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4-Chloro-2-Fluorophenylboronic Acid

    • Product Name 4-Chloro-2-Fluorophenylboronic Acid
    • Alias 4-Chloro-2-fluorophenylboronic acid
    • Einecs 813-899-3
    • 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

    390459

    Productname 4-Chloro-2-Fluorophenylboronic Acid
    Casnumber 511297-32-2
    Molecularformula C6H5BClFO2
    Molecularweight 174.37 g/mol
    Appearance White to off-white solid
    Meltingpoint 125-130°C
    Purity Typically ≥97%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles B(C1=CC(=C(C=C1)Cl)F)(O)O
    Inchi InChI=1S/C6H5BClFO2/c8-4-1-2-5(9)6(3-4)7(10)11/h1-3,10-11H
    Storagetemperature 2-8°C, protected from moisture
    Synonyms 4-Chloro-2-fluorobenzeneboronic acid

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

    Packing & Storage
    Packing White, opaque, screw-cap bottle labeled "4-Chloro-2-Fluorophenylboronic Acid, 5g" with hazard pictograms, lot number, and supplier details.
    Shipping 4-Chloro-2-Fluorophenylboronic Acid is typically shipped in tightly sealed containers, protected from moisture and light. It should be transported following all regulatory guidelines for chemicals, ensuring labels indicate proper handling and hazard information. Temperature control may be recommended to prevent degradation, and packages should be cushioned to avoid physical damage during transit.
    Storage 4-Chloro-2-Fluorophenylboronic Acid should be stored in a cool, dry, well-ventilated area, tightly sealed in its original container, and protected from moisture and direct sunlight. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature and avoid conditions that could generate dust or fumes. Ensure proper labeling and restrict access to trained personnel only.
    Application of 4-Chloro-2-Fluorophenylboronic Acid

    Applications of 4-Chloro-2-Fluorophenylboronic Acid in Industrial Manufacturing

    As a direct manufacturer specialized in high-purity boronic acid derivatives, we deliver 4-Chloro-2-Fluorophenylboronic Acid for critical intermediate roles across advanced fine chemical industries. Below we detail the primary industrial application fields where this compound provides essential value, outlining compliance benchmarks, recommended formulation dosing, precise production integration stages, and the resulting finished products delivered to end markets.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Drug substance production plants utilize this compound as a building block in Suzuki–Miyaura cross-coupling to generate API scaffolds, especially within targeted oncology and anti-infective pipelines. Its stable halogenated structure facilitates controlled introduction of aryl groups during the late-stage assembly of small-molecule APIs, maintaining stringent trace impurity and residual metal limits from the very first kilo lab batch through to GMP scale.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia 11.0, Monographs for synthetic organic APIs
    • US FDA 21 CFR Part 211 – cGMP for Finished Pharmaceuticals
    • ChP (Chinese Pharmacopoeia), API raw material directives

    Typical usage ratio

    • 0.6–1.2 molar equivalents in Suzuki–Miyaura coupling reactions; precise amount set by the downstream substrate ratio and desired conversion efficiency to minimize by-product profile.

    Downstream process integration

    • Introduced during Stage 2–3 of multi-step API synthesis, after initial aromatic ring functionalization; compound is added directly to the palladium-catalyzed coupling vessel under nitrogen with the partner aryl halide.

    Final product types

    • Advanced pharmaceutical intermediates (e.g., fluorinated biphenyls)
    • Small-molecule cytostatics for targeted therapies
    • Antimicrobial active ingredients
    • Agrochemical actives with medicinal chemistry backbones

    2. Custom Fine Chemical Synthesis for Agrochemicals

    Formulators in agrochemical intermediate synthesis rely on 4-Chloro-2-Fluorophenylboronic Acid to build complex crop-protection molecules where halogenated aryl motifs improve bioactivity and photostability. It is particularly valued in the development of novel herbicides and fungicides where precise substitution patterns are required by regulatory and performance-driven design.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006 for chemical registration
    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 Quality Management System (for consistent batch supply)
    • China ICAMA pesticide intermediate production permits

    Typical usage ratio

    • 0.8–1.1 equivalents per coupling unit operation; modified based on structure–activity relationship optimization and avoidance of excess boron content in waste streams.

    Downstream process integration

    • Reagent addition at the key aryl–aryl bond formation step within multi-step pesticide intermediate synthesis by Suzuki coupling, introduced post-halogenation but prior to protection group removal.

    Final product types

    • Complex herbicide actives and intermediates
    • Fluorinated systemic fungicides
    • Insecticide molecular scaffolds
    • Seed-coating agent intermediates

    3. Specialty Material Monomer Preparation for Electronic Chemicals

    Producers of high-performance polymers and advanced electronic materials employ this compound to introduce halogen- and fluorine-functionalized aromatic rings essential for targeted dielectric and UV-resistance properties. The material supports synthesis of monomers for specialty polymers used in flexible printed circuit boards, photoresists, and organic semiconductors.

    Industry compliance standards

    • IEC 61249-2-7: Materials for PCBs, Quality Specifications
    • RoHS Directive (2011/65/EU) for hazardous substances in electronics
    • ISO 14001:2015 Environmental Management
    • Japan Industrial Standards (JIS) for electronic chemicals

    Typical usage ratio

    • 1.0 equivalent in targeted monomer synthesis; adjusted to molecular design and to avoid excess unreacted species that could influence polymer chain uniformity.

    Downstream process integration

    • Charged during monomer assembly as the arylboronic acid for Suzuki polymerization or arylation coupling steps; introduced before the final condensation or polymerization.

    Final product types

    • Aromatic monomers for specialty polymerization
    • Photoresist resin intermediates
    • Polymeric coatings for microelectronics
    • Flexible PCB substrate materials

    4. Advanced Dye and Pigment Intermediate Manufacturing

    Dye and pigment producers utilize this raw material to synthesize halogenated biphenyl and fluorinated aromatic intermediates that serve as chromophore regulators and lightfastness boosters in specialty pigments and high-stability dyes. Its role is critical in obtaining consistent color shade, resistance to photodegradation, and fine-tuned solubility.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006 REACH for dye registration
    • Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers (ETAD) Guidance
    • China National Standards GB/T 21866 for colorants
    • ISO 1248:2016 for pigment quality grading

    Typical usage ratio

    • 0.7–1.3 equivalents depending on target chromophore structure, balance between cost and hue depth, and impact on final dye purity level.

    Downstream process integration

    • Introduced prior to azo coupling or condensation reactions within aromatic ring functionalization sequence; precise dosing ensures color matching and batch-to-batch reproducibility.

    Final product types

    • High-stability textile and plastic dyes
    • Specialty pigments for coatings, inks, and plastics
    • Lightfast varnishes
    • Electronic display colorants
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    Certification & Compliance
    More Introduction

    4-Chloro-2-Fluorophenylboronic Acid: Practical Experience Behind a Key Building Block

    Chemists know that every detail matters when working with intermediates, especially when planning routes for complex synthesis. Having spent years running large-scale production and handling quality control from our own reactors, we’ve formed a grounded perspective on what 4-Chloro-2-Fluorophenylboronic Acid offers. Unlike traders or resellers, we approach each compound as a producer who sees strengths, variations, and real-world differences in every batch. We watch the process from raw material selection, through every cleaning and filtration step, to the final packaging. This means our understanding of this boronic acid isn’t just theoretical. It’s shaped by real production runs, conversations across R&D, and feedback from colleagues in industries as diverse as pharmaceuticals, agrochemicals, and materials science. Every batch reflects this experience.

    The Pattern in Production: Consistency and Genuine Differences

    4-Chloro-2-Fluorophenylboronic Acid stands apart from simpler boronic acids. The installation of chlorine and fluorine on the aromatic ring brings both benefits and challenges. We make this compound with a focus on the little choices that change the end result: temperature control during lithiation, the slow addition of boronic acid ester, careful workup to avoid decomposition. Anybody in the lab can run a theoretical synthesis with lab-grade glassware and small flasks. What’s harder — and where the manufacturer’s perspective matters — is keeping each large batch inside the same tight quality range, especially as trace impurities can disrupt downstream applications.

    We have seen firsthand that moisture and trace metal contaminants will ruin a whole lot, even at low detection levels. It’s taken years to fine-tune our drying steps, to catch every insoluble particle as we scale. Many end users don’t want extraneous chlorinated byproducts that sneak past standard purification. That’s why our control steps for residual solvents and chlorides go beyond the usual spot checks. To those in R&D, a “clean” batch may mean faster reaction kinetics, fewer filter complications, and cleaner spectra the moment the first NMR scan runs. Customers involved in Suzuki-Miyaura cross-couplings remark that reproducibility, from the first gram to the hundredth kilo, saves them costly delays. They sometimes bring reaction complaints when competitors supply an off-white, sluggish material; in our own supervision, we’ve learned the coloring often signals over-oxidation or breakdown from prolonged exposure to air or old packaging.

    About the Model and the Role of Specification Choices

    Some users prefer to handle high-purity crystalline forms; others are fine with a slightly impure powder if it means a cost reduction for early stage research. In our facility, 4-Chloro-2-Fluorophenylboronic Acid comes with a purity specification above 98 percent by HPLC; we often discuss with procurement teams whether to provide more detailed analyses like GC-MS, ICP, or elemental microanalysis. The model we ship can vary if you need larger crystalline batches for automated dosing or a finer powder for hand-scooping in gloveboxes. We hear stories from pilot plant engineers who want particle size distributions to match their dosing units, while synthetic chemists focus on purity and batch-to-batch NMR compatibility.

    This isn’t just about ticking boxes on a spec sheet. Small differences in how a compound behaves during storage or blending make a real-world difference. Some boronic acids clump or absorb moisture after repeated handling in open air. To address this, we’ve learned how to optimize the drying and packing process. Sometimes we recommend using nitrogen-purged containers or suggest shipment schedules customized for the user’s work rhythm. That kind of thinking comes straight from hands-on production — not from reselling a product you’ve never carried through a shift.

    Where It Fits: Applications in Industry and Academia

    The true utility of 4-Chloro-2-Fluorophenylboronic Acid emerges in applied chemistry, both in patent-protected pharmaceutical syntheses and in the development of novel agrochemicals. The electron-withdrawing character of the fluorine and the chlorine makes this boronic acid valuable for building aryl fluorides, which are increasingly common in new generation drugs to enhance metabolic stability. Our partners in medicinal chemistry departments trust this intermediate as a linchpin for quickly assembling more complex molecules. They use it to reliably create biaryl linkages that resist metabolic breakdown, often reporting higher yields due to its fine particle consistency and batch purity.

    We receive feedback from material science teams tackling new polymers. The chlorinated and fluorinated phenyl units transmit desirable electronic properties into the final products. In these settings, the difference between our compound and a generic offering comes down to both quality metrics and communication. Our technical staff have explained details like how trace water content can cause unexpected polymerization problems; we try to troubleshoot before any issue derails a run. For academic researchers, the combination of aromatic substitution patterns enables new ligand systems for catalysis and fine-tuning electronic effects in more complex molecular systems.

    What Sets 4-Chloro-2-Fluorophenylboronic Acid Apart from Other Boronic Acids

    We handle many types of boronic acids in-house, from simple phenylboronic acid to more elaborate functionalized derivatives. In our experience, 4-Chloro-2-Fluorophenylboronic Acid often requires more careful attention during both synthesis and storage than non-halogenated analogues. Some users underestimate just how different the purification process can become when dealing with multiple halogen substituents. Unlike simple phenylboronic acid, which may be tolerant of a wider pH range in subsequent reactions, the dual halide version often prefers tighter control on aqueous workups and may show different solubility in organic solvents.

    We’ve watched how even the orientation of chlorine and fluorine on the aromatic ring will tweak the reactivity in cross-coupling. It’s the difference between a smooth high-yielding assembly and an unexpected byproduct. Our staff have compared NMR and HRMS readings from various sources and identified impurity patterns unique to this boronic acid, mainly stemming from over-chlorination or poor quenching. For customers looking at pricing, there’s also a real-world factor — creating these dual-functionalized molecules usually results in lower yields and higher raw material costs compared to simpler boronic acids. Our own learning curve has led us to optimize reaction pathways and invest in automated filtration, since manual separations waste both product and time with these more nuanced intermediates.

    Daily Production Realities: Practical Insights from the Manufacturing Floor

    Inside the plant, each lot’s journey starts long before the barrel leaves our warehouse. For 4-Chloro-2-Fluorophenylboronic Acid, the story often revolves around risk management and safety, due to the toxicity of some chlorinated and fluorinated starting materials. Crews wear more protective gear. Supervisors sign off fresh safety reviews as procedures evolve. Gas handling systems are routinely checked to avoid leaks of volatile intermediates. As a producer, we see not just a chemical identifier or a CAS number — we see the need for reliable logistics, safe storage, and packaging that controls light and moisture ingress.

    After production, warehousing teams keep close track of shelf life, using sealed containers and light-blocking packaging to extend stability. Minor lapses, such as storing the acid at room temperature for too long, could seed degradation and contaminate future batches. Our ongoing quality audits flag any off-standard color, particle clumping, or odor, prompting immediate investigation. We operate this way not because a regulation demands it — but from hard experience with compound loss and reprocessing.

    Whenever users encounter reaction stalls, filter problems, or analytical surprises, our technical specialists step in. Many times, it isn’t a major impurity but small handling details that trigger issues: static buildup during container transfer, improper desiccant use, or underestimated impacts from storage humidity. As manufacturers, our troubleshooting checklists reflect hundreds of internal observations. Over time, these patterns teach us to anticipate both the new and the unexpected, to fix root causes and build real practical knowledge about our product’s behavior under different work conditions.

    Our Learnings Shape Real-World Performance

    Continuous improvement isn’t just a corporate slogan for us; it’s a necessity. Each round of production offers the opportunity to spot errors and drive innovation. We frequently swap insights between synthesis and analytical departments. Chemists, operators, and packaging staff all help spot trends, from how a cooling rate affects crystallization to how a subtle tweak in solvent wash changes drying requirements. Open communication across teams leads to gradual, substantial quality improvements over time.

    Customers often approach us with process feedback and quality complaints from other suppliers. They’ve witnessed sluggish reactions, unexpected TLC smears, or excess solids in solution, sometimes traced back to overlooked handling steps. We recognize that even rigorously defined specifications won’t eliminate all surprises. That’s why we equip our teams to share observations and document problems as they arise. Our process chemists directly compare analytical spectra, particle images, and solubility data, searching for variation sources and striving for consistency in future batches. For us, rigorous attention to these production subtleties is the biggest factor keeping our boronic acid a preferred choice for research, development, and scale-up applications.

    Typical Usage Patterns: Where and How End Users Rely on Us

    Pharmaceutical chemists use 4-Chloro-2-Fluorophenylboronic Acid to make active pharmaceutical ingredients with special metabolic profiles. This involves reliance on predictable Suzuki coupling, where trace impurities could lead to downstream isolation headaches or regulatory hold-ups. Agrochemical researchers value the molecule for its dual halogen pattern, allowing access to advanced herbicide and fungicide candidates with improved environmental persistence. Material scientists describe how the acid’s distinctive substitution pattern enables custom architectures in electronic polymers, often pushing for tighter controls on bulk impurities and residual metals due to the sensitivity of their final products.

    We listen to stories from small university labs where budgets are tight and every gram counts. Here, reproducibility takes the spotlight — researchers can’t afford ruined reactions. They often contact us to discuss batch reservation or supply timing, wanting certainty before starting a long, multi-step synthesis. Industrial scale clients have their own priorities: bulk cost, consistency, and support for rapid troubleshooting if anything goes astray. We run extra retention samples for these partners, allowing retroactive investigation should any discrepancy surface over months of storage. Real experience in the production seat means we can quickly review batch records, check analytical data, and advise partners with confidence.

    At higher production volumes, the logistics of handling chlorinated and fluorinated intermediates adds an extra layer of planning. Our warehouse teams stay aware of chemical compatibility, storage temperature, and packaging configuration, flagging any deviation before it can snowball into user problems. We ship under inert atmosphere where needed and pre-schedule deliveries to match site storage cycles, often collaborating with procurement teams on-site to adapt as project timelines shift.

    Constantly Evolving: Meeting New Challenges with Every Batch

    Over the past decade, demands have intensified. Customers need faster delivery, tighter quality targets, and more granular understanding of their purchased intermediates. Research partners want not only purity certificates, but detailed impurity profiles, trace metal data, and physical form specifications. Our investment in analytical technology reflects this shift. By keeping mass spectrometry, elemental analysis, and automated moisture analysis running on every lot, we can bring more detail to every delivery.

    The challenges aren’t only technical. Environmental, health, and safety regulations govern every aspect of our operation. We have lived through shifting waste management policies, periodic audits, and the need to justify every chemical waste stream with supporting data. For a halogenated compound such as 4-Chloro-2-Fluorophenylboronic Acid, the bar for transparency sits higher. We run staff training on spills, personal exposure, and emergency scenarios. Our continuous dialogue with regulatory authorities keeps us up to date, ensuring that our product can be shipped wherever end users need it, with supporting paperwork and certifications already prepared.

    No two runs look exactly alike. Weather affects yields, starting materials can shift in purity, and supply chain hiccups force quick adaptation. Whether we’re revalidating a reactor batch after a supply change or troubleshooting a slight off-odor in a recent lot, the learnings feed straight back into revised procedures. Each of these steps helps us to adjust our SOPs, invest in better equipment, and most of all, maintain honest communication with our partners who depend on 4-Chloro-2-Fluorophenylboronic Acid for their projects’ success.

    A Relentless Focus on Quality, Safety, and Practical Use — Every Step of the Way

    Taking 4-Chloro-2-Fluorophenylboronic Acid from concept to kilo-scale batch means living with every triumph and mishap along the way. Unlike product brokers or middlemen, our teams carry responsibility from early-morning shift handoffs to late-night inventory checks. That perspective changes how we collaborate, how we troubleshoot, and how we pass information to our end users. For us, product quality isn’t only represented by spec sheets or purity percentages. It’s the culmination of careful process choices, continuous observation, technical expertise, and honest feedback loops running between plant, lab, and customer. The goal is predictable, reliable material that adds value from pilot scale to full production — with every batch representing a sum of lessons learned, ongoing collaboration, and manufacturing experience that only a true producer can provide.