2-Bromoaniline

    • Product Name: 2-Bromoaniline
    • Alias: o-Bromoaniline
    • Einecs: 202-121-1
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    876558

    Chemicalname 2-Bromoaniline
    Molecularformula C6H6BrN
    Molarmass 172.02 g/mol
    Casnumber 578-57-4
    Appearance Pale yellow to brown solid
    Meltingpoint 29-33 °C
    Boilingpoint 255-258 °C
    Density 1.66 g/cm³
    Solubilityinwater Slightly soluble
    Flashpoint 110 °C
    Smiles C1=CC=CC(=C1N)Br
    Pubchemcid 10360

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

    Packing & Storage
    Packing A 100g amber glass bottle labeled "2-Bromoaniline," featuring hazard warnings, chemical formula, CAS number, and manufacturer details.
    Shipping 2-Bromoaniline is shipped as a hazardous chemical, typically in tightly sealed containers made of compatible materials to prevent leaks. It must be packaged and labeled according to relevant regulations (such as DOT, IATA, or IMDG). Handling requires proper documentation, and transport should avoid heat, moisture, and incompatible substances.
    Storage 2-Bromoaniline should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances, such as strong oxidizing agents and acids. Keep the container tightly closed and properly labeled. Store in a corrosive-resistant, chemical safety cabinet. Avoid exposure to heat and ignition sources, and ensure storage at room temperature to prevent degradation or hazardous reactions.
    Application of 2-Bromoaniline

    Applications of 2-Bromoaniline in Industrial Manufacturing

    2-Bromoaniline serves as an essential aromatic amine intermediate in the fine chemical industry, supporting large-scale and batch production for specialized downstream segments. Our manufacturing expertise ensures chemical consistency and strict adherence to industry-specific regulatory demands. Below, we outline its established roles across diverse but specialized sectors, including key standards, usage levels, routes of integration, and actual end products manufactured with this raw material.

    1. Pharmaceutical Intermediate Synthesis

    As a crucial building block for active pharmaceutical ingredient (API) synthesis, 2-Bromoaniline is primarily adopted in the preparation of antipyretic-analgesic and antimicrobial molecules at pilot and plant scales. Its ortho-substituted halogen configuration enables targeted reactions — including the Ullmann condensation and Buchwald–Hartwig aminations — leading to framework extension, heterocycle development, or further substitution. Stringent GMP-compliant handling and validated traceability are mandatory throughout this scenario’s workflow.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex, Volume 4 - GMP Guidelines (Part II)
    • USP–NF and EP monographs on process impurities and intermediates
    • 21 CFR Part 210/211 (FDA cGMP regulations)

    Typical usage ratio

    • Applied from 0.5 to 2.5 molar equivalents based on N-arylation or coupling requirements; process chemists adjust ratio depending on downstream substitution pattern and purity control demands.

    Downstream process integration

    • Charged during early-stage reaction steps (halogenation, acylation, or amination setup), often prior to ring closure or heterocycle development.

    Final product types

    • Analgesic and antipyretic APIs such as paracetamol analogs
    • Sulfonamide-based antibacterials
    • Benzimidazole antifungals and associated generic intermediates

    2. Agrochemical Active Ingredient Manufacturing

    2-Bromoaniline acts as a selective precursor for constructing substituted aniline frameworks required in modern agrochemical actives, including herbicidal and fungicidal agents. Its electronic and steric effects enable process selectivity during the synthesis of phenylurea, benzoxazinone, or triazole derivatives. Precise formulation and hazard management practices ensure all downstream formulations comply with local and global agrochemical registration directives.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • ISO 9001:2015 Quality Management Systems in chemical manufacturing
    • REACH Registration (EC 1907/2006) for use in plant protection products
    • BPR (EU Biocidal Products Regulation) for certain fungicidal preparations

    Typical usage ratio

    • Ranges from 0.8 to 3.0 molar equivalents per batch, determined by synthetic route and desired derivative; higher ratios are applied in multi-step coupling sequences to drive reaction to completion.

    Downstream process integration

    • Introduced at initial coupling or amidation stages in crude synthesis of target actives, prior to further functional group modifications or ring closures.

    Final product types

    • Phenylurea herbicides (e.g., linuron analogs)
    • Triazole fungicides
    • Benzoxazinone-based seed treatment formulations

    3. Dye and Pigment Intermediate Production

    Within the specialty colorants industry, 2-Bromoaniline enables the synthesis of azo dye intermediates and diarylamine pigments, providing targeted shade control and high tinting strength. Its suitability derives from controllable diazotization and subsequent coupling steps, allowing formulation of both water-soluble and high-fastness dyes. Our material meets stringent controls for trace metal, insolubles, and byproduct amines to comply with sector-specific standards.

    Industry compliance standards

    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals, Manufacturing Restricted Substances List)
    • OEKO-TEX® Standard 100 (chemical purity for textiles)
    • DIN EN ISO 9001 and 14001 for colorant synthesis plants
    • REACH SVHC (Substances of Very High Concern) avoidance protocols

    Typical usage ratio

    • Typically 1.0 to 1.2 equivalents in diazotization systems targeting monoazo dye production; ratios are recipe-dependent according to shades and fastness parameters demanded by clients.

    Downstream process integration

    • Fed into the diazotization unit upstream of azo coupling or during the initial condensation with diaryl precursors for pigment synthesis.

    Final product types

    • Solvent dyes for plastics and synthetic fibers
    • Acid and disperse dyes for textile applications
    • Diarylamine-based organic pigments for coatings and inkjets

    4. Synthesis of Specialty Polymers and Resins

    In the polymer and advanced materials sector, 2-Bromoaniline enters as an aromatic nucleophile or halide donor in step-growth polymerizations, notably in the fabrication of functionalized polyamides and high-performance resins. Its presence introduces thermal stability and offers sites for further cross-linking or grafting. Downstream buyers typically require traceability for all inputs and adherence to established monomer purity thresholds for electronic, photonic, or engineering plastics.

    Industry compliance standards

    • UL 94 Flammability Standard for Polymer Materials
    • EN ISO 10993 for medical-technical polymers
    • RoHS Directive 2011/65/EU compliance (for electronics)
    • ISO 14001 environmental management for resin production

    Typical usage ratio

    • From 0.7 to 1.5 equivalents as a comonomer or chain-extension agent, depending on desired molecular weight and functional group loading; adjusted by reaction chemists for end-use mechanical properties.

    Downstream process integration

    • Dosed into polymerization reactors during the monomer preparation or polycondensation step, often pre-dissolved in suitable solvents for homogeneous mixing.

    Final product types

    • Functional polyamides for filters and separations
    • High Tg aromatic resins for circuit boards and encapsulants
    • Specialty coatings with enhanced solvent resistance

    5. Fine Chemical and Performance Material Building Blocks

    The specialty fine chemicals industry incorporates 2-Bromoaniline as a customizable scaffold in the development of advanced performance additives, stabilizers, and laboratory reagents. It acts as a reactive starting point for constructing nitroanilines, diarylamines, and other functional intermediates, supporting downstream customization for catalysis, lubrication, or high-temperature applications. Manufacturers demand precise analytical profile and impurity control for compliance with local chemical handling and hazard communication mandates.

    Industry compliance standards

    • GHS/CLP Regulation (EC No 1272/2008) for hazard communication
    • ISO 17025 laboratory accreditation for QC testing of intermediates
    • REACH Annex XVII Restrictions for certain downstream uses
    • National fire safety codes (NFPA, GB 15603-1995 for China)

    Typical usage ratio

    • Utilized at 0.2 to 1.0 mole per mole of targeted additive or intermediate; adjusted during early R&D throughput or custom synthesis scale-up.

    Downstream process integration

    • Employed at initial nucleophilic substitution, cross-coupling, or reduction steps; integrated in both batch tank and continuous flow systems.

    Final product types

    • Specialty stabilizer packages for lubricants or coolants
    • Photoinitiators for electronic and 3D printing inks
    • Reference reagents and calibration standards for analytical labs

    Free Quote

    Competitive 2-Bromoaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Email: admin@ascent-chem.com

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    Certification & Compliance
    More Introduction

    Understanding 2-Bromoaniline: Experience from a Chemical Manufacturer

    The Role of 2-Bromoaniline in Chemical Synthesis

    2-Bromoaniline has become a familiar sight in our facilities, not just as a simple reagent, but as a core part of life in chemical manufacturing. We have watched the growing interest in this compound over time, especially from fine chemicals and pharmaceutical teams. Our process brings 2-Bromoaniline to customers with specifications that reflect real manufacturing conditions. The product appears as a colorless to light brown liquid, with a molecular formula of C6H6BrN and a molecular weight of 172.02. From batch to batch, we track purity and water content with every run, because the work done with 2-Bromoaniline relies on these details. We check parameters like melting point and assay; typically, we see purity levels of 99% or more by GC, and the melting point falls within a narrow 62-65°C range. Such focus isn’t just for compliance. It’s essential for downstream reactions, for yields, and for consistency in demanding schemes where people don’t get second chances.

    How Our Production Experience Shapes Quality

    Over the years, most of the requests for 2-Bromoaniline from our clients involve multi-step syntheses where a brominated aromatic amine is a linchpin. Many pharmaceutical intermediates begin with this compound. What sets it apart from other brominated aromatics often comes down to how smoothly nucleophilic substitutions run or how predictable coupling reactions behave. Anyone with a background in QC knows: an impurity profile, even a minor one, changes the outcome down the line. In manufacturing, issues like metal content and isomer presence make the most difference, so our process runs with this in mind. Each step, from the selection of raw aniline to the bromination stage, draws on years of experience balancing efficiency with safety. We use technology that limits byproducts, and we review GC traces before release. It sounds simple but reaching this level of routine precision takes repeated investment in controls and a willingness to adjust to the quirks of scale-up chemistry.

    Application Stories: What Happens Beyond Our Factory

    Most of the 2-Bromoaniline leaving our site ends up in processes making dyes, pigments, or medical compounds. We’ve worked with dye houses who use 2-Bromoaniline to build more complex aromatics; a run with our 2-Bromoaniline in their hands can mean the difference between a dye that fades and one that keeps its color. In pharmaceutical work, chemists value how the amino group and the bromine atom can be swapped or protected at different points in a lengthy synthesis. Our clients feed 2-Bromoaniline into Buchwald-Hartwig couplings, Suzuki reactions, and beyond. More than a few times, we’ve received feedback from synthesis teams who noticed fewer byproducts or shorter purification steps thanks to consistent input quality. Not all substitutions or coupling agents tolerate a high impurity load. The fewer contaminants in the starting material, the less rework, the clearer the final product, and the less waste to haul away.

    We can draw a sharp contrast with other brominated anilines, for example, 4-Bromoaniline or 3-Bromoaniline. Edge cases do arise when a reaction demands a different regioisomer. Sometimes a new drug design absolutely requires the para- or meta- rather than ortho-substituted form. The issues with misidentification or cross-contamination are practical. We mark and segregate inventory so the right isomer gets pulled. In our view, the differences between these isomers go deeper than structure; they alter the behavior in coupling reactions, impacting regioselectivity and the byproducts you see. Our customers who use more than one type recognize this too—they watch reaction outcomes closely, sometimes side by side, and know that even trusted procedures can yield surprises if the isomer is wrong.

    Consistency and Trust: The Result of Practice, Not Chance

    No bottle or drum of 2-Bromoaniline comes with a badge proclaiming “reliable,” but our team’s reputation follows each shipment. We’ve had urgent calls from partners in the middle of a process, needing urgent answers about a result or variance. Sometimes it comes down to trace elements—it only takes a tiny amount of catalyst poison to throw off a yield. In these cases, we pull archived samples, review records, and share what we find. Our approach involves a three-part QC system: in-process monitoring, final goods testing, and retained samples for every lot. Not every competitor invests the time or resources here, and some leave testing to a third party with unpredictable standards.

    Take moisture, for instance. The amine’s reactivity pairs badly with water during some reactions—coupling steps are especially sensitive. Those who have run hundreds of reactions know the headache small amounts of moisture cause. To address this, we manage both internal drying and atmospheric controls throughout packaging. Our teams test moisture by Karl Fischer titration, and anything out of spec gets retested before it leaves the floor. This prevents the stress of an unexpected reaction outcome on our client’s bench.

    Real-World Handling and Storage Experience

    People who store and use 2-Bromoaniline know that handling isn’t just about paperwork. Our years of experience have taught us some lessons: the compound deserves careful storage, away from excess heat and direct sunlight. Ventilation is key, as 2-Bromoaniline can emit odors if allowed to warm up or degrade. We work with steel or HDPE drums and clearly mark storage areas to keep incompatibilities at bay. These steps aren’t transferred through safety data sheets alone—it’s from one operator to another, through training and habits built into the routine.

    Sometimes our customers in smaller labs have asked about storage strategies or how to limit loss from evaporation or spillage. We recommend opening containers only as needed, resealing tightly, and using septa for repeated sampling. Over time, these little habits cut costs and preserve quality—a lesson we learned from day-to-day handling here.

    Supporting Customer Processes, Not Just Selling a Product

    Years ago, a customer switched suppliers and came back to us after struggling with batch-to-batch variability. Their yields fluctuated even after purifying their new supplier’s 2-Bromoaniline, which cost them both product and time. They weren’t the first, or last, to find that source reliability trumps a lower quote. We stepped in with side-by-side sample runs and open dialogue about their process, tracking down issues together. The experience reinforced one of our guiding principles: our involvement doesn’t end after the product is loaded onto a truck or container. Most of the feedback we get is detailed and specific—sometimes with suggestions or requests for modifications. With every cycle, we learn more about how 2-Bromoaniline performs out in the world, and this back-and-forth improves the next batch.

    Customization matters, but only up to a point. We’ve been asked about changing packaging or modifying specifications to suit a new process. Here, we work alongside partners, troubleshooting challenges in real time. Chemicals like 2-Bromoaniline rarely fit a single use case; each application brings new questions and drives subtle adjustments in the chemistry and logistics. Experience with pharmaceutical manufacturing has shaped the way we prepare documentation and track regulatory standards. Sometimes, new methods or compliance needs reshape our batch records or purity testing. We treat each as a chance to double-check that the product matches the end-use, not just a number on a specification.

    Comparing with Similar Compounds: Insights from Daily Practice

    2-Bromoaniline’s closest relatives in our lineup—4-Bromoaniline and 3-Bromoaniline—often get compared for their use in related reaction schemes. The differences between the ortho, meta, and para isomers drive much of our daily planning. Each isomer moves differently through purification equipment; they show different stabilities and affect catalytic reactions with their steric and electronic differences. For example, 2-Bromoaniline’s ortho-bromo position brings both advantages and challenges. This substitution pattern offers unique reactivity for ortho-directed lithiation or cross-couplings but can slow some substitutions because of steric hindrance near the amine group. Customers who run aromatic substitutions note higher selectivity or yield from one isomer compared to another, depending on the downstream pathway.

    Unlike some specialty chemicals, the market for 2-Bromoaniline has remained steady year over year. We adjust plans based on actual demand from downstream users in pharma, dyes, and agrochemicals. Knowing the requirements of each industry means we sometimes field questions around residual metals, DMSO solubility, or even alternative packaging. We look at actual performance, not just specs, so those approaching us with a new synthesis route can trust the results aren’t a coin toss.

    Practical Lessons from Years in the Industry

    Several lessons repeat. The best results follow from a mixture of adherence to process and listening to end-users. Anyone who has struggled with yield loss, inconsistent purification, or unexplained byproducts appreciates what reliable input means. We keep track of changes in regulatory environments and update our documentation as needed for exports or audits. Over the years, demand for detailed impurity data has grown, especially from pharmaceutical researchers preparing for regulatory submissions. We expanded analytical capabilities, running HPLC and GC-MS for full impurity profiling.

    Our approach to shipping has changed, too, prompted by real stories from the field. More than a few partners reported delays or off-spec material due to poor transit conditions. We started using insulated containers or expedited shipping in summer, reduced the risk of high-temperature degradation, and built stronger packaging. Each adjustment reflects what users face outside our plant—not just what worked in a controlled storage room.

    Environmental Responsibility: Our Continuous Focus

    The bromoaniline family has unique issues for handling and waste management. We have installed advanced waste capture for both bromine-containing byproducts and spent mother liquors. Reducing environmental footprint comes back to the same habits that improve quality—closed system transfers, careful monitoring of tanks and air, on-site neutralization units. Our team participates in regular training to spot early signs of leaks or off-spec batches, feeding lessons back into procedure books. We have invested in odor controls and improved ventilation for operator safety. Over time, fewer spills and better emergency readiness have reduced both regulatory risk and real-world harm.

    Customers sometimes ask about end-of-life disposal for empty containers or product that has passed its shelf life. We offer advice shaped by both local rulebooks and practical experience: neutralization under controlled conditions, use of authorized incinerators, and avoidance of sewer disposal. With each shipment, we support clients in meeting both performance and regulatory goals.

    Looking Ahead: 2-Bromoaniline in a Changing Chemical Landscape

    Regulations in global trade, restrictions on hazardous compounds, and rising expectations for traceability have shifted the ground beneath all chemical manufacturing. With 2-Bromoaniline, traceability is more than a formality—it allows downstream processors and finished goods manufacturers to prove compliance, safety, and performance. Our traceability system integrates batch records and materials control, designed through years of customer collaboration and audit experience.

    Recent trends toward green chemistry and solvent reduction have affected the way 2-Bromoaniline is handled and applied. Customers show interest in routes that generate less waste, use less water, or avoid chlorinated solvents. Whenever possible, we support process adaptation, testing alternative extraction or purification steps, and collaborating on pilot-scale trials. The shared aim: making strong products, minimizing negative impact.

    The team at our plant sees every kilogram of 2-Bromoaniline as connected to someone’s process, whether a dye, drug, or intermediate. Our direct experience shapes every decision, from sourcing to analytics to packaging. Each lesson along the way—every success, every challenge—gets built into what we offer next.

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