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2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide

    • Product Name 2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide
    • Alias 2-Fluoro-3-(trifluoromethyl)benzyl bromide
    • Einecs 701-393-8
    • 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

    104043

    Product Name 2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide
    Cas Number 181276-54-8
    Molecular Formula C8H5BrF4
    Molecular Weight 257.02 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 74-76 °C at 11 mmHg
    Density 1.687 g/cm³
    Purity Typically ≥97%
    Smiles C1=CC(=C(C(=C1)F)C(F)(F)F)CBr
    Refractive Index n20/D 1.497
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Solubility Soluble in organic solvents (e.g., DCM, THF)

    As an accredited 2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 2-Fluoro-3-(trifluoromethyl)benzyl bromide, sealed with a screw cap, labeled for laboratory use.
    Shipping 2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide is shipped in tightly sealed, chemically resistant containers to prevent leakage and exposure. It is packed according to hazardous materials regulations, kept away from heat and incompatible substances, and accompanied by appropriate safety documentation. Transport is conducted via certified carriers specializing in dangerous goods.
    Storage Store **2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide** in a tightly sealed container under a dry, inert atmosphere such as nitrogen or argon. Keep it in a cool, well-ventilated area, away from moisture, heat sources, and incompatible materials like strong bases or oxidizers. Protect from light. Handle in a fume hood and avoid prolonged exposure to air, as the compound is moisture-sensitive.
    Application of 2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide

    Applications of 2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide in Industrial Manufacturing

    2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide is a specialty halogenated aromatic employed in advanced chemical synthesis. Its unique structure supports the creation of value-added intermediates in targeted segments of the pharmaceutical, agrochemical, and specialty chemical industries. As an established manufacturer, we focus on real-world production needs, offering compliant supply solutions across multiple precise downstream sectors.

    1. Pharmaceutical API Intermediate Synthesis

    This compound supports the development of selective pharmaceutical intermediates, especially for drugs featuring fluorinated aromatic motifs. Manufacturers rely on it for nucleophilic substitution steps when building benzyl-functionalized scaffolds in cardiovascular and central nervous system (CNS) therapies. Precise handling and trace impurities control are crucial for maintaining process quality in GMP environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • EU GMP EudraLex Volume 4
    • Ph.Eur. General Monographs (where relevant)

    Typical usage ratio

    • 0.8–1.2 molar equivalents per target intermediate, depending on the nucleophile loading and step yield
    • Batch sizes flexibly scaled from 1 kg to 100+ kg output modules

    Downstream process integration

    • React in the nucleophilic aromatic substitution (SNAr) stage downstream of initial core building-block synthesis
    • Follow substitution by purification, then esterification or amide bond formation
    • Strict final impurity and residual bromide removal protocols before further API elaboration

    Final product types

    • Advanced pharmaceutical intermediates for CNS agents
    • Key side chains for antihypertensive APIs such as angiotensin II receptor antagonists
    • Lead compounds for oncology research pipelines
    • Aromatic fragments for antidiabetic drugs in preclinical stages

    2. Agrochemical Active Ingredient Precursor

    Chemical producers apply this intermediate in the synthesis of crop protection agents, especially for incorporating fluorinated aryl units into selective herbicides and fungicides. The halogenated benzyl structure enables strong binding interactions and metabolic stability in targeted active substances. Process teams monitor strict residue thresholds and environmental rules to ensure regulatory acceptance of finished products.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • REACH Annex XVII (EC 1907/2006) restrictions on halogenated aromatics
    • ISO 9001:2015 Quality Management System
    • Environmental risk assessment under OECD guidelines

    Typical usage ratio

    • 0.95–1.1 molar equivalents per pesticide active, optimized based on downstream target yield
    • Reaction charge ratio tailored considering co-reactant excess for complete conversion

    Downstream process integration

    • Used in the benzylation step after coupling of the core heterocycle
    • Followed by halide elimination and purification in solvent phases
    • Final clean-up according to GLP residue standards prior to formulation

    Final product types

    • Fluorinated triazole-based fungicides
    • Selective post-emergence herbicidal active ingredients
    • Precursor to pyrazole and pyridine crop protection agents
    • Plant growth regulator synthesis intermediates

    3. Specialty Fluorinated Polymer Monomer Manufacturing

    Producers of advanced specialty polymers utilize this compound as a reactive monomer precursor, introducing fluorinated aromatic units for enhanced chemical and thermal resistance in finished materials. Controlled bromide introduction affects chain-termination behavior, offering process control for ring-opening or cross-linking polymerizations. Quality teams verify minimal residual halide to meet application-specific performance metrics in high-value fluoropolymer segments.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing process consistency
    • RoHS Directive (EU 2015/863) regulatory review for electronics-focused materials
    • ASTM D4000 Classification for Systematic Coding of Plastics
    • Customer-defined specification agreements for purity and performance

    Typical usage ratio

    • Normally 2–6% by weight as functional monomer in copolymer resin formulation
    • Fine-tuned based on desired fluorine loading and end-use thermal properties

    Downstream process integration

    • Feeds into the initiation stage of step-growth polymerization
    • May undergo pre-functionalization via nucleophilic substitutions before integration
    • Final resin blending follows to adjust mechanical and heat-resistance attributes

    Final product types

    • High-performance fluorinated polyesters
    • Fluorinated polyaryl ether resins
    • Chemical-resistant coatings for electronics
    • Polymeric binders for specialty filtration membranes

    4. Advanced Organic Electronic Material Construction

    Developers of organic electronic materials, such as OLED emitters and organic photovoltaic absorbers, incorporate this compound when synthesizing electron-transport and light-emitting molecules. The specific fluoro-trifluoromethyl substitution pattern raises electron-withdrawing capability, supporting balanced optoelectronic behavior in target molecules. Clean-room and moisture-free conditions remain vital in these syntheses, as trace halide or water can impede device-grade purity and long-term stability.

    Industry compliance standards

    • IEC 62321 screening for restricted substances in electronic components
    • ISO 14644-1 (Cleanroom Class 7+) standards for semiconductor facilities
    • Customer-specific electronic material grade purity protocols
    • RoHS-compliant material declaration for end-use devices

    Typical usage ratio

    • Introduced at 1:1 molar ratio relative to the core substrate in coupling reactions
    • May adjust loading by up to ±10% to ensure electronic functionality within narrow tolerances

    Downstream process integration

    • Enters the final arylation or alkylation step of OLED or OPV material synthesis
    • Strict dry and oxygen-free protocols for substrate and reagent handling
    • Post-synthesis purification via sublimation or gradient chromatography for electronic grade output

    Final product types

    • Hole-blocking and electron-transport layer molecules in OLED panels
    • Active absorbers for organic solar cells
    • Low-voltage organic transistor materials
    • Fluorinated aromatic dopants for display color enhancement

    5. Fine Chemical Intermediate for Perfluoroalkylated Synthesis

    Manufacturers specializing in high-value perfluoroalkylated compounds use this raw material as a benzylation agent for architecturally complex molecules where standard alkyl halides lack the needed reactivity profile. These multi-step processes for specialty intermediates demand narrow by-product profiles and careful control over substitution patterns to meet end-market purity and registration requirements.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management System
    • REACH registration for specialty intermediates (where volume thresholds apply)
    • Specific customer-restricted substance declarations
    • UN transport classification for fluorinated intermediates

    Typical usage ratio

    • Usually 1.05–1.2 equivalents per active nucleophile group in the target molecule
    • Process chemists adjust loading depending on degree of benzylation required for step yield/side product minimization

    Downstream process integration

    • Applied during late-stage benzylation to avoid overbromination of sensitive moieties
    • Reaction monitored in-line via GC or NMR to ensure completion and minimize residuals
    • Final intermediate isolated via solvent extraction and recrystallization

    Final product types

    • Fluorinated building blocks for custom surfactants
    • Specialty ligands in catalytic processes
    • Precursors for advanced lubricating agents
    • Intermediates for custom-engineered fluorinated compounds
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    Certification & Compliance
    More Introduction

    2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide: Practical Experience From Direct Manufacturing

    At our facility, we handle the production of 2-Fluoro-3-(Trifluoromethyl)Benzyl Bromide from the raw starting materials through to finished packaging. Over decades, our chemists studied how every reaction step influences purity, safety, and consistency. Rather than accept variable supply, we control the synthesis and all purification steps on-site.

    The molecular structure, carrying both fluorine and trifluoromethyl substituents, introduces a particular set of reactivity and stability factors. Our team first observed that this unique motif alters both electron distribution and reaction speed when compared with standard benzyl bromides. Direct experience shows that these two groups, at the two and three positions respectively, do more than change a chemical formula. They shift everything about the downstream chemistry — something no catalogue ever illustrates.

    Specifics of In-House Manufacture

    Day in and day out, we see the importance of exact environmental control. This compound's preparation involves more than a basic bromination. On paper, the reaction route looks simple: construct the fluoro-trifluoromethyl benzyl core, then add the bromide. In the plant, tiny differences in water content, temperature ramp rates, or even glassware selection can tweak product yield and trigger rough separation challenges.

    We've adapted all equipment to address specific handling. Employees who run these lines notice immediately if a vessel's trace residue from a prior batch causes color changes or slows crystallization. Our investment in drying and inert-atmosphere transfers has paid off; for halogenated aromatics like this, even small traces of moisture or oxygen shift assay results. Over the years, these on-the-ground adjustments ensured that every drum — whether packed for domestic partners or for export — measured up in purity and appearance.

    Assessing Quality: Not Just Numbers

    Standard purity readings measured by GC and NMR never tell the whole story. Only through direct reactivity testing with actual customer intermediates do we spot underlying performance differences. Our chemists periodically use a split-batch strategy: they send samples from the same synthesis lot through parallel downstream reactions, which reveals which side processes produce fewer byproducts or require less solvent cleanup.

    Another detail arises from the analytical side. The dual presence of fluorine and bromine induces strong mass spec signals, incredibly useful during trace analysis in downstream research. Each batch gets a fingerprint based on retention times and isotopic blends. What emerged from these practices is surprising: subtle shifts in trace metals or residual solvents can impact the reactivity of this compound in pharmaceutical settings, far more so than with traditional benzyl bromides. So it's not just purity or assay that matters — the invisible impacts of our process optimization change the success rate in end-use chemistry.

    Usage Patterns: What Industry Actually Wants

    Experienced process chemists in pharma, agro, and electronics segments trust this molecule as a building block for complex organic synthesis. The strong electron-withdrawing effect of the trifluoromethyl, combined with para-fluoro orientation, brings unique reactivity to aryl alkylations. For those building aryl-heterocycle connections, this molecule opens up selectivity options that regular benzyl bromide cannot achieve.

    Over time, we’ve learned where the real demand comes from. Research into fluorinated pharmaceuticals often starts with a handful of unusual building blocks. Several of our long-standing partners report that replacing standard benzyl bromide with 2-fluoro-3-(trifluoromethyl)benzyl bromide speeds up introduction of the CF3 unit into later synthesis steps, sealing in greater metabolic stability for candidate drugs. Those who craft advanced organofluorine compounds for electronics also report vastly different behaviors in film formation, dielectric constants, and chemical vapor deposition processes.

    Young startups sometimes ask about the difference between this product and more common halogenated benzyl bromides. In real-world campaigns, we’ve seen that the double halogenation — fluorine and bromine — creates a chemical lever for selective coupling. Substitution pattern matters: ring orientation alters steric effects, which in turn provides control over reaction pathways. Our in-house bench chemists frequently collaborate with the synthesis teams at customer labs, sharing old reaction logs or alternative purification protocols that we’ve refined over the years.

    What Sets This Product Apart

    Generics stockists and bulk traders often cannot see beyond the specification sheet. Deep familiarity with production chemistry uncovers real distinctions. Anyone handling benzyl bromide derivatives recognizes issues with hydrolysis sensitivity, color stability, and volatility. Our blend of synthetic precursors, pre-conditioning, and high vacuum distillation creates a product that remains stable on the shelf longer than less-rigorously purified alternatives.

    Our operators and technical managers keep records of every deviation. Past trials with variants lacking the trifluoromethyl group resulted in more side reactions during downstream alkylations, especially under mild base conditions. Without the ortho-fluoro group on the aromatic ring, the resultant product showed higher sensitivity to nucleophilic attack, especially during multi-step synthesis in scaled reactors.

    This compound’s halogen set uniquely tailors it for site-selective alkylation, such as introducing arylmethyl patterns on medicinal scaffolds. Chemists crafting APIs (active pharmaceutical ingredients) appreciate the way these substituents slow down undesired rearrangements, which keeps yields optimal and workups less demanding. Over hundreds of batches, our staff observed product from our own reactors delivering more predictable performance through every major scale range.

    Process Safety and Reliability

    Much has changed in the past decade about how the industry views hazardous intermediates. We have led process safety revision cycles for each new regulatory demand — not because it’s required, but because improvements always return value in uptime and risk reduction. The strong reactivity of benzyl bromide motif requires skill at every transfer and storage point. We replaced decades-old tanks with modern pressure-controlled, lined vessels specifically to prevent trace metallic contamination.

    Training frontline staff pays off. Attention to detail during bromination or crystallization avoids hotspots, charring, or off-gas formation. We learned that only constant monitoring and knowledge sharing enables a safe workplace. Process updates aren’t top-down; they come from careful listening to the best operators and bench analysts. Over the course of numerous process hazards analyses, we phased in new solvent management systems and bleed controls along each pipeline. Direct feedback from experienced line operators guided us toward solutions that shortened turnaround, reduced downtime, and cut batch variability.

    Meeting Changing Demands: Sustainability and Traceability

    Markets change every year. Research centers now demand more origin data and sustainability credentials for their feedstocks. We’ve responded with digital batch tracing and waste minimization practices, not just talk. Our plant logs environmental metrics for water consumption, solvent recovery rates, and energy usage per batch. Auditors visit twice yearly. Our records and process flows are open for inspection by accredited partners. The efforts to refine waste handling, recycle solvents, and reduce emissions lead to lower costs in the long run — and help meet tightening global sustainability standards.

    Raw materials sourcing presents another challenge. We work with longstanding suppliers who provide full traceability on halogen precursors and ensure conflict-free supply. These relationships reduce the risk of unseen impurities that can derail high value downstream campaigns for our customers. In fact, some partners rely on our certification system as part of their own procurement audits. Over time, chemical buyers told us that regular reports and open doors matter more than any marketing tagline.

    Long-Term Partnerships and Continuous Improvement

    We stay close to the people who rely on our 2-fluoro-3-(trifluoromethyl)benzyl bromide. Lab directors often contact us directly about yield drops or side-product profiles. Instead of hiding behind a distributor’s chain of custody, our technical support teams revisit the plant batch logs, retest stock in real-time, and deliver site-specific advice to solve actual process problems. In practice, most competitors lack this level of follow-up, especially if they don’t control the entire synthesis.

    Manufacturing reveals the subtleties ordinary spec sheets never explain. Take the effect of tiny changes in bromine feed source, or how humidity on a single shift can drive a color change in bulk product. Or the way early lots from off-site producers once suffered clogging during transfer, forcing us to switch drying methods altogether. The hands-on experience gained from listening, adjusting, and re-validating every process informs every lot we produce now.

    Our approach adapts every year. We sponsor new evaluation programs for our customers — sometimes even running trial synthesis campaigns inside our plant for their research teams. Rather than resist feedback, we adjust our practices, retrain staff, and improve maintenance schedules. That mindset, grounded in the real needs of the market and shaped by years of accumulated plant records, continues to sustain our reputation with global research buyers and major industrial partners alike.

    Responsibility in a Chemically Complex World

    We know firsthand the responsibilities that come with producing potentially hazardous intermediates. Our safety data sheets, risk assessments, and staff protocols update after every near-miss or customer-reported challenge. Clarity on storage, reactivity, and waste handling emerges from tested, logged procedures. The company culture encourages every operator to question, report, and document all events, large or small.

    Community engagement has become just as important as technical compliance. Local outreach programs involving our plant management and staff demonstrate our transparency. We believe that the best way to address societal concern about chemicals is with openness and continuous learning.

    Looking Ahead: Innovation Grounded In Experience

    New synthetic methods and tighter regulations reshape the chemicals industry every year. We keep pace by revisiting our purification steps and refining in-line analytical control. By collaborating closely with clients and tracking every feedback point, we continue to push for higher process yields, greater environmental performance, and more reliable downstream outcomes, not just for this product but across our production lines.

    People outside the industry rarely see this product’s full story. Beyond molecular diagrams and specification sheets, true quality comes from understanding what chemists in the real world need: rock-solid supply, proven performance, the ability to respond quickly if things go wrong. Open dialogue, grounded technical support, and transparent process management have allowed us to serve both established industry leaders and the brightest emerging teams. Every batch out the door draws on lessons earned the only way that matters — in the plant, not in the brochure.

    Closing Thoughts on the Value of Experience

    In thirty years of direct manufacturing, we’ve faced every challenge from raw material shocks to new impurity regulations. The combined knowledge of our operators, analytical chemists, and process engineers means problems are solved before they reach our customers’ benches. Our practice remains clear and consistent: listen to users, optimize every small detail in production, and stay ready for whatever new demands research and industry bring. That’s the path that keeps our 2-fluoro-3-(trifluoromethyl)benzyl bromide trusted around the world.