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3,4-Difluorobenzyl Bromide

    • Product Name 3,4-Difluorobenzyl Bromide
    • Alias Benzyl bromide, 3,4-difluoro-
    • Einecs 852-969-6
    • 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
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    Specifications

    HS Code

    321357

    Productname 3,4-Difluorobenzyl Bromide
    Casnumber 85118-10-7
    Molecularformula C7H5BrF2
    Molecularweight 207.02 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 74-76°C at 0.5 mmHg
    Density 1.613 g/cm³ at 25°C
    Meltingpoint -5°C
    Purity Typically ≥ 97%
    Storagetemperature Store at 2-8°C (Refrigerated)
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms α-Bromo-3,4-difluorotoluene

    As an accredited 3,4-Difluorobenzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3,4-Difluorobenzyl Bromide, tightly sealed with a screw cap and hazard labeling.
    Shipping 3,4-Difluorobenzyl Bromide is shipped in tightly sealed containers, protected from moisture and light. The packaging complies with regulatory standards for hazardous chemicals, typically including secondary containment and appropriate labeling. Transport follows guidelines for flammable, irritant substances, with documentation for safe handling and emergency procedures provided. Suitable for ground and air shipment.
    Storage **3,4-Difluorobenzyl Bromide** should be stored in a cool, dry, well-ventilated area, tightly sealed in its original container to prevent moisture absorption. Keep away from heat, strong acids, bases, oxidizing agents, and direct sunlight. Store in a dedicated poison control cabinet or a secure chemical storage area, and label clearly to prevent accidental misuse. Handle under a fume hood.
    Application of 3,4-Difluorobenzyl Bromide

    Applications of 3,4-Difluorobenzyl Bromide in Industrial Manufacturing

    3,4-Difluorobenzyl Bromide serves as a specialized intermediate for regulated sectors requiring halogenated aromatic building blocks. This section details distinct downstream applications implemented by industrial manufacturers.

    1. Pharmaceutical Active Ingredient Synthesis

    Major pharmaceutical producers incorporate 3,4-Difluorobenzyl Bromide in the synthesis of specialty APIs, notably within antiviral, anticancer, and psychiatric medications. It introduces a difluorinated building block for benzyl functionalization via nucleophilic substitution reactions. Medicinal chemists use it to develop new drug candidates or scale up commercial APIs where the 3,4-difluorobenzyl motif provides target binding specificity or alters metabolism. Strict GMP and ICH Q7 compliance guide its qualification and batch traceability. Production batches use validated protocols, with comprehensive QC for halogen content, residual solvents, and bromide ion monitoring prior to API coupling steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210/211 (US FDA)
    • EU GMP (EudraLex Volume 4)
    • USP, Ph. Eur. reference standards for raw material testing

    Typical usage ratio

    • Typically used at 0.8–1.5 molar equivalents per targeted functional group, adjusted based on substitution efficiency and route selectivity

    Downstream process integration

    • Charged during stepwise nucleophilic substitution or alkylation stage prior to API key intermediate formation
    • Utilized with phase-transfer catalysts or in polar aprotic solvents (DMF, DMSO, acetonitrile) to control reactivity and yield

    Final product types

    • Antiviral agents (e.g., difluorobenzylated heterocycles)
    • Oncology targeted molecules
    • Central nervous system modulators
    • Diagnostic and imaging probes

    2. Agrochemical Intermediate Production

    Large-scale agrochemical manufacturers utilize this material for preparing difluorinated benzyl moieties within advanced herbicide, fungicide, and insecticide formulations. Its performance in ring substitution provides selectivity and persistence critical to modern crop protection actives. Dedicated closed-system synthesis lines support operator exposure limits. Batch records include raw material origins, impurity profiling, and environmental health parameters, tested for conformity with national and international agchem legislations, such as REACH and EPA guidelines.

    Industry compliance standards

    • Directive 91/414/EEC and Regulation (EC) No 1107/2009 for pesticide ingredients
    • REACH (EC 1907/2006) Registration, Evaluation, Authorisation, and Restriction of Chemicals
    • US EPA FIFRA (Federal Insecticide, Fungicide, and Rodenticide Act)
    • ISO 9001:2015 certified quality management practices

    Typical usage ratio

    • Employed at 1.0–1.2 molar equivalents; fine-tuned case-by-case for active loading, impurity profile, and cost efficiency

    Downstream process integration

    • Introduced during synthesis of acylated, etherified, or aminated benzyl intermediates for further chlorination or cyclization
    • Continuous flow or batch-wise alkylation, depending on desired downstream incorporation rate and scale

    Final product types

    • Difluorinated crop protection actives (herbicides and fungicides)
    • Benzyl-derived insecticidal agents
    • Intermediates for seed treatment formulations
    • Growth regulator precursors

    3. Advanced Material Monomer Synthesis for Specialty Polymers

    Chemical manufacturers serving electronics and high-performance coatings sectors use 3,4-Difluorobenzyl Bromide to introduce difluorinated aromatic units in monomer design. These structural motifs substantially enhance chemical resistance, low dielectric properties, and thermal stability for polymers used in electronic substrates, photoresist resins, and membrane fabrication. In-house polymer R&D teams maintain complete source-to-polymer batch traceability, including halogen-containing residues and byproduct control in compliance with electronics sector material restrictions.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive) 2011/65/EU; monitoring trace bromine and fluorine
    • IEC 61249-2-21 (laminate specifications for printed circuit boards)
    • ISO 9001:2015 for documentation and process validation
    • UL 94 flammability testing for downstream polymer products

    Typical usage ratio

    • 0.25–0.75 mole per difluorinated monomer repeat unit; tuned to achieve target copolymer composition, dielectric constant, and crosslink density

    Downstream process integration

    • Used in the initial aromatic substitution or Grignard formation stage for monomer functionalization
    • Integrated before condensation or polymerization step for direct transfer of difluorinated benzyl groups

    Final product types

    • High-durability electronic encapsulants
    • Photoresists and advanced circuit board laminates
    • Polymeric membranes for gas separation
    • Resistant coatings for specialty optical fibers

    4. Fine Chemical Synthesis for Aroma & Flavor Ingredients

    Producers of fine chemical intermediates for fragrance and flavor houses formulate with 3,4-Difluorobenzyl Bromide to introduce fluorine functionalities into aromatic aldehydes, esters, and alcohols. These groups modulate volatility, stability, and perceptual notes, especially in compounds destined for high-end perfumery or heat-stable flavors. Manufacturing occurs under FSSC 22000 and IFRA (International Fragrance Association) protocols, with traceability and allergen screening in the supply chain to meet end-customer requirements. Key analytical methods confirm bromine and fluorine residue removal before final blending for consumer markets.

    Industry compliance standards

    • IFRA Standards for restricted aromatic and halogenated ingredients
    • FSSC 22000 for food and aroma ingredient manufacturing
    • Food Chemical Codex (FCC) for food-grade contributors
    • 21 CFR §172.515 for synthetic flavoring substances (US FDA)

    Typical usage ratio

    • 0.1–0.5 molar equivalents per synthetic batch, dependent on the target aroma/flavor note and downstream reactivity

    Downstream process integration

    • Applied during alkylation, etherification, or Friedel–Crafts steps for aromatic core modification
    • Final product purified to eliminate bromide residues before downstream formulation

    Final product types

    • Fluorinated aroma aldehydes and ketones for perfumery
    • Heat-stable flavor intermediate esters
    • High-purity aroma chemicals for fine fragrances
    • Traceable flavor compounds for food and beverage

    5. Crop Protection Formulation Additives

    Formulation plants for advanced pesticide products employ this raw material as a key modifier in proprietary adjuvant systems. These systems require tightly controlled physical and chemical characteristics, such as volatility, soil adsorption, and metabolic stability. In-house QC confirms absence of trace regulated impurities post-processing. Blending adheres to national standards for agrochemical adjuvants, with environmental monitoring to fulfill residue and groundwater safety requirements. Compliance management documents the raw material chain-of-custody to strengthen registration dossiers.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications
    • US EPA 40 CFR Part 180 (adjuvant residue limits)
    • ISO 17025 accredited testing for composition/impurity tracking
    • OECD Series on Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • Blended at 0.5–2.0% by weight in adjuvant concentrate, determined by efficacy screening, compatibility, and risk assessment

    Downstream process integration

    • Added during final blending of adjuvant packages for tank-mix formulations
    • User-specific customization for anti-drift, adhesion, or stability boosters prior to market release

    Final product types

    • Drift-control agents
    • Penetrant adjuvants for post-emergence sprays
    • Tank-mix compatibility additives
    • Soil binding enhancer blends

    6. Custom Synthesis for Medicinal Chemistry CROs

    Chemical custom synthesis organizations serving pharmaceutical R&D utilize this raw material for targeted small-scale projects. Medicinal chemists integrate the building block into hit-to-lead and lead optimization programs, focusing on SAR (Structure Activity Relationship) expansions involving fluorinated benzyl groups. Stringent cGMP protocols regulate each isolation step, with full documentation for regulatory submissions and patent filings. Material traceability supports process transfer into client pilot labs or clinical supply chains.

    Industry compliance standards

    • US FDA cGMP (21 CFR 210/211)
    • International Council for Harmonisation Q11: Development and Manufacturing of Drug Substances
    • Synthesized to meet customer’s proprietary analytical specifications and patent requirements
    • ISO 13485 where medical device chemical use is involved

    Typical usage ratio

    • Varies from 0.05–1.0 mmol per synthesis batch, based on screening plate sizes and targeted SAR library scale

    Downstream process integration

    • Deployed at intermediate or late-stage functionalization steps for high-value analog libraries
    • Integrated to maximize analog diversity and intellectual property differentiation

    Final product types

    • SAR analog libraries for screening
    • Clinical trial candidate molecules
    • Patent-protected intermediates
    • Reference standards for preclinical and clinical research
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    Certification & Compliance
    More Introduction

    Introducing 3,4-Difluorobenzyl Bromide: Insights from the Manufacturing Floor

    Shaping Performance Through In-House Craftsmanship

    In our production halls, every batch of 3,4-difluorobenzyl bromide begins with a commitment to pure chemistry and transparent results. Over the decades, we've seen how subtle changes in a molecule rewrite the rules of entire syntheses. The industry relies on the straightforward bromide function of this compound—operative, reliable, and unambiguous in its reactions. This material steps into key roles for pharmaceutical intermediates, crop protection chemicals, and advanced materials. Unlike kitchen-sink blends or standardized packages pulled from generic supply networks, each lot we prepare reflects intentional, direct control from raw feedstock to the last sealed container.

    Why Fluorine Makes the Difference—Not All Benzyl Bromides Behave Equally

    3,4-difluorobenzyl bromide brings its own logic to the laboratory bench. We've handled every variant: unsubstituted benzyl bromide, monofluorinated analogues, even the tricky dichloros. Chemists in R&D or on the plant floor look for consistency batch over batch, but subtle differences reveal themselves. Two fluorines at the 3 and 4 positions stiffen the aromatic ring and modulate electron distribution. These fluorines don’t just change the reactivity profile—they rewrite how downstream nucleophilic substitutions proceed. Researchers have come to us after frustrating results with plain benzyl bromide, and they report sharper, more selective alkylation when switching to our product. That’s not only theory; we’ve confirmed reaction kinetics in controlled pilot runs, and the improvement stands out.

    Direct Applications—Why Labs and Plants Select This Version

    3,4-difluorobenzyl bromide finds favor where requirements go beyond textbook transformations. In pharmaceutical synthesis, protecting groups and structural motifs often hinge on precise halogen placement. The 3,4-difluoro pattern brings unique physicochemical properties—lower metabolic vulnerability, altered solubility, and distinctive pharmacophores emerge with this template. Agrochemical innovators value the material for its role in constructing active molecules that withstand environmental breakdown yet remain effective in the field.

    Several large-scale projects used our difluorinated benzyl bromide to reach higher target yields and reduce process steps. One client scaling up a key intermediate for specialty pesticides swapped out their previous reagent, reporting not only a boost in product purity but also a smoother purification process. Our real edge comes from a granular understanding—direct contact and problem-solving with chemists facing bottlenecks in real time. People want more than specification listings or standard purity claims. They ask where the feedstock originated, what potential byproducts could interfere with downstream steps, and how close our process holds to their needed reactivity window.

    The Manufacturing Edge—What We Control, Others Guess

    There’s a comfort in handling your own process from start to finish. The bromination step, especially, determines the fate of the product. We handle reactions in batches designed for traceability, using monitored feeds and in-house purified solvents. Quality shows not just in published numbers, but in the way samples stand up to stress testing. Chemists running scale-ups scan for residual metals, non-volatile impurities, or traces of unreacted starting materials; recent analytical profiles from our batches confirm single-digit ppm levels for residual organics, allowing reactors to run cleaner and limiting the need for repeated washes down the line.

    Customers sometimes bring us “market samples” of the same compound from other channels. Side-by-side, our 3,4-difluorobenzyl bromide typically gives sharper NMR and GC profiles—reduced baseline noise, essentially no extraneous halo-aromatics. These aren’t just claims. Over the past year, two collaborations began with comparative trials; both resulted in adjustments to the competitors’ process based on purity markers spotted initially in our analytical lab. This kind of direct feedback loop—between our production, QC, and the end users’ bench—not only saves time, it shaves whole failure modes from complicated synthetic cycles.

    Balancing Throughput with Customization

    On the factory end, producing 3,4-difluorobenzyl bromide consistently takes more than following a fixed protocol. Market needs shift—sometimes labs require smaller lots for screening, while scale-up pushes demand for multi-kilogram deliveries with matching purity. Our plant runs single-reactor lines for high purity, tapping into deep-well cooling and temperature staging to tame side reactions. Analysts periodically adjust purification routines, especially if a subtle feedstock difference or seasonal impurity finds its way into the process. This flexibility allows for tailored minima of bromine residues and tight limits on water content, crucial for high-sensitivity pharmaceutical routes.

    We also monitor storage arrangements. 3,4-difluorobenzyl bromide prefers cool, sealed conditions, away from excessive light. Shelf life isn’t just marketing—degradation profiles over 12-month intervals can impact downstream product stability, which end users have confirmed in stability trials. Maintaining these standards means more than ticking boxes; it means direct responsibility if a batch falls short once it leaves our gates.

    Sustainability—Moving the Needle Forward

    Chemical production holds a direct line to environmental responsibility. The bromination steps and subsequent washes release byproducts, so we invested in solvent recovery and close-looping. Where traditional production sent spent halides directly to disposal, our setup routes these streams to both in-house neutralization and recycling. Over the past three years, these process changes dropped waste volumes by over 20 percent and improved overall atom economy. The pursuit of cleaner processing routes isn’t an afterthought—we see real reductions in raw material input and burdens on downstream effluent treatment.

    Clients increasingly ask for data on carbon footprint, life cycle analysis, and supply chain transparency. While regulatory demands push everyone toward tighter reporting, we see competitive advantage in demonstrating actual, process-level improvements that customers can reference to satisfy their own compliance teams. We open facility doors to partner site auditors, demonstrating how reclamation and waste minimization bear out in regular production runs.

    Consistency and the Human Element

    A process isn’t only as good as its written protocol; people make every difference along the chain. Our senior chemists have kept logs on every run, tracking process tweaks and batch outcomes, handing down adjustments that step far beyond what a process flow diagram could convey. A lesson learned from a single off-spec batch years back led to a revision in the washing protocol, now standard in every run, reducing the risk of potential bromide carryover. Having operators and analysts with long-term experience cuts both training time and the risk of missed details. This level of hands-on experience minimizes deviations, delivers more reliable products, and encourages open reporting if issues arise.

    Transparency carries through to problem-solving with clients. When a partner reported unanticipated side products in a multi-step synthesis, our technical team retraced steps, reviewed every analytical certificate, then dispatched a fresh lot with full impurity mapping attached. The client’s own in-house work confirmed that a trace contaminant in a generic batch had interfered, something that hadn’t occurred with our material. These little victories—rooting out issues through shared expertise—build trust far more than price or theoretical data sheets ever could.

    Innovation Drives Improvement

    The chemistry behind 3,4-difluorobenzyl bromide hasn’t stood still. Each year brings tighter requirements—higher tolerance to process stress, lower detection limits for impurities, and shifting downstream transformations as new pharmaceuticals and materials are developed. In response, our labs trial new purification media, revisit process parameters, and test product performance under a range of storage and transport scenarios. We’ve worked with clients evaluating solid-state stability to find new packaging options. Feedback cycles between our plant and their R&D fronts accelerate these improvements, cutting months off technology transfer schedules.

    Research teams in both pharma and agro fields use our product to construct fluoroaromatic building blocks with higher reliability each round. Several API candidates in trials owe their success to switchovers from less-pure or less-consistent benzyl bromides. Our internal teams study how these differences impact rate, selectivity, and downstream product polishing—then adapt our process to keep each batch ready for the most sensitive routes.

    Differences—Fluorination Isn’t Just a Label

    It’s tempting to see all benzyl bromides as interchangeable commodities. The two fluorines at the 3 and 4 positions change more than just analytical numbers—they alter the electronic dynamics of reactions, giving different intermediate profiles and offereing chances to discover new reactivity. Comparing our difluorinated bromide to standard or other dihalogenated variants, end users have seen different rates of arylation, lower sidestream formation, and altered chromatographic behavior. These effects manifest in the lab, the pilot plant, and the downstream purification rooms.

    Our experience reinforces that subtle chemical changes call for methodical production. The more crowded the aromatic system, and the more tightly controlled each reaction step, the deeper the implications for route optimization. That exchange with users—talking directly about what works and what doesn’t—crafts each improvement. In the world of specialty chemicals, this iterative process keeps R&D work ahead of market curveballs.

    Beyond the Bench—Delivering Trust Alongside Product

    Working at the source of 3,4-difluorobenzyl bromide production, the most frequent requests from partners sound simple: “Make sure it works every time.” Consistency isn’t just about purity figures on a certificate—it’s about no surprises during late-stage development, pilot scale, or commercial rollout. Every season, feedback returns from around the globe—a new API candidate clearing preclinical hurdles, an agrochemical team scaling up a promising lead, or a polymer lab discovering better functionalization. These aren’t stories of faceless batches on a distributor’s shelf. They reflect a partnership between the hands who make each liter and the minds scaling up innovative products.

    Today’s R&D frontiers demand tighter specifications, honest reporting, and readiness to face the unexpected. Our commitment remains clear: maintain direct control, adapt with purpose, and listen to the needs that arise beyond the process flow charts. 3,4-Difluorobenzyl bromide produced under these principles keeps chemical innovation moving forward, one reliable lot at a time.