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4-Benzyloxybenzeneboronic Acid

    • Product Name 4-Benzyloxybenzeneboronic Acid
    • Alias 4-(Benzyloxy)phenylboronic acid
    • Einecs 623-591-6
    • 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

    229504

    Name 4-Benzyloxybenzeneboronic acid
    Cas Number 511054-37-0
    Molecular Formula C13H13BO3
    Molecular Weight 228.06 g/mol
    Appearance White to off-white solid
    Melting Point 195-199 °C
    Purity Typically ≥97%
    Solubility Slightly soluble in water; soluble in organic solvents
    Synonyms 4-(Benzyloxy)phenylboronic acid
    Structure Contains a boronic acid group attached to a para-benzyloxyphenyl ring
    Smiles B(C1=CC=C(C=C1)OCC2=CC=CC=C2)(O)O
    Boiling Point Decomposes before boiling
    Storage Conditions Store at 2-8°C, protected from light and moisture

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

    Packing & Storage
    Packing The chemical is packaged in a 5-gram amber glass bottle with a secure screw cap and clear hazard and identification labeling.
    Shipping The shipping of 4-Benzyloxybenzeneboronic acid complies with standard chemical transport regulations. It is packaged securely in sealed containers to ensure stability and prevent contamination. The chemical is shipped at ambient temperature, typically labeled as non-hazardous, though care is required to avoid moisture and prolonged exposure to air. Safety documentation accompanies all shipments.
    Storage 4-Benzyloxybenzeneboronic acid should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Store separately from incompatible materials such as strong oxidizers and acids. Use appropriate personal protective equipment when handling to avoid contact and contamination.
    Application of 4-Benzyloxybenzeneboronic Acid

    Applications of 4-Benzyloxybenzeneboronic Acid in Industrial Manufacturing

    4-Benzyloxybenzeneboronic Acid serves as a specialized building block for advanced synthesis in fine chemicals, pharmaceuticals, agrochemicals, OLED intermediates, and specialty polymer sectors. As a manufacturer, we enable direct incorporation into tightly regulated downstream processes relying on aromatic boronic acids for high-yield performance and stringent quality systems.

    1. Pharmaceutical API Intermediate Synthesis

    Global pharmaceutical manufacturers use 4-Benzyloxybenzeneboronic Acid as a key arylboronic acid intermediate in palladium-catalyzed Suzuki-Miyaura cross-coupling reactions for the synthesis of complex active pharmaceutical ingredient (API) scaffolds. Process engineers introduce it at the aryl coupling stage to achieve high-purity biaryl compounds in anti-cancer, anti-inflammatory, and CNS active molecules. Rigorous traceability and impurity profiles are mandatory, especially when downstream purification steps must meet ICH Q3A/B guidelines for APIs. Formulation teams validate ratio adjustments during scale-up to control side products and maintain quality metrics for regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • USP <467> Residual Solvents
    • EMA Guideline on the Chemistry of Active Substances

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to aryl halide in Suzuki coupling
    • Adjusted in process development based on target API, catalyst turnover, and purification route
    • Maintained at controlled excess for impurity management in pilot and commercial scales

    Downstream process integration

    • Dissolved in mixed organic solvents with base before Suzuki coupling stage
    • Monitored for reaction completion by HPLC; isolated during crystallization or chromatography
    • QC validates for boron and benzyloxy impurities before moving to API finalization stages

    Final product types

    • Biaryl oncology drugs (e.g., kinase inhibitors)
    • Non-steroidal anti-inflammatory pharmaceuticals
    • Central nervous system modulators containing biaryl motifs
    • Advanced pharmaceutical intermediates for further derivatization

    2. Agrochemical Active Ingredient Synthesis

    Commercial agrochemical companies integrate 4-Benzyloxybenzeneboronic Acid into process routes for producing aryl-substituted herbicides and fungicides via palladium-catalyzed coupling. Plant engineers optimize addition at the preparative stage, often following pre-functionalization of the benzene ring to ensure selective coupling. Regulatory compliance, especially in the management of residual solvents and process catalysts, is strictly monitored for downstream product safety and international market acceptance. Tailored blend ratios support diverse aryl halide reactants and scale from pilot to full commercial operation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EPA FIFRA Guidelines (for US registration)
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • ISO 9001 quality management across batch records

    Typical usage ratio

    • 0.9–1.15 molar equivalents based on target aryl halide substrate
    • Process control adjusts based on reaction kinetics and crude yield in pilot validation

    Downstream process integration

    • Added to intermediate solution reactors, combined with aryl halides under specific pH
    • Purified through distillation or solid-phase extraction ahead of formulation
    • Residual boronic acid content checked prior to formulation of actives and bulk storage

    Final product types

    • Aryl-based herbicide active ingredients
    • Fungicidal intermediates for broad-spectrum applications
    • Precursor molecules for insecticide synthesis
    • Multi-site action agrochemical actives

    3. Organic Light Emitting Diode (OLED) Intermediate Manufacturing

    Specialty electronics manufacturers apply 4-Benzyloxybenzeneboronic Acid to synthesize advanced aryl-based intermediates crucial for the structure of high-performance OLED materials. R&D teams utilize this boronic acid in controlled Suzuki-Miyaura cross-coupling at the aryl diversification stage, directly influencing device efficiency and color stability. Every batch follows electronics-grade purity protocols to prevent conductivity loss from residuals. Process engineers maintain specific equivalencies for custom optoelectronic materials, and QC oversight documents compliance at every step.

    Industry compliance standards

    • IEC 61249-2-21 standards for base materials in electronic devices
    • RoHS (EU Directive 2011/65/EU) for heavy metal restrictions
    • ISO 9001 for electronics manufacturing consistency
    • Internal customer-specific quality agreements for OLED raw material traceability

    Typical usage ratio

    • 0.95–1.05 molar equivalents per aryl halide used in coupling; precisely controlled for batch reproducibility
    • Adjusted to minimize conductive residue and maximize final optical performance

    Downstream process integration

    • Mixed with diaryl or triaryl halides under inert atmosphere in anhydrous media
    • Purified via sequential silica column and vacuum sublimation for electronics grade
    • Integrated into downstream monomer or oligomer synthesis units for OLED layers

    Final product types

    • OLED emitting layer monomers
    • OLED charge-transport materials
    • Light-active oligomers for display panels
    • Blue and green emission intermediates for consumer electronics and automotive displays

    4. Specialty Polymer Additive Synthesis

    Producers in the specialty polymer market employ 4-Benzyloxybenzeneboronic Acid for functional modification of advanced polymer materials, where aromatic boronic acid groups enable further polymer-analogous reactions or surface modifications. Formulation chemists dose it at the block copolymer or cross-linker addition stage, facilitating subsequent steps such as surface grafting or fluorescent tagging. Quality requirements often reference regulated absence of residual catalyst and polymerizable contaminants, and process teams optimize ratios based on target functional group density and downstream performance tests.

    Industry compliance standards

    • ISO 9001 certified specialty chemical manufacturing
    • Regulated by customer-specific purity and safety specifications for polymer additives
    • FDA 21 CFR 177.1520 when intended for food-contact or medical-grade polymers
    • SDS/CLP Regulation (EU) No 1272/2008 for material safety classification

    Typical usage ratio

    • 0.3–1.0 weight % based on target copolymer or as designated by desired functionalization degree
    • Ratio adjusted in pilot projects for surface reactivity and polymer molecular weight distribution

    Downstream process integration

    • Incorporated late in polymerization or modification sequences for maximum group presence
    • Processed under nitrogen to minimize moisture impact on sensitive polymer scaffolds
    • Polymer QC checks for residual acid and determines batch release for downstream blending

    Final product types

    • Functionally modified block copolymers for research and industry
    • Reactive polymer resins for surface functionalization of plastics
    • Fluorescent or sensor-tagged specialty polymers
    • Medical polymer intermediates for diagnostics and device coatings
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    Certification & Compliance
    More Introduction

    4-Benzyloxybenzeneboronic Acid: A Reliable Building Block from an Experienced Source

    Proven Capabilities with Boronic Chemistry

    Bringing boronic acids from the lab to the plant floor takes more than just accurate chemical reactions. Our own experience with 4-Benzyloxybenzeneboronic Acid (CAS 5122-93-6, C13H13BO3) stretches beyond a decade, marked by continual fine-tuning of every stage—coupling steps, crystallization, purification. The compound's clean profile distinguishes it from other boronic acid derivatives, simplifying process development and cutting headaches at scale. Consistently high purity with minimal byproducts reflects the benefits of in-house synthesis, strict control of moisture, and deep understanding of the compound’s chemical temperament. As a manufacturer with hands on the line every day, we recognize which small process shifts push up yields and which raw materials actually hold up in scale batches.

    Key Specifications Backed by Consistent Output

    We consistently produce 4-Benzyloxybenzeneboronic Acid as a free-flowing white to off-white powder, with HPLC purity levels regularly above 98 percent. Each batch runs through a battery of checks—from ¹H-NMR for structural verification to water content analyses that often reveal traces below 0.5 percent. The molecular weight stands at 226.05 g/mol, and we hold process and packaging standards to avoid accidental hydrolysis or contamination. Years of synthesis experience show that halogenated impurities and oligomerization can sap reactivity, so we enforce strict limits on both.

    Why Direct Purchase Matters for Synthesis Projects

    Development chemists building new drugs and advanced materials often run into a common roadblock: surprises in the chemical supply chain. Without direct access to the people making the key intermediate, there is little opportunity to resolve issues or request specific tweaks to the process. Our team works beside kilo-scale reactors, not in distant offices, so conversations about project needs shape improvements right at the source. With 4-Benzyloxybenzeneboronic Acid especially, end users have asked for narrow melting ranges—often 150 to 154°C for the monohydrate form—and trace impurity certificates to ensure compliance with strict downstream quality requirements. Customization requests, from packaging in tryptamine-free environments to special documentation for regulated industries, happen regularly and don't get lost in a web of brokers or overseas agents.

    Usage: Modern Applications Guided by Real Feedback

    Research teams have given constant feedback about this boronic acid’s performance in Suzuki-Miyaura cross-coupling and related routes, especially for constructing carbon–carbon bonds in biaryl or diaryl ether frameworks. With the benzyloxy protecting group on the para position, the molecule resists harsh conditions yet deprotects smoothly under hydrogenolysis. This resilience brings clear advantages for stepwise synthesis. Over countless campaigns, not only in pharma but also in agrochemical and material science developments, the compound’s robust lot-to-lot consistency lets chemists skip re-qualification headaches after scale-up. Many see notable reductions in side reactions traced back to impurities or inconsistent moisture levels—issues that often crop up with poorly tracked or re-bottled material. Our batch records and supply chain transparency let end users quickly verify that previous issues with reactivity or discoloration are no longer a concern when working with material made at the source.

    Comparison with Other Substituted Boronic Acids

    4-Benzyloxybenzeneboronic Acid sits apart from more basic boronic acids, such as phenylboronic acid or p-tolylboronic acid, not just in functionality but in versatility during late-stage synthesis. A simple methyl or methoxy group modifies reactivity in predictable ways, but the benzyloxy substituent does more. It toggles solubility and electronic character, opening doors for chemists chasing higher selectivity in complex systems. Protective group chemistries in particular benefit from this unique profile because the benzylic ether group can be peeled off right before the final union, preserving intermediates that would otherwise suffer side reactions.

    On the factory floor, such differences are not trivial. The stickiness or easy lumping that plagues some boronic acids in humid conditions is less of a worry because our process steps counteract hydrolysis—giving a product that stores well, dispenses efficiently, and handles safely even in larger drums. Over time, direct side-by-side pilot work with research partners revealed that this product stands up better than p-methoxyboronic acid in Suzuki reactions needing precise electronic properties, and outperforms phenylboronic acid when steric protection is critical to a synthetic route.

    Real-World Troubleshooting: Challenges and Solutions

    Every manufacturer recognizes the headaches involved in boron chemistry. Solubility mismatches, batch-to-batch inconsistency, and instability during storage have caused more than a few late nights. Early on, our teams ran into batch failures when subtle shifts in pH during aqueous workups created excess boroxine byproducts. Fixing the root causes, not just treating symptoms, made a real difference. Tighter process controls, antisolvent approaches, and rigorous solvent drying actually show up in lower impurity peaks—even several months out in long-term stability tests.

    Some chemists report persistent clumping in their previous suppliers’ batches, leading to uneven dosing or inconsistent mixing on multi-gram scales. Our plant tackled this by refining both drying and milling conditions and ensuring sealed packaging. The change was simple: less time spent breaking up lumps and more time running productive campaigns. Our shipments now reach customers without the ‘mystery melt’ problem seen when moisture sneaks in during transit and caking forms.

    Unwelcome color changes during transport, sometimes signaling side reactions or oxidation, created questions about shelf stability. By switching oxygen-barrier packaging and tracking transit temperatures, we cut these incidents to near zero. If a batch arrives outside agreed specs, our technical team is already familiar with the batch history and can support root-cause troubleshooting rather than repeating standard answers.

    Safety Practices Gained Through Actual Experience

    Handling of boronic acids bears a different risk profile than simple aromatics or halides. Over years of operating at scale, our workers logged and investigated every instance of skin or respiratory contact, revising protocols in response. Unlike some boronic esters or stronger acids, 4-Benzyloxybenzeneboronic Acid shows relatively low volatility and manageable toxicity, but not zero hazard. Standard gloves and goggles remain mandatory in our processing rooms, and dust minimization strategies—by way of controlled transfer and mild negative pressure—protect everyone in the workspace. Regular practical drills reinforce the message, shown in near-zero lost time since these protocols were upgraded.

    Our in-house teams work directly with waste partners and authorities to keep disposal safe and legal. Used filtration media or solvent residues receive deactivation before landfill disposal, and every step is logged against the manifest, not farmed out to unverified handlers. Over the years, local compliance officers have seen and audited all aspects of our procedures, which holds our team accountable and helps keep end users protected from regulatory surprises down the line.

    Supporting Demand for Genuine Quality—Not Just Documentation

    Researchers and production chemists continually emphasize actionable transparency, not just paperwork. Every outgoing batch of 4-Benzyloxybenzeneboronic Acid links back to full records—synthesis dates, analytical data, purification logs. This practice removes uncertainty about substitution or off-brand mixing seen on the open trading market. We give end users both authentic CoA and the opportunity to see or request raw data for their own analysis, which has settled plenty of debates about batch equivalence in ongoing development programs.

    Documentation aside, repeat clients value our willingness to work together as long-term partners. Large pharmaceutical firms and academic synthesis labs bring specific purity needs, unique sampling criteria, or just questions about historical lots. Our history of handling sensitive intermediates gives customers confidence that the physical product matches the promises. No generic description could ever substitute for the direct insight that comes from manufacturing involvement, whether investigating a trace impurity or finding material optimized for a one-off kilogram run.

    Adaptations in Response to Market Pressures

    Markets for boronic acids change with the ebb and flow of pharmaceutical research focus, regulatory hurdles, and global sourcing bottlenecks. Early in our experience, price fluctuations and chemical shortages called for creative shifts—tweaks to raw material procurement, development of back-up synthesis schemes. This agility has proven its worth in keeping customer supply steady during periods of international transport congestion or when custom specs and volumes spiked with little notice. Direct manufacturer relationships have smoothed plenty of last-minute bumps that would otherwise stop an urgent R&D program cold.

    We routinely get asked to deliver specialized packaging—glass bottles for milligram samples, fiber drums for multi-kilo campaigns. Requests for security seals or double packaging come up for material sent overseas, and we've responded by working with logistics partners hand-in-hand. Storing stable inventory on-site, tied to robust batch QC audits, lets us keep a step ahead of demand surges or transport slowdowns. In sum, adaptability, not just adherence to spec, proves critical to fulfilling evolving needs.

    Insights from Decades of Direct Synthesis

    Manufacturing boronic acids such as 4-Benzyloxybenzeneboronic Acid day in, day out, produces a finer sense of what works and what falls short. Each plant operator, chemist, and technician carries a lived memory of challenging campaigns—some dogged by stubborn impurity profiles, others lifted by a minor process tweak that unlocked days of smoother production. Feedback from these front-line experiences—mixing, filtering, packaging, and shipping—loops right back into process and product refinement.

    As strict regulatory demands gain ground, we draw on protocol upgrades, frequent internal audits, and ongoing material testing, sometimes years after lot release. This day-to-day investment in the product becomes apparent to our clients. They describe sharper, more predictable results in Suzuki couplings and fewer regulatory headaches when moving into pilot stages. Our technical support team worked directly with a university lab recently whose yields leaped after optimizing toward our product's unique impurity and solubility traits.

    Pushing Ahead: Responsible, Real Manufacturing for Reliable Supply

    Today’s chemists need more than a spec sheet; they need true reliability. By taking full ownership of every 4-Benzyloxybenzeneboronic Acid batch, from reactor preparations to analytical sign-off, we deliver a product that keeps research and commercial programs moving forward. Technical questions met with practical know-how, not just templated advice, have repeatedly closed the gap between development and dependable supply.

    Direct manufacturing attention allows customers to avoid common pitfalls—cross-contamination, inconsistent documentation, shipment mix-ups. Every process step, from weighing raw aromatic inputs to final packing under controlled atmosphere, reflects an ingrained commitment to safety, integrity, and improvement. We stay close to the actual product, not cut off by layers of intermediaries, so surprises get handled before they affect the customer.

    Conclusion: Dependability Through Direct Manufacturing Experience

    Supplying 4-Benzyloxybenzeneboronic Acid isn’t just about keeping drums in a warehouse. Progress depends on detail—batch checks, process tweaks, safety refinements, real corrective action when problems arise. Tracing every lot to its source, verifying each analytical signal, and learning from real-world use, we maintain a product trusted by labs and factories worldwide. Our approach trades short-term savings for lasting value, and that confidence shows each time our 4-Benzyloxybenzeneboronic Acid takes part in building new medicines, new materials, or new research breakthroughs.