|
HS Code |
141901 |
| Chemical Name | 4-Fluorophenyl Acetate |
| Molecular Formula | C8H7FO2 |
| Molecular Weight | 154.14 g/mol |
| Cas Number | 454-13-3 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 41-43°C |
| Boiling Point | 229-231°C |
| Density | 1.21 g/cm3 |
| Solubility | Slightly soluble in water |
| Purity | Typically >98% |
| Storage Temperature | Store at room temperature |
| Smiles | CC(=O)OC1=CC=C(C=C1)F |
As an accredited 4-Fluorophenyl Acetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g quantity of 4-Fluorophenyl Acetate is packaged in a sealed amber glass bottle with a secure screw cap. |
| Shipping | 4-Fluorophenyl Acetate is shipped in tightly sealed chemical-resistant containers under ambient conditions. It should be clearly labeled and handled according to standard chemical safety protocols. During transit, packages must be protected from physical damage, extreme temperatures, and moisture. Compliance with local and international regulations for shipping chemicals is required. |
| Storage | 4-Fluorophenyl acetate should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it separate from strong oxidizing agents and incompatible materials. Store at room temperature and protect from moisture. Clearly label the container and ensure it is kept out of reach of unauthorized personnel. |
Applications of 4-Fluorophenyl Acetate in Industrial Manufacturing4-Fluorophenyl Acetate serves as an intermediate in several targeted processing routes within specialty chemical synthesis, fragrances, pharmaceutical precursors, and fine chemical end-products. Below, we detail representative downstream applications emphasizing actual industry adoption, regulatory standards, formulation considerations, processing integration, and real end-use types. 1. Pharmaceutical Intermediate Synthesis: Non-Steroidal Anti-Inflammatory Drug (NSAID) ProductionAs a key building block for specific NSAID molecules, 4-Fluorophenyl Acetate integrates into the synthetic route during active pharmaceutical ingredient (API) assembly. Synthetic chemists use it mainly in nucleophilic substitution reactions to introduce fluorinated aromatic groups that modulate bioactivity. Strict adherence to quality benchmarks is critical throughout processing, and residue monitoring ensures compliance for downstream human use APIs. Industry compliance standards
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2. Aroma Chemical Manufacturing: Synthesis of Fluorinated Ester Fragrance IngredientsProducers of specialty fragrance compounds use 4-Fluorophenyl Acetate as a starting material in the construction of rare-fluorine aromatic esters. Its reactivity enables downstream conversion to complex fragrance esters with increased volatility, longer-lasting top notes, and unique olfactory properties prized in luxury perfumery. Attention to IFRA and REACH rules is required due to the introduction of fluorinated aromatics. Industry compliance standards
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3. Agrochemical Synthesis: Herbicide Precursor ProductionDownstream agrochemical manufacturers rely on 4-Fluorophenyl Acetate as a coupling partner for formulating fluorinated phenoxyacetic acid derivatives, which display improved leaf uptake and tailored selectivity in modern post-emergent herbicide formulations. Recipe balancing and impurity monitoring are conducted in accordance with global agrochemical regulations and product registration requirements in major agriculture markets. Industry compliance standards
Typical usage ratio
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4. Specialty Polymer Modification: Incorporation in High-performance Co-polyestersIndustrial polymer producers employ 4-Fluorophenyl Acetate to introduce fluorinated aromatic units into co-polyester chains, targeting enhanced chemical resistance and thermal properties for engineering plastics. Stringent monitoring of additive content and polymer-RoHS compliance is observed to satisfy demanding downstream applications such as electronics encasings, filtration membranes, and automotive components. Industry compliance standards
Typical usage ratio
Downstream process integration
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Working in chemical synthesis for over a decade, we have handled a broad range of phenyl acetates and fluoroaromatic compounds. Among them, 4-Fluorophenyl Acetate (model: 4-FPA) stands out for its clean profile and distinct applicability in research and manufacturing. Our team values this compound for its unique chemical balance—a stable ester bond paired with the strategic placement of a fluorine atom on the aromatic ring. Its code in our plant's order system is 4FPA-101.
Our chemists produce 4-Fluorophenyl Acetate as an off-white crystalline powder, exhibiting sharp melting and consistent solubility. We maintain a purity threshold above 99% by GC and NMR checks. Moisture content always stays below 0.5%, and typical batch yields stay close to 98%. We have invested in tight control over melting point and color because such minor details, drawn from real plant experience, keep downstream reactions manageable and yields reliable.
The key molecular formula for 4-Fluorophenyl Acetate is C8H7FO2, and the CAS registry number is 459-64-3. We select high-purity acetic anhydride and 4-fluorophenol as starting materials, run each batch under inert atmosphere, and use vacuum drying to eliminate trace solvents, as even minor contamination can undermine later reactions. This attention to baseline purity emerged from repeated feedback from labs and production houses relying on consistency.
4-Fluorophenyl Acetate serves as both a stand-alone intermediate and a building block. We often receive requests from pharmaceutical R&D, where chemists employ it in the preparation of fluorinated phenols after selective hydrolysis. Because fluorine atoms modulate biological activity, many biotech teams add this small acetate group as a temporary masking group, only to remove it after other functionalizations are complete.
Research teams synthesizing agrochemical actives also seek 4-Fluorophenyl Acetate for its influence on lipophilicity and metabolic stability. Some medicinal chemists use it in fragment-based drug design. Our manufacturing history shows robust demand for this molecule in pilot and full-scale runs, especially as companies search for fluorine-containing scaffolds with predictable reactivity.
Comparing 4-Fluorophenyl Acetate to bulk phenyl acetate, the difference is distinct in both reactivity and outcomes. The fluorine atom in the para position tunes aromatic reactivity, meaning chemists can carry out substitutions and hydrolyses with more control. This single-atom switch, as we’ve seen in repeated plant runs, allows for more predictable yields when converting to downstream phenols or in cross-couplings.
In workshops and feedback calls, seasoned users point out the difference from ortho- or meta-fluorinated analogs. The para-substituted version displays more manageable melting and better shelf stability. Chemically, it resists unwanted side reactions, like hydrolysis during storage—even in regions with high humidity—saving both headache and cost.
Against 4-fluorophenol itself, the acetate offers the benefit of a protected hydroxyl group. That protection streamlines multi-step syntheses, as acetates are less prone to oxidation and side-chain reactions than free phenols. Once the desired chemistry is complete, standard saponification or acid hydrolysis cleanly yields the needed 4-fluorophenol. We perfected our work-up procedure to preserve both high overall yields and reproducibility, even at kilo scale.
With 4-Fluorophenyl Acetate, even 1% impurities can sabotage research or scale-up projects. There have been situations where inconsistent reactor cleaning in other facilities brought about trace catalysts or by-products—those residues cripple downstream hydrogenations or coupling reactions. To avoid surprises, we built a purification protocol that includes both column chromatography and recrystallization. Our operators then check each fraction using NMR, GC-MS, and UV-Vis. Any off-spec product is immediately recycled, not blended.
Stability also became a focus after some feedback on product packed in suboptimal containers. Moisture and traces from plasticizers once crept in. We switched to glass and high-density inert polymer packaging, developed internal QC triggers tied to every batch, and track all containers by unique ID. In our experience, these extra controls pay for themselves by improving yields in customer reactions.
Several academic teams used our 4-Fluorophenyl Acetate to synthesize advanced inhibitors for kinase assays. Their feedback confirmed cleaner hydrolytic deprotection and fewer downstream purifications compared with unprotected fluorophenols. Another group adapted it as a precursor in Suzuki coupling, attaching more complex boronic acids to the aromatic ring. The acetate group showed selectivity, avoiding unwanted transesterification.
Our own pilot lines tested 4-Fluorophenyl Acetate in the manufacture of specialty polymers. Results showed improved control over molecular weight distribution due to the acetate acting as both a reactivity moderating group and a leaving group at a later step. In flavor and fragrance labs, researchers tried acetylated fluorophenols for selective aroma profiles. In each field, minor adjustments in purification or process saved costs and time, something we learned to standardize after dozens of scale-ups.
Producing and isolating 4-Fluorophenyl Acetate brings safety and environmental concerns specific to fluorinated materials. Even waste acetylation by-products require careful handling. We designed our facility’s scrubbers and solvent recycling to capture volatile organic compounds and recycle solvent streams, reducing overall waste.
Operators undergo training in fluorine-sensitive reactions, as exothermic steps during acetylation can runaway without attention. Automated monitoring and manual oversight by experienced shift supervisors prevent spills and ensure consistent product output. We invested in data tracking for each batch, so each shipment leaves a transparent paper trail. We’ve seen too many industry cases where lax process control led to downstream recalls; history taught us to stay ahead with documentation and hands-on vigilance.
Within the same ester family, methyl, ethyl, and phenyl acetates see broader bulk distribution, but 4-Fluorophenyl Acetate shows critical advantages when specificity counts. Reactivity trends observed in the lab demonstrate faster cleavage rates—catalyzed hydrolysis proceeds more cleanly without generating colored by-products. Our chemists have tested batches from multiple suppliers and compared their output post hydrolysis; only those with high 4-FPA quality matched pure 4-fluorophenol recovery, without post-treatment, dryness, or yield loss.
Some researchers approach us requesting comparison trials between 4-fluorophenyl benzoate and the acetate. Throughout dozens of reactions, the benzoate leaves a heavier by-product toll and demonstrates sluggish hydrolysis, especially in mild or buffered systems. The acetate wins out every time in ease of protection and deprotection steps. The upshot: the right functional group at the right place can save weeks in total synthesis time.
On the ground, process chemists opened up about bottlenecks: batch-to-batch variability was the leading cause of lost time. Fluctuations in melting behavior, particle size, and off-odors cast a long shadow. So we reviewed each work-up step—from initial mixing, in-situ temperature logging, phase separation, and filtration—then upgraded drying equipment and swapped filter presses. As a result, product uniformity case after case has met customer specs, not by accident but by systematic hashing and improvement.
Chemical plants that neglect modification in the face of repeated technical failures find themselves cut out of critical markets. We listened to client pain points and adopted suggestions about packaging alternatives and shipment scheduling—shipping out on Fridays reduced transit time and storage under sub-optimal conditions for overseas clients. Our technical staff learned to take pride in feedback, realize its value, and drive change.
Areas like green chemistry and sustainable synthesis have sparked new conversations about organofluorine intermediates. Emerging applications in fluorinated monomers and functionalized polymers depend on uncompromised raw materials. Some researchers anticipate new bioactive libraries will hinge on the acetate group’s strategic removal to unmask critical active centers. In the environmental chemistry field, screening for transformation products from fluorinated aromatic esters centers on predictable, traceable starting materials—like the ones we craft.
As we scale further, we focus on agile process adjustments to handle custom derivatives—a task only possible with a deep knowledge of base 4-Fluorophenyl Acetate quality. We deploy internal analytics and open communication with clients, enabling more seamless adjustments to match their project cycles. Real problems in custom chemistry get solved by a sharp eye on both plant floor realities and changes in regulatory trends.
With expanding environmental and safety oversight, each batch goes through in-house documentation of physical and chemical properties. Certificates are reviewed by QA staff, who understand both synthesis routes and real risks. We document each step and sampling point from raw material through to release, as regulatory compliance can’t tolerate “black box” manufacturing. Inspection auditors flagged documentation lapses as the root cause for rare product recalls years ago; since then, tracking and archiving improved, making client audits smooth and predictable.
Academic partners approached us with requests for alternative protection groups and even higher purity levels. Iterative projects in medicinal and industrial labs gave us the experience to fine-tune not just yield, but also pale color, melting behavior, and scalability. We adopted better documentation, took in small tweaks for reduction in side products, and realized that the best product doesn’t come from the equipment alone.
In recent years, client laboratories required batch-specific mass spectra and digital melting trace data. Our technical crew responded by improving software integration and analytical calibration. Real collaboration in research and scale-up has improved both our offerings and customer project outcomes.
We regularly analyze shipment returns, sample reviews, and production anomalies—these operational lessons build the next procedure or tweak the recipe. Site engineers meet monthly to dissect even minor irregularities, such as trace color in some batches tied to specific drum sources. Local knowledge carries over into new team member training, embedding each lesson learned into plant culture.
Upgrading analytical protocols, improving safety training, and soliciting operator feedback—these steps trim inefficiency and bolster product reliability. Every year brings new customer requirements and evolving scientific expectations; meeting these means not leaning on past achievements, but committing to ongoing problem-solving.
4-Fluorophenyl Acetate stands as more than just a laboratory chemical. Lessons from hundreds of production cycles, continual feedback, and troubleshooting shaped it into a reliable, practical tool for both daily synthesis and new research demands. As scientific discovery moves forward, the value of a well-made—never generic—4-Fluorophenyl Acetate will only grow.