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4-Methoxy-2-(Trifluoromethyl)Benzaldehyde

    • Product Name 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde
    • Alias 4-Methoxy-2-(trifluoromethyl)benzenecarbaldehyde
    • Einecs 629-281-3
    • 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

    824047

    Chemical Name 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde
    Chemical Formula C9H7F3O2
    Molecular Weight 204.15 g/mol
    Cas Number 867-37-2
    Appearance White to pale yellow crystalline solid
    Melting Point 46-49°C
    Density 1.332 g/cm3 (approximate)
    Solubility In Water Slightly soluble
    Smiles COC1=CC=C(C=C1C=O)C(F)(F)F
    Inchi InChI=1S/C9H7F3O2/c1-14-7-3-2-6(5-13)8(4-7)9(10,11)12/h2-5H,1H3
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C in a tightly sealed container
    Synonyms 4-Methoxy-2-(trifluoromethyl)benzaldehyde; 2-(Trifluoromethyl)-4-methoxybenzaldehyde

    As an accredited 4-Methoxy-2-(Trifluoromethyl)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 "4-Methoxy-2-(Trifluoromethyl)Benzaldehyde, 25g" with hazard and handling information.
    Shipping 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is handled as a laboratory chemical, typically transported via ground or air, following all relevant chemical safety regulations and labeling requirements. Ensure compliant documentation and avoid extreme temperatures during transit to maintain product integrity.
    Storage 4-Methoxy-2-(Trifluoromethyl)benzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Protect from moisture and incompatible substances such as strong oxidizers and acids. Store at room temperature and clearly label the container to prevent accidental misuse. Use appropriate chemical safety practices at all times.
    Application of 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde

    Applications of 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde in Industrial Manufacturing

    As an advanced aromatic intermediate, 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde plays a key functional role in multiple downstream sectors where selective reactivity and stability under stringent process conditions are essential. Its chemical properties underpin various high-value transformations that result in differentiated materials and compounds across fine chemicals, pharmaceutical intermediates, agrochemical synthesis, and specialty material production.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    Downstream API manufacturers utilize this aldehyde as an essential building block in the synthesis of complex heterocyclic compounds for innovative CNS and cardiovascular drug candidates. Its electron-withdrawing trifluoromethyl group and methoxy group facilitate selective condensation and functional group installation steps. Addition occurs most often at the targeted imine or aza-heterocycle formation stage, providing a reliable point for introducing fluorinated motifs while maintaining process validation and batch-to-batch quality consistency demanded by regulated pharmaceutical environments.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF and EP monograph requirements (for intermediates)
    • FDA 21 CFR Part 211 (where applicable to CMOs)
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 0.8–1.3 molar equivalent relative to nucleophile in main condensation step; exact ratio depends on target API structure and impurity profile optimization

    Downstream process integration

    • Charged to reaction vessel during imine, amide, or oxime formation, often following azeotropic drying and controlled nucleophile addition; followed by purification via chromatography or crystallization

    Final product types

    • Intermediates for CNS-active agents (e.g., selective serotonin modulators)
    • Key intermediates for cardiovascular or diabetes drug research
    • Fluorinated synthetic building blocks for new chemical entities (NCEs)

    2. Agrochemical Synthesis for Herbicide and Fungicide Intermediates

    4-Methoxy-2-(Trifluoromethyl)Benzaldehyde serves as a crucial aromatic precursor within the crop protection sector, supporting the development of selective agrochemical actives, especially those requiring a fluorinated aromatic scaffold for enhanced persistence and bioactivity. In these formulations, it enters downstream at the core coupling or condensation stage, where its steric and electronic effects enable precise modifications of final pesticide molecules. End-use manufacturers rely on its consistent reactivity profile to maintain regulatory compliance and environmental stewardship goals.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration for intermediates
    • ISO 14001:2015 for Environmental Management

    Typical usage ratio

    • Typically 0.9–1.5 eq in Knoevenagel-type condensation steps or aromatic substitution; adjusted according to yield and downstream activity requirements

    Downstream process integration

    • Introduced after initial activation or halogen exchange in the main aromatic functionalization step; followed by hydrolysis, esterification, or sulfonation as needed

    Final product types

    • Herbicide intermediates for fluorinated amides and ethers
    • Fungicide precursors for triazole and strobilurin derivatives
    • Active ingredient scaffolds for research-stage crop protection molecules

    3. Fine Chemical Intermediate for Liquid Crystal Materials

    Manufacturers of specialty display materials employ this benzaldehyde derivative as a tailored precursor in synthesizing fluorinated biphenyl and terphenyl units, essential to the performance of advanced nematic and chiral nematic liquid crystal mixtures. Its stable trifluoromethyl and methoxy substitutions promote strong dielectric anisotropy and high clearing points, which are critical for new-generation LCD technology. Dosage is tightly controlled to meet batch uniformity and application performance metrics for display manufacturers in consumer electronics.

    Industry compliance standards

    • RoHS EU Directive 2011/65/EU (for electronic display compliance)
    • IEC 61249-2-21 (halogenated substances control)
    • ISO 9001:2015 Quality Management (chemicals for electronics)

    Typical usage ratio

    • Ranging from 2–10% w/w in precursor feedstock blend depending on targeted alignment and electro-optic properties of the liquid crystal mixture

    Downstream process integration

    • Employed in Suzuki or Heck coupling with halogenated aryl units; integrated via automated dosing systems before hydrogenation to lock-in desired optoelectronic characteristics

    Final product types

    • Biphenyl and terphenyl-based fluorinated liquid crystals
    • Chiral dopants and alignment regulators for LCDs
    • Mesogenic precursors for next-generation flat-panel displays

    4. Chemical Intermediate for Specialty Fragrance Synthesis

    This aromatic aldehyde plays a specific role in the manufacture of advanced fragrance ingredients within the fine chemicals domain, particularly fluorinated aromatics that provide enhanced volatility and olfactory effects not achievable with conventional benzaldehydes. Its entrance point in the downstream supply chain is at the aldehyde-alkene reaction or etherification phase, maximizing the creation of stable, high-intensity fragrance molecules for use in luxury perfumery and selected home care segments.

    Industry compliance standards

    • IFRA Code of Practice (fragrance ingredient safety)
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • Good Manufacturing Practices (GMP) for fragrances: ISO 22716

    Typical usage ratio

    • Typically 1–7% by mass in aromatic condensation, depending on target odor profile and volatility requirements

    Downstream process integration

    • Charged during key aldol or Wittig reactions; followed by extraction and rectification to isolate pure fluorinated aromatic notes

    Final product types

    • Fluorinated aldehyde fragrance bases
    • Functionalized musk and floral note compounds
    • Luxury perfume concentrate bases and fine home fragrance ingredients
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    Certification & Compliance
    More Introduction

    4-Methoxy-2-(Trifluoromethyl)Benzaldehyde: A Practical Perspective from Our Lab Floor

    Meeting the Needs of Modern Chemistry with Confidence

    We have spent years refining the processes behind aromatic building blocks, and 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde stands out in daily production for its reliability and consistent reactivity. Our own product, carrying the molecular formula C9H7F3O2, bridges several needs in both pharmaceutical and agrochemical synthesis. We have seen orders shift from basic substituted benzaldehydes to this particular compound as research grows more specific, especially for those developing advanced intermediates that call for both electron-donating and electron-withdrawing effects in the same molecule.

    In our workflow, purity tops the list of priorities. We target a GC purity above 98%, with the water content kept below 0.3%. Consistent results stem from carefully monitored crystallization procedures and rigorous analytical controls. Over years of production, we have learned that slight deviations leave too much risk of batch rejection for downstream users. This attention shows itself not just in numbers, but in the reliable yields and the clarity of the colorless to pale yellow solid our chemists know to watch for during final quality inspections.

    Why 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde Makes a Difference

    This benzaldehyde derivative finds its role as a versatile intermediate. Customers from pharmaceutical labs frequently request it for developing heterocyclic scaffolds, where its trifluoromethyl group serves both to improve metabolic stability and influence electronic properties. The methoxy group on the ring gives additional synthetic options, often acting as a protecting group or opening doors to further functionalization.

    On our manufacturing floor, we see that the trifluoromethyl group introduces a level of reactivity that simplifies design logic for medicinal chemists. Where older unsubstituted or mono-functionalized benzaldehydes fall short, the dual-substitution pattern here makes a direct difference. Analysts bring new structures forward faster because this intermediate reduces synthetic routes and favors desired electronic effects in drug candidates.

    In crop protection research, we supply this compound to agrochemical development teams. Their focus frequently ties to the persistence, lipophilicity, and controlled reactivity the trifluoromethyl group can bring. Our plant operators know that consistent supply translates into short lead times for these research teams, often critical as they run parallel trials for competitive submissions.

    Specification: Our Approach, Not a Statistic

    Every batch starts with raw materials vetted by our in-house procurement — once inside, chromatography and NMR keep synthesis on target. Quality assurance runs hands-on, not just by-the-numbers: technicians handle sampling and documentation, and weekly meetings review any deviation or suggestion from the line. Through this system, we have found that keeping melting points within the expected range, checking for color consistency, and verifying typical spectral signatures remove ambiguity later.

    Logistics runs smoother since we standardized on a crystalline product with a melting range at the upper end, preferred by formulators who want manageable storage. Packing and transport departments report fewer complaints from customers dealing with caking or premature degradation, because we developed and scaled up our own filtration and drying process.

    We supply in gram to multi-kilogram quantities, often packing under inert atmosphere for larger batches, since shelf-life extends when exposure to moisture is minimized. Ensuring the product leaves our plant according to the specifications our chemists rely on in their own lab work keeps re-orders straightforward; nobody wants unplanned re-validation in downstream synthesis.

    Comparing with Other Benzaldehydes: The Key Differences

    It would be simple to list numbers, but real-world experience shapes preferences. Comparing this product to similar molecules, such as unsubstituted benzaldehyde, 4-methoxybenzaldehyde, or 4-(trifluoromethyl)benzaldehyde, offers insights missed by spreadsheets.

    Unsubstituted benzaldehyde is known for reactivity, though its lack of electron modulation often restricts applications. 4-Methoxybenzaldehyde raises nucleophilicity and solubility, but lacks the unique stability and lipophilicity stemming from trifluoromethyl substitution. 4-(Trifluoromethyl)benzaldehyde increases hydrophobicity and metabolic stability, yet does not provide a second synthetic handle for transformations available in our product. The combination present in 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde makes a difference where versatility and precisely tuned reactivity matter.

    Our chemists—many with factory and R&D experience—remark that yields improve in multi-step pharmaceutical synthesis when using this intermediate compared to mono-substituted benzaldehydes. Reaction conditions often demand less adjustment, and protecting group strategies become more flexible. This saves time in product development cycles, a sentiment echoed back by our regular clients.

    Supporting Our Customers Through Upscaling and Innovation

    Upscaling always brings learning opportunities. Running hundred-gram pilot batches often reveals the quirks missed in research-scale syntheses, such as solvent swaps, byproduct issues, or the nuances of temperature control. As manufacturing chemists who repeatedly move from glassware to reactors, we adapt processes to fit changing volumes. Our control over raw materials and reaction atmospheres ensures the same high-purity outcome whether filling a small drum or a kilogram bottle.

    We work directly with research scientists at customer labs who sometimes request tailored filtration, drying, or packaging. Our R&D team discusses these modifications, and we have adopted feedback to refine filtration techniques, pack with moisture indicators, or switch to specialty containers for specific projects. For large-scale needs, storage stability becomes critical; we invested in climate-controlled warehousing to reduce risk of temperature excursions.

    Sustainability and Responsible Practices in Scale-Up

    Scaling up halogenated aromatic compounds often impacts both waste management and energy use. Over the years, we have introduced solvent recycling and byproduct recovery systems. These steps reduce cost and lower environmental loading, important as regulatory pressure grows. Employees at every step ensure waste streams meet strict discharge criteria—colleagues from our environmental unit regularly join meetings on batch planning.

    We also monitor workplace exposure with routine air sampling and offer safety training for all operations involving volatile aromatics. These steps protect the people working with us and build confidence with partners who visit our site for supplier assessments.

    Building Trust Through Transparency and Documentation

    Traceability forms the backbone of our operation. For every shipment, batch records include raw material origins, analytical data, synthesis and work-up parameters, and storage logs. Customers often ask for these records, and we share them without delay—especially those running regulated synthesis for clinical or market registration.

    In practice, traceability lets us resolve questions quickly. On two occasions, post-market pharmacovigilance flagged odd impurities in finished products, which we traced through documentation and confirmed stemmed from unrelated synthetic steps far downstream. Accurate records and open communication let both sides resolve issues without delay.

    Reliable Support and Forward Planning

    Regular audits and on-site visits from client technical teams are the norm. We engage with them directly, discussing not just the current order but also future needs or upcoming modifications in protocols. These conversations drive our own internal improvements and help anticipate demand trends. With pharmaceutical pipelines shifting toward fluorinated scaffolds, many outreach requests over recent seasons focus exactly on this kind of dual-functional intermediate.

    Feedback prompts us to keep stocks prepared for urgent deliveries, reducing downtime for researchers. Our plant managers relay direct supplier relationships for core raw materials, which avoids delays caused by market shifts. Because many of us moved from bench chemistry to plant operations, the connection to downstream user frustration over shortages or specification variability holds personal meaning.

    Applications Our Team Knows Well

    We see the impact of our work in published research and patent filings, particularly in advanced pharmaceutical chemistries. Researchers report that 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde supports both Grignard and reductive amination reactions, essential for quick analog synthesis. In other settings, agrochemical work references the same compound for early-stage herbicide and fungicide lead identification.

    Beyond these mainstream uses, specialty reagents and dye manufacturing have incorporated this intermediate for its unique handling of electronic effects, allowing tailored absorption properties. Graduate students and industrial chemists alike confirm that product consistency and specification compliance mean fewer failed reactions and more reproducible results—the kind that actually make it into supporting information sections of journals and development reports.

    Supply Chain Resilience and Flexibility

    Market disruptions tested supply arrangements over the past several years. We have maintained raw material reliability by working closely with long-term suppliers of both basic aromatic precursors and trifluoromethyl sources. Our procurement staff regularly visit these suppliers, reviewing not only quality and documentation but also labor practices and process controls to ensure sustainable sourcing.

    The logistics team tracks each shipment closely, adjusting routes during extreme weather or regulatory bottlenecks. Dedicated shipment monitoring software flags risk before it affects delivery. Strength in logistics shows in our on-time arrival rate and in swift communication with clients if shipments face unexpected delays. These contingencies build confidence and support long-term partnerships.

    Continuous Improvement Through Direct Feedback

    Open communication lines with customers drive improvement. We host regular roundtables where formulation chemists, purchasing managers, and our production leads discuss performance in end-use applications. Good and bad feedback both matter. Several major manufacturing upgrades, such as extended drying times and upgrades to air-handling systems, resulted directly from these frank exchanges.

    We take these sessions as opportunities to dig into results beyond our own internal testing. Many of the best process refinements began outside R&D planning documents, springing from real-world use in our partners' facilities. In several cases, side-by-side trials with different substituents have led us to bolster analytical capacity, catch trace byproducts sooner, and offer updated certificates of analysis on every lot.

    Sharing Knowledge, Building Expertise

    Our workforce brings together plant chemists, quality specialists, and process engineers—many with academic and industrial backgrounds. This experience guides our technical support. When customers encounter rare synthetic difficulties or challenging scale-up puzzles, the technical team offers the insight learned from daily production, not just from product bulletins.

    We invest in in-house training on evolving techniques in aromatic chemistry, supporting workshops on trifluoromethyl group reactivity and advances in protecting group strategies. This allows immediate deployment of improvements when new publication data demands it, closing the gap between state-of-the-art research and manufacturing reality.

    Handling and Responsible Use: Lessons from the Floor

    Working directly with methylated and trifluoromethylated aromatics requires sensible handling. Our standard safety protocols involve local exhaust, double-glove sampling, and closed transfer into weighing hoods. These measures come not from regulation, but from hands-on learning accumulated over long stretches at the plant. Minor spills or fugitive vapors caused by poor technique prompted process changes, regular refresher courses, and investments in detection equipment.

    For new users, we provide detailed handling recommendations tailored from our own operations experience. Processing departments take pride in low incident rates, using visual inspection and routine instrumentation checks to keep production safe. We have also implemented buddy systems on critical shifts, ensuring two sets of eyes for each important step—one more safeguard built from actual operational lessons.

    Staying Ahead Through Research Collaboration

    Collaboration with academic laboratories helps us track the frontiers of aromatic intermediate chemistry. Cooperative projects often explore new uses for 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde, from novel cross-coupling protocols to emerging applications in material science. Results from these projects create a feedback loop, guiding minor adjustments in synthetic method or purification step at our own plant.

    These productive partnerships not only improve quality, but also build bridges into next-generation chemistry. One recent project led to an improvement in the yield of a key pharmaceutical intermediate, following direct exchange of technical insights between graduate researchers and our process team.

    Why Our Team Sticks With 4-Methoxy-2-(Trifluoromethyl)Benzaldehyde

    After years making, handling, and supporting chemistry with this product, confidence comes as much from experience as from analytical data. Customers stay loyal because we offer consistency, open dialogue, and targeted improvements that reduce failures and speed up development time. Many members of our operations and technical teams came up running reactions on the bench; that knowledge translates directly into better solutions for complex, evolving synthesis needs.

    The journey from raw material to finished shipment reveals surprises with each production cycle. We've learned that adapting quickly, asking the right questions, and preserving institutional knowledge lets us serve researchers and manufacturers with more than just a chemical—what matters most is the support, reliability, and experience growing behind every bottle leaving our warehouse. That’s the true value of what we produce every day.