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4-Cyano-3-Fluorobenzoic Acid

    • Product Name 4-Cyano-3-Fluorobenzoic Acid
    • Alias 4-Cyano-3-fluorobenzoic acid
    • Einecs 841-555-1
    • 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

    670491

    Productname 4-Cyano-3-Fluorobenzoic Acid
    Molecularformula C8H4FNO2
    Molecularweight 165.12 g/mol
    Casnumber 870987-64-1
    Appearance White to off-white solid
    Meltingpoint 150-154°C
    Solubility Slightly soluble in water
    Purity Typically >98%
    Smiles C1=CC(=C(C=C1C#N)F)C(=O)O
    Inchi InChI=1S/C8H4FNO2/c9-7-2-1-5(4-10)3-6(7)8(11)12/h1-3H,(H,11,12)
    Storagetemperature Store at 2-8°C
    Synonyms 3-Fluoro-4-cyanobenzoic acid

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

    Packing & Storage
    Packing A 25g amber glass bottle sealed with a screw cap, labeled “4-Cyano-3-Fluorobenzoic Acid, ≥98%,” featuring hazard symbols.
    Shipping 4-Cyano-3-Fluorobenzoic Acid is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with chemical safety regulations, ensuring no leaks or contamination. The container is clearly labeled with hazard and handling information. During transit, it is stored in cool, dry conditions and handled by trained personnel.
    Storage 4-Cyano-3-Fluorobenzoic Acid should be stored in a tightly sealed container, away from direct sunlight, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing or reducing agents. Always ensure proper labeling, and avoid exposure to air and humidity to prevent degradation. Store at recommended temperatures, typically room temperature.
    Application of 4-Cyano-3-Fluorobenzoic Acid

    Applications of 4-Cyano-3-Fluorobenzoic Acid in Industrial Manufacturing

    As a direct manufacturer, we supply 4-Cyano-3-Fluorobenzoic Acid to specialized industry sectors where its unique structure supports targeted synthesis pathways, especially in regulated and performance-driven production environments. The following application scenarios reflect its real, long-standing use across key chemical and pharmaceutical industries, highlighting precise compliance protocols, technical formulation requirements, process integration points, and resultant finished product types.

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

    Organic synthesis teams in the pharmaceutical industry utilize 4-Cyano-3-Fluorobenzoic Acid as a core heterocyclic building block for a range of active pharmaceutical ingredients. This acid’s cyano and fluoro functionalities enable specific substitution patterns on benzene rings, necessary for target molecules in advanced cardiovascular, anticancer, and anti-inflammatory drug analogs. These applications demand stringent adherence to industry quality and traceability measures.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • EU GMP Part II (Active Substances Used as Starting Materials)
    • USP-NF and Ph. Eur. monograph specification for impurity profiles
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • Employed at 0.5–3.5% molar ratio, based on the targeted synthetic route complexity and specific intermediate yield demands; always determined by stoichiometry in route design and adjusted during scale-up validation.

    Downstream process integration

    • Triggered at the third or fourth step of multi-stage chemical synthesis, frequently as a nucleophilic aromatic substitution reactant; introduction occurs in coupled batch reactors under nitrogen with controlled solvent systems, followed by workup and isolation ahead of downstream amidation or cyclization steps.

    Final product types

    • API intermediates for kinase inhibitors
    • Precursors in non-steroidal anti-inflammatory drug (NSAID) synthesis
    • Starting materials for oncology compound families
    • Finished APIs subject to final purification and crystallization

    2. Agrochemical Active Ingredient Development

    Crop protection chemical manufacturers use this raw material primarily as a functionalized aromatic acid in the development of fluorinated herbicide and fungicide molecules. Its ability to impart both metabolic stability and plant-specific activity through tailored molecular scaffolds provides substantial benefits in new generation product pipelines, especially under tightening regulatory controls for pesticide residues and by-products.

    Industry compliance standards

    • OECD Test Guidelines for Residue Chemistry (OECD GLP)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 Quality Management System for agrochemical production
    • REACH Registration and Safety Data Sheet (SDS) requirements under ECHA

    Typical usage ratio

    • Dosage level ranges from 1–6% in the technical concentrate; final ratio depends on target molecule structure and efficacy optimization with adjuvants through pilot formulation trials.

    Downstream process integration

    • Introduced during the aromatic coupling step in synthesis of pyridine- or triazole-based agrochemical actives; the acid enters post-chlorination reactor trains and proceeds through controlled esterification or amidation, ahead of microencapsulation processes for finished dose forms.

    Final product types

    • Selective herbicide technicals for post-emergence weed control
    • Fungicide actives designed for cereal crop protection
    • Technical grade intermediates for insecticide formulation
    • Pesticide formulation concentrates and ready-to-use suspension concentrates

    3. Electronic Chemicals for Liquid Crystal Intermediate Production

    Manufacturers in the display materials sector select 4-Cyano-3-Fluorobenzoic Acid as a controlled precursor in multi-step processes to generate high-purity intermediates used in LCD and OLED liquid crystal compositions. The presence of both cyano and fluorine substituents ensures defined dipole moments and alignment properties, vital for optical clarity and fast switching displays. Only producers with advanced QC and contamination controls can support the demanding purity needs of this application.

    Industry compliance standards

    • SEMI C67.1–0708 (Standard for Electronic Grade Chemicals)
    • ISO 14001:2015 (Environmental Management Systems in electronics manufacturing)
    • IATF 16949 for electronic component supply chains
    • RoHS (Restriction of Hazardous Substances) compatibility validation

    Typical usage ratio

    • Incorporated at 0.3–2.8% wt/wt as a precursor within multicomponent reaction streams; the actual proportion adapts to specific LC molecule series and end-use optical requirements.

    Downstream process integration

    • Enters as a raw matrix input in phase-transfer catalyzed coupling steps, followed by high-vacuum purification and column chromatography to achieve sub-ppm impurity control prior to downstream isomer separation and final blending.

    Final product types

    • Liquid crystal intermediates for nematic and smectic phase displays
    • Purity-defined compounds for active matrix LCD panel assembly
    • OLED intermediate materials for large-format display modules
    • High-transmittance monomers for specialty screen technologies

    4. Fine Chemical Synthesis for Specialty Dye and Pigment Manufacture

    Specialty pigment producers leverage the unique electron-withdrawing properties of this functionalized benzoic acid in the controlled synthesis of high-stability dye intermediates, especially where colorfastness, solvent resistance, and molecular tunability are critical. The material’s halogenated-cyano aromatic ring structure supports diazo compound routes and condensed ring systems not achievable with other acids, particularly for technical textile and polymer coloration.

    Industry compliance standards

    • OEKO-TEX Standard 100
    • ISO 18314-3 (Analytical color measurement in dye products)
    • EN 71-3 (Toy safety – Specification for migration of certain elements, for pigment use in plastics)
    • ISO 9001:2015 in fine chemical manufacturing

    Typical usage ratio

    • Utilized at 1.2–4.5% by weight in the initial dye precursor batch, modifiable based on desired chromophore intensity and molecular design for downstream coupling or condensation.

    Downstream process integration

    • Integrated after initial aromatic amination, often as the acid component in controlled diazotization or Friedel-Crafts coupling reactions; typically followed by sequential purification, precipitation, and filtration steps before stabilization additives.

    Final product types

    • High-stability pigment precursors for engineering plastics
    • Solvent-resistant dyes for fiber and yarn processing
    • Specialty colorants for performance inks
    • Lightfast pigments for automotive and industrial coatings

    5. Advanced Polymer Modification for High-Performance Resins

    Producers of specialty polymers and engineering resins use this benzoic acid derivative to introduce controlled polarity and molecular rigidity in advanced resin synthesis, notably in the polyimide and polyamide-imide sectors. Its incorporation modifies thermal and dielectric properties, supporting formulations for demanding applications such as electronics, aerospace, and high-barrier films. Integration requires robust batch controls and analytical verification to meet application-specific performance benchmarks.

    Industry compliance standards

    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • ISO 11357 (Differential scanning calorimetry in polymers)
    • ASTM D3418 (Thermal transitions of polymer resins)
    • RoHS and REACH for end-use in electronic applications

    Typical usage ratio

    • Blended in the 0.7–2.5 mol% range relative to total monomer content in step-growth polymerization; the specific percentage adapts based on targeted glass transition temperature (Tg), mechanical reinforcement, and dielectric constant requirements.

    Downstream process integration

    • Added during initial monomer charge or as a pre-reacted salt in the polycondensation reaction vessel, followed by controlled imidization or amide formation and solvent casting or extrusion for final shaping.

    Final product types

    • High-thermal-stability polyimide films
    • Engineered thermoplastic resin pellets
    • Dielectric materials for flexible printed circuits
    • Barrier films for flexible packaging applications
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    Certification & Compliance
    More Introduction

    4-Cyano-3-Fluorobenzoic Acid – A Core Building Block for Innovation

    Understanding 4-Cyano-3-Fluorobenzoic Acid

    As a chemical manufacturer specializing in the development and large-scale production of key organic intermediates, we've seen shifts in both the pharmaceutical and chemical industries that demand a greater level of reliability from raw materials. 4-Cyano-3-Fluorobenzoic Acid, often referred to by its CAS Number 57381-36-5, fills a growing need for highly pure, versatile building blocks in advanced synthesis. Across our facilities, we produce this compound with an eye toward strict quality standards and the rigor required for sensitive downstream reactions.

    Production Approach and Quality Experience

    Years of practice with benzoic acid derivatives taught us the value of controlled reaction conditions. Not all manufacturers execute multi-step syntheses with the same consistency, especially where handling strong cyano and fluoro substituents is concerned. We designed our process to prevent cross-contamination and degradation, using closed systems that maintain the integrity of both the cyano and fluorine groups. We know that subtle impurities can carry through to final APIs or electronic chemicals, so every stage gets monitored by HPLC and NMR, not just at the end. Material coming out of our reactors passes tests for color, crystallinity, and residual solvent. Batch records stretch back years for full traceability. Analysts in our labs review melting point, identification, and assay before packaging. This direct control helps assure that lab-scale results match what R&D and production chemists see when using our material.

    What Sets This Compound Apart?

    We have worked with dozens of benzoic acid derivatives, and each one has personality. 4-Cyano-3-Fluorobenzoic Acid distinguishes itself by its unique arrangement of functional groups, offering both a strong electron-withdrawing cyano at the para position and a fluorine at meta. Many compounds offer just one of these features. That specific substitution pattern produces a balance of reactivity and selectivity that chemists demand, enabling more controlled downstream transformations like amidation, esterification, and cross-coupling. In synthesis routes where both electron density and positional activation matter, chemists find that ortho or para fluorine substitutions change the game. The cyano group allows for further elaboration via nucleophilic addition or palladium-catalyzed couplings our customers want to attempt without fussing over unwanted side reactions. We pick raw materials and solvents that suit this application profile, not only purity for its own sake, but practical end-use in mind.

    Physical Characteristics and Consistency

    The material typically forms as an off-white to light tan crystalline powder. After years in production, we've experienced how minor color shifts can signal process deviation or exposure to moisture during packaging. Employees at our plant have adjusted handling to minimize exposure, employing quick drying cycles and double-layered bags for every shipment. We calibrate analytical scales daily so our packaging stays true to stated net weight. Melting point sits reliably in the expected range around 178-182°C, every batch confirmed by three-point measurements. In earlier years, batches sometimes exhibited trace color or polymorphic forms; we traced those back to subtle changes in cooling rates after filtration. Changes in water content were remedied only by investing in lower-humidity storage rooms. Our internal standards for appearance and purity exceed most published pharmacopeia references. This effort helps downstream chemists avoid starting material surprises that bump back project timelines.

    Practical Use – A Chemist's Perspective

    Chemists at pharmaceutical and agrochemical companies have told us repeatedly: predictable performance trumps novelty. We’ve sat in meetings with formulation teams who want reliable compound behavior, whether working on gram scales or moving toward metric tons. 4-Cyano-3-Fluorobenzoic Acid’s acid group allows for easy salt or ester formation, useful for intermediate steps in small molecule drug synthesis. Its cyano and fluoro groups set the stage for selective bond formation in both Suzuki and Buchwald-Hartwig couplings. The combination unlocks C–N or C–O bond creation while minimizing meta- and para- side reactions. Even beyond pharmaceuticals, R&D groups in liquid crystal manufacturing reach for this material because its functional groups offer rigidity yet permit further functionalization. In every application, chemists ask for a starting material that comes clean, packaged to avoid static and clumping, and ready for direct weighing. Our reputation has grown less through splashy materials than from delivering cargo that works for bench chemists and process engineers alike.

    Safety and Handling Experience

    This compound enters our operations with regularity, so operational safety is non-negotiable. Through firsthand handling, we know that powders in this class can create airborne dust if handled roughly on the line. We train staff to charge vessels with slow, deliberate pour rates and to wear fitted masks. After one near miss in a pilot suite, we shifted to smaller, double-walled drums that reduce physical stress on each lot. Our teams learned early that minimizing skin contact, even with mild irritants, protects long-term health. Cleaning protocols ensure no residues persist beyond each shift—a detail that non-manufacturers too often miss.

    Applications Shaped by Direct Feedback

    Our relationships with application chemists shape what and how we produce. Pharmaceutical developers explained how 4-Cyano-3-Fluorobenzoic Acid serves as an intermediate for synthesizing kinase inhibitors, anti-inflammatory drug candidates, and even antibiotics. We saw agrochemical researchers employ it as a precursor in herbicide synthesis, manipulating the cyano and acid groups for tailored biological activity. Electronic material manufacturers described its use as a scaffold for OLED and advanced polymer R&D. Technical feedback arrives in all kinds of forms—sometimes a casual email, other times a full process report. In one such exchange, a medicinal chemistry group asked for lower residual solvents because their next reaction stage used base-sensitive catalysts; we introduced an extra rotary evaporation step at our end, shaving ppm levels well below their threshold. These long-term partnerships mean our modifications address real-world process constraints, not just theoretical improvements.

    Supply Reliability Under Pressure

    Supply risk has become a hot topic, especially with global disruptions affecting raw material sourcing. Our procurement teams learned some lessons during the last major border closures, when certain reagents became restricted or delayed. We maintain dual sourcing for primary starting materials. If a critical fluorinating or cyanating agent runs short in one region, we have a framework to switch to an alternate supplier with pre-approved quality. We keep extra inventory of strategic intermediates on-site, using just-in-time production only where it doesn’t threaten downstream consistency. Annual maintenance shutdowns factor heavily into long-term customer relationships; we communicate blackout dates months ahead, enabling our partners to adjust purchase orders and plan alternative batch schedules. These supply chain decisions stem from the plant floor, not just a remote scheduling office.

    Environmental and Regulatory Realities

    Handling benzoic acid derivatives with cyano and fluoro functional groups involves real regulatory and waste challenges. Local and regional authorities scrutinize process effluent containing cyano byproducts. Over time, we invested in dedicated waste neutralization for cyanide species, opting for both pH adjustment and catalytic decomposition prior to discharge. Fluorinated wastes bring their own complexity. We maintain a closed-loop distillation system to recover spent solvents and any fluoro byproducts. Even with new updates to local emissions reporting, our facility data shows well below mandated release thresholds. Our auditing team works with environmental consultants to pre-empt changes and avoid unwelcome surprises. Auditors call for granular logs on material in/outflows; we maintain them in real time. Regulatory pressure continues to increase, but by addressing these needs ahead of inspection cycles, we sustain approvals and customer confidence.

    Comparing to Other Benzoic Acid Derivatives

    4-Cyano-3-Fluorobenzoic Acid stands out from many other substituted benzoic acids through its dual functionalization. Some competitors offer mono-functionalized acids, but those lack the additional control over electronic properties and downstream reactivity. Other products like 3-fluorobenzoic acid or 4-cyanobenzoic acid each bring only one aspect of tuning, making them less adaptive in stepped syntheses. Through direct feedback, we’ve learned that combinatory effects from cyano and fluorine allow for reactivity not available from methyl, methoxy, or simple halogenated analogs. This is not just a theoretical advantage; it plays out in higher yields and fewer byproducts in real pilot batch reports. Years ago, bench chemists compared products head-to-head in model Suzuki couplings and shared the results; our combined cyano-fluoro profile led to fewer purification steps. For larger producers, this shrinks waste streams and accelerates time-to-market in route scouting and scale-up.

    Solutions and Continuous Improvement

    Direct manufacturing experience fosters an attitude of continuous, targeted improvement. The realities of working with reactive organics led us to develop specialized drying processes and anti-static packaging. Monitoring yield drift and impurity profiles over multi-year cycles taught us which process points drive variability; we act faster now, not waiting for QC failures. In one pivotal year, a minor solvent swap in early synthesis introduced a new trace impurity. Only routine NMR flagged the change, letting us fix the protocol and maintain trusted supply. These practical tools beat grand strategies: we keep close links between QC labs, process chemists, and plant operators so nothing gets lost in translation. Listening to the line chemists has helped us identify new pain points and adapt shipping methods to match both bulk and small-lot customer preferences.

    Sharing Knowledge Across the Supply Chain

    A manufacturer doesn’t succeed in a vacuum. We work side-by-side with users who encounter downstream bottlenecks, whether in HPLC purification or scale-up heat management. Shared technical roundtables sometimes reveal tweaks to particle size or solubility that once seemed trivial. We incorporate this feedback directly—sometimes changing milling methods, other times adjusting filter drying. Industry events and technical workshops let us trade insights with peers, staying aware of alternate synthetic routes and new application spaces. Several years back, after one technical exchange, a customer challenged us to deliver milled lots with a narrower particle size. The shift shaved hours off their own downstream filtration time. No catalog or specification could have predicted this improvement; it emerged through direct dialogue and willingness to listen.

    Embracing the Realities of Scale

    Producing 4-Cyano-3-Fluorobenzoic Acid at both small and industrial scale involves unique decisions at every step. At lab scale, fine temperature and reagent control comes easily. As batch size grows, even slight changes in solvent loading, agitation, or recrystallization temperature show up in the finished bulk powder. We now use automated sensors to track temperature gradients in real time, trimming variability across 100 kilo batches. We keep pilot lots aside when running new process modifications, guaranteeing our customers can test lots side-by-side before committing to a new bulk order. Managing scale also means thinking through logistics—pallet sizes, moisture-proof liners, paperwork for regulated transport. Our warehouse staff, who handle both outbound drums and custom-packed small containers, understand how every order reflects on customer trust.

    Looking Ahead – Where Does Improvement Lead?

    As the fields of pharmaceutical and electronic materials synthesis continue to evolve, demand for reliable, functionally rich intermediates is only rising. Customers bring new process ideas and tougher end-use conditions every year. We remain committed to adapting our facility and analytical capabilities, keeping both flexibility and output quality at the core. Our future investments target even higher purity levels and real-time analytics so material properties stay consistent batch after batch. Collaboration with downstream partners, technical workshops, and feedback sessions drive us toward even leaner, more predictable supply chains. Our record with 4-Cyano-3-Fluorobenzoic Acid sets a benchmark by which we judge progress, not just with this item, but across all our specialty intermediates.