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2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol

    • Product Name 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol
    • Alias 2-Chloro-3-(trifluoromethyl)benzyl alcohol
    • Einecs 697-739-7
    • 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

    319902

    Product Name 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol
    Cas Number 261762-57-6
    Molecular Formula C8H6ClF3O
    Molecular Weight 210.58
    Appearance Colorless to pale yellow liquid
    Density 1.42 g/cm³
    Purity Typically ≥97%
    Synonyms α-Hydroxy-2-chloro-3-(trifluoromethyl)toluene
    Smiles C1=CC(=C(C(=C1)Cl)C(F)(F)F)CO
    Inchi InChI=1S/C8H6ClF3O/c9-6-2-1-5(4-13)3-7(6)8(10,11)12/h1-3,13H,4H2
    Storage Temperature 2-8°C

    As an accredited 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tightly sealed with screw cap; labeled with chemical name, molecular formula, and hazard warnings.
    Shipping 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol is shipped in tightly sealed containers, protected from light and moisture. It is transported as a hazardous material according to international regulations. Appropriate labeling and documentation are required. Handle with care; avoid physical damage. Store in a cool, well-ventilated area, away from incompatible substances and ignition sources.
    Storage **2-Chloro-3-(trifluoromethyl)benzyl alcohol** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers and acids. Ensure the storage area is clearly labeled and restrict access to authorized personnel. Avoid moisture ingress and handle under a chemical fume hood if possible.
    Application of 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol

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

    2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol is a key intermediate in chemical synthesis for advanced industrial applications. As the original manufacturer, we deliver consistent, high-purity material to enable precise downstream performance for specialty sectors. Below are the main industrial application scenarios, supported by direct process insights, compliance requirements, and details for each manufacturing segment.

    1. Agrochemical Active Ingredient Synthesis

    This intermediate enters the manufacture of complex crop protection agents, particularly fluorinated pyridine and benzyl-containing herbicides. Production facilities use it during core condensation and coupling stages, contributing selectivity and stability to the target molecule. Downstream synthesis demands strict batch traceability and purity control for regulatory registration in major agriculture markets.

    Industry compliance standards

    • China GB 2763-2021 Maximum Residue Limits
    • EU Regulation 1107/2009 (authorisation of plant protection products)
    • US EPA 40 CFR Part 180 (tolerances for pesticide residues)
    • ISO 17025 (analytical laboratory validation for pesticide registration)

    Typical usage ratio

    • 5–15% of molar input per batch depending on the synthetic route and replacement group required for the finished active.
    • Ratio adjusted based on route efficiency and downstream coupling yields.

    Downstream process integration

    • Used in the nucleophilic substitution or alkylation steps before final halogen exchange.
    • Frequently enters reactor with other heterocyclic or substituted aromatic precursors.
    • Integrated as an input to multi-step, closed-system reactions followed by in-process solvent removal and crystallization.

    Final product types

    • Herbicide technical concentrates (e.g., for broadleaf weed control)
    • Insecticidal active intermediates
    • Seed coating compounds containing fluorinated groups
    • Regulatory-submitted active ingredient samples for GLP field trials

    2. Pharmaceutical Intermediate for API Synthesis

    Pharmaceutical firms specify this compound as an advanced intermediate for APIs in neurodegenerative, anti-inflammatory, and respiratory therapeutic classes. It provides valuable functionalization, allowing controlled incorporation of halogen and fluorine elements. Customer processes require rigorous documentation, batch segregation, and compliance with international GMP for regulated drug ingredients.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF monograph suitability for reference standards
    • EDQM CEP (European Certificate of Suitability) starting material definition
    • FDA CFR Title 21 Part 210/211 for cGMP production environments

    Typical usage ratio

    • Ranges between 8–25% of the total input mass in multi-stage synthesis, dependent on API structure and coupling efficiency.
    • Higher ratios for late-stage intermediates; adjusted for purification yield.

    Downstream process integration

    • Charged into reactor during key halogenation or etherification stages before closure or ring formation.
    • QC performed on isolated intermediate before transfer to API purification step.
    • Material flows through validated, closed-system lines with audit trails.

    Final product types

    • Pharmaceutical active pharmaceutical ingredients for CNS or anti-inflammatory medicines
    • Research-stage bulk drug substances for scale-up trials
    • Regulatory submission batches for new chemical entity applications
    • Contract development finished dosage forms (tablets, capsules)

    3. Electronic Chemical Synthesis

    Specialty electronics and semiconductor material manufacturers incorporate this compound within the synthesis framework for high-performance fluorinated monomers. These monomers impart dielectric strength and thermal resistance in advanced polymer films. Material purity and control of trace contaminants are critical for downstream microelectronics processing reliability.

    Industry compliance standards

    • SEMI C3-0818 (Specification for High Purity Chemicals)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 60749-20 (Semiconductor device quality standards for assembly)
    • ISO 9001:2015 (Quality Management Systems for electronic intermediates)

    Typical usage ratio

    • 3–10% by weight in copolymer synthesis lines, variable according to formula and application (e.g., low-k dielectric or heat-resistant films).
    • Ratio tuned for molecular weight control and electronic property requirement.

    Downstream process integration

    • Fed into polymerization kettles during fluorinated monomer introduction.
    • Used under inert atmosphere to prevent moisture-induced side reactions.
    • Downstream blending precedes film extrusion or wafer surface coating.

    Final product types

    • Dielectric polymer films for integrated circuit substrates
    • High-temperature resistant insulator foils
    • Specialty coatings for semiconductor packaging
    • Optoelectronic device components

    4. Fine Chemical Building Block for Fragrance Ingredients

    Fragrance formulation manufacturers employ this advanced benzyl alcohol to create high-performance aroma molecules for use in both industrial and premium consumer products. Its trifluoromethyl and chloro groups enable the synthesis of rare, nuanced top notes that enhance thermal and oxidative stability for detergent and cleaning applications. Formulations operate under IFRA guidelines with specific batch qualification testing.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • REACH Registration (EC 1907/2006) for European fragrance raw materials
    • ISO 9001:2015 for flavor and fragrance ingredient manufacturing
    • Japan Flavor & Fragrance Materials Association requirements

    Typical usage ratio

    • 0.1–2.5% by weight in fragrance intermediate synthesis, dependent on formula intensity and volatility characteristics needed.
    • Adjusted for batch quantity and downstream product profile.

    Downstream process integration

    • Added at the esterification or acylation stage to produce complex aroma molecules.
    • Directly involved in modification steps yielding unique olfactory profiles.
    • Material purity and byproduct qualification tested before bulk blending.

    Final product types

    • Specialty fragrance intermediates for detergent bases
    • High-affinity aroma compounds for luxury consumer goods
    • Functional scent components for industrial cleaners
    • Perfumery-grade chemical stocks
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    Certification & Compliance
    More Introduction

    Introducing 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol: A Reliable Asset from the Lab Bench to Production

    Product Overview

    From the manufacturer’s side of the bench, every compound we produce is more than a set of numbers on a certificate of analysis. Over the years, we’ve developed, optimized, and consistently scaled up 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol, which carries the model identifier CTBA-99 based on its minimum assay by area normalization. What started as a bench-scale pilot batch after requests from medicinal chemists has grown into routine batches crafted to support research, clinical, and scale-up needs.

    The structure of CTBA-99 merges a chlorinated aromatic core with a benzyl alcohol group and the electronegative punch of a trifluoromethyl moiety. Each substitution alters the electronic profile, creating distinct advantages and reactivity for modern synthetic applications. Our production follows a robust chlorination and selective trifluoromethylation sequence, monitored by multi-step purification to minimize levels of residual chlorotoluene or unconverted alcohol.

    Quality and Specifications

    Every batch of 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol undergoes a systematic quality inspection before release. HPLC analysis regularly shows purity above 99% with residual solvents far below the ICH Q3C thresholds. Water content typically measures well below 0.15% by Karl Fischer, and color remains consistent—no measurable yellow tint that complicates downstream processing in sensitive syntheses.

    We have stuck with glass-lining for the final isolation, which controls off-odors and preserves the alcohol’s clarity. By maintaining strict nitrogen blanketing and monitoring for peroxide formation, we keep batches stable over months in tightly closed amber bottles at room temperature. Researchers need material that performs the same way—week after week, quarter after quarter.

    Distinctive Performance in Synthesis

    Direct input from API, crop protection, and material science partners shaped our scale-up. 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol delivers unique value because of a combination of its functional groups. The benzylic alcohol opens access to ether and ester derivatives through straightforward alkylation or acylation. The ortho-chlorine modifies reactivity for directed ortho-metalation or cross-coupling, somewhat rare with standard benzyl alcohols. The trifluoromethyl group offers both electron-withdrawing effects and significant sterics, modifying NMR signatures and facilitating differentiation for monitoring conversions.

    Pharmaceutical customers tell us they value the alcohol’s role as an intermediate for CNS-active molecules and innovative kinase inhibitors, where the steric environment governs selectivity. In agrochemicals, it yields more robust analogs with improved metabolic stability. Electronics manufacturers noted improved fluorine introduction in specialty monomers where alternatives bring only one or two of these effects to the table. The unique pairing of a benzylic alcohol with both chloro and trifluoromethyl enhancements transforms the landscape for derivatization.

    Comparing Analogues and Substituted Benzyl Alcohols

    In practice, CTBA-99 stands out from other benzyl alcohol variants, like unmodified benzyl alcohol, 2-chlorobenzyl alcohol, or those substituted only with trifluoromethyl. Standard benzyl alcohols tend to be more nucleophilic and less sterically hindered, but they don’t offer the same stability or unique reactivity. In cross-coupling reactions or directed ortho-metalation, CTBA-99’s additional functional groups enable transformation pathways that unadorned benzyl alcohols simply cannot tolerate.

    Substitution pattern matters. Take trifluoromethylbenzyl alcohols: while they grant some electron withdrawal and improved lipophilicity, they lack the ortho-chlorine’s directing effect, which fundamentally changes how the molecule interacts with metal catalysts or bases. On the other hand, 2-chlorobenzyl alcohol misses the stability and electronic tuning that the CF3 group contributes. The combination in CTBA-99 has proven flexible and resilient, often allowing for milder conditions, streamlined workups, and more predictable outcomes at the scale where time matters most.

    Supporting Modern Chemistry With Consistency and Transparency

    Years of producing this specialty intermediate revealed that end users experience frequent batch-to-batch variability from smaller resellers or traders. Over-oxidized lots, excessive water, or micro-impurities such as 3,5-bis(trifluoromethyl) byproducts tend to sneak in via insufficient purification or inconsistent control of starting materials. By manufacturing everything under a single batch record—tracked from raw 3-chlorotoluene to final packed alcohol—traceability exists at every checkpoint.

    Feedback from scale-up labs informed our emphasis on color, solubility, and impurity profile. We rely on GC-MS and NMR confirmation for each bulk lot, not just HPLC purity. As our own teams run kinetic studies and derivatizations in parallel, insights trickle straight back into the process—shaving time from each filtration or reducing downstream column chromatography for customers. The goal has always been to clarify where this intermediate fits reliably in the synthetic chemist’s toolbox.

    Environmental guidelines push the industry toward cleaner profiles and less hazardous waste. By designing for low residual solvents and improving aqueous workup steps, we built a process that minimizes chlorinated waste generation. Researchers appreciate a compound that lets them focus on the next coupling, not cleanup complications stemming from unstable or inconsistent starting materials.

    Applications in Research, Development, and Production

    Most of the CTBA-99 batches support pharmaceutical research. Medicinal chemists use it to generate ethers, acetals, and esters with unique three-dimensional shapes and electronic environments that standard alcohols can’t match. The compound’s performance in classic Williamson ether synthesis proves reliable. Its liquid consistency enables accurate pipetting and blending, essential in automated synthesis platforms.

    The agricultural sector wants intermediates that handle radical initiators, strong bases, and variations in temperature profile without decomposing. Formulating more metabolically stable agrochemical actives relies on the CTBA-99 core for better persistence in complex environmental matrices. Our own early collaborations in this space highlighted the difference just one or two byproducts can make—yield drops, color shifts, or minor activity losses show up fast at scale.

    We have also partnered with specialty polymer groups, where the combination of aromatic halogen and fluoroalkyl substituents broadens thermal and chemical resistance in monomers. Material scientists explore CTBA-99 derivatives for their role in electronics, optoelectronics, and advanced coatings. Each field values the compound’s reproducibility, which only direct manufacturer control can assure batch after batch.

    Addressing Customer Experiences and Challenges

    Buyer feedback drives most process tweaks. Stories about delivery delays, partial crystallization, or impurity headaches direct our focus each quarter. Material sourced from the field sometimes reaches us with troublesome color or unexpected residual solvent levels, usually due to inconsistent bottling or changes in solvent mixtures during transit. Early on, we realized that rigid QC and close attention to packaging made a difference in how reliably customers can use the alcohol without secondary purification.

    Researchers look for information on shelf life, reactivity under light, and compatibility with a range of bases and acids. Having run accelerated aging studies ourselves, CTBA-99 in sealed glass bottles shows full integrity for more than a year at ambient temperature, limiting peroxide formation and avoiding hydrolysis under humid conditions. There are always lessons to pull from real-world feedback, whether that’s the impact of storage near open bench tops or recommendations to avoid metal containers that catalyze slow decomposition.

    Troubles sometimes arise in the transfer from discovery to kilogram production. Scale can change everything: cooling rates, agitation methods, or even the order of addition. Working alongside development chemists, our technical staff routinely troubleshoots bottle-to-drum transitions. Accurate assay labeling, updated safety, and prompt technical bulletins keep misunderstandings to a minimum and shorten the learning curve as customers scale their syntheses.

    Commitment to Transparency and Ongoing Process Improvement

    Direct engagement with our customers led to early moves away from simple COA printouts to richer datasets—NMR spectra, impurity tables, residual solvents reporting, and ongoing stability studies. End users gain full batch traceability due to integrated tracking from hydrogenation, halogenation, and purification right through to final bottle fill. Sometimes customers push for analytical data beyond the standard panel, such as LCMS for trace-level impurities or tests for residual inorganic acids. We keep flexibility in our QC pipeline to address custom requirements, and our open attitude to analytical transparency has helped avoid surprises.

    Scaling up always reveals cracks that small batches hide. Moving from flasks to reactors reshapes impurity profiles, and the water handling needed for a 100-liter run doesn’t mirror that of a 1-liter flask. We designed our manufacturing process for modularity, so it adapts to requirement shifts without forcing a full plant rework. Changes from one customer’s order sometimes produce insights that improve consistency or cut cycle time for everyone.

    Handling Regulatory, Safety, and Logistics Questions Up Close

    Dealing with regulatory demands and logistics flows falls right at the production line. Safety data—fire points, health hazards, reactivities—are documented from hands-on testing and regular literature review. Our technical team clarifies labeling and packaging before any shipment, fielding direct questions about compatibility, transport, and regulatory documentation needed for smooth import and local approvals.

    Some customers require smaller cleavable packs for R&D; others seek bulk drums for pilot or commercial manufacture. Our logistics team learned early that wrong bottle material or leaky closures create problems that ripple all the way to the lab bench. Every bottle leaves with tamper-evidence seals, lot tracking, and certificates right from the source, not duplicated downstream. Direct communication keeps confusion low and trust high.

    Ongoing dialogue with customs brokers and regulatory agencies reduces shipment delays. Where regulatory or hazardous classification raises questions, technical staff provides updated testing and compliance reports to support ports, shippers, and warehouse teams. Chemistry doesn’t move forward if paperwork lags. Keeping both QC and regulatory data under one roof helps resolve issues quickly and keeps our product in motion.

    Responsiveness to Emerging Science and Market Needs

    Half of our process improvements in the last two years have emerged from customer problems or advancing science elsewhere. We stay connected to the literature on CF3-substituted aromatics, new cross-coupling methods, and downstream transformations demanding extra purity or compatibility. Direct input lets us pivot our process or batch characteristics as soon as the market steers a new direction.

    For example, demand for even lower residual halide or higher stability under light and heat prompted a move to in-house recrystallization in some product lines, alongside further improvements in oxidative stability. Whenever a research group publishes a new downstream route with CTBA-99 as a key intermediate, we use internal test runs to check for subtle issues that may emerge at process scale.

    Collaborations with university groups, early-stage pharma, and downstream innovation hubs help us keep the product ahead of new regulatory asks and shift process economics as supply chain costs swing. That hands-on mindset—adapt, test, learn—keeps our 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol performing, whether it’s destined for a gram-scale pilot or multi-tonne production supply.

    Practical Advice and Ongoing Support for End Users

    Reliable intermediates only stay valuable when you have open channels for feedback and troubleshooting. Patterns in incoming questions—a crystallization issue here, a color shift there—drive weekly meetings among our technical, QA, and logistics teams. We find small problems early and push incremental improvements batch by batch rather than waiting for change to come from the outside.

    We advocate a hands-on approach: clear instructions for re-sealing, handling, and analysis; open offers of reference spectra; and on-call support for customers scaling up or adapting to new requirements. Our team appreciates direct feedback, whether it’s as technical as a subtle impurity pattern or as practical as improving bottle design to avoid solvent permeation. That response loop ensures the product’s long-term dependability.

    By working out front as the manufacturer, we witness how every detail—a controlled raw material source, a slightly cleaner solvent, a difference in storage temperature—matters to researchers at every step. Scientists trust 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol when it arrives consistent and with real data in hand, not just promises on a sheet.

    Shaping the Future Together in Chemical Manufacturing

    We see 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol as more than a boxed commodity. Relentless focus on process transparency, regular data sharing, and hands-on troubleshooting elevates the product for all who depend on it. As more science shifts to complex, multi-substituted intermediates and demands for cleaner, more controlled syntheses grow, those of us making the material need to stay agile—responding with transparency, speed, and reliable performance.

    Direct manufacturing experience teaches us that no intermediate sits in isolation. Feedback from every batch, every customer, and every emerging synthetic challenge shapes our evolution. As projects grow in ambition and scope—from small-molecule pharmaceutical campaigns to advanced materials for electronics—customers benefit from a close partnership with the source, not another layer of abstraction in the chain.

    Our ongoing partnership with the scientific community ensures a streamlined flow of knowledge, improvements, and high-quality material for the most demanding tasks. Each bottle of 2-Chloro-3-(Trifluoromethyl)Benzyl Alcohol we send bears the legacy of that approach—one batch at a time, rooted in practical experience, ready for what’s ahead in research and innovation.