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4-(Trifluoromethyl)Benzyl Bromide

    • Product Name 4-(Trifluoromethyl)Benzyl Bromide
    • Alias 4-(Bromomethyl)benzotrifluoride
    • Einecs 216-755-8
    • 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
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    Specifications

    HS Code

    955345

    Productname 4-(Trifluoromethyl)Benzyl Bromide
    Casnumber 402-43-7
    Molecularformula C8H6BrF3
    Molecularweight 239.03
    Appearance Colorless to pale yellow liquid
    Boilingpoint 124-126°C at 17 mmHg
    Meltingpoint -6°C
    Density 1.539 g/cm3 at 25°C
    Purity Typically ≥98%
    Refractiveindex n20/D 1.511
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms p-(Trifluoromethyl)benzyl bromide
    Smiles C1=CC(=CC=C1CBr)C(F)(F)F
    Inchi InChI=1S/C8H6BrF3/c9-5-6-1-3-7(4-2-6)8(10,11)12/h1-4H,5H2
    Storagetemperature Store at 2-8°C

    As an accredited 4-(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 25 grams of 4-(Trifluoromethyl)Benzyl Bromide, tightly sealed, labeled with hazard warnings and handling instructions.
    Shipping Shipping of 4-(Trifluoromethyl)benzyl bromide requires secure, sealed containers, compliant with hazardous materials regulations. It should be transported under controlled temperature, away from moisture and incompatible substances. Proper labeling, documentation, and use of absorbent packing to prevent leaks or spills during transit are essential for safe and compliant delivery.
    Storage 4-(Trifluoromethyl)Benzyl Bromide should be stored 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 direct sunlight, moisture, heat sources, and incompatible substances like strong oxidizers or bases. Properly label the storage container and use secondary containment to prevent leaks or accidental spills.
    Application of 4-(Trifluoromethyl)Benzyl Bromide

    Applications of 4-(Trifluoromethyl)Benzyl Bromide in Industrial Manufacturing

    As a direct manufacturer of 4-(Trifluoromethyl)Benzyl Bromide, we collaborate with industrial partners who integrate this specialty intermediate into core chemical synthesis workflows. The following sections outline the real downstream sectors that require this material, each characterized by well-defined industry standards, precise formulation practices, distinct process incorporation points, and specific end product outcomes.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies use 4-(Trifluoromethyl)Benzyl Bromide to introduce the trifluoromethylbenzyl group into drug intermediates, supporting the synthesis of advanced building blocks in antihypertensive, antiviral, and central nervous system drug pipelines. Formulation chemists adjust addition rates for structure–activity optimization, while robust regulatory control governs raw material introduction at pre-GMP or GMP synthesis steps. Manufacturing teams require batch-level traceability to meet strict final product safety and purity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • Chinese Pharmacopoeia, European Pharmacopoeia (relevant for APIs and intermediates)
    • EU GMP EudraLex Volume 4

    Typical usage ratio

    • 0.5%–4% of reaction mass, depending on target API intermediate and specific substitution efficiency; usually determined by stoichiometric calculations and route design.

    Downstream process integration

    • Introduced during SN2 alkylation or substituted benzyl group installation after core ring assembly, often in Stage 2 or Stage 3 synthesis, followed by purification and validation steps.

    Final product types

    • Pharmaceutical intermediates for proprietary APIs
    • CNS drug scaffolds containing trifluoromethylbenzyl motifs
    • Precursors for anti-infective and oncologic agents

    2. Agrochemical Synthesis: Herbicide and Fungicide Intermediates

    Agrochemical companies use this raw material to construct high-value pesticide intermediates by selectively introducing the trifluoromethylbenzyl moiety, which improves bioactivity and environmental persistence in finished crop protection products. Synthesis teams adjust charge ratio in early-stage laboratory optimization, and scale-up in compliance with chemical safety and environmental management standards common to pesticide active manufacturing.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No. 1907/2006
    • China GB/T 1600–2001 Pesticide Technical Standards
    • ISO 9001:2015 Quality Management Systems for agrochemical production

    Typical usage ratio

    • 1.5%–6% of total formulation batch for intermediate coupling; adjusted downward in cases of high-potency final actives or up for bulk synthesis campaigns.

    Downstream process integration

    • Typically charged during N-alkylation or aromatic substitution stages prior to ring closure, followed by downstream oxidation, chlorination, or formulation into technical products.

    Final product types

    • Trifluoromethyl-substituted herbicide pre-products
    • Fungicide technical intermediates
    • Active ingredient analogs for broad-acre use

    3. Specialty Chemical Building Blocks for Electronic Materials

    Manufacturers in electronics and advanced material sectors rely on this compound as a fluorinated benzyl source for producing high-performance polymers and liquid crystalline monomers needed for LCD and OLED displays. Integration occurs under precisely controlled conditions to ensure molecular integrity and reproducibility across downstream functionalization stages, in full alignment with cleanroom and sectoral quality standards.

    Industry compliance standards

    • IEC 60749 for semiconductor device production
    • ISO 14644 Cleanroom Standards
    • QC080000 IECQ HSPM for hazardous material management
    • RoHS Directive 2011/65/EU for finished electronics

    Typical usage ratio

    • 0.2%–2.5% by monomer feed mass, depending on polymerization requirements and targeted electronic property enhancements.

    Downstream process integration

    • Feeding at the functional monomer preparation stage, often via base-catalyzed benzylation; subsequent processing into liquid crystalline or fluorinated polymer systems.

    Final product types

    • Liquid crystal display monomer precursors
    • Fluorinated specialty polymers for optoelectronics
    • OLED device intermediates with substituted benzyl functionality

    4. Fine Chemical Synthesis for Fragrance and Flavor Compounds

    Producers of fine fragrance and aroma ingredients value the tailored reactivity of this benzyl source for synthesizing fluorinated aromatic building blocks, especially where unique scent signatures and stability enhancements are needed. Formulators closely monitor ratios based on olfactory and purity specifications, and operations adhere to food-grade or perfumery GMP as required for downstream flavor and fragrance applications.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • EU Regulation No. 1334/2008 (Flavorings and food ingredients)
    • ISO 9001:2015 for flavor and fragrance manufacturing
    • US FDA 21 CFR Part 172 (Food Additives permitted for direct addition to food)

    Typical usage ratio

    • 0.1%–1% of formulation mass, subject to IFRA safety and organoleptic requirements and adjusted in lab-scale trials for yield and sensory properties.

    Downstream process integration

    • Added during aromatic benzylation of alcohol or phenolic substrates to form new fragrance or flavor backbones, typically before distillation and purification.

    Final product types

    • Fluorinated fragrance components for consumer perfumery
    • Aroma chemicals for processed flavor systems
    • Scent ingredients for fine fragrances and toiletries

    5. Synthesis of Advanced Materials: Functionalized Surfactants

    Manufacturers of specialty surfactants for oilfield, coatings, and high-end cleaning agents deploy this intermediate in the synthesis of trifluoromethyl-functional surfactant molecules, yielding end products with enhanced hydrophobicity and chemical resistance. Technical formulation teams set dosage based on critical micelle concentration goals and integrate at controlled reaction stages to meet final performance and regulatory QC tests.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • ISO 14001:2015 for environmental management of surfactant production
    • REACH Annex XVII (Restrictions on surfactant use in EU)
    • US EPA TSCA Inventory status

    Typical usage ratio

    • 0.35%–2% by total reaction volume; exact loading refined through pilot scale evaluation for fatty alcohol or amine substrate modification.

    Downstream process integration

    • Charged during the late-stage alkylation or benzylation step after core surfactant chain assembly; followed by neutralization or salt formation.

    Final product types

    • Trifluoromethylated nonionic and cationic surfactants
    • Oilfield performance additives
    • Surface-modified detergents for critical cleaning
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    More Introduction

    4-(Trifluoromethyl)Benzyl Bromide: Core Insights from the Manufacturing Floor

    Introduction to 4-(Trifluoromethyl)Benzyl Bromide

    Some chemicals carry more weight on the production floor than they do on the spec sheet. 4-(Trifluoromethyl)Benzyl Bromide is one of these difference-makers. As people who turn raw ingredients into finished molecules day in and day out, we see the true value of each compound in the way it changes reactions, controls outcomes, and helps innovation cross the finish line. The daily focus comes down to one thing: what this molecule actually does in the hands of chemists, and how its unique features meet real-world needs.

    Model, Appearance, and Core Attributes

    This product comes in the pure, colorless-to-pale yellow liquid form that experienced bench chemists recognize by its sharp, biting odor. Each new batch runs through strict GC and NMR checks before it leaves the production site. The molecular structure, marked by a benzyl bromide skeleton and a trifluoromethyl group locked in the para position, isn't just for show. That fluorinated group is what sets this compound apart, amplifying its performance in places where traditional benzyl bromide would fall short.

    From the moment we scale up from pilot to run production, quality means more than just hitting a percentage marker. Our teams keep long shifts on the lines, running controls for water, acidity, and packing density, trimming off batches that show even the faintest impurity spike. For the end user, this translates to a reagent they can measure and trust every time.

    Reactivity and Role in Advanced Synthesis

    The world of organic synthesis has no shortage of brominated intermediates. Still, few handle with the consistency or power of 4-(Trifluoromethyl)Benzyl Bromide. The presence of the trifluoromethyl group adds volatility and alters electron density, giving reactions new pathways and sharper selectivity. One would expect benzyl bromide, on its own, to perform as a workhorse alkylating agent; that's the general rule. When you switch to the trifluoromethyl derivative, reactivity patterns start shifting. You'll see faster alkylation, stronger electrophilic activity, and, almost everywhere, enhanced compatibility in complex multi-step syntheses.

    We've watched researchers take on tough projects with the singular goal of fine-tuning a molecule's physiochemical profile using fluorination. In many cases, 4-(Trifluoromethyl)Benzyl Bromide has delivered answers where milder analogues would lead to lower yields or fussy purification. The results go beyond theory—the actual batch data tells the story. In one run, our partners boosted conversion efficiency by half and halved their waste by switching from standard benzyl bromide to this product. No extra catalysts. No more post-reaction headaches. Just a cleaner workflow, from mixing tank to crystallization tray.

    Comparisons with Other Benzyl Bromides

    Many ask: Why not just use typical benzyl bromide? The chief difference shows up in the moment of application. The trifluoromethyl group dramatically shifts both solubility and reactivity. We've run head-to-head trials. Benzyl bromide tends to deliver lower selectivity, and residual byproducts stick around in the crude mix. With the trifluoromethylated compound, the reaction mixture often runs clearer, and purification steps finish faster, especially in pharmaceutical or agrochemical intermediates.

    There's no mystery about the cost difference. Fluorinated intermediates take more energy and more specialized conditions to produce. Many operations have settled for unfussy molecules to hit budget targets. Still, rigorous testing and hands-on troubleshooting have proven—time and again—that the higher initial investment frequently pays off. Improved yields, higher active ingredient loading, and cleaner overall processing can open the door to new product lines that simply weren’t feasible with more basic reagents.

    Downstream Applications and Long-Term Impact

    Over the years, we've tracked where our batches end up. Drug discovery, specialty agrochemicals, industrial process catalysts—all rely on intermediates that can withstand tough conditions. 4-(Trifluoromethyl)Benzyl Bromide stands up to those demands. Medicinal chemistry, in particular, leans heavily on the fluorine effect. Adding a trifluoromethyl group to core scaffolds boosts bioavailability and shifts binding affinity in ways that non-fluorinated benzyl groups cannot match. The compound’s unique reactivity profile allows medicinal chemists to build complexity without risking excess side reactions or product loss.

    Agrochemical innovators value this molecule for similar reasons. In herbicide or fungicide active design, backbone modification using 4-(Trifluoromethyl)Benzyl Bromide delivers products with improved soil stability and longer field persistence. Customers have compared pre-fluorinated products against legacy recipes and logged longer shelf life, better formulation performance, and more predictable spray patterns. These wins come from the unique interaction between the trifluoromethyl group and target substrates—something cheaper bromides simply can’t provide.

    Industrial Process Reliability

    Batch-to-batch consistency is the mark of a strong manufacturing operation. We invest in advanced instrumentation and automated in-line controls so every drum matches the one before it. That means customers don’t have to carry out extra verification; the spec sheets always match the actual drum contents. This level of dependability takes patience and vigilance. In production, we catch occasional lot variability tied to ambient temperature or shipping times. The fix comes from quick response procedures and on-site pre-shipment testing, keeping reliability at the top of the list.

    Customers return to products like 4-(Trifluoromethyl)Benzyl Bromide not just for what it can do but for the sense of certainty it brings to scale-up and commercial production. Bench chemists regularly mention smoother set-ups, lower rates of rework, and better cost control over long timelines. Reliable product quality means fewer breakdowns and reruns, especially when every hour on a big reactor carries a premium cost.

    Safe Handling and Worker Experience

    Over the years, safety systems surrounding bromides have advanced a lot. Older generations of chemical makers learned the hard way from exposure—burns, skin irritation, respiratory trouble. Now, closed system loading, multi-level PPE, and local VOC scrubbers keep workers safe throughout the shift. Trifluoromethylated benzyl bromide has its own handling challenges given its higher vapor pressure and strong odor. We employ vented transfer piping and full containment at every handover stage. Routine training drills and constant review sharpen the team’s ability to avoid accidents. The work can get intense. The payoff: zero sustained injuries in our primary production lines for multiple years running.

    On the customer end, the benefits continue. Consistent formulation and careful packaging protect both small pilot-lab operations and scalable commercial runs from product loss or accidental exposure. We ship in packaging designed specifically to maintain integrity through long-haul transport, cutting down evaporation and preventing unnecessary risk in the warehouse or on the dock.

    Environmental Considerations

    All brominated and fluorinated compounds deserve close scrutiny for their environmental impact. 4-(Trifluoromethyl)Benzyl Bromide isn’t exempt. From start to finish, we monitor emissions, control waste, and recycle solvents at every opportunity. Our plant operates with a closed-loop system to capture residuals and reduce direct-to-air releases. Spent mother liquors move through dedicated incineration units, minimizing landfill waste and keeping groundwater impact close to zero.

    We have worked with regulators and downstream partners to document the life cycle of the product. Every part of the operation ties back to a larger goal: reducing footprint without cutting output. For chemists in pharma or agroscience, this translates to better compliance with health, safety, and environmental standards—a growing priority in every market.

    Insights on Product Differentiation and Research Value

    It's easy for people outside manufacturing to see all benzyl bromides as interchangeable. From our vantage point, every structural tweak offers a new tool for research. The trifluoromethyl group is never a simple flourish—the way it changes boiling point, polarity, and nucleophilic substitution rates has concrete effects on experimental outcomes.

    Over multiple cycles of feedback from research teams and process development groups, we’ve documented sharper end-point conversion and less product drag through chromatography columns. Most strikingly, some labs using standard bromides found unexpected side products or sticky contaminants, while those who used 4-(Trifluoromethyl)Benzyl Bromide reported smoother post-reaction workups, cutting several processing hours per batch.

    The value of these improvements is more than academic. Each hour trimmed from workup saves both labor and operational overhead. Each increase in target yield means fewer raw materials, lower solvent consumption, and, in the end, more sustainable operations at every level. The compound’s profile has let researchers move forward with challenging projects—from next-generation pesticides to advanced specialty polymers—projects that would have remained stalled if not for these exact features.

    Long-Term Supply and Global Collaboration

    Today’s chemical supply chain faces regular stretch and strain. Disruptions—whether natural, political, or logistical—test every producer’s resilience. We take pride in building redundant sourcing for raw fluorinated toluenes, working with long-standing partners to create a secure inventory buffer. This policy emerged from past lessons. A single missed shipment in a key quarter caused months of lost research in customer labs. We learned to over-stock certain precursors, never hesitating to invest in storage capacity or alternative logistics. Customers trust us to keep product moving even during global snarls.

    This level of preparation makes a difference in real research continuity. During demand spikes, we launch extra shifts and prioritize high-need orders without sacrificing quality controls. We share production timelines and troubleshoot alongside customer R&D teams. One of the reasons pharma and agrochemical partners return year after year is the ability to access crucial intermediates without interruption—even when global conditions shift.

    Innovation from the Manufacturing Perspective

    Refining production of 4-(Trifluoromethyl)Benzyl Bromide has taken years of live experimentation and feedback from chemists on multiple continents. Small process changes—modifying the temperature ramp, shifting purification solvents, or re-optimizing bromination timing—each contribute to a better, more reliable product. The lessons go both ways. Chemists share reaction bottlenecks, and we translate that into factory-level tweaks. It’s this constant back-and-forth that keeps the process sharp and the product fit for increasingly complex research needs.

    This compound sits at the crossroads of tradition and progress. Older synthetic methods leaned heavy on brute-force conditions—high heat, excess base, hours at reflux. Modern protocols, built around exact reactivity of fluorinated benzyl halides, favor shorter reaction times, lower environmental loads, and, crucially, fewer unplanned deviations. We keep the line open to those building the next class of pharmaceuticals, crop protection agents, or specialty materials, always pushing the process to deliver safer, cleaner, and higher-value outcomes.

    Continuous Improvement

    No manufacturing protocol remains static. We review in-process data, audit customer outcomes, and solicit troubleshooting reports from every corner of the market. If a customer flags crystallization trouble at 20°C or observes unexpected degradation during late-stage reactions, our quality and R&D teams dig in. Sometimes, the fix points to a minor contaminant; other times, a tweak in storage temperature solves the issue. These constant checkpoints build resilience into the supply chain and produce a more refined material over time.

    We invest in advanced analytical methods—LC/MS, FTIR, and high-resolution NMR—to probe for even the rarest impurities. Each new insight adds another layer of certainty before the product heads out the door. Clear lines of communication keep corrective actions fast and direct. For large-volume or specialty buyers, we run custom syntheses, dialing production parameters to fit the exact requirements of a new research cycle. Customers see this hands-on approach as an essential part of long-term partnership, not just as good service.

    Real-World Value: Beyond Price and Purity

    To the untrained eye, all drums of benzyl halides might look the same. Yet the true value of 4-(Trifluoromethyl)Benzyl Bromide shows up where reliable performance meets the demands of live production. Customers have told us that consistency—batch-to-batch, quarter-to-quarter—matters more than small price gaps. By ensuring a stable supply and integrating customer feedback into workflow, we support not only safer and more efficient operations but also genuine progress in fields where every innovation counts.

    As people who manufacture the products researchers rely on each day, we see that every improvement in product performance, safety protocol, or environmental stewardship delivers gains all the way down the line. Our role doesn’t end with loading the tanker truck or crating the last drum. We view the entire collaborative chain—from our floors to the scientist’s bench—not as an obligation but as a mission to advance both technology and safety, one project at a time.

    Looking Forward: A Manufacturer’s Pledge

    Every chemical carries a life story. For 4-(Trifluoromethyl)Benzyl Bromide, the journey—the daily effort to improve, ensure supply, and support customers—defines its place on the market. Whether optimizing another batch, fielding a customer troubleshooting report, or evaluating a new green chemistry protocol, we treat every step as a direct investment in research, trust, and safety. By holding equipment, staff, and partnerships to high standards, we build more than a product line. We support an industry that thrives on innovation and reliability in equal measure.