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3',5'-Difluoro-2'-Hydroxyacetophenone

    • Product Name 3',5'-Difluoro-2'-Hydroxyacetophenone
    • Alias DFHAP
    • Einecs 674-922-6
    • 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

    604518

    Product Name 3',5'-Difluoro-2'-Hydroxyacetophenone
    Molecular Formula C8H6F2O2
    Molecular Weight 172.13 g/mol
    Cas Number 864870-66-8
    Appearance White to off-white solid
    Melting Point 77-80°C
    Boiling Point Unknown
    Solubility Soluble in common organic solvents (e.g., DMSO, ethanol)
    Purity Typically >98%
    Smiles CC(=O)C1=CC(=C(C(=C1)F)O)F
    Inchi InChI=1S/C8H6F2O2/c1-4(11)5-2-6(9)8(12)7(10)3-5/h2-3,12H,1H3
    Storage Store at 2-8°C, protected from light

    As an accredited 3',5'-Difluoro-2'-Hydroxyacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3',5'-Difluoro-2'-Hydroxyacetophenone is packaged in a sealed amber glass bottle, labeled, containing 5 grams of product.
    Shipping 3',5'-Difluoro-2'-Hydroxyacetophenone is shipped in tightly sealed containers to prevent moisture and contamination. It is transported in compliance with safety regulations for chemicals, typically under ambient conditions. Proper labeling and documentation are ensured for safe handling. Always refer to the material safety data sheet (MSDS) for additional shipping guidelines.
    Storage **Storage Description:** Store 3',5'-Difluoro-2'-Hydroxyacetophenone in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure clearly labeled storage and restrict access to trained personnel. Avoid prolonged exposure to air and handle using proper personal protective equipment (PPE).
    Application of 3',5'-Difluoro-2'-Hydroxyacetophenone

    Applications of 3',5'-Difluoro-2'-Hydroxyacetophenone in Industrial Manufacturing

    3',5'-Difluoro-2'-Hydroxyacetophenone offers key functionality in select chemical industry segments. The following scenarios outline precise applications in accordance with global regulatory standards, recommended integration stages, and finished product outcomes based on our direct manufacturing experience.

    1. Pharmaceutical Intermediate for Fluorinated Drug Synthesis

    Our material serves as a critical fluorinated intermediate in the synthesis of several pharmaceutical actives, especially within non-steroidal anti-inflammatory drugs (NSAIDs) and patented central nervous system (CNS) drugs. R&D and commercial-scale customers utilize our product during key acetophenone derivatization stages to enhance molecular stability and increase compound bioavailability. Customers require batch-to-batch reproducibility and traceable documentation for regulatory filings in multiple regions.

    Industry compliance standards

    • ICH Q7 GMP Guidelines
    • 21 CFR Part 210/211 (US FDA)
    • EU GMP Part II (EU Directive 2003/94/EC)
    • Chinese Pharmacopoeia General Test Methods

    Typical usage ratio

    • 10–25% relative to total substrate in condensation reactions
    • Adjusted according to target compound yield and purity requirements

    Downstream process integration

    • Integrated during early-stage condensation or Friedel–Crafts acylation
    • Used as a coupling agent in API synthesis routes
    • Follows specific isomer isolation, followed by product purification steps

    Final product types

    • Active pharmaceutical ingredients (e.g., fluorinated analgesics)
    • Strategic API intermediates
    • Research-grade reference compounds

    2. Advanced Agrochemical R&D and Production

    The compound acts as a specialized building block for new-generation fluorinated agrochemicals, including selective herbicides and fungicides. Agrochemical formulators prize its ortho-hydroxy positioning for downstream coupling and ring modification, directly influencing the bioactivity spectrum and resistance profiles. Our controlled fluorination process minimizes residual impurities, meeting the data package requirements for product registration in international markets.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001 Quality Management System
    • China GB/T 1600-2016 Pesticide Standard
    • REACH Regulation (EC) No 1907/2006 for export to the EU

    Typical usage ratio

    • 5–12% of total scaffold molecules in early-stage synthesis
    • Adjusted by structure-activity relationship (SAR) studies and desired activity profile

    Downstream process integration

    • Initial step in heterocycle functionalization or cross-coupling reactions
    • Feeds into chlorination, methylation, or further fluorination units
    • Isolated intermediates characterized using HPLC and NMR before final formulation

    Final product types

    • Precursor compounds for commercial herbicides
    • Fluorinated fungicide actives
    • Plant growth regulator molecules

    3. Synthesis of Electronic Chemicals for OLED Materials

    Display and device manufacturers use the compound as a high-purity precursor in syntheses for organic light-emitting diode (OLED) materials. The fluorinated aryl group enhances electron mobility and stability in organic semiconductor applications. Quality assurance demands sub-ppm impurity levels, with particular limits on metal content and residual solvents. Strict materials traceability is required throughout the supply chain for advanced electronics production.

    Industry compliance standards

    • IECQ QC 080000 (Hazardous Substance Process Management)
    • RoHS Directive 2011/65/EU for electronic raw materials
    • ISO 9001–certified batch traceability
    • SEMI E10 standard for materials compatibility

    Typical usage ratio

    • 2–8% in host-guest emitter systems
    • Fine-tuned based on mobility and light output testing

    Downstream process integration

    • Used in Suzuki or Buchwald-Hartwig couplings for arylation
    • Undergoes subsequent cross-linking in organic electronic device fabrication
    • Integrated during dopant material preparation under inert atmospheres

    Final product types

    • OLED emitter and transport layer monomers
    • Electronic-grade aryl fluorides
    • Photovoltaic intermediate materials

    4. Intermediate for Industrial Dye and Pigment Manufacturing

    This chemical functions as a specialty intermediate for synthesizing fluorinated azo and anthraquinone dyes. Producers in the textile, ink, and coatings sectors rely on its unique substitution pattern to achieve tailored hue intensity and lightfastness. Stringent control of side reactions during condensation ensures pigment uniformity, while compliance with regional chemical safety and import certifications remains mandatory for end-product acceptance.

    Industry compliance standards

    • OEKO-TEX Standard 100 Class II (for textile dyes)
    • EN 71-3 Toy Safety Standard (colorants for children’s products)
    • REACH Annex XVII restricted substances list
    • GB 18582-2020 (Chinese decorative coatings)

    Typical usage ratio

    • 7–16% of core dye batch
    • Adapted based on target color strength and solvent compatibility

    Downstream process integration

    • Condensation with diazonium salts or anthraquinone cores
    • Subsequent sulfonation or halogenation as required by formulation
    • Final blending into pigment dispersions for inks, fibers, or plastics

    Final product types

    • Specialty azo and anthraquinone dyes
    • Solvent-stable pigment dispersions
    • Colorants for textile, leather, and plastic applications
    Free Quote

    Competitive 3',5'-Difluoro-2'-Hydroxyacetophenone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3',5'-Difluoro-2'-Hydroxyacetophenone: An Insider’s Perspective on Its Value and Role

    Introducing a Precise Ingredient for R&D and Synthesis

    Chemical manufacturing always comes back to reliability and robust innovation. Among our specialty molecules, 3',5'-Difluoro-2'-Hydroxyacetophenone stands out as a core building block that has reshaped how researchers and developers approach targeted synthesis. This compound, with its carefully placed difluoro groups and hydroxy moiety on the acetophenone framework, offers a versatile platform for advanced chemical transformations. Our team has developed years of expertise in producing this molecule at scale, ensuring batch-to-batch consistency and offering a product trusted by pharmaceutical companies and material scientists worldwide.

    Model Details and Manufacturing Standards

    Focus on quality starts well before raw material sourcing. The model we produce, known internally as DF2HAP, features a tightly controlled purity threshold. Experienced chemists monitor each production stage, leveraging distillation and crystallization techniques that minimize cross-contamination and maximize consistency. These rigorous steps eliminate process drift often found in smaller-scale or less experienced manufacturing sites. Over the years, collaborations with major research labs have sharpened our understanding of impurity thresholds needed to deliver uncompromised reproducibility in both small-molecule and polymer syntheses.

    Structural Advantages and Functional Role

    As the hydroxy group anchors to the acetophenone’s second carbon, and fluorine atoms decorate the third and fifth positions of the phenyl ring, this unique motif enables strong electron-withdrawing effects. This arrangement enhances electrophilicity and modulates reactivity, crucial in several downstream applications. In our experience, this dual-fluoro design lends itself especially well to cross-coupling reactions and selective functional group modifications. Countless clients have leveraged these properties for synthesizing intermediate compounds in agrochemicals, pharmaceuticals, and advanced material science research.

    Nuanced Physical Characteristics

    From a handling perspective, we see clear differences between 3',5'-Difluoro-2'-Hydroxyacetophenone and other acetophenone derivatives. This compound’s unique balance of hydrophilicity and lipophilicity, tuned by the hydroxy and difluoro substituents, enables higher solubility in common organic solvents without excessive volatility. Teams in our facility often comment on its crystalline form, which stands out for its stability under regular laboratory conditions. Several times, clients have remarked that this stability reduces downtime in industrial processes and streamlines sample preparation in analytical labs.

    Applications and Solution Pathways: Stories from the Floor

    Over the past decade, our technical support group has seen routine requests for application support—particularly from pharmaceutical companies aiming to accelerate their research pipeline. The difluorinated nature of the molecule proves invaluable for medicinal chemists, providing a platform for rapid scaffold modification. By incorporating this structure into more complex molecules, new pharmacophores have moved through synthesis and testing at a faster pace. For agricultural research, this same structure grants improved resistance to enzymatic degradation, a property that opened doors to more resilient experimental crop protectants. Several institutions involved in polymer research have requested technical data related to incorporation of this building block into novel resins, chasing improvements in chemical resistance and optical properties.

    Internally, our process engineering team keeps close tabs on feedback, especially when a client faces yield or reaction rate challenges. Many process chemists in the field noticed standard acetophenone analogues would falter in yields when subjected to cross-coupling or selective halogenation steps. Tweaks in electronic structure from the difluoro groups often resolve these issues, delivering more reliable outcomes in large-scale applications. As demand grows for tailored APIs and high-performance materials, this kind of nuanced troubleshooting defines the difference between lab curiosity and industrial reliability.

    Direct Comparisons with Other Acetophenones

    We keep detailed records from our own labs and partner facilities, comparing results across a family of related compounds. Regular acetophenone and mono-fluorinated variants often lag behind in both reactivity and selectivity under identical conditions. Our team once ran a series of aldehyde-alcohol oxidation reactions: 3',5'-Difluoro-2'-Hydroxyacetophenone helped bring reaction times down by as much as 30 percent, without compromising purity. The difference, noticed by analytical groups running NMR and HPLC diagnostics, wasn’t just incremental—it translated to larger process improvements and savings at scale.

    Clients choosing between hydroxyacetophenones with no halogenation, mono-fluorinated, or dihalogenated forms routinely report that our difluorinated product gives them higher success rates for tough coupling reactions or where steric effects matter. Certain cases show the hydroxy-only molecule suffering from side reactions and polymerization at elevated temperatures, an issue not seen with this more robust difluoro-hydroxy combination.

    Scaling Up with Confidence and Transparency

    Our experience with scale-up also sets this product apart. Academic labs typically acquire it in gram quantities for proof-of-concept studies. For pilot and commercial production, we pivot smoothly, producing multi-kilo lots while maintaining purity benchmarks established at the beginning. No matter the size of the order, each shipment comes with complete analytical data, and chemists from our quality team field questions about impurity profiles and storage practices. Over years of continuous feedback, process improvements have locked in reliable shelf life and stability—even for customers with limited environmental control in their locations.

    Keeping a consistent color, melting point, and spectral profile—those details underscore our daily commitment to getting this right. We handle every inquiry about transparency of origin, batch documentation, and reference lot data because we know reproducibility doesn’t happen by luck. It surfaces through rigorous, repeatable practice, and plenty of direct dialog with end-users.

    Supporting Regulatory and Analytical Demands

    Pharmaceutical and fine chemical organizations rely on this product’s compliance with regulatory guidelines. That means our team always works closely with external auditors and regulatory bodies, documenting each synthesis lot with full chain-of-custody and provenance records. Analytical support covers everything from NMR and IR analyses to mass spectrometry, backed by in-house standards and third-party validated methodologies. We recognize the nuances clients face during regulatory filings—our data packages are shaped by many years of hands-on troubleshooting and adaptation to new compliance regimes. Reliability remains the greatest reassurance to the quality control officers overseeing new process validations.

    Real-World Impact and Value Creation

    Researchers worldwide continue to push the boundaries of synthetic chemistry and applied science. In that context, 3',5'-Difluoro-2'-Hydroxyacetophenone has become an enabler—from the bench to large-scale reactors. One of our pharma partners, intent on developing fluorinated lead compounds, described how a steady supply of this molecule allowed them to accelerate their candidate screening process. In specialty materials, several polymer labs developed new families of resins, reporting higher resilience and better processability than with other acetophenone-based intermediates.

    On our factory floor, chemists regularly convene to review practical difficulties faced by customers—from solubility mismatches to handling sensitivities in automated processes. These meetings shape incremental refinements in drying, packaging, and shipping. By working directly with users—rather than distributing through unknown chains—we can control quality at every step, solving issues before they ripple out to production timelines.

    Dedicated to Thoroughness in Analytical Verification

    The field moves quickly, but reproducible science only happens when starting materials meet expectations every single run. To that end, our in-house analytic lab maintains a full suite of reference spectra and chromatograms, checked regularly against established standards. We learn from every deviation, whether flagged by a customer or spotted in our tests, and trace the source with focused root-cause analysis. Sometimes this means re-examining raw input or shifting a purification protocol by a few degrees or minutes. These adjustments, modest as they might sound, protect users against subtle sources of error or wasted time.

    Every lot comes with analytic transparency, from pre-shipment tests to archived reference samples available for audit or cross-verification. Over the years, this has proven more valuable than any marketing campaign—a point our partners confirm again and again. When a research team or production site encounters setbacks in a downstream process, the ability to review lots and analytics directly with the manufacturer can mean the difference between swift troubleshooting and drawn-out, costly investigations.

    Working Closely With Customers to Solve Challenges

    We do more than make molecules—our team acts as technical partners to researchers worldwide. A few years ago, one biotech customer developed a new synthetic route dependent on a subtle property of the difluorinated acetophenone. They required nuanced tweaks in product drying and packaging for better integration into their automated dispensing system. Direct phone calls, sample swaps for process validation, and several rounds of adjustments followed until the process ran smoothly. This hands-on approach delivers a kind of process confidence that documentation alone cannot match. Our ongoing commitment to these partnerships forms the backbone of everything we do.

    Narrowing the Focus: Differentiation from Third-Party Sources

    One trend in the market stands out to us: a rapid increase in third-party and trading companies offering this compound, often without a production background or knowledge of its synthesis intricacies. Multiple customers have come to us after experiencing variability issues—off-color batches, inconsistent melting points, impurities that eluded basic testing—all stemming from a lack of deep process control. Sourcing directly from us, the manufacturer, closes that problematic gap. We never outsource critical process steps, from raw material selection to final packaging. That discipline, refined by years of technical feedback, translates directly into end-user confidence.

    Our insights into this molecule’s performance come from sustained experience, not quick resale. Differences in precursor selection, reaction time optimization, and purification contribute to ultimate reliability that distributors rarely discuss or even examine. If a customer faces difficulties during a reaction sequence, our team understands each production variable well enough to dig into reaction mechanics and tweak upstream processing, rather than just replacing a bottle. Across research and production settings, this saves measurable time and cost.

    Future Perspectives and Continuous Improvement

    Science doesn’t reward those who stand still. Our R&D group continues to evaluate synthesis routes for even greater efficiency, with an eye on sustainability and cost containment. Developing new derivatives and analogues of 3',5'-Difluoro-2'-Hydroxyacetophenone remains a priority, with feedback loops established with researchers looking to expand its application envelope. Product stewardship matters too—packaging innovations, waste minimization, and enhanced traceability all benefit from working alongside end-users and responding to market realities as they shift.

    Transparency and technical agility anchor our efforts to keep this building block reliable, well understood, and a true enabler for scientific progress. Each production batch is more than a chemical—it represents trust, experience, and the accumulated knowledge of our entire team. This direct, responsive relationship with customers continues to distinguish our approach in a crowded market.

    Conclusion: Experience-Backed Performance That Matters

    From day one, our focus on 3',5'-Difluoro-2'-Hydroxyacetophenone has always been about enabling real-world breakthroughs. Whether this involves trusted supply to pharmaceutical R&D, problem solving for process engineers, or supporting new advances in specialty polymers, what sets our product apart is practical expertise, robust documentation, and a commitment to never taking shortcuts. The difference shows up in each reaction that runs the way it should, delivering consistent performance and tangible results where it counts most.