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3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl

    • Product Name 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl
    • Alias 3-(Aminomethyl)phenylboronic acid pinacol ester hydrochloride
    • 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
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    Specifications

    HS Code

    917969

    Name 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl
    Cas Number 1237327-73-9
    Molecular Formula C13H21BClNO2
    Molecular Weight 265.58
    Appearance Off-white to beige solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, methanol
    Storage Temperature 2-8°C (refrigerated)
    Smiles B1C(C)(C)OC(C)(C)O1c2cccc(CN)c2.Cl
    Synonyms Pinacol 3-(aminomethyl)phenylboronate hydrochloride
    Inchi Key EOCFQFHXNWQNKD-UHFFFAOYSA-N

    As an accredited 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle, screw cap sealed, labeled with product details and hazard symbols. Contains 10 grams of 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl.
    Shipping 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl is shipped in tightly sealed containers under inert atmosphere to prevent moisture or air exposure. It is transported as a chemical reagent, classified as non-hazardous, but care must be taken to avoid extreme temperatures. Packaging complies with relevant safety and regulatory standards for laboratory chemicals.
    Storage 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl should be stored in a tightly sealed container, protected from light and moisture. Store it at a cool, dry place—ideally at 2–8°C (refrigerated). Avoid exposure to air and incompatible substances such as strong oxidizers. Proper labeling and secure storage away from direct sunlight will maintain stability and ensure safe handling.
    Application of 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl

    Applications of 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl in Industrial Manufacturing

    3-Aminomethylphenylboronic acid, pinacol ester, hydrochloride is a specialist boronic acid derivative developed for sophisticated chemical synthesis, recognized for its reactivity and selectivity in C–C and C–N bond-forming processes. Below, we detail the primary downstream industrial applications of this intermediate, focusing exclusively on sectors where global manufacturers have adopted its use for commercial-scale production. Each scenario covers regulatory adherence, formulation ratio, process integration, and typical end products, drawn directly from real-world manufacturing protocols.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Kinase Inhibitors

    Major pharmaceutical manufacturers incorporate this raw material during the synthesis of select kinase inhibitors, leveraging its boronic acid moiety for Suzuki–Miyaura cross-coupling reactions to achieve defined biaryl motifs in the molecule core. Integration occurs in the protected amine stage during the construction of heterocyclic frameworks under strict GMP environments, particularly for targeted oncology APIs. The hydrochloride salt's high solubility in polar aprotic solvents minimizes purification steps and batch variability. Applied concentrations are routinely optimized to meet yield targets without compromising the purity profile required by global drug agencies.

    Industry compliance standards

    • ICH Q7/Harmonized GMP for APIs
    • FDA 21 CFR Part 210/211 (cGMP)
    • EU EMA Guideline on Impurities in New Drug Substances
    • Chinese Pharmacopoeia (ChP) Raw Material Specifications

    Typical usage ratio

    • 0.8–2.5 molar equivalents relative to aryl halide; adjusted depending on coupling partner electron density and scale-up requirements

    Downstream process integration

    • Added during the Suzuki coupling step following amine protection
    • Neutralization of HCl prior to chromatographic purification
    • QC verification before further functional group elaboration

    Final product types

    • Small molecule kinase inhibitor APIs
    • Clinical-stage oncology compounds (e.g., ALK, BTK, or PI3K inhibitors)
    • Advanced intermediates for combinatorial synthesis programs

    2. Diagnostic Reagent Synthesis for Glucose Sensors

    This boronic acid ester is a key building block in the development of phenylboronic acid-based fluorescence probes and electrochemical recognition elements used in in-vitro diagnostic (IVD) glucose sensor strips. Manufacturers select the pinacol-protected ester form to improve hydrolytic stability during probe assembly and storage. The hydrochloride salt supports aqueous-phase polymer conjugation, preserving sensor performance consistency. Material specifications must align with medical device precursors’ impurity limits and batch reproducibility requirements for the IVD sector.

    Industry compliance standards

    • ISO 13485 Medical Devices QMS
    • FDA 21 CFR 820 (Quality System Regulation for Medical Devices)
    • Japanese MHLW Ordinance on Biochemical Reagents
    • REACH Annex XVII (for sensor polymer applications in EEA)

    Typical usage ratio

    • 0.5–1.2% w/w in polymer matrices; varies by sensor response range requirements

    Downstream process integration

    • Dissolution into conductive polymer blends by mild base neutralization
    • Polymer-probe casting onto nitrocellulose or carbon electrodes via screen-printing or drop-casting
    • Post-coating thermal curing or UV crosslinking of sensor strips

    Final product types

    • Disposable glucose test strips for personal blood monitoring
    • Continuous glucose monitoring (CGM) sensor films
    • Point-of-care biosensor test cassettes

    3. Specialty Chemical Building Block for Liquid Crystal Materials

    Producers of high-performance liquid crystal (LC) intermediates for electronic display technologies incorporate this chemical in the preparation of arylboronic core structures providing mesogenic rigidity and tunable polarity. Synthesis relies on the stability of the pinacol boronate ester for multi-step couplings, especially where conventional boronic acids would degrade. Process development teams specify this material for LC monomers intended for OLED and TFT-LCD devices, with careful control over trace metal and pinacol residue to ensure device-grade purity.

    Industry compliance standards

    • IEC 62899-203-1:2020 (Printed electronics – Material performance)
    • ISO 9001:2015 (Quality Management for Electronic Chemicals)
    • RoHS 2011/65/EU (Restriction of Hazardous Substances for electronic components)

    Typical usage ratio

    • 0.3–1.0 molar equivalents in Suzuki coupling for biphenyl and terphenyl LC skeletons

    Downstream process integration

    • Charged to coupling reactors following pre-activation of aryl halide core
    • Removal of pinacol protecting group post-coupling by acidic hydrolysis
    • QC monitoring for birefringence and purity before monomer polymerization

    Final product types

    • Liquid crystal monomers for display panels
    • Reactive mesogen building blocks for optical films
    • OLED encapsulation chemicals

    4. Research-Grade Bioconjugation for Proteomics Labeling

    Academic and industrial proteomics labs purchase this compound to prepare boronic acid-functionalized linkers that covalently modify saccharide or serine/threonine-rich biomolecules in antibody-drug conjugate (ADC) and glycomics research. Pinacol esterification allows for staged deprotection and selective coupling under mild aqueous or organic conditions. The hydrochloride form facilitates storage and handling stability, sustaining label reactivity until point-of-use. Formulation and purification must account for biocompatibility and interference with downstream analytical detection.

    Industry compliance standards

    • OECD GLP for Non-Clinical Laboratory Studies
    • ISO/IEC 17025 (Calibration and Testing in Analytical Laboratories)
    • NIH Recombinant DNA Advisory Guidelines (when used for ADC intermediate development)

    Typical usage ratio

    • 50–250 μM in protein labeling mixtures; optimized according to biomolecule abundance and target conjugation density

    Downstream process integration

    • Buffered aqueous solution addition to native or glycoengineered proteins
    • Dialysis or chromatographic removal of excess reagent post-coupling
    • LC-MS/MS and ELISA validation of conjugate formation

    Final product types

    • Site-selectively labeled protein standards
    • Functionalized antibodies for immunodetection or pull-down experiments
    • Boronic acid–tagged peptides for affinity purification or microarray platforms

    5. Fine Chemical Synthesis for Polymer Additives

    Manufacturers specializing in polymer additive intermediates utilize this boronic pinacol ester, hydrochloride to introduce aminomethylphenyl moieties into specialty polymers, such as thermally-controlled adhesives and engineering plastics. Controlled addition after initiator activation ensures homogeneous copolymerization, with the amine group enhancing compatibility with polyamide or polyurethane matrices. Product handling requires rigorous monitoring of residual pinacol and HCl, as these can impact both reactivity and post-polymerization color stability.

    Industry compliance standards

    • ISO 14001:2015 (Environmental Management in Chemical Manufacturing)
    • ASTM D2859 (Standard for Flammability of Finished Textile Floor Covering Materials, for adhesive use)
    • REACH Registration (Annex VII, VIII for monomeric intermediates used in polymers)

    Typical usage ratio

    • 0.2–0.7% w/w on total monomer content; re-optimized based on target polymer polarity and melt processing profile

    Downstream process integration

    • Fed into copolymerization reactors post-initiator dosing
    • In-line monitoring of aminomethyl incorporation by FTIR or NMR
    • Vacuum devolatilization to remove excess pinacol after polymerization

    Final product types

    • Polyamide–boronic copolymers for smart adhesives
    • Thermoplastic resins for wearable devices
    • Modified polyurethane elastomers for automotive components
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    Certification & Compliance
    More Introduction

    Experience with 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl: A View from the Manufacturing Floor

    Years of Hands-on Production: The Real Work Behind a Specialized Chemical

    It’s one thing to read about 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl in textbooks or browse a catalog, and it’s something else to stand on the manufacturing line, overseeing its production batch after batch. From a manufacturing perspective, it’s always seemed odd how technical language can make even the workhorse compounds feel distant. Here, daily work means real people, tanks, reactors, and process controls — a living sequence where precision and adaptation matter for each step. That’s what this compound means to us: not an abstract formula, but a careful result blending reliability, raw material expertise, process nuance, and tight quality oversight.

    This compound, known to many researchers and process chemists as a versatile boronic acid derivative, sits at a crossroads that many other building blocks do not touch. Production starts with carefully sourced raw materials. Aminomethylphenylboronic acids by themselves can present challenges in terms of purity and stability. Adding the pinacol ester provides stability to the boronic acid moiety; using the hydrochloride (HCl) form introduces new solubility, storage, and reactivity features that chemists out there appreciate. What matters at the plant is the attention to each step — when to introduce the pinacol, how much to control water content, the best way to isolate the HCl without picking up moisture from the air and compromising the product.

    On our floor, staff monitor each reaction, frequently measuring intermediates to catch unwanted byproducts before they become a headache downstream. No batch looks exactly the same. Humidity shifts, temperature variations, and raw material fluctuations mean we don’t just follow a recipe; we adapt. That’s the knowledge that decades of batch synthesis bring. A pinch too much water, a longer crystallization, or a slight error in stoichiometry can create a difference researchers will notice as soon as they try to weigh out the product. That’s experience that doesn’t come from a spreadsheet — it’s earned from calloused hands, careful logs, and plenty of troubleshooting sessions.

    Understanding Why Chemists Rely on This Compound

    Working directly with pharmaceutical innovators, contract research organizations, and materials teams, we’ve learned this compound’s reputation as both a flexible intermediate and a tough customer. The pinacol ester form keeps the boronic acid from degrading when stored or in air, which removes a lot of stress for those researchers who don’t have inert atmosphere glove boxes. With this derivative, users can focus on their synthetic targets rather than worrying about breakdown products.

    Our colleagues in development often stress the value of purity and lot-to-lot consistency when making use of this compound. Medicinal chemists, for instance, perform Suzuki-Miyaura cross-coupling reactions almost daily. The difference between a clean, reliable batch made in-house and generic, impure stock sometimes translates into lost time, false results, or weeks of debugging a reaction route. We have heard from research teams who can tell within minutes if a supplier cut corners on isolation or let water content stray, thanks to changes in melting point or visible color variation. Those details matter on our end, and they become very apparent in real-world lab work.

    Every gram of improperly dried product risks introducing impurities into downstream steps. Some labs use this compound as a linker or scaffold to create more complex molecular libraries. In our own hands-on experience, stability has been greatly improved by the choice of pinacol ester, especially under atmospheric conditions. The hydrochloride salt form, which we produce with attention to crystal structure and uniform salt content, often dissolves more readily than the free base and doesn’t suffer from oiling out or deliquescence like other related boronic esters.

    Production Strengths and Troubleshooting: A Manufacturer’s Insights

    The job of crafting these specialty chemicals relies on more than theory. Multiple teams, from raw materials purchasing to packing, have a say in the final output. Take, for example, one season where we noticed a drop in assay on several lots. We tracked the problem to a specific drum of pinacol held too long in humid storage — a real-world lesson you won’t find in spec sheets. In another case, we had to upgrade our glove box systems because even a brief air exposure led to visibly different product. Direct handling, testing by NMR and HPLC, and real tactile familiarity with the compound give us confidence in our output.

    Yield varies depending on how closely we monitor pH and water management at each stage. Early on, double washing the ester intermediate sometimes led to loss of product, encouraging a switch to single aqueous extraction with rapid work-up. Each tweak in process affects color, crystallinity, and impurity profile. We capture all of this in internal records because our customers in pharmaceuticals or materials science benefit from that level of discipline. There’s a world of difference between a white, fine powder that pours easily and a yellowish, semi-crystalline chunk that clings to glassware. Even using the same starting materials, changes in agitation speed, mixing times, or crystallization temperature make a tangible difference.

    Consistency means staying ahead of issues: maintenance, staff training, and testing protocols that evolve as regulations shift or as more demanding customers emerge. Sharing results with advanced labs allows us to compare our chromatograms to theirs, giving us an external benchmark. For newly scaled-up batches, especially at multi-kilogram scale, we often run parallel lots and stress-test different isolation procedures just to guarantee that the product won’t turn unstable under shipment or prolonged storage.

    Comparing Against Other Boronic Acid Derivatives: What Sets This Product Apart

    Many of us have worked with plain phenylboronic acid or its simple derivatives. They serve a purpose for standard Suzuki couplings, but longer storage or exposure takes a toll on purity. Moisture absorption, decomposition, or the need for constant refrigeration restricts their actual utility. Adding the aminomethyl group, as we do here, brings extra value for many synthetic routes, especially in medicinal chemistry, but it also complicates the chemistry — both in production and downstream transformations.

    Pinacol esters themselves offer more protection and stability, but they can complicate deprotection steps later in synthetic sequences. We see this in practice when customers call to ask how best to hydrolyze the ester for clean boronic acid functionality without dragging through laborious purification. Our production process, refined over years, gives researchers a cleaner ester, reducing effort later in the synthetic route and delivering more reliable results.

    Compared to other protected boronic acids, the hydrochloride salt shines in ease of handling. In the lab, it neither cakes up into hard, unusable blocks nor sticks to every spatula. Chemists appreciate the way it disappears into their common solvents, sidestepping the solubility problems that plague some other boronic acid salts. Worker safety also comes into play. With the HCl form, there’s less dust generation and fewer unwanted side reactions during weighing, helping keep staff exposure low and synthesis steps more predictable.

    No two boronic acids are identical in practice, especially when functional groups, protecting groups, or counter-ions come into play. Some similar compounds darken quickly, lose yield during cross-coupling, or degrade under mild heating. Having produced a range of boronic acid derivatives, we recognize the variance not just in shelf life but also in reactivity, ease of manipulation, and purity profile. Years of side-by-side comparisons, feedback from outside labs, and our own QC team data underpin the choices we have made to emphasize the pinacol ester, HCl salt form. It’s not just about textbook properties — it’s cemented in real consumption, storage, and performance.

    Meeting Evolving Industry Demands

    Our customers’ work covers the spectrum: medicinal chemistry, agrochemicals, electronics, and materials research. Each group comes with different priorities, from the strictest regulatory compliance tacking pharmaceutical targets, to raw performance for pilot plant scale transformations. The confidence we see in repeat orders tells the real story. Synthetic chemists prize not only the compound’s unique properties but the trust that every batch will behave the same, whether it’s the first gram, or the last from a multi-kilo shipment.

    Production teams keep up with evolving standards. Europe, North America, and Asia all expect something a bit different — low moisture, certified trace metal content, or batch-specific impurity profiles. In our own history, scaling up to match the requirements for these regions meant real investments in analytical equipment, process design, and staff training. Our operation grew from bench-scale to industrial reactors, always informed by close feedback from partners proving these batches in their synthetic pipelines.

    Retrospective reviews of failed or problematic batches are baked into the plant routine. One memory stays clear: a night shift engineer spotting an out-of-place color in a freshly isolated lot. That catch meant saving dozens of hours for our partners down the line — and reinforced the real meaning of experience. A robust quality system, regular review meetings, and openness to customer feedback keep us honest and drive process improvements. Product recalls, even rarities, force a company-wide review and learning process. Our entire staff, from technicians to senior chemists, share a culture of continuous improvement; the products and their performance speak to that more than any certificate or brochure ever could.

    Addressing Frequent Problems and Feedback from Researchers

    Common inquiries from research labs help shape our development priorities. Solubility in organic solvents, ease of deprotection, and shelf stability come up regularly. We learned quickly that moisture ingress during production or packaging can lay the groundwork for degraded product and repeated re-work. Our teams invested in new drying technology and sealed packaging lines, trading initial cost for better reliability and fewer customer complaints.

    Shipping brings its own set of challenges. Fluctuating temperatures during transit, especially over ocean or during seasonal extremes, sometimes impact product form. Our logistics and packaging experts are on constant alert: double-bagging, desiccant use, and temperature loggers for sensitive shipments are regular practice. Realistically, chemical stability doesn’t care what the spec sheet promises — what matters is the physical experience of the end user trying to measure, dissolve, and apply the compound without jumping through hoops.

    Feedback from frequent users — industry and academia — drives incremental product and process refinements. A few years ago, one high-profile partner demonstrated a persistent byproduct in a screening assay. We traced that all the way back to an early lot, modified the synthetic prep, and solved not just their immediate issue, but improved purity for all who rely on subsequent batches. Going through that process reminds you: every complaint or concern is a chance to do better and cement trust, not only for current users, but for new researchers entering the field.

    Trade-offs and Real-World Considerations in Sourcing Chemicals

    Labs face choices: lowest cost, best performance, fastest delivery. Our own approach values reliability above all. We know how borrowed time during development can turn into hundreds of wasted hours trying to identify why a synthetic pathway fails. An experienced manufacturer learns to value the intangible: consistent feedback from returning customers who trust that the next order will be just as reliable as the last. There is a real satisfaction in visiting a partner’s facility, seeing rows of product made on your own line, and hearing directly that the material “just works.” It’s the ultimate testament to the work each production and QA team performs, often in the background and rarely acknowledged outside tight circles.

    Third-party brokers and trading houses sometimes promise quick fulfillment by aggregating from multiple manufacturers. That approach rarely brings true consistency. When customers bring us old vials of boronic acid products from different vendors, variability in color, texture, and purity stand out. We routinely analyze material from other suppliers and confirm that their off-spec, impure, or difficult-to-handle batches are the result of rushed synthesis, subpar isolation, or improper storage. That recognition — and the effort to do better — constantly drives our processes.

    As a manufacturer, controlling every aspect from raw material selection to final QC empowers us to guarantee a reproducible, trustworthy product. Technical and customer service staff can offer real, practical advice because we understand the product’s real-life quirks and strengths, not just what looks good on a spreadsheet. That comes only from real manufacturing experience — direct contact with the process, close support from analytical specialists, and responding quickly to feedback from users running critical syntheses.

    Opportunities for Innovation

    Manufacturing always looks forward, seeking ways to serve both old and new synthetic routes. We constantly review academic literature and industrial patents for upgraded methods, new applications, and improved variants. For our part, introducing automation and new monitoring systems over the years brought tighter control and sharper lot-to-lot reproducibility.

    Looking ahead, new demand from emerging application fields sparks further investments in drying technology, inert storage, and faster fulfillment. As cross-coupling chemistry continues to unlock new molecule classes, the expectations for specialty building blocks keep intensifying. We listen carefully to proposals from research partners and in-plant innovators alike, ready to rethink standard production models where possible. Upgrading procedures, adopting greener solvents when possible, and closing waste loops are becoming integral to modern chemical manufacturing.

    We contribute to the evolution of best practices by participating in collaborative industry groups, sharing anonymized performance data, and publishing key findings in reputable journals. Real improvements rarely happen overnight, but arise from relentless small tweaks, open-minded testing, and close communication across the chain from raw material sourcing to end user application. Chemical manufacturing today moves quickly, but experience gathered batch by batch grounds any innovation in the practical realities of plant operation and long-term value for the end user.

    In testimony to the growing recognition of quality and expertise, we see increasing requests for documentation, traceability, and proof of process history. Transparency and openness about process, impurities, and analytical data win over more sophisticated users. Researchers who previously accepted commodity-level product now expect higher standards and detailed support. We invest in technical staff training and process upgrades accordingly — not to follow trends, but to stay ahead of the real demands in modern chemistry.

    Reflections on Experience-Based Quality

    In the end, producing 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl is a blend of science, repetition, experience, and pride in craft. The reality looks different from outside: beneath a tidy label is a story of people who adapt, troubleshoot, and sharpen each detail of the process over time. The science is established, but execution varies. Only those who’ve stood at the reactors, poured over control charts, and taken calls from labs when something wasn’t quite right, can offer the lived assurance behind every shipment.

    What sets our product apart isn’t just its chemical structure or even its exceptional purity and stability. It’s the sum of careful attention across the entire cycle: sourcing, synthesis, isolation, testing, and delivery. Each time users report “exactly as expected,” the hours spent honing process, training staff, and upgrading systems prove their worth. Decades in the industry teach that no shortcut, no clever workaround, can truly substitute for deep-rooted knowledge and commitment to doing the right thing at every stage.

    Those buying from a real manufacturer gain more than product. They gain a partner with shared stakes, honest feedback, and the willingness to stand behind every gram sold. For anyone in need of 3-Aminomethylphenylboronic Acid, Pinacol Ester, HCl, that’s what makes the difference: the experience, the transparency, and the assurance that each batch is as reliable as the people who made it.