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

2-(4-Bromomethyl)Phenylpropionic Acid

    • Product Name 2-(4-Bromomethyl)Phenylpropionic Acid
    • Alias BMPPA
    • Einecs 841-073-3
    • 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

    991421

    Product Name 2-(4-Bromomethyl)Phenylpropionic Acid
    Molecular Formula C10H11BrO2
    Molecular Weight 243.10 g/mol
    Cas Number 117155-26-9
    Appearance White to off-white powder
    Melting Point 98-102°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥ 98%
    Storage Condition Store at 2-8°C, protected from light and moisture
    Synonyms 4-(Bromomethyl)-α-methylbenzeneacetic acid
    Chemical Structure Contains a bromomethyl group attached to the 4-position of a phenylpropionic acid
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract

    As an accredited 2-(4-Bromomethyl)Phenylpropionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 2-(4-Bromomethyl)Phenylpropionic Acid is supplied in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 2-(4-Bromomethyl)phenylpropionic acid is shipped in tightly sealed containers to prevent moisture and contamination. It is usually packed in inert, chemical-resistant bottles, cushioned for safe transit. The shipment complies with regulations for hazardous materials, requiring appropriate labeling, documentation, and temperature control if necessary. Handling instructions and safety data sheets accompany each shipment.
    Storage 2-(4-Bromomethyl)phenylpropionic acid should be stored in a tightly sealed container, away from light and moisture. Keep the container in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to strong acids, bases, and oxidizing agents. Wear appropriate protective equipment when handling, and ensure good laboratory practices are followed to prevent contamination or accidental release.
    Application of 2-(4-Bromomethyl)Phenylpropionic Acid

    Applications of 2-(4-Bromomethyl)Phenylpropionic Acid in Industrial Manufacturing

    2-(4-Bromomethyl)Phenylpropionic Acid serves as a critical building block in advanced chemical syntheses across several industrial sectors. Our manufacturing expertise ensures high-purity batches that support stringent customer requirements for both quality and traceability. Below, we provide detailed application insights for key, verifiable downstream segments utilizing this specialty chemical.

    1. Pharmaceutical Intermediate for Nonsteroidal Anti-Inflammatory Drugs

    This molecule is frequently deployed in the multi-step synthesis routes for select NSAID active pharmaceutical ingredients, targeting the modification of aromatic frameworks and side-chain introduction, especially within the class of phenylpropionic acid derivatives. Customers integrate our material early in their reaction sequence, employing its functionality to introduce a bromoalkyl group critical for downstream couplings or cyclizations. Process chemists adjust the addition stage based on target molecule complexity, with reaction conditions tailored for controlled bromine reactivity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monograph 2.9.40 for impurities
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • Chinese Pharmacopoeia processing directives for intermediates

    Typical usage ratio

    • 0.35–1.05 molar equivalents per batch, determined by target NSAID molecular structure and intended yield optimization

    Downstream process integration

    • Introduced after initial aromatic compound protection steps; bromomethylation performed under controlled temperature, in closed reactors with in-line HPLC verification

    Final product types

    • Naproxen analogues
    • Flurbiprofen intermediates
    • Other phenylpropanoic NSAID actives and research candidates

    2. Advanced Agrochemical Synthesis (Herbicide Precursors)

    Custom synthesizers and contract manufacturers utilize this intermediate when constructing complex aromatic rings within pre-emergent and post-emergent herbicide candidates. Its bromo substituent enables regioselective addition or functional group transformation under mild conditions, typically during the late-stage approach to the active ingredient’s skeleton. Farmers and end-users do not encounter this substance in its raw form, given its conversion into final actives before formulation.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for chemical production
    • REACH (EC 1907/2006) downstream user obligations

    Typical usage ratio

    • Ranges from 0.25–0.8 weight% relative to the total mass of precursors, adjusted to optimize conversion efficiency and minimize waste byproduct formation

    Downstream process integration

    • Charged after initial formation of the core aromatic scaffold, with bromo-functionalization enabling final side-chain coupling; stepwise batch monitoring via GC-MS throughout

    Final product types

    • Aromatic herbicide intermediates
    • Selective grass and broadleaf weed control actives
    • Pre-formulated agrochemical active concentrates

    3. Specialty Chemical Synthesis for Liquid Crystal Materials

    Manufacturers of advanced display and optical materials employ this compound in the early stages of synthesizing arylpropionic derivatives needed for precise molecular alignment in liquid crystal applications. The high bromine reactivity allows direct integration into aromatic frameworks during the formation of mesogenic core structures, facilitating production of intermediates with defined polarity and rigidity essential for display performance.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • ISO 14001:2015 for environmental management in chemical synthesis
    • IEC 60450 for purity and handling in electronic material supply chains
    • Customer-specific purity grades (≥99.0%) as per custom supply agreements

    Typical usage ratio

    • 0.10–0.45 weight% in the total monomer formulation, depending on required mesogenic unit length and desired electro-optical response

    Downstream process integration

    • Fed directly into the coupling stage during mesogen synthesis; subsequent dehalogenation or functionalization performed in continuous or semi-batch reactors, monitored via NMR

    Final product types

    • Liquid crystal monomers for TFT-LCD panels
    • Phase-retardation materials for optical films
    • Specialty intermediates for next-generation display prototypes

    4. Building Block in Custom Organic Synthesis (Fine & Performance Chemicals)

    The compound is widely requested by custom synthesis organizations and contract R&D labs seeking a reactive handle for further derivatizations, including carboxyl, ester, and amide transformations. Its functionalized aromatic structure ensures controlled site-selective reactions for high-value intermediates, and clients often require kilogram-to-ton quantities with tailored impurity profiles for precise downstream reactivity in pilot and commercial projects.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical manufacturing
    • REACH registration for Europe-directed shipments
    • IPEC GMP Guide for Pharmaceutical Excipients (where applicable)
    • Chemical Weapons Convention Schedules (for export/import compliance)

    Typical usage ratio

    • Typically 0.5–2.0 molar equivalents based on designed downstream reaction stoichiometry and final yield requirements

    Downstream process integration

    • Undergoes initial aromatic bromination, followed by targeted carboxylate conversions, either in batch or flow reactors as dictated by complexity and purity needs

    Final product types

    • Custom functionalized aromatic acids
    • Pharmaceutical fine chemical intermediates
    • Performance additives for coatings and adhesives
    • Specialty ligands for catalyst development
    Free Quote

    Competitive 2-(4-Bromomethyl)Phenylpropionic 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

    Our Perspective on Manufacturing 2-(4-Bromomethyl)Phenylpropionic Acid

    Building the Right Foundation: Purposeful Chemistry from Start to Finish

    At our chemical manufacturing plant, the development of compounds such as 2-(4-Bromomethyl)Phenylpropionic Acid takes place on the back of decades of technical experience and practical knowledge. This compound, known in some circles as a key intermediate for several advanced applications, has found its niche due to its reliable structure and the versatility of the bromomethyl functional group anchored to the aromatic ring. What makes it stand out in our lineup has never been the name itself but the hands-on work that happens from the minute we source raw materials to the moment the product ships out of our controlled storage facilities.

    2-(4-Bromomethyl)Phenylpropionic Acid carries the chemical formula C10H11BrO2. As a manufacturer, we’ve leaned into every step required to deliver high-quality material: purification, moisture control, minimizing contamination, and confirming consistent molecular structure. There’s much discussion in the industry about grade and reproducibility, but the devil is always in the details. The true quality of this compound only becomes clear when you see how well it performs as a building block for pharmaceuticals or as an intermediate for specialty chemicals.

    What the Finished Product Delivers

    People working in advanced synthesis know that the difference between success and failure comes down to how clean a reaction runs and how reliably the starting materials behave batch after batch. For 2-(4-Bromomethyl)Phenylpropionic Acid, slight impurities—undetectable without stringent analytical processes—can sideline an entire production run. The melting point shifts ever so slightly, possibly triggering trouble in downstream coupling or alkylation reactions.

    Our team members have spent years working out protocols for recrystallization, which resulted in controlled crystal habits and improved handling properties. Anyone dealing with benzylic bromides recognizes the inherent instability of these compounds; they can darken over time due to light exposure or trace metal catalysis. We batch and pack in low-light, low-humidity environments using amber vessels for long-term stability. With every lot, our technical staff reviews gas chromatography and NMR spectra to confirm that the product’s identity matches the rigorous standards expected in regulated markets.

    With this approach, our 2-(4-Bromomethyl)Phenylpropionic Acid obtains a level of batch uniformity that reduces customer troubleshooting costs. Researchers and production engineers often comment on the way our batches dissolve at predictable rates and how their own downstream yields improve with our material. Companies synthesizing non-steroidal anti-inflammatory drugs, certain agrochemical compounds, or specialty linkers for custom molecules can push their projects ahead without losing time to repeat purification work caused by out-of-spec raw materials.

    Tested Methods for Reliable Results

    Our facility addresses every production run with strict in-process controls. One recurring challenge lies in the scale-up from laboratory grams to process-scale kilograms. Just increasing the mass of reactants without adjusting mixing protocols or controlling thermal gradients brings trouble—so we record every deviation and calibrate our reactors accordingly. Not once, but batch after batch.

    We validate our process reproducibility through retained samples stored for periodic analysis. Over time, we refined our bromination protocols using dry, high-purity reagents, carefully titrating quantities to avoid over-bromination (which can form unwanted di-bromoderivatives). Following each run, we filter, wash, and dry the material under vacuum to reduce traces of solvent, which, in our experience, can alter the physical consistency and risk shipment delays—especially in summer when temperatures fluctuate.

    What we ship to our customers doesn’t just leave our plant with a quality certificate. Representatives from R&D, production, and analytical testing sign off, confirming that the specific lot meets our expected standards—not a generic industry benchmark. We invite audits from clients who want to look behind the curtain because trust grows from transparency, not just compliance.

    Where 2-(4-Bromomethyl)Phenylpropionic Acid Excels Versus Other Compounds

    Years of manufacturing experience showed us that benzylic bromides don’t all behave the same way. 2-(4-Bromomethyl)Phenylpropionic Acid sits apart from similar molecules like 4-bromobenzyl derivatives or unsubstituted phenylpropionic acids because of the location of the bromomethyl functionality on the aromatic ring and the additional propionic tail. This structure strikes a unique balance—providing reactivity at the benzylic position while maintaining steric flexibility for reactions targeting the carboxylic group.

    Clients in the pharmaceutical sector often compare benzylic bromides for their reactivity profiles. We’ve received feedback from across the globe: some alternatives degrade in storage, others provide inconsistent yields in nucleophilic substitution. Our compound’s robust response to controlled substitutions, combined with the reduced by-product content achieved via our workup process, directly impacts the value it brings to these sectors.

    One key application area involves synthesis of target ligands used in drug discovery. The carefully positioned bromomethyl group opens direct access routes for elaboration into ether or amine side chains. The carboxyl group increases solubility in polar organic solvents, which supports transformations that demand a balance between reactivity and stability.

    Manufacturing teams often ask about bromine content, trace impurity levels, and solubility profiles because these parameters impact final formulation work. Each batch of our material ships with supporting spectra—giving project leads the confidence they need to troubleshoot less and synthesize more.

    Quality as Learned through Years at the Bench

    Some newcomers to benzylic bromide chemistry focus on catalog specs, but as a manufacturer, we learn far more from customer field reports than from paper metrics. For example, we’ve implemented inline spectroscopic analysis based on feedback from formulators performing scale-up under tight regulatory oversight. Being able to confirm the consistency of our batches — even when produced months apart — matters more than simply producing according to specification.

    We receive questions on storage and handling, especially for larger scale customers staging material for several months. Bromine-based compounds have always warranted extra care — amber glass, desiccant, and cool temperatures. Our packaging team developed custom containers that minimize headspace without increasing atmospheric exposure. There has been a strong push in the market for greater traceability and batch-level accountability; this is no trend for us — every drum and bottle links back to a record that details not just manufacturing date but conditions of processing and storage.

    Why Experienced Teams Seek This Compound

    Anyone working a synthetic route that demands selective benzylic reactions deals with the limits of side-product formation and sensitivity to environmental conditions. Reactivity at the benzylic position can trigger unwanted ring chlorination or dehalogenation under less controlled conditions, costing time and lost materials. Our long-term stability tests provide a record—months at controlled temperatures with precise colorimetric readings confirm that the compound resists decomposition better than less-refined grades.

    Scientific teams, at bench and plant scale, look for products that give them flexibility. They routinely tell us they can reach targeted analogs via one or two steps, thanks in part to the compatibility of our compound with a wide range of nucleophiles. To us as producers, the best validation comes when these same teams reorder for their next campaign.

    Working with 2-(4-Bromomethyl)Phenylpropionic Acid often lets research groups shorten their synthesis time by avoiding excess purification. We keep our focus on minimizing halogen-exchange side reactions, which means our customers spend less time on post-reaction clean-up. The propionic acid tail improves solubility relative to shorter-chain analogs, so it does not require as aggressive measures for dissolution, giving process chemists greater latitude in their downstream steps.

    Environmental Responsibility in Everything We Do

    Discussions about chemical intermediates frequently lead to worries over waste and environmental impact, especially with halogenated materials. For us, responsible bromination means solvent recycling, closed-system transfers, and effluent monitoring. Operators on our production floor receive regular training to handle bromine safely, which cuts both accident risk and environmental footprint.

    Some competitors opt for cheaper, less-efficient processes that generate more by-product, but cost overruns and stricter disposal regulations make this a shortsighted view. Our process recovers and reuses the majority of solvents, and our waste-handling protocols exceed common industry guidelines. In reality, preventing leaks and unplanned emissions during manufacture are the only sustainable way to keep quality high and impact low. We believe this ongoing investment pays back in customer trust and plant safety, especially when customers require paperwork for regulatory audits or environmental reviews.

    Consistent Communication: Technical Support Built on Experience

    Our technical support group includes people who’ve run both kilo lab and production-scale reactors. Customers appreciate speaking to someone who has handled the same issues—stirring efficiency, temperature calibration, bottleneck removal, and analytic troubleshooting—in the trenches. With every delivered drum or bottle, we offer honest, no-nonsense guidance on storage, reactivity, and compatible transformations.

    Requests for custom packing sizes, special documentation, or direct consults with our chemists happen almost every week. New customers commonly ask for recommendations on solvent usage during solution-phase synthesis or clarification on permissible storage durations. We share insights grounded in direct experience, not just synthesized technical bulletins. Over the years, this approach reduced miscommunications and helped develop a shared language between the lab and operations teams.

    Reducing Complexity: Downstream Impact and Feedback

    Feedback tells us production engineers use 2-(4-Bromomethyl)Phenylpropionic Acid as a starting material for pain management molecules, agrochemicals, and advanced intermediates. These developments rarely occur in isolation. Each batch enables dozens of additional transformations, each with separate regulatory and analytical hurdles. Production teams favor intermediates they can trust not to bring surprises—an area where our focus on batch consistency truly pays off.

    One customer in the generic pharma space described how repeated use of our compound lowered their product variability scores by nearly 20 percent. This improvement did not come from blind luck but from controlled process changes stemming from ongoing dialogue between our groups. Such concrete, on-the-ground results highlight the difference between manufacturing with intent and simply filling orders.

    Handling large lot sizes, especially for multinational clients who stage production in multiple regions, stretches our logistics capacity. Yet we invest in dedicated tracking and backup inventory so critical new batch requirements do not stall downstream launch timelines. The best batches not only ship fast but arrive ready to use, reducing sample testing delays and allowing clients to stay in pace with shifting market pressures.

    Meeting and Exceeding Regulatory Demands

    Chemicals destined for regulated industries answer to audits from multiple global agencies—often on short time frames. Our files, from initial QC checks through long-term stability data, stand ready for inbound requests. Years of crossing regulatory checkpoints sharpened our ability to document every step, from material sourcing through to final packing and shipment. Pharmaceutical customers note that supporting files, like flowcharts of our bromination and purification profiles, enable smooth passage through their own compliance reviews.

    Increasingly, customers ask for deeper insight into trace impurity profiling. Responding to these requests requires ongoing investment in both equipment and staff retraining. Mass spectrometry and HPLC are fixtures on our QC bench, matching the level of scrutiny demanded by evolving marketplace standards. Each report comes with clear annotations so review teams get the context behind every metric tested—not just numbers on a page.

    Adapting to a Changing Chemical Supply Chain

    Global circumstances shift supply chains daily, putting added pressure on procurement managers and research teams. As a manufacturer, we counter this uncertainty by building redundancy into our own supplier network and maintaining ongoing relationships with all input vendors. Changes in bromine or base chemical prices get managed through buffer agreements, so our production calendars remain largely intact. Several clients have mentioned that, even during the COVID-19 pandemic, our shipments remained on schedule when others faltered.

    Keeping communication open matters as much as producing high-quality substances. Our commercial and technical teams continually monitor for signals of upstream or downstream constraints—getting ahead of unforeseen delays means fewer missed deadlines and more predictable batch launches for clients. Transparency, built day after day in consistent interactions, keeps these relationships strong.

    Ongoing Development: Innovations Rooted in Shop-Floor Experience

    Staying competitive in the global chemical market requires more than following the same script with every batch. Each year, our synthesis group pursues process improvements—tweaking stoichiometry, updating equipment, and retraining operators. Many of these changes stem from after-action meetings where technical managers and shop-floor staff compare final batch reports, troubleshoot problem runs, and propose new approaches.

    As a result, our process for making 2-(4-Bromomethyl)Phenylpropionic Acid improved not by accident but by conscious analysis of what works and what does not. Minor changes, like adjusting filtration times or revising crystallizer settings, compressed production cycles by hours. These gains let us respond to customer emergencies and seasonal demand spikes with confidence. Ultimately, it’s this feedback loop—from pilot batch to full-scale delivery—that keeps our compound’s quality and reliability ahead of what others in the market can offer.

    Real-World Differences: Going Beyond the Catalog Page

    Discussing technical grade versus high-purity material, many groups overemphasize theoretical specs. In our facility, the proof comes through firsthand use cases—how clean the material appears upon arrival, how predictable it behaves when weighed, and how much labor it saves on post-reaction separation.

    For those pursuing tight Active Pharmaceutical Ingredient (API) specifications, the difference between meeting a parts-per-million limit for halide contamination and missing it can rest on the consistency of the supplier’s batch process. Over the years, we’ve invested in high-grade analytical reference standards and upgraded our detection capabilities—giving us and our clients confidence that each shipment supports seamless workflow integration. Our hands-on engagement with clients and focus on transparent reporting made us a preferred partner for some of the world’s leading pharmaceutical innovators.

    Summary: Confidence Grown from Manufacturing Knowhow

    2-(4-Bromomethyl)Phenylpropionic Acid serves as a textbook case for what years of direct manufacturing experience add to a simple chemical structure. Its value, measured not only in high purity and reliable functionality but in the absence of surprises, is something that catalog descriptions simply cannot convey. Our ongoing pursuit of better process controls, hands-on customer support, and honest engagement makes a real-world difference, ensuring every shipment out of our plant helps move our clients’ projects one step closer to commercial realization.

    In an industry shaped by continual change, quality and reliability become the natural byproducts of rigorous work and a culture focused on learning, improvement, and accountability. Each batch stands as proof that expertise at the manufacturer’s bench keeps value and trust flowing down the supply chain, from chemical foundation to final breakthrough.