|
HS Code |
832903 |
| Iupac Name | 3-(1,1,2,2-Tetrafluoroethoxy)phenol |
| Cas Number | 886762-58-5 |
| Molecular Formula | C8H6F4O2 |
| Molecular Weight | 210.13 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | Estimated ~210°C |
| Density | Estimated ~1.38 g/cm3 |
| Solubility In Water | Low |
| Smiles | C1=CC(=CC(=C1)O)OCC(F)(F)C(F)F |
| Inchi | InChI=1S/C8H6F4O2/c9-7(10)8(11,12)14-6-3-1-2-5(13)4-6/h1-4,7,13H |
As an accredited 3-(1,1,2,2-Tetrafluoroethoxy)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle, 25g quantity, tightly sealed with a screw cap, labeled with chemical name, hazard pictograms, and batch information. |
| Shipping | **Shipping Description:** 3-(1,1,2,2-Tetrafluoroethoxy)phenol should be shipped in tightly sealed containers, protected from light and moisture. It must comply with chemical shipping regulations, using appropriate hazard labeling. Transport at ambient temperature unless otherwise specified. Ensure documentation conforms to local, national, and international regulations for safe handling of organic chemicals. |
| Storage | **3-(1,1,2,2-Tetrafluoroethoxy)phenol** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect from light and moisture. Use secondary containment to avoid leaks or spills, and clearly label the storage area to prevent accidental misuse or exposure. |
Competitive 3-(1,1,2,2-Tetrafluoroethoxy)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615380400285
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Every year brings new technical challenges in the laboratory and on the manufacturing floor. Managing those daily, we rely heavily on the chemicals that drive modern processes forward. Working directly with 3-(1,1,2,2-tetrafluoroethoxy)phenol, I get to see firsthand what this unique phenolic ether brings to our customers and partners.
3-(1,1,2,2-Tetrafluoroethoxy)phenol, sometimes shortened in technical discussions, stands out for its molecular architecture. The four fluorine atoms on the ethoxy group aren’t just a curiosity—they’re the reason this compound occupies a specialized place in synthesis and formulation. The presence of these electron-withdrawing groups shapes many of the compound's reactivity patterns. In practical terms, it remains stable under conditions that break down similar compounds. We measure that stability in batch records, not in theory, and customers see it in higher-yielding reactions and fewer shutdowns.
Our production team works closely with R&D to keep improving process reliability. The tetrafluoroethoxy functionality blocks many side reactions that slow down other phenolic ethers in strong acid or alkaline environments. Many of our customers come to us after trying standard ethoxyphenol or even trifluoroethoxy derivatives. In pharmaceutical intermediate manufacture, that resistance to unwanted reactivity translates to purer end products and lower costs because it cuts out unwanted byproducts that drain time and money.
Another distinguishing factor comes from its physical behavior. 3-(1,1,2,2-Tetrafluoroethoxy)phenol possesses a distinctive melting point and solubility profile. Years of careful scale-up allow us to tune crystallization steps for consistency lot to lot. The compound dissolves effectively in solvents that fail to accommodate less fluorinated phenols, supporting applications in custom coatings and surface treatments where other additives fall short. Our QC team doesn’t just report numbers—they tune handling and shipping protocols to preserve quality through the entire supply chain.
Commercial chemists working with aromatic ethers quickly notice the effect fluorine has on chemical resistance. The 1,1,2,2-tetrafluoroethoxy group’s strong bond strength keeps out water and aggressive species much more effectively than a plain ethoxy. For production chemists scaling up fluorinated organics, every step matters: halogen-based side reactions are a constant headache with other compounds, but not here. This is the kind of reliability that matters on a quarterly downtime report.
On structure, the phenolic hydroxyl group’s reactivity—already well known—pairs with electron-withdrawing power from fluorine atoms to provide a different balance during nucleophilic substitution or oxidative steps. This expands the toolbox for anyone building advanced molecules for material science or healthcare. The compound’s altered acidity can be quantified using standard titration and confirmed through bench-scale runs, and frequent application feedback from our partners ensures our process keeps pace with their changing demands.
Every sector brings its own set of challenges. In electronic materials manufacturing, subtle changes in solvent compatibility make or break whole production runs. Our experience producing multi-ton quantities of 3-(1,1,2,2-tetrafluoroethoxy)phenol has shown a significant uptick in demand from companies developing advanced dielectric films. Here, high breakdown voltage and low dielectric loss require more than just a general-purpose phenol. The unique fluorinated tail attached to the aromatic ring delivers superior electrical insulation properties, which in turn allows slimmer device designs and higher reliability in the field.
Pharmaceutical researchers appreciate this molecule’s influence on molecular scaffolds, especially where metabolic stability and reduced off-target binding remain high priorities. The phenolic function stays available for conjugation, but the presence of four fluorines reduces oxidative metabolism. That translates to more predictable performance in drug candidates and process intermediates. Our technical staff have discussed cases where switching from a non-fluorinated analogue to our 3-(1,1,2,2-tetrafluoroethoxy)phenol improved not only the yield but also the selectivity of late-stage synthetic steps—feedback collected up and down the supply chain.
It's tempting to lump all fluoroalkoxyphenols together on a spreadsheet, but experience shows that differences in atom count and position shape reactivity and usability. Compared to simple ethoxyphenol, our product carries dramatically enhanced resistance to acid- and base-catalyzed hydrolysis. For customers dealing with the trifluoro version, adding one more fluorine makes a noticeable jump in resistance to both chemical and thermal stresses. Side-by-side pilot runs show less discoloration over time—a clear readout for quality assurance teams monitoring polymer additives.
Among custom material developers, the additional fluorine atoms in this structure open up new export markets where regulatory thresholds for environmental persistence or toxicity have grown stricter. The route we use to build this molecule ensures trace impurities remain tightly controlled, cutting compliance risk. Production managers often stress-test these phenols for extraction resistance using their own blend of solvents and the feedback cycle continuously informs our manufacturing protocols. We rarely ship a specification that hasn’t already been field-tested by end users.
Consistent batch performance doesn’t happen by accident. Sourcing fluorinated feedstocks, managing waste byproducts, and scaling up synthesis from a flask to a reactor train introduces dozens of variables. Between each step, we push for in-process controls armed with lessons learned through years of commissioning new capacity. After years of direct feedback, we have established container materials and shipment packaging that don’t compromise chemical integrity, keeping oxidation and hydrolysis at bay well beyond published shelf life.
In our own storage areas, strict climate control has become standard, informed by long-term stability tests. Each drum receives a unique identifier, allowing us to trace any lot through the full history of production and QC interventions. Customers with their own audit programs often request our stability data, and we’re proud to have minimized deviations through investment in analytical methods and deliberate risk management practices.
Having produced thousands of kilograms over the years, our team has catalogued nearly every quirk and advantage of 3-(1,1,2,2-tetrafluoroethoxy)phenol. Unlike many commercial suppliers who treat such products as commodities, our status as the manufacturer means firsthand interaction with the molecule itself. We have adapted synthesis protocols for tailored particle size, which directly influences blending and reaction efficiency downstream. These are not theoretical improvements—a line supervisor can recount improved throughput based on more controlled drying and milling methods on our equipment.
Customers often face hurdles adapting lab-scale chemistries to kilo-scale plants. Early project stages benefit from detailed process notes, including filtration techniques specific to this compound’s physical form. Some end users blend it to create novel resins; others use it in surface-modification steps for specialized membranes. As those needs evolve, we share real-time process updates—sometimes adjusting our operation windows to serve a particularly demanding requirement, rarely encountered with conventional phenolic ethers.
The manufacture of specialty organofluorines demands careful stewardship. Our process development teams have made significant progress reducing waste by leveraging recycling streams within the plant. We actively monitor fluorinated byproduct formation at each stage, not just for cost control but to meet tightening environmental expectations. The regulatory environment across Europe, North America, and Asia continues to shift. Sharing environmental data with customers has become more routine—most recently, full life-cycle emissions profiles including scope three impacts. It’s a point of pride for operators and leadership alike that we’ve slashed process water consumption without compromising purity.
Downstream customers are asking harder questions about end-of-life fate for fluorinated compounds. Drawing from our own EHS audits and third-party environmental research, we regularly update technical sheets with the latest on thermal degradation pathways and recommended disposal strategies. Where possible, we work directly with customers to recover off-spec lots or expired materials. Safe, responsible handling matters more than brand or price.
One fact sets manufacturers apart: resolving the problems that never show up in patents or journals. Early on, we encountered scale-up challenges involving the selective alkylation of the phenolic group. Having built dozens of runs to address specific customer concerns, we now provide a much tighter specification than most bulk traders on moisture, halide content, and residual catalyst. Those tweaks are documented in daily logbooks; they don’t just live in marketing copy.
More recently, we’ve backed research into the application of 3-(1,1,2,2-tetrafluoroethoxy)phenol in creating low-surface-energy polymers. This comes from relationships built on timely technical advice and the willingness to adjust production schedules. Contract researchers feed back results in real time, allowing us to tighten controls on process variables that influence downstream reproducibility. It’s never a matter of simply shipping a drum and moving on; each step is tracked to ensure the chemical meets the specific goals set out in the customer’s development cycle.
No two projects draw on the same properties to the same extent. A coatings manufacturer might prioritize compatibility with high-boiling solvents and resistance to chemical breakdown, while a pharmaceutical team values predictable reactivity and regulatory transparency. Either way, we support these efforts by running small, targeted custom synthesis batches in parallel with larger-scale routine production. That flexibility means we can transition from kilogram evaluation samples to full-scale drum shipments without the risks of batch-to-batch drift.
Because we control every aspect of production, traceability remains ironclad. This includes full documentation on raw material sourcing and in-house analytical verification. In some cases, we engage directly in troubleshooting new formulations, leveraging both our maintainers’ observations and chemists’ process data. Rapid technical response means small issues rarely become project-stalling headaches for our partners.
The advanced performance of 3-(1,1,2,2-tetrafluoroethoxy)phenol didn’t emerge through luck or guesswork. It’s rooted in years of hands-on improvement, market feedback, and data-driven process control. Over time, we’ve come to rely on open customer relationships, honest feedback, and a clear-eyed view of chemical safety and environmental impact. Our direct experience with scale-up and new application support means we keep improving—not because it’s the easiest path, but because that’s where long-term value for both manufacturer and user really lies.
Those selecting a phenolic ether for next-generation products face an array of options. Taking a shortcut on source or process knowledge often ends up costing more due to unreliable supply or inconsistent performance. We invite customers to reach out—not to a faceless distributor, but to the team responsible for every flask, drum, and reactor run that goes out our doors. Our commitment to technical detail, operational safety, and shared success has shaped every kilogram of 3-(1,1,2,2-tetrafluoroethoxy)phenol we’ve ever produced, and we look forward to helping shape future successes across industries.