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HS Code |
314314 |
| Product Name | 8-(Trifluoromethyl)Quinolin-4-ol |
| Cas Number | 515855-33-1 |
| Molecular Formula | C10H6F3NO |
| Molecular Weight | 213.16 |
| Appearance | Solid, powder |
| Melting Point | 183-187°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically >98% |
| Synonyms | 8-(Trifluoromethyl)-4-quinolinol |
| Smiles | C1=CC2=C(C=CN=C2C(=C1)C(F)(F)F)O |
| Inchi | InChI=1S/C10H6F3NO/c11-10(12,13)7-3-1-2-6-8(7)9(15)4-5-14-6/h1-5,15H |
| Storage Conditions | Store at room temperature, away from moisture and light |
As an accredited 8-(Trifluoromethyl)Quinolin-4-ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 8-(Trifluoromethyl)Quinolin-4-ol, labeled with safety information and chemical identifiers. |
| Shipping | 8-(Trifluoromethyl)Quinolin-4-ol is shipped in tightly sealed containers, protected from light and moisture. The package complies with chemical safety regulations, labeled as a laboratory reagent. Transportation follows all hazardous material guidelines, and safety data sheets are included to ensure proper handling. Suitable for delivery by approved chemical carriers only. |
| Storage | Store 8-(Trifluoromethyl)quinolin-4-ol in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Store at room temperature or as recommended by the supplier, and ensure proper labeling. Follow all laboratory safety protocols and maintain access to appropriate spill cleanup materials. |
Applications of 8-(Trifluoromethyl)Quinolin-4-ol in Industrial Manufacturing8-(Trifluoromethyl)Quinolin-4-ol is a specialized intermediate with strong electron-withdrawing fluorine attributes, regularly incorporated by manufacturers in targeted synthesis and formulation workflows. Below, we outline key downstream application tracks where this raw material integrates into established industrial practices, with details on compliance, formulation, process entry, and the end-use goods our global clients manufacture. 1. Pharmaceutical API Intermediate for Fluorinated AntimicrobialsMany pharmaceutical firms specify 8-(Trifluoromethyl)Quinolin-4-ol as an advanced intermediate in multi-step synthesis of next-generation quinoline-derived antimicrobial APIs. The fluorinated moiety improves metabolic stability and enhances target selectivity in pathogen control agents. Typically, this substance undergoes condensation, cyclization, and substitution reactions under strictly controlled cGMP protocols. The intermediate stands as a key building block in developing active ingredients for regulated therapeutic applications, particularly where trifluoromethyl substitution is crucial for product registration and lifecycle extension. Industry compliance standards
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2. Agrochemical Intermediate for Broad-Spectrum FungicidesAgrochemical manufacturers utilize this quinolinol derivative in the synthesis of advanced fungicidal actives targeting systemic and contact fungal pathogens in high-value crops. Its trifluoromethyl group supports resistance management and enhances soil persistence through robust C–F bonds. Process chemists implement this material in alkylation, complexation, and hydrolysis stages to yield active compounds. Crop protection R&D teams favor this intermediate for its impact on new product registrations and label extensions across major markets. Industry compliance standards
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3. Specialty Dye and Pigment Synthesis for Electronic DisplaysSpecialty dye manufacturers leverage 8-(Trifluoromethyl)Quinolin-4-ol as a precursor in producing quinoline-based pigments essential for advanced optoelectronic materials. The trifluoromethyl substituent introduces unique polarity and color-fastness, enabling the synthesis of high-purity dyes that meet stringent flat-panel display and OLED device specs. The compound is incorporated at critical nucleophilic substitution points, leading to colorants with tailored emission properties and minimized ionic contamination—critical for long-life display panels. Industry compliance standards
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4. Laboratory Reagent for Analytical and Research ChemistryResearch institutes and contract labs employ 8-(Trifluoromethyl)Quinolin-4-ol as a high-purity reagent in method development and trace analysis. Its distinct fluorinated quinoline core acts as a fluorine label or molecular probe in NMR, LC-MS, and fluorometric testing. Labs value its well-characterized impurity profile for calibration and kinetic studies in medicinal and synthetic organic chemistry, supporting both academic and regulatory research requirements. Industry compliance standards
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5. Synthesis of Advanced Materials for PhotocatalysisProducers of functional nanomaterials utilize this compound to introduce fluorinated motifs into quinoline frameworks for next-generation photocatalysts. The trifluoromethyl group increases UV-stability and enhances electron transfer capabilities. Material synthesis labs introduce this intermediate in sol-gel or metal-complexation processes, targeting use in environmental catalysts, water splitting units, and pollutant degradation modules. This integration enables the production of catalytically active frameworks meeting strict durability and efficiency benchmarks. Industry compliance standards
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Years on the manufacturing floor have shown us that reliable chemical quality unlocks breakthrough results, not just minor advantages. Our 8-(Trifluoromethyl)Quinolin-4-ol—sometimes recognized by its chemical shorthand, 4-hydroxy-8-(trifluoromethyl)quinoline—has earned its place on countless research benches and in production vats because of its distinctive properties and reproducibility. Every batch emerges from precise synthesis standards refined through experience, not just following theory but iterating recipes based on what truly works in the reactor and on the end-user’s bench.
Diving beneath the surface, the presence of a trifluoromethyl group at the eighth position isn’t just a matter of nomenclature. In real-world usage, fluorination at this position gives this compound a resilience and chemical reactivity quite different from its non-fluorinated analogues. Subtle electronic effects affect aromaticity and hydrogen-bonding in downstream reactions, facts routinely confirmed in organic syntheses and medicinal research projects. These are the kinds of differences that count when yield, purity, and intricate selectivity all depend on the nuances of the starting material.
As a manufacturer, our team controls quality from sourcing of raw fluorinating agents to finished compound. Techniques like recrystallization and multi-stage distillation run as standard, but direct hands-on observation carries equal weight with analytical numbers. We’ve seen that a few tenths of a percent impurity or subtle solvent residue can wreck someone's library screening or block a reaction downstream. Thus, we designed our process to drive impurities below thresholds that matter in real-world reaction kinetics and bioassays.
Our latest lot typically offers purity exceeding 98 percent by HPLC, checked batch by batch. The model designation—Q4OL-TFM-8—marks this particular synthetic route, letting researchers track reproducibility back to the core process, not generic off-the-shelf sources. Stability holds in ambient storage if exposure to moisture and sunlight is minimized, yet we include moisture indicator cards in each primary package, reflecting the lessons of supply chain transit over continents and climate bands.
From our vantage point, the real measure of a chemical’s worth arrives in the stories that come back from the lab: more robust SAR data, greater confidence in high-throughput medicinal chemistry, or new material prototypes built on a quinoline scaffold. Research partners share successes synthesizing new ligands, performing cross-coupling reactions, or modifying the quinoline ring for diverse functional studies.
Routine shipment destinations include bioactive compound screening labs, specialty pigment developers, and polymer R&D lines. In drug discovery, this quinolinol supports development of kinase inhibitors and antibacterial scaffolds, where the trifluoromethyl group promotes both metabolic stability and membrane permeability. Our own technical staff field questions that can only come from hands-on users—on eliminating particulates, adjusting crystallization solvent systems, or managing static charge in weighing rooms. Feedback like this shapes ongoing process improvements; it’s not theory, it’s the lived reality of scaling from bench to pilot reactor.
Not all quinolinol compounds play the same role in synthesis or formulation. The trifluoromethyl group at the eighth position brings a unique combination of electron-withdrawing power and increased lipophilicity. This alternation in charge distribution can direct reactivity toward desired sites, or slow down enzymatic degradation in medicinal applications. Many quinolines without this specific group fall short, especially where reaction selectivity or metabolic half-life matters.
Comparing directly with regular 4-hydroxyquinoline, the trifluoromethyl variant resists classic oxidative breakdown better under forcing conditions. In pigment chemistry, it delivers sharper color definition due to its electronic effects on the aromatic ring—results we’ve measured in both solution testing and finished pigment dispersion. And when it comes to advanced polymer formulation, this variant grants distinct solubility and processability advantages, suited for microelectronic or performance plastic innovation.
Over the years, we’ve worked through the challenges of transitioning from bench glassware to full-jacketed reactors. What looks simple at a flask level can become a bottleneck when reactor fouling, heat transfer variation, or impurity persistence enters the picture. Scale brings out every weakness in a synthetic route—and only iterative production, feedback, and optimization drive out the failure points.
A decade ago, a batch ruined by moisture ingress led to an overhaul of our solvent degassing system. Later, a production hiccup during a scale-up trial prompted us to refine agitation speeds and cooling rates. Each lesson feeds into the next run, improving not just the process for 8-(Trifluoromethyl)Quinolin-4-ol but deepening our understanding of aromatic trifluoromethylation and hydroxy group retention under real factory pressures. We refuse to cut corners, and our longest-standing customers trust that diligence they can taste in the reproducibility of their results.
Quality starts with raw material certification and ends only after a final shipment passes HPLC, GC-MS, and NMR checkpoints laid out by both industry standards and our stricter house rules. Every drum or vial ships with batch-specific spectra, matching finished product identity to known reference compounds without exception.
We’ve stood beside customers troubleshooting spurious melting points or unexpected UV/Vis spectra, helping them trace differences to solvent residue or missed drying steps. Years of working shoulder-to-shoulder with experienced chemists make us quick to spot and explain the odd impurity or color shift, offering informed solutions rather than disclaimers.
Our roots as a primary manufacturer lets us generate and update technical data based on direct production experience, not hearsay or handed-down certificates. Every new regulatory development triggers a review of process steps, safety assessments, and environmental controls. In cross-border shipments, we’ve learned the unique documentation and hazard labeling expectations of customs in North America, Europe, and Asia.
Customers in regulated environments—whether academic, contract research, or development labs—receive access to real-world batch traceability and full audit trails. Should project requirements change, our in-house compliance team assists in adapting supplies to meet revised storage or disposal stipulations, with guidance based on direct field feedback from several continents.
No amount of laboratory-grade purity means a thing if packaging introduces contamination or instability. Over the years, research chemists have pointed out that only robust primary barriers and smart closure designs keep the material viable on their benches. We package 8-(Trifluoromethyl)Quinolin-4-ol under nitrogen to limit oxidative change. Our moisture and oxygen indicators show at a glance whether the contents have experienced transit stress.
When projects demand large volumes, we use heavy-wall containers and secondary tamper evidence, limiting the risk of cross-contamination in storage or batch use. All labels print with solvent-resistant inks that resist chemical attack in real-world workspaces, rather than fading after a single spill.
A good manufacturing philosophy never stands still. Every inquiry about shelf life or solubility prompts new tests. We’ve adjusted drying parameters after a customer’s synthetic intermediate turned cloudy, and we diverted a whole batch when a single point of anomalous color appeared in a QC test. Our process R&D team runs regular pilot-scale trials based on user feedback, each time aiming not just to minimize cost, but to refine reliability under the varied, sometimes rough reality of diverse end uses.
Feedback from academia and the pharmaceutical industry alike have led us to update our documentation packages, offering more detailed solubility curves, recommended reconstitution solvents, and safety handling checklists built on more than regulatory compliance—built on habits proven by hands-on engagement and post-project debriefs with primary investigators and production chemists.
Progress in fine chemical manufacturing relies on partnership and candor. From early-stage medicinal chemistry to scale-up projects for advanced coatings companies, our team pays close attention to shifts in reaction design and analytical techniques. When collaboration calls for customized batches—modified purification, alternative salt forms, unusual packaging—we commit resources and staff time for practical experimentation.
Recent years have seen growing requests for variant lots tailored to match specific process tolerances or analytical signatures. In the spirit of continuous improvement, we log every special request and customer insight, using that feedback loop to shore up weaknesses, anticipate new needs, and develop complementary synthetic intermediates based on the 8-(Trifluoromethyl)Quinolin-4-ol core.
No one enjoys production halts. Over decades, disruptions ranging from raw material shortages to shipping delays have taught us the absolute necessity of contingency. Our supply agreements for key fluorination agents include redundant sourcing, and warehouse protocols make traceability and stock rotation more than a paperwork exercise. Fast recall of any batch, right back to original reactant delivery tickets, supports peace of mind for large-scale research projects and recurring orders alike.
We handle surge requirements without stretching production beyond its robust limit, thanks to a steady investment in spare reactor capacity and experienced technical operators. Frequent supply-side disruptions in specialty chemical markets only reinforce our approach: keep buffers high, communicate timelines with honesty, and deliver exactly what the researcher needs, without drama.
Too many end-users have shared frustrations with resellers who can’t answer detailed synthesis questions or trace a problem batch back to the source. As the true producer, we offer firsthand knowledge—whether that means helping a process chemist rerun a stalled reaction, or drilling deep into the question of why two different lots seem to behave differently in a chromatographic separation.
We see stories emerge from the field showing the impact of small, often-overlooked tweaks in manufacturing or packaging. The little things matter—solvent history, drying duration, even the skill of the technician operating the final vacuum oven load. Our team stands ready to collaborate, bringing direct manufacturing knowledge to solve challenges quickly.
A successful synthesis route for 8-(Trifluoromethyl)Quinolin-4-ol reflects years of iterative adjustment, careful sourcing, and an unwavering focus on user outcomes. It supports breakthrough work in drug discovery, materials design, and advanced manufacturing—not because it follows a paper protocol, but because its reliability in actual user hands uncovered and drove out weaknesses batch by batch.
We invest in this compound because we know firsthand how chemical quality, documentation, and consistent batch performance shape the front lines of research and production. This is how high-value chemistry is done—with open communication, technical transparency, and respect for the craft and challenges of manufacturing specialty chemicals in a changing world.