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4-Aminobenzo-2,1,3-Thiadiazole

    • Product Name 4-Aminobenzo-2,1,3-Thiadiazole
    • Alias 4-Aminobenzo[c][1,2,5]thiadiazole
    • Einecs 219-122-6
    • 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
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    Specifications

    HS Code

    816060

    Productname 4-Aminobenzo-2,1,3-Thiadiazole
    Iupacname 4-aminobenzo-2,1,3-thiadiazole
    Molecularformula C6H5N3S
    Molecularweight 151.19 g/mol
    Casnumber 5335-95-5
    Appearance Off-white to light yellow solid
    Meltingpoint 216-218 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Density Approximately 1.43 g/cm³
    Purity Typically ≥98%
    Synonyms 2,1,3-Benzothiadiazol-4-amine
    Smiles c1cc2c(cc1N)nsn2
    Inchi InChI=1S/C6H5N3S/c7-4-1-2-5-6(3-4)10-9-8-5/h1-3H,7H2

    As an accredited 4-Aminobenzo-2,1,3-Thiadiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed, amber glass bottle containing 25 grams, labeled with product details, safety symbols, and lot number.
    Shipping 4-Aminobenzo-2,1,3-thiadiazole is shipped in tightly sealed containers to prevent moisture and contamination. During transit, it should be stored in a cool, dry, and well-ventilated environment, away from incompatible substances. Packaging complies with chemical transport regulations to ensure safe handling and prevent spills or leaks.
    Storage 4-Aminobenzo-2,1,3-thiadiazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances, such as strong oxidizing agents. Protect it from moisture and direct sunlight. Store at room temperature and label appropriately. Avoid sources of ignition, heat, and static discharge. Use proper personal protective equipment when handling.
    Application of 4-Aminobenzo-2,1,3-Thiadiazole

    Applications of 4-Aminobenzo-2,1,3-Thiadiazole in Industrial Manufacturing

    4-Aminobenzo-2,1,3-Thiadiazole finds utility as a specialty intermediate in several downstream chemical industrial sectors. Extensive process know-how and precise production control make it essential for targeted molecule synthesis and functional materials. The following sections detail key industry application scenarios, with a focus on compliance, processing integration, and finished goods manufacturing.

    1. Pharmaceutical Intermediate for Antibacterial Agents

    As a building block for heterocyclic pharmaceutical compounds, 4-Aminobenzo-2,1,3-Thiadiazole enables synthesis of select antibacterial drugs, particularly in the sulfonamide and related classes. Production batches require careful management of raw material purity and reaction temperatures to achieve consistent molecular structures for API manufacturing, supporting regulatory filing processes. The intermediate supports targeted substitution patterns, entering the synthesis pathway after initial starting material preparations, often via amide coupling or cyclization steps, leading to regulated final APIs for human or veterinary use.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. 10.0 and USP-NF Monographs (where applicable to derivative APIs)
    • FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • REACH Registration (EC No. 1907/2006) for raw material import and downstream safety data

    Typical usage ratio

    • 10–40% molar fraction in targeted heterocycle synthesis
    • Exact dosage depends on desired API structure and process yield; adjusted by process development through route optimization and impurity profiling

    Downstream process integration

    • Post-initial precursor synthesis as a key ring formation element
    • Introduced during controlled heating and solvent management steps prior to final crystallization and purification
    • QC laboratories briefed on handling, with documented batch traceability

    Final product types

    • Active pharmaceutical ingredients (APIs) for sulfonamide derivatives
    • Antibacterial finished drug formulations in oral or parenteral dosage forms
    • Veterinary drug intermediates

    2. Precursor in Organic Electronic Materials Manufacturing

    4-Aminobenzo-2,1,3-Thiadiazole supports development of electron-transport materials and donor–acceptor polymers for use in next-generation semiconductors and organic light-emitting diode (OLED) display materials. Performance in final devices depends on controlled incorporation of the aminothiadiazole motif during monomer synthesis, ensuring uniformity in conjugation and charge-transport properties. The material enters at the monomer or co-monomer synthesis stage via advanced coupling protocols, leading to production of electronic-grade polymers and thin film deposition solutions for OLED assembly lines.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substance restrictions
    • ISO 9001 Quality Management Systems for raw material traceability
    • IPC-4101E for base material qualification in electronic laminates
    • Customer- or consortium-based material specification sheets for organic electronic applications

    Typical usage ratio

    • 5–20 wt% relative to other monomers in copolymer synthesis
    • Ratio optimized according to charge transport performance and targeted band gap in device design

    Downstream process integration

    • Activated as a co-monomer during solution-phase or melt polymerization steps
    • Reacted under inert atmosphere to prevent oxidation-sensitive group degradation
    • Integrated into material supply chains for OLED fabrication and device prototyping

    Final product types

    • High-purity electron transport polymers for OLED and OPV (organic photovoltaic) layers
    • Semiconducting thin films for display panel manufacturing
    • Functionalized monomers intended for advanced organic circuits

    3. Intermediate for Corrosion Inhibitor Formulations

    Many metalworking fluid and water treatment companies use this thiadiazole derivative as a precursor in corrosion inhibitor synthesis for ferrous and non-ferrous materials. The compound imparts sulfur and nitrogen donor sites into formulated inhibitors, boosting film adhesion to metal surfaces in aggressive industrial environments. Strict process control ensures the correct functionalization occurs during formulation, as incompatibility with other additive chemistries can reduce product stability. The intermediate enters the blending stage after pre-formulation of carrier solvents, often post-neutralization, improving batch-to-batch consistency.

    Industry compliance standards

    • ASTM D7667 Standard Test Method for Corrosion Inhibitor Formulations
    • European Chemicals Agency (ECHA) CLP Regulation for hazardous raw material classification
    • ISO 9001 for manufacturing and lot traceability
    • EN 12925-1 for lubricants, industrial oils, and related products (mechanical engineering applications)

    Typical usage ratio

    • 1–5% weight basis in finished corrosion inhibitor concentrate
    • Dosage tailored based on metal type, exposure time, and compatibility with other lubricity or biocidal additives

    Downstream process integration

    • Added post-solvent and carrier blend, prior to package homogenization and final pH adjustment
    • Batch QC includes solubility and film formation tests on metallic coupons
    • Supplied as technical-grade or higher purity for industrial blending lines

    Final product types

    • Aqueous and oil-based rust inhibitors
    • Metalworking fluids for drilling, cutting, or rolling applications
    • Chemical protection films for pipes, tanks, and storage vessels

    4. Specialty Dye Intermediate in Textile Industry

    Selected dye houses integrate 4-Aminobenzo-2,1,3-Thiadiazole into advanced azo and heterocyclic dye synthesis for textile coloration. Its unique electron donor attributes enable chromophore tuning during molecule assembly, yielding high-colorfastness and specialty hues tailored for demanding fabric performance. Production processes incorporate the material during the diazotization or coupling step, with close monitoring of reaction kinetics to prevent unwanted byproduct formation. Final product performance is validated through exhaustive fastness and wash stability testing.

    Industry compliance standards

    • OEKO-TEX Standard 100 for absence of hazardous amines
    • ISO 105-series for colorfastness testing
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • REACH Annex XVII for dye composition in EU markets

    Typical usage ratio

    • 5–18% molar substitution in multi-component dye formulations
    • Adjusted according to target shade, bath reactivity, and final product brightness requirements

    Downstream process integration

    • Fed into dye precursor batch reactors during chromophore assembly
    • Requires temperature and pH control during diazotization/coupling
    • Intermediate storage under controlled ventilation to prevent sublimation losses

    Final product types

    • High-performance disperse and reactive textile dyes
    • Custom color shades for polyester and polyamide fibers
    • Wash- and lightfast finishes for apparel textiles

    5. Additive for High-Performance Lubricant Formulations

    In the lubricant and grease industry, this aminothiadiazole derivative acts as a multifunctional additive precursor, particularly for high-pressure applications. It undergoes functionalization steps to form performance modifiers that enhance anti-wear and extreme pressure characteristics in finished lubricant blends. Controlled reaction with base oils or additional sulfur donors is required to prevent thermal decomposition during blending, ensuring consistent product stability and tribological properties in heavy machinery operating environments.

    Industry compliance standards

    • DIN 51517-3 (Lubricants – Lubricating oils – Part 3: Requirements for lubricants for gears)
    • API 1509 (Engine Oil Licensing and Certification System)
    • ISO 14001 for environmental management of lubricant production
    • SAE J183 for chemical and physical property validation

    Typical usage ratio

    • 0.5–2% by weight in finished oil or grease formulations
    • Adjusted based on operating load, temperature, and compatibility with metal surface chemistries

    Downstream process integration

    • Dosed post-base oil blending, ahead of thickener or viscosity improver addition
    • Blending conducted under inert gas to limit oxidation pathways
    • Routine batch QC includes anti-wear and high-pressure bench testing

    Final product types

    • Extreme pressure gear oils
    • High-load greases for industrial bearings
    • Specialized lubricants for mining and construction equipment
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    More Introduction

    4-Aminobenzo-2,1,3-Thiadiazole: An Introduction from the Manufacturer’s Perspective

    Understanding the Core of 4-Aminobenzo-2,1,3-Thiadiazole

    In our years of experience synthesizing fine chemicals, a compound like 4-Aminobenzo-2,1,3-thiadiazole (often called ABTD) stands out for its versatility and reliability in a range of demanding applications. Behind every batch, our team navigates the complexities of heterocyclic chemistry, aiming not just for high yield but for repeatable purity levels that meet the scrutiny of quality-driven researchers. As we focus on heterocyclic compounds, we understand the little things—impurities, particle size, solubility, batch stability—that make ABTD suitable for ongoing R&D or process recipes. Our manufacturing practice relies on solid process control and batch traceability, not shortcuts. Our ABTD usually appears as a solid, off-white or slightly yellow powder, with purity standards exceeding 98% by HPLC. Every step, from raw material sourcing to final dry-down, reflects a commitment to minimizing contaminants, ensuring consistent melting points and ease of handling. The CAS number 6973-09-7 means something to those looking for traceable, documented chemical substance—one less complexity in the chain of custody.

    What Sets Our ABTD Apart

    Technical teams recognize 4-Aminobenzo-2,1,3-thiadiazole for the reactive amino and thiadiazole groups on the benzene ring. The molecule brings together the nucleophilicity of the amino group and the aromatic stabilization from the thiadiazole, creating a combination that’s tough to match in other intermediates. We hear from our formulation partners in agrochemicals and pharmaceuticals that this core skeleton allows them to build out a range of functional derivatives—each tailored for different biological activities. Some intermediates on the market cut corners with purity, which backfires with stubborn side-reactions or unreliable downstream yields. We’ve seen shipments of “generic” ABTD with trace organosulfur byproducts muddy up target reactions, often costing weeks in purification and trouble-shooting.

    One key differentiator is control over isomer impurities and residual solvents. A controlled synthesis route means consistently low levels of 2-Aminobenzo-2,1,3-thiadiazole—a similar compound but with notably different reactivity. We’ve invested in proprietary crystallization techniques that reduce these isomer impurities below 0.2% on a finished batch basis. That’s not marketing language; it’s the result of routine HPLC runs, methodical wash steps, and actual on-the-floor inspection at critical points. Other players sometimes skip these checks to save time, but the cost appears later in lost batch value or regulatory headaches.

    On the Critical Role in Synthesis

    Most ABTD grades on the market, including ours, target synthetic chemists developing functionalized derivatives. The real utility comes when the amino group undergoes diazotization, halogenation, or coupling for targeted synthesis. One of the well-documented fields is its journey as a building block in active pharmaceutical ingredient (API) scaffolds—where heteroaromatic rings offer selectivity points for kinase inhibitors or as intermediates for CNS-active drugs. We notice increasing demand from specialty pigment manufacturers as well, where the sulfured core interacts interestingly with metal ion centers.

    Not all ABTD is equal in build quality for these diverse routes. Our involvement goes past shipping barrels; we batch-release only after confirming low water content (Karl Fischer titration, typically <0.2%), and ensure batch-to-batch homogeneity by retaining batch samples for post-delivery troubleshooting. Many colleagues recall labs where reactivity collapsed due to unseen traces of iron, copper, or persistent organosulfurs; in our line, we use dedicated, non-reactive vessels for thiadiazoles to sidestep these trace metal contamination issues.

    Specifications That Matter in Real Work

    To move quickly in experimental work, end-users demand not just chemical nameplates but clear physical and chemical parameters. Our ABTD comes with a molecular formula of C6H5N3S, molecular weight of 151.19 g/mol, and melting point range of 141-145°C—well within the boundaries expected for this compound. Proper solubility is essential: it dissolves readily in DMSO and DMF, limited solubility in water under ambient conditions, which matches published solvent compatibility. Some clients wonder about its behavior in organic-acid functionalizing environments; we’ve tested stability against oxidation and hydrolysis, providing documented dry storage and handling conditions. We package only in moisture-barrier containers, reducing the risk of hygroscopic clumping or oxidative color change.

    One aspect—often missing from off-the-shelf material—is the confirmation of polymorphic stability, which shapes the solid-state properties and downstream process reproducibility. Working with university collaborators, we’ve screened several polymorphs and ensure that what we provide represents the most stable, easily processable form for further transformations.

    Comparisons with Other Building Blocks

    It’s tempting to compare ABTD with well-known building blocks like 4-aminobenzoic acid or phenylenediamine. While close structurally, each brings a different clutch for process engineers and bench chemists. 4-Aminobenzoic acid offers easier carboxylate reactions and is widely used in basic arylamine chemistry, but lacks the sulfur-based reactivity of the thiadiazole group. The 2,1,3-thiadiazole ring, present in ABTD, gives a rigid, electron-rich structure that interacts differently in condensation or coupling—opening up chemistry that classic aminobenzoic acids or benzenediamines cannot reach. Where phenylenediamine might trigger quick oxidative darkening, ABTD offers greater stability and less air sensitivity, making it preferable in workflows sensitive to oxygen or where handling over longer timescales is needed.

    We’ve worked with catalyst manufacturers who report that ABTD resists conditions that lead to rapid degradation in other aromatic amine reagents. In preclinical API synthesis—especially where late-stage functionalization takes place—these differences save significant time and raw material. The sulfur and nitrogen-rich ring in ABTD creates specific metal-ligand coordination patterns, which benefit certain catalyst syntheses that 4-aminobenzoic acid cannot support. These choices matter for managers tracking yield, safety, and waste disposal margins, and not just for academic curiosity.

    Supporting End-to-End Reliability

    From the early days, we noticed end-users often struggled with inconsistent grade materials. Even minor deviations—say, a small spike in water content or a blip in particle size—could throw off entire reaction sequences or disrupt process validation. This reality led us to bake routine wet-chemistry tests into our release requirements, not just relying on numbers from the analyzer. Rather than chasing lowest-cost throughput, we prioritize predictable reactivity and shelf-stability, even if it adds a step or two to scale-up. Our experience is that fixing downstream failure costs more than prevention at the synthesis stage.

    We continuously work on process upgrades too. For example, early batches years ago sometimes developed faint odors due to trace thiols; refining our purification strategy eliminated that problem. Such hands-on process improvements reflect ongoing collaboration with veterinarians in the field, who report odors as a compliance risk in animal drug manufacture. Between feedback loops with our lab and customer use-cases, we target real-world functional performance—not theoretical values.

    Pushing Boundaries in Application Development

    ABTD’s unique reactivity profile opens doors in multiple sectors. In pharmaceuticals, sulfonamide derivatives of ABTD feature in broad-spectrum antimicrobial research. The combination of amino functionality and the thiadiazole ring enables the development of new enzyme inhibitors and receptor modulators. Several university partnerships focus on derivatives of ABTD for anti-tumor and anti-inflammatory agents. Our material provides the backbone for their library synthesis, where purity and lot consistency become critical. Research groups often prefer our batches after testing less predictable alternatives, owing to consistent reaction outcomes and reproducibility in their assays.

    In agrochemical synthesis, the thiadiazole scaffold serves as a starting point for creating novel fungicides and pesticides. Agricultural researchers turn to ABTD when looking for sulfur and nitrogen donor effects that modulate biological activity. We see repeat demand due to the compound’s performance in field trials and pilot-plant production. Unlike other building blocks that break down under field-use stressors, ABTD derivatives maintain potency and resist photodegradation, improving shelf life and effectiveness in real-world conditions.

    Material scientists value ABTD’s role in developing advanced polymers and coatings. Its heteroaromatic ring introduces thermal and oxidative stability into specialty resins used for electronics and high-performance films. We work with chemical engineers to match ABTD lots to specific end-product requirements, verifying impurity profiles and stability via extended aging tests. End-users often share success stories—like improved shelf stability or enhanced electrical insulation properties—thanks in part to the core stability of ABTD within their product matrices.

    Reliable Supply and Practical Packaging

    Meeting customer timelines means more than just producing quality material—it requires reliable logistics and practical packaging. We pack ABTD in moisture-proof, chemical-resistant containers, ranging from laboratory-scale vials to drum quantities for pilot and full production. Our experience has shown that open contact with air or bulk packaging in standard plastic bags often introduces degradation or moisture uptake—easy pitfalls that plaque users of cheaper, repackaged thiadiazole. By using lined drums and nitrogen backfilling for bulk orders, we cut down oxidative risks and support long-term storage needs.

    Traceability and regulatory compliance run through every shipment. Each delivery comes with clear COA documentation, batch-specific impurity profiles, and SDS reports—removing guesswork for purchasing or health-safety teams. We retain batch samples for every shipment, supporting quality investigations or regulatory audits on demand. In our field, clear records and transparency mean no confusion when the inspector calls or a process engineer needs information about a six-month-old lot.

    Collaborative Problem-Solving and Technical Support

    The real value of a chemical manufacturer shows up when customers hit real-world roadblocks. Because we synthesize ABTD at commercial scale, our technical support goes far beyond generic advice. Over the years, we’ve helped research teams debug side reactions, recommended compatible solvent systems, and optimized addition rates to avoid precipitation or unwanted byproduct formation. This collaboration often leads to new ideas or tweaks that improve overall process efficiency and yield.

    For example, several labs reported inconsistent coupling results using ABTD from unnamed sources. After reviewing their procedures and analyzing their remnants, we traced the issue to isomeric and sulfoxide contaminants. Adjusting their purification steps and switching to cleaner ABTD from our line led to reproducible product formation, reduced wasted batch time, and better downstream analytics. Every process has its quirks, and we document customer solutions to build a knowledge base that informs improvements for others facing similar barriers.

    Supporting Sustainable Chemistry and Safety

    Safety and sustainability ring loudly in today’s chemical industry, especially with regulatory tightening in Europe, North America, and Asia. Safe scale-up of ABTD production starts with thoughtful solvent selection and containment, strict emissions controls, and closed handling where possible. Manufacturing progress comes through cutting hazardous waste and reducing worker exposure—goals we pursue not for compliance departments, but because we’ve seen the difference at the operational level.

    We continue to shift to cleaner solvents and have invested in recovery and recirculation systems, which limit waste and cut overall costs over time. Colleagues at regulatory bodies appreciate detailed hazard analysis and operational history, so we maintain up-to-date documentation for all handling and storage procedures. Safe use of ABTD in downstream facilities gets direct in-plant training, technical briefs, and real-world guidance—not just theory or paperwork.

    Putting It All Together: The Value of Experience

    Along the supply chain, ABTD’s value isn’t just in its molecular structure, but in the consistency and reliability our manufacturing brings. Researchers, process chemists, and product engineers depend on repeatable outcomes—whether they are tackling late-stage API synthesis or optimizing high-performance coatings for industrial electronics. We have seen that patience in refining batch protocols, active problem-solving in the face of unanticipated failures, and commitment to end-to-end documentation give our ABTD an advantage.

    We don’t claim every problem gets fixed overnight, but having lived through hundreds of production campaigns, pilot plant issues, and customer troubleshooting calls, we respond with on-the-ground knowledge and a view of the whole process from reaction vessel to final application. It’s this focus on practical experience—coupled with openness to innovation and willingness to revisit process design—that grounds our approach to manufacturing 4-Aminobenzo-2,1,3-thiadiazole.

    Looking Ahead

    As chemical applications continue to diversify, the need for reliable, well-characterized intermediates remains steady. 4-Aminobenzo-2,1,3-thiadiazole is evolving from a niche building block into a workhorse across life sciences, agritech, and advanced materials. We stay alert to feedback, track regulatory changes, and invest in process upgrades that help our customers move from proof-of-concept to pilot plant and full commercialization.

    Every new batch continues the cycle of improvement and partnership that defines our work as actual manufacturers. Our promise remains simple: consistent, traceable ABTD, made with care and supported with real-world experience. Together with our partners in research and industry, we’ll keep pushing what this remarkable compound can achieve—one batch at a time.