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3-Fluoro-4-(Trifluoromethyl)Benzaldehyde

    • Product Name 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde
    • Alias 3-Fluoro-4-(trifluoromethyl)benzenecarbaldehyde
    • Einecs 721-107-3
    • 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

    305591

    Product Name 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde
    Chemical Formula C8H4F4O
    Molecular Weight 192.11 g/mol
    Cas Number 881049-25-0
    Appearance Colorless to pale yellow liquid
    Boiling Point 92-94°C at 15 mmHg
    Purity Typically ≥98%
    Density 1.425 g/cm³
    Refractive Index n20/D 1.484
    Smiles O=Cc1ccc(C(F)(F)F)cc1F
    Inchi InChI=1S/C8H4F4O/c9-6-3-2-5(4-13)1-7(6)8(10,11)12/h1-4H
    Storage Temperature 2-8°C
    Solubility Slightly soluble in water; soluble in organic solvents

    As an accredited 3-Fluoro-4-(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 containing 25 grams of 3-Fluoro-4-(trifluoromethyl)benzaldehyde, sealed with a PTFE-lined cap and labeled for laboratory use.
    Shipping `3-Fluoro-4-(Trifluoromethyl)Benzaldehyde` is shipped in tightly sealed chemical containers, protected from moisture and light. It is classified as a hazardous material and handled according to safety regulations. Shipping utilizes UN-approved packaging, and includes necessary documentation for safe handling, storage, and emergency procedures during transit. Temperature control may be applied if required.
    Storage Store **3-Fluoro-4-(trifluoromethyl)benzaldehyde** in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, oxidizing agents, and incompatible materials. Ensure proper labeling and access to appropriate spill containment. Use in a chemical fume hood and follow all relevant safety protocols for handling aromatic aldehydes and fluorinated compounds.
    Application of 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde

    Applications of 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde in Industrial Manufacturing

    3-Fluoro-4-(Trifluoromethyl)Benzaldehyde serves as a building block for various high-value chemical syntheses. Our direct production and stringent process control ensure batch-to-batch consistency, supporting integration into specialized downstream segments. Below we detail industry-recognized scenarios, referencing compliant operational parameters and finished goods directly consuming our product.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical producers incorporate this compound as a fluorinated aromatic aldehyde for synthesis of active pharmaceutical ingredient (API) scaffolds and lead candidates, particularly for oncology and CNS drugs. The electron-withdrawing properties and ready reactivity in condensation and reductive amination steps promote selective introduction of pharmacophores. Manufacturers consistently validate its identity and purity under regulatory requirements, leveraging our lot traceability for submission batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia General Methods 2.4.14 (Identification tests)
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • Specification conformity to USP <467> Residual Solvents for raw materials

    Typical usage ratio

    • 0.2–1.8 molar equivalents relative to target API precursor
    • Adjusted depending on yield optimization and side-reaction profiles
    • Strict maximum content limits for residuals in final API, typically under 0.05% w/w

    Downstream process integration

    • Charged in initial coupling reactions in medicinal chemistry scale-up
    • Enter at aldehyde-to-ketone oxidation or imine formation steps
    • Subjected to column purification post-condensation for process R&D batches
    • Integrated into validated batch records for GMP documentation

    Final product types

    • Antitumor agent intermediates
    • Central nervous system drug starting materials
    • Selective serotonin reuptake inhibitor (SSRI) precursors
    • API analogues with fluorinated aromatic rings for patent extension

    2. Agrochemical Intermediate Synthesis

    Crop protection and pesticide manufacturers use this compound for constructing fluorinated benzaldehyde moieties in advanced herbicides and fungicides. Fluorinated functional groups improve product stability and bioactivity in target molecule design. Manufacturing processes require analytical verification of content and impurity profile before coupling with amines or phenolic units. Our material supports robust synthesis with low byproduct formation under typical agrochemical production conditions.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines on Residue Analysis
    • OECD GLP Principles for chemical intermediate manufacture
    • REACH Regulation (EC) No 1907/2006 for substance registration
    • ISO 9001:2015 Certified Quality Management System

    Typical usage ratio

    • 0.5–2.0 molar equivalents per target active compound backbone
    • Optimized according to product-specific synthetic pathways
    • Residual precursor thresholds: typically <0.1% in technical active ingredient

    Downstream process integration

    • Introduced during primary amination or condensation step
    • Handled in closed-system reactors for process safety
    • Incorporated into semi-continuous or batch process streams
    • Samples tested for purity and absence of regulated impurities before formulation

    Final product types

    • Triazole-based fungicides
    • Pyridine herbicide intermediates
    • Fluorinated insecticidal compound precursors
    • Seed treatment and soil fumigant chemical intermediates

    3. Liquid Crystal and Display Material Synthesis

    Electronics manufacturers working in the advanced materials sector employ this molecule for the targeted production of fluorinated aromatic building blocks used in liquid crystal (LC) compounds. Its trifluoromethyl and fluoro substituents impart specific alignment and dielectric properties crucial for nematic and smectic phase stabilization. Downstream users rely on analytical grade purity and rigorous contaminant screening to prevent device performance drift.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Hazardous substances in electronics)
    • JIS C 6100-2-4 (Japanese Electronic Display Standards)
    • IEC 61249-2-41:2017 for display substrate materials
    • ISO 17025 accredited analytical verification at incoming QC

    Typical usage ratio

    • 15–60% weight fraction in LC intermediate syntheses
    • Adjusted based on electronic phase and blend viscosity specifications
    • Residual threshold in LC formulation under 0.05% as per panel device standards

    Downstream process integration

    • Enter at backbone core synthesis for LC mesogen production
    • Reacts with extended chain alcohols and phenoxy derivatives
    • Purified intermediates proceed to blend with other LC compounds
    • Post-integration quality analysis for dielectric constant and birefringence values

    Final product types

    • Twisted nematic (TN) and in-plane switching (IPS) LC mixtures
    • Specialty fluorine-containing LC aligner chemicals
    • Active-matrix liquid crystal display (AMLCD) panels
    • Organic light-emitting diode (OLED) display pre-polymers

    4. Fluorinated Aroma Chemical Precursor

    Manufacturers in the flavors and fragrance segment utilize this raw material for synthesizing rare fluorinated aldehyde notes, enhancing aromatic profile intensity and volatility. Process chemists deploy strict analytical controls on residual fluorine content to ensure compliance with global food additive guidelines. Uses focus on specialized compositions where stability and distinctive note delivery are required.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • EU Regulation (EC) No 1334/2008 (Flavorings and certain food ingredients)
    • US FDA 21 CFR 172.515 (Synthetic flavoring substances and adjuvants)
    • ISO 11014 for Material Safety Data Sheet (MSDS) compliance

    Typical usage ratio

    • Max 0.05–0.2% by mass in finished aroma mix
    • Determined by olfactory panel thresholds and toxicological review
    • Strictly monitored to keep cumulative daily intake within regulatory limits

    Downstream process integration

    • Condensation with other aromatic aldehydes in blending reactors
    • Purified by low-temperature distillation to isolate functional aroma intermediates
    • Enter into GC-MS analysis stages for trace impurity verification
    • Finished blends submitted for IFRA and allergen labelling approval

    Final product types

    • Designer fragrance components for personal care
    • Premium flavor enhancers for beverage concentrates
    • Novel air care and scent diffusion agents
    • Custom perfumery top-note aldehydes

    5. Fine Chemical Synthesis for Specialty Polymers

    Producers of advanced performance materials integrate this fluorinated benzaldehyde as a co-monomer or chain modifier, contributing to enhanced weatherability and chemical resistance in specialty polymers. Product acceptance relies on stringent control of end-group reactivity and residual monomer content. We offer consistent intermediate quality, supporting high-yield reactions and reliable polymer characteristics in downstream compounding.

    Industry compliance standards

    • ISO 9001:2015 Quality management for chemical manufacturing
    • REACH Annex XVII (restrictions on specific hazardous substances)
    • ASTM D638 (Mechanical properties of polymers)
    • RoHS compliance for use in electronics encapsulants

    Typical usage ratio

    • 0.7–3.5% by weight in polymer blend, subject to chain length and structure
    • Optimized for desired UV resistance and tensile properties
    • Final residuals below 0.1% by GC-MS to meet electronic-grade requirements

    Downstream process integration

    • Charged with other monomers in step-growth or radical polymerization reactors
    • Used as functional end-capper in perfluoropolyether syntheses
    • Post-synthesis purification to remove unreacted aromatic units
    • QC tested for full conversion and absence of extractable impurities

    Final product types

    • Fluorinated polyacrylates for coatings
    • Specialty thermosets for electronics encapsulation
    • UV-resistant fiber treatment agents
    • High-durability adhesive matrix resins
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    Certification & Compliance
    More Introduction

    Introducing 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde: Reliable Consistency from the Production Floor

    Direct from the Manufacturer’s Line: Perspective on Crafting 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde

    Anyone who spends years synthesizing specialty aromatic compounds picks up a unique perspective on how slight tweaks in structure deliver real differences in reactivity, stability, and downstream versatility. Having overseen batches of 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde through all production stages—from initial fluorination through the isolation of that crystalline, faintly pale solid—there’s a level of intuition that comes with monitoring each small shift in pH, temperature, and pressure. You can spot the difference in final purity and batch-to-batch homogeneity with a practiced eye, both before and after analytical runs confirm it.

    Our work happens at the heart of synthetic research, not in the office or boardroom. You feel the aromatic bite of benzaldehyde and witness just how much the introduction of fluorine atoms and a trifluoromethyl group changes everything. Not just in the physical properties, but in how this molecule slots into broader synthesis plans—especially in the pharmaceutical and agrochemical worlds. Over the years, I’ve fielded requests for higher and lower impurity thresholds and demands for scale-up without a shift in analytical profile. Real hands-on experience has taught me where corners get cut and quality starts to slip.

    The Model We Produce: Specifics Forged by Real Process Experience

    Our typical product runs as 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde with the CAS number commonly recognized throughout R&D and commercial supply chains. Each batch comes with high-performance liquid chromatography results including area percentages and absolute residual solvent data—you won’t find this in shipments from middlemen who never see the production floor. Usually, we target GC purities consistently above 99%, because even small increases in byproducts can derail multi-step syntheses.

    Melting points tend to fall around the predicted range, but we keep an eye on any outliers, since those often signal subtle process drift or contamination. Appearance—the color, the state—immediately tells an experienced manufacturer if the reduction or oxidation conditions shifted too far. Water content, measured using Karl Fischer titration, also gets documented in detail, especially for projects where moisture might trigger unintended side reactions later on.

    Usage in Complex Synthesis: Built for Chemists Who Push Boundaries

    Many of us on the production side are regularly in touch with medicinal, crop science, and materials researchers who depend on our benzaldehyde variant as a core building block. They trust these halogenated aromatics for introducing selective reactivity or polarity where carbonyl and fluoro substituents offer handles for further functionalization. One recurring example involves the molecule’s capacity to participate in Grignard or Suzuki couplings, creating diversity for downstream lead development.

    A key point: our 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde doesn’t just serve as an off-the-shelf aldehyde. Its structural design, pairing electron-withdrawing fluorine and trifluoromethyl groups, sharply increases resistance to oxidation yet keeps the aldehyde reactive enough for typical condensation and addition chemistry. This matters in scale-up: inconsistent or over-reactive intermediates slow down process development and pile on costs. Over the years, we’ve observed that this benzaldehyde’s very specific pattern of fluorination leads to clean, controlled progress in synthetic steps, reducing troubleshooting and material waste.

    Distinguishing Features: Why Our Batch Differs from Generic Aldehydes

    Every chemist knows the scene: you order from a catalog, a third-party warehouse ships a bottle. What turns up might have variable moisture, yellowed appearance, or detectably off GC profile. Being direct manufacturers, we’re well aware of how chain-of-custody errors, improper storage, or blending with inadequately inert atmosphere leads to product degradation. This affects both shelf-life and the reliability of your experiments.

    We store and ship our 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde under controlled conditions, making sure to eliminate extended atmospheric exposure and rapid, unprotected temperature swings. Our storage protocols stem from years of hands-on trial and error, not from guesswork. Time and again, we hear feedback from researchers who switched to our material after running into batch failures with resellers providing product outside recommended storage guidelines.

    Manufacturing in-house means sampling every batch for trace impurity analysis—down to less than 0.1%—as even microscopic foreign species impact reaction outcomes at scale. Years ago, we revised our purification protocol after spotting an unidentified side product in a downstream process for an API precursor. Trials with minor process changes made clear how sensitive both the pharmaceutical and specialty polymer end-users are to even small shifts in starting material quality.

    Controlling Quality: Continuous Monitoring, Not Just End-Point Checking

    QC for us means more than running a few checks near the end of the production line. We validate every critical stage, including preliminary fluorination prior to introduction of the formyl group, with real-time analytics. Having overseen hundreds of batches across multiple years, I’ve learned that drifting just a couple of degrees in temperature profile or mismanaging local pH during extraction triggers out-of-spec results fast.

    Our analytical team—engineers who also train in solvent recovery and waste neutralization—regularly retest retained samples, often months after dispatch. This practice gives us confidence that shelf stability lines up with reality, rather than just hitting spec at the moment of shipment. For end users, confidence in reordering based not only on documentation but lived experience of product performance is a key reason we keep customers for years rather than sales cycles.

    Process Improvements over the Years

    When you spend enough time making a narrow set of halogenated aromatics, process improvements turn into a daily goal, not an occasional exercise. We’ve experimented with incremental solvent system changes, switching bases, and reoptimizing water wash protocols. These seemingly small changes deliver sharper color profiles and push impurities below detection. As a result, our benzaldehyde often appears as a brittle, clean-looking solid rather than a sticky, off-white clump.

    Extraction efficiency, solvent use, and temperature harmonization reduce both raw material consumption and batch-to-batch variability. We discovered early on that minimizing exposure to trace transition metals—copper, iron, or nickel—eliminates byproduct formation that otherwise slipped past early detectors and caused problems in scale-up. Having production chemists involved in the QA loop caught these details well before they caused delays in critical pharmaceutical projects.

    Responsibility doesn’t end with the synthesis itself. We regularly reexamine byproduct streams to lower waste volumes, finding partners for reprocessing viable fractions and reclaiming solvents with the latest recovery equipment. Our team notices when even the minor impurities—less than 0.05%—might influence sensitive catalytic steps. Consistency and reliability always win out over volume or output rates in our plant.

    Taking Feedback from Downstream Users

    The learning curve of direct manufacturing includes a steady stream of feedback from analytical labs and synthetic chemists. Researchers often tell us about downstream reactions that fail due to invisible impurities, or about changes in NMR spectra that correlate perfectly with tiny contaminant peaks we spotted weeks earlier. Having full chain-of-custody control, our QC team can reanalyze retained samples from historical batches, trace the origin of issues, and refine both raw material screening and final purification.

    Occasionally, customers ask for modified specifications, such as alternative crystal forms, or for custom washing and drying to support process development. We’re able to accommodate these thanks to maintaining direct control over both process and QA steps, something wholesalers and blenders rarely support. Open lines of technical communication let us constantly benchmark and refine each production run, instead of aiming just for basic conformity.

    Supply Chain Integrity

    The value of direct manufacturing becomes clearest during global raw material disruptions or regulatory adjustments. We source fluoroaromatic precursors directly from trusted suppliers and keep safety stocks based on years of demand patterns. Process transparency helps us update partners immediately about delivery windows, adjusting lots based on real output rather than speculative wholesaler projections.

    During periods of constrained logistics—shortages of key solvents, shifts in regulatory handling of fluoroalkyl sources—our ability to recalibrate the process means we keep product moving with minimal gaps. Adaptability comes from working directly on the reaction floor, not from negotiating with layers of middlemen who rarely see the actual chemistry in play.

    Safety, Environmental and Regulatory Compliance: Not Optional

    Real-world manufacturing of halogenated benzaldehydes brings unique safety and environmental challenges. Our in-plant training combines chemical handling, ventilation management, and solvent re-use with a strong culture of ongoing learning. We install detection systems for volatile organic compounds and keep real-time records, matching our internal standards with evolving national and international regulations.

    Compliance for us has grown into a cornerstone rather than a check-mark. Inspection-readiness means ongoing documentation review and periodic audits—whether internal or by external accredited labs. Having to implement recalls or corrective actions over a decade ago taught us the value of continuous review, both of process and culture. Our in-house team maintains close dialogue with regulators and external technical advisors, keeping every part of the operation above-board and secure.

    Why 3-Fluoro-4-(Trifluoromethyl)Benzaldehyde Stands Apart in the Chemist’s Toolkit

    Compared to non-halogenated benzaldehydes, this compound offers increased selectivity and resistance to unwanted over-oxidation. Where other benzaldehydes risk rapid change in open air or in the presence of trace catalysts, the trifluoromethyl and fluorine groups used in this product stabilize both the aromatic system and carbonyl functional group. This makes the molecule dependable when developing novel chemotypes, especially for targets where tight control over intermediate oxidation states matters.

    We’ve seen this compound open pathways in medicinal chemistry that standard aldehydes simply can’t match. Researchers working on kinase inhibitors, antiviral agents, or advanced crop protection products often report employing our benzaldehyde as the originating scaffold. Functional diversity, fostered by the electron-withdrawing groups, gives more flexibility in stepwise modifications and substitution. It’s not just about reactivity—physical predictability during purification and crystallization steps also saves time.

    For those working in electronics materials or specialty polymers, the presence of these halogenated functional groups offers new entry points for building high-performance structures. Years of supplying directly to these fields have taught us about both the chemical and logistical needs, including proper inert gas packing and documentation of batch-specific trace elements.

    Meeting the Future: Trends and Manufacturing Challenges Ahead

    Global demand for increasingly complex fluorinated intermediates continues to rise—not simply due to new discoveries, but thanks to regulatory tightening and customer demands for more predictable, scalable purity. Our team constantly evaluates feedstock availability, reassesses environmental controls, and refines purification sequences. Having hands-on oversight over every production and shipping detail allows us to adjust and improve on short notice, avoiding the lag that affects less integrated suppliers.

    Innovation in the field comes from deeper chemical understanding, not just scaling up for volume. Our laboratory works closely with equipment manufacturers on custom reactors and in-line analytics that catch anomalies earlier. We routinely test newer, environmentally safer extraction and purification systems to lower emissions and reduce hazardous waste material.

    Because our production chemists also contribute to customer support, we field real-world questions on synthetic bottlenecks and propose refinements rooted in process experience. That connection between the bench and production floor gives us a practical sense for what works and what needs improvement, whether for R&D scale multi-gram orders or for multi-ton commercial runs.

    Community and Knowledge Sharing

    One rewarding aspect of direct manufacturing is the ongoing exchange with academic groups and industrial process teams. Over the years, we’ve hosted plant visits, supported consortia tackling solvent recovery and green chemistry, and worked on joint publications tackling analytic and process challenges. These connections keep us alert to emerging trends and foster innovation in both small-batch and high-volume production.

    Our production lines do not operate in isolation—partnerships with reagent makers, equipment suppliers, and research consortia enrich our technical base and keep our methods on the cutting edge. Transparency about process, not just product, has earned us long-term collaborations with forward-thinking synthetic teams around the globe.

    The Real Difference: Manufacturing With Integrity

    Direct manufacturing creates a culture of craft, accountability, and steady improvement impossible to match by resellers or brokers removed from the process. Experience tells us that small divergences in starting material purity, process conditions, or storage protocols dictate outcomes all the way down the chemical supply chain. Our ongoing commitment is to keep refining and supporting chemists with material that works, every batch, every shipment.

    3-Fluoro-4-(Trifluoromethyl)Benzaldehyde isn’t just another aromatic intermediate. From the first grams to commercial lots, we take pride in the performance, reliability, and integrity of our product and processes. For chemists seeking predictable results and a partner that understands the realities of hands-on synthetic work, the difference shows in every bottle.