|
HS Code |
112249 |
| Iupac Name | N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide |
| Molecular Formula | C20H16N6O4S |
| Molecular Weight | 436.44 |
| Cas Number | Unavailable |
| Appearance | Solid (assumed) |
| Solubility | Unknown, likely soluble in DMSO or DMF |
| Structure Features | Contains: pyrazine, oxadiazole, pyridine, sulfonamide, and methoxy groups |
| Pubchem Cid | Unavailable |
| Synonyms | None commonly found |
| Chemical Class | Sulfonamide derivative |
| Smiles | COC1=NC=NC(C)=C1NC2=NC=C(C3=CC=C(C=C3)C4=NN=CO4)S2(=O)=O |
| Inchi | InChI=1S/C20H16N6O4S/c1-13-12-22-20(29-2)25-17(13)23-19-10-18(31(27,28)24-19)16-6-4-15(5-7-16)14-21-26-30-11-14/h4-7,10-12H,1-2H3 |
| Logp | Unknown, likely moderate |
| Primary Uses | Research and development |
As an accredited N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a sealed 10g amber glass bottle, featuring a tamper-evident cap and clearly labeled for laboratory use. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide ensures safe, moisture-proof bulk transport. |
| Shipping | This chemical, N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide, is shipped in tightly sealed, chemically resistant containers, protected from light, heat, and moisture. Standard ground or air shipping applies, with compliant documentation and adherence to regulatory requirements for laboratory chemicals. Handle with care during transport. |
| Storage | Store **N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide** in a tightly sealed container, protected from light and moisture. Keep at 2–8 °C (refrigerated), in a well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure proper chemical labeling and access only to trained personnel. Avoid sources of ignition and excessive heat. |
| Shelf Life | Shelf life: Stable for at least 2 years if stored tightly sealed, protected from light, moisture, and at 2–8°C (refrigerated). |
|
Purity 99%: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized impurity profiles. Molecular Weight 423.45 g/mol: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with molecular weight 423.45 g/mol is used in drug formulation development, where accurate dosing and reproducibility are achieved. Melting Point 215°C: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with a melting point of 215°C is used in solid-state pharmaceutical research, where thermal stability is required for processing. Stability Temperature 60°C: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with stability at 60°C is used in high-temperature storage studies, where it maintains structural integrity during accelerated stability testing. Particle Size 10 μm: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with 10 μm particle size is used in tablet manufacturing, where uniform powder flow and compaction are essential for dose consistency. Viscosity Grade Low: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with low viscosity grade is used in liquid formulation processes, where rapid solubilization and homogeneity are required. Solubility in DMSO 50 mg/mL: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with solubility in DMSO at 50 mg/mL is used in bioassay sample preparation, where high concentration solutions enable effective screening. HPLC Assay ≥98%: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with HPLC assay ≥98% is used in analytical reference standards, where precise quantification and validation are necessary. Moisture Content ≤0.5%: N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide with moisture content ≤0.5% is used in lyophilized product formulation, where stability and shelf-life are enhanced. |
Competitive N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
At the heart of chemical manufacturing lies a responsibility to ensure that every batch, every molecule, and every delivery stands up to scrutiny—not just on paper, but under the microscope and in the hands of end users. Producing N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide brings together both technical mastery and practical know-how. Our team focuses on precision, clarity, and consistent reproducibility, which matter to anyone relying on specialty chemicals. Each successful synthesis run speaks to years of process development, hands-on lab work, and careful sourcing of raw materials.
Delivering a complex molecule like this isn’t about chasing novelty for its own sake. On the production line, every step—whether it’s the control of solvent quality, the tuning of reaction temperature, or the purification after each stage—serves the final performance. We have invested in high-efficiency reactors that handle scale-up without sacrificing traceability. Analytical tools play their part as well: Our HPLC, NMR, and mass spectrometry results help us maintain a narrow band for key specifications like purity, water content, and particle size. Laboratory experience tells us that when you control these factors, you cut down on batch rejections and unscheduled plant downtime.
This sulfonamide derivative offers a unique combination of functional groups—pyrazinyl, oxadiazolyl, and pyridinesulfonamide. Each piece brings its own chemical reactivity: for example, the methoxy and methyl substituents on the pyrazine ring affect electronic properties significantly. In our process, we take special care during condensation steps to safeguard these delicate substituents, as any deviation can lead to byproducts that show up in chromatography data. We run every lot through strict validation—confirming both the molecular structure and checking for residual solvents and side products.
Customers in pharmaceutical research often comment on the way this compound performs in lead optimization and SAR studies. The combination of a robust aromatic system and polar functionalities seems to support strong target binding, while maintaining solubility profiles needed for preclinical experimentation. This feedback has impacted our in-process checks, encouraging us to keep water and solvent residues below 0.5% using advanced drying cycles and tightly controlled filtration systems.
Offering a molecule of this complexity at scale means confronting real-world manufacturing variables. In one of our earliest production runs, even a minor change in batch size produced unexpected differences in crystal morphology, which in turn affected purity after filtration. Learning from these setbacks, our engineers adjusted solvent ratios, cooling profiles, and drying parameters to balance yield and purity. To make this process reproducible, we track and document every parameter in digital batch records, giving our customers a clear line of sight from raw material to finished product.
Spec sheets and certificates of analysis only tell part of the story. Laboratory technicians and process chemists rely on rapid access to analytical data—whether that’s melting point range, HPLC purity, or mass balance from NMR. This product, as manufactured in our facility, typically meets or exceeds the 98% purity mark, as demonstrated by both chromatographic and spectroscopic analysis. We have tailored our grinding and sifting steps to deliver a consistent flow property—a detail that matters for downstream formulation work.
Researchers choose N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide for its distinctive chemical scaffold, which enables the exploration of new modes of biological activity. We have followed customer publications describing its selection as a core structure in early-stage medicinal chemistry campaigns, particularly where a balance of lipophilicity and hydrogen bonding capability is critical. Our product finds its way into screening programs, structure-activity relationship investigations, and solid-state chemistry research.
For those developing solid formulations, the crystal form of this compound plays a decisive role. We have invested in both X-ray diffraction and polymorph screening to provide data supporting formulation scientists’ efforts to achieve desirable stability and dissolution profiles. Customers in material science and analytical labs have pointed out the clean thermal decomposition and sharp melting point, making the compound a candidate for more advanced applications beyond drug discovery.
There’s a crowded field of specialty chemical suppliers, but our approach sets us apart in a number of tangible ways. As a manufacturer, we maintain control over raw material sourcing, with strict vendor qualification programs limiting impurities at the origin. Our chemists design multistep syntheses for both scale-up and periodic revalidation, ensuring that each part of the process stands up to repeated scrutiny. In our operation, we avoid batch amalgamation or split-batch processing—a practice that lets us provide full traceability on every vial, drum, and container.
Customer audits and regulatory inspections form part of our daily life. These aren’t box-ticking exercises. For each production lot, we keep written and electronic logs, tracking adjustments in real time. This helps us pinpoint sources of variability—from subtle changes in a reaction’s exotherm to the presence of micro-impurities in a filtration aid. Drawing from real process failures and subsequent improvements, we are able to anticipate and avoid similar challenges in the future, increasing reliability for customers.
Some suppliers focus purely on offering low prices and fast delivery, but we see reliability and transparency as fundamental. If a customer requests an atypical particle size range or a custom packaging configuration, we provide these not as an afterthought but as a planned extension of our mainline manufacturing process. End users receive real samples with attached batch data—not generic statistical averages—and are free to call on our technical staff for support during their method development or troubleshooting.
Our company fosters ongoing dialogue with customers, academic partners, and industry peers. New requests, such as for alternative salt forms or fresh analytical data, prompt direct interaction with the same team that runs the plant. Project managers and senior chemists remain accessible, defining and testing improvements in process safety, scale, or product cleaning. When a customer’s end application raises new regulatory questions or demands tighter impurity profiles, we respond by revisiting our route of synthesis, trying new intermediates, and field-testing our results.
Chemical manufacturing at this level of complexity can’t run on autopilot. We’ve faced and solved difficult questions in real time—for instance, a recent need for lower metal content in the final product led to the integration of specific scavenging steps, which now come standard in every lot. These modifications spring from constant engagement with the people who use our compounds in research, product development, and manufacturing partnerships.
Early pilot runs for this sulfonamide revealed areas for improvement. Fluctuating yields at scale prompted a deeper look into reactor design, agitation rates, and temperature gradients. Our engineers introduced segmented stirring and automated controls, boosting yield reproducibility while keeping the impurity profile in check. We climbed a learning curve, but now our large-scale production runs deliver the same molecular integrity as laboratory-scale syntheses.
Every operator on our plant floor understands that small lapses can have outsized consequences. Cross-contamination checks, line clearances, and final drum labeling all receive the same attention as the core chemical transformations. Our product leaves the facility only after senior chemists review the batch record and confirm the results of a full suite of chemical and physical tests—giving our partners confidence from research bench to commercial pilot plant.
Safe production forms the backbone of our operation. The process for N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide involves the use and control of multiple reagents, each with its own hazards. Real-time monitoring of ventilation, effluent, and waste streams forms a daily practice, not a theoretical standard. Where possible, we substitute greener solvents and use closed-system filtration to limit worker exposure and environmental footprint. Our team reviews every incident or spill, adjusting training or equipment to prevent repeat events.
Solvent recycling, energy management, and water usage reductions don’t just trim costs—they mean less impact on the local community and a better long-term relationship with regulatory agencies. Our plant leaders meet regularly with local environmental authorities to review and renew permits, ensuring compliance and a spirit of mutual trust. Longer-term investments—like automating hazardous step addition, installing waste heat recovery, and developing in-line monitoring—have paid off by reducing downtime and improving the working environment.
Customers often bring us new challenges tied to their own technical or regulatory requirements. In the last year, clients have asked for documentation supporting both genotoxic impurity testing and extractables/leachables evaluations. Our analytical group validated additional testing protocols, adding supplemental data as standard for each request. Supply chain disruptions and shifting lead times have forced us to build tighter partnerships with freight partners and secondary suppliers for critical reagents.
Innovation isn’t just about delivering a new compound—it’s about finding practical solutions when timelines shrink and requirements shift. We’ve produced custom solution concentrations, participated in blinded comparability studies, and coordinated joint technical meetings to ensure smooth technology transfer. These steps establish trust and deepen our understanding of the real-world environments our molecules enter.
Producing N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]-3-pyridinesulfonamide means more than shipping out a well-labeled bottle. We take pride in knowing where every component originates, how every step unfolds, and what each data point shows. Our staff learn from setbacks, build on successes, remain accessible to customers, and take part in continuous improvement projects. This approach yields a product that stands up to scrutiny—in research, development, and regulatory review.
The market for specialty chemicals grows more demanding every year. Regulatory scrutiny increases, supply chains become less certain, and customer expectations rise. In this environment, reliability trumps pure speed. Our team’s expertise and transparency set a clear standard; knowledge gained in the plant and lab translates directly to confidence at the customer site.
Every year brings new requirements—tighter impurity control, expanded regulatory submissions, and ever-faster delivery cycles. Rather than playing catch-up, we use lessons from each synthesis to improve the next. Regular reviews of both process and analytical failures have led to upgraded filtration systems, better documentation practices, and streamlined quality assurance protocols. Our engineers lead quarterly training sessions for both junior and senior staff, making sure fresh ideas get woven into proven routines.
Direct manufacturer experience offers insights that no outsourcing or agency relationship can match. We document small changes and major redesigns alike, sharing both what worked and what failed. Customers benefit from these insights in tangible ways—fewer production delays, more consistent material, and a point of contact who knows both the chemistry and the context for its application. This product, like every one that leaves our facility, stands as a testament to careful craftsmanship, to the pursuit of practical improvement over empty technical flourish, and to the belief that genuine quality builds trust across every level of the business.