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2-Aminothiazole-5-Sulfonamide

    • Product Name 2-Aminothiazole-5-Sulfonamide
    • Alias 2-Aminothiazol-5-ylsulfonamide
    • Einecs 221-314-1
    • 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

    704460

    Casnumber 3034-18-0
    Molecularformula C3H5N3O2S2
    Molecularweight 179.23
    Appearance Off-white to light yellow solid
    Meltingpoint 213-217°C
    Solubility Soluble in water and DMSO
    Boilingpoint Decomposes
    Purity Typically ≥98%
    Storageconditions Store at 2-8°C, protected from light

    As an accredited 2-Aminothiazole-5-Sulfonamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Aminothiazole-5-Sulfonamide, 25g: Supplied in a sealed amber glass bottle with tamper-evident cap and detailed hazard labeling.
    Shipping 2-Aminothiazole-5-Sulfonamide is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with regulations for handling chemicals. The product ships via ground or air transport, depending on destination, while adhering to safety standards for hazardous materials. Documentation, including safety data sheets, accompanies each shipment for regulatory compliance.
    Storage 2-Aminothiazole-5-sulfonamide should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep it in a cool, dry, and well-ventilated area, preferably at room temperature (15–25°C). Store away from strong oxidizers and acids. Ensure proper labeling and restrict access to authorized personnel. Use appropriate personal protective equipment when handling this chemical.
    Application of 2-Aminothiazole-5-Sulfonamide

    Applications of 2-Aminothiazole-5-Sulfonamide in Industrial Manufacturing

    As a dedicated producer of 2-Aminothiazole-5-Sulfonamide, we supply this advanced intermediate to specialized sectors with stringent quality and compliance needs. Our technical team works directly with downstream manufacturers, sharing application-specific knowledge to ensure success from scale-up through finished goods production. See below for detailed use cases across key industrial fields.

    1. Pharmaceutical Intermediate for Sulfonamide Antibiotic Synthesis

    In pharmaceutical manufacturing, this compound serves as a core intermediate in the multi-step synthesis of thiazole-based sulfonamide antibiotics. Companies use it to introduce the thiazole and sulfonamide motifs during active pharmaceutical ingredient (API) assembly. It enters the process after initial ring formation but before coupling with specific amines or aryl groups, ensuring correct chemical lineage and purity at this critical transformation step. Reliable performance in this stage supports API batch consistency, meeting regulators’ demands for strict quality control and full traceability.

    Industry compliance standards

    • United States Pharmacopeia (USP) monographs for final APIs
    • European Pharmacopoeia (EP) standards
    • Current Good Manufacturing Practice (cGMP, ICH Q7 guidelines)
    • FDA 21 CFR Part 210/211 for finished antibiotics

    Typical usage ratio

    • 0.85–1.20 molar equivalents per antibiotic API synthesis batch, adjusted to downstream coupling partners and desired API yield

    Downstream process integration

    • Employed in protected intermediate stage following initial heterocycle construction; often purified then coupled with functionalized aromatic/amino reagents

    Final product types

    • Sulfonamide antibiotics (oral tablets, injections, topical solutions)
    • Thiazole-containing antibacterial agents

    2. Agrochemical Intermediate for Fungicide and Herbicide Formulation

    In the agrochemical sector, downstream producers rely on this material as a heterocyclic building block for new thiazole-sulfonamide-based fungicides and herbicides. Fine chemical formulators introduce it during the late-stage condensation or sulfonation steps, helping generate active ingredients with targeted crop protection properties. Raw material purity and controlled dusting are critical to avoid batch yield loss or off-target bioactivity.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • EPA 40 CFR Part 180 (US pesticide residue limits)
    • REACH (EC 1907/2006) compliance for agrochemical intermediates
    • ISO 9001:2015 certified quality management systems

    Typical usage ratio

    • 1.0–1.5 molar equivalents per active ingredient batch, adjusted for condensation efficiency and crop-specific activity targets

    Downstream process integration

    • Introduced during pre-final condensation or sulfonamide moiety installation, usually after primary aromatic backbone assembly; may require solvent exchange or acid-neutralization steps

    Final product types

    • Systemic fungicides (granules, wettable powders, suspension concentrates)
    • Selective herbicides for cereals or legumes

    3. Dye and Pigment Intermediate in Specialty Textile Processing

    Manufacturers of specialty thiazole dyes use this chemical for coupling reactions that produce reactive dye intermediates with enhanced light and washfastness. It functions in the sulfonamidation phase, where thiazole units are installed to alter chromophore absorption, helping textile processors comply with ecological standards while achieving persistent coloration. Production lines require controlled feed rates and solvent compatibility assessments to ensure reproducible color development.

    Industry compliance standards

    • OEKO-TEX Standard 100 for non-toxic dyes
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals)
    • EU REACH Annex XVII (restricted substances in dye stuff)
    • ISO 14001:2015 for environmental management

    Typical usage ratio

    • 0.6–1.0 molar equivalents per batch, depending on target chromophore density and color intensity requirements set by textile end-users

    Downstream process integration

    • Utilized at the reactive coupling stage, usually post-azo or anthraquinone core synthesis; subsequent purification critical for washfast dye quality

    Final product types

    • Reactive thiazole dyes for cotton and blended fabrics
    • High-performance inks for technical textiles

    4. Intermediate in Specialty Polymer Additive Manufacturing

    Industrial polymer producers incorporate this compound as a precursor for sulfonamide-functionalized thiazole additives, enhancing polymer flame retardance or UV stability. The chemical enters the side-chain grafting or copolymerization phase, reacting with monomers or pre-polymers via controlled temperature and catalyst dosing. Each stage requires stringent monitoring to ensure the additive’s compatibility with the host polymer matrix, with special attention given to end-use safety and migration limits.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (flame retardant exclusion)
    • UL 94 (flammability standards for plastic materials)
    • EN 71-3 safety for toy and children’s product polymers
    • ISO 9001 process control for specialty chemicals

    Typical usage ratio

    • 0.4–2.0 wt% of total polymer mass, varied according to desired flame retardance or UV-blocking effect; lower dosages for thin films, higher for bulk plastics

    Downstream process integration

    • Added during compounding, reactive extrusion, or as a co-monomer feed during solution/solid-phase polymerizations

    Final product types

    • Flame-retardant engineering plastics (PA, ABS, PC blends)
    • UV-stabilized polyester packaging films

    5. Intermediate for Analytical Reagent Manufacturing

    Producers of analytical reagent kits utilize this thiazole derivative to prepare select colorimetric and chelating agents. It is essential for constructing molecular probes that react with trace metals or biologically relevant ions. The substance’s controlled purity supports reproducibility, matching rigorous analytical standards in QC laboratories or clinical diagnostics.

    Industry compliance standards

    • ISO 13485 for medical device (IVD) reagents
    • EN 14885 (standards for chemical disinfectants and antiseptics)
    • GLP (Good Laboratory Practice, OECD)
    • Analytical reagent-grade specification (ACS, ISO)

    Typical usage ratio

    • Precisely titrated at 0.1–1.5 mmol per formulation, based on target ion selectivity and sensitivity requirements of the diagnostic kit

    Downstream process integration

    • Entered at the probe synthesis phase, after backbone assembly, followed by purification for direct use in reagent cartridge or test strip preps

    Final product types

    • Colorimetric trace metal detection kits
    • Ion-selective reagent packs for clinical chemistry analyzers
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    Certification & Compliance
    More Introduction

    2-Aminothiazole-5-Sulfonamide: A Closer Look from the Manufacturer’s Perspective

    Practicality Built into Every Batch

    From the very start, manufacturing 2-Aminothiazole-5-Sulfonamide demands careful attention. We recognize this compound’s value across research, pharmaceuticals, and innovative chemical synthesis. Every decision in our process, from choosing the right grade of raw thiazole to adjusting the crystallization steps, shapes what ends up in our customers’ hands. We don’t treat this as just another sulfonamide derivative—its purity and performance often make the difference in whether a pharmaceutical experiment goes smoothly or a specialty coating does what it promises.

    What Sets Our 2-Aminothiazole-5-Sulfonamide Apart

    Not all chemical products measure up the same, even if they carry the same name on paper. Over years of manufacturing, we have learned that trace impurities in sulfonamide chemistry tend to haunt downstream results. We keep these in check, especially through filtration protocols that do not rob the material of its integrity. From repeated feedback and our own in-process analytics, a consistency in color, particle size, and moisture content makes our batches easy to work with in lab and plant conditions. Lab directors and process technicians have explained how haze or trace discoloration in similar compounds from other sources can throw off analyses or delay further processing steps.

    We produce our 2-Aminothiazole-5-Sulfonamide with assays above 99.0%, measured by HPLC. While making it, our team has never considered shortcuts that could jeopardize stability in storage. Degradation products cause headaches that extend far beyond our warehouses. Our investments in closed-system handling and real-time spectroscopic monitoring help keep the profile tight and predictable from shipment to shipment.

    Batch Sizes and Customization: Real-World Demands

    Smaller lots for university programs rarely mirror the specifications of pilot plants or commercial pharmaceutical facilities. For us, that means managing both custom and standard batch runs. If researchers order a few hundred grams, requests sometimes ask for additional documentation—NMR, melting point—and we’re equipped to provide these details, thanks to in-house capability and long relationships with accredited testing labs. Scaled-up batch runs, reaching tens of kilograms, push our team to optimize crystallization and containment protocols so even large orders don’t suffer in terms of product stability or flow characteristics.

    There’s no universal granule size that works for everyone using sulfonamide derivatives. In custom work, if a powder with a coarser cut has made weighing easier for one client, another may need more free-flowing material for a chute-feed process. Over time, we have adjusted drying times and milling approaches based on practical handling feedback rather than one-size-fits-all guidance.

    Niches and Applications Backed by Real Experience

    Most buyers we speak with use 2-Aminothiazole-5-Sulfonamide for its intermediate role in synthesizing various drugs, pesticides, or specialty chemicals. Sometimes, even a small impurity unexpectedly blocks a downstream reaction or changes a pharmacological profile. We’ve worked alongside end users who noticed issues trying off-the-shelf material from other producers. A case stands out—a generic supplier’s sample once stalled an antiparasitic drug synthesis due to sulfonamide breakdown under heat. Our version, processed with careful pH control and minimal mechanical stress, prevented those bottlenecks.

    For pesticide developers, the balance between reactivity and storage stability matters just as much. Environmental labs also count on it as a reference standard in analyte identification. The structure lends itself to targeted modifications, and our teams track shifts in reactivity when handling slightly altered analogs. Having run tens of kilograms through pilot synthesis stages ourselves, we know what impurities matter most and have tuned our testing accordingly.

    Constantly Improving Purification and Handling

    No manufacturing method stays static. We have altered our purification steps as analytical tools reveal new insight. Water content, for instance, once hovered closer to 0.5% in older production runs. That gave us trouble with storage cakes and lumping. Fine-tuning our vacuum drying system—guided by inspection later in the supply chain—brought most new lots under 0.2%. That level matures each shipment, reducing caking and improving shelf life for everyone needing to store bulk containers.

    Dust and powder management issues taught us valuable lessons, too. Airborne fines in batch rooms made for cross-contamination risk. Steps like gentle tumble-blending and double filtration now all but eliminate foreign particle transfer—a point our long-term buyers asked us to prioritize.

    Comparing to Similar Sulfonamide Products

    The world of thiazole and sulfonamide compounds covers plenty of structures, each promising something unique. 2-Aminothiazole-5-Sulfonamide’s profile gives it distinct advantages for certain syntheses over well-known alternatives such as sulfanilamide or 2-aminobenzothiazole. We’ve noted that its reactivity, anchored by both the amine at position 2 and the sulfonamide at position 5, opens specific chemical routes that wouldn’t otherwise be accessible with simpler analogs. A benzothiazole ring, for example, introduces extra resonance stability but lowers the rate of some desired transformations; 2-aminothiazole-5-sulfonamide encourages rapid sulfonylation or N-alkylation, which aligns with the goals of many medicinal chemists.

    Buyers working on structure-activity relationship studies tell us they skip other sulfonamides due to solubility issues. Our product, thanks to the way we fine-tune the final crystallization step, dissolves reliably in standard lab solvents—something that isn’t true for less carefully handled material. That saves time at the bench and improves accuracy of analytic and scale-up experiments.

    Specifications that Support the User’s Needs

    We’ve built our reputation not around flashy numbers but by listening to the actual pain points customers face. That pushed our finished product to meet or exceed the most critical analytical parameters, including high assay confirmation by HPLC, tightly controlled residue-on-ignition results, and consistent melting point. Stability tests, both at accelerated and room temperature conditions, prove valuable for users needing longer shelf lives. Our QC team runs these in every major batch and publishes these details for any user with regulatory or internal compliance requirements.

    As a chemical manufacturer, we know that supplying crystalline powders to the pharmaceutical industry brings a host of scrutiny. Trace metals, especially copper, zinc, and iron, can be especially problematic in fine chemical synthesis. We minimize these by sourcing carefully-certified reagents and running additional metal screening beyond what many producers perform. From customer audits, this has helped us remain a trusted source when others in the supply chain have struggled.

    Handling and Logistics: Lessons from Hard Experience

    Anyone who has actually packed and shipped 2-Aminothiazole-5-Sulfonamide can attest: chemical handling, especially at scale, brings real challenges. Moisture, static electricity, and temperature swings in transit all impact how powders behave and settle. We package in multi-wall bags with a moisture barrier or in lined fiber drums for larger quantities, a change we made after early shipments picked up ambient humidity during transport to rainy regions.

    We track customer complaints as closely as production yields. Years ago, complaints about minor lumps or agglomerated powder led to a redesign of our post-drying blending and packing stages. A more uniform product today traces back to real talks between our technical team and the operators who load the trucks. In each improvement, the end-user’s handling complaints guide practical steps, rather than the reverse.

    Supporting Research and Validation

    Our facility serves as the backbone for multiple ongoing collaborations with leading research institutions. Requests for lot-to-lot consistency in this compound keep us attentive to detail. Some researchers require additional documentation showing infrared, UV-VIS, and LC-MS spectra, particularly if running a regulated pre-clinical study. We have responded by integrating more automated batch records and additional sampling checkpoints, to keep results as consistent as possible. Having worked through several multi-year research agreements, we learned that sometimes, a single odd result in a multi-year program can send teams back to square one. Sharing full QC data in real time, not just on request, has saved time for our customers—and avoids miscommunication about what a “typical” batch really means.

    For chemical suppliers who work broadly across commodity and specialty products, these kinds of support steps can seem tedious. Still, based on our experience, every page of validation and transparency builds real trust with our customers. The cost to over-communicate about a batch profile pales compared to a contract disrupted by inconsistent material or product recalls.

    Environmental and Workplace Considerations in Production

    The production of sulfonamide derivatives like 2-Aminothiazole-5-Sulfonamide involves handling corrosive agents and volatile organic solvents. Safety for our workers and the surrounding community shapes every equipment investment. Installing segmented air extraction and routinely updating PPE requirements help prevent cross-contamination and exposure incidents. Spills or leaks have been extremely rare in our facility over the last decade, and we trace this record back to employee-driven safety suggestions.

    Effluent from our process contains manageable loads of organics and sulfur compounds, which we neutralize and treat before discharge. These investments, though expensive, prevent both regulatory issues and community complaints. Responsible chemical stewardship guides how we plan expansion or technology upgrades. That pays dividends in a good relationship with local agencies and a strong safety culture onsite.

    Anticipating Regulatory and Customer Trends

    Markets for thiazole and sulfonamide intermediates keep evolving. Regulators demand lower impurity profiles and more rigorous traceability than ever. We believe transparency is not just about fine print compliance; it builds the backbone for real partnerships in R&D and commercial manufacturing. To that end, our enterprise resource management system records materials sourcing and process settings at a granular level. That way, if a customer ever questions a specific analytical result, we can trace every input and adjustment used in that batch.

    Most buyers don’t see the constant revision process behind-the-scenes. Each quarter, we compare our practices with updated guidance from agencies such as the European Medicines Agency and the U.S. Food and Drug Administration. If new impurity thresholds or documentation standards emerge, we adjust protocols preemptively, not only after customer pressure.

    Supply Chain Resilience in an Unpredictable World

    Supplying specialty chemicals in today’s volatile environment requires more than just production expertise. Disruptions upstream—from raw solvent shortages to unexpected regulation—can undercut the best-laid production plans. We established secondary supply lines for our core raw materials. This took investment, but keeps both small batch and high-volume orders moving even when global logistics falter. Most importantly, we share early heads-up alerts with our buyers during bottlenecks.

    Lessons from recent years, like the global shipping disruptions, reminded us how fragile just-in-time chemical supply chains can be. We have expanded on-site inventory for key intermediates, lowering lead times and reducing last-minute customer angst. While this burdens working capital, the stability it brings outweighs the cost.

    Direct Customer Support and Knowledge Sharing

    Questions don’t stop at the point of sale. Synthesizing with 2-Aminothiazole-5-Sulfonamide rarely runs textbook-smooth for every lab. Our technical service team fields questions ranging from solvent compatibility to risk mitigation in scale-ups. Sometimes, we can direct a customer to a better solvent system or suggest purification tweaks to improve conversion rates. These suggestions come from lab-scale trials run with material from our own pilot plant. We stand behind our product beyond shipment, a practice that has reduced customer complaints—and made collaboration easier.

    Some new buyers, uncertain whether this compound or a related one fits their planned chemistry, reach out for comparative insight. Instead of offering canned answers, we use our process data and experience to explain similar past requests, helping them avoid wrong turns that waste time and budget.

    Understanding What Users Really Value

    The best specifications look good on paper, but we know customers—and their quality assurance teams—care more about reliability and responsiveness. What matters most in specialty chemical manufacturing is whether a batch meets application goals not just the day it arrives, but months later. That’s why we routinely review past performance records, repeat stability testing, and invest in technical training for every team member involved.

    We watch the market and adapt based on feedback. Whenever a customer points out a packaging improvement, a preferred particle cut, or asks for a new analytical method, we evaluate it seriously. The demands change; the core commitment—delivering a dependable, useful product—remains.

    Looking Forward: Innovation with Real Purpose

    We believe that continuous improvement must ground itself in the needs of both present and future customers. Expanding process automation, fine-tuning synthetic routes, and increasing the transparency of our operations belong not just to efficiency drives but real-world accountability. Every batch of 2-Aminothiazole-5-Sulfonamide tells a story of adaptation—each cycle shaped by technical learning, customer necessity, and regulatory movement.

    Our hope is to keep building on these experiences, growing with the scientists, formulating chemists, and production engineers who rely on our product. We measure success by how seamlessly buyers put 2-Aminothiazole-5-Sulfonamide to use in their own breakthroughs, knowing the foundation rests on expertise built with every run in our plant.