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3-Aminobenzeneboronic Acid

    • Product Name 3-Aminobenzeneboronic Acid
    • Alias 3-Aminophenylboronic acid
    • Einecs 629-435-7
    • 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

    610976

    Product Name 3-Aminobenzeneboronic Acid
    Cas Number 87199-17-5
    Molecular Formula C6H8BNO2
    Molecular Weight 136.95 g/mol
    Appearance White to off-white solid
    Melting Point 233-238°C
    Purity Typically ≥ 98%
    Solubility Soluble in water and polar organic solvents
    Density 1.32 g/cm³ (estimated)
    Iupac Name 3-aminobenzeneboronic acid
    Synonyms Meta-Aminophenylboronic acid
    Storage Conditions Store at room temperature, tightly sealed, protected from moisture
    Smiles B(C1=CC(=CC=C1)N)(O)O
    Ec Number 617-288-3

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

    Packing & Storage
    Packing 3-Aminobenzeneboronic Acid, 5g, supplied in a sealed amber glass bottle with tamper-evident cap and detailed labeling.
    Shipping 3-Aminobenzeneboronic Acid is shipped in tightly sealed containers to prevent moisture and air exposure. It is transported under ambient conditions, but protected from extreme temperatures and physical damage. All shipments comply with regulatory guidelines for chemical transport, accompanied by proper labeling, safety documentation, and Material Safety Data Sheet (MSDS) for safe handling.
    Storage 3-Aminobenzeneboronic acid should be stored in a tightly sealed container, protected from moisture, light, and incompatible substances. Store it in a cool, dry, well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to strong oxidizing agents and acids. Ensure proper labeling and keep the chemical away from sources of ignition, heat, and incompatible materials.
    Application of 3-Aminobenzeneboronic Acid

    Applications of 3-Aminobenzeneboronic Acid in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Aminobenzeneboronic Acid to diverse industrial segments that require specialized aromatic boronic acids for advanced synthesis. Below, you will find rigorously detailed scenarios showcasing the real-world deployment of this raw material in high-value downstream manufacturing environments.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Small-Molecule Targeted Therapeutics

    Pharmaceutical companies integrate 3-Aminobenzeneboronic Acid into the synthesis of specific kinase inhibitors and targeted oncology drugs, where the molecule participates as a boronic acid building block in Suzuki–Miyaura cross-coupling reactions. In these processes, our product enables precise construction of complex phenyl rings within active ingredients, maintaining molecule integrity to meet strict regulatory profiles for human medicinal applications.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP/NF and Ph. Eur. reference standards
    • FDA 21 CFR Part 210/211
    • EU EMA pharmaceutical ingredient directives

    Typical usage ratio

    • For Suzuki–Miyaura cross-coupling: 1.0–1.2 molar equivalents relative to halogenated aromatic intermediate; actual ratio refined based on yield optimization and impurity profile in medicinal chemistry flows.

    Downstream process integration

    • Introduced during the construction of biaryl frameworks, following protection of amino groups and prior to deprotection/purification steps in the multi-step API synthesis pipeline.

    Final product types

    • Small-molecule kinase inhibitors (e.g., proteasome inhibitors)
    • Novel antitumor agents containing boron functionalities
    • Research-use-only APIs for preclinical development

    2. Diagnostic Reagent Manufacturing for Bioanalytical Kits

    Producers of diagnostic and bioanalytical kits utilize 3-Aminobenzeneboronic Acid to synthesize conjugated probes for glycoprotein or sugar detection in advanced immunoassays. The amine and boronic acid functionalities allow for selective immobilization on sensor platforms, supporting sensitive, quantitative biochemical detection in clinical laboratory kits and in vitro diagnostic reagents.

    Industry compliance standards

    • ISO 13485 quality system for medical device and diagnostic reagent manufacturing
    • CLSI standards for in vitro diagnostic system performance
    • FDA 21 CFR 820 QSR for IVD devices
    • REACH registration in the EU for laboratory chemical suppliers

    Typical usage ratio

    • Applied at 0.1–0.5 mmol per gram of polymeric carrier or sensor substrate; loading optimizes probe sensitivity in ELISA and lateral flow platforms based on surface area and intended analyte concentration range.

    Downstream process integration

    • Coupled onto activated surfaces via amide or Schiff base linkages; subsequent crosslinking and stabilization complete immobilization prior to assembly of detection cartridges or microplates.

    Final product types

    • Glycoprotein detection kits (colorimetric or fluorescence detection)
    • Sugar-binding analytical sensor strips
    • Affinity chromatography columns for glycan isolation

    3. Organic Electronic Material Precursor for OLED and OFET Components

    In the field of organic electronics, material manufacturers introduce 3-Aminobenzeneboronic Acid into the synthesis of advanced arylamine-boronic derivatives, which serve as monomers for conjugated polymers or as intermediates for hole-transporting materials. The fine control over substitution patterns enables tuning of energy levels and charge mobility within devices such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs).

    Industry compliance standards

    • IEC 62341 for OLED display device performance
    • RoHS Directive (2011/65/EU) for restricted substances in electronics
    • IPC-6012 for rigid printed board fabrication
    • In-house QC and purity requirements for low ionic and metallic impurities

    Typical usage ratio

    • In polymer synthesis: 0.8–1.1 equivalents versus dibromo-aryl partners; excess managed to optimize polymer yield and minimize side reactions under Pd(0) catalysis.

    Downstream process integration

    • Enters reaction system at monomer introduction stage in high-purity organic synthesis reactors. Post-synthesis, end-use device manufacturers refine and dope resulting polymers or molecular semiconductors.

    Final product types

    • OLED hole-transport and emission layer formulations
    • OFET active layer precursor materials
    • Conjugated copolymers for advanced display panels

    4. Fine Chemical Intermediate for Agrochemical Synthesis

    Agricultural chemical producers use 3-Aminobenzeneboronic Acid as a building block in multi-step synthesis of phenylboronic acid-substituted herbicides or plant growth regulators. The compound’s dual aminated and boronic functionalities expand the palette for engineered molecules with enhanced selectivity and environmental compatibility, supporting the formulation of crop protection agents under stringent regulatory scrutiny.

    Industry compliance standards

    • FAO/WHO pesticide specifications for active ingredient content and purity
    • ISO 9001-certified process control
    • REACH/CLP Regulation compliance for European agrochemicals
    • China GB2763 food safety standards for permissible residue levels

    Typical usage ratio

    • Reacted at 1.0–1.3 equivalents with halogenated benzene intermediates in key coupling steps; optimized to product yield and downstream purification strategy for scale-up production.

    Downstream process integration

    • Feeds directly into the main coupling reaction during multi-stage synthesis before final formulation and microencapsulation of agrochemical active concentrates.

    Final product types

    • Boron-containing herbicide actives targeting broadleaf weeds
    • Plant growth regulation compounds with boronic modifications
    • Pre-emergence weed control agents

    5. Specialty Polymer Modification for High-Performance Materials

    Advanced polymer manufacturers employ 3-Aminobenzeneboronic Acid to graft boronic acid functionalities onto aromatic polymer backbones, yielding materials with tailored chemical recognition and hydrophilicity. This targeted modification broadens application in membrane separation, selective adsorption, and responsive hydrogel platforms for high-end industrial and environmental filtration systems.

    Industry compliance standards

    • ISO 9001 for total quality management in materials production
    • ASTM D638 for mechanical testing of polymeric materials
    • EPA TSCA for premarket chemical review in the United States
    • EU WFD/REACH regulations for polymer additives

    Typical usage ratio

    • Grafting concentrations: 0.5–2.0 wt% relative to polymer feedstock, adjusted according to target membrane selectivity and mechanical property profiles for end-use systems.

    Downstream process integration

    • Introduced during post-polymerization grafting or as a comonomer via solution or melt phase reaction; downstream blending or casting forms membranes, beads, or films.

    Final product types

    • Affinity membranes for glycoprotein purification
    • Boronic acid-functionalized hydrogels for biosensing
    • Adsorbent resins for water treatment
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    Certification & Compliance
    More Introduction

    3-Aminobenzeneboronic Acid: Behind the Glass of the Reactor

    Putting Experience Into Every Batch

    Not all chemicals are created the same, and nowhere does this ring truer than with specialty boronic acids. I’ve spent years working in the plant—charging reactors, weighing out crystalline intermediates, tightening every control point. Over that time, 3-Aminobenzeneboronic Acid has proven itself as a backbone molecule for medicinal, agrochemical, and materials research. Chemists walk in chasing new targets; what they often need is a building block that delivers consistent reactivity, especially when exploring new catalysts or substituent effects. That is where hands-on manufacturing makes a difference.

    Local Process, Global Standards

    Our production of 3-Aminobenzeneboronic Acid, with a model designation of 98% min assay on dry basis, bridges reliable upstream sourcing with precision downstream finishing. No shortcuts or batch blending here—each run begins with high-purity aniline and boronic acid building blocks, reacting under clean conditions, watched over by operators whose boots have worn grooves in the plant floor. Scale matters less than control; we focus on nucleophilic and electrophilic substitutions that introduce the boronic group precisely where needed without biaryl byproducts.

    Moisture content typically stays below 0.5%. Residual starting materials and heavy metal impurities get reduced through careful crystallization and washing steps. The result is a pale to light brown powder, not sticky, not clumped, flowing evenly onto the scale. Our own researchers regularly check melting point, NMR, and HPLC so we know exactly what’s going into customers’ labs. There's little patience for guesswork when a few tenths of a percent impurity can ruin a multi-stage synthesis.

    Inside the Tank—Why Quality Control Isn't Marketing Fluff

    Our laboratory doesn’t hand out passing results lightly. Every tank, every drum, faces scrutiny. Operators pull samples at critical points; if color, solubility, or TLC fingerprint drifts, we stop and investigate before shipping any material. Colleagues in the plant know why: a missed impurity in our 3-Aminobenzeneboronic Acid could sabotage a pharmaceutical screening step, force process chemists to retrace weeks of work, or even clog up precious catalysts. Quality control isn’t for the brochure—it answers to hard experience.

    We've been through far more than one external audit. Compliance involves documentation, not just raw data. We keep every record for traceability, from source vessel to finished package. Chemists working in the trenches spot the difference between storytelling and technical proof. That’s why lab notebooks from process to QC are just as valuable as the drums that eventually arrive at your loading dock.

    What Makes 3-Aminobenzeneboronic Acid Valuable

    Ask a hundred chemists for the use of 3-Aminobenzeneboronic Acid and you’ll get a spectrum of answers. From my perspective on the manufacturing floor, its main value lies in cross-coupling chemistry. The amino group brings unique opportunities: Suzuki-Miyaura couplings, for example, become less straightforward compared to plain phenylboronic acid, and require better control of pH and solvents. The amine function can chelate palladium or serve as a hydrogen-bonding handle for designing lead candidates in drug discovery.

    Outside pharmaceuticals, we field regular questions from materials scientists developing sensors, OLED displays, and polymers. The boronic acid group attaches to sugars, diols, and alcohols. Industrial partners demand a product that survives storage but remains reactive enough to function at bench scale. Waste isn’t tolerated. Research budgets rarely stretch to reordering material because an earlier lot didn't perform as expected.

    Specifications Aren’t Just Numbers

    From our side, an assay of 98% minimum means a laboratory and process team stands behind every figure. This value is not plucked from a competitor’s website or a data sheet template. The low water content stems from investing in vacuum ovens and gentle drying conditions. Melting points are checked batch-to-batch—not assumed based on tenure. What ultimately gets packed—often in amber bottles or double nylon bags—must meet stated limits on chloride, sulfate, heavy metals, and volatile organics.

    No drying agents are thrown in as afterthoughts. No anti-caking agents dilute the powder. We use low-iron process vessels and monitor air quality continuously, out of experience—not theory—that trace contaminants can sabotage a Grignard, Buchwald-Hartwig, or Suzuki reaction. Our assurance comes from knowing what actually goes on in the chemist’s flask afterward.

    Why This Product Isn’t Interchangeable With Its Cousins

    Customers sometimes compare 3-Aminobenzeneboronic Acid with similar compounds, such as 4-Aminobenzeneboronic Acid or unsubstituted phenylboronic acid. These differences matter, especially for late-stage functionalization. Take regioselectivity: the position of the amino group shapes electron density, impacts cross-coupling rates, orthogonality, and even patent coverage. Our product undergoes synthesis routes that avoid rearranged byproducts, so downstream chemistry doesn’t suffer surprises.

    A chemist working on a conjugated polymer might find 4-amino isomers less effective in chain-growth processes. Pharmaceutical researchers often prefer our 3-amino version for specific kinase or proteasome inhibitor scaffolds. From manufacturing experience, we learned that demands for positional isomers are not just about price or purity—they relate directly to performance. The time spent isolating these isomers during synthesis would not be justified if processed by an inexperienced or inconsistent team.

    Working Through the Reality of Large-Scale Production

    Lab-scale syntheses look clean on paper but rarely translate smoothly to bulk reactors. The amino group is notoriously sensitive to oxidation and must be protected from air and light during workup. We cap reaction vessels with dry nitrogen and check seals the old-fashioned way: with detergent solution and a steady eye. If water control slips, you’ll see clumpy, darkened product that won’t pass even a basic NMR screen. Our hands-on crew uses in-line monitoring alongside old-school TLC plates.

    Solubility remains a challenge—3-Aminobenzeneboronic Acid won’t dissolve as benignly as some of its alkylated cousins. We choose solvents as carefully as any downstream user. No step gets rushed; the biggest mistakes happen when someone ignores the intermediate’s sensitivity. The plant houses separate lines just for boronic acids, cutting down on risk and keeping cross-contamination at bay. After each batch, cleaning validation runs ensure nothing else rides in the next tank.

    From Drum to Flask—What End Users Notice

    Supply chain hiccups tested us over recent years—raw material shortages, price surges, shipping gridlocks. What kept our shipments moving has always been extra steps at the packaging bench. Seals get checked twice. Desiccant packs regularly ride with every container, even on orders that cost more to finish out than they bring in. Repeat customers point out that, in a world full of “me-too” suppliers and traders, knowing where and how your chemicals are really made makes all the difference in their project timelines.

    Feedback from medicinal chemistry groups tells us they value homogeneity—not just batch-to-batch, but within a drum. You shouldn’t have to remix material to get even samples. Each package gets filled, checked, and finished in our own plant, not in a shipping container or repackaging warehouse. Every operator on that bench has earned their stripes. It’s a human process, built by men and women who care because they’ve seen what happens when neglected corners come back to haunt the synthetic route.

    Supporting Responsible Innovation

    We’ve watched the landscape around arylboronic acids shift. Regulatory scrutiny tightens while research ambitions keep expanding. Our plant sits inside a special chemical park, so environmental controls mean more than paperwork—they’re tied to the local groundwater and air. We made the decision to install scrubbers for both amines and boron-based offgassing. These changes came before they appeared in any regulation because we see what happens when a wetland or a drinking water source gets contaminated with process waste.

    Our staffers complete regular training, not as a box-ticking drill but recognizing that one thing always leads to another. Waste drums carry RFID tags; every kilogram of boronic process waste gets logged and tracked so an inspector finds the evidence long after the lot leaves our floor. All wastewater goes through dedicated boron-removal systems, with routine checks against local utilities and independent labs. This wasn’t driven by outside pressure but by the knowledge that chemical manufacturing can’t exist in a vacuum from its surroundings.

    Solving Problems Before They Hit the End User

    Customers will point out issues, but frontline workers usually find them first. During the last heat wave, higher impurity loads cropped up in finished batches—tied to subtle shifts in cooling water temperature. We revamped chiller circuits, not because anyone demanded it but because running the plant for the long haul means seeing possible failures before they cascade.

    Solubility tweaks can make or break an entire multi-step project. One polymer group asked for extra documentation on byproducts, concerned about background interference in fluorescence spectra. Chemists and engineers partnered up; extra LC-MS runs dug into the details. That open-door approach has pulled us out of potential recall situations more than once. We’ve learned to see shipping as part of the product, not an afterthought.

    Continuous Investment and Future Readiness

    What looks routine—white powder in a drum—is the result of years of tough learning and steady reinvestment. Our plant replaced its oldest crystallizer with a low-energy, programmable unit. We moved away from manual weighing on open benches toward ventilated, closed-feed systems—not for show, but to keep dust in check and employees healthier. Orders might arrive for a single kilogram or jump to a ton; each size gets the same commitment, and each customer’s next round of results influences our next round of process improvements.

    Demand for 3-Aminobenzeneboronic Acid expands each year. Analytical requests now often mention green chemistry targets or C-H borylation methodologies. We’ll keep adapting syntheses and equipment to stay ahead, knowing that tomorrow’s reaction logic will need yesterday’s attention to detail. Our commitment comes from living alongside the chemistry—not treating the process as abstract or distant. For us, every order connects back to time spent walking the lines, inspecting glassware, and learning from the batch record’s hard numbers and hard lessons.

    The Manufacturer’s Perspective: A Living Product

    Each shipment of 3-Aminobenzeneboronic Acid carries more than grams and assay slips. It travels out of our plant with practical experience built in: from operators who train new hires, to chemists who probe every spectrum, to environmental teams who take their responsibilities home at night. The product’s strength and reliability survive long after the last label goes on, affecting not just the next experiment but the bigger cycles of discovery and innovation.

    Labs rely on more than the name stamped on the box. They need proof in each reaction flask—proof that every step was respected, every tank cleaned, every sample honestly reported. Anyone who’s stood next to a pilot reactor on a humid Monday or scrambled to adjust controls at two in the morning understands that real manufacturing doesn’t happen on paper or in sales copy. It comes from living with the material, over time. That’s how our team sees 3-Aminobenzeneboronic Acid: as a living product, one you know by hand, by sight, by smell, from batch to batch and decade to decade.