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HS Code |
118937 |
| Iupac Name | 1-Phenyl-1,1,2,2,3,3,4-heptafluorobutan-1-one |
| Cas Number | 350-14-3 |
| Molecular Formula | C10H3F7O |
| Molecular Weight | 274.12 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 136-138 °C at 760 mmHg |
| Density | 1.543 g/cm³ at 25 °C |
| Melting Point | -13 °C |
| Refractive Index | 1.386 |
| Flash Point | 64 °C |
| Solubility In Water | Insoluble |
| Synonyms | Heptafluorobutyrophenone |
| Ec Number | 206-495-0 |
As an accredited (Heptafluorobutyro)Phenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL amber glass bottle with tamper-evident cap, chemical label displaying “(Heptafluorobutyro)Phenone,” hazard symbols, and handling instructions. |
| Shipping | (Heptafluorobutyro)phenone should be shipped in tightly sealed containers compatible with fluorinated organics. It must be packed according to hazardous material regulations, avoiding sources of heat or ignition. Transport should be via licensed carriers with appropriate hazard labeling and documentation. Handle with gloves and goggles, and ensure compliance with all relevant local, national, and international shipping regulations. |
| Storage | (Heptafluorobutyro)phenone should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from moisture, heat, and ignition sources. Protect from light and incompatible substances such as strong oxidizers. Use proper chemical storage cabinets, and clearly label the container. Always follow all relevant safety regulations and guidelines for storage. |
Applications of (Heptafluorobutyro)Phenone in Industrial Manufacturing(Heptafluorobutyro)phenone is utilized by advanced chemical manufacturers across select specialized industries. Our facility delivers consistent batch quality, allowing B2B customers to comply with stringent downstream process requirements. The following application segments outline established uses by sector, integrating compliance, dosage, process flow, and finished product considerations. 1. Fluorinated Pharmaceutical Intermediate Synthesis(Heptafluorobutyro)phenone functions as a key intermediate in the synthesis of select fluorinated pharmaceutical compounds, especially for active pharmaceutical ingredients requiring high fluorine content. It enters as a building block for carbonyl-functionalized aromatics, influencing pharmacokinetics and metabolic paths. Process lines control moisture and temperature to stabilize reactive intermediates, safeguarding product integrity throughout multi-step synthesis. Industry compliance standards
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2. Advanced Liquid Crystal Material ProductionManufacturers harness (heptafluorobutyro)phenone for synthesizing high-performance liquid crystal materials, benefiting from its rigid, electron-withdrawing structure. Its incorporation targets nematic phase stability and enhances dielectric anisotropy. Processing occurs under dry nitrogen, using phase-transfer catalysis for high-purity intermediates suited to large-scale LCD panel material output. Industry compliance standards
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3. Photoinitiator and Photoacid Generator ManufacturingThe material is critical in synthesizing commercial photoinitiators and photoacid generators deployed in UV-curable resins, inks, and microelectronics. Its high fluorine density provides superior volatility control and UV absorption tuning. Batch processes require precise addition in the reaction setup for aryl–trifluoromethylation, monitored via HPLC or GC-MS for trace-level impurity control. Industry compliance standards
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4. Specialty Polymer Surface Modification AgentsDirect users in the high-performance polymer sector select this compound to introduce fluorinated aromatic residues onto polymer surfaces via grafting or copolymerization. It enhances surface energy, solvent resistance, and dielectric properties for engineering plastics and films. Only nitrogen-purged, jacketed reactors meet required safety and purity for the coupling step, and continuous inline FTIR checks verify process targets. Industry compliance standards
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(Heptafluorobutyro)Phenone draws a lot of attention in the roster of fluorinated ketones. Chemists know this molecule by its distinct properties, which come from its seven fluorine atoms attached to a four-carbon butyro group, conjoined with a phenone core. As manufacturers, our close connection to the synthesis process gives us a detailed look at what sets this substance apart in labs and production lines.
Producing (Heptafluorobutyro)Phenone demands rigorous control at every stage. Our team has invested in process monitoring, and batch consistency checks. We take samples during key phases to verify structure and purity through NMR and GC-MS, because any minor deviation can affect downstream reactions. The physical form—usually a clear to pale yellow liquid—helps with visual inspections during quality control. Experience tells us that when the color shifts, impurities or by-products are often at play, alerting our staff before formal analysis even begins.
We use high-purity starting reagents and a closed system to control contamination risks. The reaction itself runs under inert atmosphere to prevent moisture or oxygen from spoiling yields. Typical specifications for (Heptafluorobutyro)Phenone include a purity of no less than 99%, since lower purity creates complications in sensitive pharmaceutical and agrochemical syntheses. Final packaging steps use amber glass to shield the compound from ultraviolet light, a lesson learned from several batches degraded by warehouse skylights in previous years.
Lot-to-lot consistency comes down to process discipline. Our senior operators know, for example, that a longer reaction time at a reduced temperature improves selectivity and eases purification. They track yield drift and identify where operator technique matters—manual handling of sensitive intermediates makes the difference more often than SOP writers would like to admit.
Those seven fluorine atoms do more than add weight; they bring chemical stability and lipophilicity that most non-fluorinated analogs cannot match. The high electronegativity of fluorine pulls electron density from the carbon skeleton, making the phenone core both less reactive and more interesting to medicinal chemists looking for metabolic stability. Over the years, we have partnered with R&D teams in both pharma and crop science, who come to us after exhausting standard phenones that either break down too fast or show insufficient activity.
Customers share clear success stories. Several agrochemical projects hit milestones only after switching to heptafluorobutyro substitution, which protected the core structure in field trials plagued by photodegradation and microbial attack. Our technical sales group spends time reviewing lab data and real-world test results, then relays feedback so we can tweak specs or handling instructions as new application nuances emerge. It is not just about meeting a static standard; our focus lies in reinforcing support from the chemist’s bench to the pilot plant.
(Heptafluorobutyro)Phenone sees extensive use in advanced synthesis, particularly where standard phenones break down or react too freely. API development groups favor it during lead optimization, because the presence of fluorine tends to suppress metabolic pathways that would strip or modify the phenone. Unlike generic phenyl ketones, the heptafluorobutyro variant stays intact longer in biological assays. More stability means fewer re-runs, lower sample losses, and less wasted time—a difference only regular users truly appreciate.
Material scientists approach us for its high thermal and chemical resistance. In one battery electrolyte project, replacing a non-fluorinated analog with our product eliminated the formation of a troublesome by-product. Researchers reported that this shift let them scale pilot runs with much lower risk of hazardous side reactions. The broad adoption in this sector owes much to real-world trial-and-error rather than abstract theoretical promise; our job involves constant troubleshooting and adapting to lab findings reported by customers worldwide.
Owing to its volatility profile and solubility traits, (Heptafluorobutyro)Phenone gives process chemists a flexible platform for multi-step synthesis. Its resilience in the presence of strong acids and bases widens the operational window for key transformations. Years ago, we received batches of criticism about vapor losses in open reactors. Since then, we recommend using sealed systems and offer best-practice guidance for headspace monitoring to stem unnecessary yield losses.
Decades of experience in chemical packaging make us shine where off-the-shelf distributors falter. Standard drum and bottle materials can leach or degrade in contact with highly fluorinated organics; we choose specific high-barrier polymers and pre-test all closure materials with simulated storage conditions. Years ago, a poorly designed cap cost a pilot campaign thousands in lost inventory after an unnoticed vaporscape led to product loss. Since tightening these protocols, customer complaints on container integrity have fallen to near zero.
Routine storage guidance—keep sealed, out of direct sunlight, below 30°C—comes from hard lesson not from generic templates. On several occasions, extended high-temperature storage warped seals and let air into containers, degrading content over time and confusing buyers. Proactive contact with our users unearthed these pain points early, letting us adjust shipment and warehouse instructions before problems started eating into profits or timelines. Technical bulletins on pitfalls and prevention bore fruit through repeat orders rather than paperwork.
One challenge with fluorinated ketones relates to worker safety. Our production staff wears specialized gloves and respiratory gear during high-volume operations, since overexposure can irritate skin or respiratory tracts. We engage occupational health teams and share risk learnings with our professional clients, many of whom install additional engineering controls on our recommendation. A direct approach to sharing real incidents—rather than just MSDS sheets—has done more to build trust and protect users than years of generic compliance checklists.
Comparing this compound to less-fluorinated or hydrocarbon ketones reveals its distinct role. The heavy fluorination not only influences boiling and melting points—it shapes reactivity patterns, environmental fate, and safety protocols. We have conducted controlled side-by-side trials—not just literature reviews—that show conventional methyl or acetyl phenones degrade quickly or persistently off-gas under even moderate storage conditions, while the heptafluorobutyro group brings resilience and cleaner mass spectra.
Competitors often offer lower-fluorinated analogs, touting easier synthesis, but customers inevitably return to our product when they need predictable performance under demanding chemical regimes. In one instance, a manufacturer of specialty intermediates switched back to our compound after their downstream yield cratered by over 20% using a shorter fluoro-chain alternative. They cited superior process-throughput and waste reduction—which we confirmed through shared batch records.
(Heptafluorobutyro)Phenone shows a unique combination of low nucleophilicity and steric shielding. In cross-coupling and Friedel–Crafts-type reactions, its reduced reactivity to attack saves costs by curbing side products. Labs running environmental exposure studies echo anecdotes from large-scale buyers: the compound’s persistence in soil, while controlled, can be mitigated with photolysis steps or managed incineration, and our technical staff assists with thoughtful disposal planning. Unlike simpler ketones, this molecule demands a different mindset from users, one that aligns with safety, performance, and stewardship across sectors.
Our experience leads us to invest heavily in process optimization. As raw material pricing for fluorinated compounds remains volatile, we monitor supply chains closely and secure long-term agreements to guarantee uninterrupted plant operations. Where early batches sometimes showed variable color or odor, we overhauled purification columns and adopted better drying techniques, greatly improving shelf stability and appearance. Old records from the plant floor underscore that even minor process levers—particle size of reagents, water content, agitation speed—reshape product outcome. Continuous operator training and hands-on oversight outperform automation alone.
Our approach includes scenario planning, from raw material shock to rare customer usage accidents. Over years, product recalls have been exceptionally rare, not due to luck but from early detection systems embedded at QA/QR checkpoints. Any off-spec findings trigger root-cause investigations managed directly by our seasoned supervisors. Unlike volume resellers or casual handlers, a manufacturer’s direct engagement with feedback reveals failure patterns, so fixes happen before field escalation tarnishes reputation.
To meet evolving regulatory and sustainability standards, we've focused on green-chemistry enhancements without sacrificing batch consistency. Through research partnerships, we're piloting methods to recover and recycle process fluorides, closing loops and easing environmental impacts. Pressures to curb emissions and shrink waste affect our decisions on solvent choices and energy supply, and by tracking emissions, we align with best-in-class environmental norms, reflecting conscious stewardship as the market expects.
Direct relationships with laboratories and downstream producers anchor our ongoing improvements. We have dedicated field technical representatives who visit customer sites, review procedural setups, and provide troubleshooting. These team members pass practical intelligence from the user environment—clogged lines, glassware etching, filter fouling—directly back into our process design. Customer pain points shape not only batch standards but also how we instruct end-users, how we design containers, and how we time deliveries to match lean inventory systems downstream.
Feedback loops translate into revised handling protocols or upstream purification tweaks. A program we rolled out last year asks for post-delivery feedback within thirty days, usually catching minor handling or storage confusion before it becomes costly. Customers find value in this manufacturer-direct approach; they gain fast, fact-backed troubleshooting, not canned advice off a PDF. Our best product improvement ideas come from these conversations—not from an echo of site audits or sales pitch cycles.
Manufacturing (Heptafluorobutyro)Phenone presents ongoing challenges and rewards that reflect the high standards of today’s specialty chemical industry. The drive for purity, reliability, and responsible operation emerges from a mix of technical know-how and hard-won lessons learned through years at the production line. The specifics—control of each fluorine addition, attention to worker safety, relentless tracking of storage environments—shape a real difference for customers, evident not just on lab reports but across the full journey from raw material to end application.
Broad familiarity with both intended uses and typical hurdles gives us the drive to go beyond routine supply, to act not as distant vendors but as partners invested in our customers’ ongoing success. We regard every feedback, every technical challenge as a cue to respond and refine. By retaining a direct, hands-on approach and investing in both process innovation and people, we continue to earn our place as trusted suppliers in this demanding field.