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4-Hydrazinobenzene-1-Sulfonamide Hydrochloride

    • Product Name 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride
    • Alias PABSA·HCl
    • Einecs 241-356-5
    • 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

    382399

    Product Name 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride
    Synonyms Sulfanilhydrazide hydrochloride
    Cas Number 90034-79-2
    Molecular Formula C6H9ClN4O2S
    Molecular Weight 236.68 g/mol
    Appearance White to off-white powder
    Melting Point 250-254°C (decomposes)
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, tightly sealed
    Chemical Class Sulfonamide derivative
    Application Analytical reagent, pharmaceutical intermediate

    As an accredited 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in a 25g amber glass bottle, labeled with chemical name, purity, safety warnings, batch number, and handling instructions.
    Shipping 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride is shipped in tightly sealed containers, protected from light and moisture. This chemical is classified as hazardous and requires compliant packaging, proper labeling, and documentation in accordance with international and local transport regulations. Shipment occurs via specialized couriers, ensuring safe and secure delivery to authorized recipients only.
    Storage 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated). Avoid exposure to heat, incompatible substances, or excessive air to prevent degradation. Proper labeling and separation from oxidizers and acids are essential for safe storage.
    Application of 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride

    Applications of 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride in Industrial Manufacturing

    We supply 4-Hydrazinobenzene-1-sulfonamide hydrochloride to manufacturers seeking reliable performance in specialized chemical synthesis and downstream industrial processes. Below, we outline key application sectors with detailed information on compliance, recommended addition levels, integration strategies, and the actual end products you can achieve using our material.

    1. Pharmaceutical Intermediates for Sulfonamide Drug Synthesis

    Major pharmaceutical companies utilize this compound as a building block in multi-step syntheses to produce certain sulfonamide-based drugs, particularly those in the antibacterials segment. The sulfonamide group enables targeted molecular modification during active ingredient assembly stages. Adherence to process control standards is critical due to the regulated nature of API production; addition ratios must be calibrated to batch size and impurity thresholds as specified by validated process sheets.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP)
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) Monographs for Sulfonamide APIs
    • European Pharmacopoeia (Ph. Eur.) for intermediates

    Typical usage ratio

    • 0.2–1.5 molar equivalents per target API molecule, optimized during route validation and based on yield/purity benchmarks for the desired pharmaceutical intermediate

    Downstream process integration

    • Feeds into the condensation step of the synthetic route, usually following initial aromatic substitution and prior to final API crystallization. Reacts with acyl chlorides or activated esters in controlled reactors under nitrogen atmosphere.

    Final product types

    • Sulfonamide-based antibiotics (e.g., sulfadiazine, sulfamethoxazole)
    • Custom R&D pharmaceutical intermediates for new chemical entity (NCE) development

    2. Dyes and Pigment Intermediate Manufacturing

    Our product serves as a critical diazo component in the azo coupling process, which is foundational to the synthesis of high-performance dyes and organic pigments. The compound’s sulfonamide function groups ensure color stability and desired reactivity during pigment customization for coating and plastics industries. Manufacturers must conform to global colorant specifications regarding purity and migratory substance control.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile raw materials
    • EN 71-3: Safety of Toys – migration of certain elements for colorants used in plastics and paints
    • REACH Regulation (EC) No 1907/2006 for EU market chemicals
    • ISO 9001:2015 for pigment production QMS

    Typical usage ratio

    • 1.0–2.0 equivalents relative to diazotizable amines per batch; precise ratio depends on the target color strength, solubility, and chroma value of the final pigment

    Downstream process integration

    • Charged into diazotization reactors before coupling with aromatic amines or phenols; applied directly in batch or semi-batch reaction steps under acidic conditions, with careful pH and temperature monitoring to prevent side reactions

    Final product types

    • Azo dyes for textile, leather, and paper coloration
    • Organic pigments for plastics and printing inks
    • Specialty effect pigments for coatings industries

    3. Analytical Reagent Production for Diagnostic Kits

    Chemical manufacturers use this material as a precursor for reagents in colorimetric and enzymatic diagnostic assays. Its structural integrity and sulfonamide functionality allow for modified reagent synthesis, supporting precision in clinical and agricultural diagnostics. Compliance with analytical reagent purity and safety standards ensures downstream kit reproducibility and accuracy during end-user testing.

    Industry compliance standards

    • ISO 13485: Medical Devices – Quality Management for diagnostic reagent manufacturing
    • CLSI (Clinical & Laboratory Standards Institute) Guidelines
    • USP 40-NF 35: Reagent Specifications
    • RoHS Directive 2011/65/EU regarding hazardous substances in test kits used in the EU

    Typical usage ratio

    • 0.01–0.10% w/w in premixed batch formulations; concentration tailored according to detection thresholds and background signal requirements for each assay type

    Downstream process integration

    • Incorporated into pilot-scale synthesis of colorimetric reagents prior to blending with stabilizers and excipients; filtered and dried as part of the final reagent powder or liquid formulation step

    Final product types

    • Blood diagnostic test kits (reagent strips, enzymatic color tests)
    • Veterinary field test reagents
    • Food safety analytical kits

    4. Corrosion Inhibitor Formulation for Industrial Water Treatment

    Producers in power plants and heavy industry employ sulfonamide derivatives as raw materials for formulating water-soluble corrosion inhibitors. The compound acts as an intermediate to modify inhibitor molecules, improving metal surface passivation and lifespan of system components. Rigorous adherence to health, safety, and environmental regulations is required due to direct discharge or recycling of treated water streams.

    Industry compliance standards

    • ANSI/AWWA B100-16: Standard for Chemicals for Water Treatment
    • OSHA (Occupational Safety and Health Administration) Chemical Safety Regulations 29 CFR 1910
    • ISO 14001: Environmental Management for chemical production sites
    • Registration, Evaluation, Authorisation, and Restriction of Chemicals (REACH) for use in EU member states

    Typical usage ratio

    • 0.05–0.2% in corrosion inhibitor concentrate formulations; adjustment based on required metal protection efficiency and plant water chemistry

    Downstream process integration

    • Introduced at the intermediate synthesis step before neutralization and blending with other inhibitor actives; emulsified or dissolved in aqueous solution as part of the inhibitor concentrate make-up

    Final product types

    • Circulating water system corrosion inhibitors
    • Closed-loop cooling system formulations
    • Anti-scaling blends for industrial boilers and chillers

    5. Specialty Synthesis for Custom Research Chemicals

    Contract research organizations and advanced chemical suppliers rely on this compound as a tailored synthon in multi-stage synthesis protocols where modifications of aromatic sulfonamides are required. Quality requirements for this sector demand batch-level documentation, traceability, and precise adjustment to chemical reactivity in downstream customized molecules.

    Industry compliance standards

    • ISO 17034: General Requirements for the Competence of Reference Material Producers
    • Good Laboratory Practice (GLP) OECD Guidelines
    • Material Safety Data Sheets (MSDS) and globally harmonized labelling for chemical research materials
    • Documentation and traceability under ISO 9001:2015 for specialty synthesis

    Typical usage ratio

    • 0.05–1.0 equivalents adjusted for specific reaction schemes and final molecule targets as per customer research protocols

    Downstream process integration

    • Added at early-stage substrate modification or late-stage derivatization steps, depending on target compound structure; often handled in sealed, nitrogen-purged reactors to prevent air/moisture exposure

    Final product types

    • Analytical standards for laboratory research
    • Experimental bioactive molecules and enzyme inhibitors
    • Custom small-molecule libraries for screening projects
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    Certification & Compliance
    More Introduction

    Introducing 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride

    Experience from Real Production: Understanding and Using 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride

    Working as a chemical manufacturer, we find our perspective is shaped not by abstract ideals, but through the daily experience of continuous batches, careful quality checks, and the demands of real customers. In our world, chemicals are not commodities picked from a shelf, but compounds shaped by precise processes, strict material selection, and an unwavering eye for unwanted byproducts. Among the host of refined intermediates we produce, 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride holds a distinctive place. Its unique structure—an aromatic ring, a hydrazino group at the para position, and a sulfonamide moiety balanced with a hydrochloride counterion—means we pay careful attention to synthesis, storage, and onward use.

    What Sets This Compound Apart in Real Manufacturing

    Over the years, we have seen 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride requested for advanced pharmaceutical synthesis, research-scale dye chemistry, and more recently for probe molecule development. Its chemical model, C6H9N3O2S·HCl, often draws questions: what is so important about this compound, with its carefully placed substituents? Unlike simple hydrazine derivatives or benzenesulfonamide units on their own, this molecule brings together two moieties that can open up advanced routes of reaction. The para-hydrazino group offers a reactive handle not just for diazotization, but for constructing linkers, conjugating with carboxylates, or setting up intermediates in heterocycle formation. The sulfonamide, meanwhile, provides both stability and solubility, but also influences how the compound behaves in water or polar organic solvents. In our manufacturing process, we focus on retaining the identity of the sulfonamide group, protecting it during all synthesis stages, and avoiding unwanted hydrolysis under variable temperature and pH during workups.

    Handling Quality and Consistency—An Insider’s Perspective

    If you step into a chemical plant or a targeted kilo lab, you know the relentless focus on color, purity, and remaining solvent traces. Each batch of 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride pressures us to get the melting point right, eliminate residual starting materials, and document even low-level impurities. Customers in API research and specialty chemicals inspect the certificate of analysis as closely as we do; if we cut corners, the consequences can show up later in someone else’s reaction. Our staff tests samples with both HPLC and, where possible, NMR—relying on clear ^1H signals for the aromatic protons, unmistakable hydrazino resonances, and clear sulfonamide signatures in both ^1H and ^13C spectra. Each lot comes under scrutiny for chloride content and water uptake, which can change solubility and reactivity for downstream users.

    Production Knowledge: Scale, Storage, and Real-World Logistics

    Scaling up from grams to multi-kilogram lots, we have adjusted our methods to remain true to the original chemistry. We do not use just any hydrazine or benzenesulfonamide salt. Raw materials undergo additional drying and purity screening before charging into reactors. The hydrochloride counterion adds a step—neutralizing, filtering, and then securing the correct hydration level before final packing. Errors in this stage bring in not just handling complications, but also analytical surprises down the line. Years of practical experience have taught us which containers limit moisture intrusion, and why rapid sealing makes such a difference. Our warehouse crew labels by batch, not blindly, because the hydrazino group makes oxidized byproducts a genuine risk during extended storage, especially if humidity creeps up in the warehouse.

    Applications That Demand Reliability

    Researchers developing emerging treatments or analytical standards trust our process because in pharmaceutical synthesis, one out-of-spec batch can derail weeks of work. Our customers have used 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride in N-heterocyclic ring constructions, coupling with a range of carboxylic acid derivatives, or as a functional group transfer reagent in stepwise organic synthesis. In dye chemistry, it acts as a precursor for assembling a variety of diazo linkages, expanding color palettes and solubility profiles. Its hydrochloride salt form, compared to the free base or other counterions, offers better crystalline stability—a factor that makes purification less aggressive and the compound itself safer to handle on bench scale. When researchers mention consistency from bottle to bottle, we know our attention to the salt form and the purification protocol pays off.

    How 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride Differs from Other Reagents

    Over the past decade, industry demand has shifted. There is no shortage of sulfonamide-based intermediates or hydrazino aromatics in the market, but very few meet the combined needs for stability, solubility, and targeted reactivity that our compound achieves. Compared to unsubstituted hydrazinobenzenes, the para-sulfonamide further limits side reactions; in paired functionality, it often delivers superior yields in multi-step syntheses. We have seen alternative hydrazino derivatives suffer from handling difficulties—prone to oxidation, uneven crystallization, or even safety issues due to higher volatility. Our hydrochloride salt brings a manageable odor profile and more predictable shelf life, qualities that set it apart from the base form. For those sensitive to regulatory compliance (especially handling requirements for hazardous materials), the hydrochloride salt simplifies logistics compared to unprotected hydrazine derivatives.

    Quality by Experience—Solving Downstream User Problems

    Beyond basic analytics, we learned from customers struggling with other suppliers. Common complaints include low yield after extended storage, off-color powder that signals partial decomposition, or sticky lots that hint at excessive moisture content. Early in our production of 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride, we saw similar challenges until we tuned drying procedures, switched desiccant materials, and refined our packaging protocol. One research group, working with a competitor’s lot, contacted us after losing an entire run to side reactions. When we supplied them with freshly produced material, not only did their yield improve, but analytical results proved cleaner and more reproducible. This kind of feedback shapes our QA/QC focus and pushes us to maintain tight control over each lot.

    Some users care most about solubility; others need a granular solid for ease of handling in semi-automated apparatus. Our aggregated production logs show there is no one-size-fits-all solution, but transparent feedback channels have let us tweak slurry drying or crystal sizing in response to repeated requests. Sometimes, a small adjustment, like optimizing drying curve endpoint or packing smaller aliquots, leads to noticeable performance upticks for the end user. We keep an archive of requests—from improved free-flowing powder to minimal static cling on dispensing—which guides changes for future production runs.

    Supporting Claims with Evidence, Not Hype

    As a manufacturer, it is easy to promise quality, but much harder to prove consistency by numbers. In the labs, our monitoring of purity and identity always starts with validated reference standards. By reporting real HPLC trace data and performing periodic third-party cross checks, we ensure customers don’t just take our word on assay claims. Our worst critic remains our own R&D team; they push for the lowest total impurity numbers, driven by their knowledge of how batch-to-batch differences can compound in larger scale syntheses. Long term, tracking the performance of each lot from plant to customer application gives us a map of what works and what brings challenges. This pragmatic approach gives our technical support team the kind of insight that makes problem-solving effective—rooted in real data, not fluff.

    For chemists using the compound in medicinal research or analytical methods, the absence of trace hydrazine or benzene-related byproducts means fewer purification headaches and more reliable downstream reactions. Because so much depends on stability, our warehouse protocols separate materials sensitive to moisture or light, a simple but crucial real-world practice. Without this discipline, even the cleanest batch can gradually degrade, undermining synthesis results just by sitting too long on a shelf. These are not theoretical risks, but problems learned over dozens of runs and hundreds of kilos shipped.

    Practical Solutions to Production and Storage Challenges

    Throughout our history with 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride, technical obstacles rarely resolve on their own. They respond to direct intervention. Moisture uptake proved important—prompting upgraded dehumidifiers, improved vacuum sealing, and barcode tracking for time out of controlled storage. Temperature swings can condense water from humid warehouse air, so real-time sensors now inform us before a batch risks degradation. Customers working in climates markedly different from ours receive advance consultation on secondary packaging, and we send clear instructions on minimizing exposure before use.

    Occasionally, researchers run into reactivity differences using material from different suppliers. Our commitment remains to eliminate those concerns by matching particle size, maintaining clear trace elements reporting, and guaranteeing reproducible results in core organic transformations. When difficult-to-measure characteristics like minor polymorphism variation arise, we collaborate with partners on both sides: analytical labs and end users. The key to lasting solutions lies not in theoretical fix-it-lists, but in persistent effort, open dialogue, and willingness to adjust even small steps. For our team, these habits are learned through trial and, occasionally, error. These lessons show up in our production notes, not just our marketing materials.

    Meeting Compliance—Beyond Paperwork

    Work with us long enough, and you see compliance as more than boxes on an audit checklist. Regulations exist to keep people safe, but process discipline does the real work. Our plant follows systematic cleaning routines between all production runs involving hydrazine intermediates. Staff training emphasizes not only the required procedures, but the reasons behind them—eliminating cross-contamination, spotting early signs of off-color powder, and documenting deviations before they spiral into quality lapses. Auditors can catch slip-ups, but the true test comes when a customer uses our product in a critical step and finds the outcome repeatable, cycle after cycle.

    Why We Maintain Direct Relationships with Researchers

    Over the years, feedback from real users has steered our upgrades and process adjustments far more than abstract trend reports or listless specification sheets. When a research group stumbles on an unexpected incompatibility—be it in a new dye route, a pharmaceutical precursor, or a diagnostic reagent—we respond directly. Our technical support logs signal recurring questions on solubility, application in diazotization, or coupling yields. In every case, the solution comes from a granular look at batch history and customer dialogue. Where an issue lies in trace-level moisture, we tweak drying schedules; when particle size causes weighing inconsistency, a calibrated grinder resolves the issue. This cycle—listen, test, refine, and revalidate—sits at the core of how we operate.

    The Practical Impact of 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride

    Our compound’s greatest merit resides where the sums of its parts make a real impact: high yield in critical syntheses, minimized waste, and process stability under everyday conditions. In continuous runs, researchers report less clogging, smoother filtrations, and more reliable endpoint detection. Compared to other intermediates, our salt form means less downtime required for purification or reprocessing due to inconsistent product quality. Such advantages may not show up in glossy brochures, but in lower costs, higher throughput, and more confident project planning.

    To those working daily in organic synthesis, specialty pigment formulation, or advanced diagnostics, 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride means more than a name on a bottle. It carries weight as a trustworthy input—performing as expected, batch by batch. Our manufacturing experience makes this consistency possible and shapes every decision from sourcing to quality assurance. In evolving research, where a single synthetic stumble can disrupt an entire project, we have learned there is no substitute for sustained attention to detail and honest engagement with those who depend on our work.

    Open Channels, Ongoing Improvements

    We do not treat 4-Hydrazinobenzene-1-Sulfonamide Hydrochloride as a static commodity. As manufacturing methods evolve and research pushes boundaries, we continue to refine both how the compound is made and how it is supported. Open communication with end users, real-world observation, and rapid technical feedback loops define how we stand behind our product—avoiding excess jargon or hollow assurances in favor of facts from the production floor. Over time, these habits build trust and ensure our output does not just meet today’s expectations, but is ready for tomorrow’s challenges.