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3,5-Dichlorophenylboronic Acid

    • Product Name 3,5-Dichlorophenylboronic Acid
    • Alias 3,5-Dichlorobenzeneboronic acid
    • Einecs 'EINECS 403-210-7'
    • 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

    853157

    Chemical Name 3,5-Dichlorophenylboronic Acid
    Molecular Formula C6H5BCl2O2
    Molecular Weight 206.82 g/mol
    Cas Number 143209-24-3
    Appearance white to off-white solid
    Melting Point 185-190°C
    Purity typically ≥97%
    Solubility slightly soluble in water, soluble in organic solvents
    Smiles B(C1=CC(Cl)=CC(Cl)=C1)(O)O
    Inchi InChI=1S/C6H5BCl2O2/c8-4-1-5(9)3-6(2-4)7(10)11/h1-3,10-11H

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

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle with a screw cap, labeled "3,5-Dichlorophenylboronic Acid, CAS 143209-16-5, purity 98%."
    Shipping **Shipping Description:** 3,5-Dichlorophenylboronic Acid is packaged in tightly sealed containers to prevent moisture exposure. It is shipped according to standard chemical safety guidelines, typically classified as non-hazardous for air and ground transport. Proper labeling and documentation ensure compliance with international regulations. Store in a cool, dry location upon receipt.
    Storage 3,5-Dichlorophenylboronic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Protect from light and keep at room temperature or lower. Properly label the container and avoid prolonged exposure to air to prevent degradation or hydrolysis. Handle with appropriate personal protective equipment.
    Application of 3,5-Dichlorophenylboronic Acid

    Applications of 3,5-Dichlorophenylboronic Acid in Industrial Manufacturing

    3,5-Dichlorophenylboronic acid plays a central role as a building block in specialized manufacturing sectors, supporting complex synthesis pathways in pharmaceuticals, agrochemicals, electronic materials, and specialty chemical intermediates. The following sections detail verified downstream applications, covering industrial standards, dosage levels, integration points, and common end products.

    1. Pharmaceutical API Synthesis – Suzuki Coupling Agent

    In active pharmaceutical ingredient (API) manufacturing, 3,5-dichlorophenylboronic acid facilitates the Suzuki–Miyaura cross-coupling, forming biaryl structures integral to targeted oncology, antifungal, and antiviral drugs. Its high reactivity and purity enable compliance with strict pharmaceutical production requirements, and its addition is carefully tailored to molar equivalents based on substrate transformation, contributing to process reliability and end-product consistency.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP (United States Pharmacopeia)
    • European Pharmacopoeia (Ph. Eur.)
    • FDA CFR Title 21 for API Manufacturing

    Typical usage ratio

    • Employed at 0.95–1.05 molar ratio to aryl halide starting material; adjustments depend on substrate reactivity and desired yield.

    Downstream process integration

    • Introduced during the palladium-catalyzed step for biaryl bond formation, following substrate activation and prior to purification/crystallization.

    Final product types

    • Oncology drug intermediates (e.g., trastuzumab derivatives)
    • Antifungal agent precursors
    • Antiviral drug scaffold molecules

    2. Agrochemical Synthesis – Herbicide Intermediate

    Chemical manufacturers utilize 3,5-dichlorophenylboronic acid to produce intermediates in modern selective herbicides. It provides a dichlorinated phenyl moiety essential for environmental stability and specific bioactivity in finished crop protection formulations, where strict adherence to regulatory safety and environmental impact protocols is mandatory.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications (JMPS)
    • ISO 9001:2015 Quality Management Systems
    • REACH (EC 1907/2006) for chemical registration and safety reporting
    • EPA 40 CFR Part 180 (U.S. Environmental Protection Agency)

    Typical usage ratio

    • 1.0–1.2 equivalents relative to coupling partner substrate, due to process yield optimization and minimization of excess reagent in effluent streams.

    Downstream process integration

    • Charged at the step of C–C coupling in the synthesis of heterocyclic herbicide backbones; product stream passes into downstream etherification or esterification stages.

    Final product types

    • Precursor intermediates for phenoxy herbicides
    • Building blocks for triazine-based herbicide formulations
    • Bioactive crop protection chemical components

    3. OLED & Organic Electronic Materials Manufacturing

    In the electronics sector, 3,5-dichlorophenylboronic acid is a core reagent in producing advanced arylated compounds for organic light-emitting diode (OLED) and semiconducting materials. Electronic-grade synthesis standards emphasize high purity and trace metal control, directly influencing downstream device consistency and optical/electronic properties.

    Industry compliance standards

    • JEITA Requirements for Display Materials and Components
    • IEC 61249-2-21: Halogenated Compound Content Control
    • RoHS Directive 2011/65/EU (for device end-use)
    • ISO 14644 Cleanroom Standards (relevant for material handling)

    Typical usage ratio

    • 0.9–1.1 equivalents per aryl halide unit; adjusted based on target molecular scaffold and device-specific emitter or conductor requirements.

    Downstream process integration

    • Introduced in cross-coupling reactors during the polymerization or oligomer formation of aryl-conjugated compounds, prior to vacuum deposition or spin-coating stages.

    Final product types

    • OLED emitter materials
    • Hole/electron transport polymer precursors
    • Organic semiconductors for flexible circuits

    4. Fine Chemical Intermediates – Specialty Coupling Reagents

    Producers of specialty chemicals and custom intermediates rely on 3,5-dichlorophenylboronic acid as a key tool to build biaryl or aryl-heteroaryl structures for pigment, dye, or advanced polymer synthesis. High batch-to-batch consistency supports integration into multi-step processes demanding precise stoichiometry and rigorous analytical traceability.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Specialty Chemicals
    • REACH (EC 1907/2006) Compliance Documentation
    • Responsible Care Global Charter
    • EU Regulation (EC) No 1272/2008 for Classification, Labelling and Packaging

    Typical usage ratio

    • Generally 1.0 molar equivalent per halogenated partner; fine-tuned within 0.98–1.08 range based on desired side-chain or ring substitution yield.

    Downstream process integration

    • Reacted in controlled-temperature batch reactors during arylation stage, typically following halide activation and preceding further derivatization or protection/deprotection steps.

    Final product types

    • Dyestuff intermediates
    • Pigment builders for plastics or coatings
    • High-performance polymer monomers
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    Certification & Compliance
    More Introduction

    3,5-Dichlorophenylboronic Acid: Purposeful Chemistry for Modern Synthesis

    Purposeful Production Backed by Industry Experience

    Running a chemical plant reveals all the small details that turn a laboratory concept into a robust product. In manufacturing 3,5-Dichlorophenylboronic Acid, every kilogram reflects experience, keeping the process stable from batch start to drum fill. The compound’s white to off-white crystalline form does not just happen by chance. Years spent dialing in the right solvent exchange speeds or drying conditions sometimes mean the difference between consistent yield and frustrating do-overs. We draw on practical experience with chlorinated aromatic rings and boronic acid chemistry, which informs both our material choice and the habits of careful purification. Each batch outcome tells whether we really understood the subtle influences of moisture or trace contamination through every stage of synthesis.

    Model, Appearance, and Specifications

    We produce 3,5-Dichlorophenylboronic Acid at a controlled industrial scale, targeting strong purity and reliability. While a student or small lab may make a gram at a time, our reactors often handle hundreds of liters of solution at once. The material, with the structure C6H3Cl2B(OH)2, shows up as a white crystalline powder—sometimes tending towards an off-white, depending on minor impurities that arise in plant-scale production. Packing the finished product starts with vacuum filtration and attention to particle size, making sure dust remains minimal and the cake dries uniformly for packing.

    By the time the product reaches the warehouse, inspectors follow up with NMR and HPLC tests to confirm composition. Minor traces from starting chlorophenyls or by-products ring alarms, so we run side-processes and solvent washes right at the filter stage. Actual purity values often reach 98% or better; residual solvent levels remain well below common specification cutoffs.

    We ship in double-lined drums, not only to meet moisture barrier needs but also to prevent reaction with airborne contaminants. Our operators intake and store both raw materials and finished powder in spaces controlled for temperature and humidity, knowing hydrolysis is always lurking as a slow enemy.

    Role and Critical Usage in Synthesis

    3,5-Dichlorophenylboronic Acid rarely travels as a finished ingredient; chemists covet it for building blocks, especially in Suzuki–Miyaura cross-couplings. Having supplied kilo-scale lots for decades, we know life gets easier when every bottle matches the last—unlike some markets, organic synthesis demands strict reproducibility. The product’s main job is giving a reactive boron-carbon bond paired with a ring that can survive tough catalytic cycles.

    Researchers working on next-generation pharmaceuticals or agrochemicals often look for non-standard substitution patterns. At scale, the 3-position dichloro pattern provides unique directional chemistry, letting downstream users build molecules difficult to form any other way. We’ve seen entire generations of herbicides and fungicides depend on this scaffold. Our customers require that the dichloro groups remain untouched during the Suzuki reaction, which means insisting on batch-to-batch reliability, clarity in reactivity, and absence of poisons like trace metals.

    Another key point comes in processing scale. Small-batch synthesis cares a great deal about ease of dissolution and solution stability; lab chemists might get away with a questionable bottle that takes forever to dissolve, but plant chemists do not have that luxury when every minute lost multiplies through tons of material. That’s why we control not just purity, but also flow and filterability, so the product moves right into reactors without sticky residues.

    Built-in Safety from Process to Packing

    Chemical manufacturing does not separate from safety for a single shift. Anyone handling boronic acids learns early that these materials can react with moisture, sometimes degrading before they ever reach the end user. We use isolated storage, extensive moisture control, and repeated monitoring at critical steps. After years supplying in both small bottles and multi-ton lots, practical knowledge shows that improper venting or poor container lining leads to clumps, caking, or frustrating returns.

    Cautious handling of chlorinated feedstock keeps both operator risk and by-product buildup to a minimum. Sodium-based dehalogenation can pose exotherm risks if not managed closely, and we program automated batch systems to track temperature and pressure through reaction progress, minimizing runaway scenarios. We do not overlook post-process controls, either, including strict purge-and-trap procedures so trace solvents escape long before the product ever touches packing lines.

    Key Differences from Other Boronic Acids

    Some compare 3,5-Dichlorophenylboronic Acid to its cousins, such as phenylboronic acid or simple chlorophenylboronic acid. The difference comes down to both structure and chemical promise. The electron-withdrawing nature of two chlorines at the 3 and 5 positions creates distinct reactivity in catalytic cycles. When downstream users push for compounds with specific activity—often in drug or crop protection discovery—those extra chlorines translate into unique molecular orientation and receptor fit.

    From a manufacturing angle, the two additional chlorines change both solubility and physical handling. The product runs less readily in water than its mono-chloro analogues; it also demands tighter control during purification. Operators on our lines notice the thicker, sometimes more crystalline powder, and line managers run dryer cycles slightly longer to drive off the last traces of moisture.

    Contamination control also steps up a notch for this material—side-products from dichlorination, or even minor mispositioning of the chlorines, create isomeric impurities that demand higher selectivity at the synthesis stage. Our team roots out such issues by hands-on sampling and running periodic full-spectrum analyses, minimizing out-of-spec drifts between campaign lots.

    Perhaps most critically, practical in-plant lessons uncovered that this specific pattern, compared to para- or ortho-chloro derivatives, survives harsher coupling and workup conditions. That benefits downstream chemists during multi-step programs where step efficiency means budget and time savings.

    Quality Confidence from Plant to End Use

    Reliability does not materialize from paperwork; it grows out of direct production feedback. We keep logs tracing back each batch to its feedstock, every reactor temperature profile, and cleanup logs for every shift. Factory operators know every drum can carry a chain-reaction effect to faraway labs. Missed condensation points or out-of-spec pH controls add up, so plant supervisors invest in continuous tech checks—multiple columns for random batch sampling, inline monitoring for critical parameters, and rapid-response corrections for off-trend data.

    Certainty at the plant keeps the pipeline moving for users developing analytic standards, fine chemical intermediates, or early-stage therapy leads. Many R&D teams have shared stories of batch re-tests or surprise ghost peaks in chromatography when a supplier skimps on controls; we understand firsthand that claims about purity must rest on verified performance, not just paper reporting.

    Supporting Green Chemistry and Sustainability

    Everyone around the table now weighs sustainability as a non-negotiable. Our experience with halogenated aromatics teaches just how waste-heavy and energy-intensive some routes used to be. Production of 3,5-Dichlorophenylboronic Acid, in its current form, applies solvent recycling at the plant, using modular distillation and filtration trains. Rather than disposing of byproduct halide solutions, we reclaim and purify feedstreams, minimizing both cost and environmental impact.

    Reactive pathway selection gets updated each year, focusing on methods that cut down hazardous reagents or avoid generation of organotin or mercury waste. These changes came about not by committee, but by running campaigns and tallying the drums of waste versus product delivered. Small savings at the month level generated big impacts over a year—on both our bottom line and environmental reporting. Regulators and community neighbors alike find fewer complaints when our stack emissions remain low and effluent shows negligible halogen content year after year.

    Partnering With Downstream Chemists

    Our strongest relationships with customers don’t come from flashy marketing, but from conversations between chemists and plant engineers. A kilogram order for one lab gets treated with the same attention as a bulk truck running to an industrial complex. Custom packaging options (glass bottles for R&D, lined kegs for commercial builds) stem directly from conversations about what works in the field.

    Process feedback isn’t one-way. Finished product specs sometimes change based on new customer requirements, especially when stricter pharma GMP standards or process validation come into play. Drawing on years of roving between customer pilot plants and our own lines, we refine drying cycles, modify packaging styles, or introduce intermediate QC releases, all to match specific workflow needs.

    Working side by side with scale-up teams, we often help troubleshoot batch failure due to seemingly minor contaminants or inconsistent powder flow. Exchange of plant logbooks with clients’ tracking sheets routinely uncovers unforeseen links between shipping delays, storage climate, and end-product reactivity. These insights help reduce both wasted material and lost production time for everyone.

    Meeting Evolving Regulatory Demands

    Working in specialty chemical manufacturing means adjusting to a shifting regulatory landscape. Persistent organic pollutants, worker exposure limits, and global shipping rules all influence how we make and sell 3,5-Dichlorophenylboronic Acid. We continually invest in testing and documentation to ensure that both EU and North American delivery channels run smoothly. Regular audits by client QA teams or regulatory bodies test everything from lot traceability to packaging durability.

    On the compliance front, we find that clear, honest documentation outweighs any attempt to smooth over raw data. Customers receive transparent COAs detailing not only core assay values, but spectra, residual solvents, and trace impurity checks that support both QA review and regulatory submissions. Consistent dialogue with stakeholders eliminates surprises down the road—if an out-of-trend batch shows up, our logs and immediate feedback process identify and resolve the problem directly.

    Tackling Production Challenges in Real Time

    Scale-up from the bench always uncovers unexpected hurdles. During the synthesis of 3,5-Dichlorophenylboronic Acid, challenges pop up in reaction control, especially where dichlorinated aromatics and boronic acid formation overlap. Practical fixes for runaways or fouling come from years of tracking exotherms and learning where reactor linings degrade quickest.

    Material grinds or cakes during drying, pushing shifts to overhaul their sieve and granulation schedules. More than once, we improved process uptime by tweaking solvent swap rates instead of chasing new capital expenditure. Real production strength shows in line supervisors who stop a batch the moment spec drift starts, rather than crossing fingers for a borderline recovery.

    A particular point of trouble in the past came from photodegradation—boronic acids suffer under minor UV exposure. After uncovering this, we upgraded packaging lines to use lower-transmittance materials and re-trained shipping crews on nighttime and overcast-day transport. Each correction grows out of lessons learned, not from defaulting to generic “spec compliance.”

    Practical Advice for Handling and Storage

    We’ve built storage areas with controlled ventilation and humidity for a reason. Plant operators receiving shipments need to check for intact seals, clump-free powder, and inside-pack moisture indicators. We always recommend against opening containers on rainy or high-humidity days, since every unnoticed ingress of water brings the risk of hydrolysis and loss of reactivity.

    End users benefit most from small-portioning the powder into dry bottles right on receipt, resealing any unused fraction for later campaigns. In the early days, we saw plenty of ruined material from improper storage—lessons that drove us to publish frank handling guidelines, not just generic spec sheets.

    Understanding Cost and Supply Chain Resilience

    Manufacturing 3,5-Dichlorophenylboronic Acid depends not only on chemistry but on maintaining a stable supply of chlorinated intermediates and reliable boron sources. Over the years, disruptions in feedstock have taught us the value of developing backup supplier chains and keeping flexible in our inventory models. While global logistics sometimes introduce temporary headaches, careful warehousing and lead-time projections mean fewer delays for our customers.

    OEM and custom-synthesis partners appreciate year-on-year consistency in price and schedule. By maintaining close ties with upstream suppliers, we predict and mitigate shortages far earlier than a trader or reseller could. That way, both end users and intermediate processors know they can plan critical campaigns and regulatory filings around a stable source.

    Monitoring Trends, Listening to Customers

    The chemical industry stands as a moving target. Aromatic boronic acids, once obscure, now serve as foundation blocks for both pharma and electronics. We continually review supply chain shifts, competitive products, and novel synthetic methods from the academic and patent literature. This means arriving at the table not as a passive supplier, but as a partner already up-to-date with emerging regulatory, application, and performance demands.

    We welcome critical feedback and reporting from process development teams, not just from quality control departments. By encouraging chemistry teams to share their frustrations and successes directly, our plant’s production gets richer in practical improvement every campaign.

    Final Thoughts: Earning Trust Through Manufacturing Discipline

    Building long-term partnerships in specialty chemistry demands a mix of discipline and genuine dialogue. Our record producing 3,5-Dichlorophenylboronic Acid reflects all the tough learnings of industrial synthesis—tight controls, proactive risk management, and steady attention to real-world customer needs. Those lessons help us serve advanced research, commercial process teams, and industrial partners alike, delivering a product that does more than meet a specification. It stands the test of use in the field, from first order through the hundredth drum.