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3-(Trifluoromethoxy)Benzyl Alcohol

    • Product Name 3-(Trifluoromethoxy)Benzyl Alcohol
    • Alias 3-(Trifluoromethoxy)phenylmethanol
    • Einecs 629-586-7
    • 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

    574792

    Cas Number 827-94-1
    Molecular Formula C8H7F3O2
    Molecular Weight 192.14 g/mol
    Iupac Name 3-(Trifluoromethoxy)benzyl alcohol
    Appearance Colorless to pale yellow liquid
    Boiling Point 211-213 °C
    Density 1.34 g/cm³
    Refractive Index 1.470
    Flash Point 95 °C
    Purity Typically ≥97%
    Solubility Slightly soluble in water, soluble in organic solvents
    Synonyms m-(Trifluoromethoxy)benzyl alcohol, 1-(Hydroxymethyl)-3-(trifluoromethoxy)benzene
    Smiles C1=CC(=CC(=C1)CO)OC(F)(F)F
    Inchikey XWQAJHRIKAPSFA-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-(Trifluoromethoxy)Benzyl Alcohol, tightly sealed with a screw cap and labeled for laboratory use.
    Shipping **Shipping Description:** 3-(Trifluoromethoxy)benzyl alcohol is shipped in sealed, chemical-resistant containers, protected from moisture and direct sunlight. Packaging complies with hazardous material regulations (if applicable). Containers are clearly labeled with product and hazard information. Shipment is handled by certified carriers, ensuring safe transit, and typically includes safety data documentation. Temperature control may be specified if required.
    Storage Store 3-(Trifluoromethoxy)benzyl alcohol in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat, ignition sources, and incompatible materials like strong oxidizers. Protect from direct sunlight and moisture. Ensure proper labeling and keep out of reach of unauthorized personnel. Follow all relevant safety and regulatory guidelines for organic chemical storage.
    Application of 3-(Trifluoromethoxy)Benzyl Alcohol

    Applications of 3-(Trifluoromethoxy)Benzyl Alcohol in Industrial Manufacturing

    Our 3-(Trifluoromethoxy)Benzyl Alcohol serves as an essential intermediate for downstream industries with stringent requirements for purity, traceability, and process efficiency. Below, we detail key application scenarios where this raw material demonstrates critical functional value, supported by regulatory adherence and precision formulation knowledge from an actual manufacturing perspective.

    1. Pharmaceutical Intermediate in Active Pharmaceutical Ingredient (API) Synthesis

    Global pharmaceutical manufacturers utilize 3-(Trifluoromethoxy)Benzyl Alcohol as a building block in the synthesis of fluorinated APIs, particularly within small-molecule drug development pipelines. The alcohol group provides a reactive handle for selective etherification or esterification steps, introducing the trifluoromethoxy motif to targeted molecular scaffolds. Production batches must conform to strict process controls, and trace levels of starting material are monitored throughout GMP-compliant environments to ensure patient safety in the final drug formulations.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs
    • United States Pharmacopeia (USP) guidelines for process intermediates
    • FDA 21 CFR Part 211 for API manufacturing controls

    Typical usage ratio

    • 0.5–8 wt% of total reactant mass, adjusted according to required yields and scale-dependent step-up protocols in multi-step syntheses

    Downstream process integration

    • Added as a key intermediate during the initial building block assembly or at selective fluorination steps; the material enters closed reactor systems under inert atmosphere, followed by in-line purification and QC monitoring before further conversion or coupling

    Final product types

    • Pharmaceutical APIs incorporating the trifluoromethoxyphenyl group (e.g., antineoplastic agents, CNS active compounds)
    • Advanced pharmaceutical intermediates used for clinical trial material supply

    2. Agrochemical Synthesis for Herbicide and Fungicide Actives

    Producers of advanced agrochemical actives employ 3-(Trifluoromethoxy)Benzyl Alcohol during core scaffold construction and functionalization of phenyl-substituted active ingredients. Its fluorinated group increases metabolic stability and provides enhanced target specificity in field applications. The compound is dosed according to downstream chlorination or nitration sequence requirements, with all steps integrated in environmental management systems for compliance with agricultural chemical regulations.

    Industry compliance standards

    • Food and Agriculture Organization of the United Nations (FAO) pesticide specifications
    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals
    • ISO 9001 quality management system for agrochemical production

    Typical usage ratio

    • 1–10 mol% relative to the phenyl ring precursor, tailored according to the targeted fungicide or herbicide active’s design and reaction scale

    Downstream process integration

    • Fed into high-shear batch reactors during the aromatic substitution step or as an alkylation precursor in the synthesis of target molecules; removed post-reaction by aqueous work-up or solvent extraction for yield maximization

    Final product types

    • Post-emergence herbicide technical concentrate
    • Broad-spectrum fungicide technical grade substances
    • Granular agrochemical formulations ready for field blending

    3. Specialty Polymer Synthesis (Trifluoromethoxy-Modified Resins)

    Specialty polymer manufacturers apply 3-(Trifluoromethoxy)Benzyl Alcohol in the functionalization of aromatic polyesters and polycarbonates, exploiting the trifluoromethoxy group for hydrophobicity and chemical resistance enhancements. It is introduced during the monomer modification stage or as an end-group capping agent, ensuring high uniformity in backbone incorporation. Stringent process validation maintains polymer performance, with each batch documented for traceability according to advanced materials industry standards.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for chemical synthesis)
    • ASTM D256 test methods for plastics
    • REACH compliance for polymer and monomer safety
    • RoHS Directive when polymers target electronics enclosures

    Typical usage ratio

    • 2–5 mol% of total monomer feed for backbone modification, depending on desired polymer end properties and application standard requirements

    Downstream process integration

    • Injected into continuous stirred-tank reactors during polycondensation, often pre-dissolved in compatible organic solvents for homogeneous mixing; in end-capping, introduced in the final reaction step prior to polymer precipitation and pelletization

    Final product types

    • High-performance engineering plastics (insulation covers, microfluidic chips)
    • Fluorinated coating resins for anti-graffiti or anti-corrosion layers
    • Specialty polycarbonate or polyester films for optical and electronic uses

    4. Fluorinated Fragrance and Aroma Intermediate

    Manufacturers in the fine chemicals sector include 3-(Trifluoromethoxy)Benzyl Alcohol as a reactive intermediate for crafting high-value fluorinated aromatic compounds, which add unique olfactory notes or stability to luxury fragrance blends. The regulated manufacturing environment demands detailed process documentation and control over trace flavorant residues, given their potential carryover into end-use consumer goods.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU Cosmetics Regulation (EC) No 1223/2009
    • ISO 22716 (Cosmetics—Good Manufacturing Practices)
    • IFRA/IOFI Labelling Manual for flavoring substances

    Typical usage ratio

    • 0.2–2 wt% in aroma intermediate synthesis, fine-tuned per distinctive scent profile or regulatory allergen requirements

    Downstream process integration

    • Participates in the acylation or methylation stages of aroma chemical production, most frequently handled under cold or controlled temperature regimes to protect reactive functional groups, followed by rigorous distillation and fragrance profile assessment

    Final product types

    • Fluorinated aldehyde or ketone fragrance molecules for use in perfumery bases
    • Specialty aroma compounds for premium household and personal care products
    • Fine flavour intermediates used in compounded scent blends

    5. Advanced Liquid Crystal Material Synthesis

    Liquid crystal display (LCD) manufacturers rely on precise molecular engineering to achieve consistent electro-optical performance. 3-(Trifluoromethoxy)Benzyl Alcohol acts as a precursor for the synthesis of trifluoromethoxyphenyl-based mesogens, where the electron-withdrawing trifluoromethoxy enhances dielectric anisotropy and thermal stability. Entry at early synthetic stages permits optimal control over phase transition behavior, essential for downstream device uniformity and operational longevity.

    Industry compliance standards

    • IEC 61290-1-3 for display screen material assessment
    • RoHS and REACH directives for electronic materials
    • ISO 9001:2015 for specialty chemicals quality management
    • Japanese Industrial Standards (JIS) for display panel components

    Typical usage ratio

    • 1–4 mol% during initial mesogen precursor coupling, modifiable depending on final LC material structural requirements and dielectric performance targets

    Downstream process integration

    • Fed into Grignard or Suzuki coupling steps at the outset of mesogenic molecule synthesis, followed by purification, then integration into LC material compounding and device encapsulation lines

    Final product types

    • Advanced liquid crystal compounds for TFT-LCD and OLED displays
    • Novel LC mixtures for high-frequency opto-electronic devices
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    Certification & Compliance
    More Introduction

    3-(Trifluoromethoxy)Benzyl Alcohol: Confidence Through Careful Chemistry

    Knowing the Product—Inside and Out

    Manufacturing chemicals is not just about mixing raw materials. It means understanding the fine details of every molecule that leaves the reactor. We spend years working with substances like 3-(Trifluoromethoxy)Benzyl Alcohol, learning from each batch, each analysis, and every step that turns a set of feedstocks into a specialty product. This compound, also called 3-(Trifluoromethoxy)phenylmethanol, carries specific traits that make it stand out to chemists looking to build more persistent, highly functional molecules. Our model for this product, defined by consistency and low impurity, reflects our belief that even basic intermediates benefit from sharp attention and real expertise.

    Why Use 3-(Trifluoromethoxy)Benzyl Alcohol in Synthesis?

    Many industries, especially pharmaceuticals and agrochemicals, look to trifluoromethoxy groups for their unique effect on chemical behavior. Fluorinated aromatic compounds tend to increase metabolic stability and improve physicochemical properties. By introducing a trifluoromethoxy substituent on the benzene ring at the meta position and keeping the benzyl alcohol functional group accessible, chemists gain a flexible handle for downstream transformation. The compound’s structure supports the introduction of polar or reactive elements into complex molecules, which is a crucial step in drug discovery projects, as well as in the design of crop protection agents.

    Our team has worked on dozens of fluoroaromatic syntheses. We've seen that 3-(Trifluoromethoxy)Benzyl Alcohol responds reliably during alkylation, oxidation, or condensation. In the laboratory, you don’t want unpredictability to derail a synthetic sequence. In our experience, inferior or mixed-isomer grades often lead to hard-to-separate byproducts, compromising the integrity of subsequent reactions. Reliable single-isomer material, produced with strict attention throughout the process, means less workup and higher yields downstream.

    What Goes Into the Manufacturing Process?

    Every reaction step gets monitored, from the selection of trifluoromethoxybenzene precursors to the controlled reduction that yields the benzyl alcohol. Our chemists look for trace contaminants, often below 0.1%, using both gas and liquid chromatography. Solvent residues or elemental impurities do not belong in the finished product. We invest in frequent instrument calibration, as even the smallest variation in retention time or mass spectral match provides a clue about possible process drift. Customers that order from us can expect a narrow range for every parameter that matters—color, clarity, assay, and water content.

    We rarely see complaints about crystalline quality with this compound, mostly because we manage all the final drying and filtration ourselves. Moving away from third-party finishing gave us direct control over how the product hits the bottle—whether the customer needs a pure solid for weigh-and-add batching or a clear, particulate-free solution.

    The Details That Matter—Specifications

    Our current batches typically show an assay of over 98%. Spectra show no more than trace levels of related benzyl derivatives. Unlike commodity versions from less specialized sources, ours carry a certificate confirming the single isomer status. Moisture content by KF titration stays below 0.2%. Most groups who require this chemical for coupling, reduction, or as an intermediate are focused as much on the elimination of chromatic or proteic impurities as on the actual numerical purity. Our batches regularly outperform industry standards, and customers consistently prefer them in critical contexts where failed reactions mean wasted research hours or costly rework.

    The difference comes from the level of in-house technical attention. Finer solvent controls, better atmospheric handling, and a commitment to keeping every piece of equipment maintained and documented. We believe in batch-to-batch comparability, which matters just as much for the pilot user as it does for those scaling towards registration or even commercial production.

    Not Just Another Benzyl Alcohol—Key Differences

    Chemists sometimes assume all benzyl alcohols behave similarly, but the addition of a trifluoromethoxy group creates meaningful changes. The electron-withdrawing effect of the CF3O- group not only increases resistance to oxidation but also modifies solubility and reactivity in common organic solvents. During side-chain modification or nucleophilic substitution, this positioning limits unwanted side reactions. Unlike simple unsubstituted benzyl alcohol, which tends to over-oxidize or form tars in harsh conditions, our 3-(Trifluoromethoxy)Benzyl Alcohol stays clean and shows excellent recovery.

    We constantly test competitor samples from global markets and regularly find higher levels of cresols, methylbenzenes, or positional isomers. Such impurities undermine SOI (Structure of Interest) formation and undermine the hard work your R&D team invests. A tailored process gives our product the needed edge—an edge verified directly by both in-process and finished product analysis.

    Experience Brings Real-World Solutions

    One can’t gauge product value based solely on a certificate or catalog listing. On more than one occasion, customers have brought us their reaction troubles—sometimes as off-color solutions, sometimes as low isolated yields. They trace the problem to a poorly controlled impurity profile in intermediate chemicals. In nearly all cases, simple substitution with our well-characterized 3-(Trifluoromethoxy)Benzyl Alcohol resolves the bottleneck. The practice of open, responsive technical dialogue with chemists not only improves our product but helps us support those working at the sharp edge of discovery and manufacturing.

    For custom applications, teams often ask about solvent compatibility. Our experience shows the product maintains stability not just in polar aprotics such as DMSO, but also in common alcohols and aliphatic solvents. We have even supported applications where extended storage stability was critical. Here, packaging under inert gas, along with low-moisture containment, maintains long-term integrity—confirmed by real-time and accelerated aging studies run in-house.

    Beyond Chemical Identity—Supporting Innovation

    Every year, new classes of pharmaceuticals reach clinical trials. Each wave brings more complexity, more challenging toxicological endpoints, and tighter quality demands. Aromatic building blocks like this one form the foundation for thousands of research projects worldwide. Many of our partners send feedback after running their first kilo: cleaner mass spectra, simpler purification, more predictable reactivity. In recent agrochemical development, for example, we’ve helped formulators by providing material allowing for selective halogenation downstream—a reaction that failed repeatedly with lower-grade commercial samples.

    Libraries of trifluoromethoxy-substituted molecules keep expanding. Our ongoing role is not just to supply liters or kilograms but to help navigate the real-world constraints of time, cost, and batch reproducibility. Laboratory relationships matter more than anonymous purchasing channels. When chemists can trust their raw materials, they push projects further with fewer setbacks.

    Why Consistency is Non-Negotiable

    There is no shortcut to consistent manufacturing. Traceability—tracking each batch of precursor chemicals, each process parameter log, each QC result—forms the backbone of our daily work. We use validated processes rather than rely on “tuning” at the operator level. No matter if you order a sample or a full drum, you get a product with the same spectral and physical profile every time.

    Working with the same reagent from disparate sources almost always reveals gaps that lead to research setbacks. We’ve stepped in countless times where a high-throughput screening campaign stumbled due to inconsistent reactant lots. By maintaining a stable and transparent supply chain, we minimize the risk of batch-to-batch surprises for our partners.

    Hands-On Technical Support—Not Just a Sales Goal

    We keep a technical team available to consult directly with users. This includes sharing best practices for storage, handling, and even reaction troubleshooting, based on firsthand experience rather than just theoretical data. If a novel application requires alternate packaging or adjusted specification, we are ready to customize—not just in theory, but by quickly reallocating production resources or tweaking the purification protocol. This customer-driven flexibility allows our clients to focus on what they do best, knowing we stand behind each order.

    Returns due to off-spec batches remain vanishingly rare, and when questions arise, it’s our experienced chemists who respond directly. This ongoing feedback loop means a better product, time after time.

    Safe Handling and Realistic Packaging Options

    3-(Trifluoromethoxy)Benzyl Alcohol does not pose the severe reactivity of many functionalized aromatic compounds. Safe handling comes down to standard organic laboratory practice: avoid skin contact, work in a fume hood, and prevent accidental ingestion. Based on user feedback, we now offer both amber glass and fluoropolymer-lined containers, each sealed to limit oxygen ingress and prevent hydrolysis.

    Shipment from our facility follows local and international regulations. Documentation includes full batch traceability and composition data for your records. For larger production plans, our logistics team collaborates closely with on-site staff to design schedules that fit into wider project timelines—less risk of delay, less administrative complexity.

    Feedback Drives Refinement

    Chemistry is a living discipline—it changes as new discoveries emerge and as market needs evolve. We listen closely to the teams using our products on a daily basis. If a reaction stalls, or a formulation needs higher concentration or purer intermediate, we make those needs our challenge. One recent case involved a customer working on a late-stage functionalization of a lead compound. Their standard supplier provided material with trace levels of meta and para isomers, enough to complicate HPLC separation and create new peaks in the mass spectrum. Within days, we adjusted our process, implemented targeted crystallization, and delivered isolate with a single prominent peak on both NMR and HPLC, solving their problem.

    This kind of experience builds real trust. People come back and share their new requirements or challenges, so we integrate these into process updates and regular quality reviews. The feedback loop means improvements don’t get delayed by bureaucracy or lost in channels; they show up in the next batch, or even in-week if urgent needs dictate.

    Why Customers Rely on Us—Day-After-Day

    There is a reason returning partners make up the bulk of our business. Many of them have run the same synthesis for years, but as end-user specifications tighten, they need supply partners who stay one step ahead. We pride ourselves on stable leadership, technical staff who know the difference between theoretical and applied chemistry, and a production culture that never settles for “good enough.” Each batch tells a story of careful attention and lived experience in making sure customers get not only what they need, but what they expect.

    Requests for technical data—ranging from stress testing under elevated humidity to customized impurity profiling—do not get passed off or ignored. The process reflects how we value open, direct communication. We keep learning and adapting, and each customer inquiry gets treated as an opportunity for further improvement.

    Conclusion—The Chemist’s Perspective

    What sets our 3-(Trifluoromethoxy)Benzyl Alcohol apart comes down to practical, daily discipline. Every kilogram that leaves our facility reflects a commitment to both product and customer. From the first sample to long-term contract supply, we stay grounded in the knowledge that chemistry is both an art and a discipline. The lab results, the feedback, and the ongoing collaboration drive us to keep raising the bar each year, supporting teams across research, scale-up, and production.

    We invite feedback, collaboration, and technical consultation. Our production team’s experience grows with each batch, making us not just a supplier but a real manufacturing partner for those who refuse to compromise on material quality in the pursuit of new discoveries.