Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Bromo-2-Nitrobenzoic Acid

    • Product Name 4-Bromo-2-Nitrobenzoic Acid
    • Alias 4-Bromo-2-nitrobenzoic acid
    • Einecs 214-486-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    914771

    Product Name 4-Bromo-2-Nitrobenzoic Acid
    Cas Number 50813-99-9
    Molecular Formula C7H4BrNO4
    Molecular Weight 246.02 g/mol
    Appearance Yellow to light brown solid
    Melting Point 220-225°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Boiling Point Decomposes before boiling
    Purity Typically ≥98%
    Synonyms 2-Nitro-4-bromobenzoic acid
    Density 1.892 g/cm³
    Smiles C1=CC(=C(C=C1Br)C(=O)O)[N+](=O)[O-]
    Inchi InChI=1S/C7H4BrNO4/c8-4-1-2-5(7(10)11)6(3-4)9(12)13/h1-3H,(H,10,11)
    Storage Conditions Store at room temperature, in a dry and well-ventilated place
    Ec Number 610-075-7

    As an accredited 4-Bromo-2-Nitrobenzoic Acid 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-Nitrobenzoic Acid, labeled with hazard symbols and product information.
    Shipping **Shipping Description:** 4-Bromo-2-Nitrobenzoic Acid is shipped in tightly sealed, chemical-resistant containers, labeled according to hazardous material regulations. It is transported under controlled temperature and protected from moisture, light, and physical damage. Proper documentation and Material Safety Data Sheet (MSDS) accompany each shipment to ensure safe and compliant handling during transit.
    Storage 4-Bromo-2-Nitrobenzoic Acid should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Avoid exposure to moisture and incompatible materials such as strong bases and reducing agents. Proper labeling and secondary containment are recommended to prevent accidental spills or contamination.
    Application of 4-Bromo-2-Nitrobenzoic Acid

    Applications of 4-Bromo-2-Nitrobenzoic Acid in Industrial Manufacturing

    4-Bromo-2-Nitrobenzoic Acid serves as a critical raw material in several specialty chemical production streams. Its unique molecular scaffold introduces bromine and nitro substituents facilitating selective transformations in downstream synthesis. The following sectors integrate this compound into their manufacturing processes under strict compliance standards and controlled dosage protocols to produce advanced intermediates and end-user products.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers integrate this compound as a key intermediate for generating substituted benzoic acid derivatives used in API synthesis, especially for anti-inflammatory and anti-bacterial drug candidates. The bromine and nitro groups offer reliable points for subsequent amination, reduction, or halogen exchange steps conducted under cGMP-compliant settings to assure critical quality attributes in regulated drug substance manufacturing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and EP monograph requirements for pharmaceutical intermediates
    • EU and US FDA regulatory guidelines for starting materials
    • ISO 9001 Quality Management Systems for chemical manufacturing

    Typical usage ratio

    • Batch synthesis protocols apply 4-Bromo-2-Nitrobenzoic Acid at 0.8–1.2 molar equivalents per target molecule. Ratios adjust depending on downstream substitution yield and impurity profile control.

    Downstream process integration

    • Material enters at step one or two of multistage API intermediate synthesis, commonly following coupling or esterification with protected amino groups. It undergoes further transformation via metal-catalyzed reductions or nucleophilic aromatic substitutions.

    Final product types

    • Sulfa drug intermediates
    • Nonsteroidal anti-inflammatory drug (NSAID) intermediates
    • Quinolone precursor fragments
    • Specialty contract-manufactured generic APIs

    2. Agrochemical Synthesis

    Agrochemical companies utilize 4-Bromo-2-Nitrobenzoic Acid to produce pre-emergent and post-emergent herbicide intermediates and selective fungicidal agents. The compound enters chlorination or methylation reactions to build novel aryl benzoic acid analogues providing crop protection. Formulation chemists monitor residue profiles and reaction completeness to ensure compliance with agricultural actives regulations during scale-up and continuous process operation.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius requirements for pesticide active ingredient precursors
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products Regulation)
    • ISO 9001 process traceability for agrochemical raw material handling
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EC 1907/2006)

    Typical usage ratio

    • Applied at 1.0–1.5 molar equivalents relative to target ring system, depending on desired selectivity and conversion in halogenation/methylation operations.

    Downstream process integration

    • Introduced in the core structure formation of benzoic acid-based herbicides or fungicidal actives via metal-catalyzed coupling and selective oxidations using continuous flow or batch reactors under ex-proof conditions.

    Final product types

    • Benzoic acid-derived herbicidal actives
    • Triazole fungicide intermediates
    • Precursor to substituted aryloxyacetic acids
    • Active ingredient blends for broad-spectrum plant protection

    3. Dyes and Pigments Industry

    Specialty dye producers deploy this compound in synthesizing azo and anthraquinone colorants with enhanced stability and specific absorption profiles. Its nitro and bromo functionalization facilitates regioselective coupling and diazotization during chromophore extension, yielding pigments for plastics, fibers, and coatings. The batch-optimized process ensures low contaminant carryover and compliance with global colorant standards.

    Industry compliance standards

    • EN 71-3: Safety of Toys — migration of certain elements (for pigment safety in consumer goods)
    • OEKO-TEX Standard 100 for textile chemicals
    • REACH regulations on restricted aromatic amines
    • ISO 9001 for colorant production management

    Typical usage ratio

    • Applied between 0.5–1.5 equivalents per target pigment precursor, adjusted by required color depth, application concentration, and byproduct suppression efficiency.

    Downstream process integration

    • Material introduced in diazotization or bromination steps during synthesis of high-purity dye intermediates, followed by coupling with aromatics to finalize pigment backbone; protocols integrate solvent recovery and batch analytics.

    Final product types

    • Disperse dyes for polyester and polyamide fibers
    • Azo pigment intermediates
    • Solvent-stable colorants for plastic compounding
    • Industrial inks and coatings with UV stability

    4. Specialty Polymer Modifier Manufacturing

    Polymer manufacturers incorporate the material to introduce functionalized aromatic groups during chain modification or crosslinking in high-performance plastic formulations. The compound’s substituents participate in step-growth polymerizations and nucleophilic aromatic substitution, enabling targeted modification of resin architectures for electronic and engineering applications. The raw is strictly handled under polymer-grade impurity protocols to preserve dielectric and thermal behaviors.

    Industry compliance standards

    • UL 94 flammability standards for polymer materials
    • ISO 9001 production batch documentation
    • RoHS Directive 2011/65/EU for restricted substance use in electronics plastics
    • EU Regulation (EC) No 1935/2004 for materials in food contact, if applicable

    Typical usage ratio

    • Incorporated at 0.1–0.8% by weight of resin, tuned by performance requirement, crosslinking degree, and targeted mechanical property profile.

    Downstream process integration

    • Injected into polymer batch at modifier blending stage, undergoes in-situ aromatic substitution or radical-initiated grafting at melt or solution phase, with subsequent extrusion, pelletizing, or molding.

    Final product types

    • High dielectric plastics for electrical housings
    • Heat-resistant polymer films
    • Crosslinked engineering resin masterbatches
    • Functionalized plastic additives

    5. Advanced Electronic Chemical Synthesis

    The electronics sector employs this compound in synthesizing bench-stable intermediates for liquid crystal display (LCD) materials and other advanced aromatic compounds needed for semiconductors. Its functional groups enable further selective reactions under tightly controlled process conditions and purity control, ensuring compatibility with microelectronic manufacturing protocols and preventing dopant or residue contamination.

    Industry compliance standards

    • IEC 62474 for substances in electronics
    • IPC-4101 for base materials in printed boards
    • ISO 14001 for environmental management in electronics chemical processing
    • JEDEC JESD625B for handling of electronic grade materials

    Typical usage ratio

    • Applied at 0.2–0.7 equivalents relative to target functional molecule; adjusted based on reactivity with aryl halide/coupling partners and desired purity.

    Downstream process integration

    • Material deployed at halogenation or nitration stage to prepare mesogenic core intermediates. These then participate in Suzuki or Stille cross-coupling for complex functional group assembly used in display materials.

    Final product types

    • Liquid crystal monomer precursors
    • OLED and LCD display base substrates
    • Semiconductor chemical intermediates
    • Specialty electronic resins for sensor applications
    Free Quote

    Competitive 4-Bromo-2-Nitrobenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    4-Bromo-2-Nitrobenzoic Acid: Experienced Production for Reliable Applications

    A Manufacturer’s Perspective on 4-Bromo-2-Nitrobenzoic Acid

    Every chemist in this industry knows the value of consistency. Our experience producing 4-Bromo-2-Nitrobenzoic Acid has shown us that the core foundation for a sustainable business lies in integrity, clarity, and a focus on the end-use requirements of technical customers. On our shop floor, workers encounter first-hand the challenges of reproducible crystallinity, color uniformity, and reliable delivery timelines. We have come to trust that good chemistry is only as strong as every batch that leaves the plant.

    What Sets 4-Bromo-2-Nitrobenzoic Acid Apart

    Our product, CAS 5081-87-8, has been at the core of our aromatic acid manufacturing for years. Teams at our facility have developed an intimate familiarity with its demanding synthesis. They know the difference in handling requirements when compared to simpler halobenzoic acids. Starting from ortho-substituted aromatics, we select only materials with correct impurity profiles. Controlling the bromination so it doesn’t trigger unwanted di-substitution takes daily attention—not just at the reactor, but all the way through to the final drying and storage.

    Many customers ask how this compound diverges from plain benzoic acids or isomers with other functional groups. From our work developing synthetic pathways, it is clear: that nitro and bromo substitution in the ortho and para positions result in distinct reactivity. For example, replacement attempts on the bromine site react differently depending on nitro group orientation. With this product, selectivity isn't only about process controls but also about knowing the subtle chemistry at play.

    Specifications That Reflect Real-World Demands

    Clients count on purity levels not just because their analysts demand it, but because these tiny differences drive yields and downstream impurity profiles. In recent years, we’ve seen a shift: quality inspections have become far more stringent for pharmaceutical precursor grades. Where a 98% assay once sufficed, requests for 99% and higher are now the standard for many applications. We don’t hide behind such numbers. Every batch is sampled across the drying trays, and data is logged so that future reference points are available for process improvement.

    Melting point consistency also matters in practical terms. We keep records of every thermal analysis. Any deviation can signal a process hiccup. Years ago, we worked with a partner who had issues with two-degree variations between lots from a different manufacturer. After switching to our regularly verified process, their crystallization yields stabilized, undermining the notion that fine details don’t matter in bulk production.

    End Uses: Not Just a Lab Curiosity

    4-Bromo-2-Nitrobenzoic Acid is more than a catalog entry—it’s a backbone in the development of high-value intermediates used in crop protection, pharmaceuticals, and specialty pigment synthesis. We have worked with customers developing novel anti-inflammatory APIs where our acid acts as the substrate for Suzuki cross-couplings. Some formulators rely on it as a building block in the manufacture of fluorescent dyes. The carboxylic acid moiety enables coupling reactions, while the reactivity of the bromine and nitro groups unlocks avenues into further functionalization.

    We’ve tracked several research projects over the years from partner institutions, watching as this aromatic acid unlocks synthetic possibilities that other benzoic acid derivatives simply do not provide. In our records, we see patents and publications describing ring-opening reactions, modulated coupling efficiencies, and selective hydrogenations. Feedback tells us that downstream users benefit from knowing precisely what is coming in with each batch—so we keep impurities tightly controlled, based on both our own analytics and customer-driven specs.

    Manufacturing Practices Rooted in Experience

    There’s no shortcut to process optimization. Over time, we optimized our conversion yields by tweaking temperature ramps, solvent ratios, and the rate of bromine addition. Earlier runs delivered inconsistent particle size—one lesson learned was the importance of controlled agitation throughout the crystallization step. With 4-Bromo-2-Nitrobenzoic Acid, even drying rates affect solubility downstream, especially for HPLC quantitative users. We now document every critical step, understanding which levers result in a finished product that meets the grade.

    Multi-step syntheses build up impurity profiles—sometimes invisible to standard tests, but not to downstream chemistry. We routinely screen for halogenated byproducts, trace isomers, and moisture. Purity isn’t a slogan; it’s an operational checkpoint addressed at each filtration and wash stage. The drive to reduce variable residues led us to source advanced filtration material and adjust solvent polarity. We also invested in spectroscopy for final confirmation of structure and identity, going beyond what many basic suppliers might provide.

    Strict Quality Benchmarks

    Most users approach us with their own needs—one chemist might prioritize low palladium residue, while a pigment processor may look for reduced iron content. Our QA operators work side-by-side with R&D and production to set practical acceptance limits, not just for the lot in question but also for trends that emerge month to month. For pharmaceutical intermediates, we keep a reference stock. Regular cross-testing with external labs confirms our in-house data.

    Particle size and solubility sometimes cause problems for specific customers. Our hands-on work has taught us the importance of sieving and milling before final packing. Reports from one pigment application customer showed how inconsistent particle sizes led to flawed coloration. We altered our milling approach and set up end-use feedback lines that allow us to respond to these needs in real time.

    Reliability—A Result of Investment and Continuous Learning

    Long-term customers stick with a manufacturer who proves able to troubleshoot, anticipate needs, and adapt to feedback. When an inquiry comes in for a custom specification, our team sits down to review past batches, evaluate current capacity, and recommend solutions. In some cases, this means tweaking crystal habit or handling protocols. Old challenges, like solvent recovery issues and scaling up batch sizes, led us to rethink plant layout and invest in robust thermal control systems.

    Experienced teams know that keeping documentation straight isn’t a bureaucratic nuisance; it allows for root-cause analysis if a deviation occurs. Over the last decade, as batch numbers and lot tracking have grown in complexity, we implemented a digital backbone for every step from raw materials to finished goods. Traceability is not an option—it underpins customer trust and regulatory compliance.

    Positioning in the Broader Market: Not All 4-Bromo-2-Nitrobenzoic Acids are Built Equally

    Buyers looking for 4-Bromo-2-Nitrobenzoic Acid can find offers at nearly every price and quality point. Our work in the field has demonstrated that, despite the presence of many suppliers, few offer the manufacturing depth and transparency we maintain. Traders and resellers often cannot guarantee origin, traceability, or post-shipment support. On several occasions, we’ve been approached by end users who encountered major setbacks due to unexplainable impurities traced to non-manufacturer sources.

    Over time, customers learn the hard way that a lower price rarely compensates for lost batches or unpredictable performance. Our plant’s scale provides cost competitiveness, but never at the expense of core quality or data transparency. When supply chains grow tight, we maintain stocks rather than cut corners on process verification or skip critical analyses. We learned early that the market punishes shortcuts; experience has shown a steady hand and open lines solve real-world problems.

    Safety, Environmental Responsibility, and Regulatory Alignment

    Anyone involved in halogenated aromatic acids recognizes the potential hazard profile. Over years of operation, we’ve instilled a culture of safety and risk management grounded in reality. Our facility meets strict environmental controls, with scrubbers, effluent treatment, and documented incident reporting embedded in normal operation. All chemicals are handled with the view that worker safety and environmental compliance come before volume or speed.

    Waste reduction and resource efficiency reflect a commitment to the community as well as the customer. Initiatives to recover solvents and minimize hazardous waste are not marketing slogans—over years, small projects add up to real impact. For a product like 4-Bromo-2-Nitrobenzoic Acid, proper control not only protects the workforce, but ensures supply is never interrupted due to regulatory missteps. We prioritize processes that have withstood audit scrutiny and keep in contact with regional authorities to confirm ongoing compliance.

    Difference From Other Comparable Chemicals and Analogues

    From the shop floor out to the R&D bench, our team repeatedly compares this acid against other nitro- or bromo-substituted aromatic acids. It stands distinct by offering a combination of two activating substituents in controlled positions, enabling selectivity for further aromatic substitutions not possible with many other derivatives. Unlike mono-substituted acids or those bearing less reactive halogens, synthetic chemists use our product to unlock demanding coupling processes and controlled reductions. Its handling characteristics—moisture content, solid-state stability, filtration time—differ plainly in side-by-side comparison, as any operator grinding 4-Nitrobenzoic versus 4-Bromo-2-Nitrobenzoic acid will quickly realize.

    Several past customers started with a bromo- only or nitro- only acid, found themselves struggling with low conversion in palladium-catalyzed reactions, and came back for this dual-substituted version. We run ring-substitution tests in-house, logging conversion rates and purity before and after. For a pigment manufacturer we partnered with, almost undetectable traces of a meta isomer from a third-party supplier led to a product recall, revealing why certified identification from the manufacturer is essential.

    Supporting Our Partners at Every Step

    Our focus is always on genuine partnership—from technical questions before the order, through to after-sales follow-up. Researchers bring unique project needs, and we respond with technical insight earned from years of hands-on handling. There is transparency in every specification, with data and literature available for the properties most relevant to specific applications.

    We stay available to discuss process adjustments and help troubleshoot scale-up issues. Sometimes a batch doesn’t behave as predicted, and a flexible team with real manufacturing background can suggest practical changes—whether a slight increase in recrystallization wash volume to improve downstream solubility, or advice on controlling exotherms in coupling reactions. All this comes not from a playbook but from years working with 4-Bromo-2-Nitrobenzoic Acid at kilogram and ton scale.

    Unpacking Demand Drivers and Looking Ahead

    Market demand for this acid reflects growth across pharmaceuticals, crop science, and specialty materials. As more clients push forward with innovative synthetic routes, feedback returns to us through technical reports, performance notes, or even requests for impurity studies on new byproducts. We see the best outcomes when users engage early—sharing what they need each time so our process can support those goals. Our plant’s flexibility enables us to respond to shifting requirements quickly, adjusting batch sizes, particle characteristics, or analytical support as needed.

    The role of this product will keep evolving, and we invest accordingly. Experience covering decades has proven that companies outlive trends by focusing on real requirements and understanding the deeper chemistry that underlies success for our customers. For new projects, we offer insight into alternate synthetic routes, best practices for handling, or analytical tips beneficial to both experienced users and those just starting out with this compound.

    The Value of Direct Manufacturer Relationships

    People trust factories with experience. Over the years, we’ve seen customer projects recover from otherwise fatal setbacks because a manufacturer stood by with process knowledge, a willingness to investigate, and the records to support corrective action. Distributors might offer more products but lack the connection to origin and accountability. Our team puts in the hours, day and night, understanding what it takes to guarantee a steady supply—and a partner who will still be answering the phone long after a delivery is made.

    Trust matters. Reliability grows out of years delivering not just chemical, but technical value. We keep our ears open to customer feedback—auditing results, real-world process successes and failures, and evolving use cases all shape how we improve. Our commitment is visible not only in the technical specifications but equally in our willingness to share what we know, deliver what we promise, and learn from every new challenge a customer brings forward.

    Conclusion: Why Source 4-Bromo-2-Nitrobenzoic Acid From an Experienced Manufacturer

    Relying on practical experience and ongoing investment, we consistently produce 4-Bromo-2-Nitrobenzoic Acid batches that underpin complex chemistry in challenging industries. Our operation has weathered volatile supply chains, regulatory shifts, and advancing customer requirements. This stability comes from an ingrained respect for process discipline, frank communication, and constant learning.

    With us, you don’t just buy a chemical, you gain a collaborative partner committed to your long-term success—because every batch is a reflection of what matters most: skilled people working to earn customer trust, one reaction and delivery at a time.