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2-(Trifluoromethyl)Benzyl Alcohol

    • Product Name 2-(Trifluoromethyl)Benzyl Alcohol
    • Alias Benzyl alcohol, 2-(trifluoromethyl)-
    • Einecs 249-388-2
    • 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

    816772

    Chemicalname 2-(Trifluoromethyl)Benzyl Alcohol
    Casnumber 402-46-0
    Molecularformula C8H7F3O
    Molecularweight 176.14
    Appearance Colorless to pale yellow liquid
    Boilingpoint 202-204°C
    Density 1.276 g/cm3
    Refractiveindex 1.501
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Flashpoint 93°C
    Smiles OCc1ccccc1C(F)(F)F
    Inchi InChI=1S/C8H7F3O/c9-8(10,11)6-3-1-2-5-7(6)4-12/h1-3,5,12H,4H2

    As an accredited 2-(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 containing 25 grams of 2-(Trifluoromethyl)Benzyl Alcohol, securely sealed, labeled with chemical name, hazard symbols, and batch information.
    Shipping 2-(Trifluoromethyl)Benzyl Alcohol should be shipped in tightly sealed containers, protected from moisture and light. It must be packed and labeled as per relevant chemical transport regulations. Use appropriate cushioning and secondary containment to prevent leaks, and transport under ambient temperature while accompanying the shipment with the proper safety documentation (SDS).
    Storage 2-(Trifluoromethyl)Benzyl alcohol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep the storage area free from moisture and direct sunlight. Properly label the container and ensure it is protected from physical damage and excessive heat. Use appropriate safety precautions when handling.
    Application of 2-(Trifluoromethyl)Benzyl Alcohol

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

    As a direct manufacturer, we supply 2-(Trifluoromethyl)Benzyl Alcohol for performance-critical industrial processes. This compound delivers specific functional advantages in selected downstream industries that demand stringent regulatory compliance, precise formulation protocols, and seamless process integration for end-product consistency.

    1. Agrochemical Intermediate for Selective Herbicide Synthesis

    Major agrochemical formulators use this compound as a key intermediate in the synthesis of trifluoromethyl-substituted benzyl-based herbicides. Its chemical structure enables targeted reactivity during condensation and halogenation reaction stages. Custom batch recipes require close ratio adjustments to balance crop selectivity, regulatory traceability, and environmental release limits. The final synthesis routes maximize yield and minimize unwanted side products, ensuring compliance with agricultural chemical registration standards and improving the purity of commercial herbicidal products.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 on plant protection product authorizations
    • US EPA pesticide registration quality and traceability requirements
    • China GB 2763 Maximum Residue Limits for Pesticides in Food
    • ISO 9001 for consistent batch production quality

    Typical usage ratio

    • Inserted at 0.2–1.8 mol per synthesis unit, depending on target molecule complexity and desired herbicide concentration; ratios determined by downstream conversion efficiency and environmental controls

    Downstream process integration

    • Added during aromatic coupling or etherification stages for active ingredient core scaffold assembly
    • Subject to in-process QC verification of purity and reaction completeness

    Final product types

    • Selective post-emergent herbicide technicals
    • Water-dispersible granules (WDG) and suspension concentrate (SC) formulations
    • Ready-to-use liquid herbicide products

    2. Pharmaceutical Intermediate for CNS-Active Compound Synthesis

    Active pharmaceutical ingredient (API) manufacturers employ this material in multi-step syntheses to introduce trifluoromethylbenzyl moieties into CNS-targeted drug candidates. Its unique electronic profile facilitates specific ring substitutions and side chain modifications required for optimized pharmacokinetic profiles. All reactions involving this intermediate comply strictly with cGMP batch control, with stepwise monitoring for residual solvents and trace impurities. Scale and dosage vary by molecule class, regulatory submission status, and target therapy indication.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7, 21 CFR Part 210/211)
    • ICH Q3A/B guidelines for impurity management in APIs
    • Ph. Eur./USP/NF monographs for relevant drug substances
    • ISO 13485 for drug-device combination systems, if integrated downstream

    Typical usage ratio

    • 0.03–0.22 molar equivalents per API batch, depending on synthetic design and desired substitution degree; proportion tailored to downstream therapeutic index and route of administration

    Downstream process integration

    • Introduced during early or mid-stage API assembly (e.g., Grignard reaction or alkylation step)
    • Purified via column chromatography and analyzed for structure confirmation by NMR, MS, and HPLC

    Final product types

    • CNS drug intermediates (including investigational new drugs with trifluoromethylbenzyl subunits)
    • Final APIs for neurodegenerative and psychiatric therapies
    • Advanced pharmaceutical intermediates (APIs under process validation)

    3. Specialty Polymer Modification and Performance Additives

    Specialty polymer formulators leverage this raw material to functionalize aromatic polymer chains, introducing trifluoromethyl groups that enhance hydrophobicity, UV stability, and chemical resistance. Its alcohol group acts as an anchor for transesterification and copolymerization steps, yielding modified resins for extreme environments. The downstream process tightly controls feed ratios and reaction temperatures to minimize unreacted monomer content and achieve uniform polymer chain distribution, producing resins specified in advanced coatings, electronics, and automotive components.

    Industry compliance standards

    • REACH compliance for polymer additives (EC No 1907/2006)
    • UL 94 (flammability standards for plastics)
    • ISO 14001 for environmental management in plastics processing
    • RoHS Directive (2011/65/EU) for electronic-grade applications

    Typical usage ratio

    • 0.5–5 wt% loading in base monomer or prepolymer feedstocks, adjusted for target film or molded part performance requirements

    Downstream process integration

    • Co-fed in melt-phase or solution polymerization reactors before curing or crosslinking stages
    • Blending and compounding with other additives as part of resin masterbatch preparation

    Final product types

    • UV-resistant coatings and topcoats
    • High-performance engineering plastics
    • Fluorinated polymer dielectrics for electronics components
    • Automotive trim and exterior applications

    4. Liquid Crystal Intermediate for Advanced Display Materials

    Advanced materials suppliers utilize this compound to synthesize specific liquid crystal molecules, exploiting the trifluoromethylbenzyl structure for desired optical and electrochemical characteristics. Downstream, precise synthetic control, including temperature, solvent choice, and stoichiometry, underpins the high purity and anisotropic ratios demanded by thin-film display technologies. Strict adherence to electronics industry standards ensures component safety, reliability, and supply chain traceability for high-value OEM panel integration.

    Industry compliance standards

    • IEC 61249-2-21 (halogen-free material content for electronics)
    • JEITA ET-5006 (Japanese LCD display material guidelines)
    • IPC-4101 for base materials protocols in electronic interconnections
    • ISO 9001 with additional supplier audits for display-grade material lots

    Typical usage ratio

    • 0.1–2.5 mol per synthetic batch, tailored according to the phase transition thresholds and dielectric alignment properties of each display formulation

    Downstream process integration

    • Reacted during the fine synthesis of liquid crystal precursors or terminal group modifications, often within multi-stage condensation protocols
    • Subject to repeated recrystallization and spectroscopic verification to confirm isomeric purity

    Final product types

    • Nematic and smectic liquid crystal compounds
    • LCD panel active matrix materials
    • OLED alignment layers for high-resolution displays
    • Specialty optical retarders and modulators
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    Certification & Compliance
    More Introduction

    2-(Trifluoromethyl)Benzyl Alcohol: Experience-Driven Insights from the Manufacturer's Floor

    This is Not Just Another Benzyl Alcohol

    Over the years of scaling up batch after batch of fine and specialty chemicals, one compound stands apart in our daily operations: 2-(Trifluoromethyl)Benzyl Alcohol. Every step, from raw material sourcing to the last QC check, gives our staff a first-hand look at why this molecule keeps drawing strong demand. Plenty of alcohol derivatives roll out of manufacturing plants, but there’s something distinctive about this compound beyond a simple tweak in molecular structure.

    What Sets 2-(Trifluoromethyl)Benzyl Alcohol Apart

    As a team responsible for loading reactors and monitoring the columns, we see structural elements directly impact reaction handling. The trifluoromethyl group alters both the behavior and the versatility of the end product. Regular benzyl alcohol serves as a solid building block, but swapping in the CF3 group at the ortho position shifts the game. The difference shows up less in glossy brochures and more in how our technicians manage purification or adjust parameters during scale-up runs. The chemistry shifts in subtle but real ways. The electron-withdrawing effect of trifluoromethyl tightens control over nucleophilicity and makes the alcohol more robust under oxidative conditions. Many customers report sharper selectivity and fewer downstream byproducts.

    We monitor water content, acidity, and possible trace metal contamination batch by batch, since some catalytic processes demand near-zero impurity profiles. In our experience, clients from pharma and agrochemical labs often ask for specs beyond industry minimums, so we keep equipment standards higher, frequently verifying through GC-MS and NMR. We typically supply material as a colorless transparent liquid, with purity above 99%. Melting and boiling points land in ranges consistent with reference literature and client feedback. Even minute deviations are flagged for internal review before shipping.

    Why the Molecular Structure Matters on the Manufacturing Line

    Some folks might think making 2-(Trifluoromethyl)Benzyl Alcohol is simply a variation on regular benzyl alcohol. That assumption misses reasons this compound behaves differently in reactors and product lines. The trifluoromethyl group introduces distinct physical properties: its high electronegativity influences solubility and volatility, which in turn, affects storage, handling, and delivery. Our tank operators notice these differences while mixing or transferring. Over time, we saw how these changes let the compound fit better into certain innovative chemistries.

    Several downstream users, especially those working on complex organic syntheses or developing new active pharmaceutical ingredients, comment on how cleanly the product integrates into multi-step processes. Not every alcohol manages to go through chlorination, oxidation, or cross-coupling without introducing low-level side-products. The trifluoromethyl group’s stability under a range of typical process conditions means fewer surprises on both our plant floor and the chemist’s bench. In catalyst-driven reactions, less background noise from impurities gives consistent yields.

    Every Kilogram Tells a Story

    Our operators remember the first time they handled sizable requests from research divisions pushing fluorinated compound innovation. Shifts in heat evolution, altered volatility profiles, and faster stirring endpoints meant retraining in practical plant routines—not just rewriting SOPs. Equipment compatibility sometimes needed evaluation: seals, sensors, and valves respond differently to this molecule than to regular benzyl chain alcohols.

    We never treat any variant as "just another alcohol." Our focus stays on measurable quality: purity, moisture content, and chromatographic profile. Each product lot passes not just regulatory requirements, but also our in-house benchmarks. This involves hands-on testing and prompt data review, rather than defaulting to paperwork alone.

    Where End Users Find the Value

    Talking with labs developing APIs and crop protection intermediates, we hear why 2-(Trifluoromethyl)Benzyl Alcohol features in their shortlists. Medicinal chemists value it for the way the trifluoromethyl group enhances lipophilicity, enabling better performance in targets needing metabolic stability and selective permeability. The OH group serves as a functional handle for esterification, ether formation, and halogenation. The product easily adapts to several coupling reactions: Suzuki, Heck, and even selective reductions—thanks to that balance of rigidity and reactivity added by CF3.

    Compared to similar fluorinated benzyl alcohols, the ortho placement in 2-(Trifluoromethyl)Benzyl Alcohol opens up unique pathways. Alternative isomeric placements—and non-fluorinated counterparts—don’t replicate this same reactivity profile. In our own manufacturing review, we've seen clients confirm that ortho-trifluoromethyl substitution allows them access to intermediates they couldn't reach with other analogs.

    How the Specifications Translate into Real Lab Performance

    We track feedback from process teams working with small and multi-kilo lots. Purity thresholds above 99% reduce the risk of unwanted peaks in GC-HPLC traces, a factor that saves days in downstream purification for many. Residual solvents must be negligible; we routinely measure and limit chlorinated solvent levels to far stricter standards than the bulk chemical market expects. The majority of feedback we receive signals appreciation for low water and halide contents, as these improve shelf life and reduce the need for tricky drying steps before sensitive reactions.

    The compound retains stability at ambient storage but does require light-avoidance and moisture-tight containment for long-term holding. Our facilities use double-sealed drums, detailed inventory tracking, and temperature logging to ensure no surprises occur in finished product sent worldwide. Customers, especially those inbound portions of supply chains, value lot-to-lot consistency. Stories keep coming in about how "the big drum from your plant saved us an extra QA clean-up step”—a direct testament to our focus on practical batch results.

    Regulatory Reality and Market Trends

    In the fine chemical world, regulatory scrutiny climbs year on year. We improved record-keeping and increased batch-level traceability after seeing more questions directed our way by buyers working under cGMP or similar frameworks. 2-(Trifluoromethyl)Benzyl Alcohol finds direct use in regulated synthesis routes, so we keep full documentation—from starting material origins to NMR printouts—on hand. No one wants a regulatory audit to flag a missing impurity profile or unexplained process deviation.

    Our experience tells us not every competitor delivers the same level of embedded traceability. Several users switching to our product end up doing so after facing questions from their own QA or technical transfer teams. We've handled site visits and remote audits from client-side auditors keen on seeing exactly where in the plant each drum was filled and what critical controls got logged. No spot gets left unchecked or unverified.

    Process Development: Meeting Customer R&D Demands

    Research groups at both established players and startups call up looking for specific customization—whether it’s ultra-low metal content for catalysis or adjusted solvent profiles for pilot plants. Our process chemists and production supervisors team up to tailor every batch. We've run campaigns targeting residual metal levels in the low ppm and worked directly with synthetic teams to match solvent tolerances exactly. The plant’s flexibility and staff experience enable these targeted campaigns.

    Newer entrants often ask us about upscaling from grams to kilos, or batch-to-continuous transfer. We share case stories from our own plant floors—how temperature gradients in crystallizer columns shifted just enough to require a recalibration before tackling mega-liter batches. Sharing real-world lessons from scaling up 2-(Trifluoromethyl)Benzyl Alcohol saves clients wasted effort.

    Differences from Other Alcohols: Why the Choice Matters

    Plenty of buyers, especially those starting out or switching from bulk sources, wonder why costs and lead times vary so much compared to simple benzyl alcohol. In practice, we show them how the manufacturing process diverges. The introduction of trifluoromethyl group means longer synthesis steps. This calls for more tightly defined reaction environments, extra distillation passes, and those glowing NMR and GC traces our QC team gets used to chasing.

    Solubility in polar and nonpolar media also tells a story. Users running two-phase or micellar chemistry projects notice how the product remains predictable under changing temperatures—there’s more value here than just a substitution on a ring. Some clients relay feedback that switching to para- or meta-substituted versions altered reaction rates or byproduct formation, with ortho placement offering a tighter, more reproducible result.

    Even after shipping, the differences persist. End-users processing similar alcohols discover that the reactivity, volatility, and even scent can change, potentially altering workplace or process conditions. We’ve documented workplace adjustments based on the slightly higher volatility or the different boiling range compared to standard products.

    Day-to-Day Reality: Batch Management and Troubleshooting

    Producing this molecule teaches our teams plenty about process discipline. Small setbacks—unexpected color drift, off-spec pH, or minuscule solvent retention—demand on-the-spot troubleshooting anchored in hands-on know-how. This differs from running more “commoditized” alcohols, where quality swings make less of a dent in downstream performance.

    We bring in real-world turnaround stories to every training session: how a technician caught a contamination issue early, how switching from one grade of raw material shifted our purification timeline, or how a minor heater setting change produced a smoother final distillation cut. These lessons turn into plant-wide best practices, benefiting the next sets of orders.

    Solutions for the Next Generation of Chemisty

    Our position as a producer means we do more than synthesize and ship. We work directly with users, sharing not just COAs but manufacturing insights. Some recurring challenges—like minimizing solvent residues or eliminating trace neutral impurities—get solved on the production line, tweaking temperature regimes, column packing or feedstock choices after each campaign. Our R&D staff often sits in on customer calls, translating real plant observations into actionable ideas for scale-up or pilot projects.

    We welcome the push for even tighter impurity profiles, and higher compliance. This encourages a culture of continual improvement, not just ticking boxes for certifications. Onboarding wider digital tracking, integrating new analytics, and adopting advanced drying or containment methods all happened because end users cared about actual outcomes, not industry slogans.

    What the Future Holds for Our Production, and for End Users

    We’ve learned to keep our focus on the interplay between production discipline and end-user priorities. As chemical synthesis grows more specialized, demand feeds back: requests for even rarer isomers, ultra-pure grades, and solutions tailored to exotic synthesis conditions. Our plant’s hands-on experience with 2-(Trifluoromethyl)Benzyl Alcohol sits at the foundation for tackling these new challenges. We refine processes after each campaign, minimizing waste, improving energy efficiency, and dialing in consistency at every turn.

    As one of the few manufacturers deeply embedded in fluorinated building blocks, we see customers pushing the boundaries of what's possible, and we share in those ambitions. Whether it's offering technical support for a brand new process development campaign, tweaking specs to shave down time in quality assurance, or racing to fulfill rush orders, our role remains clear: deliver pure, consistent, and fully traceable 2-(Trifluoromethyl)Benzyl Alcohol batch after batch.

    A Product Molded by Real-World Experience

    There’s no shortcut in delivering consistent, high-purity specialty chemicals. Each kilogram of 2-(Trifluoromethyl)Benzyl Alcohol reflects cycles of practical experience, lessons learned during upscaling, and above all, a sharp focus on what chemists and process engineers actually need. Staying in close touch with real feedback—not just certificates and paperwork—grounds our daily work. Maybe it’s less glamorous than flashy ads, but for those who measure batch success by yield, purity, and reactivity, that’s what matters most.