Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Bromo-4,6-Difluoroiodobenzene

    • Product Name 2-Bromo-4,6-Difluoroiodobenzene
    • Alias 1-Bromo-3,5-difluoro-2-iodobenzene
    • Einecs 843-885-9
    • 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

    249705

    Product Name 2-Bromo-4,6-Difluoroiodobenzene
    Cas Number 62269-17-6
    Molecular Formula C6H2BrF2I
    Molecular Weight 319.89 g/mol
    Appearance Solid
    Purity Typically >98%
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 1-Bromo-3,5-difluoro-2-iodobenzene
    Smiles C1=C(C(=CC(=C1Br)F)I)F
    Inchi InChI=1S/C6H2BrF2I/c7-3-1-4(8)6(10)5(9)2-3/h1-2H

    As an accredited 2-Bromo-4,6-Difluoroiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, sealed with a PTFE-lined screw cap, labeled, containing 10 grams of 2-Bromo-4,6-Difluoroiodobenzene.
    Shipping 2-Bromo-4,6-Difluoroiodobenzene is shipped in tightly sealed, chemical-resistant containers to ensure stability during transit. The package is labeled according to relevant hazardous material regulations (such as UN2811, Toxic Solid, Organic, N.O.S.), and handled with care to avoid exposure to moisture, light, and incompatible materials. Documentation accompanies each shipment.
    Storage 2-Bromo-4,6-Difluoroiodobenzene should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep in a cool, dry, and well-ventilated area, separate from incompatible substances such as strong oxidizers and bases. Store at room temperature, and ensure proper labeling. Use chemical-resistant containers and follow standard safety protocols for halogenated organic compounds.
    Application of 2-Bromo-4,6-Difluoroiodobenzene

    Applications of 2-Bromo-4,6-Difluoroiodobenzene in Industrial Manufacturing

    As a specialized manufacturer, we supply 2-Bromo-4,6-Difluoroiodobenzene to advanced sectors that require high-purity halogenated aromatics for reliable downstream innovation. Below are key, substantiated industry application scenarios, including regulatory and process insights for formulation teams and plant engineers.

    1. Pharmaceutical Intermediate for Heterocyclic API Synthesis

    This compound is widely utilized by innovative pharmaceutical manufacturers as a halogenated building block in the synthesis of complex heterocyclic active pharmaceutical ingredients (APIs). Its precise electronic effects enable selective coupling and substitution steps during the multi-stage assembly of fluoroaryl-based drug candidates, essential for oncology and antiviral research pipelines. The high reactivity of the bromo-iodo motif facilitates palladium-catalyzed cross-coupling reactions, often in Suzuki, Buchwald-Hartwig, or Sonogashira pathways, ensuring high yields and minimal side products.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 US FDA cGMP
    • European Pharmacopoeia (EP 11.0)
    • China Pharmacopoeia (ChP 2020)

    Typical usage ratio

    • Applied at 1.0–5.5 mol% in multi-step synthesis; exact quantity determined by target API scaffold and conversion requirements in each coupling cycle.

    Downstream process integration

    • Introduced during the early-stage or mid-stage reaction block in palladium-catalyzed cross-coupling (e.g., Suzuki), typically in a controlled inert atmosphere, to form core heterocycles or biaryl intermediates.

    Final product types

    • Fluorinated API intermediates for oncology drugs
    • Building blocks for small-molecule antivirals
    • Advanced intermediates for CNS drug discovery

    2. Agrochemical Research & Synthesis

    Leading agrochemical development firms incorporate this raw material into the synthesis of advanced fluorinated and brominated aromatic scaffolds, targeting efficient structure-activity modification in new fungicide and herbicide candidates. Its dual halogenation allows for precise control in sequential halogen-metal exchange and transition metal-catalyzed functionalization, essential for producing analogues with improved photostability and bioactivity profiles for regulatory field trials.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • REACH Regulation (EC) No 1907/2006 for new active substances
    • ISO 9001:2015 Quality Management Systems
    • OECD Good Laboratory Practice (GLP) for agrochemical R&D

    Typical usage ratio

    • 1.0–4.0 mol% per batch in pilot-scale synthesis; ratio tailored to targeted scaffold, based on combinatorial chemistry protocols and substrate availability.

    Downstream process integration

    • Dosed during the selective aryl halide step to enable subsequent nucleophilic aromatic substitution or Stille coupling during lead compound derivatization, prior to formulation into emulsifiable or water-dispersible concentrate prototypes.

    Final product types

    • Advanced herbicide and fungicide candidates
    • Lead molecules for pre-registration field tests
    • Structural analogues for insecticide SAR libraries

    3. Key Reagent in OLED Material Development

    Electronic material producers use this compound in the synthesis of π-conjugated, fluorine-enriched building blocks for organic electroluminescent devices. Its halogen atoms enable sequential cross-coupling to introduce donor and acceptor groups, crucial for improving charge injection and stability in blue or green light-emitting layers. Producers monitor purity and handle the raw material using moisture-free conditions to ensure defect-free film deposition in downstream fabrication.

    Industry compliance standards

    • IPC-4101B: Specifications for Base Materials for Printed Boards
    • IEC 60068: Environmental testing requirements for OLED reliability
    • RoHS Directive 2011/65/EU for downstream electronic compatibility
    • ISO 14001:2015 Environmental Management

    Typical usage ratio

    • Used at 0.5–2 mol% for functional layer precursor synthesis; actual dosage adjusted to balance donor–acceptor architecture and control device photoluminescence efficiency.

    Downstream process integration

    • Added during the late-stage precursor modification step, ahead of purification and vacuum deposition to form emissive layers in OLED substrates or solution-processable inks for display panels.

    Final product types

    • Small-molecule OLED emitters for display and lighting
    • Precursor intermediates for printable electroluminescent layers
    • Functionalized organic semiconductors for flexible touchscreens

    4. Intermediate for Agrochemical Analytical Standards

    Chemical reference laboratories use this compound for certified reference material (CRM) production due to its defined molecular structure and dual halogen substituents. It is vital for generating analytical standards by derivatization or as a spiking agent to calibrate LC-MS and GC-MS quantification methods in residue testing, ensuring method validation in regulated agrochemical control programs.

    Industry compliance standards

    • ISO 17034:2016 Requirements for Reference Material Producers
    • SANCO/3029/99 EU Guidelines for Analytical Quality Control
    • EPA Method 8081B for organochlorine pesticide residues
    • GLP as per OECD No.1 for residue analysis laboratories

    Typical usage ratio

    • Typically applied at 0.05–0.1 mol% in CRM synthesis; precise mass verified via quantitative NMR or gravimetric calibration for trace-level standard preparation.

    Downstream process integration

    • Processed during CRM formulation and purified via chromatography or recrystallization; final material undergoes homogeneity and stability testing before batch release.

    Final product types

    • Certified reference materials for pesticide residue testing
    • Analytical standards for regulatory quality control
    • Calibration solutions for LC-MS/GC-MS validation

    5. Raw Material for Specialty Fluorinated Polymers

    Research divisions within polymer manufacturing operations utilize the dual-halogen motif of this molecule for the synthesis of specialty fluorinated monomers. The material allows for site-specific functionalization via lithiation or halogen-exchange reactions, which is critical in tailoring polymer branches or main chains with desirable dielectric and chemical resistance characteristics, especially for applications in high-frequency electronics and membrane technologies.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Specialty Chemicals
    • ASTM D6288-18 Standard Practice for Polymer Purity Assessment
    • FDA 21 CFR 177.1550 (for fluoropolymer food-contact components, if relevant)
    • REACH pre-registration for new polymer precursors

    Typical usage ratio

    • Used at 1–3 mol% in monomer functionalization protocols; adjusted based on target polymer molecular weight and required halogen incorporation per repeat unit.

    Downstream process integration

    • Added during the initial or mid-phase of monomer building block assembly, often via metal-halogen exchange or nucleophilic substitution, directly preceding polymerization (e.g., via free-radical or polycondensation method).

    Final product types

    • Fluorinated aromatic co-monomers
    • High-performance dielectric films for microelectronics
    • Specialty membranes with enhanced chemical resistance
    Free Quote

    Competitive 2-Bromo-4,6-Difluoroiodobenzene 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Bromo-4,6-Difluoroiodobenzene: Manufacturer’s Perspective on Performance, Reliability, and Value

    Real-World Experience Directs Chemical Innovation

    Every day on the production floor and in our formulation labs, the story of 2-Bromo-4,6-Difluoroiodobenzene continues to evolve. We have spent decades navigating the delicate balance between reactivity and durability in halogenated aromatics. Out of that process, this product has earned a strong position as a cornerstone for synthesis where selectivity cannot be left to chance. We control our processes in-house, overseeing everything from raw material sourcing to final drum sealing. That in-house oversight means we don’t simply ship barrels and bags: we ship chemical performance and consistency forged by years of experience and market feedback.

    What Sets 2-Bromo-4,6-Difluoroiodobenzene Apart?

    2-Bromo-4,6-Difluoroiodobenzene distinguishes itself with its dual halogen functionalities arranged on the aromatic ring, bringing together bromine, iodine, and fluorine in a pattern that drives reactivity in organic transformations. In contrast with monohalogenated benzenes or alternate substitution patterns, this specific compound responds to catalysts and reagents in predictable, efficient ways that shed light on new routes for C–C and C–N bond creation. Many of our partners in pharmaceutical research point to this unique substitution as a decisive advantage when building molecules with precise electronic tuning or designing scaffolds for agrochemical screening.

    We often observe that 2-Bromo-4,6-Difluoroiodobenzene behaves with a reliability that other highly substituted benzenes struggle to match. The ortho- and para- positions relative to the iodo group offer direct points for functionalization. The electron-donating and -withdrawing nature of these halogens, drawn from their placement, guides selectivity in Suzuki-Miyaura, Buchwald-Hartwig, and other palladium-catalyzed cross-couplings. Chemists on our teams choose this material over less-substituted or differently configured benzene rings after seeing sharper conversion rates, fewer byproducts, and smooth upscaling in gram-to-kilogram volumes.

    Specifications Backed by Manufacturer Experience

    Our batches of 2-Bromo-4,6-Difluoroiodobenzene stay within tight specification windows by design. Years of process refinement have taken has minimized the formation of single- and double-substitution positional isomers, and we devote high-performance analytical suites to batch release. Typical purity exceeds 98 percent by GC and NMR, as ensured by internal data from every lot. Moisture control has become integral to long-term stability; we dry under reduced pressure and monitor all outgoing lots for water content below stringent thresholds, a decision based on early feedback from our partners engaged in sensitive metal-catalyzed reactions.

    We realized early on that trace metal contamination and non-volatile residues complicate downstream processing. Control points throughout synthesis, filtration, washing, and crystallization were installed to address this very issue. Many clients who migrated from distributor stock to direct manufacturer supply report fewer surprises: less fouling of glassware, reduced color contamination, and improved yields in sequential process steps.

    Main Fields of Use and Practical Experience

    The most active requests for 2-Bromo-4,6-Difluoroiodobenzene come from pharmaceutical and crop protection R&D segments. Multiple discovery projects have shared data with us showing this molecule as a key building block for kinase inhibitor libraries. In complex heterocycle assembly, the interplay between the bromo and iodo functions means selective manipulation produces challenging scaffolds without excessive protecting group choreography. This advantage saves steps in synthetic routes, bringing down total project time and cost—a benefit we hear about directly in feedback sessions and process consultations.

    Process engineers at active ingredient manufacturing hubs tell us that alternatives, like 2-fluoro-5-bromoiodobenzenes or 3,5-difluoro-4-bromoiodobenzenes, tend to require extra purification or slower reaction rates. During scale-up operations moving from bench-scale to plant reactors, our 2-Bromo-4,6-Difluoroiodobenzene maintains its product profile without introducing trace impurities that complicate regulatory submissions on impurity profiles.

    Beyond small molecules, several advanced materials developers running on-site test reactions use it to install functional fluorinated and halogenated groups in ligands and monomers. The raw material costs, process predictability, and downstream compatibility were cited in procurement audits as deciding factors for long-term offtake agreements with our manufacturing group.

    Why Our Manufacturing Matters

    Trust develops because we control every step and respond to the realities of our customers’ operations. Simple distribution or repackaging cannot replicate the understanding gained from actually running reactors, monitoring curves, and tuning cleaning cycles. Over the years, we have installed real-time monitoring to capture every fluctuation and anomaly. Our line technicians have learned that product color drift and odor warnings correlate with sources of impurity, so corrective actions now take place in-line, not at QC reinspection.

    Manufacturing this compound requires careful temperature and solvent control during halogenation and coupling steps. Training and retention of experienced staff mean the actual handling and management of hazardous or corrosive intermediates stay consistent. Feedback from process chemists in North America, Europe, and Asia highlighted long ago that poorly managed manufacturing campaigns result in frustrating batch-to-batch variability. Our experience has honed timelines and supplier relationships for upstream raw materials, cutting risk for last-minute substitutions or technical-grade feedstocks.

    Differences from Other Products—A Chemist’s Perspective

    Direct substitution patterns and electron-rich aromatic rings perform differently compared to this 2-Bromo-4,6-Difluoroiodobenzene. With other highly halogenated benzenes—especially those where chlorine substitutes for either bromine or iodine—reaction conditions can drift, and yields wobble. Our technical liaisons have noted that in Suzuki couplings, the iodo position on this compound can be cross-coupled efficiently at lower temperatures, preserving sensitive motifs downstream. Switch to a 2-bromo-3,5-difluoroiodobenzene or 4-iodo-2,6-difluorobromobenzene and the selectivity falters, especially in large multi-step sequences requiring robust intermediates.

    Fluorinated aromatics derived from legacy commercial processes often fail to replicate this performance because they either lack dual activation sites or introduce inconsistent halogen placement. The arrangement on this molecule delivers both reactivity potential and stability, translating to fewer byproducts in downstream transformations. Users developing high-throughput libraries in early-stage pharma R&D and late-stage gram-to-ton scale-up for API manufacturing both benefit, as reaction reproducibility carries from microplate to reactor.

    As the original manufacturer, we also field queries about potential applications outside classic domains. Recent inquiries from specialty polymer research groups explored the compound's capacity as a functional monomer for specialty plastics where robust fluorinated and halogenated building blocks introduce new properties. Our team supports these developments with analytical support, process optimization assistance, and practical tips that have emerged from years of handling the subtleties of this compound’s behavior.

    Manufacturing Practices: Hard Lessons and Harder Wins

    Achieving purity and consistency across thousands of kilograms takes more than adherence to a standard recipe. Decades ago, trace contamination issues forced a re-evaluation of washing and drying protocols. Now, the facility design compartmentalizes each synthesis step. Raw materials undergo dual-stage validation before ever reaching production tanks. Any fluctuations in upstream halogen sources prompt direct supplier engagement and, if necessary, process redesign. The goal: eliminate surprises and maintain integrity. As a result, we have watched defect rates drop whereas competing products from non-integrated sources often introduce delays and troubleshooting cycles on the user end.

    After years of running side-by-side comparisons and managing multi-ton campaigns, our technical services group has documented rare but critical process upsets: cross-contamination, photodegradation, and agglomeration. Learning from those events, we introduced end-of-line light shielding, batch segregation, and inert-atmosphere storage not just for compliance but for end-user clarity. Now, we routinely receive requests for lots manufactured after these process changes, as field results generate confidence across development teams.

    Solutions for User Challenges

    We receive numerous reports from formulation and process development teams about how product performance reveals itself during actual runs. If a lot spends too much time in transient warehousing, moisture uptake can become a problem, leading to hydrolysis in sensitive downstream syntheses. In direct response, we ship with humidity controls and recommend storage in original, sealed containers under dry nitrogen. Users in tropical or high-humidity regions frequently ask for tips—our experience suggests transfer to desiccator-equipped storage and limiting open times on drums reduces risk for scale-up reactivity issues.

    Unanticipated crystallization or caking has at times disrupted direct metering into reactors. Through ongoing feedback, we adjusted compound milling and packaging parameters, landing on particle sizes that flow when required, yet resist dusting. Formulators appreciate the reduced wastage and safer transfer. Whenever we see repeated complaints from the field, we feed them directly into root-cause investigations. Direct engagement with customers enables improvements at the source, not just fixes after the fact.

    Supporting Employee and Environmental Safety

    Production of highly halogenated aromatics once carried risks of occupational and environmental exposure—particularly during chlorination or fluorination steps. Our teams have encountered, and resolved, issues around waste stream handling and air emissions. Engineering controls now route halogen offgassing through dedicated scrubbers. Management of reaction residues, mother liquors, and cleaning solvents runs on verified protocols updated after every audit. Operators in full process gear work shifts under constant visual supervision, and company safety statistics have steadily improved.

    As regulatory frameworks around hazardous chemicals grow more rigorous, we recognize that compliance cannot stop with documentation. We build process and training redundancies that are validated annually. We invite audit teams and third-party chemical safety officers into our plants to scrutinize both day-to-day reality and accident contingency preparedness. No amount of final product value justification can overlook worker and environmental health, and our own operational evolution testifies to that priority.

    Market Demand and Future Directions

    Global demand for specialty halogenated aromatics is trending upward, driven by the search for new therapeutics and advanced materials. Venture-backed startups and established pharmaceutical producers alike now seek intermediates with more precise substitution and higher reliability. We note a pattern: once chemists trial our grade of 2-Bromo-4,6-Difluoroiodobenzene, repeat orders follow at steadily growing scale. Some of these clients enter early R&D with grams; within a year they call for drum lots and collaborative support for kilo lab and pilot plant transition.

    Our strategy for the next half-decade follows industry needs: reduce environmental footprint, further drive down impurity levels, and keep turnaround times in tune with customer development cycles. To do that, we are investing in lean manufacturing upgrades, closer analytics partnership with reference labs, and direct customer support for validation studies.

    Building Reliability Into the Product Lifecycle

    Customers entering new chemical space encounter unknowns, whether evaluating the impact of fluorine distribution on metabolic fate or the kinetic profile of bromo–iodo exchanges. By producing 2-Bromo-4,6-Difluoroiodobenzene in an integrated environment—from raw material intake through packing and release—we buffer against avoidable surprises. Projects that call for additional documentation, custom labeling, or modified packaging for regulatory or operational reasons get direct support from our logistics teams, with process traceability extending back to the originating lot.

    Real relationships with process users allow us to push improvements forward. Open feedback cycles have given rise to nuanced adjustments: process cooling rates that trim impurity peaks, holding tank modifications that extend shelf life, and order batching—sometimes at short notice—to match customer plant schedules. We view every customer contact as a chance to learn and iterate, embedding those lessons back into manufacturing, safety, logistics, and documentation.

    Concluding Reflections: Beyond the Catalog Listing

    For us, manufacturing 2-Bromo-4,6-Difluoroiodobenzene is not a matter of catalog numbers, generic purity B, or arbitrary batch stamping. It functions as a benchmark of what direct production oversight, industry knowledge, and feedback-driven improvement can achieve. Technical and commercial partners alike return because they have witnessed, in their own plant data, the gap between directly manufactured and third-party sourced material.

    Looking ahead, we remain focused on the concrete realities of chemical development. Efficiency, reproducibility, safety, and compliance are achieved not through shortcuts or jargon but through rigorous, day-in, day-out application of experience gained on the factory floor and in the formulation lab. As long as our own teams field hard questions, troubleshoot tough projects, and stand beside users when things do not go as planned, we will continue to build the kind of reliability that makes products like 2-Bromo-4,6-Difluoroiodobenzene engines for discovery and innovation.