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5-Amino-1,3,4-Thiadiazole-2-Thiol

    • Product Name 5-Amino-1,3,4-Thiadiazole-2-Thiol
    • Alias 5-AT
    • Einecs 242-047-3
    • 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

    343044

    Product Name 5-Amino-1,3,4-Thiadiazole-2-Thiol
    Cas Number 15893-52-4
    Molecular Formula C2H3N3S2
    Molecular Weight 133.19 g/mol
    Appearance Light yellow to yellow crystalline powder
    Melting Point 187-189°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Boiling Point Decomposes before boiling
    Storage Conditions Store in a cool, dry place away from light
    Synonyms 2-Mercapto-5-amino-1,3,4-thiadiazole
    Smiles NC1=NN=C(S1)S
    Inchi Key VQIOQOGLMQDLSF-UHFFFAOYSA-N
    Usage Intermediate for pharmaceuticals and agrochemicals

    As an accredited 5-Amino-1,3,4-Thiadiazole-2-Thiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with secure screw cap, labeled “5-Amino-1,3,4-Thiadiazole-2-Thiol” and hazard symbols displayed.
    Shipping **Shipping Description for 5-Amino-1,3,4-Thiadiazole-2-Thiol:** This chemical is typically shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be classified and handled as a laboratory chemical, compliant with applicable regulations, including labeling and documentation. Transport must ensure secure packaging to prevent spills, contamination, or accidental exposure during transit.
    Storage Store **5-Amino-1,3,4-thiadiazole-2-thiol** in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight and moisture. Keep it separate from oxidizing agents and strong acids. Handle under inert atmosphere if necessary to prevent degradation. Label properly and use appropriate precautions to prevent inhalation, ingestion, or contact with skin and eyes.
    Application of 5-Amino-1,3,4-Thiadiazole-2-Thiol

    Applications of 5-Amino-1,3,4-Thiadiazole-2-Thiol in Industrial Manufacturing

    5-Amino-1,3,4-Thiadiazole-2-Thiol serves as a specialty intermediate with established roles across industrial sectors such as pharmaceuticals, agrochemicals, dyestuffs, and corrosion inhibition. As a primary manufacturer, we focus on sector-specific integration of this compound, supporting customers with technical process know-how and regulatory-compliant raw materials. Below are the main industrial scenarios in which our material enables differentiated downstream production.

    1. Pharmaceutical Synthesis of Heterocyclic Intermediates

    Pharmaceutical ingredient manufacturers adopt 5-Amino-1,3,4-Thiadiazole-2-Thiol as a key heterocyclic building block when developing advanced intermediates for APIs such as thiosemicarbazones, cephalosporin derivatives, and other bioactive molecules requiring sulfur-nitrogen moieties. Material introduction typically occurs in the ring closure or substitution step, where strict control of impurity profiles and traceability is mandatory. Usage rates depend on the stoichiometric requirements of the targeted active intermediate, with special handling protocols to comply with GMP documentation and change control. Batch-specific specifications support audit trails, ensuring compatibility with regulated market filings.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • Ph. Eur., USP, JP monographs (for relevant intermediates)
    • EDQM/EMA guidelines regarding process impurities
    • FDA 21 CFR Part 211 (where US market entry is required)

    Typical usage ratio

    • 0.5–1.2 molar equivalents per target intermediate, adjusted according to reaction stoichiometry and impurity clearance after process optimization

    Downstream process integration

    • Direct charge to reactor during early-stage heterocycle formation or thiol functionalization of pharmaceutical intermediates
    • Strict in-process controls for residual solvents and elemental impurities

    Final product types

    • Beta-lactam antibiotics intermediates
    • Thiadiazole-containing antifungal actives
    • Thiourea derivatives for diagnostic agents
    • API intermediates for research and generic scale-up

    2. Agrochemical Active Ingredient Precursor

    In pesticide and fungicide manufacturing, the compound acts as a primary raw material to generate sulfur- and nitrogen-enriched scaffolds essential for bioactivity in modern crop protection chemistry. Toll formulating sites feed it in at the condensation or cyclization step, paying close attention to impurity stripping and conversion rates because downstream regulatory dossiers specify threshold levels of process-related impurities. Dosing rates get fine-tuned during field validation and stability assessment, reflecting the need for consistent batch performance and compliance with agricultural chemical directives.

    Industry compliance standards

    • FAO/WHO specification guidelines for technical raw materials
    • REACH registration (EU)
    • China National Standard GB (e.g., GB 2763 for max residue levels)
    • ISO 9001:2015 quality systems for manufacturing

    Typical usage ratio

    • 2–4% w/w relative to total batch mass in active ingredient synthesis, adjusted after small-scale versus pilot scalability trials

    Downstream process integration

    • Incorporated at the initial formation of N-S heterocyclic nuclei for sulfonylurea and triazole compound classes
    • Pre-crystallization purification to minimize process contaminants

    Final product types

    • Herbicide and fungicide technical concentrates (e.g., triazole fungicides)
    • Seed treatment actives containing thiadiazole motifs
    • Agrochemical intermediates for further derivatization

    3. Synthesis of Corrosion Inhibitors for Industrial Water Treatment

    Formulators in the industrial water treatment sector use this material as a core building block in synthesizing organic corrosion inhibitors, especially in settings such as boiler water systems, closed-loop cooling circuits, and oilfield injection fluids. The thiol and amino functionalities enable targeted chemical grafting onto inhibitor backbones via condensation or substitution reactions. Usage concentration depends on metal exposure, system size, and performance testing during inhibitor formulation. Regulatory audits require precise input records and substance tracking to meet regional water safety and discharge standards.

    Industry compliance standards

    • ANSI/AWWA B600 (for materials in water systems)
    • OECD guidelines for water treatment product environmental impact
    • EU Biocidal Products Regulation (BPR)
    • ISO 14001 environmental management systems

    Typical usage ratio

    • 1–6% by weight within total inhibitor matrix, adjusted according to target system metallurgy and inhibitor lifetime

    Downstream process integration

    • Functionalization during blending of multicomponent corrosion inhibitor packages for large-scale cooling and boiler circuits
    • Tested post-synthesis in bench-scale corrosion coupons

    Final product types

    • Customized organic corrosion inhibitor additives for power plants
    • Oilfield brine treatment chemicals
    • Multi-metal protection blends for industrial circulating water

    4. Synthesis of Dyes and Pigment Intermediates

    Dye and pigment manufacturers rely on this compound’s electron-rich heterocyclic ring to introduce sulfur and nitrogen atoms into azo, monoazo, and other complex dye precursors. Material addition occurs during diazotization, coupling, or direct arylation processes, where color shade, purity, and light fastness properties depend on both the synthetic route and precise input quality. Usage ratios reflect color depth and formulation solids requirements, and strict compliance documentation is maintained to respond quickly to textile, plastic, and ink sector audit requests.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substance content (textiles)
    • ISO 9001:2015 for pigment and dyestuff manufacturing
    • EU REACH (Annex XVII, restricted dyes list)
    • FDA 21 CFR Parts 74 & 82 (for colorants in food-contact plastics, US market)

    Typical usage ratio

    • 0.8–3% by weight relative to co-reactive amines or phenols, optimized by desired hue and strength in industrial pigment/dye synthesis

    Downstream process integration

    • Batch addition during diazotization or subsequent aryl coupling reactions in dye/pigment formulation
    • In-process purification for shade and clarity control

    Final product types

    • High-performance azo dyes for textile printing
    • Monoazo pigment dispersions for inks and plastics
    • Custom dyestuff intermediates for specialty colorants
    Free Quote

    Competitive 5-Amino-1,3,4-Thiadiazole-2-Thiol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    5-Amino-1,3,4-Thiadiazole-2-Thiol: A Chemical Manufacturer’s Perspective

    Introduction to 5-Amino-1,3,4-Thiadiazole-2-Thiol

    Every chemist remembers the first time they opened a drum of 5-Amino-1,3,4-Thiadiazole-2-Thiol. We manufacture this compound with a focus on purity, minimizing batch variation and unwanted byproducts at each stage. This chemical, model ATD-98, comes to us as a free-flowing crystalline powder, off-white and immediately recognizable by its slightly sulfurous scent when handled in bulk. We regularly verify its molecular weight and melting range—crucial benchmarks for both in-house quality checks and customer trust.

    Model and Specifications

    Our plant produces 5-Amino-1,3,4-Thiadiazole-2-Thiol under the model designation ATD-98. The primary control is keeping impurity levels below 0.5%, which means running multiple purification steps and careful drying under vacuum conditions to prevent any hydrolysis or degradation. The material’s main specification, C2H3N3S2, aligns with our high-precision elemental analysis. We test each lot for precise melting point (206°C–208°C) and assay values (typically above 99%) so that clients can use it directly in synthesis without extra purification. As any experienced manufacturer will tell you, reaching these targets involves more than polished marketing language—it’s a question of keeping every step controlled.

    Why This Compound Matters

    A practical discussion of 5-Amino-1,3,4-Thiadiazole-2-Thiol always circles back to one fact: its direct role as a building block in pharmaceutical and agrochemical synthesis. In our labs, chemists rely on it for thiosemicarbazide replacements, or as a precursor to more complex substituted thiadiazole derivatives. Pure, reliable input chemicals keep syntheses reproducible, yields predictable, and side reactions minimal. We’ve seen production lines come to a halt just from a slight change in starting material color or melting point—painful evidence that a 98% assay isn't always enough when the rest is unknown trace contaminants.

    Our teams have watched demand for this compound shift as research on thiadiazole rings uncovers fresh antibacterial, antifungal, and anticancer applications. We field questions from large-scale pharmaceutical organizations and custom synthesis houses alike, each hoping to avoid paperwork headaches or supply chain problems. Imagine a research group waiting on one missing barrel to begin a months-long molecule screening campaign - our role in delivering what they need becomes personal, especially knowing the downstream consequences.

    Handling and Usage Insights

    Handling this chemical means paying attention to moisture sensitivity and compatibility with synthesis solvents. Our wealth of experience confirms it dissolves readily in DMF and DMSO, but resists solubility in water and common nonpolar solvents. Unlike more sensitive organosulfur compounds, it stores well under nitrogen and ambient room temperature, as long as exposure to direct sunlight or moisture remains minimal. In reality, a batch left open in a humid storeroom quickly forms lumps, which dissolve the advantage of precision feeding in automated reactors.

    Downstream customers typically use 5-Amino-1,3,4-Thiadiazole-2-Thiol in multiple steps: as a nucleophile in condensation reactions, as a sulfur source in ring-building, or for direct coupling with acyl halides and heterocyclic intermediates. The strong nucleophilicity of the amino group, paired with thione’s distinctive reactivity, opens up a wide menu of functionalization strategies. We’ve followed our product into the heart of patent filings and academic projects, each novel pathway adding to its deepening value.

    Comparisons With Similar Products

    Having worked hands-on with thiadiazole analogs, we see how 5-Amino-1,3,4-Thiadiazole-2-Thiol differentiates itself from its closest relatives. 2-Amino-1,3,4-thiadiazole, for instance, lacks the key thiol function that makes our compound a valuable linchpin for metal ion chelation studies or sulfur-crosslinking reactions. Unlike 5-methyl or 2-alkyl derivatives, our molecule steers clear of steric hindrance challenges and accompanies a cleaner, more predictable reaction profile in most coupling steps.

    In pharmaceutical and agricultural spheres, it outpaces other ring systems for ease of further modification. For every chemist who has scrapped project ideas over cost or purity issues with obscure intermediates, we see steady satisfaction when they return to this workhorse. Cheap, reliable, and straightforward to scale—all possible when a manufacturer invests in synthesis routes that deliver a clean, single-phase product. Most of our long-term clients comment on this stability: once a synthetic process switches to our ATD-98, troubleshooting yields or impurity-drift episodes almost vanish from their notebook records.

    Quality and Traceability

    Our materials science team never takes shortcuts with traceability. Each drum carries a batch number etched into its side. We keep spectrographic data, elemental analysis, and impurity profiles accessible on request because problems can begin with just a stray half-percent contaminant. With regulations tightening year after year, traceability means less downtime for our clients, who sometimes face regulatory scrutiny or unexpected audits mid-project.

    Internally, our labs perform repeated HPLC assays and moisture checks across the production cycle. Storage and transport use double-sealed liners, and we monitor all shipments for temperature and humidity exposure. These measures grow from years seeing what works and what exposes flaws as soon as someone in the field opens an overdue container.

    Real-World Challenges and Solutions

    On the production line, making 5-Amino-1,3,4-Thiadiazole-2-Thiol seems straightforward on paper. The truth looks different under the hood. Sulfur sources vary batch-to-batch. Each brings unique odors and secondary products unless you use controlled lots and iron-clad inventory discipline. Skipping vacuum drying can cause oxides or bound water to creep above 0.5%, which wreaks havoc downstream in diazotization or alkylation steps. We've lost whole runs to minor contamination—wasting time, raw materials, and crew effort.

    Solving these headaches means sticking to in-line monitoring for each stage: starting materials, processing temperatures, drying curves, finished product. We also calibrate detection methods every week. Working closely with our analytical chemists, we find potential issues before the drying stage, not after shipping faulty lots. Solvent recycling and careful waste capture prevent any carryover that could sully subsequent syntheses.

    Sometimes, customers order bis-molecular blends or demand oversight in reaction scale-up. In these cases, our technical teams sit with their chemists, comparing notes, swapping real-world stories. We adapt process parameters, improve filtration setups, or suggest slight temperature shifts during coupling—drawn straight from our own bench trials, not just from literature values or isolated academic studies.

    Few people outside the plant floor realize how handling conditions in one season, or how starting material shifts from a new upstream supplier, can ripple out as subtle artifacts in the final product. Our ongoing raw material audits and cooperation with vetted suppliers form the backbone of product consistency.

    Environmental and Safety Considerations

    The chemistry world keeps a sharp eye on environmental performance. Our output of 5-Amino-1,3,4-Thiadiazole-2-Thiol adheres to local and global legislation, not out of obligation but from internal risk controls. Byproducts get neutralized; effluent streams get filtered and tested before discharge. Workers wear the proper gear, and we schedule exposure monitoring for anyone handling open containers for extended periods. Training runs monthly with direct feedback from previous incidents—every inch of spilled product or excess dust triggers a process review and staff discussion.

    Transport uses certified sealed packaging. Trucks go out with manifests double-checked by our safety team. Once, a valve flaw caused minor powder loss during a cross-country shipment—we revised our drum clamp process and added chemical tracers to match each batch precisely.

    Customer Feedback and Ongoing Improvements

    Customer voices shape a large part of how we refine both production and delivery. One pharmaceutical researcher pointed out slight changes in color and flow properties over a six-month stretch, helping us revise our crystallization step. Another organization, using our compound for agricultural fungicide R&D, noticed minor clumping from late-season humidity; their input led us to reinforce our desiccant packing and develop revised humidity tagging for sensitive drum lots.

    More clients now demand digital certificates and advanced impurity panels—far beyond the basic COA—so our analysis suite has grown to meet these requests, adding full LC-MS and FTIR capabilities. Dialogue with end users often leads us to fresh improvements, like container-sizing options, split shipment scheduling, or rebalancing our inventory in response to new research trends.

    The Road Ahead for Thiadiazole Chemistry

    The chemical industry adapts constantly, and so do our strategies for producing reliable intermediates. Areas like targeted pharmaceuticals, advanced agrochemicals, even material science coatings now draw on 5-Amino-1,3,4-Thiadiazole-2-Thiol as a versatile platform. Our R&D division reviews new literature monthly, examining published applications and refining synthesis to minimize waste and maximize batch reproducibility.

    Research institutes and companies bring us practical challenges: requests for higher purity, alternate packaging, or direct shipment to global trial sites. Each new requirement prompts us to revisit process workflow and raw material selection, always through the lens of field results. Our role as a manufacturer stays focused on bridging lab-scale insights with robust, large-batch production—and remaining open to meaningful change when quality or safety demand it.

    Closing Insights—Trust Tempered by Experience

    Sourcing and producing 5-Amino-1,3,4-Thiadiazole-2-Thiol never sits on autopilot. We’ve learned from every hours-long analytical run, every operator shift, and every post-mortem on a failed batch. Whether the client focuses on a high-value pharmaceutical or a gram-scale custom synthesis, reliability and transparency guarantee continued trust. Differences in quality and consistency always trace back to the factory—the best results come when manufacturing adapts with each new challenge, never simply relying on the way things have always been done.

    We never lose sight of the bigger picture: the compound may be an intermediate, but its role compounds through whole chains of value, from bench-top breakthroughs to final formulations that touch people and industries worldwide. That responsibility drives us to sharpen every part of our process, to keep learning, and to continue delivering what researchers and producers actually need, not just what fits a catalog description. Every batch tells a story, and for us, each one is a fresh chance to reaffirm our role not as generic suppliers, but as committed partners in every step of chemical innovation.