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4-Bromo-2-Fluorobenzyl Alcohol

    • Product Name 4-Bromo-2-Fluorobenzyl Alcohol
    • Alias (4-Bromo-2-fluorophenyl)methanol
    • Einecs 826-425-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    237264

    Product Name 4-Bromo-2-Fluorobenzyl Alcohol
    Cas Number 863870-49-5
    Molecular Formula C7H6BrFO
    Molecular Weight 205.03
    Appearance Colorless to light yellow liquid
    Purity Typically ≥97%
    Solubility Soluble in organic solvents such as DCM and ethanol
    Smiles OCc1cc(Br)ccc1F
    Inchi InChI=1S/C7H6BrFO/c8-6-2-1-5(4-10)3-7(6)9
    Synonyms α-(4-Bromo-2-fluorophenyl)methanol
    Storage Conditions Store at 2-8°C, protected from light

    As an accredited 4-Bromo-2-Fluorobenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25g, with tamper-evident cap, hazard label, product name, batch number, and safety information clearly displayed.
    Shipping **Shipping Description for 4-Bromo-2-Fluorobenzyl Alcohol:** This chemical is shipped in tightly sealed containers, protected from light and moisture, and typically packed with absorbent material. Transport complies with relevant regulations for hazardous substances, including proper labeling and documentation. Shipping is conducted via authorized carriers, ensuring safety and compliance with local, national, and international guidelines.
    Storage 4-Bromo-2-Fluorobenzyl alcohol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it separated from incompatible substances such as strong oxidizers and acids. Store at room temperature, avoiding excessive heat or moisture. Ensure proper labeling and handle according to standard laboratory safety protocols to prevent exposure or contamination.
    Application of 4-Bromo-2-Fluorobenzyl Alcohol

    Applications of 4-Bromo-2-Fluorobenzyl Alcohol in Industrial Manufacturing

    As a manufacturer dedicated to the development and supply of specialty aromatic intermediates, we provide 4-Bromo-2-Fluorobenzyl Alcohol to the global market for well-established downstream sectors. Below we outline its primary industrial applications, with specific consideration of industry standards, real formulation practices, integration with downstream synthesis, and end-use product types supported by our QC and technical documentation.

    1. Pharmaceutical API Intermediate Synthesis

    This compound supports the manufacture of active pharmaceutical ingredient (API) intermediates, especially for advanced heterocyclic drugs requiring fluorinated and brominated aromatic moieties. The alcohol functionality provides strategic leverage for functional group interconversion, used by HPAPI and oncology molecule manufacturers for final API assembly under strict quality control. Its batch traceability aligns with US FDA and EU regulatory audit requirements for pharmaceutical synthesis chains.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • EU GMP Directive 2011/62/EU for starting materials
    • 21 CFR 211 (US FDA cGMP for finished pharmaceuticals, for traceability)
    • Chinese Pharmacopoeia for intermediate handling (where required for export registration)

    Typical usage ratio

    • Used at 0.7–3.2 molar equivalents, adjusted according to final API batch size and route of synthesis
    • Exact charge depends on downstream nucleophilic substitution step and desired conversion yield

    Downstream process integration

    • Enters as a building block in Suzuki, Buchwald-Hartwig, or etherification reactions for assembling fluorinated biaryls or fused ring intermediates
    • Undergoes oxidation, chlorination, or direct alkylation prior to core coupling stage in API labs

    Final product types

    • Targeted oncology drugs
    • Neuropsychiatric agents
    • Antiviral small molecules
    • Advanced synthetic intermediates for regulatory filings

    2. Agrochemical Active Ingredient Precursor

    Agricultural formulation companies apply this molecule in the synthesis chain for new-generation herbicides and insecticides that incorporate halogenated benzyl motifs. Its unique substitution pattern supports selective bioactivity tuning through direct chemical transformation, contributing to sustainable crop protection agents compliant with international safety and residue requirements. Our extensive batch documentation directly aids customer regulatory submissions in both developed and emerging markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • European Regulation (EC) No 1107/2009 (placing on the market of PPPs)
    • US EPA FIFRA requirements for technical grade active ingredients
    • ISO 9001:2015-certified QA traceability for export-oriented supply

    Typical usage ratio

    • Common addition of 1–5% w/w in multi-step synthesis of targeted agrochemical actives
    • Adjusted based on desired functional group transformation and precursor reactivity

    Downstream process integration

    • Introduced during alkylation or esterification steps forming core pesticide scaffolds
    • Undergoes subsequent halogen exchange, oxidation, or protective group chemistry as part of the active’s assembly

    Final product types

    • Selective herbicidal active ingredients
    • Systemic insecticide precursors
    • Advanced fungicide intermediates
    • Formulated concentrate for regulated market distribution

    3. Specialty Chemical and Performance Materials Synthesis

    Producers of advanced performance materials use this bromofluoroaromatic alcohol as a scaffold starter in the manufacture of specialty monomers and resins. Its dual halogen substitution enables precise electronic property modulation for engineered polymers, adhesives, and liquid crystals. These properties are essential for applications demanding strict electrical or thermal characteristics, with downstream QC documentation ensuring traceable quality for high-value sectors.

    Industry compliance standards

    • ISO 9001:2015 certification
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • RoHS 2011/65/EU for electrical/electronic materials (where applicable)
    • CFR Title 21 for indirect additives in processing (in certain polymer applications)

    Typical usage ratio

    • Usually 2–10 phr (parts per hundred resin) in polymerization feedstock
    • Concentration varies with desired substitution density and chain functionality

    Downstream process integration

    • Feeds as an initiator or comonomer in resin or oligomerization reactors
    • Incorporated by etherification, direct halogen exchange, or alcohol-to-aldehyde conversion prior to polymer chain extension

    Final product types

    • Liquid crystal intermediates for electronic displays
    • High-performance adhesives and engineering plastics
    • Specialty coatings for electronics or optical films
    • Advanced resins for sensor and semiconductor encapsulants

    4. Fine and Custom Chemical Synthesis

    Custom synthesis service providers and fine chemical manufacturers utilize this intermediate in the development of fluorinated and brominated compounds needed for niche life science research, analytical standards, or proprietary molecule design. Our material offers distinct reactivity for rapid scaffold diversification driven by specific project needs and strict analytical traceability, helping R&D clients fulfill both synthetic and reporting obligations efficiently.

    Industry compliance standards

    • ISO 17025:2017 (analytical testing traceability for standards production)
    • OECD Principles of Good Laboratory Practice (GLP)
    • Local chemical registration—TSCA (US), IECSC (China), or other jurisdictions
    • Internal customer protocols for custom molecule qualification

    Typical usage ratio

    • Ranges from 0.5–10 mmol scale for R&D batches, scaling up to kilogram level as project progresses
    • Modified according to the specific synthetic route, functionalization degree, or required intermediate purity

    Downstream process integration

    • Enters at the scaffold-building phase for aryl functionalization, usually via direct arylation, cross-coupling, or selective protection/deprotection steps
    • May undergo iterative derivatization for SAR (structure-activity relationship) campaigns in early drug discovery

    Final product types

    • Reference standards for analytical labs
    • SAR tool compounds for pharmaceutical discovery
    • Diagnostic reagent intermediates
    • Custom fluorescent or probe molecules for research
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    Certification & Compliance
    More Introduction

    4-Bromo-2-Fluorobenzyl Alcohol: A Manufacturer’s Insight

    Trust Grows from Experience and Quality

    Every batch of 4-Bromo-2-Fluorobenzyl Alcohol leaving our site carries the imprint of discipline, attention, and practical know-how. This fluorinated benzyl alcohol isn’t just a chemical on a catalog—it is the result of carefully tuned protocols, consistent sourcing, and years spent refining each production step. As a manufacturer, we do more than replicate a structure: we chase purity, reproducibility, and safe handling at every turn.

    The chemical—known in shorthand by its model designation, sometimes referenced by CAS number 179898-41-2—finds its place within a tightly woven supply chain. Laboratories working on aromatic substitution reactions and intermediate synthesis reach for this molecule because it brings something extra: the bromine and fluorine atoms placed on the benzene ring lend new properties not found in unsubstituted benzyl alcohols. That means greater selectivity, altered reactivity, and new possibilities in custom synthesis projects. Chemists value differences like these. As we’ve partnered with R&D teams and process chemists around the world, we’ve seen firsthand how the right substitution pattern on an aromatic alcohol opens shortcuts, saves purification cycles, and sometimes makes unthinkable projects possible.

    Look Beyond the Cas Number

    Benzyl alcohols as a group sometimes seem generic at first glance, especially in fine chemical catalogs. But production experience with compounds like 4-Bromo-2-Fluorobenzyl Alcohol makes one point clear: small differences in substitution carry huge practical importance. Our team has adjusted solvent profiles and run dozens of crystallization tests to hit a consistent appearance—usually an off-white crystalline powder or sometimes a viscous liquid, depending on production scale and storage temperature. A small impurity spike, often invisible during one-off R&D-scale runs, can snowball during scale-up. Impurities such as unreacted starting material, or regioisomers arising from halide crossover, cost time and money later.

    Real-world projects, especially in pharmaceutical custom synthesis or advanced materials, rarely leave margin for guesswork. Every order of 4-Bromo-2-Fluorobenzyl Alcohol that leaves our site carries a full analytical report, generated in-house: NMR—both proton and fluorine—HPLC purity trace, and occasional GC-MS confirmation on request. We’ve learned these checks matter. R&D teams come to us, asking for this alcohol by specification, because they’ve been burned elsewhere by sidestream isomers or suspicious color. Replicability comes from obsessive monitoring of every distillation, wash, and crystallization, and we own that responsibility—it never gets delegated or rushed.

    Application Drives Our Thinking

    This compound appears as an intermediate in the synthesis of heterocycles and functionalized aromatics. Biotech teams and medicinal chemists rely on the electron-withdrawing bromine and fluorine for targeted halogenation reactions. Those substituents change electron density, which means a seasoned chemist can build more control into selective cross-coupling, nucleophilic substitution, or Grignard reactions. Rather than just reacting as a generic benzyl alcohol, our product supports intricate route design—when downstream intermediates require selectivity or halogen retention, that matters a lot.

    We’ve heard from process engineers seeking to optimize yields in Suzuki or Sonogashira cross-coupling steps who prefer our product because retention of the bromine and fluorine controls downstream reactivity. The alcohol group brings reactivity that can be strategic, especially when converted to esters, ethers, or halides as needed—each with a clear, documented pathway. As the manufacturer, we coordinate with these clients to ensure scale-dependent parameters are considered: what works for a 5 g trial may need serious vitamin D (dedication) on the drum scale. We’ve adapted, learning to strip batch-to-batch variations from our runs, and we never hide behind specs. If a customer hits a problem, we look at our batch data and answer honestly.

    Comparing to Other Benzyl Alcohols: What’s Distinct About 4-Bromo-2-Fluorobenzyl Alcohol?

    This alcohol stands out for its substitution pattern. With a bromine at the 4 position and fluorine at the 2 position, the molecule assumes a different kind of personality compared to more common benzyl alcohols such as the unsubstituted version or mono-substituted entries like 4-bromobenzyl alcohol and 2-fluorobenzyl alcohol. Bromine and fluorine together do not just add molecular weight—they shift the electron density, alter the polarity, and open doors to unique synthetic strategies.

    Bench chemists can make quick substitutions for mono-halogenated or unsubstituted benzyl alcohols. But multistep syntheses requiring selectivity—especially when crafting complex pharmaceuticals or agrochemicals—demand tools like 4-Bromo-2-Fluorobenzyl Alcohol. Here, both the reactivity and the final chemical fate of each substituent matters. Fluorine introduces metabolic stability in drug discovery, shifting the pharmacokinetic profile of a candidate compound. The bromine, on the other hand, allows transformations via coupling or displacement. We know because our technical service teams discuss these transformations with partners every week.

    As a manufacturer, we measure product lifespan on the shelf, batch consistency, and the absence of contamination. These characteristics distinguish a chemical you can scale—confidently—from a mere research curiosity. Our history with this product proves that not all benzyl alcohols are interchangeable. Analysts and route designers regularly report that switching to our grade not only raises their yield but saves time wasted troubleshooting off-spec color or managing unknown by-products. One kilogram of off-odor or darkened batch can cost a whole campaign. Our plant personnel stay up late, fine-tuning everything to prevent that outcome.

    Why Rigorous Control Beats the Shortcut

    Production of halogenated benzyl alcohols like 4-Bromo-2-Fluorobenzyl Alcohol can look deceptively simple, especially to those who have run small-scale syntheses. Error margins grow as scale rises. Precise feed rates, temperature ramps, solvent dryness, and post-synthesis isolation all play critical roles in the final outcome. We learned this after observing slight changes in product color and NMR impurity level when running larger batches for new pharmaceutical campaigns. Even storage logistics can nudge purity specs downward: trace moisture or UV exposure gradually shifts the balance, introducing minute decomposition products that jeopardize long-term application.

    Our lab follows production runs with rigorous in-house analysis—not to chase standards, but because we’ve witnessed projects derailed by an off-spec batch. Our investment in analytical tools and staff training stemmed from these hard lessons. Many off-site suppliers or third-party traders cannot offer this kind of assurance. Here, every bottle or drum can be tracked by in-process data trialed against decades of real-world results. Changes in appearance or analytic output are flagged, reformulated, or reprocessed before reaching any client.

    This level of vigilance isn’t only about compliance. Our credibility, team pride, and long-standing partnerships depend on it. Missing NMR peaks, traces of by-product, or visible color changes set off alarms that drive us to review solvent sources, reaction conditions, and even packaging protocols. We run old-school thermal cycling storage tests and real-time shelf-life analysis because field returns and customer complaints are the most expensive lessons of all.

    Applications: Building New Chemistry, Step by Step

    Demand for 4-Bromo-2-Fluorobenzyl Alcohol arises most strongly from pharmaceutical and specialty chemical sectors. Drug discovery groups target this molecule for its dual-halide substitution as it offers two handles for downstream derivatization. Some projects use it as a core for constructing drug-like molecules featuring increased metabolic stability, because fluorine resists enzymatic attack. Processes for synthesizing agrochemicals or advanced materials also benefit—this alcohol serves as a launchpad for introducing complex bioactive or functional motifs. The alcohol group transforms directly to aldehydes, acids, amines, or even more elaborate architectures via established chemistry.

    Having supplied this product to several new drug development campaigns and custom synthesis programs, we know the stakes. A major pharmaceutical partner building selective kinase inhibitors used our product for installing both halogens in a key aromatic intermediate. Another customer in advanced polymer development reported improved process control because contamination risk decreased. Where projects depend upon reliable, halogenated building blocks, every gram of authenticity matters.

    We adjust our production not just to make the molecule but to deliver a product fit for late-stage synthesis. Downstream reactivity depends on more than the chemical structure alone; it’s about purity, solvent residue, and reproducible physical characteristics. We maintain validated storage and transport procedures, cutting oxygen and moisture exposure whenever transfer or packaging takes place. That’s how we keep product specifications firm not just at dispatch, but throughout storage and delivery.

    Limitations and Responsible Use

    Practical knowledge recognizes specific limitations. 4-Bromo-2-Fluorobenzyl Alcohol contains two reactive halogens, making it sensitive to over- or under-handling during transformation. Some chemistries, such as oxidative conditions or extreme nucleophiles, require special attention to prevent loss of function or mixture of side products. On the plant floor, we pay extra attention to minimizing contaminants that might catalyze unwanted transformations. Temperature stability, inner packaging, and routine retesting of inventory keep our stocks within spec.

    Environmental and regulatory compliance are not optional afterthoughts. Halogenated compounds fall under increased scrutiny for disposal and handling. All outgoing shipments feature complete documentation not because of regulatory paperwork, but because customers need clarity for local compliance, hazard communication training, and safe operational protocols. Technical support doesn’t end at shipment dispatch—our team regularly answers questions from partners about best practices in reactivity, solvent compatibility, and safe storage. Those conversations loop back to our internal procedures, driving each improvement cycle.

    Continuous Improvement, Not Standing Still

    Making 4-Bromo-2-Fluorobenzyl Alcohol is a challenge. Process chemists on our team update protocols to keep pace with feedback from users. We adjust for feedstock variability, solvent profiles, and exact product appearance based on client needs—always guided by analytic evidence, not just paper specs. Sometimes that means holding a batch back for additional purification, or even changing lots because color drift or minor odor points to a storage problem. We treat those adjustments as part of our job, not exceptions to it.

    Industry hasn’t stood still since this molecule entered the market. New coupling methods, greener synthetic protocols, and regulatory shifts push us to keep learning. Our technical group pursues continuing education in both upstream and downstream technologies. From solvent waste reduction to new crystallization techniques, we chase incremental gains at every step. Field failures or off-spec returns serve as signals for root cause analysis—we use lessons learned to fortify process controls.

    Speaking Plainly: What Sets a Good Manufacturer Apart?

    Trust builds gradually. Customers remember when orders ship with full documentation, precise analytics, and prompt technical support. Chemists talk among themselves, measuring service as much as product. We complete the circle by tracking every shipment, maintaining tight records, and being up front if something falls short. Rarely, we field questions from customers burned by off-brand or grey-market intermediates—chemicals with the right name but a very wrong set of surprises in the flask.

    The core difference between a manufacturer and a mere supplier stems from this commitment. We handle every synthesis, purification, analysis, and shipment without shortcuts. Long-running partnerships depend on follow-through: full traceability, no skipped steps, and real engagement when technical questions arise. As new chemistries and advanced synthetic pathways emerge, we adapt and inform our clients about changes affecting 4-Bromo-2-Fluorobenzyl Alcohol quality or application.

    Safety extends to the shop floor and the user’s lab. Production hygiene, exposure monitoring, and training align with evolving global standards. Every employee on our line—from chemists to operators—understands the importance of careful handling, batch isolation, and routine verification. That culture finds its way into every bottle shipped. Customers sense the difference, not just in the lab but in the sense of certainty about what they receive.

    Last Mile: Shared Knowledge and Open Channels

    Questions about reactivity, batch parameters, or best storage practices never bother our staff. Practical requests drive innovation. Each application—whether bulk synthesis or a single academic project—adds to our knowledge base. We treat follow-up technical support as an essential part of the service: reliable data sheets, honest feedback, and straightforward communication.

    Our experience as a direct manufacturer means no detail goes unnoticed or unattended. Any substitution on the benzene ring, change in alcohol content, or drift in physical characteristics leads to technical investigation. Achieving consistent, high-quality 4-Bromo-2-Fluorobenzyl Alcohol is more than matching paperwork; it’s the sum of collaborative effort, rigorous habit, and a respect for real-world consequences. Feedback from the field, whether praise or criticism, guides our every improvement.

    This commitment to improvement delivers tangible results. Major process improvements—like greener solvents or waste-minimizing workups—came directly from conversations with partners. Tracking returns, comparing cross-lab batch data, and rapid root-cause analysis all ensure tighter controls with each production cycle. Whether the market demands higher volume, stricter purity, or creative reaction support, our team carries that responsibility with both hands.

    Moving Forward: Practical Solutions to Persistent Issues

    Supply reliability, quality consistency, and technical transparency remain the most critical factors for synthetic projects depending on halogenated benzyl alcohols. We focus on in-house validation, transparency with technical reports, and fast troubleshooting when the unforeseen occurs. Stronger cross-checks between plants and labs shorten the distance between production and end-user goals.

    Scale-up challenges, waste disposal, solvent management, and intermediate purity all shape how we manufacture and supply 4-Bromo-2-Fluorobenzyl Alcohol. By partnering directly with technical leads and formulation chemists, we shorten feedback loops and close the gap between request and delivery. Investment in staff training, analytic infrastructure, and documentation translates to better product experience for every partner.

    We believe that as chemistry grows more complex and projects face tighter timelines, real partnership—marked by openness, technical strength, and honest support—will remain the backbone of supplying quality intermediates. Our track record with 4-Bromo-2-Fluorobenzyl Alcohol illustrates what direct engagement and constant learning can achieve, not just for one product but for future generations of chemical innovation.

    Every synthesis tells a story. With each bottle of 4-Bromo-2-Fluorobenzyl Alcohol we deliver, we stand behind the results—batch after batch, day after day.