|
HS Code |
665772 |
| Chemical Name | 4-(1,1,2,2-Tetrafluoroethoxy) Phenol |
| Cas Number | 353-55-9 |
| Molecular Formula | C8H6F4O2 |
| Molecular Weight | 210.13 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 72-75 °C |
| Boiling Point | 226-228 °C |
| Density | 1.48 g/cm³ |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% (commercially available) |
| Storage Temperature | Store at 2-8 °C |
| Flash Point | 107 °C |
| Smiles | C1=CC(=CC=C1O)OCC(F)(F)C(F)F |
As an accredited 4-(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 | White plastic bottle containing 100 grams; tightly sealed, labeled with chemical name, hazard warnings, CAS number, and manufacturer information. |
| Shipping | 4-(1,1,2,2-Tetrafluoroethoxy) Phenol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is transported under ambient conditions with appropriate hazard labeling. Handling complies with safety regulations, protecting from moisture, heat, and physical damage during transit. Shipping methods align with local and international chemical transport standards. |
| Storage | Store 4-(1,1,2,2-Tetrafluoroethoxy)phenol in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers or bases. Protect from direct sunlight and moisture. Clearly label the container and ensure appropriate chemical spill containment is available. Use only in a fume hood or well-ventilated workspace. |
Competitive 4-(1,1,2,2-Tetrafluoroethoxy) Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Navigating the ever-evolving field of specialty chemicals demands both strong technical expertise and a practical understanding of how materials behave at the molecular level and in real-world applications. Developing and manufacturing 4-(1,1,2,2-tetrafluoroethoxy) phenol involves hands-on experience with fluorinated moieties, phenolic frameworks, and a consistent pursuit of purity and reproducibility. In practice, this compound serves both as a critical intermediate and as a performance enhancer in fields such as agrochemical formulation, electronic materials, and specialty polymer synthesis.
Here in the manufacturing plant, every step — from raw material qualification to final quality release — reflects lessons learned from years of running fluorination chemistry at scale. The distinctive property profile of this molecule stems from its tetrafluoroethoxy substituent. Four fluorine atoms on the ethoxy chain create a combination of high hydrophobicity, chemical inertness, and a distinct electronic effect on the phenolic ring. This sets up both synthetic advantages and practical considerations for downstream use.
Experience in chemical production reveals that handling perfluorinated ethers offers unique challenges. These compounds dislike variability in reaction conditions. A robust process controls water content, temperature drift, and even batch-to-batch subtlety in starting materials. Customers rely on our mastery of phase separation, vacuum distillation, and precision in catalyst charging to deliver product with minimal off-flavors, stable melting point, and no surprise peaks in the chromatogram.
Our team emphasizes traceable QC protocols backed by in-process monitoring. Any residual impurities can create headaches for downstream users, particularly in catalytic processes or analytical fields. Once, an upstream supplier changed a drying solvent without warning, triggering a week-long investigation into shifts in FTIR baseline. Lessons like these forge attention to detail and reinforce the value of handling all key steps in-house.
Long-term supply partnerships only work when each drum, each bag, each liter leaving the gate performs like the batch before it. Scale-up introduces surprises: sometimes minor agitation changes affect crystal habit, or a slight difference in reactor surface changes reaction rate. Consistent product gives formulators confidence to pursue demanding applications such as photosensitive resist additives or custom agrochemical actives.
Many customers ask how 4-(1,1,2,2-tetrafluoroethoxy) phenol differs from phenol itself, or from other alkoxy- or perfluoroalkoxy- substituted phenols. The difference starts at the molecular level. The tetrafluoroethoxy group is a bulky and strongly electron-withdrawing functional group. It sits at the end of a relatively flexible side chain, changing both reactivity and physical profile.
Contrast this with non-fluorinated phenolics, which often lack the hydrophobicity required for advanced coatings or the thermal stability for certain electronic uses. The tetrafluoroethoxy chain also distinguishes this product from mono-fluorinated or trifluoro versions, which do not provide the same degree of chemical inertness or resistance to oxidative attack. Chemists rely on this attribute to push the performance envelope — whether that means boosting resistance in polymer blends or prolonging the function of active pharmaceutical intermediates.
Another point is volatility and odor. Standard phenol and simple alkoxyphenols present risks in open processing due to vapor emissions, workplace complaints, and regulatory restrictions on both workplace exposure and finished product residuals. Tetrafluoroethoxy substitutions dial back volatility without driving up molecular weight excessively. This translates to safer handling and broader process compatibility.
In applications requiring strong hydrogen bonding, methyl or ethyl ethers of phenol lose value as they interrupt these interactions. The tetrafluoroethoxy chain, by contrast, offers a balance of hydrophobic push and electron-withdrawing pull, realigning the acid-base and solubility characteristics of the phenolic oxygen. In practice, this manifests as improved compatibility in crosslinked resins, better solubility for active dispersion in high-performance solvents, and greater process flexibility at manufacturers’ sites.
Manufacturers trust this compound because it stands up to challenge after challenge. Few building blocks can deliver both the electron-withdrawing strength and the non-stick characteristics that today’s advanced composites, semiconductor materials, and specialty coatings demand. Engineers and chemists in plants across the world value its combination of high purity and reproducible behavior in bench- and plant-scale reactions.
Year after year, the reality is clear: Choosing the right intermediate or additive in product design shapes not just final performance, but the ease and economics of manufacture. Working with 4-(1,1,2,2-tetrafluoroethoxy) phenol gives teams leeway to build more durable photoinitiators, tailor their surfactant or dispersant profiles, and engineer interfaces in ways that simple hydrocarbon chemistry can’t match.
Another subtle but crucial advantage involves regulatory and sustainability compliance. Fluorinated materials draw scrutiny due to environmental persistence concerns. Responsible manufacturers use generation- and application-specific risk assessments, rigorous emissions controls, and robust waste streams tracking to ensure safe stewardship from drum to device. Downstream users draw confidence from knowing their suppliers do not just focus on sales, but on full lifecycle management and regulatory alignment.
In recent years, collaborative projects between our technical teams and downstream partners have led to valuable process innovations. Sharing analytical methods to identify trace byproducts in high-purity applications, retooling solvent systems to maximize yield and minimize environmental load, and supporting users in regulatory filings all tie back to the knowledge built up in years of on-the-ground running of fluorinated-ether processes.
What sets 4-(1,1,2,2-tetrafluoroethoxy) phenol apart is its track record in high-barrier applications. Semiconductor fabrication, optical material synthesis, and leading-edge agricultural chemistry all place special requirements on intermediates. A simple impurity may short-circuit months of downstream work, especially in high-resolution photoresist formulations or pharmaceutical intermediate synthesis.
Over time, the feedback loop between laboratory-scale users and plant-scale producers gets tighter. Bringing on new clients from R&D labs often means closer scrutiny and higher expectations. Sharing benchmarking results, opening up production data, and fielding specific customized specifications — that kind of flexibility and technical dialogue only comes from manufacturers with day-to-day hands-on control over each lot.
End-use areas continue to expand, from robust non-stick coatings to fluorinated block copolymer architectures, to designer surfactants with low surface tension and high oxidative tolerance. Some customers use it as a coupling agent; others value its utility as a polymer stabilizer or as a starting point for advanced pharmaceutical active ingredients. Our understanding of its precise reactivity informs not only our own process design but our support for customers driving new applications.
Synthesizing and purifying 4-(1,1,2,2-tetrafluoroethoxy) phenol brings a set of real-world complications. For example, the exothermic nature of the etherification step means small miscalculations in temperature control can propagate through to the next distillation, raising work-up times and possibly requiring extra cycles of purification. Plants with an eye toward thermal balance and real-time monitoring avert these problems and keep sidestreams recyclable.
Another concern appears in the handling of gaseous fluorinated byproducts. Strong air abatement systems, paired with routine leak checks and scrubbing units, have become standard. Operators monitor emissions not just for regulatory compliance, but for plant safety and to maintain workplace air quality. These measures feed directly into sustainable production — a basic concern among both producers and buyers as scrutiny of PFAS-type substances grows worldwide.
In the warehouse, proper material handling makes or breaks an efficient operation. Tetrafluoroethoxy-substituted phenols show low reactivity with standard container materials, but long-term storage behavior still depends on controlled humidity and temperature. This attention to physical stability ensures long shelf life and trouble-free on-site transfer, a point that downstream users value for integration into their logistics flows.
Kilogram-to-metric-tonne scale-up exposes unplanned hiccups. Careful scale-down and stress-testing help smooth transitions between laboratory and plant production runs. Sometimes subtle rate changes, temperature ramps, or agitator settings resolve problems that neither process simulation nor simple scale arithmetic foresee. Ongoing optimization forms the basis for both reliability and innovation, benefiting users as well as manufacturers.
In recent years, regulatory agencies and industry groups have pushed for more transparency around fluorinated intermediates in the supply chain. Our response involves full-spectrum traceability from raw material acquisition through closed-loop production and analytical release. Documenting batch genealogy, routine impurity profiling, and detailed process logs arm clients with the information they require for product registrations and compliance dossiers.
Innovation in purification has been a key driver for improved cost-position and supply reliability. Our process chemists re-examine solvent systems, distillation cut points, and chromatography protocols to tighten specifications and address client feedback on purity and consistency. As new product grades emerge for ultra-high purity electronics, medical uses, and niche performance chemistry, we adapt by modifying protocols rather than relying on borrowed off-the-shelf processes.
Collaboration forms the core of our approach. Whether the industry is pushing for lower impurity specifications, faster delivery on pilot-scale lots, or more detailed environmental data, we engage technical and production teams to ensure changes are reflected throughout the process, not tacked on at the end. That hands-on philosophy comes directly from years of close work with operational chemists and engineers — our own included — who see both the practical issues and the long-term opportunities.
Regulatory headwinds, changing compliance expectations, and shifts in customer product profiles mean this class of compounds faces continual evaluation for both risk and opportunity. Our work does not stop at meeting specification sheets; it continues into supporting client innovation, troubleshooting technical questions, and responding to market signals with process improvements and knowledge sharing.
Chemists and engineers designing new products do not work in isolation; they benefit from feedback rooted in actual production realities. The resin chemist troubleshooting solubility, or the process development team benchmarking thermal stability, both draw on supplier knowledge as much as published literature. Publishing reaction constraints, providing sensory feedback from actual product trials, and disclosing solution behavior in real solvents allows technical conversations to move forward with confidence.
One of the most rewarding aspects of making 4-(1,1,2,2-tetrafluoroethoxy) phenol involves the open dialogue between makers and users. Sometimes a product that met specification two years ago needs tuning as downstream application methods evolve. We routinely tune process parameters, review data from client labs, and shift quality release points. That flexibility and responsiveness prove crucial in building partnerships that last across product generations.
Feedback on application performance sometimes surprises. What looked like a minor impurity on the spec sheet may show up as haze in a polyurethane blend or as an inhibitor in a UV-cure system. Real-time sharing of issues — and collaboration on root causes — delivers practical results faster than any abstract data exchange. It also builds trust: clients understand that a manufacturer handling problems head-on becomes a partner in technical and commercial progress, not just a supplier of a commodity.
Day-to-day, refining the process for 4-(1,1,2,2-tetrafluoroethoxy) phenol becomes a technical challenge and a business driver. Changing global demand, new regulatory focus on fluorinated substances, and the push to reduce process environmental impact drive ongoing optimization of every part of our system — from raw material sourcing and energy consumption to end-of-pipe controls. Innovating with green chemistry and investing in energy efficiency not only answers immediate regulatory questions but future-proofs the product offering.
Working with partners who understand that process capability ties directly to supply chain resilience, quality stability, and costs keeps both sides competitive. Each round of process improvement — whether a tweak to purification, a logistics breakthrough, or a new analytical method — adds value from the production line to the customer’s finished goods. We see every product shipment as an opportunity to reinforce that bond, provide technical support, and capture new application knowledge for the cycle to continue.
Moving forward, the link between technical insight and practical know-how only deepens. Users can count on steady access to a trusted specialty intermediate, backed by a manufacturing partner that understands the chemistry, the process variables, and the importance of clear, honest communication.
Materials like 4-(1,1,2,2-tetrafluoroethoxy) phenol might never become household names, but they underpin innovation across many industries that shape our daily lives. Manufacturing and supplying this compound at scale relies on technical rigor, attention to detail, and a continuous conversation between the plant floor and the lab bench. Customers value not just what arrives on the shipping dock, but the deeper skill set and know-how that make reliable, high-purity production a reality.
Through decades of practical experience and a commitment to ongoing improvement, our team continues to help our partners solve tough molecular puzzles, bring new products to market, and respond to a world where the chemistry — and the expectations — grow more sophisticated year after year.