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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 | 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. |
Applications of 3-Benzyloxybenzotrifluoride in Industrial ManufacturingOur 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 SynthesisPharmaceutical 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
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2. Agrochemical SynthesisMajor 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
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3. Advanced Material Monomer ModificationProducers 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
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4. Fine Chemical and Flavors IntermediateManufacturers 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
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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.
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.
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:
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.
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.
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.
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.
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.
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.
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.