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Sulfaphenazole

    • Product Name Sulfaphenazole
    • Alias Ro 4-3074
    • Einecs 200-634-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    394786

    name Sulfaphenazole
    CAS_number 83-48-7
    molecular_formula C13H12N4O2S
    molecular_weight 288.33 g/mol
    IUPAC_name 4-Amino-N-phenylbenzenesulfonamide
    appearance White to off-white crystalline powder
    solubility Slightly soluble in water
    melting_point 192-195°C
    pubchem_CID 5336
    pharmacological_class Sulfonamide antibacterial

    As an accredited Sulfaphenazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sulfaphenazole, 1 gram, is supplied in a sealed amber glass vial with a white label indicating chemical name, purity, and safety warnings.
    Shipping Sulfaphenazole is shipped in tightly sealed containers, protected from light and moisture, and labeled according to hazardous material regulations. It is typically transported at ambient temperature unless otherwise specified. Ensure compliance with local, national, and international shipping guidelines for laboratory chemicals, including proper documentation and safety precautions during handling and transit.
    Storage Sulfaphenazole should be stored in a tightly closed container, away from moisture and incompatible substances. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Protect from light and sources of ignition. Avoid exposure to heat, humidity, and direct sunlight to maintain its stability and chemical integrity over time.
    Application of Sulfaphenazole

    Applications of Sulfaphenazole in Industrial Manufacturing

    Sulfaphenazole serves as a specialized chemical intermediate with key roles in pharmaceutical synthesis, veterinary medicine formulation, analytical research laboratories, and biomedical assay development. As an experienced manufacturer, we focus on real-world applications supporting regulated industries and stringent quality systems. The following sections detail main downstream use cases, each described in terms of operational standards, typical incorporation ratios, processing stages, and finished product formats found at the industrial level.

    1. Pharmaceutical Intermediate for Sulfonamide Antibiotic APIs

    Pharmaceutical companies employ sulfaphenazole primarily as an intermediate in the synthesis of certain sulfonamide-class active pharmaceutical ingredients (APIs). Its selective incorporation into synthetic routes helps deliver target compounds meeting high-purity standards required for regulated generic and branded formulations. Stringent compliance with pharmacopeial and GMP guidance governs both its procurement and downstream integration to ensure reproducibility and product traceability from raw material to final dosage forms.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (EP)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • Stoichiometric to 1.2-fold molar ratio as a key intermediate step, depending on the specific downstream synthetic route and targeted API purity profile

    Downstream process integration

    • Introduced at intermediate condensation or sulfonation stage during multi-step antibiotic API synthesis, followed by purification via crystallization or chromatography systems

    Final product types

    • Sulfonamide bulk APIs (e.g., sulfamethoxazole, sulfathiazole)
    • Oral solid and parenteral pharmaceutical formulations
    • Veterinary antimicrobial medicines (formulated from sulfonamide APIs)

    2. Analytical Reference Standard in Pharmaceutical and Toxicological Testing

    Quality control laboratories and contract analytical centers use sulfaphenazole as a certified reference and internal standard for chromatographic calibration, particularly in clinical pharmacokinetic, toxicology, and quality release testing. Its defined purity profile and availability as a traceable standard enable method validation and compliance with global regulatory frameworks for pharmaceutical testing workflows.

    Industry compliance standards

    • ISO 17025 Laboratory Accreditation
    • FDA Good Laboratory Practice Regulations (21 CFR Part 58)
    • OECD Principles of Good Laboratory Practice

    Typical usage ratio

    • Standard preparation at 1–100 µg/mL, adjusted to analytical method sensitivity and matrix effects; calibration curves typically employ serial dilutions across four to seven concentration points

    Downstream process integration

    • Direct addition into control samples, plasma, tissues, or environmental matrices prior to LC-MS/MS, HPLC, or GC-MS analysis to ensure traceability and quantitation accuracy in validated methods

    Final product types

    • Pharmaceutical QC sample kits
    • Bioanalytical test panels for clinical research
    • Environmental residue monitoring kits

    3. Preclinical Drug Metabolism Inhibitor in CYP450 Enzyme Studies

    In preclinical pharmacology research, sulfaphenazole functions as a selective cytochrome P450 2C9 (CYP2C9) inhibitor for in vitro and in vivo metabolic studies. Research labs and pharmaceutical R&D teams incorporate it into assays to delineate specific drug-drug interaction pathways, inform dose selection, and fulfill regulatory expectations for mechanistic metabolism profiling under controlled study protocols.

    Industry compliance standards

    • FDA Guidance for Industry: Drug Interaction Studies — Study Design, Data Analysis, Implications for Dosing, and Labeling Recommendations
    • OECD Test Guidelines for the Testing of Chemicals
    • EMA Guideline on the Investigation of Drug Interactions

    Typical usage ratio

    • 5–100 µM final concentration in enzyme inhibition assays; ratio selection based on enzyme abundance and comparative substrate competition protocols established in relevant metabolism studies

    Downstream process integration

    • Added to human or animal liver microsome preparations, recombinant enzyme assays, or in certain perfused organ models prior to substrate administration or co-incubation for drug interaction quantification

    Final product types

    • Preclinical assay kits for CYP enzyme inhibition testing
    • Validated drug screening services
    • Standardized metabolic research protocols for regulatory submission

    4. Reference Compound for Biomarker and Medical Diagnostic Assay Development

    Diagnostic assay developers and biomedical research firms utilize sulfaphenazole as a model compound in exploratory biomarker discovery and in the calibration of drug monitoring systems, particularly in studies involving anti-infective therapies. Its defined reactivity supports establishment of robust calibration curves, background controls, and trace-level physician-ordered tests in clinical diagnostic instrument platforms.

    Industry compliance standards

    • ISO 13485 Medical Devices – Quality Management Systems
    • CLIA (Clinical Laboratory Improvement Amendments) Requirements
    • FDA 21 CFR Part 820 – Quality System Regulation

    Typical usage ratio

    • Varies between 0.1–5 mg/mL based on analytical platform—manual assays, microfluidic lab-on-chip, and high-throughput immunoassay calibrators deploy different working concentrations according to sample input and required LOD (limit of detection)

    Downstream process integration

    • Incorporated as a control or standard during test cartridge assembly or integrated into multi-analyte kit production lines at the calibration phase; material traceability maintained across batches to support audit requirements

    Final product types

    • Finished reference standards for clinical chemistry analyzers
    • Pre-loaded calibration vials for point-of-care test systems
    • Ready-to-use diagnostic panel components
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    Certification & Compliance
    More Introduction

    Sulfaphenazole: Consistent Performance for Advanced Research and Production

    The Role of Sulfaphenazole in Modern Chemistry

    In the world of chemical manufacturing, sulfaphenazole (CAS number 63-16-5) stands out because of its reliability in both pharmaceutical and laboratory applications. Our factory has spent years refining the production of this compound, learning through trial and direct feedback from the science community. We know first-hand how vital high-purity reagents are for researchers and formulators. Every day, we see requests from professionals who want to control variables tightly in their experiments. They don't just need “any” version; they’re searching for a material that won't introduce silent errors or contaminants.

    Sulfaphenazole started as a sulfonamide antibiotic but, over the years, has become much more than that in chemical laboratories. Its primary role today is as a cytochrome P450 inhibitor, especially notable for CYP2C9. This specificity allows researchers to tease apart metabolic pathways in mammals and design safer, more predictable medicines. R&D chemists reach for it when seeking to understand how particular drugs get metabolized, absorbed, or blocked in the human body. By controlling for one metabolizing enzyme, scientists can isolate effects that would otherwise be masked by overlapping biological processes.

    Consistency Through Precise Manufacturing

    Maintaining a high-grade supply takes more than basic chemical synthesis. We monitor solvent quality, batch reaction times, filtration settings, and storage temperature to avoid subtle impurities that might skew bioassay outcomes. The final product leaves our factory as a pure, low-moisture crystalline powder (C13H12N4O2S, MW: 288.33), packaged to hold its stability even in long-distance transport. Years ago, a major clinical client flagged trace-level carryover from a faulty drying process; we scrapped that batch and overhauled the procedure line. Every audit since then checks for these tiny risks. That relentless focus on detail means the chemist can move straight to their experiments without cross-checking unknowns in every jar.

    The specifications we meet stem from industry requests and evolving pharmacological needs. Pharmacopeia standards and internal research protocols align closely in purity control. Our analytical verification (HPLC, NMR, MS, and IR) runs on every lot, and our lab guarantees a purity level over 99%. We don’t shy away from customer audits, nor questions about stability or potential contaminants. When problems arise, we discuss root cause analysis in person with end-users and adapt workflows, rather than hiding behind stock answers.

    Understanding Real-World Applications

    Here in the factory, we see orders for sulfaphenazole from a mix of sources: university labs, pharmaceutical developers, government projects, and even specialty veterinary researchers. Each has a slightly different approach, but they all need a reliable compound. Some expect single-gram vials for screening studies; others order in multi-kilogram lots for scaling up potential therapies. As a manufacturer, it’s clear to us that this molecule does far more than treat infections. Its inhibition of enzyme CYP2C9 makes it an irreplaceable control in metabolic studies. Chemists can suppress a specific leg of a metabolic pathway and, by doing so, illuminate the broader mosaic of drug interactions and toxicities.

    Teaching labs use our product in student protocols where precise concentrations and dissolution rates must match the written curriculum. In pharmaceutical discovery, teams add sulfaphenazole in vitro to pinpoint reactions that might otherwise be lost in a fog of cellular crosstalk. For contract researchers designing drug screens, it offers a tool to measure the impact of metabolism on drug half-life and potency. Even production-scale formulations sometimes deploy this inhibitor to test for product stability under simulated metabolic stress.

    Comparisons to Other Sulfonamides and Research Reagents

    Having produced a range of sulfonamides, we’ve learned each compound brings something unique to the bench. Sulfaphenazole differs from more common agents like sulfamethoxazole, sulfadiazine, and sulfanilamide in both molecular structure and application focus. Most classmates see broader use as antimicrobials; laboratories add those to biological media to inhibit bacteria growth. Sulfaphenazole rarely makes it into direct microbial treatments, since its strength lies not in killing pathogens but in shaping mammalian enzyme systems.

    Direct chemical structure affects both solubility and target selectivity. For instance, sulfamethoxazole has a different substitution at the aniline group, leading to distinct metabolic stability and binding profiles. Labs seeking to compare sulfonamide activity rely on these small but crucial differences. The selectivity of sulfaphenazole for CYP2C9 gives it an edge when researchers need to rule out overlapping enzyme contributions found in alternative sulfonamides.

    Our production team regularly receives questions from labs that have worked with generic sulfonamides but find erratic assay results. They discover that purity gaps, improper storage, or mislabeling cause batch-to-batch variability. With sulfaphenazole, we’ve tackled this by keeping our supply chain tight and batch records transparent. Supporting direct communication between manufacturing and bench science teams builds mutual trust—the only real safeguard against errors creeping into research output.

    Handling, Usage, and Storage Insights

    Using sulfaphenazole correctly often comes down to the basics: accurate weighing, proper dissolution, and safe handling. Our staff trains clients on how to avoid light-induced or moisture-related product degradation. Once you open a container, always rescale and recap tightly. As a dry powder, it responds poorly to ambient humidity, and we’ve documented how improper sealing can cause small but measurable shifts in potency. We supply material with drying agents in custom packaging for high-humidity shipping routes, based on direct instruction from long-term customers in tropical climates.

    The compound dissolves best in organic solvents like DMSO or methanol but can also be suspended in buffered aqueous solutions for biological work if pH levels are monitored. End uses may demand stock solutions for serial dilution or microplate application. Several pharmaceutical researchers rely on our material because it keeps its clarity and doesn’t precipitate unexpectedly under controlled conditions.

    Safe handling in labs remains a priority. All our shipments include clear preparation and disposal guidelines. Every operator in our own facility follows strict ventilation and PPE protocols, and our documentation reflects what actually works rather than offering generalities. Several partner labs have requested demonstration batches, enabling their staff to witness the handling procedures we use daily.

    Quality Oversight and Meeting Regulatory Needs

    Our supply agreements serve universities, medical companies, and government scientists meeting strict regulatory requirements. Yearly independent audits check not only our site’s sterility and environmental controls but also our documentation trail from raw input through to final shipping. We’ve never seen an inspection without actionable feedback, so we encourage repeat transparency checks to keep the system honest and evolving.

    Recent years saw tightening of documentation for research APIs sent across borders. We keep digital and physical batch traceability available at any moment. Teams faced with surprise requests from their country’s health department receive backup records within hours. Our internal auditing caught a labeling inconsistency a few years ago, prompting a shift to tamper-evident containers and numbered seals. As a result, repeat customers now have greater confidence in the material they’re receiving.

    We refuse to list sulfaphenazole as a direct human drug ingredient or for over-the-counter use in our catalogs, echoing the guidance of global regulatory agencies. Most researchers use it under strict supervision in settings where precise dosing and endpoint monitoring take place. We ensure those requirements translate into real manufacturing and labeling systems, not just paper checkboxes.

    Supporting Innovation and Responsible Use

    Our role does not end the moment a shipment leaves the plant. We routinely discuss application feedback and troubleshooting with clients when they see anomalous results. Collaborative relationships lead to iterative improvements—sometimes in packaging material, other times in analytical method validation. We have, for example, adapted our drying process to reduce crystal aggregation after scientists at a clinical research center noted slight handling trouble in automated dispensing systems. Instead of offering blanket reassurances, we ran side-by-side comparisons and then rebuilt our standard operating protocol with their input.

    Waste stream control and responsible disposal form a key part of our long-term commitments. Chemical byproducts can’t always be removed from municipal water with standard treatments, so we work with local agencies to devise specialized filtration for our site and issue precise disposal instructions to customers. We stress this topic frequently in client newsletters and Q&A sessions, knowing from experience how small-scale actions can add up over thousands of labs.

    Responsible chemical supply goes beyond ticking compliance boxes. During global supply chain disruptions, we have prioritized ongoing orders for educational and research facilities, working with partners to secure necessary transportation permissions. More than once, emergency shipments required overnight labelling and documentation reviews to satisfy customs and central authorities. These moments prove the value of direct manufacturer-to-user communication, saving researchers weeks of downtime.

    Real Manufacturing Challenges and Solutions

    Batch scale-up brings out the particularities of sulfaphenazole production. While gram-scale reactions run well in standard laboratory glassware, metric-ton scale demands robust controls to maintain temperature and mixing uniformity. As producers, we know the risks: exothermic reactions can surge past safe limits if monitored poorly, leading to decomposition or excessive byproducts. To fight this, we use staged addition, reactor cooling jackets, and real-time analytics instead of relying on end-point testing alone.

    Controlling moisture throughout the process means continuously calibrating drying ovens and rotating stock based on observed hygroscopicity patterns. There’s no substitute for walking the floor and checking physical product instead of just reviewing digital meters.

    As more end users incorporate automation and robotics to streamline their workflow, we get requests to modify granulation and particle size to suit specific dispensing mechanisms. We adjust crystallization parameters on request but keep strict records so clients can trace all changes affecting their data. Direct feedback from users operating high-throughput plate readers helps us calibrate our own particle size controls, ensuring the material flows smoothly and doesn’t jam delicate instruments.

    Building for the Future

    After years of manufacturing sulfaphenazole, we remain rooted in practical, experience-driven choices. Tightening standards and new scientific ambitions present a moving target. Some days, the challenge is meeting a new university’s criteria for animal studies. Other weeks, it’s troubleshooting a chromatographic issue for a hospital research side project. The constant: open channels with those who depend on the reliability of our material.

    We invest in new instrumentation not only because a regulation requires it but because each upgrade sharpens our visibility into what we’re delivering. Meticulous documentation, ongoing third-party analysis, and real-world client engagement support product trust that cannot be bought or spun with marketing. The reward comes in the messages we receive from teams who publish breakthrough data, knowing their results won’t be undermined by off-batch variables.

    Every lot we ship carries not just our label but years of improved practices and shared learning. The goal—always—is to align with the high expectations of the scientific community. For us as manufacturers, the most important feedback never comes through a website form; it arrives through a phone call from a researcher who noticed something in their experiment, asking if we saw the same thing during our own quality checks. That cycle of direct, down-to-earth communication keeps the process honest and ensures that the sulfaphenazole we supply remains reliable for every project, from the teaching bench to the frontiers of drug discovery.