Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2,4,6-Tribromoaniline

    • Product Name 2,4,6-Tribromoaniline
    • Alias 2,4,6-Tribromo-1-aminobenzene
    • Einecs 219-320-0
    • 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

    435157

    Chemicalname 2,4,6-Tribromoaniline
    Molecularformula C6H4Br3N
    Molarmass 345.82 g/mol
    Casnumber 615-36-1
    Appearance White to off-white crystalline powder
    Meltingpoint 148-152 °C
    Density 2.53 g/cm³
    Solubilityinwater Insoluble
    Pubchemcid 12178
    Iupacname 2,4,6-tribromoaniline
    Smiles C1=C(C=C(C(=C1Br)N)Br)Br
    Inchi InChI=1S/C6H4Br3N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2

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

    Packing & Storage
    Packing 2,4,6-Tribromoaniline is supplied in a 25g amber glass bottle with a screw cap, labeled with hazard and handling information.
    Shipping 2,4,6-Tribromoaniline is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as a hazardous material and handled per relevant transport regulations (such as DOT, IATA, or IMDG). Appropriate labeling and documentation are required, and only trained personnel should manage the shipping process.
    Storage 2,4,6-Tribromoaniline should be stored in a tightly sealed container, protected from light and moisture. Store it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents and acids. Clearly label the container and ensure secondary containment to prevent spills. Follow all appropriate safety and regulatory requirements for handling hazardous chemicals.
    Application of 2,4,6-Tribromoaniline

    Applications of 2,4,6-Tribromoaniline in Industrial Manufacturing

    2,4,6-Tribromoaniline serves as a core intermediate in organic synthesis for specialty chemical manufacturing. Our production integrates stringent quality control and traceability, supporting diverse industry needs in high-value end-use sectors.

    1. Pharmaceutical Intermediates for Antibacterial and Anticancer Agents

    Manufacturers use 2,4,6-Tribromoaniline in multi-stage syntheses as a building block for active pharmaceutical ingredients including certain antibiotics and anti-tumor molecules. Its rigid aromatic structure and bromination facilitate specific coupling and substitution reactions vital for creating target pharmacophores. Customers request material with consistent purity ≥ 98% to ensure reproducibility for medicinal chemistry and process scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs (where applicable for intermediates)
    • 21 CFR Part 211 (US FDA cGMP regulations for finished pharmaceuticals, relevant for API manufacturing)
    • EudraLex Volume 4 GMP Guidelines (EU)

    Typical usage ratio

    • 10–25 mol% of total starting aromatic amine charge, depending on downstream target molecule complexity and yield optimization objectives.
    • Process chemists adjust molar ratio based on side product minimization and isolation efficiencies.

    Downstream process integration

    • Used during the early stage amidation or Suzuki coupling steps.
    • Fed directly to the main synthesis vessel in batch or semi-continuous conditions following in-house or contract QC release.
    • Subsequent transformation typically involves palladium-catalyzed reactions or nucleophilic substitution to complete the core scaffold.
    • Multi-kilogram quantities processed with rigorous intermediate sampling for reaction completion monitoring.

    Final product types

    • Antibiotic intermediates for cephalosporin and macrolide families
    • Precursors for kinase inhibitor active ingredients
    • Building blocks for radiolabeled probes (research and early-phase pharmaceuticals)
    • Specialty antineoplastic agent scaffolds

    2. Synthesis of High-Performance Dyes and Pigments

    Colorant producers utilize 2,4,6-Tribromoaniline as a halogenated aniline precursor in the synthesis of azo dyes, anthraquinone and phthalocyanine pigments. Direct substitution on the aromatic ring allows for controllable color depth and fastness properties. End-users demand traceable lot release and low-level metal impurity specifications to ensure final pigment compliance, especially for textile and printing applications in regulated markets.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textiles, restrictions on banned amines and heavy metals)
    • REACH Annex XVII (regulation on certain hazardous substances in finished pigments/dyes)
    • ISO 9001:2015 certified pigment manufacturing QMS
    • ASTM D4287 (Color strength and shade test method, pigment dispersion)

    Typical usage ratio

    • 8–16% by weight in dye synthesis reaction mixtures, depending on target chromophore structure and final hue intensity requirements.
    • Adjusted according to desired color strength and stability in textile or coating formulations.

    Downstream process integration

    • Introduced at the diazotization or coupling stage for mono- or polyazo dye synthesis.
    • Integrated into pigment reaction batches before final metal salt chelation and grinding processes.
    • Manufacturers deploy batch release testing for shade, purity, and heavy metal analysis before shipping to downstream blenders or finishers.

    Final product types

    • Textile and leather dyes (direct, acid, reactive grades)
    • High-performance organic pigments for automotive and industrial coatings
    • Color concentrates for plastic compounding
    • Inkjet and digital print ink formulations

    3. Flame Retardant Additive Intermediate

    Chemical manufacturers use 2,4,6-Tribromoaniline as a reactive intermediate for synthesizing brominated flame retardants. Its high bromine content enhances fire resistance in polymers by facilitating free radical quenching mechanisms. Downstream blending requires tight control of residual amines to avoid migration in finished materials used in electrical or construction sectors. Customers audit entire production runs for batch consistency and halogen content stability.

    Industry compliance standards

    • UL 94 (Standard for Safety of Flammability of Plastic Materials)
    • IEC 60695-2 (Fire hazard testing, part of electrical safety requirements)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • ISO 17896 (Assessment of the release of components from polymeric materials)

    Typical usage ratio

    • 15–30 wt% relative to base resin batch, with proportions optimized for target Limiting Oxygen Index (LOI) and mechanical property trade-offs.
    • Adjusted for the presence of co-monomers or stability boosters in specialty compound formulations.

    Downstream process integration

    • Formation of brominated flame retardant monomers via direct amination or acylation in closed reactors.
    • Subsequent isolation, washing, and high-shear incorporation during pelletizing or masterbatch blending stages.
    • Continuous QC checks on halogen content and residual amine for compliance before integration into larger polymer runs.

    Final product types

    • Polyamide (PA), ABS, and polypropylene flame-retarded compounds
    • Foam insulation components for building envelopes
    • Wire and cable insulation coatings
    • Flame-retardant masterbatches used in automotive interiors and electrical device housings

    4. Agricultural Chemical Synthesis (Pesticide Active Ingredients)

    Producers of crop protection chemicals use 2,4,6-Tribromoaniline as a core aromatic intermediate for agrochemical active ingredient synthesis. Its halogenated structure is crucial in creating molecules with selectivity and enhanced environmental stability. Suppliers must guarantee low metal contaminants and strict lot retention for traceability in line with global agrochemical regulations and stewardship policies. Material batches undergo independent laboratory analysis for purity and potential nitrosamine precursors before downstream conversion.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA 40 CFR Part 158 (Data requirements for pesticide registration, US)
    • ISO 17025 accredited laboratory release for active ingredient synthesis
    • REACH registration dossier requirements for intermediates

    Typical usage ratio

    • 5–12 mol% in initial synthesis reactors, adjusted based on required yield and byproduct profile.
    • Lower ratios preferred for batch processes; higher ratios for continuous in-line reactions targeting higher output.

    Downstream process integration

    • Charged at the initial halogenation or condensation step for HPPD inhibitor synthesis.
    • Incorporated in closed-loop continuous reactors for selective coupling or further bromination steps.
    • Followed by isolation, washing, formulation, and packaging for crop protection end-uses.

    Final product types

    • Herbicide active ingredient intermediates
    • Insecticide and acaricide aromatic scaffolds
    • Fungicidal precursor molecules
    • Custom synthesis products for contract agrochemical research
    Free Quote

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

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2,4,6-Tribromoaniline: Experience from the Manufacturer’s Plant Floor

    The Nature of 2,4,6-Tribromoaniline

    Anyone who has spent time in the business of brominated aromatics knows that 2,4,6-tribromoaniline is not just another specialty compound. Our team has worked with this material for years, and each batch reflects attention to preparation and experience handling bromination reactions. This solid compound, typically presenting as a pale to off-white crystalline powder, carries the unique fingerprint of its three bromine atoms strategically fixed on the aromatic ring. The amino group at the para position enables a striking profile for downstream chemistry, cementing its niche in fields that need controlled reactivity and a solid backbone.

    Manufacturing Mindset

    At the chemical plant, production of 2,4,6-tribromoaniline means more than following recipes. Bromine’s reactivity demands experience and precision. Our operators monitor temperature, agitation, and addition sequences to avoid unwanted side products, especially those nagging traces of dibromoaniline or over-brominated tars. It can take years to hone protocols that offer reliable purity and low impurity profiles batch by batch. The difference? A floor manager who has seen hundreds of cycles and knows by eye and smell when conditions start to slip. Customers notice the consistency this brings—not just numbers on a certificate, but results in their syntheses.

    Specifications and What They Signal

    We generally target a purity exceeding 98% by HPLC or GC, but it’s not just about the headline number. Impurities can disrupt downstream reactions or impact the color and stability of produced materials. Particle size has practical consequences. Too fine and dust-handling becomes a real issue; too coarse and customers struggle with solubility or uniform mixing. Our standard practice is to keep a balance that flows well but suspends without clumping, shaped by feedback from longtime partners in the dye and pharmaceutical sectors. Moisture shouldn’t exceed 0.5% as measured by Karl Fischer titration because water alters reactivity and storage properties.

    Where 2,4,6-Tribromoaniline Makes an Impact

    End users reach for 2,4,6-tribromoaniline as a key intermediate for more complex molecules. Developers in agrochemicals, dyes, and drug candidates routinely use this building block to introduce dense bromine substitutions that other approaches find difficult. It stands out in the synthesis of highly functionalized aniline derivatives, where mixed-halogen patterns are critical. We’ve seen customers design custom ligands, specialty pigments, and even novel flame retardants around this core. What seems like an ordinary compound at a glance can unlock unique properties—thermal stability, rigid backbone, or fresh binding sites—for new molecular architectures.

    Differences from Other Brominated Anilines

    In our experience, the placement of bromines makes a world of difference. Some processes work with 2,4-dibromoaniline—a product we also make—but 2,4,6-tribromoaniline brings rigidity and planarity that change how the ring interacts with electrophiles or bases. Tri-bromination at the ortho and para positions sets up steric shielding, which can help in subsequent substitutions or protection from oxidative conditions. Chemists notice how the three bromines influence aromatic reactivity, leading to cleaner outcomes in coupling, azo-dye formation, or Suzuki-type cross-coupling. In contrast, mono-brominated analogs lack this robustness and leave certain synthetic doors closed.

    Real-World Use Cases from the Factory

    Over years, we’ve had conversations with formulators and process chemists who share their production challenges. In organic pigments, a consistent supply of 2,4,6-tribromoaniline saved one specialty ink customer hours of adjustment in their downstream coupling reactions. They reported brighter, more stable magenta shades because bromine placement prevented unwanted byproduct formation. Pharmaceutical research teams rely on our product to anchor lead development, building scaffolds for kinase inhibitors and β-lactam antibiotics. Since tribromoaniline can act as either a base or nucleophile, it opens paths closed to lighter-halogen analogs. As flame retardant regulations tightened, customers explored tribromoaniline derivatives for electronics applications, appreciating the balance of bromine weight and molecular rigidity.

    Production Challenges and Opportunities

    Producing tribromoaniline means navigating exothermic reactions, bromine fumes, and safe handling protocols day in and day out. The key to minimizing byproducts and maximizing yield is incremental bromine dosing, strong stirring, and reliable temperature control. Scale-up from pilot to bulk takes the most finesse, as temperature gradients and mixing uniformity become much more complex. We moved to glass-lined reactors with robust seals after experiencing pitting and leaks in basic steelware. Waste management isn’t a minor detail either—aqueous waste streams with bromide salts require careful neutralization. In response to environmental regulations, we’ve upgraded our effluent treatment to handle these salts more efficiently. These operational details often fly under the radar but spell the difference between a reliable supplier and a recurring headache for end-users.

    Stability, Storage, and Shelf Life in Practice

    2,4,6-Tribromoaniline demonstrates impressive shelf stability, provided the storage conditions are right. Our warehouses maintain sealed, light-protected bins in climate-controlled sections to prevent caking or color degradation. Exposing the powder to humid, bright environments shortens shelf life, leading to yellowing and sometimes caking that interferes with dosing. Our drum packaging and multi-layer liners reflect years of customer feedback on storage issues. Small changes here can prevent costly material losses on the final user’s end.

    Environmental and Safety Considerations

    We recognize the gravity of working with heavy halogenated compounds. Even skilled operators face challenges managing spills or bromine exposure. Regular training, real-time monitoring of vapors, and emergency protocols shape the daily workflow. We invest in air filtration, dedicated PPE, and double containment for all fuming reagents. Continuous improvement of our neutralization tanks and waste handling not only keeps us compliant but also supports local community health. Customers ask about our environmental track record, and we share clear benchmarks of emissions, effluent quality, and ongoing reduction projects. Years ago, issues with odor emissions led us to invest in scrubber systems, which cut local complaints down to zero.

    Upstream Decisions Matter to Downstream Outcomes

    Manufacturing choices have real consequences. Brightness of finished azo dyes or the crystalline purity of synthesized drug intermediates often tie directly to tribromoaniline’s purity or moisture content. In our own R&D labs, small changes to washing or recrystallization steps often yield big gains in downstream consistency. We test every lot in model coupling reactions before shipment. These “real world” stress tests show how material will perform in kinases, pigments, or trial syntheses for other clients. Our experience reminds us that the lab notebook can only go so far—full-scale plant feedback means more.

    The Role of 2,4,6-Tribromoaniline in Innovation

    The pace of product development in pharmaceuticals and advanced materials keeps picking up. Most recent successes we’ve seen from customers start with small tweaks—better halogen control, finer particle size, or tighter moisture specifications on raw intermediates. Years ago, an agricultural customer shifted from 4-bromoaniline to 2,4,6-tribromoaniline to improve field stability and minimize photodecomposition in their fungicide. The result was fewer recalls, longer shelf life, and increased yield per hectare. These gains rarely come from flashy advertising; they’re the result of tireless optimization and a willingness to trial “one more run” with a slightly different input. We keep lines open for these discussions, treating each packaging tweak or batch trial as a chance to pioneer the next solution.

    Feedback Loop with Long-Term Partners

    Decades in chemical production teach a lot about what actually matters to folks in formulation or synthesis. Customers need more than a high-purity, well-documented product—they look for swift, clear communication about variability or expected profiles. We embrace requested changes in lot size, package type, and documentation. Once, a pigment customer flagged dusting as a major plant issue. We ran several trials with granulation and rollout timing to settle on a particle profile that met their process needs without generating excess fines. Direct feedback has driven a number of improvements—from stricter in-process moisture checks to modified labeling after a user requested batch-by-batch traceability. Our philosophy remains to learn directly from those handling, blending, and reacting our material every day.

    Comparisons with Other Manufacturers

    Every plant develops its own signature fingerprint—no two batches from different suppliers are quite the same, even on paper. Having seen incoming samples from across the globe, we know how subtle differences in process control, washing protocols, and impurity handling show up in the final performance of the material. While some producers trim corners to maximize throughput, our operation focuses on minimizing downtime for cleaning cycle, which means fewer cross-contaminations and more uniform product quality. The end result is a material that shows up in customer QC as “trouble-free,” with consistent performance, reliable storage, and no unpleasant off-odors. Frankly, experience and a long memory of process hiccups guide improvements—years of steady hands and sharp eyes produce a more robust product than automation alone.

    Real Costs and Returns for the User

    End users in the pharmaceutical and pigment sectors often ask about the “true” cost of their intermediates. From our vantage, cost is measured in more than dollars per kilogram. It’s downtime from a clogged filter press, waste from inconsistent crystallization, or lost batches from unexpected side reactions. A high-purity, clean 2,4,6-tribromoaniline supply moves easily through most reaction setups, minimizes line cleaning and waste disposal headaches, and lets chemists focus on new product development rather than troubleshooting. Our error rate and reclamation effort dropped significantly after we invested in secondary screening and finer moisture control measures. That investment shows up as smoother customer audits and fewer complaints, not just lower manufacturing risk.

    Supply Chain Stability and Responsiveness

    Global sourcing and changing logistics grow tougher each year. Raw bromine isn’t always available on demand, and shipping heavy, hazardous goods brings unique regulatory hurdles. We've set up back-up sources for key reagents and agonized over stocking levels. Consistency in the supply of intermediates like 2,4,6-tribromoaniline saves every customer in the value chain money and headache. Our direct production model, rather than a broker approach, means real visibility and direct accountability with no gaps. It lets us react quickly to weather events, logistics delays, or special runs required for a new development project. Years of direct relationships with international regulators have helped smooth document flow and resolved tricky import questions before they could derail critical shipments.

    Potential Improvements, Research, and Looking Ahead

    Innovation never sits still in an active chemical plant. We constantly experiment with greener alternatives for solvents, researching ways to minimize energy input without sacrificing reaction efficiency. Pilot studies on recycling bromide streams aim to reduce environmental footprint further and deliver cost benefits back to users. We tinker with higher throughput batch reactors, evaluating each trial not only for yield but ease of cleaning, waste reduction, and operator workload. As customer requirements grow stricter—whether by regulatory mandate or technical necessity—we adapt specifications, document byproducts, and validate new test methods to offer full transparency. The drive to support new molecular formats in pharma and materials science, as well as to support customers in regulatory compliance, steers our ongoing research choices.

    Listening and Responding for Shared Success

    The work producing 2,4,6-tribromoaniline brings together chemistry, logistics, and real personal relationships. End users stop by our plant to see scale-up trials or send in samples for reanalysis. We’ve noticed the best results come from early, straightforward conversations about project requirements, not from chasing the lowest cost per kilo. Experience—earned by years of navigating process upsets, raw material shortages, and unexpected regulatory questions—teaches a simple truth: reliable, safe production supports everyone downstream. Every batch represents a chance to learn from mistakes, preferences, and successes, each one bringing us closer to products that solve end-user challenges. Our whole team feels a responsibility to keep raising the bar, so the next generation of chemists can count on their inputs to support the future’s discoveries.