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4-(3-Fluorophenyl)Benzaldehyde

    • Product Name 4-(3-Fluorophenyl)Benzaldehyde
    • Alias MFBA
    • Einecs 831-099-7
    • 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

    296534

    Chemical Name 4-(3-Fluorophenyl)Benzaldehyde
    Molecular Formula C13H9FO
    Cas Number 136040-16-3
    Appearance White to off-white solid
    Melting Point 66-68°C
    Boiling Point 344.7°C at 760 mmHg
    Density 1.18 g/cm3
    Purity ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC=C(C=C1)C2=CC(=CC=C2)F
    Inchi InChI=1S/C13H9FO/c14-13-5-3-4-11(10-13)9-12-2-1-6-15-7-8-12/h1-10H

    As an accredited 4-(3-Fluorophenyl)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 4-(3-Fluorophenyl)Benzaldehyde, sealed with a screw cap, labeled with hazard warnings.
    Shipping 4-(3-Fluorophenyl)Benzaldehyde is shipped in secure, airtight containers to ensure stability and prevent contamination. Packaging meets all regulatory and safety requirements for hazardous chemicals, including clear labeling. During transit, temperature and handling precautions are maintained to protect product integrity and ensure safe delivery to the customer.
    Storage 4-(3-Fluorophenyl)benzaldehyde should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from light and moisture. Store at room temperature or as specified on the MSDS. Ensure proper labeling and keep out of reach of unauthorized personnel.
    Application of 4-(3-Fluorophenyl)Benzaldehyde

    Applications of 4-(3-Fluorophenyl)Benzaldehyde in Industrial Manufacturing

    As a direct manufacturer, we supply 4-(3-Fluorophenyl)Benzaldehyde to multiple advanced chemical sectors. The compound serves as a critical intermediate for downstream synthesis in pharmaceuticals, fine chemicals, agrochemical actives, specialty polymers, and liquid crystal materials. Below, we present detailed application channels, including compliance demands, process approaches, and target end-products deployed by industry leaders.

    1. Pharmaceutical Intermediate for API Synthesis

    4-(3-Fluorophenyl)Benzaldehyde functions as a key starting material in the synthesis of selective serotonin reuptake inhibitor (SSRI) and kinase inhibitor actives. API manufacturers employ this compound in multi-step routes, using controlled hydrogenation and condensation stages for final molecule construction. Effective process control and traceability are essential due to strict pharmacopoeial and cGMP demands.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • United States Pharmacopeia (USP) for relevant APIs
    • European Pharmacopeia (Ph. Eur.) monographs
    • FDA 21 CFR Part 211 (if destined for regulated markets)

    Typical usage ratio

    • Employ as a limiting reagent; dosage varies 0.8–1.2 molar equivalents depending on the synthesis step
    • Adjustment based on API target purity and byproduct profile

    Downstream process integration

    • Introduced at the condensation or coupling phase after halogenation or nitration pre-steps
    • Subjected to catalytic hydrogenation and/or reductive amination in downstream reactors
    • QC sampling for residual aldehyde prior to final crystallization

    Final product types

    • Fluorinated antidepressant APIs
    • Tyrosine kinase inhibitor molecules (oncology sector)
    • Other CNS-active pharmaceutical compounds

    2. Advanced Agrochemical Building Block

    Crop protection manufacturers use 4-(3-Fluorophenyl)Benzaldehyde as a structural unit in high-performance herbicides and insecticides. Its fluorinated aromatic system enhances binding affinity in new actives. Downstream blending and formulation typically involves alkylation or imine formation, with strict impurity and traceability requirements for regulatory approval.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • ISO 9001:2015 Quality Management
    • REACH registration for import/export into the EU
    • Environmental Protection Agency (EPA) guidelines for pesticide manufacturing

    Typical usage ratio

    • Standard input: 15–30% of advanced agrochemical intermediates by weight
    • Adjusted according to proprietary crop protection formulations and structure-activity relationship studies

    Downstream process integration

    • Charged into synthesis reactors during key condensation or cyclization stages
    • Purification and microfiltration before formulation to minimize residual contaminants
    • Batch documentation per lot for regulatory traceability

    Final product types

    • Fluoroaromatic herbicides
    • Systemic insecticides
    • Seed treatment formulations

    3. Precursor for Specialty Polymer Monomers

    Polymer manufacturers select 4-(3-Fluorophenyl)Benzaldehyde for the creation of high-performance polyimides and fluorine-containing polyesters. Its aromatic core and electrophilic aldehyde functionality enable further derivatization, critical for engineering specialty materials used in electronics and aerospace sectors. Strict monomer purity and batch-to-batch consistency are crucial in this segment.

    Industry compliance standards

    • ASTM D3418 for Glass Transition Temperature analysis
    • ISO 14001:2015 for Environmental Management
    • TSE (Total Specific Element) control for fluorinated materials
    • RoHS Directive 2011/65/EU (if used in electronics)

    Typical usage ratio

    • Feedstock level: 5–12% by weight for target copolymers
    • Adjusted for desired glass transition temperature and mechanical strength endpoints

    Downstream process integration

    • Condensation polymerization with diamines to yield pre-polymers
    • Post-reactor purification and devolatilization to achieve low residual monomer
    • Blending with other comonomers prior to extrusion or film casting

    Final product types

    • High-performance polyimide films
    • Fluorinated polyester resins
    • Dielectric coatings for microelectronics

    4. Intermediate for Liquid Crystal Display (LCD) Material Synthesis

    Producers of liquid crystal intermediates use 4-(3-Fluorophenyl)Benzaldehyde in the synthesis of aromatic esters and biphenyl derivatives. These units impart improved phase stability and low viscosity for advanced display applications. Critical control of isomeric purity and low trace metals is mandatory to prevent display performance issues.

    Industry compliance standards

    • IEC 61249-2-21:2012 (For Halogen-Free Components in Electronics)
    • JIS C 5016 for display-grade material analysis
    • Internal QC for isomer specification (purity >99.5%)
    • RoHS compliance for finished display panel supply chain

    Typical usage ratio

    • Component ratio: 8–16% in high-value liquid crystal intermediate mixtures
    • Modified as required for specific optical/thermal properties in the final LC blend

    Downstream process integration

    • First-stage derivatization via esterification or Suzuki coupling
    • Follow-up cyclization under inert, absolutely anhydrous conditions
    • Fractional distillation or preparative HPLC for refining to electronics grade

    Final product types

    • Biphenyl-based nematic liquid crystals
    • Cholesteric liquid crystal mixtures
    • LCD panel intermediate materials

    5. Fine Chemical Intermediate for Fragrance Synthesis

    Manufacturers in the fragrance and aroma industry utilize this fluorinated benzaldehyde for synthesizing unique musks and specialized odorants. The aldehyde functionality offers selective reactivity in condensation and acetalization steps, allowing for the creation of rare scents not achievable with non-fluorinated analogues. High traceability and purity are mandatory due to consumer safety and REACH reporting.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • REACH substance registration and safety data documentation
    • ISO 22716:2007 (Cosmetic GMP for relevant blends)
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients

    Typical usage ratio

    • 0.5–5% on batch weight for specialty fragrance molecule synthesis
    • Adjusted for reaction yield and olfactory strength desired in the final blend

    Downstream process integration

    • Enters acetalization or aldol condensation step as primary aromatic aldehyde
    • Post-reaction vacuum distillation for impurity removal
    • GC/MS analysis prior to blending with essential oil carriers

    Final product types

    • Synthetic musks for premium perfumes
    • Specialty aroma compounds for luxury consumer products
    • Fragrance ingredients for personal care items
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    Certification & Compliance
    More Introduction

    Introducing 4-(3-Fluorophenyl)Benzaldehyde: Direct From the Manufacturer

    A Closer Look at 4-(3-Fluorophenyl)Benzaldehyde

    In the chemical production field, 4-(3-Fluorophenyl)benzaldehyde offers clear advantages when customers seek consistent reactivity and fine-tuned selectivity. At our manufacturing facility, we synthesize this compound under conditions that emphasize precision, reproducibility, and transparency of source. Unlike procurement channels that rely on intermediary warehouses or repackagers, every batch we produce remains under our direct quality oversight, ensuring full traceability from raw materials to drum.

    4-(3-Fluorophenyl)benzaldehyde, commonly identified by its structure—a benzaldehyde group substituted with a 3-fluorophenyl ring—has proven itself in a range of core organic synthesis strategies. Pharmaceutical researchers value this molecule’s unique placing of the fluorine atom, because it opens up new routes in the design of biologically active compounds. The placement modifies both electronic properties and steric factors in downstream molecules, often altering biological affinity or metabolic resistance. The organic electronic materials sector and advanced polymer researchers have found similar advantages by favoring this precise substitution pattern.

    Reliable Production Rooted in Experience

    Our approach to manufacturing 4-(3-Fluorophenyl)benzaldehyde comes from years spent refining aromatic fluorination and aldehyde-forming processes. Developing a scalable pathway took effort at every step—from identifying stable, high-purity fluorinated precursors to designing reactors that sustain clean transformations without byproduct carryover. We focus on exacting catalyst choices, tightly controlled temperatures, and solvent systems that minimize unwanted side reactions. With this groundwork, we consistently attain a product with greater than 99% GC purity for customer applications, with impurity profiles that remain stable batch after batch.

    This isn’t just about meeting a datasheet value. In uses such as medicinal chemistry, where minor impurities can derail assays or mask the real effect of a lead compound, researchers depend on knowing exactly what they’re putting into their experiments. The main aldehyde envelope must hold, with minimal formation of overstated oxidized or reduced byproducts. Subtle differences in trace phenolic or fluoro-ketonic residues can mislead development teams, contributing to failed downstream experiments and lost time.

    Specifications With a Practical Purpose

    Direct manufacturers understand that a set of specifications isn’t just an exercise in paperwork. Every parameter we publish connects to a real concern from the field. Our standard format includes a product assay using gas chromatography, moisture analysis by Karl Fischer titration, and targeted limits for specific fluorinated aromatic impurities. Most labs receive our product in either sealed amber glass bottles or inert-lined steel drums, depending on the scale, to shield the sensitive aldehyde group from ambient moisture and photodegradation.

    We have found that handling and storage matter. Aldehydes carrying fluorinated aromatics tolerate less thermal cycling and exposure to open air than many analogues. We keep the process airtight and chilled through final packing, and suggest users do the same to prevent loss of potency. Shelf life testing under various storage regimes shows that minimizing oxygen and light extends usability for months without observed degradation or formation of acid byproducts—data we make available to interested clients on request. For those scaling up, support includes recommendations drawn from our experience on vessel materials and transfer line compatibility.

    Comparing Against Other Aromatic Aldehydes

    The market for substituted benzaldehydes includes a wide spread of analogues—some with halogens, some with methyl or alkoxy substituents, or even with combinations. Many customers ask how our 4-(3-fluorophenyl)benzaldehyde stands against similar molecules like 4-fluorobenzaldehyde or 3,4-difluorobenzaldehyde. From the seat of a manufacturer, we see differences manifest physically in yield stability, odor, and even the feel of crystallized product during scaling or reslurrying.

    Our 4-(3-Fluorophenyl)benzaldehyde distinguishes itself in several key respects. The meta-fluorine substitution introduces effects not seen with purely para- or ortho-substituted compounds. It adjusts the electron density of the aldehyde’s reactive carbonyl, tuning the nucleophilicity and making select reactions—like Wittig condensations or enzyme-catalyzed transformations—run cleaner and faster. Some analogues give inconsistent end-point readings or unexpected exotherms; our customers report more predictable handling and reproducible conversions in pilot runs. Production chemists at several mid-sized pharma firms have told us that switching to our direct-source material has cut down on weeks lost to analytical troubleshooting.

    On the physical chemistry side, crystallization behavior and melting points vary in subtle but tangible ways. Our method consistently produces material with a melting point in the expected 60-62°C range, yielding solid, easily handled product that fits seamlessly into automated systems or manual weighing environments. By comparison, some suppliers of similar fluorinated aldehydes report broader melting ranges, clumping, or even partial liquefaction at controlled ambient temperatures—complications that create headaches in compounding labs or automated feed bins.

    Sourcing Directly Brings Clarity and Confidence

    As a dedicated manufacturer, we often hear from customers who switched from trading houses only after repeated failures in purity claims, batch composition, or supply reliability. Our business rests on keeping production under one ceiling. This means no relabeling, no batch-roundtripping, and no unknown storage environments from intermediate distributors. Buyers welcome the transparency—each certificate tracks the journey from raw feedstock right to the end crate.

    Somewhat uniquely, we field technical questions not only about the product but about its origins and handling. Lab project leads often want to know which fluorinating agents we choose, if we recycle or incinerate non-product streams, and how we verify process safety. Forward the most detailed science query—our senior synthesis chemists engage directly. We believe this level of interaction separates true manufacturers from badge-sellers. Peer-to-peer discussions have led to product improvements, helped customers solve stubborn process bottlenecks, and let younger chemists hone their own analytical skills.

    Practical Applications Unlocked by Our Product’s Profile

    Consumers of 4-(3-Fluorophenyl)benzaldehyde fall into several key groups. Pharmaceutical innovators leverage the compound’s high purity and stable meta-fluorine for anything from initial hit-to-lead screening through to scale-up intermediates in complex arylation or alkylation steps. Fine chemicals houses use it when formulating designer aryl-aldehydes, targeting agrochemical actives or advanced electronic motifs. Material scientists have started exploring this fluorinated aldehyde as a building block in new classes of conjugated polymers and OLED structures—citing its impact on hole injection layers and photostability profiles.

    Feedback from these diverse users usually centers on two themes. First, reliable, reproducible input quality reduces cycle time, especially in regulated environments where each gram needs full documentation. Second, our product supports both bench-scale screening and plant-scale synthesis without changes to analytical targets or product handling. One global contract manufacturer reported fewer failed shipments of API intermediates after switching to our directly sourced lot, compared to inconsistent results through traders.

    There’s another population that values direct-from-producer sourcing: environmental and compliance officers at downstream companies. By demonstrating that a product’s entire lifecycle—starting with fluorinated raw materials and specialty solvents, moving through closed-loop reactors, and ending in recoverable or recyclable waste—is tracked and engineered to minimize emissions, we contribute to sustainable chemistry targets enforced worldwide by both private contracts and public policy.

    Addressing Challenges Seen in the Broader Market

    Producing fluorinated aromatics calls for skill and focus. We have seen market entrants who purchase non-fluorinated base arenes and attempt late-stage direct fluorination, often introducing hard-to-detect isomeric impurities. From our own experience, such approaches deliver inconsistent yields and complicated downstream purification. Incidents of uncontrolled fluorine release and uncontrolled exotherms have cropped up across the industry—problems avoidable with designs honed over years, rather than months.

    By controlling upstream supply and maintaining full traceability, our manufacturing keeps these risks tightly bounded. Workers at our facility undergo ongoing training in both process safety and analytical troubleshooting. Any deviation in reactor profile triggers root-cause analysis overseen by a team of senior chemists. Documented lessons from near-misses and field-returns filter back into standard operating procedures. This proactive investment pays off both in day-to-day running and in solid customer trust—validated by years of incident-free distribution.

    Supporting Next-Generation Synthesis and Discovery

    The future of specialty benzaldehydes, especially those featuring strategic fluorination, depends not just on technical competence but on responsiveness to new requests. Our technical teams invest in collaborations with end users, regularly exploring derivative syntheses that extend beyond the base product. Requests range from stable-isotope labeled versions for tracing metabolic pathways, to derivatives where the fluoro substituent shifts position or pairs with another electron-withdrawing group for expanded reactivity.

    Our facility handles these requests through flexible reactor trains and an analytical suite built for high-throughput screening—tools that third-party traders can’t offer. Organic synthesis itself keeps evolving, and involvement at this manufacturing level gives us insight into the practical needs of both research chemists and process engineers: understanding volatility shifts, batch-to-batch color changes, or minor solubility quirks before they matter downstream.

    We also pay close attention to environmental and regulatory shifts worldwide. As production criteria tighten and solvent or emissions thresholds drop, we respond by redesigning waste capture, switching to greener solvents, and updating compliance reporting in real time. Direct manufacturers can pivot faster, since feedback loops from field to factory are short.

    Customer-Focused Culture Backed By Knowledge and Experience

    Customers who source directly with us often mention one cultural difference: they benefit from the collective experience of staff who have worked this chemistry for years. Many of our team cut their teeth on less forgiving halogenation or oxidation runs before moving to the bench or plant floor production of specialized aldehydes. We believe this matters because it shapes how the product is checked at every stage. A drum of 4-(3-Fluorophenyl)benzaldehyde isn’t just a number on a specification sheet—it’s the converged outcome of hundreds of decision points, all made possible through lived know-how and peer-to-peer support.

    By choosing direct sourcing, researchers, process chemists, and procurement departments sidestep the uncertainties brought by long supply chains. They receive the benefit of open science and candid conversation. If a formulation problem arises, staff who made or analyzed the batch can jump in with guidance drawn from deep chemical familiarity. We routinely host customer audits, provide full traceability reports, and engage in data-sharing sessions to support regulatory filings across pharmaceutical and industrial contexts. This environment generates trust and keeps both our team and our clients at the forefront of discovery.

    Why Product Differences Matter in the Lab and Plant

    In our industry, details drive outcomes. No two lots from generic traders exhibit identical performance because their upstream controls vary. As a manufacturer, we see firsthand how tight process control influences both on-paper specifications and real-world handling. For instance, when customers feedback that a rival’s benzaldehyde “smells off” or gives inconsistent melting points, we look up our chromatogram archives and help diagnose the likely route or stability issue. A data-driven approach shapes not just product confidence, but also supports method transfer, scale-up processes, and compliance in highly regulated environments like pharmaceuticals or electronics.

    Physical handling matters as much as molecular structure. Pharmas and electronic materials producers need products that maintain clarity and purity through days-long reactions, temperature shifts, and careful catalysis steps. We have found that automated reactors and process lines operate best when each lot aligns with the last. Color, particulate load, and even subtle viscosity properties feed back into system reliability. Production runs using off-spec aldehydes—sometimes accepted out of procurement urgency from middlemen—often cost more in wasted runs and post-run purifications than direct sourcing would have.

    Continual Improvement Through Real-World Experience

    We view every manufacturing chemist’s job as a journey of continual learning. Every reaction run, every analysis, and every customer feedback cycle brings new insights about what matters on the end user’s bench. That’s why we invest in ongoing development across our operations. Regular production meetings evaluate trends in test data, shipping feedback, and analysis of reported outliers. Problems are solved with tools honed by years in the field—whether the fix calls for adjusting a purification cut, changing a filtration material, or implementing a new final rinse before packing.

    Direct interaction with customers shapes both practice and pride. When a pharmaceutical researcher requested better light protection for shorter-scale shipments, our team experimented with multiple glass vials and found a solution that worked through chilling and UV-proof transit. When a chemical engineer flagged minor changes in aldehyde content after a supplier change, our team ran stability tests, isolated the root cause in a raw input impurity, and provided a modified certificate to support new regulatory filings.

    Conclusion: Why Experience and Directness Count

    Every gram of 4-(3-Fluorophenyl)benzaldehyde reaching a customer’s facility carries with it layers of expertise, transparency, and dedication. True manufacturers treat product as the sum of knowledge, effort, and continual adaptation—not a commodity moving through the warehouse. Differentiation by source, purity, consistency, and user support has become central as industries demand both technical performance and supply chain clarity. Direct engagement, process investment, and open exchange of knowledge define our approach; these translate to real-world advantages for every customer and every application, today and in the next wave of chemical innovation.