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

4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester

    • Product Name 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester
    • Alias ANPBA Pinacol Ester
    • Einecs 425-210-7
    • 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

    930715

    Product Name 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester
    Chemical Formula C12H17BN2O4
    Molecular Weight 264.09 g/mol
    Cas Number 1092395-69-1
    Appearance Yellow solid
    Purity Typically ≥97%
    Melting Point 114-120°C
    Solubility Soluble in organic solvents (e.g., DMSO, methanol)
    Storage Temperature 2-8°C (refrigerated)
    Synonyms 4-Amino-3-nitrophenylboronic acid pinacol ester
    Smiles B1(C2=CC(=C(C=C2N)[N+](=O)[O-])O1(C(C)(C)C)C(C)(C)C)
    Inchi Key QXJQANRPXLWYGO-UHFFFAOYSA-N

    As an accredited 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 1-gram amber glass vial, sealed with a PTFE-lined cap, and labeled with hazard and product details.
    Shipping 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester is shipped in secure, sealed containers to prevent contamination and moisture exposure. Packaging adheres to chemical safety regulations. The product is dispatched with appropriate labeling and documentation, and transport is arranged to comply with relevant national and international hazardous material guidelines, ensuring safe and timely delivery.
    Storage 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester should be stored in a cool, dry, and well-ventilated place, away from direct sunlight and sources of ignition. Keep the container tightly closed and store under an inert atmosphere, such as nitrogen or argon, to prevent hydrolysis and degradation. Avoid exposure to moisture and incompatible materials, such as strong oxidizing agents.
    Application of 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester

    Applications of 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester in Industrial Manufacturing

    4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester serves as a key intermediate in several high-value industrial processes. Our direct production approach ensures strict material traceability, batch-to-batch consistency, and process scalability. Below, we present primary downstream sectors using this compound, detailing specific compliance, formulation, integration technologies, and delivered end products.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies utilize this compound during late-stage Suzuki-Miyaura coupling reactions to introduce amino- and nitro-substituted phenyl rings into targeted molecules. In precision API synthesis, chemists adjust stoichiometry based on substrate reactivity, regulatory guidelines, and impurity control plans. Pinacol ester stability aids in storage and delivery while the amino group increases compound diversity. Our material integrates into multi-step GMP routes where documentation, analytical QC, and validation remain mandatory from raw material receipt through final CrP isolation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF Monographs for relevant drug substances
    • 21 CFR 210/211 cGMP (FDA)
    • EDQM Certification of Suitability (CEP)

    Typical usage ratio

    • 0.85–1.25 equivalents relative to aryl halide coupling partner
    • Adjustment based on targeted yield and allowed impurity profile
    • Reaction scale ranges from 5 g to several kilograms per batch

    Downstream process integration

    • Introduced during Suzuki coupling step in the synthetic route
    • Reaction monitored via HPLC/TLC for completion
    • Followed by aqueous workup and crystallization
    • Full documentation in batch production records

    Final product types

    • NCE (New Chemical Entity) intermediates
    • Small molecule APIs for oncology, CNS, and anti-infective drugs
    • Key process intermediates for regulatory submission DMFs
    • Chemical probes for preclinical drug discovery

    2. OLED Emissive Material Manufacturing

    Display and lighting industries incorporate this boronic acid ester in the production of advanced OLED (organic light-emitting diode) materials. The compound acts as a building block for creating aryl-amine and nitro-functionalized molecules required for tuning emission spectra and charge transport properties. Manufacturers exert tight control over molar charge ratios and solvent selection to avoid defects in emissive layers. Pinacol ester’s compatibility with anhydrous processing and its suitability for vacuum and inert conditions enhance device reliability and commercial yield.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronic chemicals
    • REACH Regulation (EU) No. 1907/2006 registration status
    • IEC 62321: Determination of Certain Substances in Electronics
    • Internal customer specifications for residuals and metals

    Typical usage ratio

    • Typically 1.0 equivalent relative to coupling halide in synthesis
    • Solution concentrations 0.05–0.3 M depending on substrate solubility
    • Batch sizes from 500 g to 10 kg per synthesis campaign

    Downstream process integration

    • Used in Pd-catalyzed cross-coupling to form target OLED emitters
    • Integrated into multi-step small molecule synthesis or polymer chain extension
    • Purification follows via column chromatography or preparative HPLC
    • Customer conducts residue and purity testing prior to device deposition

    Final product types

    • Blue and green OLED emitters
    • Hole-transport and electron-transport materials
    • Flexible display panel components
    • OLED lighting sheet films

    3. Agrochemical Intermediate Production

    Crop protection chemical manufacturers incorporate this material to synthesize advanced heterocyclic intermediates for selective herbicides and fungicides. The boronic acid ester functionality enables efficient coupling with halogenated heterocycles. Exact feed ratios depend on the desired yield and downstream tolerance for process-related impurities. Implementation in continuous production lines necessitates compliance with environmental, safety, and quality norms specific to agrochemical synthesis and formulation.

    Industry compliance standards

    • FAO/WHO specifications for technical active ingredients
    • ISO 9001:2015 Quality Management System
    • REACH pre-registration for environmental safety
    • National regulatory requirements for new actives (EPA, ICAMA, etc.)

    Typical usage ratio

    • 1.0–1.2 equivalents relative to coupling substrate
    • Adjusted for reactivity and impurity cutoff based on pilot trial data
    • Production campaigns typically 10–50 kg per batch

    Downstream process integration

    • Charged during synthesis of heterocyclic precursors via metal-catalyzed cross-coupling
    • Followed by extraction, phase separation, and vacuum drying
    • QC sampling according to agrochemical traceability protocols
    • Intermediate often granulated or milled for technical grade use

    Final product types

    • Precursor intermediates for triazole fungicides
    • Key building blocks for phenyl-pyridyl herbicides
    • Formulation actives for post-emergence sprays
    • Technical material for further downstream derivatization

    4. Advanced Polymer Crosslinker Synthesis

    This compound functions in the specialty polymer sector as a precision crosslinker precursor, particularly for high-performance aromatic polymer networks. The boronic ester group facilitates controlled Suzuki coupling with di- or tri-halogenated monomers. Polymer manufacturers select loading ratios to achieve targeted crosslink density and mechanical properties. Purity specifications ensure downstream polymer performance, especially when targeting high glass transition or chemically resistant resins for automotive or electronics encapsulation.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical production sites
    • ISO 9001:2015 for production consistency and QC
    • Customer-specific monomer impurity and trace metal specifications
    • Restriction of Hazardous Substances (RoHS) for electronics-related polymers

    Typical usage ratio

    • 0.5–1.0 mol equivalents relative to halogenated crosslinker base resin
    • Adjusted by desired degree of crosslinking and target mechanical specs
    • Polymerization batch sizes: 1 kg to 100 kg scale

    Downstream process integration

    • Added in melt or solution phase to resin monomer mixture
    • Catalyst system added simultaneously or in staged fashion
    • Mixture polymerized under inert atmosphere to limit oxidation
    • End-use sheet or molded product formed by subsequent downstream operations

    Final product types

    • Aromatic crosslinked polymer sheets
    • Thermoset encapsulants for microelectronics
    • High-performance structural composites
    • Specialty films for chemical barriers

    5. Specialty Analytical Reagents Manufacturing

    Producers of high-purity analytical and diagnostic reagents integrate this boronic acid ester into the design of molecular probes and tagging reagents. Its unique substitution profile enables covalent bonding to aromatic- or amino-functionalized biomolecule scaffolds. Reagent manufacturers maintain precise additions and batchwise molarity for purity and reactivity. Stability under refrigeration and low moisture environments remains critical for ensuring shelf-life and analytical consistency, with validation standards tied to instrument calibration and clinical performance.

    Industry compliance standards

    • ISO 13485:2016 for medical device and diagnostic quality systems
    • Analytical Reagent Grade (AR) per ACS standards
    • Clinical and Laboratory Standards Institute (CLSI) standards for diagnostic reagents
    • Customer specification for purity, endotoxin, and trace metal levels

    Typical usage ratio

    • Typically 0.9–1.1 equivalents for probe conjugation reactions
    • Concentration between 0.01–0.3 mmol depending on target probe size
    • Lot sizes from 10 mg to 1 kg scale per customer order

    Downstream process integration

    • Used as coupling partner in chemical dye/probe synthesis
    • Integrated into multi-step synthetic routes with purification at each step
    • Final formulated with stabilizers and lyophilized for shipment
    • Released upon full QC including mass spec, HPLC, and functional assay

    Final product types

    • Fluorescent tagging reagents
    • Affinity labeling probes for proteomics
    • Bioanalytical standards for clinical labs
    • Point-of-care diagnostic kit components

    6. Industrial Fine Chemical Synthesis

    Manufacturers specializing in fine chemicals for photographic, electronic, and specialty coatings industries employ this compound for site-selective arylation steps. The amino and nitro substituents support subsequent functionalization or reduction schemes. Plant engineers routinely calculate feed molarities to control regioisomer formation and downstream impurity profiles. Applications often outline compliance with chemical handling safety and environmental discharge norms during both batch and continuous processing.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for specialty chemicals
    • REACH registration for volume band and application group
    • Occupational health regulations: Globally Harmonized System (GHS) implementation
    • Environmental site permits (local EPA or EU Environmental Agency)

    Typical usage ratio

    • 1.0 equivalent relative to substrate in arylation or reduction
    • Adjusted by in-process yield and impurity thresholds
    • Plant batch sizes from 2 kg to 20 kg, larger for campaign runs

    Downstream process integration

    • Added to reactor after initial halide substrate charge
    • Pd-catalyzed or Cu-catalyzed coupling in inert/reactive atmospheres
    • Process followed by organic extraction and solvent recovery
    • Final QC performed on refined product before sale or shipment

    Final product types

    • Specialty difunctional intermediates
    • Precursor compounds for photographic imaging chemicals
    • Monomers for advanced electronic coatings
    • Color developer intermediates
    Free Quote

    Competitive 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester 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

    4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester: Shaping Specialized Chemistry

    Opening Our Doors: What Goes Into Manufacturing this Reagent

    Inside the production facility, our story with 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester starts long before packaging or shipping. Every batch comes together under strict supervision. We monitor the environment, work through careful boronation, and never lose sight of moisture control. You learn pretty quickly that pinacol esters are more than entries in a catalog—small changes in process can spell big shifts in the final outcome. The structure, a boronic acid masked with a pinacol group, resists hydrolysis and gives a stable alternative to free boronic acids. That matters to our customers, so it matters to us.

    This molecule—the model most are referring to carries the CAS 874778-12-2—combines an aromatic ring with amino and nitro functionalities, and the pinacol ester group stands out in cross-coupling work. Once you’ve seen these reactions up close, you notice subtle things: purifying the product can challenge even seasoned chemists if the boron moiety drifts from equilibrium, or if residual salts sneak in from earlier steps. In our plant, you can literally smell the vigilance in the air. Our team regularly scrutinizes each drum, comparing it to both last week’s batch and decade-old standards we still reference. If the color veers even a shade, or if the powder clumps, we stop and reset.

    Why This Ester Stands Out for Synthesis

    Chemistry at this level depends on predictability. Researchers in medicinal chemistry, for example, lean heavily on 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester for Suzuki-Miyaura coupling to build complex molecules. The nitro and amino groups open up divergent pathways. With the protected boronate, people skip the headaches that come with unprotected boronic acids—pinacol shielding cuts back on unwanted side reactions. Rogues like oxygen and water can spoil delicate intermediates, but properly prepared pinacol esters can hold up on the shelf, giving users time to plan rather than react. Working with the raw powder, our staff routinely checks for melting point drift and solubility quirks, since subtle impurities can derail a multi-step synthesis. These lessons only emerge when you’ve run enough cycles and seen what can go wrong.

    There's a lot of theory about why this ester should function smoothly in organic synthesis, but nothing substitutes for the evidence you get from actual reaction runs. Many users report fewer side products or tarry residues when compared to the base boronic acid, especially in scaled-up batches. From our own lab trials, we noticed reactions finish faster with the ester, and isolation after reaction goes easier. Precipitation and column chromatography both move along without gumming up. The data line up with our customers’ accounts: yield, color, odor, and ease of evaporation all show real improvement. Every kilo that ships out represents hours of sweat and attention, not abstract potential.

    Understanding the Pinacol Ester Model

    There’s a tradition among technicians to respect the fine differences in reactivity—even small tweaks in the substrate can open or close downstream steps. The pinacol ester we make comes as a pale yellow to tan powder; color fluctuations can mean contamination or improper storage. We watch for particle size because fine powders disperse more evenly and react more fully. Our own routine includes FT-IR and NMR checks after drying, so that shipping crews never send off a questionable lot.

    Pinacol esters stay reliable under normal handling, resisting hydrolysis better than unprotected boronic acids, which tend to break down from ambient moisture. This fact shapes how we package and store materials—every drum is nitrogen-flushed, every bag sealed in foil. Free-flowing powders get the job done in automated dispensers, saving valuable time during process development or pilot runs. In our experience, clumpy, moisture-prone batches cost far more in lost labor than any up-front investment in good handling protocols.

    Differences From Other Boron Reagents

    Boronic acids often come up as competitors, but anyone using both side by side knows pinacol esters store longer and handle better in the lab. Unlike the parent boronic acid, the pinacol ester endures in more solvents, including tetrahydrofuran and many alcohols, which means more flexibility for chemists moving from lab scale to kilo production. Some similar boronates can hydrolyze under basic or neutral conditions, yet pinacol versions stay put until the chemist applies strong acid or base. That means longer working times and less hurry during scale-up. From our perspective as manufacturers, pinacol esters also ship well—less packing drama, lower risk of caking, fewer returned shipments.

    You see plenty of options marketed for C-C bond formation, but pinacol esters—like our 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester—offer a better tool for late-stage diversification, especially in competitive drug discovery or high-end material science. Customers working under tight regulatory scrutiny especially value consistent performance, and we build traceability right into every batch of ester we make. With typical boronic acids, we field more questions about reactivity drift or unseen impurities, since open boron sites draw in moisture and degrade over time. The pinacol group cuts those headaches way down.

    Challenges We Tackle in Production

    Raw material sourcing remains the backbone of everything we do. Feedstock reliability spells the difference between smooth campaigns and frantic troubleshooting. Nitro and amino groups both bring their quirks to the process, and you can’t cut corners with purification. Sometimes, an impurity gets stubborn, and the only fix is to rerun the whole batch. Over years, we’ve fine-tuned purification—recrystallization, column work, and drying—so our esters avoid trace metals, halides, or solvent residues. Analytical techniques like LCMS and advanced NMR help us ensure nothing gets through the cracks.

    Scaling up from flask to reactor brings its own set of hurdles. Reaction exotherms can spike quickly; if you don’t manage cooling and agitation, you lose consistency in the pinacol addition step. We’ve invested in variable-speed mixers and jacketed reactors to stay one step ahead. Regular maintenance means less downtime and more product in spec. Training counts here too—our operators log every correction and tweak, building a playbook of best practices that gets thicker every quarter.

    Supporting Innovation With Reliable Materials

    Research teams using boron chemistry count on steady, versatile building blocks. 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester plays a key part in cross-coupling, functionalization, and library construction. We’ve supplied this ester for work in pharmaceuticals, specialty polymers, and advanced dyes. Several research groups let us know their protocol calls for high purity, since contamination at the borylation stage leads to losses downstream. We answer these demands with rigorous in-process control. Our lab checks every batch with HPLC, checking for trace starting material and checking by-products. We never ship a drum unless numbers match the specs developed from decades of batch data.

    Other boron compounds—like trifluoroborates, MIDA boronates, and simple boronic acids—each have their place, but pinacol esters offer a sweet spot for daily research. Trifluoroborates store even longer, but struggle in some conditions where pinacol esters stay stable. MIDA boronates give clever control in iterative cross-coupling but usually break the budget for large runs or routine prep. By holding the line on cost and reliability, we’ve watched our pinacol ester find use in hundreds of distinct syntheses, from complex heterocycles to new ligands and catalysts. In storage tests, we’ve documented stability over months—powder still loose, melting point steady. That consistency matters for customers running against the clock, with deadlines and grant cycles on the line.

    Solubility, Handling, and Downstream Reactions

    Chemists switching to our pinacol ester quickly notice the ease of measuring out the powder—no sticky residue or glassware clinging, thanks to a solid-fluid interface that resists static and clumping. We’ve observed higher solubility in polar organic solvents, and our feedback log fills with reports of practical benefits: transfers without loss, short dissolution times, predictable mixing in automated weigh stations.

    In practical Suzuki-Miyaura and Chan-Lam couplings, our product activates well under standard bases and ligands, showing clean conversion and easy work-up. We often run our own “shadow” reactions alongside customer recipes, confirming expected behavior in both staged and one-pot protocols. Column purification seldom hitches; we’ve improved particle size by careful grinding to suit both manual pipetting and automated process lines. Over time, these small choices in manufacturing feed straight into real productivity for project chemists and process engineers.

    Field Examples and Continuous Feedback

    Through ongoing feedback, we follow our ester's path from university labs to startup innovation hubs. Several pharmaceutical researchers shared accounts where our material replaced less stable boronic acids, speeding up multiple-step campaigns for kinase inhibitor analogs. In another case, a materials science group used the ester to produce new polymers with high dielectric constants, reporting shorter processing times and cleaner film formation.

    Sometimes, a perfectly clean batch isn’t enough—users run into bottlenecks with solvent selection, work-up routines, or post-reaction purification. We respond directly: changing the crystalline form, fine-tuning moisture levels, or advising on storage. A senior process chemist once called us after a humid summer caused a shipment to arrive more compacted than expected. We overhauled the packaging, shipped extra desiccants, and ran follow-up checks; that attention paid dividends in their next order.

    Proactive Quality Management

    Reflecting on past mistakes, we keep quality at the center of operations. There’s no substitute for vigilant staff and functional instrumentation. Every technician receives training on not just analytical protocols, but the “feel” and look of finished powder—intuitive skills passed down from mentor to apprentice on the production floor. We stage “what-if” drills for common mishaps, revisiting packaging specs to protect against cap cracks or humidity spikes in transit. Customer trust builds batch by batch. Even a single return gives us lessons, and we log fixes for real, measurable improvement.

    Batch-to-batch consistency isn’t an abstract claim for us—it’s a goal we chase through meticulous record-keeping, real sampling, and strict documentation. Our team meets weekly to review control charts, spot trends, and catch subtle drifts before they bloom into real defects. That vigilance supports our customers’ own regulatory and reporting requirements—no one likes scrambling for paperwork days before a major filing or submission. Nothing builds trust like open, prompt action when issues arise. We invite audits, share regulatory filings, and never run silent in the face of new questions.

    Sharpening the Edge: Research, Development, and Customer Partnership

    Turning out high-quality 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester takes more than following SOPs by rote. Our R&D team pilots incremental improvements, testing greener solvents or milder reaction conditions. Where possible, we recycle or recover pinacol to minimize waste streams. Whenever a new synthetic route emerges—like ligand-free couplings or microwave-accelerated protocols—we supply researchers with material in custom lots, quicker than bigger companies wedded to their own processes. One collaborative project with a leading industrial lab led us to adjust particle sizing for compatibility with a new automated dispensing system. Later orders from other customers benefited from that knowledge.

    Some research partners challenge us, requesting new package sizes, tailored flow rates for automated plants, or blends pre-mixed with stabilizers. We take on these requests, brainstorming solutions on the fly. This sort of dialog shapes the future direction of our production lines. Customers providing real-world field data fuel our continuous improvement, and their trust strengthens our resolve to deliver materials that anticipate new directions in chemistry.

    Ethics and Sustainability in Modern Chemical Manufacturing

    Modern manufacturing faces scrutiny—not because industrial chemistry is new, but because the stakes keep growing. We track environmental responsibility, aiming for waste reduction, safer solvents, and energy conservation. Recycling pinacol scrap and recovering solvent not only makes sense for the planet, but keeps costs in check. Strict emission controls, reduced use of halogenated materials, and constant vigilance over workplace health create a culture where workers feel secure and proud.

    Sustainability commitments also steer our supplier choices—we favor raw material vendors with clear ethical records and documented traceability. Customers routinely ask us about trace elements and residual solvent levels, both from a regulatory angle and a sustainability one. We adapt by maintaining detailed records, participating in industry benchmarking, and prioritizing improvements that cut waste or reduce toxic risk.

    Sharing best practices is part of our open policy. We collaborate with peers to raise standards across the specialty boron landscape, boosting reliability for the wider customer community. Each improvement, whether in energy consumption or material recovery, filters through to better, safer compounds for innovators everywhere.

    Why a Manufacturer’s Experience Matters

    Traders and catalog resellers don’t see the full risk or the detail in production. At our end, each adjustment—temperature, feed rate, stirring profile—makes a difference that ripples outward. We recognize familiar faces among our repeat customers: project chemists, lead scientists, pilot plant managers, all finding value in consistent, transparent materials. Direct experience shapes every step from raw material to packaged product. That closeness to the chemistry means we develop real solutions, keeping our esters sharp and our standards high.

    Listening to detailed feedback from people actually wielding the product inspires a continuous drive toward perfection, not window-dressing. Over time, our accumulated “shop floor intelligence”—tool modifications, tweak logs, observation journals—becomes a living record of what actually works. That edge shows in every order filled and every drum inspected.

    Final Thoughts: Serving Chemistry in Practice

    Every molecule of 4-Amino-3-Nitrophenylboronic Acid, Pinacol Ester produced in our facility gets more than a lot number. It carries the experience, learning, and pride of a company bent on doing things right. The process, and all the details that go into it, reflects the realities of modern chemistry—precision, openness, stewardship, and steady partnership. We’ve seen our product pave the way to patent filings, published studies, and new materials with demonstrated value. Each successful application, from university bench to industrial pilot, tells us our approach—patient, detail-driven, never satisfied—delivers more than just a chemical. It delivers the trust and confidence every researcher, process chemist, and innovator deserves.