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HS Code |
819755 |
| Iupac Name | 1,1,1-Trifluoro-2-(trifluoromethyl)pent-4-en-2-ol |
| Molecular Formula | C6H6F6O |
| Molecular Weight | 210.10 g/mol |
| Cas Number | 351001-47-5 |
| Appearance | Colorless liquid |
| Smiles | C=CCC(C(F)(F)F)(C(F)(F)F)O |
| Inchi | InChI=1S/C6H6F6O/c7-5(8,9)6(13,4-3-2-1)10(11,12)14/h2,13H,1,3-4H2 |
| Pubchem Cid | 25196317 |
As an accredited 1,1,1-Trifluoro-2-(Trifluoromethyl)Pent-4-En-2-ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g net weight, sealed with PTFE-lined cap, labeled with chemical name, structure, hazard warnings, and supplier details. |
| Shipping | 1,1,1-Trifluoro-2-(trifluoromethyl)pent-4-en-2-ol should be shipped in tightly sealed, corrosion-resistant containers. Store and transport under cool, dry conditions away from heat and incompatibles. Comply with applicable hazardous material regulations. Ensure proper labeling and include safety data sheets with the shipment. Handle to prevent leaks or spills during transit. |
| Storage | 1,1,1-Trifluoro-2-(trifluoromethyl)pent-4-en-2-ol should be stored in a tightly sealed container, away from moisture, heat sources, and direct sunlight. Store in a cool, dry, well-ventilated area, separated from incompatible materials such as strong acids, bases, and oxidizing agents. Ensure proper labeling and avoid storing near ignition sources. Use secondary containment to prevent leaks or spills. |
Applications of 1,1,1-Trifluoro-2-(Trifluoromethyl)Pent-4-En-2-ol in Industrial ManufacturingAs a specialized manufacturer, we supply 1,1,1-Trifluoro-2-(Trifluoromethyl)Pent-4-En-2-ol to support sophisticated industrial processes requiring reliable fluorinated intermediates. Below, we outline established applications, sector-specific compliance, and integration details essential for production planning and downstream success. 1. Agrochemical Synthesis IntermediatesThis compound functions as a critical fluorinated building block in the custom synthesis of selective herbicides and fungicides, especially for modern active pharmaceutical ingredients where a trifluoromethyl functional group is required to confer resistance to metabolic breakdown in field use. Chemical process engineers utilize it for late-stage functionalization reactions delivering crop protection agents with targeted biological profiles. The fluorinated structure improves product longevity and application effectiveness under varying climatic conditions. Industry compliance standards
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2. Pharmaceutical Fluorinated Intermediate ManufacturingPharmaceutical R&D relies on this compound as a precursor for constructing advanced fluorinated motifs within small-molecule APIs and investigational agents. Its distinct structural elements aid in metabolic stability, increased binding affinity, and effective organ targeting, especially for CNS and oncology indications. Integration of this compound in medicinal chemistry enables downstream innovators to streamline lead optimization with improved pharmacokinetic properties guided by regulatory standards. Industry compliance standards
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3. Specialty Polymer MonomersChemical engineers source this material for copolymerization in high-performance fluorinated polymers where its unsaturated group accelerates crosslinking during polymer design. The resulting polymers present superior chemical resistance, enhanced weatherability, and lower dielectric constants, addressing specifications for electronics encapsulation, fluorinated coatings, and membrane materials. Using this compound, downstream manufacturers obtain bespoke molecular architectures for demanding end markets. Industry compliance standards
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4. Advanced Electronic Chemical PrecursorsLeading microelectronics producers demand high-purity fluorinated intermediates like this compound as specialty building blocks in the development of photoresist materials and as additives for improving dielectric properties in next-generation semiconductors. Its presence modulates etch resistance and supports thermal stability during fabrication cycles, helping wafer fabrication facilities meet tight process parameters and ensuring precision in critical device layer creation. Industry compliance standards
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5. Fluorinated Surfactant Synthesis for Industrial CleanersThis compound serves as a precursor in the production of next-generation fluorinated surfactants, which impart unique surface-tension lowering and chemical stability properties vital for cleaning formulations used in precision manufacturing and process equipment maintenance. Its structure enables synthesis of surfactant molecules with defined hydrophilic-oleophobic balance, directly influencing cleaning effectiveness on sensitive equipment and in critical processes. Industry compliance standards
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Competitive 1,1,1-Trifluoro-2-(Trifluoromethyl)Pent-4-En-2-ol prices that fit your budget—flexible terms and customized quotes for every order.
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Year after year, demand surges for new fluorinated building blocks. Customers push to synthesize more selective agrochemicals, tougher specialty polymers, or active pharmaceutical ingredients with unique properties. Our journey began in a modest synthesis workshop—handling, refining, and tuning molecules like 1,1,1-trifluoro-2-(trifluoromethyl)pent-4-en-2-ol long before their potential made headlines. Behind every batch, we pursue not only consistent reactivity but also functional reliability through cycles of adjustment and analysis.
This compound delivers a smart mix of structure and reactivity. Featuring both trifluoromethyl and trifluoropropenyl groups, it balances resistivity to unwanted side reactions with an attractive handle for custom chemistry. Fluorine substitutions in molecular frameworks have a well-documented impact on bioactivity, stability, and metabolic resistance, opening doors for industrial labs developing next-generation fine chemicals.
Over the decades, our team has learned that specifications do not just sit on paper. They play out in every pump, vessel, and control system we run. The 1,1,1-trifluoro-2-(trifluoromethyl)pent-4-en-2-ol we send to your lab is produced in facilities designed around dry, oxygen-free conditions to preserve the alcohol functional group and a clean carbon–carbon double bond. We set GC purity requirements that routinely exceed 98%, prioritizing not just peak area but also detectable by-products. Analytical staff constantly re-examines our purity and impurity profiles, matching them with customer feedback.
What sets our lot tracking apart starts at batch numbering and carries through shipment. We implement retesting schedules, bottle-to-bottle checks, and freeze-thaw cycle samples. In some years, we have had to address agitation, oxygen ingress, and even line swelling; our data shows these issues can jeopardize both purity and yield. We trained operators to spot subtle signs of moisture or contamination before any product leaves the warehouse. Many of us have stood next to drums and wondered about winter condensation or trace solvent introduction, so we commit to documented, reproducible packaging protocols.
The power of this molecule lies in its molecular duality. Chemists in pharmaceutical discovery reach for it to unlock rapid routes for fluorinated piperidines or pyrrolidines, key motifs in drug scaffolds. Our own pilot studies have shown that a single step with an appropriate cyclization agent can yield a variety of heterocycles that feature both CF3 and alkene groups. This structure, rare just a few years ago, lets medicinal chemists tune electronic properties and metabolic fate in one step.
Agrochemical customers do not just ask for a bottle—they request custom packaging and direct support with process development. The terminal alkene allows selective additions, including hydroboration or epoxidation. For some partners developing crop protection molecules, we have helped set up safety and compatibility discussions around the strong electron-withdrawing trifluoromethyl group. Direct feedback from formulation teams has pushed us to standardize handling guides and create collaborative trouble reports for reactivity or solubility questions.
In materials science, we have received growing interest from researchers needing robust blueprints for next-generation organic semiconductors and advanced fluorinated coatings. Their processes favor the balance between volatility, manipulation, and storage lifetime. Our in-lab studies tested evaporation rates under both nitrogen purge and open bench conditions, giving us a better understanding of handling losses and safe bottle design.
Progress does not come from news announcements—it comes from failures we have adapted to and challenges we have confronted. Not every attempt resulted in perfectly isolated 1,1,1-trifluoro-2-(trifluoromethyl)pent-4-en-2-ol. One setback involved batch reactions in glassware contaminated by legacy cleaning agents; yields collapsed until protocol changes and tighter vessel auditing solved the problem. At another point, we saw unexpected polymerization from trace acids introduced during capsuling. That cycle of setbacks and refinement now means better checkpoints, targeted in-line monitoring, and tighter standard operating procedures.
We have also been approached to reduce environmental footprints and pursue closed-loop recycling in line with green chemistry goals. Handling perfluorinated building blocks remains a responsibility, and we have begun pilot programs to minimize vented emissions, recover solvent, and re-condition raw material containers. Within our process team, direct input from shift operators, lab managers, and analytical chemists becomes part of every year’s process improvement cycle.
Supply chains have brought us their own challenges. Shortages of fluorinating reagents in past years pressed us to develop new backup processes and identify secondary sources, in order to keep customer timelines intact. Some partners needed documentation for new regulatory filings, and we responded by upgrading archive retention and providing additional impurity profiles as the market matured.
Many customers ask how this material differs from more common fluoroalcohols or trifluoromethylated alkenes. The arrangement of functional groups matters. The primary competition—compounds with terminal CF3 or internal alcohols—offers either higher volatility or more limited downstream chemistry. In our own alkylation tests, the presence of a secondary alcohol next to a terminal alkene provides synthetic flexibility that crucially expands both the number of reactions possible and the regioselectivity achieved. Unlike some perfluoroalcohols that require extensive protecting group strategies, this molecule allows direct access to derivatives, minimizing step count and byproduct formation. Customers have reported higher yields when using it in Michael additions, direct transpositions, and catalytic cross-couplings.
Other building blocks sometimes force users to choose between thermal stability and reactivity. The trifluoromethylated pentene structure resists premature degradation while presenting the alcohol where it most benefits subsequent transformations. Handling this product becomes more forgiving, provided exposure to sources of strong acid or base is minimized. Compared to pure hydrocarbons, this structure resists common degradation pathways triggered by oxygen or moisture, which means longer shelf life and safer staged storage.
Analysis within our facility shows typical impurities include trace alkenes, isomeric fluoroalcohols, and residual starting reagents. We document these so synthetic chemists do not lose time on troubleshooting. We learned to filter final lots to remove trace polymeric material difficult to catch with only standard chromatography. In the first year of development, customer feedback about reactivity differences between our batches and resellers’ prompted further root-cause investigation—resulting in changes to purification and increased investment in analytical standards.
Our historical experience with fluorinated products gives us a practical sense of what features make a difference in daily lab work. Products like 1,1,1-trifluoro-2-(trifluoromethyl)pent-4-en-2-ol deliver. They provide a balance: not so volatile as to cause storage headaches, not so reactive as to demand cumbersome safety handling, and not so limited as to constrain routes for innovation.
No product, no matter how pure or stable, can perform if neglected. Over the years, users have learned to avoid extended exposure to light or air in the lab. While the molecule stands up well against ambient conditions, excess moisture can introduce hydrolysis and reduce the efficiency of sensitive subsequent steps. We recommend drawing product under dry, inert atmosphere and resealing containers immediately. Team members who have worked from bench to drum can vouch that diligent handling practices, such as using dry syringes and degassed solvents, help achieve outperforming yields and process reproducibility.
Our chemists designed bottle and drum closures to minimize oxygen ingress, informed by headspace monitoring trials performed over several seasons. Customers operating at both milligram and multi-kilogram scale benefit from the same closures, re-labelling, and traceability practices we apply internally. We advocate training for new technicians, emphasizing safe material transfer and chemical hygiene, particularly with perfluorinated species that can irritate skin or mucous membranes.
Laboratory-scale development investigators often return to us after trial, documenting reaction temperatures, solvent compatibility, and reactivity profiles. Feedback loops from these cycles drive incremental improvements. Our fluoride-analysis group investigates any anomalous reactivity that is reported, providing front-line support and proposing technical alternatives for tricky transformations.
Supplying 1,1,1-trifluoro-2-(trifluoromethyl)pent-4-en-2-ol is only the visible surface of our commitment. Twenty years of manufacturing specialty molecules mean we recognize every branch in a synthetic pathway represents cost, timeline, and opportunity. We work with process teams, not just procurement staff, bridging the gaps that open between research, scale-up, and regulatory submission. During long projects, we provide continuity in lot release, repeat analysis, and root-cause troubleshooting to minimize surprises down the line.
Chemists—like us—rely on more than packaging and COAs. Our team’s experience spans failed runs, scale-up surprises, and last-minute analytics. We know handing off incomplete data breeds delay and confusion. Modern synthetic chemistry demands verified raw materials, transparency in trace impurity disclosures, and a support structure able to respond when unforeseen variables upend a project timeline. Our record shows that both established manufacturers and startups benefit from open, technical exchange—and sharper documentation built on honest reporting.
Our group tracks industry guidance, international regulatory trends, and pushes to implement new analytics when partners request them. We do not shy away from questions about vendor-of-record documentation, impurity disclosures, or bulk shipment validation. It is easier to fix a documentation gap now than to endure weeks of missed production or regulatory holdup. Our experience with risk mitigation lets chemists spend more hours inventing and fewer chasing down supply issues.
Trends in the chemical industry push toward smarter functionalization, aggressive timelines, and tighter environmental compliance. In response, we work to streamline our synthetic routes for 1,1,1-trifluoro-2-(trifluoromethyl)pent-4-en-2-ol and to cut waste at every stage. Twenty years ago, remote monitoring, digitized batch records, or rapid trace impurity screening barely existed at plant level. Today, this data feeds our improvement cycles, boosts transparency, and enhances our ability to meet both customer and regulatory expectations.
The rise of fluorinated molecules in pharmaceuticals, electronic materials, and advanced catalysts will keep this class of chemicals in demand. Our ongoing work includes adapting to new regulatory requests, fine-tuning emission controls, and searching for lower environmental impact in both sourcing and packaging. These changes stem not from outside pressure alone, but from our own drive to keep raising the bar in reliability and technical support.
Customers continue to challenge us with questions and needs nobody imagined at the start of our manufacturing journey. Whether responding to inquiries about scalability or how downstream waste can be handled, our technical staff sits ready, drawing from thousands of production hours and live batch data. As expectations about documentation, environmental responsibility, and performance rise, our team pushes our analytical and quality systems forward, letting us offer more than just a product—offering a partnership grounded in science, reliability, and direct human experience.
The story of 1,1,1-trifluoro-2-(trifluoromethyl)pent-4-en-2-ol reflects decades of adaptation, learning, and practical craft. Rather than treating each batch as a commodity, our process encapsulates shared expertise between operators, chemists, and engineers. This approach delivers advantages in the lab and on the plant floor.
The work remains unfinished. Every new regulatory request or feedback call means one more opportunity to improve. Each bottle delivered represents not only grams of a specialty intermediate but a record of technical steps and the know-how to keep chemistry practical, safe, and moving forward. With this foundation, innovation doesn’t just happen—it thrives.