging during their acylation step, linked to impurity carryover from a non-fluorinated benzonitrile. Their troubleshooting eventually led to incorporating our 3-Fluoro-4-Aminobenzonitrile, and the difference in reaction clarity and post-synthesis filtration rates was immediate. Not every fix requires a fancy new catalyst or reactor upgrade—sometimes, it takes rethinking the input material.

    Other buyers who made the switch saw faster lab turnaround, easier analytical reconciliation against USP standards, and fewer wash cycles during cleanup, which lowers both cycle times and utility consumption. Better reproducibility ripples through every stage, from early drug discovery to full-scale commercial output. These hidden cost savings accumulate, freeing resources for more value-adding R&D downstream.

    Looking Forward: Partnership and Progress

    3-Fluoro-4-Aminobenzonitrile is more than just a chemical compound to us. Decades of hands-on experience have shaped not just how we make it, but how we think about serving the scientists who put it to work in new therapies, materials, and industrial innovations. No shortcut replaces thoroughness at each process step. No regulatory file looks after itself; every detail gets checked, rechecked, and signed off by staff as invested in your results as you are.

    We’ve learned that the most effective advances happen with open technical exchange between manufacturer and customer. The challenges tackled yesterday—from impurities and packaging to custom handling and analytical support—dissolve when trust and transparent problem-solving lead the relationship. Each run of 3-Fluoro-4-Aminobenzonitrile reflects a partnership built on real experience and a shared commitment to getting it right, today and for every new innovation in the years ahead.