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1-Bromo-4-(Trifluoromethoxy)Benzene

    • Product Name 1-Bromo-4-(Trifluoromethoxy)Benzene
    • Alias 4-(Trifluoromethoxy)bromobenzene
    • Einecs 205-614-4
    • 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

    301288

    Chemical Name 1-Bromo-4-(Trifluoromethoxy)Benzene
    Cas Number 461-97-2
    Molecular Formula C7H4BrF3O
    Molecular Weight 241.01
    Appearance Colorless to pale yellow liquid
    Boiling Point 173-175°C
    Melting Point -8°C
    Density 1.68 g/cm3
    Refractive Index 1.504
    Flash Point 62°C
    Solubility Insoluble in water, soluble in organic solvents
    Synonyms 4-Bromophenyl Trifluoromethyl Ether
    Pubchem Cid 94024
    Smiles C1=CC(=CC=C1Br)OC(F)(F)F
    Inchi InChI=1S/C7H4BrF3O/c8-5-1-3-6(4-2-5)12-7(9,10)11/h1-4H

    As an accredited 1-Bromo-4-(Trifluoromethoxy)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 mL, screw cap. Labeled with chemical name, formula, hazard symbols, and supplier details for 1-Bromo-4-(Trifluoromethoxy)Benzene.
    Shipping 1-Bromo-4-(Trifluoromethoxy)benzene is shipped as a hazardous chemical. It should be packed in secure, leak-proof containers, clearly labeled according to international regulations. The substance requires ground or air transport with relevant documentation, including Safety Data Sheets (SDS). Handling and shipping must comply with all applicable chemical and hazardous material regulations.
    Storage 1-Bromo-4-(Trifluoromethoxy)benzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and bases. Protect from moisture and direct sunlight. Proper labeling and storage in a designated corrosive/halogenated organics cabinet is recommended to ensure safety and chemical integrity.
    Application of 1-Bromo-4-(Trifluoromethoxy)Benzene

    Applications of 1-Bromo-4-(Trifluoromethoxy)Benzene in Industrial Manufacturing

    1-Bromo-4-(Trifluoromethoxy)Benzene serves as a key intermediate in several precision-driven sectors within the chemical industry. Our production technology supports reliable downstream integration, offering consistent high-purity material for demanding synthesis and formulation environments across custom organic synthesis, agrochemical active design, pharmaceutical development, fine electronic chemical production, and specialty polymer manufacturing.

    1. Pharmaceutical Intermediate for Active Compound Synthesis

    Pharmaceutical companies employ this brominated trifluoromethoxy benzene derivative as a structural building block during the synthesis of advanced pharmaceutical intermediates, especially for molecules in the anti-inflammatory and antiviral categories. The compound introduces electron-withdrawing functionality to aromatic systems, enabling precise molecular tuning in multi-step API synthesis routes. It enters the process during halogen-lithium exchange or cross-coupling reactions, ensuring reliable downstream transformations for strict regulatory compliance in drug development.

    Industry compliance standards

    • ICH Q7 (GMP for Active Pharmaceutical Ingredients)
    • EU GMP Annex 8 (Sample retention and reference standards)
    • USP <795> (Pharmaceutical Compounding—Nonsterile Preparations) for handling
    • REACH registration for intermediate production

    Typical usage ratio

    • 0.15–0.35 molar equivalents per batch in Suzuki–Miyaura or Buchwald–Hartwig couplings; adjusted based on target molecule's halogen to carbon ratio

    Downstream process integration

    • Introduced during halogen exchange or metal-catalyzed coupling steps in multi-stage synthesis cascades for complex pharmaceutical intermediates

    Final product types

    • Anti-inflammatory API intermediates
    • Antiviral lead compounds
    • Chemically modified small molecule library entries for drug discovery
    • Solid dosage forms (following further downstream synthesis)

    2. Agrochemical Synthesis: Herbicide and Fungicide Intermediates

    The compound acts as a strategic starting material for synthesizing advanced agrochemical actives, such as trifluoromethoxy-substituted benzenes incorporated into new herbicidal and fungicidal frameworks. It is typically involved in nucleophilic substitution and cross-coupling reactions during process R&D and scale-up for active ingredient production. Its electron-withdrawing properties enable downstream formulation of high-performance crop protection agents.

    Industry compliance standards

    • FAO/WHO Specification Guidelines for Pesticides (including impurity limits)
    • ISO 9001:2015 for production batch traceability
    • REACH registration as chemical intermediate
    • China GB 2763 (MRLs for pesticide residues) — reference for formulation constraints

    Typical usage ratio

    • 20–60% by weight of total raw material charge in herbicide and fungicide actives; the precise ratio depends on downstream molecular structure and desired functionalization level

    Downstream process integration

    • Feeds directly into nucleophilic aromatic substitution or palladium-catalyzed coupling units during active ingredient synthesis; process optimized for impurity profile and reactivity

    Final product types

    • Trifluoromethoxyphenyl-based herbicides
    • Systemic fungicide intermediates
    • Pre-emergence weed control concentrates
    • Granular and liquid agrochemical formulations (after active ingredient isolation)

    3. Specialty Polymer Modifiers for Advanced Materials

    Polymer producers utilize this aromatic bromide as a functional comonomer or end-group modifier to introduce trifluoromethoxy functionality into specialty poly(arylene ether) or polyimide chains. These modifications enhance chemical resistance, lower dielectric constants, and fine-tune glass transition temperatures, particularly in performance films and fluoropolymer composites. Integration occurs by direct copolymerization or post-polymerization modification during resin manufacturing.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Resin Production)
    • UL 94 (Tests for Flammability of Plastic Materials)
    • RoHS 2 Directive (2011/65/EU) in downstream electronics
    • ASTM D3159 (Standard Specification for Polyimide Films)

    Typical usage ratio

    • 0.5–8% by weight as co-monomer or functional additive in engineered polymer resins; adjusted to balance dielectric and mechanical properties

    Downstream process integration

    • Charged during melt-phase copolymerization or used as functional end-capper in step-growth polymerizations; enables direct incorporation of trifluoromethoxy moiety into macromolecular backbone

    Final product types

    • Low-loss polyimide and poly(arylene ether) films
    • Flexible printed circuit boards (FPCBs)
    • High-frequency insulation layers
    • Engineering plastics for aerospace and electronics

    4. Advanced Electronic Chemical Intermediates

    Electronics chemical manufacturers employ this halogenated aromatic as a precursor for producing trifluoromethoxy-functionalized monomers and intermediates needed in high-end liquid crystal displays (LCDs), OLED devices, and other miniaturized electronic components. It features prominently in cross-coupling and substitution steps, supporting the fixation of unique fluorinated motifs in advanced small molecules used for high breakdown voltage and low leakage current materials.

    Industry compliance standards

    • IEC 61249-2-7 (Halogen-free materials for electronic applications)
    • ISO 14001:2015 (Environmental Management in chemical processing)
    • REACH SVHC regulations on aromatic intermediates
    • JIS C 5016 (Material standards for electronic devices, Japan)

    Typical usage ratio

    • 5–25% in key monomer or intermediate batches, varying with formulation for final dielectric and optical requirements

    Downstream process integration

    • Used in early-stage halogen–metal exchange and cross-coupling synthesis steps for manufacturing liquid crystal and organic semiconductor intermediates before final functionalization and purification

    Final product types

    • Small-molecule liquid crystal intermediates
    • OLED display building blocks
    • Photoresist additives
    • Specialty electronic grade fluorinated compounds
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    Certification & Compliance
    More Introduction

    Introducing 1-Bromo-4-(Trifluoromethoxy)Benzene: A Critical Intermediate from a Manufacturer’s Perspective

    Building Reliable Chemistry—Our Direct Experience

    Manufacturing 1-Bromo-4-(Trifluoromethoxy)Benzene isn’t just a matter of filling barrels or meeting a spec sheet for us. This compound, often recognized as a specialized aromatic intermediate, leaves our reactors with intentions far beyond our own gates. Creating it means a commitment: process accuracy, consistent purity, and supporting industries that need the unique performance this molecule brings. We see direct feedback from downstream users, which shapes the way we handle its entire production cycle. At our site, each reactor run for this compound tells its own story—of process controls, filtration decisions, and quality check routines that aren’t just copy-pasted from general chemistry textbooks.

    Understanding the Core: Specification and Characteristics

    The identifier 1-Bromo-4-(Trifluoromethoxy)Benzene describes a specific structure—a benzene ring bearing a bromo group at the 1 position and a trifluoromethoxy group at the 4 position. In manufacturing language, that particular core translates to challenges with halogen handling, vigilant moisture control, and specialized purification—especially when prepping high-purity grades. Final products come as colorless to pale yellow liquids or solids, depending on exact storage conditions and batch, but we always measure purity by gas chromatography, pushing well above 98% unless a different grade is expected. Water content, residue on evaporation, and individual impurity profiles have to meet each customer’s expectations; the feedback loop with purchasing chemists is direct and ongoing.

    Why the Trifluoromethoxy Group Changes the Game

    The trifluoromethoxy group draws a sharp line between 1-Bromo-4-(Trifluoromethoxy)Benzene and more standard halogenated benzenes. This isn’t only a synthetic tweak—CF3O shifts physical properties, influences electronic effects, and ultimately, allows for transformations that plain bromo derivatives can’t always match. Chemists downstream count on these effects to drive reactivity or introduce the kind of metabolic stability other substituents don’t offer. During scale-up, our equipment gets tested by the reagent’s volatility and reactivity, especially because traces of water and oxygen can short-circuit yield or affect color and purity.

    Many who use this product want the trifluoromethoxy group precisely for its electron-withdrawing nature, which lets them install more complex groups through palladium catalysis or manage selectivity in reactions that don’t behave the same way with traditional bromo benzenes. Those advantages shape our quality criteria as much as they influence downstream choices in pharmaceuticals, agrochemicals, and materials. We receive requests for specific impurity limits not because they fill out a regulatory document, but because one contaminant in the aromatic region can make or break a catalyst’s function. That’s real-world impact for a single substituent change.

    Scale-up: Lessons from the Field

    Years spent moving from flask to plant reactor show where things slow down or go sideways. Bromination and trifluoromethylation protocols differ across the industry, but as a producer, we know even batch-to-batch consistency can throw curveballs when it comes time to scale. Our operators keep detailed logs noting pressure spikes or color shifts, since these might not show up if you’re just running a few grams in the lab. We also find that slight changes in solvent grade or agitation rate show up in the final purity figures, so process validation goes deeper than “good enough” checks; we weigh and verify critical controls each day.

    We don’t ignore the handling aspects either. This product requires smooth logistics for everything from specialized glassware to packaging that keeps out stray moisture and light. Our tank farms and bottling lines have upgraded seals and humidity monitors for this class of intermediate. Each improvement doesn’t just keep our operation tidy—customers often tell us that a broken seal on a shipped drum set their R&D back by weeks. Solving that means listening, upgrading equipment, and treating packaging as part of the synthesis, not an afterthought.

    Differentiation: Standing Apart from Standard Bromo Benzenes

    People sometimes ask why not use less substituted bromo benzenes—why pay extra for a trifluoromethoxy version? From years of talking to application chemists, the answers are practical, not abstract. The impact on molecular polarity, reactivity, and downstream safety or biological profiles is significant. A fluoroalkoxy group isn’t just a checkbox in a chemical catalog; it opens doors for regulatory approval or lets a molecule survive stressful environments. We supply several related intermediates, but buyers consistently return to this product for projects with no tolerance for extra reactivity at the wrong ring positions. The difference in downstream success rates is traced directly to our product’s structure and the controls we implement in-house.

    We also notice that some customers run side-by-side tests, tracking not only physical properties but also catalyst lifetimes and reaction reproducibility. We spend time in dialogue with these teams so that our quality parameters reflect lab reality and not just legacy commodity specs. Having handled both general brominated aromatics and this specialized molecule, we see the critical difference starts before the material even leaves the plant.

    Methods and Challenges—Going Beyond Routine Synthesis

    The plant runs for this compound aren’t generic. Each reaction step ties together cost pressures, operator safety, regulatory compliance, and customer audits. The trifluoromethoxy group’s installation demands selectivity—side reactions, if left unchecked, eat into batch yield or slip in contaminants with chromatographic tails that drag out purification. Our chemists invest in pre-batch planning, running small-scale pilots for every raw material lot, and calibrating endpoint detection equipment before each campaign.

    For us, these processes are never divorced from reality. Our experience with new raw material supplies has taught us to avoid last-minute substitutions. A small impurity in a bromo source or solvent can become a significant chromatographic ghost in the finished product. The plant’s process documents run deep, and root cause analysis is a regular practice, not a rare event. The technical and commercial teams check incoming data daily, alert for slight drifts in analytical signatures—especially as new suppliers enter the market and regulations shift.

    Market Trends, Real-World Applications, and Customer Feedback

    Applications for 1-Bromo-4-(Trifluoromethoxy)Benzene have trended upward as pharmaceutical and crop protection chemistries seek more robust and bioavailable motifs. We see usage in SAR (structure-activity relationship) studies, library synthesis, and more recently, in advanced materials where fluorinated groups improve chemical resistance or fine-tune physical characteristics. The molecule’s adoption often emerges from incremental lab wins—a medicinal chemist swapping out a chloro for a trifluoromethoxy, then seeing an order-of-magnitude boost in metabolic stability.

    Feedback loops from our major clients shape the priorities in our labs. Pharmaceutical buyers emphasize the need for detailed analytical packages, trace impurity tracking, and letters of access for regulatory filings. We collaborate openly, providing certificates backed up by full batch traceability. For us, a successful shipment isn’t a mailed drum, it’s a project milestone for a partner. Our engagement with these teams has led us to develop specialized batches with even tighter impurity control, and sometimes to modify the process for a particularly sensitive downstream application.

    When dealing with R&D teams, speed and responsiveness mean as much as purity. We maintain reserve inventory for pilot trial support, and have streamlined documentation to minimize administrative slowdowns. If a customer’s application flags a trace contaminant, we cross-reference plant batch logs and immediately replicate GC data to pinpoint any anomaly. This direct line between plant and user builds trust—something no standard chemical description can capture.

    Environmental Awareness and Risk Management

    Handling halogenated trifluoromethoxy aromatics introduces a set of environmental and safety obligations. Our plant meets strict emission controls, and we’ve learned from experience which abatement systems yield the lowest environmental footprint. Waste handling, VOC control, and closed system transfer get regular review. Operator training goes beyond canned safety videos—we incorporate feedback from near-misses and successful mitigations to keep both our people and our neighbors protected.

    Recent regulatory updates targeting perfluoroalkyl and polyfluoroalkyl substances (PFAS) encourage ongoing process development. We apply advanced analytics to every plant discharge stream, even if regulations don’t directly call for it yet. Proactive controls help us stay ahead, rather than scrambling for compliance as rules evolve. Clients often ask about product stewardship, and our investment in closed-loop recovery or alternative solvent use comes from real experience managing the intersection of cost, compliance, and community responsibility.

    Supply Chain Insights from a Manufacturer’s Standpoint

    1-Bromo-4-(Trifluoromethoxy)Benzene’s market price often moves with the availability of core reagents and specialty intermediates upstream. Any trader or distributor can see price changes, but as manufacturers, we feel every ripple immediately. Weather events, regulatory shakeups in key raw material geographies, or unexpected shutdowns in neighboring plants all flow through our supply chain. The difference isn’t just academic; it impacts batch scheduling, overtime needs, and even maintenance plans.

    To buffer these shocks, we diversify suppliers, but only after rigorous onboarding—every new source gets trial runs and deep-dive QA. Dual-sourcing and local storage build resilience, but maintaining a ready supply of key inputs comes at a cost. Our on-site warehousing isn’t empty risk management; it’s a safety margin that lets us quote tighter lead times or offer consistent contract fulfillment even if the wider market seizes up.

    Continuous Improvement Driven by Customer Needs

    Real-world success for us doesn’t hang on legacy recipes or inertia. Our lab and scale-up chemists meet regularly with customer technical teams—these discussions go beyond checking boxes on pre-shipment paperwork. We gain early notice of novel applications, new compliance thresholds, or tighter impurity budgets from pharmaceutical partners. Those signals shape capital investment decisions and direct our own R&D priorities.

    For example, several years ago, a major pharmaceutical developer flagged a minor impurity that standard QC had missed, traceable to a degradation pathway not previously considered. Instead of a costly recall, joint troubleshooting led us to install an updated in-line filtration module and shift a distillation endpoint. That single feedback loop not only secured the partnership, but also prompted us to extend the filter upgrade throughout the entire plant, raising the baseline for all subsequent batches. These aren’t theoretical case studies—they’re our living workflows, as real as a shift change in the plant.

    Supplier-customer relationships, in our experience, thrive on this two-way flow. Technical and QA teams regularly visit our site for joint audits or on-the-fly troubleshooting. Their real-life use cases help us prioritize investments. Even small improvements in batch-to-batch color or micro-impurity spectra can mean a faster regulatory submission for a drug candidate or streamline an agrochemical’s downstream processing.

    Analytical Rigor and Traceability

    Every production batch comes paired with a full analytical suite—main product purity, water content, residual solvents, UV/Vis traces, and, where required, specialized NMR and MS confirmations. Our lab team participates in global proficiency testing, calibrating against international standards and peer manufacturers. The same applies to impurity fingerprinting—customer R&D departments often submit their own reference substances, and our lab team responds with targeted analysis before dispatching barrels or bottles.

    Traceability isn’t just a buzzword. Our records let clients match every drum or bottle to raw material lots, operator teams, and even in-process notes. Troubleshooting, root cause analysis, and process improvement draw on these records, closing the feedback loop. Any deviation or customer return triggers direct action—resampling, root cause workshops, and if needed, process modification. Our operational standards beat industry norms because real-world use cases expose gaps long before regulators do.

    Supporting Next-Generation Research and Applications

    From our vantage point, 1-Bromo-4-(Trifluoromethoxy)Benzene has seen increased use not just in well-trodden pharmaceutical syntheses, but also in exploratory research on advanced materials. Material scientists contact us with requests for large-batch samples to run screening series that test durability, hydrophobicity, or unique optical properties. These collaborations don’t feel like simple vendor calls—they draw on our team’s organic synthesis experience and upstream supplier relationships.

    Academic and industrial research teams value reliability and documented lot histories almost as much as purity. Streamlining these requests into our plant scheduling and batch archival systems is ongoing work—often an early indicator of trends that will become standard in a few years. Our site regularly hosts technical workshops, welcoming cross-organization input to push process boundaries. These collaborative efforts have led to incremental but critical improvements: reduced solvent use, faster cycle times, and improved intermediate isolations.

    Concluding Observations from a Manufacturer’s Daily Reality

    Producing 1-Bromo-4-(Trifluoromethoxy)Benzene goes beyond running reactors and sending out drums. It means engaging directly with research, process chemistry, regulatory, and commercial challenges in a field where each detail counts. Impurities that hide on the chromatogram, drum seals that don’t hold up, supply shocks that ripple through warehouses—our team handles each issue with lessons drawn directly from daily practice. Direct communication with users who need a dependable source for this intermediate shapes our approach with rigor and adaptability, all grounded in the chemistry and logistics we manage each day.

    The demands from the market place us in a position of problem-solver and process optimizer, not just molecule maker. Every truck that leaves our loading dock demonstrates the collective experience of operators, chemists, engineers, and logisticians whose routines only pay off when the drum lands right and the end user’s reaction goes as planned. For us, that's how manufacturing earns its place—by delivering not just molecules, but measurable, repeatable outcomes for our customers and their industries.