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3-Fluorocinnamicacid

    • Product Name 3-Fluorocinnamicacid
    • Alias 3-Fluoro-cinnamic acid
    • Einecs 219-924-4
    • 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

    199305

    Chemical Name 3-Fluorocinnamic acid
    Cas Number 261952-41-4
    Molecular Formula C9H7FO2
    Molecular Weight 166.15
    Appearance White to off-white crystalline powder
    Melting Point 128-130°C
    Boiling Point 292.7°C at 760 mmHg
    Density 1.279 g/cm3
    Solubility Slightly soluble in water; soluble in most organic solvents
    Smiles C1=CC(=CC=C1C=CC(=O)O)F
    Inchi InChI=1S/C9H7FO2/c10-8-4-1-3-7(6-8)2-5-9(11)12/h1,3-6H,2H2,(H,11,12)
    Storage Conditions Store in a cool, dry place, tightly closed
    Purity Typically ≥98%
    Synonyms m-Fluorocinnamic acid; 3-Fluoro-cinnamic acid

    As an accredited 3-Fluorocinnamicacid 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 screw cap, labeled "3-Fluorocinnamic acid" and safety information, securely sealed.
    Shipping 3-Fluorocinnamic acid is shipped in sealed, chemical-resistant containers to ensure stability and prevent contamination. Packages are labeled according to regulatory standards, handled with care, and accompanied by safety data sheets. Transport is conducted via dedicated chemical carriers, compliant with applicable regulations for hazardous materials, ensuring safe and secure delivery.
    Storage 3-Fluorocinnamic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from moisture, light, and incompatible substances such as strong oxidizing agents. Store at room temperature, away from direct sunlight and sources of ignition. Ensure the storage area is labeled appropriately and, if possible, use a desiccator to minimize hydrolysis.
    Application of 3-Fluorocinnamicacid

    Applications of 3-Fluorocinnamic Acid in Industrial Manufacturing

    Our 3-fluorocinnamic acid supports core chemical transformations in advanced manufacturing, enhancing molecular frameworks across select industrial sectors. As the original manufacturer, we supply this material for downstream processes where precise structure-activity relationships, functionalization, and regulatory compliance drive production value.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Non-Steroidal Anti-Inflammatory Drugs

    3-Fluorocinnamic acid’s aromatic structure with fluorine substitution offers a valuable intermediate in the synthesis of non-steroidal anti-inflammatory drug precursors, such as modified fenamates and related APIs. Pharmaceutical companies leverage this intermediate for regioselective coupling reactions, constructing fluorinated scaffolds where biological activity and metabolic stability are critical. The intermediate stage focuses on reproducible transformations for scalable commercial supply, addressing both structural requirements and regulatory approval in final drug substances.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <795> for pharmaceutical compounding
    • European Pharmacopoeia (Ph. Eur.) monographs for related pharmaceutical substances
    • FDA CFR Title 21, Part 211 for finished pharmaceuticals production (data traceability and material ID)

    Typical usage ratio

    • 5–15% molar equivalent in condensation and coupling reactions; precise proportion depends on targeted API structure and functional group tolerance.

    Downstream process integration

    • Enters the batch synthesis after first-step carboxylation, acting as a precursor in halogenated aromatic substitution, followed by amidation or esterification under controlled temperature and pH.

    Final product types

    • Fluorinated fenamate derivatives (API)
    • Experimental NSAIDs with tailored pharmacokinetics
    • Reference standard substances for pharmaceutical research

    2. Synthesis of Agrochemical Crop Protection Intermediates

    Agricultural chemical manufacturers utilize 3-fluorocinnamic acid to introduce fluorinated aromatic rings in pre-emergent herbicide and fungicide synthesis. The compound enables formation of oxime or amide intermediates, imparting UV resistance and improved soil stability in agrochemical formulations. Downstream producers select this building block for its electronic effects, influencing the final molecule’s environmental degradation profile and bioactivity on targeted plant enzymes. All production steps must comply with strict agricultural chemical regulations.

    Industry compliance standards

    • FAO/WHO Specification for Agrochemicals (JMPR)
    • ISO 9001:2015 for quality management in agrochemical production
    • REACH (EC 1907/2006) for chemical substances registration in Europe
    • China GB 2763—National Food Safety Standard for maximum residue limits

    Typical usage ratio

    • 3–10% of batch formula depending on desired degree of fluorination and crop protection molecule backbone.

    Downstream process integration

    • Undergoes acylation or cross-coupling with nitrogen-containing scaffolds via Suzuki or Heck reactions post-hydrolysis, preceding sulfonation or chlorination as required by the finished product strategy.

    Final product types

    • Selective pre-emergent herbicide intermediates
    • Fluorinated fungicide building blocks
    • Stabilizers for post-harvest chemical treatments

    3. Specialty Fragrance and Flavor Synthesis

    Manufacturers in the aroma chemistry sector source 3-fluorocinnamic acid for the controlled production of specialized fragrance molecules and flavor precursors. The aromatic carboxylic acid enables synthesis of functionalized aldehydes and alcohols with unique olfactory properties, expanding the palette for high-value perfumery and fine flavor applications. Addition levels and process steps are determined by final olfactive performance and IFRA (International Fragrance Association) compliance.

    Industry compliance standards

    • IFRA Code of Practice and Guidelines
    • EU Regulation (EC) No 1223/2009 on cosmetic products (for fragrance use)
    • US FEMA GRAS assessment for flavors (21 CFR, Food Additives)
    • ISO 9235 for aromatic natural and synthetic substances

    Typical usage ratio

    • Variable between 0.2–2% of total synthetic batch, set by target note intensity and matrix volatility.

    Downstream process integration

    • Input into catalytic hydrogenation or olefination as an intermediate; further downstream, the material is distilled and fractionated during aldehyde or ester formation prior to compounding.

    Final product types

    • Fluorinated fragrance aldehydes
    • Base notes for fine perfumes
    • Flavoring components in premium food and beverage formulations

    4. Advanced Organic Electronic Materials Synthesis

    The electronics industry employs 3-fluorocinnamic acid for introducing fluorine-containing motifs into organic semiconductor materials and photonic polymers. Its role in precursor macromolecule synthesis supports high-performance coatings and layering in OLED devices, thin-film transistors, and photovoltaic applications, where electron-withdrawing groups impart improved charge mobility, solubility, and thermal resistance. Material integration relies on tightly controlled workflow steps to maintain purity and film quality, in line with international electronics standards.

    Industry compliance standards

    • IPC-4101 for base materials specification in electronics
    • IEC 61249 for electronic substrates
    • RoHS Directive (2011/65/EU) for hazardous substance limits
    • ISO 9001 for electronics production traceability

    Typical usage ratio

    • 1–5% in the total precursor mixture, adjusted based on desired film morphology and device efficiency requirements.

    Downstream process integration

    • Combined in step-growth polymerization or Friedel–Crafts functionalization after monomer synthesis; followed by purification and solution casting or vapor deposition onto active device platforms.

    Final product types

    • Organic light-emitting diode (OLED) intermediate materials
    • Photonic and conducting polymer films
    • Active layers for flexible displays and photovoltaic cells
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    Certification & Compliance
    More Introduction

    Introducing 3-Fluorocinnamic Acid: A Manufacturer’s Perspective

    Our Experience with 3-Fluorocinnamic Acid

    Day in and day out, every batch of 3-Fluorocinnamic Acid that leaves our plant carries the story of painstaking attention and a craftsman’s commitment to reliable quality. Over the past decade, we have watched the fluoroarene derivatives market shift and regroup as pharmaceutical, agrochemical, and fine chemical industries look for more specific building blocks that pack both efficiency and selectivity. We have been hands-on in scaling up this compound, from the lab bench where our chemists troubleshoot hydrogen fluoride compatibility to the industrial reactors where each process step gains scrutiny for safety and purity. Among dozens of fluorinated aromatics that run through our reactors, 3-Fluorocinnamic Acid holds a special place thanks to its combination of simplicity and synthetic utility.

    Our production workhorse for this item features a high-purity, white to off-white crystalline solid, with assay values guaranteed upwards of 98.5%. Whether it’s for research-scale requests or multi-kilo synthesis, every batch comes through a filtration and recrystallization program that’s been honed over multiple campaigns. Product lot files get checked by GC-MS and NMR, every single time. We only ship product that passes tight control limits for residual solvents and heavy metals. This focus on analytical rigor stems from daily feedback we get from groups actively performing hydrogenation, coupling, and condensation chemistry with this acid. Even one trace impurity showing up in downstream transformations can waste an entire week of their work. We think a focus like this builds trust with chemists who need reliable intermediates, not just chemical names on a catalog.

    Understanding the Structure and Its Impact

    Every chemist who purchases fluoro-substituted aromatics looks for different things—some want higher reactivity on the ring, some need stability in acidic or basic conditions, some worry about proper alignment for cross-coupling or amide bond formation. The structure of 3-Fluorocinnamic Acid brings together a phenyl ring substituted at the meta position with a fluorine atom and an acrylic acid tail that offers broad compatibility in coupling reactions.

    Fluorine’s electronegativity is not a small thing—it affects electron density across the aromatic ring in ways that can make or break a synthetic sequence further down the line. Chemists appreciate meta-fluoro substitution, like in 3-Fluorocinnamic Acid, for the careful balance it creates. Ortho and para-fluorinated versions hit different reactivity trends and steric environments; the meta position, by contrast, often offers the greatest versatility for downstream arylations, oxidations, and halogen-metal exchanges. Our feedback from pharma and agricultural innovators often focuses on how cleanly this molecule reacts compared to its cousins, and that feedback has helped guide several process tweaks over the years.

    Compared with unsubstituted cinnamic acid, the fluorinated version demonstrates noticeably increased resistance to oxidative degradation. This is crucial not only in the synthesis itself but during storage and handling—quality managers report fewer issues with shelf stability, which lets R&D teams spend less time worrying about starting material degradation and more time running experiments. From a manufacturing stance, that means less product lost to off-specification complaints, and fewer requests for returns, reprocessing, or technical troubleshooting.

    Product Specifications Informed by the Realities of Scale-Up

    Deciding on production parameters for 3-Fluorocinnamic Acid was not quick or easy. The old pilot-scale method—thermal condensation of 3-fluorobenzaldehyde with malonic acid—threw up scale-dependent exotherms and inconsistent purity once we tried charging raw materials at metric ton volumes. Careful temperature control, solvent selection, and the switch to continuous filtration instead of batch crystallization solved most of those issues. We keep water content under 0.5% by employing vacuum drying with active inline monitoring after final isolation. Achieving this demanded investment in drying equipment specifically rated for fluorinated aromatic materials; other plants sometimes overlook vapor phase losses in exotic substitutions, but we track the numbers and minimize plant emissions through closed-loop recovery as part of our quality commitment.

    Packing always comes up in client technical calls. Some researchers need 100g sealed glass jars for glovebox use; chemical process teams routinely ask for steel-lined drums to avoid moisture ingress during ocean shipments. For us, flexibility in packaging doesn’t mean a one-size-fits-all approach—it’s the result of years of listening to user complaints about clumping, caking, or contamination. Every drum, every bottle, gets nitrogen-flushed as the last step, based on feedback from clients who store materials for long periods or who handle multi-ton lots. Shipping 3-Fluorocinnamic Acid safely, with certificates showing not only the assay but also impurities below 0.1%, reflects our commitment to supplying a trustworthy product.

    Supporting Applications: Where Lab and Industry Meet

    Phone calls with process chemists often start with very specific questions—solubility in polar aprotic solvents, compatibility with chiral catalysts, or thermal stability at 110°C for several hours. Our technical group keeps track of dozens of these reports every quarter to improve both the product and the documentation that goes out the door. We know this compound gets used as a precursor in the production of a wide range of pharmaceuticals, especially those where aryl-fluorinated backbones lead to new biologically active molecules. From diaryl ethers to biphenyl motifs, 3-Fluorocinnamic Acid frequently serves as a coupling partner in Suzuki and Heck reactions, as well as in acylation sequences for peptide and polymer intermediates.

    Outside of pharma labs, we see research activity focused on the design of advanced materials—liquid crystals, MXene modifiers, and novel photoactive polymers all make use of meta-fluorinated cinnamic acids. Often, this product finds a place in small-molecule research where electron-withdrawing character and partial fluorine shielding provide a route to chemical entities not easily accessed via other pathways. Our experience collaborating with university groups has shown many of these applications emerge from custom synthesis projects that turn into semi-commercial scale runs after just a few months of promising lab results.

    One lesson learned over years of filling orders for 3-Fluorocinnamic Acid: reproducibility matters. Whether a customer is collecting NMR data on a 25mg run or charging 2kg to a production reactor, they expect the same melting point, consistent crystal habit, and a full set of analytical documentation, every single time. To deliver on that, we employ double-lot testing, where a retained sample from each production batch gets compared by FT-IR and DSC to a long-term reference lot held in cold storage. This direct comparison avoids drift in characteristics from campaign to campaign, which can show up as yield drops or side product formation in high-sensitivity synthetic applications.

    How 3-Fluorocinnamic Acid Stands Apart

    Competing products on the market include simple cinnamic acid, as well as the ortho- and para-fluorinated isomers. Our process and our experience show why meta substitution draws such specialized attention. Ortho-isomers invite more steric interference in coupling and metalation reactions, affecting yields and reaction selectivity, especially when incorporated into rigid frameworks or hindered systems. Para-isomers, while useful, don’t allow for the same electron delocalization and present different patterns in further aromatic substitution or oxidation steps. Years of client feedback suggest the meta-fluorinated option consistently serves a broader swath of reaction types, delivering more controlled electronic influence on the aromatic ring without excessive destabilization.

    Compared with the more commoditized forms of cinnamic acid, our 3-Fluorocinnamic Acid finds specific favor in medicinal and crop science settings, where even minute impurities or incorrect isomer ratios derail long-term research or regulatory approval. From our own manufacturing perspective, holding the line on purity, isomeric consistency, and documentation creates ongoing value for those downstream clients. If a batch gets flagged for any deviation—even cosmetic—our team investigates and resolves the root cause before anything more leaves the facility.

    We get asked why pricing for 3-Fluorocinnamic Acid can sometimes exceed what researchers expect for similar-looking molecules. The reasons stem directly from its chemistry. Handling fluorinated intermediates at scale presents extra environmental and safety hurdles—not only in terms of hydrogen fluoride management during synthesis, but also with scrupulous waste handling as dictated by both local and international regulations. Our plant abides by these standards through routine audits and regular retraining for all operators. Further, the choice of specialized glass and fluoropolymer surfaces in reactors, filtration units, and storage tanks means higher upfront and maintenance costs that go into every shipped kilo. We stand by these decisions and walk our customers through regulatory or quality questions, reflecting the real-world complexities they face in their own businesses.

    Listening to Our Customers and Evolving with Demand

    Every technical support ticket, every feedback form, feeds straight into our improvement loop. We’ve learned, for example, that some research groups working on polymer additives value denser, smaller particle size distributions for better solubility and handling. Others dealing with nonpolar solvent systems seek out batches dried below 100ppm water. Over the years, we have reshaped our crystallization protocols and offered batch-specific certificates—not just standard ones written by a generic compliance team. The information customers get has roots in direct production and analytics insight, allowing them to plan, troubleshoot, and innovate more confidently.

    From the earliest days of our work with 3-Fluorocinnamic Acid, we have refused to treat it as a commodity. We team up with R&D chemists to discuss how changes in supply, seasonal fluctuations in raw material quality, and environmental requirements can affect output over the long term. During global supply shocks or regulatory crackdowns on fluorinated intermediates, we have kept communication going with clear updates about expected lead times, production slowdowns, or alternative sourcing. Consistency, even outside the plant gates, helps establish the trust essential in high-stakes synthesis workflows.

    Security and sustainability remain front-of-mind as regulations change and environmental scrutiny grows. In producing 3-Fluorocinnamic Acid, we rely on closed-loop solvent recycling and minimize hazardous byproduct formation, both to lower costs and because our workers and customers expect it. Auditors visit our shops regularly to check compliance and proper safety controls—a process that might seem tedious, but which backs up the claims we make about responsible chemical stewardship. We encourage researchers and industrial users to ask about these steps; informed partners drive progress faster than detached speculation ever could.

    The Importance of Documentation and Technical Guidance

    For every order shipped, we include real NMR, GC, and HPLC chromatograms describing the material in detail. Not every manufacturer does this—some rely solely on lot numbers and generic spec sheets. Our policy is to provide as much context as possible: impurities, storage notes, recommended handling to avoid moisture pickup. Before a new lot gets released, our team guarantees it has passed both internal and external reference checks, a practice born from years of feedback about unexplained yield losses or inconsistent results in downstream reactions bought from lesser sources.

    Building strong technical documentation does more than avoid phone calls about returns or troubleshooting. It means that researchers, scale-up teams, and QC laboratories all arrive at the same place from the first attempt. Synthetic success shouldn’t rely on luck or heroic workarounds. In practice, robust paperwork saves time and money for everyone in the chain—failures happen even with good starting material, but they should never trace back to an unknown inconsistency in a supplied building block.

    Our technical team helps customers plan for safe scaling and process adaptation, answering questions about byproduct trends, color changes under different storage conditions, or compatibility with particular solvents or catalysts. If unusual results show up in a customer run, we walk through assay files and historical batch data together, giving advice based on years of both small-scale work and ton-scale campaigns in our own plant. These relationships form over repeated transactions, not one-off sales, and help both sides make better choices in a changing world.

    Building Long-Term Value Through Quality and Transparency

    Experience shows that consistency trumps short-term savings over the lifespan of a project. Savings realized by buying lower-cost, off-spec material rarely stand up to the hidden costs of failed runs, lost time, or regulatory headaches. That reality motivates us to invest in diagnostics, staff training, and careful raw material vetting. During leaner years, we have chosen to carry extra inventory of 3-Fluorocinnamic Acid to protect customers from raw material swings—sometimes at a financial cost, always with transparency as our guide. We openly discuss these choices with buyers, because predictability for their projects depends directly on decisions made on our floor.

    Quality here means attention at every stage. Incoming raw materials go through identity confirmation and purity checks, not just barcode scanning. Operators handling critical steps of the reaction and isolation process train with reference to past deviation reports, so small problems spotted early get fixed before they snowball. Our maintenance team monitors temperature, pressure, and environmental data points for every run to ensure the process window always matches established safe operating space. Accidents or failed batches happen less when every layer of staff owns their part of the job.

    Regulations for fluorinated organics change with evolving environmental understanding and global scrutiny. We stay in front of those changes, updating safety data sheets and process limits while working with external auditors and compliance bodies both at home and abroad. These partnerships come from many years of dialogue on emission standards, waste treatment, and cross-border documentation for regulated compounds. Customers, both new and old, ask for this transparency; we deliver it as a matter of course.

    How We See the Road Ahead

    Supplying 3-Fluorocinnamic Acid involves more than filling orders. Our approach builds on experience with challenging syntheses, investments in reliable analytical infrastructure, and a long series of conversations with leaders in pharmaceuticals and materials development. We fine-tune particle size upon request, agree to advanced stability testing, and provide in-depth analytical reports that go beyond industry minimums. Our willingness to address difficult questions rather than provide canned answers reflects a work culture shaped by listening and technical rigor.

    In our view, work with 3-Fluorocinnamic Acid rewards careful process control, collaborative improvement, and a willingness to outlast market trends. We draw insight from every project—every complaint, every request for documentation, every run that reveals a way to tighten controls or improve handling. Our customers shape what we offer, pushing us to improve, investigate, and anticipate demands before they arise. The future for this product isn’t static—it's shaped each season by the evolving needs of researchers, innovators, and markets. Our commitment remains: deliver the clearest, most reliable 3-Fluorocinnamic Acid, produced with responsible stewardship and open dialogue, batch after batch, year after year.