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5-(Aminomethyl)-3-Isoxazolol

    • Product Name 5-(Aminomethyl)-3-Isoxazolol
    • Alias AMPA
    • Einecs 627-093-9
    • 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
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    Specifications

    HS Code

    931423

    ChemicalName 5-(Aminomethyl)-3-Isoxazolol
    MolecularFormula C4H6N2O2
    MolecularWeight 114.10 g/mol
    CASNumber 24802-57-1
    Appearance White to off-white solid
    MeltingPoint 135-137°C
    BoilingPoint No data available
    Solubility Soluble in water
    Purity Typically ≥98%
    StorageConditions Store at 2-8°C
    Synonyms AMPA, 3-Hydroxy-5-(aminomethyl)isoxazole
    SMILES NCC1=NOC(O)=C1
    InChIKey IBJIZUKVRXZZSG-UHFFFAOYSA-N

    As an accredited 5-(Aminomethyl)-3-Isoxazolol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle with a secure screw cap, clearly labeled "5-(Aminomethyl)-3-Isoxazolol, 25g, for research use."
    Shipping 5-(Aminomethyl)-3-Isoxazolol is shipped in tightly sealed, chemical-resistant containers to ensure stability and prevent contamination. All handling follows standard regulations for laboratory chemicals, including proper labeling and documentation. The shipment is expedited and protected from extreme temperatures and moisture, complying with all pertinent safety and transport guidelines.
    Storage 5-(Aminomethyl)-3-Isoxazolol should be stored in a tightly sealed container, protected from light and moisture. Keep at 2–8°C (refrigerated) in a well-ventilated, dry area away from incompatible substances such as strong oxidizers and acids. Ensure the storage location is secure, clearly labeled, and complies with local chemical safety regulations. Avoid prolonged exposure to air or heat.
    Application of 5-(Aminomethyl)-3-Isoxazolol

    Applications of 5-(Aminomethyl)-3-Isoxazolol in Industrial Manufacturing

    As a manufacturer with extensive experience in producing 5-(Aminomethyl)-3-Isoxazolol, we supply this intermediate for critical transformation processes across multiple regulated downstream sectors. The following application scenarios are based on our practical supply documentation, regulatory registration, and customer collaboration in industrial production environments.

    1. Pharmaceutical API Synthesis: CNS Active Compounds

    Pharmaceutical companies utilize 5-(Aminomethyl)-3-Isoxazolol as a core intermediate in CNS drug discovery, particularly for the synthesis of isoxazole-based small molecule APIs targeting neurotransmitter pathways. Researchers depend on its unique isoxazole scaffold to introduce aminomethyl functionality at stepwise points in heterocyclic compound assembly, especially for investigating novel ligands with NMDA antagonistic or selective GABAergic activity. The compound integrates during N-alkylation or amidation steps, allowing precise modification of pharmacophore properties. Downstream API manufacturers select the usage ratio based on desired molar equivalence for each route, with adjustments to minimize regulatory impurity levels before moving the semi-finished intermediate to final API finishing and purification.

    Industry compliance standards

    • ICH Q7 GMP Guidelines
    • USP, EP, JP Pharmacopoeial Monographs (as required by API designation)
    • EU REACH Registration for intermediates
    • FDA DMF Type II (if incorporated in US-marketed drug)

    Typical usage ratio

    • 0.8–1.1 molar equivalents per target API molecule, subject to process yield and side-reaction profiles

    Downstream process integration

    • Addition after initial heterocyclic ring preparation via N-alkylation or acylation steps in batch or continuous stirred-tank reactors
    • Integration at the stage of key intermediate coupling, followed by selective crystallization and purification before final API synthesis

    Final product types

    • CNS pharmaceuticals (e.g., potential NMDA receptor antagonists, GABA modulators, isoxazolone-derived drug candidates)
    • Other experimental neuropharmacological reference compounds supplied to research laboratories

    2. Agrochemical Active Ingredient Synthesis

    Specialty agrochemical producers incorporate 5-(Aminomethyl)-3-Isoxazolol as a building block when synthesizing heterocyclic active ingredients targeting pest or fungal resistance. Its aminomethyl group enables key functionalization during ring closure or side-chain introduction, particularly in the later phases of active compound design. These steps support the customization of molecular structure for improved target affinity and biological stability in field application. Typical formulation processes include the compound in targeted condensation or cyclization reactions, with subsequent extraction and purification involving solvent partitioning or chromatography.

    Industry compliance standards

    • FAO/WHO JMPR Technical Specifications
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • ISO 9001:2015 Quality Management Systems
    • OECD Guidelines for Testing of Chemicals

    Typical usage ratio

    • 0.9–1.2 molar equivalents, depending on the target heterocyclic core and functional group efficiency required for downstream biologically active components

    Downstream process integration

    • Addition during the key heterocyclic core formation stage, specifically in stepwise condensation or ring closure reactions
    • Integrated into the intermediate synthesis route, followed by post-reaction workup and large-scale column purification

    Final product types

    • Isoxazole-structured herbicides and fungicides
    • Biologically active pesticide intermediates
    • Custom agrochemical active ingredients for registered crop protection formulations

    3. Advanced Chemical Building Blocks for Fine Chemicals

    Manufacturers of fine chemicals and custom synthesis intermediates employ 5-(Aminomethyl)-3-Isoxazolol as a precursor for functional specialty molecules in dyes, electronic materials, and chemical research standards. Its reactive aminomethyl group, combined with the isoxazole ring, facilitates post-modification through acylation, sulfonation, or regioselective substitution. Production teams introduce the intermediate at stages requiring selective nitrogen installation, while process chemists tailor the feed ratio to reaction kinetics or downstream functionalization efficiency. End products rely on consistent quality and trace impurity controls, particularly for specialty applications in electronics or analytical reference materials.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • RoHS Directive 2011/65/EU (for electronic and analytical chemicals)
    • REACH Regulation (EC) No 1907/2006
    • Internal corporate quality documentation for specialty fine and analytical chemicals

    Typical usage ratio

    • 1.0–1.5 equivalents, adjusted for downstream coupling or modification efficiency

    Downstream process integration

    • Inserted during core modification steps—such as N-alkylation, acylation, or sulfonation in multi-step synthesis cascades
    • Used as an initiator or terminating intermediate in fine chemical custom reactions

    Final product types

    • Specialty dyes and pigment precursors for textile and polymer coloration
    • Analytical reference standards for QC laboratories
    • High-purity intermediates for electronics manufacturing (e.g., organic semiconductors, sensor materials)

    4. Research-Grade Intermediate Synthesis for Academic & Industrial R&D

    Academic institutions and industrial research labs purchase 5-(Aminomethyl)-3-Isoxazolol to construct focused isoxazole derivatives for mechanistic studies, structural activity relationship (SAR) investigations, and novel compound libraries. Its defined aminomethyl group on the isoxazole ring allows researchers to probe site-specific transformations and test newly synthesized molecular scaffolds for applications in catalysis, molecular recognition, or receptor binding studies. Users incorporate the intermediate at early stages of combinatorial synthesis, with quantities and reproducibility verified by strict analytical and documentation protocols.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for chemical synthesis in research settings
    • ISO/IEC 17025:2017 for laboratory competence (applied to QC and characterization)
    • Institutional safety and handling regulations (local and international)

    Typical usage ratio

    • 0.5–2.0 equivalents, depending on experimental design, scaffold complexity, and parallel reaction scale

    Downstream process integration

    • Often utilized at the initial stage for primary isoxazole library assembly in small-scale batch reactors or parallel synthesis platforms
    • Enters combinatorial mix-and-match protocols for rapid generation of compound variants

    Final product types

    • Novel heterocyclic compounds for academic or industrial screening
    • Research-grade standards for chemical reactivity or mechanistic benchmarking
    • Custom intermediates for internal project development in chemical and pharmaceutical R&D divisions
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    More Introduction

    5-(Aminomethyl)-3-Isoxazolol: Exploring a Specialty Molecule from the Manufacturer’s Bench

    Introduction to 5-(Aminomethyl)-3-Isoxazolol

    On the shop floor, where glassware, reactors, and hands-on attention direct each step, specialty molecules like 5-(Aminomethyl)-3-Isoxazolol demand a specific kind of care. Over the years, working through synthesis runs of heterocyclic compounds, we’ve built up a relationship with this molecule—a relationship shaped by handling the demands of real quality control and the harsh realities of delivering chemistry that meets researchers’ toughest standards. While many compounds look similar on paper, 5-(Aminomethyl)-3-Isoxazolol holds a unique value, both for its reactivity and for the trust researchers place in it.

    Choosing a Molecular Building Block

    Our experience as a manufacturer starts with understanding that every synthetic chemist wants predictability in their building blocks, no matter how tricky the chemistry. 5-(Aminomethyl)-3-Isoxazolol isn’t a simple, run-of-the-mill amine or basic isoxazole. Its scaffold features an amine functional group tethered directly to a robust five-membered isoxazolol ring. That core doesn’t just give stability; it unlocks a particular reactivity that’s rare to find, which is why it finds its way into medicinal, agrochemical, and material science research. Every time a new inquiry about this molecule comes in, the conversation is direct: what’s been needed is chemistry that enables formation of more complex structures—whether those are targets for CNS-active pharmaceuticals or custom ligands for materials discovery.

    Most teams requesting 5-(Aminomethyl)-3-Isoxazolol work at a fine line: scaling up feasibility studies, or pushing lead optimization for a drug program. Small batch inconsistencies sabotage months of work, something we’ve seen firsthand from calls and urgent emails after a bad lot disrupts downstream steps. Years of running our reactors, monitoring every stage with real-time analytics, and pulling off successful purifications at both gram and multi-kilo scales, have shown us where the pitfalls lurk. Purity isn’t a paper number—it’s something tested by the most sensitive methods, confirmed batch after batch.

    Process Control and the Quality Edge

    5-(Aminomethyl)-3-Isoxazolol has different physical characteristics than simpler amines. During drying and storage, this molecule stays stable and resists decomposition better than many primary amines with similar structures. That resilience comes from the way the isoxazolol ring helps dissipate stress in the molecule. We've measured moisture uptakes and track trace-metal levels religiously, knowing how impurities sabotage even the cleverest chemistry in a med-chem pipeline.

    In labs and production bays where we synthesize this molecule, controls run tighter than a textbook's margin. Raw material screening heads off rogue impurities. We use closed systems throughout, since aminomethylated heterocycles can be sensitive to ambient conditions. Data from gas and liquid chromatography, NMR, and trace analysis feed directly into batch monitoring. If a run starts to drift, our team investigates before the lot ever hits packaging. We reject out-of-spec product, not just on purity, but on byproduct fingerprint and color. Our quality team regularly tell stories of catching problems that trace back to starting materials—something commercial suppliers sometimes miss.

    Specifications Born in the Field

    The specs that matter most developed over dozens of batches. We’ve learned that reaction byproducts specific to this skeleton, like over-oxidized or incomplete aminomethylation products, sneak into the process other vendors don’t always flag. By getting the synthesis just right—controlling stoichiometry, catalyst activity, and temperature profiles—we repeatedly drive the reactions to near-quantitative yield, followed by purification methods that strip out problematic side-products instead of just polishing the main peak. We maintain single-digit ppm impurity profiles, which lets researchers avoid downstream extrapolation errors and unexplained biological results.

    Handling kilogram or larger campaigns changed what we thought was possible with 5-(Aminomethyl)-3-Isoxazolol. Stability under long-term refrigerated storage matches lab data; open vials from even 12-month-old inventory come out clean by analysis. We run ongoing stress and stability checks and keep a library of reference data. Every time a research partner builds out a custom protocol—a unique solvent, addition order, or coupling partner—we collect the results and feed them back into our specs and recommendations. That’s a real difference from generic products off a shelf.

    Differences from Other Aminomethyl Compounds

    Compared to benzyl or aliphatic aminomethyl derivatives, the isoxazolol ring of this molecule gives it a different polarization and electronic structure. This translates to distinct cross-coupling reactivity and higher selectivity in certain bioactive scaffolds. Direct experience in scale-up pretty quickly highlights how the ring system resists hydrolysis and unwanted side reactions on standing, something not all analogous heterocycles can claim.

    There’s a tendency to think amines are interchangeable. Our customers’ feedback and internal project work prove otherwise. Minor tweaks to the core—removing oxygen, shifting nitrogen—can change crystallinity and melt points. 5-(Aminomethyl)-3-Isoxazolol brings predictable solid-state properties. On filtration, it leaves minimal residue. On dissolution, it behaves consistently across standard polar aprotic solvents—even during high-throughput automated pipetting, clogging and drift remain rare. Many hours spent troubleshooting different analogs showed us that the hydrophilic-lipophilic balance (HLB) of the isoxazolol core helps this molecule dissolve where others sludge up. This makes formulation, downstream chemistry, or high-throughput screening significantly easier for end users.

    Real-World Usage in Drug Discovery and Synthesis

    The main customers for this molecule sit at the intersection of discovery and translational research. Synthetic chemists have deployed it for direct amide coupling in CNS lead scaffolds, and pharmacologists have explored its isoxazolol ring for receptor-targeting properties. One research group published results using 5-(Aminomethyl)-3-Isoxazolol as a fragment for kinase inhibitor development—a project that demanded gram-quantity lots with zero trace metals, since even sub-ppm copper or palladium can poison parallel reactions. By staying in direct communication with their teams, we adjusted purification steps, running extra chromatography cycles and extending drying times to drive metals lower than standard specs. That single tweak renewed the group’s contract for future campaigns, a testament to real-world customization in manufacturing.

    Agrochemical teams explore its structural motifs when scouting new bioactive molecules, due to its amenability to fine-tuning through downstream functionalization. In one ongoing multi-client collaboration, the robust isoxazole ring enabled lead diversification—all stemming from the reliable delivery of a pure and reactive aminomethyl precursor. Only through direct feedback from their process optimization trials—covering solvent systems from acetonitrile to specialized greener alternatives—have we been able to refine our isolation procedures. Most generic catalogs lack this feedback loop, leaving teams to troubleshoot at their own cost.

    Materials science projects, although more niche, demand even higher consistency. We’ve heard from polymer chemists incorporating this building block into responsive networks, describing batch-to-batch variation in melting behavior as a deal-breaking issue from previous suppliers. Our team’s hands-on oversight—tracking polymorph forms and performing parallel crystallization experiments—built the confidence that ultimately keeps these projects on track.

    Handling, Packaging, and Storage Backed by Experience

    Every shipment of 5-(Aminomethyl)-3-Isoxazolol leaves our facility in custom-sealed containers, based on lessons learned from years of exposure and testing. Once, after handling a batch that arrived from a third-party lab showing off-target HPLC peaks caused by microleaks in transport, we overhauled our seals and now fit every unit with tamper-evidence. We recommend refrigerated storage based on stress test reports; our pilot plant data shows physical and chemical stability retained for over a year if conditions match protocol.

    Customers routinely call with concerns on reactivity or crystal habits. Our tech support group—seasoned process chemists, not just sales staff—pull from archives of batch logs and real-use case studies. For teams worried about solubility, we have run additional solvent screenings and supply detailed solubility tables on request, featuring results in solvents from DMSO to methanol and water. This isn’t a generic commodity—teams want to see the actual behavior observed by those making the molecule, not just reference numbers pulled from historic databases.

    Addressing Key Challenges: Consistency, Purity, and Process Updates

    Sourcing critical intermediates like this means customers either get a smooth research run or a string of costly headaches. Often, customers tell us about batch-to-batch differences from bulk commodity sources, like inconsistent melting points, color, or slow reaction rates when scaling up. No product is immune, but our years of attention to solvent residues, minor side-products, and material handling reduce these issues. For larger requests, we produce under campaign mode—assigning a single production team, a single set of analytical runs, and standardized packaging for every lot. This focus lessens run-to-run drift and helps teams with documentation during regulatory review, patent filing, or early clinical input.

    As process chemistry evolves, so do our protocols. We regularly evaluate greener synthetic routes, waste minimization, and yield enhancements. After seeing an uptick in green solvent requests, our R&D team ran comparison syntheses of 5-(Aminomethyl)-3-Isoxazolol, using various solvent classes. By logging outcomes—yield correction, impurity levels, reaction times—we now provide select lots fully synthesized under these updated conditions, making product available for environmentally conscious end-users, without undermining our established specs.

    Customers sometimes worry about regulatory or compliance hurdles. While every industry has its own standards, we draw from recurring audits at our facility. Necessary compliance—traceability, batch archiving, or key documentation—happens alongside chemistry, not as an afterthought. This helps researchers build stronger project justification and streamline tech transfer, from discovery into process development.

    Collaboration and Customized Service: Stories from Our Factory Floor

    The story of 5-(Aminomethyl)-3-Isoxazolol at our facility is built from regular collaboration. We continue improving our in-process monitoring based on chemists who love to challenge specs. One client needed a tight control on basicity for their microfluidics project, something rarely requested in standard specs. Our lab team developed an additional titration protocol, verifying every lot to meet this constraint. Nobody does this sort of work out of obligation—it grows from years of working directly with research chemists and understanding the stakes when experimental runs go wrong.

    We also field frequent requests for documentation support: full impurity profiles, sample spectra, residual solvent analysis, and even details on packing material compatibility. Due to our experience with specialty chemistries, we can supply this data within hours, not days—a small point, but something teams in rapid-paced industries consider essential. Each time a customer shares a downstream synthesis snag, whether that’s an unexpected byproduct or a failed scale-up, our in-house chemists respond not with generic advice but practical troubleshooting steps and, where justified, protocol tweaks that other manufacturers might shy away from.

    Commitment to Transparency and Continuous Improvement

    One of the strongest lessons learned over years handling 5-(Aminomethyl)-3-Isoxazolol is the value of full transparency. Teams that know exactly what goes into each lot—down to trace analytical data—can adapt protocols confidently. Our philosophy is not to withhold or gloss over uncertainties: every certificate comes with batch-specific data, and we archive full runs for repeat customers. If a client comes back with a question about a lot from years past, we retrieve and share the original records, matching any follow-up analytical needs without delay.

    Continuous improvement shapes our daily work. Every misstep, every lot that fails an internal spec, prompts a review and often results in revised in-process checks or procedural changes. Sometimes, an expected upset—like a cooling system miscalibration—leads to new best practices, and these changes roll out to every future batch, not just the one that brought the issue to light. Rather than waiting for customer complaints, we review process telemetry and batch logs, seeking minor trends before they become problems. This keeps our product in line with the requirements of modern research and manufacturing teams.

    Understanding the Importance of Trust in Research Chemistry

    Manufacturing specialty chemicals is as much about reliability as it is about technical know-how. Over years of supplying 5-(Aminomethyl)-3-Isoxazolol, we have learned that researchers care most about being able to count on a molecule behaving the same way every time. Whether that’s in a rush synthesis for a patent race or a carefully tuned mechanism study, any hiccup affects project timelines and bottom lines. Our record stands on consistent supply, thorough technical support, and openness about product characteristics. Long-term partnerships with discovery labs and scale-up teams demonstrate how trust grows from getting these details right.

    Moving Forward: Supporting Innovation with Quality Chemistry

    The landscape for applied chemical research keeps shifting—automation, green chemistry, and tighter regulatory controls all raise the stakes for manufacturers of building blocks like 5-(Aminomethyl)-3-Isoxazolol. By remaining rooted in hands-on experience and direct conversations with users, we contribute not just a reliable product, but a legacy of service and technical insight. Every challenge, from a tricky isolation to an outlier analytical result, shapes the way this molecule gets manufactured, packaged, and supported. Our commitment remains: delivering specialty chemistry that enables innovation, improves outcomes, and keeps research moving—batch after batch, year after year.