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4-(Bromomethyl)Phenylacetic Acid

    • Product Name 4-(Bromomethyl)Phenylacetic Acid
    • Alias BMPAA
    • Einecs EINECS 616-046-7
    • 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

    807331

    Cas Number 32672-94-7
    Molecular Formula C9H9BrO2
    Molecular Weight 229.07 g/mol
    Appearance White to off-white solid
    Melting Point 91-95 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=CC(=CC=C1CC(=O)O)CBr
    Inchi InChI=1S/C9H9BrO2/c10-6-8-3-1-7(2-4-8)5-9(11)12/h1-4H,5-6H2,(H,11,12)
    Synonyms p-(Bromomethyl)phenylacetic acid
    Storage Temperature 2-8°C (refrigerated)
    Ec Number 251-148-5

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

    Packing & Storage
    Packing White HDPE bottle containing 25 grams of 4-(Bromomethyl)phenylacetic acid; features a tamper-evident cap and hazard labeling.
    Shipping 4-(Bromomethyl)phenylacetic acid is shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. It is labeled as a hazardous material, requiring handling and transportation according to local, national, and international regulations. Store and ship at ambient temperature, away from incompatible substances and protected from moisture and light.
    Storage 4-(Bromomethyl)phenylacetic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the chemical away from incompatible substances such as strong oxidizing agents. Recommended storage temperature is 2-8°C (refrigerated). Ensure proper labeling and secondary containment to prevent leaks and contamination.
    Application of 4-(Bromomethyl)Phenylacetic Acid

    Applications of 4-(Bromomethyl)Phenylacetic Acid in Industrial Manufacturing

    As an experienced manufacturer, we support multiple specialized sectors with high-purity 4-(Bromomethyl)Phenylacetic Acid, produced to strict quality specifications. Below are core industrial applications proven through real usage by leading downstream manufacturers.

    1. Pharmaceutical Intermediate for Antihistamine Synthesis

    Pharmaceutical firms utilize this compound as a key intermediate for the synthesis of selective H1-antihistamines, particularly second-generation agents. The para-bromomethyl group facilitates site-specific alkylation reactions during the formation of advanced pharmacologically active intermediates. Manufacturers scale up batch production in closed reactor systems for multi-step synthesis, supporting the formulation of prescription allergy medication APIs according to strict cGMP regulations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice
    • European Pharmacopoeia 11.0 (Ph. Eur.)
    • United States Pharmacopeia (USP) compliance
    • EMA and FDA record traceability

    Typical usage ratio

    • 0.8–1.2 molar equivalents per active pharmaceutical ingredient target, adjusted per synthetic yield optimization and impurity profile requirements

    Downstream process integration

    • Incorporated in the amide bond formation step following Grignard or Friedel-Crafts reactions; monitored for conversion and residual bromide by validated HPLC

    Final product types

    • Antihistamine API (e.g., cetirizine and analogs)
    • Coated oral tablets
    • Pediatric chewable pharmaceuticals
    • Liquid formulations for clinical use

    2. Building Block in Agrochemical Active Ingredient Synthesis

    Agrochemical formulators require this brominated compound for producing advanced selective herbicides and insect signal disruptors. The benzyl precursor acts as a reactive synthon for etherification or aminomethylation during late-stage modification of agricultural actives. Downstream processors employ multi-kilogram scale charge reactions with solvent control in closed environments, maintaining environmental and personnel safety compliance.

    Industry compliance standards

    • ISO 9001:2015 Quality Systems
    • REACH Registration (EC 1907/2006)
    • OECD Test Guideline Documentation
    • FAO specification for active component containment

    Typical usage ratio

    • 5–20% w/w of target molecule in synthesis batch; refined based on crop-protection performance, residue level, and targeted field application method

    Downstream process integration

    • Charged at the nucleophilic aromatic substitution stage; isolated, purified, and validated via GC-MS for field safety evaluation batches

    Final product types

    • Herbicide technical concentrates
    • Pesticide active ingredient formulations
    • Granular and liquid agricultural products for field application
    • Emulsifiable concentrates for large-scale farm use

    3. Custom Monomer Precursor for Functional Polymer Synthesis

    Specialty polymer firms select this compound as a core monomer precursor for tailoring polymer side-chain functionality. Incorporation of brominated aromatic groups enables site-specific crosslinking and post-polymerization functionalization. Downstream manufacturers utilize proprietary feed ratios in solvent-based copolymerization reactors, ensuring batch consistency, reactivity, and thermal performance in final specialty materials.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management
    • ISO 9001:2015 Quality Assurance
    • EU Regulation (EC) No 1907/2006 (REACH) for monomer traceability

    Typical usage ratio

    • 0.2–5% by mass of total monomer charge depending on desired bromine content and polymer characteristics

    Downstream process integration

    • Loaded at the chain-propagation stage in step-growth or free radical polymerization, allowing precise introduction of functional groups before resin curing

    Final product types

    • Functionalized engineering thermoplastics
    • Photocurable dental composites
    • Printed circuit board laminates
    • Specialty films for electronics and optics

    4. Intermediate for Fine Fragrance Ingredient Manufacturing

    Aroma chemical producers integrate this intermediate into the synthesis of aromatic aldehydes and esters used in luxury fragrance blends. The benzyl structure allows regioselective transformations for generating high-value olfactory ingredients. Large-scale fragrance factories conduct precise batch conversions under controlled temperature and ventilation, ensuring high purity for direct use in personal care market formulations.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • ISO 9001:2015 for raw material traceability
    • EU Cosmetic Regulation (EC) No 1223/2009 for ingredient safety
    • Good Manufacturing Practices for Cosmetic Ingredients (ISO 22716)

    Typical usage ratio

    • Typically 1–10% of total batch mass; determined by target ingredient yield, by-product control, and intensity profile testing

    Downstream process integration

    • Utilized during oxidation and esterification steps; fully converted resin undergoes vacuum distillation prior to blending into fragrance concentrates

    Final product types

    • Fine fragrance bases
    • Perfume oils for high-end segments
    • Personal care fragrance additives
    • Scented consumer goods (air care and personal hygiene)

    5. Intermediate for Dye and Pigment Precursor Manufacturing

    Dye manufacturers employ this chemical for the preparation of brominated intermediates used in synthesizing high-performance azo and anthraquinone colorants. It serves as a critical linker for donor-acceptor molecular structures, providing enhanced solubility and colorfastness. Vetted manufacturers repeat the process under controlled agitation and pH, optimizing for batch-to-batch consistency and eliminating heavy metal residues.

    Industry compliance standards

    • ETAD Eco-Toxicological Guidance for Colorants
    • OEKO-TEX Standard 100 for textile applications
    • ISO 105-A02 for color fastness assessment
    • REACH Annex XVII (restricted substances)

    Typical usage ratio

    • 5–15% of total precursor load; optimized based on target dye class, process yields, and required saturation for specific textile or plastic use

    Downstream process integration

    • Introduced in the diazotization or coupling reaction stage; excess reagent removed by controlled filtration and solvent washes

    Final product types

    • Synthetic dyes for polyester and nylon textiles
    • Organic pigments for inks and coatings
    • High-purity intermediates for specialty colorants
    • Chromophore building blocks for digital printing
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    Certification & Compliance
    More Introduction

    4-(Bromomethyl)Phenylacetic Acid: Bridging Chemistry and Practical Innovation

    In chemical manufacturing, we spend a lot more time than most realize listening and learning from what the industry actually needs. We make 4-(Bromomethyl)phenylacetic acid not because it’s just another chemical on the shelf, but because it shapes solutions for several targeted syntheses. Over years of making specialty intermediates for researchers, pharmaceutical developers, and material scientists, we’ve seen the range of requirements that come up with a building block like this. Each time a customer requests this acid—with its bromo-substituted methyl group—they’re chasing after a very specific reactivity profile. And since we synthesize it ourselves, we control everything from starting raw materials right through to the consistency of the final batch.

    Where Our Product Fits in the Synthetic Chain

    Ask around in any busy research lab: reliable intermediates are the currency of progress. 4-(Bromomethyl)phenylacetic acid sits on many bench shelves for good reason. Its two functional groups—the carboxylic acid and benzyl bromide—drive its popularity. Whether someone is interested in coupling reactions, nucleophilic substitution, or preparing more complex structures, this molecule delivers a level of versatility. During custom synthesis projects for the fragrance, pharmaceutical, and agrochemical fields, we’ve seen it underpin routes to compounds that ordinary phenylacetic acids simply can’t reach. The bromomethyl handle allows for direct and clean substitution, something our clients use when speed, yield, and reduced byproducts all matter.

    Traditional phenylacetic acid derivatives lack the leaving group power you find with a bromomethyl substituent. We watch chemists turn to our material when they want to skip tedious multi-step protection and activation. The bromo group boosts reactivity but doesn’t bring the instability or fussiness found in some halogenated materials. It stores and handles without the headaches usually linked to more sensitive species, yet it steps up in the flask and provides clean conversions when the right nucleophile enters the scene.

    How Specifications Affect Real-World Results

    We manufacture 4-(Bromomethyl)phenylacetic acid in different grades, but purity is a direct concern every time we get a new batch request. Unlike traders or third-party brokers, we know exactly how small levels of unreacted precursors or heavy-metal residues can torpedo sensitive downstream chemistry. That’s why we go beyond basic melting point and assay testing. We track halide content, residual solvent, and look for trace color-formers or sideline aromatic compounds. Years of feedback taught us that a seemingly minor contaminant, overlooked by less careful suppliers, turns into major headaches—lower yields, separation issues, or even regulatory hiccups.

    Let’s break it down: a pharmaceutical team needs the intermediate for an active ingredient, so low trace metals and high chemical purity become central. On the other hand, a materials group might prioritize a certain particle size for blending or better processability.  We’ve supplied both, adjusting our crystallization and filtration to target their specific needs. Our operators keep detailed production logs, and every process tweak comes from hands-on experience making the batch work for its end use.

    Comparing with Other Substituted Phenylacetic Acids

    Chemists often ask whether to use 4-(Bromomethyl)phenylacetic acid or a different substituted phenylacetic acid. Maybe the choice is para- versus ortho-substitution, or swapping bromine for chlorine. It’s tempting to see these as simple alternatives, but we’ve watched projects live or die based on these structural differences. The bromo-methyl para position on the aromatic ring changes reactivity compared to meta or ortho positions. In electrophilic aromatic substitution or cross-coupling, that para location stabilizes intermediates and gives different selectivity than other isomers.

    Replacing bromine with chlorine can lower cost, but it softens the reactivity. We’ve had clients switch back to the bromo version mid-project because the chloro-analogues couldn’t meet conversion efficiency standards, or left stubborn side products behind. Our acid’s balance of reactivity and stability stems directly from its exact substitution pattern. After repeated trial, customers settle on ours when a more sluggish halogen undermines throughput or isolation.

    Then you get the cases where someone’s trying to avoid the acid handle altogether—they’ll ask for methylated analogues or esters, usually to simplify downstream handling or to avoid acidic environments. Our acid remains the choice when teams need phase-transfer reactions, or coupling steps that leverage the carboxyl’s inherent activation potential. And for some, the free acid lets them derivatize in-situ, with full control over how and when the transformation takes place.

    Hands-On Experience: Batch Consistency Makes or Breaks Complex Syntheses

    In our factory, achieving consistency in 4-(Bromomethyl)phenylacetic acid is about more than just safety checklists or regulatory paperwork. We’ve seen the difference batch quality makes in kilo-to-multitonne scale runs, especially if you’re building libraries for lead discovery, or running a long sequence with minimal room for error. Tiny changes in the bromomethyl group’s reactivity—stemming from uneven purity, mixed isomers, or rogue trace contaminants—show up in column loadings, NMR spectra, or even GC-MS traces.

    We trace every batch through more than one set of eyes and several analysis methods. Two decades ago, customers flagged issues with color and off-odors that later correlated with tiny impurities we hadn’t tracked as closely. Now, our process emphasizes multi-stage purification and closed-loop tracking. Our staff knows the analytical markers and they catch small deviations before they reach a client’s doors. Chemists who’ve synthesized it themselves in the past tell us our product saves them cleanup time and failed reaction cycles, simply by being right the first time.

    Application Stories from the Laboratory and Industry Floor

    Walk into a synthetic chemistry lab and you’ll find 4-(Bromomethyl)phenylacetic acid taking part in everything from peptide coupling to custom drug discovery scaffold builds. In pharma R&D, it serves as a bridge in forming active pharmaceutical ingredients that rely on direct aromatic functionalization. We’ve worked alongside teams using it as the bromo handle in Suzuki or Heck-type couplings, where speed and clean conversion keep costs and solvent use in check.

    On our plant scale, a customer once pushed for a multi-tonne run with batch-after-batch reproducibility and a tight spec for halide content. Their downstream partner detected yield losses tied to minor off-types—compounds that slipped in from a supplier that cut corners. After they redirected sourcing to us, consistency improved and the cost per gram dropped. These lessons stay with us because quality standards set in the manufacturing hall echo downstream, whether the product winds up in pilot plant runs or registration batches for regulatory submission.

    Our experience tells us to track and adjust based on what’s genuinely going on in the field. Whether a team preps a few grams or several hundred kilos, they want the starting input to behave the way it did last order. We’ve responded by updating our documentation, keeping retained samples from each lot, and providing matched data on request. It takes more effort, but customers recognize the difference each time they avoid troubleshooting failures caused by unpredictable raw materials.

    Addressing Industry Challenges with Manufacturing Transparency

    Some pain points are baked into the supply chain: supply fluctuations, purity drift between lots, regulatory shifts, and documentation lags. We’ve addressed these by keeping our process in-house and investing in training alongside automation. With 4-(Bromomethyl)phenylacetic acid, outside noise about market price swings or shortage rumors stay off our production floor. If a global event disrupts raw materials or logistics, we have backup stock and alternate suppliers checked for equivalency. Over the years, we’ve watched buyers lean into shorter lead times and “just in case” procurement. Staying flexible and open about true capacity gives partners real planning confidence—not just spec sheets or catalog promises.

    On a few occasions, project deadlines forced us to adapt manufacturing schedules or cleaning protocols to deliver custom lots ahead of planned runs. Our technical staff isn’t locked into rigid standard operating procedures if unusual requirements come through. Not every request makes sense on paper, but we learn from direct dialogue. We keep channels open, especially when partners uncover new uses or need custom packaging, track/trace details, or extra analytical proof for regulatory filings.

    Manufacturing protocols have evolved since the early days, but every new regulatory detail or customer feedback cycle sharpened our approach. For example, as global limits on halide levels in finished pharmaceuticals tightened, we revisited our own specifications and upstream checks. Updating internal QC against the real compliance landscape isn’t optional, it’s what keeps the product trusted and in demand. This flexibility doesn’t come from reselling someone else’s material, it comes from owning the process end-to-end.

    Meeting Safety and Environmental Expectations

    Every batch of 4-(Bromomethyl)phenylacetic acid we prepare has to pass a set of controls that reflect current environmental and worker safety standards. Some buyers worry that bromo-containing intermediates present a disposal risk downstream, or that manufacturing involves harsh reagents and problematic byproducts. Where possible, we source smarter reagents, and our purification strategy aims to lower the use of aggressive solvents or specialty acids.

    Our facility includes solvent recovery and waste minimization circuits. Our teams handle waste salts with clearly documented protocols that meet or surpass legal standards, and ongoing audits double-check that routine production never leaks non-compliant waste. We’ve invested in closed filtration and dust containment to minimize exposure for workers and protect neighboring spaces. By re-assessing everything from batch size to reagent flow rates, we’ve trimmed surplus waste streams and reduced off-spec discard to negligible levels.

    We publish annual reviews of our handling of halide-containing wastes, and keep our partners informed about our approach to green chemistry. Forward-thinking customers want to see not just a cleaner intermediate roll off the line, but tangible progress toward more sustainable chemistry in practice. Our documentation and transparent compliance processes give project managers the confidence to build their own safety and sustainability cases for their review boards.

    Why End Users Stick with Direct Manufacturers

    People who buy direct from us usually started by testing out a few samples against competitor batches. They report less trouble with out-of-spec issues, and deeper technical support. If something isn’t right for their application, they talk to our process team straight away, instead of dealing with layers of distributors or faceless catalog reps. Sometimes we get feedback for things standard datasheets didn’t even mention: how our product grinds, how it solubilizes at a particular pH, or how it handles if blended with thermolabile actives. These cues help us tighten specifications where it matters most.

    Supplying directly also roots out surprises. Our customers run their own incoming QC, but knowing that the producer stands behind every gram shipped takes pressure and uncertainty out of their projects. If a lab flags an odd result, it doesn’t take days to track down who’s responsible. We respond directly, pulling batch records or running side-by-side analyses in our own labs. It’s this transparency and readiness to collaborate, not anonymous supply chains, that pulls repeat customers into long-term partnerships.

    With intermediates like 4-(Bromomethyl)phenylacetic acid, there’s no substitute for real-world technical follow-up. We’ve sent out replacement samples, walked through reaction troubleshooting calls, and shared tips on optimizing workup steps at scale. This interaction produces a feedback loop that keeps making our product better and more reliable. Direct manufacturing gives us the agility to respond in days, not months or quarters.

    What Sets Our 4-(Bromomethyl)Phenylacetic Acid Apart

    Plenty of suppliers list 4-(Bromomethyl)phenylacetic acid, but not all can guarantee process traceability, tailored pack sizes, and continuity across multi-year projects. Our in-house synthesis, purification, and packaging ensure that each order fits the project—no long wait times, no batch mixing, and a single source of accountability. Every improvement in our process comes from listening to the actual chemists and engineers using these materials. Challenges like maintaining a consistent crystalline phase, improving shelf life, and supporting specialized analytical requests aren’t afterthoughts; they’re part of the production routine.

    Some clients notice performance differences only after long-term storage or secondary processing. We test for product stability and offer guidance on handling, whether customers plan to use the batch immediately, or need to keep inventory for regulatory resubmission later. Real experience means real answers. A material that works reliably in hundreds of gram batches, and that passes industry-driven scrutinies, does more than keep projects running—it builds mutual trust between supplier and end user.

    We’ve built our business producing true specialty intermediates. Our focus remains on the details that matter to practitioners: batch reproducibility, documentation you don’t have to chase, flexibility to scale up or scale down, and honest communication. 4-(Bromomethyl)phenylacetic acid is just one example from our catalog, but it reflects decades of learning from real synthesis, not just rote sales calls or catalog listings.

    Looking Ahead: Future Needs in Custom Synthesis

    Tomorrow’s chemical projects will push all of us to deliver intermediates that are both technically precise and ecologically responsible. Our ongoing investment in process controls, on-site analytics, and greener reagent sourcing reflects this reality. 4-(Bromomethyl)phenylacetic acid will likely remain an in-demand building block for any number of functionalized aromatics, biologically active compounds, or advanced materials. The requests will keep getting more challenging, as downstream applications grow in complexity and scale.

    We’re preparing for these changes not with promises, but by building robust, flexible manufacturing and reinforcing the technical dialog that has earned long-lasting partnerships. If the mix of specifications, certification needs, or handling guidance changes, we’ll adapt. We encourage our partners to treat us not just as a supplier, but as a part of their technical ecosystem—one with deep knowledge of how 4-(Bromomethyl)phenylacetic acid performs across a real spectrum of applications. That’s how progress happens, batch after batch, project after project, and it’s how we deliver genuine value from the manufacturer’s bench to the customer’s achievement.