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3,4-Dimethylisoxazol-5-Amine

    • Product Name 3,4-Dimethylisoxazol-5-Amine
    • Alias 5-Amino-3,4-dimethylisoxazole
    • Einecs 810-069-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    237030

    Chemical Name 3,4-Dimethylisoxazol-5-Amine
    Molecular Formula C5H8N2O
    Molecular Weight 112.13 g/mol
    Cas Number 114772-55-1
    Appearance White to off-white solid
    Melting Point 60-64°C
    Solubility Soluble in organic solvents such as DMSO and methanol
    Storage Conditions Store at room temperature, protected from light and moisture
    Smiles CC1=CON(N1)C
    Inchi InChI=1S/C5H8N2O/c1-3-4(2)8-7-5(3)6/h1-2H3,(H2,6,7)
    Purity >95% (typical for commercially available samples

    As an accredited 3,4-Dimethylisoxazol-5-Amine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle of 3,4-Dimethylisoxazol-5-Amine is supplied in a sealed amber glass container with a clear hazard label.
    Shipping 3,4-Dimethylisoxazol-5-Amine is shipped in tightly sealed containers, protected from light and moisture. It may be classified as a chemical reagent and handled according to standard laboratory safety protocols. Packaging ensures containment and labeling for transport. Consult local and international regulations for specific shipping requirements and hazard classifications if applicable.
    Storage 3,4-Dimethylisoxazol-5-amine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, and follow all relevant safety protocols, including appropriate labeling and secondary containment where necessary to prevent accidental release or contamination.
    Application of 3,4-Dimethylisoxazol-5-Amine

    Applications of 3,4-Dimethylisoxazol-5-Amine in Industrial Manufacturing

    3,4-Dimethylisoxazol-5-Amine serves as a specialized intermediate within multiple value-added sectors. As a direct manufacturer, we provide this compound with quality consistency and technical support, enabling efficient incorporation into precise industrial processes. Outlined below are key downstream scenarios verified by industry usage, describing integration points, compliance frameworks, and preferred formulation strategies based on actual customer requirements.

    1. Active Pharmaceutical Ingredient (API) Building Block

    Pharmaceutical manufacturers employ 3,4-Dimethylisoxazol-5-Amine as a heterocyclic amine component for synthesizing certain registered APIs, where its isoxazole ring lends selective bioactivity in the final molecule. Synthesis routes often deploy it during intermediate steps to introduce precise substitutions of the isoxazole core, contributing to the pharmacologically active moiety of small-molecule drugs, particularly in anti-inflammatory and CNS categories.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia Reference Standards for final APIs
    • EU REACH Registration for chemical intermediates

    Typical usage ratio

    • 0.6–1.3 molar equivalents relative to the target core scaffold, with adjustment based on target yield maximization and impurity control

    Downstream process integration

    • Reacted in mid-stage condensation or cyclization steps within a multi-step synthesis, typically in batch reactors under nitrogen atmosphere at 40–80°C, followed by filtration and solvent exchange protocols before subsequent coupling

    Final product types

    • New chemical entity (NCE) API intermediates
    • Final APIs for CNS and anti-inflammatory drugs
    • API technical-grade intermediates for nonclinical development

    2. Agrochemical Intermediate for Herbicide Synthesis

    Chemical crop protection formulators use 3,4-Dimethylisoxazol-5-Amine as a nucleus for constructing selective herbicidal actives. Its functional groups enable coupling onto aromatic rings or carboxylic acids to yield high selectivity isoxazole-based herbicides, reducing crop phytotoxicity. Formulators value the compound for delivering high conversion in multistep synthetic routes and process yields critical for large-scale herbicide manufacture.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for agrochemicals
    • REACH Annex VII–IX chemical safety
    • OECD Good Laboratory Practice (GLP) for development phase toxicology

    Typical usage ratio

    • 10–18% (w/w) of the starting material mix in the herbicide active ingredient synthesis, tailored as per target compound and rate-limiting coupling efficiency

    Downstream process integration

    • Introduced during aromatic substitution or amidation stages; controls are maintained for moisture and pH to optimize yield and minimize side reactions

    Final product types

    • Isoxazole herbicidal actives for broadleaf and cereal crops
    • Bulk technical-grade herbicide intermediates
    • Registered formulated herbicide concentrations

    3. Specialty Dye and Pigment Precursor

    Producers in the specialty chemical sector utilize 3,4-Dimethylisoxazol-5-Amine as a precursor to synthesize advanced dye intermediates, specifically for pigments demanding thermal stability and tailored absorption spectra. The amine functionality participates in custom diazotization or coupling reactions, supporting the design of novel chromophores for plastics coloration, textile dyeing, and industrial ink production.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006 (REACH) for chemical substances
    • ISO 9001:2015 for manufacturing quality systems
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) guidelines for dye safety and environmental responsibility

    Typical usage ratio

    • 5–15% (mol/mol) in dye synthesis batches, based on pigment structure and desired color fastness

    Downstream process integration

    • Added during main coupling reaction after initial diazotization, typically neutral or slightly acidic conditions around 25–35°C, followed by purification through solvent extraction or recrystallization

    Final product types

    • High-performance azo dyes
    • Thermally stable pigments for plastics and industrial coatings
    • Reactive dye intermediates for fiber and synthetic textile applications

    4. Electronic Chemical: Functional Polymer Modifier

    In advanced material production, this compound modifies functional polymers designed for electronic applications. Specialty polymer manufacturers integrate the isoxazol-amine moiety to tailor electrical, thermal, or mechanical response profiles, crucial for dielectric films, microelectronic adhesives, and semiconductor encapsulation materials. Its incorporation improves end-use properties such as surface polarity or chemical resistance with minimal impact on polymer bulk properties.

    Industry compliance standards

    • RoHS Directive (Restriction of Hazardous Substances in Electrical and Electronic Equipment)
    • IEC 61249-2 for base materials in electronics
    • UL 94 flammability classification for plastics
    • ISO 9001:2015 for advanced polymer production

    Typical usage ratio

    • 0.2–3% (w/w) relative to base polymer, selected by target application: lower end for dielectric coatings, higher for adhesives requiring functional group density

    Downstream process integration

    • Incorporated in the functionalization stage, through solution blending or melt compounding, under inert gas to prevent oxidation, followed by post-treatment cure or film-casting

    Final product types

    • Dielectric polymer films for PCB manufacture
    • Microelectronic-grade reactive adhesives
    • Specialty encapsulants for semi-device packaging

    5. Developmental Chemical Probe Synthesis (R&D)

    Medicinal chemistry and chemical biology research teams rely on this raw material to construct custom probe molecules where bi-functional isoxazole derivatives serve as analytic tools for receptor studies and pathway elucidation. It provides a stable scaffold for further modification, leading to probe candidates suitable for structure-activity relationship (SAR) studies, fluorescent labeling, or affinity tagging in preclinical assays.

    Industry compliance standards

    • IUPAC and ACS standards for chemical purity designation
    • ISO/IEC 17025 laboratory accreditation for analytical verification
    • REACH Annex I for R&D chemical use under tonnage exemption

    Typical usage ratio

    • 1:0.8–1:1.2 functional substrate ratio, determined per synthetic scheme calibration and compound library size

    Downstream process integration

    • Utilized in parallel synthesis to build analytic probe libraries, generally automated by liquid handling workstations in multiwell formats, followed by purification and structural verification

    Final product types

    • Fluorescent or tagged chemical probes for binding studies
    • Reference standards for receptor-ligand screening panels
    • SAR probe sets for preclinical target validation
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    Certification & Compliance
    More Introduction

    3,4-Dimethylisoxazol-5-Amine: A Direct Perspective from Our Manufacturing Facility

    What Makes 3,4-Dimethylisoxazol-5-Amine Stand Out

    In the world of chemical manufacturing, reputation and reliability grow from the ground up. Every batch of 3,4-Dimethylisoxazol-5-Amine we produce carries with it the weight of practical, day-in and day-out experience. We see the full process, from sourcing raw materials to final quality checks, every time this compound moves through our plant. Over years spent on the production floor and in the quality control lab, we’ve learned a lot about how and why this amine plays an essential role for our customers and how it truly differs from the crowd of similar heterocyclic amines.

    Compound in Focus

    3,4-Dimethylisoxazol-5-Amine occupies a niche demand that keeps growing in both pharmaceutical research and advanced material science. This isn’t an amine that floats in and out of relevance with shifting trends. Its structure—a five-membered isoxazole ring with methyl groups at the 3 and 4 positions and an amino group at the 5-position—gives it distinct chemical behavior. The electronic properties and steric structure here aren’t an academic matter; they translate directly to how this molecule reacts, and to the kinds of compounds you can efficiently build around it.

    Chemists who have worked with other isoxazole derivatives quickly notice the impact of those two methyl groups. They’re not just bulky side chains—they dial down the reactivity of adjacent positions, offering more selectivity during substitution or coupling reactions. In medicinal chemistry, selectivity and controlled reactivity save both time and resources. We’ve seen research teams avoid extra purification steps after synthesizing more complex analogues, and it usually starts with careful choices at this stage of intermediate selection.

    Specifications That Matter on the Floor

    Our typical output of this amine ships as a white to off-white crystalline powder, providing a stable format for further reactions. With a melting point that falls within a closely checked range and tight controls on residual solvents and trace impurities, our batches remain consistent. These specs don’t come from a marketing department—they come from practical demands. Synthetic steps downstream depend on predictability, and unpredictable outcomes spell lost time and discarded product.

    We’ve tested how our production output behaves under scale-up, not just bench-scale synthesis, and tracked performance in different solvents. Users see less batch-to-batch variability because our raw input audits catch problematic suppliers, and our plant layout prevents cross-contamination with amines carrying different ring substitutions. This focus means our technical teams can respond clearly and quickly to customer validation requests, not only with paperwork but with actual retained samples and re-tests.

    Applications That Drive Real-World Impact

    We regularly speak with formulators using 3,4-Dimethylisoxazol-5-Amine in development of kinase inhibitors, protease modulators, and a growing spread of central nervous system drug candidates. In recent years, interest from agrochemical developers has picked up as well, with demands for building blocks that allow introduction of tailored substituents at specific sites on aromatic or heterocyclic cores. Teams working on crop protection agents appreciate the compatibility of the isoxazole motif, especially when aiming for selective targets with minimal off-site impact.

    Material science teams have reached out for custom batches where higher color purity or lower sodium trace levels affected downstream catalyst performance. We’ve seen photonic materials applications as well, where even subtle differences in impurity profiles lead to changes in physical behavior. The wide range of technical requests has pushed us to adapt upstream and midstream controls, keeping both traditional pharma-grade and bespoke high-purity requirements within our reach.

    Each application offers its unique set of hurdles. Medicinal chemists might complain about unwanted side reactions or difficult isolations with lower purity material from other sources. Agricultural researchers often require larger-scale batches, pushing our reactor design and supply chain to respond in kind. Across these challenges, direct lines of communication—chemist to chemist—carry more weight than broad claims. We listen, and we adapt the production recipe if it means better yield or cleaner output for the user’s purposes.

    How 3,4-Dimethylisoxazol-5-Amine Compares to Close Relatives

    Few other heterocyclic amines rival the versatility this compound demonstrates in cross-coupling and functional group modification. Compare the 3,4-dimethyl variant to base isoxazol-5-amine, and the contrast in steric protection becomes clear. The pair of methyl groups on positions 3 and 4 doesn’t block all unwanted reactivity, but they do nudge reactions toward greater selectivity—less byproduct, clearer chromatography, easier isolation. Because we control every step of the production line, from early-stage methylation through amination, our technical staff can talk customers through the risks and quirks that come with alternative substitution patterns or isosteric replacements.

    Some customers have tried shifting to the monomethyl version, thinking a single methyl could serve a similar protective effect. It isn’t the same. We’ve run those experiments ourselves for customers evaluating cost trade-offs, and the resulting impurity profile and yield loss usually do not justify the swap. Where higher reactivity matters, and when synthesis routes demand earlier ring modifications, those alternatives have appeal. But for downstream coupling and for pharmaceutical or agrochemical contexts where contamination and yield losses hit budgets fast, experience has shown the fully methylated version offers better value over the long run.

    Lessons Learned in Scaling and Safety

    Having managed scale-up runs of 3,4-Dimethylisoxazol-5-Amine, we know the real challenges begin long before final shipment. The chemistry can appear straightforward on paper: methylation, ring closure, amination, purification. Yet until you have watched reaction temperature surge or filtration steps slow to a halt when impurity levels rise, it’s easy to underestimate the craftsmanship required. We allocate extra time to temperature ramp controls and monitor byproduct formation with in-line spectroscopy, not only during validation but every run.

    It’s not uncommon for teams new to this compound to overlook cross-reactivity hazards or overstate the thermal stability at various process stages. Bench-top data doesn’t always scale. We’ve had to adjust for exotherms and solvent compatibility issues that arose only when moving from kilogram to multi-ton production. Our safety reviews extend beyond MSDS paperwork; lab chemists and production engineers meet before each batch for a real conversation about new findings and edge cases that went wrong in earlier runs. In our experience, that kind of communication cuts accident risk and makes troubleshooting possible on short notice.

    Waste management sits right alongside production in our facility planning. You don’t see that in most brochures, but active amine wastes and isoxazole byproducts demand specialty disposal rather than catch-all solvents. We reclaimed solvents by in-plant distillation, further cutting our resource footprint. Over the last five years, we’ve reinvested savings from lower waste costs into tighter chromatography columns and better analytical tools—direct benefits to both output quality and environment.

    Supporting Customers Beyond Paperwork

    The most valuable feedback rarely appears in formal tender documents or regulatory requests. Customers working through synthetic challenges know they can call and get a direct answer from someone who’s run these reactions. We won’t recite generic storage or handling guidance—we’ll give real details about reaction kinetics at different scales, side reactions we’ve trapped, and purification steps worth the time investment. One formulations lead recently flagged an unexpected discoloration in a late-stage intermediate. Our technical team walked through potential sources, drew on years of troubleshooting similar cases, and found a trace impurity at a level undetectable by generic HPLC testing. That insight didn’t just fix the immediate batch; it sharpened future runs for everyone.

    Building trust with development chemists has taught us the value of routine retention sampling, rapid re-testing access, and upfront transparency about supply limitations. These lessons didn’t come cheaply— they took years of occasional misfires and hard-won corrections. Today, we encourage partners to send their staff to our site for batch review and in-house QC analysis if they want a closer look. Sometimes, the way forward comes from those face-to-face exchanges rather than lengthy threads of paperwork and email.

    Delivering Real Consistency

    Running a chemical plant means everything counts at scale. A single off-profile batch doesn’t just slow down one research group—it can bottleneck entire projects, throw off schedules, and strain budgets. To keep 3,4-Dimethylisoxazol-5-Amine output tight, our teams revisit batch records and raw material supply reports after every run. Discrepancies don’t get buried; we bring them to the surface before they land on the customer’s bench.

    We’ve made strides in automated analytics, leveraging in-line NMR and real-time chromatographic feedback to alert staff to drift in process control. Upgrades like these emerged not from distant labs but from specific production blockages and repeated conversations with downstream users. Regular customer audits bring us up to speed on evolving application needs, allowing us to tweak specifications and address new documentation standards without falling behind.

    Regular handling of shipping logistics keeps us grounded in the realities our customers deal with every day. Delays at port or last-minute re-routing remain serious risks for any global supplier. Direct involvement with packaging, hazardous labeling, and container management has taught us the value of redundancy and pre-emptive planning. Cutting corners on packaging or QC never pays off in this business; a contaminated or opened container can ruin months of work for a partner. We test seals, batch labels, and stability under different transport conditions, informed by field failures that only came to light after deep analysis of transit conditions and arrival inspections.

    Continuous Learning and Process Improvement

    No process reaches perfection. Every production cycle brings lessons, whether through unexpected impurities, equipment wear, or shifts in market demand. Through decades of continuous production, we’ve built a knowledge archive spanning synthetic method tweaks, troublesome side reactions, and handling recommendations rooted in field experience. These insights feed directly into production refinements that make practical differences—fewer repeat runs, tighter product specs, and lower customer complaint rates.

    Collaborating with small research labs and leading multinational groups both bring their own pressures. Smaller teams often need rapid turnaround of modest batch sizes, placing stress on our scheduling, but providing invaluable feedback on changes in compound application. Larger buyers may want analytics much more robust than standard. Our process engineers and QC chemists work together to meet these demands. Often, a small tweak in purification flow or additional post-reaction washing improves not just one batch, but all future output.

    Transparency and Trust: Our Commitment

    Experience has taught us the long-term value of transparency. Manufacturing a specialty intermediate like 3,4-Dimethylisoxazol-5-Amine doesn’t just end at the fence line of our facility. Our customers expect clarity on sourcing, batch origin, and processing conditions. They demand real COA support—not just a box-ticking exercise, but deep access to analytical data and explanations behind specification ranges. We invite critical questions and review any findings with thorough documentation.

    We open our records for regulatory or customer inspection, giving access to all historical batch data and deviation logs upon reasonable request. Confidence in product quality isn’t built in isolation, and ignoring the realities of compliance and repeatability only invites headaches. Over time, these habits forge a consistent, reliable partnership with our users, ensuring the material we produce does its job without surprises.

    Meeting Evolving Market Demands

    Markets change quickly. Over the past decade, regulatory expectations on trace impurities and solvent residues have grown more restrictive, with an increasing focus on documentation and environmental footprint. As demand for 3,4-Dimethylisoxazol-5-Amine ramps up in new therapeutic and agrochemical leads, we’ve had to push both analytical boundaries and process control tighter. What satisfied regulators and users last year might not stand up to scrutiny this year.

    Customer requests for more detailed impurity profiles led us to upgrade HPLC and GC-MS infrastructure. Detailed records now extend to residual solvent logs and incremental retention sampling after each batch stage. For users worried about evolving guidance and stricter future regulations, we offer clear support in adapting paperwork and product release standards, never just meeting the baseline but staying one step ahead. This reduces risk not only for our production, but for every partner reliant on our compound.

    Final Thoughts from the Factory Floor

    Every milestone in developing, scaling, and shipping 3,4-Dimethylisoxazol-5-Amine ties back to the lessons we’ve learned from past projects and customer relationships. Building trust and ensuring reliability don’t come from marketing copy or boilerplate assurances; they grow through frank conversation about what works, what fails, and how every gram of this compound will behave under stress.

    Having operated the same production lines, monitored the same reagent trends, and traced the same analytical data through hundreds of batches, we know where promises meet real constraints. That honesty shapes our relationships with partners around the world, helping them move projects from pilot scale to production with confidence in what their starting materials will deliver. For us, 3,4-Dimethylisoxazol-5-Amine isn’t just a line item—it’s the result of continuous craft, critique, and improvement.