Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

(2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride

    • Product Name (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride
    • Alias AMBF-HCl
    • Einecs 721-161-5
    • 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

    634271

    Product Name (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride
    Cas Number 1446758-98-0
    Molecular Formula C8H11BClNO4
    Molecular Weight 231.44
    Appearance White to off-white solid
    Purity Typically >=98%
    Solubility Soluble in DMSO and methanol
    Storage Store at 2-8°C, protected from moisture
    Synonyms 2-Amino-4-(methoxycarbonyl)phenylboronic acid hydrochloride
    Smiles COC(=O)c1ccc(B(O)O)cc1N.Cl
    Inchi InChI=1S/C8H10BNO4.ClH/c1-14-8(11)5-2-3-6(9(12)13)7(10)4-5;/h2-4,12-13H,10H2,1H3;1H

    As an accredited (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle with secure screw cap containing 25 grams of (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride, labeled with product details and safety warnings.
    Shipping (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride is typically shipped in tightly sealed containers, protected from moisture and light. It is packed according to regulated guidelines for hazardous chemicals, often accompanied by safety data documentation. Temperature control may be required; shipment is generally via ground or air in compliance with local and international regulations.
    Storage (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride should be stored in a cool, dry, and well-ventilated area, away from moisture and sources of ignition. Store in a tightly sealed container, protected from light and incompatible substances such as strong oxidizers. Refrigeration (2–8°C) is recommended for extended shelf life. Follow all relevant chemical safety protocols when handling and storing this compound.
    Application of (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride

    Applications of (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride in Industrial Manufacturing

    As a direct manufacturer of (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride, we supply this specialized boronic acid compound for established advanced chemical synthesis routes in regulated sectors. Our material supports mission-critical transformations and coupling in high-value production environments where process traceability, batch consistency, and integration with downstream manufacturing protocols are mandatory.

    1. Active Pharmaceutical Ingredient (API) Synthesis – Oncology Research Compounds

    This boronic acid derivative serves as a pivotal intermediate for Suzuki-Miyaura cross-coupling reactions during the assembly of complex heteroaromatic backbones in targeted oncology drug candidates. Researchers integrate it at the early stage of medicinal chemistry routes, forming key building blocks for bioactive small molecule APIs subjected to clinical evaluation and commercialization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.) Section 5.2
    • Current Good Manufacturing Practice (cGMP)

    Typical usage ratio

    • In Suzuki coupling reactions, used at 1.0–1.2 molar equivalents relative to the aryl or heteroaryl halide substrate. Ratio adjusted according to scale-up batch optimization and reagent throughput requirements in multistep synthesis.

    Downstream process integration

    • Introduced during palladium-catalyzed coupling step after initial halogenation; intermediate is further processed through purification and isolation for inclusion in subsequent synthetic transformations.

    Final product types

    • Early- and late-stage clinical trial oncology APIs
    • Reference standards for synthetic route validation
    • Fine chemicals for medicinal chemistry screening

    2. High-Purity Agrochemical Intermediate Production

    Major agrochemical manufacturers use this compound as a selectively reactive boronic acid for synthesizing functionalized heterocyclic intermediates. These intermediates are further transformed into proprietary herbicide and insecticide actives that enhance selectivity and degradability profiles for field applications, meeting escalating regulatory requirements for residue and toxicity.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FAO/WHO specifications for pesticide active ingredients
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance for agrochemical registration
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • In functional group transfer, used at 0.8–1.1 equivalents, based on the stoichiometric needs of the cyclization or substitution step and the nature of the target agroscaffold.

    Downstream process integration

    • Charged after initial aromatic functionalization to provide boronic acid motif required for further cyclization or coupling; isolation and QC verified before further chemical elaboration.

    Final product types

    • Precursor molecules for selective herbicides
    • Advanced intermediates for systemic insecticides
    • Custom intermediates for crop protection synthesis routes

    3. OLED and Advanced Material Monomer Sourcing

    Device and advanced material manufacturers leverage this boronic acid for constructing monomeric units in organic electronic and photoactive polymers. Its well-defined functional groups offer precise reactivity control, enabling developers to tailor electronic and optical properties in OLED materials, organic semiconductors, and high-performance coatings required for reliable optoelectronic applications.

    Industry compliance standards

    • RoHS 2015/863/EU (Restriction of Hazardous Substances for electronics)
    • IEC 62474: Material declaration for products of and for the electrotechnical industry
    • ISO 14001:2015 Environmental Management Systems
    • Quality protocols specified by key multinational electronics OEMs

    Typical usage ratio

    • Polymer synthesis protocols call for 0.5–1.0 equivalents to match targeted chain-end functionalities, fine-tuned based on the desired molecular weight and the number of boronic acid units required in polymer backbones.

    Downstream process integration

    • Incorporated at the coupling/condensation step for co-polymerization with halogenated electronic monomers to achieve specified chain architectures; thorough in-process QC ensures batch-to-batch consistency before formulation.

    Final product types

    • Organic light-emitting diode (OLED) emitter monomers
    • Organic photovoltaic active layers
    • Thin-film transistor (TFT) functional coatings

    4. Custom Dye and Pigment Intermediate Development

    Dye manufacturers introduce (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride during the semi-synthesis of high-purity azo and anthraquinone-based dyes, enabling site-specific substitution patterns and enhanced colorfastness in specialty pigment products. The boronic acid group facilitates directed metalation or cross-coupling to achieve tailor-made chromophore structures for application in technical textiles and high-definition printing systems.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile safety)
    • EN 71-3:2019 Safety of Toys (Migration of certain elements for inks/dyes)
    • ISO 9001:2015 for dye and pigment manufacturing
    • REACH Annex XVII for azo dye restrictions

    Typical usage ratio

    • Typically dosed at 0.7–1.3 equivalents in metal-catalyzed coupling, adjusted depending on the complexity of the dye moiety and the targeted hue intensity or fastness properties.

    Downstream process integration

    • Added in the nucleophilic aromatic substitution phase to generate intermediate chromophores; intermediates are subsequently purified and reacted with various functional amines or acids to extend the dye structure.

    Final product types

    • Colorants for high-performance textile fibers
    • Specialty printing inks for technical substrates
    • Lightfast pigments for plastics and automotive coatings

    5. Reference Standards and Analytical Reagent Manufacturing

    Accredited laboratories and chemical testing kit producers require this compound as a primary or secondary standard for calibration of analytical equipment and for validation studies in both pharmaceutical and environmental method development.

    Industry compliance standards

    • ISO/IEC 17025:2017 for testing and calibration laboratories
    • USP Reference Standard material requirements (USP–NF)
    • Ph. Eur. General Chapter 5.12 Reference Standards
    • Good Laboratory Practice (GLP) as defined by OECD

    Typical usage ratio

    • Used as pure material (≥98% assay) with absolute quantity determined by instrument-specific calibration requirements; weighed to develop standard curves or as a check sample for system suitability.

    Downstream process integration

    • Batched directly into packaging and QC testing steps as reference material; undergoes independent certification and documentation prior to distribution to laboratories and testing centers.

    Final product types

    • Certified reference standards for HPLC or LC-MS
    • Calibration kits for quality assurance laboratories
    • Analytical reagents for pharmaceutical and agrochemical testing
    Free Quote

    Competitive (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride: Real-World Manufacturing Perspective

    This Compound’s Role in Industry

    If you walk the floors of a production plant, you learn that basic descriptions never capture the full story. (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride, which we sometimes shorten as AMB-HCl for our own convenience, earned its reputation through contribution, not marketing. It doesn’t just fill a line on the order list—real output flows from careful synthesis and proven purity standards, achieved batch after batch. We work daily with AMB-HCl, observing hundreds of grams shifting to kilograms and sometimes up, all feeding into larger streams for organic synthesis or active pharmaceutical ingredients.

    It stands out as a boronic acid derivative, one that pairs an amino group with a methoxycarbonyl (or methyl ester) on a phenyl ring, then stabilizes as a hydrochloride salt. Each of those features shapes its handling and reactivity. The hydrochloride function helps with shelf stability and dust control, avoiding volatility issues we sometimes face with free acids. The amino functionality opens cross-coupling pathways, linking up for Suzuki-Miyaura chemistry, which drives many modern pharma and material science advances. More subtle chemical building blocks lack this reliability or present more handling hazards.

    Our Day-to-Day with AMB-HCl

    Handling this compound in production never feels like a side project. Our line techs and QC teams recognize AMB-HCl right away—a white to slightly off-white crystalline solid, easy to transfer under nitrogen, not nearly as sticky as some analogous boronic acids. From synthetic experience, we know boronic acids often suffer from oligomerization, reducing their effectiveness and complicating purification. The hydrochloride form holds the boronic acid in check, keeping batches consistent from the drum’s top layer down to the last gram at the bottom.

    We target purity levels above 98% by HPLC and NMR, and our batches routinely cross that mark. Achieving this comes from hands-on control over the reaction steps: starting with cleanly protected ortho-nitro or ortho-bromo methyl esters, controlled borylation under inert conditions, and a crystallization process that rejects common side-products. Any deviation finds us backtracking to the root, not skipping over issues for speed. The salt form avoids easy hydrolysis and sets our product apart from more temperamental boronic acids.

    Specifications in Context

    It’s worth stepping into the lab to see how we check every batch. Besides visual inspection, we run HPLC purity, ^1H NMR, ^13C NMR, mass spec, and water content by Karl Fischer. Absence of unwanted peaks becomes a matter of pride and necessity. Even minor impurities in a boronic acid will derail a cross-coupling, producing false starts, low yield, and project delays for our customers’ chemists. A single failed coupling run wastes time and solvents, introduces extra purification, and can throw off R&D or early API campaigns.

    Our AMB-HCl typically flows from the dryer below 0.5% water. This level makes it easy to transfer in gloveboxes or under an argon manifold, reducing clumping. We monitor melting point both for quality and to quickly rule out over-crystallization or salt formation errors. The hydrochloride imparts a slightly higher melting point than the free acid, a detail that matters once you’re managing drums at scale.

    Batch-to-batch reproducibility means more to end-users than any isolated test metric. Our on-site chemists keep strict logs, tracing every raw material back to its source lot. We examine each synthesis record, tightening controls as needed. This oversight keeps surprises away from customers’ R&D groups, who count on every package to behave the same way as the last.

    Usage: Drawing on Manufacturing Experience

    Clients count on AMB-HCl as a core intermediate. Suzuki-Miyaura coupling represents the most common downstream reaction, and it’s where most of our product is headed. Projects targeting kinase inhibitors or emerging bioactive scaffolds draw from this compound’s unique profile. The boron-phenyl bond enables formation of complex aryl-aryl or aryl-heteroaryl architectures without scrambling core functionalities.

    We don’t just ship and forget—our technical support often gets involved in troubleshooting process chemistry. AMB-HCl’s salt form simplifies many common headaches. Free boronic acids sometimes decompose or form sticky residues during work-up; our hydrochloride salt remains easy to filter or redissolve. This keeps reaction margins higher and saves time during purification. We field multiple requests each year for alternative packaging or shipment protection because researchers understand the value of this enhanced stability.

    Many clients purchase this molecule to build out libraries for SAR (structure-activity relationship) studies. It holds up under microwave conditions, survives long coupling times, and tolerates a wide window of pH and temperature conditions compared to less robust boronic acids. For pilot-scale runs, it avoids batch failures that can derail months of planning. That sort of reliability keeps the requests coming year after year.

    How AMB-HCl Differs from Other Boronic Acids: Field-Based Observations

    Chemists have dozens of boronic acids to choose from, and newer catalog entries pop up all the time. Despite the apparent variety, only certain boronic acids give strong enough performance for regular demand. AMB-HCl stands out from the usual crowd, owing to its stability profile and functional group arrangement.

    In other cases, we’ve handled plain (unprotected) aminophenyl boronic acids, which arrive as hygroscopic powders, degrading within days unless refrigerated or stored with desiccant. Free acids sometimes clump, lose purity, and scatter fine dust, leading to spills or exposure risks for technicians. By contrast, AMB-HCl’s salt form packs cleanly, offering much better shelf life and safety.

    Traditional boronic esters don’t serve in the same way. Pinacol or glycol boronate esters, routine in cross-coupling, trade away reactivity for greater shipping stability. Our compound allows direct use in coupling reactions, skipping pre-activation or hydrolysis steps, avoiding unnecessary solvent usage and cutting down on time-sensitive manipulations in the glovebox or fume hood.

    This difference becomes clear on scale-up. Our process engineers note that AMB-HCl avoids many moisture sensitivity issues. Customers synthesizing hundreds of grams for an early tox lot or scale-up campaign don’t face the same loss ratio or failed reactions that crop up when managing less stable boronic acids. The hydrochloride form mitigates air and water uptake, meaning outside packaging performs an important but secondary role. It simplifies planning for manufacturing, especially in variable humidity or temperature conditions.

    Corporate Responsibility and the Manufacturing Commitment

    Within our operations, every bit of incoming raw material and outgoing product faces scrutiny. Compliance with international standards isn’t just a checkbox—our reputation and the safety of everyone on site ride on it. All hands along the line, from reactor operators to final QA, contribute to a repeatable standard. We pay close attention to regulatory guidance from ICH, REACH, and local agencies, steering us to restrict and track all relevant starting materials.

    Traceability runs deep through our inventory system. Every drum that leaves the warehouse matches full documentation, and we maintain tightly controlled records for years. This effort builds the kind of trust that keeps projects running. Our repeat clients count on us not to cut corners or chase minimal compliance.

    Feedback flows both directions. Process chemists regularly update us with practical challenges in coupling optimization or purification. Their needs push us to refine synthesis, minimize unknown byproducts, and maintain a reliable stock of the highest purity. Minor changes in feedstock or new regulatory thresholds don’t get swept aside—they become the focus of updated SOPs and retraining.

    Environmental Awareness: Improving Methods

    Every gram synthesized generates some degree of waste, so our production goals focus on process intensification and waste minimization. We adapt our synthetic method to require less solvent per kilogram of product, using greener alternatives where possible. Our R&D teams invest in rework protocols to repurpose any rejected lots, extending life cycle value. Washing byproducts out of the main product stream with safer reagents reduces the risk faced by downstream processors.

    Waste collection doesn’t happen out of sight. We allocate floor space to segregate halogenated streams, boronic residues, and cleaning fluids for proper disposal. Each year, updates from environmental agencies compel us to find even better ways to lower our emissions. It’s a challenge, but we recognize chemical manufacturing as a stewardship task as much as a business.

    Shipping and packing materials draw the same care. We select containers and liners that minimize risk of environmental contamination or worker exposure. Adjusting pack size to customer need trims excess waste and prevents chemical aging. By shortening the time from plant to user, less product goes off-spec, and less ultimately reaches waste streams.

    Supporting Advanced Research

    In drug discovery and advanced organic synthesis, details matter. Minor batch-to-batch differences, once ignored, can mean failed experiments or misleading data sets now. Our technical staff keeps open lines with R&D clients, not just for troubleshooting, but to incorporate their suggestions into our manufacturing process. After years supplying AMB-HCl, we don’t just view it as a catalog item—we treat it as a living product that adapts with changing research frontiers.

    The structure of AMB-HCl makes it adaptable. Research groups modifying aryl scaffolds count on the amino and ester functionalities to serve as entry points for further transformations, like amide couplings or selective reductions. The boronic acid function sits at a reactivity sweet spot for many cross-coupling catalysts, avoiding the sluggishness or instability sometimes seen with bulkier or more electron-poor versions.

    Our direct collaboration with project chemists gives us an edge in anticipating demands: whether for solid-state particle distribution, alternate polymorphs, or novel salt forms. Manufacturing consistently at scale requires constant feedback and willingness to adapt routes and processing windows at short notice, all without compromising on final purity or batch reliability.

    Quantities for Every Stage: From Bench to Kilo Lab

    Our facilities scale output to match research needs, from gram vials suited for bench chemistry to kilo lots destined for pilot plants. Larger batches bring unique challenges—mixing, drying, and packing for bulk shipment require more planning than producing dozens of analytical samples. We use direct feedback from kilo run clients to place added controls on residual metals, solvent traces, and long-term shelf life.

    Our instruments monitor every phase, from raw material checks with FT-IR to end-stage particle sizing. Each step shapes the final utility for end users. Often overlooked, final micronization or packing steps can introduce variability; we run additional quality checks to lock in reproducibility. Frequent requalifications keep our standards aligned with evolving customer needs.

    Every bulk user receives a dedicated technical contact, ensuring last-mile issues don’t hamper larger campaigns. If a client requests alternate mesh size, added blending precautions, or specialized anti-static packaging for AMB-HCl, we handle those adaptations in-house. Regular performance reviews and customer audits hold us accountable to the standards we set.

    Supporting Safe and Sustainable Chemistry

    Chemical stewardship means more than a checklist attitude. Our staff undergoes ongoing safety and handling training that covers both established best-practices and updates for new procedural recommendations. We invest in real-world hazard assessment, not just theoretical assessments pulled from databases. Surface cleaning, spill response, and worker PPE controls receive regular scrutiny and hands-on training.

    We also benefit from internal incident reviews, tracking every close call and adjusting protocols. For AMB-HCl, we maintain manufacturing zones with zero-tolerance cross-contamination policies, especially relevant due to the compound’s strong affinity for glass and metal ions.

    Ensuring no cross-contamination from halogenated boronic acid derivatives leads us to dedicate certain glassware, gloveboxes, and transfer lines for exclusive use. Safety interlocks and routine calibration cut down on handling lapses, lowering downstream risk.

    Continuous Improvement and Industry Collaboration

    Real improvement stems from cooperation, not just competition. We talk directly with other manufacturers, academic researchers, and industrial partners to exchange best practices. Participation in standardization efforts pushes us to adopt more precise titration and analytical methods.

    By sending samples for independent testing and validating our QC with external labs, we ensure that our AMB-HCl stands up to scrutiny beyond our own walls. That ongoing transparency builds confidence both internally and throughout the supply chain.

    When sector-wide data points to process improvements—such as reducing environmental byproducts or controlling energy consumption—our engineering team pilots those advancements and rolls them out to production swiftly. Even minor changes to stirring speed or neutralization agents can drive notable gains over long multikilogram campaigns.

    Shaping the Future of Specialty Reagents

    Investment in continuous flow methods, in-line monitoring, and solvent recycling sets the direction of tomorrow’s AMB-HCl output. Research into greener borylation reagents, less hazardous protection groups, and automated drying techniques signals the way forward. We commit to translating those lessons to the production floor and keeping quality high while minimizing resource use and impact.

    Direct relationships with our users encourage us to refine both specification and support tools—whether adopting smarter barcoding, digital batch tracking, or rapid requalification procedures. Success follows from adaptability and a constant eye on end-user realities, not just theoretical metrics.

    Trust from Factory Floor to Research Bench

    Confidence in (2-Amino-4-Methoxycarbonylphenyl)Boronic Acid Hydrochloride endures because it draws from practical control, responsive support, and careful attention to detail, not marketing spin or generic catalog claims. We carry lessons from the plant floor, combine them with chemists’ needs, and shape each drum and bottle to serve real-world goals—reliable synthesis, safe handling, and environmental responsibility.