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HS Code |
961284 |
| Cas Number | 75-89-8 |
| Molecular Formula | C2H3F3O |
| Molar Mass | 100.04 g/mol |
| Appearance | Colorless liquid |
| Density | 1.370 g/cm³ |
| Melting Point | -43 °C |
| Boiling Point | 78 °C |
| Solubility In Water | Miscible |
| Refractive Index | 1.301 |
| Vapor Pressure | 54 mmHg (20 °C) |
As an accredited 2,2,2-Trifluoroethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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Purity 99.5%: 2,2,2-Trifluoroethanol with purity 99.5% is used in pharmaceutical synthesis, where it ensures high yield and product consistency. Boiling Point 78°C: 2,2,2-Trifluoroethanol with a boiling point of 78°C is used as a solvent in peptide coupling reactions, where it facilitates easy removal by evaporation and reduces contamination. Molecular Weight 100.04 g/mol: 2,2,2-Trifluoroethanol of molecular weight 100.04 g/mol is used in protein denaturation studies, where it allows precise control of unfolding kinetics. Stability Temperature up to 120°C: 2,2,2-Trifluoroethanol stable up to 120°C is utilized in high-temperature organic reactions, where chemical integrity is maintained throughout the process. Water Content ≤0.1%: 2,2,2-Trifluoroethanol with water content ≤0.1% is applied in moisture-sensitive fluorination reactions, where it prevents undesired side reactions and improves final product purity. Low UV Absorbance: 2,2,2-Trifluoroethanol with low UV absorbance is used in spectroscopic protein analysis, where it minimizes background interference for accurate measurements. Viscosity 1.5 cP: 2,2,2-Trifluoroethanol with viscosity 1.5 cP is employed as a chromatographic solvent, where it ensures efficient flow and sharp separation peaks. Density 1.37 g/cm³: 2,2,2-Trifluoroethanol with density 1.37 g/cm³ is used in extraction applications, where it enables efficient phase separation and high extraction rates. Acid Value <0.01 mg KOH/g: 2,2,2-Trifluoroethanol with acid value below 0.01 mg KOH/g is used in polymer synthesis, where it avoids acid-catalyzed side reactions and enhances polymer quality. Storage under Nitrogen: 2,2,2-Trifluoroethanol stored under nitrogen atmosphere is utilized in sensitive chemical processes, where it prevents oxidation and extends shelf life. |
| Packing | 2,2,2-Trifluoroethanol is packaged in a 500 mL amber glass bottle with a secure, chemical-resistant screw cap for safety. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2,2,2-Trifluoroethanol: 160 drums × 250 kg per drum; net weight 40,000 kg per container. |
| Shipping | 2,2,2-Trifluoroethanol is shipped in tightly sealed containers, typically glass or suitable plastic, to prevent leakage and degradation. It is transported as a hazardous material due to its flammability and potential health hazards. Proper labeling, documentation, and compliance with all relevant transport regulations (such as DOT, IATA, or IMDG) are required. |
| Storage | 2,2,2-Trifluoroethanol should be stored in a tightly closed, clearly labeled container, in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Store separately from oxidizers, acids, and bases. Protect from moisture and direct sunlight. Use appropriate corrosion-resistant materials for containers and ensure proper grounding to prevent static discharge. Observe all relevant safety protocols when handling. |
| Shelf Life | 2,2,2-Trifluoroethanol typically has a shelf life of two years when stored tightly sealed in a cool, dry, and dark place. |
Competitive 2,2,2-Trifluoroethanol prices that fit your budget—flexible terms and customized quotes for every order.
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Every day on our line, 2,2,2-Trifluoroethanol moves from raw materials to high-purity final product under careful watch. In our business, this fluorinated alcohol stands out for its blend of volatility, miscibility, and select chemical reactivity. Instead of listing generic features, we focus on what 2,2,2-Trifluoroethanol means in hands-on chemical processes and what sets it apart from other solvents and reagents.
The product’s molecular formula, C2H3F3O, tells only a fraction of its story. Trifluoroethanol brings together a short ethyl backbone and three fluorine atoms bound to the same carbon. Fluorine’s presence boosts both acid strength and solvent power. That means working with 2,2,2-Trifluoroethanol delivers results that differ sharply from simple ethanol or isopropanol.
On the production line, maintaining a reliable assay—usually upwards of 99.5%—proves vital. Even small variations in purity show up in both NMR solvents and downstream reactions. Water content, often less than 0.05%, matters. Precise measurement, regular Karl Fischer titration, and gas chromatography remain constant habits rather than optional extras.
Chemists look at trifluoroethanol for its balance of hydrogen bonding and high polarity. It dissolves both organic and inorganic compounds, making it more versatile than many alcohols. Unlike ethanol, it will often keep fluorinated or highly halogenated molecules dissolved long after others fall out of solution. For biochemists, this means easier handling of peptides and proteins. For organic synthesis, the combination of acidity and polarity speeds up several types of reactions—especially Friedel–Crafts, oxidations, and cyclizations.
Peptide synthesis, a notoriously challenging process, often finds improved yields with trifluoroethanol as co-solvent. In pharmaceutical development, clients choose it to denature proteins or refine active pharmaceutical ingredients. Medicinal chemists point to clear spectral signatures in NMR analysis when using trifluoroethanol, thanks to reduced background reactivity compared to less specialized alcohols. In research labs, even small changes in solvent polarity can spell the difference between failure and success; our customers share that using trifluoroethanol gives them more reproducible outcomes and reaction rates.
Producing 2,2,2-Trifluoroethanol requires not just attention to basic protocols but persistent care in each step. Hydrofluorination, rigorous drying, and multistage distillation take skill and patience. Raw material quality makes a difference. Even a slight drift in upstream hydrofluoric acid content can introduce impurities that standard distillation can’t remove. So, our team keeps intake checks as strict as release testing, measured every batch rather than per shipment.
Safety stands as a daily concern. Trifluoroethanol’s volatility shows up with every tank transfer; leaks hit sensors quickly, and so do temperature shifts. Venting systems need regular checks, since small leaks become obvious through the pungent odor before meter readings leap up. Personal safety on the floor isn’t abstract—respirators, splash goggles, double gloves always in place—because exposure risks include both the alcohol and breakdown products.
Someone new to trifluoroethanol may ask why not use ethanol, which costs less and looks similar on paper. Two main reasons stand out. Trifluoroethanol brings higher acidity—roughly pKa 12.4 compared to ethanol around 15.9—and that acidity changes how molecules interact in solution. Peptide chemists, in particular, watch for alpha-helix formation, and find that trifluoroethanol stabilizes their target conformations better than any other common solvent.
Compare it next to methanol or isopropanol. Neither matches the unique balance of high dielectric constant and strong hydrogen bonding delivered by trifluoroethanol. This allows it to act as both solvent and reactant in a broader swath of transformations, especially those needing activation of electron-poor centers. Some competitors carry similar names—1,1,1-trifluoroethanol and 1,2,3-trifluoropropanol—but substitution patterns mean chemical properties shift. For example, positional isomers often lack the acidity and solubility profile that makes 2,2,2-Trifluoroethanol effective in peptide and pharmaceutical labs.
After shipping hundreds of tons worldwide, we have learned about trifluoroethanol’s temperament. It absorbs atmospheric moisture—not as rapidly as some reagents, but enough that drums require nitrogen-blanketing if partial use is planned over weeks. Bulk storage always draws customer questions. Stainless steel resists corrosion nearly as well as glass. Over time, seals and valves degrade faster than with ethanol. Routine inspection is not just a checklist item but crucial for safety and product quality. Temperature control makes a difference. Sub-ambient storage can reduce evaporation losses, especially given trifluoroethanol’s relatively low boiling point.
University labs and corporate R&D teams often move from milliliter-scale experiments to bulk kilogram and ton purchases. We help bridge the scale-up gap by drawing on years of batch data and lessons about temperature, equipment compatibility, and local regulations. In early-stage medicinal chemistry, trifluoroethanol gives a way to test new synthetic routes before locking in a process. In process development, recipes using trifluoroethanol often transition to industrial reactors with minimal adjustment, provided agitation and reflux are well-controlled.
Over time, we have collected customer questions, from minor odorous byproduct formation to issues with extraneous color. Usually, issues emerge from improper closure or minor storage lapses. Our feedback: minimize headspace, seal tightly, purge with dry nitrogen, and avoid prolonged exposure to direct sunlight. Purity and stability remain highest under these practical storage conditions.
As regulations shift, production teams face increasing scrutiny from both national and international agencies regarding solvent emissions and worker exposure. Our own emission controls reflect those pressures. Closed transfer and vapor recovery systems have become standard practice, replacing open drum techniques common decades ago. We track all solvent waste, including process-generated residues, through approved hazardous waste channels.
Trifluoroethanol’s relative toxicity warrants separate mention. Unlike simple alcohols, it poses targeted risks—central nervous system effects, mild corrosivity to eyes and skin, and potential for bioaccumulation in certain settings. Practical risk mitigation extends from the production floor to every downstream handler. Proper training and regular review of control measures keep staff and customers safer.
We find that trifluoroethanol integrates well into Suzuki and Heck cross-coupling reactions, particularly when more conventional solvents like DMF or toluene underperform. Its capacity to activate substrates and promote homogeneous mixing translates into higher conversion rates and lower byproduct formation. In our direct manufacturing, this means less stress on downstream purification. Waste reduction starts not just at disposal, but right at the choice of solvent.
For materials science, thin-film deposition and polymer chemistry exploit its rapid evaporation and moderate dielectric constant. These characteristics lead to consistent film morphologies and fewer pinholes than those observed with methanol or isopropanol. Some of our advanced manufacturing customers report increased throughput and consistent batch quality, directly tied to solvent performance.
Over the years, we have fielded countless requests for troubleshooting. Chemists want to know why their yield dropped in a condensation step or why a crystalline peptide failed to precipitate. Often, water ingress or minor impurities are to blame. We take an active role in reviewing customer process details and shipping records to identify root causes. Our routine involves sharing suggestions rather than just selling a drum and stepping back.
Several years ago, a client reported lower NMR resolution than their historical baseline. Closer inspection of solvent lots and careful review uncovered a trace halide contaminant from a raw material source. In response, we tightened input controls and modified a purification step to eliminate repeat issues. Such process improvements, while often invisible to buyers, drive higher quality over time.
Scale-up projects bring their own surprises. One pharmaceutical customer, moving from pilot to production, found distillation recovery rates less than projected in process simulations. Our engineers visited the site, reviewed their columns, and found condenser capacity was mismatched to trifluoroethanol’s latent heat. Advice: reassess condenser design and upgrade cooling loops, minimizing vapor loss and reducing overall batch times. Results followed in the next campaign: higher recovery, less downtime, no off-spec charge.
Price volatility has surfaced repeatedly in the last decade. As the upstream supply of hydrofluoric acid and fluoroalkanes tightens, so do cost curves. Transparent discussions with our partners—explaining both raw material pressures and efficiency gains from good solvent choice—help our customers make informed purchase decisions. We encourage buffer stock planning, and, where volume justifies, multi-shipment agreements. This shields projects from short-term spot pricing spikes and allows more predictable R&D budgets.
Questions about shelf life arise regularly. In controlled conditions, unopened drums last at least two years with retention of purity, based on our stability studies and customer returns data. For in-use containers, best practice means recording every puncture, purging after use, and limiting oxygen or moisture ingress. Realistically, opening and closing drums more often raises contamination risk; we recommend transfer to smaller, inert-lined bottles for bench-scale use, mirroring what we practice in our pilot facility.
Analytical chemists seek out trifluoroethanol for its clear NMR background and useful chemical shift profile, especially in peptide and nucleic acid work. Experience tells us that high purity standards, near absence of extraneous peaks, and reliable batch-to-batch composition all contribute to sharper spectra. The slight acidity helps in sample dissolution, especially for amphipathic molecules resisting more traditional solvents.
Synthetic protocols have broadened as well—cyclization, azide-alkyne click reactions, and oxidative couplings find consistent performance. Our collaboration with process development teams yields insight on reaction times, optimal additive selection, and streamlined work-ups. Reagents and catalysts function more efficiently in the presence of trifluoroethanol under controlled pH and moisture content.
Direct manufacturing allows us to control each narrow cut in fractional distillation. By analyzing both heads and tails, we keep unwanted byproducts below specification. We do not re-bottle third-party material or blend off-spec lots. Taking full ownership means investing in better instrumentation, updated hazard detection, and long-term staff continuity. Our NMR and Karl Fischer data support this hands-on technical approach. Each drum bears the quality and security of a vertically integrated workflow.
This depth of technical oversight brings repeat clients from biotech startups to global manufacturers. Our confidence in our product stems from what we measure, not only what we promise. Most chemical buyers ask about analysis certificates and traceability; we deliver both, and track customer feedback to guide continuous improvement.
Trifluoroethanol’s range of uses keeps expanding. Researchers trialing new bioactive compounds report positive outcomes tied to reliable solvent interactions. Emerging applications in green chemistry and biofuel research suggest further growth. Our own process R&D explores recovery and recycle opportunities, aiming for less downstream waste and ongoing cost reduction.
We see academic groups trialing alternative fluorinated solvents, and our team keeps pace by benchmarking every new candidate against trifluoroethanol. Some alternatives offer lower toxicity or volatility, but seldom match the performance envelope—especially in protein chemistry or precision polymer synthesis. Through direct feedback and method sharing, we seek to encourage transparent, fact-based discussion about both strengths and potential improvement areas.
On the shop floor, in the analytical lab, and throughout distribution, we have witnessed firsthand what 2,2,2-Trifluoroethanol brings: predictable results, unique reactivity, and persistent technical challenges that are manageable by good practice. Handling it well starts with disciplined storage, regular monitoring, and honest communication between manufacturer and user.
Every innovation, every adjustment, and every batch improvement we make reflects years of technical problem-solving and open discussion with synthetic and analytical chemists alike. That experience shapes the promise we offer: a solvent grounded in direct manufacturing knowledge, delivering value through each stage of research and production.
In summary, 2,2,2-Trifluoroethanol stands out for those who need more than a commodity solvent. As both a manufacturer and technical partner, we commit to ongoing process improvement, transparent communication, and support shaped by real-world experience.