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HS Code |
198621 |
| Iupac Name | N-methylpyridin-4-amine |
| Molecular Formula | C6H8N2 |
| Molar Mass | 108.14 g/mol |
| Cas Number | 10402-20-1 |
| Appearance | White to light yellow solid |
| Melting Point | 73-75°C |
| Boiling Point | 265°C (estimated) |
| Solubility In Water | Soluble |
| Density | 1.12 g/cm³ (estimated) |
| Pubchem Cid | 13308 |
As an accredited N-Methyl-4-Pyridinamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of N-Methyl-4-Pyridinamine supplied in a sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Shipping | N-Methyl-4-Pyridinamine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. Packaging complies with local and international hazardous material transportation regulations. The chemical is protected from moisture, heat, and direct sunlight. Proper labeling and documentation ensure safe handling during transit by ground, air, or sea. |
| Storage | N-Methyl-4-pyridinamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from light and moisture. Clearly label the container and keep it away from heat sources and ignition. Ensure proper safety equipment is available and follow local regulations for chemical storage. |
Applications of N-Methyl-4-Pyridinamine in Industrial ManufacturingAs a direct manufacturer of N-Methyl-4-Pyridinamine, we supply this specialty intermediate to multiple advanced chemical industries. The following application segments reflect areas where this material becomes an essential building block in commercial downstream processing, supported by industry-specific standards, distinct input levels, and precise integration methods to realize tangible finished goods. 1. Pharmaceutical Intermediate SynthesisCommercial pharmaceutical manufacturers rely on N-Methyl-4-Pyridinamine as a key starting reagent in the preparation of several small-molecule active pharmaceutical ingredients (APIs), especially within antihypertensive and CNS-targeted drug classes. It enters as a strategic intermediate—typically at the nucleophilic substitution or reductive amination stage—contributing to the core pyridine ring modifications required by drug master files. Owing to strict global regulatory oversight, the use, traceability, and residual control of this compound remain essential for cGMP validation and post-synthesis purification. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingThe crop protection sector employs N-Methyl-4-Pyridinamine in the synthesis of selective herbicides and fungicides, especially those requiring pyridine-based frameworks for mode-of-action enhancement or improved environmental stability. Its role as a key methyl amino donor improves downstream selectivity and biological activity in pyridinylurea and related syntheses. Production facilities maintain detailed batch records for traceability as required by international agrochemical safety evaluations. Industry compliance standards
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3. Specialty Dye and Pigment ManufactureIn specialty dye and pigment production, N-Methyl-4-Pyridinamine functions as a core amination agent for the creation of high-value pyridine-containing chromophores, especially in the development of vat and disperse dyes. It enters directly into coupling reactions with diazonium salts or acyl chlorides, enabling manufacturers to target specific color indices, lightfastness, and solubility profiles demanded by textile and plastics sectors. Industry compliance standards
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4. Electronic Chemicals for Semiconductor ProcessingManufacturers of advanced electronic chemicals incorporate N-Methyl-4-Pyridinamine as a ligand and intermediate in the development of metal-ion scavengers and specialty etchants. The compound’s electron-donating properties facilitate specific chelation behaviors with transition metals, essential for preparing ultra-pure cleaning compounds and photoresist auxiliaries in integrated circuit fabrication. Strict impurity profiling and batch certification are necessary throughout supply and use. Industry compliance standards
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5. Fine Chemical Catalysts and Ligand PreparationCatalyst manufacturers deploy N-Methyl-4-Pyridinamine in producing tailored pyridine-based ligands used in homogeneous and organometallic catalyst systems, such as those for fine chemical synthesis or cross-coupling reactions. Its methylated amine group enables high coordination stability and unique electronic effects, directly impacting catalyst turnover rates and selectivity in downstream specialty syntheses. Industry compliance standards
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N-Methyl-4-Pyridinamine doesn’t pop up much in everyday conversation, but it comes into play where reliability, purity, and chemical insight matter. Having handled pyridine derivatives for years, we have seen laboratories and process engineers wrestle with overall yield, batch stability, and handling safety. Manufacturing N-Methyl-4-Pyridinamine requires attention to each of these concerns. Small inconsistencies in raw material purity or process temperatures quickly show up as batch loss or unexpected reactivity downstream. Since we manufacture this compound ourselves, we control the entire process—from sourcing methylating agents free of problematic side components, right down to careful temperature ramps and solvent handling during amination. That’s why what you receive in the drum always matches the quoted assay.
Chemists often glance at a TDS and see a compound with a melting point around 55 degrees Celsius and an assay exceeding 98%. From a manufacturer’s standpoint, these numbers do not capture the details that matter day-to-day. Inconsistent feedstocks and skipped purification steps sometimes mean unwanted color, higher water content, or low-level contaminants with unpredictable impact. Consistently producing white crystalline N-Methyl-4-Pyridinamine with minimal odorous by-products calls for active management each step of the way. We have invested in multi-stage vacuum distillation and on-site GC-MS, not just for a passing certificate, but to guarantee downstream processes won’t clog filters or leave behind tars.
N-Methyl-4-Pyridinamine finds its home mostly in organic synthesis, pharmaceutical intermediates, and dyes. In our experience, its appeal often boils down to the methyl group at the nitrogen and the reactivity bump that brings. Labs synthesizing API building blocks rely on it for controlled N-alkylation reactions that call for selectivity—switching to this compound can trim steps off multi-stage syntheses and help maintain product purity, saving both time and waste solvent. When dye or pigment manufacturers approach us, the need for batch-to-batch reproducibility always tops the list. Our material stands out in those lines: no unpredictable color carryover or sulfurous trace residues means less risk of costly recalls or downstream performance drift.
Direct contact with certain amines gives headaches, literally and otherwise. We have learned from direct feedback that proper fume management and clear transfer systems make the biggest daily difference for operators. By tuning the particle size of our solid product and improving drum lining, we reduce cake formation and accidental exposure during batch charging. We’ve worked alongside industrial hygienists during plant audits. This lets us offer practical advice on minimizing exposure beyond basic SDS guidance, promoting both regulatory compliance and consistent staffing.
There are several chemical suppliers selling N-Methyl-4-Pyridinamine, many as repackagers drawing from the same bulk producers. If you buy from the real source, you get traceability, technical support, and full chain-of-custody documentation. We monitor everything in-house: yield adjustments after methylation, ammonia feedstock quality, and storage conditions for the crystalline product. Any customer inquiry about lot-to-lot performance or unusual analytical readings goes directly to the same technical team signing off on the COA.
A few details make our process distinct. Our approach to temperature control during N-methylation ensures no hot-spot formation—a common cause of yellowing and ammonium salt contamination. We reject shortcut solvent recycling that leaves residues. Our water-removal systems ensure almost no hydrate formation, critical for those needing dry, free-flowing powder. We do not cut corners on testing: GC-MS, NMR, and Karl Fischer titration—run by on-site staff, not outsourced—catch low-level side products long before they can affect finished product performance.
Pharmaceutical research groups have told us minor impurities in this molecule either slow their reaction rate or create by-products tough to separate. A key step in custom synthesis for them is avoiding salt build-up and by-product amines, which can drag down purification yields. By controlling amination with precise stoichiometry and using only reagent-grade feedstocks, we limit these contaminants. In our recent multi-ton batch, the sum of all non-target isomers remained below 0.2%, resulting in direct feedback from one European partner who saved weeks by skipping additional recrystallization.
The specialty dye industry brings its own pressure points. Color matching over thousands of kilograms leaves no room for variation. Unintended copper or sulfur traces have derailed production in the past, something we've minimized through segregated process lines and routine audits. Thanks to decades of purifying and blending at this scale, we supply the material in packaging tailored for clean transfer. Our engineers tested multiple fiberboard and lined drum options to keep water out and transfer fast. That may seem like a detail, but it keeps production lines running without delay.
Our industry sits in the crosshairs of product safety and environmental performance. We put our experience to use developing process water recycling and solvent reclamation that don’t compromise product purity. By investing in closed-loop systems for our methylation steps, we reduced both overall emissions and hazardous waste generation. This took investment upfront in process control, and our operators developed protocols from lessons learned during trial runs where off-specification material cost us production time. We now send less to incineration and see a cleaner facility, both of which matter to our staff and surrounding community.
Clients and regulators alike want real visibility into product composition and sourcing. Relying only on basic lot numbers and safety datasheets leaves too many questions unanswered. We provide a full analytical packet for each batch, including all GC and NMR traces and impurity checks. Pharmaceutical partners often send their own auditors; we have nothing to hide, so visitors can watch as we run analytical checks on in-process and finished product. Our documentation process tracks from incoming raw material down to each output drum—there are no black-box processes.
We often work with clients running pilot runs for new pharmaceutical intermediates, surfactants, or materials for electronics applications. Development teams have asked for input on handling, purification, or melt processing. Rather than quoting a standard response, we pass on what has worked best in our own plant—be it temperature-controlled storage, best bulk transfer equipment, or lessons from filter selection. Our familiarity with every step of N-Methyl-4-Pyridinamine’s journey, from reaction initiators to final packaging, means suggestions are rooted in experience, not guesswork. This collaboration extends to adjusting specs when projects move from lab to plant scale so partners keep their yields high.
It helps to know why researchers and process chemists specify this pyridine derivative over close cousins. N-Methyl-4-Pyridinamine’s additional methyl group at the nitrogen fundamentally changes its behavior. Its reactivity often matches primary amines, but with greater resistance to over-alkylation—a headache in similar compounds, like 4-aminopyridine, that readily double-react and force tricky purification. Unlike its non-methylated counterpart, our compound’s increased basicity and altered solubility simplify certain condensation reactions and make it a better candidate where water or alcohol as solvent is required.
Looking at similar N-alkyl pyridines, you run into tradeoffs between boiling point, stability, and reactivity. N-Methyl-4-Pyridinamine’s moderate melting point and crystalline form make weighing and transferring straightforward, while liquid analogues create headaches during measuring and can cause leaks or volatilization losses. Each customer has their own end-use in mind, some chasing maximum selectivity in catalysis, others needing a reliable intermediate for dye manufacture. We regularly advise on whether the purity grade or crystalline form will offer a meaningful advantage for their process; often, the details under the hood—such as low water content or minimal aminal by-products—are more critical than a one-dimensional purity number.
N-Methyl-4-Pyridinamine manufacture isn’t without headaches. We have faced issues such as crystallization fouling, off-spec color, and even drum storage failures during humid spells. Sometimes small changes in ambient temperature shift the product toward clumping, which has caused downstream dosing inconsistencies. Our team has engineered dehumidified zones and flexible packaging to head off these problems after years of experience with lost time and some frustrated line workers. Early on, shipping delays or overly ambitious batch sizes led to corner-cutting on quality checks. Feedback loops with our customers have prompted us to double the frequency of in-process notebooking and batch reviews, ensuring not only compliance but actual reliability.
A frequent request—especially from those scaling up production—centers on better transfer methods for large volumes. Solid product shipped in bulk often cakes or bridges in hoppers, so we sourced new anti-static liners and trialed flow agents. Our in-house maintenance crews developed rapping and vibration methods that keep product moving. These aren’t textbook engineering solutions—they arose from collaborating across packaging, logistics, and plant floors, and the result is smoother, more reliable charging in your process facility.
We expect tighter impurity limits and environmental regulations for all chemical production, especially those entering pharmaceutical and high-tech supply chains. Rather than waiting for rule changes, we test our synthetic route with newly available catalysts and even bio-derived methyl donors. This reduces dependency on older, multi-hazardous reagents while supplying the same exceptional quality. Real improvement sometimes only comes by walking down the process floor, catching off-odors or faint discoloration, and brainstorming with the staff daily in the plant. Instead of assuming the process is optimized, we’ve set aside resources for small-scale pilot plant testing whenever clients propose a use-case beyond pharmaceutical or dye intermediates. Knowledge from these trials feeds directly into both our production and the recommendations we provide to new industry partners.
Our team brings a manufacturer’s mindset to every container of N-Methyl-4-Pyridinamine that leaves the facility. The historical knowledge—mistakes made, solutions tried, and incremental tuning applied—doesn’t pass along when you buy through a middleman. Technical advice from a manufacturer carries the weight of direct experience, sometimes bypassing pitfalls discovered the hard way. Working directly with users, we get early visibility into their formulation plans or technical pain points, which lets us recommend the best grade, packaging, and transfer protocol based on actual needs, not just theoretical compatibility.
Customers often value this partnership model during audits, process troubleshooting, or specification reviews. They know that feedback shared here can prompt real action. If an issue with color, odor, or even supply timing appears, dialogue isn’t filtered through layers of bureaucracy, so problems get solved quickly. By dedicating staff with years on our production line to incoming requests or complaints, we don’t just protect our own processes; we help safeguard your final application’s quality and consistency as well.
For today’s chemical market, quality and transparency make a difference. Each lot of N-Methyl-4-Pyridinamine reflects process controls developed from direct plant experience—starting from supplier qualification, through reaction tuning, to batch-by-batch logs and analytical checkpoints. Our operators, quality control staff, and technical support teams stand behind every drum, motivated by hands-on involvement in the manufacturing process and a commitment to both product safety and sustainability.
Those details accumulate over time. Batches of N-Methyl-4-Pyridinamine aren’t just a product; they’re a result of deep technical know-how, ongoing investment, and countless problem-solving meetings. Customers, whether large multinational plants or smaller innovators, draw on this practical expertise to realize steady, high-yielding processes. By purchasing directly from the source and engaging openly, you access not only a chemical but also a support system ready to tackle the unique challenges that come with your industry’s next breakthrough.