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4-Tert-Butylphenylboronic Acid

    • Product Name 4-Tert-Butylphenylboronic Acid
    • Alias 4-(tert-Butyl)phenylboronic acid
    • Einecs 632-747-0
    • 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

    843283

    Chemicalname 4-Tert-Butylphenylboronic Acid
    Casnumber 2609-39-6
    Molecularformula C10H15BO2
    Molecularweight 178.04 g/mol
    Appearance White to off-white powder
    Meltingpoint 168-172°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents like ethanol and methanol, slightly soluble in water
    Boilingpoint Decomposes before boiling
    Density 1.10 g/cm³ (approximate)
    Synonyms 4-(tert-Butyl)phenylboronic acid; p-Tert-butylphenylboronic acid
    Storagetemperature Store at 2-8°C
    Smiles CC(C)(C)C1=CC=C(C=C1)B(O)O
    Inchikey QWGRIXPOJBIPKK-UHFFFAOYSA-N

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

    Packing & Storage
    Packing 4-Tert-Butylphenylboronic Acid is packaged in a 25g amber glass bottle, sealed with a screw cap, and labeled with safety information.
    Shipping 4-Tert-Butylphenylboronic acid is shipped in tightly sealed containers to prevent moisture ingress and contamination. It is typically transported under ambient conditions unless specified otherwise. Proper labeling ensures compliance with regulatory guidelines, and packaging is designed to prevent breakage and leakage during transit. Safety data sheets accompany each shipment.
    Storage 4-Tert-Butylphenylboronic Acid should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from direct sunlight. Store at room temperature, and avoid exposure to high heat or open flames. Use appropriate containers to avoid contamination and ensure safe handling and storage.
    Application of 4-Tert-Butylphenylboronic Acid

    Applications of 4-Tert-Butylphenylboronic Acid in Industrial Manufacturing

    4-Tert-Butylphenylboronic Acid serves as a specialized organoboron reagent across advanced manufacturing sectors. With well-established reactivity in Suzuki-Miyaura cross-coupling and related transformations, it plays an integral role in the synthesis of sophisticated intermediates for specialty chemicals, agrochemicals, and pharmaceutical preparations. Downstream applications require strict adherence to process specifications, regulatory frameworks, and batch consistency.

    1. Pharmaceutical Intermediate Synthesis

    Leading pharmaceutical manufacturers use this material for constructing advanced biphenyl frameworks and other substituted aromatic motifs within active pharmaceutical ingredient (API) backbones. It participates in Suzuki coupling reactions with a variety of aryl halides, supporting the manufacture of kinase inhibitors, antivirals, and third-generation antihypertensive APIs. Integration into API workflow follows rigorous validation to maintain identity, purity, and low residual boron content in final products.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • European Pharmacopoeia monographs Annex 3 (for residual solvents and elements)
    • Japanese PMDA GQP/GMP Inspection Standards

    Typical usage ratio

    • Ranges from 1.05 to 1.3 equivalents relative to the halide substrate
    • Adjust ratio based on reaction scale, conversion yield, and downstream purification needs

    Downstream process integration

    • Enters as the boronic acid component in Suzuki-Miyaura cross-coupling step
    • Reacts in presence of palladium(0/II) catalyst and a base under controlled temperature
    • Followed by sequential workup, chromatographic purification, and analytical QC integration

    Final product types

    • Aromatic biphenyl intermediates for oral anti-diabetic APIs
    • Precursors to selective kinase inhibitors
    • Building blocks for anti-HIV and anti-HCV actives
    • Sidechain fragments for central nervous system drugs

    2. Agrochemical Synthesis and Crop Protection Formulations

    Chemical synthesis groups in crop protection leverage this compound during late-stage synthesis of fungicide and herbicide actives containing complex biphenyl or alkylated phenyl rings. Sophisticated coupling mechanisms enable tight control over regiochemistry and minimize side products, which is necessary for regulatory compliance in downstream commercial registrations of agrochemical actives. Environmental and technical standards govern raw material traceability throughout the synthesis.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (JMPS)
    • ISO 9001:2015 Quality Management Systems for agrochemical production
    • REACH Regulation (EC) No 1907/2006
    • US EPA 40 CFR Part 158 (data requirements for pesticides)

    Typical usage ratio

    • 1.0 to 1.5 equivalents versus halogenated coupling partner
    • Variations based on molecular complexity of downstream actives and minimization of post-reaction waste

    Downstream process integration

    • Introduced at late-stage Suzuki-coupling for biaryl herbicide/fungicide core structure formation
    • Parameters: anhydrous conditions, controlled and monitored pH, and chromatographic purity tracking
    • Follow-up: full work-up, crystallization, and solid-state stability verification

    Final product types

    • Biphenyl fungicides (e.g., strobilurins series)
    • Selective herbicides with tert-butylphenyl substituents
    • Intermediates for post-emergence crop protection agents
    • Aromatic additives for seed coating formulations

    3. Specialty Polymer and Functional Resin Modification

    Polymerization specialists incorporate this raw material for the targeted synthesis of advanced resin modifiers and specialty phenolic additives. Boronic acid groups can be converted or coupled to introduce alkyl-aryl functionalities, which provide improved heat stability, chemical resistance, or hydrophobicity in final resin systems. Stringent process controls guarantee batch reproducibility and trace-level boron detection in end-product analytics for industrial and electronics-grade resins.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (environmental management) for industrial resin production
    • RoHS Directive 2011/65/EU for electronic component applications
    • ASTM D5319 (Standard Specification for Phenolic Resins Used for Laminates)
    • REACH SVHC monitoring for restricted organoboron content

    Typical usage ratio

    • 0.3–2.0% by weight as functional modifier, with optimization per target property and cross-link density
    • Ratio selection depends on compatibility with base polymer (epoxy, phenol-formaldehyde, or acrylic systems)

    Downstream process integration

    • Added at the oligomer stage or during endcapping/cross-linking steps
    • Maintains stability up to 160°C in batch and continuous polymerizations
    • Subsequent finishing includes devolatilization and quality screening for spec compliance

    Final product types

    • Modified phenolic resins for electrical insulation
    • Heat-resistant coatings and adhesives in automotive segments
    • Acrylic composite resins enhancing weatherability and UV performance
    • Specialty molding plastics for high-performance applications

    4. Electronic Chemicals and Advanced Material Synthesis

    Integrated circuit and flat-panel manufacturers deploy this boronic acid in organic synthesis routes to fine-tune aromatic structures for semiconducting and optoelectronic polymers. Its high reactivity and steric effects enable selective aryl-aryl linkages that influence charge transport characteristics and electrical performance in OLED and OFET fabrication. Precision in input quality and batch serialization supports the demanding reliability standards of electronic component supply chains.

    Industry compliance standards

    • IPC/JEDEC J-STD-033B for handling sensitive chemical materials
    • ISO 9001:2015 for microelectronic precursor manufacture
    • TSCA (US Toxic Substances Control Act) for chemical suppliers to electronics fabricators
    • IEC 62474 compliance for hazardous substance restrictions in electronics

    Typical usage ratio

    • 0.5 to 1.2 equivalents in organic synthesis for aryl-containing semiconductor precursors
    • Adjustment based on target molar mass and minimization of electronic impurities

    Downstream process integration

    • Introduced at key monomer-coupling steps under inert atmosphere
    • Palladium-catalyzed coupling forms the base for subsequent polymerization or device layering
    • Final purification involves extensive recrystallization, sublimation, or zone refining

    Final product types

    • Organic light-emitting diode (OLED) blue/green emitters
    • OFET (organic field effect transistor) base polymers
    • Specialized hole-transport materials for display and photovoltaic modules
    • Sensing layers for wearable and flexible electronics

    5. Fine Chemical Intermediates and Advanced Synthesis Projects

    Contract synthesis operations and fine chemical manufacturers use this compound for the creation of high-value intermediates with defined steric or electronic properties. This includes production of customized ligands, polymer initiators, and specialty aryl derivatives for research and pilot-scale production. Each batch processed ties closely to project-specific documentation, customer-end validation protocols, and targeted impurity profiles to match research-to-pilot scale-up requirements.

    Industry compliance standards

    • ISO 9001:2015 for fine and specialty chemical synthesis
    • cGMP (current Good Manufacturing Practices) for pilot and small-volume production
    • REACH registration for intermediate supply, per Article 18/19 (if applicable)
    • Customer-specific COA/QC parameter alignment

    Typical usage ratio

    • Custom ranges: usually 1.0–1.2 equivalents for targeted transformations
    • Ratio is project-specific, determined based on substrate reactivity and product purification yield

    Downstream process integration

    • Enters at the designated cross-coupling step for aryl unit construction
    • Used with in-house or customer-specified catalytic systems
    • Downstream includes preparative separation, solvent exchange, and full-spectrum characterization (NMR, HPLC)

    Final product types

    • Custom ligands for homogeneous catalysis
    • Initiators for living polymerization techniques
    • Substituted aromatic compounds for pigment, dye, and specialty monomer research
    • Advanced intermediates for pilot drug or material synthesis
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    Certification & Compliance
    More Introduction

    Understanding 4-Tert-Butylphenylboronic Acid from the Manufacturer’s Bench

    4-Tert-Butylphenylboronic Acid has shown itself to be an indispensable tool across different chemistry benches, from academic research to industrial process development. As a chemical manufacturer with years of experience in aromatic boronic acid production, watching how the needs of chemists and engineers shift shapes the way we approach quality, consistency, and scale in making this compound. Let’s walk through what we’ve seen with this product, why it matters in real-world applications, and how it compares to its relatives in the same family.

    The Chemistry of 4-Tert-Butylphenylboronic Acid

    The molecular structure of 4-tert-butylphenylboronic acid, C10H15BO2, features a boronic acid group attached to a phenyl ring, with a bulky tert-butyl group at the para position. That tert-butyl group doesn’t just sit there for show—it offers real chemical advantages. It influences reactivity, solubility, and selectivity. Anyone who’s handled arylboronic acids knows that small tweaks in substitution patterns change a lot about a reaction’s fate. In this case, the tert-butyl group can help control side reactions that plague similar compounds.

    Across our manufacturing line, we maintain tight thresholds for moisture, residual metals, and purity—factors that make or break performance in things like Suzuki-Miyaura cross-coupling reactions. We keep boronic acid monomer content high and look out for unwanted boroxine formation, especially in longer storage. Researchers frustrated with batch variance or erratic yields often share their positive experience with our material, which helps reinforce why investing effort in fine-tuning each production parameter isn’t wasted labor.

    Why Synthetic Chemists Reach for this Compound

    Reaction reliability matters most in the lab and plant. With 4-tert-butylphenylboronic acid, chemists get a reagent that tends to deliver consistent coupling even over a wide temperature or solvent range. Our teams have taken notes directly from customers—pharmaceutical chemists, agrochemical process experts, and new material developers—to understand what causes hiccups in their runs. One chemist pointed out that getting a complete conversion on an electron-deficient aryl bromide became easier when switching from basic phenylboronic acid to the tert-butyl variant. That direct user feedback pushed us to invest in stricter process controls and additional re-purification steps, even at the expense of throughput. No product spec sheet alone tells the story of why actual practice sometimes outpaces theory.

    Scale-up capability is another common concern. Some research-grade reagents behave perfectly well at milligram scale, but inconsistency shows up quickly when batches grow to kilograms or more. Our approach often means running side-by-side reactions using lots from different months and analyzing yields and product purities through headspace GC, LC-MS, and HPLC. These studies highlight why a manufacturer’s consistency matters. A key learning: multi-ton production campaigns for OLED intermediates or pharmaceutical building blocks demand a product free of boroxine and heavy metal residues. That led us to invest in upgraded boronic acid purification lines and keep a “gold standard” retained sample from each batch.

    How it Stands Apart from Other Boronic Acids

    Early in my career, I worked mostly with plain phenylboronic acid—abundant, cheap, quite reactive but prone to hydrolysis and sometimes tricky to handle after long storage. Substituted versions, including 4-tert-butylphenyboronic acid, solve more than a few practical issues. The bulky tert-butyl group blocks oxidative dimerization, which in plain phenylboronic acid sometimes leads to variable purity batches and unpredictable behavior in scale-up. There’s also reduced tendency for protodeboronation, a persistent problem when scaling reactions for pharmaceutical intermediates.

    Other arylboronic acids, even with alkyl or alkoxy groups, may not provide the same steric shielding. From synthetic experience, tert-butyl substitution makes the reagent more robust under Suzuki-Miyaura cross-coupling conditions. The difference shows up in yield, isolation, and overall throughput. The question of “which arylboronic acid to use” rests on more than just molecular weight and melting point. Reaction workups often go easier with tert-butylpnenylboronic acid. It sometimes prevents troublesome side products that complicate post-reaction purification. We’ve seen process teams save hours on scale-ups by switching to this compound from less hindered analogs.

    Delivering Consistency at Scale

    The “small differences” in chemical quality that look trivial on a certificate of analysis can shift entire process economics. Countless projects end up delayed or over budget because a kilogram lot of boronic acid came off spec by just a fraction of a percent. In our factory, every kilogram run for large pharmaceutical companies or OEM electronics suppliers gets its own record—from raw material lots, to reactor log sheets, to isolated fractions. Our staff know just how much headaches grow when a process shows drift from batch to batch, so our process control follows what happens across every vessel and dryer. Our in-process QC lab doesn’t just check purity—it checks the trace water and boroxine contents before final drier steps.

    Getting to that level takes hard lessons. In the early days, we’d get emails from academic groups puzzled why their Suzuki or Chan-Lam couplings performed beautifully one month, then dropped off the next. We learned to correlate these stories with subtle drifts in water content, storage environment, tiny lots of catalyst poisons, or mechanical breakdowns in filtration. Each time, process redesign and staff training closed the gap, but no one reaches that state without taking a few tough phone calls. Over time, we built extended stability protocols and developed custom packaging: glass-lined steel or high-barrier bottles for higher volume shipments, clear desiccant choices, and tight labeling on “opened shelf life”. No trader or distributor can vouch for every detail—only hands-on manufacturers track each step, from boronate ester synthesis to the final powder on the shelf.

    Meeting Standards for Regulatory and R&D Applications

    Pharmaceutical and advanced material companies require traceability and quality above all else. For API precursor manufacturing, the specifications for boronic acids go beyond just appearance and GC purity—our end users require elemental analysis, heavy metal screening, and tight batch traceability. We developed PCR and NMR documentation packages both for the internal team and for submission to regulatory bodies. Yearly, we review our manufacturing protocols, update hazardous raw material registers, and validate cleaning steps to avoid cross-contamination.

    Once, a pharmaceutical customer flagged a single lot for mild pink coloration after opening—QC flagged no impurities by standard GC, but post-mortem tracked it to minimal iron carryover, invisible on routine scans. The fix wasn’t in marketing, or on a website, but on our production floor: new filter media, adjusted reactor surfaces, and post-drying nitrogen purges. We see every mistake as a push to improve, since end users depend on chemical consistency in drug substance or electronics assembly. By remaining transparent and direct with customers, we maintain trust and keep the quality bar high.

    Purity, Storage, and Shelf Life: Learned from Actual Use

    Customers frequently ask about optimum storage for boronic acids. In our experience, the tert-butyl variant holds up better than simpler analogs. Its solid-state and low tendency for self-condensation makes it less prone to forming crystals of boroxine, which can reduce reactivity or complicate handling. We recommend that customers use airtight vials or drums, away from heat, and humidity—same advice we follow before shipping.

    There’s no substitute for hands-on stability trials. Before ever launching commercial production, we test our own output under temperature cycling and forced humidity conditions. Only when the material’s integrity matches expectations does it leave the plant. If a customer flags changes after storage, we break out retention samples and run additional purity and NMR checks. Decisions on shelf life, packaging specs, and recommended handling only come after this kind of real-world, multi-month observation. As manufacturer, every data point ties back to manufacturing practice.

    Environmental and Occupational Health Considerations

    Environmental safety remains top of mind in chemical manufacturing. The shift in regulations, especially for boron-containing wastes, prompts regular review of our emissions, water treatment, and solid waste streams. We invested in solvent recovery and in-plant scrubbing, and have adjusted purification steps to reduce mother liquor and excess boronic acid in filtrates. Waste minimization isn’t only cost control—it means building a practice that stands up to changing waste codes and audits. Worker health is central, too: we transitioned to better ventilation, closed system transfers, and real-time air monitoring, not only to comply but to avoid surprises that can sideline a competent team.

    Years of process knowledge let us anticipate where dust or off-gassing can pose a risk, especially as batch sizes grow. The best standard operating procedures are built not just for auditors—but for the line chemists, mechanics, and warehouse teams who interact with the product each day. We’ve learned from every safety incident to update our training and leave room for team feedback when issues show up. Product stewardship doesn’t stop at getting the chemistry right.

    Improvements Through Partnerships with Industry and Academia

    The chemical world doesn’t stand still, and neither do our development plans for 4-tert-butylphenylboronic acid. Academic partners share their experience with catalyst systems or newly developed ligands, and we replicate their results in our pilot labs to check how our product behaves in these new settings. Collaborative R&D with electronics, coatings, or agrochemical firms highlights requirements for tailored particle size, dustiness, or packaging. The dialogue isn’t one way—the best improvements come when end users flag a need, and we trial changes, share batch samples, and gather direct feedback.

    We support both large-scale process plants and smaller innovation teams with custom documentation, specialized analysis, and confidential batch history review. Our long-term partnerships push each lot of boronic acid closer to the needs of the end chemistry—there’s no bureaucratic gap or loss of context compared to what a trader or external distributor knows. For new or tricky projects, we’re often called on to adjust process solvent systems or change reactor parameters to supply new boronic acid derivatives, and our experience with the tert-butylphenyl compound serves as a starting template.

    Challenges and Continual Improvement in Manufacturing

    Consistent high quality doesn't arise from automation alone—it comes from lived experience. Every batch that leaves the plant carries the fingerprints of process development work: reactor optimization, purification tweaks, packaging redesigns. We run each synthesis as a tightly controlled sequence, tracking temperatures, agitation speeds, and downstream handling. Our batch records and in-line sampling help us spot issues before they reach the final customer.

    Challenges do crop up: cross-contamination, scale-up inconsistencies, trace impurity drift, changes to reagent suppliers, and weather-driven swings in ambient humidity. Having a responsive, tightly knit production and QA team means we adapt fast. I remember a time when an unexpected impurity spiked just as we expanded production for a new electronics client. We stopped the line, traced the problem back to a new grade of sodium carbonate, reviewed supplier certifications, and swapped it out. The fix cost a day of output, but saved months of troubleshooting and customer headaches.

    Continual improvement means more than “good enough.” In boronic acid manufacture, even small process gains—a more efficient condenser, a custom-built filter, a tweak in crystallization temperature—cut both waste and user issues. We maintain close ties with suppliers, emphasizing that small changes on their end ripple through to our customers. It’s the detail work that distinguishes a manufacturer’s product from generic versions.

    Sustainability, Supply Security, and Future Directions

    Supply chain security ranks high among user concerns—the COVID pandemic taught the industry not to rely on single-point overseas sources. We qualified multiple upstream suppliers, maintain buffer raw materials, and support local (sometimes domestic) raw material integration for key intermediates. Our routine disaster recovery drills and parallel warehousing mean ongoing customer projects avoid disruption, even as logistics take unexpected turns.

    We continue to explore greener synthetic routes, aiming to cut solvent and energy consumption, move to catalysts with lower toxicity and recycle waste wherever possible. These steps often fly under the radar for the market but matter for real-world implementation. For example, a recent change to a new catalytic system not only improved selectivity in the coupling step, it also reduced byproduct formation and decreased cycle time in the dryer. These process gains, passed on to end users, mean higher throughput and less environmental load per kilogram of product.

    Real Users, Real Results

    The best case for choosing 4-tert-butylphenylboronic acid comes from those who’ve put it to work. Users report high yields and clean conversions in Suzuki coupling reactions, especially with sterically hindered or deactivated aryl halides. Others highlight smoother workup and fewer residual byproducts, speeding downstream processing in both pharma and advanced material synthesis. Reproducibility, one of the most valued qualities for process chemists, depends not only on chemical structure but on every detail of manufacturing protocol and QA oversight.

    Looking through years of feedback, improvements, and side-by-side trials, our takeaway is simple: sourcing directly from a chemical manufacturer with hands-on process control and a track record in aromatic boronic acids changed the reliability of end uses for many partners. It’s less about glitzy marketing and more about the quiet, persistent refinement that comes from direct feedback and long-term partnership. For anyone considering which arylboronic acid to use or which supplier to trust, the difference grows clearer over time: careful process practice turns a reliable molecule into a reliable solution on every scale.