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4-Bromo-2-Ethylaniline

    • Product Name 4-Bromo-2-Ethylaniline
    • Alias 4-Bromo-2-ethylbenzenamine
    • Einecs EINECS 216-103-2
    • 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

    999953

    Productname 4-Bromo-2-Ethylaniline
    Casnumber 183158-42-1
    Molecularformula C8H10BrN
    Molecularweight 200.08
    Appearance Light brown to tan solid
    Meltingpoint 41-44°C
    Boilingpoint Unknown
    Density Unknown
    Purity Typically ≥98%
    Synonyms 2-Ethyl-4-bromoaniline
    Smiles CCc1cc(Br)cc(N)c1
    Inchi InChI=1S/C8H10BrN/c1-2-6-4-7(9)3-5-8(6)10/h3-5H,2,10H2,1H3

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Bromo-2-Ethylaniline, sealed with a screw cap, labeled with hazard and identification details.
    Shipping 4-Bromo-2-Ethylaniline is shipped in tightly sealed containers to prevent exposure to air and moisture. It is classified as a hazardous material, requiring proper labeling and adherence to chemical transport regulations. Shipments are typically made by certified carriers, with documentation ensuring compliance with safety and environmental guidelines during transit.
    Storage 4-Bromo-2-ethylaniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. The storage area should be clearly labeled, and the chemical should be kept away from sources of ignition. Follow all relevant safety guidelines and local regulations for hazardous chemicals.
    Application of 4-Bromo-2-Ethylaniline

    Applications of 4-Bromo-2-Ethylaniline in Industrial Manufacturing

    As an established manufacturer of specialty aromatic amines, we supply 4-Bromo-2-Ethylaniline for integration in advanced chemical synthesis across key sectors. Our technical team supports clients in scaling up downstream formulations that demand consistent reactivity, tailored purity profiles, and documented traceability. Here, we detail principal real-world application scenarios, with specific focus on sector standards, dosage guidelines, critical process steps, and representative end-use products.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Leading pharmaceutical manufacturers incorporate this compound as a halogenated aniline building block during the synthesis of several small-molecule APIs, particularly for targeted therapeutic agents requiring selective substitution patterns. Incorporation typically occurs during multi-step organic routes, optimizing molecular scaffolds for downstream transformation and ensuring process compliance for regulated markets.

    Industry compliance standards

    • ICH Q7 GMP guidelines for API manufacturing
    • 21 CFR Parts 210/211 (FDA cGMP regulations)
    • EP/USP monograph requirements (as applicable for APIs synthesized)
    • EU REACH registration for workplace and environmental safety

    Typical usage ratio

    • Used at 0.6%–2.5% of total batch mass in the key condensation or Suzuki coupling step, with precise quantity adjusted based on desired yield and downstream reagent molar ratios

    Downstream process integration

    • Introduced during the functionalization stage of heterocyclic ring assembly, directly participating in palladium-catalyzed cross-coupling or amide formation sequences

    Final product types

    • Antihypertensive agent intermediates
    • Kinase inhibitor precursors
    • Anti-infective bulk compounds
    • Custom small-molecule research compounds

    2. Intermediate for Agrochemical Synthesis

    Major agrochemical producers utilize this halogenated aniline in the synthesis of selective herbicide and fungicide molecules, specifically where controlled substitution on the aromatic ring is required for biological activity and environmental stability. The input enables efficient construction of target molecules with regulatory traceability for commercial formulation.

    Industry compliance standards

    • FAO/WHO specification procedures for technical material
    • ISO 9001:2015 certified quality management in production
    • Globally Harmonized System (GHS) for labeling and safe handling
    • National EPA registration requirements for active ingredients

    Typical usage ratio

    • Added at 1.2%–4.0% by weight in the primary chlorination or amidation sequence, with upper limit determined by both solubility and targeted functionalization degree in the active ingredient structure

    Downstream process integration

    • Charged into the reaction vessel during the initial aromatic substitution or cyclization step, preceding further alkylation or sulfonation for final active

    Final product types

    • Triazole-based fungicides
    • Bipyridylium herbicide intermediates
    • Custom formulation additives for crop protection
    • Industrial pesticide actives

    3. Advanced Dye and Pigment Intermediate

    Producers of high-performance dyes source this compound for targeted synthesis of brominated anthraquinone or azo dye systems, where electron-donating and -withdrawing group positioning is essential for color intensity, lightfastness, and thermal stability in specialty textile and plastic applications. Its precise structure supports reproducible chromophore formation in proprietary formulations.

    Industry compliance standards

    • REACH (EC) No. 1907/2006 Annex XVII for restricted substances
    • OEKO-TEX® regulations for eco-friendly textiles
    • ISO 9001:2015 for dye manufacturing process control
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals) requirements

    Typical usage ratio

    • Used at 0.8%–3.1% (w/w) within the azo coupling or condensation polymerization blend, with dosage set according to target hue strength and bath exhaustion properties

    Downstream process integration

    • Added during the pre-condensation phase or as a protected group donor in diazotization or acylation reaction, followed by dilution and finishing for dye block isolation

    Final product types

    • Brominated azo dyes for synthetic fiber
    • Anthraquinone pigment intermediates for plastics
    • Water-based inkjet textile inks
    • Special-purpose printing colorants

    4. Building Block for Electronic and Functional Material Synthesis

    Manufacturers of organic electronic materials employ this aniline derivative in the construction of semiconducting polymers and specialty monomers used for display, sensing, and optoelectronic applications. The selective halogenation patterns directly impact charge transfer properties, making batch consistency and traceability critical.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substances in electrical/electronic applications
    • ISO 14001:2015 for environmental management in electronics industry
    • PAT (Polymer Additive Technology) regulatory documentation requirements
    • IECQ Certified Process for supply chain traceability

    Typical usage ratio

    • Blended at 1.5%–3.8% based on monomer feedstock, adjusted to achieve specific molecular weight and conductivity in conjugated polymer synthesis

    Downstream process integration

    • Introduced as a primary aromatic amine during the initial oxidative polymerization or Stille coupling, setting the base for subsequent film casting or device fabrication

    Final product types

    • OLED emitter and host materials
    • Organic photoresistors
    • Flexible printed sensor substrates
    • Anti-static polymer coatings

    5. Fine Chemical Synthesis for Research and Custom Synthesis Houses

    Contract research organizations (CROs) and custom synthesis labs utilize this compound as a specialized precursor in exploratory synthetic routes, supporting structure-activity relationship (SAR) studies, novel heterocyclic library creation, and pharmacophore optimization. Its defined substitution enables the exploration of innovative molecular scaffolds with tight analytical control.

    Industry compliance standards

    • GLP (Good Laboratory Practice) in chemical synthesis R&D
    • IUPAC naming and reporting conventions for new entities
    • ISO/IEC 17025 for analytical method validation
    • Material safety and handling: GHS/CLP compliance

    Typical usage ratio

    • Charged at 0.2%–1.0% of total reactant mass in lab-scale high-throughput synthesis batches; ratio varies in optimization screens based on targeted scaffold complexity

    Downstream process integration

    • Utilized during the initial scaffold construction via halogen-metal exchange, nucleophilic substitution, or amide coupling, prior to purification and characterization phases

    Final product types

    • Innovative bioactive compound libraries
    • Chemical probe reference standards
    • Proprietary research intermediates
    • Analytical calibration substances
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    Certification & Compliance
    More Introduction

    Introducing 4-Bromo-2-Ethylaniline: Developing Consistent Quality and Practical Performance in Chemical Manufacturing

    Meeting Precise Needs Through Experience and Focused Manufacturing

    Here in the plant, every batch of 4-Bromo-2-Ethylaniline starts with the same question: how do we achieve the level of purity, consistency, and stability that research and industry labs rely on? This compound—often shortened simply to 4B2EA—has found its way into targeted organic syntheses, pharmaceutical intermediates, and the development of complex molecules. The backbone of this molecule—a bromo-substituted ethylaniline—offers a unique entry point that synthetic chemists lean on for further transformation.

    Years of tight process control mean we have built productivity into our workflow without losing sight of the details. Operators oversee each step with a mix of automation and hands-on inspection. Whether someone is manning our glass-lined reactors or checking the results of a gas chromatography test, there's a clear understanding: the value of 4B2EA for our partners hinges on unwavering product quality. We’ve streamlined the workup to minimize impurities and to keep the water content low, so every shipment supports demanding laboratory and industrial practices.

    Specifications That Reflect Real-World Demands

    We handle 4B2EA as a pale to light orange solid, typically melting between 52 to 56 degrees Celsius, showing the consistency expected for this structure. Purity routinely meets or exceeds 98%, a result reached by careful distillation, crystallization, and stringent monitoring. For storage and transport, we pack the product in airtight, light-protected containers. This attention to detail reduces the risks of decomposition or moisture uptake, issues that can cost hours in a bench-scale lab or thousands of dollars in a production environment.

    The defined density and molecular weight—core parameters for stoichiometry in the lab—are double-checked for each lot. Labs running micro-scale synthesis or factories scaling up both need assurance that values align with the literature and regulatory needs. Consistency in these metrics tells researchers they can trust what comes through their doors, reducing time spent on trial and error and increasing the focus on discovery or manufacture downstream.

    Applications—Enabling Synthesis and Discovery

    In the world of specialty aromatics, flexibility matters. 4B2EA’s specific substitution pattern—where a bromo atom sits at the 4-position of a 2-ethylaniline backbone—makes it much more than a basic building block. It’s the starting point for a cascade of fine chemical transformations, from Suzuki-Miyaura cross-couplings to amide or urea formation in pharmaceutical research.

    Custom peptide work and the creation of advanced dyes also sometimes call for this structure because of the way the ethyl and bromo groups interact in small-molecule scaffolds. The push to discover new agrochemicals and materials often centers on versatile intermediates like this one, where selectivity in reactivity saves both time and reagents.

    Over the years, feedback from development chemists and process engineers has shaped our approach. Some labs want micron-level grind for dissolving the compound quickly. Others ask about larger crystals to feed into solid-handling systems. Awareness of solvent compatibility, thermal behavior, and even the color of the product features heavily in our continual improvement, not just because it’s about compliance, but because it’s about achieving a trouble-free workflow for every scientist and plant manager.

    How 4-Bromo-2-Ethylaniline Stands Out From Similar Products

    Comparing 4B2EA to its simpler relatives—plain anilines or the more common 4-bromoaniline—draws a hard line. That extra ethyl group changes the game. Not only does it shift the reactivity profile for most electrophilic aromatic substitutions, it offers synthetic chemists a level of control not possible with unsubstituted rings. The presence of both bromine and an ethyl tail leads to regioselectivity in transformations, making product isolation and purification far more straightforward in many sequences.

    With rising demands on purity and reproducibility, we don't just rely on textbook processes. For instance, earlier methods often tolerated higher resistant impurity levels, especially when producing 4-bromo derivatives in smaller batch plants. Our adjustments—such as two-stage crystallization and inline moisture testing—came directly from the headaches reported in customer labs, like inconsistent NMR spectra or residue sticking on glassware. Surfaces that look clean by eye can still trip up scale-ups; flagged issues prompt immediate conversation between production crews and our quality control team.

    In handling safety, we have gone beyond MSDS summaries. Regular reviews led us to standardize PPE across all shifts and implement local exhaust ventilation during the isolation process. While the compound isn’t the most volatile aromatic out there, long-term exposure data has guided improvements in both operations and documentation. We factor in not only occupational safety but also transportation and storage protocols, in order to reduce both rupture and spillage risk from door to door.

    Compared to bulk brominated anilines, 4B2EA has gained a spot as a preferred intermediate in select acetylation and acylation pathways. The ethyl group throws predictable but useful steric effects, meaning side-product formation usually takes a back seat. This makes it easier to pursue cleaner downstream conversions, which end-users—especially those working on regulatory filings or patent submissions—regard as essential to business success.

    Listening to Users, Responding Through Practice

    Our role doesn’t stop with finished product filtration and packaging. The team here creates a line of communication with researchers and operational chemists, learning from hiccups and repeat purchases alike. For example, one pharmaceutical pilot plant flagged a periodic rise in particulate in filtered solutions. Rather than send back a pre-written apology, our technical group locked in with theirs, ran both our material and their solvents through dual-filtration, and isolated the cause to drum static from winter shipping delays. Now, protective drum liners are standard, and return rates due to this issue have all but vanished.

    Decades in batch chemistry have taught us that keeping written feedback logs and cross-referencing those against production records gives us the truest sense of what matters to the user down the line. If a synthetic step fails reproducibility or a purification stretches out by two days, this is not a minor scheduling lag, but dollars lost and deadlines missed. We adapt our manufacturing sequence or supply timing accordingly, aiming for less downtime and more output at the customer site.

    Problems do arise: variability in raw bromine shipments, container shortages, or sudden spikes in demand from regulatory-driven restarts. Having a blend of stable local vendors and international supply partners gives us built-in redundancy. Facility audits and regular staff training support a culture where everyone recognizes their stake in each kilo sent out.

    Addressing Industry Challenges with Solutions Built on Experience

    The specialty chemicals industry contends with more regulation, environmental monitoring, and data transparency than ever before. As demand for 4B2EA grows, especially in sectors aiming for low-volume, high-value products, the spotlight falls on traceability and responsible sourcing.

    We respond to this by implementing complete chain-of-custody documentation and independent third-party batch testing. Each shipment ships with a detailed certificate of analysis and—where requested—full impurity profiling. Questions about sources or grades get direct, data-backed answers traced to the plant floor or raw supplier, never generic boilerplate. In a world of copy-paste MSDS sheets and speculation, this real-world specificity means that industrial partners can face audits and product registrations with more confidence.

    Energy, chemical handling, and waste treatment costs all climb in tandem with higher purity expectations. Our approach brings together old-school chemistry with modern tools, such as in-line spectroscopic purity assessment and automated dosing valves that minimize rework. Waste reduction targets are more than monthly targets—they translate to reclaimed solvents, energy reduction, and better plant morale. When staff can point to kilograms saved from landfill, it makes sustainable production tangible, not abstract.

    Supporting Innovation With Transparent Practice

    Partnerships with academics and startups have brought unexpected innovations to our operations. Through collaborative research, we’ve tested alternative synthesis methods that bypass expensive solvents or hazardous byproducts. These small-scale studies, run hand in hand with external labs, go on to influence standard operating procedures. Sharing what failed, just as much what worked, creates trust and pushes us forward. As a result, pilot runs can ramp up to manufacturing scale faster and with lower risk.

    For new users—whether niche pigment developers or fine chemical firms entering new territory—our technical expertise becomes a resource. We share real response data, highlight known challenges with product solubility, and openly discuss optimal storage conditions. By keeping these discussions grounded, feedback becomes actionable, promoting problem-solving instead of blame-shifting.

    We support skill development at every level. Staff undergo in-depth training, focused not only on compliance but on understanding why each step matters—be it temperature control, vacuum regulation, or close monitoring of coloration during recovery. Ongoing education in chemistry, safety, and analytical techniques means the plant’s collective expertise moves forward as new methods and regulations arise.

    Continuous Improvement: Learning from Every Batch

    There is no one perfect method for producing 4B2EA, and mistakes teach as much as successes do. By tracking reactivity anomalies, side-product trends, or problems during large-scale filtration, we build a repository of do’s and don’ts. On-site process engineers routinely review logs, recommending minor tweaks—sometimes a shift in batch quenching order, sometimes a replacement of sealing materials on glassware.

    Vendor negotiations center on documented outcomes, not marketing claims. When raw material purity fluctuates, we call for extra analytics before incorporating new batches into main production. The time invested here cuts down on recalls or substandard shipments farther down the road.

    Routine post-production meetings between production, technical, and logistics teams allow rapid identification of bottlenecks. Experienced staff often spot trends in off-gassing rates or product color shifts before automated charts register an alert. Periodic third-party calibration of weighing and testing equipment helps prevent drift over time, keeping reported assay values honest and consistent.

    Years of feedback, successful launches, and yes, the occasional recall have together formed our practical approach to 4B2EA supply. By carrying forward lessons learned batch by batch, we minimize problems for each new customer and create products chemists want to work with.

    Outlook: Sustaining Value in a Competitive Market

    The demand for specialty aromatic amines like 4B2EA continues to rise, spurred by innovation in pharmaceuticals, material science, and chemical research. To not only keep pace but set the standard, we focus on problem-solving at every stage: sourcing, synthesis, testing, and shipping. By remaining open with our data, methods, and experiences—instead of hiding behind catchphrases or blanket assurances—we help customers overcome their own challenges faster.

    Not all chemistry can be automated—many decisions still rest on the trained eyes and practiced judgment of staff on the floor. This blend of hands-on skill and technical feedback creates a manufacturing culture where product improvements arrive naturally, not by corporate decree. When customers share their successes—a yield increase, a new compound, a finished patent—they add to a shared story of progress.

    Every bottle or drum of 4B2EA that leaves our site carries the work of a team built around authenticity and adaptability. That translates into real results for those in the lab or on the line, who in turn drive discovery, efficiency, and value in their own fields.