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4-Fluorophenyl Acetate

    • Product Name 4-Fluorophenyl Acetate
    • Alias p-fluorophenyl acetate
    • Einecs 252-092-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 4-Fluorophenyl Acetate

    Applications of 4-Fluorophenyl Acetate in Industrial Manufacturing

    4-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) Production

    As 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

    • EU Good Manufacturing Practice (GMP) EudraLex Volume 4
    • U.S. FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • Chinese Pharmacopoeia (ChP) API intermediate quality controls

    Typical usage ratio

    • Utilized at 0.08–0.25 molar equivalence relative to primary amine or phenol coupling partner, adjusted based on specific target molecule reaction yield and functional group tolerance.

    Downstream process integration

    • Introduced at the step of aromatic esterification or fluoroarene coupling prior to cyclization or further derivatization to achieve the required NSAID backbone structure.

    Final product types

    • Active pharmaceutical ingredients (APIs) for NSAIDs such as diflusinal or analogues incorporating fluorinated phenyl groups
    • Bulk intermediates for contract pharmaceutical manufacturing

    2. Aroma Chemical Manufacturing: Synthesis of Fluorinated Ester Fragrance Ingredients

    Producers 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

    • International Fragrance Association (IFRA) Standards
    • European Chemicals Agency (ECHA) REACH Regulation (EC) No 1907/2006
    • ISO 9235 (Aromatic Natural Raw Materials and Isolated Natural Aromatic Compounds)

    Typical usage ratio

    • Added at 1–5% by weight within the esterification reaction mixture; final percentage reflects target volatility and regulatory threshold of resulting aromatic ester compound in fragrance bases.

    Downstream process integration

    • Reacted in select esterification or transesterification steps following initial aromatic acetylation, prior to blending or fractionating the isolated fragrance molecule.

    Final product types

    • High-purity aroma chemicals for fine fragrance manufacturing
    • Fluorinated ester compounds for use in eau de parfum and premium colognes

    3. Agrochemical Synthesis: Herbicide Precursor Production

    Downstream 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

    • FAO/WHO Specifications for Plant Protection Products (FAO Pesticide Specifications)
    • U.S. EPA 40 CFR Part 180 (Tolerances and Exemptions for Pesticide Chemical Residues in Food)
    • China National Standard GB 2763 (Maximum residue limits for pesticides in food)
    • OECD Principles of Good Laboratory Practice (GLP) for pesticide development

    Typical usage ratio

    • Applied at 0.10–0.34 mole fraction relative to other phenoxy precursors, refined based on desired herbicidal spectrum and molecular scaffold.

    Downstream process integration

    • Combined during salt-forming or condensation reactions ahead of acid hydrolysis and formulation into technical concentrates.

    Final product types

    • Technical grade herbicide intermediates for further downstream formulation
    • Active ingredient concentrates for cereal and broadleaf weed control

    4. Specialty Polymer Modification: Incorporation in High-performance Co-polyesters

    Industrial 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

    • IEC 62321 (RoHS test methods for hazardous substances in electrical and electronic equipment)
    • ISO 9001 (Quality management for polymer compounds)
    • ASTM D638 (Standard Test Method for Tensile Properties of Plastics)
    • REACH SVHC (Substances of Very High Concern) regulatory review for final resin products

    Typical usage ratio

    • Used at 0.5–2.2 wt% in polyesterification reaction mix, tailored to the length of copolymer chain and level of desired property modification.

    Downstream process integration

    • Fed during polycondensation step, reacting with diol and dicarboxylic acid monomers, and followed by extrusion or pelletizing for final copolymer granule production.

    Final product types

    • High-performance co-polyester resins for specialty plastics
    • Precision-molded engineering thermoplastic parts for electronics and automotive sectors
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    Certification & Compliance
    More Introduction

    4-Fluorophenyl Acetate: A Versatile Intermediate with Real-World Utility

    Overview and Our Perspective on 4-Fluorophenyl Acetate

    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.

    Physical Properties and Quality Benchmarks

    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.

    Direct Uses in Synthesis and Industry

    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.

    In-Lab Handling Versus Related Chemicals

    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.

    Why High Purity Matters—and How We Achieve It

    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.

    Application Cases from Our Plant and Partners

    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.

    Environmental Responsibilities and Process Safety

    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.

    Comparisons with Commonly Encountered Phenyl Esters

    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.

    Our Plant’s Recipe for Consistency

    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.

    Looking Ahead: Where 4-Fluorophenyl Acetate Will Matter Most

    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.

    Differences in Regulatory and Documentation Aspects

    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.

    Partnering with Research: Feedback Makes a Better Product

    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.

    Continuous Improvement: Getting Better with Every Batch

    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.

    Closing Thoughts from a Working Manufacturer

    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.