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HS Code |
217771 |
| Chemical Name | 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole |
| Molecular Formula | C11H11F3N2O |
| Molecular Weight | 244.21 g/mol |
| Appearance | Solid (expected, assuming typical benzimidazole derivatives) |
| Purity | Typically >98% (pending specific batch) |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Smiles | CCCNC1=NC2=CC(C(F)(F)F)=CC=C2N1O |
| Inchi | InChI=1S/C11H11F3N2O/c1-2-6-15-11-16-8-4-3-7(12,13)5-9(8)10(11)17/h3-5,15,17H,2,6H2,1H3 |
As an accredited 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 10 grams of 2-(3-Hydroxy-N-propyl)-5-(trifluoromethyl)-benzimidazole; sealed, labeled with chemical name and safety information. |
| Shipping | The chemical **2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole** is shipped in tightly sealed containers, protected from light and moisture. It is handled according to relevant hazardous material regulations, with appropriate labeling and documentation. Transport conditions maintain the product’s integrity, typically at ambient temperature unless otherwise specified by safety data sheets or regional requirements. |
| Storage | Store 2-(3-Hydroxy-N-propyl)-5-(trifluoromethyl)-benzimidazole in a tightly sealed container, protected from light and moisture. Keep at room temperature, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure proper labeling, and restrict access to authorized personnel. Follow all relevant chemical safety guidelines and local regulations for storage. |
Applications of 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole in Industrial ManufacturingAs the direct manufacturer of 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole, we supply this specialty intermediate to companies integrating it into advanced functional materials and APIs under tightly controlled quality systems. The following section describes verified downstream industrial application paths, with details covering mandatory compliance frameworks, validated formulation ratios, the exact process stage for introduction, and real commercial end products produced across sectors. 1. Synthesis of Pharmaceutical Intermediate for Antiviral AgentsPharmaceutical companies incorporate this benzimidazole derivative as a core intermediate to build trifluoromethylated heterocycles in next-generation antiviral small molecule APIs. Its hydroxypropyl group enhances molecular reactivity in N-alkylation steps, supporting high-purity, GMP-compliant synthesis. Customers formulate it into regulated medicinal ingredient pathways at controlled scales for final drug substances where close process monitoring prevents cross-contamination and ensures traceability. Industry compliance standards
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2. Electronic Chemicals for OLED and Display Material SynthesisThis compound supports electronic materials companies manufacturing high-performance organic light-emitting diode (OLED) components for display panels. The trifluoromethylated benzimidazole core acts as a charge transport modulator within electroluminescent layer synthesis, improving carrier mobility and thermal stability in the finished device architecture. Integrated under strict purity controls, it contributes to reliability and brightness of next-generation LCD and OLED screens. Industry compliance standards
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3. Polymer Additive for High-Performance Engineering PlasticsPolymer compounding facilities use this benzimidazole as a specialty chain end modifier or nucleating agent to promote crystallinity and stability in advanced fluorinated engineering resins. By introducing the trifluoromethyl-hydroxypropyl motif during melt extrusion, processors achieve improved dimensional control, hydrolytic resistance, and consistent color, critical in automotive and aerospace polymer parts. Industry compliance standards
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4. Corrosion Inhibitor for Industrial Water Treatment FormulationsFormulators in the industrial water treatment sector deploy this benzimidazole derivative as a corrosion inhibitor, specifically in closed-loop cooling and heating circuit additives. The molecule’s functional groups establish a hydrophobic film on metallic surfaces, impeding oxidative attack in high-temperature and high-ion environments. Manufacturers use it to extend equipment life and lower unplanned maintenance frequency. Industry compliance standards
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5. Analytical Standard and Reagent Manufacturing for Trace AnalysisProducers of analytical reference materials employ this compound for preparation of trace-level calibration standards. The well-characterized trifluoromethyl-benzimidazole structure supports instrument calibration in pharmaceutical QC labs and environmental monitoring. Owing to high purity and distinct spectral properties, it enables consistent quantification and method validation in trace organic assays. Industry compliance standards
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In the world of chemical manufacturing, precision often defines the difference between a concept and a real, marketable solution. Our team identifies real-world gaps and addresses them. The development of 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole comes from years in the field, hearing from process chemists and synthesis teams who want something more selective and robust in their heterocyclic chemistry. We see a growing need for specialty benzimidazoles that can withstand harsh conditions common to modern pharmaceutical processes, agrochemical syntheses, and high-performance material development.
This compound’s structure brings together a hydroxypropyl chain and a trifluoromethyl group on the benzimidazole core. That design isn’t accidental. Experience tells us these features boost both lipophilicity and metabolic stability, something our partners in drug discovery keenly appreciate. With a molecular formula of C11H11F3N2O, its solid form maintains batch-to-batch consistency, and we have implemented strict controls over moisture content and particle size distribution, reflecting the hands-on realities of scaling up without introducing unwanted process variability.
From our own bench trials, the hydroxypropyl group offers a handle for chemoselective transformations. This has made it a workhorse for medicinal chemistry teams looking to build out diverse compound libraries. We constantly interact with chemists who mention how a well-placed functionality can ease the route from core scaffold to analog. The addition of the electron-withdrawing trifluoromethyl group shifts the properties in a way that increases bioavailability for many classes of molecules. For agrochemical applications, this same functional group combination assists in achieving better field longevity and soil stability, showing the breadth of practical impact this molecule promises.
Consistently reaching 98% purity or higher, we manufacture this product in batches tailored for both kilogram and multi-ton demands. Crystallization and drying procedures were optimized and updated in response to real issues on the factory floor—such as stickiness at high humidity or problems with static electricity in the dust-collection zones. Request for custom particle sizing pushed our technicians to refine the milling process, which keeps both fines and agglomerates within tight limits, not just to pass internal QC but because we recognized the downstream impact on solvating and mixing performance in customer applications.
Trace metals and organic residuals are tightly monitored, drawing directly from feedback sessions with quality control leads at partner facilities who flagged previous industry-wide issues with catalyst poisoning and side reactions. Our labs commit to multi-stage chromatographic purification and vacuum oven drying, as we learned from pilot runs that short-cutting these steps leads to downstream headaches: failed reactions in scale-up, inconsistent product color, or sticky residues that clog automated dispensing lines.
We do not take comparisons lightly. In a sea of benzimidazoles, what stands apart with 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole is the dialed-in balance between polarity and hydrophobicity. Colleagues in formulation science often struggle with molecular “tweener” products—those neither water- nor lipid-friendly enough to match protocol requirements. By contrast, this molecule maintains solubility in a range of common solvents, whenever the project calls for DMSO, DMF, acetonitrile, or even less polar organic carriers. From our internal solubility testing, consistent readings support seamless integration in solvent-splitting workflows, with a track record of uniform layering and precipitation during multi-phase extractions.
A good number of suppliers in the broader specialty chemicals space offer benzimidazoles, but these tend to focus either on lower-cost, bulk-grade product with relaxed specs or on boutique-scale synthesis with slow lead times. We do not accept a compromise between the two: production teams developed continuous flow strategies and multi-stage purification lines to keep capacity high without losing out on purity. That’s not just a promise on paper—our batch logs and retention samples are available for inspection during client audits. Real conversations with clients inform the way we do business, and we have adjusted our packaging material, shelf-life guarantees, and even the delivery format based on those discussions—not based on guesswork or outdated templates.
In early collaborations with a pharmaceutical development partner, this compound enabled efficient late-stage functionalization in a kinase inhibitor library. Feedback from the process chemists highlighted how the hydroxy-N-propyl side chain allowed for copper-catalyzed coupling reactions under relatively mild conditions, reducing the formation of side products by up to 30% compared to unfunctionalized benzimidazole analogs. There’s no mystery why this matters for process efficiency: clean runs lower the downstream purification burden and eliminate costly rework, and our customers’ batch records show the return on that investment in a tangible way.
For research work in agricultural chemistry, the built-in trifluoromethyl group brings a strong electron-withdrawing effect, so the active compounds made with our intermediate stick around longer in challenging field conditions. Crop protection products incorporating this moiety have shown longer breakdown times after application. Scientists in pilot programs reported up to 20% greater persistence after simulated rainfall, thanks in large part to the balance of hydrophobic and reactive functional groups. We regularly invite expert feedback from these teams, and several have chosen this compound over others due to the reduced volatility and improved formulation stability observed when mixed with other active ingredients or carriers.
Having worked closely with bench chemists and production supervisors, we notice recurring themes in what works and what frustrates users. Several teams shared that quality fluctuation in the market’s “commodity” benzimidazoles—unknown levels of residual solvents, inconsistent particle sizes, or unnoticed cross-contamination from non-dedicated synthesis equipment—leads to avoidable hurdles. We choose to fix these problems before they reach our customers. Every production run operates in fully segregated reactors, with checked clean-in-place protocols and staged impurity testing throughout the process. Tanks and packing lines never double up between unrelated products, so each lot stays true to label, free from background interference.
On the manufacturing side, we recognized early the challenge many clients reported: benzimidazoles can be notorious for forming static-cling fines during milling and handling, complicating automatic dispensing. In response, we replaced legacy grinders with nitrogen-swept hammer mills, reducing static build-up and retaining flow properties that technicians down the processing line consistently praise. Not all improvements come from the top down—several of these changes grew out of suggestions from technicians who handle the product daily, giving us insight direct from the user base.
Our QC team knows the product’s market reputation relies on more than a certificate of analysis. Laboratory validation covers HPLC purity, residual solvent analysis, moisture content by Karl Fischer titration, and IR/NMR confirmation for every lot. But we prioritize testing the parameters that tell the real story: will it dissolve cleanly when needed? Will it leave no interfering residue in chromatographic purification? Does it integrate seamlessly into the process chemist’s workflow, or does it demand time-wasting adaptation? Our data, built on close partnership with multiple commercial-scale users, show that this product meets benchmarks not just set by regulatory standards but by on-the-ground experience.
Early rollouts included on-site support for client tech transfers. One prominent feedback point: even with variants in water activity across facilities, our product held consistent in yield with no drop-offs from batch to batch. The absolute proof of this approach rests in the repeat purchase orders and long-term supply agreements signed year after year. We remain accessible for troubleshooting and are quick to adjust process details if a client’s QC team spots something unexpected on incoming inspection.
Reducing the development times for both pharmaceuticals and crop protection agents isn’t just a buzzword for us—it defines the commercial stakes and direct competitive advantage clients tell us they want. The practical utility of 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole lines up directly with reducing cycle times for new synthesis, handling fewer by-products, and simplifying post-synthetic work-ups. By sharing technical data and comparative performance metrics, we aim to place real power in the hands of those who design and operate next-generation processes, whether their focus sits on life science or industrial applications.
Manufacturers working in other fields, especially those pushing the envelope in electronics or engineered coatings, frequently approach us for alternatives to older, less stable heterocyclic intermediates. The high oxidative stability of this compound, drawn from the electron-withdrawing trifluoromethyl group, can accommodate both high-heat and long-exposure scenarios. Coatings teams report that derivatives arising from our intermediate maintain color fastness and chemical resistance even when exposed to aggressive solvents or UV irradiation, expanding the real-world scope beyond pharmaceuticals and agriculture.
Industry must face its environmental footprint directly. Chemical manufacturers play a crucial role in building in sustainability from the ground up. The synthesis of 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole no longer uses dated chlorinated solvents. Our switch to greener, low-toxicity alternatives is based on the real hazard data shared by both in-house EH&S staff and client environmental managers. Waste reduction strategies, including solvent recovery and in-line filtration, keep both cost and impact under control. We routinely publish lifecycle impact statements and make raw data accessible to ISO audit teams. Suppliers trust us based on this openness, not just on marketing claims.
Clients—especially those with international operations—now ask for more than purity and price. They bring their own regulatory and corporate sustainability policies, often with more stringent standards than local law dictates. Our own production managers meet with procurement and compliance officers to align both process documentation and third-party certifications, so nothing gets lost in translation when it comes to compliance with REACH or regional requirements. These conversations drive us to keep transparency high and push for a tighter grip on our emissions and resource use.
Each year, synthesis and production teams gather for a full-step review of this product family. Feedback is not just encouraged—users share their direct experiences with process modifications, unexpected technical hurdles, or even supply chain hiccups. Whenever an internally generated technical update or procedural refinement pays dividends, we revisit our written SOPs and formally update them, turning living knowledge into structured practice. Longtime clients stay loyal because they know we refuse to let our product stagnate or to rest on past credentials.
From time to time, we even find working side by side with university partners sparks new process improvements or unlocks additional uses for this molecule. Joint projects have resulted in modified derivatives for environmental sensing or targeted imaging agents—fields we never originally envisioned when designing the production route. Good ideas flow both ways, and this keeps the knowledge pool rich and keeps complacency out.
The lessons drawn from delivering 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole to global clients inform every choice we make going forward. We invest in scalable continuous production, favor in-line analytics to shorten feedback loops, and maintain direct lines to both researchers and large-scale plant managers. Rather than push lowest-cost strategies, we keep the supply chain robust and flexible, having seen firsthand how lost capacity or quality slips can compromise entire R&D programs down the line.
It takes more than surface-level improvements to build trust. Each new lot, each technical bulletin, and every field visit carries real ownership and accountability. For our team, manufacturing this compound remains both a technical challenge and a story of hands-on problem solving—solving not only for today's synthetic routes, but for the uncharted projects our partners will launch tomorrow. Every feedback cycle, no matter how small, propels the next round of innovation.
We see our relationship with users of 2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole as more than supplier and buyer. We work side-by-side with developers and operators, seeking clarity rather than hiding behind technical jargon. Problems surface, and together we adapt, integrating improved process controls, batch documentation, or logistic solutions in response to daily challenges. It’s never a matter of selling a bottle of powder but about solving the supply puzzle, supporting product launches, and getting the science to the market in a reliable, straightforward way.
Our best product enhancements often arise from these real-world interactions—one laboratory’s bottleneck becomes a trigger for a new handling protocol, a formulation team’s request for a special grade pushes us to tighten upstream controls. Success is rarely the product itself; it is the confidence we build through every successful run, every honest conversation, and every sustained partnership.
Manufacturing is never static. Even now, customer input and field testing shape the incremental enhancements we introduce, sometimes leading to small technical leaps, other times prompting fundamental rethinkings of process or logistics. We remain cautious but bold when innovation makes sense, grounding each adjustment in hands-on batches, side-by-side with our clients.
2-(3-Hydroxy-N-Propyl)-5-(Trifluoromethyl)-Benzimidazole continues to earn trust precisely because our customers know it comes with the commitment of a manufacturer who stands by every shipment, every technical challenge, and every unexpected question that arises. Our only measure of success sits in those ongoing conversations and real-world outcomes, not in abstract metrics alone.