|
HS Code |
200954 |
| Productname | 4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide |
| Molecularformula | C13H8F3N3OS |
| Molecularweight | 311.29 |
| Appearance | Solid |
| Purity | ≥98% |
| Solubility | DMSO, Methanol (predicted) |
| Storagetemperature | 2-8°C |
| Smiles | C1=CC(=CC=C1C(=S)N)OC2=NC=C(C=C2)C(F)(F)F |
| Inchi | InChI=1S/C13H8F3N3OS/c14-13(15,16)10-5-3-9(17-7-10)21-12-4-1-2-8(6-12)11(20)18/h1-7H,(H2,18,20) |
| Canonicalsmiles | C1=CC(=CC=C1C(=S)N)OC2=NC=C(C=C2)C(F)(F)F |
As an accredited 4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, sealed cap, labeled with chemical name, CAS number, hazard pictograms, and storage instructions. |
| Shipping | The chemical `4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide` is shipped in secure, airtight containers compliant with safety and regulatory requirements. Packaging ensures protection from moisture, light, and contamination. Material safety data and labeling accompany the shipment. Transport follows all relevant local and international chemical handling and shipping regulations for hazardous materials if applicable. |
| Storage | 4-[5-(Trifluoromethyl)Pyrid-2-yloxy]thiobenzamide should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from sources of heat and ignition. Protect from direct sunlight, moisture, and incompatible substances such as strong oxidizers or acids. Store at room temperature, and ensure that proper chemical labeling and safety precautions are in place. |
Applications of 4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide in Industrial Manufacturing4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide is primarily utilized as an advanced intermediate in downstream sectors including agrochemical formulation, pharmaceuticals, specialty coatings, photographic chemicals, and fine chemical synthesis. Manufactured under stringent in-plant controls, our material meets precise industrial requirements and supports value-added production workflows at global scale. The following application scenarios outline exact integration points, regulatory frameworks, and downstream conversion processes for industrial users. 1. Herbicide Active Ingredient SynthesisThis compound functions as a crucial building block in the synthesis of targeted post-emergence herbicides for crop protection. Its structural features provide chemical stability during main route coupling reactions, enabling selective inhibition mechanisms in finished active ingredients. Producers incorporate this intermediate at critical stages of multi-step synthesis, guided by national and regional agrochemical safety regulations ensuring residue control in the food supply. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical API Intermediate ManufacturingThe thiobenzamide scaffold, with its trifluoromethyl-pyridyl group, is favored in the formation of advanced intermediates for new-generation anti-inflammatory and CNS-active pharmaceutical molecules. Contract manufacturers source this compound for late-stage functionalization or ring fusion steps, maintaining batch-to-batch consistency required for registration under global pharmacopoeias and cGMP validation audits. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Functional Coating Additives in Electronic MaterialsAs a specialty additive, this compound imparts increased chemical resistance and tailored surface energy in advanced electronic coatings. OEMs and coating formulators use it within dielectric topcoat recipes for printed circuit boards and precision devices, where purity and homogeneity impact downstream assembly yield and long-term reliability. Contribution to key electrical properties and moisture protection requires tight process controls and adherence to electronics industry safety protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Light-Sensitive Compound for Photographic Chemical FormulationsThe compound’s aromatic and trifluoromethyl-substituted core enables reliable photoreactivity in specialty photographic and imaging chemicals. Commercial photo-chemical formulators employ it for silver halide stabilization and to fine-tune spectral response in modern photolithographic processes. Integration requires compliance with environmental safety profiles and tight control of handling and residual levels in end products destined for professional and industrial imaging markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Fine Chemical Intermediate for Heterocyclic Compound SynthesisThis thiobenzamide derivative offers synthetic flexibility and high reactivity within specialized organic synthesis operations producing target heterocycles for research and specialty markets. Laboratories and custom synthesis workshops use it as a key precursor in the stepwise assembly of high-value scaffolds, where traceability and reagent purity underpin downstream application in discovery chemistry and analytical standards production. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Daily production and quality control in fine chemicals show us how subtle changes in molecular structure reshape outcomes in research and industrial applications. 4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide brings a unique chemical profile that leverages both the electron-withdrawing trifluoromethyl on the pyridyl ring and the reactivity of the thiobenzamide core. In countless conversations with experienced chemists and process engineers, the drive for targeted performance and process safety always brings the specificity of such molecules to the fore. Unlike off-the-shelf analogs, our synthesis focuses on delivering high purity and reliability batch after batch, reducing downstream purification costs and helping labs focus on what matters—adding value by moving a project forward, not repeating prep work.
The presence of a trifluoromethyl group alters polarity, metabolic stability, and interaction with biological targets. The oxygen bridge between the pyridine and thiobenzamide offers new binding possibilities. Chemists who specialize in medicinal and agrochemical synthesis have asked for compounds that offer both chemical stability in storage and reliable integration during reaction steps. More standard thiobenzamides or pyridyl derivatives can fall short—some break down under common coupling conditions, others leave problematic side-products. We see these problems in returned samples, in technical calls, and when scientists share notes about frustrating stalls in their own optimization runs.
We protect against these pitfalls by using controlled crystallization and precisely timed reagent addition during final synthesis. The extra rigor pays off in smoother downstream operations. Analytical feedback shows minimal byproducts and consistently tight purity ranges, often below 0.2% total impurity content, even on large scale. This translates as fewer analytical headaches and almost no batch-to-batch performance swings, which in turn supports teams working under pressured schedules.
Teams involved in new molecule discovery and intermediate design need robust building blocks. In the field, we’ve seen this compound find a dependable role in heterocycle elaboration, lead candidate refinement, and late-stage diversification. The chemistry behind the oxygen-linked pyridine is less prone to unplanned side reactions, especially when compared to structurally similar molecules with direct carbon-pyridine or thioether connections. The trifluoromethyl group improves chemical shielding, which we’ve observed produce better yields in fluorination and cross-coupling studies.
Feedback from development partners illuminates the pathway from bench to pilot scale. Reaction screens experiment with different nucleophiles and electrophiles, and the molecule resists hydrolytic decomposition in conditions that quickly degrade less sophisticated structures. The product’s stability under scalable reaction temperatures makes it fit for use not only in research-scale flask work but also in automated flow setups. End users rarely comment on solubility issues or filterability—our in-house drying protocol decreases residual solvent to negligible levels, easing downstream purification and analysis.
Quality is more than a headline statistic. The product’s specified purity opens doors for confident analytical work, high-yield transformations, and regulatory compliance in sensitive areas like pharmaceutical ingredient discovery. Internal standards from our QC team rely on multiple orthogonal methods including HPLC, NMR, and MS. Over years of production, we have noticed that small shifts in impurity profiles can introduce real unpredictability into follow-up chemistry, especially during scale-up or late-stage reactions.
By consistently controlling impurity levels and residual solvents, we take uncertainty out of the equation. Histories and batch logs connect directly to compliant process documentation, which supports our clients’ internal tracking and regulatory reports. Every client using this compound for GLP or regulatory-submission chemistry points back to this consistency as an asset for both commercial and research environments.
Substitution patterns govern reactivity and application success in specialty intermediates. Some alternative thiobenzamides swap out the CF3 group or use a different linkage position on the pyridine ring. In our experience, the 5-position trifluoromethyl substitution does more than make a subtle change—it shifts lipophilicity, metabolic pathway resistance, and improves coupling to a wider range of electrophiles. Our synthetic chemists constantly review new publications and patent filings, confirming that this substitution strategy keeps pace with evolving market needs.
Off-patent or resold intermediates often miss these performance touches. In process optimization sprints, the margin between a project that advances and one that stalls can hinge on small changes in solubility, decay rates, or ease of isolation. Customers who run comparative trials with other suppliers report fewer failures to complete reactions and higher reproducibility when using this particular intermediate. For teams under budget or time constraints, every percent higher yield—every hour gained by smoother workup—accumulates real value over a campaign.
Other vendors sometimes offer lower-cost pyridyl thiobenzamides missing the structural refinement or QC controls. During client site visits, spot analysis of competing lots frequently reveals inconsistent purity, trace metals, or a different counterion. These translate to troubleshooting, rework, or lost productivity. We’ve learned this lesson standing shoulder-to-shoulder with process chemists, watching as a supposedly routine step gets bogged down from batch to batch. Removing that frustration defines the value of our approach.
Every step in our production has grown from direct experience solving both expected and subtle process challenges. Sourcing starting materials with verified origins backs up traceability. Reactor charging sequences follow protocols that prioritize operator safety while minimizing the risk of cross-contamination—a lesson reinforced by earlier, less controlled runs that once forced costly recalls and added clean-up steps.
To avoid batch heterogeneity, we rely on calibrated feedback from in-line analytical monitoring—not just end-of-line checks. This trims reaction time and sharpens control over color and particulate formation in the product slurry. The first time we stepped to continuous production from manual batch work, tighter impurity containment became possible. This led not only to better product quality but also to increased sustainability by lowering waste and energy use.
Improved drying and storage protocols, adopted after some difficult freeze-thaw cycles in earlier years, now keep our inventory ready for prompt delivery. Time after time, customers confirm the lot they received lasts well during staged usage and doesn’t degrade after a container has been opened multiple times.
The chemicals sector can no longer treat safety and sustainability as afterthoughts. Active monitoring of waste minimization and emissions reductions has become a central pillar in our operations. By switching to greener solvents and reusing process water, we reduce both hazard and cost. In the specific context of 4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide, careful reagent selection cuts down on persistent byproducts that can challenge conventional waste streams.
Employee training keeps technicians attuned to potential hazards associated with fluorinated intermediates. Every new production cycle draws on technician feedback and incident reporting, supporting a cycle of genuine improvement. Our focus on process design—especially in handling and neutralization of thiol-containing intermediates—has enhanced both environmental responsibility and worker protection.
Tracking the product’s supply chain impact, from raw materials to packaging, pushes us to engage suppliers committed to similar standards. The resulting traceability allows our largest buyers, particularly those in regulated markets, to meet their own sustainability goals with substantiated reporting. Over the past two years, these efforts have saved significant energy, cut inadvertent release events, and shrunk our carbon footprint per kilogram delivered.
No process runs in a vacuum. Long-term partnerships with both academic and industry clients highlight common issues: moisture sensitivity, analyte degradation, and variable filtration rates have all appeared in customer feedback. Routine engagement with user teams led us to refine both crystalline form and particle size distribution. Early feedback, for example, identified problems with slumping and clumping when left on the bench in humid climates. In response, we altered post-drying handling and revised packaging design, which led to much happier downstream experiences.
It’s also not uncommon to see unexpected hot spots or color bleed during scale-up. Process analytical technology caught early signs of both issues in our own upscaling attempts. We responded by refining jacket temperature control and cleaning validation, securing batch uniformity through improved process automation.
Once or twice, customers encountered byproducts associated with batch aging. This led us to revise time management from reaction end-point to packaging—a move that cleared up issues and confirmed both short- and long-term stability under recommended storage.
Customer priorities have always shaped where we invest our energy. Client feedback flags not just what works but what frustrates teams on the ground—be it during method validation or late-phase pilot runs. The need for on-time shipment and batch documentation spurred us to invest in both logistics and traceability. Product support doesn’t end at delivery: repeated technical exchanges help unlock best practices for integrating this intermediate into varied chemistries.
We used to treat customer questions as troubleshooting. With time, experience taught us that many requests represent testable improvements. Tweaks in particle size, alternative solvent delivery, and batch-specific application notes have sprung from actual requests. Some teams ask about structural derivatives or ways to leverage observed reactivity in parallel discovery programs—this open channel shortens iteration time and deepens mutual trust.
Decades of shared process insight show us that practical knowledge, rooted in evidence and built up from repeated use cases, offers more value than any single spec sheet. That’s where discovery happens—in the lab, in the plant, and in direct technical exchange.
Chemical innovation never static; it relies on stepping stones built from reliable intermediates and teamwork between manufacturers and users. Delivering 4-[5-(Trifluoromethyl)Pyrid-2-Yloxy]Thiobenzamide at reliable purity and scale supports projects ranging from new pharmaceutical candidates to advanced agrochemical barriers. As partners refine their own research and process steps, the details we build into our production sharpen their edge in meeting tight project deadlines and ambitious discovery goals.
Teams involved in lead optimization and structure-activity relationship studies frequently need derivatives or analogs. Drawing on our own process development experience, we engage early on new structure requests, making use of modular synthesis pathways built around this molecule’s core. Investments in production flexibility, raw material sourcing, and technical onboarding deliver solutions that draw from both our portfolio and our continuous learning in scale-up chemistry.
In parallel, investment in digitized quality tracking and advanced analytics supports not just “what” gets delivered but “how”—accelerating response times and clearing the path for regulatory and client audits.
The story of this molecule in our production reflects broader truths about modern chemical manufacturing. Every gain in process efficiency, purity, or application success comes from direct engagement with challenging problems that real users face in application and scale-up. Stale process assumptions impede progress; our development pipeline improves by listening and adapting, not just by chasing lower cost or minimum compliance.
By putting genuine technical experience ahead of templated claims, we continue to meet complex client requirements, support forward-looking research, and provide products that shape the next generation of synthesis. In every interaction—from trouble-shooting a tricky coupling to consulting on analog design—our role as manufacturer and problem-solver sets the course for safer, smarter, and more sustainable chemistry.