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2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol

    • Product Name 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol
    • Alias 2-Fluoro-3-(trifluoromethyl)benzyl alcohol
    • Einecs 642-196-8
    • 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
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    Specifications

    HS Code

    561823

    Product Name 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol
    Cas Number 886371-42-6
    Molecular Formula C8H6F4O
    Molecular Weight 194.13 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically >98%
    Synonyms 2-Fluoro-3-(trifluoromethyl)phenylmethanol
    Smiles C1=CC(=C(C(=C1)CO)F)C(F)(F)F
    Inchi InChI=1S/C8H6F4O/c9-7-3-1-2-6(8(10,11)12)5(7)4-13/h1-3,13H,4H2
    Storage Conditions Store at 2-8°C

    As an accredited 2-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 Amber glass bottle, 25 grams, airtight cap, chemical label with hazard warnings, product name, CAS number, supplier logo, and barcode.
    Shipping **Shipping Description:** 2-Fluoro-3-(Trifluoromethyl)benzyl alcohol is shipped in a tightly sealed, chemical-resistant bottle within secondary containment to prevent leaks. The package is labeled with hazard warnings and handled as a laboratory chemical, avoiding exposure to moisture, heat, or direct sunlight. Transportation complies with all relevant safety regulations for chemical substances.
    Storage Store 2-Fluoro-3-(trifluoromethyl)benzyl alcohol in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizers and acids. Keep container tightly closed and clearly labeled. Use appropriate chemical-resistant containers to prevent moisture ingress. Handle under an inert atmosphere if possible, and follow all standard laboratory safety procedures for storage.
    Application of 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol

    Applications of 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol in Industrial Manufacturing

    2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol is a specialized fluorinated benzyl alcohol widely used as a chemical building block in advanced industrial manufacturing. Its unique structural features make it valuable to several high-end downstream sectors, enhancing product properties and supporting innovation in demanding production environments.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol as a structural precursor for synthesizing fluorinated heterocyclic compounds and substituted benzimidazoles. Research and development departments rely on its reactivity in nucleophilic substitution, esterification, and ether bond formation. The raw material supports active pharmaceutical ingredient (API) synthesis pipelines requiring fluorine-bearing fragments to enhance metabolic stability and modify pharmacokinetic performance. Integration into the process occurs at intermediate coupling reactions where controlled fluorination is critical for the target molecule’s biological profile.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur., USP, and JP quality specifications for starting materials
    • FDA 21 CFR Part 210/211 for finished pharmaceuticals
    • EMA and FDA impurity profiling guidelines

    Typical usage ratio

    • 2%-8% weight by weight in key coupling reactions depending on the molecular scaffold of the target compound; exact ratios determined by stoichiometry and scale-up batch design

    Downstream process integration

    • Added during nucleophilic aromatic substitution with halide reagents
    • Participates in base-assisted etherification or esterification steps to form functionalized intermediates
    • Follows strict process analytical control for by-product minimization

    Final product types

    • Fluorinated API intermediates
    • Pyridine- and benzimidazole-based drug molecules
    • Precursor units for anticancer and CNS pharmaceuticals
    • Fine chemicals for preclinical compound libraries

    2. Agrochemical Active Ingredient Manufacturing

    2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol serves as a core intermediate for synthesizing fluorinated phenyl-containing herbicides, insecticides, and fungicides. Agrochemical producers incorporate it into multi-step organic synthesis workflows that prioritize fluorination to optimize bioactivity, rainfastness, and soil stability. Process chemists rely on its stability in aggressive reaction media and precision in yielding desired substitution patterns during aryl alkyl ether or amide bond formation. The compound’s contribution enables downstream production scale-up while ensuring product performance in agricultural environments.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • OECD Good Laboratory Practice (GLP) guidelines
    • REACH registration and hazard communication (Europe)
    • EPA 40 CFR Part 158 data requirements for pesticides (US)

    Typical usage ratio

    • 3%-12% of the total raw chemical input by molar ratio, with optimization based on target active ingredient and batch yield

    Downstream process integration

    • Incorporated in Williamson ether synthesis for aryl-alkyl ether pesticide structures
    • Used in amide coupling steps to introduce functionalized benzylamine moieties
    • Undergoes in situ purification for impurity removal prior to formulation

    Final product types

    • Fluorinated herbicide actives
    • Systemic and contact fungicides
    • Broad-spectrum insecticidal compounds
    • Seed protective formulations

    3. High-Performance Polymer Synthesis

    Specialty polymer manufacturers select 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol as a functional monomer or end-group modifier in the design of polymers with superior thermal and chemical resistance. Chemical engineers value its integration to introduce fluorinated benzyl groups, improving barrier properties and reducing surface energy in finished materials. The compound enters controlled polycondensation or esterification reactions, where precise feed ratio adjustments regulate molecular weight and distribution to meet end-use application performance.

    Industry compliance standards

    • ISO 9001:2015 quality management for polymer manufacturing
    • ISO 14001 environmental system compliance
    • ASTM D543 chemical resistance testing for plastics
    • FDA 21 CFR 177 for indirect food contact (where applicable)

    Typical usage ratio

    • 0.5%-5% of monomer units by mole, higher for end-functionalization or specialty surface performance; adjusted via stoichiometric control

    Downstream process integration

    • Added during polycondensation to form block and random copolymers
    • Post-polymerization surface treatment for low-energy coating resins
    • Utilized as a chain-terminating agent to fine-tune polymer properties

    Final product types

    • Fluoropolymer membranes
    • High-durability coatings
    • Low-permeability packaging materials
    • Specialty engineering resins

    4. Liquid Crystal and Advanced Electronic Material Manufacturing

    Producers of high-performance display and electronic materials use 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol as a key chemical for creating custom liquid crystalline compounds applied in OLED, TFT-LCD, and organic electronic devices. Its fluorinated backbone imparts increased birefringence, dielectric anisotropy, and environmental durability to molecular architectures. Entering the synthesis via etherification and arylation reactions, this intermediate ensures precise control over thermal range and phase transition characteristics that are crucial for advanced display performance and miniaturization.

    Industry compliance standards

    • IEC 61249-2-21 for electronic materials
    • RoHS Directive 2011/65/EU for hazardous substances
    • IPC-4101E for base materials in electronic laminates
    • ISO 9001:2015 for materials supply chain traceability

    Typical usage ratio

    • 0.3%-2.5% by weight in molecular design formulations, adjusted for target birefringence and viscosity thresholds

    Downstream process integration

    • Built into mesogenic core synthesis via ether or ester functionalization
    • Utilized in final tuning cycles for phase transition temperature calibration
    • Integrated into monomer streams for thin-film fabrication

    Final product types

    • Liquid crystal display fluids
    • Organic light-emitting diode (OLED) functional layers
    • Advanced polarizing films and filters
    • Photonic crystal assemblies
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    Certification & Compliance
    More Introduction

    2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol: Value in Chemical Synthesis

    Experienced Chemical Manufacturing in Benzyl Alcohol Derivatives

    Creating and supplying specialized benzyl alcohols is both a challenge and a point of pride for any chemical manufacturer focused on precision and reliability. Among these, 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol stands out due to its unique molecular structure, which brings together fluorination at the 2-position with a trifluoromethyl group at the 3-position of the benzyl ring. This combination impacts both chemical stability and reactivity. The presence of multiple fluorine atoms sets it apart from conventional benzyl alcohols or simple monosubstituted analogues. In our work, differences like these are not trivial—they affect everything from production scale to downstream application performance.

    Molecular Structure and Implications

    The CAS number commonly cited for this compound is 72433-78-0. Its chemical formula, C8H6F4O, sums up the distinctive features: four fluorines, six carbons in the aryl ring, and one primary alcohol group. The interplay between the electron-withdrawing trifluoromethyl and fluoro substituents can tune physical and chemical properties. Those familiar with synthetic organic chemistry notice that such electronic effects can either boost or moderate the reactivity in nucleophilic substitution, oxidation, or cross-coupling reactions. This makes it an attractive option for customers seeking more selective or reliable performance in advanced synthesis.

    As a manufacturer, we have learned how adjusting batch conditions—choice of solvent, temperature control, purity management—will impact both yield and quality. Selectivity, product color, and by-product control require vigilance. With fluorinated benzyl alcohols, precise process control helps avoid hydrolysis or rearrangement reactions that might otherwise complicate downstream conversion. Over time, we have developed purification techniques, including fractional distillation under reduced pressure and silica gel chromatography, to ensure the finished product exhibits the purity necessary for demanding pharmaceutical and agrochemical synthesis.

    Key Points in Handling and Purity

    Handling a compound with both a benzylic alcohol and electron-withdrawing substituents demands care at all stages. The trifluoromethyl group in the 3-position raises the volatility somewhat compared to 2-fluorobenzyl alcohol alone. We have observed that moisture exclusion and oxygen management extend shelf-life and preserve clarity. Standard product offerings often reach 98% or higher GC purity, with residual solvent limits consistently kept below 0.5% by mass. Achieving this means real investments in analytical equipment—GC-MS, NMR, and Karl Fischer titration all play roles in everyday work to validate purity, confirm structure, and monitor water content.

    From a manufacturer's standpoint, every coating on a flask or residue in a line can sap batch yields. To address this, we maintain procedures for full line washing and tracking batch numbers at every production scale, from pilot batches up to metric ton shipments. This might sound routine, but it forms the backbone of quality assurance. As we have seen, a small slip in process discipline with fluorinated intermediates can easily compromise an entire synthesis campaign, costing time and material.

    Usage Across Sectors: Synthesis Building Block

    2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol serves as a niche yet vital building block primarily in the pharmaceutical and fine chemical industries. It is less common in bulk polymer synthesis, but truly shines in complex molecule construction. Medicinal chemistry teams reach for this alcohol to design molecules with adjusted metabolic profiles, taking advantage of the metabolic stability and lipophilicity imparted by fluorinated aryl groups. This functionality helps in the early investigation of lead compounds, especially in oncology, central nervous system, or anti-inflammatory drug research.

    In-house, our experience shows that this alcohol, once protected or functionalized, can be driven smoothly into esters, ethers, or benzylic halides. Such intermediates are prime candidates for further elaboration through Suzuki-Miyaura coupling, Mitsunobu reactions, or reductive aminations. The presence of the fluorine and trifluoromethyl substituents sometimes lowers nucleophilicity at the benzylic position, permitting more controlled transformations than are often possible with unsubstituted analogues. Experts in agrochemical research also recognize the value of these electronic effects, using such building blocks to tweak both biological activity and degradation pathways of crop protection candidates.

    Selection Factors: Differences From Other Benzyl Alcohols

    Several important differences distinguish 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol from traditional benzyl alcohol or even simple fluoro-substituted variants. First, the combination of fluoro and trifluoromethyl groups at ortho and meta positions leads to dramatically decreased aromatic electron density. This reduces susceptibility to autoxidation—a real problem for some benzylic alcohols stored for extended periods. Incorporating both substituents also increases molecular weight and dramatically alters logP values, making the compound more suitable for design of molecules requiring increased lipophilicity.

    From a process chemistry perspective, we know this alcohol often carries a higher boiling point and lower water solubility than its parent benzyl alcohol. This impacts solvent choices, purification strategies, and crystallization methods. The halogenated framework also promotes stability under acidic or oxidative conditions, adding flexibility to downstream process choices. A team experienced in handling these nuances avoids headaches with phase separation, recovery, or solvent removal.

    Safe Use and Sustainable Practice

    Sustainability pressures and cost efficiency concerns apply even to niche specialty chemicals. We have seen increased requests for green chemistry protocols and lifecycle information regarding fluorinated products. Waste minimization is a challenge, as the disposal of fluorinated byproducts demands special care due to their persistence in the environment. In response, we've invested in solvent recovery systems and filter cakes designed for full traceability and minimized loss.

    As the manufacturer, regular reviews ensure we’re keeping pace with environmental and safety demands. Sharing best practices with peer companies and academic partners—how to handle spent solvents, how to minimize reactor cleaning cycles, how to recover and reuse precious fluorinated materials—benefits both bottom line and sustainability reporting. We routinely audit our protocols, track emissions, and refine our energy management, not only because of legislation but also because waste reduction often aligns with lower production costs.

    Scale, Reliability, and Quality: Lessons Learned in Manufacturing

    Consistency is more than a slogan in specialty chemical production. Year after year, pharmaceutical customers remind us that validated batch records and transparent supply chains matter as much as molecule quality. Copying a literature procedure rarely matches the needs of industrial production. The devil is in the details: agitation rates, order of addition, precise solvent composition—all these can swing yields by five percent or more, an enormous effect at production scale. We run material in both glass and Hastelloy reactors, understanding that metal ion leaching or trace impurities can show up in unanticipated batch-to-batch variation if not tightly controlled.

    A key lesson: don’t neglect the packaging. Leak-proof, fluoropolymer-lined containers, careful inerting with nitrogen, and segregated storage paths keep the alcohol stabilized until customer labs open it. On the documentation side, years of feedback from regulatory teams underline the value of full, transparent certificates of analysis. This is not a paperwork exercise—trace residual metals, impurity profiles, and shelf-life validation help keep research and manufacturing schedules on track for our customers.

    Looking Forward

    As new medical and agrochemical entities require even finer control over their performance and safety, molecules like 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol play a growing role. We continue investing in both analytical capability and process safety, not out of abstract planning but from real-world feedback: customers need reliability, rapid response, and a partner who understands the complexity from raw material to finished formulation. Analytical data guides process refinement, letting us scale successfully without losing micro-level quality. By working directly in manufacturing, we gain insights that go beyond following specifications—we adapt quickly and continuously, anticipating the shifting needs of research and industry.

    The specialty chemical sector increasingly depends on products derived from complex, multifunctional intermediates. We are reminded regularly that price is only a starting point; technical support, batch consistency, and future-ready compliance matter just as much. As manufacturers, our commitment is to deliver that full package, from molecular innovation to hands-on support, wherever and whenever this compound becomes a critical part of the next discovery or application.

    Process Optimization and Problem Solving

    Every batch tells its own story. Practical challenges, like the occasional incomplete conversion or stubborn color impurity, show up despite detailed planning. With this particular benzyl alcohol, adjusting reaction time and base concentration can resolve most conversion issues. Color persistence often points to trace metal contamination or low-level side reactions; switching to high-purity reagents or cleaning glassware with fluoride-neutralizing solutions usually solves the problem. Long-term partners appreciate the extra effort, as it lets them focus on innovation rather than cleaning up after inconsistent suppliers.

    Another key improvement area stems from solvent compatibility testing. Some customers require this alcohol in specialized dry or anhydrous grades. Custom drying lines, inline moisture analyzers, and use of molecular sieves help us hit those low water targets, often below 200 ppm. Careful monitoring of each step means we can handle custom orders without derailing production efficiency or raising new contamination risks.

    Working Directly with R&D Customers

    We take a hands-on approach to supporting R&D teams who rely on 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol in their own labs. These researchers often want quick turnarounds, custom packaging, or specific documentation to match their regulatory environment. Direct conversations with synthetic chemists reveal application-specific tweaks—crystallization solvents, shelf-life extension via stabilizers, or special handling guides for air-sensitive manipulations. Since we produce at scale, our team’s feedback feeds back into our in-house R&D, powering a continuous loop of process refinement.

    Working closely with formulation scientists also means responding quickly to quality queries or unexpected findings in downstream testing. Our technical staff shares NMR spectra, GC chromatograms, and impurity lists freely, cutting the time lost to back-and-forth paperwork or generic help-desk answers. Customers recognize the difference: a partner who knows how to solve production bottlenecks is as valuable as the purity of the product itself.

    Long-Term Impact: Performance and Regulatory Trends

    Across newer regulated markets, we see an upward trend in demand for complete impurity profiles and toxicological assessments for fluorinated intermediates. Historically, manufacturers could ship with a simple COA and basic validation. That is rapidly changing, as new pharmaceutical and environmental standards call for far more transparency about side products, potential genotoxins, and unknowns. We have adopted data management systems and digital records storage, making it easier for our partners to access full production histories and batch traceability.

    The mounting attention to environmental persistence of fluorinated compounds sometimes leads to tough discussions about necessity versus risk. We do not ignore these issues; we encourage open discussions, and, where alternatives exist, we help customers evaluate options. Still, for certain advanced materials or therapeutics, no substitutes match the performance benefits delivered by this family of building blocks.

    Innovations in Purification and Waste Minimization

    Learning directly from manufacturing lines, we have adopted several newer technologies to reduce waste, cut solvent use, and handle purification with less downtime. In the past, many specialty fluorinated benzyl alcohols required large volumes of chlorinated solvents or multi-stage distillation. Working with newer stationary phases, reverse-phase preparative chromatography, and safe, non-halogenated solvents, we have decreased both environmental footprint and production bottlenecks.

    On the laboratory side, reconstructing solvent flows has led us to build integrated solvent recycling and in-line purity testing, slashing both cost and process downtime. This makes it easier to respond dynamically to changing purity targets or unexpected process deviations, with less risk of scrapped material.

    Supporting the Next Generation of Molecule Makers

    Chemical engineering and synthetic research are moving fast. As a manufacturer, we sense a responsibility to train the next generation of chemists and production engineers in best practices for handling, purifying, and transforming complex fluorinated intermediates. Vendor training, joint webinars with academic groups, and shared troubleshooting sessions give everyone a chance to learn from the real-world hiccups and successes that define chemical manufacturing today.

    In summary, 2-Fluoro-3-(Trifluoromethyl)Benzyl Alcohol speaks to both the complexity of modern organic chemistry and the attention to detail required in contemporary chemical manufacturing. Delivering quality at scale, adjusting quickly to new process or regulatory demands, and maintaining transparent, hands-on technical support have proven to be the foundation for reliable partnerships and continued growth in this sector.