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2,5-Difluorobenzyl Alcohol

    • Product Name 2,5-Difluorobenzyl Alcohol
    • Alias 2,5-DFBA
    • Einecs 701-177-6
    • 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

    210636

    Cas Number 26792-93-2
    Molecular Formula C7H6F2O
    Molar Mass 144.12 g/mol
    Iupac Name 2,5-difluorobenzyl alcohol
    Appearance Colorless to light yellow liquid
    Boiling Point 218-220 °C
    Melting Point Unknown
    Density 1.28 g/cm³
    Solubility In Water Slightly soluble
    Refractive Index 1.512
    Synonyms 2,5-Difluorophenylmethanol
    Smiles C1=CC(=C(C=C1F)F)CO
    Flash Point 98 °C
    Storage Conditions Store at 2-8°C
    Purity Typically ≥98%

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

    Packing & Storage
    Packing Amber glass bottle containing 100g of 2,5-Difluorobenzyl Alcohol, securely sealed with a tamper-evident cap and labeled for laboratory use.
    Shipping 2,5-Difluorobenzyl Alcohol is shipped in tightly sealed containers to prevent leakage and contamination. It should be transported as a chemical reagent, complying with relevant local and international regulations. Store and ship in a cool, dry place, away from heat and incompatible substances. Handle with appropriate safety precautions during transit.
    Storage **2,5-Difluorobenzyl Alcohol** should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Keep in a cool, dry, well-ventilated area. Avoid contact with strong oxidizing agents and acids. Properly label the container and follow all standard chemical storage and safety protocols to prevent contamination and degradation.
    Application of 2,5-Difluorobenzyl Alcohol

    Applications of 2,5-Difluorobenzyl Alcohol in Industrial Manufacturing

    2,5-Difluorobenzyl Alcohol is a key intermediate serving specialized synthesis requirements across several advanced industrial sectors. Our manufacturing expertise ensures precise control over purity and supply consistency to support secure downstream integration for demanding technical applications.

    1. Pharmaceutical Intermediates: Sartan Antihypertensive Synthesis

    Pharmaceutical manufacturers use 2,5-difluorobenzyl alcohol as a core intermediate during the preparation of sartan-based antihypertensive APIs, including losartan and candesartan. In practice, our product acts as the glycosylation precursor, providing crucial di-fluoro aromatic substitution for robust angiotensin receptor antagonist activity. Controlled impurity profiles and process-scale batch reproducibility receive regulatory scrutiny throughout medicinal synthesis.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, JP, and EP monograph guidelines on API intermediates
    • 21 CFR Part 211: Finished Pharmaceuticals (as component supplier)
    • EDQM CEP documentation for downstream API registration

    Typical usage ratio

    • 0.95–1 molar equivalent per candidate sartan core in glycosylation
    • Adjustment based on target API molecular weight and route efficiency
    • Excess up to 1.05 equivalents for improved yield in scale-up runs
    • Regularly monitored by HPLC for impurity carryover risk

    Downstream process integration

    • Charged during etherification/glycosylation stages on substituted biphenyl scaffolds
    • Used in closed reactors with controlled anhydrous conditions
    • Pre-concentration and dehydration requirements prior to coupling reactions
    • Final API purified by crystallization or flash chromatography

    Final product types

    • Losartan potassium
    • Irbesartan
    • Candesartan cilexetil
    • Other structurally related sartan antihypertensive APIs

    2. Agrochemical Synthesis: Fluorinated Herbicides and Fungicides

    In agrochemical development, 2,5-difluorobenzyl alcohol enters the synthesis of advanced phenoxy-based pesticides and systemic fungicides. The di-fluoro benzyl ring increases bioactivity and chemical stability in environmental exposure. Downstream producers implement the material via esterification and halogenation steps before final formulation and encapsulation. Throughout the workflow, compliance with monitoring of residual solvents and trace fluorinated byproducts remains essential.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC No 1907/2006) Annex XVII – fluorinated compounds
    • EPA 40 CFR Part 158: Data Requirements for Pesticides
    • ISO 9001/14001 quality systems for environmental security

    Typical usage ratio

    • 0.85–1.1 equivalents per target esterified or alkylated product
    • Recipe varies depending on active ingredient load and molecular architecture
    • Occasional excess alcohol to ensure complete conversion in batch
    • Limits set below 500 ppm for alcohol residue in final technical concentrate

    Downstream process integration

    • Reacts with acid chloride or activated acid to form key benzyl esters
    • Integrated into automated batch reactors with in-line solvent recovery
    • Post-reaction distillation and solvent stripping for product isolation
    • Incorporated in further halogenation for active ingredient enhancement

    Final product types

    • Difluoro-phenoxy herbicide esters
    • Systemic fluorinated fungicides (technical grade)
    • Granule and wettable powder crop protection formulations
    • Seed treatment actives with improved field persistency

    3. Specialty Chemical Precursors: Polymer Modifiers

    2,5-difluorobenzyl alcohol supports specialty manufacturers as a structural modifier in high-performance fluorinated polymer resin syntheses, influencing dielectric properties and chemical resistance. It is utilized in nucleophilic substitution and chain extension steps for engineered applications such as electronic encapsulants and high-frequency circuit materials. Strict traceability and batch consistency are vital, particularly for use in electronics and aerospace composites.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronics applications
    • ISO 10993–18 for material chemical characterization
    • ASTM D543: Chemical Resistance of Plastics
    • UL 94: Flammability testing for polymers

    Typical usage ratio

    • 3–6% w/w as a functional monomer or comonomer in polymer resin feed
    • Ratio depends on targeted dielectric constant and polymer chain length
    • Process engineers adjust formulation to balance flexibility and resistivity
    • Material evenly dispersed during melt or solution polymerization step

    Downstream process integration

    • Added during pre-polymerization as reactive benzyl alcohol functional group
    • Initiates copolymerization with fluoroaromatic monomers
    • Thermal curing phase crosslinks modified polymer architecture
    • QC sampling for molecular weight and dispersion uniformity

    Final product types

    • Low-loss circuit board prepregs
    • Encapsulant systems for semiconductors
    • Chemical-resistant composite laminates
    • Specialty adhesive films for electronics assembly

    4. Advanced Material Synthesis: Liquid Crystal and Specialty Dye Intermediates

    Producers in the advanced materials industry apply 2,5-difluorobenzyl alcohol for the synthesis of liquid crystal intermediates and structure-specific dyes, taking advantage of its di-fluoro aromatic motif for desired orientation and stability. This alcohol is engaged in etherification and condensation reactions under anhydrous conditions, producing compounds for display technology and high-stability pigments. Quality control focuses on byproduct minimization and color standardization.

    Industry compliance standards

    • EN 71-3: Safety of Toys – migration of certain elements (for display coatings)
    • ISO 9001 for material synthesis traceability
    • Restriction of Hazardous Substances (RoHS) for electronics dyes
    • REACH pre-registration for new dye intermediates

    Typical usage ratio

    • 0.75–1.2 molar equivalents depending on arylation or condensation reaction
    • Batch-to-batch variation monitored by GC-MS purity testing
    • Adjusted in small-scale pilot batches for new chromophore synthesis
    • Purity maintained above 99.0% for optical grade materials

    Downstream process integration

    • Introduced during initial etherification for liquid crystal core buildup
    • Combines with halogenated aromatic partners for extended conjugation
    • Frequent in-situ monitoring by UV-Vis and chromatography
    • Final intermediates purified under reduced pressure to minimize discoloration

    Final product types

    • Biphenyl-type nematic liquid crystals for display panels
    • High-performance fluorescent dyes
    • Infrared-absorbing pigment intermediates
    • OLED colorant bases for electronics
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    Certification & Compliance
    More Introduction

    2,5-Difluorobenzyl Alcohol: A Manufacturer’s Perspective on a Key Intermediate

    Direct experience with raw chemical production brings a different outlook than simply moving molecules on paper. Over the years, we have watched 2,5-Difluorobenzyl Alcohol grow in demand across industries, particularly in pharmaceutical, agrochemical, and specialty chemical fields. As manufacturers, we see the value and nuance of this compound firsthand—from exacting synthesis to meeting the quality standards that researchers and producers expect.

    What Sets 2,5-Difluorobenzyl Alcohol Apart

    2,5-Difluorobenzyl Alcohol stands out for its unique structural motif. With two fluorine atoms positioned at the 2 and 5 locations of the aromatic ring, it offers reactivity patterns not seen in non-fluorinated or mono-fluorinated analogs. The presence of the benzyl alcohol moiety also allows synthetic chemists to use it as a starting point or intermediate in a variety of complex syntheses. Our direct involvement in its production cycles has highlighted an important fact: even small changes in substituent positions create strong differences in downstream chemical behavior.

    Our chemists have long noted the way these fluorine atoms influence both the chemical stability and the polarity of the molecule. Their electron-withdrawing effect can alter reaction mechanisms and influence the selectivity of transformations, which is of critical importance during both scale-up and application. Compared to standard benzyl alcohol, or even other difluorinated isomers, the 2,5-configuration brings significant synthetic advantages in medicinal and agricultural compound development.

    Production Experience and Manufacturing Considerations

    Manufacturing 2,5-Difluorobenzyl Alcohol requires a thorough understanding of reaction chemistry and tight process controls. During our own scale-up process, controlling the selectivity of fluorination and protecting the benzyl alcohol group have presented challenges. Yields and purity depend on careful distillation, judicious use of protecting groups, and targeting optimum temperature and pH conditions during hydride reduction steps.

    What sets experienced manufacturers apart is the ability to replicate results batch after batch. Not every producer runs high-vacuum purification steps or analyzes content down to trace impurities using 1H and 19F NMR. We have found that skipping even one extra round of purification can compromise both the performance and safety of finished formulations. Sourcing from original producers who align with these standards has a measurable impact on final product quality for any buyer downstream.

    Our process often makes use of advanced instrumentation—not only for the main product but for closely monitoring byproducts and precursors. For example, incomplete fluorination leaves behind mono-fluorinated or non-fluorinated benzyl alcohols, which can react differently and compromise reaction efficiency in later synthetic steps. As manufacturers, eliminating these through targeted purification gives us confidence in the material we provide, and in turn, gives our customers more reliable performance.

    Specifications: Purity and Practical Qualities

    In direct factory environments, attention to detail is everything. For 2,5-Difluorobenzyl Alcohol, the most frequent focus is on achieving high chemical purity—typically above 98 percent, with low moisture content and minimal color. Impurities pose a problem in organic synthesis, particularly in pharmaceutical projects, where unknowns become critical regulatory concerns. Our operators routinely run HPLC and GC analysis to confirm purity and assess contaminant profiles after each step.

    Color and odor also reflect the compound’s quality. We monitor for off-notes or discoloration, which indicate process inconsistencies or potential side reactions. While some think of aromatics as relatively benign, improper storage or slow reactions can generate byproducts that skew performance. Storage in cool, dry conditions with tightly sealed containers helps prevent unnecessary degradation or moisture uptake. We’ve developed packaging protocols to minimize exposure to air and humidity, ensuring a consistent product from warehouse to the customer’s bench.

    How 2,5-Difluorobenzyl Alcohol is Used

    Pharmaceutical chemists often reach for 2,5-Difluorobenzyl Alcohol as a versatile building block. Its structure supports the development of bioactive molecules, including kinase inhibitors and central nervous system drugs. The fluorines can alter metabolism rates, improving half-life or shifting biological activity. Researchers working on anti-infectives and herbicides also value this scaffold, as it helps finetune target binding or adjust volatility in agricultural formulations.

    Our clients frequently report the alcohol group acts as an entry point for etherification or esterification, leading to a broader library of analogs. In lab practice, 2,5-Difluorobenzyl Alcohol reacts cleanly with acid chlorides or anhydrides to form esters, or with alkyl halides for ether derivatives. We regularly advise researchers on solvent selection and activation strategies based on firsthand pilot plant data. Good manufacturing experience translates to meaningful technical input for those exploring new routes or scaling production for trials.

    Differences from Related Products and Isomers

    Not all difluorobenzyl alcohols are created equal. Our direct synthesis work has illuminated key contrasts between the 2,5-isomer and other positional isomers like 3,5- or 2,4-difluorobenzyl alcohol. Subtle changes in fluorine placement affect reactivity under typical substitution, oxidation, or reduction conditions.

    For example, the 2,5-arrangement frequently enhances electron delocalization within the aromatic system. This impacts coupling reactions on the ring and influences outcomes in Suzuki or Heck chemistry. Researchers using other isomers have reported sluggish or unexpected reactivity compared to the reliable performance of the 2,5-isomer.

    Storage stability also benefits from the dual fluorine presence at those specific positions. Other benzyl alcohols may oxidize or discolor more readily under light or on exposure to air. Through routine batch QC and stress testing, we have found that 2,5-Difluorobenzyl Alcohol keeps its clear appearance and characteristic odor much longer than non-fluorinated analogs, simplifying storage and reducing product loss for our clients.

    Quality Control and Reliability in Supply

    Having our own reactors and labs means we control the entire process, from raw fluorination agents through to the finished drums. This consistency underpins each shipment, giving our partners confidence in continuity of supply. We’ve invested in calibration procedures for our analyzers and run reference standards at key checkpoints in the process to anticipate deviations before they become a problem.

    Packaging and shipping present unique challenges. Some buyers underestimate the impact of minor temperature excursions, which can shift product specifications during transit. Our team uses climate-controlled transport solutions for longer lead times and insulates product containers for sensitive cargo. Years of feedback from active pharmaceutical partners drove us to refine these approaches, because supply integrity directly affects project timelines and the trust our customers place in us.

    Supporting Sustainable and Safe Manufacturing

    The discussion about sustainability and environmental impact has reached every corner of chemical manufacturing. In our production of 2,5-Difluorobenzyl Alcohol, we continually seek greener solvents and waste minimization strategies. The fluorination step, in particular, often involves specialized reagents. Our facilities have invested in containment and recycling programs to capture fluorinated byproducts, ensuring safer handling for both operators and the environment.

    Process safety guides plant layout and operator training. We’ve adapted Best Available Technology principles within the plant—not simply because regulations say so, but to foster resilience against upsets and human error. Emergency quench systems, leak detection, and operator drills are part of daily life, not an afterthought. Reliable production of specialty organofluorine compounds comes from this commitment to operational discipline.

    Meeting the Needs of Pharmaceutical and Agrochemical Innovation

    The pace of medicinal chemistry moves faster than ever. Each new scaffold needs to meet demanding standards and withstand ever-tighter timelines. We see 2,5-Difluorobenzyl Alcohol as a molecule that helps bridge this gap; its performance enables bench chemists, pilot plant scientists, and regulatory teams alike to test more hypotheses with less troubleshooting.

    Clients often ask about downstream impurity formation when synthesizing candidate molecules. Our own experience in pilot programs has taught us that fluorinated benzyl alcohols can occasionally form trace acid byproducts if exposed to open air for prolonged periods or during protracted reactions. Mitigating these risks lies in sound laboratory technique and attention to solvent quality. We share our stability data to help alleviate concerns and reduce the risk of failed syntheses.

    Scaling from grams to kilograms or metric tons exposes process weaknesses. Chemical reactions that work perfectly in a beaker sometimes behave unpredictably at the 100-liter mark. As manufacturers, we have refined batch documentation, mixing systems, and purification equipment through each scale-up cycle. Uninterrupted supply keeps research moving forward—delayed shipments mean missed project milestones, not just procurement hassles.

    Technical Support: Drawing from Experience

    Supplying this compound to hundreds of customers on multiple continents has exposed us to a wide array of questions and challenges. Some concerns are technical—solvent compatibility, residual solvent content, or waste stream management. Others focus on documentation, such as thorough lot records and trace impurity profiles. Each request hones our approach to quality and responsiveness.

    Direct communication between manufacturer and researcher goes a long way. We draw from a legacy of troubleshooting: selecting the right catalyst for an etherification, conquering batch-to-batch color variation, even working with specialized packaging for trial locations with unique local conditions. These are not hypothetical scenarios—they are part of daily life for both producer and end user.

    Feedback loops matter. Regular post-delivery check-ins and open lines for technical discussions help us refine both process and product. That partnership enables breakthroughs—when customers trust that what arrives will perform as expected, critical paths shorten, and projects advance more quickly.

    Going Beyond the Bottle: The Human Side of Chemical Manufacturing

    Behind every drum or bottle of 2,5-Difluorobenzyl Alcohol is a story of careful planning, personnel dedication, and hard-won expertise. From early morning QC rounds to late-night shipment sign-offs, manufacturing teams commit themselves to getting every detail right. Many on our staff have spent years, even decades, handling aromatic alcohols and understand the subtleties that separate premium goods from merely adequate options.

    Internal collaboration powers our ability to innovate and respond. Chemists, process engineers, and plant managers pool their insights after each batch run: what went smoothly, where potential improvements linger, what new analytical techniques we might deploy. This continuous improvement feeds directly into the reliability our customers expect.

    Challenges for the Future and Community Collaboration

    The global landscape for specialty chemicals continues to evolve. Supply chain interruptions, regulatory changes, and increasing performance requirements all place new demands on raw material suppliers. Those working with 2,5-Difluorobenzyl Alcohol will likely see stronger integration with digital tracking systems, enhanced transparency in production records, and even greener synthetic routes as the field advances.

    Our experience suggests that a productive manufacturer-customer partnership depends on candor and agility. Openly sharing production challenges—whether related to raw material access, yield fluctuations, or evolving safety standards—builds a stronger base for everyone relying on this molecule. Community forums, consortia, and joint research initiatives could help drive innovation while maintaining supply resilience.

    Why 2,5-Difluorobenzyl Alcohol Remains a Reliable Choice

    Years of supplying this compound from our own reactors have crystallized its value. Whether for medicinal chemistry programs seeking next-generation treatments, crop protection companies searching for higher-performance actives, or specialty chemical users needing tailored intermediates, 2,5-Difluorobenzyl Alcohol keeps showing its strengths.

    Direct manufacturing ties let us enforce quality, provide technical insight, and anticipate demands. Our facility’s location, process controls, and skilled workforce deliver not just a product, but a partnership rooted in attention to detail. That care pays off for every formulation, every synthesis, and every new idea our customers bring to the table.

    Commitment to the Next Generation

    Growing with customer needs means putting legacy and learning into practice. New applications for organofluorine compounds emerge every year, and innovation at the production level keeps pace. By supporting curious minds and careful hands—on both sides of the customer relationship—we build pathways for safer workflows, stronger results, and better chemistry.