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2,5-Bis(Trifluoromethyl)Benzyl Alcohol

    • Product Name 2,5-Bis(Trifluoromethyl)Benzyl Alcohol
    • Alias 2,5-Bis(trifluoromethyl)phenylmethanol
    • Einecs 216-927-2
    • 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
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    Specifications

    HS Code

    611110

    Product Name 2,5-Bis(Trifluoromethyl)Benzyl Alcohol
    Cas Number 328-74-5
    Molecular Formula C9H6F6O
    Molecular Weight 244.13 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically >98%
    Boiling Point 115-117°C at 20 mmHg
    Density 1.474 g/mL at 25°C
    Refractive Index n20/D 1.443
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles OCc1cc(C(F)(F)F)ccc1C(F)(F)F
    Inchi InChI=1S/C9H6F6O/c10-8(11,12)6-1-2-9(13,14,15)7(3-6)4-5-16/h1-3,16H,4-5H2
    Synonyms 2,5-Bis(trifluoromethyl)benzyl alcohol
    Storage Temperature 2-8°C

    As an accredited 2,5-Bis(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, sealed with a plastic screw cap and labeled with product name, CAS number, and safety information.
    Shipping 2,5-Bis(Trifluoromethyl)Benzyl Alcohol ships in tightly sealed, chemical-resistant containers under ambient conditions. Packaging ensures protection from moisture, light, and physical damage. All shipments comply with relevant chemical transport regulations, and safety documentation, such as SDS, accompanies each order. Temperature and handling instructions are provided as required by the compound’s stability profile.
    Storage 2,5-Bis(Trifluoromethyl)Benzyl Alcohol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area. Protect from light, heat, and moisture. Store away from incompatible materials such as strong oxidizing agents, acids, and bases. Label containers clearly, and avoid prolonged exposure to air to prevent degradation. Handle using appropriate personal protective equipment.
    Application of 2,5-Bis(Trifluoromethyl)Benzyl Alcohol

    Applications of 2,5-Bis(Trifluoromethyl)Benzyl Alcohol in Industrial Manufacturing

    2,5-Bis(Trifluoromethyl)Benzyl Alcohol serves as a specialized intermediate favored for its electron-withdrawing trifluoromethyl groups, enabling the synthesis of high-value fluorinated compounds. Downstream industries apply this raw material in tightly regulated processes to achieve distinct properties in advanced chemical, electronic, and pharmaceutical end-products. The following sections detail its actual industrial deployment across select application scenarios.

    1. Pharmaceutical Synthesis: Fluorinated Active Pharmaceutical Ingredients (APIs)

    Pharmaceutical companies leverage this fluorinated benzyl alcohol as a building block in multi-step syntheses of APIs, particularly where metabolic stability and bioavailability enhancement require fluorinated aromatic moieties. The compound undergoes precise coupling, alkylation, or oxidation reactions in GMP-controlled environments, contributing fluorinated functionality in the late-stage assembly of patented drug substances targeting central nervous system, oncology, and antiviral indications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) monographs and supplementary chapters
    • Chinese Pharmacopoeia ChP (as applicable for local markets)

    Typical usage ratio

    • Applied at 0.5–5% molar ratio in stepwise synthesis, varying by target molecule structure and route optimization in the API process route.

    Downstream process integration

    • Introduced during advanced intermediate coupling or side-chain installation to the precursor scaffold, followed by purification and regulated handling in final API crystallization.

    Final product types

    • Patent-protected small molecule APIs containing trifluoromethylated aromatic rings
    • CNS drug candidates with enhanced metabolic profiles
    • Targeted kinase inhibitors and antiviral drug substances

    2. Agrochemical Intermediate Manufacturing

    Leading agrochemical formulators utilize this alcohol for the custom synthesis of fluorinated intermediates that form the backbone of next-generation herbicide and fungicide actives. Its chemical structure enables selective substitution and oxidation steps to construct molecules resistant to photodegradation, critical for improving field persistence and lowering application rates in advanced crop protection formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Principles of Good Laboratory Practice (GLP) for pesticide intermediate synthesis
    • REACH Regulation (EC) No 1907/2006 for intermediate registration and tracking
    • ISO 9001:2015 Quality Management in chemical intermediates

    Typical usage ratio

    • Usage ranges from 1–3% w/w of the total reaction mixture during initial ring substitution, subject to target molecule and batch process scale.

    Downstream process integration

    • Added to chlorination or nucleophilic aromatic substitution reactors where functionalized aromatic rings are assembled prior to further derivatization and formulation.

    Final product types

    • Fluorinated herbicide intermediates
    • Trifluoromethyl-based fungicide precursor compounds
    • Crop protection agent synthesis blocks for large-scale agrochemical production

    3. Electronic Chemicals: Liquid Crystal Monomer Synthesis

    In the field of display and electronics manufacturing, specialty chemical producers deploy this compound in the precise synthesis of high-purity fluorinated monomers for advanced liquid crystal (LC) mixtures. Its structure improves thermal and voltage stability, supporting the performance demands of LC display matrices utilized in automotive, medical, and high-definition consumer screens. End users require detailed batch traceability and ultra-low impurity levels for downstream integration.

    Industry compliance standards

    • SEMATECH/SEMI S2 Safety Guidelines for Electronic Materials
    • JIS C 62704 (Japanese Industry Standards for Electronic Materials)
    • ISO 9001:2015 for quality assurance in specialty monomer production
    • RoHS (Restriction of Hazardous Substances Directive, EU)

    Typical usage ratio

    • Applied at 2–8% molar fraction in mixed aromatic LC monomer synthesis, with ratio adjusted based on viscosity and birefringence requirements for end-use display type.

    Downstream process integration

    • Integrated during custom monomer functionalization and co-polymerization prior to LC blending and final mixture purification; contamination control critical at all stages.

    Final product types

    • Fluorinated liquid crystal monomers
    • High-contrast, wide-temperature-range LC mixtures
    • TFT-LCD and automotive display base materials

    4. Performance Polymer Synthesis: Fluorinated Resin Modifier

    Manufacturers in the performance polymer sector exploit the electron-withdrawing and hydrophobic properties of this compound as a specialty modifier for fluorinated resins. During polymer backbone construction or chain-end functionalization, this alcohol introduces trifluoromethyl aromatic segments, imparting chemical resistance and low dielectric constant essential for wire/cable jacketing, electronic encapsulants, and high-durability coatings. Process parameters remain tightly controlled to ensure uniform incorporation and end-use property targets.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics Materials
    • IEC 61249-2 (Base materials for printed boards—Fluorinated polymers)
    • American Society for Testing and Materials (ASTM D543, chemical resistance)
    • ISO 14001:2015 for environmental management in polymer manufacturing

    Typical usage ratio

    • Typically incorporated at 0.2–1.5% by mass as a co-monomer or end-group modifier, ratio determined by required dielectric properties and mechanical durability of the finished resin.

    Downstream process integration

    • Dosed during pre-polymer synthesis and chain-end functionalization steps in batch or continuous bulk polymerization processes, ahead of extrusion or compounding.

    Final product types

    • Fluorinated wire/cable jacketing resins
    • Hydrophobic encapsulant compounds for microelectronics
    • Specialty anti-corrosion and dielectric coatings for industrial use

    5. Specialty Fine Chemicals: Fluorinated Fragrance Intermediate

    In the sector of fine chemicals and specialty perfumery, compound houses utilize this raw material to synthesize novel fluorinated fragrance intermediates that deliver enhanced longevity and volatility in premium formulations. The trifluoromethylated benzyl structure contributes olfactive notes with unique persistence, suitable for high-end perfumes and scent additives, achieved through controlled etherification or esterification reactions and subject to strict IFRA and customer specification-driven controls.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • EC Regulation No 1223/2009 (Cosmetics Products Regulation, EU)
    • ISO 9235 for chemically defined fragrance ingredients
    • REACH Registration for fragrance raw materials

    Typical usage ratio

    • Integrated at 0.1–0.8% in fragrance intermediate synthesis, adjusted according to intensity and volatility requirements of the target aromatic profile.

    Downstream process integration

    • Utilized during key fragrance intermediate etherification or esterification reactions, followed by fine purification and direct formulation into top-note components.

    Final product types

    • Fluorinated fragrance intermediates for perfumery blends
    • Long-lasting aroma compounds for luxury consumer products
    • High-purity scent bases for personal care applications
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    Certification & Compliance
    More Introduction

    2,5-Bis(Trifluoromethyl)Benzyl Alcohol: Insight from the Manufacturer’s Floor

    Bringing Precision to Fluorinated Benzyl Alcohols

    Most chemists see the name 2,5-Bis(Trifluoromethyl)Benzyl Alcohol—sometimes referenced by its CAS number—and immediately recognize the value in those two CF3 groups positioned on the benzene ring. Years of manufacturing specialty fluorinated intermediates have shown us how even a subtle change in substitution pattern can profoundly affect performance downstream. In this segment, I want to share not only what this molecule offers, but why those details matter to innovators in pharmaceuticals, agrochemicals, and advanced materials.

    Molecular Features: What Sets It Apart

    This product, which we typically deliver with GC purity above 99%, features a benzyl alcohol core flanked by trifluoromethyl groups at the 2 and 5 positions. That configuration doesn’t appear by chance; it took us several pilot runs before we established a reliable synthesis pathway. While other benzyl alcohol derivatives might offer either electron-withdrawing or donating groups in various positions, the combined electronic effect and steric protection of the 2,5-bis(trifluoromethyl) motif stand out. The molecule delivers a unique blend of hydrophobicity and oxidative durability, making it less reactive in some undesired side-reactions compared to mono-substituted variants.

    Each batch runs under carefully controlled conditions, with precise temperature monitoring and inert atmosphere workflows. Any deviation in conditions threatens the selectivity—fluorinated reactants demand attention to detail. Consistency weighs more than speed; we've found that rushing steps introduces minor impurities that become headaches later in process scale-up or regulatory submission.

    Applications in Advanced Synthesis

    It didn’t take long before pharma partners started sending requests for this compound. The strong electron-withdrawing groups create a platform for structural analogues that resist metabolic breakdown, which matters a great deal for oral bioavailability in medicinal chemistry. Teams working on kinase inhibitors or CNS-active drugs often prioritize CF3-rich scaffolding, knowing it can mean the difference between a viable candidate and one buried by rapid Phase I metabolism. The alcohol functional group invites further derivatization—it can be oxidized, esterified, or serve as a handle for Suzuki or Buchwald–Hartwig coupling.

    On the agricultural side, the same features appeal to formulation scientists who ask for “rain-fast,” persistent backbones. Pesticide discovery platforms increasingly push for actives that bind selectively and resist sunlight-induced breakdown. Placing those CF3 groups on the aromatic core improves not only environmental stability but also increases uptake through waxy plant cuticles, according to several field studies we've reviewed. Our technical team frequently collaborates with formulation chemists to optimize process parameters for new analogues using this core building block.

    Manufacturing Challenges Only Producers Face

    Traders and third-party resellers discuss product lists, but rarely contend with what we face on the synthesis floor. The starting materials for 2,5-Bis(Trifluoromethyl)Benzyl Alcohol often come from overseas sources with varied quality. Before the first batch runs, our analytical chemists scrutinize every incoming drum—iron contamination, moisture, or trace halides can undermine catalytic steps. Scaling up from grams to kilos, we learn new lessons about heat removal, proper mixing, and gas evolution. Early mistakes taught us which reaction glassware holds up to these conditions, and why oxygen exclusion matters more for some solvents than others.

    Waste management presents another challenge. Trifluoromethylation steps produce residues that are not tolerant of lax handling. Our facility invests in solvent recovery and compliant incineration. These investments raise costs compared to bulk benzyl alcohol makers, but responsible production underpins reliable long-term supply. Our clients invest their trust on the idea that what leaves our plant meets agreed specs and secures environmental due diligence.

    Quality You Can Trust—Why Origin Matters

    Our documentation starts long before a product gets its label. We build traceability into every notebook page, every instrument log, and every container label. This enables us to troubleshoot any issue, whether it pops up in a research bench or commercial-scale application. On two occasions, our partners brought us feedback on slightly out-of-spec melting points. Routines for root-cause analysis went to work and traced the issue to small variances in one solvent lot. By correcting upstream controls, subsequent batches met the expected range. Such details separate real producers from traders.

    We keep rigorous batch records, not because regulations demand it, but because experience shows how subtle variables—like humidity over a weekend or operator shift change—can shape yield and purity. Each batch undergoes NMR, GC-MS, and Karl Fischer titration. Supply interruptions or inconsistent profiles set research and production back. Our approach focuses on zero-defect delivery, knowing that our partners build their business on consistent intermediates.

    Distinguishing Factors from Other Benzyl Alcohols

    As a producer, side-by-side comparisons come up often when customers transition projects between related fluorinated alcohols. While standard benzyl alcohols, such as para- or ortho-substituted types, serve many mainstream needs, our 2,5-Bis(Trifluoromethyl)Benzyl Alcohol offers much stronger electron-withdrawing influence. This alters downstream reactivity in a way that opens access to chemistries otherwise unavailable. Chemists have used this for finer-tuned active site orientation in complex molecule syntheses or to adjust crystallinity in specialty polymers.

    The dual CF3 groups do more than tweak physicochemical data—they give tangible advantages in formulation longevity, metabolic halflife, and, for bulk processes, solvent compatibility. Standard benzyl alcohols or mono-trifluoromethyl analogues often fall short in delivering the desired hydrophobic protection. User experience tells us that moving to the bis-substituted product isn’t just a step up, it’s a move into a new performance category.

    Addressing Supply Chain and Sustainability Questions

    Chemicals containing multiple CF3 groups historically relied on raw materials with geopolitical sourcing risks. We have invested in diversifying suppliers and developing some in-house fluoride and trifluoromethyl reagent production capacities. This keeps project timelines reliable in the face of market disruptions—an asset our partners recognized during the last few years marked by unexpected transport delays.

    Our sustainability policies address solvent recycling, energy-efficient batch protocols, and rigorous waste stream analysis. Instead of sending waste streams down the drain, we reclaim solvents with vacuum distillation and treat fluorinated residues with certified incineration. Operators undergo continuous training on process safety, and new equipment undergoes risk assessment before deployment. These investments help assure partners that production adheres to current expectations for environmental responsibility.

    Supporting Innovation through Manufacturing Know-How

    We frequently collaborate with R&D and process engineering teams seeking to adapt this intermediate to new synthetic routes. It’s more than “sell and forget”—our chemists remain available for technical troubleshooting, alternative synthetic planning, and scale-up adjustments. Supporting IP-protected or confidential projects, we sign NDAs and deliver custom specs, drawing on decades of process adjustment experience. This includes real-world parameters for scale-up, not just lab-scale data.

    One key area where our direct experience pays off concerns crystallization and isolation. Lab-scale protocols may mislead even the most careful researchers; at the kilo scale, solvent choice and temperature gradients start to matter much more. We advise on process windows that maximize yield and minimize color impurities—lessons that come only from repeated, hands-on runs.

    Bringing Consistent Outcomes to Industry

    The end-users for 2,5-Bis(Trifluoromethyl)Benzyl Alcohol extend beyond pharmaceuticals or agrochemicals. Teams developing specialty coatings use this molecule as a precursor to high-performance surfactants with custom solubility profiles. Polymer researchers incorporate the building block into side chains that modify glass transition temperature and weatherability. Advanced electronic material manufacturers find value in the robust C-F backbone, which imparts dielectric strength and oxidative resistance to device components.

    We have supplied this product to custom synthesis labs looking to prototype new materials, as well as to scale-up teams setting up robust flows for commercial active ingredient production. In every sector, project leaders find that having access to an authentic, traceable producer unlocks growth and reliability in product development pipelines.

    Direct Dialogues Make the Difference

    Being a specialist manufacturer puts us in direct conversation with both laboratory and industrial stakeholders. Many clients expect technical support on reaction mapping or impurity tracking. Experience with adjacent products—like mono- or tri-substituted trifluoromethyl benzyl alcohols—gives us a frame of reference, so we can suggest alternative routes or troubleshoot reaction stalls. We routinely run side-by-side stability tests to guide choice of solvent or reaction conditions. These data-driven conversations focus not on theory but on what truly works when you move from flask to reactor.

    Feedback cycles move fast. If a partner runs into an unexpected chromatographic issue in downstream purification, we bring in our analytical chemists directly, compare actual lot data, and suggest actionable process tweaks. This saves weeks in project troubleshooting, gets better results in purity, and often points toward next-generation products.

    Facing Future Demand for Fluorinated Intermediates

    Demand for advanced fluorinated intermediates continues to rise, driven by new drug candidates, more resilient crop protection solutions, and novel material science projects. Market analysis predicts growth in the CF3-benzyl segment, especially for scaffold diversification and specialty polymer production. As a full-scale chemical manufacturer, we stay ready to respond both to planned increases and sudden surges in need. Our operations prepare extra capacity for flexible batch sizes, adapt process layouts for custom specs, and maintain critical stocks of starting materials.

    We’ve observed that as regulatory scrutiny grows over per- and polyfluoroalkyl substances, buyers seek suppliers that already comply with emerging environmental and product safety expectations. Our internal policies do not wait for legal mandates—proactive management of fluorinated waste and ongoing process improvement meet today’s, and tomorrow’s, challenges.

    Conclusion: A Trusted Link in the Innovation Chain

    Years on the shop floor reveal that success doesn’t just hinge on chemistry textbooks or sales brochures—it comes from watching reaction mixtures, tracking every variable, and treating every delivery as a small testament to professional integrity. 2,5-Bis(Trifluoromethyl)Benzyl Alcohol doesn’t just enter our inventory as a number or SKU. Every batch draws on deep process knowledge, safety vigilance, and a sense of partnership with innovators who demand reliable, high-performing intermediates. We find satisfaction not just in shipping quality molecules, but in knowing our experience helps shape the next wave of life-changing discoveries.