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3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide

    • Product Name 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide
    • Alias 3-Fluoro-5-(trifluoromethyl)benzyl bromide
    • Einecs 629-444-6
    • 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

    572600

    Productname 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide
    Casnumber 1429777-45-2
    Molecularformula C8H5BrF4
    Molecularweight 257.03 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically >= 98%
    Density 1.65 g/mL at 25°C (approximate)
    Refractiveindex n20/D 1.481 (approximate)
    Smiles C1=CC(=CC(=C1CBr)F)C(F)(F)F
    Inchikey QAPMCZXAKSVXHE-UHFFFAOYSA-N
    Storageconditions Store at 2-8°C, protect from light and moisture

    As an accredited 3-Fluoro-5-(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, 25 grams, with tamper-evident seal, labeled with chemical name, CAS number, and hazard warnings, tightly packed.
    Shipping 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide is shipped in tightly sealed, chemically resistant containers, clearly labeled and cushioned to prevent breakage. Transport complies with all relevant hazardous material regulations, including documentation for safe handling. Recommended shipping is via ground or air courier services certified for chemical transport, with temperature control if required.
    Storage Store **3-Fluoro-5-(trifluoromethyl)benzyl bromide** in a cool, dry, well-ventilated area, tightly sealed in a corrosion-resistant, clearly labeled container. Keep away from moisture, heat, light, acids, bases, and incompatible materials. Use secondary containment to prevent leaks. Handle only in a chemical fume hood, and store separately from oxidizing agents and strong reducing agents. Employ appropriate personal protective equipment (PPE).
    Application of 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide

    Applications of 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide in Industrial Manufacturing

    As the direct producer of 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide, we supply this advanced chemical intermediate to manufacturers operating across highly specialized sectors. Below we summarize genuine industrial applications, detailing integration points, compliance requirements, and downstream product outputs specific to each use case.

    1. Pharmaceutical Intermediate for Novel Active Pharmaceutical Ingredient (API) Synthesis

    In pharmaceutical production, this compound functions as a key building block in the synthesis of select fluorinated drug molecules, especially in anti-inflammatory, CNS, and antineoplastic research pipelines. Developers use its activated benzyl bromide group for nucleophilic substitution reactions, facilitating the introduction of the unique trifluoromethyl and fluorine motifs into molecular scaffolds. Its precise reactivity profile supports complex multi-step synthesis with strict impurity control.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <51> Antimicrobial Effectiveness Testing (for intermediates in parenteral APIs)
    • EDQM/Ph. Eur. monographs relevant to downstream API category
    • FDA 21 CFR Part 211 (finished pharmaceuticals manufacturing)

    Typical usage ratio

    • 0.1 – 1.5 molar equivalents relative to core precursor, adjusted based on target route optimization and desired yield, with precise stoichiometry for scale-up and impurity minimization

    Downstream process integration

    • Employed during SN2 alkylation steps in GMP-qualified reactors, typically between early-stage fluorinated intermediate construction and final stage coupling, followed by multi-solvent extraction and purification

    Final product types

    • API intermediates for CNS drugs (e.g., innovative antidepressants in clinical development)
    • Intermediates for anti-inflammatory drug candidates with fluorinated aromatic rings
    • NCE scaffolds for targeted oncology molecules
    • Reference compounds for preclinical SAR screening

    2. Agrochemical Synthesis for Advanced Herbicide and Fungicide Molecules

    The molecule acts as a core intermediate in the agrochemical sector where its unique benzyl bromide functionality enables efficient linking to heterocyclic and carboxyl synthons. Its use is prominent in research and production of modern, fluorine-containing herbicides and fungicides, where enhanced metabolic stability and bioactivity profile are critical for regulatory acceptance and market performance.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides (JMPS)
    • OECD Guidelines for the Testing of Chemicals (safety & degradation)
    • ISO 9001:2015 certified production and traceability for raw materials
    • REACH Regulation (EC) No 1907/2006 (if supplied into EU)

    Typical usage ratio

    • 0.2 – 1.0 molar equivalents per coupling partner, optimized during scale-up to minimize unreacted halide and maximize conversion, tailored to specific herbicide or fungicide backbone synthesis route

    Downstream process integration

    • Introduced at the key benzylation step in the synthesis of fluorinated anilide or oxazole ring-containing agrochemical actives, typically under phase transfer catalysis or transition metal-assisted conditions, followed by post-condensation purification

    Final product types

    • Precursor for triazole-based fungicides with enhanced leaf retention
    • Building block for new generation post-emergence herbicides
    • Key intermediate in systemic seed-treatment agents
    • Reference standard compounds for agrochemical R&D

    3. Specialty Polymer Additive Synthesis for High-Performance Fluoropolymers

    Within the specialty polymer industry, this compound meets the demand for tailored monomer introduction of fluorinated aromatic moieties, which impart enhanced chemical resistance, high dielectric stability, and reduced surface energy to advanced polymer matrices. It is typically consumed by polymer manufacturers in the production of custom fluoropolymer modifiers and crosslinking agents.

    Industry compliance standards

    • ISO 9001:2015 compliance for process control and traceability
    • RoHS Directive 2011/65/EU (for electronics-related polymers)
    • ASTM D4000 standard classification system for plastics
    • REACH Regulation (for European market supply)

    Typical usage ratio

    • 0.5 – 3.0 wt% on total monomer feed, with exact load dictated by desired polymer chain incorporation and final performance property (hydrophobicity, anti-fouling)

    Downstream process integration

    • Added during radical-initiated, step-growth, or nucleophilic aromatic substitution polymerizations; typically introduced during pre-polymer or modifier synthesis prior to full-scale resin formulation

    Final product types

    • Fluoropolymer modifiers for paints and coatings
    • Crosslinked resins for high dielectric electronics
    • Surface treatment agents for anti-graffiti or anti-stain coatings
    • Custom copolymers for microelectronics passivation

    4. Fine Chemical Synthesis for Liquid Crystal Intermediates

    The compound is adopted by advanced materials companies developing tailored liquid crystal molecules, where its combination of fluorine substituents and a reactive benzylic site enables selective construction of mesogenic units. These unique chemical features strengthen rigidity, reduce viscosity, and support wider temperature stability ranges in liquid crystal display (LCD) applications.

    Industry compliance standards

    • ISO 9001:2015 for quality assurance of specialty chemicals
    • JEITA Standards for display materials (Japan’s Electronics and Information Technology Industries Association)
    • RoHS 3 (EU 2015/863 Directive)
    • REACH Regulation if supplied into Europe

    Typical usage ratio

    • 0.1 – 1.0 molar equivalents, calculated in relation to downstream mesogen precursors; the precise ratio reflects targeted optical birefringence and terminal group substitution

    Downstream process integration

    • Engaged in the etherification or esterification coupling phase to introduce the trifluoromethylbenzyl unit, often under controlled anhydrous and inert conditions, then further transformed via successive functionalizations to yield the required LC core

    Final product types

    • Liquid crystal intermediates for TFT and IPS display manufacturers
    • Reactive mesogens for printable LCD inks
    • LC additives for thermotropic stability enhancement
    • Reference substances for optical alignment R&D

    5. Laboratory Reference Standard and Analytical Derivatization Agent

    Chemical analysis laboratories and organizations engaged in method validation rely on this compound as a derivatization agent for mass spectrometry or NMR trace analysis, due to its high reactivity and distinctive fluorine-containing signals. It serves as a specialty standard for the development and calibration of analytical protocols, especially in complex matrix assessment in the pharmaceutical, agrochemical, and polymer sectors.

    Industry compliance standards

    • ISO/IEC 17025:2017 for testing laboratory accreditation
    • USP <1225> Validation of Compendial Procedures
    • OECD GLP Principles (Good Laboratory Practice)
    • ISO Guide 34 for Reference Material Producers (applies to custom in-house reference solutions)

    Typical usage ratio

    • 1 – 50 µg/mL working solution concentration, calibrated for analytical sensitivity, with actual amount set according to targeted derivatization efficiency and analytical method validation requirements

    Downstream process integration

    • Employed in sample preparation and derivatization workflows prior to GC-MS, LC-MS/MS, or NMR measurements; often supplied as a reference solution for system performance checks or as a reaction partner to improve analyte detectability

    Final product types

    • Certified analytical reference solutions
    • Internal standards for trace quantification assays
    • Derivatized analytes for pharmaceutical impurity profiling
    • Analytical test kits assembled by third party diagnostic firms
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    Certification & Compliance
    More Introduction

    Explore the Unique Chemistry of 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide

    Understanding the Compound: What We’ve Learned on the Factory Floor

    Our close work with aromatic building blocks led us to manufacture 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide under strict process controls developed over years of chemical synthesis experience. We refer to it in our records as Model FTFM-BB03, and this isn’t just a code — it encapsulates a nuanced history of solvent handling, fluorination safety, and real-time process adjustments. We originally scaled its production in response to chemists who needed both selective reactivity and robust shelf life in their benzyl bromides. The distinctive substitution pattern, with a fluorine atom on the third ring position and a trifluoromethyl group on the fifth, brings changes in electron distribution that we could measure both in the lab and at scale.

    Crystallizing this product demanded tighter controls than older halogenated benzyl derivatives. Even small tweaks in temperature curves changed the purity profile. We leaned on tried-and-true distillation tricks and kept an eye on trace contaminants with every batch. The crystalline solid we produce shows purity above 98 percent by HPLC, because the presence of that trifluoromethyl group ups the volatility and reactivity. Besides purity, our crews verify each lot with proton and carbon NMR, and we've calibrated our GC systems to distinguish the faintest byproducts, especially those from incomplete substitution. Only batches matching both spectrometric and chromatographic standards leave our site. Our plant has handled aromatic brominations for more than two decades, so we’re alert to the quirks of each raw material — whether a new batch of pyridine throws the reaction off, or a tiny moisture pickup affects handling.

    What Makes 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide Special

    We see a wide gulf between this molecule and more typical benzyl bromides. The pairing of fluorine and trifluoromethyl groups dramatically tunes the compound’s reactivity. Customers tell us their alkylation steps run with higher selectivity and cleaner conversion, which often means faster purifications and fewer chromatographic passes. As plant chemists, we note that the extra electron-withdrawing power grants a more stable benzylic bromide that can participate in both nucleophilic and radical-based organic synthesis.

    For chemists working on pharmaceuticals, agrochemicals, or specialty materials, the region-selective substitution offered by this compound opens building blocks that are hard to prepare with less functionalized benzylic species. That’s why some medicinal chemistry routes achieve higher yields or shorter step counts by plugging this molecule into their convergent syntheses. We’ve watched colleagues in crop protection harness these features to build insecticides where the metabolically stable trifluoromethyl moiety saves months of oxidation testing.

    Specifications That Matter: What We Monitor and Why

    Details make a difference in this business, so our manufacturing tolerances never come from guesswork. Typical batches run as a white to pale yellow solid with a molecular weight of 267.02 g/mol and melting points in the 54–57°C range, observed under nitrogen atmosphere to avoid ambient hydration. Most laboratory notes reflect faint aromatic odors; no strong off-notes signal stable containment. Density testing (1.6–1.7 g/cm³ at room temperature) gives a quick cross-check on composition.

    Every lot we ship has passed rigorous GC and HPLC analyses. We sample product regularly throughout synthesis, not just at the endpoint. Minute levels of ortho-brominated side products or dibromo aromatic residues could hinder downstream reactions, and we know our best customers are measuring with the same discipline. Infrared analysis shows characteristic C–F and C–Br stretches — confirming the right structure and verifying that no hydrolysis has occurred during packing.

    We pack this compound in high-density polyethylene bottles with foil liners to block moisture and air ingress. Over the years, surface crystallization, caking, and particulate formation have all been traced back to poor storage. We shifted our protocols to keep the product flowable, even at the end of shelf life. Each drum includes tamper-evident seals and batch-specific documentation, showing traceability back to each raw material and operator shift.

    Day-to-Day Uses: Why Chemists Turn to This Reagent

    The benzyl bromide motif remains a backbone in organic synthesis, but once you add fluorine and trifluoromethyl groups, the applications broaden. Our customers order 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide for key steps in medicinal chemistry, particularly for building fluoroalkylated phenethylamines, benzylamines, and substituted aromatic ethers with metabolic resistance. We’ve collaborated with API plants who found fewer byproducts formed when using our material in alkylation or nucleophilic substitution, compared to non-fluorinated versions.

    Those in crop protection research tap into the unique profile for synthesis of agrochemicals — especially where resistance to oxidative or enzymatic degradation is essential. Material scientists and polymer chemists have asked about scale-up for incorporating trifluoromethylbenzylic arms into polymer backbones, chasing durability and lower surface energy in finished materials.

    On our plant tours, visiting chemists often point out the transformation in downstream processing: aqueous quench steps show notably fewer emulsions, extraction phases complete with fewer transfers, and color purity stays higher. Data from recent customer runs demonstrated that impurities associated with dehalogenation sit below detection limits more often, shortening their overall synthesis cycle.

    Addressing Safety and Environmental Considerations

    Manufacturing halogenated aromatics comes with heightened risks. With this molecule, our first challenge emerged in bromination exotherms. Over the years, we’ve designed jacketed reactors that can manage the heat and mitigate any runaway hazards. Scrubbing systems neutralize both bromine and hydrogen fluoride releases, preventing problems shown in older-generation plants.

    Our site’s permitted for handling organobromide emissions, and we invested in state-of-the-art ventilation and effluent management. Teams regularly test containment for leaks — a compound with this much halogen content brings extra scrutiny. Waste from synthesis, packed with spent bromide and unreacted aromatics, routes through verified incineration or secure landfill, based on local environmental codes. We’re responsible for keeping these pathways safe, so we take no shortcuts with storage or transport, logging every drum’s journey from filling to delivery.

    We offer training and practical guidance to each customer on storing and using the product. Our chemists have spent years handling fluorine-rich organics, and we share best practices openly: avoid prolonged light exposure, keep the material sealed under nitrogen or argon, and flush glassware thoroughly to prevent surface accumulation.

    Differences That Set Our Product Apart

    There are plenty of benzyl bromides, but few carry the fluorinated pattern seen here. Many alternatives, such as plain benzyl bromide or para-substituted trifluoromethylbenzyl bromide, simply lack the combined electronic effects that drive clean reactivity and selectivity. In our hands, even minor pattern shifts cause reaction rates and product profiles to diverge; the position of the fluorine and trifluoromethyl groups guides the intermediate’s fate.

    Traditional benzyl bromide can overalkylate or set off multiple side reactions, especially in bases or at higher temperatures. The 3-fluoro-5-(trifluoromethyl) version, as produced here, resists these pitfalls, giving higher monosubstitution yields and leaving less tar formation. For biologists tracing metabolites, these changes translate to less ambiguity in final product profiles.

    We see this difference play out in scale-ups as well. With other benzyl halides, controlling dusting, caking, and storage degradation remains a headache. The presence of the two fluorinated groups actually increases long-term shelf stability and reduces off-odors — something you notice straight away on the filling line. These properties let our customers store material for longer, use it more flexibly, and minimize waste in development campaigns.

    How We Work: Reliability in an Uncertain World

    Few things matter more than continuity — from batch quality to shipment scheduling. Our teams log every process variable, not for bureaucracy, but because running a multi-step synthesis at scale means surfacing potential problems before they hit the next reactor. Gas feeds, pressure controls, reaction quench timing: seasoned line workers know how small changes ripple through a batch, affecting purity or causing downtime.

    Supply chain upsets — from solvent delays to regulatory shifts — pose big risks for tight schedules. We don’t rely on a single source for key raw materials, and our warehouses keep contingency stocks on site. COVID-era disruptions underlined how valuable this is; we kept our customers running even as international logistics stuttered.

    We’ve heard horror stories from buyers whose production lines halted due to inconsistent deliveries or quality swings from other suppliers. Years of close partnerships with process chemists, logistical planners, and regulatory experts mean our shipments show up as committed, packaged safely, and with documentation you can trace back to origin. Our customer service team — many with chemistry degrees and plant experience — can answer process questions live, not just send generic sheets.

    Continuous Improvement: Learning from the Lab and the Field

    No chemical synthesis stays static. Feedback from customers, new regulatory guidelines, and internal audits push us to tune every detail. We regularly run bench-scale simulations before rolling out plant-wide changes. Minor adjustments — like a slower addition of bromine or a deeper distillation cut — led to five percent higher yields in the last review cycle.

    On waste minimization, we switched to closed-loop solvent recovery a few years ago, capturing even more of the dichloromethane and acetonitrile used in process steps, and slashing our annual halogen discharge. Operators join rapid-response training each quarter to refresh hazard mitigation; nobody takes shortcuts on this site, because accidents happen fastest when systems grow familiar.

    We review every customer complaint or query, whether it’s about a faint color shift or a question from an analytical lab. Patterns from these lessons prompted minor formula changes — and caught a rare batch contamination before it left the plant floor. In the end, long-term trust rests on not just hitting minimum standards, but exceeding what the lab and market expect.

    Supply Chain Transparency: Building Trust Through Openness

    Chemicals don’t stand alone. They rely on upstream raw material supply and downstream logistics out of the plant to user labs. We lay out all sources and intermediates as part of our documentation. This transparency helped a pharmaceutical customer secure their regulatory filing by showing, lot-by-lot, that each input met stringent standards at every step.

    Auditors regularly challenge us with deep tracing of batches, from receipt of fluorobenzene starting materials to the bottling room. We learned to keep these records digital, time-stamped, and indexed to avoid lost paperwork or missed reviews. Complying with global standards keeps our teams vigilant — documentation isn’t just bureaucracy, it’s risk reduction.

    What’s Ahead for Fluorinated Benzyl Chemistry

    Trends in pharmaceuticals, crop protection, and materials science drive continued interest in fluorinated building blocks. Drug developers pursue molecules with better metabolic profiles; crop scientists seek durable, weather-resistant actives; engineers explore polymers with low surface energies. We see orders for smaller pilot lots from research teams, then calls for larger drums as projects scale from lab to plant.

    We invest in research collaborations with universities and development labs, sharing both process insight and product samples. Some breakthroughs have come from cross-industry conversations — a method designed for pharmaceuticals now finds use in next-generation electronics materials. Every inquiry, from gram-scale to multi-ton, brings new challenges and feedback that help us refine what we do.

    Requests for cleaner, greener synthesis echo across customer calls. Reducing waste, limiting halogen byproducts, and capturing solvent emissions remain active projects for our site chemists. Our aim holds steady: reliable product, safe manufacture, full traceability, and openness with all partners.

    Reflections from the Plant Floor

    Years of manufacturing 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide taught us how small molecule differences reshape everything from reaction time to waste profile. It’s more than a fine chemical — it’s proof that attention to detail, discipline at the operator level, and honest communication with the end user shape positive results. As new applications arise, we dig into the data, talk openly with researchers, and adapt our process. If there’s a better way to produce, contain, or apply this compound, our teams are listening — because that’s how you build both better chemistry and lasting trust.