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3-Bromo-4-Fluorocinnamic Acid

    • Product Name 3-Bromo-4-Fluorocinnamic Acid
    • Alias (E)-3-Bromo-4-fluorocinnamic acid
    • Einecs 841-711-0
    • 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

    107458

    Productname 3-Bromo-4-Fluorocinnamic Acid
    Casnumber 1209456-15-4
    Molecularformula C9H6BrFO2
    Molecularweight 245.05
    Appearance White to off-white solid
    Meltingpoint 140-144°C
    Purity 98% (typical)
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=CC(=C(C=C1C=CC(=O)O)Br)F
    Inchi InChI=1S/C9H6BrFO2/c10-8-5-7(3-1-2-6(8)11)4-9(12)13/h1-5H,(H,12,13)
    Synonyms 3-Bromo-4-fluoro-phenylacrylic acid
    Storagetemperature 2-8°C

    As an accredited 3-Bromo-4-Fluorocinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3-Bromo-4-Fluorocinnamic Acid, 5g, is packaged in a sealed amber glass bottle with a chemical-resistant screw cap and safety labeling.
    Shipping 3-Bromo-4-Fluorocinnamic Acid is shipped in secure, chemical-resistant containers to prevent contamination and ensure stability. Packages comply with international regulations for hazardous materials. During transit, the chemical is kept in cool, dry conditions and labeled appropriately to ensure safe handling and prompt delivery to laboratories or research facilities.
    Storage Store **3-Bromo-4-Fluorocinnamic Acid** in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect the chemical from moisture, heat, and direct sunlight. Label containers clearly and handle with proper protective equipment to avoid inhalation, ingestion, or contact with skin and eyes.
    Application of 3-Bromo-4-Fluorocinnamic Acid

    Applications of 3-Bromo-4-Fluorocinnamic Acid in Industrial Manufacturing

    3-Bromo-4-Fluorocinnamic Acid serves as a critical intermediate across a range of industrial fields, particularly in the synthesis of high-value compounds. As a direct manufacturer, we supply this material to advanced chemical industries where stringent requirements on purity, reactivity, and regulatory compliance drive end-market performance. Below are key downstream applications with focused technical application information.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical compound developers incorporate this acid into targeted syntheses for creating novel small-molecule drugs and as a building block for active pharmaceutical ingredients (API) requiring halogenated aromatic scaffolds. Synthesis occurs under high-purity conditions, supported by full traceability and documentation. Production lines utilize continuous flow or batch reactors to maintain precise molar feeds, and all intermediates undergo in-process GC/HPLC controls before moving to final API processing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) Monograph Compliance
    • 21 CFR Part 211—Current Good Manufacturing Practice for Finished Pharmaceuticals (US FDA)

    Typical usage ratio

    • Ingredient feed: 0.5–2.5 equivalents in condensation or coupling reactions, optimized by API synthesis pathway and yield requirements

    Downstream process integration

    • Entry point: stepwise addition during heterocycle assembly or side-chain modification following initial aromatic halogenation
    • Used as a coupling partner in Suzuki, Heck, or Sonogashira cross-coupling reactions before isolation and purification

    Final product types

    • Halogenated pharmaceutical intermediates
    • Small-molecule APIs targeting CNS, oncology, and infectious disease applications
    • Precursor to further functionalized active molecules including amides and esters

    2. Agrochemical Active Ingredient Development

    Technical formulators in the crop protection sector use 3-Bromo-4-Fluorocinnamic Acid in the synthesis of novel fungicides and herbicides. The aromatic ring structure supports molecular modifications that improve bioactivity and selective toxicity. Production involves batch blending and fine control of reaction temperatures to maximize conversion rates, while compliance documentation supports export to regulated markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • Commonly 0.1–0.8 moles per mole of agrochemical product, adjusted for formulation yields and target molecule design

    Downstream process integration

    • Introduced during early chemical synthesis steps to construct extended aromatic or heteroaromatic frameworks
    • Serves as a coupling component in microwave-assisted or solvent-free synthetic protocols

    Final product types

    • New generation fungicide actives
    • Herbicidal intermediates with enhanced field stability
    • Structural precursors to patent-protected crop protection agents

    3. Specialty Dye and Pigment Manufacturing

    Specialty colorant manufacturers leverage this acid for the targeted modification of diaryl and heterocyclic dye compounds used in technical textiles, electronics, and plastics. The halogen and aromatic moieties provide anchoring points for sulfonation, azo coupling, or metal complex formation. Quality assurance covers batch purity tests and compliance with heavy metal content limits to fulfill textile and electronics industry requirements.

    Industry compliance standards

    • Oeko-Tex Standard 100: Certification for Textile Products
    • EN 71-3:2019—Safety of Toys (Migration of certain elements)
    • RoHS Directive 2011/65/EU—Restriction of Hazardous Substances

    Typical usage ratio

    • Used at 1–5% weight of total dye synthesis batch, dependent on targeted chromophore and required shade intensity

    Downstream process integration

    • Added to core dye mixture during condensation or coupling reaction prior to crystallization and filtration
    • Engages in high-temperature esterification or amidation for pigment dispersions

    Final product types

    • High-purity specialty colorants for plastics and fibers
    • Electronic-grade dyes for imaging and displays
    • Custom pigment intermediates for inkjet and screen printing markets

    4. Advanced Organic Electronic Material Synthesis

    Producers of organic semiconductors, OLED precursors, and conductive polymers use this compound for backbone construction, benefiting from its conjugated system and halogen substitution pattern. Processing lines use controlled temperature and solvent conditions to assemble polymerizable monomers or charge-transfer complexes. The process incorporates advanced analytical testing (e.g., NMR, FTIR) at each conversion step for quality and batch-to-batch consistency, meeting electronics raw material procurement standards.

    Industry compliance standards

    • IEC 62899-2016—Printed Electronics Standards
    • ISO 14001:2015—Environmental Management Systems
    • REACH Substances of Very High Concern Exclusion Protocols

    Typical usage ratio

    • Integration at 0.2–1.8 equivalents in monomer synthesis, tunable for polymer chain length and final charge mobility

    Downstream process integration

    • Functionalized during monomer building prior to chain-assembly polymerization
    • Used as key substrate in palladium-catalyzed C–C coupling

    Final product types

    • Precursor monomers for OLED and OFET fabrication
    • Substituted cinnamic acid-based organic semiconductors
    • Functionalized intermediates for printable electronic inks

    5. Fine Chemical Intermediates for Fragrance Synthesis

    Fragrance chemical developers incorporate 3-Bromo-4-Fluorocinnamic Acid for the synthesis of advanced aromatic aldehydes and ketones serving as key notes in perfumery and flavor compounds. The material supports regioselective substitutions and controlled chain extension, enhancing molecular complexity for high-value fine fragrance ingredients. Plants employ multi-step batch processing with rigorous impurity profiling and consistent lot release analysis.

    Industry compliance standards

    • IFRA Standards and Guidelines (International Fragrance Association)
    • ISO 9235:2013—Aromatic Natural Raw Materials Vocabulary
    • EU Regulation No 1223/2009 on Cosmetic Products

    Typical usage ratio

    • Incorporated at 0.3–1.0 mole per mole in the desired synthetic fragrance route, controlled by formulation and volatilization profile

    Downstream process integration

    • Main feedstock during alkylation, oxidation, or further halogenation towards aldehyde or ketone synthesis
    • Blended prior to final distillation and purity adjustments

    Final product types

    • Aromatic aldehyde and alcohol intermediates for perfumery
    • Fine flavor compounds for food-grade applications (with additional purification)
    • Complex scent molecules for home fragrance essentials
    Free Quote

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    Certification & Compliance
    More Introduction

    3-Bromo-4-Fluorocinnamic Acid: Our Experience as Direct Manufacturers

    We've spent years on the production line, pushing the boundaries of small molecule synthesis. Out of the hundreds of compounds we grind, crystallize, and purify on a daily basis, 3-Bromo-4-Fluorocinnamic Acid stands out as a valuable building block in the world of specialty chemicals. We commit ourselves not just to the simple repetition of a reaction scheme, but to careful, hands-on attention each step of the way, ensuring reliability for our clients in pharma, agrochemicals, and advanced material fields.

    Model and Specifications Grounded in Practice

    The model we routinely supply carries a CAS registry number of 90719-34-3, and we aim for a minimum purity of 98%, measured by HPLC. Crystalline powder with a white to off-white appearance is what we expect at the end of a consistent, well-controlled batch. Purity and physical integrity rely on how tightly we control temperature ramps during bromination, which itself is a lesson in patience: rushing the heating step drives up byproducts and slows later purification challenges. The compound’s melting point lands close to 170°C, and we’ve found even small deviations to signal contamination or incomplete reactions. We run silica gel columns and check every batch by proton NMR and mass spectrometry, refusing to send out anything that doesn’t match our detailed spectra. Our staff handles the material with nitrile gloves at every stage, keeping any potential for contamination in check.

    Why Sourcing From a Direct Manufacturer Matters

    There’s a world of difference between direct production and dealing through a chain of traders. We navigate the entire process – from raw material sourcing to reaction and isolation, to drying, packing and even customer feedback. Years ago, we ran into a run of unreliable p-fluorocinnamic acid from a supplier, and learned firsthand how quickly quality issues can snowball. Since controlling every stage, we’ve eliminated erratic particle size and batch-to-batch variation. With 3-Bromo-4-Fluorocinnamic Acid, one recurring concern from R&D groups is lot consistency, especially for gram-to-kilogram scale-up. Our batches reach consistent 98-99% purity, and the reproducibility eases method validation for anyone downstream.

    Having all steps under one roof speeds up troubleshooting too. If a customer sees spots on their HPLC after doing Suzuki or Heck coupling, we don’t send emails around looking for an answer. Instead, we sit down in the production lab, retrace the lot data, and call the chemists who ran the drying curves themselves. That’s the difference when the manufacturer stands behind each product. Boxed bulk flasks sent out of our plant have passed through the hands of workers who know the end use may spark an entirely new agrochemical intermediate or a targeted kinase inhibitor.

    Comparing to Conventional Substituted Cinnamic Acids

    Chemically, 3-Bromo-4-Fluorocinnamic Acid is a unique hybrid—the conjugation of the aryl ring maintains the classic cinnamic backbone, while specific substitution brings about notable changes in reactivity. Introducing both a bromine and a fluorine on the aromatic ring creates opportunities for orthogonal transformations. Compared to monosubstituted cinnamic acids (like 4-fluorocinnamic acid or 3-bromocinnamic acid), the di-substituted structure of this compound unlocks selectivity in cross-coupling reactions. The bromine atom, sitting ortho to the carboxylic acid, responds predictably in palladium-catalyzed processes, allowing for further elaboration with boronic acids, stannanes, or simple direct arylation. Meanwhile, the fluorine atom’s electron-withdrawing nature tunes the reactivity, often leading to higher chemo-selectivity in nucleophilic aromatic substitution. Such behavior sets our product apart for chemists looking to build diversity and complexity in a single synthetic step.

    Traditional sources rely on single-step halogenations from cinnamic acid, resulting in non-selective mixtures and residual side-products. Our process, informed by years of in-house R&D and scale-up work, makes use of careful, sequential halogenation—introducing fluorine and bromine at key stages under controlled conditions. The outcome is a purer, single-isomer product, without the tangle of regioisomers that muddle peptide synthesis or hinder crystallographic characterization. In our plant, we anchor our sodium bisulfite washes and re-crystallization to remove even trace-level impurities, because we’ve tested firsthand how these can poison metal catalysts or complicate downstream steps for our customers.

    Transformative Applications in Industry and Research

    For our clients, 3-Bromo-4-Fluorocinnamic Acid serves as much more than a reagent: it acts as a flexible handle in cutting-edge organic synthesis. In pharmaceutical labs, it often sits at the foundation of custom small molecule design. The double substitution paves the way for targeted modifications, especially in structure-activity relationship (SAR) work on bioactive molecules. Medicinal chemists appreciate the options: attach alkyl or aryl groups at the bromine position, then fine-tune electronic properties through the fluorine, all while maintaining carboxylic acid functionality for further conjugation or salt formation. We’ve worked with several teams developing new non-steroidal anti-inflammatory drugs (NSAIDs) where this compound plays a critical role, both in patent-protected scaffolds and in open research probes.

    In agricultural chemistry, the molecule brings similar advantages. Pesticide and herbicide discovery often starts with scaffolds allowing for late-stage diversification, especially where bioisosteric exchange is necessary. The ability to selectively transform either the bromine or fluorine region expands the toolkit for lead optimization. Based on feedback from agrochemical collaborators, robust handling, stability during long-term storage, and consistent melting behavior make for smoother regulatory documentation and easier pilot-scale runs.

    We keep in touch with university research groups exploring advanced electronic materials. The electron-rich and electron-poor character of this aromatic acid yields interesting charge transport properties when incorporated into oligomers or conjugated polymers. Researchers spin films and crystals from our product, then tune performance by modifying the aryl backbone. Any batch-to-batch difference in purity or substitution pattern can show up in device trial results, so delivering repeatable, verifiable material remains a point of pride for our entire technical crew.

    Addressing the Inconveniences in Sourcing and Handling

    Sourcing specialty aromatic acids often brings hidden headaches—unexpected impurities, shifting color, and lumpy crystallinity that resists dissolution. We learned early on to expect these challenges, especially for molecules involving complex halogenation steps. Moisture control has been one of the toughest battles in keeping 3-Bromo-4-Fluorocinnamic Acid pure on a practical scale. We run controlled atmosphere drying, using nitrogen streams to keep humidity below 1% during the final stage; this approach prevents hydrolysis of sensitive sites and staves off micro-degradation that leads to acid smell or yellowing. Our production team documents each batch’s drying curve and water content by Karl Fischer titration, and unusual outliers prompt a full review before packing for shipment.

    Transportation poses another test. The bulk powder can clump under excessive vibration. Over several years, we optimized packaging in double-lined bags with desiccant, all packed in sturdy HDPE drums meant to withstand both local shipping and overseas container transit. Product arrives to customers—small sample vials or multi-kilo bulk—without the dust and fines that clog dissolution steps or foul HPLC injectors. Our clients working on kilo-scale synthesis prefer this reliability since every step downstream depends on easily weighing and dissolving repeatable solids.

    Safety stays on our minds at every stage. Aromatic halides like this demand careful handling, as dusting and exposure can cause respiratory or skin irritation over prolonged work. Our plant emphasizes thorough training and protective gear compliance among all operators. We use local dust extraction both at grinding and filling. Each drum leaves our site with clear labeling and handling advice, based on years of in-plant experience.

    Why We Emphasize Demonstrable Experience

    Direct experience shapes every improvement in our process. More than once, unexpected results during a batch’s work-up forced us to rerun analytical tests beyond the standard methods. During one upgrade, we noticed that using a cheaper solvent for crystallization shaved a few hours off the timeline but led to unseen co-crystallization with byproducts, upending batch repeatability. Rather than chase quicker gains, we adopted a straight-laced recovery process that may take longer but always delivers the bench-mark spectra and melting behavior from the product. Such attention to detail only pays off for the operator who actually runs the reactor and supervises the last filtration—not from a distanced trading desk.

    We answer calls from customers directly. Questions about solubility, reactivity, or unexpected TLC spots land with the same production chemists who built the batch, not with a sales intermediary. Over the years, this direct feedback loop has helped us refine every step, from purification to bottling. One customer flagged trace benzaldehyde as an impurity years ago; since then, we redesigned our reactor quenching method to fully address this risk. These improvements don’t show up in standard datasheets, but result in a better performing product once it’s placed in the client’s hands.

    Understanding Regulatory and Compliance Considerations

    More labs request documentation about residual solvents, heavy metal levels, organic impurities, and batch traceability. We have responded by integrating systematic testing protocols. Each manufactured batch includes a detailed Certificate of Analysis (COA) backed by firm analytical data: HPLC chromatograms, NMR spectra, and residual solvent panels. We maintain samples from every manufactured lot in our QC archive. Several clients, working under GMP-like requirements, need lot traceability and detailed impurity profiles. Our plant tracks each drum’s route from raw material warehouse, through each production step, into packaging and shipping. This traceability enables rapid response if questions arise—no relying on distant, incomplete datasets.

    For researchers submitting grants, renewing licenses, or preparing publications, up-to-date regulatory alignment—such as proof of absence of controlled substances, environmentally persistent pollutants, or unacceptable levels of brominated or fluorinated side-products—can be critical. Our technical team can supply supporting documentation, regulatory statements, and impurity breakdowns so that review boards and collaborators stay satisfied and projects move forward without delay.

    Continual Process Innovation: Lessons from the Factory Floor

    Improvement stems from identifying weak points as batches scale from tens to hundreds of grams, or even kilo production. We realized that scaling up the bromination step invited side-product formation that earlier, in smaller runs, could be stripped away with silica columns. A few years back, we invested in new glass-lined reactors that hold temperature within tighter ranges and reconfigured pumps for more responsive dosing of brominating agents. We promptly recorded steadier yields and cleaner LC-MS profiles per batch. This change came from evaluating actual batch notes, not guesswork.

    Waste handling is another area where hands-on experience matters. Brominated and fluorinated waste streams attract regulatory scrutiny, so we invested in onsite neutralization facilities. Plant operators received additional training to neutralize and minimize hazardous releases, both for compliance and environmental responsibility. Customers appreciate transparent reporting in this area, since many now require sustainability statements as part of long-term supply agreements.

    Continuous feedback from our production and QC team narrows down sources of minor impurities or batch-to-batch drift. We scrutinize each manufacturing run to spot signs of catalyst carry-over, residual solvent, or even tiny levels of regioisomeric impurities, and make iterative adjustments. This results in lots that match exactly between pilot and bulk, sparing downstream chemists the headache of re-calibrating conditions for every new drum.

    Supporting the Chemist’s Workflow

    Our clients span discovery chemists screening for bioactivity, project leads scrambling to deliver next-stage intermediates, material scientists looking for reliable film-forming building blocks, and scale-up specialists needing robust logistics. Each group values predictability backed by experience. Chemists on tight timelines or working on grant-anchored deliverables find less downtime chasing batch artifacts or supplier miscommunications. The compound’s chemical features—precision in substitution, batch reproducibility, controlled particle size—link directly to smoother experiment setup and cleaner data analysis.

    We understand that technical support is just as valuable as raw material supply. Our team provides confidential advice on solubility improvement, reactivity patterns, and alternative purification strategies using the insights we gained while synthesizing, storing, and shipping the very same batches our clients receive. We see our product not as a standardized commodity, but as a project enabler whose performance shapes the innovation it supports.

    Many of the advances we’ve made came at the suggestion of clients who, encountering a bottleneck, reach out directly to our technical team. By cultivating these long-term, trust-based relationships, we tailor future runs, adjust physical parameters, and implement suggestions that ultimately serve the needs of a practical lab or production environment. This approach stands apart from faceless, warehouse-driven supply chains, where requests often vanish into a helpdesk ticketing abyss.

    Facing the Unknown: Forward-Thinking Chemical Manufacturing

    Reliability builds on honest communication about both strengths and limitations. In creating 3-Bromo-4-Fluorocinnamic Acid batches, we are sometimes challenged by new reaction pathways, unpredictable impurity profiles, and the practical obstacles of scale. Having a trained team, analytical systems, and customer-driven continuous improvement helps us meet these challenges directly and transparently.

    The future of specialty chemical manufacturing centers on tighter integration between those who produce compounds and those who apply them—whether in discovery, process development, or product commercialization. Our years spent running, refining, and scaling up 3-Bromo-4-Fluorocinnamic Acid have given us not only technical mastery, but also a deep respect for the day-to-day needs of people who rely on quality, reliability, and direct support from the manufacturer’s side. Growing together with our customers, we keep raising the bar on transparency, traceability, and technical responsiveness.

    Those who look beyond standard catalog entries see the value in a manufacturer’s direct experience, careful oversight, and an ongoing dialogue about improvement. We supply not just 3-Bromo-4-Fluorocinnamic Acid, but a partnership that anchors technical progress and supports the ambitions of modern research and industrial innovation.