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2,6-Dibromo-4-Tert-Butylaniline

    • Product Name 2,6-Dibromo-4-Tert-Butylaniline
    • Alias 2,6-Dibromo-4-(tert-butyl)aniline
    • Einecs 249-984-5
    • 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
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    Specifications

    HS Code

    741554

    Productname 2,6-Dibromo-4-Tert-Butylaniline
    Casnumber 51252-09-8
    Molecularformula C10H13Br2N
    Molecularweight 321.03
    Appearance White to off-white solid
    Meltingpoint 90-94 °C
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Density 1.59 g/cm3 (predicted)
    Smiles CC(C)(C)c1cc(Br)c(N)c(Br)c1
    Inchi InChI=1S/C10H13Br2N/c1-10(2,3)6-4-7(11)9(13)8(12)5-6/h4-5H,13H2,1-3H3
    Storagetemperature Store at 2-8 °C
    Hazardstatements H315, H319

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

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    Application of 2,6-Dibromo-4-Tert-Butylaniline

    Applications of 2,6-Dibromo-4-Tert-Butylaniline in Industrial Manufacturing

    As a manufacturer with extensive production capacity of high-purity 2,6-Dibromo-4-Tert-Butylaniline, we focus on industrial segments where this raw material’s brominated aniline structure contributes to specific chemical synthesis and advanced materials. Here we outline proven, regulatory-compliant downstream uses with relevant operational insights.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Our 2,6-Dibromo-4-Tert-Butylaniline is widely utilized as a core intermediate in the multi-step synthesis routes of certain APIs. The brominated positions enable selective further functionalization by coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig aminations, providing access to pharmacologically active benzaniline derivatives. Given the strict process control required, manufacturers incorporate our material at defined stages to ensure high purity of subsequent reaction products before final crystallization of APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines for Active Pharmaceutical Ingredients
    • Ph. Eur./USP Monograph compliance for trace impurity limits
    • REACH Registration and Substance Evaluation
    • ISO 9001:2015 Certified Quality Management Systems

    Typical usage ratio

    • Used at stoichiometric or slight molar excess in coupling steps, ranging from 0.9:1 to 1.2:1 equivalent molar ratios according to route optimization and yield targets

    Downstream process integration

    • Charged after primary amination or bromination stage; purified by extraction and distillation before entering next step
    • QC analysis for trace metals and halide residues before API conversion reactions
    • Batch records maintained for traceability under GMP protocols

    Final product types

    • Cardiovascular drug intermediates
    • Oncology-targeted active substances
    • CNS (central nervous system) pharmaceutical compounds
    • Specialty antiretroviral raw materials

    2. High-Performance Dye Manufacturing

    This raw material enters dye synthesis where its molecular structure assists in achieving enhanced color fastness and stability for high-end applications such as specialty disperse and reactive dyes for polyester textile finishing. Downstream dye manufacturers utilize its aniline core for high-purity diazotization and coupling with diazonium salts, followed by media purification to reduce halogen emissions and waste.

    Industry compliance standards

    • OEKO-TEX® Standard 100: Residual aromatic amine restrictions
    • ZDHC (Zero Discharge of Hazardous Chemicals) guidelines
    • EU REACH Annex XVII compliance for dye intermediates
    • ISO 14001:2015 Environmental Management Systems for effluent control

    Typical usage ratio

    • Applied at 0.6-1.0 molar equivalent relative to coupling agents; adjusted per color strength and target application depth

    Downstream process integration

    • Introduced post-nitration/purification, then converted to diazonium salts in ice-cooled reactors
    • Subjected to high-shear mixing and pH stabilization before final azo-coupling
    • Routine in-process chromatography for structural purity and color index consistency

    Final product types

    • Disperse dyes for polyester fiber
    • Reactive dyes for cellulosic blends
    • High-lightfast textile pigments
    • Heat-transfer printing inks

    3. Specialty Agrochemical Synthesis

    Leading agrochemical producers select 2,6-Dibromo-4-Tert-Butylaniline as a building block for selective herbicide and fungicide synthesis. Its tert-butyl group improves target compound solubility and activity spectrum. This raw material acts as a nucleophile in SNAr reactions or as a ligand precursor for novel actives. Careful reaction monitoring ensures conversion efficiency, especially in chlorination or alkylation steps.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications and Evaluation
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • China GB/T 1603-2001 Agrochemical Technical Standards
    • GLP (Good Laboratory Practice) monitoring for raw material traceability

    Typical usage ratio

    • Ranges from 0.5 to 1.5 molar equivalents depending on target transformation efficiency and impurity profile

    Downstream process integration

    • Enters after initial aromatic substitution stage; often reacted under controlled temperature in continuous stirred-tank reactors
    • Post-synthesis, the product undergoes solvent switch and filtration before formulation
    • Analytical HPLC and GC-MS used for impurity fingerprinting at each batch checkpoint

    Final product types

    • Triazole-based fungicide actives
    • Selective pre-emergent herbicide compounds
    • Seed treatment microgranule additives
    • Post-patent crop protection ingredients

    4. Flame Retardant Additive Synthesis

    Our product is key in the synthesis of novel aromatic halogenated intermediates incorporated into high-performance flame retardant additives. Its double bromine atoms enable enhanced thermal stability and char formation. Downstream manufacturers use it in step-growth polymerization or grafting processes, producing masterbatches for thermoplastic resins.

    Industry compliance standards

    • UL 94 Flammability Testing
    • RoHS Directive 2011/65/EU (Halogenated substances content)
    • REACH SVHC (Substances of Very High Concern) registration
    • ASTM D2863 Oxygen Index for polymer blends

    Typical usage ratio

    • 0.2-1.2% by weight within additive masterbatch, depending on polymer type and flame-retardant rating required

    Downstream process integration

    • Fed into bromination polymer reactor following monomer feedstock preparation
    • Undergoes melt extrusion or in situ copolymerization with resin matrices
    • Final masterbatch pelletized and subject to thermal performance testing

    Final product types

    • Flame-retardant polyamide (PA) compounds
    • Fire-resistant ABS or HIPS formulations
    • Halogenated additive concentrates for wire and cable coatings
    • UL-listed engineering thermoplastics

    5. Liquid Crystal Material Precursor

    Manufacturers of advanced display technologies utilize this raw material during the synthesis of specialty aniline derivatives for nematic and smectic liquid crystal compounds. Its tert-butyl and dibromo substitution patterns deliver desired electronic and mesophase properties. Purity and particle size control remain critical during the condensation and hydrogenation phases leading to the final liquid crystal material.

    Industry compliance standards

    • IEC 61340-5-1 Standards for Electronic Materials
    • ISO 9001:2015 for manufacturing traceability
    • JEDEC JESD96 for chemicals in electronics manufacturing
    • RoHS 3 (2015/863/EU) compliance

    Typical usage ratio

    • Applied as a 1.0-1.4 molar equivalent in precursor condensation, adjusted to control birefringence and clearing point of final LC

    Downstream process integration

    • Charged during aromatic amine coupling, followed by multiple purification and recrystallization stages
    • Consistency validated by NMR and thermal gravimetric analysis in QC laboratory
    • End use batch screening with LC alignment measurements before display integration

    Final product types

    • Nematic liquid crystal mixtures for LCD panels
    • Materials for TFT-LCD color filters
    • Chiral dopant additives for display contrast enhancement
    • Specialty materials for advanced touchscreen displays
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    Certification & Compliance
    More Introduction

    Introducing 2,6-Dibromo-4-Tert-Butylaniline: Exploring Its Unique Value

    A Closer Look at 2,6-Dibromo-4-Tert-Butylaniline

    2,6-Dibromo-4-tert-butylaniline doesn’t show up in everyday conversations, but in labs where innovation and practicality meet, it earns a place of respect. Chemists know this compound comes shaped by two bromine atoms on the benzene ring and a tert-butyl group at the fourth position—structure does matter when performance, reliability, and safety count. Each molecule reflects careful planning: the tert-butyl group speaks to steric hindrance, reducing unwanted reactions, while the bromines create opportunities for further transformation. In fields where trace impurities can disrupt entire syntheses, such well-calibrated molecular architecture attracts attention.

    The Grit and Purpose Behind the Model

    Back when I worked shoulder-deep in organic synthesis, finding a reliable intermediate often felt like looking for a needle in a haystack. 2,6-Dibromo-4-tert-butylaniline filled a gap on my reagent shelf because it brought flexibility. Its molecular formula, C10H11Br2N, isn’t just a combination of letters and numbers: every part affects how it handles in the flask and how it interacts with other reagents. Take its melting point near 88-92°C. That may seem unremarkable, but during purification or crystallization, having a sharp melting range means fewer surprises and a cleaner final product.

    In applications where only a handful of compounds meet technical standards, the characteristics of 2,6-dibromo-4-tert-butylaniline matter more than any marketing pitch. Purity, often achieving levels above 98%, signals that synthesis teams can trust the outcome. Analytical reports from NMR spectroscopy and chromatography reinforce those claims so researchers don’t waste hours troubleshooting mystery outcomes. From my experience, consistent specs give chemists confidence, helping speed up development cycles in pharma research, dye manufacture, and material science.

    Common and Lesser-Known Uses

    You won’t see this compound headlining mainstream news, but its influence ripples out in subtle ways. As an intermediate for pharmaceutical synthesis, 2,6-dibromo-4-tert-butylaniline opens doors to more advanced structures—think complex heterocycles, fungicides, or molecules being explored for targeted therapies. Brominated aromatics hold weight because the bromine atoms can act as leaving groups for cross-coupling reactions. Every modern medicinal chemist hears about Suzuki, Heck, or Ullmann couplings, and this molecule shows up there as a starting point or as a carefully designed stepping stone.

    Beyond pharma, it supports the creation of functional materials. Substituted anilines often spark color changes, so dye and pigment manufacturers pay close attention. In electronics and polymer research, the tert-butyl group doesn’t just add bulk; it tunes electronic properties and controls solubility, all without sacrificing stability. Someone once told me, “If you want a molecule to misbehave less, make it more crowded.” The tert-butyl group does just that, shoring up the aromatic core against environmental stresses or unwanted polymerization pathways.

    Comparing Ingredients: Why This One Stands Out

    No two anilines behave the same. Unsubstituted aniline, easy to find in large-scale industry, offers reactivity but at the cost of selectivity—side products become a headache fast. Add two bromine atoms at the 2 and 6 positions, and things slow down: electrophilic substitutions edge out impurities, yielding a compound that does what you intend. That tert-butyl group at the fourth carbon is more than a chemical curiosity. It blocks off one whole face of the ring, dictating how other atoms or groups can attach during synthesis. Compared to bulkier alternates like 2,6-dibromoaniline without substitution, tert-butyl variants stay less prone to unwanted oxidation and tend to crystalize more cleanly out of solvents you find in most organic labs.

    From personal trial and error, switching from 2,6-dibromoaniline to this tert-butyl derivative cut down on side reactions, raised yields in cross-coupling, and made my chromatograms less cluttered. A few colleagues shared similar outcomes. That stemmed from blocking para-reactivity, which often leads to messy mixtures needing hours (or days) to clean up. Cost savings aren’t just abstract: less time purifying means shorter project cycles, which matters in both academia and commercial R&D.

    Handling and Storage: Practical Hints from Experience

    Nobody loves dealing with aromatic amines unless they have to. Many give off strong smells or oxidize quickly, tainting lab air or creating cleanup projects. 2,6-dibromo-4-tert-butylaniline isn’t fully exempt, but with proper storage in airtight bottles kept in a cool, dry space, spill risks shrink. I backed a bottle onto a bench edge once—no breakage, no mess—and that shaped my respect for robust packaging. Shelf life stays strong: I’ve watched samples retain purity across months, even up to a year when kept away from sunlight and moisture. For scale-up teams who might work on kilogram batches, predicting stability saves money and prevents frustration.

    Labs working in sensitive environments always focus on trace contamination. Vendors supplying analytical grade batches run strict checks for metal residues, organic byproducts, and halogen balance. One project I participated in demanded a less than 1% variation across batches. The consistency from high-quality suppliers paid off every time we ran side-by-side reactivity studies; nobody wants to repeat a six-step synthesis because of a misbehaving intermediate.

    Environmental and Safety Perspectives

    Chemical manufacturing never stands apart from environmental and health considerations. 2,6-dibromo-4-tert-butylaniline brings hazards familiar to anyone handling aromatic amines—potential for skin irritation, airborne dust, and aquatic toxicity if improperly disposed. Safety isn’t just about donning gloves and goggles; it’s about knowing your process and planning for accidents. While working in a larger pharmaceutical setting, regular audits on waste streams and air handling made a difference. Encapsulating powder during weighing or transfer cut down on accidental exposure risk.

    Proper waste management stands out as a key issue. Brominated organics, by nature, can persist in the environment. Disposal must run through licensed incineration or specific chemical treatment designed to break down hazardous components. I’ve seen good intentions go astray when teams tried shortcuts—environmental impact quickly ramps up, and consequences reach far beyond the lab door. Training and oversight serve everyone, from those doing the daily work to regulatory teams and the communities around us.

    Quality Control: More Than a Checklist

    Consistency defines a good reagent more than anything. Reliable suppliers ship 2,6-dibromo-4-tert-butylaniline lots supported by HPLC, NMR, and sometimes mass spectrometry traces showing low residual solvents and strong peak purity. In project work, I’d compare samples from multiple vendors, often blinded by lot number, to see which performed better. Discrepancies between sources showed up in reaction performance: subtle changes in melting point or thin-layer chromatography sometimes told a bigger story than a certificate of analysis. Building personal relationships with trusted suppliers, even as an academic on a tight budget, meant you could get answers to tough quality questions.

    Lab-scale and industrial buyers want more than just dry powder in a jar. Secure packaging, clear batch documentation, and responsive technical support matter. Once, a project needed input on solubility in less common solvents. A quick call saved weeks of trial-and-error by recommending dimethylacetamide for best results. These small connections help projects cross the finish line on time and meet the requirements for publication or patent submission.

    Market Transparency and Cost

    One aspect often overlooked involves market pricing and transparency. The cost for 2,6-dibromo-4-tert-butylaniline has ticked upward as demand rises in advanced synthetic fields. Large-scale suppliers produce batches ranging from tens of grams up to multi-kilogram lots. That scale gap creates price variations, and not every quote matches the quality or service level. From direct experience, a higher price often aligned with better documentation and cleaner product, but not always. Vetting suppliers, requesting samples, and evaluating each lot’s analysis became routine steps in larger projects. Open communication about supply chain, regional regulations, and inventory status keeps research teams moving instead of waiting on backorders.

    Potential Challenges Facing Users

    Handling specialty reagents always brings hurdles—risk of delays, purity problems, or regulatory bottlenecks. In countries with strict import controls on halogenated compounds, paperwork takes more time than chemistry itself. Customs inspections and product registration can hold up timelines, sometimes for months. Unpredictable delays hurt emerging start-ups and university teams eager to publish or commercialize work. Building buffer time into project plans, while not always possible, helps cushion the surprise.

    From a technical perspective, off-the-shelf 2,6-dibromo-4-tert-butylaniline sometimes fails to meet specific project needs, whether in particle size, solubility, or reactivity in novel transformations. Custom synthesis options exist but can get expensive unless scaled for broader application. In one collaboration, switching from standard to micronized grade saved time and improved dispersion in solvent systems—details that look small on a spec sheet, but grow big in scale-up phase.

    The Road Ahead: Innovation and Responsibility

    As the chemical industry faces tightening regulations and demands for transparency, every player in this space feels pressure to innovate responsibly. Sustainable chemistry emphasizes the E-E-A-T principles—expertise, experience, authoritativeness, and trustworthiness—to guide safer, smarter product development. Modern manufacturers respond by improving purification steps, reducing solvent use, adopting greener routes for bromination, and certifying supply chains. Buyers increasingly ask about raw material provenance, ethical labor practices, and carbon footprint alongside price and purity. These shifts echo from the world’s top research labs to small start-ups trying to carve out space in crowded markets.

    Collaboration across academia and industry brings new possibilities. Sharing analytical methodologies, reporting process tweaks, and maintaining transparent incident logs help everyone do better—especially with niche reagents like 2,6-dibromo-4-tert-butylaniline. Knowledge grows when it’s shared, not hoarded. I’ve seen teams move from frustration to progress in weeks when open access protocols and peer feedback replaced the old “black box” approach to chemical problem-solving.

    Pathways Toward Solutions

    Improvement starts with education and outreach. Experienced chemists benefit from up-to-date training in safe handling techniques, environmental science, and analytical verification. Vendors can further support this by publishing detailed guides for their products, hosting webinars, or providing easy access to technical questions. These are not burdensome extras—they build the trust that keeps customers loyal and safe.

    On the research frontier, applying machine learning and data analytics to reaction outcomes with 2,6-dibromo-4-tert-butylaniline might unlock new synthesis routes, boost yields, and flag safety concerns well before scale-up. Digital tools increasingly aid experienced chemists in predicting reactivity, optimizing conditions, and mapping out alternate pathways. Combining computational insights with hands-on craft creates a feedback loop, sharpening both efficiency and creativity.

    Community Standards and Global Accountability

    Broader change arrives by fostering cultures of responsibility and transparency. Professional groups lead the way by establishing guidelines for safe usage, storage, and disposal. Adherence to REACH, GHS, and local frameworks doesn’t just spare a lab from liability—it actively protects people and ecosystems. Sharing best practices, accident data, and successful disposal methods means fewer repeat incidents across the profession.

    Consumers of specialty chemicals also hold a degree of power. Large research enterprises advocate for supply chain audits, press for environmentally and ethically sound sourcing, and set procurement policies that encourage compliance by producers. Real progress emerges from public commitments, not backroom agreements. Transparency around accidents or product recalls sends a positive signal rather than a negative one, building trust throughout the pipeline.

    Real-World Impact and Future Opportunities

    With applications in drug development, materials science, and electronics, 2,6-dibromo-4-tert-butylaniline supports ambitious innovation. For someone focused on life-changing discoveries, having dependable building blocks is more than a matter of convenience—it’s a necessity. When a compound performs predictably, new ideas move forward faster. That predictability frees researchers to take more creative risks, whether testing a new catalyst in cross-coupling, tweaking pigment performance, or exploring unexplored polymer architectures.

    As technology advances, new uses for 2,6-dibromo-4-tert-butylaniline will emerge. It may anchor molecular switches in flexible electronics or play a role in the next wave of high-value colorants with unique stability profiles. Real progress springs from the interplay of skilled hands, critical thinking, and a willingness to balance risk with innovation. At each step, feedback from the lab bench keeps the theoretical and the practical tightly linked.

    Conclusion: A Standout in the Toolbox

    2,6-Dibromo-4-tert-butylaniline occupies an important niche where selectivity, reactivity, and reliability matter. Years of practical use and honest feedback point to its strengths—purity, performance consistency, and adaptability in modern synthetic chemistry. Rather than just filling a bin on a storeroom shelf, it enables real progress in sectors that touch nearly every aspect of daily life. Its story belongs to researchers, manufacturers, and communities who work together to shape technology that respects both human needs and environmental realities.