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(4-Tert-Butoxycarboxyphenyl)Boronic Acid

    • Product Name (4-Tert-Butoxycarboxyphenyl)Boronic Acid
    • Alias (4-(tert-Butoxycarbonyl)phenyl)boronic acid
    • Einecs 629-708-7
    • 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

    770431

    Productname (4-Tert-Butoxycarboxyphenyl)Boronic Acid
    Casnumber 1025506-71-7
    Molecularformula C11H15BO4
    Molecularweight 222.05 g/mol
    Appearance White to off-white solid
    Meltingpoint Approx. 200-205°C
    Purity Typically ≥97%
    Solubility Soluble in DMSO, slightly soluble in water
    Storagetemperature 2-8°C (Refrigerated)

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

    Packing & Storage
    Packing White, labeled screw-cap vial containing 5 grams of (4-Tert-Butoxycarboxyphenyl)boronic acid; features hazard symbols and product information.
    Shipping (4-Tert-Butoxycarboxyphenyl)boronic acid is shipped in tightly sealed containers, protected from light and moisture, and typically packed with inert cushioning materials. It is transported at ambient temperature unless specified otherwise, following all relevant regulations for handling chemicals. Appropriate hazard labeling and documentation are included to ensure safe and compliant delivery.
    Storage (4-Tert-Butoxycarboxyphenyl)boronic acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from moisture, as boronic acids can be sensitive to hydrolysis. Store at room temperature and avoid exposure to air to maintain product stability.
    Application of (4-Tert-Butoxycarboxyphenyl)Boronic Acid

    Applications of (4-Tert-Butoxycarboxyphenyl)Boronic Acid in Industrial Manufacturing

    (4-Tert-Butoxycarboxyphenyl)boronic acid supports specialized synthesis in advanced sectors including pharmaceuticals, electronic materials, agrochemicals, and specialty polymers. Detailed below are downstream manufacturing areas where this boronic acid derivative plays an integral, differentiated role. Each scenario reflects actual customer use cases, defined quality criteria, dosing practices, and points of process integration.

    1. Pharmaceutical API Manufacturing: Suzuki-Miyaura Coupling Processes

    Drug manufacturers utilize this boronic acid in Suzuki-Miyaura cross-coupling to create biaryl pharmacophores essential for targeted therapies, such as oncology and CNS medications. Regulatory-driven process control and precise dosing are required to meet stringent impurity thresholds and batch reproducibility demanded by international health authorities.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF and EP monographs for residual solvents and related substances
    • US FDA 21 CFR 210/211 for finished dose manufacture
    • ICH Q3A/B guidelines for impurity profiling

    Typical usage ratio

    • 0.8-1.2 molar equivalents versus halogenated aromatic partner, adjusted according to catalyst turnover and substrate reactivity

    Downstream process integration

    • Compound charged in batch or flow reactors during Pd-catalyzed C–C bond formation; usually post-hydration and prior to aqueous work-up/purification

    Final product types

    • Active pharmaceutical ingredient intermediates for antineoplastic drugs
    • Finished APIs featuring substituted biphenyl or heteroaryl structures
    • Patent-protected CNS therapeutics utilizing biaryl subunits
    • GMP-grade reference standards for approved drugs

    2. OLED Material Synthesis for Display Technology

    Boron-containing aryl building blocks are pivotal in constructing conjugated molecules for organic light-emitting diode (OLED) emitters and host materials. Downstream electronic material producers demand exceptional trace metal purity and consistent reactivity to prevent unwanted quenching and device performance losses.

    Industry compliance standards

    • JEITA EDA technical requirements for OLED chemicals
    • CQC quality audits for electronic-grade materials
    • Semi S2 standards for chemical sourcing in device manufacture
    • RoHS Directive (EU) for hazardous substance limitations in displays

    Typical usage ratio

    • 0.95-1.1 molar equivalents, typically matching stoichiometry of aryl halide under palladium catalysis

    Downstream process integration

    • Introduced during organic synthesis of blue/green/red emitter units and hole-transport materials; integrated in multi-step coupling cascades

    Final product types

    • OLED emitter molecules for smartphone and TV panels
    • Light- and electron-transport layer intermediates
    • Purified small molecules for display module ink formulation
    • Functionalized oligomers for flexible screen substrates

    3. Agrochemical Active Ingredient Development

    Crop protection formulators incorporate this boronic acid to build biaryl or heteroaryl motifs within herbicides, fungicides, and select insecticides. Integration occurs under tightly controlled conditions to assure field compatibility and environmental profile compliance, while balancing cost and byproduct minimization.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • FAO/WHO Food and Agriculture Standards (JMPR)
    • REACH (EC) for new agrochemical intermediates
    • ISO 9001 certification for process and batch consistency

    Typical usage ratio

    • 0.85-1.3 molar equivalents, based on aryl halide loading and product selectivity goals

    Downstream process integration

    • Reagent added in main biaryl coupling—either batch or telescoped with protection/deprotection steps—prior to downstream formulation or micronization

    Final product types

    • Precursor molecules for post-emergence herbicides
    • Biaryl fungicidal active substances
    • Chemical building blocks for safener compounds
    • Registration-standard reference compounds

    4. Specialty Polymer and Resin Modifier Synthesis

    Advanced polymer producers apply this boronic acid as a functional comonomer or end-group modifier, targeting improved mechanical and thermal characteristics, and enabling new structural arrangements for specialty coatings and adhesives. Traceability and batch records support downstream ISO compliance and reproducibility needs.

    Industry compliance standards

    • ISO 9001/14001 for polymer materials management
    • ASTM D256 and D638 for finished polymer performance
    • EU REACH compliance for polymer additives
    • UL94 test protocols for flame-retardant polymers

    Typical usage ratio

    • 0.5–2% by weight for functionalization reactions, with exact content tailored to target molecular weight and end-use mechanical strength

    Downstream process integration

    • Incorporated in controlled-molecular-weight polymerizations or post-synthesis chain-end modifications, prior to blending and extrusion

    Final product types

    • Functionalized thermoset resins for electronic encapsulation
    • Adhesive base polymers with enhanced toughness or processability
    • Cross-linkable coating precursors
    • Block copolymers with tailored chain architecture

    5. Fine Chemical Building Block for Molecular Sensors

    Research and diagnostics manufacturers employ this boronic acid derivative in the synthesis of biaryl motifs for fluorescent probes, chemosensors, and receptor molecules. Downstream integration mandates precision in molecular connectivity and batch purity, validated by spectroscopy and analytical testing, with lot traceability for laboratory or clinical supply chains.

    Industry compliance standards

    • ISO 13485 for diagnostic reagents and laboratory consumables
    • GLP (Good Laboratory Practice) guidelines for chemical traceability
    • HSQ (Health and Safety Quality) management in research settings
    • National Research Council chemical safety policies

    Typical usage ratio

    • Generally 1.0 molar equivalent, with potential adjustment down to 0.9 for high-purity syntheses requiring rigorous side-product elimination

    Downstream process integration

    • Participates as a synthetic step in multi-component probe or sensor molecule assembly, typically after halogenated intermediate introduction

    Final product types

    • Fluorescent chemosensors for biomolecule detection
    • Affinity-based molecular probes for research diagnostics
    • Spectral calibration standards
    • Screening reagents for biomedical R&D
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    Certification & Compliance
    More Introduction

    (4-Tert-Butoxycarboxyphenyl)Boronic Acid: A Closer Look from the Manufacturer's Bench

    Bringing Precision Chemistry to Modern Synthesis

    Working directly in chemical production, we see the requirements of the lab and the factory floor meet in very real terms. Every step, each new compound, means we have to deliver pure, reliable, and stable materials that perform the same with each batch. Among the specialty chemicals that receive growing attention for cross-coupling reactions, (4-Tert-Butoxycarboxyphenyl)Boronic Acid stands out. It offers a unique set of reactivities and capabilities that help chemists innovate in both research and production environments.

    Understanding the Unique Structure

    This compound features a boronic acid group linked to a phenyl ring, itself substituted with a tert-butoxycarbonyl (tBoc) group at the para position. Looking at the molecular model, the structure creates an interesting blend of stability and selective reactivity—attributes valued by pharmaceutical developers and industrial chemists alike. Handling its synthesis and purification daily, we appreciate its tangible differences from standard boronic acids, starting with solubility and extending to stability under ambient conditions.

    How It Performs on the Bench

    Few chemicals deliver such consistent coupling yields in Suzuki and similar cross-coupling reactions as this one. We have observed that the tert-butoxycarbonyl group offers predictable protection without cumbersome side reactions that sometimes hinder boronic acids bearing more common substituents. Our process engineers value the compound for the way it holds up through several synthetic steps—holding reactive boron accessible while preventing unwanted oxidation or hydrolysis. Trying to scale methyl- or phenyl-boronic acids under parallel conditions, we have seen more loss and more variation in reaction consistency. By contrast, this compound’s particular protecting group moderates the reactivity, helping teams avoid purification headaches downstream.

    Specifications and Purity: Meeting the High Bar

    Staying close to the production process, we watch every stage of the manufacture for this material—from raw feedstock qualification through final packaging. We regularly achieve purity above 98%, confirmed by HPLC, NMR, and titration. The target melting point lands between 181-186°C, and we control moisture content under 0.5% thanks to controlled storage and quick, careful handling. For each lot, consistency matters more than numbers alone; we keep analytical fingerprints for every batch and adjust process conditions as raw materials change, never relying on speculation or oversimplified claims of “grade.” In-house chemists work with the QC team to review every stage: solvents, catalysts, filtration, and packaging all impact final compound quality, so the manufacturing process never takes a back seat.

    Applications in Synthesis—From Library Generation to Scale-Up

    Across our years making boronic acids for researchers and industrial partners, few compounds get as many repeat requests as this one. It proves especially helpful in medicinal chemistry for aryl-aryl bond formation, as well as in developing targeted materials for advanced electronics and coatings. Chemists trust its performance in Suzuki-Miyaura couplings, not only for library synthesis but also for pilot campaigns. The robust character lets users handle aggressively optimized conditions—strong bases, elevated temperatures, or water-tolerant solvents—without watching the starting material disappear to tars or unidentified side-products.

    A Step Beyond Standard Boronic Acids

    Where standard boronic acids often demand dryboxes or elaborate protection, we see this compound offer straightforward bench-top handling. Experienced users working repeatedly with these chemicals often remark on the tert-butoxycarbonyl group’s clear benefit: it strikes a balance between protecting the aromatic boron while leaving aromatic and boronic reactivity open to fine control. This differs noticeably from pinacol ester-protected boronic acids or boronate esters, which need additional steps for deprotection, stirring up more waste and extending purification timelines. With (4-Tert-Butoxycarboxyphenyl)Boronic Acid, the route to deprotection is established, mild, and selective—saving chemists from retracing steps or creating more by-products.

    Storage, Shelf Life, and Handling

    Laboratories and production sites prefer compounds with shelf stability measured in months and, in some contexts, years. We rigorously monitor the stability of each batch under real-world temperature and humidity swings, not just idealized settings. By keeping packaging inert and cycling fresh lots into inventory, the acid retains its quality. The tBoc group, as part of the molecule, grants a significant buffer against accidental hydrolysis, making it resilient against brief air or moisture exposure. With standard boronic acids, a lapse in storage care can ruin entire lots; with our product, we see a tangible reduction in rejected or degraded material thanks to that in-built protection.

    Production Insights—Scale, Sourcing, and Sustainability

    Every batch we put out reflects the constraints and possibilities of modern fine chemical production. By controlling each reaction stage, starting from high-purity precursors and monitored conditions, we keep impurity profiles minute. Raw phenols, tert-butyl chloroformate, and boronate reagents pass stringent analysis before use—each batch gets chromatographed and tested before moving forward. In upstream supply, finding consistent, reliable sources for raw aromatics and protecting reagents matters, and our long-term vendor relationships minimize production interruptions. Unlike generic resins or low-grade boronic acids, which might cut costs by relaxing upstream controls, our direct synthesis means no batch leaves without confirming data and a hands-on check from a production specialist.

    Fitting into Regulatory and Quality Frameworks

    With each customer request, we face a new set of documentation, analytical, and regulatory hurdles. We work daily with global firms pursuing registrations in stricter markets—Europe, North America, East Asia—necessitating high standards for traceability, change management, and documentation. Analytical documentation, COAs, and traceability records follow every batch; this aligns with the expectations of experienced buyers, particularly those scaling pilot outputs to cGMP environments. Any deviation from published impurity patterns brings a halt until we trace the root cause—a framework born not from regulation for its own sake, but from hard-earned experience in process troubleshooting and client trust.

    Direct Manufacturer Perspective—Efficiencies and Responsibility

    Making (4-Tert-Butoxycarboxyphenyl)Boronic Acid at scale means looking at economics and efficiency up close. Powder handling, mass transfer, and reactor setup routines all shape throughput and loss profiles. On our lines, minimizing solvent use, capturing trace by-products, and recycling clean solvents reduce waste and workplace exposure. We avoid surplus packaging and monitor energy use, as even bulk chemical operations face rising scrutiny on carbon footprint and sustainable practice. Because our reputation rests on every outgoing kilogram, these choices are not abstract or secondary—they are shaped by the daily discipline of managing real-world materials.

    End-User Feedback: Improving Each Step

    Chemists using this boronic acid often share feedback about reaction times, color changes, solubility quirks, or trace impurities. Our technical support team responds with real-world, practiced solutions—suggesting solvent swaps, stirring rates, or purging protocols based on hands-on data rather than speculative advice. More than once, issues that might look like “bad starting material” have traced back to mixing, dosing, or atmospheric exposure during a scale-up. By running our own process trials alongside user input, we adapt both product and recommendations together, keeping quality transparent and communication direct.

    Innovating While Maintaining Reliability

    Every year, the push for “custom” reagents gets stronger. The market asks for subtle modifications: isotopic labeling, alternative protecting groups, or variants for process screens. Our experience as a direct manufacturer, not a reseller, puts us in a position to tune production in response. Possibilities for future improvement exist around greener solvents, quicker deprotection methods, and streamlined work-up routines, often informed by client suggestions or our own pilot runs. With every technical advance, though, reliability in the core material takes priority. No tweak gets commercialized until it passes the same side-by-side tests as the mainline compound—yield, purity, shelf life, and downstream impact all measured from the same bench.

    Comparing With Other Boronic Acids and Esters

    Chemists have their preferences: some lean toward simple phenylboronic acid when cost trumps handling or stability; others favor the relative stability of pinacol boronate esters for library work or automated synthesis. What sets (4-Tert-Butoxycarboxyphenyl)Boronic Acid apart emerges each day on the production line and in feedback from advanced users—the protective, electron-withdrawing tBoc group changes both reactivity and robustness, uniquely fitting high-stakes cross-coupling steps. Where unprotected analogues degrade rapidly on air exposure or require glovebox handling, our product withstands standard atmospheric conditions, even during long reaction cycles or when handled outside of strictly inert setups.

    Reducing Downstream Processing Burdens

    Compound and reaction purity aren’t details—they define final product yield and waste generation. In the routes we’ve validated for clients, the lower tendency for this boronic acid to form hard-to-remove side-products means fewer columns, less silica, and reduced solvent use in product cleanup. In pilot processes, turnaround proceeds more quickly, with chromatographic performance supported by the well-defined polarity and reactivity conferred by the tBoc group. This translates into economic savings and safety gains for users—points that often go unsung until scale-up or analytical bottlenecks hit.

    A Resource for Specialty Synthesis—From Early Stage to Process Chemistry

    The demand picture for such a targeted boronic acid reflects broader shifts in fine and specialty chemical industries. Life science companies and material chemists want compact, reliable building blocks to fuel innovation in smaller, more efficient workflows. This demand means greater scrutiny on material origins, quality control, and reproducibility. Our ongoing commitment matches that: developing routes that limit trace metal residues, tuning crystal characteristics for easy weighing and handling, and supporting every new order with an eye to building long-term trust.

    Facing Challenges Head-On—Stability, Consistency, and Compliance

    Direct access to our manufacturing means we catch problems early—batch-to-batch variation, emerging impurity signatures, or mechanical issues in transfer or packing. Process stability stands at the top of the list, supported by continuous training and upgrades to analytical infrastructure. Every time we adopt a new method, it responds to chemistry in the real world, not just theoretical improvements. Compliance with REACH, TSCA, and emerging regulations never gets “outsourced”—our documentation, labeling, and disposal all reflect direct accountability, removing the distance often seen with handed-off supply chains or untraceable intermediaries.

    Supporting Scientific Progress

    From the perspective of those actually making the material, (4-Tert-Butoxycarboxyphenyl)Boronic Acid is more than a SKU or catalogue entry. It is a case study in how molecular design, process discipline, and end-user focus can together yield a compound that grows with the needs of innovative chemists. As cross-coupling chemistry advances, so does the bar for starting material consistency, documentation, and sustainable manufacturing. Our commitment runs from the reaction vessel through to the packed product, always shaped by new client insights and our own ever-present demand for robust, trustworthy chemistry.