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Trans-2,5-Difluorocinnamic Acid

    • Product Name Trans-2,5-Difluorocinnamic Acid
    • Alias trans-2,5-DFC Acid
    • Einecs 678-214-6
    • 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
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    Specifications

    HS Code

    124689

    Product Name Trans-2,5-Difluorocinnamic Acid
    Cas Number 128452-01-1
    Molecular Formula C9H6F2O2
    Molecular Weight 184.14 g/mol
    Appearance White to off-white solid
    Melting Point 187-189°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=C(C=C1F)F)/C=C/C(=O)O
    Inchi InChI=1S/C9H6F2O2/c10-7-3-2-6(5-8(7)11)1-4-9(12)13/h1-5H,(H,12,13)/b4-1+
    Storage Temperature Store at 2-8°C
    Synonyms trans-2,5-Difluorocinnamic acid; (E)-2,5-Difluoro-3-phenyl-2-propenoic acid

    As an accredited Trans-2,5-Difluorocinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Trans-2,5-Difluorocinnamic Acid, 5g, is supplied in a sealed amber glass bottle with a tamper-evident cap and detailed labeling.
    Shipping Trans-2,5-Difluorocinnamic Acid is typically shipped in tightly sealed containers to protect from moisture and contamination. It should be handled as a chemical substance, following appropriate regulations. The package should be labeled, protected from physical damage, and stored in a cool, dry place during transportation. Ensure compliance with all safety and transport guidelines.
    Storage Trans-2,5-Difluorocinnamic Acid should be stored in a tightly closed container, kept in a cool, dry, well-ventilated area, away from incompatible substances such as strong bases and oxidizers. Avoid moisture and direct sunlight. Recommended storage temperature is typically at room temperature (15–25°C) unless otherwise specified by the manufacturer. Proper labeling and secure shelving help prevent accidental exposure or spillage.
    Application of Trans-2,5-Difluorocinnamic Acid

    Applications of Trans-2,5-Difluorocinnamic Acid in Industrial Manufacturing

    Trans-2,5-Difluorocinnamic Acid serves as a specialized intermediate in several advanced industrial chemical sectors. As a direct manufacturer, we supply this material strictly to established downstream industries where its unique difluorinated structure delivers performance advantages in targeted synthesis, homogenous formulation, and molecular engineering pipelines. The following sections outline core application scenarios grounded in actual regulatory standards, production integration, and end-use product types.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Fluorinated Drug Molecules

    This acid routinely features in the design routes of potent fluorinated pharmaceutical candidates, particularly where bioactivity modulation is essential. It mainly appears at the early intermediate stage for producing non-steroidal anti-inflammatory agents and receptor antagonists. API manufacturers require precise formulation and consistent quality as dictated by international pharmacopoeias and regulatory filings. Our material feeds directly into selective hydrogenation or amide coupling steps, supporting subsequent purification and conversion to finished drug compounds.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) for chemical intermediates
    • European Pharmacopoeia (EP) monograph requirements for related synthesis steps
    • FDA Drug Master File (DMF) traceability protocols

    Typical usage ratio

    • Ranges from 5%–15% mole ratio, calculated on the limiting reagent for target API synthesis; specific adjustment based on targeted molecular substitution pattern and process yield optimization.

    Downstream process integration

    • Charged as a building block in Grignard-type coupling, hydrogenation, or amidation reactions at the intermediate manufacturing stage for clinical-phase APIs.

    Final product types

    • New chemical entity (NCE) APIs featuring difluorinated motifs
    • Selective enzyme inhibitors
    • Advanced-stage investigational pharmaceuticals

    2. Organic Electronic Materials: OLED Emissive Layer Precursors

    Manufacturers of organic light-emitting diode (OLED) devices exploit the conjugated fluorinated scaffold for enhanced electron mobility and stability in blue and green emissive layers. This raw material enters the customization of organic small molecules deployed in advanced display and illumination technologies. Strict materials purity, as well as compatibility with high-vacuum deposition, is required.

    Industry compliance standards

    • IEC 61249-2-21:2017 for halogen-free electronic materials safety
    • RoHS Directive (2011/65/EU) restriction of hazardous substances
    • ISO 9001:2015 certified process control for electronic material synthesis
    • REACH SVHC compliance for pre-registered fluorinated chemicals

    Typical usage ratio

    • Used at 2–8% by mass in the organic formulation, tailored according to required photoluminescent profile and molecular weight of the downstream functional molecule.

    Downstream process integration

    • Condensation and palladium-catalyzed cross-coupling with substituted aryl units, leading directly to OLED-active compounds, then purified for vacuum evaporation or solution-casting onto substrate films.

    Final product types

    • Blue and green emissive organic layers for OLED displays
    • Custom fluorinated dopants in display and backlight modules
    • Organic photonic materials for flexible screen technology

    3. Agrochemical Intermediate for Fungicide Synthesis

    Producers of specialty crop protection agents incorporate this acid as a precursor for the construction of difluorinated benzenoid and cinnamamide derivatives used in next-generation fungicides. Compliance with pesticide precursor management and environmental control is critical. The compound enters amidation and esterification reactions to yield actives for seed treatment and foliar application formulations.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • OECD Principles of Good Laboratory Practice (GLP) for agrochemical synthesis
    • ISO 17025:2017 for analytical quality control
    • China ICAMA (Institute for the Control of Agrochemicals, Ministry of Agriculture) registration for technical materials

    Typical usage ratio

    • 3–6% molar equivalent as a substrate, variable by the target compound’s core structure and desired spectrum of biological activity.

    Downstream process integration

    • Integrated via direct amidation with amine nucleophiles or esterification with alcohols, feeding into formulation of technical concentrate or granule pre-mix.

    Final product types

    • Fungicide technical concentrates (TCs) with difluorinated aromatic features
    • Wettable powder and suspension concentrate (SC) formulations for field application
    • Seed coating actives with enhanced environmental persistence

    4. Specialty Polymer Modifier for High-Performance Fluorinated Resins

    In the specialty polymers sector, this difluorinated acid acts as a chain-modifying monomer for producing performance resins with improved chemical resistance and dielectric properties. Production adheres to polymer industry quality systems and requires rigorous thermal history control. Resin manufacturers employ the acid in melt or solution copolymerization alongside styrenics, acrylates, or vinyl monomers.

    Industry compliance standards

    • ASTM D638 for polymer tensile property qualification
    • ISO 9001:2015 and ISO 14001:2015 for environmental management
    • RoHS/REACH compliance for electronics-grade polymer use
    • UL 94 flammability rating requirements for finished materials

    Typical usage ratio

    • Generally loaded at 0.5–2.5% by weight, modulated to balance physical property enhancement with processability in copolymer blends.

    Downstream process integration

    • Introduced during bulk polymerization or post-polymerization grafting, then subjected to compounding, extrusion, and pelletizing for downstream fabrication.

    Final product types

    • Dielectric layers for printed circuit boards
    • High-frequency communication cable jacketing
    • Flame-retardant and chemical-resistant engineered plastics

    5. Fine Chemical Intermediate in Liquid Crystal Material Synthesis

    Trans-2,5-Difluorocinnamic Acid finds essential use in producing core building blocks for advanced nematic and smectic liquid crystals used in information displays. The fine chemical sector demands extremely high purity levels and tight batch consistency due to optical and electrochemical criticality. Integration targets specified substitution at the aromatic cores through catalytic coupling and non-aqueous esterification.

    Industry compliance standards

    • ISO 9001:2015 quality management in fine chemical manufacture
    • ISO 14001:2015 environmental control certifications
    • RoHS/REACH registration for display-use intermediates
    • JEITA (Japan Electronics and Information Technology Industries Association) performance evaluation

    Typical usage ratio

    • Typically dosed at 1–4% by weight based on chain length and mixture optimization for voltage-holding ratio and clearing point.

    Downstream process integration

    • Deployed for aryl coupling and ester formation as a stepping stone towards halogenated biphenyl or phenylcyano derivatives, subsequently fractionated for custom liquid crystal mixes.

    Final product types

    • Nematic liquid crystal mixtures for TFT-LCD panels
    • High-purity intermediary compounds for custom display formulations
    • Electro-optical switchable glass devices
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    Certification & Compliance
    More Introduction

    Trans-2,5-Difluorocinnamic Acid: A Closer Look from the Manufacturer’s Bench

    Direct Manufacturing Insight Into Trans-2,5-Difluorocinnamic Acid

    Trans-2,5-Difluorocinnamic Acid has become increasingly relevant for specialty synthesis in pharmaceuticals and agricultural research. From our manufacturing floor, we see its practical value every production run. We understand the compound because we handle its process from raw material to final packaging, seeing firsthand what close quality control delivers. In a landscape where every impurity can muddy downstream synthesis or cloud analytical profiles, running the actual reactor makes us keenly aware of what separates a fine product from a merely acceptable one. Years of watching the crystals grow and the numbers on the HPLC readout enables us to speak directly on practical matters and challenges, not marketing theory.

    Production, Character, and Practical Use Cases

    The molecule’s structure looks simple at a glance—a benzene ring bearing fluorines at two positions, tied to an unsaturated carboxylic acid side chain. That chemical layout does more than decorate a catalog or appeal to theoretical models; it shapes reactivity, solubility, and reliability in synthetic steps for a variety of industries. Run after run, we see how the trans configuration favors certain cross-coupling reactions and provides more predictable behavior in Diels-Alder and aromatic substitution chemistry.

    Trans-2,5-Difluorocinnamic Acid doesn’t just sit in a bottle—it drives real R&D, affecting yields and reproducibility. As a manufacturer, we observe researchers gravitating toward this compound for prep of building blocks with electron-withdrawing profiles. Medicinal chemists frequently use it as a scaffold for custom fluorinated phenyl derivatives, driven by the altered lipophilicity and metabolic stability conferred by fluorine atoms on the ring. Agricultural formulation teams have tapped it for advanced screening to create more robust lead compounds against broad classes of fungi and weeds.

    In our hands, we notice that the acidification and crystal formation steps require a careful eye to temperature and solvent use to ensure the end product stays pure—not just visually, but in terms of trace metal and residual solvent content. We can point to batches where a careless squeeze on the filter or a slightly too-hasty solvent switch led to a drop in purity or an increase in isomer formation. Batching and filtration at the plant force a continual focus on yield and impurity rejection, not academic ideals.

    Model and Physical Attributes That Impact Real-World Processing

    Each drum or bottle that leaves our factory passes a true set of hands-on inspections. The number everyone asks about is the purity threshold, which for us regularly exceeds 98.5% by HPLC. We crystallize it as a white to slightly off-white powder, typically providing stable flow and easy handling even when scaling up to dozens of kilos. The melting range tends to fall between 151–154°C, and the product resists rapid hydrolysis or degradation at room temperature. In solution, it shows considerable advantages over mono-fluorinated or non-fluorinated cinnamic acids, particularly when preparing downstream amides or esters that often prove sensitive to trace byproducts.

    Packing lines can become bottlenecks if particle size distribution drifts out of spec. We monitor this to minimize dust and clumping, both for safety reasons and for ease of use in high-throughput settings. The acid’s dense, crystalline consistency helps in accurate weighing, with little tendency towards hygroscopicity under standard storage. This matters more for bulk laboratory or kilo-lab users than is ever mentioned in most public-facing documents.

    We have engineered our production cycles to support delivery in packaging scaled to application—some clients want sealed glass for analytical grade projects; others choose lined drums for mid-scale campaign runs. All originate from a single batchwise synthesis system designed for maximum traceability. If you spot a problem, we can walk down the timeline to raw material source. That accountability can only come from decades of direct oversight.

    Key Differences from Similar Products: What We See in the Plant

    Chemically comparing trans-2,5-difluorocinnamic acid to more common cinnamic acid derivatives reveals a few points chemists and formulators rarely see without hands-on experience. Most laboratories are familiar with either non-fluorinated or mono-fluorinated cinnamic acids. Double fluorination (both ortho relative to the vinyl group and meta to the carboxyl group) alters both reactivity and downstream processing. In practical terms, this means certain coupling and condensation reactions either work more cleanly or fail less often compared to their mono-substituted counterparts. Double fluorination blocks some metabolic pathways that would otherwise deactivate or degrade the molecule under enzymatic conditions.

    Handling behavior also changes; trans-2,5-difluorocinnamic acid is less prone to forming sticky oils during solvent evaporation, compared to many closely related acids. The solubility profile in polar and slightly nonpolar solvents matters greatly for those setting up robotically managed purification systems or preparing microgram amounts for screening programs. Our feedback from scale-up chemists points strongly to more reliable retention times in preparative HPLC. This might seem minor, but in a workflow where dozens of derivatives need to be tracked and separated, small gains save hours per batch.

    Compare that to para-fluoro or 2,4-difluoro analogs, where unpredictable side reactions lead to byproducts that gum up analysis or complicate downstream hydrolysis. The trans-2,5 variant’s double fluorination pattern reduces the susceptibility to polymerization under UV light or base conditions. For manufacturing, this means less waste and smoother purification, both of which mean tighter compliance with internal and external quality standards.

    We supply research groups who have tested multiple isomers and soon settle on the trans-2,5 version for difficult arylation, acylation, or reduction development. Customer feedback loops through our technical service and process improvement teams, giving us a clear sense of which version proves most robust in each use case. Few resellers experience this level of direct, practical data. Our process teams collaborate with clients aiming for novel crop protection agents or fluorinated drug intermediates, refining process specs to best fit actual working conditions, not just theoretical purity targets.

    Supporting High-Value Research: Reliability as a Critical Element

    Most advanced research today—especially in pharmaceuticals—demands more than a simple reagent. Regulatory review, patent filings, and scale-up trials impose an extra set of requirements not apparent to those new to custom synthesis. Any deviation in isomeric purity, trace metal profile, or batch-to-batch consistency carries through every stage of molecule development. By running our process steps in-house, from raw material validation to reaction monitoring and quality assurance, we control every possible variable. Beyond generic testing like melting point, IR, or NMR, we use LC-MS to check for micro-impurities and confirm structural identity. In our labs, product reliability means never having to worry whether an analytical discrepancy traces back to a vendor.

    Research teams increasingly worry about supply chain transparency and reproducibility. We maintain long-term contracts for fluoroarene sourcing, certify each lot, and keep thorough shipment histories. The value here lives in real-world research timelines—a missed delivery date or bad batch wastes weeks in a modern discovery campaign, far more than a slightly lower catalog price could justify.

    Sustainability and Evolving Production Standards

    Our plant keeps pace with environmental and regulatory trends, both because we care about our staff and because our clients increasingly require full documentation. The production of fluorinated organics has unique waste and emission concerns—perflourinated compounds feature in environmental debates for good reason. In our operation, solvent choice prioritizes lower toxicity and improved recyclability; we recover, recycle or appropriately neutralize fluorinated byproducts at every stage possible. On-site capture and careful effluent monitoring ensures we stay well within evolving regulatory guidelines.

    Each kilo produced represents a balance between demanding synthetic chemistry and responsible waste management. Unlike remote trading houses, we continually upgrade our reactor designs and purification equipment based on real throughput and yield data. Our process knowledge is drawn from both accident reviews and day-to-day troubleshooting, not just engineering handbooks. Our on-the-ground staff can point to specific protocols that lowered emissions or improved yields last quarter—concrete details that collectively push the field forward.

    Feedback from our clients on sustainability gets folded into real projects. We track which sectors—like agrochemical development—face the most scrutiny and adjust our transparency tools accordingly. This stretches beyond annual audits; we push for complete disclosure on precursors, handling, and risk mitigation, since any future restriction on fluorinated chemicals will impact us and our customers together. Our commitment to responsible chemistry gets measured not by slogans but by day-to-day manufacturing decisions, disposal records, and supplier audits.

    Practical Challenges: Sourcing, Storage, and End Use

    Every synthetic campaign has bottlenecks and surprises; we see this play out from both our factory and the client’s own feedback. Procuring high-purity fluorinated arenes requires more than just spot negotiation; a missed impurity in the source material can translate into byproducts that take months to track down in an end-use formulation. We contract directly with fluorinated benzene synthesis plants, sometimes pursuing annual or biannual delivery cycles to guarantee uninterrupted supply, especially during cycles of heightened geopolitical or market volatility.

    Warehouse storage guides our packaging decisions. Though trans-2,5-difluorocinnamic acid doesn’t present major hazards, cross contamination, moisture ingress, or UV exposure can still create measurable losses in yield or purity. We triple-seal our lab-scale containers and use lined industrial drums with data loggers for bulk movements. By doing so, we aim to stop issues before they reach the bench—saving researchers from days spent chasing down unexplained analytical blips.

    Clients in high-throughput screening, scale-up medicinal chemistry, and custom intermediate programs return to us for predictable, clean supply. Each group faces unique challenges: some require compound for milligram-to-gram screening; others for hundreds of grams per trial batch. Many formulation scientists now ask about reactivity under green chemistry conditions or compatibility with new catalyst systems. We perform small-batch tests in our own labs to verify claims before making recommendations. In cases where a researcher develops an entirely new process, we share real spectra and process details, not just a data sheet.

    Supporting Researchers: Collaboration, Feedback, and Customization

    Being a manufacturer makes us far more than a remote producer—we’re an ongoing partner in process troubleshooting, scale-up, and method transfer. It’s not uncommon for a project head to call us and describe an unexpected color change in a test run, only for our chemists to identify and solve the root cause within a day. Years of running our own reactors teach us to anticipate these issues ahead of time, reducing both wasted time and materials.

    Each year, we tune our synthesis and purification based on the feedback loop created by direct collaboration with our clients. When a new regulatory issue emerges, or a specific analytical parameter shifts in importance, we fold that into the next round of process improvements. Customization is not a slogan here; it means actually reworking a batch, retesting a new solvent system, or sourcing a more robust precursor. Our ability to deliver on these fronts stems from process ownership, persistent troubleshooting, and real familiarity with the day-to-day demands of R&D.

    Academic groups pursuing novel synthetic pathways, or industry partners scaling up next-generation fluorinated products, benefit from this responsive, iterative system. In our role, process robustness goes hand in hand with adaptability. This living knowledge base cannot be replicated by resellers or trading houses, no matter how closely they stick to data sheets and catalog descriptions.

    Product in the Real World: From Bench to Pilot Plant

    Our experience with trans-2,5-difluorocinnamic acid doesn’t end at the last batch test. We support users moving from laboratory-scale proof-of-concept all the way to pilot and production scale. Issues like solution color drift, unexpected precipitation, or shifts in spectroscopic signatures at large scale have all appeared in client plants. We answer these challenges by sharing real-time process insight, from temperature controls to solvent recovery practices. Our technical team often walks partners through filtration, drying, and packing techniques that preempt quality deviations.

    In high-stakes sectors such as new agrochemical lead discovery or advanced pharmaceutical intermediate synthesis, researchers value the ability to raise processing or quality concerns and receive original analytical data straight from our QC labs. Our long-term relationships with both established pharmaceutical manufacturers and agile contract research outfits mean our product and knowledge both move quickly, tailored to the rapidly changing needs of innovation-driven organizations.

    Summary: Why Manufacturing Experience Counts

    Handling, manufacturing, and delivering trans-2,5-difluorocinnamic acid demonstrates the difference between supplying a chemical and supporting real-world research outcomes. Our team sees every step of the process, learns from each challenge, and responds with improvements that show up in future batches. The true value, as we’ve seen across hundreds of client processes and production cycles, is in trustworthiness, adaptation, and accountability. Real process knowledge drives everything from the reactor on our shop floor to the reaction flask in your lab.

    Each bottle that leaves our door has been shaped by thousands of hours of expertise, countless process adjustments, and feedback from partners who rely on us when the stakes are high. This ongoing dialogue creates a product experience far more nuanced and reliable than catalog numbers or generic descriptions. Trans-2,5-difluorocinnamic acid, in our practice and in the hands of leading researchers, doesn’t just serve as another reagent—it’s a key enabler for successful, responsible, and high-impact science.