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(6-Ethoxypyridin-3-Yl)Boronic Acid

    • Product Name (6-Ethoxypyridin-3-Yl)Boronic Acid
    • Alias 6-Ethoxy-3-pyridinylboronic acid
    • Einecs 803-716-6
    • 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
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    Specifications

    HS Code

    992681

    Product Name (6-Ethoxypyridin-3-Yl)Boronic Acid
    Cas Number 1032764-89-4
    Molecular Formula C7H10BNO3
    Molecular Weight 166.97 g/mol
    Appearance White to off-white solid
    Solubility Slightly soluble in water; soluble in organic solvents like DMSO and methanol
    Purity Typically >97%
    Smiles B(C1=CN=C(C=C1)OCC)(O)O
    Inchi InChI=1S/C7H10BNO3/c1-2-12-7-4-3-6(8(10)11)5-9-7/h3-5,10-11H,2H2,1H3
    Storage Conditions Store at 2-8°C, protect from moisture
    Synonyms 6-Ethoxypyridin-3-ylboronic acid

    As an accredited (6-Ethoxypyridin-3-Yl)Boronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing (6-Ethoxypyridin-3-Yl)Boronic Acid, 1g, is supplied in a tightly sealed amber glass vial, labeled with product details for laboratory use.
    Shipping (6-Ethoxypyridin-3-yl)boronic acid is carefully packaged in sealed containers, protected from moisture and light. It is shipped in compliance with relevant chemical transport regulations, typically under ambient conditions unless specified otherwise. Appropriate labeling and documentation accompany the shipment to ensure safe handling and delivery to the destination.
    Storage (6-Ethoxypyridin-3-yl)boronic acid should be stored in a tightly sealed container, protected from moisture and light. Keep in a cool, dry, and well-ventilated area, ideally at 2–8 °C (refrigerated conditions). Avoid exposure to air to prevent degradation, and store away from strong oxidizing agents. Ensure that the storage area is secure and appropriately labeled for laboratory chemicals.
    Application of (6-Ethoxypyridin-3-Yl)Boronic Acid

    Applications of (6-Ethoxypyridin-3-Yl)Boronic Acid in Industrial Manufacturing

    (6-Ethoxypyridin-3-Yl)Boronic Acid enables precision synthesis in modern industrial sectors, playing a crucial role as a coupling intermediate in several advanced downstream processes. Our clients utilize this intermediate to achieve selective connectivity and consistent molecular architecture in high-confidence production environments. Below we detail the application contexts, compliance requirements, optimal incorporation ranges, production steps, and the end-sector finished goods resulting from its industrial integration.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    This substance secures a position in API synthesis, particularly for heterocyclic-based small molecule drug candidates. Its boronic acid functional group participates in Suzuki-Miyaura cross-coupling, allowing medicinal chemists to construct complex pyridine-containing drugs such as kinase inhibitors and neuroactive compounds with controlled regioselectivity. Adoption directly impacts final yield reproducibility and structural purity.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • EU GMP Part II for API manufacturing
    • USP and EP Monograph requirements for impurity profiles
    • FDA 21 CFR Part 211—Pharmaceutical Manufacturing Controls

    Typical usage ratio

    • Used at 1.0–2.5 molar equivalents relative to the halide reactant in cross-coupling steps; amounts adjusted to reactant excess or reaction scale

    Downstream process integration

    • Integrated in the mid-stage synthesis step following nitrogen protection; enters the reactor after palladium catalyst charging and before base addition

    Final product types

    • Synthesized pharmaceutical APIs classified as BCS class I-IV compounds
    • Drug substance intermediates for central nervous system and oncology therapies
    • Research reference standards of drug candidates
    • Advanced intermediates for regulatory submission batches

    2. Agrochemical Active Ingredient Production

    Chemical engineers in the agrochemical industry employ this boronic acid derivative for building substituted pyridine rings key to the structure of next-generation crop protection agents. Its use ensures precision in the manufacture of fungicide, herbicide, and insecticide active substances, with the ability to align with region-specific residue limits and technical grades.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications (JMPS)
    • ISO 9001 Certified process quality systems
    • REACH regulation (EC) No 1907/2006
    • China GB 2763: Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • Applied at 0.8–1.8 molar equivalents relative to halogenated aromatic partners, determined by desired product yield and process impurity control

    Downstream process integration

    • Charged into multipurpose reactors during the key bond-forming steps immediately after base and solvent loading in batch or semi-batch flow

    Final product types

    • Registered actives for use in commercial fungicide SCs and ECs (Suspension Concentrates and Emulsifiable Concentrates)
    • Technical material concentrates for post-synthetic formulation
    • Seed treatment ingredients for integrated pest management
    • Proprietary herbicide intermediates required for patent-protected products

    3. OLED and Advanced Display Material Synthesis

    Materials engineers in the display and electronics industry use this compound as a key building block for constructing conjugated systems in organic light-emitting diodes (OLED) and related displays. Its reactivity in forming pyridine-linked polyaromatic chains directly impacts the efficiency and color range of the final emissive layers, supporting manufacturers’ targets for high yield and precise stoichiometry in molecular electronics.

    Industry compliance standards

    • RoHS Directive 2011/65/EU and amendments on Restriction of Hazardous Substances
    • IEC 61249-2-21: Halogen-free electronic materials
    • ISO 9001:2015 for optical material production
    • JEDEC Standard JESD96 for organic electronic materials

    Typical usage ratio

    • Added at 1.2–2.0 molar equivalents relative to bromo- or iodo-aromatic reactants, tuned for chain extension and device layer thickness design

    Downstream process integration

    • Step-integrated in solution-phase coupling prior to purification and thin-film application; timing adjusted for batch reaction harmonization in pilot or industrial scale

    Final product types

    • OLED small molecules and polymeric light-emitting molecules
    • Pyridine-based host materials for blue and green emitters
    • Charge transport layers for phone, television, and signage display assemblies
    • Precursor molecules for research-grade printable electronics

    4. Specialty Fine Chemical Synthesis for Heteroaromatic Compounds

    Custom synthesis providers and fine chemical manufacturers integrate this reagent for producing structurally-defined heteroaromatic intermediates, often destined for dye, pigment, or specialty laboratory use. The ethoxypyridine structure broadens substitution possibilities, resulting in custom molecules difficult to assemble by alternative routes.

    Industry compliance standards

    • ISO 9001:2015 certified synthesis procedures
    • Responsible Care and ICCA Global Product Strategy adherence
    • REACH registration for new chemical notification and supply within Europe
    • Chemical Facility Anti-Terrorism Standards (CFATS) for US custom manufacturers

    Typical usage ratio

    • Utilized at 1.0–2.0 equivalents versus the reaction partner, with tailoring for batch vs. continuous flow synthesis and final purity target

    Downstream process integration

    • Coupled in cyclization steps or aromatic substitution during the assembly of intermediates with multiple functional groups, prior to isolation and QC

    Final product types

    • Heteroaromatic dye precursors for analytical or textile applications
    • Chromophore intermediates used in sensor and detection devices
    • Chemical building blocks for academic and in-house R&D markets
    • Intermediates sold to contract research and custom synthesis organizations for proprietary uses

    5. API Impurity and Degradation Product Reference Standard Synthesis

    Reference laboratories and pharmaceutical quality control facilities synthesize trace level impurity and degradation product standards incorporating this aryl boronic acid, facilitating regulatory compliance in impurity identification and quantification during routine drug product testing and stability studies.

    Industry compliance standards

    • ICH Q3A/B: Impurities in New Drug Substances/Products
    • US Pharmacopeial Convention (USP) Reference Standard qualification
    • EDQM Certification of Suitability (CEP) requirements
    • ISO/IEC 17025:2017 accreditation for testing and calibration laboratories

    Typical usage ratio

    • Employed at 0.5–1.5 equivalents as needed for the controlled synthetic routes of impurity standards, depending on complexity and specific impurity structure target

    Downstream process integration

    • Initiated in the impurity standard assembly step, entering after main API synthesis route adaptation for targeted isomer or trace variant formation

    Final product types

    • Certified impurity reference standards for HPLC/GC analytical validation
    • Degradation marker standards for stability indicating methods
    • Pharmacopoeia-compendial standards for regulatory dossier submissions
    • Traceable reference compounds for pharmaceutical release and compliance testing
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    Certification & Compliance
    More Introduction

    (6-Ethoxypyridin-3-Yl)Boronic Acid: Advancing Chemical Synthesis with Purpose

    Experience at the Source

    After years working directly with boronic acids, our perspective as the manufacturer is shaped by our hands-on interaction with both starting materials and the finished compounds themselves. (6-Ethoxypyridin-3-yl)boronic acid stands out not through a clever catalog description, but through what it actually delivers on the benchtop. In every batch, we tweak solvent conditions, adjust temperatures, and troubleshoot how trace impurities could affect catalytic performance. Knowing every step from the reactor to the drum gives us a finely tuned sense of this compound’s real-world behavior and value.

    What Defines this Boronic Acid

    This boronic acid, based on a 6-ethoxy modification of pyridine, exhibits properties that set it apart from both its methyl- and unsubstituted pyridine analogs. In simple terms, attaching the ethoxy group at the 6-position suppresses some of the volatility that can frustrate scale-up chemists. The compound’s physical form—a reliable solid with predictable handling—makes it especially amenable for routine or automated dosing. Over the years, this exact product model has become a favorite among medicinal chemists seeking boron-containing building blocks that actually survive real processing conditions.

    The distinguishing feature for people at the bench revolves around how this functional group influences reactivity in cross-coupling reactions. We have found that, compared to its methyl analog, the ethoxy group’s electron-donating nature perks up the ring and shifts the outcomes in some of the more challenging palladium-catalyzed couplings. Process chemists appreciate this because it can mean the difference between a reaction that fizzles out and one that pushes through, especially at larger scales. It’s not simply another reagent, but one that changes synthetic possibilities for those trying to modify pyridine motifs.

    The Manufacturing Perspective

    Fresh quality begins at the earliest synthesis step. Our plant follows the same strict protocols at the kilo lab and commercial scale. Every procedure, whether in glass or steel, is mapped for consistency. In our experience, moisture control is not a theoretical concern—traces of water can destroy a boronic acid’s usefulness before it even arrives at the user’s door. Each lot undergoes rigorous analytical testing, including HPLC and NMR, with in-house benchmarks that go beyond just passing COAs. We pull samples across different points in the batch, not just the end, to track where impurities start to show up or sneak through purification. The extra effort returns in the reproducibility labs report back to us in the field. Authentic traceability built into our process sets our material apart, not as a claim but as a fact we monitor daily.

    From a production engineer’s view, the physical nature of (6-ethoxypyridin-3-yl)boronic acid helps reduce headaches many users report with similar compounds. The powder packs well, flows evenly, and resists the clumping that can frustrate attempts to dispense accurate dosages into reactors. This consistency makes a noticeable difference for formulation chemists and those setting up automated preparation robots. We routinely consult with customers who ran into inconsistent delivery from competing sources—one week their material comes as a fine powder, the next as soggy lumps or sticky chunks. Through direct process adjustments at our own site, we’ve dialed in procedures that give robust flow and stability under a range of transport and storage conditions.

    Synthetic Applications That Matter

    Initially, demand for this boronic acid came mostly from small-molecule pharmaceutical research. Its reliability in Suzuki–Miyaura coupling reactions, particularly those targeting pyridine scaffolds with challenging substitution, led to enthusiastic adoption in high-throughput medicinal libraries. In our ongoing technical dialogues with users, we’ve learned where the compound saves time and money. For example, the ethoxy group’s influence makes it easier to install various functional groups onto the pyridine core without winding up with decomposition or scrambling that plagues similar reagents.

    Over time, its applications broadened to agrochemical development and even some specialty electronic dyes. In every case, the core benefit comes down to consistent cross-coupling efficiency paired with cleaner side-product profiles, which means less downstream purification. Our own R&D teams, applying the compound in both small and pilot plant syntheses, see fewer purification steps and faster throughput on account of better selectivity in the key transformations. Feedback from industrial users led us to revisit our purification process, cutting out contaminants that would otherwise cause headaches in subsequent reactions.

    Formulation and Integration

    Solid handling and compatibility with a spectrum of standard solvents make our (6-ethoxypyridin-3-yl)boronic acid friendly to a variety of synthetic methods. Our production staff spends real time dialing in the moisture content. Powder falls within a narrow window, neither too dry (causing dust) nor too moist (leading to clumping), reducing waste and cleanup. Consultants tell us this has given them better downstream yields by avoiding “hot spots” of reactivity or uneven dissolution in solution-phase chemistry. This is not a boast, but repeated feedback from scientists working with the actual lots.

    Unlike some boronic acids that degrade quickly, especially in the presence of trace acids or heat, our product withstands the short-term exposures typical of routine handling routines. Years coordinating with shipping logistics have prompted us to design packaging that resists ingress from humidity during transit, another point of real-world difference against less carefully prepared material sold by bulk traders or repackagers.

    Reliability in Scale-up and Automation

    From a manufacturing point of view, scale brings new challenges. Smaller lots that work in a research lab do not always translate seamlessly to multiple-kilogram reactor runs. (6-Ethoxypyridin-3-yl)boronic acid sidesteps some of the surprises with good shelf stability and batch-to-batch uniformity. We regularly support pilot plant campaigns where even small blips in physical form or impurity content can ripple out into lost days and extra costs. Our technical staff, including those with deep experience in process chemistry, has put time into working out protocols that forecast issues before they hit the customer’s facility.

    In discussions with automation specialists, we see how demanding robots are about granule size and powder free flow. Variable powder quality causes jams, bad dosing, or screen clogging. Over the years, we worked with in-house and customer teams to optimize particle size distribution, improving consistency for both manual and automated workstations. Real-world experience, not catalog marketing, drives these decisions. Our team gets regular feedback from repeat industrial users—comments about reduced downtime and fewer cleaning stops came only after shifting to our consistently controlled supplies. These improvements stem from hands-on engineering solutions, not theory.

    Comparisons: What Sets (6-Ethoxypyridin-3-yl)boronic Acid Apart

    People familiar with boronic acids know that pyridine-based varieties often introduce headaches in both storage and application. The addition of the 6-ethoxy group, as seen in our material, distinguishes it sharply from standard pyridin-3-yl boronic acids. This structural detail produces real effects, not just on the reactivity but also on how the compound behaves in storage. We’ve cross-compared in-house and competitor materials; our boronic acid’s performance holds up even after months in controlled storage. By contrast, unsubstituted pyridinyl boronic acids from other sources sometimes dissolve into sticky residues or degrade after repeated opening of the package.

    We are often asked about differences between this compound and its close relatives, such as the 5- or 2-ethoxypyridine variants. Our research revealed that both the position and electronic properties of the ethoxy group strongly affect the kind of bonds users can form through Suzuki coupling as well as the tendency towards protodeboronation—a common side reaction that eats up precious material in longer syntheses. In contrast to other positions, the 6-ethoxy group tempers this unwanted reactivity, reflecting in noticeably better recoveries in gram to kilogram runs.

    In every real-world test against similar commercial products, including common methylpyridin-3-yl boronic acids, our (6-ethoxypyridin-3-yl)boronic acid turns out purer coupled products with fewer chromatographic headaches. This is supported not just by laboratory analysis but by repeated user reports after multistep, diverse process chains. Clean output pays off in lower purification costs and higher overall yields for those scaling up.

    Supporting Sustainable and Repeatable Chemistry

    Long-term consistency matters for repeat campaigns. We track feedback from users seeking sustainable processes with fewer rejects and cleaner mother liquors. From our viewpoint as the original producer, only rigorous attention to raw material control and reaction environment delivers the batch consistency research and production teams depend on. Our facility owners and operators track real-time data from every production lot, so we can back up each shipment with auditable records. This puts direct responsibility and traceability on our shop floor—something traders and resellers simply cannot replicate.

    The increasing move towards green chemistry relies on high-purity, stable reagents that minimize waste downstream. We’ve worked with environmental engineers to tune purification and solid handling systems, steadily reducing solvent losses and VOCs in our own operations. Our clients in regulated industries, especially pharmaceuticals and high-end materials, return year after year because every lot matches or exceeds prior delivery. That kind of reliability stems from manufacturing discipline, something only a hands-on chemical producer can sustain.

    Meeting New Challenges and Demanding Purity

    New synthetic targets require not just strict purity but careful consideration of trace metals, residual solvents, and process breadcrumbs that may compromise a reaction or regulatory acceptance. Users, especially those in regulated markets, demand open data about residual metals, particle size range, and solvent residues. Teaming with downstream partners, we deploy ICP-OES, residual solvent screening, and impurity fingerprinting on every production run. Our analytical chemists collaborate with external QC labs to cross-check findings, ensuring users do not uncover surprises after delivery.

    Process innovations come directly from addressing recurring pain points that only reveal themselves in actual use. As original manufacturers, we gather technical feedback, then loop it directly back into continuous improvement. By actively engaging with customer challenges, we develop not just products, but solutions that simplify how laboratories and plants run. If there’s ever an off-spec result, our technical services team, loaded with practical experience, attacks the problem at the molecular and operational level—no passing the buck to a nameless upstream source.

    Looking Forward: Keeping Innovation Real

    Every kilogram we produce ties back to workflow improvements and synthetic wins that our customers achieve. From method scouting in early research to pilot plant optimization, (6-ethoxypyridin-3-yl)boronic acid delivers quantifiable results. Even as new boronic acids enter the market, we see persistent demand for this structure thanks to its blend of physical manageability and reaction performance. Advances in catalyst technology continue to make its use more widespread, but it is our job to keep refining supply and reliability so chemists aren’t caught out by avoidable variability.

    Experience shows that only through ownership of the entire process can a supplier bring the real-world knowledge required to solve user problems before they escalate. Each year, increased expectations for sustainability, legal compliance, and process resilience refine the standards of manufacturing required. By directly controlling every step, from precursor sourcing to drum filling, we can respond both to regulatory shifts and to new demands like digitized supply chain traceability or stricter analytical verification. Our team stands ready to make incremental, real-world driven upgrades based on what shows up in the reaction flask, not just what makes it into a PowerPoint.

    What Our Hands-on Involvement Brings Users

    There’s no substitute for getting your gloves on a product batch. Direct experience at the reactor bank, regular sampling, process tweaking—these steps yield a final product that brings peace of mind to chemists and production managers alike. Our real-world perspective means our insights touch actual process variation, seasonal environmental quirks, and operator habits—factors missed by plug-and-play distributors. In side-by-side user trials, our lots are called out for their reproducibility, hassle-free handling, and, most of all, reaction success.

    By investing in both materials science and client relationships, we keep ahead of routine supply challenges and shifting technical standards. As a manufacturer, we know that each decision made in our facility echoes downstream. We invite every user to engage directly with us, not just so we can deliver reliable supplies, but so we can learn and adapt with the practical needs of every chemistry project our product powers.