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3-(Trifluoromethyl)Benzhydrol

    • Product Name 3-(Trifluoromethyl)Benzhydrol
    • Alias 3-(Trifluoromethyl)Diphenylmethanol
    • Einecs 237-325-0
    • 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

    899352

    Chemicalname 3-(Trifluoromethyl)Benzhydrol
    Casnumber 348-74-9
    Molecularformula C14H11F3O
    Molecularweight 252.23
    Appearance White to off-white solid
    Meltingpoint 72-75°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.22 g/cm³ (approximate)
    Smiles C1=CC(=CC(=C1)C(C2=CC=CC=C2)O)C(F)(F)F
    Inchi InChI=1S/C14H11F3O/c15-14(16,17)11-7-6-10(8-12(11)13(18)9-4-2-1-3-5-9)9-4-2-1-3-5-9/h1-8,13,18H

    As an accredited 3-(Trifluoromethyl)Benzhydrol 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 screw cap; white printed label displaying chemical name, CAS number, safety warnings, and supplier logo.
    Shipping **Shipping Description:** 3-(Trifluoromethyl)Benzhydrol is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. Packages are labeled per regulatory requirements and transported under ambient temperature. Handle with care, following all safety and hazardous material guidelines. Ensure accompanying documentation includes safety data and emergency procedures for secure and compliant transit.
    Storage Store **3-(Trifluoromethyl)benzhydrol** in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible materials such as strong oxidizers and acids. Protect from light and moisture. Ensure proper labeling, and keep it away from heat or ignition sources. Use appropriate chemical storage cabinets, preferably in a designated area for organic compounds.
    Application of 3-(Trifluoromethyl)Benzhydrol

    Applications of 3-(Trifluoromethyl)Benzhydrol in Industrial Manufacturing

    As an experienced manufacturer specializing in high-purity fluorinated intermediates, we supply 3-(Trifluoromethyl)Benzhydrol to leading industrial customers supporting advanced synthesis and specialty formulation projects. Below are primary downstream applications, each requiring careful adaptation to industry-specific requirements and stringent regulatory frameworks.

    1. Pharmaceutical Intermediate for Antipsychotic APIs

    Major pharmaceutical synthesis routes for select atypical antipsychotic agents rely on trifluoromethylated benzhydrol scaffolds. Production chemists use our material for key Grignard additions and reductive coupling stages within multi-step API syntheses. During process scale-up, manufacturers deploy it in stepwise, controlled reactions under cGMP protocols to prevent by-product formation and ensure high batch purity. Such applications demand secure traceability and integrated quality assurance from raw material to final active pharmaceutical ingredient release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, Ph. Eur. residual solvent and impurity thresholds for intermediates
    • EU REACH registration for pharmaceutical precursors
    • FDA DMF (Drug Master File) referencing raw material batches

    Typical usage ratio

    • Applied at 0.95–1.05 mole equivalents per coupling step
    • Final ratio determined by batch scale, Grignard reagent excess, and downstream yield optimization

    Downstream process integration

    • Introduced into the stepwise Grignard or Friedel–Crafts alkylation under inert atmosphere
    • Subjected to controlled temperature ramps and monitored for conversion completion
    • Intermediate’s presence confirmed via in-process HPLC or NMR

    Final product types

    • Bulk pharmaceutical intermediates (Phase II/III clinical)
    • Marketed API (e.g., select antipsychotics or CNS actives)
    • Pharmaceutical reference standards

    2. Agrochemical Synthesis: Fluorinated Herbicide Precursor

    Manufacturers of advanced crop protection agents incorporate fluorinated aromatic alcohols as vital intermediates. 3-(Trifluoromethyl)Benzhydrol enters hydroxy-functionalization pathways conferring metabolic stability and soil persistence to final actives. Suitable for pilot and commercial synthesis under multi-ton batch regimes, this compound demonstrates reactivity in aromatic ring substitution and handles oxidative process stresses. Downstream users require diligent impurity profiling and validation of carryover in final technical-grade herbicides.

    Industry compliance standards

    • OECD test guidelines for agrochemical intermediates
    • FAO/WHO specification for technical material purity
    • ISO 9001:2015 production quality assurance
    • REACH pre-registration for environmental impact assessment documentation

    Typical usage ratio

    • Introduced at 1.0–1.2 equivalents relative to target aromatic core
    • Adjustments made to compensate for conversion efficiency and raw material purity

    Downstream process integration

    • Added during aromatic ring chlorination or alkylation under controlled temperature and pH
    • Reactant flow regulated in semi-continuous reactors for consistent yield
    • Resulting intermediates purified via solvent extraction and crystallization

    Final product types

    • Technical-grade pre-emergent and post-emergent herbicides
    • Intermediate compounds for fungicide active ingredients
    • Analytical standards for regulated field residue testing

    3. Electronic Chemicals: OLED and Liquid Crystal Intermediates

    Production of next-generation display materials such as OLED emissive layers and liquid crystal compounds leverages trifluoromethyl aromatics for enhanced electron mobility and chemical resistance. Downstream clients specify our benzhydrol derivative for use in synthesis of advanced aromatic cores and carrier molecules, requiring batch consistency and extremely low metal and halide residues. QC laboratories conduct routine spectroscopic qualification to meet demanding optoelectronic industry benchmarks.

    Industry compliance standards

    • JEDEC purity requirements for electronic-grade materials
    • RoHS Directive 2011/65/EU for hazardous substance limits
    • IPC-5701A guidelines for material batch traceability
    • Internal panel-maker proprietary specifications

    Typical usage ratio

    • Formulation levels span 5–25% by mass (w/w), depending on molecular design and active layer composition
    • Fine-tuned according to target luminance, response time, and viscosity parameters

    Downstream process integration

    • Introduced as a condensation or substitution partner in small-molecule OLED core synthesis
    • Utilized in liquid-phase or solid-state fabrication protocols
    • Undergoes further coupling before device fabrication commences

    Final product types

    • OLED emitter and host materials for display panels
    • High-purity liquid crystalline intermediates for screen manufacturing
    • Functional polymers with tunable optical properties

    4. Fine Chemical Synthesis: Specialty Fragrance Intermediates

    Fragrance compound formulators require stable, high-purity aromatic alcohols as building blocks for luxury perfumery and aroma compounds. This benzhydrol derivative supports the synthesis of fluorinated musk and woody tonalities by serving as a nucleophile in acylation or etherification steps. Downstream blending houses test batches for odor neutrality, low peroxide formation, and residual solvent content to comply with IFRA and international fragrance regulations.

    Industry compliance standards

    • IFRA Standards and Amendment notifications (International Fragrance Association)
    • EU Regulation (EC) No 1223/2009 for Cosmetic Ingredients
    • RIFM safety assessment for new aroma chemicals
    • ISO 9001 production records for traceability audits

    Typical usage ratio

    • Engaged at 0.2–2.5% by total batch mass in fragrance intermediate synthesis
    • Ratio determined by end-note intensity and reactive yield in musk/woody base synthesis

    Downstream process integration

    • Deployed in Friedel–Crafts acylation or Williamson ether synthesis with continuous monitoring of reaction by-products
    • Adjusted for by-product isolation during distillation of aroma intermediates
    • QC includes odor profile and peroxide testing before integration into high-value blends

    Final product types

    • Musk and animalic fragrance materials
    • Signature compound intermediates for designer perfumes
    • Encapsulated aroma microcapsules for home and fabric applications
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    Certification & Compliance
    More Introduction

    Real Handling, Real Chemistry: 3-(Trifluoromethyl)Benzhydrol

    A Manufacturer’s View on Performance, Quality, and Use in Industry

    Creating specialty chemicals for advanced industries comes down to precision and know-how, especially for intermediates like 3-(Trifluoromethyl)Benzhydrol. We produce this compound in our own controlled facilities, following time-tested synthesis routes, because we see every day how the smallest impurity in this material can swing downstream yields or lead to unpredictable reactions. Our chemists have refined the process for years in-house, learning through every batch where side products form, how to suppress them, and how our control impacts the kind of purity researchers depend on. Our 3-(Trifluoromethyl)Benzhydrol arrives at your door without the hesitation that comes from trading or uncertain sources.

    The structure—two phenyl rings and an alcohol group, punctuated by a trifluoromethyl at the meta position—isn’t chosen for show. That trifluoromethyl group opens up real practical differences, which makes this intermediate matter for high-value pharmaceuticals, agrochemicals, and advanced material syntheses. Over years of batch optimization, our team has found that certain downstream catalytic couplings run cleaner when this specific meta pattern is present instead of an ortho or para. It’s not just theory: we’ve seen reduced side-reactions compared to benzhydrols with fluorine in other spots or with simpler methyl groups.

    You might see 3-(Trifluoromethyl)Benzhydrol listed in fine chemical catalogs, lumped in a group with substituted diphenylmethanols. The reality for producers, not just resellers, is that this compound requires a different handling philosophy at scale. Fluorinated aromatics behave in reactors with their own set of quirks. During purification, our operators engage with volatility and resistance to moisture uptake—a bonus for those who need anhydrous conditions in precise coupling or alkylation steps downstream. We build every kilogram batch with this future use in mind, shipping product that consistently resists the clumping or solvent retention common in less-refined outputs.

    Specifications guide the lab, but our experience shows that the best way to establish trust with demanding customers lies in routine documentation and transparency. Every synthetic lot gets analyzed against GC, HPLC, and NMR benchmarks, with a spectroscopic fingerprint unique to our synthesis route. While on paper this product carries the same CAS number and molecular structure as anyone else’s batch, actual impurity profiles separate producers who take shortcuts from those who monitor each crystallization or distillation. We see strong demand from customers manufacturing APIs where regulatory filings make these analytical details non-negotiable. We run older analytic archives in tandem with current spectra to keep process drift under constant review.

    We started working with 3-(Trifluoromethyl)Benzhydrol for a handful of local research customers a decade ago, and since then, the use cases have multiplied. Today, medicinal chemistry programs reach for this molecule when studying new benzyl alcohol derivatives, because the electron-withdrawing effect of CF3 tunes molecular reactivity and bolsters metabolic stability. Crop science developers leverage this compound to build new agrochemical scaffolds, exploiting its unique interaction with enzyme targets. Each sector pushes us to further customize purity grades, and we’ve responded by segmenting product lines—offering material suitable for exploratory synthesis, pilot-stage preclinical development, and full regulatory filing applications.

    Experience has shown us that even small changes to the synthetic route alter how the product behaves in storage and processing. Some clients require crystalline product for direct weighing and formulation; others favor a semi-solid or dissolved form for immediate integration into automated synthesis systems. In our facilities, we tailor the isolation and packaging steps to meet those requests. Every production run gives us a new lesson in what makes handling easier for formulation chemists or pilot plant operators. Not every 3-(Trifluoromethyl)Benzhydrol supplier can, or will, match product form to customer workflow—but as manufacturers, we see it as a responsibility to support those nuances.

    Many industrial applications rely not just on molecular structure, but on the story behind material quality. For example, in the manufacture of select anti-inflammatory drugs, the way residual solvents or trace metal impurities linger through multiple synthetic steps can influence not only yield, but also regulatory compliance. We invested in solvent recovery and purification systems, specifically to cut down these contaminants. Over time, our teams shared data with downstream formulators showing that lower solvent residues in our 3-(Trifluoromethyl)Benzhydrol shortened their downstream purification protocols and resulted in cleaner API lots. Direct feedback like this triggers process improvement cycles directly at the source, long before shipping.

    Compared to benzhydrols with different substituents, the trifluoromethyl group at the 3-position creates a challenging target for some synthetic routes, especially via classic Grignard or Friedel-Crafts approaches. Our scale-up chemists learned that raw material purity and reagent preparation needed tighter control for this intermediate, because unreacted starting materials or regioisomeric byproducts could complicate downstream application in medicinal chemistry libraries. We’ve spent years refining not only the main product, but also the precursor purification steps—removing trace mono-fluorinated byproducts or isomeric impurities rarely tracked by third-party sellers.

    The explosion in demand from contract research organizations over the last several years showed us another angle: researchers look for reliable, repeatable quality, but also suppliers who can scale from grams to multi-kilogram lots without the “surprise” batch-to-batch variation. We take those scale challenges seriously. Our batch records and blending tanks track each run’s output, and we hold material for additional analytical runs if we spot trends. Consistency matters to synthesis teams running dozens of coupling reactions on fast timelines, racing to meet project deadlines. Every delay from unpredictable quality flows upstream in wasted time and resources.

    We recognize that the shelf life and stability profile of 3-(Trifluoromethyl)Benzhydrol impacts long-term inventory management for large organizations. Our process engineers dial in product water content, reject material showing phasing or crystallization inconsistencies, and blend stock at controlled humidity before packaging. Learning from early logistics hiccups, we adapted our packaging process to use moisture-barrier containers and UV-resistant barrels for companies storing material for six months or more. Those incremental changes stem from first-hand reports—solid product for an entire season, free of technical headaches.

    Bridging Gaps Between Small-Scale Research and Industrial Manufacturing

    There’s a temptation to lump chemicals like 3-(Trifluoromethyl)Benzhydrol into bulk-organic catalogs, but real-world handling points out the gaps between research consumables and industrial intermediates. Unlike straightforward aromatic alcohols, the trifluoromethyl group’s high electronegativity and steric impact steer reactivity in unique ways. Customers synthesizing specialty ligands or building blocks encounter differences in reaction rates, selectivity, or even color change during workup. Our application chemists talk to R&D teams about specific case studies—catalytic reductions, Suzuki couplings, or stereochemical outcomes in asymmetric reactions. Each use teaches us more about what production choices ripple outward.

    Talk to any bench chemist who’s handled a gram of high-purity 3-(Trifluoromethyl)Benzhydrol after years of running standard benzhydrol, and you’ll see the difference in ease of handling, especially in moisture-sensitive or air-sensitive assemblies. Because we produce this material in dedicated fluorinated-aromatic suites, we can guarantee low cross-contamination—even trace carryover from other production lines can make a difference in high-throughput synthesis environments. We audit washing protocols and build in extra safety checks to protect the material and users alike.

    Process safety has taken on new significance as demand shifts toward fluorinated building blocks. Our risk teams identified the exothermicity of certain substitution steps and modified reactor cooling to prevent runaway reactions. We’ve trained line workers and technical support staff to recognize the smell, feel, and flow properties of the intermediate at various stages, adding a human filter in parallel to automated sensors. Feedback from packaging teams spurred a redesign of our filling equipment, reducing exposure risk and ensuring repeatable fill weights for export shipments subject to strict customs scrutiny.

    Some customers need solid pellets, while others ask for dry flakes or fine powders, each form requiring distinct isolation steps after synthesis. We saw that customers exploring continuous-flow synthesis preferred certain particle sizes for optimal solubility and dosing accuracy, prompting us to invest in custom crystallizers instead of one-size-fits-all protocols. We now provide several selectable formats, guided by feedback from process chemists who have tested our material through their own equipment. Those adjustments let researchers and production engineers move right from delivery to application without frustrating transfer losses.

    Looking across the market, the difference between our 3-(Trifluoromethyl)Benzhydrol and knockoff or “no-name” variants grows more obvious as end-uses get more specialized. We’ve fielded calls from teams wrestling with unidentified contaminants traced to poor material; some turned to us after failed batches halted R&D or clinical trial programs. For each new customer, we invest time in onboarding, discussing use-case specifics, reviewing their analytic findings, and issuing technical bulletins to help troubleshoot or identify improvements. Our data-sharing approach has built trust with regulated companies where transparency isn’t just a bonus, but a norm.

    Every bottle or drum of our benzhydrol derivative gets a tracking code that links all production, analytic, and packaging data back to the lot level. We believe in direct accountability, and over years of open feedback, we’ve helped many labs identify bottlenecks, fix protocols, and realize higher reliability in their synthetic routes. This mindset requires more investment on our part, but it pays tangible dividends for chemists counting on material consistency to develop new products or meet regulatory expectations around reproducibility.

    Direct manufacturing means we see both the technical challenges and the end-user pressures firsthand. Our operators are attuned to common pain points, from bottle crystallization during long shipping routes, to minor appearance shifts after storage near plant utility lines. Chemistry doesn’t pause at the border—material shipped globally must keep its specification profile through humidity, temperature swings, and human handling on docks. Based on lessons from early export projects, we reinforced packaging procedures, developed layered climate-resistant wraps, and created protocol sheets for receivers on best handling practices at arrival.

    For process innovation, our R&D team runs small pilot studies whenever there’s a suggestion from a partner or regulator about alternative synthetic routes or new analytical detection methods. We’ve dedicated production lines for these pilots, learning as we go so the next generation of product meets both external and internal benchmarks. As markets shift toward ever-purer fluorinated intermediates, we stay proactive in upgrading our capabilities, pushing ahead on crystallization and solvent-exchange equipment, and benchmarking outcomes against previous lots. We embrace dialogue with formulation and analytic chemists to keep our process rooted in practical user needs rather than theoretical minimums.

    The Real Impact of a Carefully Manufactured Intermediate

    At the core, 3-(Trifluoromethyl)Benzhydrol isn’t just another entry in a catalog. Every gram reflects years of experience, technical iteration, and close communication between production and customers. Our team supports pharmaceutical groups where every impurity could mean hours of extra work or failed regulatory filings. We talk to materials scientists building new polymers or high-electron-mobility compounds where a slight moisture uptick, caused by poor packaging or secondary crystallization, can kill an experiment or cost a project weeks of rework.

    While industry trends keep pushing toward tighter specifications and lower impurity profiles, our focus stays rooted in direct customer outcomes. Customers in the API pipeline highlight new challenges—like sub-ppm levels of halogenated or aromatic impurities, or questions about isotope labeling for specific tracking studies. Because we manufacture directly, we get involved in weighing, customizing, and adapting our protocols to help answer those questions fast, instead of filtering requests through intermediaries who lack firsthand experience.

    Comparing our hands-on manufacturing background with traders or brokers, we take direct responsibility for every aspect—from raw material sourcing through final packing. That single-source accountability means we know which batches align for a multi-year project, or which lots support registration filings under different regulatory regimes. Over several years, our production planners have built a run-book of real-world troubleshooting insights—recommending storage tips, working out delivery timelines, and advising on compatibility with solvent systems encountered during late-stage formulation development.

    The trifluoromethyl-substituted benzhydrols might appear similar on a page, but our production chemists regularly teach partners about the subtle, application-level effects that come from a clean meta-fluoro group. This influences both reactivity and compatibility across a range of synthetic operations. By providing access to historic and current spectra, collaborating with QC teams, and offering direct feedback lines, we see our customers gain confidence in both short- and long-range planning. Our reliability helps them cut down analytical uncertainty, reduce troubleshooting cycles, and accelerate research timelines.

    Support from a genuine manufacturer lifts more than numbers on an assay sheet; it supports scientists and engineers contending with pressing timelines and costly decision points. In pushing to improve how 3-(Trifluoromethyl)Benzhydrol is produced and delivered, we open up possibilities for innovation further downstream. Trust grows batch by batch, for organizations who know their critical path depends not just on molecules, but on dependable people, honest data, and a commitment to getting every detail right.

    We continue to refine our work based on honest feedback, close technical partnerships, and a willingness to address problems as they arise. With every kilogram delivered, we bring the combined experience of our team—with lessons learned from production floors, QC benches, and chemical reactors—so customers can depend on consistent, high-quality 3-(Trifluoromethyl)Benzhydrol for whatever comes next.