|
HS Code |
402550 |
| Product Name | 2-(Trifluoromethoxy)Benzyl Bromide |
| Cas Number | 42838-07-1 |
| Molecular Formula | C8H6BrF3O |
| Molecular Weight | 255.03 |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | 74-77°C at 10 mmHg |
| Density | 1.597 g/mL at 25°C |
| Refractive Index | 1.528 |
| Purity | Typically ≥98% |
| Smiles | C1=CC=CC=C1OC(F)(F)FCCBr |
As an accredited 2-(Trifluoromethoxy)Benzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, sealed with PTFE-lined cap, labeled with hazard warnings. Contains 25 grams of 2-(Trifluoromethoxy)Benzyl Bromide. |
| Shipping | 2-(Trifluoromethoxy)Benzyl Bromide should be shipped in secure, airtight containers, clearly labeled and compliant with hazardous material regulations. It must be protected from moisture and light, and handled by trained personnel. Transport is typically via ground or air with appropriate documentation, in accordance with national and international chemical shipping guidelines. |
| Storage | Store 2-(Trifluoromethoxy)benzyl bromide in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, in a cool, dry, and well-ventilated area away from light and incompatible substances (especially strong bases, acids, and oxidizers). Keep refrigerated if recommended, and handle with appropriate personal protective equipment due to its lachrymatory and reactive properties. |
Applications of 2-(Trifluoromethoxy)Benzyl Bromide in Industrial ManufacturingAs the original manufacturer of 2-(Trifluoromethoxy)Benzyl Bromide, we supply this highly specialized intermediate to industrial clients worldwide. The following sectors represent the primary downstream applications, with each process focused on the unique requirements of the respective industries. Each scenario explains compliance standards, addition ratios, integration into existing chemistries, and the finished products derived from this critical building block. 1. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisMajor pharmaceutical companies rely on our compound as a key intermediate for synthesizing various fluorinated APIs, especially in central nervous system and oncology research. Its trifluoromethoxy substituent introduces metabolic stability and unique binding profiles in novel drug candidates developed under stringent regulatory frameworks. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Ingredient ManufacturingLeading crop protection manufacturers incorporate our material as a reactive benzylating agent to construct trifluoromethoxyphenyl moieties in selective herbicides and fungicides. The electron-withdrawing characteristics impart long-lasting field efficacy and improved environmental degradation profiles after application. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Polymer Additive SynthesisSpecialty chemical manufacturers utilize this compound as an intermediate for fluoroaromatic moieties in polymer modifiers, enhancing polymer thermal stability and hydrophobicity for electronics and automotive resins. The unique trifluoromethoxy group enables targeted surface and bulk property improvements during advanced polymer development meeting modern industry protocols. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Custom Synthesis for Fine Chemical Building BlocksContract research organizations (CROs) and specialty chemical companies use this raw material to deliver advanced aromatic intermediates for proprietary synthesis projects, where the trifluoromethoxybenzyl group enables rapid molecular diversification. These projects require tight process traceability and analytical verification for downstream fine chemical portfolios. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Development of Diagnostic and Imaging ProbesManufacturers in the life sciences sector incorporate this compound into the synthesis of molecular probes, particularly for PET (positron emission tomography) and fluorescent tagging systems. The trifluoromethoxy group enhances in vivo stability and allows selective modification at the benzyl position, which is essential for probe specificity and pharmacokinetics in advanced diagnostic applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2-(Trifluoromethoxy)Benzyl Bromide prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
This year marks our eighteenth cycle producing 2-(Trifluoromethoxy)Benzyl Bromide at commercial scale. On the production floor, many chemicals run through reactors, but this compound offers something different: it delivers a combination of reactivity and functional versatility that opens doors in complex synthesis work. Each batch, engineered to the same demanding consistency, plays a role supporting research breakthroughs and industrial processing. The knowledge we’ve built up—practical lessons, successful troubleshooting, even equipment wear patterns—shapes our processes and informs every kilogram that leaves the gate.
There’s no shortage of benzyl bromides out there, but introducing a trifluoromethoxy group changes not just the chemistry, but also how the compound behaves under actual process conditions. For our model, we focus on high-purity (over 98%) 2-(Trifluoromethoxy)Benzyl Bromide, with minimal color and carefully monitored water content. Our teams draw from lessons learned scaling up bench chemistry into safe, manageable production runs. The trifluoromethoxy addition increases the electron-withdrawing power, alters lipophilicity, and allows downstream molecules to take on properties simply not possible with unsubstituted benzyl bromides. Chemists working on fluorinated pharmaceuticals or specialty agrochemicals recognize this difference immediately.
On a factory schedule, the structure of a product decides more than theoretical yield— it controls which safety systems we activate, which reactor linings hold up to repeated use, where quenching and washing steps fit. We’ve found that 2-(Trifluoromethoxy)Benzyl Bromide’s reactivity toward nucleophilic substitution demands heightened monitoring, especially when moisture levels drift or equipment cycles are off-spec. This isn’t theory; we’ve watched small process variances create measurable differences in color, purity, or downstream compatibility. That’s why strict batch logging, in-line monitoring, and a robust operator training program drive repeatable results in the hands of our crew.
Many research users look at a spec sheet and think purity is a checkbox. Nobody notices it in spot runs. But at the scale where we work, low-level impurities and moisture content alter not just reactions, but catalyst compatibility, shelf life, and waste stream management. Every percent of extra water means more hydrolysis. Side reactions multiply with only trace oxidative breakdown. To keep barrels meeting target specs, we run regular Karl Fischer titrations and tight chromatography checks, sampled directly from filling lines. It’s not just compliance: it keeps development chemists from losing hours to redissolution or downstream purification steps.
We started producing 2-(Trifluoromethoxy)Benzyl Bromide because there was a clear need for functional building blocks that deliver both reactivity and resistance to simple metabolic degradation. The trifluoromethoxy moiety increases electron deficiency on the aromatic ring, and in practice, our customers use this compound in syntheses where classic benzyl bromide would get stuck—such as blocking, protecting, or activating steps leading up to fluorinated pharmaceutical intermediates and fine chemical targets. Our longer-term partners have pointed out that this product allows them to design more stable molecules, especially in agrochemical development. Many newer synthetic plans call for fluorine-bearing groups not only for activity but also for tuning pharmacokinetics and persistence: this is a demand other benzyl bromides can’t answer.
Specifications for 2-(Trifluoromethoxy)Benzyl Bromide haven’t been lifted from generic data books. We’ve worked with process engineers in Europe, Asia, and North America troubleshooting stubborn solvation issues, emulsion separation, and thermal stability under various reaction conditions. These experiences have shaped our regular quality controls: limiting phenolic contaminants, stabilizing the product for light and air sensitivity, and facilitating storage even in seasonal temperature swings. Real-world usage tests revealed over time that a clean cut between main and trace impurities makes downstream work-up much less burdensome. We don’t just chase narrowest specs: we optimize what delivers most reliable results for process and research chemists.
In our trade, feedback doesn’t come from surveys. It comes through field reports, photos of unexpected color changes, and—occasionally—barrels returned as nonconforming. Working directly with users over the years, we’ve learned where 2-(Trifluoromethoxy)Benzyl Bromide provides extra value. One generic API manufacturer improved overall yield by over 10% after switching from a standard benzyl bromide, skipping extra purification steps for a fluorinated intermediate. Another client in agrochemical R&D highlighted trace halide content as a major stumbling block. We needed a new purification pass and in-line gas analysis, but that customer ramped up to tonnage-scale volumes. These practical experiences led us to tighten controls not because it reads well on a data sheet, but because it avoids costly shutdowns and wasted batches.
Handling 2-(Trifluoromethoxy)Benzyl Bromide has taught us plenty about simple mistakes that snowball into expensive headaches. Early on, a handful of incidents taught us the consequences of improper drum capping or exposure to atmospheric moisture. Product that cures on the drum rim or reacts slowly with humidity doesn’t just break specifications; it risks contamination in entire batches. In response, we updated packaging lines, tested alternative inert atmospheres for nitrogen blanketing, and retooled storage spaces for lower dew points. What we follow now is not only about regulations— it’s based on hard-won stories where small lapses led to downstream trouble.
In daily production, differentiating 2-(Trifluoromethoxy)Benzyl Bromide from regular benzyl bromide or p-substituted variants isn’t about trivial paperwork. The reactivity changes first hit you during small-scale syntheses. We see altered rates in SN2 reactions, compared to ortho or para-substituted analogues, and the trifluoromethoxy group’s electron pull changes selectivity in cross-couplings. In pilot runs, this means chemists working to introduce complex fluorinated blocks have more freedom to tune outcomes. The product’s unique solubility profile in polar and nonpolar solvents comes straight from its asymmetric structure; simply put, it behaves when others don’t. These distinctions matter especially in medicinal chemistry, where the difference between product profiles translates directly to patentable molecules and faster project timelines.
With this compound the utility extends across several industries. In pharma labs, 2-(Trifluoromethoxy)Benzyl Bromide serves as a key intermediate for synthesizing molecules where fluorine content improves biological activity or metabolic stability. Agrochemical developers turn to it when designing active ingredients with slow-release profiles or greater field persistence. Custom synthesis teams rely on its reactivity for installing benzyl moieties selectively in large combinatorial libraries. Each use case brings its own reaction quirks, but consistent high-quality supply keeps synthetic planning on track.
Like many specialty halides, early production ran into repeated bottlenecks. Trifluoromethoxy-based reagents sometimes cause unexpected byproducts, especially if process water control isn’t up to par. We invest in multi-stage drying and carefully guarded transfer lines, and each package batch gets in-house titration. For multi-ton runs, real troubleshooting meant hands-on meetings with reactor operators and repeated trial runs. We tracked down sources of trace contamination—sometimes as simple as residue in feed lines or less-than-ideal solvent recovery cycles—and built error-proofing into our workflow. This cycle of observation, root-cause analysis, and incremental improvement keeps the material robust enough for everything from R&D labs to multi-step plant processes.
Producing 2-(Trifluoromethoxy)Benzyl Bromide doesn’t escape the responsibilities surrounding fluorinated chemicals. Early runs produced greater waste than we found acceptable. Today’s process improvements let us capture and recycle spent halide streams, cut solvent waste, and filter off residual traces for incineration at controlled plants. We maintain careful emissions logs, including routine stack testing. Practical sustainability doesn’t come from checklists but from decisions made every production cycle—waste segregation, recovery routes, and offsite treatment each contribute. These aren’t PR initiatives. Less waste and safer handling deliver cost benefits and protect our crew and neighbors. Our commitment to responsible production reflects years spent responding directly to regulatory changes, not just ticking compliance boxes.
More products launch every year that depend on reliable fluorinated intermediates. Process chemists have used our 2-(Trifluoromethoxy)Benzyl Bromide in the creation of next-generation antifungals, cardiovascular drugs, and persistent agricultural agents. In every case, application chemists benefit from the altered electronic character. This detail—often invisible to those outside research—allows more efficient coupling reactions and selective functionalization, giving rise to levels of product purity otherwise hard to reach. Our close cooperation with users leads to process tweaks, sometimes as precise as modifying addition rates or changing base equivalents, meaning the compound adapts to ever-shifting chemistries and application demands. The result is fewer surprises in scale-up and more robust projections for time-to-market.
Our team keeps its focus on results that matter inside flasks, reactors, and pilot plants. On multiple occasions, labs comparing our material to alternatives flagged issues ranging from inconsistent melting points to residual halides that disrupt catalyst cycles. Each problem comes with a lesson. Two years ago, we incorporated automated water removal and tighter control over raw material sourcing. The direct effect: fewer rejections, higher acceptance rates, and smoother regulatory audits for the teams using our product in their filings. We avoid shortcuts—skipping stabilizer additives, taking extra time in distillation—because real performance gets measured in the downstream facility, not just in third-party files.
Navigating global regulatory frameworks requires more than a certified tick box. Recent audits by non-domestic pharmaceutical clients reminded us that quality control means direct access to analytical results and transparency when documentation trails need clarification. Our standard operation delivers complete traceability, from raw material supplier through final fill. That kind of supply chain certainty matters for customers pursuing filings with health authorities, who know their registration depends on trace impurity documentation and established process stability. We treat these requirements as integral, rather than burdensome—after years of practical work, short-term expedients hurt more than they help. Every regulatory cycle builds practical skills, as teams handle queries not with off-the-shelf responses, but with direct process data.
Many platform molecules get produced with little dialog between maker and user. We take a different approach. Over the years, we’ve developed dozens of methods side by side with synthetic chemists, iterating over solubility issues, exothermic reaction runs, and product stability tweaks. This has led, for example, to improved logistics for temperature-controlled shipping, and more tailored drum linings for longer shelf life, based on real-world shipping experiments in varying climates. Recently, a customer scaling a specialty intermediate faced repeated clogging in their transfer lines. After several video conferences and process reviews, the solution emerged through a better stabilizer protocol, not a new batch per se. We count these types of partnerships as central to advancing the value of 2-(Trifluoromethoxy)Benzyl Bromide beyond its basic chemical properties.
Like every manufacturing sector, our field participates in a dynamic global market. In the past decade, supply interruptions for key fluorinated reagents created downstream headaches, especially for groups running on just-in-time logistics. By focusing production in-house, we reduce reliance on outside suppliers for critical raw materials. This direct control shields customer projects from global transportation hiccups or sudden price spikes tied to third-party shortages. By maintaining buffer stocks and routinely requalifying equipment, we support even large, unexpected orders with minimal delay. During pandemic-related disruptions, customers with advance demand forecasts still received steady shipments, helping them maintain uninterrupted R&D and plant operations. Buying from the source, in this case, guarantees outcomes trading firms can’t match.
The research frontier advances quickly, and those on the chemical manufacturing side must keep pace. 2-(Trifluoromethoxy)Benzyl Bromide remains integral to a host of expanding fields: new diagnostics, slow-release agricultural agents, and advanced polymers with tailored performance. With each advancement, we anticipate new demands for purity, consistency, or altered physical properties. Our continuous process review and readiness to adapt keeps our offering at the industry’s front. As new application requirements emerge—think greener procedures or tighter impurity controls—we revisit both upstream and downstream process components, investing both in analytic capability and practical knowledge transfer to application teams.
Selling chemicals isn’t just about shifting stock. Our reputation stands, batch by batch, on the reliability of our production processes and the value users can extract from every shipment. With 2-(Trifluoromethoxy)Benzyl Bromide, our experience, hands-on quality control, and longtime user relationships drive an offering that goes well beyond a standard chemical listing. The demands of specialty fluorinated compounds require commitment to ongoing learning, process resilience, and fast response to end-user experience. This ongoing cycle of improvement, informed by practical results as much as by data, ensures every kilogram shipped helps chemists address the next round of complex synthesis challenges—and keeps the supply chain running with confidence, backed up by real manufacturing knowledge.