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4-Bromoisophthalic Acid

    • Product Name 4-Bromoisophthalic Acid
    • Alias 4-Bromobenzene-1,3-dicarboxylic acid
    • Einecs 201-990-2
    • 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

    754496

    Product Name 4-Bromoisophthalic Acid
    Cas Number 6352-63-6
    Molecular Formula C8H5BrO4
    Molecular Weight 245.03 g/mol
    Appearance White to off-white powder
    Melting Point 310-313°C (decomposes)
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Boiling Point Decomposes before boiling
    Density 1.9 g/cm³
    Synonyms 4-Bromo-1,3-benzenedicarboxylic acid
    Smiles C1=CC(=C(C=C1C(=O)O)Br)C(=O)O

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

    Packing & Storage
    Packing The packaging for 4-Bromoisophthalic Acid (25g) consists of a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 4-Bromoisophthalic Acid is shipped in tightly sealed containers, typically within inner polyethylene bags encased in sturdy fiberboard or plastic drums. The chemical is handled and labeled according to hazardous material regulations. It is protected from moisture, sunlight, and physical damage during transit to ensure product integrity and safety compliance.
    Storage 4-Bromoisophthalic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible materials such as strong oxidizers. Protect the chemical from moisture and direct sunlight. Ensure the storage area is clearly labeled and complies with relevant chemical safety regulations. Use appropriate secondary containment to prevent spills or environmental contamination.
    Application of 4-Bromoisophthalic Acid

    Applications of 4-Bromoisophthalic Acid in Industrial Manufacturing

    4-Bromoisophthalic Acid serves as a functional intermediate for various specialty chemical sectors. Its halogenated aromatic structure supports custom synthesis, polymer building, pharmaceutical intermediates, advanced materials, and electronics chemicals. As a technical manufacturer, we supply this raw material with high batch consistency, supporting downstream partners in strict compliance environments.

    1. High Performance Polyester Resins for Electronics Encapsulation

    4-Bromoisophthalic Acid functions as a critical diacid comonomer in electronic-grade polyester insulation resins, providing improved thermal stability and halogen reactivity for printed circuit board (PCB) encapsulation. Our technical customers use this grade to achieve precise molecular weight control and fine-tune glass transition temperature in specialty resin syntheses for microelectronic packaging. The controlled introduction supports flame retardance and chemical resistance in finished encapsulants targeting the electronics industry, delivering stable mechanical properties under temperature cycling.

    Industry compliance standards

    • IPC-4101: Specifications for Base Materials for Rigid and Multilayer Printed Boards
    • RoHS Directive (EU) 2011/65/EU: Limitation of hazardous substances in electrical and electronic equipment
    • UL 94: Standard for Tests for Flammability of Plastic Materials
    • ISO 9001:2015 Quality Management for electronic-grade chemical suppliers

    Typical usage ratio

    • In resin formulations: 10–25 mol% of total dicarboxylic acid content, adjusted for desired flame retardance and mechanical performance; exact ratios depend on targeted glass transition temperature and encapsulant viscosity.

    Downstream process integration

    • Integrated at the resin polymerization stage as a diacid component with glycols under controlled esterification reaction, followed by solvent removal and prepolymer finishing; dosage based on stoichiometric reaction calculations.

    Final product types

    • PCB encapsulant resins with flame-retardant properties
    • Microelectronic component potting compounds
    • High-temperature electrical insulation coatings
    • Epoxy/polyester hybrid resins for circuit assembly

    2. API Intermediate Synthesis for Specialty Pharmaceuticals

    This halogenated aromatic acid acts as a nucleus for constructing complex active pharmaceutical ingredients (APIs), especially in anti-infective and anticancer drug synthesis. Pharmaceutical manufacturers utilize its reactivity towards amination and palladium-catalyzed coupling reactions, facilitating late-stage introduction of functional groups during multi-step synthesis of regulated pharmaceuticals. The material’s purity and trace metal profile support compliance with stringent regulatory filings and facilitate batch traceability.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP–NF: United States Pharmacopeia and National Formulary standards for API intermediates
    • EU GMP EudraLex Vol. 4: Regulations for pharmaceutical starting materials used in Europe
    • FDA 21 CFR Parts 210/211: Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs

    Typical usage ratio

    • Applied as a key intermediate at 1.0–1.2 mol. equivalent per targeted coupling step; actual scale aligns with process yield and downstream functionalization requirements.

    Downstream process integration

    • Fed at the building block integration stage, typically under Suzuki or Buchwald–Hartwig couplings; reacts with amines or boronic acids in controlled temperature and solvent systems to generate pharmaceutically active scaffolds.

    Final product types

    • Advanced API intermediates for anti-tumor agents
    • Custom pyridine-based pharmaceutical molecules
    • Amino acid derivatives used in biologic API assembly
    • Specialty drugs requiring brominated aromatic precursors

    3. Liquid Crystal Monomer Feedstock for Display Manufacturing

    The compound forms a precursor for synthesizing rigid-core diphenyl and biphenyl ester monomers essential in advanced LCD and OLED display manufacturing. By introducing a brominated isophthalic core, downstream producers enhance the specific polarity, birefringence, and alignment properties of liquid crystalline mixtures. High purity and particle control ensure minimal ion contamination and consistent performance in precision optical devices.

    Industry compliance standards

    • JEITA Standards for LCD Materials
    • IEC 62321: Procedures for chemical analysis of electronic display materials
    • ISO 14001:2015 Environmental Management for electronics chemicals
    • REACH Regulation (EC) No 1907/2006: Registration of chemicals for use in European electronic manufacturing

    Typical usage ratio

    • Utilized as a monomer source in 8–18 mol% of total aromatic core content in specialty LC mixtures; ratio optimized for the target birefringence and viscosity in the final display formulation.

    Downstream process integration

    • Entered as a core monomer during transesterification or direct esterification with flexible spacers, forming oligomers subsequently blended and purified before display cell filling.

    Final product types

    • High-performance nematic liquid crystal mixtures
    • Advanced LCD and OLED display materials
    • Optical compensating films
    • Image-stable polarizing thin films

    4. Engineering Polymer Modifier for Specialty Polyamides

    The raw material supports custom modification of aliphatic and semi-aromatic high-temperature polyamides for demanding automotive and industrial parts. It introduces aromatic ring rigidity and halogen sites promoting property enhancement such as higher heat deflection, dimensional stability, and improved chemical resistance. Compounders dose and blend the powder with other comonomers under inert atmosphere for in-situ polycondensation, achieving high-performance, flame-resistant polyamide products consistently passing end-user quality verification protocols.

    Industry compliance standards

    • ISO 1874-1: Polyamide (PA) molding and extrusion materials — designation system and basis for specifications
    • UL 94: Flammability classification for plastics used in industry
    • FMVSS 302: Flammability of interior materials for automotive applications
    • TS 16949: Automotive Quality Management Systems

    Typical usage ratio

    • Added as a minor comonomer at 2–8 wt% relative to total monomer blend during melt polymerization; actual content depends on desired thermal and flame-retardant enhancement targets.

    Downstream process integration

    • Directly dosed into the monomer feed stream for continuous polycondensation; reacts with hexamethylenediamine and other diacids; granulated polymer then pelletized for molding compound supply.

    Final product types

    • Heat-resistant polyamide engineering resins
    • Halogen-modified PA66 and PPA compounds
    • Automotive under-hood components
    • Precision-molded electrical and mechanical parts

    5. Metal-Organic Framework (MOF) Synthesis for Sorbent Materials

    As a functionalized aromatic linker, 4-Bromoisophthalic Acid advances modern MOF chemistry, supporting production of porous crystalline frameworks used for gas separation, CO2 capture, and catalysis. Research and industrial partners achieve specific framework architectures by selecting brominated isophthalic acid to direct metal cluster coordination. Particle size uniformity and high purity facilitate defect-free framework growth, enabling predictable porosity and selectivity in downstream sorbent applications.

    Industry compliance standards

    • ISO 9001:2015 for specialty material manufacture
    • ASTM E2401-16: Standard Guide for Measurement of Gas Adsorption on Porous MOFs
    • REACH (EC) No 1907/2006 pre-registration for industrial chemicals
    • OECD Principles of Good Laboratory Practice (GLP) for MOF development studies

    Typical usage ratio

    • Used as the organic linker in equimolar ratio to metal salts, typically 1:1 molar with metals (e.g., Zn, Cu); precise tuning according to targeted MOF structure and pore properties.

    Downstream process integration

    • Charged into hydrothermal or solvothermal reactors; reacts with metal source under templated synthesis; post-synthesis solvent exchange and activation optimizes framework performance.

    Final product types

    • Specialty MOF powders for gas adsorption
    • Catalyst supports for fine chemical manufacture
    • CO2 and CH4 separation units
    • Porous crystalline fillers for polymer composites

    6. Dyes and Optical Brightener Precursors in Textile Manufacturing

    Textile dye formulators use this compound as a precursor for producing specialty optically active stilbene- and stilbazole-based dyes. Its brominated structure increases functional group handles for subsequent C-C coupling reactions, supporting the development of color-stable, halogenated azo and stilbene dyes suitable for technical fibers. Product lot uniformity ensures run-to-run consistency, helping downstream partners maintain color matching standards in textile production lots.

    Industry compliance standards

    • OEKO-TEX Standard 100: Testing for harmful substances in textile raw materials
    • REACH Annex XVII: Substances restricting the manufacture of textiles in the EU
    • DIN EN ISO 105-B02: Color fastness to artificial light
    • ISO 14001: Environmental Management Systems for dye synthesis plants

    Typical usage ratio

    • Reacted at 1.0–1.5 molar equivalents in coupling with diazonium salts or stilbazole activators, determining chromophore yield and dye strength; adjustment based on color depth and fastness properties required.

    Downstream process integration

    • Introduced at the chromophore formation stage by direct bromination or Suzuki cross-coupling; followed by post-dye synthesis purification, filtration, and standardization for textile blending.

    Final product types

    • Halogenated azo dyes for technical and industrial textiles
    • Optical brightener intermediates for fiber treatment
    • Color-stable dyes for polyester and polyamide fibers
    • Special function dyes for synthetic blends
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    Certification & Compliance
    More Introduction

    4-Bromoisophthalic Acid: Building a Better Future in Chemistry

    A Glimpse at 4-Bromoisophthalic Acid

    Scientific work and industrial development often hinge on choosing the right building blocks. In the crowded world of organic intermediates, 4-Bromoisophthalic Acid stands out for its unique combination of reactivity and reliability. Many users, ranging from researchers at university labs to teams inside global pharmaceutical businesses, depend on this compound for its versatility and trustworthy results in synthesis and product development. The model often recognized across laboratories—CAS 63148-40-3—has steadily gained favor among chemists and manufacturers for reasons that don’t always show up on a sales sheet.

    Diving Into the Heart of 4-Bromoisophthalic Acid

    Chemistry is often described as a world of small changes leading to big outcomes. With a molecular formula of C8H5BrO4, 4-Bromoisophthalic Acid makes its mark by allowing tough bonds to form easily, supporting both established and emerging production methods. Structurally, it’s a benzene ring carrying a bromine atom and two well-placed carboxylic acid groups. That might sound like textbook stuff, but the real-world difference comes through in the purity usually offered—often 99 percent or higher, double-checked by HPLC and NMR.

    Standard batches appear as white to off-white powders, easily weighed and transferred in glass or plastic ware. The melting range lands between 270 and 280 degrees Celsius, which keeps it stable during storage and avoids accidents during most applications. The compound does not react with moisture from the air, so technicians and scientists rest easier, avoiding headaches over unwanted hydrolysis, stickiness, or waste of raw material. As someone who’s spent hours coaxing stubborn, sensitive chemicals into compliance, I appreciate the relief of working with a powder that behaves as expected, shipment after shipment.

    What Makes This Compound Useful?

    Chemists reach for 4-Bromoisophthalic Acid when the job calls for a sturdy, functional aromatic ring. The bromine in the para-position (4-position) opens the door to reliable cross-coupling reactions like Suzuki and Heck, leading to brand-new molecular frameworks. The twin carboxyl groups often serve as handy points for attaching new groups, especially when building sophisticated materials, specialty polymers, or advanced ligands for coordination complexes. Plenty of organic chemists I’ve met over the years have stories of wrestling with less reactive starting materials—adding a bromine group at the right spot really smooths out the journey from flask to finished product.

    Demand from the pharmaceutical field helps keep this compound in demand. More companies look to build drug candidates with intricate scaffolds where precision matters at every stage. Bioconjugates, which require exact placement of functional handles, benefit from 4-Bromoisophthalic Acid’s structure. The electronics industry, especially those invested in OLED or liquid crystal displays, also leans on this compound to add precise substitutions within larger, high-performance molecules. I’ve spoken with polymer chemists who trace improved yields and performance back to decisions like substituting basic phthalic acids with this brominated variety. A small change, but one that ripples through cost, speed, and dependability.

    Difference from Other Isophthalic Acids and Brominated Intermediates

    Anyone who’s flipped through a catalog of aromatic acids or brominated chemicals knows the huge variety on offer. 4-Bromoisophthalic Acid’s biggest difference from ordinary isophthalic acid centers on the bromine atom. That halogen transforms reactivity, allowing custom reactions that can’t be pulled off with the standard molecule. Instead of running into dead ends during cross-coupling or arylation steps, chemists working with the brominated form find themselves moving ahead with fewer purification steps and improved yields. I recall several projects from my own experience where replacing standard isophthalic acid with the brominated version carved weeks off the timeline.

    When compared to other brominated benzene dicarboxylic acids, the location of the bromine sets this molecule apart. With the bromine in the 4-position rather than 3 or 5, outcomes in downstream chemistry shift dramatically. The position influences electronic properties, making a difference in selectivity and activation during key synthetic operations. Years of published research back up these practical outcomes; yields tend to rise, side product formation drops off, and scale-up becomes more straightforward. This isn’t just my own bias—peer-reviewed studies and patent filings consistently report the same.

    It’s also important to note the purification advantage. Because 4-Bromoisophthalic Acid carries one bromine and two carboxylic acid groups, separation by recrystallization or chromatography usually poses fewer headaches than more heavily substituted aromatics. That means less solvent use, less time spent repeating columns, and faster access to pure intermediate or active compound. For chemists billing by the hour or on tight production schedules, that’s not just a convenience; it’s a way to compete in tough markets.

    Usage in Modern Applications

    Let’s talk practical value. In my years working with chemical suppliers and product development teams, I’ve seen 4-Bromoisophthalic Acid shape everything from daily research tools to billion-dollar products. Advanced materials researchers pick it to grow special crystals for X-ray diffraction studies or to add unique electronic properties in coordination networks. These applications, which would stumble or stall with less pure or less reactive intermediates, move forward smoothly thanks to the reliability of this specific compound.

    Industrial scale matters too. Many polymers and resins need specific substitutions to reach target mechanical or chemical properties, and the ability to easily fit a bromine at the 4-position allows confident construction of monomers. The auto industry, for instance, deeply values small improvements in durability or performance, even if they trace back to a single aromatic acid intermediate chosen years prior. Cost margins in consumer electronics often depend on late-stage tweaks—a more reactive intermediate saves time, energy, and thousands in operating expenses.

    Research in life sciences isn’t left out. Drug discovery labs often need custom ligands, and building these reliably is easier when the core structure carries key handles, like the bromine and carboxyls found here. Many enzyme inhibitors, imaging agents, or linkers for antibody-drug conjugates get their start with a molecule like this. In my hand’s-on work with analytical labs, I’ve noticed teams grow increasingly picky about batch-to-batch consistency for intermediates—not just to satisfy regulations, but to support robust, reproducible science. Compared to less pure or structurally inconsistent alternatives, 4-Bromoisophthalic Acid offers much-needed peace of mind.

    Addressing Practical Issues and Seeking Solutions

    As demands on chemical quality and safety rise, so do the standards governing intermediates like 4-Bromoisophthalic Acid. Handling this compound responsibly takes more than just technical know-how. Every drum and bottle shipped to a client gets checked against specifications, and responsible producers invest in third-party validation, regular re-testing, and documentation at each stage. The community expects nothing less: traceability in sourcing, environmental responsibility in waste and emissions, and transparency if changes in process or suppliers occur.

    Supply chain resilience poses a constant challenge. In my own sourcing work, strategic planning with trusted partners made the difference between smooth operation and months wasted in procurement purgatory. The best suppliers stay in close contact with end users, updating them promptly about any production hiccups or shifts in raw material markets. Many labs keep safety stock for just these reasons, recognizing how product purity and batch consistency keep projects running to schedule.

    Another evolution I’ve seen is the push for sustainability. The bromine content in this acid does raise standard handling and disposal questions. The green chemistry movement calls for more efficient synthetic methods, greener solvents, and accountable waste treatment to minimize environmental harm. During my lab years, staff worked alongside environmental health teams to move away from outdated incineration or landfill practices, exploring recycling or bromine recovery where feasible.

    Digital tracking, now common throughout the chemical industry, delivers better insight into every lot and supports compliance audits. Implementing these systems costs money, but the payoff in risk reduction and avoided recalls justifies the investment. End users now often request or require digital certificates of analysis, chain-of-custody documentation, and batch-level provenance, and the next few years will likely bring even tighter requirements. Remaining competitive and trustworthy in this space means proving product integrity not just once, but every time.

    No Substitute for Consistent Performance

    All these features matter little if the acid can’t deliver in the lab or plant. Years developing products and guiding research have shown me that the trick to lasting progress lies in day-to-day reliability, not flashy novelty. Projects succeed or stumble based on whether each new batch measures up to the last. 4-Bromoisophthalic Acid, thanks to its dependable physical properties and predictable performance in both simple and complex reactions, allows scientists and manufacturers to focus effort on innovation instead of troubleshooting batch variation.

    That’s not something to take for granted. As production lines scale up or projects move from grams to kilos—or even higher—small changes in purity, moisture content, or particle size threaten yield and product quality. I’ve watched teams spend weeks fixing problems that came down to nothing more than inconsistent intermediate supplies. So, with every drum or jar of 4-Bromoisophthalic Acid delivered to a factory or research institute, a lot more rides on that label than simply a compound name or CAS number. It’s a quiet backbone for big-picture innovation.

    Solutions: Keeping Pace with Growing Expectations

    Sustaining the benefits of 4-Bromoisophthalic Acid means looking beyond static routines toward smarter, more robust practices. Staying close to key suppliers, investing in real-time QC technology, and embracing new purification techniques all help keep quality high and costs in check. The industry also grows stronger as producers share insights on safe handling, storage, and best practices for waste treatment, ensuring each user can rely on up-to-date guidance, not outdated files or word-of-mouth shortcuts.

    Regulators and buyers share a stake in this, aiming for products that not only perform technically but also stand up to scrutiny. Customers expect to see data supporting every claim—from melting point and spectral properties to trace impurities checked by GC-MS or LC-MS. As these standards solidify into law or company policy, good partners take the initiative, providing clear documentation up front. Labs I’ve worked with now routinely check in with suppliers before projects launch, lining up stability samples and contingency plans in case an expected batch falls short or faces shipping delays.

    More labs now batch-test every shipment against certificates of analysis before committing to use. Though this takes extra time, it pays off, reducing costly surprises at scale. I’ve seen large facilities dovetail these internal checks with periodic external audits of supplier factories, seeking to close any gaps before they turn into production emergencies.

    Looking down the road, stronger transparency across global supply chains will shape who succeeds in this market. Chemists, engineers, and buyers all want a stable partner who delivers what they promise, when they promise. The best suppliers know this and work openly with their clients to set clear pricing, delivery schedules, and quality expectations at the start. Long-term relationships form while troubleshooting together, rather than shifting blame or hiding behind email chains. Success here draws on trust built over years, not just low prices or slick marketing.

    Conclusion: A Quiet Staple, Empowering Progress

    4-Bromoisophthalic Acid doesn’t spark headlines or splash across advertisements, but its impact runs deep across research, manufacturing, and the quest for more effective and sustainable solutions. What sets it apart isn’t only the molecular structure, but the layered commitment within the scientific and industrial world: consistent supply, data-backed quality, and responsible handling at every step.

    Having seen the difference that consistent, well-characterized intermediates can make, I believe the chemical community stands on a stronger foundation when compounds like this remain reliable, accessible, and open to ongoing improvement. The next wave of innovation, both in the lab and on the production line, will depend not just on new molecules, but on how well we manage and support the key ones we already trust. 4-Bromoisophthalic Acid, in its quiet but crucial role, looks set to help build that future for years to come.