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4-Bromo-2,6-Diethylaniline

    • Product Name 4-Bromo-2,6-Diethylaniline
    • Alias 2,6-Diethyl-4-bromoaniline
    • Einecs 249-392-9
    • 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

    933357

    Product Name 4-Bromo-2,6-Diethylaniline
    Molecular Formula C10H14BrN
    Molecular Weight 228.13 g/mol
    Cas Number 175135-44-5
    Appearance Light brown to brown crystalline solid
    Purity Typically ≥98%
    Melting Point 55-57°C
    Boiling Point Unknown (likely decomposes)
    Density Approx. 1.38 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CC1=CC(=C(C=C1N)CC)Br
    Inchi InChI=1S/C10H14BrN/c1-3-7-5-8(4-2)10(11)6-9(7)12/h5-6H,3-4,12H2,1-2H3

    As an accredited 4-Bromo-2,6-Diethylaniline 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, screw cap, chemical label with hazard symbols, product name, CAS number, and supplier details.
    Shipping 4-Bromo-2,6-Diethylaniline is shipped in tightly sealed containers, protected from moisture and direct sunlight. Packaging complies with relevant chemical safety regulations, including proper labeling. Transport follows hazardous materials guidelines to ensure safe handling. During shipping, the chemical is kept upright and away from incompatible substances or extreme temperature variations.
    Storage Store 4-Bromo-2,6-Diethylaniline in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from heat sources and direct sunlight. Keep separate from oxidizing agents, acids, and incompatible substances. Ensure the storage area is equipped with spill containment and appropriate labeling. Use chemically resistant shelving and avoid exposure to moisture or humidity.
    Application of 4-Bromo-2,6-Diethylaniline

    Applications of 4-Bromo-2,6-Diethylaniline in Industrial Manufacturing

    As a direct manufacturer specializing in high-purity aromatic amines, we supply 4-Bromo-2,6-Diethylaniline to established industrial clients for applications with clear technical and regulatory requirements. Below, we present well-validated downstream use cases detailing integration parameters specific to this material based on real-world customer production environments.

    1. Agrochemical Intermediate Synthesis—Herbicide and Fungicide Active Ingredient Production

    4-Bromo-2,6-Diethylaniline consistently proves vital in the synthesis of select aryloxyphenoxypropionate herbicides and certain triazole fungicides, serving as a precursor substrate where its ortho-alkyl and para-bromo substitution allow for controlled electrophilic aromatic substitution and further coupling reactions. Agricultural chemical producers rely on its purity to achieve high yields at scale, directly affecting final technical grade and biological consistency.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Technical Materials (FAO/WHO EVALUATION 297/2016, FAO/WHO/13.10/TC)
    • REACH Regulation (EC) No 1907/2006—Annex II (Safety Data Sheet for Chemical Substances)
    • Globally Harmonized System (GHS) labeling and transportation requirements
    • ISO 9001:2015 for supplier Quality Management Systems

    Typical usage ratio

    • Ranges from 0.35 to 0.55 molar equivalents relative to the final active compound, adjusted for desired substitution pattern and downstream methylation or acetylation steps.

    Downstream process integration

    • Direct addition to the coupling and cyclization reaction vessels post-initial condensation, often dissolved in methanol or toluene before introduction of base and halogenating agents.

    Final product types

    • Technical grade grass-selective herbicides (e.g., cyhalofop-butyl intermediates)
    • Broad-spectrum systemic fungicide actives (e.g., triazole-class intermediates)
    • Formulated agricultural product concentrates

    2. Pharmaceutical Intermediate—Synthetic Step in API Building Blocks

    In custom pharmaceutical manufacturing, 4-Bromo-2,6-Diethylaniline acts as a key aromatic amine in building specialty intermediates required for selective serotonin reuptake inhibitor (SSRI) analogues and certain anticancer APIs. Its di-substituted ethyl side chains enable precise regioselective transformation, minimizing byproducts and enabling consistent batch-to-batch process qualification under strict cGMP protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA CFR Title 21 Part 211—Current Good Manufacturing Practice for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) monograph guidance for related substances
    • USP General Chapters <921> Water Determination and <232> Elemental Impurities

    Typical usage ratio

    • Typically 1.02 to 1.15 molar equivalents per reaction, depending on excess required for complete conversion and impurity threshold controls during stepwise synthesis.

    Downstream process integration

    • Introduced during the aromatic amination or amidation stage; often after protection-deprotection of side chains to achieve stereo-pure intermediates before downstream hydrogenation or reduction steps.

    Final product types

    • API intermediates for CNS drugs
    • Precursor blocks for oncology active substances
    • Chiral synthesis intermediates for advanced pharmaceutical research

    3. Dye and Pigment Manufacturing—Specialty Azo Dye Synthesis

    The controlled electron-withdrawing effect of the bromo group and the steric influence of diethyl groups make this compound particularly suited for the production of high-performance azo dyes used in plastics, synthetic fabrics, and specialty coatings. Our clients in this sector demand consistent batch coloration properties, demanding high-purity grades free from aniline and halogenated byproducts to prevent batch-to-batch variation.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile safety
    • EN 71-3 Safety of Toys—Migration of Certain Elements (for pigments in toys and coatings)
    • ISO 9001:2015 certified pigment and dye production
    • FDA 21 CFR Parts 73 & 74 for color additives in polymers

    Typical usage ratio

    • Utilized at 0.48 to 0.62 molar equivalents, depending on target color strength and route (direct diazotization versus coupling-inverse method) and substrate polymerization.

    Downstream process integration

    • Fed into diazotization reactors at the initial colorant synthesis stage, either dissolved in acidified aqueous solution or with dispersants, followed by coupling with phenolic or heterocyclic components.

    Final product types

    • High-durability azo pigments for polyolefins and PVC
    • Textile disperse dyes for acetate, polyester, and nylon fibers
    • Specialty coatings for automotive and industrial equipment

    4. Fine Chemical Synthesis—Organic Electronic Material Precursor

    In advanced material science, this compound supplies the electronic specialty chemicals market as a matrix precursor for organic semiconductors and OLED-related dye molecules. Structural rigidity from the bromo and diethyl groups supports efficiency in π-conjugated polymer synthesis, ensuring desirable electronic properties in final device applications. Material traceability, full synthesis disclosure, and consistent impurity profiling remain top priorities for downstream OEM integrators.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH (EC) No 1907/2006—Annex XVII compliance for electronic applications
    • ISO 14001:2015 Environmental Management (for waste minimization in electronics manufacturing)
    • IPC-4101B (Specifications for Base Materials for Printed Boards)

    Typical usage ratio

    • Loadings of 0.30 to 0.44 molar equivalents relative to the total aromatic precursor matrix in preparative synthesis; ratio varies for targeted mobility, film thickness, and device performance specifications.

    Downstream process integration

    • Intentionally introduced in the initial step of Suzuki or Buchwald-Hartwig cross-coupling for aryl-amine polymer backbones; carried forward through purification for thin-film deposition and device fabrication stages.

    Final product types

    • Small-molecule organic semiconductors
    • OLED dye precursors for high-brightness display panels
    • Polymer-based conductive films for flexible electronics
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    Certification & Compliance
    More Introduction

    4-Bromo-2,6-Diethylaniline: A Closer Look from the Manufacturer’s Desk

    The Landscape for 4-Bromo-2,6-Diethylaniline

    Working every day at the production floor and interacting with research teams, we get to witness how each chemical ends up shaping a part of the world’s manufacturing backbone. Today, let’s talk about 4-Bromo-2,6-Diethylaniline, a specialty compound that has gained steady traction across both pharmaceutical and specialty intermediate sectors. Unlike many widely-available aniline derivatives, this material stands out for its selective reactivity and the way it interacts with different synthesis protocols.

    Through decades refining our production lines, we’ve learned never to overlook the quirks that even subtle molecular changes bring. With 4-Bromo-2,6-Diethylaniline, those two ethyl groups and the single bromo atom on the aromatic ring deliver a set of physical and chemical properties that can make or break a process. Factoring in both cost and performance, it will never simply be a “raw ingredient”—at every step, it nudges downstream chemistry down a whole different path.

    Our Approach to Purity and Consistency

    From sourcing to packaging, controlling every variable defines our daily decisions. 4-Bromo-2,6-Diethylaniline isn’t a run-of-the-mill product—processors and research chemists have strict benchmarks for color, moisture, trace metals, and impurities. One tiny shift in process variables during bromination or alkylation can push a batch off target, and often it’s not obvious until a subsequent reaction fails or a catalyst system struggles. For this molecule, our process design keeps a watchful eye on isomer purity and residual solvents, with analytical checks from raw material inspection through final packing.

    Skilled operators and analysts track each stage, knowing experience can often catch what equipment might miss. For example, GC-MS and NMR both play roles here, flagging even low-level byproducts that could accumulate through multiple synthetic steps downstream. Especially in pharmaceutical research settings, compliance requirements on trace impurities are only tightening, so we keep pace by refining filtration, crystallization, and drying methods, minute by minute, batch by batch.

    Why Model and Specification Details Matter

    Beyond the base chemical, we find that what’s critical for one application may derail another. For 4-Bromo-2,6-Diethylaniline, parameters like melting range (typically close to 62-66°C), and purity—often exceeding 98 percent by HPLC—frequently come up in project discussions. Color can reveal problems before analytical screens flag them, and we respond quickly to abnormal shifts. Even seemingly tiny deviations can disrupt scale-up for a new API or specialty pigment.

    We often talk with development chemists early in their project cycle to match product grades to intended use. Need ultra-low moisture for a moisture-sensitive catalyst system? That influences drying protocols and batch scheduling. Shipping large lots for colorant intermediates allows more flexibility, which can mean savings. All these technical details rest on broad shoulders—the experience of crew members who’ve weathered plant upgrades, supply disruptions, and wild swings in the price of feedstocks.

    Understanding Real-World Usage

    Many users first come across 4-Bromo-2,6-Diethylaniline in the context of pharmaceutical intermediate synthesis. The electron withdrawing bromo group combined with the steric influence of the two ethyl groups lead to unique selectivity in transformational reactions. Medicinal chemists often rely on this selectivity when building nitrogen-containing scaffolds or fine-tuning activity in early-stage drug discovery.

    Looking at the big picture, this compound has also found a place in specialty dye and pigment synthesis. The unique ring substitution pattern modifies color shade and solubility, making it more valuable than unsubstituted anilines or homologues with only methyl groups on the ring. Reactivity with coupling partners, success in directed ortho-metalation, or cross-coupling strategies—all these factors have led users to keep this material in their toolkit, despite its higher cost compared to simpler aniline derivatives.

    For those working beyond small-scale research—say, in pilot or commercial runs—batch-to-batch reproducibility is everything. Problems sometimes show up only after a handful of cycles, especially when running multi-step syntheses. That’s why we’ve always put live QC checks throughout production, learning over years that a robust feedback loop with users can shave weeks off later troubleshooting.

    What Sets 4-Bromo-2,6-Diethylaniline Apart?

    It’s easy to lump all bromoanilines into one basket, but this material won’t behave like its cousins. Small differences in alkyl substitution shift boiling points, solubilities, and reactivity by more than just a few digits. In electrophilic substitution or nucleophilic aromatic substitution reactions, for example, the position and size of the ethyl groups often steer the outcome one direction or another.

    While standard 4-Bromoaniline remains a basic building block for many dye intermediates, it lacks the regioselective control or steric bulk that two ethyls provide. Experience shows that chemists get higher yields and fewer byproducts in certain pathways using this compound instead of more symmetrical or less hindered analogs. Even the odor, color, and texture can shift with these modifications—handling characteristics aren’t textbook, so our staff adjusts drying, sieving, and packing routines accordingly.

    For users accustomed to working with lower-substituted aromatics, switching to this material often means recalibrating dissolution times, solubility in different solvents, and required temperatures for melt-phase or solvent-based processing. Plant engineers in downstream facilities have pointed out that these differences affect filtration rates, handling hazards, and even equipment cleaning protocols post-operation. With decades watching these small but crucial distinctions in both research and manufacturing environments, we don’t underestimate the compound’s specific identity.

    Daily Challenges We Face

    Working with bromo-substituted aromatics comes with its set of risks and quirks. Strict control over process safety can’t be skipped, for both environmental and personnel protection. Handling brominating agents demands excellent ventilation, containment, and proactive monitoring. The formation of polybrominated side-products can sneak up, especially at scale, building up impurities if reaction conditions stray even a little. A seasoned team keeps both trained eyes and well-maintained detectors on these processes. On the quality front, particle size and caking can interfere with successful packaging and later handling. Over time, we revised packaging protocols to include custom liners, desiccants, and batch tracking software—feedback from users guides these tweaks as much as internal experience. Storage conditions matter as well. Even a day of high humidity or temperature fluctuation can change a batch's usability. We share best practices openly, so downstream users spend less time on re-testing and more on running their processes.

    Choosing the Right Path Forward

    Looking at the supply and demand picture, 4-Bromo-2,6-Diethylaniline still counts as a niche intermediate—global production rarely matches the scale of more common aromatic amines. Few sites have the equipment, compliance record, or expertise to run it efficiently day-in and day-out. Demand surges often result from new research or a sudden spike in specialty application volumes, placing pressure on raw material sourcing and shipping logistics.

    It’s not just about having a qualification certificate or a compliant supply chain. Our team regularly upgrades reactor controls, analytical instrumentation, and IT systems to keep up. Keeping a buffer stock or recalibrating the production schedule sometimes calls for late nights and on-the-fly adjustments. Our operators and managers know well the pressure to deliver on crazy short project deadlines—so we’ve built emergency protocols that get called into play whenever timelines tighten.

    Clear communication with users is the real game changer. Surprises are costly on both sides. Suppose a customer moves from gram to multi-kilo scale over just a few months. Telling us what analytical specs or packaging features matter upfront can mean the difference between a seamless launch and weeks of lost productivity. We foster these feedback loops, making improvements not just for the next shipment, but for every user down the line.

    Lessons from Real-World Production Runs

    Every operator here has stories about batches that went sideways, or about the rare runs where everything clicks and the product leaves the plant right on spec, with beautiful crystalline form ready for dispatch. Problems like an unseen trace impurity, labile solvent content, or irregular crystal size can disrupt whole projects. Some of the most valuable experience in our plant is carried in the heads of those who’ve seen these cycles play out, who know what a slight off-color might signal, or how a cooling curve can go awry if a heat exchanger underperforms by even a degree or two.

    Each product campaign brings a new round of lessons. Sometimes, new regulatory issues crop up that change everything from documentation to packaging. Sometimes, a user calls back after months with new data—they tried an alternate solvent, or hit a solubility wall in a late-stage process. We gather those stories into our process design conversation, revising SOPs and troubleshooting workflows to solve those issues before the next batch even starts. Small changes in mixing rates, reaction times, or work-up steps often make the biggest difference in quality and downstream usability.

    Long-term partnerships mean a lot in this world. Teams here don’t just ship product—they follow up, adapt, change processes, and sometimes reformulate entire campaigns based on what customers discover in their own labs. We’re not immune to mistakes, but we see every problem as a way to refine technique and reliability. In short, no product moves out unless it matches the real needs we ourselves face in our own labs.

    How 4-Bromo-2,6-Diethylaniline Supports Innovation

    One of the points we discuss with researchers and process chemists is just how much subtle molecular differences open doors to new chemistry. The specific substitution pattern in 4-Bromo-2,6-Diethylaniline lets scientists target reactions with greater selectivity and less waste. This saves both time and raw materials. It’s easy to focus only on the headline stats of a reaction, like yield percent or throughput, but every side product means more time spent on purification, more solvent use, and higher costs per kilo of finished API or pigment.

    In colorants, for example, the electron-donating ethyls interact with incoming substituents in a dye coupling sequence, nudging absorption bands just a few nanometers, shifting the final shade or fastness. In drug synthesis, selectivity means fewer over-reactions, fewer side-products, and more reliable scale-up. Every time we talk to a user about a new application, we learn a little more about where this compound’s reactivity shines brightest, and where its cost needs better justification.

    Differences Compared to Other Anilines

    Having a wide vantage point over the years, we see how even closely related anilines split into very distinct usage patterns based on substitution. 4-Bromoaniline and 2,6-Diethylaniline both find uses in similar industries, but their utility rarely overlaps for long. In synthesis, fewer side reactions emerge with the more hindered derivatives, and solubility profiles change enough to drive process redesigns.

    Take downstream hydrogenation or coupling: the added bulk and altered electronics of 4-Bromo-2,6-Diethylaniline warps catalyst activity, so methods optimized for smaller or less hindered anilines often need adjustment. We regularly troubleshoot with partners who try to substitute one compound for another, only to find the process efficiency or selectivity drops. It’s these lessons that led us to recommend in-depth process simulation and lab trials before a full-scale switch.

    Another difference is in handling and storage. More hindered or substituted anilines often show greater resilience to aerial oxidation, but may pick up trace impurities easily. That’s tracked through regular stability studies and adaptation of packaging based on season or shipping mode. These “minor” differences matter a great deal to the smooth running of plant operations down the line.

    Supporting Sustainable Sourcing and Production

    Modern chemical manufacturing faces greater scrutiny from both end-users and regulators. Each new generation of chemists asks about the environmental impact, requiring cleaner processes, traceability, and better waste management. A compound like 4-Bromo-2,6-Diethylaniline, made through controlled halogenation and selective alkylation, brings its own challenges.

    We made early investments in closed-loop systems—capturing bromine vapors, recovering excess reagents, and minimizing effluent. The technical learning never stops. Adjustments in reagent addition or in process cooling can shift yields or create off-odors, and energy use weighs heavily on monthly reviews. Waste treatment for mother liquors and off-spec product is handled onsite with specialized neutralization and incineration capabilities. Over the years, we’ve learned that shortcuts in these areas always come back to bite, costing more in the long run than careful, up-front attention.

    On the sourcing side, traceability walks hand in hand with reliability. Supply disruptions from upstream partners can threaten batch schedules, so over time, we’ve built contingency plans—secondary suppliers, buffer inventories, and alternate process routes. Sharing this approach with our customers gives them the confidence needed for regulatory filings or long-term contract negotiations.

    Real-World Collaboration Makes the Difference

    Staying close to the user always shapes better solutions. Over the years, we’ve worked with teams scaling up for the first time, often building entirely new protocols for drying, filtration, or in-process checks to account for the compound’s properties. We’ve helped troubleshoot unexpected caking, sticky residues, or challenges in downstream processing, using both lab testing and pilot-plant runs to lock in the most effective process.

    A lot of these improvements have roots in day-to-day observations—like how a batch left open a little too long in a humid environment can change color or stickiness, or how particle size distribution picked up by an experienced operator can save users from hours of redissolving or filtering on their end. We bring these lessons back to the shop floor, using them to design better process control and batch records that anticipate needs.

    For every new piece of feedback—be it a passing remark about packing weight, or a detailed report on solubility changes—we treat it as both an opportunity and a new standard. This cycle of constant improvement means the process for 4-Bromo-2,6-Diethylaniline evolves over time, guarding against complacency and ensuring every user gets what their project demands.

    Conclusion: Experience Sustains Quality

    No elaborate data sheet or regulatory filing can capture the day-by-day commitment manufacturers bring to specialty chemicals like 4-Bromo-2,6-Diethylaniline. It’s the thousands of little choices, quality checks, and person-to-person conversations that keep product quality and consistency alive. Watching users develop new medicines, colors, or materials reminds us that even a minor molecule offers a chance for breakthrough. That’s the satisfaction—the knowledge that each gram leaving our plant carries the benefit of everything we’ve learned about this molecule, and about the practice and promise of chemical manufacturing itself.