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HS Code |
739529 |
| Chemical Name | 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide |
| Molecular Formula | C12H13N3O2S |
| Molecular Weight | 263.32 g/mol |
| Appearance | Solid (typically powder or crystalline) |
| Solubility | Slightly soluble in water; soluble in DMSO and methanol |
| Purity | Typically available at ≥97% |
| Storage Conditions | Store in a cool, dry place, away from light |
| Smiles | Cc1cccc(Nc2cc(ncc2)S(=O)(=O)N)c1 |
| Inchikey | JYRYIGDQYIQHBU-UHFFFAOYSA-N |
As an accredited 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams of off-white powder, labeled '4-[(3-methylphenyl)amino]pyridine-3-sulfonamide,' with hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide: Securely packed in drums or bags, maximizing container capacity. |
| Shipping | 4-[(3-Methylphenyl)amino]pyridine-3-sulfonamide is shipped in secure, chemical-resistant packaging to prevent contamination and degradation. The product is labeled according to relevant safety regulations and includes handling instructions. Shipping complies with local and international guidelines for chemical transport, ensuring safe and prompt delivery to the destination. Temperature and humidity control may be applied as needed. |
| Storage | 4-[(3-Methylphenyl)amino]pyridine-3-sulfonamide should be stored in a tightly sealed container, protected from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure proper chemical labeling and restrict access to trained personnel. Follow local regulations for chemical storage and disposal. |
| Shelf Life | `4-[(3-methylphenyl)amino]pyridine-3-sulfonamide` should be stored tightly sealed in a cool, dry place; typical shelf life is 2 years. |
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Purity 99%: 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product quality. Melting Point 215°C: 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide with a melting point of 215°C is used in high-temperature medicinal chemistry applications, where it maintains compound stability during processing. Molecular Weight 265.32 g/mol: 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide with a molecular weight of 265.32 g/mol is used in medicinal formulation design, where accurate molar dosing enhances pharmacokinetic predictability. Particle Size <10 µm: 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide with particle size less than 10 µm is used in solid dosage form manufacturing, where uniformity improves tablet consistency. Stability Temperature 60°C: 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide with a stability temperature of 60°C is used in storage and transport logistics, where thermal stability reduces degradation risk. Solubility 25 mg/mL in DMSO: 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide with solubility of 25 mg/mL in DMSO is used in biochemical assays, where high solubility improves assay sensitivity. HPLC Purity ≥98%: 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide at HPLC purity ≥98% is used in research and development, where analytical accuracy supports reliable experimental outcomes. |
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Manufacturing 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide challenges even seasoned chemists. The production process draws on years of hands-on experience in heterocyclic and sulfonamide chemistry, and the product owes its reliability to small but decisive choices made by people at the bench, not marketing teams. For end users developing pharmaceutical actives, the precise nature of each input means everything. Consistency reflects not only technical controls but an awareness of what small changes can do to yield and reactivity further down the line.
Demand for intermediates that combine aromatic sulfonamides and aminopyridines has increased. Regulations and customer expectations both require careful attention to each lot’s reproducibility. Our commitment starts with raw material selection, not just for purity but also for reactivity and contaminant profiles. Not everything with the right CAS number behaves the same under actual synthesis conditions. We track subtle batch-to-batch changes, and whenever we’ve pushed for tighter control, results show up in fewer process deviations for customers.
We supply 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide in several grades, ranging from research to advanced pharmaceutical applications. Typical product is a pale beige crystalline solid, and chemical purity by HPLC exceeds 98%, verified against in-house synthesized reference material, not outsourced standards. Moisture levels fall below 0.2% because exposure risks carry over to downstream reactions, particularly amide couplings. We keep particle sizing under control to limit dust formation during handling, which users in pilot plants appreciate.
By managing temperature and pH tightly during sulfonation and coupling, we avoid generating colored side impurities that can lead to extensive purification headaches later. Shelf stability under ambient conditions exceeds two years; our own retention samples confirm this with regular follow-up testing. We understand nobody wants to waste time requalifying an input due to unexplained color change or contamination, so we work to ensure the delivered product remains consistent every shipment.
Lab workers who’ve handled similar pyridine-sulfonamides notice the difference in free-flowing powder, which minimizes loss during weighing and transfer. Customers preparing scale-up runs have told us that our material dissolves faster than off-the-shelf imports—an effect rooted in our drying regime and particle engineering, not chance. This reduces the time spent troubleshooting dissolution or filtering unreacted solids. We strive for a balance: the product must pour smoothly, but excessive milling can generate electrostatic build-up, which nobody wants in a scale production room.
Clean reaction and work-up are not luxuries in a modern synthetic route—they avoid introducing unknowns to later steps. Our process yields minimal residual solvents; GC analysis confirms this for every production batch. We’ve had users from agrochemical labs report better overall step yields because impurities that normally appear with less controlled batches are absent. Years ago, a series of customer complaints about unexpected pinkish tint led us to re-assess our sulfonation endpoint monitoring. Updating our in-cycle quality checks made for clearer product and eliminated a recurring headache for users downstream.
Distinct from simpler sulfonamide intermediates, 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide carries dual aromatic character and strong electron-donating capacity. Synthetic chemists value the compound’s ability to participate in cross-coupling and nucleophilic aromatic substitution without excessive byproduct formation. Competing products often carry traces of nitro or halogen impurities—a result of less-selective precursor sourcing—and these contaminants cause catalyst poisoning in Pd- or Ni-catalyzed couplings. Ours avoids these pitfalls by sourcing high-purity 3-methyl-aniline and pyridine derivatives.
Comparisons with conventional 3-pyridine sulfonamides show the benefit of the 3-methylphenylamino group. Electron density at key positions differs, which lets formulators fine-tune both solubility and reaction selectivity. For those optimizing process routes, the clean conversion afforded by this product in downstream steps has significantly reduced purification cycles, saving both time and solvent use. During method development, one pharmaceutical partner successfully replaced a two-step protection sequence by switching to our sulfonamide—confident that no reactive impurities would spark side chemistry in their coupling step.
In pharma, the sulfonamide serves as a versatile intermediate, feeding into heterocyclic core modification and boronate pinacol ester couplings. We’ve supplied material destined for kinase inhibitor libraries, which demand consistent amine reactivity without colored impurities. More than one medicinal chemist has pointed out that yields are more reproducible when starting from our lot versus catalog-bought, inconsistently dried powders. Process chemists have shared that scaling up our sulfonamide leads to cleaner filtrations and less waste, particularly after labor-intensive amidation steps.
Outside pharmaceuticals, the product sees use in pigments and electronics. R&D groups exploring organic thin-film transistors note that our sulfonamide’s tight melting point specification reduces the risk of batch failure. Analytical chemists find quantification straightforward—because we keep extractables and leachables to a bare minimum. This kind of control can make the difference when validating a new material for high-reliability uses, whether batch or continuous process.
For years, we have documented the real-world impact: fewer rejected lots, easier batch record reconciliation, and shorter manufacturing campaigns for end users. Time after time, tighter quality parameters mean fewer phone calls and troubleshooting sessions for technical staff, both for us and for those using our products. In a recent multi-year partnership with a leading generic manufacturer, consistent batch color and melting range helped reduce quality complaints by more than half, freeing up analytical resources to focus on more complex products.
We share current impurity profiles, not just because regulators ask, but because informed users make more reliable partners. Analytical transparency—whether in providing full NMR spectra or verifying non-detectable metal content by ICP-MS—creates trust better than any marketing brochure. We bring these practices in because we have stood on the receiving side ourselves, frustrated by lack of information or unexplained batch variation.
Sulfonamides and aminopyridines cover a broad class of molecules, but subtle changes in the aromatic system alter both physical characteristics and reactivity. 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide’s particular arrangement creates a compound less likely to hydrolyze during long-term storage. Some related species, lacking the methyl group, prove more moisture sensitive and degrade quickly outside carefully controlled environments. Users who switched from straight 3-aminopyridine sulfonamides to our product have reported less discoloration and higher final product yields.
In multi-step synthesis, each impurity can cascade, eventually affecting API crystallization or even stability. Competitors sometimes blend batches from multiple precursors, leading to unpredictable impurity profiles. We use a single, controlled synthetic route. This matters: typical contaminants like unreacted starting materials or over-sulfonated byproducts are easily spotted and controlled when using a carefully tracked process, not so with mixtures from different plants or shortcuts designed to hit only the broadest specifications.
On a physical level, some market alternatives ship as compacted lumps, making weighing and dissolution difficult on both bench and plant scale. Our commitment to carefully dried and milled product avoids these issues, minimizing waste and contamination risk. In one scale-up campaign, a partner documented a ten percent reduction in filtration time simply by switching to material with better flow properties and tighter PSD (particle size distribution). This kind of improvement shows up less in brochures and more in daily production logs.
Quality in specialty intermediates doesn’t just impact regulatory audit outcomes; it drives everyday results for formulators and production chemists. Reproducibility comes from discipline: rigorous raw material authentication, ongoing staff training, and prompt root-cause analysis whenever deviations appear. We use real-time analytical controls—HPLC/GC/IR—to catch minor lot-to-lot drift before it reaches delivery. For those mixing plants with old and new equipment, predictability in input chemical handling eliminates many headaches at the intersection of batch and continuous processing.
We engage regularly with customers, learning directly from those troubleshooting synthesis issues. Solutions often depend on more than data sheets. Recently, a customer’s unexpected drop in yield traced back to a subtle shift in recrystallization conditions on our side. Open communication allowed us to correct the problem long before it triggered downstream revalidation. This collaborative approach builds trust and maintains product quality, not only by sharing current spec sheets but by learning from real-world implementation.
As regulatory requirements tighten, whether through stricter impurity thresholds or environmental impact reporting, we keep pace not just with final product testing but with more sustainable process improvement. By actively reducing waste in our own syntheses and switching to greener solvent choices, the environmental footprint of the intermediate drops, and regulatory filings become much smoother for our customers. This enables a faster path from research to qualification—an urgent need for innovators racing both time and budget.
Supply chain resilience matters more than ever. Many users experience delays with intermediates sourced from brokers or repackagers with uncertain manufacturing controls. Our direct control and transparent batch records support faster and more confident audits. Every shipment contains both full analytical documentation and a direct line to technical support staff familiar with details down to specific batch quirks.
By minimizing rework and off-spec batches, we help downstream users reduce not only direct material costs, but also the significant resource outlay for quality investigations and root-cause analyses. Few things stall a process faster than an out-of-spec intermediate with no traceable backstory. Our manufacturing process is built around avoiding such scenarios, and the results are borne out by repeat customers working in tightly regulated API plants and other high-stakes environments.
Making 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide at scale highlights the interplay between process chemistry and practical needs on the ground. Every kilogram that moves from plant to customer reflects not just technical capability but also responsiveness to new requests: a different PSD for better blending, alternate packaging for safety, or modified drying cycles to meet strict water specification for moisture-sensitive synthesis. The best improvements often originate in conversations between our synthesis and technical support teams and the scientists working directly with the product.
Looking forward, we continue refining our process with in-line quality analytics and periodic raw material audits. As demand shifts further from bulk to custom-tailored synthesis, we apply lessons learned from each production campaign to create tighter, more reproducible products. The chemistry underpinning 4-[(3-methylphenyl)amino]pyridine-3-sulfonamide exemplifies a field where details matter, and the best results come from an ongoing, informed dialogue between producers and users.
For those looking to solve complex synthetic challenges, reliability and full transparency hold value over glossy presentations and generic promises. Our track record rests on a foundation of practical experience, documented performance in critical applications, and the willingness to keep improving both product and process. We stand by the science, the craft, and the partnerships that have made this product a preferred choice for those who know both the promise and the pitfalls of complex organic synthesis.