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1-Bromo-3,5-Difluorobenzene

    • Product Name 1-Bromo-3,5-Difluorobenzene
    • Alias 1,3,5-Difluorobromobenzene
    • Einecs 828-342-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    676481

    Chemical Name 1-Bromo-3,5-Difluorobenzene
    Molecular Formula C6H3BrF2
    Molecular Weight 192.99 g/mol
    Cas Number 64248-56-2
    Appearance Colorless to pale yellow liquid
    Boiling Point 169-171 °C
    Melting Point -6 °C
    Density 1.668 g/cm³
    Refractive Index 1.525
    Purity Typically ≥98%
    Synonyms 3,5-Difluorobromobenzene
    Flash Point 58 °C
    Solubility Insoluble in water; soluble in organic solvents
    Smiles C1=C(C=C(C=C1F)Br)F
    Inchi InChI=1S/C6H3BrF2/c7-4-1-5(8)3-6(9)2-4/h1-3H

    As an accredited 1-Bromo-3,5-Difluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Bromo-3,5-Difluorobenzene is packaged in a 100 mL amber glass bottle with a secure screw cap and hazard labeling.
    Shipping **Shipping Description:** 1-Bromo-3,5-difluorobenzene should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Label as hazardous (flammable/irritant). Comply with all relevant regulations (DOT, IATA, IMDG). Use appropriate cushioning and secondary containment to prevent leaks or spills during transit. Store at ambient temperature, away from incompatible substances.
    Storage Store **1-Bromo-3,5-difluorobenzene** in a tightly sealed container in a cool, dry, well-ventilated area away from incompatible materials such as strong oxidizers. Keep it away from sources of ignition and direct sunlight. Use appropriate chemical-resistant containers and label them clearly. Ensure access to safety equipment such as eyewash stations and spill kits in the storage area.
    Application of 1-Bromo-3,5-Difluorobenzene

    Applications of 1-Bromo-3,5-Difluorobenzene in Industrial Manufacturing

    1-Bromo-3,5-Difluorobenzene is a key intermediate in several high-value industrial segments. Its reactivity and substitution pattern make it valuable for advanced synthesis, particularly where controlled halogen and fluorine functionalities support complex molecule construction and high-performance materials manufacturing. The following application segments represent the major, real downstream industrial uses.

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

    This compound serves as a halogenated aromatic building block in the synthesis of APIs for antihypertensive, antiviral, and oncological formulations. Its bromo and difluoro substitution enables regioselective cross-coupling and further functionalization, facilitating the construction of advanced pharmaceutical cores that incorporate fluorinated rings for improved metabolic stability and target affinity. Reaction schemes often employ Suzuki or Buchwald–Hartwig couplings at the bromo position. Bulk production for API pipelines requires strict batch traceability and contamination control.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: FDA Current Good Manufacturing Practice (CGMP) for Finished Pharmaceuticals
    • EU GMP Part II: Basic Requirements for Active Substances
    • USP–NF (United States Pharmacopeia–National Formulary) monograph compliance where applicable

    Typical usage ratio

    • Used as a core intermediate at 1–4 molar equivalents in the initial coupling or ring construction steps; the precise ratio is process-dependent, determined by downstream yield studies and impurity profile management.

    Downstream process integration

    • Entry point: Early-stage halogen–metal exchange or palladium-catalyzed cross-coupling with amine or boronic acid pre-cursors, followed by downstream derivatization to give API skeletons.

    Final product types

    • Final APIs in oral, injectable, or topical dosage pharmaceutical forms, including fluorinated derivatives for cardiovascular and antiviral indications.

    2. Agrochemical Intermediate for Selective Herbicide and Fungicide Synthesis

    Producers of next-generation herbicides and fungicides incorporate this compound during multi-step synthesis of fluorinated aromatics, which show increased potency and stability in field applications. Its high compatibility with nucleophilic aromatic substitution and Grignard reactions makes it suitable for creating new actives with improved environmental safety profiles. Process flows emphasize clean conversion and minimization of halogenated by-products to satisfy environmental and worker safety regulations.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Agrochemical Manufacturing)
    • OECD Guidelines for the Testing of Chemicals (Residue, Toxicology, Fate)
    • FAO/WHO Guidelines on Specification Requirements for Plant Protection Products
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals—EU)

    Typical usage ratio

    • Applied at 0.8–1.5 equivalents based on the desired product formula and the extent of fluorination or bromo substitution required in the final agrochemical molecule.

    Downstream process integration

    • Intermediate introduced during early-stage aromatic assembly, typically via nucleophilic aromatic substitution, then channeled into further coupling or cyclization to construct the functional crop protection agent core.

    Final product types

    • Formulated liquid or solid herbicides and fungicides for pre-emergence or post-emergence crop application, with enhanced environmental resistance and biological activity.

    3. Material Intermediate for Liquid Crystal Display (LCD) Monomers

    This halogenated aromatic often enters manufacturing lines producing highly pure monomers for advanced LC (liquid crystal) materials. Manufacturers value the difluorinated structure for introducing rigidity and high dielectric anisotropy to resultant mesogens. The compound undergoes precise Friedel–Crafts or Suzuki coupling to affix onto aryl or cyclohexyl-based platform molecules, with stringent purity requirements to prevent display image defects.

    Industry compliance standards

    • IEC 61249-2-30: Materials for Interconnection Structures of LCD Panels
    • RoHS Directive (Restriction of Hazardous Substances in Electrical/Electronic Equipment—EU)
    • ISO 14001:2015 (Environmental Management for Materials Sourcing)
    • Sony SS-00259 Standard (Chemical Content Management for Displays)

    Typical usage ratio

    • Blended at 1.0 equivalent for specific monomer syntheses; often between 2–8% by weight in the multi-step assembly of advanced LC material blends, adjusted for the desired birefringence and viscosity characteristics.

    Downstream process integration

    • Integrated during the critical stage of mesogenic compound synthesis, typically followed by hydrosilylation or etherification in high-purity, trace metal-controlled environments.

    Final product types

    • Specialty monomers and oligomers for LCD panel and flexible display fabrication, applied in consumer electronics, automotive instrument panels, and commercial signage.

    4. Intermediate for Fluorinated Polymer Synthesis

    Specialty polymer manufacturers employ this compound to introduce fluorine moieties in the aromatic backbone of high-performance polymers. This modification provides chemical resistance and low dielectric constants for fluorinated polyimides and related engineered materials. Its use is critical in electronics, wire insulation, and membrane manufacturing. Careful reaction control minimizes unreacted monomer and ensures batch-to-batch reproducibility.

    Industry compliance standards

    • ASTM D7091: Standard Practice for Polymer Synthesis QC
    • UL 94: Flammability Standard for Plastics
    • RoHS and REACH (Hazardous Substance and Environmental Control—EU)
    • ISO 9001:2015 (Quality Management for Polymer Processing)

    Typical usage ratio

    • Incorporated typically at 3–10 mol% relative to total repeat units, subject to target dielectric constant, chemical resistance level, and thermal properties specified by end user application.

    Downstream process integration

    • Added at the aromatic monomer introduction stage, often participating in condensation or copolymerization with dianhydrides, diamines, or other fluorinated partners before film casting or fiber spinning.

    Final product types

    • Fluorinated polyimide films, chemical-resistant membranes, and insulating layers for microelectronics and high-temperature industrial applications.

    5. Fine Chemical Intermediate for Advanced Dye and Pigment Precursors

    Producers of specialty dyes and pigments utilize this compound for introducing precise halogen and fluorine patterns into aromatic frameworks used in high-stability colorants. These features contribute to improved lightfastness and solvent resistance in end-use paints, coatings, and printing inks. Process stages focus on controlled halogenation and subsequent tailored coupling with chromophoric groups to maintain batch consistency and regulatory traceability.

    Industry compliance standards

    • EN 71-3: Safety of Toys—Migration of Certain Elements (relevant for colorants in toys)
    • ISO 9001:2015 (Quality Systems in Fine Chemical Production)
    • REACH Annex XVII (Restrictions on Organohalide Pigments and Dyes—EU)
    • GHS/CLP Regulation (Classification, Labelling, and Packaging of Substances and Mixtures—EU)

    Typical usage ratio

    • Applied at 0.5–1.2 equivalents as the halogenated precursor in dye synthesis, adjusted based on pigment purity targets and desired chromatic properties.

    Downstream process integration

    • Introduced at the halogenation or aromatic substitution stage and followed by azo-coupling, condensation, or metallation to complete the pigment or dye molecule.

    Final product types

    • High-stability dyes for textile printing, organic pigments for automotive and industrial coatings, and inkjet ink formulations.
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    Certification & Compliance
    More Introduction

    1-Bromo-3,5-Difluorobenzene: A Closer Look from the Manufacturer’s Bench

    Work in chemical manufacturing reveals how a compound like 1-Bromo-3,5-difluorobenzene leaves an imprint on both process design and end-use applications. This molecule has a way of helping customers reach targets that may not be possible with other halogenated benzenes. Having spent years overseeing its synthesis, purification, and eventual shipment, I can point out real world differences which may not pop out in a catalog but matter on the factory floor and in research labs.

    Model and Molecular Identity

    We deal with the compound C6H3BrF2, recognized as 1-Bromo-3,5-difluorobenzene, CAS number 17689-77-9. We grew familiar with slight changes in substitution patterns on the aromatic ring leading to significant shifts in physical and chemical behaviors. Place the bromine on carbon 1, then drop fluorine atoms onto the 3 and 5 positions, and you get a balance of reactivity and stability not found in its close cousins: 1,4-difluoro-2-bromobenzene or trifluorobenzenes, for instance, won’t fill the same niche.

    At room temperature, this compound presents as a colorless to pale yellow liquid with a scent some call sweet but most production staff describe simply as sharp. The molecular weight (209.99 g/mol) marks a good midpoint for a halogenated aromatic; heavy enough for manageable handling without becoming overly viscous. It shows a boiling point in the 180 °C range and melts well below freezing, so cold storage in temperate climates never brings precipitation or clogging challenges. These traits combine to make charging reactors straightforward at scale, whether by drum or smaller pack sizes.

    Handling and Purity Standards

    Maintaining high purity is not just a matter of confidence—it’s a necessity downstream. We control synthetic routes to avoid over-bromination and over-fluorination. Lab analytics using GC and NMR confirm both identity and absence of positional isomers. Our usual purity benchmarks reach at least 98%, though targeted syntheses for pharmaceutical and electronic intermediates sometimes raise that mark beyond 99%. Each batch comes with data covering residual solvents, moisture, and related substances. While some customers request custom specifications, most appreciate predictability batch-to-batch because scale-up chemistry does not allow surprises.

    On our production line, this compound resists the sort of oxidative or hydrolytic breakdown that can sabotage shipment quality on long journeys. Bromine at the 1-position holds firm—rarely does debromination show up without severe stress. The two fluorines, sitting meta to each other, keep the ring from activating toward unwanted side reactions, which is valuable in multi-step syntheses where selectivity rules. Minimizing contaminant carry-over at this stage has a domino effect for the next synthetic step, especially when working toward fine chemical APIs or advanced materials.

    Role in Synthesis and Industry Relevance

    Few benzenes with dual fluorination and monobromination have this blend of characteristics. Our chemists hear from customers developing agrochemical scaffolds, pharmaceutical precursors, and specialty functional materials. The bromine acts as a reliable leaving group for cross-coupling reactions—Suzuki, Buchwald-Hartwig, and Ullmann variants—enabling creation of more elaborate molecules. Fluorines sitting at 3 and 5 positions bring a mix of electronic effects: the electron-withdrawing fluorines slow the reaction just enough to allow for selectivity, avoiding side reactions that would crop up with monosubstituted or ortho-fluorinated benzenes.

    We have watched this compound enter projects ranging from crop protection agents to preclinical pharmaceutical candidates. One frequent use starts with palladium-catalyzed coupling to form biaryl or aryl-heterocycle linkages. Every year, we field requests from medicinal chemists who value the electron density and lipophilicity changes imparted by this exact fluorination pattern. Regulatory constraints around unwanted byproducts in these sectors mean we cannot take shortcuts or allow substitutions. What leaves our plant has to perform reliably in the context of multi-million-dollar development campaigns.

    Comparisons with Similar Chemical Building Blocks

    Switch up the halogen pattern and both laboratory outcomes and large-scale yields may change. 1-Bromo-4-fluorobenzene interacts with reactants differently, lacking the nuanced electronic push-pull balance achieved by dual meta-fluorines. Trifluoro analogs offer stability but may be too unreactive for some couplings. Dichlorinated or difluorinated benzenes without the bromine lack an easily displaced group for functionalization. We find customers often test several related halogenated aromatics early in a synthetic campaign before identifying 1-Bromo-3,5-difluorobenzene as optimal for both selectivity and process throughput.

    I have seen industrial R&D teams swapping in isomeric starting materials, chasing cleaner reactions or higher conversions, only to realize that yields slip or unwanted isomers crop up. Once they try our difluoro-bromo combination, the gains in selectivity and ease of purification often answer lingering problems. Chemistry rarely accommodates simple swaps; position and type of halogen matter. Clients working in thin film electronics value the thermal properties and chemical inertia that this compound brings to their formulations. They report improvements in device stability and performance, as compared to analogues where the core benzene sees different halogen arrangements.

    Scale-Up from Lab Bench to Plant Floor

    Lab-scale synthesis may gloss over facts about solubility, volatility, or residual byproducts. Taking 1-Bromo-3,5-difluorobenzene from grams to kilograms, then to metric tons, gives insight into what makes it practical or difficult for real world chemistry. Right from the first run, this compound distilled cleanly. The lack of tarry residues or polymeric buildup distinguishes it from certain polychlorinated benzenes. Over the years, we optimized our reactor designs—jacketed vessels, in-line drying, automated distillation cuts—because handling halogenated aromatics demands respect for both safety and product stability.

    Waste mitigation steps add another layer. The fluorine atoms help decrease the compound’s reactivity toward strong acids and bases, so we experience less corrosion and fewer disposal worries than with more reactive intermediates. By capturing or reprocessing brominated byproducts, we close the loop on environmental concerns. Regulatory authorities keep eyes on halogenated organic emissions. Early investment into vent treatment and waste reduction made a long-term difference, and those choices matter both ethically and for consistent supply.

    Storage and Packaging Realities

    Packaging brings its own set of hurdles. Aromatic bromides can degrade if stored in sunlight or if moisture sneaks in, so we store and ship under nitrogen whenever practical. Tight seals and UV-opaque drums preserve quality from plant to port. We spend time with new clients explaining the logic behind these choices, because a few days of improper storage can sabotage an entire project batch. Customers working at gram, kilogram, or ton scale should not have to reprocess or re-purify a shipment; years of experience teaches us to prevent these headaches before they happen.

    Solvent compatibility also drives packing format decisions. Glass-lined steel and high-density PE containers resist long-term leaching while keeping shipping weight low. Electronic-grade clients often require pre-rinsed and certified containers—an extra step, but experience shows it pays off with less contamination risk. Every now and then, someone asks why strict packing is necessary for a seemingly stable compound. Seeing solvent impurities or micro-particulates compromise a multi-step synthesis answers that question fast. In our line of work, consistency at every stage makes future steps smoother for everyone involved.

    Regulatory Considerations and Environmental Responsibility

    No conversation about halogenated benzene derivatives can ignore the regulatory environment. Brominated aromatics raise red flags in certain jurisdictions due to historical misuse and environmental persistence. Our facility invested in closed loop reaction systems, scrubber units for off-gasses, and solvent recovery infrastructure. These choices add upfront costs but shield operators and neighbors while supporting future market access. Shipments meet standards like REACH, TSCA, and local equivalents; certificates follow each batch out of the gate.

    Internally, waste reduction demands both routine and discipline. Trace amounts of unreacted bromine and fluorinated side-products get destroyed on site rather than sent off-site. Our environmental team audits water, air, and soil metrics quarterly. Avoiding measurable discharge is more than regulatory compliance. It gives our clients confidence that their supply chain does not bring surprises at the audit stage. Responsible production practices ensure that R&D, process development, and manufacturing continue without the reputational or real costs of regulatory backlog. Years of clean records in this sector get earned batch by batch, drum by drum—a fact often missed by third-party traders.

    Technical Support, Troubleshooting, and Process Improvements

    Process support does not end at the loading dock. Over the years, customers have brought issues ranging from micro-scale reactivity complications to scale-up thermal management. We draw on in-plant experience to provide guidance that aligns with lot-specific data, not generic technical notes. When a pharmaceutical client in Asia found trace isomer contamination in a late-stage coupling, our team traced it to a process step upstream and offered a process tweak that dropped contaminants below detection. Such support feels different from third-party advice: real ownership means being invested in the right solution, not just moving material.

    On rare occasions, users report handling issues: crystallization during winter transit, off-odors indicating oxidative degradation, or stuck valves due to vapor lock in heated tanks. We deploy troubleshooting advice that comes from seeing these issues first-hand. If a customer uses automated liquid handling, advice shifts toward minimizing air entrainment. Customers with high-throughput parallel reactors get recommendations on nitrogen blanketing. In every case, advice comes from plant experience, not website boilerplate. Ultimately, problem-solving stays personal and direct—another edge for clients sourcing from a real producer with ongoing technical involvement.

    Building for Tomorrow: Innovation and Continuous Improvement

    As applications evolve, so does our approach to manufacturing. Electronic materials R&D, for example, calls for ever-tighter impurity controls. We responded by adding multi-stage distillation during final workup. Customers seeking to drive their product quality beyond standard markets receive technical sheets and stability data, even early in feasibility studies. The partnership goes both ways: customers report needs, we adapt processes, and both sides move forward. Such feedback loops help us anticipate rather than react to demand trends in pharmaceuticals, agrochemistry, and electronics.

    Ongoing investment matters. We continue pilot runs on greener fluorination agents and alternative bromine sources. Switching to less hazardous raw materials takes time—it challenges equipment and requires years of validation. Yet these steps pay off, lowering risk for operators and reducing end-of-life environmental load. Lessons learned from scale-up campaigns on 1-Bromo-3,5-difluorobenzene shape how we deliver other halogenated aroma compounds as well. No single compound stands in isolation; each process improvement here influences a family of related products given similar scrutiny.

    Application-Driven Feedback and Achievements in Practice

    Feedback from real users shapes our innovations and even the minor tweaks to daily operations. In one instance, a customer scaling up for agrochemical trials found an unexpected emulsion forming during extraction. Process technicians from our site suggested a solvent switch and slightly raised agitation temperature, eliminating the bottleneck without introducing new risks. Another client, piloting OLED intermediate development, ran into trace water issues due to local humidity. Because our plant operates in climatic extremes, we could recommend drying protocols that had proved themselves in our bulk storage tanks.

    These are not just stories of chemistry, but of people working together—inside the plant and out in the world—making projects succeed under pressure. Problems arrive on tight timelines, and no single best practice covers every scenario. Our technical staff rotates between the plant floor and customer-facing roles. The result is a company rooted in its own craft, responsive and open, always driven by challenges arising downstream. We work on the scale of global supply chains with the mindset of personal accountability.

    What Distinguishes Us in the Market

    Where pure traders and brokers handle requests at arm’s length, the responsibilities of a chemical maker run differently. We guard continuity, not just supply. Our production plans synchronize to customer requirements: whether clients need a steady drum-per-week or occasional bulk orders, we adapt schedules to reduce lead times and harmonize with global transit realities. Real manufacturing muscle becomes apparent when disruptions strike. Raw materials go tight or port closures delay logistics; years of trusted supplier relationships and stable in-house production see us through rough patches.

    With each shipment, ownership for both quality and continuity carries forward. The batch number recorded on the side of each container connects to a chain of documentation running back to raw input. Through that chain runs our commitment to client outcomes. This level of traceability and assurance sits outside what occasional trading partners can realistically deliver. Having met with customers facing regulatory holds or multi-stage process delays, I recognize what’s at stake and put a high premium on reliability and transparency.

    Conclusions from Practice: Why Quality Matters Now More Than Ever

    Work in chemical manufacturing rarely matches the simplicity of a product list or catalog entry. Each order, each batch of 1-Bromo-3,5-difluorobenzene exits the factory loaded with choices—raw materials, synthetic routes, analytical controls, packaging protocols—each one affecting both immediate and long-term success for the customer. Hearing from users in disciplines as diverse as novel electronics, agricultural innovation, and advanced pharmaceutical chemistry grounds our adjustments and investments in day-to-day impacts, not abstract theory.

    Years spent working with this molecule show the difference between seeing a chemical as a commodity and as a strategic building block. Careful production, transparent support, flexible logistics, and ongoing innovation combine into something clients value far more than just price or availability. Each liter delivered carries an imprint of cumulative action built on hard-won experience. That combination keeps us responsive to market needs and always looking for new ways to enable customers to do more, better, for longer. True progress in this field rests on knowledge, on partnerships that run deeper than transactions, and on consistency built day in and day out—qualities 1-Bromo-3,5-difluorobenzene helps to highlight, from our plant to every place it finds application.