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4-Fluorocinnamaldehyde

    • Product Name 4-Fluorocinnamaldehyde
    • Alias 4-Fluorocinnamal
    • Einecs 741-418-6
    • 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

    776085

    Product Name 4-Fluorocinnamaldehyde
    Cas Number 403-21-0
    Molecular Formula C9H7FO
    Molecular Weight 150.15
    Appearance Pale yellow liquid
    Boiling Point 244-245°C
    Melting Point N/A
    Density 1.153 g/cm³
    Refractive Index 1.586
    Purity Typically ≥98%
    Solubility Soluble in organic solvents
    Smiles C1=CC(=CC=C1C=O)F

    As an accredited 4-Fluorocinnamaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, screw cap, 25g label: "4-Fluorocinnamaldehyde, CAS 1012255-76-9, for research use only, handle with care."
    Shipping 4-Fluorocinnamaldehyde is shipped in tightly sealed containers to prevent moisture and contamination. It should be packaged according to standard regulations for hazardous chemicals, labeled clearly with appropriate hazard information. During transport, it must be stored in a cool, dry place, away from incompatible substances, and handled by trained personnel.
    Storage 4-Fluorocinnamaldehyde should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store it in a cool, dry, and well-ventilated area, preferably under inert atmosphere (nitrogen or argon) to prevent oxidation. Keep away from incompatible materials such as strong oxidizing agents and acids. Properly label the container and follow all relevant safety and regulatory guidelines.
    Application of 4-Fluorocinnamaldehyde

    Applications of 4-Fluorocinnamaldehyde in Industrial Manufacturing

    4-Fluorocinnamaldehyde supports multiple key industrial sectors through its specialized chemistry and functional reactivity. Based on our manufacturing experience and customer collaboration, we detail integral downstream uses across the fine chemicals, pharmaceuticals, and material sciences industries.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Many pharmaceutical companies source 4-Fluorocinnamaldehyde as a core building block for synthesizing targeted therapeutic molecules, including selective enzyme modulators, potential anti-inflammatory agents, and antivirals. The compound’s predictable reactivity allows chemists to incorporate a fluorinated aromatic aldehyde into stepwise condensation, reductive amination, or cyclization routes. Process chemists monitor and control usage with validated quality control protocols to ensure regulatory compliance during API development.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU & US Pharmacopoeia references for chemical purity
    • FDA 21 CFR Part 210/211 for drug substance control
    • REACH registration for commercial scale import and use

    Typical usage ratio

    • 10–35 mol% in multi-step synthesis; adjusted per desired API framework and stoichiometry

    Downstream process integration

    • Charged in the initial condensation or alkylation stage with amines or active methylene compounds
    • Used in Grignard, Wittig, or reduction protocols downstream
    • Purified via crystallization or chromatographic separation before further synthetic transformations

    Final product types

    • Small molecule APIs containing fluorinated aromatic rings
    • Pharmaceutical intermediates for heterocyclic system construction
    • Reference standards for analytical methods

    2. Agrochemical Intermediate for Synthesis of Novel Herbicides

    Agrochemical manufacturers utilize 4-Fluorocinnamaldehyde as a reactive precursor in development of innovative pre- and post-emergence herbicides. Specific aldol or Michael addition reactions allow formulation of target-selective compounds with optimized field activity. Consistent quality, traceability, and batch homogeneity are continuously monitored to meet regulatory data requirements before field testing or final registration.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • ISO 9001:2015 certified process traceability
    • REACH compliance for environmental safety data
    • OECD guidelines for chemical safety assessment

    Typical usage ratio

    • 5–25 mol% per synthetic batch; depends on the structure–activity relationship study outcomes

    Downstream process integration

    • Condensed with substituted amines, phosphonate esters, or heterocyclic scaffolds
    • Submitted to hydrogenation, oxidation, or halogenation to generate final herbicide structures
    • Batch purity assessed using HPLC and GC methods

    Final product types

    • Novel fluorinated acyl-herbicides for post-emergent use
    • Intermediate actives for combinatorial screening
    • Field-ready technical concentrates

    3. Fragrance Ingredient for Fine Aroma Chemicals

    For specialty fragrance houses, 4-Fluorocinnamaldehyde supports the creation of niche aldehydic and spicy notes in perfumery and personal care. Skilled aroma chemists exploit its unique electrophilicity to modulate fragrance accords or mask undesirable base notes. Manufacturing attention focuses on minimizing trace contaminants, stabilizing the aldehyde functionality, and efficient blending under IFRA guidelines to safeguard performance and consumer safety.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards & Amendments
    • EU Cosmetics Regulation (EC) No. 1223/2009
    • Cosmetic Ingredient Review (CIR) Panel recommendations
    • ISO 9235 definition for natural and synthetic aroma chemicals

    Typical usage ratio

    • 0.05–0.5% in fragrance concentrate; adjusted per desired olfactory strength, IFRA maximum levels, and stability in formulation

    Downstream process integration

    • Blended into oil phase during fragrance compounding
    • Added at controlled temperatures to avoid oxidation or discoloration
    • Co-formulated with fixatives or other aldehydes for complex bases

    Final product types

    • Fine fragrance concentrates for niche perfumes
    • Functional fragrance for soap, detergent, and home care applications
    • Personal care bases such as handwash and body lotions

    4. Electronic and Advanced Material Synthesis

    Producers of advanced electronic materials and functional polymers select 4-Fluorocinnamaldehyde for introducing fluorine content and rigid aromatic units within specialty resins, liquid crystals, and optoelectronic compounds. Its well-defined purity enables reliable reaction scaling, and analytical documentation supports quality-critical semiconductor and display industry requirements. Trace metal content and moisture are tightly controlled to prevent downstream defects or electrical interference.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic applications
    • ISO 9001:2015 for quality control in specialty chemical synthesis
    • SEMATECH and JEITA guidance for material trace impurities
    • REACH compliance for all exported electronic-grade intermediates

    Typical usage ratio

    • 1–8 wt% in polymer precursor resins; altered depending on resin architecture, degree of fluorination desired, and end-use application stress testing

    Downstream process integration

    • Introduced during step-growth polymerization or as an end-group in thermostable resins
    • Utilized in synthesis of fluorinated side-chain liquid crystal monomers
    • Purified via vacuum distillation to semiconductor-grade standards

    Final product types

    • High-performance polymer resins for electronics
    • Fluorine-modified liquid crystals for display panels
    • Optoelectronic intermediate building blocks

    5. Fine Chemical Manufacture for Specialty Dyes and Optical Brighteners

    Producers in the textile and specialty dye sector employ 4-Fluorocinnamaldehyde to synthesize advanced fluorescent and chromophore systems. Its electron-withdrawing fluorine helps tailor emission wavelength and enhance dye stability. Manufacturing protocols include staged condensation, purification by column chromatography, and precise stoichiometric balancing to achieve correct chromophore geometry and maximize finished product yield. All operations are certified for chemical handling and environmental traceability.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for non-toxic dye ingredients
    • ISO 14001 environmental management for dye production
    • Registration under REACH Annex VII–IX for specialty chemicals
    • Compliance with ZDHC guidelines for input chemical verification

    Typical usage ratio

    • 5–18 mol% relative to parent aromatic amines or phenols in dye synthesis; varied for desired lightfastness or molecular fluorescence efficiency

    Downstream process integration

    • Combined via Knoevenagel or Wittig-type condensations to extend conjugation
    • Refined in small-batch reactors with process analytics for purity and hue
    • Submitted to subsequent sulfonation or alkoxylation as required by final application

    Final product types

    • Optical brighteners for textile finishing
    • Specialty fluorescent dyes for security inks and fiber labels
    • Organic pigments with enhanced photostability
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    Certification & Compliance
    More Introduction

    4-Fluorocinnamaldehyde: Experience from the Manufacturer’s Bench

    Real-World Choices: Why Chemists Turn to 4-Fluorocinnamaldehyde

    Some chemicals make their mark not by buzzwords, but because chemists reach for them repeatedly in the lab toolbox. 4-Fluorocinnamaldehyde is one such product. We have spent years on its production line, seeing its full journey from raw material to the finished, fine crystalline solid. Our everyday routines involve weighing it for precise batches, controlling storage temperatures, and verifying each lot by GC and NMR. Its distinctive pale yellow hue always seems to signal a quality difference compared to standard cinnamaldehydes—something that matters in practice, not just on paper.

    Clients usually come to us with specific needs—sometimes it’s aromatic aldehydes for pharmaceutical projects, sometimes it’s for specialty flavor compounds in fragrance R&D. 4-Fluorocinnamaldehyde stands apart within the cinnamaldehyde family due to its para-fluoro group on the aromatic ring. This substitution gives it electronic properties that differ significantly from plain cinnamaldehyde, altering both reactivity and sensory profile. In our experience, this single change often transforms reaction pathways or results in a sharper, more persistent note in formulated scents.

    This unique position means a batch of 4-Fluorocinnamaldehyde can shape the route of a multi-step synthesis or the character of a flavor component in commercial and academic laboratories. We see a strong pull for this compound in fine chemical production and early-stage drug discovery. Innovation relies on starting materials like this, which enable new reactivity. From the manufacturer's view, it's not just a line item—it's a crucial reagent that pushes forward more complex science.

    Quality Starts with the Process

    Every batch of 4-Fluorocinnamaldehyde gets more than a nod from our quality team. Incoming 4-fluorobenzaldehyde and acetic anhydride pass through preparative steps using conditions proven to avoid unwanted side products. Our reactors maintain close temperature control around 80°C, and a slow feed protocol prevents uncontrolled exotherms. Workers regularly check for color and clarity at each stage. Too dark, and we know a by-product snuck through; too pale signals incomplete reaction. TLC and in-process NMR allow us to stay ahead of the curve, so only what meets spec advances.

    Every operator recognizes the faint, sweet-spicy aroma—subtler than 4-chlorocinnamaldehyde, brighter than the parent cinnamaldehyde. That scent quickly signals to even junior lab staff that the reaction has reached its endpoint. After crystallization, we confirm purity using HPLC, and for orders requiring it, we share spectral data in detail. Our experience shows that reliable quality isn’t just about analytical numbers—machines can verify content, but a trained eye notes every nuance, catching oddities before they reach the client.

    Performance in Synthesis: Why the Fluoro Group Matters

    Our customers often ask what makes 4-fluorocinnamaldehyde more than a variation on an old classic. Years working with it highlight the effect fluorine brings—a strong inductive withdrawing group at the para position. This influences both the stability and reactivity of the molecule. Electrophilic addition reactions show notable selectivity shifts using this compound. For example, in reductive amination or cross-coupling, the para-fluorine can open up new routes entirely or change yields. Compared to 4-chlorocinnamaldehyde, the fluorinated analog brings different leaving group properties and lower steric hindrance.

    We've also noticed shifts in physical properties. 4-Fluorocinnamaldehyde runs as a slightly higher melting solid than its parent compound, which affects process storage and shipping needs. Its lower tendency to polymerize in ambient air during storage means less product loss—critical if you're handling scale beyond bench level. Customers in pharmaceutical intermediates value its more predictable shelf-life, sparing cost and rework.

    Flavor and Fragrance: What Our Partners Report

    Our fragrance and flavor partners repeatedly tell us they choose 4-fluorocinnamaldehyde for its crisp, spicy-citrus character, something you cannot easily achieve with classic cinnamic aldehydes. Sensory evaluation panels consistently describe the aroma as sharper and more persistent in finished blends, despite low use levels. That small para-fluoro change tunes volatility and perceived top note, something that matters for fine perfumery and for stable flavors in beverages and confections.

    We work with R&D groups who have tried to mimic these properties with alternative aldehydes or with higher loadings of standard cinnamaldehyde, but the results lack persistence and the balance between sharp and smooth. For instance, product formulators trying to design long-lasting cleaning products often switch to 4-fluorocinnamaldehyde after noticing their initial scents fade. Our on-site chemical engineers noticed similar effects during our own odor retention tests in polymer matrices. It takes just a little of this compound to maintain character over time.

    Working with Regulations and Logistics

    Our experience has taught us that no batch gets out the door until regulatory demands are fully met. 4-Fluorocinnamaldehyde doesn’t face as stringent oversight as some aromatics or controlled substances, but international shipping still brings paperwork and port inspections. We handle repeat audits for Asia-Pacific, North American, and European clients—every certificate request gets matched by documentation kept in our records system.

    Product labeling and MSDS preparation stay updated to reflect best practices, as global supply chains demand transparency. Sometimes, clients find themselves double-checking for halogen content or asking for clarifications on storage safety. Feedback from their sustainability teams points to the advantage of low-volume transport for this compound—its efficiency reduces the carbon footprint compared to less potent aromatic aldehydes.

    Scaling Up: Troubles and Solutions from the Floor

    The journey from bench to kilo-scale rarely goes as smoothly as process flow diagrams suggest. 4-Fluorocinnamaldehyde presented its own set of headaches at first—reactor fouling during condensation meant we needed better agitation and solvent controls. Solvent choice matters: anhydrous toluene gave far more reproducible yields than acetic acid alone. On one trial, we watched a full batch solidify mid-transfer; after that, heat tracing on all transfer lines has been required for each run.

    End-users rarely see the hours our teams spend preventing cross-contamination in shared vessels. Even minor carryover from other aldehydes ruins analytical purity, which matters most to researchers needing unambiguous downstream data. Routine solvent flushes, careful use of disposable filters, and regular operator training sessions ensure product integrity. Our troubleshooting notes fill a binder that has grown bulky, reminding us that every detail in production safeguards the end-use application.

    Purity and Analytical Control: What We’ve Learned the Hard Way

    4-Fluorocinnamaldehyde doesn’t forgive lapses in process detail. At scale, we’ve learned trace over-oxidation can form corresponding acids, which causes issues for both synthesis and scented applications—acidity disrupts some perfume formulations or causes discoloration in flavor syrups. Rigorous gas chromatography and running acid number titrations catch these problems before bulk packaging.

    Analytical monitoring goes well beyond minimum spec. We test for trace halogen impurities, unreacted starting materials, and even rare solvent residues that occasionally creep in during hot summer months. Having to recall a lot—or worse, hearing a client caught an impurity we missed—costs more than money. Our staff feel personal embarrassment if we don’t uphold reputation built through decades of chemical reliability. Customer trust makes all the late nights and double-checks worth it.

    What Sets 4-Fluorocinnamaldehyde Apart from Other Choices

    Over the years, new aromatic aldehyde analogs have come and gone. Some touted higher reactivity, some promised cost savings. Our view: 4-fluorocinnamaldehyde stands above due to its consistent, well-documented effects in both chemical synthesis and flavor performance. Chemically, para-fluorination changes the electron density profile, favoring different types of additions and couplings; experienced synthesis chemists confirm faster steps or better selectivity in their project reports to us.

    For scent or flavor work, the functional group engineering behind 4-fluorocinnamaldehyde’s structure means the aroma profile can be targeted more precisely, and the flavor notes stay brighter and longer-lasting, especially compared to 4-chlorinated or unsubstituted cinnamaldehydes. The compound’s lower volatility ensures less product evaporates in open-vat applications—something our perfumery clients appreciate, since they can reduce refill rates and avoid off-notes after prolonged usage.

    Manufacturing improvements have brought more predictable parameters than many competitive aromatic aldehydes. Where some batches of other cinnamaldehydes show wild swings in melt point or color, 4-fluorocinnamaldehyde’s outcomes remain tight. This makes it easier to meet customer recipes for downstream reactions or final goods without major reformulation. Feedback from long-term contract buyers points to this reliability as their reason for returning.

    Safe Handling Insights Gained in Daily Work

    Laboratory work with aromatic aldehydes tends to stick with you—literally and figuratively. We’ve learned to prevent eye and skin contact, despite the relatively moderate hazard profile of 4-fluorocinnamaldehyde. The characteristic spicy odor acts as an early alert if any leaks develop. Operators routinely wear nitrile gloves and use well-ventilated benches. Teaching new staff proper pipetting and weighing protocols, as well as immediate cleanup, prevents unnecessary exposure.

    Bulk storage at our facility involves stainless steel drums with nitrogen headspace to avoid oxidation and moisture uptake, which can degrade the product’s sensory notes or cause discoloration. Training focuses on transfer line integrity and prompt cleanout, since residue left behind in storage containers often causes off-odors or purity drift after a few weeks. The same level of care translates to client blending rooms, where measured, single-use sampling reduces the odds of cross-contamination.

    Frequently Asked Questions from Fellow Chemists

    We hear a broad range of questions from both industrial chemists and graduate students. Some ask about solvent compatibility in cross-couplings; others want real-world comparisons to 4-chloro or 4-methyl variants. Through working with hundreds of projects, we have seen that 4-fluorocinnamaldehyde dissolves well in typical polar organic solvents—acetonitrile, THF, DCM—and offers better shelf-life under dry conditions. Customers working in high-throughput screens value its rapid reaction rates and the stability of resulting products.

    There have also been questions on flavor compatibility with specific ingredients. Beverage clients often explore compatibility with citrus or menthol, finding that the brightness of 4-fluorocinnamaldehyde adds lift without masking delicate volatiles. We advise against use in highly acidic formulations for maximum shelf stability, as occasional aldol condensation products may cloud the blend.

    Continuous Improvement Driven by Practical Feedback

    From our own plant to end-user labs, feedback shapes how we manufacture and support 4-fluorocinnamaldehyde. One particularly useful critique pointed out risks of fine particulate formation during cold-weather shipments; we responded by adjusting storage protocols and recommending early warming for lots received below 10°C. Another application called for custom particle sizing, which led us to overhaul our sieving and packaging lines. Each improvement, whether prompted by staff observations or client input, gets baked into the next batch, creating a product that is shaped by the hands and eyes of real chemists.

    Even after years of routine manufacturing, small tweaks in filtration, drying, or even packaging materials can create downstream improvements. We find this ongoing innovation matters most to clients pushing boundaries in novel drug intermediates or eco-friendly fragrances, where consistency and predictability save them time and money. That’s the side of chemical manufacturing that rarely makes press releases but matters to every formulator and bench scientist using our product.

    The Next Step for 4-Fluorocinnamaldehyde in Chemical Manufacturing

    As trends in synthetic chemistry and consumer markets shift, so does demand for reliable specialty aldehydes. We have seen growth in orders from fine chemical makers working on heterocycle development or green chemistry catalysts, where the precise behavior of the para-fluoro variant opens doors to milder reaction conditions and previously inaccessible scaffolds. Universities and smaller research firms often reach out for samples to run exploratory screens, test new condensation strategies, or probe reactivity series. Production scale-ups routinely rely on our technical support, leveraging our hard-won operational experience.

    From our side, we don’t view 4-fluorocinnamaldehyde as just another generic chemical. Every container that leaves our facility represents years of process optimization, hands-on adjustments, and continuous dialogue with end-users. Decades in the business have shaped our standards for quality, consistency, and reliability, and 4-fluorocinnamaldehyde continues to earn its place on every serious chemist’s supply list.