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HS Code |
848513 |
| Product Name | 3-Amino-2-Methoxydibenzofuran |
| Cas Number | 210690-56-5 |
| Molecular Formula | C13H11NO2 |
| Molecular Weight | 213.23 g/mol |
| Appearance | Light yellow to beige solid |
| Melting Point | 168-170°C |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Purity | Typically >98% |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
As an accredited 3-Amino-2-Methoxydibenzofuran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a tightly sealed, amber glass bottle containing 25 grams of 3-Amino-2-Methoxydibenzofuran, labeled with hazard warnings. |
| Shipping | 3-Amino-2-Methoxydibenzofuran is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. The package is clearly labeled with hazard information, handled by trained personnel, and shipped following relevant regulations for laboratory chemicals to ensure safe and secure delivery. Temperature and safety precautions are maintained as required. |
| Storage | 3-Amino-2-Methoxydibenzofuran should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat sources and direct sunlight. Store it separately from incompatible substances such as strong oxidizers and acids. Ensure appropriate chemical labeling and restrict access to trained personnel only. Use secondary containment to prevent spills and accidental exposure. |
Applications of 3-Amino-2-Methoxydibenzofuran in Industrial Manufacturing3-Amino-2-Methoxydibenzofuran serves as a specialized intermediate in several industrial sectors, supporting the synthesis and functionalization of advanced chemical products. As the original manufacturer, we supply this material in strict accordance with industry-specific quality standards and application requirements. The scenarios below outline its authentic downstream integration in commercial operations. 1. Pharmaceutical Intermediates for Kinase Inhibitor DevelopmentLeading pharmaceutical manufacturers incorporate this compound during the multi-step synthesis of diaryl ether core structures necessary for kinase inhibitor APIs. Its electron-rich aromatic system supports targeted molecular modifications. The raw material is introduced following initial etherification and before amide coupling, with dosage precisely adjusted to reaction yield needs and impurity control. Quality demands traceable batch manufacturing and compliance evidence for every shipment to API producers. Industry compliance standards
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2. OLED Materials and Organic Semiconductor SynthesisManufacturers of organic optoelectronic materials use 3-Amino-2-Methoxydibenzofuran as a controlled dopant or structural modifier during the fabrication of blue and green emitting layers for OLEDs. The compound’s electron-donating and methoxy modification enhances charge transport properties in the aryl backbone, impacting final electroluminescence parameters. It is introduced during the fine-tuning of π-conjugated polymer systems in the solution processing or vacuum deposition stages. Industry compliance standards
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3. Agrochemical Synthesis for Selective Fungicide Active IngredientsIn the agrochemical sector, this intermediate is essential for synthesizing dibenzofuran-based fungicide actives, particularly those targeting cereal and fruit crop pathogens. It is used after initial organometallic coupling with halogenated arenes, serving as a precursor for subsequent functionalization with sulfonyl or carboxamide groups. Production scale reactions require close adherence to occupational safety and post-reaction purification benchmarks. Industry compliance standards
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4. High-Performance Dye and Pigment Precursor ManufacturingProducers of specialty dyes and pigments integrate 3-Amino-2-Methoxydibenzofuran into molecular frameworks to achieve stable chromophore systems for use in textile and plastic coloration. The compound contributes to enhanced lightfastness and an expanded absorption spectrum in final dye molecules. It enters the synthetic route after initial sulfonation of the furan ring, with strict anchoring to batch traceability and regulated discharge management. Industry compliance standards
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In our decades of chemical production, certain specialty intermediates attract attention for their value across research and industry. One standout is 3-Amino-2-Methoxydibenzofuran, a compound we have refined and supplied to laboratories and synthesis plants worldwide. Laboratories and process engineers often look for chemicals that strike the right balance between stability, reactivity, and selectivity. Across synthesis routes, this molecule delivers strong performance, especially for advanced projects that push beyond commodity grade aromatics.
Our 3-Amino-2-Methoxydibenzofuran is designed with both quality and repeatability in mind. This compound, identified by its fused aromatic core and key amine and methoxy functional groups, brings unique chemical behavior that is hard to match with more basic intermediates. Structurally, the methoxy group at the second position supports electron-donating effects, while the amine at the third increases reactivity for further derivatization. Synthetic chemists look for these features when working on pharmaceutical leads, advanced pigments, and certain specialty polymers.
The production of 3-Amino-2-Methoxydibenzofuran at our site relies on tightly-controlled conditions—from precise feedstock selection to managed reaction parameters. With consistent input materials and a carefully monitored process, batches remain uniform and traceable. This consistency means research teams receive a product they know will perform, and that forms the bedrock of reliable data. For process chemists, minimizing batch-to-batch variations prevents setbacks and reduces costly scale-up mistakes.
Purity represents more than a number on a certificate. In practical terms, impurities act as roadblocks in a synthesis route, sometimes giving rise to unexpected side reactions or even outright product failure. Our track record in purifying aromatic amines includes several years actively developing new separation techniques, including column chromatography, fine-tuned washing protocols, and advanced crystallization methods. Chemists invested in drug discovery repeatedly stress how overlooked impurity profiles cripple downstream work, leading to misleading bioactivity data or, worse, the generation of toxic byproducts.
With 3-Amino-2-Methoxydibenzofuran, we typically reach purities of 98% or higher through a multi-step process, including detailed analytic runs by HPLC and NMR. Each batch undergoes stringent review, since we have seen firsthand how even minor contaminants complicate structure-activity relationships in pharmaceutical research. This obsession with trace characterization comes from both regulatory requirements and the hard lessons delivered by missed project deadlines or failed patent defenses.
Beyond chemical structure and purity, practicality demands attention to physical characteristics. The melting point of this compound enables users to easily assess identity, but it also dictates suitable solvents, storage conditions, and the logistics of scale-up. We have worked through several challenging scenarios in which a subtle shift in melting point—caused by uncontrolled cooling or exposure to light—changed performance in solid-phase synthesis.
Our experience shows that 3-Amino-2-Methoxydibenzofuran benefits from storage under nitrogen with protection from light and moisture. In ambient conditions, certain batches suffer from discoloration or slow formation of trace decomposition products, ultimately lowering yields for end-users. As manufacturer, we pack the material in amber glass bottles sealed under inert gas, based on repeated analysis of degradation kinetics under simulated shipping stress.
Among specialty aromatic amines, 3-Amino-2-Methoxydibenzofuran has emerged as a reliable building block. The amine group opens up broad utility in the formation of amides, sulfonamides, ureas, and azo compounds. Methoxy substitution influences both electronic and steric properties, often making selectivity easier to fine-tune than with unsubstituted analogs. For example, during catalytic cross-coupling, the methoxy group mitigates some of the harshness that would otherwise degrade the dibenzofuran scaffold.
We’ve seen this compound applied as an intermediate in the synthesis of several investigational drugs and custom fluorescent dyes. Its electron-rich core also supports the formation of charge-transfer complexes, opening pathways into organic electronics. In pigment chemistry, 3-Amino-2-Methoxydibenzofuran acts as a precursor for vibrant, lightfast colorants. In every case, its distinctive reactivity can mean fewer synthetic steps or higher overall yield compared with basic aminated aromatics.
Years of feedback from clients reveal clear distinctions between this compound and other substituted dibenzofurans. While plain dibenzofuran stands out as a cost-effective backbone in industrial chemistry, the addition of the amino and methoxy groups brings pronounced changes in reactivity. Take the case of 2-Aminodibenzofuran or 2-Methoxydibenzofuran: their single substitution patterns present limited functionality compared with the dual-substituted 3-Amino-2-Methoxydibenzofuran, which simultaneously boosts solubility and nucleophilicity.
For research teams driven by selectivity, this dual substitution creates a unique window of reactivity—many transformations that fail or run inefficiently on less-substituted analogs work more smoothly here. We identified these patterns early through collaboration with academic labs, where iterative experiments highlighted the impact of even minor modifications to the dibenzofuran ring. Complex multistep syntheses especially benefit from substrates that withstand oxidative, reductive, or basic conditions without excessive side-product formation.
Scaling the synthesis of specialized dibenzofurans was not a straightforward exercise. Early pilot runs with 3-Amino-2-Methoxydibenzofuran surfaced several bottlenecks: incomplete conversions, issues with impurity carryover, and occasional safety events from exothermic reactions. Our R&D team addressed these by redesigning reactor profiles, incorporating in-line monitoring, and prioritizing operator safety at each decision point.
One of the thorniest obstacles involved optimizing solid-liquid separation after the reaction. The fine particle size routinely clogged conventional filtration equipment, slowing production and endangering timelines for customer projects. We introduced a staged centrifugation process, which allowed us to recover pure product more efficiently, reduce solvent losses, and lower the risk of contamination. Over time, sustained process improvements cut turnaround times by nearly half and increased throughput far beyond initial projections.
Environmental stewardship forms an important part of modern chemical manufacturing, and we learned that certain dibenzofuran synthesis routes create waste streams or expose operators to harsh reagents. Rather than following industry norms, we piloted greener oxidants and less aggressive catalysts, validating them with quantitative lifecycle assessments. Our current synthesis method reduces the generation of halogenated byproducts and achieves higher atom economy than processes popular a decade ago.
We rebuilt waste capture systems, integrating modern scrubbers and distillation units that allow for partial recovery and recycling of solvents. We also take care to limit the use of persistent organic contaminants, after observing their environmental persistence in earlier generations of dibenzofuran chemistry. Our waste is tracked and documented, with periodic third-party reviews to ensure compliance and meet growing sustainability expectations from our customers and regulatory authorities.
Hundreds of project teams have brought challenging requests to our door, seeking not only pure 3-Amino-2-Methoxydibenzofuran but guidance on reaction mechanisms, handling nuances, and trouble-shooting. Our strong ties with leading pharmaceutical and materials science groups allow us to gather direct feedback. For example, a partner in the OLED sector relayed how minor batch impurities affected device lifetime, prompting us to install upgraded chromatographic columns for tighter purification.
Close work with academic laboratories helped us refine our packaging protocols. Moisture ingress, for instance, was a recurring theme in reports from tropical regions. We responded by switching out common stoppers for crimp-sealed, fluoride-lined closures, and documented subsequent decreases in failed experiments. Such iterative changes do not come from manuals or abstract specifications, but real-world frustration and iterative dialogue between our teams and end users.
We often receive inquiries about recommended safe-handling practices. Although 3-Amino-2-Methoxydibenzofuran presents relatively low volatility, dust generation during transfer causes headaches, especially for labs with open-bench operations. We instituted a policy of delivering pre-weighed, sealed ampules for more sensitive customers, based on their reports of inconsistent results from makeshift scoops and jars. This style of manufacturing partnership, shaped by the ground truth of active researchers, leads to fewer failed runs and higher confidence in outcomes.
Relying on published reference spectra often leaves chemists guessing about purity, stereochemistry, or minor isomeric contaminants lurking in their samples. To address this, we maintain a dedicated analytical team that routinely shares up-to-date HPLC, NMR, and mass spec data with interested clients. Our typical cycle involves detailed documentation with each lot, including retention times, integration profiles, and comparative spectra from previous runs. The program arose not from regulatory mandates, but from direct suggestions in customer calls and technical visits.
In one collaboration, a research team detected subtle endpoint drift in their assays, which we traced to batch-level trace oxidation of the amino group. Our chemists modified post-synthesis stabilization steps, validating the improvements through weeks of side-by-side physical and analytic trials. Such personalized interaction surpasses “specification sheet” thinking—it forms a dynamic cycle of feedback and improvement central to how we view chemical manufacturing.
Shipping specialty chemicals brings a unique set of complications. Temperature swings, vibration, and humidity wreak havoc on high-purity aromatics. In response, we established a dedicated logistics team that regularly stress-tests shipping protocols. For 3-Amino-2-Methoxydibenzofuran, shipments travel in insulated, vibration-dampened secondary containers. For long hauls or extreme climates, we supplement with cold packs and include real-time data loggers to track conditions from loading dock to destination.
On occasion, delayed customs inspections cause concerns about potential degradation or regulatory compliance. By building close relationships with logistics partners and keeping all paperwork in order, we mitigate these risks and accelerate clearing times. Repeat customers often request custom batch sizes, which we accommodate through flexible lot management. For particularly sensitive projects, we arrange hand delivery to ensure both chain-of-custody and material handling protocols meet on-site expectations.
The landscape for specialty dibenzofurans continues evolving as new fields—such as organic electronics, green catalysis, and biomedicine—demand ever more sophisticated intermediates. We observe growing requests for even higher purity, more tailored functionalization, or alternative salt forms. Requirements around environmental safety and responsible sourcing also shape how we operate and plan investments in process R&D.
Looking ahead, we see a rising market for enantiomerically-enriched and isotopically-labeled variants. STEM researchers press us for increasingly specific material grades to support mechanistic studies or advanced imaging. Our role as manufacturer extends beyond reactors and barrels: we are technical partners in innovation. We remain committed to sharing expertise, opening our facilities to controlled short-run pilot production, and investing in the analytical tools needed to continue exceeding baseline requirements.
3-Amino-2-Methoxydibenzofuran represents more than just another aromatic intermediate to us. Our commitment to quality, technical transparency, and responsive customization stems from direct experience supporting discovery science and scale-up operations. Chemists returning for multiple projects offer the best endorsement of our approach—one rooted in real-world learning, process discipline, and open lines of communication.
As a manufacturer, we know successful chemistry starts with reliable inputs. We take pride in delivering 3-Amino-2-Methoxydibenzofuran at standards that meet the highest demands of science and industry. Through ongoing investment in quality systems, sustainable practices, and technical partnerships, we aim to advance both the science and business of fine chemical manufacturing. For every barrel or vial we ship, the message remains clear: precision in production, accountability in partnership, and a genuine respect for the researchers and engineers who trust us with their work.