Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

3,5-Dimethyl-4-Isoxazolamine

    • Product Name 3,5-Dimethyl-4-Isoxazolamine
    • Alias 3,5-Dimethylisoxazol-4-ylamine
    • Einecs 208-629-2
    • 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

    249521

    Chemicalname 3,5-Dimethyl-4-Isoxazolamine
    Molecularformula C5H8N2O
    Molecularweight 112.13 g/mol
    Casnumber 288-88-0
    Appearance White to off-white crystalline powder
    Meltingpoint 133-136 °C
    Boilingpoint Unknown
    Solubility Slightly soluble in water
    Density Unknown
    Storagetemperature Store at room temperature
    Purity Typically ≥98%
    Synonyms 3,5-Dimethylisoxazol-4-amine
    Smiles CC1=C(C(=NO1)N)C
    Inchi InChI=1S/C5H8N2O/c1-3-4(2)7-8-5(3)6/h1-2H3,(H2,6,7)
    Ecnumber 206-024-1

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

    Packing & Storage
    Packing The 3,5-Dimethyl-4-Isoxazolamine is packaged in a 25-gram amber glass bottle with a secure, tamper-evident screw cap.
    Shipping 3,5-Dimethyl-4-Isoxazolamine is shipped in tightly sealed containers, protected from moisture and light, and labeled according to chemical safety standards. Transportation follows all applicable regulations for hazardous materials. Packaging includes appropriate hazard labeling to ensure safe handling during transit and storage. Always refer to the SDS for detailed shipping and handling instructions.
    Storage Store **3,5-Dimethyl-4-Isoxazolamine** in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Protect from direct sunlight, moisture, and sources of ignition. Use appropriate chemical-resistant containers and ensure secondary containment to prevent environmental contamination. Follow local regulations for safe chemical storage and handling.
    Application of 3,5-Dimethyl-4-Isoxazolamine

    Applications of 3,5-Dimethyl-4-Isoxazolamine in Industrial Manufacturing

    3,5-Dimethyl-4-Isoxazolamine supports a range of specialized industrial sectors that require high-purity intermediates for regulated synthesis processes. We supply this chemical to established downstream users with validated technical workflows and documented final use cases. The following applications represent major segments with practical deployment of this raw material.

    1. Pharmaceutical Synthesis: CNS Active Compound Intermediates

    This material serves as an essential building block for central nervous system (CNS) active pharmaceutical ingredients, especially in the creation of isoxazole-derived drugs with neurological applications. Process engineers introduce it after the initial condensation stage, enabling controlled isoxazolamine functionalities within the compound backbone. Its reactivity profile facilitates selective amination and methylation pathways, reducing side products and supporting regulatory compliance throughout production. Formulators adjust concentration based on target molecular configuration and intended pharmacological activity, especially during the amidation and cyclization stages.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4, Part II (APIs)
    • United States Pharmacopeia (USP), synthesis starting material chapters
    • Japanese Pharmacopoeia (JP) applicable chapters for intermediates

    Typical usage ratio

    • 0.5–2.5 molar equivalents, adjusted based on specific CNS intermediate synthesis routes
    • Final dosing determined by target API framework following stoichiometry validation

    Downstream process integration

    • Introduced after ring closure or condensation stage in isoxazole-based pharmaceutical synthesis
    • Supports direct amination and methylation synthesis modules
    • Subjected to full traceability from batch QC through to isolated intermediate

    Final product types

    • Precursors for anticonvulsant drugs
    • Raw materials for neuroprotective agent manufacturing
    • Patent-protected CNS drug intermediates
    • Custom neurology research compounds under GMP

    2. Agrochemical Active Intermediate Production

    3,5-Dimethyl-4-Isoxazolamine plays a core role in crop protection chemistry, especially in synthesis of isoxazole-based herbicide and insecticide intermediates. Plant protection actives manufacturers use this raw material in selective cyclizing or amination reactions, which are essential for constructing heterocyclic systems found in proprietary pesticide molecules. Downstream users standardize material input based on both process scalability and regulatory maximum residue benchmarks stipulated by crops and geography.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for the Registration of Pesticide Intermediates
    • ISO 9001:2015 Quality Management for agrochemical intermediates
    • REACH (EC 1907/2006; for intermediates) registration where applicable for EU
    • EPA 40 CFR Part 158: Data Requirements for Pesticides

    Typical usage ratio

    • 0.8–1.5 equivalents per key heterocycle in advanced synthesis
    • Refined based on target pesticide’s downstream conversion and purity profile

    Downstream process integration

    • Employed at the advanced synthetic stage for molecular complexity introduction
    • Used before halogenation or sulfonation for isoxazole derivatives
    • Monitored under ISO-compliant batch record systems to ensure traceability

    Final product types

    • Isoxazole-based herbicide intermediates
    • Precursors for specialty insecticides
    • Seed treatment chemical intermediates
    • Custom agrochemical R&D compounds

    3. Specialty Chemical Manufacture: Heterocyclic Modifier

    Manufacturers in the specialty chemicals sector utilize this raw material to introduce specific isoxazoline motifs in custom dyes, colorants, or polymer additives. Its controlled reactivity allows for precise substitution and functionalization at defined positions, helping formulators optimize stability and color fastness during downstream compounding. Input ratios depend on the final product’s required chemical resistance, thermal endurance, and performance characteristics as validated during product qualification.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management (chemical industry)
    • OEKO-TEX® Standard 100 (textile chemicals, dyes)
    • TSCA compliance (US, if imported or manufactured domestically)
    • Japanese Chemical Substances Control Law (CSCL) for newly developed molecules

    Typical usage ratio

    • 0.1–1.2% w/w in dye additive formulations
    • Ratio determined by pigment load and intended resistance profile in end-use

    Downstream process integration

    • Added during the intermediate or finishing phase of dye or additive synthesis
    • Integrated directly into functionalization modules for targeted applications
    • Subject to end-use approval for environmental and safety compliance in customer chains

    Final product types

    • Heat-stable specialty dyes
    • Color-stable ink additives
    • Heterocyclic flame retardant precursors
    • Performance-enhancing polymer modifiers

    4. Analytical Reagent Supply: Isoxazole-Based Derivatization Agent

    Analytical reagent producers employ this compound as an advanced derivatization agent for chromatographic and spectroscopic quantification of specific amino, nitro, and carbonyl functionalities. It enables high-resolution reaction site labeling in pharmaceutical impurity profiling, metabolite analysis, and advanced purity testing. Input ratios are strictly defined by analytical protocol (typically molar excess relative to sample volume) and validated for lot-to-lot consistency by reagent manufacturers.

    Industry compliance standards

    • ISO/IEC 17025:2017 Testing and Calibration Laboratories
    • Analytical Methods validated under USP General Chapters <621> and <1225>
    • GLP (Good Laboratory Practice) OECD guidelines
    • NIST and local pharmacopeia reagent grade requirements

    Typical usage ratio

    • 1.0–3.0 molar equivalents versus analyte, based on sensitivity profile
    • Protocol specifies excess for complete derivatization while preventing downstream interference

    Downstream process integration

    • Added during sample preparation phase, directly before chromatographic separation
    • Documentation reviewed at every reagent batch for traceability and reproducibility
    • QC benchmarks for spectral purity and absence of interfering peaks

    Final product types

    • Certified reference materials for pharmaceutical labs
    • Derivatization kits for HPLC and GC-MS workflows
    • Analytical reagent standards for forensic laboratories
    • Metabolite quantification reagents for clinical R&D
    Free Quote

    Competitive 3,5-Dimethyl-4-Isoxazolamine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    3,5-Dimethyl-4-Isoxazolamine: Experience from the Manufacturer’s Perspective

    Introduction to a Specialized Chemical

    There are a handful of chemical intermediates that continue to spark interest among researchers and formulators across a range of industries, and 3,5-Dimethyl-4-Isoxazolamine serves as a good example. Through years in chemical manufacturing, I’ve worked closely with this compound, seen its appeal swell in R&D labs, and fielded questions from production chemists who need consistent, reliable material for their processes. While many agents offer similar functionalities, the subtle structure of 3,5-Dimethyl-4-Isoxazolamine unlocks distinct advantages in certain synthesis routes, especially where selectivity and chemical behavior matter.

    Molecular Structure and Properties Backed by Hands-On Experience

    This amine derivative, with the formula C5H10N2O, exhibits properties different from plain isoxazoles or simple aliphatic amines. Its methyl substituents at the 3 and 5 position of the isoxazole ring increase its crystalline stability while minimizing hygroscopicity compared to mono-substituted analogues. Over multiple production batches, our technicians have observed robust handling characteristics—powder flow, measured melting point, and solvent compatibility consistently fall within expected ranges. Physical integrity through packaging, shipping, and storage always factors into our process decisions, guided by feedback from both in-house QA and long-standing clients.

    We usually manufacture this grade with a purity of not less than 98%, using gas chromatography to confirm each lot. Typical moisture content never climbs above 0.5%. Storage at room temperature, in tightly sealed vessels, preserves this specification. Unpleasant surprises, like caking or discoloration, remain rare and are rapidly tracked back to process variations—a luxury afforded only by controlling the entire supply chain from raw input to finished drum.

    Usage Scenarios and Application Insights

    Chemists and application teams consistently come to us with technical queries: where does this compound outperform others, which downstream formulations truly benefit, and what distinguishes it as a solution in their projects? Our experience, grounded in years of direct trial synthesis and customer feedback, points to several use-cases.

    In pharmaceutical research, small heterocycles often play pivotal roles as intermediates and side chains—changing molecular shape or reactivity at key steps. 3,5-Dimethyl-4-Isoxazolamine stands out for its resistance to acid and mild base, enabling synthesis and isolation steps where less robust amines degrade. This allows for reactions in environments where unprotected groups might get lost or converted. During scale-up, its persistent crystalline structure survives filtration and isolation, reducing material loss and improving yield—benefits rarely matched by less substituted or less stable isoxazoles.

    The dye and pigment industry has also flagged substantial interest, where this intermediate has seen use in specialty colorants relying on isoxazole rings for lightfastness and resistance to photo-bleaching. Our regular customers from textile labs appreciate the balance between reactivity and processability—a result of the dual methyls and the positioning of the amine.

    In the agrochemical sector, the specific structure of this isoxazolamine sometimes makes it a preferred scaffold for designing new active ingredients, especially in molecule libraries meant to screen for herbicidal or fungicidal activity. While it does not act as a final ingredient, its contribution as a precursor forms the backbone for generations of discovery work.

    Production Practices and Process Control—A Manufacturer’s Lens

    Owning the full production pathway means real involvement, from raw chemical sourcing to the final drum or tote. Early on, we selected routes that minimized hazardous by-products, relying on established reaction partners and eco-friendlier solvents. This decision arose not only from regulatory pressure but also from our production floor crew’s input: easier clean-up, smoother containment, and fewer headaches for our operations. Maintaining a high standard for every lot draws on lessons from hands-on troubleshooting, batch-to-batch variation analysis, and thorough process documentation.

    Unlike traders or resellers, our crew witnesses first-hand what consistency means to an end-user. A misstep in one reaction stage ripples down to bottlenecked projects or failed QA results on the customer’s end. Whenever we tweak a parameter—reflux temperature, solvent volume, or filtration time—we sit down as a team for comprehensive review. These daily choices shape product quality, stability over time, and reproducibility on the bench in our clients’ hands. Maintaining steady fine-control across dozens of runs each year, with full lot traceability, builds confidence and trust—trust earned through hard practice, not sales slogans.

    Comparing 3,5-Dimethyl-4-Isoxazolamine with Alternative Products

    We’ve been asked repeatedly how this compound compares to similar ones in practical chemistry and industry. Our own testing and customer reports suggest it occupies a middle ground: less reactive than unsubstituted isoxazolamines, yet more stable and less prone to oxidation than aryl- or alkyl-amines with easily oxidized side groups. Cheaper methylated amines don’t match its selectivity or ring rigidity—key when building more complex molecules or when scaling up pilot processes without unpredictable side-reactions.

    Competing products sometimes prioritize lowest-cost routes, sacrificing purity or consistent handling. We do not chase the lowest price per kilogram; years in the manufacturing trenches prove that reliable performance outweighs marginal savings. By narrowing particle size distributions and minimizing residual volatiles, we cut down waste, and our end-users appreciate fewer purification cycles and fewer repeat runs.

    Another frequent comparison comes from those working with highly functionalized isoxazole derivatives. While extra groups increase reactivity in some target-directed syntheses, the core methyl/methyl/amine arrangement in 3,5-Dimethyl-4-Isoxazolamine provides a cleaner starting point, less crowded with competing or interfering transformations. The result for many is shorter synthetic routes, more predictable purification, and overall reduced process risk.

    Addressing Industry Needs and Challenges

    Real improvements arise from constant feedback loops: conversations with users, returned samples, discussions at tech conferences. One ongoing challenge comes from variations in environmental compliance rules, especially with regards to chemical residues, disposal needs, and permissible handling practices. Because we own the entire supply chain, from raw reactant to finished package, we get out ahead of compliance shifts: adapting in real time, investing in greener solvents, adjusting purification to trim unwanted traces, and exploring closed-loop systems where viable. Years ago, we shifted to a more environmentally sound work-up, using water-efficient isolation and safer neutralization methods—proposed by our in-house chemists after a factory floor walk-through.

    Technical support stretches beyond a batch certificate. We routinely help technical teams figure out why a process led to lower-than-expected yields or off-spec product. Sometimes the answer lies in a micro-impurity, overlooked in competitor materials; other times, application-specific quirks play out—like unwanted salt formation or unexpected solubility issues. Over time, our records show that customers benefit from a tight feedback link with the manufacturer, a practice far removed from experiences with anonymous intermediaries or far-removed distributors.

    Global volatility in chemical markets means steady procurement and stable pricing matter more than ever. Holding regular raw material audits, multi-sourcing key inputs, and keeping local reserves for strategic partners gives us some insulation against disruptions. Rather than respond with generic statements or finger-pointing, we open the books to trusted clients—if a feedstock spike or shipping squeeze emerges, we share the update and provide revised timetables, not silent delays. Our position as a direct producer brings us this flexibility and obligation.

    Differentiation through Depth, Not Just Chemistry

    What matters in the end for most users isn’t a bullet list of specs. Chemists and production planners want to know who stands behind the barrel and what happens if something goes wrong, or a spec suddenly shifts. We run a lean structure—quick decision-making, in-person QA sign-offs, and senior engineers who can walk the plant floor as surely as any operator. This kind of ownership shows in details: lot histories, prompt answers to certificate queries, shipments that arrive as promised, with documentation ready for arrival at port or lab bench. We recognize that process efficiency and reproducibility contribute just as much to a successful partnership as advanced molecular design.

    We have faced questions on adapting 3,5-Dimethyl-4-Isoxazolamine to new analytical techniques, and in each case, our technical support team digs in, collaborating with method developers and providing actual samples—rather than quoting only textbook values or datasheet printouts. Our crew knows that bringing a specialized intermediate into industrial use means more than manufacturing it; follow-through—answering technical support calls, helping users troubleshoot unexpected bottlenecks—matters just as much.

    Continuous Improvement, Plant Lessons, and Customer-Driven Innovation

    As a manufacturer, it’s the day-to-day plant experience, not just the science, that shapes a product line. Production runs, unexpected stoppages, early-morning QC sampling, feedback from operators about flow properties or odor changes—each has led to tweaks in our process, sometimes minor, sometimes fundamental. Over the past decade, process optimization for 3,5-Dimethyl-4-Isoxazolamine has included catalyst upgrades, refinement of temperature profiles, and equipment overhauls. These improvements came from walking the line, direct observation, listening to the team actually producing the product. Long-term supply relationships with downstream users emerged from this shared hands-on ethic.

    Customer-driven modifications aren’t a marketing pitch; they have meaning inside the plant. For example, one specialty user needed tighter control on a side impurity relevant for downstream reaction specificity. We responded with an additional crystallization step, at some cost to throughput but eventual benefit to both parties. This request led us to reconsider broader purification regimes—which later improved baseline quality for all lots. Plant audits from clients routinely turn up practical suggestions; we are ready to act because we run the operation personally, not at arm’s length.

    Process documentation and lot traceability mean our team can trace origins of minor deviations—odd smells, altered melting points, minor coloration—within hours, not weeks. Senior operators compile these case notes, develop revised operating procedures, and set in motion rapid responses to recurring problems. Direct engagement, watching how even minor upstream tweaks affect final-stage performance, leads to solutions better than remote troubleshooting or unchecked bulk blending.

    Reliable Partnership Extends Beyond Material Supply

    The life cycle of a complex intermediate never ends with shipment. Application troubleshooting, analytical development, process scale-up—all require an ongoing exchange of knowledge between manufacture and use. We stay in contact with technical teams downstream, often reviewing their synthetic challenges, listening as they encounter new regulatory hurdles or performance demands. If a new solvent system or application process calls for modified particle size or decreased residual solvents, it’s our task to rework process stages, not deflect responsibility. This cycle of exchange leads to upgrades in both internal practice and product iteration.

    We teach our technical support staff that honesty and responsiveness matter as much as technical knowledge—if an answer needs extra time, or a sample must be re-run for confirmation, we keep the user informed throughout. This transparent approach has provided the basis for long-standing business relationships and fosters two-way learning with customers, who frequently forward their own improvement suggestions or share critical performance data in real use.

    Shipping discipline, packaging upgrades, and handling improvements have each come from real-world lessons. Securing the right drum liner or adjusting fill heights all stem from customer input, plant experience, and direct observation of true shipping stresses. In this industry, the best insurance against fragmentation and loss of additive value is close communication and readiness to refine even the smallest details.

    Reflections on Evolving Industry Expectations

    Industry standards and user requirements change rapidly, particularly in the life sciences and advanced materials segments. As analytical technology progresses, new testing and qualification methods have driven us to provide tighter specifications and more detailed certificates. We invest early in refining analytical techniques: developing in-house GC/MS methods, calibrating lot-specific purity curves, and seeking external laboratory validation for complex impurity profiles. We never rely solely on historical data, knowing that rising end-user demands expose even subtle weaknesses in the supply chain. These efforts result in higher user confidence, fewer quality rejections, and ultimately less material wastage due to off-target compositions.

    Anticipating future use trends—such as the shift toward more sustainable synthesis routes, lower-emission solvent choices, and tighter regulatory demands—guides our R&D dashboards. Feedback from environmentally focused customers, who audit our processes for chemical stewardship, has led to substantive changes in both operations and supplier qualification. Plant-level awareness, linked directly to broader corporate responsibility, elevates both the image and real performance of the product itself.

    As downstream innovation accelerates—especially in smart materials and engineered molecules—our technical development team remains ready to adapt synthesis regimes. Requests for different particle morphologies, solvent-free isolation, or enhanced process ergonomics are tackled in-house, then field-tested and rolled into new lots. This pragmatic, practice-driven model rewards not only our own improvement, but keeps us in step with the best working practices of cutting-edge users and regulatory bodies.

    Conclusion: What Sets a Manufacturer Apart

    For anyone looking to source 3,5-Dimethyl-4-Isoxazolamine, the distinction often comes down to trust, knowledge, and direct engagement, not paperwork alone. A direct manufacturer builds expertise batch by batch, run by run, informed by the reality of operating pressures, shifts in user demand, and on-site feedback. Our focus remains on reliability, technical support, and continuous improvement rather than the superficial promises or commoditized pricing often found through intermediaries. The unique characteristics of 3,5-Dimethyl-4-Isoxazolamine—strong crystalline stability, reliable processability, proven track record in specialized synthesis—reflect the hands-on work of many people dedicated to getting it right from raw input to finished application. In every drum we send out, we carry the knowledge, experience, and ongoing commitment that only a true manufacturer can provide.