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4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol

    • Product Name 4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol
    • Alias 4-Fluoro-3-(trifluoromethyl)benzyl alcohol
    • Einecs 410-120-8
    • 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

    993722

    Product Name 4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol
    Cas Number 142842-49-1
    Molecular Formula C8H6F4O
    Molecular Weight 194.13
    Appearance Colorless to pale yellow liquid
    Boiling Point 73-75°C at 0.6 mmHg
    Purity Typically ≥98%
    Density 1.40 g/cm³ (approximate)
    Solubility Soluble in organic solvents such as dichloromethane, ethanol
    Smiles OCc1ccc(C(F)(F)F)cc1F
    Refractive Index n20/D 1.450 (approximate)

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

    Packing & Storage
    Packing 100 grams of 4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol, securely sealed in an amber glass bottle with tamper-evident cap.
    Shipping 4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol is shipped in tightly sealed, chemical-resistant containers to prevent contamination and evaporation. Packaging complies with international regulations for hazardous materials. The chemical is transported under controlled conditions, protected from moisture, heat, and direct sunlight, ensuring safety and product integrity throughout the shipping process. Delivery includes required safety documentation.
    Storage Store 4-Fluoro-3-(trifluoromethyl)benzyl alcohol in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents and acids. Store at room temperature or lower, and follow all relevant chemical safety protocols, including proper labeling and secondary containment where appropriate.
    Application of 4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol

    Applications of 4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol in Industrial Manufacturing

    As a specialized upstream manufacturer, we supply 4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol to downstream sectors where advanced fluorinated benzyl structures are essential for precision synthesis and high-value material innovation. This section details the focused, real-world industrial uses of this intermediate, connecting its role to compliance, dosage, process integration, and the nature of finished products in each segment.

    1. Agrochemical Active Ingredient Synthesis

    Downstream agrochemical producers employ this benzyl alcohol as a key building block in the synthesis of advanced fluorinated crop protection agents. Its unique functional profile enables the introduction of both fluoro and trifluoromethyl groups into herbicide and fungicide active components, imparting superior metabolic stability and targeted field performance. Our material enters schemes specifically tailored to diversification in modern synthetic agrochemical molecules, facilitating optimizations in product half-life and selectivity parameters set by increasingly demanding agricultural efficiency requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • REACH Regulation (EC) No 1907/2006 – Annex XVII restrictions on intermediates
    • ISO 9001:2015 Quality Assurance in chemical synthesis
    • EU Biocidal Product Regulation (BPR, Regulation (EU) 528/2012)

    Typical usage ratio

    • Normal input: 0.45–1.2 molar equivalents per synthesis batch, adjusted based on active ingredient scaffold and downstream functionalization steps.

    Downstream process integration

    • Direct nucleophilic addition or Friedel-Crafts functionalization to prepare core scaffolds, followed by chlorination or further fluorination and esterification as required for final active ingredient structure.

    Final product types

    • Selective herbicide actives for cereal and oilseed crops
    • Fungicide compositions for resistance management in horticultural applications
    • Custom pesticide intermediates with multi-fluorine motifs

    2. Pharmaceutical Fluorinated Intermediate Manufacturing

    This benzyl alcohol serves innovation-driven pharmaceutical companies as a core intermediate in synthesizing high-purity fluorinated building blocks for APIs. Its electronic properties promote precision in the introduction of fluorine atoms to aromatic rings, meeting rigorous structural requirements for next-generation drug candidates. Our tightly-controlled supply enables downstream partners to achieve high-yield transformations during the early stage or side-chain elaboration phase of complex molecule assembly, directly impacting the active pharmaceutical ingredient's pharmacokinetic and selectivity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs applicable to fluorinated intermediates
    • 21 CFR Part 211 US cGMP for pharmaceutical manufacturing
    • USP General Chapter 1086 (Impurities in Drug Substances and Intermediates)

    Typical usage ratio

    • 0.2–0.8 molar equivalents per reaction step; specific charge adjusted according to synthetic strategy of target API or intermediate.

    Downstream process integration

    • Early-stage building block for side-chain introduction or substitution reactions, often via Mitsunobu or Suzuki coupling routes when assembling fluorinated aromatic motifs in API candidates.

    Final product types

    • Pharmaceutical intermediates featuring fluoro- and trifluoromethyl-substituted benzene units
    • Targeted oncology and CNS drug substance scaffolds
    • Drug discovery lead compounds with fluorinated pharmacophores

    3. Specialty Liquid Crystal Material Production

    Manufacturers of advanced display technologies employ this compound for precision synthesis of high-performance liquid crystal intermediates. The incorporation of fluoro and trifluoromethyl functionalities at specific aromatic positions enhances dielectric anisotropy and temperature-range stability, making it indispensable for downstream processing of liquid crystal mixtures used in high-spec television, monitor, and instrumentation displays. The compound's performance in maintaining structural purity and stability during multi-stage chemical modifications directly affects optical rotation and electro-optical behavior of the final materials.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic and electrical equipment
    • ISO 9001:2015 Quality Management Systems in specialty chemical manufacturing
    • IEC 60825-1 for safety in electronic displays
    • IEC 61290-1-3 Performance standards for optoelectronic liquid crystal devices

    Typical usage ratio

    • 2–6% mol fraction in core-formulated liquid crystal synthesis batches, depending on required dielectric and optical parameters in target blend.

    Downstream process integration

    • Stepwise etherification or carbamation followed by coupling to heterocyclic systems during the pre-assembly of liquid crystal mesogen units preceding final mixture blending.

    Final product types

    • Twisted nematic (TN) and super-twisted nematic (STN) liquid crystal display materials
    • Active-matrix (AM) LCD alignment layers
    • Custom high birefringence liquid crystal mixtures for precision optical instrumentation

    4. Advanced Polymer Modifier Synthesis

    Producers in the high-performance polymer sector use this alcohol for functionalizing specialty resins and engineering plastics. Its introduction as a pendant group delivers enhanced surface energy, chemical resistance, and thermal performance to polymers like fluorinated polyesters and specialty polycarbonates. Our formulation-grade material supports tunable incorporation rates and delivers precise performance enhancements in applications such as filtration housings, wire insulation, and solvent-resistant coatings, where traditional additives fail to match end-product requirements.

    Industry compliance standards

    • ISO 14001 Environmental Management in chemical processing
    • ASTM D638 and D790 for polymer mechanical property verification
    • UL 94 Flammability testing for plastics
    • FDA 21 CFR 177 Subpart B for indirect food contact polymers (for qualified applications)

    Typical usage ratio

    • 0.5–2.5 wt% as a functional monomer or chain modifier; dosing determined by target polymer architecture and desired surface/chemical property outcomes.

    Downstream process integration

    • Introduced into pre-polymer reaction mix before esterification or condensation polymerization; serves as a terminator or side-group donor in reactive extrusion or solution polymerization.

    Final product types

    • High-performance fluorinated polyesters
    • Chemical-resistant polymer coatings and films
    • Specialty extruded engineering plastics for electronics and filtration

    5. Fine Chemical Intermediate for Fragrance Ingredient Synthesis

    Specialty fragrance chemical companies procure this compound for synthesizing rare fluoroaromatic motifs in novel aroma molecules. The presence of both fluoro and trifluoromethyl substituents enables the production of complex, high-value musk and green-note raw materials for premium perfumery. Its high chemical purity and defined substitution pattern ensure batch-to-batch reproducibility in multi-step, structure-driven olfactory ingredient synthesis, meeting the sensory and quality demands of downstream fragrance formulators.

    Industry compliance standards

    • IFRA Standards and Amendments (International Fragrance Association)
    • EU Regulation (EC) No 1223/2009 on cosmetic products (for fragrance use in cosmetics)
    • ISO 9235:2013 for natural and synthetic aromatic chemicals
    • Good Manufacturing Practice for Fine Chemicals

    Typical usage ratio

    • 0.1–0.9 molar equivalents per fragrance molecule synthesis, set based on target note intensity and desired volatility or fixative effect within the composition.

    Downstream process integration

    • Utilized at key aldehyde or esterification stages to build fluorinated aromatic ring systems before incorporation into complex synthetic musks, aldehydes, or green-toned ingredients used in fine fragrance and flavor bases.

    Final product types

    • High-value synthetic fragrance ingredients for luxury perfumery
    • Specialty aromatic chemicals with unique freshness or musk character
    • Complex multi-component fragrance accord bases
    Free Quote

    Competitive 4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol prices that fit your budget—flexible terms and customized quotes for every order.

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    More Introduction

    4-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol: Real-World Insights from the Manufacturer’s Perspective

    Understanding the Core Structure

    4-Fluoro-3-(trifluoromethyl)benzyl alcohol stands out in our catalog for several reasons. Its chemical structure—aromatic core, fluorine at position 4, trifluoromethyl at position 3, and a benzyl alcohol moiety—lends distinct reactivity that organic chemists appreciate. This is not a compound that sits unused in the warehouse. It is requested directly by researchers and production supervisors who have experience with other benzyl alcohols and see limitations in more basic analogues.

    We keep our batches consistent by maintaining rigorous quality standards, because impurities at the ppm level shift the characteristics in a way that downstream users do not find acceptable. Over the years, our QC team has learned that minor inconsistencies in the trifluoromethyl group or contamination that introduces other positional isomers can quietly alter reaction yields. Our continuous investment in NMR and GC-MS testing ensures that each drum and bottle meets the bar set by process development teams at our client facilities.

    Model, Purity, and Appearance

    The 4-fluoro-3-(trifluoromethyl)benzyl alcohol you receive from our plant comes with a purity level regularly exceeding 98%, typical for pharmaceutical intermediates and specialty chemicals. There isn’t much debate among process chemists that a pale yellow or clear liquid is preferable—any tint or cloudiness prompts questions. Buyers don’t just call for “high purity”—the demand is for reproducible batches, tightly specified moisture content, and detailed impurity profiling. Our reactors and distillation units are dedicated to fluorinated benzyl derivatives during campaign production, and our operators have seen firsthand how cross-contamination with non-fluorinated products affects reactivity and long-term storage.

    The molecular formula C8H6F4O places it in a niche of specialty chemicals: small enough for fast, controllable reactions, but functionally robust for several synthetic schemes. The molecular weight (208.13 g/mol) works well for mass spec detection. Chemists tell us that accurate MW and tight melting point ranges support process optimization.

    Usage in Synthetic Chemistry

    We have tracked over a decade of purchase records and technical feedback, and the top four uses consistently emerge: building block for pharmaceutical active intermediates, functional monomer for polymers, custom ligand development, and agri-chemical side-chain assembly.

    In pharmaceutical synthesis, substitution at the 3- and 4-positions on the aromatic ring, especially with electron-withdrawing groups, allows for predictable regioselectivity in subsequent steps. Medicinal chemists rely on the modulation of metabolic stability and membrane permeability provided by the fluoro and trifluoromethyl groups, while the benzyl alcohol moiety participates efficiently in etherification and oxidation reactions. We have seen teams use this compound as a precursor for aryl fluorides, phenols, or benzylic acids—it plays a central part in process development where small changes to the structure could mean patentability or improved therapeutic profiles.

    Custom polymer manufacturers are increasingly turning to this compound for applications where polar fluorinated chains change surface energies or chemical resistance. The CF3 and F groups impact bulk properties. In our dialogues with technical buyers, it’s clear they regard conventional benzyl alcohols as insufficient for advanced applications requiring strong electronegative groupings on the ring. Projects involving low-surface-energy coatings, ion-exchange membranes, or unique prepolymers benefit from the tailored fluorinated structure.

    In ligand synthesis, the presence of both a benzylic hydroxyl group and multiple fluorine atoms offers a versatile handle. Research teams point out that fluorinated benzyl alcohol derivatives are gaining a presence in catalysis and material science, particularly because they confer interesting electronic effects that tweak reactivity in transition metal complexes.

    For agrochemical synthesis, the site selectivity driven by both electronic and steric effects enables predictable downstream chlorination, nitration, or coupling reactions. Our records show this intermediate featuring in the development of herbicide and fungicide candidates—not in high tonnage, but where customization and functional testing are more important than price per kilo.

    What Sets This Product Apart

    Direct comparison with standard benzyl alcohol highlights the differences between simple, unfunctionalized alcohols and those featuring heavy halogenation. Fluorinated variants like 4-fluoro-3-(trifluoromethyl)benzyl alcohol exhibit both increased lipophilicity and decreased hydrogen bonding, which can dramatically alter solubility in organic solvents and performance in synthetic routes. A user who attempts a direct substitution with an unsubstituted benzyl alcohol will notice changes in both yield and byproduct profile.

    Across many years of customer feedback—ranging from small pilot syntheses to kilogram-scale campaigns—the clear message is: the presence of trifluoromethyl and fluoro group offers greater control over both the pace and selectivity of classic transformations. Halogenated aromatics, especially those with a trifluoromethyl group, are not easy to clean up if contaminated, and operators report substantial time savings when working with a reliable supply lot compared to generic alternatives.

    Unlike some other benzyl-derived intermediates, storage stability is enhanced due to the electron-withdrawing character of the substituents. This not only minimizes the risk of peroxide formation but also slows unwanted side reactions during long-term inventory holding. After speaking with several formulation chemists, a recurring issue with simple benzyl alcohols lies in their susceptibility to oxidation; the electron-poor ring structure in this molecule offers more stable shelf life and more robust process reliability.

    Handling and Operational Insights

    Plant operators communicate regularly about challenges in scaling up reactions involving highly fluorinated aromatics. Trace byproducts can catalyze difficult side reactions or interfere with downstream purification. Our technical teams emphasize careful monitoring of reaction temperature, especially during Grignard or lithium-halogen exchange steps. Unlike simple benzyl alcohols, a slight temperature overshoot can degrade the compound, which presents differently on TLC and HPLC. Customers with experience processing this material reflect an appreciation for clear technical data on flash point, recommended inert atmosphere protocols, and solvent compatibility.

    Loading and metering present no unique safety hazards compared to other aromatic alcohols, but dust formation during transfer of drummed or bulk-packaged material raises operator concerns. Our SOPs address this with dedicated extraction systems and PPE guidelines adopted from fluorochemical handling best practices. There are occasional requests for specific particle size or pre-diluted solutions to simplify transfer and boost process consistency. We accommodate when the order volume covers the dedicated setup, but the majority prefer receiving material in standard flasks or drums, monitored for headspace oxygen levels.

    Waste disposal also crops up frequently in technical discussions, as local regulations increasingly recognize the environmental effects of fluorinated organics. Customers value detailed SDS and waste-handling documentation and appreciate upfront clarity about any specific decomposition products formed under heat or acid. We work with downstream users to identify the most cost-efficient and compliant pathways for responsible disposal, drawing on our own plant waste-stream management records.

    Common Issues in Procurement and Solutions from Our Perspective

    Among the top procurement pain points voiced by direct buyers: inconsistent purity, unreliable lead times, and poor technical support from suppliers that don’t manufacture the actual product. Over nearly two decades, our team has developed tighter process scheduling, in-house analytical validation, and extensive batch record-keeping that minimizes disruptions. We communicate honestly about capacity constraints. If we can’t deliver a requested lot size immediately, we provide realistic timelines that help our customers avoid unnecessary downtime.

    One technical lead at a mid-sized pharma company reported a series of failed batches after sourcing this compound from an unknown supplier, citing unexpected side-products and unstable reaction profiles. After switching to our supply, their process reproducibility returned. We see this not as proof of our own excellence, but as evidence that real manufacturer oversight—starting from raw material QA to final packaging—makes the critical difference when dealing with reactive, sensitive compounds.

    Communication gaps often account for the largest delays. Some procurement teams do not relay the full intended application to their supplier, missing an opportunity to request a specific impurity profile. As manufacturers, we try to build these conversations early—clarifying needs around water content, storage temperature, and shipping environment. Our shipping coordinators have overcome many logistical hurdles associated with sending specialty chemicals to both established and developing markets, reducing customs hold-ups and temperature excursions.

    Regulatory and Compliance Considerations

    With exponentially increasing scrutiny from regulatory agencies worldwide, especially regarding persistent organic pollutants and fluorinated intermediates, we have integrated robust compliance reviews into every step. Documenting full lot traceability, from fluorinated starting materials down to final container labeling, builds confidence with our customers and their regulatory reviewers. This function rarely wins awards but avoids costly recalls and import restrictions.

    Reach, TSCA, and country-specific chemical control frameworks affect how we register and ship this compound. Our procurement office keeps updated registration dossiers, routinely checked against spot audits. We maintain open channels with compliance officers in customer organizations, so that any changes in hazard classification or packaging regulations are communicated rapidly. Chemists and EHS managers often thank us for not simply providing a generic safety data sheet, but also for outlining real-world risks and workable mitigations drawn from long-term handling experience.

    Operational Experience: Lessons from the Line

    One shift leader summed it up: "Any change we make, we document. We tweak the reaction parameters, log every yield, and note the least expected impurity.” That mindset has helped us respond quickly to customer batches that present new technical challenges. In scaling up, reaction exotherms behave differently in fluorinated aromatics compared to regular benzyl alcohols—it’s not enough to extrapolate from literature data. We share this operational reality in technical briefings to avoid missteps in customer scale-up campaigns.

    Fielding tech support calls, we’ve realized how often unexpected process bottlenecks originate upstream. One production manager approached us with unexplained filter fouling during a coupling step, traced to trace iron contamination in their purchased material. Based on our manufacturing QA logs, we suggested a revised purification sequence that eliminated the problem. Few distributors offer this depth of root-cause tracing, but for customers running multi-shift production lines, actionable advice saves both time and raw material.

    Internal feedback drives many of our continuous improvements, whether it’s from a batch operator tightening up a drying step or a chemist asking us to investigate a persistent impurity. We keep a policy of sharing these incremental upgrades with long-time customers, as each improvement in purity or storage stability directly impacts end-use reproducibility. When the process improves, the whole downstream network benefits.

    Collaboration & Technical Support

    Customers doing first-time evaluations appreciate not only our product, but also guidance and troubleshooting to integrate the compound into their unique process schemes. We view our responsibility as extending beyond simple supply: operational walk-throughs, advice on process optimization for benzylic alcohols in fluorinated systems, and periodic check-ins to capture ongoing challenges.

    We regularly receive requests for application notes and real-world case studies—from organizations ranging from early-stage R&D, pilot plants, to multinational formulation groups. Our internal application chemists maintain an archive of anonymized success stories and lessons learned, disseminating select methods or process hints that can save months of costly, redundant experimentation.

    We have developed cross-functional teams comprising synthetic chemists, EHS experts, and plant operators to quickly evaluate and resolve complex technical issues for customers. By doing so, we avoid the confusion and misinformation that sometimes plague the supply of specialty chemicals from traders or bulk resellers with no firsthand production knowledge.

    Tracking Market and Technology Trends

    Fluorinated benzyl alcohols are no longer simply niche reagents for specialist labs. Across the past five years, demand has grown due to the rapid expansion in medicinal and material chemistry applications. The ongoing trend toward higher fluorine content in drug discovery, combined with polymer innovation, has pushed both awareness and sophistication of purchasers. Customers are asking deeper technical questions—about secondary impurities, long-term storage, and even the global sourcing of fluorinated raw materials.

    We monitor shifts in regulatory priorities—whether focused on environmental persistence, worker exposure, or final product safety—and adjust our internal production procedures accordingly. This agility equips us to respond quickly to evolving expectations and keeps both our operation and our customers in compliance.

    Future Directions and Challenges

    Looking ahead, customer expectations regarding both transparency and technical support will only rise. Some clients now request extensive analytical documentation with every batch, beyond ordinary CoA or SDS, seeking customized reporting and periodic trend analysis. We see this as a welcome development that helps raise standards across the industry.

    One perennial challenge: securing a stable supply of high-quality fluorinated raw materials amid a volatile market. Prices and lead times for upstream fluoroarenes fluctuate under new regulatory controls, and suppliers have learned to cement long-term contracts or establish qualified dual sources to shield production schedules from unexpected interruptions. Our own production planning reflects these market realities.

    Our team continues to invest in training and process digitization. Recording every decision—every lot, operator shift, purification tweak—builds long-term knowledge and reduces unplanned downtime. As a direct manufacturer, everything we improve upstream ultimately helps the process chemist at the other end of the supply chain achieve better batch-to-batch consistency, fewer surprises at scale-up, and a richer foundation for innovation.

    Concluding Thoughts from the Factory Floor

    4-Fluoro-3-(trifluoromethyl)benzyl alcohol reflects very real trends happening in synthetic and process chemistry—greater reliance on electronically tuned aromatics, increasing demands for predictable supply and documentation, and a shared expectation that manufacturers bring not just product, but real operational intelligence to the table. We remain committed to evolving with our customers, supporting their process needs, and communicating both the triumphs and hurdles that come from manufacturing advanced chemical intermediates.