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3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol

    • Product Name 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol
    • Alias 4-Hydroxyphenylboronic acid pinacol ester
    • Einecs 701-509-7
    • 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
    VTB
    Specifications

    HS Code

    170902

    Iupac Name 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
    Cas Number 105847-10-7
    Molecular Formula C12H17BO3
    Molecular Weight 220.08
    Appearance White to off-white solid
    Melting Point 110-114°C
    Solubility Soluble in organic solvents (e.g., DMSO, dichloromethane)
    Smiles CC1(C)OB(B2=CC=CC(=C2)O)OC1(C)C
    Inchi InChI=1S/C12H17BO3/c1-11(2)15-13(10-7-5-6-9(14)8-10)16-12(3)4/h5-8,11-12,14H,1-4H3
    Density 1.12 g/cm³
    Synonyms 3-Hydroxyphenylboronic acid pinacol ester

    As an accredited 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 1-gram amber glass bottle labeled "3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-yl)phenol," with chemical structure, hazard and safety information.
    Shipping The chemical **3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol** is shipped in tightly sealed containers to prevent moisture ingress and degradation. It is packed according to standard chemical shipping regulations, ensuring protection from light and temperature extremes. Proper labeling and documentation accompany the shipment for safe and compliant handling during transit.
    Storage Store **3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol** in a tightly sealed container, protected from air and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Store at room temperature and keep out of direct sunlight. Use only in a chemical fume hood and avoid prolonged exposure to light and air.
    Application of 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol

    Applications of 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol in Industrial Manufacturing

    3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol plays a key role as a boronic acid derivative in specialty organic synthesis, particularly within pharmaceutical, agrochemical, and advanced material sectors. As a direct manufacturer, we provide material tailored for integration into diverse process streams where regulatory compliance and consistent quality metrics are critical for downstream efficiency and certification.

    1. Pharmaceutical API Intermediate Synthesis

    In pharmaceutical manufacturing, this boron compound enables Suzuki-Miyaura cross-coupling to construct biaryl structures that form core scaffolds in selective kinase inhibitors and non-steroidal anti-inflammatory drugs. Process engineers use it as an electrophilic partner, focusing on reaction purity to reduce side-product formation, which aligns with cGMP process controls and stringent residual boron specs required for advanced pharmaceutical intermediates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210 & 211 (GMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) synthesis quality rules
    • Chinese Pharmacopoeia (ChP) for raw material controls in APIs

    Typical usage ratio

    • 0.8-1.2 equivalents relative to aryl halide, adjusted based on reaction scale and stoichiometry for the targeted intermediate.

    Downstream process integration

    • Introduced after batch verification of aryl halide; coupling carried out in palladium-catalyzed, base-mediated systems under inert conditions; followed by in-process QC on boron residue and isolated yields.

    Final product types

    • Non-steroidal anti-inflammatory drug intermediates
    • Kinase inhibitor building blocks
    • Small molecule oncology API precursors
    • CNS active pharmaceutical ingredient fragments

    2. Agrochemical Synthesis for Herbicide and Fungicide Development

    Formulation chemists rely on this material during process development for modern agrochemical actives that contain biaryl, diaryl ether, or aryl-heteroaryl motifs. It participates in catalytic coupling to introduce precise phenol-boron fragments, which support consistent biological performance standards and compliance with agrochemical registration frameworks.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for pesticide synthesis
    • ISO 9001:2015 for quality management in agrochemical manufacture
    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC) No 1907/2006 requirements for chemical safety reporting

    Typical usage ratio

    • 1.0-1.3 equivalents relative to halogenated partner; adjusted for reactivity of substrate and palladium loading for scale-up runs.

    Downstream process integration

    • Added to agitated reaction vessel post-activation of base; undergoes Suzuki coupling under controlled temperature; byproduct removal and post-reaction purification via crystallization or liquid extraction.

    Final product types

    • Selective pre-emergence herbicide precursors
    • Triazole fungicide intermediates
    • Pyrazole-based insecticide building blocks
    • Active ingredient conjugates for integrated crop protection

    3. OLED and Advanced Material Monomer Production

    Manufacturers of organic light-emitting diode (OLED) emitters and functional polymer monomers integrate this phenol-boronate ester for the formation of electron transporting units and high-stability aromatic frameworks. Process development chemists target precise monomeric purity to support reproducibility in thin-film deposition and end-use device lifespan.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substance limits in electronics
    • ISO 9001 certified quality system for functional material synthesis
    • UL 94 (flammability for polymeric materials) for end-use certification
    • IEC 62321 (Screening for hazardous substances in manufactured products)

    Typical usage ratio

    • 1.0 equivalent relative to dibromo or diiodo monomeric partner; batch adjusted for process throughput and degree of polymerization control.

    Downstream process integration

    • Enter polymerization or oligomer synthesis step following prior monomer activation; coupling performed in dry organic solvent, typically under argon, to ensure high molecular weight and functional group integrity.

    Final product types

    • OLED emitter monomers
    • Conjugated polymer precursors for display applications
    • Organic semiconductor building blocks
    • Functional coating additives for optoelectronics

    4. Specialty Fine Chemical Synthesis for Research Reagents

    Chemical suppliers serving research institutions utilize this boronate ester in the scalable production of specialty biaryl reagents, fluorescent tags, and analytical standards. Its high chemical selectivity allows for modification of sensitive substrates and tailored ligand construction for advanced screening applications.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • ISO/IEC 17025 laboratory accreditation for QC testing
    • GHS (Globally Harmonized System) chemical labeling protocols
    • Sigma-Aldrich/Acros Organics purity specification benchmarks

    Typical usage ratio

    • Variable, commonly 0.9-1.1 equivalents in reagent synthesis; stoichiometry refined by research chemist according to desired functional group density and downstream labeling efficiency.

    Downstream process integration

    • Integrated following initial aromatic activation; used in batch or flow chemistry coupling modules to tune yield and minimize cross-contamination in sequential labeling or probe assembly steps.

    Final product types

    • Biaryl research reagents
    • Fluorescent labeling compounds
    • High-purity analytical standards
    • Diagnostic assay probe intermediates
    Free Quote

    Competitive 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol: Consistency and Reliability from a Dedicated Manufacturing Perspective

    Inside the Factory: Our Journey with 3-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol

    For those of us in chemical manufacturing, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol represents more than just another specialty reagent. We have put in years fine-tuning its synthesis, improving purity by careful process monitoring, and troubleshooting every batch anomaly ourselves. The personal stories coming out of our plant floor usually revolve around ensuring this product delivers clean, reproducible results every time. Our chemists know, from repeated hands-on experience, what it means to chase down a stray impurity, monitor water content, and work the reactors so that this important phenol boronate meets the rigid standards demanded by process chemists downstream.

    Everyday Production Brings Real-World Insight

    In theory, making a boron-containing intermediate looks straightforward: react phenol derivatives with the dioxaborolane, keep everything dry and oxygen-free, then purify. Only when you're scaling up the process does reality set in. Phenol’s sensitivity to oxidation often challenges us, so we monitor reaction temperatures closely and keep an eye on air ingress. Each run gives us fresh data on color and melting point, subtle shifts that mean something in the long run. Scaling from lab glassware to kilo-lot production forced us to reinforce our equipment against trace water and choose glass-lined reactors over less expensive steel. We’ve learned solvents matter, not just for yield, but for the ease of downstream isolation. Problems solved at odd hours—like a sudden haze in the filtrate—turn into notes for every batch record.

    Why This Boronate Stands Out in Synthesis

    Other phenol boronic acid derivatives don't match the reactivity profile or reliability we’ve coaxed from the dioxaborolan-2-yl pairing. Direct partners for Suzuki-Miyaura cross-coupling, this compound’s cyclic dioxaborolane ester protects the boron center, giving stability that simple boronic acids don’t offer. It doesn’t decompose as easily during storage, and we’ve noticed users appreciate not having to redry or reprocess material that’s been sitting on the shelf. That stability traces back to the compact, shielded cage created by the tetramethyl dioxaborolane; we've measured fewer hydrolysis byproducts compared with standard open-chain organoborones. Years of feedback from our synthetic partners tell the story of time saved and higher reaction throughput.

    Real Chemistry Needs Consistent Materials

    We hear from research labs and production teams who use this intermediate at all scales. Chemists rely on our ability to deliver a uniform product, batch after batch—and we don’t take that lightly. Every order begins with selecting fresh raw materials, monitoring moisture, and controlling reaction time. Purity targets come from real-world demands: reactions that hinge on the absence of residual solvents or trace boric acid. Our internal GC and HPLC teams run every sample we release, checking for more than just assay; they flag any deviations and feed those learnings back to the plant floor. By working directly with the material, we see how consistency means more reliable coupling outcomes for our customers and fewer reworks in the lab.

    A Closer Look at Specifications and What They Mean for You

    With every batch of 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, specification means more than a printed data sheet. Inside our plant, each white crystalline material gets checked for melting range, visual purity, and hygroscopic behavior. We recognize that even a few tenths of a percent in residual water changes how well the product dissolves and reacts. Every shipment heads out packed against moisture, never just bagged and labeled. Controlled storage and monitored production history matter to us because they matter to you. The differences can appear subtle—texture, color, time to dissolve in THF or dioxane—but experienced hands quickly spot the real-world impact on downstream chemistry.

    Handling, Storage, and Logistics: Lessons Learned on the Plant Floor

    We have seen what happens when specialty boronates travel rough: containers exposed to humidity, seals that leak, and material compacted by vibration. Our approach comes from the school of hard knocks. Practical steps like double-bagging, nitrogen flushing, and minimizing warehouse exposure protect material integrity. We load outbound deliveries with the same attention given to in-plant transfers. Over time, we’ve found even dedicated cold storage pays off, especially during humid stretches. All these measures feed back into product quality, not from a checklist, but from real, tested outcomes witnessed in our operation.

    How Our Boronate Supports Your Synthesis Goals

    People come to us with a range of applications. In pharmaceutical R&D, the boronate group unlocks new scaffold synthesis, creating routes to active molecules that used to be off-limits. Materials chemists reach for this compound as a bridge to complex polymers, taking advantage of the ready compatibility with organometallic systems. Each time someone succeeds with a cleaner transformation or a new route because of reliable boron chemistry, we hear about it. It’s never just about a single reaction. It builds confidence project after project—less downtime in the glove box, fewer reruns due to starting material variability, and less guessing whether new batches will match old ones.

    Comparison to Other Boronic Esters and Acids: Direct, Not Generic, Differences

    We see requests for a variety of boronic esters and acids. But each has a unique profile of reactivity and stability. The tetramethyl dioxaborolane cage in our product imparts a moisture resistance that traditional phenylboronic acids can't offer, even under conditions that push the limits of bench chemistry. Years ago, side-by-side coupling trials in our pilot lab showed cleaner conversions and less byproduct formation with the ester form. Unprotected boronic acids can sometimes win on price, but they lag behind when process reproducibility matters. In practical terms, this means less time spent troubleshooting failed couplings, less product waste, and—most importantly—more predictable outcomes when moving from milligram to kilogram scale.

    The Value of Feedback Loops: Chemists and Plant Operators Working Together

    From the first days of launching this product, we’ve gone beyond just manufacturing and shipping. Plant operators shadowed scale-up runs in partner research groups, taking firsthand notes on dissolution times, color changes, and even odors. Chemists brought us rejected batches and stuck filters, and our team worked alongside them to fix the origin, not just the symptom. This ongoing feedback loop teaches us which raw material lots perform best, which purification steps pull out hidden contaminants, and how seemingly minor tweaks in drying cycle make a major difference in purity. We adapt processes not because a committee decrees it, but because real data points convince us it needs to be done.

    Production Scalability: Lessons from the Trenches

    Scaling up specialty organoboron chemistry takes more than lab notebooks and theory. As plant engineers, we’ve invested in controlled feeding pumps for steady reagent addition, leading to smoother reaction curves and lower risk of hot spots. Juggling the timing of quenching phases, controlling pressure drops, and fine-tuning the drying steps make for efficient turnarounds between campaigns. We track every variable on the shop floor: line pressures, tank cleaning frequencies, and finished product handling time. This hard-won knowledge reduces unexpected downtime and keeps batch yield targets within reach. The stories we trade in the break room all circle back to how well each run matched its lab-scale promise.

    Trust Built on Reliable Supply

    We know that reliability counts every time someone orders material for a critical synthesis. That’s why we devote shop floor resources to order tracking and batch documentation, not just for regulatory compliance, but so buyers and users can see the chain of care and custody. Any issue—query on a label, an unfamiliar smell, or clumping in the last shipment—gets escalated straight to the production manager, reviewed before the next lot releases. Trust builds over hundreds of shipments, and we consider every client’s process success as part of our own record.

    Learning from Unexpected Challenges

    No process runs perfectly every time. Over the past few years, we’ve run into surprises—precipitation that didn’t match spec, temperature sensors drifting off, or batches that took longer than usual to dry. Each hiccup became a lesson. We set up internal root cause meetings, brought in the raw materials team, and issued plant memos based on what we learned. Not every fix costs a fortune—tightening seals, switching vendors for glassware, or adding a sample port to a reactor. Larger adjustments, like investing in closed-hood packaging, paid off over time. Building a culture that spots, discusses, and solves problems in real-time moves quality forward far beyond minimum requirements.

    Safety Is Built-In, not Just Filed in Binders

    Personally handling this compound for years, we know the best precautions for safe storage and use. Dioxaborolane esters carry low volatility but still need ventilation—so our loading dock and blending rooms run special exhaust fans. Direct training with PPE sets the standard; every operator understands the risks and the right approach, and more than one new hire learned from a seasoned crew member about spill response and cleanup routines. Safety protocols don’t sit on a shelf. Audits come frequently, and any incident review turns into a refresher for everyone. Our team’s well-being comes before speed, and we accept slower batch release instead of cutting corners.

    One Product, Many Applications: Meeting the Needs of Today's Synthetic Chemistry

    Over time, demand for 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol spread from classic organic synthesis into new fields. In medicinal chemistry, it finds use in constructing biaryl frameworks, opening new space for scaffold hopping. For electronics and polymer applications, we learned first-hand how this boronate builds blocks for conductive and specialty materials. Bioconjugation chemists seek it out for linking aromatic units to biologically relevant substrates, valuing its selective reactivity under mild conditions. Direct feedback on reaction clean-up and post-coupling workup lets us optimize for new uses. The decades of collaboration with users tells us that listening to emerging application needs keeps this product relevant far beyond its origins.

    Technical Support from the Source

    Supplying specialty reagents today means more than shipping material. We share practical tips, like which solvent systems dissolve it fastest, and which conditions give the sharpest product spots in TLC. Our technical team fields calls about unexpected color or crystal form, offers advice based on thousands of in-house pilot reactions, and often suggests tweaks that save hours in troubleshooting. Customers tell us those hands-on fixes, straight from the manufacturing floor, make a difference. Knowledge isn’t abstract for us; it comes from working with real material, not just reading protocols.

    Why Small Variations Matter in Specialist Chemistry

    People sometimes ask why a product like 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol shouldn’t just be swapped for any boronic ester on the shelf. In our experience, small changes in protecting group bulk, phenolic substituents, or water content have outsize impact on coupling efficiency, shelf life, and byproduct formation. Long conversations with medicinal chemistry groups told us low-level impurities—sometimes below what standard specs catch—show up later as ghost peaks in screening steps or downstream in analytical results. We use what we learn from these reports to tighten our specs, run extra purity screens, and share best practices for storage and handling. In critical projects, that last trace of confidence can mean the difference between progress and delay.

    Continuous Improvement: How Plant Learnings Turn into Product Evolution

    Manufacturing isn’t static. New requests push us to improve: higher purity, finer particle size for slurry handling, or custom packaging for high-throughput screening. Operators flag minor issues, like caking or dusting, that standard specs miss but customers quickly notice. Additions to our process lab—better drying ovens, inline sensors, new analytical standards—arose because users shared what they saw downstream. Every plant-wide change, from minor tweaks in solvent ratios to major equipment upgrades, reflects the steady flow of hands-on feedback we gather. Adaptability comes from being deeply involved at every stage, seeing firsthand what real users encounter in the field.

    Outlook: Real-World Confidence Built from Experience

    The story of 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol in our facility is grounded in practical daily work—checking purity, solving storage puzzles, and learning directly from users. Our role as manufacturer puts us shoulder to shoulder with the chemists and engineers pushing the boundaries of synthesis. We know a lot rests on the dependability of every lot we produce. Delivering this compound with confidence comes from decades invested in tight controls, direct technical support, and a willingness to respond rapidly to evolving application needs. Real strength in chemistry comes from that combination of knowledge, care, and daily dedication.