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2-Amino-3-Bromobenzoic Acid

    • Product Name 2-Amino-3-Bromobenzoic Acid
    • Alias 2-Amino-m-bromobenzoic acid
    • Einecs 249-753-6
    • 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
    VTB
    Specifications

    HS Code

    515203

    Chemical Name 2-Amino-3-Bromobenzoic Acid
    Cas Number 32943-89-2
    Molecular Formula C7H6BrNO2
    Molecular Weight 216.03
    Appearance Light yellow to brown solid
    Melting Point 193-197°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store at room temperature, keep container tightly closed
    Synonyms 3-Bromoanthranilic acid
    Inchi Key HSRRBEFOSXZHDD-UHFFFAOYSA-N
    Smiles C1=CC(=C(C(=C1N)Br)C(=O)O)

    As an accredited 2-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 2-Amino-3-Bromobenzoic Acid is packaged in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 2-Amino-3-Bromobenzoic Acid should be shipped in tightly sealed containers, protected from light and moisture. Transport under ambient conditions unless otherwise specified. Ensure proper labeling and compliance with all applicable regulations for handling organic chemicals. Use appropriate packaging materials to prevent leaks or contamination during transit.
    Storage 2-Amino-3-bromobenzoic acid should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep it at room temperature and protect from moisture. Proper labeling and secure placement in a designated chemical storage cabinet are recommended to prevent accidental exposure or contamination.
    Application of 2-Amino-3-Bromobenzoic Acid

    Applications of 2-Amino-3-Bromobenzoic Acid in Industrial Manufacturing

    Our 2-Amino-3-Bromobenzoic Acid plays a critical role as an advanced intermediate within several high-value chemical supply chains. The following industrial application areas reflect real downstream use-cases where our materials directly contribute to the creation of end-use products through controlled formulation, process integration, and adherence to sector-specific regulatory regimes.

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

    In regulated pharmaceutical manufacturing, companies utilize 2-Amino-3-Bromobenzoic Acid as an essential building block for synthesizing specific active pharmaceutical ingredients, especially those within the non-steroidal anti-inflammatory and antihypertensive drug classes. Chemists form amide and urea derivatives by coupling the amino group while leveraging the bromo functionality for selective halogen-metal exchange or substitution steps. Quality control throughout the multi-step API synthesis meets ICH Q7 guidelines for GMP, and raw material traceability is mandatory.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU GMP Volume 4 Part II
    • USP/NF and Ph. Eur. monograph criteria for related APIs

    Typical usage ratio

    • Starting material, typically 0.8–1.2 molar equivalents relative to target API intermediate
    • Batch ratios determined by stoichiometry and anticipated yield; may adjust up to 10% excess to drive conversion

    Downstream process integration

    • Integration at early stage amidation or Suzuki coupling stages in the multi-step synthesis
    • Subjected to purification via recrystallization or preparative chromatography as required by impurity profile control

    Final product types

    • Antihypertensive drug substance intermediates
    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Specialty pharmaceuticals for clinical development
    • Research-grade APIs for preclinical projects

    2. Agrochemical Synthesis Building Block

    The agrochemical sector relies on this material for the targeted assembly of key heterocyclic structures, such as brominated anilines and benzoic acid derivatives in pre- or post-emergence herbicides and fungicides. Industry formulators combine it with specific catalyst systems to introduce functionalized groups, driving selectivity in active ingredient production. Compliance with environmental and product safety regulations is required at all facility and product distribution stages.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Crop Protection Chemicals
    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH (EC) No 1907/2006 for hazardous intermediates
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • Typically 0.5–1.5 molar equivalents per active ingredient intermediate
    • Ratio varies by intended halogen content in final product; may use up to 20% excess for stepwise reactions

    Downstream process integration

    • Charged during the intermediate synthesis step, often under inert atmosphere
    • Employed in halogen exchange, acylation, or condensation reactions for further elaboration
    • Processed with recovery and safe disposal of waste streams as required by environmental standards

    Final product types

    • Brominated herbicide intermediates
    • Fungicide precursors for soil and seed treatment
    • Intermediate components in broad-spectrum pesticide formulations
    • Seed coating chemical components

    3. Dye and Pigment Intermediate for Specialty Colorants

    Manufacturers in the colorants industry employ 2-Amino-3-Bromobenzoic Acid for synthesizing azo and anthraquinone dyes. The compound’s amino and bromo substituents facilitate both diazotization and subsequent coupling, resulting in high-purity dye intermediates for technical textiles, plastics, and specialty coatings. The plant’s batch records, colorimetric quality controls, and effluent treatments adhere to strict European REACH regulations on dye intermediates.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical substances
    • OEKO-TEX® Standard 100 for textile-related applications
    • ZDM (Zero Discharge of Hazardous Chemicals) Manufacturing Restricted Substances List
    • ISO 9001:2015 for process quality assurance

    Typical usage ratio

    • As a key ring component, used at 0.6–1.4 molar equivalents depending on target chromophore yield
    • Adjustments based on coupling partner reactivity and purity of starting materials

    Downstream process integration

    • Introduced during dye precursor synthesis, especially in diazotization and subsequent coupling reactions
    • Control of pH and temperature ensures stability of the resulting azo or anthraquinone bond formation

    Final product types

    • Azo dye intermediates for fiber dyeing
    • Anthraquinone pigments for technical plastics
    • Disperse dye intermediates for polyester fibers
    • Special effect pigments for automotive coatings

    4. Synthesis of Liquid Crystal Materials for Display Technology

    Specialized electronic chemicals producers use this compound as a precursor for constructing tailored aromatic carboxylate and aniline derivatives necessary for nematic and smectic liquid crystal phases. Careful integration of amino and bromo substituents enables subsequent C-N and C-O bond formations, critical for achieving the dielectric anisotropy and viscosity profiles required by display panel manufacturers. All material shipments conform to rigorous purity and trace metals criteria under ISO and RoHS standards for the electronics sector.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic raw materials
    • ISO 9001:2015 and ISO 14001:2015 for electronics chemicals
    • IEC 61249-2-21 for halogen-free electronic substrates
    • IPC-4101 for base materials for printed boards

    Typical usage ratio

    • 0.7–1.3 molar equivalents as a starting monomer for liquid crystal intermediate formation
    • Flexibly adjusted based on product’s chain length and targeted phase transition temperature requirements

    Downstream process integration

    • Used in initial condensation or substitution reaction for assembling functionalized mesogenic units
    • Undergoes purification via distillation, crystallization, or preparative HPLC to achieve electronic grade purity
    • Lot traceability for all input streams that feed display matrix manufacturing lines

    Final product types

    • Nematic liquid crystal intermediates for LCD panels
    • Chiral dopants for display modulation
    • Specialty aromatic carboxylates for TFT displays
    • Polymerizable monomers for plastic LC alignment layers
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    Certification & Compliance
    More Introduction

    2-Amino-3-Bromobenzoic Acid: Experience from the Manufacturer’s Perspective

    Practical Insights on 2-Amino-3-Bromobenzoic Acid Production

    Working directly in the plant, the routine of manufacturing 2-Amino-3-Bromobenzoic Acid becomes familiar, but each batch still carries its own lessons. Chemical synthesis, while straightforward on paper, rewards attention to detail and a willingness to adapt to conditions. For those less familiar, 2-Amino-3-Bromobenzoic Acid carries the structure of a benzoic acid substituted at the 2 and 3 positions with amino and bromo groups, respectively. The most common reference for this material in our sector is its CAS number, 40363-57-9. Unlike materials processed in massive tonnage, 2-Amino-3-Bromobenzoic Acid finds use in niche, high-value chemical fields, primarily in pharmaceutical intermediates and specialty dyes.

    Colleagues often ask why this specific substitution pattern draws so much interest from synthetic chemists and process developers. The bromine atom at the 3-position activates the molecule toward a range of cross-coupling and substitution reactions that help build more complex aromatic systems. The amino group, being strongly electron-donating, gives extra leeway in downstream reactivity. Combining these groups on a benzoic acid core means the molecule serves as a diverse building block. Our experience with real-world customers reveals a consistent pattern: companies rely on this compound to unlock synthetic routes that would otherwise stall with more common isomers like 3-bromo-4-aminobenzoic acid or other benzoic acid derivatives.

    Process Details That Matter: How the Choice of Raw Materials Shapes the Product

    Each production cycle for 2-Amino-3-Bromobenzoic Acid begins with selecting the right ortho- and meta-substituted precursors. From the chemical plant floor, small choices about solvent selection, bromination temperatures, or purification steps echo through every kilogram produced. On many days, the difference between a lot that crystallizes cleanly and one that needs extra reprocessing boils down to these details. Standard practice calls for bromination under controlled cooling, followed by careful workup to avoid over-bromination or byproduct formation.

    Purity levels can noticeably influence the usability of the end material. We consistently target assay levels of 98% or higher, verified by HPLC and NMR, not just for appearance on paper but because lower purities have caused customers downstream headaches in the form of reaction quenching or unexpected side products. Even trace metal contamination from catalysts can interfere in certain pharma applications. That’s why filters and traceability logs see as much attention as reactor temperatures.

    Meaningful Specifications: More Than Just Numbers

    It’s tempting to treat chemical specification sheets as a box-ticking exercise, but years on the factory side show that true reliability means more than posting standard numbers. Particle size, while not always specified for this product, becomes relevant when customers handle the acid in multi-kilogram synthesis; too much powder fines and dust management turns into a struggle, too coarse and dissolution or reactivity slows. Moisture content can creep up in humid transport, even with proper drum liners, and cause clumps or early hydrolysis. That’s why our packaging crew stays strict about double-layer drum sealing, and why we maintain a reserve of fresh sample lots for emergency troubleshooting.

    Color and appearance tell their own stories. Genuine 2-Amino-3-Bromobenzoic Acid, as made in our reactors, carries a pale yellow to beige color, a function of both the synthetic route and post-reaction workup conditions. Heavily oxidized or impure lots run darker, and we’ve learned to spot adjustment needs by sight long before any instrument returns a reading.

    We occasionally receive requests for ultra-high-purity versions. The approach doesn’t just involve extra recrystallization: it demands alterations to filtration speed, recovery solvents, and additional drying cycles. Each tweak forces the team to consider yield-impact, labor time, and raw material management.

    Tangible Uses: What Goes On Beyond Our Factory Gates

    2-Amino-3-Bromobenzoic Acid serves as an intermediate for a select group of pharmaceuticals. Actual end-uses consistently reflect the value-add of specialized aromatic acids compared to their more basic benzoic cousins. Whether customers pursue the production of anti-inflammatory agents, APIs targeting rare diseases, or advanced materials with dye or pigment properties, the core value lies in the benzene ring, half-modified, half-ready for tailored derivatization. During customer audits, questions often center on how consistently we can maintain reactivity, which mirrors as “how likely are impurities to interfere with downstream synthesis?”

    Clients in our experience choose this molecule not as a generic alternative but for its precise reactivity profile. For instance, compared to 2-Aminobenzoic Acid, adding a bromine at the 3-position both shifts the electronics and introduces a reliable site for further modification. In cross-coupling protocols—Suzuki, Buchwald-Hartwig, Heck—the bromine position dictates yield and byproduct profile. Missing a critical impurity or shifting the bromine further along the ring changes not just yield, but safety and scalability as well.

    How 2-Amino-3-Bromobenzoic Acid Stands Apart from Similar Compounds

    From the day-to-day perspective of a chemical engineer, the differences between this compound and other aminobenzoic or bromobenzoic acids run deeper than labels. Each substitution pattern, even within the same isomeric family, imparts unique physical and chemical behaviors. For example, 4-amino-3-bromobenzoic acid, while similar on paper, tends to show different solubility and higher tendency to form hard-to-dissolve aggregates. Substituting at the ortho positions rather than ortho/meta substantially changes melting point, lightfastness for dyes, and — most critically for the pharma sector — compatibility with protecting-group strategies.

    Our teams have tracked repeated customer feedback where switching from another isomer to 2-Amino-3-Bromobenzoic Acid solved persistent problems in purification or process yield. Long-term partners value the reproducibility as well as the profile of side-products, especially in multi-step synthetic routes. Over the past decade, our in-house data show that the market demand for this specific molecule tracks closely with the rise of advanced cross-coupling chemistries at the R&D scale.

    Challenges in Manufacturing Consistency and Quality

    In practice, the biggest hurdle to consistency comes not from core chemistry, but from subtle shifts in ancillary conditions. One rainy season in the plant, atmospheric humidity crept into storage drums and pushed moisture content up enough to cause one batch to set hard in the drums—a lesson to triple-check desiccant condition and liner seals. Minor changes in utility supplies, particularly water quality, have also altered crystallization rates, shifting particle sizes and eventually affecting filtration speed. Each instance, while frustrating at the time, underscores the importance of constant process monitoring, not just end-point quality testing.

    Maintaining competitive and reliable yields remains a daily focus. Access to stable precursors and select halogenating reagents influences everything from production cost to waste profiles. On-the-ground experience tells us the volatility of global supply chains—bromine pricing, bulk organic acids, solvents like DMF—demands flexible planning and stock management. Sustainable practices, including solvent recovery and minimizing chlorinated waste, have stayed on our agenda, in part driven by both regulation and simple economics.

    End-User Support and Ongoing Collaboration

    As the original producer, our responsibility doesn’t end when the shipment leaves the plant. We notice a growing trend toward closer supplier-customer partnerships, particularly where technical trouble-shooting is concerned. Pharmaceutical teams regularly ask for collaborative runs with process samples so they can screen for potential trace impurities. Dye manufacturers share feedback on crystal behavior in solution, which informs our production team’s choice of drying temperature and packaging type.

    We remain mindful that downstream uses often dictate our own internal standards. A formulation team in the pharma sector once flagged a minor change in melting point as a cause for concern—driven by slight variations in batch crystallization rates during the drying phase. This case highlighted the value of traceable batch records and an open feedback cycle, not just as a check-box for audits, but to ensure quality meets real-world application demands.

    Technical support, built on direct communication between plant chemists and R&D partners, smooths out many potential bottlenecks. Customers know the names behind the emails and calls. This trust—gained over years of solving unique problems and staying open with shipment or production issues—reinforces why buyers prefer manufacturers with genuine experience.

    Upgrading and Streamlining the Manufacturing Process

    As demand for high-purity aromatic acids grows, our plant continually invests in both knowledge and equipment. Deciding between batch and continuous processes depends on flexibility needs and the scale of customer orders. In the last upgrade cycle, switching to more efficient filtration presses halved cycle times and allowed better retention of fine solids. This kind of real-world improvement, supported by feedback from both operations and end-users, keeps the product in line with ever-higher expectations from pharma and chemical R&D.

    Implementing digital monitoring has also translated to fewer deviations and tighter lot-to-lot control. We now archive key process parameters—pH during extraction, temperature, agitation speeds, transfer timelines—across all production runs. This digital backbone supports both troubleshooting and regulatory reporting, particularly for customers who audit not just the product, but the manufacturing culture driving it.

    The manufacturing environment rewards those who engage directly with both technical details and practical realities. Training production operators to recognize subtle shifts in product behavior—slightly sluggish filtrations, unusual color shading, a sudden uptick in lot moisture—often prevents problems before they leave the plant.

    Packaging and Handling: Lessons Learned Over Time

    Standard packaging for 2-Amino-3-Bromobenzoic Acid remains the fiber drum with double-layer liners, a decision born from too many cases of product caking or accidental moisture ingress. Some clients expressed interest in specialty containers, such as custom polyethylene drums or high-barrier bags, particularly for air- or light-sensitive applications. While each format adds complexity on our side, actual product stability during long-term shipping matters more than short-term cost savings.

    Handling in-plant and in client facilities works best with clear protocols, especially when unloading and weighing product for transfer into synthesis. Fines control makes a marked difference for worker comfort and safety. Staff wear dust-filtering masks as standard, and we recommend that all customers prepare a dedicated workspace for opening and transferring, given the tendency of fine powders to disperse.

    Improper packing or rough handling risks both caking and unwanted changes to flow character. Real-world experience with dropped drums or unsealed bags—sometimes the result of turbulent shipping routes—reminds us to reinforce routines in both plant and distribution warehouses. Inspection upon receipt at customer sites, with quick feedback to our team, closes the loop and drives incremental improvement.

    Compliance, Sustainability, and Responsibility

    True expertise in chemical manufacture emerges in how companies manage compliance without sacrificing day-to-day practicality. Our regulatory team works directly with production to ensure all documentation traces back both to raw material origin and shopfloor conditions. For a chemical like 2-Amino-3-Bromobenzoic Acid used in advanced markets, maintaining up-to-date information on handling hazards, safe use protocols, and downstream compatibility becomes non-negotiable. Regular internal safety drills and updated training support this goal.

    On the environmental side, efforts continue to optimize solvent recovery and waste minimization. The specialty chemicals sector faces constant scrutiny over emissions and effluent control; the plant monitors both to avoid local impacts and unexpected shutdowns. Engaging with third-party auditors, driven by both regulation and customer demand, incorporates outside perspectives and raises the bar for internal practices. Over the past few years, successful integration of more energy-efficient drying and reduced negative-impact solvents has already lowered our per-kilogram environmental footprint.

    Accepting customer audits and stabilizing supply only solves part of the puzzle. Product stewardship means anticipating questions from customers about exposure, reactivity in their target application, and end-of-life options. Having a plant team equipped to address these questions proves more effective than relying solely on sales channels or generic technical bulletins.

    Looking Forward: Innovation Driven by Real-World Collaboration

    Innovation in aromatic acid manufacture doesn't come from theoretical advances alone. Feedback loops between our operations and customer R&D have pushed the plant to explore both new crystallization protocols and alternative synthetic routes. In one instance, collaboration with a pharma process team suggested a solvent swap that reduced impurities and shortened workup, saving days in scale-up scenarios. The plant view keeps such improvements grounded—not just in hits to the bottom line, but in reduction of rejected batches or improvement in lot approvals.

    Experience demonstrates that direct dialogue, batch transparency, and a practical attitude to change—rather than rigid adherence to old protocols—leads to both higher product value and stronger trust. Open exchange over even minor lot challenges, especially through real examples and batch histories, ensures reliability when it matters most.

    As a chemical manufacturer, the real value delivered by 2-Amino-3-Bromobenzoic Acid comes not just from structure or specification sheets, but from comprehensive attention to process, people, and ongoing support. This approach, rooted in everyday experience and continuous learning, forms the backbone of why our partners return—seeking not only high-purity product, but the confidence that comes when challenges are handled by those who shape the compound from raw material to final drum.