Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing sales7@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide

    • Product Name 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide
    • Alias sulfoxaflor
    • Einecs 629-536-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    104030

    Iupac Name 2-[4-Aminosulfonyl-phenyl]-ethyl-5-methylpyrazinecarboxamide
    Molecular Formula C14H16N4O3S
    Molecular Weight 320.37 g/mol
    Cas Number 58-32-2
    Appearance White to off-white powder
    Melting Point 164-166°C
    Solubility Slightly soluble in water
    Logp 0.74
    Chemical Class Sulfonamide derivative
    Synonym Sulfamethazine
    Storage Conditions Store at room temperature, protected from light

    As an accredited 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle with safety seal, labeled "2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide, 25g", hazard symbols and batch number.
    Shipping This chemical is shipped in tightly sealed containers, compliant with hazardous materials regulations. Packaging ensures protection from moisture, heat, and light. Proper labeling, including hazard identification, is provided. Shipment occurs via certified carriers with all documentation, ensuring safe handling during transit. Temperature control and secure outer packaging are maintained if required by the compound’s stability profile.
    Storage Store 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide in a tightly sealed container, away from direct sunlight and moisture, in a cool, dry, and well-ventilated area. Keep at room temperature unless otherwise specified. Avoid contact with incompatible substances such as strong oxidizing agents. Ensure proper labeling and access is restricted to trained personnel. Follow all relevant safety protocols and local regulations.
    Application of 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide

    Applications of 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide in Industrial Manufacturing

    As a direct manufacturer specializing in advanced chemical raw materials, we supply 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide for distinctly industrial downstream segments. This compound supports strict quality, regulatory, and product performance benchmarks within synthesis workflows, driving process reliability and repeatable end-use functionality.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    Our material serves as a key synthetic intermediate in the multi-step manufacturing of cardiovascular drug substances, particularly for certain antihypertensive agents in the pyrazinecarboxamide family. It fits established multi-kilogram GMP process trains by integrating directly into early-stage condensation reactions and subsequent purification steps. Manufacturers select this compound for its high purity and traceability, supporting API registration and quality validation aligned with global pharmacopoeias.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs related to pyrazinecarboxamides
    • United States Pharmacopeia (USP)
    • China National Medical Products Administration (NMPA) API registration guidelines

    Typical usage ratio

    • Used at 0.15 – 0.32 molar equivalents relative to the primary amine substrate, adjusted based on target stoichiometry in stepwise synthesis and batch size scaling

    Downstream process integration

    • Incorporated at the initial heterocyclic condensation step, commonly in acetonitrile or DMF solvents, followed by subsequent amide coupling and sulfonamide protection/deprotection procedures

    Final product types

    • Crude and purified antihypertensive API intermediates
    • Registered final APIs for tablet and capsule dosage forms

    2. Diagnostic Reagent Synthesis for Enzyme Immunoassays

    In clinical diagnostics manufacturing, this compound acts as a labelled building block for the chemical linkage of sulfonamide group-based haptens or enzyme substrates, particularly those adapted for colorimetric immunoassays. Its structure enables precise covalent attachment to carrier proteins or reporter molecules, delivering stable behaviour in aqueous conjugation and subsequent detector performance.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices – Quality Management Systems
    • CLSI EP25-A Liquid Reagents: Preparation, Stability, and Storage
    • EU In Vitro Diagnostic Regulation (IVDR) 2017/746
    • FDA 21 CFR Part 820 (Quality System Regulation for Diagnostics)

    Typical usage ratio

    • Commonly utilized at 0.05 – 0.2% (w/w) within protein conjugation buffer, ratio based on molar activity and desired reagent sensitivity calibration

    Downstream process integration

    • Reacted with activated protein carriers using carbodiimide-mediated conjugation or via maleimide, incorporated during the conjugate synthesis stage in diagnostic kit production

    Final product types

    • Immunoassay detection reagents for ELISA and CLIA platforms
    • Pre-formulated diagnostic kit conjugates

    3. Specialty Pigments for High-Temperature Polymeric Coatings

    Paint and industrial coatings formulators employ this aromatic sulfonamide derivative as a high-performance precursor for the synthesis of pigment dispersants or colorant intermediates used in heat-resistant polymers. The compound enters condensation and amidation batch processes to alter solubility, chromatic stability, and interfacial behaviour in engineering coating systems for automotive and electronics applications.

    Industry compliance standards

    • ASTM D7767-11: Standard Guide for Selection of Coating Raw Materials
    • RoHS Directive (2011/65/EU) for hazardous substances in electronic coatings
    • ISO 9001:2015 Quality Management System for Coatings Manufacture
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • 0.2 – 1.2% by weight in pigment dispersion premixes; level determined by substrate reactivity and target viscosity during milling

    Downstream process integration

    • Added during the pigment synthesis or pre-dispersion step in the colorant batch, prior to resin blending and curing stages in coating manufacture

    Final product types

    • Thermally-stable polymeric paints for automotive surfaces
    • Electronic device protective coatings with enhanced color stability

    4. Sulfonamide-Functionalized Monomer for Polymeric Membrane Production

    This compound acts as a functional comonomer in the formulation of advanced separation membranes, especially for gas and solvent filtration in chemical and pharmaceutical processing. Its incorporation brings specific sulfonamide pendant groups into polymer backbones, increasing hydrophilicity, selectivity, and mechanical strength in cast or extruded membrane systems.

    Industry compliance standards

    • EN ISO 9001:2015 for membrane production facilities
    • USP Class VI Biological Reactivity Tests for Polymeric Materials (for pharmaceutical contact)
    • NSF/ANSI 61 for potable water systems (if used in water filtration)
    • ISO 14001:2015 Environmental Management in chemical processing

    Typical usage ratio

    • 5 – 20 mol% as a co-monomer relative to base polymer feedstock, regulated to balance membrane pore size, mechanical stability, and permeability

    Downstream process integration

    • Co-polymerized via solution or interfacial polymerization, introduced during the initial monomer blend prior to casting, phase inversion, or film extrusion processes

    Final product types

    • Flat-sheet or hollow fiber nanofiltration membranes for chemical process filtration
    • Pharma-grade separation membranes requiring specific sulfonamide group presence
    Free Quote

    Competitive 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide 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 sales7@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide: Proven Performance, Consistent Quality

    Practical Innovation in Pyrazinecarboxamide Chemistry

    Over the past several years, 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide has become a mainstay in laboratories and industrial facilities where high-performance intermediates are valued. We have dedicated significant resources into optimizing the synthesis route, ensuring every batch meets predictably high standards. Unlike many aromatic sulfonamide derivatives, the combination of the pyrazinecarboxamide core and ethyl-linked aminosulfonyl group offer unique applications. Chemists and engineers rate this molecule for its structural stability and ease of handling.

    From a manufacturer’s standpoint, reproducibility matters most. Our team has refined every process stage. By controlling raw material purity, reaction conditions, and purification stages, we minimize batch-to-batch variability. This consistent output benefits downstream synthesis, allowing customers to integrate our product seamlessly into their own processes without revalidating each lot. Confidence in the supply chain liberates technical teams to focus on innovation rather than troubleshooting.

    Model, Purity, and Batch Reliability

    Our predominant production model features 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide with a nominal purity surpassing 99%. Analytical teams use HPLC, NMR, and elemental analysis at multiple points during production. Some competitors cut corners on impurity profiles, routinely running single-step purifications that leave residual starting materials or isomers. In contrast, we carry all batches through staged recrystallization and chromatography, eliminating detectable side products. Consistency relates not just to specification, but to actual day-to-day performance. Over thousands of kilograms produced, chromatograms show a clean signal, with no evidence of aromatic impurities or polysulfonated byproducts.

    Our technical staff saw early on how minor impurities impact certain synthetic steps. Example: in heterocycle coupling reactions, even fractions of a percent contamination can cause yield drops or purify issues in the customer’s plant. Providing a clean, single-species intermediate allows customers to scale up without running into bottlenecks or reduction in overall process efficiency. As a result, long-term clients frequently report lower reject rates and greater overall productivity.

    Manufacturing Process Integrity—Lessons from Experience

    Real-world manufacturing often presents issues that don’t show up on paper. Sulfonamide intermediates are prone to color changes, due to oxidation or trace side reactions. By using closed reactors and safeguarding the process environment from moisture and oxygen, we avoid off-spec color bodies and maintain a bright, uniform powder. Workers in our facilities monitor all steps, not just at the lab bench but right on the production floor. They intervene promptly if there’s a deviation in temperature or mixing speed, based on daily experience rather than just SOPs.

    We invest in preventative maintenance on all synthesis kettles and filtration equipment. Small leaks or ‘dead legs’ near valve outlets can collect residue, which over weeks produces dark particles, off-smells, and hard-to-remove contaminants. Eliminating these design flaws has paid tremendous dividends. The plant has not produced a reject batch in over two years. Customers benefit directly—no sudden need to revalidate their formulations or waste time chasing analytic ghosts.

    Why the Product Outperforms Simplified Analogues

    There’s a trend in the chemical industry to streamline synthesis by choosing the lowest-cost raw materials and intermediates. Yet this approach often leads to more headaches later. 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide stands apart from simpler aryl sulfonamides because of the specific arrangement of its functional groups. The ethyl bridge provides better solubility in common organic solvents and improved stability during both acidic and basic reactions.

    Commonly available aryl sulfonamide pyrazines lack the methyl group at the 5-position, which makes them less stable under thermal stress. We have tested several analogues head-to-head in thermal cycling protocols and found that our product resists decomposition and maintains its color and melting point even under extended heating. This resilience reduces problems in customers’ high-temperature reactions.

    Other manufacturers sometimes sell “free base” or amorphous forms with variable hydration levels. We chose to supply the compound in a well-defined crystalline form. This ensures tight control over weight measurements, stoichiometry calculations, and handling properties. Hygroscopic materials cause headaches—clumping in drums, measurement drift, and unpredictable reactivity. The crystalline material flows readily and re-dissolves without delay.

    Supporting Advanced Applications: Not Just a Simple Intermediate

    2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide plays a direct role in the synthesis of complex pharmaceuticals and specialty chemicals. We have ongoing collaborations with research teams working on kinase inhibitors, new sulfa-drugs, and diagnostic reagents. Our chemists participate in periodic reviews with client R&D teams, making recommendations on both the use of the product and purification steps for their own processes. These exchanges have allowed us to refine our procedures and, in some cases, develop new grades tailored to specific reactivity thresholds or impurity exclusions.

    Pharmaceutical clients, in particular, have strict demands for residual solvent and heavy metal content. By validating our solvent recovery and raw input sources, we have held true to best-in-class benchmarks on these metrics. For years, we have maintained analyses that show residual solvents far below ICH guidelines and non-detect levels for regulated metals. Clients rarely encounter unpleasant regulatory surprises. Many see this as a deciding factor in choosing a supplier.

    Safety and Regulatory Assurance—Proven in Practice

    From the ground up, we address safety—not only in terms of regulatory documentation, but real operational controls. All production shifts must log environmental parameters, operator interventions, and chemical usage. Batch history can be traced back in detail for customer review. We work proactively with our logistics teams, ensuring packaging integrity and safety documentation meet international shipping guidelines.

    We never treat these requirements as a paperwork exercise. Our safety managers evaluate every customer complaint and conduct root-cause analysis for near-miss incidents. The most important lessons have often come from real incidents, like condensation building up in storage leading to caking or warehouse temperature swings affecting product color. Solutions implemented—improved moisture barriers, better internal linings—have eliminated most of these issues. Field feedback informs everything about how we make and deliver this product.

    Perspective on Industry Trends—Quality as a Necessity, Not a Luxury

    As supply chains in the chemical sector become more global and price pressures intensify, quality assurance sometimes gets treated as a box-ticking exercise. Our long-standing clients have told us stories of abandoned projects and sunk costs, all because an intermediate from a “cheaper” source failed halfway through validation. We hear regularly how products labelled as “identical” actually show significant performance gaps—yield drops, new toxic byproducts, and hard-to-trace odor issues.

    In client after client, it’s become evident that the long-term cost of confronting inconsistent or subpar intermediates far outweighs the small savings from cheaper sourcing. Our team has built its reputation around predictable, documented, and transparent quality. The value isn’t just in the test results, but in the lack of drama—a drum arrives, passes inspection, and works as expected. Every repetition builds trust.

    Process Adaptability: Lessons from Client Partnerships

    No synthetic process lasts forever, and even for established products like 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide, we constantly adapt. Over the last decade, customers developing new API pathways have come to us requesting variations in particle size, solvent residue profiles, or customized labeling schemes. In each case, we’ve worked directly with customer technical teams, running joint trials across several pilot batches, measuring how process tweaks influence downstream reactivity.

    Our openness to feedback means process chemists or production managers can call us directly, even on weekends. They don’t get outsourced support or runaround—they speak with senior technical staff who know both the chemistry and the factory floor realities. Years ago, one large-volume client noticed a trace impurity drifting up above their tolerance. A short plant visit and raw input audit traced the problem to a small change in our own solvent supplier—rectified within two weeks. Collaboration solves problems faster than finger-pointing or denial.

    Sustainability Practices in Synthesis: Doing More Than What’s Required

    Government regulations on emissions, waste, and process residues keep changing, raising the stakes for compound manufacturers. We have tackled both local and global compliance issues, voluntarily exceeding minimum guidelines to limit environmental impact. Solvent recovery units capture over 95% of process solvents, and our wastewater treatment plant operates with multi-stage filtration and biological digestion. Manifest records and third-party audits show reductions in both total and hazardous waste output.

    Sustainability is not just about compliance or signage for customers. It lowers costs over time and builds resilience. Efforts to minimize off-spec batches and frequent equipment cleaning directly reduce water and chemical usage. Stable long-term supplier relationships allow us to choose raw materials from sustainable sources, cutting transportation emissions and increasing supply predictability. Employees working in a well-run, environmentally conscious facility bring more focus and pride to their roles—translating to consistently better products.

    Delivering More than a Compound—Backing Every Parcel With Experience

    Clients often ask for technical support on integrating the product into pilot plant runs or scale-up campaigns. We approach these needs as fellow chemists, not just vendors. Our application specialists assist with sample preparation, dissolution profiling, and even custom packaging for specific automation systems. Once, a client requested support on a Friday night during a scale-up—our head of manufacturing walked through their plant’s protocol by phone to troubleshoot a mixing anomaly.

    Over decades, this approach keeps the relationship long and the benefits mutual. Problems shared early are simpler to resolve, and hard-won experience travels in both directions. Our process records and feedback mechanisms create an ongoing improvement cycle, keeping us aware of changing regulatory, technical, and market demands.

    Looking Forward—Continuous Improvement Remains the Path

    As demand grows for next-generation pharmaceutical intermediates and specialty chemicals, the role of high-performance products like 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide will only expand. Variable product quality, delivery delays, and inconsistent documentation remain the biggest pain points in the industry. We stay focused on what works: technical expertise, open communication, and constant upgrades of machinery and workflow.

    Our goal isn’t just to meet the current need, but to foresee what process chemists or plant engineers will require as their own ambitions set new benchmarks. As molecules get more complex and development cycles shorten, it becomes more crucial to have chemical partners who understand not just the structure or assay of a compound, but its real-world impact on cost, safety, and success.

    We take pride in the discipline and curiosity of our staff, the high standards of our production teams, and the open, direct conversations we continue to have with the scientists and engineers who move this industry forward. Every container of 2-[4-Aminosulfonyl-Phenyl]-Ethyl-5-Methylpyrazinecarboxamide we ship represents not just chemical expertise, but an investment in the success of our partners.