|
HS Code |
193911 |
| Product Name | 1-Bromo-2,3,5-Trifluorobenzene |
| Cas Number | 175650-72-7 |
| Molecular Formula | C6H2BrF3 |
| Molecular Weight | 210.98 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 146-148°C |
| Melting Point | -21°C |
| Density | 1.755 g/cm3 at 25°C |
| Refractive Index | 1.497 |
| Purity | ≥98% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Synonyms | 2,3,5-Trifluoro-1-bromobenzene |
| Smiles | C1=C(C(=CC(=C1Br)F)F)F |
| Inchi | InChI=1S/C6H2BrF3/c7-3-1-4(8)2-5(9)6(3)10/h1-2H |
| Ec Number | 696-188-1 |
As an accredited 1-Bromo-2,3,5-Trifluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with screw cap containing 100 mL of 1-Bromo-2,3,5-Trifluorobenzene, labeled with hazard warnings and product details. |
| Shipping | **Shipping Description:** 1-Bromo-2,3,5-Trifluorobenzene is shipped as a hazardous chemical under appropriate regulations. It should be packaged in sealed, labeled containers, protected from light, moisture, and physical damage. Transport must comply with local, national, and international regulations, including UN number, hazard class, and proper documentation for safe handling and delivery. |
| Storage | 1-Bromo-2,3,5-trifluorobenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from light and moisture. Store at room temperature, and ensure containers are properly labeled. Follow standard chemical storage guidelines for hazardous materials to minimize risk. |
Applications of 1-Bromo-2,3,5-Trifluorobenzene in Industrial ManufacturingWe directly supply 1-Bromo-2,3,5-Trifluorobenzene to specialized sectors that require reliable quality and consistent chemical performance. In each established downstream segment, this raw material supports advanced synthesis processes governed by stringent technical and regulatory standards. Below, we detail its core applications, industry compliance, formulation guidance, integration points, and the principal end-use products across recognized industrial chains. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisAPI manufacturers rely on this compound as an essential halogenated aromatic intermediate when developing advanced fluorinated drug structures. Its stable trifluorinated ring structure enhances molecular selectivity and metabolic stability during target modification, specifically in channels demanding precise positional control of the bromine and fluorine atoms for later stage Suzuki or Buchwald–Hartwig cross-couplings in complex molecule assembly. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate for Herbicide and Fungicide SynthesisMajor agrochemical synthesis plants employ this trifluorobromobenzene as a fundamental phenyl building block for new generation herbicides and fungicides, leveraging its electron-withdrawing properties to obtain improved bio-efficacy and environmental persistence in crop protection agents. Downstream chemists select this compound to create specific halogen-substituted aromatic motifs with tailored activity profiles in specialty actives. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fluorinated Polymer Monomer Sourcing for Specialty MaterialsProducers of high-performance specialty polymers incorporate this molecule into functionalized monomer synthesis, leveraging its trifluorinated aromatic features to improve chemical resistance and dielectric properties in end-use resins. It supports the synthesis of application-specific polyarylenes and copolymer intermediates where precision in aromatic halogenation patterns is critical for final performance in demanding industrial environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Synthesis for Liquid Crystal and OLED MaterialsManufacturers producing advanced display materials use this halogenated trifluorobenzene structure as a crucial intermediate for liquid crystal monomer and OLED material fabrication. This raw material provides necessary position-selective fluorination that imparts tunable refractive index, photo-stability, and defined electronic properties to high-purity intermediates essential in modern optical and display device markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Building Block for Custom Synthesis in Medicinal Chemistry ResearchOur compound is widely sourced by contract research organizations (CROs) and biopharma for method development projects requiring unique trifluorophenyl motif insertion. Research chemists employ it during late-stage derivatization, probe molecule preparation, and when screening structure-activity relationships in discovery projects demanding high-purity and consistent supply to ensure reproducibility across medicinal chemistry campaigns. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 1-Bromo-2,3,5-Trifluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
At our chemical plant, 1-Bromo-2,3,5-Trifluorobenzene catches the attention of experienced chemists, project managers, and specialty formulators alike. For professionals used to working with halogenated aromatic compounds, the structure and reactivity of this fluorinated bromobenzene open doors to demanding organic synthesis projects and next-generation material developments. With years spent refining our own production methods, we’ve learned exactly how this molecule serves as more than just a stock chemical—it's a cornerstone for transformations where precision and reliability define success.
This compound, identified by the systematic structure—bromine at the 1-position with fluorines at the 2, 3, and 5 positions on the benzene ring—stands out in the crowded field of substituted aromatics. Unlike straightforward bromobenzenes or difluorobenzenes, the trifluoro substitution delivers unique electron-withdrawing effects, impacting both reactivity and selectivity during cross-coupling or nucleophilic substitution reactions. Over the years, our team has observed how these differences ripple through every stage from design to finished product. Benchmark applications keep growing, crossing from agricultural intermediates to pharmaceutical syntheses, and into specialty coatings or electronics.
Experience in chemical manufacturing means seeing more than just purity targets or basic assay statistics. We’ve developed and fine-tuned our purification techniques—distillation under reduced pressure, gas-phase monitoring, and chromatographic validation—to deliver batches that meet the highest criteria set by both R&D labs and scaled-up processing lines. Internal GC and NMR analysis confirm that trace halide and aromatic impurities remain below limits demanded by today’s synthetic chemists. Consistency matters in demanding applications, where even small side products can compromise product yields or downstream processing ease. Our operators understand exactly what a tight specification means for groups counting on reaction reproducibility further down the supply chain.
Each run is built around a deep understanding of the reaction mechanisms and side products involved in this chemistry. Cutting corners leads to difficult-to-remove byproducts or unstable lots. By dedicating reactor time, optimizing residence periods, and maintaining rigorous temperature control, we avoid these pitfalls. Our familiarity with the common pain points of isomeric contamination and incomplete halogen exchange translates into batches trusted by process engineers year after year.
It’s common for newcomers to ask why not just swap in a less expensive bromobenzene or one with fewer fluorine atoms. Years of direct customer feedback and collaborative problem solving have shown us the consequences of such shortcuts. In cross-coupling chemistry—whether Suzuki-Miyaura, Buchwald-Hartwig, or Negishi—the unique substitution pattern of 1-Bromo-2,3,5-Trifluorobenzene controls the rate and site of activation. The electron-withdrawing influence of the trifluorinated backbone stabilizes reactive intermediates, reducing the likelihood of uncontrolled side reactions compared to mono- or difluorinated analogs.
Our team’s synthetic experience further confirms that downstream modifications—such as nucleophilic displacement or functional group interconversion—respond differently with this compound than with others in the family. The presence of bromine at the 1-position remains highly activating in organometallic routes, while judicious placement of fluorines at 2, 3, and 5 improves selectivity, depending on the catalyst system engaged. Researchers aiming for highly functionalized, densely fluorinated end-products know the challenges of byproduct formation and the cost of separating inseparable mixtures. Only a well-chosen starting material prevents wasted resources, trial runs, and delayed scale-up.
Chemists driving innovation in pharmaceutical intermediates rely on 1-Bromo-2,3,5-Trifluorobenzene for good reason. The substituent effects create new possibilities in heterocyclic synthesis and functionalization, especially when building advanced motifs for lead compounds. Over the past decade, our major customers have consistently sought this product for precursors to kinase inhibitors, fluorinated amino acids, and bioisosteric analogs. The push for drugs with improved metabolic stability or altered lipophilicity often begins with a fluorinated aromatic scaffold, and trifluorinated systems present a sweet spot between reactivity and downstream compatibility.
The agrochemical industry treats reliable access to specialty building blocks as a competitive edge. Our ongoing cooperation with field formulation teams shows how the introduction of three precisely placed fluorines into crop protection and herbicide molecule libraries frequently alters potency, persistence, or environmental profile. Unlike less-functionalized bromobenzenes, this compound’s electron-rich nature can boost activity or enhance selectivity for target organisms, depending on the biological system in play.
Increasingly, materials researchers and electronics developers turn to 1-Bromo-2,3,5-Trifluorobenzene while pushing boundaries for next-generation polymers, OLEDs, and fluorinated specialty coatings. Here, our production control guarantees absence of trace metals and undesirable halide contaminants. This type of reliability only comes from hands-on production experience, especially when purifying highly volatile and reactive intermediates.
Feedback from our plant’s technical service group reveals where unexpected challenges often trip up production lines or laboratories. Switches in starting material sources may introduce subtle contaminants or affect reaction kinetics, leading to hours lost troubleshooting or, worse, failures of scale-up runs worth tens of thousands of euros. Our reputation builds on transparent batch documentation, ongoing dialogue with client chemists, and proactive adjustments based on feedback.
Test results from real-world customers often expose differences invisible to superficial glance. During scale-up for a major electronics client, minor differences in impurity profile between lots caused substantial variation in yield of a trifluorinated monomer. Our team responded by modifying a purification stage and prioritizing the shipment of consistently performing material for sensitive runs. These interventions ensure researchers meet deadlines, avoid expensive rework, and keep intellectual property efforts protected.
Another common pain point solved through our expertise addresses residue management and work-up efficiency. Some alternative sources produce batches difficult to isolate, with non-volatile halide and tar-like impurities complicating solvent exchange or crystallization steps. Because we strictly monitor and minimize byproducts throughout synthesis—not simply in a last-minute flash column—formulators and process chemists spend less time fighting problematic isolation, gaining an edge in cycle-time reduction.
Technical literature may outline basic use cases, but hard-won knowledge only comes through repeated production and real-world troubleshooting. Night and weekend calls from customers with late-stage synthesis questions reveal a recurring truth: subtle shifts in reagent ratios, feed rates, or solvent choices during manufacturing leave a permanent mark on the suitability of the product for downstream chemistry.
Our plant managers, many with decades of fluorinated compound experience, constantly iterate on batch processing to minimize waste and enhance recovery of all starting materials. When handling molecules as reactive as 1-Bromo-2,3,5-Trifluorobenzene, even ambient humidity, trace oxygen, or impurities in commonly used solvents create costly knock-on effects. Fielding these variables in actual plant operation, not just lab benches, sets apart our product portfolios in the eyes of experienced buyers.
For specialty chemical users, that reality translates directly into time saved, fewer failed batches, and a smoother path to commercialization. Open channels between our QC team and end-users clear up ambiguity fast. Instead of shipping standard lots and keeping fingers crossed, we cycle back lessons learned from every returned sample and project note, tightening controls in ways that abstract lab reports or summary specs never capture.
Beyond technical merits, responsible manufacture defines our approach to 1-Bromo-2,3,5-Trifluorobenzene. Regulatory compliance, environmental stewardship, and workforce safety all shape each batch. Direct production enables traceability from basic raw material through every step of synthesis. Traceable, closed-loop records help us respond swiftly if a customer flags a batch concern—not just to track lots but also to assure corrective actions prevent recurrence.
Collaboration with local authorities ensures that waste management systems, air handling, and effluent controls keep our environmental footprint to a minimum. Rather than viewing compliance as a box to check, our operators see these practices as core to product quality, team safety, and the trust that underpins our role as supplier. By internalizing best practices, we generate less off-grade waste, reduce hazardous output, and preserve the conditions that enable safe, reliable, long-term operation of specialty plants.
Where sustainable chemistry principles offer alternatives or process gains, our plant adopts them. Continuous review of solvent recovery and catalysis drives ongoing improvement, both in economic terms for our partners and for broader environmental benefit. This connection between tighter process control and higher product quality is clear to experienced clients, who value uninterrupted supply chains as much as outcome predictability and documentation.
Engagement with technical users, synthetic chemists, and formulation leads has always pointed us toward better product outcomes. Clients regularly seek our insight on optimal use conditions, whether troubleshooting an unexpected byproduct or optimizing for greener process conditions. Internally, we stage pilot trials and collaborate directly with laboratory scientists to better understand unanticipated failures or improvement opportunities as they emerge.
No plant run or customer workflow stays static for long. Emergence of new catalyst systems, process regulations, or raw material volatility means we must anticipate, not just react, to shifting demands in specialty benzene derivatives. Our clients rely on these open exchanges to future-proof their materials pipelines—especially in tech-centric industries where margins for error shrink as complexity rises.
Our investments bear fruit in the success stories of end-users who move from bench scale to full commercialization. Material scientists developing next-generation membranes, for instance, have shared data showing how even subtle changes in the starting aromatic scaffold impact performance in demanding separation processes. The well-controlled reactivity profile and impurity spectrum of our 1-Bromo-2,3,5-Trifluorobenzene offers them a baseline for reliable polymerization and modification.
Research teams focused on modern medicinal chemistry, especially those chasing patent-protected molecular patterns, demand transparency in sourcing starting materials. For their programs, lengthy vetting of supplier capability is as important as price or delivery speed. Open technical files, extended impurity profiling, and willingness to adapt batch records help accelerate these teams beyond regulatory hurdles or patent office queries. Our investment in people, equipment, and dialogue addresses these real-world requirements, improving their time to discovery.
One collaboration with a leading agrochemical innovator showcased how careful selection of starting materials shaped an entire product launch. Faced with inconsistency from multiple suppliers, the customer approached us to standardize inputs across laboratory and production scale. Our batch-to-batch traceability and adaptability enabled their R&D group to cut development time by weeks, setting a new internal benchmark and cementing a trusting partnership built on reliability, transparency, and technical acumen.
On the pharmaceutical front, a contract manufacturer specializing in advanced oncology molecules turned to us after facing unexplained batch failures and inconsistent final conversion rates with other suppliers’ material. After an engineering review, we identified that the root cause centered on microimpurities undetected by standard assay, but flagged by our extended analysis procedures. Adjustments in our plant’s filtration and drying steps produced subsequent batches that maintained downstream reaction yield above 98 percent, opening the door to successful commercial launch.
We believe continuous investment in both facility and staff knowledge remains the crucial edge in staying ahead of industry shifts. Specialists join our team not just to maintain routines, but to embed curiosity and iterative learning into every product cycle. This mindset drives our search for improved synthesis routes, greener alternatives for solvents, and better controls for batch-to-batch purity.
Feedback loops run from plant operator notes to lab trial records, up through direct client conversations. This direct, iterative loop is where we see the next advances in substituted benzenes emerging—not as top-down decrees, but as shared innovation with the market. Looking back, major shifts in process technology have all stemmed from an openness to listen, adapt, and improve. Our experiences with 1-Bromo-2,3,5-Trifluorobenzene stand as proof of this approach in action.
Building lasting, productive relationships doesn’t happen without years of shared successes, honest assessments, and mutual learning. Our plant’s journey with this compound illustrates that deep technical skill, consistent process, and personal accountability all combine to deliver not just a better molecule, but a more seamless, trustworthy supply chain. The customers who stick with us cite these values again and again as the reasons their programs move forward on time and on target.
By focusing on real production experience, solution-oriented dialogue, and hands-on learning, we support the world’s leading chemists as they turn 1-Bromo-2,3,5-Trifluorobenzene into tomorrow’s medicines, materials, and agricultural solutions. Our work doesn’t end at the warehouse door, but extends into every trial run, production batch, and troubleshooting session. Together, with our customers, we push the boundaries of what’s possible—one batch, one project, and one success at a time.