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4-Fluoro-3-Amino-Acetophenone

    • Product Name 4-Fluoro-3-Amino-Acetophenone
    • Alias 4-FAA
    • Einecs 629-213-7
    • 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

    464737

    Productname 4-Fluoro-3-Amino-Acetophenone
    Casnumber 333-27-7
    Molecularformula C8H8FNO
    Molecularweight 153.16
    Appearance Off-white to light yellow solid
    Meltingpoint 62-66°C
    Purity Typically ≥98%
    Solubility Soluble in organic solvents like DMSO and ethanol
    Smiles CC(=O)C1=CC(=C(C=C1)F)N
    Inchi InChI=1S/C8H8FNO/c1-5(11)6-2-3-7(9)8(10)4-6/h2-4H,10H2,1H3
    Storage Store at room temperature, protected from light and moisture

    As an accredited 4-Fluoro-3-Amino-Acetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, white screw cap, tamper-evident seal, with clear hazard labels and product information printed on the label.
    Shipping 4-Fluoro-3-Amino-Acetophenone is shipped in secure, tightly sealed containers to prevent leaks and contamination. It is stored under cool, dry conditions, away from direct sunlight and incompatible materials. The packaging complies with international regulations for chemical transport, and includes clear labeling and relevant safety documentation for safe handling and delivery.
    Storage 4-Fluoro-3-Amino-Acetophenone 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. It should be kept away from incompatible substances such as strong oxidizers and acids. Avoid exposure to moisture, and store at room temperature. Always follow local regulations and safety guidelines for chemical storage.
    Application of 4-Fluoro-3-Amino-Acetophenone

    Applications of 4-Fluoro-3-Amino-Acetophenone in Industrial Manufacturing

    As a specialized manufacturer, we supply 4-Fluoro-3-Amino-Acetophenone for well-established industrial sectors that leverage its aromatic and reactive profile for high-value downstream synthesis. The following application scenarios highlight where this intermediate is reliably used at commercial scale, along with details on regulatory standards, formulation strategies, process integration, and end-market finished goods.

    1. Pharmaceutical Intermediate for Kinase Inhibitor Synthesis

    Pharmaceutical companies utilize this compound as a key building block in targeted synthesis routes for kinase inhibitor molecules, especially in oncology research pipelines. Medicinal chemists apply its amine and fluoro functionalities to introduce pharmacophores via selective coupling or cyclization, typically during the early to mid-stages of active ingredient manufacture.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • EU EudraLex Volume 4
    • Ph. Eur. and USP General Standards for Intermediates

    Typical usage ratio

    • 0.5% – 2% of total batch mass input at the intermediate synthesis stage, adjusted according to the desired molecular scaffold and yield optimization studies

    Downstream process integration

    • Charged into solution or reaction vessel post-halogenation stage, followed by amide or urea coupling and subsequent purification before final API salt formation

    Final product types

    • Selective kinase inhibitor drug substances (e.g., aurora kinase, BTK, or ALK inhibitors)
    • Pharmaceutical research intermediates for small molecule libraries
    • Pre-clinical candidate compounds

    2. Advanced Agrochemical Active Ingredient Production

    Crop protection manufacturers incorporate this material into the synthesis of advanced herbicidal and insecticidal actives where selectivity and functional group tolerance are crucial. The raw material acts as an aromatic amine source, entering key reaction steps where fine structure-activity relationships are established for new actives.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Products
    • ISO 9001:2015 Quality Management (for process traceability)
    • GB/T 1600-2001 (Chinese Pesticide Technical Regulation)
    • OECD Principles of Good Laboratory Practice (GLP) for pesticide registration

    Typical usage ratio

    • 1.0% – 4.0% of total formulation batch, depending on specific chemical entity and downstream derivatization pathway

    Downstream process integration

    • Introduced during the aromatic nucleophilic substitution or condensation step within technical-grade active synthesis, followed by granulation or emulsification for finished formulations

    Final product types

    • Herbicide and insecticide active ingredients (e.g., fluoro-aryl substituted phenoxy compounds)
    • Chemical intermediates for further agrochemical functionalization
    • Granular, liquid, and concentrated suspension concentrates for commercial farming

    3. Organic Pigment and Dye Intermediate Manufacture

    Dye and pigment producers employ this raw material in the production of structurally unique azo and anthraquinone colorants. Its reactivity allows selective diazotization and direct coupling reactions, delivering hues with enhanced fastness and unique chromatic properties for specialty plastics and textile applications.

    Industry compliance standards

    • REACH (EC 1907/2006) Registration, Evaluation, Authorization and Restriction of Chemicals
    • Oeko-Tex Standard 100 (Textile and Leather)
    • EN 71-3 (Safety of Toys — Migration of Certain Elements)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 1.5% – 5% of the pigment or dye batch, with precise adjustments based on target shade intensity and molecular weight

    Downstream process integration

    • Used in the diazotization stage, immediately followed by coupling to form the azo or anthraquinone chromophore prior to crystallization and milling

    Final product types

    • High-performance dyes for fibers and plastics
    • Specialty pigments for electronic device coatings
    • Colorant dispersions for printing inks and toners

    4. Specialty Chemical Intermediate for Liquid Crystal Materials

    Producers of advanced liquid crystal (LC) compounds for display panels use this aromatic amine to confer precise electronic and polar properties needed in key LC molecules. The compound is leveraged early in multi-step syntheses as a functionalized core, granting desired mesogenic behavior once incorporated into liquid crystal monomers or dimers.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electronics)
    • ISO 14001 Environmental Management Systems
    • JPCA Quality Standard for Liquid Crystal Materials
    • REACH Pre-registration for intermediates

    Typical usage ratio

    • 0.2% – 1.2% in LC intermediate synthesis, quantity determined by target optical anisotropy and blending ratios in final mixtures

    Downstream process integration

    • Introduced during the initial aromatic amine condensation step before further alkylation, purification, and alignment modification for final LC formulation

    Final product types

    • Active LC monomers and dimers for TFT and OLED display panels
    • Custom mesogenic compounds for advanced display technologies
    • Intermediate blends for specialty LC device components
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    Competitive 4-Fluoro-3-Amino-Acetophenone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 4-Fluoro-3-Amino-Acetophenone: A Perspective from the Manufacturer

    Real-World Chemistries Start with Dependable Intermediates

    In the world of chemical manufacturing, every raw material tells a story of precision, scale, and patient refinement. 4-Fluoro-3-Amino-Acetophenone sits among a category of specialty acetophenones that sees demand across pharmaceutical, agrochemical, and materials science sectors. Over the years, our facility has made countless tonnes of this molecule, recognizing the nuanced challenges and possibilities that come with fluorinated intermediates.

    Understanding the Model: 4-Fluoro-3-Amino-Acetophenone's Place in Synthesis

    Our experience with 4-Fluoro-3-Amino-Acetophenone has grown from the frequent requests of research chemists and process engineers seeking more reliable and higher-purity sources. This compound, known by its structure—bearing both a fluoro and an amino group on the aromatic ring—offers unique reactivity that opens access to complex heterocycles, tailored pharmaceuticals, and specialty polymers. Its chemical behavior, compared to its non-fluorinated or mono-substituted analogues, often translates to reaction routes that exhibit better selectivity, improved stability in subsequent steps, and in many cases, enables entirely new transformations.

    The presence of the fluorine atom on the ring modulates electron density, setting the stage for reactions where selective activation or protection is key. The amino group at the meta position imparts greater flexibility in further functionalizations. In the synthetic lab, you get a starting block with fewer detours—an asset that scales well in an industrial setting.

    Up Close: Specifications and Consistent Quality

    Years of manufacturing this intermediate have taught us that consistency does not come easily. For 4-Fluoro-3-Amino-Acetophenone, purity marks a hard boundary between routine results and costly troubleshooting. Each batch leaves our reactors with a typical purity exceeding 98% by HPLC, a tight melting range, and a color that reflects minimal by-product formation. The technical team tests each lot for residual solvents and moisture, making sure the product can go straight from packaging into your next synthetic step. Whether you process in multi-kilogram batches or scale out to tonne lots, the importance of trace impurities cannot be overstated—especially in regulated industries.

    We opted for packaging solutions that address both the hygroscopic and photoreactive tendencies of the compound. Heavy-gauge, double-layer bags inside sealed drums guard against contamination and degradation without lacing your facility with the aroma that sometimes tags along with aminated aromatics. Shipments head out only after passing a battery of checks: purity, residual solvents, and mechanical integrity of the packing. For customers facing challenging regulatory documentation, our team provides full traceability to raw material lots and process conditions that matter most for reproducibility.

    From Synthesis to Scale: Our Manufacturing Approach

    Lab bench synthesis scales to factory output only when each stage of production makes peace with yield, safety, and process time. We have optimized the nitration, selective reduction, and fluorination processes over the years to reduce side-products and improve atom economy. Each step remains under careful scrutiny, since changes in temperature profiles or reagent sources can send impurity profiles in unpredictable directions. We use in-line monitoring during the key reduction and substitution stages; this allows for rapid correction before a barely-perceptible shift turns into lost product or search for a costly clean-up.

    Production lines integrate solvent recovery wherever possible, and waste streams are treated with the same attention given to product output. This means we see fewer disruptions due to environmental bottlenecks, and customers know that the product purchased today will match a repeat order next quarter. Our reactors run under strict temperature and pressure controls, with trained operators overseeing every run—not just automated monitors. Hands-on adjustments and an openness to feedback from downstream chemical users drive continual improvement.

    Why 4-Fluoro-3-Amino-Acetophenone Makes a Difference

    Every molecule serves a purpose, but fluorinated acetophenones carve out a special space due to their combined electronic, steric, and metabolic effects. Compared to 3-amino-acetophenone, the addition of the fluorine at the four position offers more than just incremental variation. In medicinal chemistry, this means subtle tweaks in metabolic stability. In crop protection, the altered aromatic profile shifts how a molecule interacts with plant or pest enzymes. That extra layer of molecular control helps R&D teams reach new patentable space, and process engineers run their steps at cooler temperatures or higher yields.

    There are plenty of acetophenone derivatives out there. Some cost less, some deliver interchangeable results for basic transformations. What we have seen is that downstream chemistries—in both bench and plant scale—often uncover bottlenecks with less pure or less specifically substituted intermediates. Nitration and reduction sequences require careful pH and temperature management to avoid over-reduction or mixed products. The presence of fluorine, in this layout, changes more than the draw of electrons—sometimes you avoid whole classes of unwanted byproducts. For customers repeatedly frustrated by the clean-up required from mixed substitution patterns, our version of 4-Fluoro-3-Amino-Acetophenone often means fewer headaches and shorter purification times.

    Applications: Where Reliability Matters Most

    Chemists working in scale-up synthesis rarely have time for trial-and-error purification. 4-Fluoro-3-Amino-Acetophenone migrates into a sequence, enabling the formation of key heterocycles or acting as a handle for next-step modifications. Its use stretches across medicinal compound libraries, preclinical candidate synthesis, and new agrochemical backbone design. Research clients often comment not just on how the molecule behaves in their coupling step, but on the time saved by predictable melting points, consistent reactivity, and reproducibility from batch to batch.

    In our own trials—and from direct client feedback—running amide coupling or aromatic substitutions benefits from the electron-withdrawing effects of the fluorine substituent. Yields in some Suzuki or Buchwald-type couplings show measurable improvements compared to non-fluorinated amino-acetophenones. The molecule enters processes as a reliable participant, less sensitive to slight variations in temperature or solvent than more temperamental intermediates.

    Our production philosophy prioritizes these downstream results. Each process update considers not just cost per kilo, but also the experience in the client’s flask or reactor. When orders come in for kilogram or tonne-scale deliveries, we appreciate the stakes: a failed batch means delayed enrollment in a trial, or lost field-testing windows for a new agricultural product. That’s why our schedule and verification procedures run ahead of procurement drives.

    Addressing Common Challenges in Manufacturing and Use

    Not all 4-Fluoro-3-Amino-Acetophenone on the market performs equally. We have watched competitors grapple with inconsistent purity, or batches that degrade in transit. Our process insisted on robust controls for residual solvents and moisture, since amines notoriously attract water or react in subtle—and costly—ways during storage.

    From the start, our technical group learned to overinvest in analytical verification. Every routine HPLC trace reveals more than quantitative purity—it flags isomeric byproducts, which, at scale, can tail-into next-step reactions, compounding losses or fouling expensive catalysts. These headaches have led us to refine our recrystallization procedures, adjust holding times, and monitor each run far more closely than if we shipped “commodity-grade” material.

    Packaging selection consumed real hours and costs, shaped by feedback from plant chemists across industries. Our solution marries protection from moisture and light, with containers strong enough for global shipping, yet easy to open and meter accurately. Whether the customer runs an under-ventilated plant in a humid region or a temperature-controlled pharma campus, the goal is the same: deliver consistency at the point of use, not just at the factory gate.

    One overlooked challenge comes from the interfacing of production scheduling with last-mile delivery. Large multinationals and fast-moving small enterprises both need flexibility in volumes and delivery timelines. We developed modular production blocks to turn out made-to-order or standard inventory more responsively; gaps in demand do not force us into excessive minimum batch sizes or long lead times. The result is the right quantity, delivered close to your use date, limiting both waste and warehouse space.

    Innovations Gained from Real-World Experience

    In the early years, our facility managed 4-Fluoro-3-Amino-Acetophenone as just another fine chemical. Frequent feedback from the lab benches and pilot plants indicated that this perspective missed opportunities. Chemists wanted more than purity—they wanted insight into physical properties, verification of isomeric integrity, and detailed information about possible contaminants.

    With that, we introduced more robust quality analysis: expanded NMR, FTIR, and GC traces accompany every batch, and client-facing chemists on our staff provide consultation on expected reactivity and potential in-process variations detected during scale-up. Our research division tracks new synthetic uses, and where possible, feeds back improvements into the process to improve throughput and minimize side-product formation. Rather than treat the product as a black-box output, we pursue a two-way relationship where adaptation and vanishing downtime dominate.

    These investments benefit more than just our own operation. Consider a scale-up campaign where impurities lead to cloned side products—catching a 1% contaminant upstream can prevent a 10% yield loss or the need for full chromatographic separations downstream. We have seen teams rescue schedules previously threatened by batch-to-batch variation, simply by switching to a process with reliable trace impurity disclosure. Judicious spending on real QC replaces firefighting with confident production planning.

    Why Direct Manufacturing Matters

    Too often, intermediates change hands through multiple brokers or repackers. Trouble arises when neither the end user nor the vendor can speak to the batch’s life story—raw material source, process parameters, transit conditions. Over the years, we found direct relationships with users drove shorter feedback loops and fewer “mystery contaminant” reports.

    By controlling the full lifecycle of 4-Fluoro-3-Amino-Acetophenone, from raw input to delivery, we guarantee traceability, not as a checkbox but as a real response to regulatory and performance demands. Several customers, especially in regulated markets, require audit trails confirming every stage of manufacture. Our site logs every batch; we keep reference samples for each production, allowing retroactive analysis if a question emerges months or even years later.

    This level of detail delivers more than peace of mind. It gives researchers the confidence to design new chemistries, regulatory officers a clear audit path, and production engineers backup during troubleshooting. Because control and transparency form the bridge between a custom intermediate and its real-world applications, our customers find fewer surprises and greater continuity no matter the project scale.

    Comparing 4-Fluoro-3-Amino-Acetophenone to Other Intermediates

    In direct side-by-side trials, we have seen the differences between 4-Fluoro-3-Amino-Acetophenone and its relatives become obvious. For projects needing the amino functionality alone, unsubstituted acetophenones carry risks of unwanted ortho or para substitution during subsequent steps. Adding a methyl or methoxy, rather than a fluorine, reshapes reactivity in less predictable ways—reactions may run faster but at cost to product selectivity or downstream stability.

    Fluorinated variants catch attention for their metabolic robustness and bioavailability in case of pharmaceuticals, or altered uptake and translocation in agrochemical applications. Where projects lean on tailored aromatic substitutions, only the correct placement of both the amino and fluoro groups delivers the mix of electronic effects and backbone rigidity required. Customers who switched from simple amino-acetophenones often report cleaner product isolation and reduced cost for subsequent purification—less solvent, less labor, better output per dollar spent.

    Building Trust with Reliable Delivery and Long-Term Support

    Our job extends beyond shipping labeled drums. Regular follow-up with end users uncovers application-specific problems. Where batch splitting or just-in-time delivery makes a difference, we adjust schedules or packaging. The team stays up to date on new industry requirements—whether documentation or process validation—so our product never becomes the rate-limiting step in your development timeline.

    Continuous contact with process chemists, process validation teams, and R&D leadership means we gather insights beyond routine batch notes. An uptick in solvent handling warnings might trigger packaging modifications; news of a new patent application involving novel downstream chemistry might lead to closer surveillance of trace by-products or a custom batch run tailored to experimental needs.

    Driving Future Development through Chemical Integrity

    Specialty intermediates like 4-Fluoro-3-Amino-Acetophenone anchor both commercial and experimental pipelines across pharmaceuticals, agriculture, and material science. Our commitment: high specification, reproducibly manufactured, and reliably delivered intermediates provide the difference between delays and breakthroughs in tough, competitive markets.

    Every improvement in purity, traceability, and customer support at our plant finds its way into better results for the end user—a cycle of improvement that moves from kilogram batches on the bench to full-commercial-scale campaigns that deliver new therapeutics and advanced crop treatments. Direct experience has shown us that shortcuts in the supply chain cost more in lost opportunity than rigorous, transparent, and attentive manufacturing.

    To those seeking a difference in their synthetic outcomes, the details of who makes your intermediate matter as much as the molecules themselves. Working with a manufacturing team that knows not just the chemistry, but the context of its use, often spells the difference between routine supply and real partnership in innovation.