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2-Bromo-5-Fluorobenzyl Alcohol

    • Product Name 2-Bromo-5-Fluorobenzyl Alcohol
    • Alias (2-Bromo-5-fluorophenyl)methanol
    • Einecs 823-541-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    989040

    Name 2-Bromo-5-Fluorobenzyl Alcohol
    Cas Number 847488-34-8
    Molecular Formula C7H6BrFO
    Molecular Weight 205.03 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically >98%
    Synonyms α-(2-Bromo-5-fluorophenyl)methanol
    Smiles C1=CC(=C(C=C1F)CO)Br
    Inchi InChI=1S/C7H6BrFO/c8-6-2-1-5(9)3-7(6)4-10/h1-3,10H,4H2
    Storage Conditions Store at 2-8°C, protected from light
    Solubility Soluble in most organic solvents

    As an accredited 2-Bromo-5-Fluorobenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 2-Bromo-5-Fluorobenzyl Alcohol

    Applications of 2-Bromo-5-Fluorobenzyl Alcohol in Industrial Manufacturing

    2-Bromo-5-Fluorobenzyl Alcohol serves as an efficient intermediate in chemical synthesis for multiple industrial segments. Our manufacturing process supports high-quality output for regulated downstream industries, addressing complex requirements for purity, batch consistency, and compliance critical to advanced end-use applications.

    1. Pharmaceutical Intermediate Production

    Pharmaceutical manufacturers employ 2-Bromo-5-Fluorobenzyl Alcohol as a key intermediate during the synthesis of several active pharmaceutical ingredients (APIs), especially for selective serotonin reuptake inhibitor (SSRI) classes and fluorinated benzyl-substituted pharmaceuticals. The compound allows for precise introduction of bromo and fluoro substituents, ensuring specificity and yield in multi-step organic synthesis. Downstream process control at this stage includes continuous monitoring for trace impurities in compliance with pharmacopeial standards, with material entering after protection/deprotection chemistries and preceding primary coupling or functionalization steps in drug manufacture.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF (United States Pharmacopeia – National Formulary)
    • European Pharmacopoeia (Ph. Eur.) monographs for process chemicals
    • Chemical safety standards as per REACH (EC 1907/2006)

    Typical usage ratio

    • Used in stoichiometric or slight excess amounts depending on API target; commonly 0.95–1.15 molar equivalents per linking step, varying based on catalyst loading and desired byproduct minimization.

    Downstream process integration

    • Utilized post-halogenation and before etherification or amination steps. Material feeds into batch or semi-batch reactors where purity is critical for step yield.

    Final product types

    • Antidepressants (e.g., paroxetine analogs)
    • Fluorinated benzyl drug substances
    • Intermediates for targeted oncology APIs
    • Other fluoro- and bromo-derived pharmaceuticals

    2. Agrochemical Synthesis

    In the agrochemical sector, 2-Bromo-5-Fluorobenzyl Alcohol supports synthesis of pyridine-based and benzyl-fluoride derivatives utilized in advanced crop protection agents. It enters as a coupling agent for forming C–O and C–N bonds adjacent to fluoro and bromo groups, enabling specific activity profiles in custom pesticide and fungicide molecule development. Our consistent supply maintains downstream batch reproducibility demanded by regulated agrochemical manufacturing environments.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 certified quality systems for agrochemical intermediates
    • REACH registration for intermediates

    Typical usage ratio

    • Usually 1.05–1.25 molar equivalents in condensation reactions; dosage adjusts for yield optimization and catalyst sensitivity depending on end molecule complexity.

    Downstream process integration

    • Password input into synthesis line after halogen integration, followed by oxidation, esterification, or ring-closing steps specific to active ingredient construction.

    Final product types

    • Fluorinated benzyl-based insecticides
    • Systemic fungicides employing bromo-fluoro building blocks
    • Herbicide intermediates for halogenated aromatic compounds
    • Active crop protection substance precursors

    3. Specialty Chemical Synthesis for Electronic Materials

    Manufacturers of specialty chemicals for electronic and photoresist industries use 2-Bromo-5-Fluorobenzyl Alcohol to introduce functional groups into high-performance organic compounds. The material’s incorporation enables fine-tuning of dielectric properties and enhances chemical resistance in downstream monomer or oligomer synthesis for printed circuit board resins and photolithography formulations. Our material feed consistency enables tight control over molecular structure and batch quality in this high-purity application domain.

    Industry compliance standards

    • SEMI C3-0819 (Specifications for High Purity Chemicals)
    • ISO 9001 for specialty chemical manufacturing
    • RoHS Directive 2011/65/EU for process materials
    • Internal customer quality and purity agreements for electronic materials

    Typical usage ratio

    • Integrated at 0.8–1.2 molar equivalents in functional unit synthesis; level varies with target final properties and degree of substitution required in oligomer chain extension.

    Downstream process integration

    • Material enters resin backbone assembly after initial monomer creation; further modified via etherification, crosslinking, or ring-substitution steps, preceding purification and formulation.

    Final product types

    • Photoresist monomers for microelectronics
    • Dielectric polymers for circuit boards
    • Functionalized benzyl ethers for organic electronics
    • Specialty resin intermediates

    4. Fine Fragrance and Aroma Chemical Production

    In the fine chemical sector, 2-Bromo-5-Fluorobenzyl Alcohol acts as a tailored precursor to novel aroma molecules and specialty fragrance intermediates. Its distinctive substitution pattern provides unique olfactory notes when converted to aldehyde and ester derivatives through selective oxidation and acylation. This enables perfumers and aroma product manufacturers to develop patent-protected molecules with high tenacity and performance required for designer scent and flavor compositions.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • FEMA GRAS (Flavor and Extract Manufacturers Association Generally Recognized as Safe)
    • ISO 9001 systems for flavor and fragrance ingredient production
    • REACH inventory and notification for downstream use

    Typical usage ratio

    • 0.6–1.1 molar equivalents based on end aroma compound; sensitivities adjusted to control olfactory note intensity and byproduct profile during downstream synthesis.

    Downstream process integration

    • Input immediately before target aldehyde synthesis or as feedstock for esterification and ether formation; further purified through fractional distillation, impacting final fragrance quality and compliance.

    Final product types

    • Aldehydic aroma molecules for fine perfumery
    • Benzyl-based esters for fragrance concentrates
    • Specialty intermediates for aroma boosters in home and body care products
    • Compounded flavors for food and beverage applications
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    Certification & Compliance
    More Introduction

    Introducing 2-Bromo-5-Fluorobenzyl Alcohol: A Reliable Intermediate for Modern Applications

    Understanding the Role of 2-Bromo-5-Fluorobenzyl Alcohol

    Chemistry, much like cooking, relies on reliable ingredients to get the reaction just right. Anyone working in pharmaceutical research or fine chemical synthesis knows the hunt for a reagent with the right balance of reactivity and selectivity. 2-Bromo-5-Fluorobenzyl Alcohol offers a unique structure—a benzyl alcohol with bromine and fluorine atoms at precise positions. It goes beyond the basic benzyl alcohol, opening doors for targeted reactions where both steric and electronic effects are important. The presence of fluorine and bromine transforms the core molecular skeleton, making this compound an effective building block for advanced synthesis.

    From years spent in synthetic labs, I’ve come to value intermediates that deliver consistency. Some substances might look similar on paper, but just a small difference in the arrangement of atoms can cause a big swing in outcome. 2-Bromo-5-Fluorobenzyl Alcohol stands out because it’s specifically suited for producing molecules where both halogenated and hydroxylated functionality matter. Whether you’re developing new active pharmaceutical ingredients, agrochemicals, or specialty materials, the position of the bromine at the ortho and the fluorine at the meta position relative to the alcohol group gives this compound reactivity that ordinary benzyl alcohols do not supply.

    Specifications Shaped for Practical Synthesis

    The purity of 2-Bromo-5-Fluorobenzyl Alcohol is essential. Impurities don’t just risk batch rejection in commercial settings—they can lead to unwanted side-reactions that waste valuable time. Typically, high-purity grades, often above 98%, are offered in solid or liquid forms, clear or pale yellow, depending on storage conditions and batch history. Molecular weight lands near 221.02 g/mol. Often, you’ll see it offered by its chemical formula C7H6BrFO, giving a clear nod to its balanced structure: seven carbons, six hydrogens, one bromine, one fluorine, and one oxygen.

    Storage advice tends to align with industry norms: keep it dry, out of strong light, and away from oxidizing materials. Sealed amber glass bottles remain the standard for safeguarding sensitive organics like this one. After years of handling similar chemicals, I’ve learned that even though some bottles seem overpacked, suppliers do that for good reason—oxidation or hydrolysis can quickly degrade a batch and make it unusable. Working with the pure material improves yields and reduces post-reaction cleanup.

    Why Chemists Prefer 2-Bromo-5-Fluorobenzyl Alcohol

    What makes this compound such a versatile choice? It’s all about the interplay of functional groups. With bromine in the ortho-position, the alcohol group becomes more reactive toward certain nucleophiles and electrophiles. The fluorine atom in the meta-position brings added stability and can fine-tune both electronic and steric profiles of intermediates. Whether the focus is Suzuki couplings, nucleophilic substitution, or reductive amination, starting with a substrate like this cuts down on unwanted byproducts.

    Researchers developing fluorinated drugs see major advantages in this structure. Compared to non-halogenated benzyl alcohols, this compound provides a direct entry point for introducing both fluorine and bromine in a single synthetic step—something that would require several protection and deprotection cycles with other precursors. A fluorine atom, small but strongly electronegative, can drastically affect the bioavailability, metabolic stability, and binding affinity of drugs. Adding bromine raises reactivity for further modification through palladium-catalyzed couplings or halide exchange.

    Having worked with a range of substituted benzyl alcohols, I’ve run into issues with poorly characterized materials stalling progress. Halogenated alcohols sometimes play “hard to get”—reacting sluggishly or unpredictably. But with 2-Bromo-5-Fluorobenzyl Alcohol, chemists report a consistent balance: neither too reactive to handle nor so inert that extra forcing conditions are needed. For labs with tight timelines, this reliability saves weeks, sometimes months, during project work.

    Comparing to Other Benzyl Alcohols

    On the surface, 2-Bromo-5-Fluorobenzyl Alcohol looks like just another entry in a long line of benzylic alcohols. The difference emerges in its dual halogen modification. For example, plain benzyl alcohol is a classic workhorse but lacks the enhanced reactivity needed for many targeted syntheses. Monosubstituted benzyl alcohols, such as 4-fluorobenzyl alcohol or 2-bromobenzyl alcohol, offer incremental advances. Neither, though, captures the synergy that comes from both halogen positions.

    The pharmaceutical sector often requires “metabolic handles”—functional groups that tweak the way a molecule behaves both in vitro and in vivo. Here, the fluorine atom acts as a metabolic modifier, often slowing down oxidative degradation. The bromine gives a convenient site for coupling, allowing for diversification down the line. Chemists pursuing structure-activity relationship studies get a flexible scaffold for rapid analog development. Compared to older intermediates, efficiencies add up across the workflow: reduced step count, improved selectivity, and lower purification costs.

    In specialty polymers and material science, halogen substitution can also influence properties like refractive index, thermal stability, and electronic conductivity. The inclusion of both bromine and fluorine extends the tuning range possible with 2-Bromo-5-Fluorobenzyl Alcohol, giving formulators extra control compared to single-halogen compounds.

    Supporting Quality in Manufacturing

    Consistency is king, especially for companies scaling up from gram bench tests to multi-kilogram pilot runs. While regulatory filings and downstream processing often focus on active agents, the quality of intermediates can make or break a project. Reliable 2-Bromo-5-Fluorobenzyl Alcohol feeds the pipeline for downstream processes like esterification, oxidation, and coupling reactions. When purity slips, issues like catalyst poisoning or side reactions pop up, increasing costs and regulatory headaches.

    In my experience, supply chain disruptions expose weak points in sourcing and quality assurance. During the pandemic, for example, projects ground to a halt not because of the final APIs, but over gaps in reliable intermediates. Trustworthy sourcing partners for specialized reagents such as this compound help maintain project momentum and keep teams focused on innovation—rather than emergency fixes.

    Handling and Safety Considerations

    Working with halogenated benzylic alcohols means paying close attention to handling protocols. These substances can cause skin or eye irritation, so gloves and goggles remain non-negotiable in any professional setting. Volatility isn’t especially high, but I’d still avoid open flask procedures unless proper fume extraction is in place. Over the years, I’ve seen too many junior chemists underestimate the risks—one slip-up with even moderate irritants can mean lost lab time.

    Waste management calls for collecting residues and unused material. Disposing of halogenated organics requires following strict guidelines to prevent environmental contamination. Labs typically coordinate with certified disposal services; melting points and boiling profiles for 2-Bromo-5-Fluorobenzyl Alcohol depend a bit on storage and batch, but this doesn’t excuse shortcuts in disposal routines.

    Environmental and Regulatory Perspective

    The presence of halogens in chemical products brings extra scrutiny under environmental regulations. Both brominated and fluorinated organics face evolving restrictions depending on geography. Manufacturers have the responsibility of providing clear paperwork—specifically safety data sheets and certificates of analysis—that accurately represent the compound’s composition and ensure traceability. Working through regulatory reviews, especially in the EU and North America, means being ready for questions about trace impurities, routes of synthesis, and downstream fate of the halogen atoms.

    One manufacturer’s report noted that close attention to solvent choice during synthesis and purification can significantly lower risk of introducing persistent organic pollutants. Having spent time on such compliance tasks, I’ve seen that rigorous control from raw materials through waste management eases the burden when audits happen, allowing R&D teams to stay focused on advancement rather than regulatory firefighting.

    Case Applications in Drug Discovery and Materials Science

    For drug discovery projects, 2-Bromo-5-Fluorobenzyl Alcohol slips neatly into strategies where scaffold-hopping or late-stage functionalization are needed. Medicinal chemists take advantage of the reactive bromine handle to explore diverse analogs by Suzuki, Buchwald-Hartwig, or Ullmann cross-coupling. Fluorine, prized for tuning potency or reducing dosage requirements, fits squarely into “rule-of-five” strategies aimed at optimizing drug-like properties.

    I recall a project aiming to improve metabolic stability in a CNS-active lead. Switching from a chlorinated to a fluorinated benzyl alcohol intermediate made all the difference—resulting in cleaner analytical profiles and a longer plasma half-life. The shift took some adjustment in reaction conditions, but the end result was worth the upfront effort. 2-Bromo-5-Fluorobenzyl Alcohol offers that same promise for research teams: it lets creative chemists dial in features that older intermediates might not easily support.

    Materials science groups also draw on this compound’s structure, building block by block, when tailoring polymers or electronic materials. The bromine and fluorine segments enable the inclusion of advanced properties into base polymer chains, such as enhanced thermal resistance or optical tunability. It’s exciting to see how a reagent, sometimes thought of just as an intermediate, can have a ripple effect through final material performance and end-use characteristics.

    Challenges with Specialty Chemicals

    Sourcing specialty intermediates often forces chemists to choose between cost, availability, and reliability. Low-volume production sometimes leads to delays or quality swings. Market demand for fluorinated and brominated compounds has grown, putting pressure on upstream supply chains. A few years ago, a sudden spike in demand for a related halogenated benzyl alcohol led to long lead times and price jumps. Labs relying on just-in-time procurement lost productivity as projects stalled. Securing trustworthy, responsive suppliers makes a big difference.

    From a broader perspective, economic volatility affects both acquisition of rare starting materials and the logistics of moving chemicals safely from manufacturer to lab. In my experience, building a network of backup suppliers and confirming lot consistency with in-house QC teams pays dividends. Collaboration between R&D, supply chain managers, and regulatory experts helps minimize project interruptions due to missing or inconsistent intermediates.

    Pushing Innovation Forward

    Modern product pipelines in pharmaceuticals and advanced materials get more complex every year. The days of one-size-fits-all reagents are long gone. Custom-tailored intermediates like 2-Bromo-5-Fluorobenzyl Alcohol help R&D teams meet new challenges head-on. Its structure brings together desirable properties that speed up discovery and enable precision modification. Past experience tells me that innovative teams win not by using the most exotic starting points, but by working with dependable tools that strike the right balance between flexibility and control.

    Recent advances in synthetic chemistry continue to benefit from compounds like this. Automated platforms for high-throughput reaction screening demand robust inputs—compounds that provide reproducible behavior under a wide range of conditions. 2-Bromo-5-Fluorobenzyl Alcohol’s track record in academic publications and patents suggests that its place in the synthetic toolbox is well-earned. As projects grow in scale and complexity, its availability and trusted performance help keep the pace of innovation high.

    Responsible Practices and Ethical Considerations

    Any conversation about halogenated chemicals in research and industry circles must address responsible sourcing and use. Misuse or improper disposal carries risks—not only for the immediate team but for the public and the environment. Academic research often drives adoption of new intermediates, but industrial practice demands traceability, stewardship, and transparency. Everyone in the supply chain, from producer to end-user, shares in this responsibility.

    In my role overseeing lab operations, I have seen the positive impact of robust corporate policies: regular training, strict inventory records, and clear reporting minimize risk and set strong examples for students and junior scientists. Open discussions of batch issues, even small ones, foster a culture where researchers flag early signs of trouble rather than brushing them aside. This proactive mindset proves especially important with reactive, halogenated chemicals.

    Future Outlook for Substituted Benzyl Alcohols

    The demand for high-performance intermediates is unlikely to slow. As more research groups and companies look for efficiency and innovation, selectively substituted reagents like 2-Bromo-5-Fluorobenzyl Alcohol will shape new frontiers in science and engineering. Fluctuations in route-of-synthesis costs may impact short-term pricing, but advances in greener, more efficient synthetic routes could help level out those swings.

    With the continuing miniaturization of electronics and the pursuit of new pharmaceuticals, precision at the molecular level is crucial. Using thoughtfully designed building blocks, chemists are able to reach into previously unexplored regions of chemical space. The dual halogenation in this compound’s structure enables access to new bioactive motifs and functional materials not easily synthesized by other means.

    The conversation around specialty chemicals is evolving—more customers ask about sustainability, supply chain transparency, and regulatory compliance before placing orders. 2-Bromo-5-Fluorobenzyl Alcohol, by virtue of its versatility and reliability, stands in a strong position for future research needs, provided that suppliers and users alike maintain high standards for quality, safety, and responsible stewardship.

    Conclusion: Real-World Value for R&D

    Success in chemistry—whether in pharma, materials science, or specialty synthesis—often boils down to one thing: having the right tools for the job. 2-Bromo-5-Fluorobenzyl Alcohol offers more than a collection of atoms; it provides a foundation for precise, efficient, and controlled innovation. Chemists want more than raw reactivity; what counts is a blend of selectivity, predictability, and adaptability. This compound brings those strengths to the bench and keeps project momentum strong, even as the landscape shifts. Having worked across multiple disciplines and watched research goals evolve, I can say with confidence that intermediates designed with both function and flexibility in mind are set to play a leading role in the discoveries of tomorrow.