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HS Code |
200519 |
| Chemical Name | 3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole |
| Molecular Formula | C10H6ClF3N2O |
| Molar Mass | 262.62 g/mol |
| Cas Number | 105642-04-4 |
| Appearance | White to off-white solid |
| Solubility | Soluble in organic solvents (e.g., DMSO, DMF) |
| Smiles | C1=CC(=CC(=C1)C(F)(F)F)C2=NC(=NO2)CCl |
| Inchi | InChI=1S/C10H6ClF3N2O/c11-5-9-15-14-8(17-9)6-2-1-3-7(4-6)10(12,13)16/h1-4H,5H2 |
| Storage Conditions | Store in a cool, dry place and keep container tightly closed |
| Purity | Typically ≥98% (as specified by suppliers) |
| Hazard Classification | Handle with care; may cause irritation |
| Uses | Intermediate in organic synthesis and pharmaceuticals |
As an accredited 3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole is supplied in a sealed amber glass bottle with hazard labeling. |
| Shipping | **Shipping Description:** 3-Chloromethyl-5-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazole is shipped in sealed, chemically compatible containers under cool, dry conditions. Transport is in compliance with international chemical safety regulations. Proper labeling and documentation ensure safe handling and storage. Special precautions are taken to avoid moisture, excessive heat, and physical damage during transit. |
| Storage | **3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole** should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated place. Avoid sources of ignition and incompatible substances such as strong oxidizing agents. Properly label the storage area and ensure chemical spill containment measures are in place. Use secondary containment to minimize accidental releases. |
Applications of 3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole in Industrial ManufacturingAs the direct manufacturer of 3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole, we supply this advanced intermediate for critical applications in regulated industrial processes. The following real downstream sectors integrate this material for high-value production, each adhering to strict industry and quality standards. 1. Active Pharmaceutical Ingredient (API) Synthesis – Antimicrobial AgentsThis compound is incorporated as a key intermediate in the synthesis of modern antimicrobial APIs. It enables selective oxadiazole ring formation and aromatic trifluoromethyl functionalization in process chemistry. Manufacturers use precise charge-in strategies to control side reactions and impurity profiles. Downstream, stringent validation ensures the final API meets global pharmacopoeial requirements for human therapeutics. Industry compliance standards
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2. Agrochemical Synthesis – Crop Protection Formulated CompoundsMajor crop protection manufacturers utilize this intermediate in constructing heterocyclic scaffolds for selective herbicides and fungicides. Integration into agrochemical formulations requires strict control of precursor quality and side product minimization. Plant scale-up follows agro-sector Good Manufacturing Practices and passes all regulatory checks before field deployment. Industry compliance standards
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3. Specialty Material Synthesis for Optoelectronic PolymersIn the specialty polymer sector, this compound serves as a monomer or cross-linker precursor for high-performance optoelectronic materials. The presence of trifluoromethyl and oxadiazole groups enhances electron transport and luminescent properties. Formulators integrate this raw material in the design and scaling of photonic polymers that comply with electronics industry standards for purity and batch reproducibility. Industry compliance standards
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4. Fine Chemical Intermediate for Advanced Dye SynthesisDye manufacturers apply this molecule as a tailored intermediate to build novel fluorinated and heterocyclic chromophores. This approach enables enhancement of dye fastness, light stability, and molecular compatibility with fibers and plastics. The sourcing and dosing of this raw material are tightly regulated under textile and pigment industry protocols, assuring consistent color yield and batch reproducibility. Industry compliance standards
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During three decades of fine chemical manufacturing, experience shows that the difference between an average intermediate and an exceptional one boils down to purity, consistency, and reliability in production. 3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole is not an off-the-shelf generic compound. It enters advanced synthetic chains with unique reactivity and a chemical profile that supports demanding pharmaceutical, agrochemical, and specialty chemistry teams.
Chemists working on new molecule entities or exploring patent-protected routes often look for building blocks with specialized frameworks. The 1,2,4-oxadiazole core extends opportunities to create stable, nitrogen-rich scaffolds that maintain their behavior during downstream reactions. Our customers see value in the 3-chloromethyl group for its direct participation in alkylation chemistry, a step that makes downstream substitution, functionalization, or coupling both practical and high-yield. The meta-trifluoromethylphenyl substituent introduces strong electron-withdrawing effects, which stabilizes target compounds and influences biological activity profiles, a key aspect in both drug discovery and fine-tuning lead optimization programs.
For every batch released, the exacting process control we maintain results in typical purity levels greater than 98% by HPLC. Moisture limits stay below 0.2%. Residual solvents fall well beneath the levels specified by major pharmacopeias. That often surprises new partners who are used to variability elsewhere, especially from traders or bulk intermediates marketed with little oversight. Real-world users do not want impurities creeping into multi-step syntheses and throwing off analytical profiles. Less time troubleshooting means more time spent on actual science.
As an in-house manufacturer, every kilo originates from reactors under our roof, monitored by our own technical teams. Handling starts from the initial fluorinated aromatics, flows through chloromethylation with carefully managed safety controls, and ends at the final oxadiazole formation under standardized conditions. Customers bring their own analytical teams to audit us, and their feedback often highlights the difference: fewer surprises, cleaner NMRs, more reliable LCMS data.
The marketplace contains dozens of other 1,2,4-oxadiazole derivatives and halomethyl intermediates. The question that comes up is: why not settle for an easier-to-access compound? The value in this molecule lies in the positions selected for substitution. The 3-chloromethyl group confers higher reactivity than bromomethyl or standard methyl analogs. Introducing trifluoromethyl at the meta-phenyl site, instead of the para position or on the core, creates distinct physicochemical properties. Solubility in common organic solvents such as dichloromethane and acetonitrile increases, which streamlines purification—particularly useful for downstream flash chromatography or high-vacuum distillation.
Other manufacturers have tried pushing analogous materials, but their inconsistencies have created headaches for firms that require strict reproducibility. Misplacement of electron-withdrawing groups or the presence of trace side products has ruined more than one scale-up campaign. Resident chemists on our team remember a project where project delays stemmed from an isomeric impurity introduced by a third-party supplier. Since bringing production entirely in-house and investing in custom glassware tailored to this molecule, such problems have not resurfaced.
End users in pharmaceutical discovery depend on tightly controlled intermediates to manage both yield and regulatory scrutiny. This molecule, with its selective reactivity, fits squarely in the toolbox for developing kinase inhibitors, anti-infective scaffolds, or agrochemical candidates. Research and development facilities, including several multinational pharma clients, have integrated the oxadiazole into high-throughput screening workflows. Consistency in reactivity and sample purity directly affects SAR (structure-activity relationship) conclusions drawn by project chemists.
In applied fields, crop science researchers use this intermediate to create novel fungicidal and insecticidal prototypes. The presence of the trifluoromethyl group often increases metabolic stability in target molecules, a trait well-known from published research in pesticide chemistry. Technical-grade materials that lack proper substitution patterns risk off-target effects, toxicity concerns, or breakdown pathways that end up costing time and money. Using the correctly substituted oxadiazole at this node in synthesis can shorten development timelines, a lesson seen repeatedly in contract projects handled at our plant.
Chemical synthesis lives and dies on trust in input quality. Distributors and resellers carry products from multiple sources, and material provenance can get lost, leading to issues such as batch-to-batch inconsistency or hidden contaminants. Manufacturing the product in our own facilities allows us to guarantee traceability from basic raw material all the way to the packaged drum. Persistent demand from long-term partners often relates not just to price but to the reduction in troubleshooting hassles down the line.
Access to full documentation, including process validation reports and custom analytical packages, sets our operation apart. Visiting client chemists have witnessed quality controls at every stage, including real-time chromatography tracking. These checks catch issues early, preventing scenarios where sub-par or contaminated material enters a synthesis campaign. After a decade of producing this compound at scale—and responding to regulatory audits in markets like the EU and Asia—we now see repeat orders motivated by the avoidance of costly project delays.
Scaling up 3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole requires thoughtful handling of hazardous reagents and the maintenance of anhydrous conditions throughout certain steps. A hands-on, experienced team minimizes accident potential by employing rigorous standard operating procedures, not just checklists. Over time, process optimizations—including jacketed reactor systems and improved distillation columns—have steadily raised yields while reducing waste streams. Attention to detail during the isolation phase greatly determines downstream purification efficiency.
One ongoing challenge is the global volatility in key raw materials. Fluorinated aromatics, for instance, often fluctuate in price and availability due to regulatory dynamics overseas. By cultivating backup supply relationships and investing in sufficient on-site storage, we hedge against disruptions and secure continuity for our partners. Both production and research teams benefit from this proactive buffer system.
Another frequent issue involves post-synthesis stability. While the chloro substituent provides desired reactivity, it can also prompt gradual decomposition if exposed to moisture or direct UV light during storage. Dedicated warehouses keep drums in temperature-controlled, low-humidity environments to mitigate such risks. Drawing direct experience from a near-miss incident in our early years—where a minor warehouse leak threatened to compromise inventory—we quickly reinforced packaging requirements and upgraded spill management equipment. Since then, integrity and shelf-life have matched or surpassed the guarantees we lay out in specification sheets.
Today’s regulatory climate holds every manufacturer accountable for the composition and handling of their materials. Our team closely tracks evolving requirements in European and Asian markets. Certain industries, including drug and crop science, demand granular batch documentation, validated analytical protocols, and regular third-party audit access. We answer these with dedicated support staff available to coordinate regulatory filings or provide technical clarifications—no middlemen involved.
Feedback from regulatory inspectors has often praised the clarity and transparency of our process documentation. Early engagement with clients’ compliance teams results in smoother project approvals and minimized time spent clarifying ambiguous paperwork. Internally, we maintain digital batch records and automatically flag material issues, giving both production supervisors and customers a clear view of process pedigree. This type of transparency forms the backbone of successful, long-term partnerships.
Experienced chemists tend to give frank feedback—sometimes mid-synthesis via urgent phone calls, sometimes later through in-depth post-project reports. One recurring observation has been the sharp control over particle size and solubility profiles, especially in gram-to-multi-kilo orders. Lab automation platforms tested pilot lots, highlighting quick dissolution and ease of handling. In previous years, users did note sporadic issues during transport in extreme heat. This led to a reevaluation of summer shipping protocols and additional cold-chain logistics for certain destinations.
We also value heavy users who challenge us to consider custom formulations—smaller lots in alternative solvents, or pre-packed kits for automated screening. By pooling insights from field chemists, analytical scientists, and scale-up operators, our technical staff iteratively optimizes both the base compound and the support service that surrounds it.
Global shifts toward greener chemistry have prompted deep dives into process safety and environmental stewardship. Oxadiazole manufacturing includes high-energy steps, so minimizing energy use and waste remains a continuous priority. On-site distillation captures solvents for recycling, reducing waste disposal volumes. Working with local regulators, we maintain transparent records of emissions and effluent quality, regularly sharing this data with stakeholders involved in environmental compliance.
For end users, the environmental lifecycle of a compound matters. The trifluoromethylphenyl structure, correctly handled, minimizes persistence in non-target environments compared to less stable analogs. Yet, every material brings a responsibility to manage disposal and exposure risks. In-house training programs for plant operators emphasize both reaction safety and downstream handling knowledge. Such preventive approaches, developed from practical experience, greatly reduce incidents and improve the safety profile of the whole operation.
As the pace of chemical innovation quickens, demand for reliable, high-performance building blocks only rises. Strategic investments in plant automation and process analytics aim to keep every batch on-spec and every customer order on time. Whether supporting academic breakthroughs or large-scale commercial campaigns, the goal never changes: keep the downstream scientists focused on discovery rather than rework.
Our journey with 3-Chloromethyl-5-[3-(Trifluoromethyl)Phenyl]-1,2,4-Oxadiazole has taught that deep technical specialization, transparency in operations, and direct engagement with users create enduring value. The compound may look simple on paper, but in a modern research or manufacturing pipeline, its reliable performance turns new ideas into practical solutions.