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3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid

    • Product Name 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid
    • Alias DEAPBA
    • Einecs 688-009-1
    • 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

    211761

    Product Name 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid
    Cas Number 851387-11-6
    Molecular Formula C11H16BNO3
    Molecular Weight 221.06
    Appearance White to off-white solid
    Melting Point 120-125°C
    Purity Typically ≥ 97%
    Solubility Soluble in DMSO and methanol
    Storage Conditions Store at 2-8°C, protected from moisture
    Smiles B(C1=CC=CC(=C1)C(=O)N(CC)CC)(O)O

    As an accredited 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in a 5g amber glass bottle with a screw cap, labeled with chemical name, formula, CAS number, and hazard warnings.
    Shipping **Shipping:** 3-(N,N-Diethylaminocarbonyl)phenylboronic acid is shipped in tightly sealed containers, protected from moisture and light. Standard shipping at ambient temperature is typical unless otherwise specified. The package complies with all applicable chemical transport regulations and should be handled by trained professionals using appropriate safety precautions.
    Storage Store **3-(N,N-Diethylaminocarbonyl)phenylboronic acid** in a tightly sealed container, protected from air and moisture. Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Store at room temperature or lower, and avoid direct sunlight. Always follow laboratory safety protocols, including proper labeling and secure storage to prevent accidental exposure or contamination.
    Application of 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid

    Applications of 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid in Industrial Manufacturing

    As an active manufacturer specializing in boronic acid derivatives, we deliver 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid for critical roles in diverse industrial verticals. Our production focus aligns with real downstream applications, helping formulators and process engineers address specific challenges in small molecule synthesis, advanced material modification, and specialty intermediate preparation. Below we present principal use cases based on real industrial demand and compliance.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology Small Molecules

    This compound functions as a prized building block in cross-coupling reactions for constructing complex oncology drug intermediates, especially where boronic acid moieties improve binding or targeting. Process chemists adopt it for Suzuki-Miyaura reactions to introduce substituted aryl groups with improved metabolic stability compared to simpler boronic acids. The controlled reactivity and solubility profile streamline downstream purification during multi-step synthesis campaigns in regulated pharmaceutical environments.

    Industry compliance standards

    • ICH Q7 GMP guidelines for API manufacturing
    • USP <1092> Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211 (for intermediates and APIs destined for US market)
    • EU EudraLex Volume 4 GMP regulations

    Typical usage ratio

    • Used at 1.0–1.3 molar equivalents relative to halogenated aryl or heteroaryl coupling partners
    • Exact proportion adjusted according to desired conversion and minimization of homocoupling byproducts

    Downstream process integration

    • Introduced during catalytic Suzuki cross-coupling steps following substrate activation
    • Used in early or late stage functionalization before isolation, crystallization, and further derivatization
    • Enter purification via preparative chromatography or controlled crystallization

    Final product types

    • Oncology API intermediates
    • Small molecule clinical candidates targeting cancer cell receptors
    • Boronic acid motif-containing pharmaceutical scaffolds
    • Specialty fluorinated or substituted aromatics for research pipelines

    2. Specialty Electronics Material Monomer Synthesis

    Chemical engineers utilize this raw material in the design and manufacture of high-performance monomers destined for conjugated polymer production in organic electronic devices. Its carbamoyl-protected nitrogen enables precise control over solubility and reactivity, vital for sequential polymerization techniques required in organic field-effect transistor (OFET) and organic photovoltaic (OPV) applications. End users integrate its phenylboronic acid group for tunable optoelectronic properties and advanced charge mobility in thin-film electronics.

    Industry compliance standards

    • IEC 63004: Printed electronics materials quality
    • RoHS Directive (for restricted substances in electronics)
    • ISO 9001:2015 Quality Management System for poly-electronic material providers
    • JEITA ET-7304A: Assessment of polymer electronic material reliability

    Typical usage ratio

    • 0.5–1.2 equivalents per dihalogenated arene in step-growth or chain-growth polycondensation processes
    • Ratios depend on target polymer backbone architecture and batch scale

    Downstream process integration

    • Engaged at the monomer synthesis stage, preceding direct polycondensation or copolymerization steps
    • Undergoes purification before solid-state polymerization or solution-processable thin-film casting
    • Chemical compatibility enables co-reaction with other boronate or stannane-functionalized comonomers

    Final product types

    • Electroactive polymeric semiconductors
    • Solution-processable conjugated polymers for OFET/OPV devices
    • Patternable monomers for printed electronic circuitry
    • Functionalized polymer blends for flexible display substrates

    3. Advanced Peptide Drug Conjugate (PDC) Linker Engineering

    Molecular design teams in peptide pharmaceutical pipelines use this compound to incorporate boronic acid-derived cleavable linkers for targeted drug delivery. Its protected amide structure ensures stability during peptide chain assembly, while the boronic functionality confers programmable degradation in specific in vivo environments. This enables conjugation of cytotoxic small molecules or imaging agents to peptide carriers, improving site-specific release and minimizing systemic toxicity in advanced oncology and diagnostic applications.

    Industry compliance standards

    • USP <1047> Peptide APIs
    • EMA Guideline on quality of peptide conjugates
    • ICH Q6A Specifications: Test Procedures and Acceptance Criteria
    • ISO 13408-1 Aseptic processing for injectables

    Typical usage ratio

    • Applied at 0.8–1.1 equivalents relative to nucleophilic attachment sites on the peptide backbone
    • Fine-tuning based on peptide chain length and linker stability requirements

    Downstream process integration

    • Engaged post-solid phase peptide synthesis (SPPS) for site-specific conjugation
    • Activated under mild coupling conditions to prevent side reactions
    • Purified by preparative HPLC before payload conjugation and formulation

    Final product types

    • Peptide-drug conjugates for targeted cancer therapy
    • Biomolecule-dye conjugates for imaging diagnostics
    • Cleavable linker-equipped peptide therapeutics
    • Next-generation ADC (antibody-drug conjugate) intermediates

    4. Fine Chemical Intermediate for Agrochemical Active Synthesis

    Agricultural chemistry manufacturers apply this material in multi-step production of novel aryl boron intermediates for crop protection agents. Its unique backbone allows for construction of bioactive molecules with increased environmental stability and selective herbicidal or fungicidal function. Its use as a selective boron donor in palladium-catalyzed coupling steps enables access to complex, patent-protected agrochemical actives with predictable environmental fate and compliance with residue regulations.

    Industry compliance standards

    • FAO/WHO JMPR Pesticide Specifications (for actives and intermediates)
    • OECD Principles of Good Laboratory Practice
    • REACH Regulation EC No 1907/2006 for substances in agrochemicals in the EU
    • ISO 17025:2017 Laboratory accreditation for QC

    Typical usage ratio

    • 1.0–1.5 molar equivalents per aryl halide building block in major coupling step
    • Dosing optimized for yield and downstream impurity thresholds

    Downstream process integration

    • Added as a key intermediate during coupling reactions under inert atmosphere
    • Undergoes workup with phase separation and selective recrystallization to purify the product
    • Feeds directly into subsequent methylation, oxidation, or halogenation steps

    Final product types

    • Crop protection compound intermediates
    • Selective fungicide precursors
    • Herbicidal actives based on boronic acid functionalization
    • Formulation-compatible aryl boronic esters for agrochemical blending

    5. Polymer Crosslinker for Medical Diagnostic Assay Components

    Manufacturers in diagnostics leverage this boronic acid derivative to engineer polymeric matrices with controlled crosslinking density for sensor strips and ELISA plate coatings. Its reactive phenylboronic acid group forms stable covalent bonds with diol-containing carbohydrates, critical for forming bioaffinity-based capture surfaces. Engineering teams select this material to regulate hydrogel porosity and stability, meeting stringent requirements for batch reproducibility and analytical specificity in in vitro medical diagnostics.

    Industry compliance standards

    • ISO 13485:2016 Medical device quality management
    • CLSI MM17-A guidelines: Validation of multiplexed immunoassays
    • FDA 21 CFR 820 (Quality System Regulation for medical devices)
    • EN 13612:2002 Performance evaluation for in vitro diagnostic devices

    Typical usage ratio

    • Incorporated at 0.05–0.15 wt% relative to total polymer/monomer mix in hydrogel or coating applications
    • Amount optimized for mechanical stability versus binding functionality

    Downstream process integration

    • Added during pre-polymer blend stage before initiation of polymerization or crosslinking reaction
    • Enables in situ grafting onto sensor strip backbones or ELISA well plates
    • Careful process control required to ensure retained boronic acid functionality post-curing

    Final product types

    • Blood glucose monitoring strips with boronic acid receptors
    • Hydrogel-based biosensor matrices
    • ELISA plates for carbohydrate-binding assays
    • Diagnostic coatings for high-specificity in vitro detection
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    Certification & Compliance
    More Introduction

    Introducing 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid: A Reliable Choice for Advanced Synthesis

    A Direct Manufacturer’s Perspective

    Experience in chemical production teaches lessons every day. Among the many specialized boronic acids we have developed over the past years, 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid stands out in both quality and flexibility. Many customers ask about our rationale for advancing this molecule and why it often becomes a preferred substrate for research labs and industrial synthesis teams. Honest feedback from countless partners helped us shape the manufacturing process and continue refining purity, particle distribution, and batch-to-batch consistency. On the shop floor and in QC, we recognize quickly which products will give project chemists an easier time and which might hold up the next synthesis step.

    Key Features and Model Availability

    This compound, sold by us under model number DEAPA-001, is engineered for ease of use across multiple synthesis platforms. Chemists usually look for performance in Suzuki-Miyaura couplings, and this derivative finds regular use in pharmaceutical intermediate synthesis, bioactive molecule scaffolding, and in the fine tuning of physicochemical characteristics of complex molecules. The boronic acid’s N,N-diethylaminocarbonyl functionality brings distinct electron-donating properties to the ring, which can impact both reactivity and solubility in diverse solvent systems.

    Production involves rigorous control over reaction temperatures, reagent stoichiometry, and purification, using scalable techniques. Raw material selection has a direct hand in the outcome, as does process water quality and ambient storage conditions through the synthetic campaign. Unchecked humidity or fluctuating storage temperatures affect a boronic acid’s performance, so we design packaging and logistics down to the last detail. Specifications include a typical purity above 98% by HPLC, with controlled moisture content and a clear melting point range to help researchers feel confident opening a new drum or bottle. Close attention to these details has kept customers coming back for multi-kilo orders or the occasional urgent overnight vial for time-critical research.

    Why This Boronic Acid Deserves Attention

    Direct feedback from partners shaped why the 3-(N,N-Diethylaminocarbonyl) derivative matters. Many analogues exist in the benzeneboronic family, but not all offer the same performance. This particular product strongly resists hydrolysis, holds together well during sensitive steps, and reduces the risks of unexpected polymerization or decomposition. Working closely with process R&D teams at scale, we’ve noticed this single advantage often makes or breaks a campaign, especially when a project advances past milligram screening and into kilogram or multiton production.

    Finding boronic acids that survive storage yet activate reliably during cross-coupling isn’t always straightforward. We select this molecule specifically to cater to users who value long shelf life alongside consistent performance from trial batch to commercial run. Presence of the N,N-diethylaminocarbonyl group helps stabilize the molecule against ambient decomposition and offers a noticeable difference when comparing it with less substituted phenylboronic acids under similar storage and reaction conditions. This modification directly addresses a problem that troubled chemists for years: unwanted side reactions due to unstable boronic acid substrates.

    Head-to-Head with Other Boronic Acid Products

    Comparison to other phenylboronic acids focuses on what matters most in real laboratory settings. Working at the bench, we see teams battle variable activity or solubility—a direct result of substituent patterns on the benzene ring. Unsubstituted phenylboronic acids sometimes suffer quick degradation under moist air or variable temperature storage. Others, such as ortho-substituted boronic acids, bring handling complications due to sterics or limited solubility in standard solvents. Our compound, with the diethylaminocarbonyl positioned on the meta ring, often brings just the right balance for smooth process development.

    On the product line, we control for unwanted contaminants and focus on trace metal removal, given the strict requirements of catalytic coupling. Small trace levels of palladium, iron, or nickel in reagents can cripple the reaction, raise downstream purification costs, and block regulatory approval. We commit to regular audits of starting materials and production lines to minimize cross-contamination. Overproduction brings new challenges: holding large inventories or scaling up single campaigns involves additional risk. Freshness and aging control mean stocks rotate quickly, reducing the risk of aging-related decline in reactivity.

    Quality and Safety: Our Daily Practice

    Our QC staff checks every drum using multiple analytical techniques, running both standard and custom methods depending on the client’s needs. UV, IR, and NMR data come as standard, but much of the insight stems from staff years of practical bench work—knowing not just what numbers look right, but what unexpected signals mean for downstream performance. Safe handling practices guide us from first sourcing raw materials to final shipment. Industrial experience flags the real hazards: inhalation risks, accidental spills, or reactive containers, especially when scaling up from flask to reaction kettle.

    We participate in both internal and external audits for chemical safety, and connect directly with users who experience real-world issues. If there are reports of clumping, loss of flowability, or reaction mixtures giving unexpected byproducts, we bring that knowledge back to our process engineers and adjust—not just for a single batch, but for future production runs across the line. This commitment stands behind every pail that leaves our warehouse.

    Sustainability and Traceability Matter

    The conversations surrounding sustainable chemical sourcing and traceability have become much louder recently. As direct producers, we have both the opportunity and responsibility to reduce the environmental footprint at every stage. Solvents are selected for both reactivity and recyclability, and process water gets captured and treated in a closed-loop system as much as possible. We know direct traceability is not just a regulatory checkbox—it benefits clients who might need to prove origin and production history for downstream regulatory filings and supply chain certification.

    Questions about the lifecycle of specialty boronic acids can’t be covered with platitudes or generic supplier claim sheets. As a team that’s worked through fluctuating feedstock prices, changing global logistics, and unexpected regulatory updates, we adjust processes quickly. Our staff builds up years of experience in converting feedback and new requirements into updated work instructions and environmental protocols. Regulatory audits — be they from international pharmaceutical companies, or local inspectors — have pushed us to document everything from operator PPE to final wastewater discharge.

    Synthesizing Value for Researchers and Manufacturers

    Synthetic demands change month to month. In recent years, we see researchers working on new heterocycles, targeted pharmaceutical scaffolds, and even covalent ligand libraries, all of which rely on high-performing, consistent aryl boronic acids. Direct application knowledge means knowing where complications might arise and offering hands-on advice. Users trust our compound because it reliably couples under a wide pH range and in organic-aqueous mixed media. We support novel reaction schemes, including the pursuit of more sustainable catalysis routes that use greener solvents or less-toxic metallic catalysts.

    Research customers adapt to market and funding shifts. Sometimes urgent delivery trumps bulk economy; other times, shelf stability and long-term contract supply offer the edge. From development labs moving to clinical trial material, up to commercial bulk Active Pharmaceutical Ingredient synthesis, we tune our production planning and inventory habits to match. No generic solution exists—every client need means a new round of checking with packing, handling, and stability teams.

    Scaling Up: Factory Lessons on Efficiency and Consistency

    Large-scale synthesis presents hurdles that don’t always match what’s seen at smaller scale. Thermal management, agitation, and solvent management become as critical as raw material quality. Our staff learned through hundreds of production runs how sensitive each batch can be to heating rate, order of addition, and quenching protocol. We document not just overall yields and purity data, but intermediate handling and cleaning regimens between runs. This boots-on-the-ground knowledge flows back into our process optimization, helping us reduce waste, boost consistency, and avoid the common headaches that slow down production for high-value specialty boronic acids.

    Bulk buyers sometimes require special packaging or conditioning. We work together with them to develop lined drums to avoid reactions with metal, or customized small packs to avoid humidity ingress in high-moisture environments. Warehouse operators understand the value of a robust logistics partner, minimizing late deliveries and condition problems by working with our own staff from production to final delivery truck. Seasonal weather shifts affect global supply reliability. Our local factory teams keep lines running year-round, not just speeding product out the door but checking stock levels and prioritizing that every drum matches the same exacting production notes as a single research pack.

    Supporting Innovation: Trends and Emerging Challenges

    Modern R&D brings new challenges almost monthly. The rise in automated high-throughput synthesis, data-driven structure screening, and novel drug design all put extra pressure on chemical input supply. We listen closely as research teams describe evolving demands for more selective, robust, or exotic coupling partners. 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid has carved out its own reputation through such feedback cycles. Direct lines of communication with technical leads mean every reported issue triggers a review of both production notes and storage recommendations. Cross-checking every lot means we can trace back any anomaly and share improvements on the next baseline production run.

    We also advise clients on extending the usable shelf life of their inventory, sharing storage best practices based on our own experience. Many labs learned the hard way that even with premium packaging, local temperature or humidity spikes risk product reliability. Our experience shows that desiccant packs, temperature monitoring, and simple, clear labeling can head off years of storage headaches. Every time a team shares lessons from the field, we sharpen our recommendations and pass the changes back through both QC and logistics.

    Collaborations Driving Continuous Quality

    No chemical producer operates in isolation. Collaboration with university researchers, industrial chemists, and even competitors sharpens methods. We invest in staff education, regular training on new analytical gear, and participation in industry associations. This helps ensure our knowledge of both regulatory and technical requirements stays current. Open-door lab visits and transparent data audits keep trust alive with clients who request repeat analysis or on-site verification during audits. This willingness to share methods means our specialty boronic acids remain a trusted input in demanding projects.

    Consistent communication back and forth with the market identifies gaps—like the period when new coupling methods overwhelmed typical boronic acid stability. We saw the need for improved shelf controls and reworked storage chemistry with fresh insight from client data. Every time a lab shares their needs, including compatible solvent systems, we adapt not through theoretical consults, but by altering drum packing, shipment, and even labeling on the next batch.

    Customer-Centric Support at Every Level

    Buying from a direct manufacturer brings more than just price or speed. As a team, we answer technical questions from the bench, troubleshoot scale-up issues with process engineers, and share lessons from our own experiments with every new order. We see real demand shifts—inquiries for newer, more specialized boronic acids—coming directly from client orders and project roadmaps. Responding quickly and accurately takes more than reactive customer service; it’s the result of years of tracking every pain point and creating action plans alongside production schedules, supply management, and inventory adjustment.

    Rapid digital transformation in chemical sourcing has made detailed lot traceability the expectation. Our systems now capture and share batch analytical data with clients before they even open the drum. Documenting this information cuts downstream troubleshooting and quickens response times if issues ever arise. Direct access to both our technical team and core production staff means questions never languish in call queues. If users notice unexpected results or packaging defects, solutions get deployed at the factory level and written into future standards.

    Continuous Improvement and Looking Ahead

    Learning from every campaign, every scale-up, and every analyst call, we keep adjusting our strategy. Pushing for both higher analytical stringency and sustainable process changes in boronic acid production remains a core goal. Our willingness to pivot, document, and retrain means we stay relevant as new catalytic coupling routes emerge and pharmaceutical standards tighten. The evolution of 3-(N,N-Diethylaminocarbonyl)Phenylboronic Acid, strongly influenced by hands-on feedback and application-driven tweaks, reflects a broader trend: chemical manufacturing thrives at the intersection of field experience and production discipline.

    Active engagement with technical partners, commitment to open information sharing, and respect for regulatory and safety requirements continue to shape how we manufacture and deliver specialty boronic acids. Opportunities for growth come from staying grounded in user experience — knowing the distinct hurdles faced by chemists in both research and commercial production. Our journey with this product offers insight into the real-world value only experienced manufacturers can bring: attentive, flexible production forged by dialogue and cumulative learning, not theoretical claims.