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2-Bromo-4,5,6-Trifluoroaniline

    • Product Name 2-Bromo-4,5,6-Trifluoroaniline
    • Alias 2-Bromo-4,5,6-trifluoro-1-aminobenzene
    • Einecs 628-769-5
    • 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

    132288

    Chemicalname 2-Bromo-4,5,6-Trifluoroaniline
    Molecularformula C6H3BrF3N
    Molecularweight 226.99 g/mol
    Casnumber 328-95-0
    Appearance Off-white to light yellow solid
    Meltingpoint 54-58 °C
    Density 1.86 g/cm3 (estimated)
    Purity Typically >97%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles c1c(c(c(c(c1N)F)F)Br)F
    Inchi InChI=1S/C6H3BrF3N/c7-3-1-2(9)4(8)6(10)5(3)11/h1H,11H2
    Storagetemperature Store at 2-8 °C
    Synonyms 2-Bromo-4,5,6-trifluoro-1-aminobenzene

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams, with secure screw cap, hazard label, product name and CAS number, sealed for chemical safety.
    Shipping 2-Bromo-4,5,6-Trifluoroaniline is shipped in tightly sealed, chemical-resistant containers to prevent leaks or contamination. It is handled as a hazardous material, complying with international regulations for chemical transport. Proper labelling and documentation are included, and transit occurs under controlled conditions, often via ground or air freight, depending on destination requirements.
    Storage **2-Bromo-4,5,6-Trifluoroaniline** should be stored in a tightly closed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep away from direct sunlight and moisture. Store at room temperature and protect from physical damage. Use appropriate safety precautions and ensure proper labeling to minimize risks associated with handling hazardous chemicals.
    Application of 2-Bromo-4,5,6-Trifluoroaniline

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

    As a direct manufacturer, we supply 2-Bromo-4,5,6-Trifluoroaniline to specialized sectors that demand reliable quality and transparent supply for advanced synthesis projects. Our focus remains on real and regulated downstream industries where this intermediate plays a pivotal role in processes involving fine chemicals, agrochemical actives, specialty polymers, pharmaceutical candidates, and advanced dye systems.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical producers use 2-Bromo-4,5,6-Trifluoroaniline as a building block for creating drug candidates within the fluoroaromatic and heterocyclic compound class. Medicinal chemists react this aniline derivative in Suzuki, Buchwald-Hartwig, and nucleophilic aromatic substitution routes during scale-up. Careful control of trace impurities ensures regulatory compliance, especially when this intermediate appears in the core structure of investigational new drugs and advanced intermediates. GMP documentation and batch traceability hold paramount importance at this stage.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • EU Regulation (EC) No 1907/2006 (REACH) for registration and documentation
    • ISO 9001:2015 for quality management in manufacturing

    Typical usage ratio

    • 0.2–0.8 molar equivalents relative to target API, depending on route optimization and desired fluoro-substitution pattern
    • Adjustment based on required yield and impurity profiles during early-phase route scouting

    Downstream process integration

    • Added during multi-step batch synthesis at the nucleophilic substitution or coupling stage
    • Reacted with boronic acids, amines, or specialty carbons for the desired scaffold
    • Final purification via column chromatography or crystallization to ensure pharmaceutical grade

    Final product types

    • Pilot-scale active pharmaceutical intermediates
    • Research new chemical entities (NCEs) for oncology or CNS therapeutics
    • Reference standards for structure elucidation
    • API components for further FDF (finished dosage form) synthesis

    2. Agrochemical Active Ingredient Manufacturing

    Leading producers in the crop protection sector incorporate this trifluorinated aniline derivative into their synthetic pipelines to obtain advanced intermediates for fungicide and herbicide actives. The fluoroaromatic structure enhances metabolic stability and field performance. Processing plants use this raw material under strict residue control to meet food-chain and environmental regulations, particularly when targeting selective agrochemical triggers or halogenated scaffolds.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO JMPR guidelines)
    • OECD Guidelines for the Testing of Chemicals
    • China GB 2763-2023 Maximum Residue Limits for Pesticides in Food
    • ISO 9001:2015 for supplier traceability

    Typical usage ratio

    • 3–10% w/w in coupling or cyclization steps of actives with target fluorine content
    • Range based on design of target molecule and yield calculations in pilot or commercial batches

    Downstream process integration

    • Utilized as a halogen donor in the construction of precursor rings for active herbicide and fungicide moieties
    • Incorporated during pre-final coupling stage, followed by purification for technical grade products
    • QC testing for trace pesticide impurities and degradation products

    Final product types

    • Technical grade fungicide and herbicide intermediates
    • Active ingredients for formulation into EC (emulsifiable concentrate), SC (suspension concentrate), or WG (water-dispersible granule) products
    • Regulatory trial samples for field studies
    • Stability study references

    3. Specialty Dye and Pigment Synthesis

    Dye and pigment manufacturers employ this fluorinated building block to introduce unique chromophore features into specialty dyes used in security printing, electronic displays, and sensitive colorant applications. The distinct halogen pattern confers thermal stability and resistance to light fading, critical for long-life industrial inks targeting electronics and anti-counterfeit packaging. Material margins and reaction efficiency depend directly on traceable, high-purity intermediate supply.

    Industry compliance standards

    • OEKO-TEX Standard 100 for dye safety
    • EN 71-3:2019 (for toys colored with industrial pigments)
    • GHS/CLP labeling (Regulation (EC) No 1272/2008)
    • ISO 9001:2015 in colorant manufacturing

    Typical usage ratio

    • 1–6% w/w in final coupling reactions, adjusted depending on desired shade or fastness
    • Engineer-specific ratios during pilot color scale-up for stability testing

    Downstream process integration

    • Used in diazotization and subsequent azo coupling sequences
    • Integrated at pre-final step for tuning hue and stability characteristics before milling and formulation
    • QC control for trace halogen and unreacted amine contents

    Final product types

    • Anti-counterfeit security inks for banknotes and legal documents
    • OLED and electronic display dyes
    • High-stability textile printing pigments
    • Special effect polymers for industrial coatings

    4. Advanced Polymer and Resin Synthesis

    Producers in specialty polymer fields utilize the aniline derivative to impart tailored electronic, barrier, or thermal properties to polyimides, polyaramids, and fluoropolymer blends. Its unique substitution pattern supports advanced monomer design for next-generation materials demanded by the electronics, aerospace, and membrane industries. Consistency and documented impurity profiles matter for downstream compounders and end-users asking for RoHS- and REACH-compliant supply chains.

    Industry compliance standards

    • EU RoHS 2011/65/EU for restricted substances in electronic-grade polymers
    • REACH Regulation (EC) No 1907/2006 for monomer use registration
    • UL 94 recognition for flame retardant resins
    • ISO 14001:2015 for environmental management during production

    Typical usage ratio

    • 0.5–5% w/w in polyimide or polyaramid precursor blends, depending on target durability and fluorinated segment length
    • Adjusted per property tests of end-use film, fiber, or coating

    Downstream process integration

    • Fed into monomer condensation reactions to generate partially fluorinated intermediate polymers
    • Blended with diamines and dianhydrides during pre-polymer melt or solution polymerization
    • Regulated drying and removal of trace residuals before extrusion or film casting

    Final product types

    • Flexible printed circuit substrates
    • High-temperature resistant insulating films
    • Selective separation membranes for industrial gases
    • Specialty engineering plastics for aerospace applications
    Free Quote

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

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    Certification & Compliance
    More Introduction

    2-Bromo-4,5,6-Trifluoroaniline: Reflections From Our Production Floor

    Meeting Stringent Demands in Chemical Synthesis

    In the ever-changing world of specialty chemicals, 2-Bromo-4,5,6-Trifluoroaniline stands out as a crucial intermediate in pharmaceutical and agrochemical research. We have worked with this compound in-house for years, producing it at commercial scale as well as in custom synthesis projects based on client requirements. This substance—bearing the CAS number 328-69-8—packs together reactivity and selectivity that drive innovation across several value chains.

    Our batches of 2-Bromo-4,5,6-Trifluoroaniline typically center around purity levels greater than 98%, which helps downstream users sidestep unnecessary purification steps. Whether the research group pursues an API (active pharmaceutical ingredient) lead or an agrochemical formulation, this material provides the trifluorinated aromatic backbone that so many target molecules demand. Unlike simpler anilines or other bromo-substituted variants, this compound offers a balance of chemical handling ease and functional group reactivity. In a laboratory, you notice right away that trifluorinated rings suppress metabolic degradation; this characteristic often proves essential in optimizing drug candidates or pesticide scaffolds.

    Learning From Production Experience

    On the production floor, we move through multiple steps—bromination, controlled fluorination, and finally amination—before reaching the target. Years of batch production have taught us to manage exothermic risks during bromine addition, as trace impurities at this stage can complicate scale-up. The expertise built in recrystallization and fine-tuning reaction conditions pays off batch after batch, bringing consistency that seasoned chemists look for in their intermediates. Many customers come to us after dealing with inconsistent supplies of this compound from brokers or small labs, who might not have the in-house analytical capabilities we use daily. Each drum or jar leaving our facility comes with full HPLC, NMR, and GC reports—not only to guarantee purity but also to give researchers confidence about trace impurities and isomer content.

    We see regular interest in this product from R&D labs specializing in fluorinated building blocks. The presence of three fluorine atoms positions the molecule for high selectivity in subsequent reactions, and bromine at the ortho position (relative to the amine) opens up Suzuki, Buchwald–Hartwig, and Ullmann-type couplings. These couplings often struggle with more heavily substituted or less pure anilines. Over the years, we have supported many projects upgrading their standard bromoanilines to this trifluorinated version, usually to sharpen target specificity or dial in metabolic stability.

    In The Field: Applications and Transformation Pathways

    2-Bromo-4,5,6-Trifluoroaniline does not linger on a shelf; it forms the keystone of several active research programs. Medicinal chemists trust it to introduce a robust trifluorinated motif into kinase inhibitors, antiviral backbones, and fungicides. From our perspective, trifluoromethyl and trifluorophenyl systems have soared in relevance—regulators and markets expect next-generation pharmaceuticals and agrochemicals to combine bioactivity with environmental persistence or selective metabolic clearance. This substance delivers both, without the oversupply of unwanted byproducts that plagues less pure grades.

    End-use partners often highlight how this compound’s electronics accelerate cross-coupling or nucleophilic substitution. The amino functional group becomes a peg for diversification; the bromine’s reactivity can be channeled to build biaryl bridges, while the fluorines dramatically blunt unwanted side reactions. Over countless collaborations, we have heard how a well-prepared intermediate like this cuts down project timelines. Whether a customer aims for a novel herbicide or a CNS-active small molecule, a reliable feedstock saves both time and troubleshooting headaches.

    Product Differentiation: Beyond Commodity Anilines

    Comparing 2-Bromo-4,5,6-Trifluoroaniline to more basic anilines or even standard trifluoroanilines draws a sharp gulf. Simpler anilines easily undergo oxidation, yet our product holds its ground—its stability in storage and handling translates directly to reduced loss and higher batch reproducibility. We have observed in trials that switching from mono- or di-fluorinated anilines to this trifluoro-bromo analog consistently boosts synthetic yield and selectivity. This observation repeats itself in both gram-scale academic research and multi-kilo pilot projects for industrial partners.

    The bromine atom, stationed at the ortho position to the amino group, goes far beyond what you would get from just 2-bromoaniline. Paired with the electron-withdrawing impact of three fluorines, the reactivity zone sharpens, drawing the attention of even cautious process chemists. Reagents encounter the molecule’s precise electronic signature, sidestepping overreactions and favoring the one-bond or two-bond functionalization that designers want. The result—cleaner reactions, less column chromatography, and better control over regioselectivity—emerges time after time.

    Another aspect that differentiates this compound from the crowded field lies in solubility and crystallization profiles. As a manufacturer, we spend a great deal of time optimizing these properties, since downstream users care about how a substance handles under process stress. The tight crystal packing forced by multiple fluorines and bromine raises melting points and limits atmospheric uptake, helping users who run moisture-sensitive processes. We collect detailed physical property data from each lot in-house, so process scalability gets considered early. All this information we offer straight to our R&D contacts, not buried in technical sheets, because real-world feedback tells us what matters in a synthetic sequence.

    Purity, Safety, and Handling: Lessons Learned Over Decades

    Storing and transferring halogenated intermediates teaches caution grounded in day-to-day operation. Purity matters because impurities in bromo-fluoroanilines, even at sub-percent levels, can derail high-performance syntheses. Every batch undergoes moisture-content scrutiny and isels off in dry, inert packaging. Supplier hiccups over transport regulations arise less often when you start off as a registered, audited producer with a proven safety record. We carry decades of incident-free operations, tracked through both international audits and customer returns—real benchmarks, not just talking points tossed around in sales brochures.

    Anyone working with this product knows that safe handling goes hand-in-glove with consistent manufacturing. Our floor crews never shortcut PPE, air-handling, or trace solvent controls, and every customer tour of our plant closes the book on quality doubts. The person who signs off on release batches worked their way up from the reactor bay—not an anonymous office kilometers away. Our own experience with regulatory agencies drives us to update documentation, even when customers do not request it. These practices start as requirements, but they soon become habits. They show themselves in every drum, every lab-scale glass jar, and every feedback loop from our users.

    Improving Customer Outcomes

    We have watched customers move from unreliable suppliers or trading houses to direct chemical manufacturers for a good reason. Projects run smoother when there is a single source accountable for both quality and technical support. Over the years, the best results often came from close contact with our process chemists, not just sales staff. Researchers call us about real-world bottlenecks—solubility issues, minor byproduct complications, or questions about what solvents to use. Since we make 2-Bromo-4,5,6-Trifluoroaniline in-house, we offer more than standard operating procedures. Detailed logs capture actual conditions from start to finish. These logs sit in our hands when a customer’s lab team wants to optimize a coupling protocol or troubleshoot crystallization quirks.

    Commercial partners gain from our history of process development. We have supported tech transfers, helped speed time-to-market on patentable molecules, and updated lot packaging based on specific shipping routes and climate conditions. Every change traces back to feedback from users—cross-continental shipments or temperature-stress packaging all started from real experiences. Each adjustment makes handling this compound less of a hurdle and more of a straightforward step on the synthesis path.

    Tackling Challenges in Scale and Supply Chain Stability

    Producing halogenated aromatics at scale challenges even experienced manufacturers. You quickly learn that bulk output brings pressure to keep impurity profiles tightly controlled and maintain steady batch reproducibility. We design our production units to handle everything from pilot to full resin-kettle scale, ensuring the supply lines don’t jerk with seasonal demand swings. Global logistics have thrown sand in the gears for many specialty chemicals, especially those crossing borders during times of regulatory change or transport slowdowns. Our teams pre-empt these challenges. We plan safety stock, monitor shipping lifecycles, and adjust schedules for clients juggling multiple intermediates. Unpredictability in the chain fades when the producer controls every step—raw materials, finished goods, and every legal detailed footstep in between.

    There have been years where customs or regulatory hurdles forced us to pivot. Instead of waiting, we doubled down on local sourcing, increased buffer inventory, and worked directly with freight partners who understand packaging and compliance for halogenated substances. By owning responsibility for each link in the chain, we made sure that not a single research program stalled for lack of material. That is the standard we hold ourselves to, and we believe it makes each gram of 2-Bromo-4,5,6-Trifluoroaniline that reaches our customers a little more dependable.

    Quality Control: Building Trust Through Data

    Some clients only see white to yellowish powder in sealed jars. Underneath, every batch sits on the bedrock of elaborate QC protocols. In our labs, the analytical chemists track impurity maps, monitor byproducts, and run repeat NMR, HPLC, and gas chromatography. Many of these steps arose from direct feedback: once, a medicinal chemistry group encountered a stubborn iodo-aniline trace in a different supplier’s lot, derailing their synthesis. We answered by zeroing in on iodine sources and investing in additional raw material testing, building out a strict contaminant exclusion program. Every time an issue bubbles up in the field, we fold those lessons into the next batch’s controls.

    Trace solvent residue and water content often cause headaches downstream. We learned to address these concerns by using dual vacuum and inert-gas drying before packing. These improvements do not just stay within our plant—they show up in better yields, cleaner reaction mass, and more consistent scale-up for customers worldwide. Technical staff can consult directly with our analytic lab, skipping the usual phone tag and delays that creep in with traders or third-party reps.

    Environmental and Regulatory Pressures

    Manufacturing 2-Bromo-4,5,6-Trifluoroaniline also demands vigilance about environmental and regulatory footprints. Our teams navigate the increasing stringency on halogenated waste streams, paying up-front attention to solvent recovery and emission controls. Engineered controls have become part of our daily workflow, not afterthoughts tacked on after a regulation change. The environmental health and safety (EHS) department shapes both the upstream process and downstream waste treatment—handling every spent solvent, every solid byproduct, and every trace residual with precision.

    Customers who operate under country-specific REACH, TSCA, or customs regimes know that documentation can make or break a supply chain. Since we prepare regulatory support in-house, not a week slips by without updating certificates, safety data, and export clearances as requirements shift. Experienced buyers ask for clear lineage from raw materials up to delivered product—a demand we meet with full batch-tracking and transparent data. Regulators across the world aim for safer, cleaner processes, and we take those goals to heart. Each kilo shipped not only passes technical muster but also fits into evolving standards for responsible chemical production.

    Substance Innovation: What Sets Us Apart

    Innovation means more than a molecule diagram or theoretical benefit. With 2-Bromo-4,5,6-Trifluoroaniline, it arises from listening to feedback, tracking real-world field results, and tuning process variables until customers achieve the outcomes they seek. One R&D group used our material to push their clozapine-derivative synthesis to higher selectivity, reporting yield improvements after shifting from less pure imports. Another agricultural partner wanted low dust formation and tight particle size specs—adjustments we pulled off by altering crystallization temperature and solvent content. These are not hypothetical stories but grounded examples that grew from long-term collaboration, not one-off sales.

    Every year, new applications and research needs reshape how this compound gets used. AI-driven molecule design rarely matches real-world chemistry without clean, dependable inputs. We have seen AI models repeatedly select 2-Bromo-4,5,6-Trifluoroaniline motifs—data scientists and chemists alike prefer the clean background, reproducible functionalization, and predictable metabolic profile. Delivering these attributes takes years refining not just the synthetic route, but also how we store, pack, and follow up on delivered lots.

    Supporting the Progress of Science and Industry

    As a team rooted in the daily grind of chemical production, we understand just how critical reliability becomes when running multiple routes and adjusting to new demands. 2-Bromo-4,5,6-Trifluoroaniline brings together structural novelty and manageable reactivity, taking its place in pipelines from pharmaceuticals to crop protection. The intense competition in these spaces places a premium on intermediates that perform reliably.

    We draw on a toolkit built of more than standard operating procedures: hands-on adjustments, analytical know-how, responsive shipping, and a willingness to innovate when feedback points us to a better solution. The chemists and engineers behind every package appreciate the difference every minor impurity or packaging flaw can make. This kind of insight, drawn from hundreds of batches and diverse collaborations, stands apart from the transactional world of third-party traders. Seasoned operations show up in stable distribution, improved R&D outcomes, and repeat orders based on trust, not just price sheets.

    Final Thoughts on Value and Service

    Our work with 2-Bromo-4,5,6-Trifluoroaniline reflects the reality that every compound stands at the junction of technical possibility and production experience. The true value comes from delivering not just a chemical, but a service—one that closes the gap between process chemistry and finished product needs. Whether your team is targeting new pharmaceutical scaffolds, seeking to optimize herbicide design, or exploring novel fluorinated materials, our door remains open to technical conversations, joint development efforts, and genuine support at every stage. This compound will keep pushing boundaries, and we stand committed to ensuring every gram does its job—reliably, safely, and with insight only a dedicated manufacturer can offer.