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HS Code |
748419 |
| Product Name | 3-Aminophenylboronic Acid Hydrochloride |
| Cas Number | 61307-13-7 |
| Molecular Formula | C6H9BClNO2 |
| Molecular Weight | 173.41 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 210-215°C (dec.) |
| Solubility | Soluble in water |
| Purity | >98% |
| Storage Conditions | Store at 2-8°C, protected from moisture |
| Synonyms | Meta-Aminophenylboronic acid hydrochloride |
| Smiles | B(C1=CC(=CC=C1)N)(O)O.Cl |
| Inchi Key | KVNLMJJBCTHZIW-UHFFFAOYSA-N |
| Ph | Approx. 3-5 in water |
| Hazard Statements | Irritant |
As an accredited 3-Aminophenylboronic Acid Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25-gram amber glass bottle with a secure screw cap, labeled with product details and safety information. |
| Shipping | 3-Aminophenylboronic Acid Hydrochloride is shipped in tightly sealed containers, protected from moisture and light, and clearly labeled according to chemical safety regulations. Packages are handled according to hazardous material guidelines, utilizing appropriate cushioning materials to prevent damage, and shipped with comprehensive documentation to ensure compliance with national and international transport regulations. |
| Storage | 3-Aminophenylboronic Acid Hydrochloride should be stored in a tightly sealed container, protected from moisture and light. Store at room temperature, ideally between 2–8°C (36–46°F) in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and bases. Ensure proper labeling and keep away from direct sources of heat to maintain chemical stability. |
Applications of 3-Aminophenylboronic Acid Hydrochloride in Industrial Manufacturing3-Aminophenylboronic acid hydrochloride serves as a specialized intermediate in synthesis processes across the pharmaceutical, diagnostic, agrochemical, material science, and specialty chemical industries. Each sector applies this compound with particular process parameters and compliance expectations to achieve high-value functional end products. 1. Active Pharmaceutical Ingredient SynthesisPharmaceutical manufacturers use 3-aminophenylboronic acid hydrochloride as a key coupling partner in Suzuki-Miyaura cross-coupling for the production of advanced intermediates and APIs, especially for kinase inhibitors and antineoplastic agents. The aminophenylboronic moiety introduces unique pharmacophores into drug molecules, and process control focuses on minimizing byproduct formation during amination steps. Production lines often integrate this compound into multi-stage, automated batch reactors to maintain traceability for regulatory dossier submission. Full validation aligns with stringent ICH Q7 guidelines. Industry compliance standards
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2. Diagnostic Reagents and Biosensor DevelopmentManufacturers of diagnostic platforms utilize 3-aminophenylboronic acid hydrochloride to functionalize surfaces and polymers for selective carbohydrate-binding properties, targeting glycoproteins and saccharides in biosensor arrays. The aminophenyl group provides covalent immobilization on sensor substrates, while the boronic acid moiety selectively interacts with diols for rapid, reversible binding in signal transduction applications. Surface modification protocols require tight batch-to-batch consistency under ISO 13485 QMS. Industry compliance standards
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3. Agrochemical Intermediate SynthesisIn agrochemical manufacturing, formulators employ 3-aminophenylboronic acid hydrochloride to synthesize pre-emergent and post-emergent herbicides. Its incorporation through cross-coupling or direct amide formation creates molecular structures with targeted bioactivity and improved soil mobility. The compound's high purity and stability minimize downstream loss and environmental contamination, supporting regulatory risk assessments in finished formulations. Industry compliance standards
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4. Electronic Materials and Organic SemiconductorsProducers of organic electronic materials use 3-aminophenylboronic acid hydrochloride for the preparation of pi-conjugated monomers, particularly in the synthesis of boron-doped polymers and small molecules for OFETs, OLEDs, and photovoltaic devices. Its amine and boronic acid functionalities facilitate site-selective cross-coupling with halide monomers, imparting charge-transport and tunable optoelectronic properties. Strict process monitoring under ISO 14001 ensures batch uniformity and environmental protection. Industry compliance standards
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5. Specialty Polymer ModificationProducers in the specialty polymer sector utilize 3-aminophenylboronic acid hydrochloride as a functional group donor for grafting onto polymers to enhance molecular recognition, hydrophilicity, or biocompatibility. Covalent attachment through amide or imine formation delivers modified resins suitable for chromatographic media and affinity membranes. Precise addition is critical to ensure consistent performance after scale-up, with compliance under ISO 9001 and, for bio-grade products, ISO 10993 biocompatibility review. Industry compliance standards
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No glossy brochure ever communicates the everyday grind of running reactors, monitoring the delicate dance between temperature, pH, and purity that keeps a batch on track. There’s a stubborn wisdom we’ve picked up from decades amid the aroma of fresh chemistry, and that old lesson always returns: reliability makes the difference between making a breakthrough and making a batch of waste. With 3-Aminophenylboronic Acid Hydrochloride – known among chemists as APBA HCl – we focus on meeting this standard. This compound’s story ties closely to those of the labs, pilot plants, and manufacturing workshops that use it every day to chase something new or to keep production steady.
Let’s set it straight. In our shop, APBA HCl isn’t another off-the-shelf commodity. We don’t treat its production like it’s just mixing and filtering. Each lot goes through finely tuned steps. Over time, small tweaks to the process improved solubility and purity, and we can now meet specs that matter to pharmacologists and materials scientists alike. Model identification here means repeatable outcome – whenever the catalog says “3-Aminophenylboronic Acid Hydrochloride,” it means our process yielded the para-aminophenyl isomer. Hydrochloride salt form enhances water solubility and shelf stability. Our batches range in purity – but most regular orders demand 98% or better, often with HPLC supporting data and impurity profiles transparent to our customers.
Customers bring their own preferences. Some only need small research batches. They may order a few grams, aiming for high-throughput medicinal chemistry screens or custom building blocks. Process development chemists in scale-up demand several kilograms, asking about polymorph control, solvent residues, or trace metals. Rather than pushing a “one-size-fits-all,” we relate to each challenge and keep flexibility to adjust packaging, moisture protection, and documentation.
APBA HCl matters because of what it lets other people achieve. The boronic acid functional group opens a world of chemistry. Suzuki-Miyaura coupling – where a boronic acid reacts with aryl halides using palladium catalysts – would not happen reliably without a trusted boronic acid in the first place. The amino group increases reactivity and broadens application. I’ve watched project scientists blend APBA HCl into their candidate selection workflow, speeding their lead optimization cycles by building biaryl structures or pharmacophores that influence kinase or protease selectivity.
Hundreds of published methods list APBA HCl as the pivotal substrate. It’s found in molecular sensors for glucose, in covalent enzyme inhibitors, in the fine-tuning of organic electronic materials, and even as a linker in solid-phase peptide synthesis. We don’t just supply the chemical; we recognize its practical usefulness comes from how quickly and cleanly it reacts, and how few headaches it brings. Impurity-driven side reactions can mean the overnight demise of a medicinal chemistry route, so we track batch-to-batch consistency perhaps more obsessively than any catalog would ever list.
Most boronic acids share quirks: they pick up moisture, sometimes degrade in storage, and can be stubborn to dissolve. The hydrochloride salt form, a protonated amine, offers improvements that practical experience taught us to appreciate. Its crystalline state holds up against humidity, which is critical under steamy summer warehouse conditions or when a shipment faces delays at customs.
A few years back, a customer contacted us after their standard boronic acid degraded in a tropical climate. From then, our packing switched to the hydrochloride salt for long-distance shipments. In-house, we ensure packaging under inert gas and supply clear storage guidelines. These are the kind of real-world adaptations that keep processes possible, not just theoretically appealing.
Many product descriptions float around with data that never sees the inside of a lab notebook. The reality is, in this business, customers want data that reflects performance in their most common applications. For APBA HCl, useful specifications rise above the bland. Product color, flow, melting temperature – these aspects can all impact bench work. Some users check particle size because it influences filtration or mixing, particularly in solution-phase reactions at production scale.
Water content draws attention for two reasons: hydrolysis risk and solution accuracy. We aim for less than 0.5% water according to Karl Fischer titration, with data provided so customers can judge their own risk tolerance. Comparisons with boronic acid esters, or free base forms, regularly arise because scientists seek better handling, less batch variability, and longer shelf lives. The hydrochloride salt wins out where those needs outweigh the slightly extended workflow needed to deprotonate it, if required, prior to Suzuki couplings or other diaryl bond formations.
There’s a temptation to claim every product is unique. Instead, we stress the real-world repeatability that we’ve nurtured for APBA HCl. The compound may carry a simple name, but its reputation among chemists hinges on how reliably it works day in and day out. If a downstream experiment fails to yield because of a hidden impurity, blame falls on the supplier. So, we keep a steady focus on analytical data, and every batch leaves with its corresponding certificate – not because paperwork solves everything, but because experience has shown us what follows when papers get neglected.
We learn as much from our customers as they do from our products. Some have walked us through how APBA HCl acts as a key intermediate building block in pharmaceuticals, pairing with aryl bromides in Suzuki reactions to build bioactive molecules. In diagnostics, its boronic acid group binds to diols – such as those on sugars or glycoproteins – leading to applications in biosensor development. Materials researchers tell us about the compound’s use in constructing self-assembled monolayers, organic electronics, or as part of templated polymer synthesis.
In peptide and protein research, users appreciate its ability to serve as a site-specific tag or handle, either for purification or for immobilization on columns. One collaboration used APBA HCl to modify enzyme surfaces, improving biosensor stability. Each of these cases requires different purity or form, showing there’s no generic answer; our experience in custom synthesis and process adaptation means we regularly modify protocols to fit the intended outcome.
Looking at the big picture, manufacturing APBA HCl raises distinct hurdles. Larger batches increase the risk of byproduct contamination and keep up the pressure to maintain solid analytical controls. Shipping hazardous compounds globally involves tough logistics rules, tight customs controls, and increasing expectations for eco-friendly packaging. Over years, we’ve re-engineered our crystallization and filtration so that even at multi-kilo scale, each lot keeps to spec, free from organohalide byproducts or excess chloride.
Shipping partners may not always know the difference between boronic acid forms, but our labeling and documentation help prevent delays or confusion at borders. Our team keeps paperwork and compliance up to date, minimizing downtime when the world’s chemistry pauses at an airport warehouse. It’s not glamorous but makes a world of difference if you rely on just-in-time supply chains.
Comparing 3-Aminophenylboronic Acid Hydrochloride to other boronic acids reveals clear distinctions beyond the surface. Free base 3-aminophenylboronic acid often absorbs room moisture, clumps in storage, or degrades on long shelves. Its hydrochloride salt resists caking and survives longer during unpredictable storage and shipping. Some suppliers sell esters or alternate salts, but we find these forms react differently and sometimes introduce new handling hazards or cost issues.
From a reactivity standpoint, not all boronic acids feature the ortho- or meta-aminophenyl isomer; the para orientation influences reactivity patterns. Knowing that customers rely on precise reactivity, we take care to isolate the correct isomer and provide full structural validation, using NMR, LC-MS, and IR where needed. In daily work, this means scientists can skip troubleshooting isomeric interference.
Some chemists know the pain of unexplained side products or stuck reactions. Over repeated calls, we’ve helped partners resolve those mysteries by walking through our batch analytics and synthesis steps. Sometimes a minor impurity, at trace levels, created a side reaction under specific catalytic conditions. Through this back-and-forth, we learned to document our processes in detail and keep extra reference samples from each lot, creating a knowledge base that benefits everyone down the road.
We don’t disappear when the invoice is sent. Fielding questions about solubility in different buffers, compatibility with solvents, or even scaling the compound from laboratory to plant scale is a part of our everyday. Listening to what goes wrong or right for our customers shapes newer, more robust processes that, a few years later, might deliver the very product you now receive in every drum or bottle.
3-Aminophenylboronic Acid Hydrochloride doesn’t just present lab-scale challenges. At production scale, we pay close attention to solvent selection and waste minimization. Our process development shifted to greener solvents when possible, with in-process controls preventing the need for excessive reprocessing. The hydrochloride salt form also makes handling safer, as its higher melting point and crystalline nature reduce airborne dust and risk of inhalation. Safe handling measures include dust control, proper storage in sealed containers, and clear guidance on spill response.
Waste management isn’t glamorous, but it saves headaches in local regulatory compliance. We conduct batch wastewater analysis and support customers handling larger volumes with disposal best practices. Those who scale up can reach back to us for help with process adaptation, improving yield, or troubleshooting work-up headaches. We keep safety data current and share findings from recent production runs – because transparency here brings more useful feedback, not lawsuits or fines.
Being present in the chemical supply chain today means responding to shifting global regulations. Trade rules update, banned substance lists grow, and documentation standards tighten. Our journey with APBA HCl reflects this. We update technical documentation based on changing national and international requirements, from REACH pre-registration in Europe to import quotas elsewhere. Our logistics and compliance teams handle customs declarations so that the product’s journey from our site to your lab is as smooth as possible.
Traceability has evolved, from simple batch logs, to full digital tracking — every bottle connects to its original lot sheet and analytical profile. This lets researchers satisfy both internal audits and regulatory reviews. Where authorities ask for origin, impurity, or contaminant data, we stand ready to provide any certificate or process history needed for clear shipment. This approach didn’t emerge overnight; experience managing customer audits and government inspections drove us to set standards that keep up with the world’s best practices.
Changes in organic chemistry push us to stay flexible. Recent trends in drug discovery push suppliers to anticipate scale-up from milligram to kilogram in months instead of years. Being able to deliver APBA HCl at both research and plant scales supports dozens of industries pursuing aggressive timelines and new therapeutic targets. Sometimes this means adapting our production to accommodate regulatory changes or inventing a new purification method to improve impurity profiles.
Emerging applications excite our process team more than any catalog sales. The push toward new diagnostics, next-generation electronics, and advanced materials brings unexpected needs for boronic acids. Researchers work on cancer-targeted drug conjugates, glucose sensors for wearable tech, or biphenyl polymers for solar cells. Each new application feeds back into our operation, sometimes changing how we package, store, or even synthesize APBA HCl.
We learned that meeting specifications isn’t everything. Repeat orders hinge on how easy it is to work with our compound, from opening the bottle to finishing purification. Through years of collaboration and troubleshooting, we trimmed unnecessary steps and responded quickly to packaging or form-factor requests. Customer feedback shaped our internal checks and led to extra steps in particle size grading, packing, and even the documentation we supply.
If a recurring issue appears — like unexpected aggregation after long-term storage, or trace solvent interfering with a step — our technical team steps in, reviews, and suggests concrete changes. Sometimes the solution lies in the factory, sometimes in revised customer workflows, and occasionally in a joint experiment across both sides. This shared journey helps us push APBA HCl further in each market it enters.
The story of 3-Aminophenylboronic Acid Hydrochloride isn’t isolated. It reflects countless hours in production, troubleshooting, and partnership, where details matter much more than generic assurances. We see the result of every improvement in customer feedback and watch how a small change in process brings results across research or manufacturing projects. The compound’s journey from our bench to another lab or plant continues to shape what we make and how we make it. Offering APBA HCl isn’t a one-sided sale; it’s a meeting of real-world needs with practical chemistry made visible, batch by batch, gram by gram, project by project.