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4-Bromo-2,3,5,6-Tetrafluoroaniline

    • Product Name 4-Bromo-2,3,5,6-Tetrafluoroaniline
    • Alias 2,3,5,6-Tetrafluoro-4-bromoaniline
    • Einecs 802-419-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    674210

    Chemicalname 4-Bromo-2,3,5,6-Tetrafluoroaniline
    Casnumber 328-63-2
    Molecularformula C6HBrF4N
    Molecularweight 244.97
    Appearance Light yellow to beige crystalline powder
    Meltingpoint 56-60°C
    Purity Typically >98%
    Density 1.92 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles Nc1c(F)c(F)c(Br)c(F)c1F
    Inchi InChI=1S/C6H2BrF4N/c7-1-2(8)4(10)6(11)5(9)3(1)12/h12H
    Storagetemperature Store at 2-8°C
    Synonyms 2,3,5,6-Tetrafluoro-4-bromoaniline

    As an accredited 4-Bromo-2,3,5,6-Tetrafluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g of 4-Bromo-2,3,5,6-tetrafluoroaniline is supplied in a sealed amber glass bottle with a secure screw cap.
    Shipping 4-Bromo-2,3,5,6-Tetrafluoroaniline is shipped in tightly sealed containers to prevent moisture and contamination. It must be labeled according to chemical safety regulations and transported as a hazardous material. Handle with appropriate safety measures, avoiding extreme temperatures and direct sunlight. Compliance with local, national, and international shipping guidelines is required.
    Storage 4-Bromo-2,3,5,6-Tetrafluoroaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Avoid contact with strong oxidizers and acids. Store in a designated chemical storage cabinet, preferably one suitable for hazardous and reactive chemicals. Always follow appropriate laboratory safety protocols and local regulations when handling or storing this compound.
    Application of 4-Bromo-2,3,5,6-Tetrafluoroaniline

    Applications of 4-Bromo-2,3,5,6-Tetrafluoroaniline in Industrial Manufacturing

    As a specialized manufacturer of 4-Bromo-2,3,5,6-Tetrafluoroaniline, we supply a high-purity intermediate tailored for critical transformations across select high-tech chemical sectors. The following downstream application scenarios highlight industry-verified uses, with details on permitted compliance, formulation ranges, process positioning, and resulting product types.

    1. Fluorinated Pharmaceutical Intermediate Synthesis

    Leading pharmaceutical companies consistently utilize this molecule as a key amine building block in multiple-step syntheses of active pharmaceutical ingredients—particularly those requiring enhanced metabolic stability and bioavailability. Its unique fluorine content supports late-stage diversification strategies in aromatic amine drug candidates, with the bromine moiety enabling site-selective cross-coupling reactions for molecular elaboration.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210/211, FDA)
    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP Guide Part II

    Typical usage ratio

    • Reactant input generally 15–30 mol% of target API batch size, adjusted per synthetic route and molar requirements

    Downstream process integration

    • Introduced after core ring establishment, usually serving as an early or mid-stage intermediate in Buchwald–Hartwig or Ullmann-type amination, prior to final API stage conversion

    Final product types

    • Fluorinated pharmaceuticals (oncology agents, antivirals, CNS drugs)
    • Advanced pharmaceutical intermediates for contract development and manufacturing organizations (CDMOs)

    2. Agrochemical Active Ingredient Production

    Agrochemical manufacturers rely on this compound as a customized precursor in the creation of fluorinated aniline-based herbicides and insecticides. Its high electronegativity and halogen pattern allow for the design of actives with improved resistance profiles, photostability, and soil longevity. The intermediate enables downstream Suzuki coupling or aromatic nucleophilic substitution, expanding the diversity of crop protection blends.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for quality management in agrochemical raw material supply
    • REACH (EC) No 1907/2006 compliance for chemical registration in Europe

    Typical usage ratio

    • 5–20% w/w based on total mass of formulated active ingredient batch; precise ratio depends on herbicide scaffolding requirements

    Downstream process integration

    • Engaged during key intermediate synthesis for direct nucleophilic substitution or metal-catalyzed cross-coupling to assemble final active molecule

    Final product types

    • Fluorinated herbicides (e.g., aryl-aniline triazine derivatives)
    • Selective insecticides and seed-treatment actives incorporating perfluorinated aryl groups

    3. Specialty Polymer and Fluoropolymer Manufacture

    Producers of advanced polymers employ this aromatic amine as a highly reactive monomer for introducing fluorinated segments into specialty polyimide and polyamide structures. Its incorporation results in polymers with elevated thermal and chemical resistance, low dielectric constants, and increased weatherability—properties demanded in electronics, aerospace, and filtration membrane applications.

    Industry compliance standards

    • ISO 9001:2015 and 14001:2015 for quality and environmental management in polymer production
    • UL 94 for flammability in electronic substrate polymers
    • RoHS Directive 2011/65/EU on heavy metals and halogen content for electronics

    Typical usage ratio

    • Up to 10 mol% of total diamine feed during condensation polymerization; actual level tuned to achieve targeted fluorine content and balance processability

    Downstream process integration

    • Charged as a co-monomer with dianhydrides or diacid chlorides in high-temperature, solvent-based condensation operations, immediately prior to imidization or amide-forming steps

    Final product types

    • High-performance fluorinated polyimide films for flexible printed circuits
    • Membrane materials for ultrafiltration and gas separation
    • Polyamide and polyimide engineering plastics

    4. Electronic Specialty Chemical (ESC) Intermediates

    Manufacturers of electronic specialty chemicals value this molecule for its ability to confer distinct electronic and thermal properties in the preparation of custom arylamines used in OLED hole transport materials, photoresists, and fluorinated derivatives for circuit board laminates. The aryl bromide handle enables selective derivatization, supporting high-purity synthesis under stringent contamination controls.

    Industry compliance standards

    • IPC-4101B (laminate standards for printed circuit boards)
    • ISO 14001 for hazardous waste and emissions during ESC production
    • Grade “Electronic” or “Ultra-High Purity” as per SEMI guidelines for materials used in semiconductor applications

    Typical usage ratio

    • Supplying 2–8 mol% relative to total arylamine-based intermediate formulation; adapted according to targeted electronic structure and end-use specification

    Downstream process integration

    • Charged post-purification into metal-catalyzed amination or borylation steps, leading to final purification under cleanroom standards before downstream device integration

    Final product types

    • OLED hole transport compounds
    • Photoactive arylamines for advanced photolithography
    • Circuit board specialty coatings

    5. Fluorinated Dye and Pigment Precursor Synthesis

    Advanced dye and pigment makers use this tetrafluorinated aniline to introduce unique electronic characteristics and superior photostability into colorants for high-performance coatings and specialty inks. The molecule’s fluorine and bromine pattern provides sites for targeted cross-coupling reactions, enabling access to chromophores with specific spectral and chemical attributes for demanding environments.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances in textile and ink formulations
    • EN 71-3 (Migration of Certain Elements) for coatings on children’s toys and articles
    • ISO 787/1-12 series for pigment testing and performance in industrial coatings

    Typical usage ratio

    • Acts as a core building block in 5–18 mol% range of dye precursor blend, adjusted for target color strength and stability requirements

    Downstream process integration

    • Introduced during early stages of azo or other chromophore synthesis via direct amination or transition metal-catalyzed coupling, followed by purification and formulation blending

    Final product types

    • Fluorinated synthetic dyes for high-durability coatings
    • Advanced pigments for security inks and anti-counterfeiting markers
    Free Quote

    Competitive 4-Bromo-2,3,5,6-Tetrafluoroaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Bromo-2,3,5,6-Tetrafluoroaniline – Insights from the Manufacturer

    Our Journey with 4-Bromo-2,3,5,6-Tetrafluoroaniline

    Stepping into the synthesis and production of 4-Bromo-2,3,5,6-Tetrafluoroaniline brought us into direct engagement with some of the most demanding requirements of the specialty chemical market. From the outset, collaborating in the development of this compound has proven one of the most consistently technical ventures our team faces. Here, consistency doesn’t come from automation alone. Meticulous handling, the purity of feedstocks, and vigilance at every batch define a high-quality outcome. Quality matters for every destination: whether a customer targets electronic applications, pharmaceutical intermediates, or agrochemical innovation, small variations in this compound shift results downstream.

    Molecular Structure and Technical Nuances

    4-Bromo-2,3,5,6-Tetrafluoroaniline carries a unique set of halogen atoms—four fluorines and one bromine—attached to the benzene core, alongside the amine group. This configuration blends electron-withdrawing effects and steric hindrance unlike simpler aniline or fluorinated analogues. Most notably, the positioning reduces cross-reactivity in subsequent steps. We see this molecular rigidity benefit key reaction pathways. Compared to trifluoroanilines or straight bromoaniline, it suppresses side reactions and sometimes tempers reactivity just enough to allow selectivity.

    Measurement consistency drives our technical work. Standard specifications focus on purity (usually above 98%), single-digit ppm water content, and tight controls for heavy metals, halide residues, and trace organics. The process team regularly optimizes the crystallization step and solvent removal to exceed these. End users notice the difference in yield and reproducibility—especially in catalytic or palladium-coupled cross-coupling reactions where deviation causes headaches.

    Origins and Scale

    Our experience tells us this compound’s true complexity starts in sourcing fine-grade precursors. One shortcut in the upstream supply-chain or a slip in isomer separation induces downstream drift. From hydrofluorination to bromination and amination, we’ve run virtually every plausible synthetic method. Over the years, scalable batch processes using orthogonal purification steps gave the highest yield. High-performance liquid chromatography only became essential as end market expectations shifted from simple bulk active ingredients to electronics-grade specialty chemicals, especially in Japan and South Korea, where dynamic standards keep rising.

    It is easy to underestimate the impact of upstream consistency. Early on, a single out-of-range batch caught several clients by surprise as they scaled up their own processes and required us to trace every reagent lot going back several months. Since then, the team tracks manufacturing history with lineage the way a vintner monitors harvest. Each lot undergoes not just quality checks but also stress-testing—exposure to heat, light, different storage regimes—to document true shelf life and reactivity.

    Usage: Downstream Applications and Demands

    Users demand this building block for good reason. 4-Bromo-2,3,5,6-Tetrafluoroaniline features in a suite of complex couplings that push molecular frameworks common in pharmaceuticals and advanced agrochemicals. Researchers designing kinase inhibitors or herbicide scaffolds demand substituents that confer both metabolic stability and the ability to fine-tune bioactivity. Here, the four fluorines impart strong effects: dramatically influencing lipophilicity, serum stability, and even metabolic half-life.

    Electronic materials manufacturers also seek performance boosts. Fluorine-rich arylamines underpin certain OLEDs, semiconductors, and specialty polymers. Excess heat, light, and voltage tolerance in devices often trace back to tiny differences in monomer purity. From our lab, even single-digit ppm impurities—trace HBr or unreacted Br2—change final properties. Each client might require a slightly different isomer ratio, bulkiness, or trace-level impurity, pressing us to partner with their R&D to revise batches on demand.

    A different group of customers wants this compound neither for drugs nor devices, but for developing new ligands or catalyst precursors in transition-metal chemistry. These customers expect not only clean product, but tight analytical traceability: batch-to-batch NMR, IR, and residual solvent profiles, including the most elusive polyhalogenated trace materials. These analytical details often become gatekeepers, deciding whether an innovative catalysis protocol works at all.

    Product Differentiation: What Sets This Molecule Apart

    Many new customers ask, “What makes this compound different from the more common anilines or bromofluoroanilines?” Short response: it’s the particular interplay of the attached halogens. The four fluorines, arrayed symmetrically, draw down electron density across the entire ring. This effect dramatically lowers nucleophilicity, significantly impacting both the reactivity and ultimate pathway of downstream couplings. By comparison, single-fluorinated or non-fluorinated bromoanilines often react too quickly, trigger unwanted substitutions, or generate instability in end use. Pure tetrafluoro patterns limit these risks.

    In direct comparison, 2,3,5,6-tetrafluoroaniline without the bromo handles subsequent halogenations or Suzuki-Miyaura couplings quite differently—the selectivity, byproduct spectrum, and ease of activating the aryl ring for additional chemistry all shift. In pharmaceutical contexts, subtle differences affect how a scaffold interacts with kinases or metabolizing enzymes. Our material has routinely outperformed others in pilot studies aiming for low off-target binding and improved pharmacokinetic profiles.

    Physical properties set further distinctions. The melting point sits higher than related mono-fluoro or bromo analogues. Solubility plummets in nonpolar solvents and rises in polar aprotic systems—impacting how customers plan their workups. Clients interested in automated handling notice sensitive points: storage conditions and moisture exposure become critical above certain scales. For those scaling up reactions, the crystalline morphology and dusting behavior of our product simplify loading into reactors, cutting down both process time and loss to waste.

    Reliability and Batch Integrity: Lessons from the Shop Floor

    Each run through our production facility involves more than just following a recipe. Over time, our technicians document granular observations: how a certain solvent blend speeds recrystallization, how a subtle temperature ramp improves filtration. Keeping a sharp eye out for shifts in crystallinity or color signals small but meaningful process deviations. Rather than leaving quality solely up to the final round of testing, the team routinely audits each stage and pulls sub-lot samples for early warning.

    Teams share findings across shifts: for example, which operator noticed foaming tendencies under humid conditions, how a cooling curve accelerated or lagged by ten minutes. Our chemists collect these details. This feedback loop means our processes adapt rapidly, preventing recurrence of small faults that, left unchecked, snowball into larger downstream issues for the end user.

    Sometimes even experienced people encounter surprises. For one batch, we noticed slight brown discoloration after filtration, leading us to trace back a minute contamination in the sodium nitrite we used. Instead of shipping questionable product, these lessons prompt robust batch quarantine procedures. Subsequent root-cause analysis and corrective actions now prevent even minor contamination from slipping past the QC net. This commitment might slow output from time to time, but it has safeguarded our relationships with customers who have very little margin for error in their own processes.

    Sustainability and Responsibility

    Handling halogenated aromatics raises environmental and regulatory considerations. Our shop balances the technical imperative for purity and the social imperative for sustainability. Each stage, from sourcing solvents intended for recovery to the efficient neutralization of effluents before discharge, comes under scrutiny. We monitor waste stream composition and routinely adjust treatment regimens to prevent halogen buildup in downstream water.

    Compliance with global standards drives new investments in closed-system transfers, on-site scrubbers, and secondary containment. Rather than relying solely on paperwork or certifications, our plant team regularly inspects every containment point. This diligence has meant clean inspection histories—both self-audited and by external agencies. It also means our compound reaches customers in all regulated markets, reducing risk of process interruptions tied to regulatory scrutiny.

    During process development, the team made the decision early on to favor reagents and conditions that avoid unnecessary side-products, excess halogenated by-products, or heavy metals. These upstream decisions take more time and cost a little extra, but the long-term benefit becomes clear. Waste-handling costs fall, qualification cycles shrink, and the traceability of the final product improves. Our operators are trained in both hazard recognition and R&D techniques, which translates into fewer incidents and helps everyone stay ahead of new rules coming from environmental authorities.

    Supporting Customer Innovation

    Customers approach us for more than just a drum of chemical. Many run small-scale evaluation trials, looking for margins of improvement in their process. They send feedback on crystallization, handling, or even unexpected reactivity, and ask for fine-tuned modifications. We treat these collaborations as a two-way street; sometimes, lab-scale adjustments we make for a single innovator later become our standard for the whole product line.

    Requests come in asking for alternate crystalline forms, solutions in different carriers, or additional analytical data. In pharmaceutical and electronics R&D, the ability to tailor not only batch size, but also how the product is presented (e.g., microcrystalline vs. large-granule) can save customers weeks of validation. Our scale and flexibility let us commit to these adjustments without driving up timelines or costs. We update partners as regulatory environments shift, ensuring material remains within evolving specifications without anyone scrambling last minute.

    Not every project requires large volumes; some scientists simply need 100 grams for a pilot screen, with assurance that future batches will match precisely. Others plan multiton campaigns for months, expecting each shipment to land as identical as possible to the prior lot. Bridging these extremes, with full attention to documentation and customization, has become a core strength in our daily work.

    Building Trust by Transparency

    Our documentation parallels the rigor of our process. Every batch ships with full supporting information: not just the technical sheets, but actual chromatograms, spectra, and real-time impurity profiling. Many end users ask to witness or audit our test protocols on site. We welcome scrutiny; our lab keeps careful records spanning back over a decade, ready for the next wave of requirements, whether DMF submission or RoHS audit.

    Batch deviations, minor or major, trigger not only corrective actions but open communication with impacted customers. Even when timelines stretch or material falls outside a customer’s exact cutoff, we keep dialogue open, updating them on root-cause investigations and adjustment strategies. This practice—cemented by hard lessons from early mistakes—ensures that surprises don’t catch anyone unprepared at scale-up or regulatory review stages.

    Addressing Ongoing Challenges

    Producing and supplying 4-Bromo-2,3,5,6-Tetrafluoroaniline at scale brings a constant challenge: aligning technical ambition with commercial realities and shifting compliance targets. Halogenated aromatics of this complexity rarely offer the luxury of a single, stable process over many years. Material availability, price volatility (especially for fluorine and bromine derivatives), and evolving workplace regulations demand constant adaptation.

    We invest in cross-training for our staff so that process chemists, QA, and warehouse operators share foundational knowledge. When a supply interruption looms or a new regulation emerges, each team member can step up to keep output safe and within spec. We also run quarterly retrospectives on all finished goods—cross-checking for shifting impurity patterns or changing analytical baselines—pinpointing slow trends before they tip into major process changes.

    Since our earliest scale-ups, open channels with both upstream raw material providers and downstream end users have been essential. These relationships led us to anticipate and respond to sudden shortages, regulatory bans, or new analytical requirements. One time, when a key upstream plant shut down for months due to an industrial accident, we were able to divert resources and maintain output to our most time-sensitive customers, sparing them costly interruptions.

    Looking Ahead

    Innovation never rests. As new uses for 4-Bromo-2,3,5,6-Tetrafluoroaniline surface—be it in targeted therapeutics, new polymer backbones, or advanced electronics—rigorous production standards, transparent processes, and agile support will keep this advanced intermediate playing a leading role. With every request, revision, and delivery, our experience informs each decision. We carry forward lessons learned on the shop floor, in the lab, and from our partners to keep quality as tangible as a handshake and every barrel as trustworthy as the last.