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2-Acetylaminophenylboronic Acid Pinacol Ester

    • Product Name 2-Acetylaminophenylboronic Acid Pinacol Ester
    • Alias AAPBPE
    • Einecs 638-798-9
    • 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

    360184

    Product Name 2-Acetylaminophenylboronic Acid Pinacol Ester
    Cas Number 870803-81-1
    Molecular Formula C14H18BNO3
    Molecular Weight 259.11
    Appearance White to off-white solid
    Melting Point 104-110°C
    Purity ≥ 98%
    Storage Temperature 2-8°C
    Solubility Soluble in organic solvents (e.g., DMSO, dichloromethane)
    Smiles CC(=O)Nc1ccccc1B2OC(C)(C)C(C)(C)O2
    Synonyms Pinacol 2-acetylaminophenylboronate
    Application Suzuki-Miyaura coupling reactions
    Sensitivity Moisture Sensitive

    As an accredited 2-Acetylaminophenylboronic Acid Pinacol Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 2-Acetylaminophenylboronic Acid Pinacol Ester, sealed with a screw cap, labeled with product details.
    Shipping 2-Acetylaminophenylboronic Acid Pinacol Ester is shipped in tightly sealed containers to protect against moisture and air exposure. It is packed with cushioning materials and clearly labeled as a laboratory chemical. Shipping typically occurs via ground or air transport, with adherence to safety regulations for chemical handling and temperature stability.
    Storage 2-Acetylaminophenylboronic Acid Pinacol Ester should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerator). Avoid exposure to air and strong oxidizing agents. Store away from incompatible substances to maintain chemical stability and ensure safety during handling.
    Application of 2-Acetylaminophenylboronic Acid Pinacol Ester

    Applications of 2-Acetylaminophenylboronic Acid Pinacol Ester in Industrial Manufacturing

    2-Acetylaminophenylboronic Acid Pinacol Ester serves as a specialized building block in advanced chemical synthesis and is valued in industrial manufacturing for its consistent reactivity and defined purity. As the actual manufacturer, we deliver this raw material to established downstream sectors with stringent quality and compliance requirements. The following application sections provide detailed insight into real-world use, from synthetic pharmaceutical intermediates to specialty material production, illustrating exact compliance standards, recommended dosage ranges, integration points within processing lines, and the final products achieved.

    1. Pharmaceutical API Intermediate Synthesis

    Leading pharmaceutical producers use this boronic ester in the production of kinase inhibitors and other targeted small-molecule APIs, where its boron-centered reactivity supports Suzuki-Miyaura coupling during late-stage functionalization. Its input at this stage enables scalable modifications of aromatic rings while maintaining strict impurity control, supporting compliance with region-specific cGMP systems for high-purity drug candidates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use
    • Chinese Pharmacopoeia (CP) for Intermediate Purity and Residual Solvents

    Typical usage ratio

    • Generally used at 0.5–3.0 mol% relative to aryl halide substrate; optimization depends on the complexity of the synthetic route and coupling efficiency.

    Downstream process integration

    • Added during the palladium-catalyzed Suzuki cross-coupling step after halogenated intermediate preparation and prior to final deprotection/purification units.

    Final product types

    • Active Pharmaceutical Ingredients (APIs) including selective kinase inhibitors and heteroaryl compounds
    • Advanced pharmaceutical intermediates with tailored functionality

    2. Diagnostic Molecule Synthesis (Fluorescent Probes & Imaging Agents)

    Manufacturers of bioanalytical reagents and medical diagnostics employ this boronic acid ester structure to prepare fluorescent tags and sensors that react specifically with saccharide or diol-containing systems. Its addition ensures the generation of high-affinity probes suitable for quantitative bioassays, while production lines must conform to traceability and low-endotoxin standards found in clinical testing supply chains.

    Industry compliance standards

    • ISO 13485 Quality Management Systems for Medical Devices
    • CLSI GP44 Analysis and Preparation of Reagents in Clinical Laboratories
    • REACH (EC 1907/2006) and RoHS where product may enter EU diagnostic markets
    • USP General Chapter <1047> Testing for Endotoxins

    Typical usage ratio

    • Use level typically at 0.2–1.5 mol% in conjugation reactions; proportion varies with probe scaffold and desired signal intensity.

    Downstream process integration

    • Introduced during the boronate ester condensation step following labeling dye activation, prior to purification and lyophilization stages for stable, ready-to-use reagents.

    Final product types

    • Near-infrared and fluorescent molecular probes for biological assays
    • Saccharide-sensitive biosensors and clinical imaging agents
    • Ready-prepared diagnostic kits

    3. Agrochemical Intermediate Manufacturing

    Producers of crop protection agents integrate this raw material in the synthesis of boron‐modified heterocyclic compounds. Its role in coupling reactions enables designers to optimize plant selectivity and metabolic stability in new agrochemical candidates, demanding process controls to align with regional chemical safety regulations.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for Agrochemical Development
    • Regulation (EC) No 1107/2009 (Market Authorization of Plant Protection Products in the EU)
    • China National Standard GB 2763 (Residue Control on Edible Crops)
    • FAO/WHO Specifications for Pesticides

    Typical usage ratio

    • Employed at 0.5–2.5 mol%, selected based on the molecular structure of the target pesticidal active and catalyst turnover observed in pilot trials.

    Downstream process integration

    • Combined with halogenated aromatics in high-throughput coupling reactors, post-initial aromatic halogenation or acylation, before further functionalization and formulation.

    Final product types

    • Crop protection agents such as boron-containing herbicides and insecticides
    • Selective fungicide intermediates

    4. Synthesis of Functional Polymers for Electronic Materials

    Chemical engineers in the electronics sector utilize this boronic ester in controlled polymerization steps to construct π-conjugated systems and organic semiconductors. The compound is vital for tuning polymer backbone structure and electrical properties, integrating into batch processes that adhere to electronic-grade material standards with high reproducibility requirements.

    Industry compliance standards

    • EIE/IEC 61249-2-40 Standard for Materials Used in Printed Circuit Boards
    • ISO 9001:2015 Quality Management Systems
    • IPC-4101D Laminate/Prepreg Material Specifications
    • RoHS 2011/65/EU (Restriction of Hazardous Substances)

    Typical usage ratio

    • Added at 1.0–4.0 mol% depending on the desired degree of polymerization and electrical conductivity targets for the final polymer chain.

    Downstream process integration

    • Fed into cross-coupling reactors during the monomer synthesis stage, preceding chain propagation and molecular weight adjustment in high-shear or continuous flow polymerization units.

    Final product types

    • Organic semiconducting polymers for flexible displays and solar cells
    • Functionalized resin systems in advanced circuit board manufacturing
    • Hybrid materials for OLED device production

    5. Synthesis of Specialty Fine Chemicals (Dye and Pigment Precursors)

    Producers of high-performance dyes integrate this boronic ester in regioselective modifications to aromatic precursors, permitting unique chromophore generation for specialty colorants. This application demands full traceability and conformance to international environmental and colorant safety standards, with manufacturing calibrated to precise shade and purity targets.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System for Fine Chemicals)
    • REACH (EC 1907/2006) Registration for Industrial Dye Components
    • ETAD Code of Practice for Manufacture and Marketing of Dyes
    • OEKO-TEX Standard 100 for Textile Applications (where applicable)

    Typical usage ratio

    • Standard usage falls within 0.4–2.0 mol% based on final coloration intensity and intermediate stability requirements.

    Downstream process integration

    • Incorporated during the key aryl coupling sequence, typically after chromophoric core preparation but before metal complexation or sulfonation.

    Final product types

    • Azo and anthraquinone dyes for technical and textile applications
    • Pigment precursors for inkjet inks and specialty coatings
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    Certification & Compliance
    More Introduction

    Introducing 2-Acetylaminophenylboronic Acid Pinacol Ester: Enhancing Synthesis with Reliable Building Blocks

    Our Perspective on 2-Acetylaminophenylboronic Acid Pinacol Ester

    In the world of synthetic chemistry, every step relies on quality starting materials. Our hands-on production of 2-Acetylaminophenylboronic Acid Pinacol Ester (model: 2-AAPBAPE) speaks to the way we approach fine chemical manufacture: real materials in real reactors, guided by real process experience. The conversation around organic synthesis often circles back to the reliability and consistency of the core building blocks. With this compound, we meet a demand that doesn’t slow down, whether it’s a graduate student at the bench or a team in a production plant working toward a new class of molecules.

    Specifications Shaped by Application

    Our batches are offered in purities exceeding 98%, consistent with HPLC trace analysis. Each lot comes as an off-white to yellow powder, melting in the 105-108°C range. Moisture control keeps water content well below 0.5%. Storage in tight, light-protected containers avoids pinacol hydrolysis and degradation of the arylboronic ester group. Each step of the process, from the management of boronic esters’ air sensitivity to the thorough selection of recrystallization solvent, draws from industrial experience accumulated over dozens of lots. We know how a small shift in the water content can tip a Suzuki coupling from run-of-the-mill yield to something you actually want to publish—or bottle for scale-up.

    Application in Cross-Coupling Chemistry

    2-Acetylaminophenylboronic Acid Pinacol Ester runs front and center in Suzuki-Miyaura reactions. Whether working with halogenated heterocycles common in pharmaceutical targets or churning out scale-up batches for commercial intermediates, this molecule fills a slot that metallorganics alone can’t reach. The pinacol ester version solves a handful of the headaches associated with the parent boronic acids: it doesn’t throw up the same hydrolytic instability, it holds up under moderate heat, and it proves less finicky when set up with base in palladium coupling conditions. As a manufacturer, we see requests for this product on both pilot and kilo scales, largely because it can survive bench-top handling and routine ambient transfer without crashing or losing its luster.

    Process Realities, Not Brochure Promises

    A lot of product descriptions dance around the specifics, hinting at “innovative applications” or “high-tech relevance.” Our days in production tell us a different story. The real challenge isn’t in the “what” so much as the “how well.” Every synthetic chemist wants certainty about source materials—whether it’s consistent melting point, low trace metal contamination (usually confirmed by ICP-MS), or the ability to dry-load material to a column without worrying about sticky residue or wild TLC spots. We roll out batches that meet these standards because we grasp the difference that even a trivial impurity can spell in a multi-step synthesis.

    With 2-Acetylaminophenylboronic Acid Pinacol Ester, the most common demand is for clean, direct transfer from dry bottle to reaction flask. We take the time to sieve and vacuum-dry the powder before packaging. Feedback from users working on late-stage intermediates, particularly in the synthesis of substituted biaryls or advanced pharmaceutical substances, confirms that material showing off-the-chart purity on paper sometimes underperforms due to handling mistakes or subtle instability. So actual kiln drying and a tightly controlled packaging line matter.

    How Our Manufacturing Choices Change End-User Outcomes

    Every step of production gets logged, with real people manually checking endpoint clarity, batch-to-batch consistency, and residual solvents. We don’t outsource process validation. The source of boron reagents, organic solvents, and even drying gases play into the overall stability. Through in-house synthesis, painstaking purification, and QA sampling, we prevent surprises down the line—ours or yours. Mixing and drying gear is reserved for pinacol esters to avoid cross-contamination. Our experience shows that running multiple boronate batches in the same facility, with no separation of equipment, risks contamination by trace mnemonics (like metal halides or unreacted precursors). We take that extra step, because it isn’t hypothetical. We’ve seen it cost companies weeks—and confidence.

    Packing for shipment throws up another set of hurdles. Pinacol esters of this type actually hold quite well in glass or plastic, but exposure to atmospheric oxygen and humidity is always lurking to nibble away at the quality. Rather than sealing blindly, we purge every drum with dry argon, then seal under double-layer protection. A shelf life measured in months and years comes only through that level of vigilance—and our experience shipping material to three continents, to climates ranging from Shanghai’s summer to Boston’s February, teaches us the value of reliable packaging.

    What Sets 2-Acetylaminophenylboronic Acid Pinacol Ester Apart

    Many chemists debate the merit of boronic acids versus boronic esters for coupling. Our knowledge comes from watching people actually run the chemistry. Pinacol esters, compared to the direct boronic acids, resist hydrolysis in humid air and dissolve more smoothly in a broader range of solvents. That opens up new ways to set up Suzuki couplings, Stille reactions, and other cross-coupling approaches. Customers have switched from the acid to this ester form mid-project, sometimes after struggling with reproducibility, or after losing product to caking and premature decomposition. As a producer, we see the returns—reorders jump when customers see clear, high-conversion NMR spectra without the nagging presence of starting material.

    Compared to methyl or neopentyl boronic esters, the pinacol version tolerates more stress—thermal, photochemical, or even mechanical. We don’t make these claims lightly. Over the years, our QA department has cataloged every “failed” batch—clumped powders, darkened solids, unexplained TLC streaks—so we know where failures creep in. Pinacol stands up to these tweaks, especially in the hands of process chemists hoping to avoid late-stage purification headaches. Even routine storage on a lab shelf, exposed to the ups-and-downs of day-night temperature, shows slow and consistent aging profiles—less drift in melting point and color, compared to more sensitive boronates.

    Common Feedback from Real Labs, Not Just the Literature

    Our customers, from startups to established pharma houses, bring practical feedback. In many cross-coupling campaigns, the difference between pinacol esters and boronic acids or other boronates shows up in actual work-up. With this product, extraction, washing, and crystallization steps go with less fuss. It’s common to hear that reactions “scale linearly”—yield and purity hold as researchers run from milligram to multi-gram. That comes from a combination of the ester’s stability and our commitment to controlled process equipment cleanup.

    Lab staff appreciate the absence of foul odors and the way the powder pours clean, without static-induced mess or unexplained caking. End users running LC/MS prep columns catch on quickly if a product drops invisible impurities under strong base. We know these worries well, because our technical service gets the midnight calls when something is off—not just on paper, but in the actual TLC or mass spec trace. Our record shows that with the right boronic ester handling, most customer complaints vanish, and batch-to-batch yield variance shrinks to almost nothing.

    What the Industry Knows—And What It Overlooks

    Too many new suppliers pitch boronic esters with broad promises. The reality: consistency in supply and batch homogeneity don’t come from new equipment alone. They come from a working knowledge of trace impurity removal—byproducts, unreacted pinacol, off-color species—and a refusal to cut corners on final drying and packing. Over the years, we’ve fielded hundreds of customer requests for modifications: finer powder, alternative solvents, special storage drums. Our most successful adaptation involved implementing a post-synthesis sieve to eliminate finicky agglomerates, specifically for customers running automated powder dispensing.

    We’ve tracked the cost savings of avoiding re-purification of failed intermediates, attributing much of this to material consistency in the boronate supply itself. Purity is only one axis; reproducible handling tells the other half of the story. One large-scale customer, synthesizing biaryl pharmaceutical intermediates, cut post-reaction reprocessing by 30% using our 2-Acetylaminophenylboronic Acid Pinacol Ester, thanks not to “revolutionary chemistry” but to predictable, stable supply.

    Meeting Demands in a Fast-Moving Field

    While some chemical intermediates see sporadic demand, this product maintains a steady pace. Its use in the development of kinase inhibitors and other pharmaceutical assets underlines the ongoing importance of arylboronic esters with amino-acetyl modifications. Through dozens of custom syntheses and specialized orders, our own QC team has seen where things break down. Amide-containing boronic esters require careful purification to avoid colored impurities—particularly those tied to over-oxidation or residual pinacol. Removing those traces isn’t a hypothetical exercise; our team pulls out chromatographic columns and spectrometers day-in, day-out to confirm it. This results in powder lots that don’t just meet numbers on a spec sheet but deliver results in the real world of process scale-up and analytical checks.

    Research teams tackling novel polymerization protocols also reach out for this compound. Many benefit from its predictable solubility profile across acetonitrile, THF, and ethyl acetate. Practical handling feedback, like “transfers by spatula with no static jump,” comes not from theory but from those scooping the powder into round-bottoms and jacketed reactors. A smooth operator on kilo and larger scales, it cuts down on cycle time by eliminating extra sonication or filtration steps sometimes required with clumping or impure competitors.

    Regulatory and Quality Challenges—Based on Experience

    As more pharmaceuticals rely on boronic acid derivatives in late-stage development, compliance scrutiny sharpens. We have direct experience resolving user questions about lot traceability, packaging, or shipment under cold-chain protocols. International shipping presents challenges: EHS documentation, correct GHS labelling, post-Brexit customs. We have set up dockside QA to intercept and correct paperwork or last-minute handling issues. No two regions receive shipments the same way; we learn, adapt, and redesign as regulations change. Our delivery record reflects the impact of these changes, with rare delays tied to documented issues, not process shortcuts.

    Users worried about regulatory grades or documentation find that our COAs reflect hands-on analysis, not boilerplate copy. Specifications get backed by in-house testing, with real batch vials archived for traceability and complaint follow-up. Regular audits push us to confirm every lot to international standards, so users receiving 2-Acetylaminophenylboronic Acid Pinacol Ester aren’t left matching paperwork with inconsistent powder.

    Iterations in Synthesis—Product Development That Follows Users

    Our development team hasn’t stopped at the pinacol ester. Over the years, we have explored alternative boronic esters, betaine analogues, and protected forms for specialized applications. User feedback cycles back into improved synthesis routes, cleaner purification, and more worker-friendly handling. Improvements come not from theory, but from recognizing customer pain points: sticky intermediates causing downstream caking, colored impurities spiking under UV inspection, process bottlenecks during batch drying.

    The result: every update in our batch process shares a direct line to user outcomes. The goal stays practical—make 2-Acetylaminophenylboronic Acid Pinacol Ester more consistent, easier to handle, and faster to integrate, whether it’s the first milligram or the final multi-kilo shipment.

    Direct Differences—Beyond the Usual Comparison

    Many companies offer boronic acid derivatives, but a close look reveals meaningful differences. By running our own reaction lines, we do not get caught between trading margins, late-night sourcing, or inconsistent third-party drums arriving with compromised seals or mystery off-white powders. That kind of direct supply—responsibility for every kilo—keeps us honest and focused. The communication loop from customer to chemist to tech service to the actual plant floor makes each lot a learning experience. Every oddity, from subtle odor to the rare color drift, is an alert to double-check, retrain, or revise.

    Choosing between 2-Acetylaminophenylboronic Acid Pinacol Ester and other boronates often means examining shelf-life, ease of use, and integration with current workflows. With this product, we know exactly what leaves our gates, and we track what succeeds in our customers’ hands. Direct feedback, lined up with actionable process control, lets us close the loop quickly—no waiting for third-party QA to review distant complaints.

    Building Trust through Competence—A Final Word from the Source

    The core of our experience lies not just in the mastery of boronic ester chemistry but in refining every interaction—from raw material screening, through synthesis and purification, to packaging and shipment. Every kilogram of 2-Acetylaminophenylboronic Acid Pinacol Ester represents trust earned through long hours, repeated procedures, careful adaptation, and open listening to the actual users. Where many focus on claims, we focus on the facts: the product handles as-promised, couples predictably, and washes out of glassware with ease. Our goal with each lot is the same: put top material into the hands of chemists who know the value of a product made with care, by a team who stands behind every batch—not just on shipment day but for the entire lifetime of the project.