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4-Bromo-2-Methylbenzoic Acid

    • Product Name 4-Bromo-2-Methylbenzoic Acid
    • Alias 4-Bromo-o-toluic acid
    • Einecs 241-241-4
    • 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

    444973

    Chemical Name 4-Bromo-2-Methylbenzoic Acid
    Cas Number 28407-53-6
    Molecular Formula C8H7BrO2
    Molecular Weight 215.05
    Appearance White to off-white solid
    Melting Point 185-189°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles CC1=C(C=CC(=C1)Br)C(=O)O
    Inchi InChI=1S/C8H7BrO2/c1-5-6(8(10)11)3-2-4-7(5)9/h2-4H,1H3,(H,10,11)
    Storage Conditions Store at room temperature, dry and away from light
    Synonyms 2-Methyl-4-bromobenzoic acid

    As an accredited 4-Bromo-2-Methylbenzoic 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-Methylbenzoic Acid, sealed with a screw cap and labeled with safety information.
    Shipping 4-Bromo-2-Methylbenzoic Acid is typically shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture absorption. It should be handled as a hazardous material, with appropriate labeling and documentation, and transported according to local, national, and international regulations for chemicals to ensure safe delivery and environmental protection.
    Storage 4-Bromo-2-Methylbenzoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from direct sunlight, moisture, and excessive heat. Store at room temperature and ensure proper labeling to prevent accidental misuse. Use appropriate secondary containment to avoid spills or leaks and follow standard chemical storage guidelines.
    Application of 4-Bromo-2-Methylbenzoic Acid

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

    Our 4-Bromo-2-Methylbenzoic Acid is utilized in select advanced manufacturing fields that require precise molecular intermediates for process reliability and regulatory conformity. As a manufacturer, we support production partners across specialty chemicals, pharmaceuticals, and crop protection actives, with traceable, specification-controlled supply for each industrial application.

    1. Pharmaceutical Intermediates for Non-Steroidal Anti-Inflammatory Drug Synthesis

    This raw material is routinely adopted as a pivotal intermediate in the multi-step synthetic pathways for specialty NSAID molecules, where bromine substitution is required prior to subsequent amination, amidation, or cyclization. Pharmaceutical R&D and process scale-up groups prefer this input where para-substitution chemistry must proceed without side-chain isomerization. Compliance with current pharmacopeial standards and GMP batch traceability is essential to ensure downstream regulatory submissions.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • USP/NF (if used in US-bound APIs)
    • European Pharmacopoeia (Ph. Eur.) specifications for starting materials
    • CFR Title 21 Parts 210/211 (Finished Pharmaceuticals GMP)

    Typical usage ratio

    • Usage typically ranges from 0.18 to 0.32 molar equivalents per mole of final API, optimized according to stoichiometry of target NSAID and the efficiency of downstream halide elimination or substitution reactions.

    Downstream process integration

    • This intermediate is charged during the early-stage synthesis step, often via halogen-metal exchange or direct nucleophilic substitution, followed by controlled condensation or acylation as dictated by specific NSAID route maps.

    Final product types

    • Non-Steroidal Anti-Inflammatory Drug (NSAID) active pharmaceutical ingredients such as specific aryl propionic acids and related analogues
    • Specialty analgesic bulk intermediates
    • Pharmaceutical fine chemicals for further conversion

    2. Agrochemical Active Ingredient Precursors

    Chemical synthesis teams in agrochemical production apply this compound in the construction of selective herbicide and fungicide active molecules, where methyl and bromine functionality at fixed positions is demanded for biological target binding. Quality teams mandate adherence to contaminant and impurity thresholds as set forth by agro regulatory agencies to enable finished product registration across major planting markets.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 (Quality Management Systems for Agrochemical Intermediates)
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals – if supplied within Europe)
    • China GB 2763: National Food Safety Standard for Maximum Residue Limits for Pesticides

    Typical usage ratio

    • Most herbicide and fungicide syntheses require between 5% and 15% by weight of this intermediate relative to total batch mass, with the precise proportion set by target molecule and yield optimization stepwise through process validation.

    Downstream process integration

    • This brominated acid is introduced into the synthetic route during coupling or halogen substitution, with integration as an essential moiety prior to etherification, cyclization, or sulfonation depending on end product requirements.

    Final product types

    • Herbicide actives (e.g., specific benzoic acid-based weed control actives)
    • Fungicidal intermediates for broad-spectrum crop protection agents
    • Pesticide formulation bases for field application

    3. Liquid Crystal Building Blocks in Electronics Materials Manufacturing

    Specialty electronics chemical manufacturers employ this compound to access advanced liquid crystal intermediates for display and sensor applications. The precise aromatic substitution pattern enables predictable mesogenic behavior and thermal characteristics. Material integrity, impurity profile, and batch consistency are tracked according to sectoral quality protocols to support device reliability and certification testing.

    Industry compliance standards

    • IEC 61249 (Materials for Printed Boards and Other Interconnecting Structures)
    • RoHS (Restriction of Hazardous Substances Directive, EU)
    • UL 746 (Polymer Material Performance for Electronics)
    • ISO 9001 (for advanced materials supply chains)

    Typical usage ratio

    • In the liquid crystal precursor syntheses, loading typically runs from 8% to 22% by mass relative to aromatic input stream, subject to designer functional group density and device-specific blend targets.

    Downstream process integration

    • This compound is included in the monomer assembly or oligomerization stage, often via Suzuki, Ullmann, or other cross-coupling methodologies prior to fractionation and polymerization to achieve required purity.

    Final product types

    • Advanced liquid crystal prepolymers
    • Optical alignment layers and display functional materials
    • Component blends for OLED and sensor manufacturing

    4. Specialty Dye and Pigment Intermediates

    Manufacturers of technical and specialty dyes employ this molecule to introduce rigid aromatic segments and halogen functionality essential for colorfastness and chromophore tuning. Regulatory teams control for azo, aromatic amine by-products, and halide residuals. Finished colorant performance for textile, paper, and ink sectors relies on the integrity of intermediates processed under certified conditions.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile Chemical Safety)
    • EN 71-3 (Safety of Toys – Migration of Certain Elements for pigments in colored toys)
    • REACH Annex XVII (restrictions on azo dyes and CMR substances)
    • ZDHC (Zero Discharge of Hazardous Chemicals)

    Typical usage ratio

    • Dye and pigment formulations typically incorporate between 3% and 12% of this intermediate by mass, based on shade depth, molecular weight, and the required photostability of resulting colorant systems.

    Downstream process integration

    • Inserted during primary aromatic substitution or metal chelation stages, often by directed coupling or halogen-metal exchange prior to functionalization, sulfonation, or azo linkage formation for advanced color properties.

    Final product types

    • Disperse and acid dyes for synthetic fibers
    • Technical pigments for plastics and automotive coatings
    • High-performance ink colorants for industrial and security applications

    5. Chemical Reagents for Analytical and Research Purposes

    Analytical laboratories and contract research organizations require this compound as a reference reagent, derivatization agent, and synthesis checkpoint for trace analysis or structure-activity studies. High batch purity and low residual halides are essential for chromatographic calibration, impurity profiling, and subsequent detailed analytics. All material supplied for laboratory and research use must conform to established reagent specifications and quality documentation.

    Industry compliance standards

    • ACS Reagent Chemicals Specifications
    • ISO/IEC 17025 (General Requirements for the Competence of Testing and Calibration Laboratories)
    • GLP (Good Laboratory Practice) for analytical chemistry
    • GHS-compliant SDS and labeling for laboratory chemicals

    Typical usage ratio

    • Usage is variable and depends on analytical scale; typically 0.2–5 mmol per batch for synthetic standard preparation or chromatography calibration, with precise adjustment per method sensitivity and detection type.

    Downstream process integration

    • Applied during synthesis of laboratory standards, derivatization reactions for HPLC/GC, or as purity markers and matrix spiking compounds in research workflows.

    Final product types

    • Synthesis reference materials
    • Research reagent kits for analytical equipment calibration
    • Standard samples for purity method validation
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    Certification & Compliance
    More Introduction

    4-Bromo-2-Methylbenzoic Acid: Practical Insights from a Chemical Manufacturer’s Bench

    Ground-Level Perspective on 4-Bromo-2-Methylbenzoic Acid

    Making 4-Bromo-2-Methylbenzoic Acid in-house brings up a set of challenges and rewards most people don’t see from a catalog page. It’s not just another benzoic acid derivative on a list. The work starts long before a bottle hits a customer’s bench, and the details throughout production shape the results that researchers and process chemists get on their end.

    About Our 4-Bromo-2-Methylbenzoic Acid

    We produce 4-Bromo-2-Methylbenzoic Acid for applications in pharmaceutical building blocks, agrochemical intermediates, and materials science. The chemical formula tells a story: the bromine atom adds weight and reactivity, and the methyl group on the ring shifts its personality compared to plain benzoic acid or its other halogenated siblings. As a solid white to faintly off-white powder, this compound’s purity isn’t just for show. Every lot passes through our strictest GC and HPLC specifications, holding a minimum content of 99%. Contaminants—halides, isomers, and even trace solvents—have been the bane of both scale-up and bench-scale chemistry, so we’ve fine-tuned our washing and crystallization steps to strip out those persistent side-products. Moisture content stays low due to our multi-stage drying sequence under reduced pressure, something users in esterification reactions or Suzuki cross-coupling have thanked us for.

    The Hands-On Uses of 4-Bromo-2-Methylbenzoic Acid

    People call us asking about the difference another methyl group or a bromine atom makes. In pharmaceutical development, medicinal chemists need this molecule for selective aryl brominations, where the methyl group at position two brings both bulk and subtle electronic effects. For Suzuki couplings or Buchwald-Hartwig reactions, the ortho-methyl branching affects both rate and regioselectivity. Downstream, some of our customer’s kinase inhibitors, CNS drug candidates, or advanced material monomers start from this exact intermediate.

    Other users, working in crop protection, chose 4-Bromo-2-Methylbenzoic Acid for its reactivity in coupling with amines, hydrazines, or phenols. That bromine moiety isn’t easily swapped for chlorine in these routes; the heavier halogen makes for more reliable reactivity under milder conditions, cutting down on the harsh reagents. In custom synthesis shops building specialty polyaromatics, the methyl crowding causes the next substitution to favor certain positions, guiding synthesis where they want it to go.

    We don’t just think about the lab reactions. Packaging decisions, whether to use high-barrier bags or more traditional drums, depend on the molecule’s hygroscopicity and bulk density. We learned early that trace moisture, picked up if stored in permeable bags, can lead to degradation products—a fact that caused one unlucky scale-up to crash during a downstream Grignard. Simple choices, like keeping this acid under nitrogen or choosing rigid containers, keep users from headaches.

    How 4-Bromo-2-Methylbenzoic Acid Stacks Up Against Similar Products

    In our portfolio, 4-Bromo-2-Methylbenzoic Acid comes up against siblings such as 4-Bromobenzoic Acid, 2-Methylbenzoic Acid, and 2-Bromo-4-Methylbenzoic Acid. Why make all these variations? Each one serves a distinct chemistry problem. Compared to the parent 4-bromobenzoic acid, the 2-methyl group in our product delivers differences in both melting point and solubility. Some customers want that increased steric bulk to prevent unwanted ortho substitutions during further chemistry—the methyl group delivers that, shielding one side of the molecule.

    Against plain 2-Methylbenzoic Acid, the bromine at the para-position stands out as a functional handle. Bromine acts as a platform for halogen-lithium exchange or Pd-catalyzed coupling, options not possible with methyl-only acids. At the scale we make, keeping the bromine source pure so no dichlorinated or other halogenated analogs creep in became a must—one failed coupling reaction from an impurity can send a whole campaign back to square one.

    “Why pick bromine over chlorine or iodine?” A common question. Brominated benzoic acids strike a middle ground: higher reactivity than chlorides in metalation and coupling, but not so expensive as iodides. The methyl group plays its own role. In our experience, the combination of electron-donating methyl and electron-withdrawing bromine sets a sweet spot, letting users fine-tune their end-products’ reactivity and stability. We’ve heard from materials scientists tuning optical properties of organic semiconductors, and they needed exactly this push-pull balance.

    Manufacturing Decisions That Shape Product Quality

    The supply chain behind this product starts with raw materials selected for ultra-low heavy metals and halide impurities. We don’t cut corners because the end users pay the price in lost yield or regulatory headaches. Our reactors are fitted with glass linings so bromide salts don’t corrode steel and leave metal contaminants. Batch records track every kilogram; if a batch drifts even one percent high in residual methyl bromide, it gets pulled. People on the blending and grinding lines take pride in the texture—free-flowing, not prone to clumping. Airborne dust is controlled, so each batch gives consistent weigh-outs, whether it’s a 10-kilogram drum or a full pallet.

    Our lab people measure not just by standard melting point and spectra; we run NMR as a routine checkpoint to nail down isomer ratios and spot subtle shifts hinting at solvent inclusion or incomplete halogenation. We worked with process chemists to understand what happens when minor isomeric byproducts sneak in—sometimes a side product doesn’t matter, but certain downstream reactions shut down if it’s over a few tenths of a percent. Every tweak in our synthetic route is field-tested, not pushed to market until our partners confirm reproducibility on their end.

    Addressing Challenges in Real-World Use

    Not everything goes right in bulk production or bench-scale use. On our end, brominations can run too hot, leading to dimeric byproducts or over-bromination. Early runs brought us face to face with batches that just wouldn’t crystallize right—fine-tuning solvent ratios, cooling rates, and wash steps took iteration with every run. The hard lesson is that books and protocols only get you so far—the devil’s in the details of plant-scale behavior.

    Customers have called about color changes or odors, signs of trace debromination or impurities carried in from raw material lots. We respond by pulling retention samples and running side-by-side analyses. Sometimes humidity in a customer’s warehouse brings up hydrolysis—while the acid group itself is stable, the right storage conditions keep those edge-case degradants at bay.

    End-use complexity varies. For some, a pharmaceutical synthesis calls for strict GMP-grade intermediates, while in materials science, the focus shifts to batch-to-batch color and metal content, especially when optical clarity matters. We’re always recalibrating our thresholds, setting specifications tighter based on new feedback. Instead of chasing “minimum specs” on a data sheet, we track real user process data, adapting our purification accordingly.

    Environmental and Regulatory Outlook

    Making 4-Bromo-2-Methylbenzoic Acid safely means doing more than just ticking compliance boxes. Brominated intermediates can leave an environmental legacy if not handled correctly. Our factory recovers and reuses as much brominated waste as possible, and scrubs off-gas streams to keep emissions low. Local authorities monitor wastewater for bromide, and we invested in specialized filtration to strip these halides before discharge.

    Our downstream users need guarantees. In pharma, each kilogram must come with traceability—lot numbers tightly tracked, full analytical profiles available. Agrochemical partners want proof that no persistent organic pollutants creep in. We answer with transparent reporting, not just airy assurances. The demands go up every year; regulatory frameworks in both Europe and North America now require tighter reporting of Potentially Persistent, Bioaccumulative, and Toxic substances. With every new guideline, we evolve too.

    Pursuing Continuous Improvement

    Making chemical intermediates at this level turns into a never-ending process of tinkering and feedback. For 4-Bromo-2-Methylbenzoic Acid, we run constant trials to squeeze out solvent residues and test new cleaning protocols to boost purity. Routine doesn’t mean resting on what worked yesterday. Every batch runs through full characterization—melting point, NMR, GC-MS, HPLC, Karl Fischer titration for trace water. Any deviation triggers a root-cause hunt.

    Feedback from experienced chemists shapes our process more than anything. One customer reported variable yields not traced to our batch—turns out their base contained unknown trace metals that affected coupling. We learned to check our acid for these ions ourselves. Another noted improved downstream crystallization when particle sizing shifted; we began offering custom milled or sieved product for these exact scenarios. Rather than holding to a one-size-fits-all mentality, we adjust with demand.

    The Importance of Building Trust Through Manufacturing

    Customers want the real story, not marketing gloss. From our perspective, nobody wins by short-cutting quality or hiding process hiccups. Often, the difference between a smooth campaign and a failed scale-up comes down to the detail of a single raw material’s origin or a storage method. Being close to both the process and the users means we hear about near-misses and outright failures—these stories keep us accountable, not just proud of our certificates.

    As experienced process chemists and technologists, we stay in direct dialogue with end-users. Sample requests lead to collaborative troubleshooting on solubility, particle size, or byproduct management. Labs tell us when their reactions suffer, and we respond like partners rather than suppliers. We’ve had situations where time pressures forced us to supply out-of-spec material with full disclosure; those instances reinforced the value of transparency, as researchers trusted us to act as part of their project, not obstacles on the supply chain.

    Looking Toward Future Applications

    Trends in pharmaceuticals, crop science, and advanced materials continue to reshape the need for exacting intermediates like 4-Bromo-2-Methylbenzoic Acid. As molecular design gets more sophisticated, tiny differences in substituent patterns on aromatic rings translate to huge shifts in biological activity or physical properties. Our customers innovate at the front edge; keeping pace means constant adaptation—changing syntheses, tweaking purification, staying atop analytical advances.

    We’re seeing growing demand from OLED and photovoltaic research, sectors hunting for new electron-rich and electron-poor building blocks. Our technical team collaborates with researchers developing novel conjugated polymers, where both the bromine and methyl group drive critical properties. As these applications move from bench to pilot plant, the need for kilogram-to-tonne supply becomes critical—and the nuances of scale-up chemistry, impurity control, and logistics return to the fore.

    Supporting Research and Scale-Up Success

    Support doesn’t end with shipment. The bench-scale sample that works in a 10-gram reaction often behaves unpredictably at kilogram scale. Solvent retention, crystal morphology, static charge—these are the real-world hurdles. Users rely on us to answer questions about reprocessing, safe handling, and even creative ways to salvage difficult batches.

    We invest in generating detailed Certificates of Analysis because researchers need hard data to plan critical experiments. Our doors stay open for process audits and technical consultation. Faced with a failed reaction, it’s about more than blame—it’s a shared fight to solve the next hurdle.

    Final Thoughts from the Chemist’s Viewpoint

    Each lot of 4-Bromo-2-Methylbenzoic Acid carries a piece of the manufacturing team’s diligence. Being a manufacturer, not a distant reseller, means we wake up to the realities behind every order: raw material fluctuations, plant shutdowns, surprise customer requests. Our belief is simple—chemicals built for research and production deserve honesty, consistency, and relentless improvement. We continue producing 4-Bromo-2-Methylbenzoic Acid not just to fill an order sheet, but to partner with those pushing chemistry, medicine, and technology forward.