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Methyl 2,4-Difluorobenzoate

    • Product Name Methyl 2,4-Difluorobenzoate
    • Alias MFCD01861390
    • Einecs 240-613-6
    • 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

    501042

    Chemical Name Methyl 2,4-difluorobenzoate
    Cas Number 85118-94-5
    Molecular Formula C8H6F2O2
    Molecular Weight 172.13 g/mol
    Appearance Colorless liquid or solid
    Boiling Point 203-204°C
    Melting Point 16-18°C
    Density 1.29 g/cm³
    Refractive Index 1.483
    Purity Typically ≥98%
    Smiles COC(=O)C1=CC(F)=CC(F)=C1
    Storage Temperature Store at 2-8°C
    Solubility Slightly soluble in water; soluble in organic solvents

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

    Packing & Storage
    Packing The 100g package features a tightly sealed amber glass bottle labeled "Methyl 2,4-Difluorobenzoate," with hazard symbols and handling instructions.
    Shipping **Shipping Description for Methyl 2,4-Difluorobenzoate:** Methyl 2,4-Difluorobenzoate is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be transported at ambient temperature, in compliance with relevant chemical transport regulations. Proper labeling and documentation are required, and handling by qualified personnel is recommended to ensure safe delivery.
    Storage Methyl 2,4-Difluorobenzoate 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 oxidizing agents. Avoid humidity and sources of ignition. Keep the storage area clearly labeled and restrict access to trained personnel. Use secondary containment to prevent accidental spillage.
    Application of Methyl 2,4-Difluorobenzoate

    Applications of Methyl 2,4-Difluorobenzoate in Industrial Manufacturing

    Methyl 2,4-Difluorobenzoate serves as a valuable fluorinated intermediate in the synthesis pipelines of several specialized chemical sectors. As a direct manufacturer, we supply this high-purity ingredient primarily to the pharmaceutical, agrochemical, advanced material, and specialty dye industries. Our capabilities align with stringent downstream formulation demands and regulatory requirements, supporting seamless integration into advanced production workflows.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies incorporate this compound as a key intermediate in producing fluoroarene-based drugs, particularly where selective introduction of fluorine atoms is required for modulating bioactivity and metabolic stability. Formulators typically react it during multi-step synthetic schemes to build core structures for APIs in antiviral, anti-inflammatory, and oncology classes. Our product enters the route following halogenation and esterification workflows, catering to active ingredient manufacturers whose QC protocols depend on strict impurity control and traceability.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF Pharmaceutical Ingredient Monograph (where applicable)
    • EDQM CEP for relevant API pathways
    • 21 CFR Part 211 (US FDA cGMP)

    Typical usage ratio

    • Utilized between 0.1 mol to 1.2 mol per mol of target intermediate, adjusted by process scale and target yield in each synthesis batch

    Downstream process integration

    • Charged as a reaction substrate following fluorination or amidation steps, with purification by crystallization or chromatography prior to API assembly

    Final product types

    • Fluorinated pharmaceutical intermediates
    • Active pharmaceutical ingredients for anti-infective and anti-cancer drugs
    • Specialty reference standards

    2. Agrochemical Active Ingredient Manufacturing

    Leading crop protection manufacturers select this ester to construct difluorinated aromatic moieties found in new-generation herbicides and fungicides. Application chemists integrate it into O-alkylation or coupling reactions to optimize systemic activity and photostability within agrochemical formulations. This material enters the sequence after initial aromatic halogenation, supporting stringent residue and purity requirements dictated by agricultural agencies worldwide.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 (approval of active substances)
    • ISO 9001:2015 Quality Management (for upstream supplier management)
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.5–2.0% by weight of formulation precursor, calculated to meet targeted yield and active loading for downstream active ingredient synthesis

    Downstream process integration

    • Added during final arylation or condensation reaction, typically before product isolation and technical product crystallization

    Final product types

    • Difluorobenzoic acid-based herbicides
    • Systemic fungicide intermediates
    • Technical grade pesticide actives

    3. Advanced Polymer and Material Synthesis

    Engineered plastics and specialty elastomer producers employ this chemical to introduce fluorinated functional groups, imparting improved thermal stability and hydrolytic resistance in high-performance polymers. Compounders optimize the feed ratio based on desired chain length and fluorine content, using it in transesterification or polycondensation steps. Downstream processors rely on this intermediate to tailor mechanical properties for end applications in electronics and automotive assemblies.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • RoHS Directive (2011/65/EU) for electronic materials
    • UL 94 Flammability Standards (for polymer compounds)
    • REACH Regulation (Registration, Evaluation, Authorisation and Restriction of Chemicals)

    Typical usage ratio

    • 0.2–0.8 mol% relative to monomer mixture, adjusted by molecular design requirements for target polymer architecture

    Downstream process integration

    • Incorporated in melt-phase transesterification reactors or solution-phase polycondensation reactors, followed by devolatilization and pelletization

    Final product types

    • Fluorinated aromatic polyesters
    • Heat-resistant elastomeric compounds
    • Electronic device encapsulation films

    4. Specialty Dye and Pigment Synthesis

    Colorant manufacturers utilize this raw material to develop functional dyes with superior stability and unique colorfastness properties. It serves as a building block during functional group coupling reactions, helping designers achieve precise electronic properties essential in photovoltaic and display applications. Integration typically follows diazotization or Suzuki coupling steps, with rigorous tracking to meet analytical quality controls for dye performance in high-value markets.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) stewardship
    • REACH Regulation (EC 1907/2006) for dyes and pigments
    • ISO 9001:2015 Quality Management
    • GHS Safety Data Sheet requirements for transported dyes

    Typical usage ratio

    • 0.3–1.5 equivalents in active synthesis batch, fine-tuned according to chromophore target and process throughput

    Downstream process integration

    • Fed into coupling or acylation step as a fluorinated aromatic source, followed by post-reaction purification and spray drying

    Final product types

    • Functionalized dyes for LCD and OLED displays
    • Solar cell photoactive pigment intermediates
    • Specialty textile colorants with improved fastness
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    Certification & Compliance
    More Introduction

    Methyl 2,4-Difluorobenzoate: Reliable Performance in Synthesis

    About Methyl 2,4-Difluorobenzoate

    In our years of experience manufacturing aromatic esters, methyl 2,4-difluorobenzoate has stood out as a steady choice for research and industrial labs. The molecular formula C8H6F2O2 gives it a precise role as an intermediate. Many professionals in pharmaceutical and agrochemical sectors reach for this compound whenever the goal is to achieve selective fluorination in benzoic acid derivatives.

    This product, with CAS number 261763-19-7, features a clean, colorless liquid or sometimes a low-melting solid, depending on storage climate. Chemists often remark on the faint aromatic odor, a quick indicator that signals proper handling. Our plant maintains consistent physical attributes: purity >99% by area, low water content, and minimal residual solvents, which we confirm by both GC and HPLC in-house. Some batches run through NMR analysis for full fluorine distribution reporting, as trace contamination alters downstream product yield.

    Practical Uses Backed by Direct Production Experience

    Laboratories ask for methyl 2,4-difluorobenzoate when the project involves the generation of fluorinated aromatics. Pipeline drugs for neuropsychiatric disorders or cancer therapies regularly feature fluorobenzoic acid scaffolds. Our material often functions as a protected ester while the core ring transforms at various substitutions, adapting easy hydrolysis back to the free acid at the right stage. Agricultural research teams use our product for actives targeting insect nervous systems, leveraging the stability and reactivity profile of fluorinated aromatics.

    One of our long-term clients echoes a sentiment shared by many: switching to in-house produced methyl 2,4-difluorobenzoate from imported sources helped their process reliability and reduced costs. The absence of extraneous residue and a predictable melting point cut post-reaction cleanup by 20%. Instead of spending time purifying starting materials, their staff could focus on core synthesis steps. Every batch ships with full documentation, letting users trust the substance for GMP and R&D runs alike.

    We see a recurring demand in life science applications, especially for those synthesizing compounds with electron-withdrawing substituents. Fluorine atoms at the 2 and 4 positions allow for specific activity tuning—reactivity, metabolic stability, and target selectivity all shift as the ring’s electronic character changes. Some researchers have noted that even a single regioisomeric impurity throws off downstream product ratios; our batch tracking ensures repeatable selectivity.

    How Methyl 2,4-Difluorobenzoate Differs From Related Compounds

    Manufacturing experience has taught us the importance of controlling isomer content and maintaining identity. For example, methyl 2,6-difluorobenzoate, a close sibling, presents markedly different reactivity at both laboratory and plant scale. The electron density at the ortho positions in the 2,6-isomer causes downstream intermediates to cyclize or rearrange less predictably, throwing off yields. The 3,4-difluoro variant doesn't provide the same balance between stability and reactivity and has found less favor among our industrial clients for these reasons.

    Some may consider ethyl 2,4-difluorobenzoate, but the extra ethyl carbon changes volatility, polarity, and boiling point, complicating reactions that require tight temperature control or minimal solvent residue after workup. For those pursuing hydrolysis or aminolysis steps, our methyl ester provides a sharper breakpoint, reducing side reactions and allowing for easier pH adjustments in later stages.

    The experience from scaling up batches over years continually highlights one clear pattern: consistency in starting material translates into better optimization and lower waste in multi-step syntheses. Several customers have returned after trialing alternatives, citing frustration from process drift—slight differences in melting point or impurity spectrum might only show up after full characterization of the final product, but by then, cost and time have built up. Our quality controls have allowed teams to lock in validated methods and repeat them at hundred-gram or even kilogram scale without unexpected setbacks.

    Our Manufacturing Perspective: Real-World Challenges & Solutions

    Producing methyl 2,4-difluorobenzoate is not simply a matter of assembling reactants. Each step brings challenge: keeping moisture out to avoid unwanted hydrolysis, choosing the right catalyst to minimize formation of over-fluorinated byproducts, tightly monitoring reaction time to prevent isomer migration. We run jacketed reactors to stabilize temperature swings, especially during mid-scale production. Sometimes, borderline batches prompt secondary purification, but the priority stays on minimal solvent waste and maximum solvent recovery—environmental stewardship and budget go hand in hand.

    Years of bench and pilot experience have taught us to spot batch inconsistencies early. The aromatic esterification step, sensitive to trace water, sometimes requires molecular sieves or gentle nitrogen sparging. Early on, we refined our cleaning routines to keep cross-contamination below detection limits after several customers reported off-odors in finished batches. Adjusting our washing SOPs and switching to high-purity solvents brought those complaints down to zero, and repeat clients continue to rely on us for reproducibility.

    Every operator in the plant learns to recognize the visual signature of over-fluorinated residues—pale, oily films in glassware after a failed charge signal an upset reaction. With oversight from both QC staff and experienced chemists on the production floor, we prevent minor process hitches from snowballing into serious rework.

    Supporting the Scientific Community With Consistency

    Feedback from regular users shapes our process improvements. Several years ago, a pharmaceutical client shared their experience synthesizing a small molecule for oncology trials. Early batches, purchased from a non-specialist supplier, led to longer purification times and intermediate instability, costing an extra week during a critical milestone. Our team addressed the issue by introducing a targeted drying step in the esterification, validating the upgrade with NMR and GC-MS. Purity and yield both increased, and the client’s synthesis timeline stabilized.

    Some users have transitioned to automated synthesis systems that integrate online GC monitoring. Our product’s tight purity range allows high-throughput screening and fast hit validation, since column fouling and sticky residues become non-issues. One academic group recently published data linking reaction efficiency to ester content, showing that lower moisture batches reduce hydrolysis of active intermediates.

    Others working with radiolabeled analogs find our methyl 2,4-difluorobenzoate particularly amenable to isotopic exchange. Low background contamination and consistent fluorine distribution open routes to short-lived PET tracers or diagnostic tool molecules. Some teams producing fluorinated peptidomimetics have adapted our product as an alkylating precursor, noting that heating profiles more closely match literature data when using high-purity lots.

    Addressing Supply Chain and Environmental Responsibility

    Our direct control of every stage in the plant supports secure supply even during raw material bottlenecks. Domestic sourcing of benzoic acid derivatives and upstream fluorinating agents gives us insight into market shifts. Regular audits of our suppliers—and contingency contracts with alternate sources when needed—minimize risk for clients running time-sensitive or regulatory filings.

    On the environmental front, we’ve engineered distillation recovery units to recycle cleaning and reaction solvents. By lowering emissions and saving on disposal costs, we keep our operation lean and sustainable. Our production staff participates in routine safety and environmental training, learning the latest best practices for handling both hazardous intermediates and high-purity finished products. Chlorinated solvents never enter our methyl 2,4-difluorobenzoate process streams, and regular water testing keeps effluent within legal limits.

    Shipment to customer sites uses packaging certified for chemical compatibility and transport safety. Our logistics team recommends just-in-time delivery windows to limit storage risk at customer facilities. We regularly review feedback on packaging durability to limit incidents in the warehouse or on the road.

    Quality Control: Precision From Raw Material to Final Batch

    Our facility’s in-line analytics set us apart. Each input stream receives FTIR and NMR fingerprinting before reactors charge. Final lots go through GC for purity, LC-MS for trace contaminants, and titration for water. Repeat analysis on retained samples helps us track batch drift over time, letting us correct process drift before it impacts our customers. Some customers have specific acceptance thresholds, like halogen content below 100 ppm or residual acidity under 0.05%; we adjust final purification as needed to match these unique specs.

    Sample transparency works both ways—clients can request aliquots from production before full shipment. This lets their QC teams run independent verification, and in rare cases our technical staff advises on optimal blending for even tighter tolerances. Our approach has grown from years of responding to unique customer scenarios: one small biotech firm needed a special purity window for a combinatorial library buildout, influencing us to couple reactor selection with batch blending to hit the mark every time.

    Labeling never uses generic codes or untracked numbers; we stamp each container with a batch number linked to production logs, raw material origin, and analytical reports. Regulatory readiness isn’t an afterthought—our documentation meets both local and global standards, making the registration process easier for downstream users in pharmaceuticals, agrochemicals, and materials science.

    Commitment to Continuous Improvement

    Customer needs change as research and regulatory pressures shift. In-house process engineers regularly upgrade reactor systems, filtration trains, and analytical methods. A few years ago, market demand for purer methyl 2,4-difluorobenzoate prompted an investment in a new vacuum distillation system, which brought water content below 0.1%—a difference quickly noticed by synthetic chemists.

    Open lines of communication with buyers translate into better products. Clients can consult with us on their proposed reaction conditions, and share feedback from pilot runs. This collaboration not only strengthens our relationships but also provides real-world insight that drives further innovation in our workflow.

    Routine staff training sharpens awareness of small details—hot spots in reactors, slight pH drifts during aqueous workup, or solvent odor changes that indicate process drift. Stay vigilant and build on lessons from every batch, both successful and flawed, to ensure ongoing improvement.

    Meeting Evolving Industry Demands

    Regulatory standards for purity and traceability have grown stricter across global markets. We track each lot from starting fluorobenzene to packaged product, using digital logs verified by both in-house and third-party audits. Compliance with ISO, REACH, or other market-specific rules means customers can bring new products to market quickly without regulatory delay.

    Handling requests for non-standard packaging, concentrated batches, or custom labeling arises frequently from our international customer base. Our flexibility keeps experimental and production timelines on track, without tying up staff in rework or administrative follow-up. Some customers bulk order for a stable supply buffer, others schedule regular smaller shipments to match clinical trial or pilot production schedules. Either approach, our plant prioritizes timely responses and accurate tracking.

    With each year, application horizons expand—from API building blocks and imaging agents to specialty polymers and novel catalysts. By tuning our facilities and know-how to the nuances of methyl 2,4-difluorobenzoate production, we continue to support both established industrial workflows and the next wave of scientific innovation.

    Collaborative Growth: Perspectives for the Future

    The best improvements come from those who use the product day-in and day-out. We welcome feedback, from questions on batch history to specific challenges in scale-up or downstream processing. Over the years, partnerships with academia, pharmaceutical development teams, and chemical engineers have led to process enhancements and new application routes we hadn’t anticipated at the design stage.

    Ongoing conversations with experts in synthetic methodology, analytical chemistry, and regulatory compliance keep us tuned into new trends and regulatory shifts. This readiness to share expertise and absorb new information lays the groundwork for both product stability and competitive edge in a demanding marketplace.

    Our guiding focus remains steady: bring reliable, high-purity methyl 2,4-difluorobenzoate to connect the vision of molecular designers with consistent execution at bench or plant scale. By grounding our workflow in real-world needs and continuous learning, we aim to help every customer get the results they need, every time.