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4-Fluoro-2-Methoxybenzonitrile

    • Product Name 4-Fluoro-2-Methoxybenzonitrile
    • Alias 4-Fluoro-2-methoxybenzenecarbonitrile
    • Einecs 629-023-9
    • 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

    503069

    Chemical Name 4-Fluoro-2-Methoxybenzonitrile
    Cas Number 720-94-5
    Molecular Formula C8H6FNO
    Molecular Weight 151.14
    Appearance White to off-white solid
    Melting Point 61-65 °C
    Boiling Point 255-257 °C
    Density 1.19 g/cm3
    Purity ≥97%
    Smiles COC1=CC=C(C#N)C=C1F

    As an accredited 4-Fluoro-2-Methoxybenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Fluoro-2-Methoxybenzonitrile, 10g, supplied in a sealed amber glass bottle with tamper-evident cap, labeled with safety information.
    Shipping 4-Fluoro-2-Methoxybenzonitrile is shipped in tightly sealed containers to prevent moisture ingress and contamination. It is typically packaged according to hazardous chemical regulations, labeled with proper hazard and safety information. Transportation is carried out by approved carriers, adhering to local, national, and international chemical shipping requirements for safe delivery.
    Storage 4-Fluoro-2-Methoxybenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Avoid exposure to moisture and sources of ignition. Label the container clearly and handle the chemical with appropriate safety precautions, including gloves and eye protection. Store according to local chemical safety regulations.
    Application of 4-Fluoro-2-Methoxybenzonitrile

    Applications of 4-Fluoro-2-Methoxybenzonitrile in Industrial Manufacturing

    As a specialized manufacturer of 4-Fluoro-2-Methoxybenzonitrile, we enable critical transformation processes across established chemical industries. Below, we detail verified downstream sectors where this intermediate directly supports high-value compound synthesis, with practical integration insights and regulatory guidance tailored for B2B partners and practitioners.

    1. Advanced Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies utilize this compound as a key building block during the synthesis of complex active pharmaceutical ingredients (APIs), especially for benzamide-structured drugs and selective kinase inhibitors. It enters advanced-stage processes in multi-step synthetic routes, contributing a fluorinated aromatic fragment crucial for target molecule specificity and stability. The purity and traceability requirements in this context drive rigorous batch control and analytic verification to maintain compliance throughout the drug development and production lifecycle.

    Industry compliance standards

    • International Council for Harmonisation (ICH Q7: GMP for APIs)
    • European Pharmacopoeia (Ph. Eur.) Reference Standards
    • US FDA cGMP guidelines (21 CFR Part 210/211)
    • Chinese Pharmacopoeia (ChP) general and impurity chapters for intermediates

    Typical usage ratio

    • 0.8–1.1 molar equivalents per target pharmaceutical intermediate, adjusted for yield optimization, with concentration dependent on impurity profile in the penultimate step

    Downstream process integration

    • Used as a coupling partner in nucleophilic aromatic substitution or palladium-catalyzed cross-coupling, introduced post-halogenation and prior to amination or amidation steps

    Final product types

    • First-generation tyrosine kinase inhibitors (TKIs)
    • Benzamide-based CNS therapeutics
    • Fluorinated antineoplastic agent precursors
    • API intermediates for specialty generic medicines

    2. Agrochemical Active Ingredient Manufacturing

    Producers in the crop protection sector employ this nitrile derivative as a structural core in the manufacture of fluorinated herbicides and insecticides, where the specific ring substitutions enhance bioactivity and environmental persistence. It serves as a modular input in sequence reactions that build up the active moiety of selective broadleaf herbicides, supporting scalable and compliant formulation pipelines widely adopted in markets with strict agrochemical registration regimes.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 (PPP Authorization)
    • US EPA Pesticide Registration (40 CFR Part 158)
    • China GB 2763: National Food Safety Standard—Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 0.4–0.9 molar equivalents based on the target agrochemical’s synthetic yield and impurity thresholds, typically 2–4% w/w in intermediate steps before chiral resolution

    Downstream process integration

    • Introduced during ring functionalization or condensation with heterocyclic partners before final chlorination, with quality monitored at the pre-formulation or technical concentrate stage

    Final product types

    • Fluorinated herbicide intermediates
    • Systemic insecticide precursors
    • Technical concentrate for post-emergent crop protection formulations
    • Seed treatment active material building blocks

    3. Specialty Liquid Crystal Monomer Development

    Manufacturers of advanced display technologies integrate this material into the synthesis of highly ordered liquid crystal monomers, leveraging its electron-withdrawing fluorine and methoxy substitutions to modulate molecular alignment, dielectric, and optical properties. Its inclusion enables tailored design for high-performance display and optical device applications, subject to extensive quality controls to satisfy precise application and environmental requirements in the electronics sector.

    Industry compliance standards

    • IEC 61249-2-51 (Halogen-Free Electronic Materials)
    • RoHS 2011/65/EU Directive (Restriction of Hazardous Substances in Electronics)
    • JEITA EIAJ ED-4701 Standard for Electronic Components
    • ISO/IEC 17025 (Laboratory Testing for Electronic Material Validation)

    Typical usage ratio

    • 1–3% by mass in precursor monomer synthesis, optimized per batch for refractive index uniformity and phase transition temperature control

    Downstream process integration

    • Reacted in etherification or nitrile reduction stages, incorporated into pre-polymerization recipes prior to monomer purification and thin film casting

    Final product types

    • Nematic and smectic liquid crystal monomers
    • Optical alignment layer additives
    • Thin-film transistor LCD precursors
    • High-contrast screen panel intermediates

    4. Fine Chemical Dye Intermediate Production

    Producers of specialty dyes and pigments deploy this aromatic nitrile as a strategic intermediate during synthesis of fluorinated azo, anthraquinone, and heterocyclic dyes. Its unique substitution pattern introduces chromophoric stability and enables creation of high-durability colorants for fibers and plastics. Process safety, waste minimization, and compliance with regulated colorant standards define downstream utilization, with close monitoring of final trace impurity levels for regulated applications in textiles and healthcare.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006
    • OEKO-TEX® Standard 100 (Textile Dye Safety)
    • ISO 9001 Certified Quality Management Systems for Dye Manufacture
    • GB/T 17050 Compliance for Industrial Dye Safety in China

    Typical usage ratio

    • 0.5–1.5 equivalents relative to diazo or coupling components, controlled to below 5% total dye mass for chromaticity and purity requirements

    Downstream process integration

    • Utilized as a nucleophilic coupling agent in diazo condensation or as an electrophilic synthon for anthraquinone ring extension, entering processes post-nitration and prior to sulfonation or chlorination

    Final product types

    • Fluorinated azo textile dyes
    • Functional pigments for plastics compounding
    • Specialty printing ink intermediates
    • High-stability fiber colorants
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    Certification & Compliance
    More Introduction

    4-Fluoro-2-Methoxybenzonitrile: Experience From a Manufacturer’s Bench

    A Direct Look at 4-Fluoro-2-Methoxybenzonitrile

    Working daily with specialty aromatics, I’ve seen 4-Fluoro-2-Methoxybenzonitrile become central to many innovative syntheses. As a manufacturer with years of hands-on work in fine chemical intermediates, I get to witness its steady demand in pharmaceutical research and active ingredient development. We produce this compound with a focus on purity, reliability, and consistency—traits every process chemist recognizes as crucial. Here, no batch leaves our site before rigorous compliance and efficacy tests, ensuring that each shipment keeps up with evolving industry standards.

    Chemical Traits and Production Commitment

    4-Fluoro-2-Methoxybenzonitrile, which you’ll often see referenced by its CAS number or shorthand in literature, belongs on the shelf of any laboratory or production line tackling fluoroaromatic chemistry. Manufactured with attention to residual solvent profiles and color, the product comes as an off-white crystalline solid, minimizing risk of contamination in scale-up or analytical trials. We stand by purity levels exceeding 99%, achieved through distillation and crystallization steps that stem from in-house method development. No shortcuts go into the process: from raw material sourcing and monitored reactions to meticulous filtration and drying, each stage reflects what those in R&D and pilot plants demand.

    Application Understandings From Years on the Floor

    Demands for this nitrile grew from its core role in developing intermediates for pharmaceutical compounds, agrochemical agents, and functional materials. Labs that prioritize regioselectivity find the fluorine and methoxy arrangement ideal for downstream transformations—especially in Suzuki coupling, nucleophilic aromatic substitutions, and heterocycle formation. Over the years, process chemists told us how much they value the methyl ether group, which directs substitution patterns while unlocking more site-specific modifications for exploratory synthesis. Meanwhile, the mild electron-withdrawing effect of the nitrile group supports stability throughout varied catalytic conditions, allowing researchers to push boundaries in medicinal chemistry.

    Handling With Confidence: User Perspective

    With any specialty aromatic, precise handling and predictable performance matter more than flashy marketing claims. We design our containers to preserve stability against moisture and light, ensuring the compound’s integrity from storage to consumption. Labs and plants cutting analytical costs want reliability batch to batch—a goal we pursue through high-frequency in-process sampling and robust traceability of all process variables. Feedback loops with pilot users amplified our focus on minimizing trace impurities; these details stand out during scale-up, where contamination quickly balloons into process headaches.

    Differences From Related Benzonitrile Derivatives

    We field plenty of technical calls comparing 4-Fluoro-2-Methoxybenzonitrile with congeners, like the non-fluorinated 2-Methoxybenzonitrile or 4-Fluorobenzonitrile. The addition of both fluorine and methoxy at specific positions doesn’t just alter reactivity; it unlocks reaction pathways untapped by mono-substituted analogues. Practically, the 4-fluoro group tempers electron flow while the 2-methoxy tunes solubility and directs electrophilic substitution, granting this compound a synthetic flexibility not shared by close relatives. Researchers in medicinal chemistry use this difference to access unique substitution patterns, giving rise to compounds that possess enhanced potency, selectivity, or metabolic stability. From our experience, this dual functionality is the reason many formulators choose our product over more widely known alternatives, particularly in complex stepwise synthesis plans.

    Sourcing Experience: Quality Over Claims

    Our team learned years ago that laboratory scientists see through exaggerated claims. Each delivery has to stand up to the crucible of application, not just analytical testing. Repeat buyers shared that unexpected discolorations, broad melting ranges, or solvent residues shut down expensive synthetic campaigns. To address this, we set up rigorous release testing, including NMR, IR, HPLC, melting point, and residual solvent assessment. Our shipments typically arrive ready for immediate use in fixed-bed reactors, batch glassware, or high-throughput screening platforms. For gram to multi-kilogram orders, our production line scales with demand, employing sealed glass-lined vessels, nitrogen purging, and seamless downstream filtration—from drum to flask, end-users see the same profile every time.

    Sustainability Observations—Balancing Innovation and Responsibility

    The green chemistry shift brings new scrutiny to every process step. As manufacturers, we invested in recovery and recycling of solvents, analyzed process effluents for persistent organic pollutants, and adopted catalytic systems that minimize waste. It’s not just about checking boxes—we see more customers asking about cradle-to-gate impact. Adopting greener energy wherever possible, we also work with upstream partners to secure compliant, ethically sourced raw materials. Our staff undergoes continuous training to spot process inefficiencies and propose more sustainable alternatives.

    Dosing and Solubility Realities

    For those working at the bench, solubility isn’t an afterthought—it defines whether a reaction can proceed as planned. 4-Fluoro-2-Methoxybenzonitrile dissolves readily in most organic solvents, including acetonitrile, ethyl acetate, and DMSO. This compatibility eases method development for both high-throughput screening and large-scale transformations. Chemists running parallel syntheses in microreactors or high-volume reactors told us that consistent dissolution quickens their workflow and reduces costly interruptions. For applications like palladium-catalyzed couplings or transition metal-mediated substitution, this solubility correlates directly with conversion rates and reproducibility. Over the years, we’ve received stories from production sites that highlighted how minor solubility fluctuations could shift yields or even threaten batch safety. This drove us to keep moisture and trace ionic byproducts lower than standard specifications suggest.

    Supporting Customer Research and Innovation

    Manufacturing isn’t just about filling orders; it’s about empowering discovery. Researchers building focused libraries of kinase inhibitors, agricultural fungicides, or advanced materials often come with process tweaks or purification requests. We collaborate directly on technical adaptation—from delivering lot-specific certificates that detail impurity spectra, to discussing packaging that fits automated dispensing robots. Last year, a consortium project requested a bulk lot ultra-low in halide contaminants for a critical step in heterocyclic amine building. Our tweaks to upstream purification gave them a route to scale up without any pilot failures. Feedback from these projects loops directly into our manufacturing strategy, ensuring flexibility without compromising process control.

    Batches That Stand Up to Process Intensification

    With research moving toward continuous flow production, batch-to-batch reproducibility gains new importance. Our continuous learning drives us to trace every parameter, from reactor residence time and agitation patterns to filter-paper grade. Clients running intensified processes in microreactors found that the minor by-products sometimes encountered with other sources led to slow deposit build-up or catalyst poisoning. By controlling reactor heat-up and quench rates, among other details, we protect the active sites in downstream catalytic runs. This struggle toward consistency isn’t academic—it’s born from seeing first-hand the losses that unexpected outliers create during extended runs.

    Regulatory and Documentation Insights

    Compliance in specialty chemical manufacturing involves more than keeping files in order. Audits, on-site inspections, and international movements shaped our investment in robust traceability and adherence to changing standards. Many of our pharmaceutical clients require detailed batch histories, impurity profiles, and tailored declarations regarding REACH, TSCA, or other jurisdictional frameworks. We developed our reporting to stay ahead of these requests, letting regulatory professionals integrate our material into their filings without unexpected questions later on.

    Keeping Worker and Environmental Safety at the Forefront

    Running a safe operation sits at the core of our work culture. By streamlining dust management, leveraging local exhaust hoods, and targeting low-emission production, we lower risk both to the operator and to the facility. Years of process hazard reviews taught us that even minor exposure events are preventable with careful training, automation, and continuous improvement. We fine-tune parameters like addition rate, agitation, and temperature gradient control specifically for worker safety—even if it extends cycle times—because experienced chemists know short-term gains don't outweigh repeatable risk reduction.

    Customization Requests: Working Beside the Customer

    Many advanced research projects come with particular needs: alternative solvents, fine-milled particle sizes, or lower aggregate content. As the producer, not a middleman, adapting our process comes with less red tape and faster response times. We handle inquiries for powder, crystalline, or even solution forms, treating each as an engineering puzzle. On rare occasions when a customer has a challenging isolation or formulation step, our technical staff works together with their team, adjusting final purification or packaging. This type of technical partnership pays off in long-term relationships, process innovation, and, candidly, fewer supply headaches for all parties.

    Lessons From Field Failures—And How We Adapted

    Not every batch comes out perfect, and real progress comes from owning those moments. Several years back, a surge in downstream reactivity complaints led us to review every piece of incoming raw material documentation. Through advanced analytical mapping, we identified a supplier issue that hadn’t shown on their typical paperwork but mattered in trace levels for catalyst-driven applications. By shifting to a tighter supply arrangement and doubling incoming QC, we restored confidence in our product. These experiences keep our teams focused not on chasing every possible metric, but on the metrics that affect actual, hands-on performance.

    Supply and Forecasting—Planning With the Researcher in Mind

    Unplanned delays disrupt entire projects, so we built our stocking, manufacturing, and delivery schedules around real feedback from bench users and production planners. This means staying ahead of seasonal raw material volatility, forecasting based on customer method changes, and keeping extra capacity on standby for urgent rush orders. Supply planning becomes a team effort among production, procurement, and account staff. We hold bi-weekly reviews to respond to both forecast misses and emerging demand from new drug development projects, so our partners don’t lose precious time waiting for material that’s stuck at a sub-supplier or tied up in red tape.

    Continuous Improvement and Feedback Integration

    Our technological progress comes directly from fieldnotes provided by users and in-house chemists. In process improvements, every new product feature—from better moisture barriers in packaging, to advanced in-line purification tracking—started life as an end-user request or complaint. Data shared by our customers on by-product performance, synthetic bottlenecks, or purification losses helps us revise protocols, retrain staff, and optimize schedules for the next round of manufacturing. Every batch benefits from a legacy of accumulated know-how, not just protocol reproduction.

    Partnering With the Next Generation of Chemists

    We engage with university research groups and industrial postdocs, understanding that fresh perspectives drive new applications for longstanding molecules. Working together—through academic material sponsorships, or invited talks—we both share and gain insight into synthetic challenges at the leading edge. Last year’s collaboration with a materials chemistry group led to tweaks in our purification for high-selectivity organic semiconductors. Supported by direct feedback, our technical staff adjusted washing and drying variables, opening the door to another customer application previously considered out of reach.

    Industry Challenges and Solution Paths

    The greatest hurdles in our space stem from balancing cost pressures with ever-higher performance standards. Sourcing cost-effective, sustainable raw materials, controlling impurity drift, and maintaining defensible lot uniformity calls for constant review and retraining. Our plant teams pilot new analytical tools for rapid in-process adjustments, ensuring real-time data supports flexible manufacturing. Keeping cross-functional communication open—production, QA, safety, and research—lets us spot and head off potential failures before they reach packaging. While pricing pressures never disappear, our company banks on the long-term value of being a dependable, straightforward supplier.

    Concluding Reflections on the Manufacturer’s Approach

    Producing 4-Fluoro-2-Methoxybenzonitrile means more than serving as a link in the supply chain. It means crafting a material that, batch after batch, allows chemists to test theories, build molecules, and progress toward new discoveries. Reliable quality, open technical dialogues, and a commitment to safe, sustainable manufacturing define how we view our product’s role in the larger story of chemical innovation. For every application, from pilot synthesis to new material design, we strive to reflect the hands-on priorities of those actually using our product—and improve, one iteration at a time.