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HS Code |
505050 |
| Cas Number | 461-80-3 |
| Molecular Formula | C8H3FO3 |
| Molecular Weight | 166.11 g/mol |
| Iupac Name | 5-Fluoro-1,3-isobenzofurandione |
| Synonyms | 5-Fluorophthalic anhydride |
| Appearance | White to light beige crystalline powder |
| Melting Point | 70-72°C |
| Boiling Point | 283°C (estimated) |
| Density | 1.54 g/cm³ (estimated) |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC2=C(C=C1F)C(=O)OC2=O |
As an accredited 5-Fluoro-1,3-Isobenzofurandione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a white screw cap, labeled "5-Fluoro-1,3-Isobenzofurandione" and hazard warnings. |
| Shipping | 5-Fluoro-1,3-Isobenzofurandione is shipped in tightly sealed containers, protected from moisture and light. It is transported as a hazardous chemical, complying with relevant regulations (such as DOT, IATA, or IMDG). Proper labeling and documentation are required. Handling precautions include avoiding inhalation, ingestion, or skin contact, and using appropriate personal protective equipment (PPE). |
| Storage | 5-Fluoro-1,3-Isobenzofurandione should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep it separate from incompatible substances such as strong bases and oxidizing agents. Ensure proper labeling, and store at room temperature. Use chemical-resistant containers and follow all local regulations for chemical storage and handling. |
Applications of 5-Fluoro-1,3-Isobenzofurandione in Industrial Manufacturing5-Fluoro-1,3-isobenzofurandione acts as a key intermediate in various chemical manufacturing segments. As the original producer, we supply this raw material for multiple specialized downstream utilizations across high-value industrial fields. The following sections detail its application in well-defined industrial processes, including compliance, blend ratios, process integration points, and the range of finished products by field. 1. Pharmaceutical Active Ingredient SynthesisMajor pharmaceutical manufacturers use 5-fluoro-1,3-isobenzofurandione as a fluorinated phthalic anhydride derivative for synthetic routes in antihypertensive, antiviral, and antineoplastic APIs. This compound enters the process during functionalization stages, introducing fluorine moieties known for modifying pharmacokinetic properties. Only regulated pharmaceutical-grade batches pass batch-release and traceability controls before API conversion, ensuring compliance with monographs and strict impurity profiles. Finished APIs include several modern drugs targeting resistant hypertension and liver carcinoma, where molecular stability requires fluorinated anhydride intermediates. Industry compliance standards
Typical usage ratio
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2. Specialty Polyimide Resin ManufacturingLeading manufacturers in high-performance polymer markets utilize this compound as the fluorine-functional monomer in specialty polyimide synthesis. Its inclusion raises thermal resistance, lowers dielectric constant, and improves chemical stability required in electronics and aerospace-grade plastics. Processing occurs in controlled polymerization environments, adhering to industrial polyimide guidelines for volatile monomer handling and emission abatement. End-users require detailed Certificates of Analysis to satisfy raw material audits before resin conversion. Industry compliance standards
Typical usage ratio
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3. Agrochemical Synthesis for Fluorinated HerbicidesAgrochemical manufacturers use this compound as an advanced intermediate for selective fluorinated herbicide molecules. The fluorine-modified aromatic is incorporated to enhance field stability, selectivity, and environmental persistence. Synthesis steps demand closed-system handling with intermediates tracked for residue and traceability. Compliance focuses on environmental regulations regarding synthesis by-products and batch-specific impurity release. The product enters multi-step processes for constructing core herbicidal rings before final coupling and formulation. Industry compliance standards
Typical usage ratio
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4. Electronic Chemical Synthesis for Photoresist MonomersProducers of semiconductor processing chemicals employ this raw material as a functionalized monomer in high-purity positive photoresists. The anhydride group contributes to enhanced etch resistance and pattern fidelity required by advanced semiconductor lithography. Handling and incorporation follow electronic chemical GMP and purity controls to meet semiconductor manufacturing requirements for metal traces, ionic impurities, and residual solvents. Only lot-specific, ultra-high purity grades integrate into positive photoresist polymer backbones for next-generation chip production. Industry compliance standards
Typical usage ratio
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In the world of chemical manufacturing, the stories behind specialty intermediates often go untold, and that’s a missed opportunity. Over the years, we have come to appreciate that 5-Fluoro-1,3-Isobenzofurandione isn’t just another entry on a long list of fluorinated phthalic anhydrides. In actual production, this compound has played a pivotal role for everyone from pharmaceutical researchers to polymer engineers, and its subtle differences from other anhydrides matter more than most realize.
5-Fluoro-1,3-Isobenzofurandione, commonly recognized by its CAS number 1673-89-8, brings the specific reactivity of a fluorinated anhydride to the laboratory and plant floor. Its chemical structure—phthalic anhydride substituted at the 5-position with fluorine—sets it apart from its siblings in very tangible ways during applications. At the molecular level, fluorine’s electron-withdrawing power enhances the molecule’s reactivity profile, letting it take part in transformations that prove too demanding for plain phthalic anhydrides.
Through repeated cycles of synthesis, we have fine-tuned the process parameters that ensure a consistent melt point, confirm purity (over 99%) by GC and NMR, and achieve flow behavior compatible with modern high-throughput installations. Consistency means different things to different users. In pharmaceutical R&D, where people run reactions on a milligram scale before scaling, a batch with impurities will not only stall a project but could cut off years of work.
From our experience, packing this compound at the right moisture level prevents hydrolysis, which can occur readily if packaging isn’t air- and moisture-tight. The shelf life, which sometimes gets overlooked when specifying similar anhydrides, is critical here due to the presence of fluorine, which catalyzes slow decomposition in adverse storage conditions. Our focus always lands on protecting the chemical from ambient humidity during blending and packaging, using tested barriers and proper secondary containment.
5-Fluoro-1,3-Isobenzofurandione doesn’t play the same role as the standard phthalic anhydride you find by the drum in old resin plants. The fluorine substitution transforms its chemical personality. Chemists who have used plain phthalic anhydride often try to push the limits with ring substitutions, but without proper fluorinated analogs, many promising reaction routes fall flat at the pilot stage.
On the ground, we’ve seen firsthand how this compound’s increased electronegativity opens the door to nucleophilic aromatic substitutions that lag with unsubstituted compounds. New pharmaceuticals often require introducing fluorinated moieties to adjust metabolic stability and receptor binding. 5-Fluoro-1,3-Isobenzofurandione gives formulators a more accessible entry point for aryl-fluorinated functionalities because it undergoes ring opening and condensation under milder conditions, with fewer side products.
Polymers present another compelling case. Recent projects in high-durability copolyimides depend on selective addition of fluorinated phthalic anhydrides to balance thermal performance and flexibility. Our technicians learned quickly that standard phthalic anhydrides could not foist off the same level of stability—polyimides built on regular anhydrides broke down more quickly under test protocols. The 5-Fluoro derivative’s tight molecular geometry added both stiffness and heat resistance in repeat tests, passing qualification standards in multiple regions where competitors’ samples failed.
Customers sometimes ask whether 4-Fluoro-1,3-isobenzofurandione would do the same job. The truth, surfaced after several experimental batches, is that the substitution pattern matters. At the 5-position, fluorine places its effects in line with desired ring activation for follow-on modifications, while 4-position fluorine often frustrates regioselective synthesis downstream.
It’s easy to treat fine chemicals as commodities if you’ve never seen a synthetic route crumble due to an uncharacterized impurity. Over our years in the field, strict control over sides, non-fluorinated anhydride analogues, and ortho-isomers in finished batches saved more than one customer from discarding failed experiments. The margin for error narrows as regulatory scrutiny heightens. Projects with final applications headed for human therapeutic use face downstream audits, which dissect synthetic routes for compliance and trace impurities.
Staff at the reactor know the difference between a batch that tracked tightly to reaction endpoints and one that lingered, risking double fluorination. Consistent NMR trace spectra, IR signatures, and an eye for moisture levels contribute more to reliability than any fancy branded drum. Our protocols cut down post-processing drying steps, which means lower risk of decomposition and lower cost per kilo for labs and scale manufacturers running continuous campaigns.
5-Fluoro-1,3-Isobenzofurandione doesn’t forgive lapses in temperature control. Our technical team keeps a close eye on reactor heat profiles, especially during acylation. High-purity fluorine sources can amplify corrosion inside steel vessels; we learned to line all contact surfaces with Teflon or glass-lined steel, or accept the cost in unplanned downtime.
Waste handling presents its own puzzle. Fluorinated byproducts call for special attention during neutralization—standard base quench methods applied in non-fluorinated runs lead to incomplete destruction of fluorinated organics if left unchecked. Staff follow designated procedures, verified through monthly audits, reducing risks to both operators and the receiving water stream.
Even the simple act of transferring finished product to storage takes extra care. Our team vacuums off remaining vapors and double-checks seals on containers. No matter the efficiency of synthesis, physical handling at the margins shapes the overall safety profile of the compound’s lifecycle.
Direct user feedback has shown where this molecule justifies its cost. For example, in agrochemical research, 5-Fluoro-1,3-Isobenzofurandione grants an edge when testing lead candidates with complex binding requirements. Its reactivity pattern overcomes sluggishness in earlier-generation analogs, letting R&D teams move through candidate lists faster than before.
Polymer research groups consistently report a boost in thermal decomposition limits for samples prepared with our batches. One team scaled a polyimide program from gram benches to ton jars without revalidating for loss of fluorine content, crediting the stability of the molecule through months of storage.
In medicinal chemistry, integrating 5-fluorophthalimide cores into new drug frameworks has become popular as regulatory agencies seek metabolic stability paired with selective distribution. Teams have cited our batches for reliable conversion and clean downstream splitting, which remains a challenge for materials jammed with impurities or side-chain anhydrides.
After so many years with this compound, the key difference from simple anhydrides lies in the knowledge of what small impurities can do. Formulators chasing specific performance have told us stories of failures with cheaper, low-assay grades from unverified makers—yields crashed, unexpected byproducts clogged columns, and projects missed deadlines. By refusing to compromise on assay or try cutting corners with less expensive fluorinating agents, we guarantee certainty from gram to multi-ton runs.
Another area that sets us apart is trace documentation. Worker logs, syntheses history, and batch records accompany every lot for customers. Some may see extra records as just paperwork, but the first time a downstream client faces a regulatory inspection, they express relief at having a complete package of information. We’re not immune to paperwork fatigue, but a thorough documentation protocol means product lots stay traceable, and problems get traced back in days, not weeks.
Safety remains a practical challenge. This is not a compound you dump and walk away. Fluorinated anhydrides can negatively react with ambient moisture—some vendors offer only loosely capped bottles, but by keeping air exposure to absolute minimum during filling and sealing, we maintain batch integrity for the long haul. Delivering product with documented residual moisture levels isn’t just about meeting customer specification—over time, dry, well-sealed product means consistently clean chemistry downstream.
Each year brings new requests from downstream innovators pushing for improved reactivity, higher purity, or specialized labeling for regulatory filings. Industry-wide, requirements for green chemistry push processes away from certain reagents and toward less polluting or more efficient routes. Through long partnership with raw material suppliers, we source high-purity fluorine under tightly controlled logistics, and our in-house development chemists regularly optimize for yield while reducing process waste.
Customers have asked whether we plan to offer custom salt forms or preblended intermediates; our answer, rooted less in commercial instinct and more in practical lab insight, depends on proven technical stability. If blending with inhibitors or co-reactants yields only marginal benefits, we stick to the single-component product until stability is thoroughly demonstrated.
On-site safety training goes beyond regulatory checklists. Drills for handling spills, improvements in ventilation, and investment in automatic monitoring systems stem directly from our commitment to both community and client. To those who think chemicals like these can be commoditized, our view remains: long-term value grows from compound dependability, production integrity, and willingness to share technical know-how.
There’s a reason customers turn away from more common anhydride analogs despite their wider availability and lower cost. In real-world R&D, the additional fluorine at the 5-position amplifies selectivity, creating reaction pathways inaccessible to ortho- and unfluorinated phthalic anhydrides. Researchers using less specialized compounds spend far longer optimizing conditions. They sometimes chalk up their frustration to poor methods, not realizing substituent effects at the molecular level block their progress. Years of comparative test data in our facilities back this up—each additional layer of purification, every added separation step downstream, erodes the time and cost advantages of sourcing a “cheaper” analog.
Some have experimented with multi-fluorinated derivatives, betting that additional fluorines would bolster stability or reactivity. Feedback from these cases shows that extra substitutions often knock out fine control over reactivity, boosting unwanted side reactions instead. The single 5-position fluorine appears, after much hands-on research, to thread a needle: boosting reaction rate and selectivity without blowing apart synthetic windows with excessive electron withdrawal.
Another difference from brominated or chlorinated analogs lies in regulatory friction. Global regulations increasingly scrutinize chlorinated and brominated compounds for environmental persistence. Many teams are now requesting fewer halogenated impurities, both for compliance reasons and to anticipate future regulatory shifts. 5-Fluoro-1,3-Isobenzofurandione stands out as a preferred choice, being less persistent and easier to track during environmental testing.
The working chemist’s first experience with 5-Fluoro-1,3-Isobenzofurandione usually comes in the midst of a tough route screening or a stubborn formulation puzzle. Expectations run high; any letdown costs time and dollars. We’ve heard stories about failed reactions traced back to off-label sources whose batches didn’t hold up under scrutiny. Ours comes straight from plant reactors running controlled conditions, followed by scrupulous QA checks—melting range, spectral fingerprint, HPLC or GC confirmation, and trace metals checked down to low ppm.
As a manufacturer, we see that the true problem isn’t so much supply as consistent supply. Local incidents—weather interruptions, supply-chain hiccups, or regulatory re-inspections—can scatter timelines and strain customers’ program goals. Our on-site storage, double-redundant supply, and relationships with raw material providers mean we haven’t missed a scheduled shipment since the mid-1990s. Finding dependable partners, both upstream and downstream, turns a hazardous specialty product into a reliable tool for the customer base.
Once an order is placed and a batch readied, our engagement doesn’t stop at delivery. Technical staff follow up with laboratories to confirm the compound’s match for the intended method. Sometimes that includes working directly with R&D personnel to troubleshoot unexpected reaction profiles or help substitute solvents and reagents for improved purity downstream. No off-the-shelf specification covers all eventualities in multi-step syntheses, which is why our application chemists routinely review process plans with customers. Should a new regulation require updated hazard documentation, we support users in preparing filings on timeline.
Our commitment extends to packaging. No order leaves the site without verified seals, minimal headspace to prevent hydrolysis, and moisture-check protocols logged by serial number. Long-term relationships are built on straightforward support: the customer knows exactly what went into the batch, when it was packaged, and what QC checks confirmed its content and stability.
Over dozens of projects, the most successful applications have come when the manufacturer stays available as a partner, not just a supplier. Even outside standard hours, we take questions about storage, process, or post-use neutralization—because the difference between a successful experiment and a scrapped order often lies in timely advice and clear data.
Quality reverberates down the line. Customers challenged to prove reproducibility for scale-up runs depend on a single-source batch record that ties all variables from raw material to packed bottle. Universities developing new routes for active pharmaceutical ingredients often require extra spectral data and run side-by-side comparisons with commercial lots—those who source from us tend to see lower dropout rates at process validation. In regulatory filings, inspection teams now ask more detailed questions about provenance of all reagents along the synthetic route. Batches originating from documented, in-house lines face fewer delays.
From environmental stewardship to operator safety, our role doesn’t just end at producing 5-Fluoro-1,3-Isobenzofurandione to a stated specification. We sit down regularly to revisit and revise protocols, bringing in third-party auditors and adopting new monitoring tools. By minimizing fugitive emissions, automating cleaning, and closing open-system transfer points, we target both quality improvement and environmental risk reduction across the plant.
Expectations for specialty intermediates keep rising. Whether a customer’s focus lies in polymer high-performance composites, new frameworks for small-molecule pharmaceuticals, or the next generation of herbicides, consistent supply of reliable chemicals underpins their progress. With 5-Fluoro-1,3-Isobenzofurandione, demands for tight substitution patterns, trace control, and exceptional purity lie at the center of daily operations. Hearing about breakthroughs achieved because our material performed as described confirms the investment in careful process engineering.
Ultimately, we view our role as something a little deeper than producing a commodity: we’re active partners, working to bring new capabilities to chemistry, one validated batch at a time. Every molecule that passes through our plant carries a backstory of technical choices, real-world feedback, and pride in helping find solutions to the most difficult synthesis questions.