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2-(Trifluoromethoxy)Benzaldehyde

    • Product Name 2-(Trifluoromethoxy)Benzaldehyde
    • Alias 2-(Trifluoromethoxy)benzenecarbaldehyde
    • Einecs 223-003-2
    • 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

    301193

    Name 2-(Trifluoromethoxy)Benzaldehyde
    Synonyms o-(Trifluoromethoxy)benzaldehyde
    Cas Number 348-33-8
    Molecular Formula C8H5F3O2
    Molecular Weight 190.12
    Appearance colorless to pale yellow liquid
    Boiling Point 82-84°C at 10 mmHg
    Density 1.393 g/cm3 at 25°C
    Refractive Index n20/D 1.526
    Purity Typically ≥98%
    Smiles O=Cc1ccccc1OC(F)(F)F
    Inchi InChI=1S/C8H5F3O2/c9-8(10,11)13-7-4-2-1-3-6(7)5-12/h1-5H
    Storage Conditions Store at 2-8°C, in a tightly closed container
    Solubility Slightly soluble in water, soluble in organic solvents

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

    Packing & Storage
    Packing Amber glass bottle with secure screw cap, labeled with "2-(Trifluoromethoxy)Benzaldehyde, 25g" and hazard symbols, manufacturer details included.
    Shipping 2-(Trifluoromethoxy)Benzaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. Transport complies with relevant regulations (e.g., DOT, IATA). Packaging ensures protection from light, moisture, and physical damage. Adequate labeling and documentation, including hazard warnings and safety data, accompany all shipments to ensure safe handling and delivery.
    Storage 2-(Trifluoromethoxy)Benzaldehyde should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Use only in a chemical fume hood and handle with appropriate personal protective equipment to avoid inhalation, ingestion, or skin contact.
    Application of 2-(Trifluoromethoxy)Benzaldehyde

    Applications of 2-(Trifluoromethoxy)Benzaldehyde in Industrial Manufacturing

    2-(Trifluoromethoxy)Benzaldehyde finds established roles in several precision-driven downstream chemical industries due to its specialized electronic properties and reactivity profile. The following application scenarios outline its authentic integration as a building block in high-value manufacturing environments, grounded in real industrial practices and sector requirements.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    In pharmaceutical manufacturing, this compound acts as a key intermediate for the synthesis of complex heterocycles and fluorinated aromatic APIs, especially within anti-inflammatory and CNS (central nervous system) drug candidates. The material enters multi-step organic syntheses, imparting fluorinated motifs that enhance metabolic stability and bioactivity, with downstream QC requiring strict traceability and impurity management.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF monographs for relevant APIs incorporating trifluoromethoxy analogs
    • 21 CFR Part 210/211 (cGMP for finished pharmaceuticals)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.1–0.5 molar equivalents, as specified per step in API synthetic routes; adjustment depends on target structure and impurity profile management

    Downstream process integration

    • Undergoes condensation or coupling reactions in the context of stepwise API syntheses; charged in controlled reactor vessels following intermediate purification and in-line analytical confirmation

    Final product types

    • Anti-inflammatory drug intermediates
    • Fluorinated CNS therapeutics
    • Pyridine-based pharmaceutical actives

    2. Agrochemical Active Synthesis

    Agrochemical manufacturers incorporate this compound as an aromatic building block in the synthesis of selective herbicide and fungicide actives. Its unique electron-withdrawing trifluoromethoxy group enables downstream producers to create molecules with improved field persistence and target selectivity, conforming to regulated environmental and residue guidelines.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • OECD Test Guidelines for Chemical Substances
    • ISO 9001:2015 in crop protection chemical production
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • Used at 5–15% w/w of target molecule mass in primary active ingredient syntheses; adjustments depend on downstream efficacy ratio and formulation requirements

    Downstream process integration

    • Feeds into aromatic acylation or alkylation steps within dedicated agrochemical synthesis lines, followed by catalytic hydrogenation, workup, and continuous in-process residue testing

    Final product types

    • Selective pyrazole-based herbicides
    • Trifluoromethoxyphenyl-substituted fungicides
    • Intermediate scaffolds for crop protection actives

    3. Advanced Organic Electronic Materials

    Manufacturers within organic electronics leverage this raw material in the synthesis of specialty aryl-based monomers for high-performance liquid crystals and organic light-emitting diode (OLED) materials. Its electron-withdrawing trifluoromethoxy group modulates photophysical properties, enabling the production of materials that meet stringent stability and purity requisites for electronic displays and optoelectronic components.

    Industry compliance standards

    • IEC 61249-2-21 for materials in printed circuit board manufacturing
    • RoHS Directive 2011/65/EU for restricted substances in electronics
    • ISO 14001:2015 for environmental management
    • Industry-specific internal standards for purity (≥99.5%) and residual solvents

    Typical usage ratio

    • 0.2–3.0% by mass in monomer feed for downstream polymerization; fine-tuned based on target viscosity and light emission spectra

    Downstream process integration

    • Charges into controlled monomer synthesis, followed by polymerization and purification steps essential for OLED or display-grade material performance

    Final product types

    • OLED emitter layers
    • High-stability liquid crystal monomers for display panels
    • Charge-transport dopants in organic semiconductors

    4. Fine Fragrance and Flavor Intermediates

    Producers in the flavor and fragrance sector use this benzaldehyde derivative as a non-natural aromatic intermediate to develop new classes of synthetic fragrance ingredients and fine flavoring agents. The fluorinated aromatic character enables creation of notes with persistence and thermal stability, mainly for niche luxury applications rather than mass-market products due to regulatory considerations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for material restrictions
    • EU Regulation (EC) No 1334/2008 on flavorings
    • ISO 9235:2013 (Aromatic raw materials — General definitions)
    • ISO 22716:2007 (Cosmetics — GMP guidelines where used in perfumery)

    Typical usage ratio

    • 0.01–0.2% in concentrate formulations, with lower thresholds in fine fragrance compounds to align with toxicity and olfactory testing

    Downstream process integration

    • Functions as a starting aldehyde in synthetic fragrance routes; enters condensation or etherification steps conducted under low moisture to maintain integrity of fluorinated structures

    Final product types

    • Synthetic musk and specialty fragrance accords
    • Heat-stable aroma molecules for fine flavoring
    • Luxury perfume ingredient intermediates

    5. High-Performance Polymer Modifiers

    Polymer manufacturers use this molecule to introduce trifluoromethyl-ether substituents into custom-engineered high-performance polymers and specialty resins. Such chemical modifications enable downstream manufacturers to enhance polymer resistance to solvents, acids, and bases, which is essential in applications that demand long-term durability and thermal endurance.

    Industry compliance standards

    • ASTM D638 for polymer tensile properties
    • UL 94 for flammability of plastic materials
    • ISO 9001:2015 Quality Management in polymer production
    • REACH SVHC compliance where applicable

    Typical usage ratio

    • 0.5–2.5% by weight within copolymer or resin precursor batch; specific levels set by target specification for heat and chemical resistance

    Downstream process integration

    • Incorporated at monomer charging or post-polymerization functionalization stage, monitored by GC/HPLC to ensure uniform distribution and minimal unreacted monomer

    Final product types

    • Fluorinated engineering resins for electronics
    • Specialty coatings with high solvent resistance
    • Custom copolymers for aerospace and automotive sectors
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    Certification & Compliance
    More Introduction

    2-(Trifluoromethoxy)Benzaldehyde: Practical Insights from Our Production Floor

    On the production line, 2-(Trifluoromethoxy)Benzaldehyde—often found under the label TFBA or OTFMBA—stands out for its unique fluorinated chemical backbone. Our team has been manufacturing this compound for over a decade, and we know firsthand how a small structural tweak like the trifluoromethoxy group at the ortho position influences both its reactivity and its end-use performance. Each batch we prepare represents hundreds of hours fine-tuning both purity and consistency to support modern chemical innovation, especially in the pharmaceutical and agrochemical fields.

    Direct Experience with Synthesis and Handling

    Crafting quality TFBA isn’t a simple job. We’ve steered clear of cut-corner synthesis routes. Instead, we lean into established methods that ensure a reliable product: a clear, nearly colorless liquid with a distinct, sharp aroma typical of high-purity aromatic aldehydes. Our process control operators monitor GC and NMR results after every batch, not just the final product. In our lab, trace inorganic impurities or extra isomers don’t make the cut, because pharmaceutical chemists rely on predictable reactions for every new library screening.

    Specs on our typical TFBA include a purity above 99% with water below 0.3% by Karl Fischer titration. Each liter comes with a guarantee verified in-house. We package under dry nitrogen during cooler morning hours to prevent moisture pick-up, an approach picked up after years studying product stability. From our desks, each step from raw material inspection through reactor charging, phase separations, crude distillation, and final packing happens under one roof. You get the results of this hands-on control—no need to filter out unexpected surprises downstream.

    Observations from Customer Projects

    Feedback loops with research teams have taught us where TFBA brings value and where it stretches its limits. Our compound’s strong electron-withdrawing group pulls reactivity away from the benzaldehyde core, letting chemists direct transformations—selective condensation, reductive amination, or cross-coupling—without as much risk of side reactions typical with plain benzaldehyde. Manufacturers in the crop protection space often report fewer byproducts thanks to the fluorine-rich leaving group. In our experience, those working on bioconjugates or small-molecule probes see sharper signal-to-noise ratios, since the compound’s volatility and low background fluorescence help keep assays clean.

    We’ve watched scientists compare it to the more common 4-trifluoromethoxybenzaldehyde. Position matters: moving the CF3O group from para to ortho boosts certain selectivities but can slow down others. Ortho substitution creates more pronounced steric hindrance, an effect useful for tailoring downstream chemistry in heterocycle synthesis. It’s one of the main reasons our product draws interest from teams developing next-generation kinase inhibitors and antimicrobial agents. We’ve tracked successful use in a series of novel oxazole and imidazole analogues, shared in project updates with our QC chemists, which showed marked improvement in reaction yields compared to less hindered isomers.

    Why the Trifluoromethoxy Group Actually Makes a Difference

    On paper, the trifluoromethoxy (-OCF3) group introduces electron-withdrawing tendencies along with increased lipophilicity. In our plant, we’ve seen firsthand that this encourages greater metabolic stability—a fact proven by the number of pharma clients returning for follow-on orders after initial screens. Med chem teams often highlight how TFBA’s properties help develop drug analogues less easily broken down by liver enzymes, leading to longer half-lives and potential once-daily dosing regimes.

    From our experience, TFBA’s fluorination also helps stand up to oxidative environments typical for pre-formulation studies. Agrochemical customers mention that the ortho-trifluoromethoxy motif gives superior rainfastness and plant adherence compared to plain benzaldehyde derivatives. We’ve sent stability samples through repeated sunlight and humidity testing: TFBA holds up, with color and purity checking out well after a week in simulated tropical conditions.

    Comparing TFBA to Other Aromatic Aldehydes on the Market

    We get a lot of questions about differences between TFBA and classic benzaldehydes like 2-methoxybenzaldehyde or 4-fluorobenzaldehyde. What stands out most during practical use is how TFBA’s trifluoromethoxy group propels certain reactions or blocks others. During some Grignard or Wittig reactions, TFBA resists nucleophilic attack more than plain 2-methoxybenzaldehyde, resulting in fewer unwanted byproducts. For large-scale manufacturing, this translates into easier downstream separation and less solvent use during wash steps—real efficiencies when running 100-liter reactors.

    Chemists often reach for TFBA when they want to maintain aldehydic reactivity but moderate speed to favor selectivity. We’ve supplied batches destined for chiral auxiliary or ligand synthesis, where one misstep with a more reactive benzaldehyde would mean racemization or low yield. In many such projects, the presence of the ortho trifluoromethoxy group offers just the right tempo for complex, multi-step processes like organocatalytic cyclizations or metal-catalyzed arylations. Our technical support team can share real-world setups and process hints because we’ve walked through them ourselves and with so many clients—sometimes even running parallel lab-scale trials for academic chemists testing the boundaries.

    Consistency and Batch Validation

    In the early years, we caught batch-to-batch inconsistencies tied to subtle shifts in solvent grade and moisture control, especially during purification. Rather than chasing numbers, we doubled down on vacuum distillation protocols and switched to custom-blown glassware designed to resist acid leaching from fluorinated intermediates. Every time we dialed in tighter controls, customer complaints dropped and repeat orders went up. Now, our QA reviewers keep each batch’s fingerprint clear: IR, GC-MS, and HPLC signatures tracked against our in-house library dating back years. New lab hires run side-by-side with senior techs so practical lessons—like the smell of improper oxidation on start-up—don’t fall through the cracks.

    We also see real value in transparency with researchers. Each shipment leaves our facility with a full certificate of analysis including spectral overlays. Most working chemists appreciate this; it avoids wasted time double-checking whether minor impurities will affect their next coupling or reduction. For us, these steps aren’t marketing—we find they’ve cut down wasted cycles, shipping returns, and troubleshooting emails by more than half over the years. The sum total? Fewer headaches, fewer surprises, and products matched to real-world use cases.

    Supporting Advanced Research and Formulation

    Today, TFBA migrates into all sorts of research programs. In medicinal chemistry circles, new lead compounds based on TFBA scaffolds are popping up in anti-viral, neuroactive, and metabolic disorder research. We’ve supported academic collaborations using 2-(Trifluoromethoxy)Benzaldehyde as a key step in the synthesis of challenging natural products, particularly for adding heavy fluorine content without destroying sensitive functional groups downstream. This versatility keeps the molecule in steady demand among contract research organizations designing combinatorial libraries.

    Our chemical engineers also work with polymer innovators. For specialty coatings needing robust solvent and weather resistance, TFBA-based monomers fit the bill. Their hydrophobic yet polarizable nature offers new routes for tuning crosslink density—valuable for applications from marine paints to semiconductors. In process scale-up meetings, formulation scientists note that the compound’s low water content and stable handling profile reduce the number of filtration and drying steps. This translates to shorter plant turnaround times and less need for post-reaction tweaking, especially at scales above 50 kg. Our field engineers have stood in tank farms, running pilot batches, making sure that theory holds up under the pressures of valve leaks, unexpected foaming, or heat transfer emergencies.

    Challenges and Continuous Improvement

    Every production facility faces reality: scaling up isn’t like following a textbook. Our process technicians have worked through equipment corrosion caused by hydrogen fluoride—a known risk in trifluoromethoxy chemistry. We rebuilt much of our reactor setup with nickel-lined steel and kept our baseline maintenance schedule aggressive. Through these investments, we learned that minimizing line downtime and material losses brings better cost control, especially as fluorinated reagents drive higher raw material prices worldwide. We don’t cut corners with exhaust scrubbing or waste solvent distillation—if anything, regulations and our own standards have moved us to tighter controls year by year.

    On the logistical front, TFBA’s shipping profile remains straightforward, but we’ve learned the value of temperature tracking for long-haul packaging. Not every distributor upstream treats sensitive compounds with care, and we’ve had to shorten some supply chains to keep product quality high. Realistically, we’ve also had to educate users on proper bench handling, since TFBA can draw moisture from the air, introducing color shifts or trace acid formation in under-ventilated labs. We include these handling notes in every shipment, written in language for working chemists, not just theoretical standards.

    Beyond the Lab: TFBA's Ecological and Regulatory Outlook

    Producing a specialty benzaldehyde brings up environmental stewardship. Older generations of the industry played loose with handling fluorinated solvents; now, our facility captures and reprocesses volatile organics, aiming to keep emissions well under permitted thresholds. Our waste stream analysis—performed quarterly for external audit—shows nearly closed-loop recycling of our process solvents. We've invested in local training to ensure our staff recognizes the impact of both trifluorinated and aldehyde-laden waste, keeping compliance at the forefront. We work with certified hazardous waste reclaimers for anything leaving our site, documenting chain of custody for every kilo.

    We keep up with global regulatory shifts, following changes in REACH guidelines from Europe, import/export restrictions in Asia, and updates to US EPA listings. Many clients ask about residual solvents, origin of raw fluorine feedstock, and possible process-side contamination. To meet their rising expectations, we built in documentation at every stage, ready for cross-border shipments and customs review. More than once, our advance notice of impending regulatory carve-outs has given partners early warning to secure supply before new bans or restrictions took effect.

    Looking Forward: Ensuring a Steady Supply Chain

    The last few years have thrown supply disruptions at many chemical producers. From our plant, we saw the impact up close: raw material bottlenecks, international freight delays, and wild price swings on specialty reagents. Our solution involved longer-term purchasing contracts and more flexible vendor relationships, but also real investment in local capacity for the core steps in the TFBA build. By holding extra stock of hard-to-source intermediates, and keeping at least two alternate suppliers on file for every high-risk material, we avoid scrambling during market swings. This strategy came from hard-won lessons during sudden spot-market shortages.

    Trust between us and our research partners has only grown because of these efforts. When an urgent request comes in from a formulation scientist or scale-up chemist, our team can pull from reserve and ship within days—not weeks—thanks to a pipeline tuned for flexibility. As demand for fluorinated building blocks continues to rise across pharma and advanced materials, this approach keeps everyone ahead of schedule. Our process managers spend as much time on procurement certainty as they do calibrating reactors—because one missed shipment can derail months of development.

    Knowledge Shared Across the Industry

    We’ve been on both sides of the development cycle—supporting early discovery teams working with grams, then helping scale up to the multi-kilo level when a candidate compound moves forward. Openly sharing what we’ve learned about TFBA’s behavior—optimal storage, shelf-life, reaction quirks—helps chemists in the field avoid pitfalls and cut down time troubleshooting. Over the years, we’ve hosted technical webinars and published internal bulletins for customer labs, all based on the lived realities of making and using this compound.

    Our methods evolve with customer feedback and industry advances, but our core philosophy remains—craft a high-quality, consistent TFBA for researchers and manufacturers who need performance, reliability, and practical support. Our customers bring the drive to take molecules from bench to real-world solutions. We provide the foundation, built on years spent overcoming real chemistry and real production challenges. Our door remains open for anyone ready to design, test, and build with us, starting from the molecule up.