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5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol

    • Product Name 5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol
    • Alias 5-Chloro-2-(trifluoromethyl)benzyl alcohol
    • Einecs 630-446-2
    • 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

    117809

    Chemical Name 5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol
    Molecular Formula C8H6ClF3O
    Molecular Weight 210.58 g/mol
    Cas Number 57381-53-0
    Appearance Colorless to pale yellow liquid
    Density 1.41 g/cm3 (approximate, at 20°C)
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and dichloromethane

    As an accredited 5-Chloro-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, 25g, sealed with a screw cap, labeled with chemical name, formula, and safety information, protective outer box.
    Shipping 5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol is shipped in tightly sealed, chemically resistant containers, protected from light and moisture. It is transported as a hazardous material according to relevant regulations, with proper labeling and documentation. Ensure storage in a cool, well-ventilated area away from incompatible substances. Handle with appropriate safety precautions.
    Storage Store **5-Chloro-2-(trifluoromethyl)benzyl alcohol** in a tightly sealed container, kept in a cool, dry, and well-ventilated area. Protect from light, moisture, heat, and incompatible substances such as strong oxidizing agents. Avoid prolonged exposure to air. Label the container clearly and follow standard laboratory chemical storage protocols, including use of appropriate secondary containment and segregation from reactive chemicals.
    Application of 5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol

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

    5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol serves as a critical intermediate in the synthesis of advanced specialty chemicals. Our team supplies this high-purity raw material directly from our own plant to leading manufacturers across several regulated downstream sectors. Please find below selected industrial application scenarios, each with process-driven details tailored for end-use integration.

    1. Agrochemical Active Ingredient Synthesis

    This raw material plays an integral part in building key intermediates for the manufacture of selective herbicides and insecticides, particularly those based on substituted benzyl moieties. Its chemical structure enables targeted halogenation and fluorination patterns that enhance bioactivity in crop protection molecule frameworks during multistep synthesis campaigns.

    Industry compliance standards

    • REACH Regulation (EU) No 1907/2006 for chemical safety evaluation
    • ISO 9001:2015 quality management systems for production and traceability
    • FIFRA (US EPA) requirements for active ingredient registration and manufacturing controls
    • GB 2082-2013 (China): Safety and quality for pesticide intermediates

    Typical usage ratio

    • 0.9% to 6% by mass in the synthesis batch, depending on the target active ingredient and molecular conversion efficiency; proportion adjusted based on downstream coupling or functionalization yield in pilot and commercial scale-up

    Downstream process integration

    • Feeds directly into pre-coupling or functionalization stages as a protected intermediate or reactive alcohol in flow chemistry or batch reactors; batch charging monitored via in-line NMR and HPLC to validate purity pre-step

    Final product types

    • Selective herbicides such as fluoro-halogenated phenyl products
    • Pyrazole-based insecticidal actives
    • Intermediate molecules for broadleaf weed control formulations

    2. Pharmaceutical Intermediates Manufacturing

    Leading API producers integrate this compound into syntheses of fluorinated benzylic fragments, essential for the structural backbone of several small-molecule drugs. Its reactivity profile supports downstream functional group installation, aiding efficient construction of pharmacologically relevant motifs without protection/deprotection bottlenecks.

    Industry compliance standards

    • Good Manufacturing Practice (ICH Q7) for pharmaceutical intermediates
    • USP–NF (current edition) for related substances controls
    • 21 CFR Part 210/211 (US FDA) for finished pharmaceuticals
    • Ph. Eur. (European Pharmacopoeia) reference for purity and residual solvents

    Typical usage ratio

    • 1.5% to 4.5% by mass in the synthesis stream; ratio optimized for each drug’s core structure and yield parameters, often refined during route scouting and process scale-up studies

    Downstream process integration

    • Incorporated at the penultimate or antepenultimate step of API synthesis to introduce the protected benzylic group, followed by selective group interconversions in fully contained GMP suites; intermediate tested by LC-MS prior to next coupling or cyclization

    Final product types

    • Fluorinated pharmaceutical intermediates for CNS and oncology APIs
    • Advanced building blocks for kinase inhibitors
    • Chiral benzylic starting materials for small-molecule drugs

    3. Electronic Chemicals and Fine Chemicals Production

    Specialist electronic chemical producers deploy this raw material for the fabrication of high-purity intermediates required in the synthesis of photoresist additives, OLED precursor molecules, and electronic-grade specialty solvents. Its high halogen and fluorine density enhance targeted electron-withdrawing properties, critical for performance in demanding semiconductor process environments.

    Industry compliance standards

    • SEMI C93-0914 (Specifications for Organic Chemicals for Electronic Applications)
    • ISO 14001:2015 for environmental management in chemical manufacturing
    • RoHS Directive 2011/65/EU compliance for downstream use in electronics
    • Corporate social responsibility (CSR) supply chain audits for semiconductor sector

    Typical usage ratio

    • Usage between 0.4% and 2.5% per formulation matrix, dependent on targeted electronic performance characteristics—e.g., charge transfer rates or optical density requirements in photoresist synthesis

    Downstream process integration

    • Introduced at the initial precursor coupling stage or as a controlled nucleophile/arylating agent in multi-step organic syntheses; exact introduction point guided by in situ process validation for low ionic impurity build-up

    Final product types

    • Photoresist monomers for semiconductor lithography
    • OLED emitters and hole transport materials
    • High-purity organic etchants and electronic solvents

    4. Specialty Polymer Synthesis

    Polymer manufacturers incorporate this material as a chain-terminating agent or functional monomer precursor in the development of high-performance fluoropolymer chains. Fluorinated aromatic structures derived from this alcohol impart increased thermal stability, chemical resistance, and surface repellency to engineered resins and elastomers.

    Industry compliance standards

    • ISO 9001:2015 for quality control in specialty polymer production
    • EN ISO 1043-1 for polymer and plastics identification and reporting
    • UL 94 flame retardancy testing protocols as required by end-user specifications
    • REACH SVHC (Substance of Very High Concern) review for monomer and additive use

    Typical usage ratio

    • 0.8% to 3.2% by total monomer content in co-polymerization batches; adjusted based on chain-length target and degree of functional group introduction determined during R&D pilot extrusion trials

    Downstream process integration

    • Added as the functional comonomer or endcapper in controlled-radical or step-growth polymerizations, typically after initial molecular weight build-up to achieve terminal fluorinated aromatic incorporation; integration closely monitored by GPC and FTIR

    Final product types

    • Fluoropolymer coatings for aerospace and automotive components
    • Specialty resin binders for high-temperature electronics
    • Water- and oil-repellent textile finishes

    5. Liquid Crystal Material Synthesis

    Manufacturers of advanced liquid crystal compounds utilize this raw material as a precisely engineered precursor that enters multi-step syntheses of fluorinated aromatic cores. These structural units are essential in providing the necessary dielectric anisotropy and viscosity characteristics for high-resolution display applications.

    Industry compliance standards

    • JEITA - Japanese Electronics and Information Technology Industries Association standards for display materials
    • ISO 9001:2015 and ISO 14001:2015 for process quality and environmental control
    • RoHS Directive 2011/65/EU for hazardous substance management
    • Global LCD industry restricted substances and impurity guidelines

    Typical usage ratio

    • 0.3% to 1.0% in the synthesis of high-performance liquid crystal intermediates; ratio controlled tightly via in-process viscosity and transition temperature profiling, varied according to final mesogen design requirements

    Downstream process integration

    • Feeds as an aromatic alcohol functional group in early-stage coupling or etherification, entering at the stage where fluorination and chlorination ensure alignment properties in end-use display materials; quality tracked through DSC and 1H NMR

    Final product types

    • High-purity liquid crystal mixtures for TFT-LCD and OLED displays
    • Mesogenic intermediates for advanced display panels
    • Specialty anisotropic fluids for industrial displays
    Free Quote

    Competitive 5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol: Reliable Quality from Direct Manufacturer

    About 5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol

    5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol, commonly recognized in the chemical industry for its stable aromatic backbone, stands out among specialty intermediates. Working as a direct manufacturer, we've seen firsthand how chemists rely on this compound for consistent reactivity and high purity in complex synthesis steps. Unlike more generic benzyl alcohols, this molecule incorporates both a trifluoromethyl group and a chlorine atom on the benzene ring. This careful arrangement leads to significant changes in properties, making it an appealing building block for many advanced chemical transformations.

    Experience in scaled synthesis underlines the importance of getting every detail right in products like this. It’s not just about attaching functional groups. Managing the substitution of a trifluoromethyl group at the ortho position, alongside a chlorine at the para position, takes careful control over reaction conditions, selective catalysis, and impurity management. Due diligence at each stage influences the outcome in terms of melting point accuracy, NMR signature sharpness, and GC trace cleanliness. Through years of refining our approach, we’ve addressed common pain points linked to mixed isomer content, trace byproducts, and incomplete conversions.

    Model, Specifications, and Consistency

    The typical batch model follows an optimized process using selective halogenation, followed by stepwise introduction of the trifluoromethyl group and protection protocols to secure the benzyl alcohol moiety. Consistency trumps theoretical yield — a lesson learned through seeing what end-users value. Color, clarity, and analytical data matter, but so does keeping the product predictable from one drum to the next. Variations in benzyl alcohol derivatives often spring from shifts in raw material supply or minor process drift. Our internal quality program checks against multiple standards: in-house NMR, FTIR, HPLC purity, and comparison with established reference materials. Most shipments exceed a purity of 98%, with water content kept below target ppm, based on Karl Fischer titration.

    Regular customers who have toured our facilities know that benchmarks are set for residual solvents and halide content, since these impact reaction profiles—especially for users targeting downstream transformations such as etherification or further substitution on the aryl ring. We stick to glass-lined reactors and monitored transfer lines to prevent trace metal contamination. Several clients have reported reduced rework rates after switching to our material, mostly because we track and minimize the stuff that ruins reactions on scale.

    Common Applications and Practical Use

    This alcohol isn’t just an intermediate to us; it’s a versatile toolkit component for synthetic chemists. Pharmaceutical researchers favor this compound for constructing energetic scaffolds where electron-withdrawing substituents steer reactivity. The trifluoromethyl group both enhances metabolic stability and shifts lipophilicity, giving rise to new candidates in medicinal chemistry campaigns. The chlorine atom directs ortho and para substitution, offering reliable access to regioselectively functionalized analogs, including aryl ethers and esters.

    Beyond pharma, agrochemical producers adopt this compound as a lead for constructing novel crop protection agents. Here, halogenation patterns affect both potency and environmental persistence. Through years of feedback from end-users in different regions, we’ve learned to anticipate formulation needs — especially where the presence of non-targeted isomers or side-chain impurities might render a formulation unsuitable.

    Coatings and specialty material developers also use this benzyl alcohol as a modifying agent. It acts as an anchor point for attaching other groups, changing polymer backbones or influencing cross-linking rates. The electron-deficient aromatic system brings unique reactivity, letting users explore new surface-active compounds with finer control.

    Why Purity and Traceability Matter in Practice

    It’s easy to talk about purity as a checkbox criterion, but in our experience, the details tell the real story. Manufacturing at scale uncovers pitfalls rarely seen at pilot level. Residual chlorine or trifluoromethylated byproducts — no matter how minor — can slow down downstream reactions or create new challenges in purification. A persistent problem we’ve helped customers solve relates to variable crystallization patterns caused by invisible impurities, which throw off downstream process yields.

    We operate with real-time tracking down to every solvent lot and raw material batch, not just main reactants. Detailed provenance for major and minor components means a rapid response if a customer reports an anomaly. The supply chain for reagents, especially fluorinating agents, comes under tight watch. We regularly update both know-how and infrastructure based on shifts in market availability or regulatory changes — a lesson underscored by disruptions during raw material allocation periods and logistics interruptions.

    Being close to the actual production means we observe quality shifts before they reach customers. This lets us make on-the-fly corrections, such as adjusting purification steps or updating drying cycles when seasonal humidity spikes affect crystallization. Lab teams collaborate with operators on the floor to catch issues early, putting reliability ahead of marketing claims.

    Key Differences from Related Products

    Experience handling other benzyl alcohol derivatives has taught us that substituent effects aren’t just textbook curiosities. The combination of both the trifluoromethyl group and the chlorine imparts a unique reactivity profile. For example, compared to unsubstituted benzyl alcohol, you might notice a reduced tendency for auto-oxidation and a distinct solubility profile across common organic solvents. This can improve product shelf life and allow for broader compatibility in synthesis schemes.

    Contrast this compound with similar molecules like 5-chlorobenzyl alcohol or 2-trifluoromethylbenzyl alcohol. The simultaneous presence of both groups shifts the pKa and alters the outcomes during Grignard or nucleophilic substitution reactions. Commercial partners using single-modified alcohols often report limitations during late-stage functionalization; the double modification in this compound can bypass those sticking points, streamlining synthetic routes and cutting out extra reaction steps.

    Some competitors rely on older production lines for these molecules, leading to higher residual halides or variable fluorination levels. Over the years, we’ve modernized our facilities to provide greater control, continuously improving vent capture, waste neutralization protocols, and in-line monitoring. These upgrades translate into higher batch reproducibility and reduced variation, making the product more than just a line item in a catalog.

    Environmental and Safety Considerations

    Having boots on the ground in a manufacturing plant changes your perspective on environmental management. Compounds containing both fluorine and chlorine demand specialized handling, both for personnel health and for dealing with process residues. Upgraded scrubbing units neutralize byproducts before any vented gas leaves the site. Waste handling plans put a strong emphasis on recycling solvents and capturing fluorinated side streams. These aren’t regulatory boxes to tick — over years of experience, they’ve become recipes for reducing downtime, limiting waste disposal fees, and staying ahead of new compliance targets.

    Our internal safety protocols reflect the experience of managing reaction exotherms, especially during steps involving active fluorination or chlorination. Training builds on incidents and near-misses, sharing lessons with operators in their native languages. All plant workers participate in risk drills, and every new process undergoes a hands-on hazard analysis — no paper exercise, just real discussion about what could go wrong and how to spot the early signs.

    Handling high-purity intermediates brings a responsibility to both end-users and the wider community. We invest directly in emission control, effluent treatment, and personal protective equipment, as it creates long-term reliability for us and clients alike. Any change in reagents or process steps undergoes review by both environmental and technical teams, with changes logged in our process histories, not just buried in annual reports.

    Supply Assurance and Customer Support

    Many customers reach out not just for product, but for confidence in the pipeline. As a manufacturer with hands-on oversight, we buffer against raw material interruptions through expanded sourcing options, prequalifying every new vendor. When something interrupts our supply chain, we keep partners in the loop, flagging any possible delays before they cascade into project setbacks. This hands-on connection has kept long-standing relationships steady, especially during times when stricter export oversight or unforeseen demand spikes shake up global markets.

    Direct feedback from laboratories using our 5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol flows directly into process updates. Chemists in both R&D and production have visited to troubleshoot scale-up challenges — for example, customizing drying steps to ensure moisture-sensitive routes proceed without a hitch. By integrating these stories into our production playbook, we offer more than just a stock molecule.

    Long-Term Benefits for Innovation

    5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol has unlocked practical breakthroughs beyond core chemistry. Contract manufacturers in pharmaceuticals have streamlined multi-step processes by starting with this compound, leapfrogging unnecessary functional group interconversions. In specialty chemicals, faster-to-market timelines often hinge on having a reliable starting material. Several partners report faster project approvals when working with traceable and reproducible input chemicals, because it smooths downstream registration and documentation requirements.

    We’ve run side-by-side trials comparing our product to alternate sources with lower control standards — the results point to fewer deviation reports, a higher percentage of successful reactions, and less time spent chasing unknowns in process analytics. These advantages filter down: fewer interruptions in pilot plants, cleaner data for process validation, and steadier product launches.

    Responsibility and Ongoing Improvement

    Hands-on production keeps us close to real-world impact. We structure our business around ongoing improvement, updating specifications according to feedback, regulatory frameworks, and emerging scientific evidence. Continuous investment in staff skills and plant upgrades translates into better material. For customers pushing boundaries in synthesis, this level of involvement brings peace of mind, as they know the next batch will not disrupt current work or trigger costly troubleshooting.

    We participate in forums and technical panels, sharing both positive and hard-won lessons. For example, sharing process improvements at industry workshops and co-authoring publications on safer halogenation techniques or greener solvent systems. Our relationships are built around detailed conversation, not just standardized reports, and we stay open to collaboration for problem-solving.

    The Value of Direct Manufacturing

    Being a manufacturer means watching the process evolve from raw material reception through final quality checks. There’s no substitute for the insight gained from responding to process upsets, scaling new batches, and tracking every variable that might influence final product. Every improvement, from reactor cleaning protocols to real-time parameter logging, stems from seeing firsthand how variance affects outcome and building layers of defense to narrow those gaps.

    Direct manufacturing also leads to a different attitude toward inventory. We keep safety stock based on historical trends and coordinate with key users for surge periods. If a custom specification arises, our team has the agility to modify runs, sometimes adjusting as quickly as within a single campaign. We take pride in supplying researchers and process chemists with what they need to keep innovations moving.

    An Experienced Approach to the Market

    Over the years, collaboration with customers big and small has shaped how we produce, control, and deliver 5-Chloro-2-(Trifluoromethyl)Benzyl Alcohol. This compound, though niche, carries broad consequences for those depending on high reproducibility, reliable documentation, and responsiveness from their source. Every drum shipped reflects the years of learning, the missteps, the fine-tuning that only a manufacturer accumulates. This approach carries forward—new projects, new challenges, new possibilities for both us and our partners.