Anhui Liwei Chemical Co., Limited
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Phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]-


    • Product Name Phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]-
    • Alias 4-[(5-Bromo-2-chloro-phenyl)methyl]phenol
    • Einecs 401-040-5
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    453264

    Iupac Name 4-[(5-Bromo-2-chlorophenyl)methyl]phenol
    Molecular Formula C13H10BrClO
    Molecular Weight 313.58 g/mol
    Appearance Solid (usually powder or crystalline)
    Boiling Point Decomposes before boiling
    Cas Number 627842-89-3
    Smiles C1=CC(=CC=C1CC2=CC(=C(C=C2)Br)Cl)O
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98% (when provided commercially)
    Storage Conditions Store in a cool, dry, and well-ventilated place

    As an accredited Phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 25-gram amber glass bottle with a secure screw cap and tamper-evident seal, properly labeled.
    Shipping Phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl-] should be shipped as a hazardous chemical, securely packaged in sealed containers conforming to applicable regulations (DOT, IATA, IMDG). Ensure secondary containment, proper labeling with hazard identification, and accompanying safety data sheets (SDS). Handle with care to avoid exposure, and protect from moisture, light, and temperature extremes during transit.
    Storage Store Phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]- in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Use secondary containment to avoid spills. Label clearly and keep away from ignition sources. Handle using appropriate personal protective equipment to prevent exposure to skin, eyes, and inhalation.
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    Certification & Compliance
    More Introduction

    Phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]-: A Manufacturer’s Perspective

    Our Approach to Phenol Chemistry

    Working hands-on as a manufacturer in the fine chemicals field, I’ve spent years involved in phenolic compound production. Every new derivative adds another layer of complexity and demand. Phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]-—for some, a simple entry on a synthesis flowchart. In the plant, this compound becomes an environment where knowledge, reliable raw sourcing, controlled reaction conditions, and constant testing all intersect. Whether it’s the first kilogram from a new batch or the thousandth, the intricacies behind this phenol’s preparation never make it routine.

    Brominated, chlorinated, and methylated phenols aren’t just traditional benzenoid molecules. Each subtle change tacks on multiple considerations. The 5-bromo, 2-chlorophenyl moiety attached to a simple para-positioned hydroxyl ring lies at the center of our daily focus. Choosing starting reagents for this synthesis demands more than just commodity buying; raw material quality influences downstream purification and ultimately impacts the reproducibility of reactions when scaled. As someone who’s handled plenty of process adjustments, I’ve witnessed how one impure intermediate multiplies the workload on boiling, filtration, and chromatography lines.

    Specifications and Quality—Built from Experience

    Our most consistent batches come when all staff—chemists, engineers, analysts—share observations in real time. Specification sheets alone never tell the full story of what works. Over the years, we’ve observed that the ideal physical form falls between an off-white to faint tan crystalline solid. Moisture content strongly affects both handling and the reliability of melting point data. After separating product from mother liquor, vacuum drying below 50°C produces a consistent, free-flowing powder, suitable for both analytical and preparative usage.

    GC-MS and HPLC always confirm final purity. Our target remains above 99% organic purity, but we monitor trace halogenated impurities more closely now than a decade ago. Years back, a minor unknown impurity eluded standard TLC. We found, through collaboration with our analytical team, this side product affected some pharmaceutical partners’ downstream activity-screening. Introducing further selective crystallization steps and tweaking solvent ratios in workup produced a marked improvement in final material quality—something a spec sheet had previously failed to highlight.

    Batch-to-batch challenges often relate to the reactivity of both bromine and chlorine substituents. In my view, tightly controlled addition rates in our functionalization steps outmatch even expensive feedstock upgrades. Automated controls never replace the trained eye of a staff chemist when exotherms run slightly hotter than expected. We log each deviation, which guides consistent process improvement.

    Applications in Synthesis and Industry

    Demand centers around specialty intermediates for pharmaceuticals and agrochemicals. Over time, our phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]-, found its way as a backbone in research synthesis and eventually in pilot-scale commercial production. Medicinal chemists appreciate the activation achieved by the bromine and chlorine for further coupling reactions. It’s now a familiar unit in constructing more advanced heterocycles.

    The electron-withdrawing halogens influence reactivity in ways that aren’t obvious until testing new routes; experienced process scientists notice how selective protection or deprotection steps benefit from these substituents. We’ve seen it act as both a nucleophile under basic conditions and as a handle for Suzuki, Heck, and other palladium-catalyzed reactions. One key detail stands out: while unhalogenated analogues show easier oxidation, this specific pattern improves shelf stability, making storage and transportation more predictable.

    Some customers originally sought it as a reference compound for bioassay screening. Once confident in the batch-to-batch consistency, they scaled up for multi-kilogram preparations. A process development chemist once hesitated at using halogenated precursors, expecting a persistent odor and fouling during scale-up. With careful control and attention to finishing techniques, we consistently deliver a product free from lingering aromatic impurities, which lowers workplace exposure risk and improves satisfaction for teams working with the material daily.

    Distinctive Features Compared to Standard Phenols

    Direct comparison with simpler phenol derivatives—such as 4-methylphenol or 4-chlorophenol—often misses the nuanced difference this bromo-chloro combination brings. It changes more than just the melting point or solubility; it allows access to a wider set of downstream chemistry. Based on internal experiments and customer feedback, coupling yields often rise when using this structure as a starting point, especially in metal-catalyzed routes.

    I’ve noted that the increased molecular weight and substitution pattern grant this molecule a subtle advantage in selective transformations. Even when making sulfonates or carbamates, the byproduct profile becomes more manageable, often cutting time spent on tedious column separations. Meanwhile, our analytical team highlights a sharper, more resolved NMR spectrum compared to other crowded aromatic compounds, which speeds up purity verification for researchers.

    Differences from lower halogenated analogues show up most in the final steps. The 5-bromo substituent in the 2-chlorophenyl ring brings greater selectivity for coupling, avoiding the ambiguities encountered with overactive sites on less-protected rings. Those seeking to functionalize only one specific position find this pattern beneficial; I’ve seen synthetic routes trimmed by an entire step thanks to the reduced risk of over-substitution.

    Production Challenges and Process Improvements

    Deciding on synthetic routes for this compound is anything but trivial. Early approaches often started with direct alkylation of 4-hydroxybenzyl alcohols or their protected derivatives. As we scaled, complications in controlling side bromination, chlorination, and over-alkylation forced us to reevaluate and develop sequential addition protocols. Those who have tried large-scale halogenation understand the unpredictable nature of exothermic reactions, especially under pressure. Temperature ramp rates mean the difference between a clean reaction and a tarry, irrecoverable waste.

    We invested in reactor upgrades to improve temperature and agitation control. With better sensor integration, we cut overall impurity formation in half and brought our waste treatment costs down significantly. In-house recycling of process solvents and implementation of energy exchange systems also improved both our environmental footprint and bottom line. Neither supply chain managers nor production chemists ignore solvent availability; market fluctuations create as many headaches as shifting regulatory requirements.

    By linking our analytical output with process control feedback, outlier batches rarely slip through. We empower anyone on the line to halt production and consult with QA should discrepancy arise, fostering a workplace culture of accountability and pride in the end result. Organic chemists on-site routinely liaise with our customers, relaying real-world feedback from bench and plant. These conversations have driven persistent changes, like substituting more readily available oxidants or moving away from chlorinated solvents—improving both safety and sustainability.

    Downstream User Perspectives

    Feedback from industrial users often adds value we can’t see from the plant floor. Many buyers originally selected this compound for its halogen pattern, but now describe how its unique structure lets them build more complex targets. We take their stories seriously—one used it to accelerate a medchem structure-activity relationship (SAR) campaign, bypassing less reliable intermediates prone to side reactions. From another, we learned that lower halogen purity standards in a competitor’s batches delayed a batch release in their own plant. That led us to implement a more aggressive surveillance program monitoring halide ion residuals at the ppm level.

    Even differences in packaging and storage conditions ripple forward. This particular phenol, with its extra halogen substituents, holds up better than most against slow autoxidation. Sealed, inert-atmosphere containers remain standard, but customers report less degradation at ambient temperatures versus perishable phenol analogues. Improvements in packaging film permeability and sealing method represent incremental advances that make a difference all the way to the final benchtop in distant R&D labs.

    A recurring challenge remains the safe handling profile. Aromatic halides always bring some risk of skin or respiratory irritation. Our team’s attention extends past the reactor: we optimize line layouts for exhaust, undergo regular air monitoring, and offer clear counsel to users about minimizing exposure during bench-level operations.

    Addressing Supply Chain and Regulatory Concerns

    In recent years, raw material markets haven’t offered much predictability. Phenol feedstock prices change with global demand swings in polycarbonates and resins. Brominating agents face separate volatility as global regulations adjust to reduce harmful byproducts elsewhere in industry. As a manufacturer, I don’t wait for a crisis. Our supply team forges ongoing relationships with upstream vendors, audits storage conditions, and tracks lot consistency at every transfer point.

    Regulation—especially in Europe and North America—always shapes our planning horizon. Strict guidelines covering both the storage and disposal of halogenated organic intermediates forced us to upgrade our waste-handling systems early. Each investment returns dividends in reliability; future audits no longer provoke the nervousness seen in earlier days. By maintaining robust documentation on synthetic and purification batches, we’ve weathered both voluntary and regulatory recalls without incident.

    Our environmental commitment guides regular review of water usage and emissions across synthesis lines. Waste minimization isn’t a slogan—it’s an operational standard. Regular staff meetings focus on isolating waste streams by halogen content and adapting neutralization protocols to suit both onsite treatment and offsite disposal partners. Years of incremental tweaks saved thousands in disposal fees and protected our baseline ability to supply as standards evolve.

    Innovation and Future Uses

    Product development never pauses. Phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]- exists as a result of persistent research collaboration between process chemists, engineers, and end-users in industry and academia. We always look for ways to improve control over substitution patterns, reaction exotherms, and purity. One new approach involved switching to continuous-flow processing for certain steps, reducing both cycle time and overall energy usage without sacrificing quality. Not every pilot project pays off, but the ones that do bring major cost and quality advantages.

    Customers continue to propose new uses in emerging fields, including advanced materials and functional polymers. Some research labs experiment with this compound in photochemical and electronic applications because its rigid, halogenated ring system translates into new physical and electronic properties. Having direct dialogue with specialty compound developers speeds up our learning curve and helps forecast future scaling needs.

    On the plant floor, we’ve begun using this phenol as a training case for junior chemists to learn advanced handling and quality assurance. It builds competencies in glovebox technique, analytical sampling, and troubleshooting when reaction outcomes fall outside norms. That process tightens our quality control and raises confidence at every level of manufacturing.

    Commitment to Safety and Transparency

    Taking responsibility for each batch means refusing to cut corners—no matter the pricing pressure from buyers or volatility in marketplaces. Manufacturing a halogenated phenolic intermediate stays safe only with a full commitment to process transparency, operator education, and traceable quality assurance data. Direct communication among production, analytical, and supply teams heads off problems before they leave the plant.

    We post updated protocols for all incoming raw material checks and verify each result before release. Training programs adapt as regulations change. Sharing knowledge between sites and shifts, we protect both workers and the environment. Plant operators, warehouse staff, technicians, and support teams all play a part; in this work, one unit of product means many hours of attention, care, and shared experience.

    Real-World Lessons Learned

    In two decades working with halogenated phenolic compounds, I’ve seen the industry’s best innovations come from early recognition of problems and an openness to outside feedback. Mechanical filtration methods changed as we understood new insoluble byproducts. Methods for process temperature management improved each time we noticed endotherms slowing overall throughput. Years of scaling, troubleshooting, and learning from both our successes and failures have shaped the reliable product we ship today.

    The best measure of any specialty chemical lies in user impact. We track reports from research, scale-up, and manufacturing networks closely. Success doesn’t mean just meeting the technical spec; it means delivering a compound that performs without introducing extra difficulties or safety risks. I take pride in knowing our advances come from hard experience, teamwork, and direct feedback from those making real-world discoveries using our product.

    Looking Forward—Manufacturing in a Changing Landscape

    Producing phenol, 4-[(5-Bromo-2-Chlorophenyl)Methyl]-, calls for flexibility, observation, and a respect for evolving client demands. Whether refining process yields, cutting energy use, or meeting new regulations, we see each change as a learning moment. Every lot not only represents the accumulated skill of our team—it drives future improvements.

    We stay ready to adapt—integrating new production methods, listening closely to users, and building collaborative relationships across the industry. Consistency, safety, and responsiveness remain the foundation of our work. That’s the true difference between just shipping a compound and being a dedicated manufacturer: the daily commitment to learn, improve, and support those who rely on the quality, reliability, and insight behind every kilogram.