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3-Benzyloxybenzotrifluoride

    • Product Name 3-Benzyloxybenzotrifluoride
    • Alias 3-(Benzyloxy)trifluoromethylbenzene
    • Einecs 629-663-9
    • 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

    747801

    Name 3-Benzyloxybenzotrifluoride
    Cas Number 60918-61-8
    Molecular Formula C14H11F3O
    Molecular Weight 252.23 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 299-300°C
    Density 1.213 g/cm³
    Refractive Index 1.554
    Solubility In Water Insoluble
    Flash Point 135°C
    Smiles FC(F)(F)c1cccc(OCC2=CC=CC=C2)c1
    Pubchem Cid 44145422

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

    Packing & Storage
    Packing Amber glass bottle, 100 mL, with screw cap. White label displays chemical name, hazard symbols, manufacturer, batch number, and handling instructions.
    Shipping 3-Benzyloxybenzotrifluoride is typically shipped in tightly sealed containers to prevent leakage and contamination. It should be stored and transported in a cool, dry, well-ventilated area, away from heat, sparks, and incompatible substances. All shipments must comply with national and international chemical transport regulations. Proper labeling and documentation are required.
    Storage **3-Benzyloxybenzotrifluoride** should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling and store at room temperature, away from acids and bases, to maintain chemical stability and prevent degradation.
    Application of 3-Benzyloxybenzotrifluoride

    Applications of 3-Benzyloxybenzotrifluoride in Industrial Manufacturing

    Our facility produces 3-Benzyloxybenzotrifluoride for diverse chemical industries seeking consistent quality, traceability, and compliance assurance across high-value applications. Below, we detail where customers integrate this specialty intermediate in their manufacturing streams, with precise regulatory, operational, dose, and output guidance relevant to each sector.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers source this compound for use as a protected benzyl ether intermediate in multi-step synthetic routes, especially when building complex aromatic active pharmaceutical ingredients (APIs). The trifluoromethyl group improves metabolic stability in API scaffolds. During GMP-controlled operations, customers introduce it in key stages requiring strict purification and reaction monitoring. Hydrolysis and deprotection steps follow, releasing key final structures for advanced pharmaceutical use.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EMA Guideline on the Specification Limits for Residues of Starting Materials and Intermediates
    • US FDA 21 CFR Parts 210/211 (cGMPs for pharmaceutical manufacturing)
    • Relevant European Pharmacopoeia monographs for API synthesis quality

    Typical usage ratio

    • 10–25% molar equivalent relative to target API backbone in protected intermediate steps; varies depending on downstream multi-step synthesis scheme and target API structure

    Downstream process integration

    • Charged during protected etherification stages in the main reactor vessel, followed by stepwise functional group manipulation and eventual benzyl deprotection via catalytic hydrogenolysis or acidic cleavage prior to API salt formation

    Final product types

    • Small molecule APIs with enhanced metabolic stability
    • Specialty pharmaceutical building blocks containing trifluoromethyl aromatic systems
    • Intermediates for patented drug substances
    • Benzyl-protected pharmaceutical intermediates for custom synthesis projects

    2. Agrochemical Synthesis

    Major agrochemical producers employ this aromatic ether as a key step intermediate in complex herbicide and fungicide syntheses. Its trifluoromethyl group aids in imparting environmental persistence and bioactivity in final formulations. The compound enters amidation or coupling reactions, supporting high-purity technical material output ready for formulation into crop protection agents. All steps operate under strict process control to manage trace residue limits in compliance with agricultural chemical safety standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU REACH Registration (EC) No 1907/2006 for synthesized intermediates
    • OECD guidelines for testing of chemicals in agricultural applications
    • China GB 2763: Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • 5–18% by weight relative to the main active ingredient core; ratio adjusted per process scale and desired bioactivity profile for pre-technical and technical grade agrochemicals

    Downstream process integration

    • Added as an electrophilic coupling partner mid-stream during heterocyclic or carbamate ring closure steps, followed by aqueous work-up, extraction, and crystallization for technical grade suitability testing

    Final product types

    • Trifluoromethyl-substituted fungicides
    • Select herbicide active ingredients
    • Plant growth regulator intermediates
    • Bench reagents for registration batch production of new agrochemicals

    3. Advanced Material Monomer Modification

    Producers of specialty polymers and performance coatings incorporate this material as a functionalized monomer or co-monomer precursor, utilizing its aromatic structure for enhanced chemical resistance, surface properties, and durability. Introduction typically occurs at the monomer blend or oligomer extension stage prior to polymerization, with a tight focus on achieving precise performance specifications for electronics, automotive, or industrial coating end uses. Detailed QC ensures target incorporation rates and minimal by-products.

    Industry compliance standards

    • ISO 9001 Quality Management Systems for specialty chemical production
    • RoHS Directive 2011/65/EU for electronics sectors
    • Registration under EU REACH as an intermediate/reactant
    • Industrial coatings: OEM-specific requirements for migration and extractables

    Typical usage ratio

    • 0.5–7% by weight in final polymer resin; adjusted to achieve specific glass transition temperature, surface energy, or solvent resistance requirements

    Downstream process integration

    • Fed to reactor with solvent and catalyst during co-polymerization or as a chain extender in pre-polymer formation, prior to main polymer cure or crosslinking

    Final product types

    • Fluorinated engineering plastics
    • High-durability clear and colored industrial coatings
    • Adhesives for electronics assembly
    • Polymer modifiers for specialty films and fibers

    4. Fine Chemical and Flavors Intermediate

    Manufacturers of aroma chemicals and fine organics use this ether for synthesis of high-purity intermediates required in flavor and fragrance compounds. Its stability and aromatic structure support Friedel-Crafts alkylation and ether cleavage chemistry typical of custom fine chemicals production. Integration occurs at controlled batch stages, followed by fractionation and chromatography, ensuring product compliance with food additive quality limits or high-purity requirements for downstream flavor formulators.

    Industry compliance standards

    • FEMA GRAS (Generally Recognized as Safe) program for flavor ingredients
    • IFRA Global Fragrance Standards for fragrance compound safety
    • ISO 22000 Food Safety Management for additive ingredient production
    • High-purity criteria per customer specification for aroma intermediates

    Typical usage ratio

    • 0.2–6% by molar percent in multi-step synthesis; optimized to balance product aroma and stability while avoiding process overuse

    Downstream process integration

    • Charged as a protected aromatic substrate at the initial alkylation or acylation step, followed by downstream cleavage, purification, and fractional distillation as required

    Final product types

    • High-purity fragrance intermediates containing trifluoromethyl groups
    • Aromatic flavor prep bases for the food industry
    • Synthesized blends for encapsulated flavor release systems
    • Flavor and fragrance building blocks for further esterification or reduction
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    Certification & Compliance
    More Introduction

    Introducing 3-Benzyloxybenzotrifluoride: A Reliable Choice for Modern Synthesis

    From the first small-scale pilot lots to full manufacturing, producing intermediates for the fine chemical and pharmaceutical industries means looking beyond just quality control. Among the many aromatic intermediates we handle daily, 3-Benzyloxybenzotrifluoride stands out for its versatility and consistent performance in downstream reactions. Our team has watched customer preferences shift toward more demanding safety and environmental expectations, and this product evolved in response to those needs as much as to economic drivers.

    Understanding What Sets 3-Benzyloxybenzotrifluoride Apart

    3-Benzyloxybenzotrifluoride features a trifluoromethyl group combined with the benzyloxy functional group, fitted onto a benzene ring. The model we prepare, most commonly referenced as CAS# 455-85-6, has been produced here with tight chloride and moisture specifications, not out of habit but because downstream products—especially in pharmaceutical active intermediates—showed a marked reduction in side reactions when those impurities stay low. Technical staff who manage purification express real appreciation for a starting material that doesn’t force costly extra polishing.

    Our internal feedback loops—involving operators, synthesis chemists, and application specialists—shed light on why this compound sees increasing demand. That trifluoromethyl group doesn’t just shift electron density; its stability in hostile reaction conditions lets chemists reach for higher yields and improved selectivity in arylation, coupling, and alkylation reactions. We often hear from process engineers working in sunscreen additive production and fluorine-based agrochemical synthesis: standard benzyloxybenzenes lack the chemical resistance or volatility profile that 3-Benzyloxybenzotrifluoride delivers.

    Key Features a Chemist Actually Notices

    Many manufacturers offer aromatic ethers and trifluoromethyl compounds. Over nearly nine years in the sector, we learned that chemists care about more than purity percentages on a specification sheet. Three workhorse advantages have come up time and again for our customers:

    Real-World Applications that Benefit

    End-use companies—especially those developing new actives or specialty coatings—choose 3-Benzyloxybenzotrifluoride for reasons often overlooked in reference catalogs. It’s not just the presence of the trifluoromethyl group, but its meta placement relative to the benzyloxy group that drives unique downstream transformations. One client uses it as a scaffold for developing advanced anti-fouling coatings in marine environments; it resists harsh saline and UV conditions that would degrade less fluorinated compounds.

    In pharmaceutical process R&D, teams searching for new CNS drug candidates comment on its tractability in late-stage functionalization. Instead of switching to different intermediates for every modification, they leverage the dual reactivity of the benzyloxy and trifluoromethyl features, sidestepping lengthier multi-step syntheses. Average overall yields climb, and waste generation falls. Process validation teams emphasize that lot-to-lot consistency lowers the number of qualification runs and slashes timelines for scale-up campaigns.

    Fluorinated aromatics used to get flagged as handling risks, but a controlled boiling range and predictable stability have convinced health and safety officers otherwise. We invested in closed-loop solvent recovery and abatement specifically to address earlier concerns about fluorinated organic waste. Environmental regulators appreciate those upgrades. End-users get a material ready for today’s push for greener, cleaner processing with reduced worker exposure.

    Comparing to Other Trifluoromethylated Benzyloxybenzenes

    Not all trifluoromethylated benzyloxybenzenes offer the same reactivity or compatibility with common reaction schemes. To chemists used to working with 2- or 4-substituted analogs, switching to our 3-substituted version unlocks pathways that increase meta-selectivity in coupling and condensation chemistry. Benchmarking in our own pilot labs revealed that the 3-substituted product tends to provide better yields in amination, etherification, and cross-coupling applications when compared to the 2-position isomer. Colleagues in pigment development noted distinctly different photostability between the isomers, which translates directly to longer-lasting materials in coatings.

    Competing compounds, such as 4-Benzyloxybenzotrifluoride, bring their own specialist roles, but repeated reports from customer runs showed that they lack the same degree of stability under basic reaction conditions or in highly oxidizing environments. Our field support staff watched several customers switch their processes after side-by-side evaluation, citing fewer issues with emulsification and less fouling of reactor internals using our product. Fewer shutdowns and more uptime flow directly from these differences—less unplanned maintenance and more predictable production schedules.

    Manufacturing Know-How Matters

    With decades of hands-on experience running aromatic substitution and etherification chemistry, our production teams learned that controlling minor variables—like agitation rate, addition order, or solvent residue—makes or breaks final batch quality. Operators track everything from agitator rpm to trace acid content. These aren’t just data points for reports; they guide real-world process tweaks. The original process design for 3-Benzyloxybenzotrifluoride had to be re-tuned after pilot work exposed small, frequent chlorination byproducts from one solvent. Investment in continuous mode washing dramatically reduced impurity carryover. Documentation alone doesn’t drive improvement; team feedback and openness to field-test scale trials move products forward.

    We don’t see ourselves as just another commodity chemical supplier. Supporting real-time process consultations with end-users led us to adjust purification cut points and invest in more rigorous final product analytics. Staff share observations about batch trends, and recurring pattern analysis led directly to installing additional vapor phase fluorine abatement. Customers now see tighter consistency in physical appearance and performance metrics. That responsiveness established trust—engineers know that reporting an issue or requesting a tighter spec won't get lost in a bureaucratic black hole.

    Practical Safety and Handling Insights

    Teams managing chemical raw material warehouses think about practical handling. Our packaging choices follow edge case scenarios from years of customer audits and site visits—never a one-size-fits-all approach. Drums and containers use fluorinated liners, not to brag about investment but because deep cleaning and sample testing showed they slash contamination risks. Distribution is coordinated from a single, climate-managed warehouse, sharply cutting down on batch mixing errors or longterm storage instability.

    End-users in the pharma and agrochemical sectors expect transparent information on material origins, processing steps, and change control. We post route change notifications and offer open documentation, reducing the guesswork for customer regulatory and QA teams. Few things derail a scale-up campaign faster than a supplier introducing a new base raw material or solvent without warning.

    Feedback from manufacturing partners pushed us to create a more direct chain of custody. Each drum is barcoded at the point of filling and tracked through shipment, providing a transparent record. This process sharply reduces mix-ups during multi-vendor blending jobs and supports quick resolution in the rare event of a recall or quality investigation.

    Reliability from End-to-End

    Our history with 3-Benzyloxybenzotrifluoride dates back to its use in dye manufacture. That legacy evolved as its profile in pharmaceuticals, specialty monomers, and coatings grew. Today, its strong performance in electron-rich environments, paired with resistance to hydrolysis and oxidation, make it an easy choice for teams tired of unpredictable feedstock.

    On-the-floor chemists report fewer headaches with protocol changes because batches behave predictably. Analytical teams note quicker clearance on QC, as chromatography profiles remain stable lot-to-lot. That reliability didn’t arrive by accident; it resulted from in-process controls, proactive operator interventions, and a continuous push for smaller, but meaningful, batch improvements. The old model—shipping on spec and letting customers sort out variances—gave way to joint process development and shared goals.

    Beyond production chemistry, our team monitors emerging literature and regulatory trends. PFAS management is top-of-mind, and while 3-Benzyloxybenzotrifluoride doesn’t fall under current hot-button restrictions, the drive toward lower environmental impacts influences every production review. We’re developing new recovery and distillation methods to harvest more recyclables from spent streams, and replacing non-essential solvents with greener alternatives. Chemists appreciate transparency: providing detailed certificates of analysis and process change documentation is standard, not just a request.

    Supporting Innovation Across Sectors

    One of the more rewarding aspects of supplying 3-Benzyloxybenzotrifluoride is seeing the variety of uses developed by our customers. In electronic materials, it serves as a building block for OLEDs and specialty films, chosen for both electrical insulation and chemical durability. Agrochemical process engineers use it to build backbones for new actives that meet increasingly tough regulatory guidelines. Small differences in reactivity, made possible by the unique substitution pattern, enable creative solutions that weren’t available with other benzyloxybenzenes.

    Pharmaceutical teams experiment with site-selective halogenation and advanced protecting group strategies. They share their results with us, closing the loop that leads to feedback-driven process improvements. This open exchange sped up reaction troubleshooting and saved both our customers and us from wasted time on unsuccessful routes or undesired side products. Even in niche areas, like developing probes for chemical biology and analytical standards, the compound’s predictable reactivity and minimal batch variability justify its use.

    What the Future Holds

    Global supply chains have seen enough turmoil in the past few years to remind all of us that reliable, responsive raw material support isn’t a luxury—it’s a requirement. Our hands-on approach to producing 3-Benzyloxybenzotrifluoride—transparent batch records, deep process tracking, and continuous skill investment—keeps us ready to meet both long-term contracts and short-notice emergency needs. We’re not only shipping a molecule; we’re delivering trust built on real experience with unique chemical challenges.

    From a manufacturing perspective, progress means staying close to the needs and priorities of customers, not just today, but as regulatory and market pressures evolve. Strong materials like 3-Benzyloxybenzotrifluoride will keep earning their place on chemists’ benches and in large-scale reactors as long as suppliers invest in quality, flexibility, and honest, two-way communication. In a sector as demanding as specialty chemicals and pharmaceuticals, that’s how new breakthroughs happen—and why reliability and hands-on experience matter more than ever.