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4-Amino-3-Bromobenzoic Acid

    • Product Name 4-Amino-3-Bromobenzoic Acid
    • Alias 4-Amino-3-BBA
    • Einecs 249-746-2
    • 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

    234654

    Product Name 4-Amino-3-Bromobenzoic Acid
    Cas Number 50847-11-5
    Molecular Formula C7H6BrNO2
    Molecular Weight 216.03
    Appearance Off-white to light brown solid
    Melting Point 220-225°C
    Solubility Slightly soluble in water
    Synonyms 3-Bromo-4-aminobenzoic acid
    Smiles C1=CC(=C(C=C1Br)N)C(=O)O
    Inchi InChI=1S/C7H6BrNO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,9H2,(H,10,11)
    Storage Temperature 2-8°C
    Purity Typically ≥98%

    As an accredited 4-Amino-3-Bromobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g package contains 4-Amino-3-Bromobenzoic Acid in a sealed amber glass bottle with clear labeling and safety information.
    Shipping 4-Amino-3-Bromobenzoic Acid is shipped in tightly sealed containers, protected from moisture and light. It is labeled according to hazardous material regulations. During transit, it is handled as a chemical substance and may require temperature-controlled or dry conditions, with shipping documentation including safety data sheets and appropriate hazard labels for safe transportation.
    Storage 4-Amino-3-bromobenzoic acid should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. It should be kept away from incompatible substances such as strong oxidizers and acids. Proper labeling and adherence to chemical storage guidelines are essential to ensure safe handling and prevent contamination.
    Application of 4-Amino-3-Bromobenzoic Acid

    Applications of 4-Amino-3-Bromobenzoic Acid in Industrial Manufacturing

    As a direct manufacturer of 4-Amino-3-Bromobenzoic Acid, we serve key sectors with precise technical and regulatory demands. This intermediate supports industrial innovation through its roles in custom synthesis, specialty dye production, advanced pharmaceutical manufacturing, and agrochemical compound development. Below, we provide detailed downstream application scenarios based on real industrial market usage.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical companies employ this intermediate in the multi-step synthesis of targeted active pharmaceutical ingredients (APIs), especially for anti-tumor, anti-infective, and anti-inflammatory indications. Its amino and bromo functionalities enable selective coupling in Suzuki, Buchwald-Hartwig, and amidation reactions during GMP manufacturing. Process chemists frequently integrate it at the scaffold-building stage for molecules requiring ortho-amino-substituted benzoic acid cores. Quality control protocols ensure traceability and batch consistency for regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP General Chapter <1078> Good Storage and Shipping Practices
    • 21 CFR Part 211 (US FDA GMP for finished pharmaceuticals)
    • Ph. Eur. monographs for intermediates (scope dependent on ultimate API)

    Typical usage ratio

    • 5 – 25% relative to the main reaction substrate, adjusted for target molecular structure and yield requirements in coupling or amidation reactions

    Downstream process integration

    • Used at initial scaffold construction or during Suzuki/Buchwald cross-coupling
    • Introduced after halogenation and amidation steps for final ring closure
    • Subjected to strict in-process controls (HPLC, GC analysis)
    • Transferred under controlled storage to downstream purification or API finishing lines

    Final product types

    • Anti-cancer API intermediates (e.g. kinase inhibitors)
    • Nonsteroidal anti-inflammatory drug intermediates
    • Active pharmaceutical ingredients for infectious disease therapies
    • Custom synthetic blocks for contract API manufacturing (CDMO/CMO)

    2. Specialty Dye and Pigment Manufacturing

    Colorant producers use this benzoic acid derivative for synthesizing azo, anthraquinone, and custom specialty dyes, particularly in high-end textile and digital printing sectors. The material supplies a key ortho-aminobenzoic acid functionality to generate stable chromophors with strong colorfastness. Manufacturers adapt continuous or batchwise diazotization and coupling cycles, implementing rigorous quality checks for heavy metal impurities and residual bromide content to ensure environmental compliance.

    Industry compliance standards

    • OEKO-TEX® Standard 100 chemical restrictions for textile dyes
    • EN 71-3: Migration of certain elements, applicable for toy safety (when dyes used in children’s products)
    • REACH Annex XVII for restricted azo compounds
    • ZDHY certification for China textile inputs

    Typical usage ratio

    • 3 – 15% of total dye batch mass, modulated according to absorptivity and shade formulation needs

    Downstream process integration

    • Direct input to diazotization step for precursor anilines
    • Reactive component in coupling with naphthol or heterocycle
    • Subject to batchwise QC for purity before blending into final dye concentrate
    • Formulated with dispersing agents for high-speed digital inkjet applications

    Final product types

    • Reactive dyes for cotton and silk textiles
    • Specialty pigments for inkjet digital textile printing
    • Azo/anthraquinone dyes for industrial coatings
    • Lab-scale intermediates for colorant R&D

    3. Agrochemical Intermediate Production

    Agrochemical synthesis units incorporate this compound as a building block during the preparation of fungicide, herbicide, and insecticide active intermediates, particularly for benzoic acid-derived structures. Synthetic schemes use it in steps involving coupling with halogenated anilines or further bromination, creating backbone intermediates for crop protection agents. Quality systems manage batch segregation, impurity profiling, and documentation to comply with pesticide manufacturing standards and active ingredient registrations.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical material
    • China GB/T 1604-2008: General rules for agricultural chemical intermediates
    • ISO 9001:2015 Quality Management for chemical synthesis
    • OECD Good Laboratory Practice (GLP) for newly registered actives

    Typical usage ratio

    • 10 – 30% relative to final actives, tuned based on coupling efficiency and desired molecular substitutions in bench-top to industrial scale synthesis

    Downstream process integration

    • Incorporated at the intermediate construction stage after halogen exchange
    • Used in amidation or coupling steps for backbone extension
    • Undergoes controlled bromination or further functionalization before final API synthesis
    • Enters final formulation pipeline after purification

    Final product types

    • Benzoic-based herbicide precursors
    • Building blocks for triazole fungicide molecules
    • Intermediates for neonicotinoid insecticides
    • Custom agrochemical R&D reference standards

    4. Polymer Additive and Monomer Development

    Advanced polymer manufacturers use this aminobenzoic acid as a functional monomer or cross-linker precursor in specialty polymer resins, including polyamides, polyimides, and high-performance engineering plastics. Its unique substitution pattern allows for precise introduction of amino and bromo groups to tailor heat resistance, mechanical strength, and chemical resistance. Strict batch consistency and low impurity levels are critical for processability and downstream molding or extrusion.

    Industry compliance standards

    • ISO 9001:2015 process certification for polymer additives
    • ASTM D6910 for polymer composition analysis
    • RoHS Directive (2011/65/EU) relevant for final electronic polymers
    • FDA 21 CFR 177.1500 for polyamide components in food contact applications (dependent on downstream approval)

    Typical usage ratio

    • 1 – 8% as a co-monomer based on the desired degree of polymer chain modification and target end-use properties

    Downstream process integration

    • Integrated during high-temperature polycondensation reactions
    • Used in batchwise addition with other diamine and dicarboxylic acid components
    • Processed through extrusion or film casting lines after polymerization
    • Assessed for residual monomer content and stability under QC

    Final product types

    • High-temperature engineering plastics
    • Polyimide films for electronic and aerospace applications
    • Specialty polyamide membranes
    • Functionalized copolymer R&D samples

    5. Specialty Chemical Synthesis for Analytical Standards

    Research reagent and reference material manufacturers rely on this compound for custom synthesis of analytical standards, including labeled substances and impurity markers for chromatographic calibration. Its precise substitution promotes structural differentiation for mass spectrometry (MS) and HPLC method validation. Each batch requires documentation of impurity profiles and homogeneity to meet accreditation and analytical repeatability needs.

    Industry compliance standards

    • ISO 17034:2016 General requirements for reference material producers
    • ISO/IEC 17025:2017 Laboratory competence for testing and calibration
    • USP General Chapter <1225> Validation of Compendial Procedures
    • REACH registration for laboratory chemical use

    Typical usage ratio

    • Varies from 0.1 – 2% in multi-component reference solutions, determined by the analytical method’s calibration range

    Downstream process integration

    • Input during controlled synthesis of analytical compound libraries
    • Undergoes purification and structural confirmation by NMR, LC-MS
    • Portioned into ampules or vials under inert conditions
    • Accompanied by certificates of analysis (CoA) and safety datasheets

    Final product types

    • HPLC/MS calibration standards
    • Structural isomer markers for quality control laboratories
    • Labeled analytical reagents for forensic/toxicology lab use
    • Custom impurity standards for pharmaceutical manufacturing
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    Certification & Compliance
    More Introduction

    4-Amino-3-Bromobenzoic Acid: Real Manufacturing. Real Chemistry.

    Understanding 4-Amino-3-Bromobenzoic Acid from a Manufacturer’s Bench

    In the course of chemical production, every compound tells a story—a story of hands-on experience, repeated process adjustments, and learned techniques. 4-Amino-3-Bromobenzoic Acid, known in our line simply as “4-ABA-3-BrBA,” stands out not due to marketing, but because chemists, researchers, and formulation experts come back to it year after year. As the people running the reactors, keeping an eye on color and purity, and troubleshooting each load, we’ve seen the real-life value this compound brings to specialty synthesis and advanced material development.

    Sourcing and Processing: Why Our Approach Matters

    Anyone involved in custom synthesis knows the difference between “off-the-shelf” and quality you can put into a multi-step process without frustration. Making 4-Amino-3-Bromobenzoic Acid isn’t only a single-step reaction. There’s the issue of controlling by-product formation, making sure the amino group doesn’t get too eager to react, and ensuring that bromination targets the third position without straying. That kind of precision requires both robust equipment and a team that’s run dozens of pilot-scale batches.

    People often ask us about starting material sources or whether we rely on recycled bromine. At scale, we’ve committed to buying high-purity raw materials, not just for compliance, but because lower impurity levels mean less time spent on downstream purification. Incoming benzoic acid, with assured trace metal control, leads to more consistent results. After years in these facilities, you notice that every “small” upstream decision affects recrystallization later on. These aren’t distant procurement stories—they show up at the bottom of our reactors.

    Purity and Specifications: Not Just a Number

    Some would say an assay over 98% suffices for an intermediate like this. Our teams, working on high-value pharma and electronics applications, see why that 99%+ actually matters. An uncontrolled isomer can spell disaster during a complex multi-step synthesis. Even a small percentage of 2- or 5- position brominated impurity might impact final yields or lead to time-consuming chromatography. Whether you’re prepping an advanced heterocycle or starting from this molecule for a dye intermediate, high-grade product saves time and headaches.

    There’s a notable difference in flow tests, appearance, and melting point from lot to lot in the industry. A batch with more moisture or larger particle size slows down reaction rates. Fine white to off-white powder—not brown or speckled—shows that re-purification has been handled the right way. Our emphasis on tight melting range (with minimal residue at 196-198°C), careful water content monitoring, and trace halogen checks is based on listening to customers frustrated by inconsistent upstream supply. It’s a technical detail with real consequence.

    Why Chemists Choose 4-Amino-3-Bromobenzoic Acid: Field Usage Seen Firsthand

    We’ve supplied 4-ABA-3-BrBA to teams in both pharmaceutical synthesis and advanced polymer work. In the pharmaceutical sector, 4-Amino-3-Bromobenzoic Acid often serves as a critical intermediate for antimicrobials or anticancer candidates, especially where later-stage substitution relies on having both the amino group and the bromine in specific positions. Its value lies in reactivity. The para-amino group opens possibilities for diazotization, coupling, and condensation. The bromine makes nucleophilic aromatic substitution or Suzuki couplings possible with a minimum of sidereactions. Every batch we move out gets logged with detailed impurity profiles, which has a real impact during drug development audits.

    On the materials science front, the uses are just as diverse. 4-Amino-3-Bromobenzoic Acid allows construction of conjugated backbones for specialty dyes, liquid crystals, and functional polymers. Teams in electronics appreciate the selectivity: the dual-groups in these positions are rare, and crucial when a molecular backbone needs “orthogonal” functional handles. Years back, we helped troubleshoot a batch for a conductive polymer project. Chromatographic analysis traced an “off-color” issue back to a batch made with subpar starting material from a third party, demonstrating firsthand that process transparency and in-house QA really matter for critical applications.

    Differentiating from Similar Products

    Bench chemists know there are a dozen recognizably similar substituted benzoic acids—4-Amino-3-Chlorobenzoic Acid, 3-Bromo-4-Methylbenzoic Acid, or even 2-Amino-5-Bromobenzoic Acid—each with its quirks. The unique advantage of 4-ABA-3-BrBA is the positional synergy. The amino group at the para position enables reliable coupling or derivatization, while the bromine at the meta position resists many unwanted side reactions, surviving aggressive conditions in metal-catalyzed or high-temperature transformations.

    We’ve heard from R&D chemists who tried to substitute a para-bromo, ortho-amino variant, only to find unwanted cross-reactivity or intractable separation. Scale-up teams often start with mixed isomers, hoping yields will remain consistent, but those “shortcut” approaches nearly always require time-consuming purification, bringing costs up unexpectedly. Our experience echoes theirs—the specific arrangement in 4-Amino-3-Bromobenzoic Acid matters. It’s not just a catalog number; it’s a solution shaped by the real-world demands of modern synthesis.

    Focus on Process Reliability: Lessons Learned at Scale

    There’s ongoing talk in industry circles about the importance of reliable chemical supply chains. As a manufacturer, our biggest challenge hasn’t been sales, but process consistency batch after batch. Temperature gradients, vessel fouling, and feedstocks all vary through the year. Bromine handling, with strict environmental controls, often raises the stakes. Even something as practical as ambient humidity during recrystallization can alter drying times and powder texture.

    Through experience, we found that a longer filtration period adds clarity and batch-to-batch reliability. Years ago, a run produced a smudgy powder with higher than normal residual solvents—an error traced to reduced vacuum efficiency in our filter station and compounded by staff rotation. Each of these “little” emergencies prompted process adjustments, documented in our SOP changes, and ultimately reflected in more reliable outcomes for our customers. Our plant teams solve these issues directly—they don’t get sidestepped by middlemen or lost in inventory shuffles.

    Safety, Environment, and Compliance in the Real World

    Brominated compounds, regardless of intent, deserve careful attention beyond product performance. Our experience handling bromine, waste treatment, and by-product minimization keeps us sharp on regulatory compliance and responsible operation. Not all facilities can adjust pH handling mid-process without risk to staff or environment. Over the years, we’ve moved to closed-system bromination and introduced scrubbers and real-time emissions monitoring as routine, not as afterthoughts.

    We’ve been asked if older processes (with open bromine addition) still exist elsewhere in the field. They do, and they increase the risk of batch contamination and site emissions. Improved containment, we found, not only minimizes losses, but gives us more reproducible product. For our reagents, especially those bound for pharmaceutical and electronics use, even trace environmental contamination can result in rejected material and rework. The lessons here are won through audit cycles, not just in internal paperwork.

    Supporting Advanced Chemistry: Our Approach to Collaboration

    Research projects have a rhythm of their own—tight timelines, shifting scope, and complex analytics. We’ve seen teams’ schedules thrown off by unreliable delivery or incomplete technical support, and it always takes more than a spec sheet to get a batch approved. Whether a customer needs GC-MS, HPLC, or residual halide profiles, we run analyses ourselves rather than sending samples to a separate QA firm. Some of our best working relationships come from troubleshooting with research supervisors on late evening calls, adjusting drying times, or offering storage advice based on a specific lab’s climate.

    People expect more today—documentation, sample retention, and sometimes custom particle sizing for solid-state work. Both academia and industry clients ask us for background data, not standardized templates. We’re used to running extended impurity screens, or helping develop sample protocols to confirm product integrity post-shipment. It's the interaction between process chemist and customer, engineer and analyst, where the “special requests” shape better practice. In several collaborations, we adjusted synthesis parameters to meet one lab’s need for more fine powder and another’s need for low-chloride product, recognizing that every downstream process sets a new bar.

    Adaptation and Improvement: Lessons from the Shop Floor

    The push for continual improvement doesn’t only start in the boardroom. We owe much to the operators and supervisors noticing yield dips or hints of off-color in glassware. Many formula shifts come from daily logs, not distant management reviews. For example, we started triple-washing isolated product only after operators noticed recurring “halo” spots during drying. Process charts can tell some stories, but nothing replaces careful observation under real plant conditions.

    Another improvement came after a recurring impurity appeared in a summer batch. Ops teams spotted a subtle color change; our lab confirmed a trace side-product via LC-MS. By running parallel small-scale experiments with a new filtration aid and an adjusted solvent mix, the team solved the contamination issue in under a week. Fixes like this aren’t theoretical—they directly reduce rework, improve yield, and get customers their product on time.

    Challenges Beyond the Lab: Shipping and Storage Know-How

    Not every chemical’s journey ends at the warehouse door. Over years of distribution, we watched heat, moisture, and static charge cause changes in powder quality and flow. Someone working with 4-Amino-3-Bromobenzoic Acid in a dry European winter can find it crisp and easy to weigh; a monsoon season shipment to South Asia requires stricter moisture barriers. We don’t use generic packaging “solutions.” Our approach relies on multi-layer bags, sealed fiber drums, and even secondary desiccant for sensitive destinations.

    Outbound inspections include a physical check—every drum, every seal, every label. There’s no substitute for hands-on control, especially where climate swings alter powder handling or packaging integrity. Early on, we learned to keep ongoing logs on customer storage conditions and to offer practical advice based on prior shipments rather than textbook guidelines. Our after-delivery follow-up system catches issues in less than 48 hours, driven by plant and warehouse staff who know what can go wrong, and have the tools to address minor packaging breakdowns before they become bigger issues.

    Supporting Innovation: Custom Requests and Process Tweaks

    Not every project fits a standard order. We’ve seen synthetic chemists push for slightly larger particle size to fit a filtration step, or tighter yellow index for a particularly sensitive application. It’s possible to deliver, but it takes open communication between research chemists and our operations personnel. If a batch must pass low-chloride levels for a novel metal-catalyzed transformation, we have tested approaches with additional deionization upgrades. A request for pre-packed, glovebox-ready containers for air-sensitive work arose during a pilot run with a research partner, leading us to modify both filling and QA steps.

    This level of responsiveness distinguishes a hands-on manufacturer. Many new project leads depend on robust technical dialogue before a gram is ordered. Projects advance faster, and fewer surprises crop up on both ends, when realistic feedback guides the process—whether that means flagging reactant limitations or recommending alternative packaging based on transit temperature statistics.

    Why Manufacturer Experience Matters in the Market

    Experience in the factory and in the research supply chain sets product apart. We operate by clear process documentation, maintain open logs, and insist on product checks that stem from actual customer feedback. Our people see every batch that leaves the plant as both a technical achievement and a trust point with the next user. More than once, a customer caught an oddity at delivery, and our teams’ willingness to investigate—by rechecking chromatograms or pulling test retains—secured lasting relationships that move beyond transactional sales.

    Some may try to shave costs with minimal testing or off-label substitutes. Over the years, we’ve seen this approach backfire, with costly project delays or compromised research data. Those with hands-on manufacturing insight distinguish between “almost right” and “actually correct,” and know when to stick with proven parameters. In chemical manufacturing, these distinctions are earned through countless cycles of production, inspection, and problem-solving, not announced by a line in a catalog.

    Quality as Commitment, Not Compliance

    Quality doesn’t end at compliance certificates or successful external audits. It’s a living standard, built on repeatable work, clear traceability, and willingness to engage in continuous process improvement. For us, batch failures are learning opportunities, not just instances to meet minimum regulatory thresholds. This mindset means accepting, recording, and resolving minor deviations with full transparency and follow-up. Our QA process assures researchers that the 4-Amino-3-Bromobenzoic Acid in their bottle is the outcome of a living system—one in which all parties, from raw material auditors to plant staff to technical liaisons, collaborate to meet higher expectations.

    Working directly as the manufacturer and supplier, we build reliability by anchoring every shipment to traceable lots, documented process parameters, and feedback-driven adjustments. By operating with practical knowledge of chemical reactivity, separation, and product stability, we offer a foundation for safer and more productive research and manufacturing downstream.

    Looking Ahead: Meeting Future Needs

    As research moves forward, project demands shift and expectations rise. In the case of 4-Amino-3-Bromobenzoic Acid, the next wave of applications could stem from interaction with new coupling catalysts, biobased solvents, or entirely fresh polymer designs. We follow developments not as observers, but as participants—ready to adapt our processes, engage with both technical and regulatory advances, and provide practical advice before and after delivery.

    The story of any chemical extends beyond its label or lot number. By treating each batch of 4-Amino-3-Bromobenzoic Acid as a reflection of collective effort—from procurement through production, testing, and shipment—we ensure that our contribution to scientific and industrial progress remains rooted in direct, tangible experience. Whether supporting the work of a single bench chemist or a multinational R&D division, our manufacturing practice carries a commitment to integrity, reliability, and open dialogue—values shaped not by mandate, but by the shared progress of real-world chemistry.