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HS Code |
571749 |
| Product Name | 4-Amino-1,3,5-Trimethylpyrazole |
| Chemical Formula | C6H11N3 |
| Molecular Weight | 125.17 g/mol |
| Cas Number | 72858-79-2 |
| Appearance | White to off-white solid |
| Melting Point | 130-134 °C |
| Solubility | Slightly soluble in water |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place |
| Synonyms | 4-Amino-1,3,5-trimethylpyrazole; 1,3,5-Trimethyl-4-aminopyrazole |
| Inchi | InChI=1S/C6H11N3/c1-4-6(7)9(3)5(2)8-4/h1-3H3,(H2,7,8) |
| Smiles | CC1=NN(C(=C1N)C)C |
As an accredited 4-Amino-1,3,5-Trimethylpyrazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 100 grams of 4-Amino-1,3,5-Trimethylpyrazole, labeled with hazard and handling instructions. |
| Shipping | 4-Amino-1,3,5-Trimethylpyrazole is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is handled according to standard chemical shipping regulations, including labeling and documentation. Typically dispatched by ground or air, it is packaged to prevent leaks and complies with safety standards for non-hazardous laboratory chemicals. |
| Storage | 4-Amino-1,3,5-Trimethylpyrazole should be stored in a tightly sealed container, protected from light, moisture, and incompatible materials. Store it in a cool, dry, and well-ventilated area, away from sources of ignition and strong oxidizers. Follow standard chemical safety protocols, including clearly labeling the container and restricting access to authorized personnel only. |
Applications of 4-Amino-1,3,5-Trimethylpyrazole in Industrial Manufacturing4-Amino-1,3,5-Trimethylpyrazole supports multiple downstream processes in chemical manufacturing, serving as a key intermediate and functional material in industries where controlled chemical performance and structural integrity are essential. As an experienced raw material manufacturer, we supply to specialized sectors that use this compound based on established process requirements, regulatory standards, and targeted formulation parameters. 1. Pharmaceutical Intermediate for Pyrazole-Based DrugsThis material enters pharmaceutical synthesis as a building block for active pharmaceutical ingredients (APIs) containing a pyrazole core. Medicinal chemists select it for specific amination steps to create anti-inflammatory, anti-diabetic, and anti-cancer molecules. Its purity levels and by-product controls are monitored stringently under regulated environments to meet impurity profiles for further downstream transformation. Manufacturers must establish validated cleaning and changeover protocols when switching between APIs derived from this input to avoid cross-contamination in GMP plants. Industry compliance standards
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2. Synthesis of High-Performance Corrosion InhibitorsSpecialty coatings and oilfield chemical manufacturers use this compound to synthesize organic corrosion inhibitors tailored for harsh operational environments. Its electron-donating amino group and methyl substituents enhance adsorption and film-forming efficiency on metal surfaces. Formulators set precise reaction parameters to ensure compatibility with downstream emulsification and blending steps. Quality control includes profiling residual amines and evaluating solubility for use in water-based or solvent-based systems. Industry compliance standards
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3. Precursor in Agrochemical SynthesisAgrochemical technical producers select this material as an intermediate in the assembly of systemic fungicides and insecticides that rely on the pyrazole structure to block pest metabolic pathways. The compound undergoes ring transformations or coupling reactions, which require controlled addition temperatures and stoichiometry to maximize conversion and minimize toxic by-products. Downstream processes involve stabilization with adjuvants and microencapsulation if required for final formulation. Industry compliance standards
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4. Chemical Intermediate for Dye ManufacturingDye producers use 4-Amino-1,3,5-Trimethylpyrazole in synthesizing specialty azo and heterocyclic dyes, exploiting its amino group for diazotization and subsequent coupling reactions. Its molecular structure provides chromophore stability and tuning of optical properties. Reaction conditions require monitoring pH, temperature, and stoichiometric ratios to optimize color yield and minimize unwanted side-product formation. Post-synthesis, the dye intermediate may undergo sulfonation or alkylation for water solubility and fabric compatibility. Industry compliance standards
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5. Polymer Stabilizer ComponentsManufacturers of engineering plastics and elastomers utilize this compound as a nitrogen-containing stabilizer precursor. It supports synthesis of hindered amine light stabilizers (HALS) by introducing controlled donor-acceptor groups into the polymer matrix. Precise dosing is needed to achieve target melt flow properties without adversely impacting color or mechanical strength. Performance evaluation includes accelerated aging assays and migration testing aligned with end-use specifications. Industry compliance standards
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Every compound tells a story, but some carve out a place for themselves through sheer practicality. 4-Amino-1,3,5-Trimethylpyrazole is one of those chemicals that earns its keep on a scientist’s shelf, not through marketing claims, but straight from the workbench. At our facility, we’ve spent years producing this specialty pyrazole, watching it quietly work its way into synthesis routes and process flows that demand more than the generic.
The title says it all: three methyl groups surrounding a pyrazole ring, with a primary amine at the four position. That arrangement brings more than just a tidy molecular formula. It creates a chemical with a real personality in reactions, one we’ve gotten to know batch after batch. Its structure means less risk of unwanted side-reactions in syntheses where position and reactivity matter. For those building up heterocyclic scaffolds or modifying biologically relevant molecules, having those methyl groups flanking the core makes a difference. The amine reacts as a dependable nucleophile, and the ring’s stability stands up under a range of conditions.
We routinely produce this compound in batches measured in kilograms, each time adhering to tight control over purity. The off-white to pale yellow crystalline powder speaks for itself the moment it comes out of final drying. The melting point rarely strays outside a razor-thin range, and the NMR confirms the purity requirement—key for any process where side-products can throw off an entire downstream step.
Pyrazole derivatives can pose their own headaches, especially during scale-up. Things get trickier once amines come into play. We learned early to pay close attention to reaction safety, ensuring ventilation is always up to the mark and the exotherm from methylation or amination is never underestimated. Every finished batch leaves only after it beats our internal benchmarks for water content, which preserves stability and flow during storage. Years of hands-on production taught us the right drying stages, and the best way to pack it for transit without loss or contamination.
Shipping doesn’t just mean going from one place to another. Maintaining product quality calls for vigilance in storage and logistics. Forgetting that leads to caking, or slow hydrolysis that ruins reactivity. We rarely see returns when everything in the process is right: sealed drums, desiccant included, clear labeling straight from our packing line. Anything less and you hear about it.
Talking with researchers and application chemists has opened our eyes to how flexible 4-Amino-1,3,5-Trimethylpyrazole can be. Its direct role as a building block in agrochemical discovery shows one path—where each functional group gives medicinal or crop-protection chemists extra handles on the molecule for further steps. In pharmaceutical R&D, we’ve seen it used in kinase inhibitor development, sometimes forming the central heterocycle in the active structure.
A client working on sensors once shared their story with us. The substituted pyrazole backbone offered the precise steric bulk and electronic properties they needed for selective detection. The amine acts as a functional anchor for attaching dyes or metal-binding motifs, while methylation ensures fewer side reactions. Every user has slightly different needs—some want maximum throughput for bulk modification, others ask us for tighter particle size distributions to boost solubility or mixing in high-value formulations. We take those requests seriously, not as custom jobs but as part of our real-world partnership with formulation scientists.
Decades in chemical manufacturing have taught us that purity means more than just numbers on a COA. Even trace impurities—solvents, unreacted precursors, or salts—can scramble the results of a targeted synthesis or analytical method. Our in-house analytics cover not just NMR and IR, but also trace-by-trace HPLC and GC-MS so clients know exactly what’s in every batch. We don’t cut corners. Documentation stays up-to-date, and anyone auditing our lines can see complete batch histories stretching back years.
We watch regulatory changes closely, especially from REACH and other authorities. If local or regional guidance shifts, we act fast, working with our compliance team to revalidate specs, update safety data, or qualify new routes that avoid flagged reagents. Our customers trust that nothing enters their supply chain without full traceability and documentation, not just from our word but because the paperwork proves it.
Not all pyrazole compounds serve the same role. 4-Amino-1,3,5-Trimethylpyrazole marks itself as a practical alternative to less stable or harder-to-handle amine-substituted rings. Unsubstituted pyrazole, although common, tends to show different reactivity and usually brings extra caution around air and moisture. Introducing methyl groups around the ring, especially in the 1,3,5- positions, increases lipophilicity, decreases electron density at sensitive sites, and changes solubility in organic media—all of which excel over other isomers or unsubstituted analogues in many applications.
Our regular clients often contrast our product against trimethylpyrazole isomers, or even related tetramethylpyrazoles that start to close off available substitution sites. Each methyl, each amine brings design options for the synthetic chemist. Whether you’re after a molecule that’s less prone to oxidation or one that sits in a certain melting range to ease downstream processing, this compound proves its worth.
While some manufacturers shy away from adjusting their process, staying rigid with a one-size approach, we adapted as customers required subtle changes. A surge in demand from a domestic pharmaceutical lab prompted us to rebuild our purification routine to provide higher purity, well above the industry baseline. This meant tighter filtration, vacuum drying down to sub-percent moisture, and documenting every modification to ensure repeatability.
Requests for smaller, more consistent grain sizes led us to trial different crystallization parameters, from seeding methods to controlled cooling, making sure each new batch behaved as expected in clients’ applications. Not every tweak makes its way into standard practice, but customer feedback always steers which direction we take. If a researcher spots a minor impurity interfering in an assay, our team tackles the root cause directly—whether it means sourcing new raw materials or upgrading our equipment to eliminate cross-contamination.
Every scale-up teaches new tricks. What works in a glass flask sometimes changes completely at reactor scale. Meticulous temperature control stands out as a major challenge. Methylation reactions, for instance, can run away if cooling isn’t uniform, so we added jacketed stainless vessels and constant monitoring. Batch reproducibility, even down to the color and flow properties, owes a lot to these upgrades.
Investing in modern analytics paid off, too—HPLC chromatography remains the check on our work, not just for finished goods but also for in-process samples. The difference shows up in greater lot-to-lot reproducibility and fewer deviations from standard. Waste treatment pushed us to optimize, especially since some solvents require special disposal by law and we keep emissions below threshold levels. Partnering with waste processors, switching to greener solvents, and reusing process water when possible keeps us above board with authorities and customers alike.
Feedback from users often illustrates more than technical data ever can. Some pharmaceutical clients report that this compound works perfectly as a fragment in building new chemical libraries for screening. Its methyl groups direct further substitution, and the amine is a reliable point of connection for labeling with probes or coupling for SAR studies.
Agricultural chemists come with different needs—asking for stability against photodegradation or seeking specific melting points for mixing into formulations. Scientists in material sciences found unexpected value, harnessing the molecule as a stabilizer for certain metal complexes, or as a ligand in catalysis experiments where steric and electronic properties must hit just the right mark.
We’ve learned from years of hard-won experience that focus on occupational safety never ends. All operators wear PPE, not for compliance, but because the risk of skin or inhalation exposure doesn’t end once you know the process. Amine-laden distillates need prompt neutralization and careful exhaust management—habits formed not out of regulation but from real incidents and near misses witnessed on the floor.
Our Quality Control teams run extensive checks on each batch, scrutinizing everything from solid content to pH stability and long-term shelf-life. Training cycles never stop. Every new procedure or process improvement gets a risk assessment, walkthrough, and documented approval to make sure there are no shortcuts. That persistence has made the trust we get from our long-term clients possible.
We don’t rest on the reputation of yesterday’s batches. The drive to cut cycle times, boost yields, and trim costs propels our everyday work. Adding automation in weighing, feeding, and filtration reduced human error and improved repeatability. By digitizing batch records and production logs, our team spots trends faster—like minor batch variations or subtle shifts in impurity profiles that might otherwise go unnoticed until they affect a customer’s run.
We regularly review sustainable sourcing. Synthetic intermediates that once depended on hazardous reagents now get reevaluated for safer or renewable routes. Even disposing spent solvents became a chance to innovate—combining streams or reclaiming to cut out unnecessary waste. We keep open lines of communication with our clients: sharing data, inviting audits, and taking every investigation seriously until we can boast not just compliance, but proof of ongoing improvement.
Beyond our factory walls, we know most users don’t want just a product, but a real connection to the source. We value the conversations where chemists and engineers walk us through exactly how each bag or drum enters their process—pointing out what matters most to them. If a university team needs small samples for screening high-throughput reactions, we set aside stock in manageable packaging. Process engineers after ton-scale reliability count on our logistics, and inform us how certain transport or handling stresses play out in practice, letting us troubleshoot upstream, not after a problem hits.
Our technical support takes the time to dig into those questions, not because they come with a P.O. attached, but because that’s how we’ve built relationships in the industry. Sometimes, that means honest talk about limits: where our compound fits and where another derivative might offer better selectivity, chemical tolerance, or regulatory clearance.
Anyone can claim quality, but in our experience, it comes down to grit and transparency. We pursue independent, third-party lab testing to complement our internal checks, reinforcing confidence on both sides of the transaction. We maintain open documentation of validation results, analytical protocols, and regulatory correspondence to facilitate audits, tech transfer, and new customer evaluations. Our commitment to higher standards means we keep up with industry-led initiatives, peer discussions, and direct feedback loops so our process never falls behind.
Executives and team leads regularly review operations on the ground, not just from spreadsheets but on the factory floor. If a customer flags a supply chain bottleneck or notes an out-of-specification lot, project managers and chemists circle up to root out the cause. Our track record comes from acting quickly and decisively—not blaming variables or hiding behind process complexity.
Over the years, our relationships with clients across industries formed the backbone of continued production and product refinement. Sharing ideas, providing technical support, and responding to unforeseen challenges nurtures mutual trust. Whether the market shifts from pharmaceutical to agrochemical development, or regulations step up, we keep close tabs and communicate with customers to reset expectations and resolve issues together.
Feedback is not just welcomed; it’s central to our approach. We document and address every inquiry—whether it relates to research use, scale-up compatibility, or a need for specialized analytical support—and integrate the solutions back into the production cycle. Our lines remain open because the landscape never stops moving, and our compound’s journey continues with each new application our partners explore.
The demands on chemical suppliers keep growing, and the call for higher-purity, better-documented, and more sustainable products never lets up. Continuous improvement isn’t just jargon here—it’s a habit. We invest in employee training, new analytical platforms, and expanded capacity, all to maintain a dependable supply for users who don’t want surprises once it lands at their dock.
New applications might take shape in pharmaceuticals, materials science, or crop protection—often stretching our understanding of what this molecule can offer. We encourage our partners to reach out, share challenges, and turn to us for joint development as synthetic targets evolve. By staying in close dialogue with the scientific community, our factory adapts, improves, and delivers not just a molecule, but a valuable tool for those on the front lines of discovery.
At the end of the day, 4-Amino-1,3,5-Trimethylpyrazole remains a core component of our product lineup—the result of lived experience, collaboration, and an ongoing push to make complex chemistry more reliable, more accessible, and more responsive to the evolving needs of innovators everywhere.