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HS Code |
602883 |
| Productname | 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol |
| Casnumber | 123832-87-1 |
| Molecularformula | C3H3F3N4S |
| Molecularweight | 188.15 |
| Appearance | White to off-white powder |
| Meltingpoint | 177-180 °C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Storagecondition | Store at 2-8°C in a tightly closed container |
| Synonyms | 4-Amino-5-(trifluoromethyl)-1,2,4-triazole-3-thiol |
| Smiles | NC1=NN(C(=S)N1)C(F)(F)F |
| Inchikey | JXZKJXJHVYKMOQ-UHFFFAOYSA-N |
| Hazardstatements | May cause respiratory and skin irritation |
| Usage | Pharmaceutical intermediate |
As an accredited 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25g amber glass bottle with a tamper-evident cap, labeled for laboratory research use only. |
| Shipping | 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol is shipped in tightly sealed containers, protected from moisture and light. The package complies with all relevant chemical safety regulations. Appropriate hazard labeling and documentation are included. Shipping typically occurs via certified carriers specializing in chemical transport to ensure safe and compliant delivery. |
| Storage | Store **4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol** in a tightly sealed container, away from moisture and incompatible substances, such as strong oxidizers. Keep in a cool, dry, and well-ventilated area, protected from direct sunlight. Label the container clearly, and ensure compliance with relevant chemical safety regulations. Use appropriate personal protective equipment when handling this compound. |
Applications of 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol in Industrial ManufacturingProduced to rigorous standards, our 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol supports critical downstream industries where triazole derivatives play a key structural role. Below, we outline established application sectors, detailing how our material integrates into specific processes, with attention to compliance, formulation, workflow, and finished goods. 1. Agrochemical Active Ingredient SynthesisMajor crop protection manufacturers use this triazole derivative as a core intermediate for synthesizing advanced triazole fungicides. Production requires strict traceability of raw material purity to achieve reliable, targeted activity in final agro formulations. Its distinctive functional groups facilitate nucleophilic substitution and oxidative cyclization steps, with precise charge-transfer properties that support consistent batch yields. Downstream users closely manage blend ratios and ensure regulatory compliance at every development and registration stage. Industry compliance standards
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2. Pharmaceutical Intermediate for Heterocyclic Drug SynthesisInternational pharmaceutical companies employ this compound as a building block in the medicinal synthesis of selected triazole-class APIs, particularly antifungal agents and experimental oncology molecules. Material traceability and impurity profiling conform to pharmacopeial monographs and internal quality benchmarks. Precise dosing and controlled reaction conditions are essential, especially during high-pressure heterocyclic coupling and thiolation reactions, to minimize by-products and maximize API quality. Industry compliance standards
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3. Materials for Specialty Corrosion InhibitorsThis organic thiol triazole structure serves as a key precursor in the manufacture of industrial corrosion inhibitors used in closed-loop water treatment and oilfield applications. Downstream formulators leverage its electron-donating properties to tailor passivation films, increasing resistance to acidic and saline environments. Consistent in-feed ratios and comprehensive QC ensure repeatable anti-corrosion performance in final formulations. Industry compliance standards
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4. Electronic Chemicals: Anti-Static and ESD Protection MaterialsManufacturers in electrostatic discharge (ESD) sensitive sectors use this functional triazole-thiol in compounding specialty anti-static coatings. Its molecular structure ensures robust interaction with polymer matrices and conductive fillers, imparting controlled surface resistivity. Quality documentation and material lot traceability follow strict electronics industry norms to prevent circuit contamination and ensure device longevity. Industry compliance standards
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5. Fine Chemical Synthesis for Dye and Pigment IntermediatesProducers of selectively functionalized dyes incorporate this compound in specialized heterocyclic pigment synthesis. Its reactivity enables unique colorant structures for high-value industrial or analytical applications. Formulation specialists rely on high-purity material for efficient dye-coupling reactions, monitored under strict batch control and industrial hygiene protocols. Industry compliance standards
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Working directly in chemical synthesis for decades teaches us which molecules carry their weight during real-world formulation. One that consistently delivers on performance is 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol. Chemists recognize this compound as more than just a catalog number. Each batch we manufacture presents an opportunity to watch theory meet application—its crystalline powder, distinctive odor, and fast dissolution remind us that thoughtful process matters as much as molecular structure.
To produce this intermediate with consistent quality, we analyze raw materials and closely control reaction parameters through every step: temperature, stirring speed, pH adjustment, solvent choice, and isolation conditions. During QC, we rely on HPLC, NMR, and elemental analysis to ensure purity meets internal benchmarks—not just published industry standards. Some customers become accustomed to seeing near-spectroscopic purity and raise questions if a fresh batch differs from what they remember. This attention to detail isn’t an accident; it’s the only way to avoid headaches further down the supply chain.
We have seen 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol find a secure place in heterocycle chemistry due to the unique interaction between the trifluoromethyl group and the thiol functionality. In agrochemical research, the drive to improve safety and selectivity has brought more attention to building blocks bearing fluorinated groups. Electronics manufacturers, as well, have grown increasingly interested in the triazole core—especially in high-performance polymers and specialty coatings.
The difference compared to more basic triazole derivatives hinges on how the trifluoromethyl group interacts with key enzymes or polymer matrices, offering improved binding strength or enhanced chemical resistance. The thiol moiety allows for diverse downstream modification, which makes this compound a keystone for libraries of analogs. More basic triazoles can lack this flexibility, which shows up when customers seek site-selective sulfur incorporation or want to control electron density along the molecule.
Over the past decade, requests for 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol have shifted from small R&D orders to larger, scale-up batches. We have watched pharmaceutical teams use it to test metabolic stability in fluorinated moieties and leverage it as a substrate for kinase inhibitor exploration. We see biocidal product developers pursuing its triazole ring in the hunt for novel antifungal scaffolds—a move supported by increasing regulatory scrutiny of legacy actives. Those differences between what used to be sufficient, such as simple thiones or methyl analogs, and the current push for targeted design highlight why demand has steadily shifted in its direction.
Process chemistry teams sometimes call our technical support directly, describing incompatibilities with older triazole sources or bottlenecks when using standard aminothiols, especially when trying to scale up multistep synthesis. One regular inquiry involves the management of trace elemental sulfur or side-product formation during coupling. Over time, we’ve responded with refinements in the workup and washing protocols, not simply due to regulatory compliance, but due to recurring feedback describing how side-impurities impact crystallization downstream. Each time we solve a problem upstream, it saves time for our customers when it counts.
Lessons in handling specialty intermediates are written in the margins of lab notebooks, not just in material safety data sheets. From repeated experience, storing this triazole under dry, cool conditions—using tight-seal containers kept away from mineral acids and oxidizers—prevents slow degradation and maintains reactivity. Product managers working in scale-up appreciate seeing stable shelf life because missed expiration dates shut down entire campaigns.
Older packaging solutions occasionally brought up clumping or discoloration issues over long storage. We addressed these risks by adopting upgraded liners and moving to smaller, batch-packed bottles at customer request. Once, we experimented with vacuum-packing small samples, but after reports of static buildup in dry environments, opted for antistatic, opaque containers that maintain potency without attracting airborne dust. This level of regular modification defines our approach: adapt, note the consequences, and share feedback with those that depend on predictable results.
In practice, sulfur-bearing triazoles open doors for functional group transformation that a standard triazole seldom allows. For example, synthetic routes toward thioethers, disulfides, or sulfonic acids benefit from a thiol group’s uneven electron distribution. We’ve helped more than a few colleagues recover stalled routes by highlighting this difference. Several process chemists have been surprised at how quickly 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol engages in selective S-alkylation, providing rapid access to libraries unmanageable via less nucleophilic triazole variants.
Electronic component manufacturers push our product to its limits by introducing it into polymer networks where low dielectric constants and robust fluorine-carbon bonds matter. The trifluoromethyl group not only strengthens chemical stability but also allows for subtle tuning of surface energy in coatings. Customers have demonstrated improved resistance in harsh chemical environments compared to structures lacking the -CF3 motif. A non-fluorinated triazole simply does not match up in these endurance and performance studies.
It’s no secret that regulatory requirements drive much of chemical synthesis today. In regions with tighter environmental controls, we face more questions about route selection and solvent fate than in years past. Consistent traceability from lab records and batch certificates assures users they’re getting more than a drum of powder—they’re getting transparency. A plant manager from Eastern Europe once told us a minor labeling change saved three days at customs; details like those shape every version of our packaging and labeling today.
We see a steady increase in demand for low-residue, high-purity triazole batches in pharmaceutical use. Not all grades on the market meet this level, and switching between lower and higher grades impacts performance, especially during registration trials. It means more documentation and, sometimes, more supply chain audits. Rather than treat this as a burden, we involve customers early in any process changes, offering freshly generated analytical reports and retaining reference samples for unexpected revalidation needs.
By listening to procurement specialists, we know site-specific documentation matters just as much as the powder itself. What gets flagged in European REACH requirements differs from what state-level regulators in North America scrutinize. Regional nuances shape lot acceptance; missing a minor point can cause shipment rejection. By anticipating requests for residual solvent data, heavy metal content, and proof of absence of controlled substances, we keep projects moving for teams that can’t afford regulatory delays.
Moving from pilot to production scale surfaces new obstacles no literature review can truly predict. One memory stands out: scaling the synthesis of 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol from kilo-lab vessels into multi-ton reactors for a customer pipeline that had leapfrogged from gram screens to hundreds of kilograms in two procurement cycles. The scale-up team noted increased heat release and thicker slurries than anticipated, risking localized overreaction. Our plant’s engineering crew responded not with theoretical advice but changes to agitator speed and refined cooling set points, then monitored batch exotherms in real time.
Off-odors from batch-to-batch were traced to trace moisture shifts introduced by a new bulk solvent shipment. After repeated small test runs, the QC team implemented Karl Fischer titration during raw material intake, eliminating product variability and closing the door on future complaints. Large campaigns run through multiple tray driers improved drying uniformity, thanks to time invested in mapping powder flow and setting staged charge rates. Details like reactor geometry and the order of addition are scribbled in plant logs but become lasting process solutions that every batch benefits from down the line.
In specialty chemicals, reputation comes not from certificates on paper, but from batches that work every time. Years ago, customers switching suppliers would call to ask why yields dropped or why TLC profiles changed. By working through these troubleshooting sessions, we learned the hard lessons of lot-to-lot inconsistency—not just purity on paper, but particle size distribution, color, and minor solvation effects. Reliability arrived from tracking every process variable and learning to expect outliers, not disregarding them.
Through many campaigns, we found that certain reactor materials influence impurity carryover and that careful selection of cleaning protocols ahead of high-purity runs prevents cross-contamination. There is a reason we never rush reactor turnaround or skip a step in the cleaning checklist. Some of our most loyal customers started as skeptics, frustrated with inconsistent performance, only to return for the lack of last-minute surprises.
What ultimately secures this compound’s place in modern synthesis comes down to the combination of its trifluoromethyl group and reactive thiol. Standard triazoles without this dual substitution lack versatility in coupling and provide less robust chemical footprints in harsh conditions. In more than one customer’s hands, the difluoro or unsubstituted triazoles failed to deliver in complex, multi-step sequences or required additional protection/deprotection chemistry that slows down the whole project.
Batch after batch, the quality of our 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol supports customers chasing advanced performance, from novel agro-molecule development to antifouling surfaces. Its unique profile in nucleophilic aromatic substitution and crosslinking applications opens doors that common aminotriazoles cannot, while the enhanced hydrophobicity imparts properties crucial for high-durability coatings and polymers. These facts are not theoretical—they show up in customer returns and the technical problems solved by reliable material, made to consistent specs, from a source with a production record stretching back more than a decade.
Having fielded countless technical support calls, we’ve grown attuned to the research realities behind every request. Requests for custom packaging, unusual certificates, or small-batch runs for pilot plants do not appear on product datasheets, but responding promptly makes or breaks project timelines. Process chemists and R&D managers regularly share results from new transformations or observations about stability. Every such piece of feedback makes its way to our process improvement pipeline.
We regularly facilitate direct technical exchanges between our own process chemists and end-users. In one memorable case, a university research team encountered insoluble particulates after a protocol change; after analyzing their NMR spectra and revisiting the workup steps, we isolated the cause and provided a specific purification hint that restored yield and allowed project milestones to be met. These experiences emphasize the non-linear nature of R&D, pushing us to document more and avoid cutting corners in future runs.
Some of our earliest partnerships started with small experimental lots and grew into multi-ton per year regular orders. The needs or specifications can shift—sometimes driven by regulatory changes, sometimes by downstream customer requests or new analytical standards. We make a point of inviting iterative feedback, treating every scaled-up batch as a new opportunity for joint development rather than repeating a fixed protocol simply because it once worked.
We witness ongoing momentum in demand for heterocyclic intermediates bearing both fluorinated and sulfur-containing groups, driven by ongoing drug discovery, electronics miniaturization, and new regulatory requirements. As synthetic chemistry pushes for higher selectivity and fewer steps, intermediates like 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol give downstream teams the flexibility to rapidly test new ideas without major process overhauls. Versatility matters when submission deadlines are tight and project directions can pivot with the latest bioassay or pilot plant result.
In our production facility, we integrate both established batch processes and newer, continuous-flow platforms for increased responsiveness. In times of sourcing strain due to global events or logistics delays, these investments keep material ready for shipment with shorter lead times. End users appreciate the reassurance that process knowledge is more than “locked in a black box”—it’s a shared resource grounded in years of plant-floor adaptation, real technical troubleshooting, and unfiltered feedback from over a decade of collaboration.
Sustainability is another driver we cannot ignore. Every year, we field more questions about solvent management, waste reduction, and lifecycle analysis for specialty intermediates. We draw on practical experience to reduce resource use in drying, minimize batch rework, and reclaim process solvents wherever critical quality attributes are not compromised. Any progress in greener process integration must line up with the reality that customers still expect consistent performance and regulatory assurance at scale.
Experience at the bench and in the plant shows that successful delivery of 4-Amino-5-Trifluoromethyl-4H-1,2,4-Triazole-3-Thiol demands more than technical knowledge—it requires the humility to learn from feedback, adapt processes, and build quality into every step. Over the years, we’ve witnessed almost every kind of project: rushed scale-ups, sudden regulatory reviews, troubleshooting with international partners, and even unexpected wins as teams achieve breakthroughs with the same materials they nearly gave up on. What stands out across these stories is the trust built by being present, solving problems as they come, and never treating a batch as “just another shipment.”
Whether the need comes from advanced material development, breakthrough pharmaceuticals, or highly specialized surface treatments, this triazole intermediate backs up theory with everyday production that stands up to scrutiny—and helps more of our customers translate bold concepts into real, tangible results.