|
HS Code |
573677 |
| Productname | 4'-Fluoro-2'-Hydroxyacetophenone |
| Casnumber | 399-95-1 |
| Molecularformula | C8H7FO2 |
| Molecularweight | 154.14 |
| Appearance | White to off-white solid |
| Meltingpoint | 84-88°C |
| Boilingpoint | 273°C |
| Density | 1.28 g/cm3 |
| Solubility | Soluble in organic solvents (e.g., ethanol, DMSO) |
| Smiles | CC(=O)C1=CC=C(C=C1O)F |
| Inchi | InChI=1S/C8H7FO2/c1-5(10)6-2-3-7(9)8(11)4-6/h2-4,11H,1H3 |
| Purity | Typically ≥98% |
| Storagetemperature | Store at 2-8°C |
| Refractiveindex | 1.543 (predicted) |
| Ecnumber | 206-066-7 |
As an accredited 4'-Fluoro-2'-Hydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure screw cap, labeled "4'-Fluoro-2'-Hydroxyacetophenone", including hazard and handling information. |
| Shipping | 4'-Fluoro-2'-Hydroxyacetophenone is typically shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Packages comply with local and international regulations for handling chemicals. Ensure compatibility with shipping materials and include appropriate hazard labeling. Consult Safety Data Sheet (SDS) for specific storage and transport recommendations before dispatching. |
| Storage | 4'-Fluoro-2'-Hydroxyacetophenone should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Protect from direct sunlight and avoid excessive heat. Properly label the storage area and keep it out of reach of unauthorized personnel to ensure safety and stability. |
Applications of 4'-Fluoro-2'-Hydroxyacetophenone in Industrial Manufacturing4'-Fluoro-2'-Hydroxyacetophenone serves as a key intermediate across fine chemical, pharmaceutical, and advanced materials sectors. As a direct manufacturer, we support a range of downstream industries requiring this specialty building block for high-value synthesis and performance-critical formulations. Below, we present real-world application scenarios addressing process role, industry compliance, typical dosage, and final product profiles. 1. Pharmaceutical Intermediate Synthesis (API Development)Pharmaceutical manufacturers use this compound as a core structural motif in the synthesis of small molecule active pharmaceutical ingredients, especially those requiring selective fluorination and phenolic functionalities. The product enters the process during the convergent assembly of complex scaffolds, helping to achieve target molecular configurations necessary for bioactivity. End users frequently demand batch traceability, impurity control, and validated analytical methodologies for downstream regulatory compliance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Compound ManufacturingProducers of crop protection chemicals value the fluorinated acetophenone core for constructing herbicide and fungicide actives. This raw material supports regioselective functionalization, improving final product stability and soil persistence profiles. Processing requires stringent impurity control to meet environmental registration requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Liquid Crystal Intermediate for Display MaterialsSpecialty chemical manufacturers incorporate this molecule in the design of polar and high-dielectric liquid crystal intermediates for advanced display technologies. Strict process control ensures the achievement of high optical purity and trace halogen content required by consumer electronics downstream users. Integration typically involves multi-step synthesis under cleanroom or controlled environments to prevent contamination. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fragrance and Fine Perfume Ingredient ManufacturingIndustrial fragrance compounders utilize this material in the selective synthesis of aroma molecules, particularly where subtle fluorination confers unique odor profiles or extended shelf stability. The compound enters targeted acylation or alkylation steps, with process quality dependent on low-residual reactant levels and precise isomer control. Final compositions must comply with international fragrance safety standards, requiring batch-controlled analytical verification. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Photoinitiator Precursor Synthesis for UV-Curable ResinsProducers of UV-curable resin systems for coatings, adhesives, and inks incorporate this fluorinated hydroxyketone in the synthesis of advanced photoinitiators. Its structural attributes enhance initiation rates and enable more efficient crosslinking under UV exposure. Manufacturing environments demand accurate dosing, rapid mixing, and trace contaminant control to qualify in performance-sensitive downstream applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 4'-Fluoro-2'-Hydroxyacetophenone prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In the chemical manufacturing world, the significance of each intermediate goes well beyond catalog numbers and certificates. 4'-Fluoro-2'-Hydroxyacetophenone is one of those molecules that draws interest not only because of its reactivity but also its reliability in industry applications. With years spent tuning our production lines for this compound, we see its impact not only in terms of order volume, but in the relationships built with R&D teams, formulation chemists, and procurement specialists who seek value, repeatability, and clarity.
Every batch of 4'-Fluoro-2'-Hydroxyacetophenone, catalogued in our shop under model FA-2101, reflects careful attention to chemical purity and functional utility. Our syntheses stick to time-proven routes, optimizing conditions to minimize impurity formation. We maintain a minimum purity specification of 99%, with residual starting materials and byproducts consistently falling below detectable thresholds based on both GC and HPLC analysis. Fine-tuning isolation steps allows us to deliver product most commonly seen as a crystalline solid, faintly off-white, easily handled and weighed even in large-scale labs.
We have tracked the compound’s CAS number—403-25-0—across procurement documents and supply records, and notice it cropping up in diverse projects. Many customers flagged its low melting point, easy dissolution in standard lab solvents (DMF, ethanol, ethyl acetate), and clean spectral profiles on NMR and mass spectrometry. The hydroxyl group at the ortho position together with a para-fluoro group gives this acetophenone scaffold a unique balance between electron richness and synthetic handle.
Looking at usage trends among our recurring clients, this compound finds its place mainly in the design of pharmaceuticals, agrochemicals, and specialty organic materials. Medicinal chemists favor 4'-Fluoro-2'-Hydroxyacetophenone because the fluorine introduction at the para position tunes metabolic stability and binding profiles. Early in my career, I recall supporting an order from a team screening for kinase inhibitors—this intermediate provided both ready reactivity for further acylation and distinct fluorine signatures for tracking metabolites.
Agrochemical researchers rely on it during the synthesis of fungicides and insecticides, where the hydroxyl and fluoro functionalities create diversified binding modes. Some product developers shared that the compound's predictable reactivity streamlines coupling reactions, especially Mitsunobu-type and nucleophilic substitutions, which favor substrates with ortho-hydroxy and para-fluoro substitution patterns.
Polymer scientists incorporate this molecule for its influence on thermal and chemical properties in specialty plastics and coatings. One client engineered a copolymer with improved hydrolytic resistance, crediting the robust aromatic core introduced during copolymerization.
Behind each shipment stands a team that tracks every process, from raw material selection to final filtration. Our plant uses closed-system reactors to manage moisture and keep oxygen out where needed, since the hydroxyl on the aromatic ring can show sensitivity under high-alkali conditions. Our operators carry out constant in-process checks, and we make use of online spectroscopic monitoring to catch deviations before they influence the final product.
A consistent challenge surfaces with acetophenone derivatives: carryover of fluoride salts or incomplete methylation steps can push impurities just above acceptance levels. Over time, we responded by tightening raw material supplier audits and implementing extra sample holds at the crude precipitation stage. Some competitors ship material with minor hydrolysis byproducts, but our batches exceed these routine hurdles thanks to tweaks in solvent systems and extended drying under vacuum.
Shipment batches hold tightly to uniform color and grain size, which may seem cosmetic, but our partners in formulation repeatedly mention improved blending behavior when properties do not shift batch-to-batch. Whether delivered in double-lined drums or smaller high-density polyethylene bottles, our clients receive a product already tested for both chemical and physical mottling. We track these specifics in our manufacturing database, which has reduced quality complaints to near zero.
The acetophenone core structure appears in countless catalogs. Industry buyers sometimes ask about cheaper options: standard 2'-Hydroxyacetophenone or even the non-substituted parent compound. Our records and customer case studies illustrate why 4'-Fluoro-2'-Hydroxyacetophenone stands apart. The fluoro substituent, out at the para position, imparts significant differences in lipophilicity, electron density, and even regulatory classification in some jurisdictions. For end-users developing pharmaceuticals, this means not only a small molecular tweak, but frequently a route to improved oral bioavailability or lower clearance in animal models.
Beyond biological effects, the presence of fluorine markedly lowers the susceptibility of the aromatic system to oxidative degradation. I’ve read accounts from tincture manufacturers who experienced extended product shelf life after substituting our product for a non-fluorinated analog. Our technical support team fields questions from labs running environmental fate studies, and here the compound’s distinct mass signature helps with easier tracking of biotransformation products.
Another noticeable distinction involves handling and storage. 4'-Fluoro-2'-Hydroxyacetophenone, when compared with trifluoromethylated relatives, delivers reactivity without excessive volatility or the need for specialty cooling. Its crystalline form stores stably under normal laboratory conditions, with shelf lives exceeding three years if containers stay tightly capped, out of direct sunlight. Technical managers appreciate not having to design special logistics or upgrade warehouse ventilation—lowering hidden costs during scale-up.
Customers’ project timelines rarely wait for ideal circumstances, so scalability is a topic that comes up. Our experience growing batches from pilot runs to full-scale drums started with the unique challenges posed by ortho-substituted acetophenones. Reaction kinetics respond strongly to temperature gradients, especially during condensation and fluorination. We equipped our vessels with advanced jacket controls, finding that holding precise reaction profiles ensured smooth, debris-free crystals. This was not guesswork—trial and error with pilot lots led us to a process that consistently yields material above industry-standard purity.
We store multiple lots for stability studies at varying humidity and temperature points. Data from our own ongoing programs indicate the product does not degrade with exposure to ambient humidity for short periods, setting it apart from some highly hygroscopic acetophenone derivatives that clump and lose flow. It can withstand regular handling, aliquoting, and sampling over the course of extended multi-step projects without visible caking or browning.
Comprehensive batch records document every nuance, and for our global clients, we supply supporting regulatory paperwork, confirming compliance with REACH, K-REACH, and TSCA where relevant. Our familiarity with infrastructure audits by major pharmaceutical customers shaped our record-keeping habits, and we know from repeat visits that walking auditors through a batch’s journey, step-by-step, reassures buyers in a way that a glossy catalog description never could.
It surprises some clients to learn how subtle formulation changes influence downstream processability. We point out that 4'-Fluoro-2'-Hydroxyacetophenone can be recrystallized from a variety of solvents common to organic synthesis labs—ethyl acetate, petroleum ether, or even isopropanol. Solubility profiles show it works well for system setups used by both smaller academic labs and industrial kilo labs.
Our hands-on experience with troubleshooting proves crucial. On several occasions, collaborating teams reported unsuccessful coupling reactions attributed to low moisture control. We shared our practice of pre-drying both the product and solvents with molecular sieves, leading to improved yields and less tarry residue. Simple but effective tweaks, learned directly from our own line staff and technical leads, not through theory.
We hear from researchers concerned about trace metal content following the use of older metal-catalyzed routes. Our regular catalyst residue checks, using ICP-OES, confirm metal contamination stays well below international thresholds. These careful steps ensure that sensitive syntheses, particularly for pharmaceutical actives, do not suffer from downstream inhibition or regulatory headaches.
Operating a chemical plant entails strict attention to environmental, health, and safety protocols. Our team invests regularly in waste treatment systems, especially for effluents from fluorination. Neutralization and proper separation of halide wastes ensure nothing untoward reaches outflow streams. Plant managers train all operators in safe handling—protective gloves, splash goggles, clear labeling, and straightforward SOPs based on actual incidents, not theoretical risk.
We use air monitoring and regular emission checks, running tighter controls than some jurisdictions demand. The physical properties of 4'-Fluoro-2'-Hydroxyacetophenone allow for straightforward hazard management. Not volatile enough to pose significant inhalation risk, but like any active washer its dust can irritate skin and eyes. Pros in the trade know not to shortcut personal protective equipment, and our operator suggestions go into every site-specific guideline.
International shipments sometimes require additional documentation, especially related to fluorinated intermediates. We stay ahead of changes in chemical notification lists and supply valid export paperwork with each batch. With a presence in audits at destination sites, we see first-hand how this attention to regulatory transparency smooths customs processes and reduces clearance delays.
Feedback loops among production, quality control, and tech support shape our routines. Regular internal reviews bring up incremental changes—adjustments in solvent swaps, updated filter media for bulk handling, or new analytical standards as detection technology advances. Physically walking the plant at shift changes means management observes and acts on trends before they become quality problems.
Reliable supply remains a hot topic for our clients, especially during market swings or supply chain disruptions. We keep healthy raw material stocks and invest in dual-source planning, so client projects do not halt for want of a precursor. By understanding our clients’ project deadlines, we prioritize batch manufacturing to ensure immediate dispatch, avoiding pipeline slowdowns.
Industry partners comment on how our direct ties to the line inform our service. Instead of relaying customer feedback through distant channels, we pass those requests straight to the plant floor, where actual production improvements happen. When one customer flagged a persistent labeling confusion (due to a structural isomer), we immediately changed labeling and documentation, and trained logistics teams to check for cross-shipment risks.
Over the years, markets shifted and regulatory frameworks changed, but the essentials of process chemistry and client relationship building hold steady. We choose to focus on continuous small-step upgrades—switching to greener solvents, seeking more robust catalyst recovery methods, and training new operators on both compliance and hands-on troubleshooting. Data from our operations point to improved long-term yields and lower environmental footprint each year.
Our partnerships with universities and chemical institutes offer fresh perspectives. Academic researchers bring creative applications, while also asking for technical clarifications on off-scope specifications—questions only a manufacturer, not a distributor, can realistically answer. Working through requests for fractionally modified versions, we support pilot projects and niche formulations. This keeps our staff sharp and helps us anticipate emerging demands.
Moving forward, we keep ears open to evolving trends: regulatory shifts on fluorinated chemicals, growing attention to lifecycle analysis, and more emphasis on closed-loop manufacturing. We already pilot projects recapturing more solvent, reducing water use per kilo of product, and pursuing documentation standards in line with the best global practices.
4'-Fluoro-2'-Hydroxyacetophenone may not be the largest-volume product on our books but it represents what clients expect from a manufacturer who understands chemistry from the inside out. From raw materials to batch logs, from technical support calls to audits on the ground, our entire operation focuses on repeatability, transparency, and a willingness to adapt alongside changing technical and regulatory landscapes.
Years spent tracking process adjustments pay off not just in marginally higher yields or clearer spectral data, but in the kind of trust that brings long-term, collaborative business. As regulatory and environmental pressures increase industry-wide, genuine commitment on the manufacturer’s side is the difference between another off-the-shelf product and a strategic raw material you can count on. In the world of specialty chemicals, details matter—and it is those details, measured by real people and shaped by lived experience, that guide both production lines and future planning.