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

    • Product Name 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole
    • Alias ATFT
    • Einecs 629-576-9
    • 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

    766459

    Chemical Name 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole
    Cas Number 23629-24-9
    Molecular Formula C3H2F3N3S
    Molecular Weight 169.13 g/mol
    Appearance White to off-white powder
    Melting Point 92-94°C
    Solubility Moderately soluble in organic solvents (e.g. DMSO, methanol)
    Purity Typically ≥ 98%
    Smiles C1=NN=C(N1N)C(F)(F)F
    Inchi InChI=1S/C3H2F3N3S/c4-3(5,6)1-8-9-2(7)10-1/h(H2,7,8,9)
    Synonyms 5-(Trifluoromethyl)-1,3,4-thiadiazol-2-amine
    Storage Conditions Store at room temperature, keep container tightly closed
    Hazard Statements May cause skin/eye irritation

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

    Packing & Storage
    Packing Sealed amber glass bottle containing 10 grams of 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole, labeled with hazard, batch, and purity information.
    Shipping 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is transported according to standard chemical safety regulations, typically via ground or air, with appropriate hazard labeling. Ensure packaging prevents leaks or spills during transit and complies with all relevant chemical shipping guidelines.
    Storage 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Store at room temperature, protected from moisture and direct sunlight. Use appropriate personal protective equipment when handling, and clearly label storage containers to prevent accidental misuse.
    Application of 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole

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

    2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole delivers targeted value as an intermediate in key industrial sectors. Our direct manufacturing process ensures reliable quality and supports downstream integration across pharmaceuticals, agrochemicals, specialty dyes, and advanced material syntheses. Below, we detail its core application scenarios, focusing on unique requirements demanded by global formulation and regulatory standards.

    1. Pharmaceutical Active Ingredient Intermediate – Anticonvulsant Drug Synthesis

    Pharmaceutical manufacturers utilize 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole as a critical heterocyclic intermediate during the synthesis of select active pharmaceutical ingredients, including compounds with anticonvulsant activity. Its chemical structure enables precise introduction of a trifluoromethyl group, which is essential for tailoring drug binding and metabolic stability required in CNS therapies.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/EP/JP compendial testing (where applicable)
    • 21 CFR Part 211 (U.S. FDA Current Good Manufacturing Practice)

    Typical usage ratio

    • Varies from 0.15–0.45 molar equivalents per API batch, depending on target molecular scaffold and scale-up stage

    Downstream process integration

    • Enters as a condensation or cyclization reactant following initial core backbone construction, typically within intermediate steps preceding API finalization

    Final product types

    • Bulk pharmaceutical intermediates
    • Approved anticonvulsant and CNS drug substances (e.g. thiadiazole-based agents)
    • Regulatory-submitted API dossiers for small-molecule drugs

    2. Crop Protection Chemical Intermediate – Herbicide and Fungicide Synthesis

    Agrochemical formulators employ this thiadiazole derivative in the development of active pesticide ingredients, particularly those demanding fluorinated or nitrogen-rich aromatic rings. The compound’s nucleophilic amine and electron-withdrawing trifluoromethyl group contribute crucially to the mode of action in targeted crop protection products.

    Industry compliance standards

    • FAO/WHO: Specifications and Evaluation for Plant Protection Products (FAO/WHO Pesticide Specifications)
    • ISO 9001:2015 for process assurance in chemical synthesis
    • Agrochemical registration under REACH (EC No 1907/2006) and EPA FIFRA (U.S.)

    Typical usage ratio

    • Typically 0.1–0.6 mole per equivalent of active agrochemical core depending on the structural demands of the target molecule

    Downstream process integration

    • Introduced at the early substitution or ring formation phase to construct fluorinated thiadiazole motifs prior to functionalization and formulation

    Final product types

    • Active ingredients for registered herbicides and fungicides
    • Preformulated pesticide technical concentrates
    • Formulation-ready agrochemical intermediates for emulsion or suspension products

    3. Specialty Dye and Pigment Intermediate – Synthesis of Fluorinated Monoazo or Disazo Dyes

    Industrial colorant manufacturers integrate this compound into dye synthesis procedures, leveraging its ability to modulate color fastness and chemical resistance in textile and specialty coatings. Its presence within monoazo and disazo chromophore frameworks imparts enhanced solvent resistance and dye stability suitable for demanding textile applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 compliance for harmful substance screening
    • ISO 105:2010 series for textile color fastness
    • EN 71-3:2019 for heavy metal migration (applicable to toys and coated materials)

    Typical usage ratio

    • Ranged at 0.08–0.25 mole per mole of diazo or coupling component depending on shade depth and final dye structure

    Downstream process integration

    • Enters reaction sequence as the amine donor or heterocyclic building block preceding diazotization or coupling operations

    Final product types

    • Sulfonated and non-sulfonated fluorescent dyes for synthetic fibers
    • High-performance pigment dispersions for plastics and printing inks
    • Color-fast textile finishing agents

    4. Advanced Functional Materials – Synthesis of Specialty Polymers and Coatings

    Manufacturers serving the advanced materials sector utilize this thiadiazole compound as a monomer or functional additive for engineering high-performance fluorinated polymers and specialty coatings. Its unique scaffold provides opportunities for combining hydrophobicity, chemical resistance, and tailored electronic properties required in electronics, membranes, and automotive finishes.

    Industry compliance standards

    • ISO 9001:2015 certified quality management during polymer and coating production
    • RoHS 2011/65/EU compliance for electronics-related applications
    • REACH (EC No 1907/2006) for raw material registration and safety

    Typical usage ratio

    • Typically 0.5–2% by weight in polymer masterbatches or copolymer blends; levels are fine-tuned based on end-use property targets such as solvent resistance or dielectric constant

    Downstream process integration

    • Frequently incorporated during the pre-polymerization step or as a reactive co-monomer when synthesizing custom fluoropolymer resins

    Final product types

    • Fluorinated specialty coatings for electronics and industrial equipment
    • Advanced separation membranes
    • Custom performance polymers for automotive or aerospace.
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    Certification & Compliance
    More Introduction

    Introducing 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole: Field Experience and Practical Considerations

    Overview of the Compound

    2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole has become a steady workhorse in our lineup, reflecting changing demands from pharmaceutical research, agrochemical development, and fine chemical synthesis. The presence of a trifluoromethyl group and an amino function on the 1,3,4-thiadiazole ring creates unique chemical behavior not found in similar thiadiazoles. Chemists directly involved in optimization and scalability see everyday how its chemical scaffold supports versatility and targeted selectivity in molecular design.

    Model and Specifications

    Our standard offering of 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole comes authenticated by established quality testing, using high-performance liquid chromatography (HPLC) and NMR confirmation at every production batch. Samples hold true to a purity of no less than 98%, with a tightly controlled moisture profile. Long-term stability under standard storage conditions has supported reliable inventory management for our industrial partners. We have learned to anticipate scale-up requirements by adjusting grain size for efficient handling in automated processes.

    Current Demand from the Chemical Industry

    Feedback from both laboratory and pilot plant operations indicates that 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole continues to earn its place as a valued building block. Medicinal chemists lean on its electron-withdrawing trifluoromethyl presence to strengthen target interactions, playing a distinct role in the evolution of antibacterial, antifungal, and antiviral research. At the gram-to-kilogram scale, we have processed custom orders that required careful adjustment of crystallization protocols to support fine-milled or larger-particle product for diverse synthesis routes.

    Some customers operating at the intersection of agriculture and specialties have pointed to this compound’s functionality in the exploration of new herbicidal and fungicidal scaffolds. The amino group participates in direct coupling, simplifying downstream functionalization. As a team with years invested in custom synthesis, we found this double lever—trifluoromethyl for bioactivity, amino for reactivity—delivers results more readily than many halogenated thiadiazoles with less accessible positions or reduced solubility.

    Established Differences from Other Thiadiazoles

    Extensive in-plant evaluation and hundreds of technical interactions established important distinctions between 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole and other members of its chemical family. Adding the trifluoromethyl group at the 5-position increases lipophilicity and metabolic stability, both highly prized by modern drug and crop protection chemists. Compounds such as 2-Amino-1,3,4-Thiadiazole without the fluoroalkyl chain fail to deliver the same SAR (structure-activity relationship) insights across iterative analogue libraries. This effect is measurable in our clients’ hit-rates during early-stage screening and subsequent optimization for potency or selectivity.

    We observed, during pilot runs, that coupling reactions involving the amino group proceed with higher yields and cleaner profiles, compared to some 5-substituted alternatives featuring bulkier or less electron-withdrawing groups. This same structural motif supports coupling both by classical condensation and modern catalytic techniques, reflected in reliably high throughput both on small glassware and in jacketed reactors up to 200 kg.

    Supply Assurance, Quality, and Traceability

    End-users relying on downstream regulatory testing need full transparency along the production chain. In response to increased scrutiny over trace metal impurities and residual solvents, our plant management and QC labs now run each batch through a battery of checks for elemental analysis and GC-based residual solvent analysis. By storing representative retain samples, we provide our customers with historical batch data, simplifying their regulatory submission efforts while aligning with their DMF or REACH documentation.

    Problems with inconsistent supply or variable purity crop up when this compound is sourced via multi-layered distribution models. As a direct chemical manufacturer, we manage all steps, from raw materials to packaging. Our technical liaisons frequently provide impurity profiles to partners engaged in scale-sensitive applications, such as API intermediate synthesis or assay reproducibility studies.

    Practical Knowledge from Real-World Application

    Scaling research findings to production scale takes more than theoretical expertise. Each year’s cumulative run data shapes how we tweak process parameters to avoid common problems: excess polymorphic forms, filtration bottlenecks, reactivity shifts from subtle solvent effects. It took years of R&D to refine how the 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole crystallizes most cleanly, and to construct a washing procedure that removes residual process contaminants, delivering lots suitable for regulated pharmaceutical labs and large-scale screening facilities alike.

    Feedback has also pointed to the compound’s manageable toxicity compared to related heterocycles. Operators with direct handling experience report no special hazard concerns beyond standard ventilation and protective equipment, so long as SOPs specific to organic powders are followed. That makes integration into existing handling protocols straightforward for teams already working with aromatic heterocycles or low molecular weight intermediates.

    Research and Industry Collaboration

    Our credibility as a supplier stems from daily technical contact, collaborative R&D, and a shared understanding of timelines dictated by patent strategies or product development goals. We work with academic researchers to fine-tune material selection for structure-activity research and consulting scientists from global pharma to negotiate custom purity grades or alternate packing methods. Whether supporting EU registration of a new active or refreshing a US DMF, our contribution is based on up-to-date analytical data, direct plant oversight, and an insiders’ grasp of how synthesis choices ripple into formulation, stability, and regulatory acceptance.

    Case studies from joint product launches show where 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole outperformed simpler or more conventional heterocyclic scaffolds in providing novelty, patentability, or physical stability against hydrolysis. A well-documented project, involving lead optimization for a North American customer, saw our modified recrystallization route cut waste by 17% and increase time-on-reactor productivity—valuable lessons that brought additional insight for later custom batches.

    Physical Handling, Storage, and Long-Term Stability

    Not all chemical intermediates store with the same stability. Our direct experience—covering multiple seasons and shipping environments—has shown 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole to maintain color, assay, and performance in sealed, inert-atmosphere packaging. Sophisticated temperature cycling and shelf-life studies, performed annually, confirmed the absence of problematic hydrolysis or significant decomposition under our standard storage protocol. This aligns field performance closely with what formulation scientists see on paper.

    Bulk deliveries to process-oriented sites often call for larger, tamper-evident containers that prevent cross-contamination—a need most often raised with us by QC managers developing ISO-standard handling or traceability schemes. In practical terms, this means each mother drum comes with a certificate of analysis directly tied to lot numbers, simplifying site audits and process validation for our clients.

    Process Improvements and Customer-Driven Adjustments

    Every scale-up bears the fingerprints of customers’ evolving synthesis or formulation goals. Our technical team works alongside plant staff to review stirrer speed, solvent profiles, and temperature set-points, capturing process intelligence that benefits future batches. When late-stage purification challenges come up, we lean into real-time analytics and hands-on troubleshooting, blending classical synthetic training with practical constraints. The most useful process improvements—those that led to consistently high yields and lower utility costs—grew out of these exchanges, grounded in plant-floor realities.

    Sometimes the customer’s process brings surprising technical questions. For example, a run using alternative solvents flagged minor impurities previously below detection limits. By adapting our clean-up routine and consulting with the customer’s in-house chemists, we found a new filtration strategy that worked for both R&D and larger runs. Every technical adjustment, logged and shared, expands what we know collectively about this molecule’s practical handling.

    Understanding Regulatory and Safety Landscape

    Professional stewardship extends to full compliance with regional and global chemical regulations. Each product batch comes backed by regulatory documentation, supporting use in both discovery and lead-optimization without tripping over compliance hurdles. Conversations with QA supervisors, regulators, and tech transfer teams keep our interpretations aligned with changes in regulatory guidance, especially on topics like elemental impurities and cross-contamination prevention. In years past, regulatory complexity often delayed projects—now, solid documentation and hands-on QA have sped up qualification.

    Knowledge transfer goes beyond sending paper. We share practical advice on safe powder handling, translating lessons from the production plant to R&D floors. Information covers everything from recommended PPE and best storage conditions, to guidance on rapid resolution of product complaints or variance investigations. Building direct feedback channels reinforces safe use and keeps our technical support grounded in current realities—not just compliance, but proactive risk management.

    Applications Across Sectors

    Our customers’ projects touch every chemical sector where new molecular scaffolds push the frontier: life sciences, agrochemicals, electronic materials. In drug discovery, 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole serves as a starting material for advanced intermediates, introducing the trifluoromethyl-driven enhancements in metabolic profile and binding affinity. Chemical suppliers and custom synthesis partners favor this product for straightforward incorporation into multi-step sequences, where robust reactivity and minimal byproduct formation simplify downstream operations.

    In the crop science market, demand for novel pesticide backbones led to a measurable uptick in requests. Our experience with direct chlorination, N-amination, and Suzuki-type couplings using 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole as a core intermediate set a precedent for reliable delivery at the multi-kilo scale. Graduate students and postdocs in screening labs, for their part, value the material’s consistency, allowing their bioassay work to proceed unhampered by material variation.

    Continuous Learning and Future Potential

    No batch run gets produced in a vacuum; each reflects what the team has internalized from previous cycles. New specifications from the pharmaceutical sector in the past three years challenged us to raise purity targets and address narrower impurity windows. Scaling up for agricultural applications drove us to upgrade plant assets to handle larger volumes with stricter dust control—lessons we once treated as future possibilities, now everyday practice.

    The evolution of 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole as a platform chemical runs parallel with our own learning curve as chemical manufacturers. To support breakthroughs in molecular design, we invest in process analytics, predictive batch tracking, and customer co-development. Unforeseen synthesis difficulties, raw material fluctuations, and changing regulatory pressures push us to act with flexibility and technical honesty—qualities customers respect each day, and key to staying one step ahead in specialty chemical production.

    Facing Real-World Challenges and Building on Experience

    Problems on the plant floor rarely disappear with wishful thinking. One product shipment affected by an unexpected container breach led our packaging team to overhaul sealing protocols and invest in tamper-resistance for every pail and drum. Root-cause analysis forms part of how we approach quality; fielded product complaints or observed inconsistencies prompt deep dives into not just what occurred, but how process or design changes in future batches will prevent recurrence.

    Modern chemical manufacturing prioritizes cross-functional collaboration, not top-down mandates. It takes direct action and regular feedback loops with users to fine-tune guidance for safe use and adapt packaging or storage solutions. We field technical calls, write up use-cases, and coordinate process changes with partner sites overseas—drawing on years of practical know-how relayed through every step, from plant to bench to field trial.

    The lessons honed over years—a straightforward crystallization, an efficient filtration, or an improved impurity purge—end up reflected in the quality and consistency of 2-Amino-5-Trifluoromethyl-1,3,4-Thiadiazole that reaches our customers around the globe. Direct experience, hands-on trials, and long-term partnership guide what we offer now, providing real value to chemical researchers, formulators, and process engineers wherever agility and reliability are at a premium.