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

4,5-Difluoro-2-Methoxybenzonitrile

    • Product Name 4,5-Difluoro-2-Methoxybenzonitrile
    • Alias 4,5-Difluoro-2-methoxybenzenecarbonitrile
    • Einecs 629-509-1
    • 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

    228257

    Product Name 4,5-Difluoro-2-Methoxybenzonitrile
    Cas Number 946687-43-0
    Molecular Formula C8H5F2NO
    Molecular Weight 169.13 g/mol
    Appearance White to off-white solid
    Melting Point 49-51°C
    Boiling Point 282.8°C at 760 mmHg
    Density 1.34 g/cm³
    Solubility Soluble in organic solvents such as DMSO and methanol
    Purity Typically ≥98%
    Smiles COC1=CC(F)=C(C#N)C(F)=C1
    Inchi InChI=1S/C8H5F2NO/c1-12-8-3-6(9)7(10)2-5(8)4-11

    As an accredited 4,5-Difluoro-2-Methoxybenzonitrile 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 with a white label displaying "4,5-Difluoro-2-Methoxybenzonitrile," safety pictograms, and storage instructions.
    Shipping 4,5-Difluoro-2-Methoxybenzonitrile is shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport complies with relevant chemical safety regulations. The packaging ensures no leakage or contamination. The chemical is labeled with hazard and handling information, and shipping documentation accompanies all consignments for traceability and regulatory adherence.
    Storage 4,5-Difluoro-2-Methoxybenzonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers and acids. Protect from light and sources of ignition. Store under nitrogen or inert atmosphere if moisture-sensitive. Ensure all storage complies with local chemical safety regulations and proper labeling.
    Application of 4,5-Difluoro-2-Methoxybenzonitrile

    Applications of 4,5-Difluoro-2-Methoxybenzonitrile in Industrial Manufacturing

    4,5-Difluoro-2-Methoxybenzonitrile serves as a precision intermediate for advanced organic synthesis, supporting several high-value sectors within the pharmaceutical and fine chemical industries. As a manufacturer, we supply this compound to downstream partners for integration into established and regulated production processes, helping them streamline formulations, reduce byproduct formation, and ensure batch-to-batch consistency. Below are primary industrial application scenarios where this material supports specialized downstream synthesis and strict quality requirements.

    1. Pharmaceutical API Intermediate: Antitumor and Cardiovascular Drugs

    Pharmaceutical producers incorporate 4,5-difluoro-2-methoxybenzonitrile as a key building block in multi-step synthesis for select active pharmaceutical ingredients, particularly in anticancer agents and antihypertensive drugs. The compound's unique substitution positions enable site-selective reactions that reduce purification burden and enhance process yields in high-value medicine production. It enters processes such as Buchwald–Hartwig amination, nucleophilic aromatic substitution, and subsequent conversion to benzamide or benzoic acid derivatives.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – ICH Q7
    • European Pharmacopoeia (Ph. Eur.) monographs relevant to the API
    • 21 CFR 210/211 FDA regulations for drug substance manufacture
    • US DMF (Drug Master File) support for regulatory dossiers

    Typical usage ratio

    • Dosage varies from 0.08 to 0.4 molar equivalents per batch, adjusted based on target molecule complexity and specific reaction stoichiometry

    Downstream process integration

    • Introduced during the early to mid-stage of multi-step synthesis, usually following Halex fluorination and prior to condensation or reduction steps
    • Monitored by HPLC and GC for residual solvent and trace impurities to ensure carryover control

    Final product types

    • Antitumor agents (such as kinase inhibitors containing fluoroarene motifs)
    • Antihypertensive APIs (such as selective ARB derivatives)

    2. Agrochemical Intermediate: Selective Herbicide Synthesis

    Leading agrochemical formulators use this material as a critical precursor in the development of advanced fluorinated herbicides. Its incorporation into patented benzonitrile and triazole systems enables precise tuning of bioactivity and degradation rates, while supporting environmentally responsible synthesis via reduced halogenated waste. The compound participates in nucleophilic aromatic substitution and further coupling to yield herbicidal actives with improved field stability.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for agro input manufacturing
    • FAO/WHO Guidelines for pesticide formulation purity
    • REACH registration and compliance (EU) for chemical intermediates
    • US EPA 40 CFR Part 158 for technical grade active ingredient registration

    Typical usage ratio

    • Integrated at 12–22% w/w of technical concentrate formulation, depending on targeted substituent density and process optimization studies

    Downstream process integration

    • Charged during first synthesis stage for aromatic backbone construction, prior to triazole ring closure or further functionalization steps
    • Every batch undergoes GC-MS and NMR verification to confirm positional substitution and minimize isomer formation

    Final product types

    • Post-emergent selective herbicides for cereal and small grain crops
    • Pre-mix technical concentrates for proprietary agricultural use

    3. Advanced Material Science: Functionalized Polymer Additives

    Manufacturers of specialty polymers in semiconductor and display technology rely on this compound for the synthesis of fluorinated oligomers and crosslinkers. Its role is crucial in modulating polymer glass transition temperature and electrical properties, allowing for application in demanding electronic device fabrication. Producers precisely control the addition of the raw material to avoid phase separation and ensure uniformity at the molecular level in high-purity polyarylene ethers and related engineered plastics.

    Industry compliance standards

    • IEC 61249-2-21 standards for halogen-free materials in electronics
    • RoHS Directive (2011/65/EU) for restricted substances in electrical equipment
    • UL 94 for flame-retardant polymer certification
    • Cleanroom production ISO 14644-1 for contamination control in specialty films

    Typical usage ratio

    • Formulated at 1.8–5% w/w in polymer masterbatch, adjusted to achieve required dielectric constants or surface energy for the end-use substrate

    Downstream process integration

    • Added during initial pre-polymerization or in reactive extrusion processes, in the presence of controlled radical initiators
    • Inline FTIR and GPC help monitor functionalization completion and polymer chain distribution

    Final product types

    • Flexible printed circuit substrate films
    • Photoresist materials for lithography
    • High-performance liquid crystal display (LCD) spacers

    4. Custom Synthesis: Reference and Screening Compound Manufacturing

    Specialty chemical research and custom synthesis organizations employ this substituted benzonitrile as a foundation block for producing advanced reference standards and chemical libraries. It provides a versatile scaffold that supports rapid analog generation for drug discovery and structure-activity relationship (SAR) studies, particularly where fluorinated motifs are required for bioisosteric purposes or metabolic profiling.

    Industry compliance standards

    • OECD GLP (Good Laboratory Practice) for test material preparation
    • ISO 17025 laboratory accreditation for chemical analysis
    • IUPAC chemical nomenclature guidelines for database registration
    • National Institute of Standards and Technology (NIST) purity benchmarking

    Typical usage ratio

    • Applied at 0.02–0.12 mmol scale for screening and milligram to gram scale for library generation, depending on assay sensitivity and analytical requirements

    Downstream process integration

    • Engaged in Suzuki or Sonogashira cross-coupling reactions, then purified via flash chromatography and lyophilization for reference standard production
    • NMR, HPLC, and LC-MS used for structural confirmation and trace impurity analysis

    Final product types

    • Analytical reference compounds for regulated bioassays
    • Building blocks for in-house SAR screening panels
    • Custom labeled standards for metabolite identification

    5. Fluorinated Dye and Pigment Intermediate

    Dye and pigment manufacturers in the specialty colorant sector turn to this compound for synthesis of advanced fluorinated chromophores. It allows for the creation of colorants with high photostability and strong lightfastness, meeting the technical demands of textile, plastic, and ink industries. The raw material enters the synthetic pathway immediately before final deprotection and coupling steps, supporting the design of dyes with controlled hue and fastness properties.

    Industry compliance standards

    • OEKO-TEX Standard 100 for substances in textiles
    • REACH Annex XVII compliance for colorant safety
    • EN 71-3 standards for heavy metal content in toys and inks
    • ISO 4618 for pigment and solvent-borne coating components

    Typical usage ratio

    • Incorporated at 0.5–3.2% w/w into reaction blends, with levels refined according to target chromophore and product batch size

    Downstream process integration

    • Added prior to azo-coupling, or used in pre-functionalization steps for phthalocyanine dye synthesis
    • Color quality checked by UV-Vis and colorimetry post-synthesis, with impurity monitoring for non-compliant colorants

    Final product types

    • High-performance textile dyes
    • Special effect pigments for plastics
    • Fade-resistant inkjet printer colors
    Free Quote

    Competitive 4,5-Difluoro-2-Methoxybenzonitrile 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

    4,5-Difluoro-2-Methoxybenzonitrile: Insight from Our Production Line

    Understanding 4,5-Difluoro-2-Methoxybenzonitrile

    Every day on the production floor, we see 4,5-Difluoro-2-Methoxybenzonitrile transforming from raw materials into a key intermediate that serves demanding chemistries. Our experience manufacturing this compound has proven its reliability for downstream synthesis, especially where purity and batch consistency impact the quality of later-stage products. With a formula of C8H5F2NO and a solid appearance, its molecular design integrates the dual fluorine atoms at the 4 and 5 positions with a methoxy group at position 2, along with a benzonitrile core.

    Through careful control of each synthesis step, we achieve crystalline material free from unwanted isomeric byproducts. Rigorous attention at the reaction stage and during purification has taught us that even small residuals from incomplete fluorination can complicate chromatographic separations, so we fine-tune reaction parameters to keep side products to a minimum. Decades of scaling from grams to multi-kilogram batches have narrowed our process windows, ensuring reliable color, melting point, and NMR profile.

    Applications in Modern Synthesis

    Often in the specialty chemical industry, clients bring us new projects that demand a highly functionalized benzonitrile core for pharmaceutical or agrochemical precursors. 4,5-Difluoro-2-Methoxybenzonitrile stands out during early route scouting, thanks to its electron-withdrawing difluoro substitutions, which activate the ring for subsequent nucleophilic or palladium-catalyzed transformations. For example, chemists commonly use it for Suzuki, Buchwald-Hartwig, or amination reactions to install more complex groups, with the nitrile moiety providing further downstream options such as hydrolysis or reduction.

    Pharmaceutical developers and crop science researchers often require grams to kilograms with a high level of purity, since any unreacted feedstock can carry forward through sensitive transformations. We learned early not to compromise on solvent removal, as trace protic or halogenated residues can poison catalysts. Our operators run each batch through customized drying protocols and closed-transfer filling to preserve the required water content and minimize environmental impact.

    What Makes This Compound Distinct from Others

    On the technical side, the defining feature of this molecule lies in its substitution pattern. Its difluoro array amplifies both metabolic stability and physiochemical reactivity, especially compared with mono-fluorinated or unconjugated benzonitrile analogs. The difference is immediately apparent during customer method development, where 4,5-Difluoro-2-Methoxybenzonitrile handles base- or acid-mediated transformations more robustly than unsubstituted versions.

    We have observed that, in coupling reactions, this compound reacts more selectively and gives higher yields compared to its 3,5-difluoro- or non-fluorinated analogs. Over multiple product cycles, customers have come back reporting fewer byproducts in their chromatograms and easier scale-up procedures. That rock-solid reliability traces straight to the specific regioisomer we manufacture, and it’s something we work hard to preserve batch in and batch out.

    Down-to-Earth Insights from Daily Production

    Inside our manufacturing plant, people on the floor face the realities that don’t show on a data sheet. The reaction’s exotherm control demands constant diligence; we run temperature feedback loops, keep cooling lines clear, and check agitator loads. Every operator here knows when the color shift during crystallization tells the story of a batch going right—or heading off track. Handling fluorinated aromatic nitriles means using dedicated containment and exhausts to keep operators safe and cross contamination out of adjacent lines.

    Our drying rooms run tailored protocols because the difluoro and methoxy groups require us to balance water removal efficiently without scorching or decomposing the product. From practical experience, we only use vessels compatible with cyano and fluorine chemical environments, minimizing the formation of troublesome deposits and extending equipment life. Open communication between QC technicians and production teams has shortened our troubleshooting time; no one wants to wait for a rejected batch before fixing a process hiccup.

    Routine maintenance includes checking gaskets and valves for fluorochemical compatibility, which prevents leaks and preserves product quality. We’ve tested many filter aids and solvents for optimal removal of colored fines that sometimes form after crystallization. On the rare occasions off-spec batches occur, we study the root cause, adjust controls, and share knowledge to prevent repeat issues. It’s not theory—our operators see, touch, and measure every stage.

    Meeting Specification for the Real World

    Our customers give direct feedback on what they receive and expect. Purity isn’t just a number, it comes with real-world consequences in terms of downstream performance and regulatory audits. With 4,5-Difluoro-2-Methoxybenzonitrile, we keep a sharp focus on controlling both organic and inorganic residuals. Our HPLC maps consistently match reference standards, and we use orthogonal techniques like NMR and GC-MS. Testing covers not only purity, but also trace moisture, halide, and metals content since a stray contaminant can spoil sensitive transformations.

    The scent and color inspection step has caught more than one outlier batch before it left the warehouse. Even a slight yellow tint can signal over-oxidation or recycled solvent carryover; we trust experienced eyes and noses as much as analytical printouts. All data gets reviewed by chemists who have run the same reactions in the lab, so out-of-spec batches don’t slip through.

    Logistics gets equal attention—no one wants a drum arriving clumped or under-weight, so we calibrate scales, dry liners to spec, and regularly sanity-check lot weights. Customer audits sometimes walk through our plant with clipboards; we welcome it. We have nothing to hide in how 4,5-Difluoro-2-Methoxybenzonitrile emerges from raw material to packaged product.

    Handling and Storage Direct from the Plant Floor

    Fluorinated benzonitriles aren’t provoked by most shipping conditions, but they can cake if left exposed to moisture. From our own storage, we know to keep vessels closed, dry, and out of direct sun. Many end-users want resealable drums with a foil inner liner to keep the product from clumping. Our warehouse managers store the product at room temperature unless customers specify otherwise. During winter, we bring drums up to room temp before sampling so moisture condensation won’t spoil the top layer. We label drums with net batch weights and manufacturing dates, then ship by vetted haulers who understand how to handle specialty chemicals.

    Customers sometimes ask for custom pack sizes—smaller kegs or bulk containers—so our filling lines can adapt on short notice. Experience has shown it’s better to repack before product sits around than risk multiple exposure cycles. Inventory management ties back to production batch records, synced with customer forecasts so nobody runs short in the middle of a campaign.

    Continuous Improvement through Feedback

    Over years of production, the drive for improvement doesn’t slow. End users often try new reaction conditions and report back what works best. We’ve worked alongside chemists and engineers who request modified specifications—lower halogen residuals, narrower melting point, or finer particle size. By rolling out these changes, we’ve watched our product become a staple for synthetic programs worldwide.

    No plant operates perfectly; unplanned downtime, process hiccups, and raw material bottlenecks happen. The team tracks downtime hours, studies trends, and modifies process parameters in real time. The closer we work with direct users, the better we adapt our product features. In one case, feedback from a pharma customer led us to modify filtration procedures, since a trace impurity affected their process validation timeline. Sharing success stories and learning from failures builds the foundation for stronger supplier-customer relationships.

    Sustainability factors into every improvement. Chemical manufacturing faces increasing scrutiny for solvent use and emission controls. Over the last decade, we swapped several traditional solvents for greener options where possible and improved closed-system transfers to minimize environmental load. Our waste stream management focuses on reclaiming solvents, neutralizing spent reagents, and segregating all byproducts for offsite treatment. This isn’t just regulatory paperwork; our teams want to hand off less hazardous streams for the next generation.

    Trust Built on Experience

    Our manufacturing team recognizes that reliability matters most. Each batch of 4,5-Difluoro-2-Methoxybenzonitrile tracks back through documented raw material lots, in-process control records, and end-item testing. During customer visits or third-party audits, we walk guests through every stage, answering questions about process safety and batch homogeneity.

    Through years in the field, we’ve learned what makes a difference: fresh raw materials, well-reviewed batch sheets, and in-person checks at every critical point. Operators have the authority to halt production if anything seems off. Senior chemists mentor less experienced staff by sharing real-life examples—not textbook solutions. We keep the product pipeline flowing, but never at the expense of people, quality, or safety.

    Some customers rely on our consistency for their own regulated pipelines or high-value R&D. That trust doesn’t get built overnight. Our batch-to-batch tracking can spotlight precisely when and how a deviation happened, so we can trace root causes, issue corrective actions, and get product back on track. Most importantly, we open up about the tough lessons learned and how we use them to keep improving.

    Comparing with Related Aromatic Nitriles

    Our bench chemists often benchmark 4,5-Difluoro-2-Methoxybenzonitrile against other substituted aromatic nitriles. Mono-fluoro analogs sometimes give slower couplings or more colored byproducts, especially under air or less-than-ideal conditions. Trifluoro derivatives skew reactivity and can complicate downstream purifications. Substitution at the ortho or meta positions rather than para can shift regioselectivity and create separation headaches.

    Methoxy substitution at the 2-position, as opposed to the 3- or 4-position, changes how the molecule behaves under Pd catalysis. From lab notebooks and customer feedback, we know that this particular arrangement often provides shorter reaction times and higher isolated yields, with fewer unwanted tars. The difference shows up tangibly—less effort spent on column clean-ups or repeat recrystallizations.

    Some process developers have started directly with the difluoro-methoxy nitrile, skipping protection-deprotection cycles that slow multi-step syntheses. Faster throughput means quicker discovery timelines or lower cost per run, which our production team notices in repeat orders and growing demand.

    Supporting Downstream Innovation

    Research teams in pharma and crop protection aren’t standing still; they keep pushing for new molecular designs, faster reaction cycles, and greener process routes. 4,5-Difluoro-2-Methoxybenzonitrile meets these demands by serving as a versatile intermediate. Its broad compatibility supports both diversity-oriented synthesis and focused route optimization. Chemists can explore novel scaffolds or optimize previously established pharmacophores by capitalizing on the stability and selective reactivity of this molecule.

    We’re in conversation with development partners exploring new applications in materials science or electronics. The stability granted by difluoro substitution opens up opportunities in areas like OLED precursors or specialty polymers. The freedom to install further functionality on a robust aromatic core provides platform flexibility for innovators, much like the original pharmaceutical programs that popularized its use.

    We never stop scanning the literature, talking to collaborators, and learning what the next wave of synthesis techniques may demand. When unforeseen problems show up—solubility issues, ecological restrictions, toxicology changes—our process chemists sit down with R&D and chart alternate routes, select new solvents, or tweak purification protocols. Team conversations focus on solutions, not blame.

    Delivering More Than Just a Molecule

    From sourcing raw materials to completing QA checks, delivering 4,5-Difluoro-2-Methoxybenzonitrile means much more than manufacturing to spec. Every kilogram carries the lessons of past batches, customer insights, and continuous improvement. We know our clients depend on responsiveness and informed conversations as much as consistent product. That’s why feedback lines remain open: shipping staff, chemists, and plant managers all respond quickly when a question arises.

    Lab-scale customers experimenting with new synthetic plans can expect the same care we put into larger supply agreements. We monitor stability, package securely, and supply full documentation on request. The relationships we build have led to improvements that benefit the entire industry. By listening to direct user needs and staying transparent about our processes, we uphold trust not only in our material but in our team.

    If unforeseen issues crop up in shipping or downstream processing, our team wants to hear about it. The open exchange of technical information has real impact: less downtime, fewer campaign interruptions, and easier regulatory reviews.

    Looking Forward

    Our plant keeps evolving to meet new needs and higher standards. As the conversation around chemical safety, sustainability, and reliable supply grows, we welcome opportunities to improve both our product and our services. 4,5-Difluoro-2-Methoxybenzonitrile offers more than a line in a catalog; it comes from hands-on experience, attention to detail, and commitment to everyone who depends on what we make.

    Long-term thinking keeps us grounded—improving yields, reducing waste streams, and preparing for tomorrow’s compliance and performance demands. Each production run draws on lessons from hundreds of previous batches and finds new efficiencies when we spot them. Our team remembers that a missed step or hidden contaminant doesn’t just slow a process; it can derail an entire research program. Consistent quality, timely support, secure delivery—all make a difference you can measure.

    Continuing to work closely with users in pharmaceuticals, materials science, and specialty chemical synthesis, we remain dedicated not only to output, but to partnership. The story of 4,5-Difluoro-2-Methoxybenzonitrile doesn’t end on our loading dock. It continues in every successful synthesis, every solved technical challenge, and every innovation built on a strong, reliable foundation.